CA2085587A1 - Method of recording plural holographic images into a holographic recording material by temporal interleaving - Google Patents
Method of recording plural holographic images into a holographic recording material by temporal interleavingInfo
- Publication number
- CA2085587A1 CA2085587A1 CA 2085587 CA2085587A CA2085587A1 CA 2085587 A1 CA2085587 A1 CA 2085587A1 CA 2085587 CA2085587 CA 2085587 CA 2085587 A CA2085587 A CA 2085587A CA 2085587 A1 CA2085587 A1 CA 2085587A1
- Authority
- CA
- Canada
- Prior art keywords
- predetermined
- recording material
- holographic
- images
- holographic recording
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
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- 230000002123 temporal effect Effects 0.000 title abstract description 14
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- 229920002678 cellulose Polymers 0.000 claims description 9
- 229910052731 fluorine Inorganic materials 0.000 claims description 9
- 239000011737 fluorine Substances 0.000 claims description 9
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 9
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 9
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 9
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 9
- 239000011118 polyvinyl acetate Substances 0.000 claims description 9
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 9
- 239000000203 mixture Substances 0.000 description 18
- -1 silver halide Chemical class 0.000 description 17
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- 238000002474 experimental method Methods 0.000 description 5
- 125000001072 heteroaryl group Chemical group 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 230000004044 response Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 230000009471 action Effects 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 230000001427 coherent effect Effects 0.000 description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 4
- 238000001093 holography Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- 230000036962 time dependent Effects 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000007687 exposure technique Methods 0.000 description 3
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- QXVYTPLRWBDUNZ-UHFFFAOYSA-N 1-imidazol-1-ylimidazole Chemical compound C1=NC=CN1N1C=NC=C1 QXVYTPLRWBDUNZ-UHFFFAOYSA-N 0.000 description 2
- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- VIZORQUEIQEFRT-UHFFFAOYSA-N Diethyl adipate Chemical compound CCOC(=O)CCCCC(=O)OCC VIZORQUEIQEFRT-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- GTVWRXDRKAHEAD-UHFFFAOYSA-N Tris(2-ethylhexyl) phosphate Chemical compound CCCCC(CC)COP(=O)(OCC(CC)CCCC)OCC(CC)CCCC GTVWRXDRKAHEAD-UHFFFAOYSA-N 0.000 description 2
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
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- 239000000539 dimer Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000852 hydrogen donor Substances 0.000 description 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
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- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 2
- 238000005457 optimization Methods 0.000 description 2
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- CNLVUQQHXLTOTC-UHFFFAOYSA-N (2,4,6-tribromophenyl) prop-2-enoate Chemical compound BrC1=CC(Br)=C(OC(=O)C=C)C(Br)=C1 CNLVUQQHXLTOTC-UHFFFAOYSA-N 0.000 description 1
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- IGHDIBHFCIOXGK-UHFFFAOYSA-N (4-chlorophenyl) prop-2-enoate Chemical compound ClC1=CC=C(OC(=O)C=C)C=C1 IGHDIBHFCIOXGK-UHFFFAOYSA-N 0.000 description 1
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- CXKZIYUKNUMIBO-UHFFFAOYSA-N 1-phenylethyl prop-2-enoate Chemical compound C=CC(=O)OC(C)C1=CC=CC=C1 CXKZIYUKNUMIBO-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- HGWZSJBCZYDDHY-UHFFFAOYSA-N 1-prop-2-enoyloxydecyl prop-2-enoate Chemical compound CCCCCCCCCC(OC(=O)C=C)OC(=O)C=C HGWZSJBCZYDDHY-UHFFFAOYSA-N 0.000 description 1
- GMIUUCWUOPOETN-UHFFFAOYSA-N 2,4,5-triphenyl-1-(2,4,5-triphenylimidazol-2-yl)imidazole Chemical compound C1=CC=CC=C1C1=NC(N2C(=C(N=C2C=2C=CC=CC=2)C=2C=CC=CC=2)C=2C=CC=CC=2)(C=2C=CC=CC=2)N=C1C1=CC=CC=C1 GMIUUCWUOPOETN-UHFFFAOYSA-N 0.000 description 1
- FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- YJGHMLJGPSVSLF-UHFFFAOYSA-N 2-[2-(2-octanoyloxyethoxy)ethoxy]ethyl octanoate Chemical compound CCCCCCCC(=O)OCCOCCOCCOC(=O)CCCCCCC YJGHMLJGPSVSLF-UHFFFAOYSA-N 0.000 description 1
- SSKNCQWPZQCABD-UHFFFAOYSA-N 2-[2-[2-(2-heptanoyloxyethoxy)ethoxy]ethoxy]ethyl heptanoate Chemical compound CCCCCCC(=O)OCCOCCOCCOCCOC(=O)CCCCCC SSKNCQWPZQCABD-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- FLFWJIBUZQARMD-UHFFFAOYSA-N 2-mercapto-1,3-benzoxazole Chemical compound C1=CC=C2OC(S)=NC2=C1 FLFWJIBUZQARMD-UHFFFAOYSA-N 0.000 description 1
- OEXUTOBUVQBHCH-UHFFFAOYSA-N 2-naphthalen-2-yloxyethyl prop-2-enoate Chemical compound C1=CC=CC2=CC(OCCOC(=O)C=C)=CC=C21 OEXUTOBUVQBHCH-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- AGWWTUWTOBEQFE-UHFFFAOYSA-N 4-methyl-1h-1,2,4-triazole-5-thione Chemical compound CN1C=NN=C1S AGWWTUWTOBEQFE-UHFFFAOYSA-N 0.000 description 1
- GBJVVSCPOBPEIT-UHFFFAOYSA-N AZT-1152 Chemical compound N=1C=NC2=CC(OCCCN(CC)CCOP(O)(O)=O)=CC=C2C=1NC(=NN1)C=C1CC(=O)NC1=CC=CC(F)=C1 GBJVVSCPOBPEIT-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 241000034673 Holographis Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 101100004031 Mus musculus Aven gene Proteins 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229940123973 Oxygen scavenger Drugs 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229940106691 bisphenol a Drugs 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
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- KOWWOODYPWDWOJ-LVBPXUMQSA-N elatine Chemical compound C([C@]12CN(C3[C@@]45OCO[C@]44[C@H]6[C@@H](OC)[C@@H]([C@H](C4)OC)C[C@H]6[C@@]3([C@@H]1[C@@H]5OC)[C@@H](OC)CC2)CC)OC(=O)C1=CC=CC=C1N1C(=O)CC(C)C1=O KOWWOODYPWDWOJ-LVBPXUMQSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005329 float glass Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229940091853 isobornyl acrylate Drugs 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229940075065 polyvinyl acetate Drugs 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000007342 radical addition reaction Methods 0.000 description 1
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- 229920001897 terpolymer Polymers 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/26—Processes or apparatus specially adapted to produce multiple sub- holograms or to obtain images from them, e.g. multicolour technique
- G03H1/2645—Multiplexing processes, e.g. aperture, shift, or wavefront multiplexing
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/26—Processes or apparatus specially adapted to produce multiple sub- holograms or to obtain images from them, e.g. multicolour technique
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/26—Processes or apparatus specially adapted to produce multiple sub- holograms or to obtain images from them, e.g. multicolour technique
- G03H1/2645—Multiplexing processes, e.g. aperture, shift, or wavefront multiplexing
- G03H1/265—Angle multiplexing; Multichannel holograms
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/02—Details of features involved during the holographic process; Replication of holograms without interference recording
- G03H2001/026—Recording materials or recording processes
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H1/00—Holographic processes or apparatus using light, infrared or ultraviolet waves for obtaining holograms or for obtaining an image from them; Details peculiar thereto
- G03H1/26—Processes or apparatus specially adapted to produce multiple sub- holograms or to obtain images from them, e.g. multicolour technique
- G03H1/2645—Multiplexing processes, e.g. aperture, shift, or wavefront multiplexing
- G03H2001/2655—Time multiplexing, i.e. consecutive records wherein the period between records is pertinent per se
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03H—HOLOGRAPHIC PROCESSES OR APPARATUS
- G03H2260/00—Recording materials or recording processes
- G03H2260/12—Photopolymer
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Holo Graphy (AREA)
Abstract
Holographic images (I1 to In) are constructed in a recording material (H) in accordance with a temporal interleaving technique in which a first set of images (I1 to In) is constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the images. Thereafter, in accordance with a subsequent predetermined sequence, a subsequent set of images (I1 to In) is constructed into the same predetermined location. The image sets (I1 to In) have at least one member in common. In one aspect all of the images (I1 to In) are constructed into the same predetermined defined region (R) of the holographic recording material (H) (an angle hologram). In another aspect the predetermined defined region (R) into which each of the images is constructed is separate from all other regions (R) of the holographic recording material (H) (a spatial hologram).
Description
wo 92/~)n555 PCI'/US91/04623 ~'~r I
IIIL~
~ U 1~ 7~
~ b~n~ This invention relates generally to a method of recording holographic images and, in particular, to a method for recording a plural number of such holo~raphic images into a recording material.
~ Ib~ Optical holography, often called "wavefront reconstructionn, may be described as the recording of a holographic image within a holographic recording material. Conventional holographic r~cording materials include 20 silver halide emulsiorls, dichromated ~elatin, thermoplastic media and time-dependent diffusion media.
A standard technique of producing a holographic image is by the interference of two coherant bearns of light, respectively 25 termed an "object beam" and a l'reference beam~. Both beams are generated from the same coherent source (typically a laser) to insure sufficient mutual coherence to form a stable interference pattern. To produce the holographic image the object beam is typically spatially modulated, e. g., it is reflected from a three-30 dimensional object. The reference beam is typically a non-spatially modulated coherent beam. The object b~arn and the reference beam are br4ught together (that is, spatially overlapped) at a predetermined position within a holographic recording material. It is the coherent addition of the wavefronts 35 of the obJect beam and the reference beam within the material WO 9~/005~ , PCI'/US91/04623 that constructs a holographic image within the recording material. In a similar manner holographic images may be created with multiple reference and object beams. The holographic image so constructed may also be referred to as the interference 5 pattern, the holographic grating, the hologram, or simply, the image.
The term "multiplexed" holographic image refers to the construction of more than one holographic image within a 10 holographic recording material. A variety of wavefront reconstruction options is permitted using multiplexed holographic images. Multiplexed holographic images in some cases make efficient use of the available area or volume of the recording medium. The holographic images produced by 15 combinations of several reference and object beams may be constructed in the same physical region in the recording material.
Alternatively, each of the holographic images may be constructed in a respective region of the recording material (spatial multiplsxing) . .
Convention~l methods used to multiplex a plural number N of holographic ima~es into the same volume of the holographic recording material use two basic approaches: a simultaneous exposure technique or a sequential exposure technique. These two 25 approaches are discussed in La Macchia and Vincelette, "Comparison of the Diffraction Efficiency of Multiple Exposure and Single Exposure Holograms", Applied Optics, Vol. 7, No. 9, pp.
1857-1858, Septembar 1968) and in R. J. Collier et al., "Optical Holography", Academic press, Inc., 1971 and H. J. Caulfield, Ed., 30 "Handbook of Optical Holography1', Academic Press, Ino., 1979.
These methods are particularly important for volume holography, where multiplexing N holograms at different angles (angle multiplexing) in the holographic recording material optimizes information recording density.
WO 92t0055~ PCl-tUS91/04623 2~ r:-,3';~
Simultaneous exposure requires that the optical bearns constructing all N h~lographic images be generated simultaneously, so that only a single exposure of the holographic recording material is made. Perceived disadvantages of this 5 approach include the difficulty in simultaneously generating beams for the N holographic images when N is large, and the problem of crosstaik between reference beams and object beams when constructing the N holograms.
Holographic exposure of conventional holographic recording materials, such as silver halide emulsions, dichromated gela~in, and thermoplastic media, involves recording a latent holographic image in the material. The final holographic image is obtained by a developing and fixing process. In the course of making 15 multiplexed holographic images by sequential exposure, for example, the recording material may be left in the dark between exposures for extended periods of time while the recording apparatus is being modified. Subsequent exposures will simply add to the latent image that already exists.
Photopolymeric holographic recording materials are now known. Copending application Serial Number 07/144,281, copending application Serial Number 07/144,355, and copending application Serial Number 07!144,840, all filed January 15,1988 25 and all assigned to the assignee of the present invention disclose and claim holographic recording materials. Holographic images are recorded in a photopoiymer recording medium as a resul$ of diffusion of unexposed monomer towards areas exposed with the highest intensity cf incident light, creating a density gradient in 3 0 the material which corresponcls to the optical intensity gradient in the holographic image. After polymerization the higher density areas have a larger index of refraction than the lower density areas, thus forming a dielectric (phase) grating.
WO 92/005~;5 z~r ~ 7 PCI`/US91/04623 Identical serially recorded exposures, using typical exposure energies (ten milliJoules per square centimeter) recorded on the order of several seconds apart, are not recorded with equal strength in the material. This is due to the dynamics 5 of the diffusion mechanism. Furthermore, monorner does not flow as readily to the second exposure as it does to the first, and not as much flows per unit of inoident optical radiation.
When using a photopolymeric holographic recording material 10 based on a time-dependent diffusion mechanism the material should not, in general, be left in the dark for extended periods of time (several seconds or minutes) between sequential exposures if one expects to achieve performance comparable to oonventional holographic materials. Since in the holographic materials the 15 latent image mechanism is replaced by a process involving the dynamic diffusion of molecules in the material the possibility of reciprocity failure exists. Reciprocity failure is due to the fact that the index of refraction change is not only a funçtion of the irradiance-exposure time product, but also is dependent on the 20 magnitude of the irradiance on the exposure time. In addition, the available modulation ran~e (i.e., the possible index of refraction change) of the photopolymerizable holographic material varies with time b~cause the diffusion mechanism and polymerization continues in the dark.
Conventional sequential multiple-exposure angle multiplexing has been demonstrated in current photopolymer formulations. HQwever the resulting diffraction efficiencies are lower than predicted for this type of exposure, possibly due to 3 0 the diffusion mechanism and its reversibility properties.
In view of the foregoing it is believed advantageous to provide a sequential exposure technique for multiplexi~ng N
holograms into a photopolymerizable holographic material which WO 92/00555 PCI`/US91/04623 s can overcome or minimize the dynamic effects of the time-dependent diffusion in the material.
-o -O-o-Conventional apparatus for forming sequential multiplexed holograms typically include a manual or automated (e.g., galvanometer controlled) mirror whereby the location and/or angie of incidence of at ieast either the object beam or the 10 reference beam on the holographic recording ma~erial may be controlled. However, the degree of control over incident beam location and/or angl~ of incidence required in the formation of sequential multiplexed holograms is not a significant factor. So long as the mirror control system is able to place the incident 15 beam within the region of the recording material dedicated to a given holographic image, the control system is sufficient for the purpose of forming sequential multiplexed holograrns. Sirnilarly, the beam positioning requirements placed on conventional apparatus for reading a sequen~ial multiplexed holo~ram are not 20 unduly stringent. So long as tho rcading beam is placed within the range of Bragg angle appropriate for the thickness of the holographic material, the angle between the object and reference beam and the wavelength of the light being used, the signal-to-noise ratio of the hologram is acceptable.
~5 For reasons that become apparent hereinafter it is believed advantageous to provide an apparatus for forming holograms in which the position of either an object or a reference beam may be repeatably and precisely controlled.
~E~
The present invention relates to a method of recording a predetermined number of holographic images into a holographic 35 recording material. The method of the present invention may be w09~00555 ~ 3~~3'7 PCI/U591/046Z3 used both for an~ularly multiplexed and for spatially multiplexed holograrns.
In accordance with the present invention each one of a set 5 of N holographic images is constructed into a predetermined defined region of the recording material in accordance with a first predetermined sequence. Each holographic image is constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the 10 ima~es. Thereafter, in accordance with a subsequent predetermined sequence, each one of a predetermined number of the set of N holographic images is constructed into the same predetermined region. Each holographic image is constructed into the predetermined defined region of the holo~raphic recording 15 material for a predetermined corresponding second imaging tirne.
A predetermined second time gap is defined between each of the images in the second sequence. Preferably, but not necessarily, th~ holographic images constructed during the second sequence includes all of the images constructed in the first sequence.
In accordance with one aspect of the invention all of the images are constructed into the same predetermined defined region of the holographic rscording rnaterial (an angle hologram).
In another aspect of the present invention the predetermined 25 defined region into which each of the N images is constructed is separate from all other regions of the holographic recording material (a spatial hologram). Altarnatively, in accordance with another aspect of the invention some of the N images may be constructed in the same region of the holographic recording 30 material and each one of the others of the N images may be constructed into spatially separate regions of the holographic recording material.
The predetermined first and secsnd imaging times are 35 preferably, but need not be, equal. The predetermined first and WO 92/005~5 PCI`/US91/04623 secand sequences are preferably, but need not be, the same. To remain within the contemplation of the invention the first and the subsequent sequences should each contain at least one common member. The predetermined first and second time gaps 5 are preferably, but need not be, equal.
In the preferred instance the holographic recording material is a photopolymerizable recording material comprising (a) a polymeric binder selected from the group consisting of cellulose 10 esters, polystyrene, stryene copolymers containing at least 60%
by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl aoetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine; (b) a iiquid 15 ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (o) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
The holographic images are recorded by construc~ing hotographic imag~s sequentially with short exposure times so that rapid in~erleaving of multiple holograms occurs. By exposing the photopolymer material in a time-multiplexed manner the recording material "sees" all of the holographic images and, due to the rapid temporal interleaving, responds to each equally with the diffusion process. By temporally interleaving the holographic images at a rate much faster than the diffusion mechanism of the photopolymer, the present invention circumvents, or at least minimizes, the problems associated with monomer flow in response to subsequent exposures and the reduction in monomer flow per unit of incident optical radiation.
-o-O-o-WO 92/00555 PCI/I)S91/04623 ~J ~ ~ r ~
In another aspect, the present invention relates to an apparatus for recording plural holographic images using the temporal interleaving method summarized above. The holographic recording apparatus in accordance with the present invention 5 includes a control arrangement whereby the angle of incid~nce of either an object beam or a reference beam on the holo~raphic recording material may be repeatably and precisely controlled.
The recording apparatus comprises means for forming an object beam and a refersnce beam and a ~alvanometer controlled mirror 10 the position of which controls the angle of incidence of at least one of the object beam and a reference bearn onto the holographic recor~ing material. A laser source and associated detector are respectively located to direct a laser beam toward the mirror and to intersect the reflection of the beam therefrom. The detector 15 is responsive to the reflected beam incident thereon to generate first and second electric currents the magnitude of aach of which is functionally related to the position on the detector at which the reflected laser beam is incident and to the power output of the laser source.
~0 The holographic recording apparatus further includes a control system for generating a galvanometer position signal to control the position of the galvanometer driven mirror ~and thereby the angle of incidence of a beam onto the holographic 2 5 recording material). The control system itself comprises means responsive to the first and the second currents for forming the ratio of the sum and difference thereof thereby to form an actual mirror position signal that is independent of the power output of the laser souroe, and an integrator responsive to the error 3 0 between the signal representative of the actual mirror position and a reference signal representative of a predetermined position of the mirror for forming the galvanometer position signal at the output thereof.
.
2~ 7 The invention will be more fully understood from the foilowing detailed description thereof, taken in connection with the accompanying drawings which form a part of this application 5 and in which:
Figures 1, 2, and 3 are highly stylized pictorial representations of various arrangements of rnultiplexed plural holographic images recorded in a predeterminled defined regions 10 of a holographic recording material by temporal interleaving in accordance with the method of the present invention;
Figures lA, 2A, and 3A are side sectional views of the holographic recording media of Figures 1, 2 and 3 taken along the 15 respective section lines therein;
Figure 4 is a schematic iilustration of an apparatus in accordance with another aspect of the present invention useful for recording multiplexed plural holographic images in 20 predetermined defined region(s) of a holographic recording material by ternporal interleaving;
Figures 5A and ~B ar~ a schematic diagram of a ratioing network and of a serYo feedback control network for a 25 galvanometer control system in accordance with the apparatus of the present invention and which are used in an apparatus for implementing the method of the present invention;
Figure 6 is a timing diagram illustration the relationship 30 between a galvanometer reference signal and a shutter timing signal used in the network of Figure 5; and Figure 7 is a schematic illustration of the holo~raphic recording material as mountsd for use in the Example.
3~ :
:
, WO 92/00555 PC~/US91/04623 5~ ~
Throughout the following detailed description sirnilar reference numerals refer to similar elements in all figures of the 5 drawings.
Referring to Figures 1, 2, and 3 shown are highly stylized pictorial representations of various arrangements of multiplexed plural holographic images I recorded in predetermined defined 10 region(s) R of a holographic recording material ~enerally indicated by the reference character H using the temporal interleaving method in accordance with the present invention, while Figures 1A, 2A, and 3A are side sectional views of the holographic recording material H of Figures 1, 2 and 3 taken along 1~ the respective section lines therein. It should be understood that a given holographic recording material H may contain more than the number of region(s) R shown in Figures 1 to 3, and that a given region R of a holographic recording material H may contain more than the number images I shown in Figures 1 to 3. Figures 1 ~0 to 3 are to be construed as being illustrative of the various possible arrangements of holographic images able to be recorded within predetermined defined region(s) of the recordin~ material H using the method of the present invention. Although any holographio recording material may be used with the method of 2 5 the present invention, a photopolymerizable holographic recording material is preferred. The composition of the photopolymerizable holographic recording material preferably used in the method of the present invention will be more fully discussed hereinafter.
Figures 1 and 1A illustrate ~he arrangement of an angularly multiplexed holographic image recorded in accordance with the present invention. An "angularly multiplexed" holographic image (or "angle hologram"), as the term is used herein, denotes the presence of at least two different holographic imag~s 11 and 12 recorded in the same predetermined defined physical region R of J~ .q~ 7 the holo~raphic material H. Forming angle holograms is most useful in volume holography, where the ~rating spacing is small with respect to the thickness af the recording material, as described in Chapter 9, Section 8 of Collier text referenced 5 earlier. For simplicity of illustration the images shown in Figures 1 through 3A are the interference pattern fringe spacing with the first image 11 being indicated in solid lines while the second image 12 is indicated by dashed lines.
Figures 2 and 2A illustrate the arrangement of a spatially multiplexed holographic image recorded in accordance with the present invention. As the term is used herein a "spatially multiplexed" holographic image (or "spatial hologram") denotes the presence of only a single holographic image within a given 15 region R of the holographic material H. Thus, as seen in Figure 2, each of the holographic images 11 and 12 is recorded in a respective predetermined defined physical region R1 and R2 of the holographic material H. The predetermined defin~d region R1 f the recording material H in which the image 11 is constructed is 20 separate from the predetermined defined region R2 of the recording medium H in whioh the image 12 is constructed. By "separate" it is moant that aven though each the predetermined defined region of the material is physlcally integral with all of the other regions in the sense that a continuous sheet of 25 holographio recording material is defined, each such region is distinct from the others on the sheet.
Combinations of angularly multiplexed and spatially multiplexed holographic images are possible. Figures 3 and 3A
3 0 illustrate the combination of angularly multiplexed holographic images 11 and 12 recorded in a predetermined defined region R1 f the recording material H while a spatially multiplexed holographic image 13 iS recorded in a separate region R2 of the holographic recording material H. It lies within the 35 contemplation of this invention to record one or more additional WO 92/0~55S PCI`/US91/04623 ~,r~.~r-r. ~')1-1 image(s) in the region R2, in effect defining angle holograms (as that term is defined herein) in each of the regions R1 and R2. It should be noted that in some instances such an arrangement has been termed in the art as "both a spatially and an anglarly S multiplexed holograml'.
-o-O-o-The method of temporal interleaving of N holographic 10 images 11 to IN into a recording material H in accordance with the present invention may now be set forth.
In accordance with a first predetermined sequence each one of a set of N holographic images is constructed into a 15 predetermined defined region R of the recording material in accordance with a first predetermined sequence. Depending upon whether an angularly or a spatially multiplexed hologram is being recorded, each image may be recorded in the same predetermined defincd rcgion of the recording matcrial (i.e., an angularly 20 multiplexed hologram, e.g., Figure 1) or each image may be recorded in a predetermined defined region that is separate from all other regions of the recording material (i.e., a spatially multiplexed hologram, e.9.t Figure 2). As discussed above, a combination of the angularly multiplexed or spatially multiplexed 25 holograms in the same reccrding material H (Figure 3) lies within ~he contempla~ion of the presen~ invention.
Each holographic image in the set of N images is constructed for a predetermined first imaging time with a 30 predet~rmined first time gap being defined between each of the images. Thereafter, in accordance with a subsequent predetermined sequence, each one of a predetermined number of the set of N holographic images is constructed into the same predetermined location into which it was constructed during the 35 first sequence. During the subsequent sequence each holographic WO 92/00555 PCI`/US91/04623 '7 t3 image is constructed into the predetermined defined region of the holographic recording material for a predetermined corresponding second imaging time. A predetermined second time gap is defined between each cf the images in the subsequent sequence.
It should be understood that the subsequent sequence may be constructed more than twice. Stated alternatively, more than two exposure sequences may be used, if desired. In general, M
number of exposure sequences may be used, where M can have any 10 convenlent value ~including being equal to N).
It lies within the contemplation of the invention that any subsequent sequence(s) of exposures may include any predetermined number (i.e., subset) of the set of N ima~es 15 constructed during the first sequence. The term "sequence" as used herein is meant to denote the order in which the rnernbers of the set of holographic images is constructed into the material. It is preferable, although not necessary, that the same order of imag0 exposure occurs during any subsequent sequence as 20 occurred in the first sequence.
It is expressly noted that in some instances a subsequent set may contain a greater number of i~nages than the first set of images. The present invention is to be construed to cover such 25 situations. Thus, temporal interleaving in accordance with the present invention may be used for the exposure of two predetermined sets of holographic images, each containing some predetermined number of images N1 and N2, respectively, so long as the first and subsequent sets of holographic images have at 30 least one m0mber in common.
In all situations the construction of an image is effected by relatively short exposures. If the recording material is a photopolymerizable recording material the timing of the 35 subsequent sequence with resp0ct to the first is soverned in WO 92J00555 P~/US91/04623 accordance with (i.e., faster than) the diffusion rate of the monomer in the material.
The method of the present invention may be more clearly 5 understood from the following typical activity schedule for its practice. A temporally interleaved exposure schedule for N
images follows, with the interleaving period T denoting the time required to expose each of the N images in the sequence.
it is assumed that each sequence of exposures contains all N
10 images. If some subset of the N images are contained within a given sequence then the periods Tp of such sequences varies (assuming uniform exposure times and gap times).
WO 92/00555 P~IUS91/04623 $Ç~lE~I~
PERIOD Tl, SEQUENCE 1 expose image 1 for imaging time t gap tg1 1 expose image 2 for imaging time t12 gap tg1 2 expose image N for imaging time t1N
gap tg 1 N
PERIOD T2, SEQUENCE
expose irnage 1 for imaging time t gap tg21 expose image 2 for imaging time t22 ~ap tg22 . . .
expose image N for imaging time ~2N
gap tg2N
~0 . ~ .
PERIOD T3, SEQUENCE 3 through PERIOD T~l, SEQUENC:E M-1 PERIOD TM- SEQUEN~E M
expose image 1 for imaging time t gap tgM1 expose image 2 for imaging time tM2 gap tgM2 expose image N for imaging time tMN
3ap tgMN
WO 92~00555 PCI'/US91/04~i23 It is understood that during the second and subsequent sequences (if any) each one of a predetermined number of the set of N holographis images is constructed into the same predetermined location into which it was constructed during 5 the first sequence.
The total imaging time for a single image k is given by M
i O ~ (tjk)-i = 1 As noted earlier, it lies within the contemplation of the invention that the imaging times for each image need not be 15 equal, the time gaps need not be equal, and/or that each sequence need not contain all of the N images in the set of holographic images. It should also be understood that either an angularly multiplexed hologram (i.e., two or more images) or an spatially multiplexed hologram (i.e., one image) may be 20 constructed in a given region R of the recording material.
-o-O-o-With reference now to Figure 4 shown is a 2 5 schematic illustration of an apparatus generally indicated by reference character 10 suitable for use in accordance with the method of the present invention for recording a plural number N of two-beam holographic images on a recording material H.
Although any holographic recording material may be used, in 30 the preferred instance the recording material H is a photopolymerizable film the details of which are fully set forth hereinafter. The apparatus 10 is able to be used to form -`
both spatially multiplexed holographic images and angularly multiplexed holographic images.
wo 92/00s5~ Pcr/US9l/o4623 . .
~?`~ 7 The apparatus 10 includes a laser source 12 which produces a beam 14. The beam 14 passes thrnugh a beam attenuator 16 and a controllable shutter 18 and is incident 5 upon a variable beam splitter 20. The beam splitter 20 bifurcates the beam 14 into an object beam path generally indicated by the chàracter 24 ancl a reference beam path generaily indicated by the character 26. Suitable for use as the source 10 is a twenty (20) Watt argon laser such as that 10 manufactured by Spectra-Physics, Inc. of Mo~ntain View, California and sold as model 2045. The attenuator is preferably implemented using a device manufactured by Newport Research Corporation, Fountain Valley, California and sold as model 935-5 Attenuator. The controllable shutter 18 15 is preferably implemented using a device manufactured by Vincent Associates, Rochester, New York, and sold as model 225L2AOZ5.
The portion of the beam turned ninety degrees by the 20 action of the beam splitter 20 propagates along the object beam path 24 through a spatial filter/collimator assembly 28A
to produce a collimated object beam indicated by the reference oharacter 30. The spatial filter/collimàtor assembly 28A is preferably implemented using a 40x microscope objective and 25 a ten micron pinhole mounted in a model 910-B spatial filter and a 63.5 mm focal length achromatic lens. These devices are all available from Newport Research Corporation.
The object bearn 30 is directed by a mirror 32 onto the 3 0 holographic recording material H. The material H is itself mechanically secured by a plateholdar schematically indicated at reference character 34 in any convenient manner. The mirror 32 is arranged such that the object beam 30 deflected from the mirror impinges on the holographic recording 35 rnaterial H at a predetermined object beam angle 36. The Wo 92~00S5~ PCl'/US91/04623 surface of the recording material H is termed herein as "the film plane~'. The object beam angle 36 is measured with respect to a normal to the ~ilm plane. To form spatially multiplexed holograms the plateholder must be able to be 5 translated in mutually orthogonal directions in the film plane.
To effect such translation an actuator generally indicated by the reference character 38 is operatively associated with the plateholder 34. The actuator 38 may be implemented in any convenient fashion, such as by manual or motorized translator 10 stages, as should be apparent to those skilled in the art.
The portion of the b0am 14 that continues through the beam splitter 20 along the reference beam path 26 is turned ninety degrees by a mirror 40 toward a spatial 15 filter/collimator assembly 28B. The spatial filter/collimator assembly 28B is similar to the assembly 28A described earlier. The collimated reference beam 42 emanating from the assembly 28B is turned by a double-sided mirror 44 mounted on a galvanometer 46. Suitable for USB as the galvanome~er 46 20 is a device manufactured by General Scanning Inc., Watsrtown, Massachusetts, and sold as model G120PD Galvo.
The reference beam 42 passes throu~h a unity angular magnification Keplerian afocal telescopic ima~ing system 48 25 that directs the reference beam 42 towards the film plane at a predetermined reference beam angle 50, also measured with respect to the normal from the film plane. The sum of the object beam angle 36 and the reference beam angle 50 defines an interbeam angle 52.
The object beam 30 and the reference beam 42 are coincident at the film plane. Since both beams 30, 42 are sufficiently coherent they produce an interference pattern, or holographic image, at the film plane. The holo~raphic image is 35 recorded in the recording material H. The cornbined action of WO 92~00S5~ $, j;, PCl`tUS91/~4623 the attenuator 16 and the variable beam splitter 20 controls the intensities of the object beam and the reference bearns 30 and 42, respectively.
Rotation the mirror 44 under control of the galvanometer 46 changes the angle at which the reference beam 42 is input to the telescopic imaging system 48. Since the reflection of the reference beam 42 from the mirror 44 is irnaged by telescopic imaging system 48 at the plane of the holographic recording material H any change in the position of the mirror 44 produces a corresponding equal change in the reference beam angle 50, assuming that the reference beam 42 remains in the aperture of the imaging system 48. The reference beam 42 remains coincident with the object beam 30 for any rotation of the mirror 44. The position of the mirror 44 under control of the galvanometer 46 thereby varies and controls the reference beam angle 50, and thus the interbeam angle 52.
An interfersnce pattern (image) suitable for recording as a holographic image is constructed at the filrn plane (the surface of the holo~raphic material H) when the shutter 18 is open. The properties of the holographic image (namely the interference fringe spacing and fringe slant) are determined by the reference beam angle 50 and the object beam angle 36.
Thus a different holographic image may be recorded in the material H by changing the reference beam angle 50.
The actual position of the mirror 44 is derived from a mirror position sensing system generally indicated at reference character 56. The mirror position. sensing system 56 includes a laser source 58 and an associated detector 60.
The source 58 and the detector 60 are respectively located to direct a laser beam 58B toward the undersurface of the mirror 44 and to intersect the reflected beam 58R therefrom. The 3 5 suitable biased detector 60 is responsive to the reflected WO 92/005~i~ PCI'/US91/04623 $~
beam 58R incident thereon to generate first and second electric currents (i1 and i2, respectively) on lines 62A, 62B.
The magnitude of the signals on the lines 62A, 62B is functionally related to the position on the detector 60 at 5 which the reflected laser beam 58R is incident and also to the power output of the laser source. Suitable for use as the laser 58 is the HeNe laser device formerly manufactured by Hughes Aircraft Corporation, of Carlsbad, California and sold as 3221H-C 5 mW. Equivalent equipment is now believed 10 available from Melles Griot of Irvine, California. The detector 60 is preferably implemented by a linear position sensor such as that manufactured and sold by Quantrad Incorporated of Los Angeles, California as model PS-100-50.
Rotation of the galvanometer 46 is controlled by a galvanometer drive signal carried on a line 64 from a galvanometer position controller generally indicated by the reference character 66. The controller 66 is shown in more detail in Figures 5A and 5B. The controller 66 is responsive to 20 the signals applied thareto on the lines 62A, 62B (which eontain information as to the actual position of the mirror 44) and to a reference signal carried on a line 58 to generate the ~alvanometer drive signal on the line 64. As will be developed, the controller 66 permits the repeatable and accurate 2 5 positioning of the mirror 44 whereby temporal interleaving of holographic images in accordance with the present method may be effected.
The controller 66 itself includes means generally indicated 30 at reference character 70 (shown in Figure 5A) responsive to the first and the second currents i1 and i2 for forming the ratio of the sum and difference thereof. The ratio is implemented using a - ratio module such as that sold by Burr-Brown Inc. of Tucson, Arizona as model number DIV100. This ratio action forms on a 35 line 72 an actual mirror position signal that is independent of the WO 92/00555 ~2lr~ ~rli(r~7 PC~/US91/04623 power output.of the laser source 58. It is noted that the signal on the line 72 is also independent of any thermal responses of the detector 60.
As seen in Figure 5B, a module 74 within the controller 66 subtracts the actual mirror position signal 72 from the reference position signal on the line 68 to produce an error signal at a summing junction J. An integrator oircuit 75 ~Fi~ure 5B) produces a galvanometer position control signal at the output point K thereof. After dynamic response compensation in an amplifier 76 the galvanometer position control signal is inpu~ to the galvanometer servo amplifier 77 which produces the galvanometer drive signal on the line 64.
The integrator 75 serves to maintain at least some drive voltage level to the amplifier 76 during those times when the galvanometer error signal (point J) is zero, thus maintaining the galvanometer 46 in the position that generates the zero positlon error.
2 0 The shutt~r 18 is controlled eiectronically by a shutter control signal applied on a line 79 from a shutter controller 78. Suitable for use as the shutter eontroller 7~ is the device manufactured by Vincent Associates and sold as Model SD-10 Shutter Drive/Timer. The input timing signal to the shutter controller 78 is a timing pa~tern applied over a line 80 (typically at a standard logic level of five Volts) which controls the stat~ of ~he shutter 18, i.e., whether the shutter 18 is open or closed.
If the number of holographic images N is two the galvanometer reference signat 68 and the timing signal 80 may be generated using a square wave generator 84 and a pulse 3enerator 86. Suitable for use as the square wave ge~nerator 84 is the device manufactured by Textronix, Beaverton, Oregon 35 and sold as model FG502 while the pulse generator 86 may be WO 92/~0555 o'~ PCI`/US91tO4623 implemented using a device manufactured by Hewlett-Packard, Palo Alto, California and sold as model 811~A Pulse Generator.
The square wave output is applied as the galvanometer 5 reference signal on the line 68 and moves the galvanometer 46 ~and thus the mirror 44), as described earlier. The square wave signal from the generator 84 is also used as the pulse generator trigger applied over a line 88 to the pulse generator 86. The pulse generator 86 triggers on both the positive and 10 negative transitions of the square wave trigger signal 88, triggering one pulse during each image position (one half of the square wave). The output of the pulse generator 86 forms the shutter timing signal 80. The assertion of the shutter control signal on the iine 79 in response to the input timing signal on 15 the line 80 serves to open the normally closed shutter 18, thereby causing an image exposure to occur in the holographic recording material H. The duration of each pulse on the line 79 is equal to tjj. The relationship of the waveforms of a galvanometor reference signal 68 and a shutter timin~ signal 20 80 is shown in Figure 6 for an N equals 2 image embodiment.
It shouid be readily apparen$ to those skilled in the ar~
that the galvanometer re~erence signal on the line 68 and the shutter timing signal on the 80 may be generated by a 25 computer system, other conventional instrumentation, or any other convenient arrangement. For example, if N is greater than two, a microprocessor based system could drive, under program control, a plurality of digital-to-analog converters to provicle the N shutter timing signals on the line 80. The 30 microprocessor based system also can be used to expeditiously provide the galvanome$er reference signal on the line 68.
Moreover, if a spatially multiplexed hologram is being prep~red, the microprocessor based system could also be used to provide appropriate indexing signals to the actuator~s) 38 3 5 associated with the plateholder 34.
WO 92/00555 PCl/US91/04623 ~r~~3);j~
It should thus be appreciated from the foregoing that by providing the appropriate electronic galvanometer reference signal on the line 68 and the appropriate shutter timing signal 5 80 any sequence of holographic exposures, exposure times, an gap times between exposures may be implemented using the apparatus 10. The apparatus 10 described above is suitable for practicing the method of the pres~nt invention whereby a predetermined number N of spatially and/or angularly 10 multiplexed holographic images may be recorded into the holographic recording material H. The N difFerent angularly multiplexed holographic images may be formed at the film plane when the mirror 44 is rotated by the action of the galvanometer 46 to each of N different positions. Spatially 15 multiplexed holograms are recorded in separate regions of the material H in accordance with the translations effected by the actuator 38.
I~, as preferred, a photopolymeric holographic recording 20 material H is usad to record the N multipiexed holographic images, temporal interleaving in accordance with the present invention overcomes the dynamic effects of the grating formation time-dependent diffusion process in the film, ~nd records N hologram images in a repetitive sequential fashion.
25 The sequence periods Tp are made shorter than the diffusion mechanism in the material, thus minimizing undesired effects obtained with conventional sequential exposure of N
holograms. This method avoids crosstalk effeots of simultaneous exposure and the difficulty of generating N
3 0 reference beams sirnultaneously.
Alternate embodiments of the apparatus 10 which one skilled in the art may easily implement include, among others:
1) spatial madulation of the object beam 30 and/or reference 35 beam 42; 2) nonplanar wavefronts in the object beam path 30 WO 92/00555 PCT/US91/0~S623 f . ~.-~C..9~ 4 and/or the reference beam path 42, (e.g. the object beam 30 is a converging spherical wavefront focusing at the film plane forming a Fourier transform hologram); 3) angle adjustment for the object beam 30,as for example, using the controller 66 5 as shown in Figures 5A and 5B; 4) angle adjustment for the film plane; and 5) non-unity angular magnification in imaging system 48.
-o-O-o-The photopolymerizable materials used herein are thermoplastic compositions that upon exposure to aotinic radiation form crosslinks or polymers of high molecular weight to change the refractive index and rheological character of the composition (s). Preferred 15 photopolymerizable materials are photopolymerizable compositions, such as disclosed in United States Patent 3,658,526 (Haugh) and more preferred materials are described copending application Serial Numbers 07/144,355, 07/144,281 and 07/144,840, all filed January 15, 1988 and all assigned to Z0 E. I. du Pont de Nemours and Company, Incorporated. In these - materials, free radical addition polymerization and crosslinking sf a compound containing one or more ethylenically unsaturated groups, usually in a lerminal position, hardens and insolubilizes the cornposition. The 25 sensitivity of the photopolymerizable composition is enhanced by the photoinitiating system which may contain a component which sensitizes the composition to predetermined radiation sources, e.g., visible light. Conventionally a binder is the most significant component of a substantially dry 30 photopolymerizable base or layer in terms of what physical properties the base or layer will have while being used in the invention. The binder serves as a containing medium for the monomer and photoinitiator prior to exposure, provides the base line refractive index, and after exposure contributes to 3 5 the physical and refraGtive index characteristics needed for .
WO 92/00555 PCI'/US91/04623 '7 the base layer or buffer layer. Cohesion, adhesion, flexibility, diffusibility, tensile strength and index of refraction are some of the many properties which determine if the binder is suitable for use in the base layer.
Photopolymerizabie materials contemplated to be equivalent are photodimerizable or photocrs)sslinkable compositions such as disclosed in United States Patent 3,526,504 ~Celeste) or those compositions in which hardening 10 is achieved by a mechanism other than the free radicai initiated type identified above.
The photopolymerizable material is composed of three rnajor components, a solid solvent-soluble preformed 15 polymeric material, at least one liquid ethylenically unsaturated monomer capable of addition polymerization to produce a polymeric material with a refractive index substantially different from that of the preformed polymeric material, or binder, and a photoinitiator system activatable by 20 actinic radiation. Although the base or layer is a solid composition, components interdiffuse before, during and after imaging exposure until they are fixed or destroyed by a ~inal uniform treatment usually by a further uniform exposure to actinic radiation. Interdiffusion may be further promoted by 2 6 incorporation into the composition of an otherwise inactive plasticizer.
In addition to the liquid rnonomer, the composition may contain solid monomer components capable of interdiffusing in 30 solid composition and reacting with the liquid monomer to form a copolymer with a refractive index shifted from that of the binder.
In the preferred compositions for use in this invention, 35 the preformed polymeric material and the liquid monomer are WO 92/00555 PCS/US91/046~3 r~ ~~ r~ r- . t ~t selected so that either the preformed polymeric material or the monomer contains one or more moieties taken frorn the group consisting essentially of substituted or unsubstituted phenyl, phenoxy, naphthyl, naphthyloxy, heteroaromatic grcups 5 containing one to three aromatic rings, chlorine, and bromine and wherein the remaining component is substantially free of the specified moieties. in the instance when the monomer contains these moieties, the photopolymerizable system hereinafter is identified as a"Monomer Oriented System" and 10 when the polymeric material contains these moieties, the photopolymerizable system hereinafter is identified as a "Binder Oriented System."
The stable, solid, photopolymerizable compositions 15 preferred for this invention will be more fully described by reference to the "Monomer Oriented System" and "Binder Oriented System."
The monomer of the Monomer Oriented System is a liquid, 2 0 ethylenically unsaturated compound capable of addition polymerization and having a boiling point above 100C. The monomer contains either a phenyl, phenoxy, naphthyl, naphthoxy, heteroaromatic group containing one to thr~e aromatic rings, chlorine or bromine. The monomer contains at 25 least one such moiety and rnay contain two or more of the same or different moieties of the group, provided the monomer remains liquid. Contemplated as equivalent to the groups are substituted groups where the substitution may be lower alkyl, alkoxy, hydroxy, carboxy, carbonyl, amino, amido, imido or 30 combinations thereof provided the monomer remains liquid and diffusable in the photopolymerizable layer.
Preferred liquid monomers for use in the Monomer Oriented System of this invention are 2-phenoxyethyl acrylate, 3 5 2-ph~noxyethyl methacrylate, phenol ethoxylate acrylate, 1-WO 92/005~5 PCI/US91/0~623 27(p-chlorophenoxy) ethyl, p-chlorophenyl acrylate, phenyl acrylate, 1-phenylethyl acrylate, di(2-acryloxyethyl) either of bisphenol-A, and 2-(2-naphthyioxy) ethyl acrylate.
While rnonomers useful in this invention are liquids, they may be used in admixture with a second solid monomer of the same type, e.g., N-vinyl-carbzole, ethylenically unsaturated carbazole monomers such as disclosed in ~Q~naLQ~Q~m~
__ , Vol.. 18, pp. 9-18 (1979) 10 by H. Kamagawa et al., 2-naphthyl acrylate, penta-ohlorophenyl acrylate, 2,4,6-tribromophenyl acrylate, and bisphenol A
diacrylate, 2-(2-naphthyloxy) ethyl acrylate, and N-phenyl maleimide.
.
The solvent soluble polymeric material or binder of the Monomer Oriented System is substantially free of phenyl, phenoxy, naphthyl, naphthyloxy, heteroaromatic group containing one to three aromatic rings, chlorine and bromine.
Preferred binders for use in the Monomer Oriented System of this invention are cellulosa acetate butyrate polymers; acrylic polymers and inter polyrners including polymethyi m~thacrylate, methyl methacrylate/methacrylic aoid and methyl methacrylate/acrylio acid copolymers, terpolymers of methylmethacrylate/C2-C~ alkyl acrylate or methacrylate/acrylic or methacrylic acid; polyvinyl-acetate;
polyvinyi acetal, polyvinyl butyral, polyvinyl formal; and as well as mixtures thereof.
The monomer of the Binder Oriented System is a liquid ethylenically unsaturated compound capable of addition polymerization and having a boiling point above 100C. The monomer is substantially free of moieties taken from~the group consistin~ essentially of phenyl, phenoxy, naphthyl, WO 92/û0555 PCI/US91/04623 '7 naphthyloxy, heteroaromatic group containing one to three arornatic rings chlorine and bromine.
Preferred liquid monomers for use in Binder Oriented 5 Systems of this invention include decanediol diacrylate, iso-bornyl acrylate, triethylene glycol diacrylate, diethyleneglycol diacrylate, triethylene glycol dimethacrylate, ethoxyethoxyethyl acrylate, triacrylate ester of ethoxylated trimethylolpropane, and 1-vinyl-2-pyrrolidinone.
While monomers used in Binder Oriented Systems are liquids, they may be used in admixture with a second solid - monomer of the same type, e.g., N-vinyl-caprolactam.
The solvent soluble polymeric material or binder of the Binder Oriented System contains in its polymeric structure rnoieties taken from the group consisting essentially of phenyl, phenoxy, naphthyl naphthyloxy or heteroaromatic group containing one to three aromatic rings as well as chloro or 20 bromo atoms. Contemplated as equivalent to the groups are substituted groups where the substitution may be lower alkyl, alkoxy, hydroxy, carboxy, carbonyl, amido, imido or combinations thereof provid~d the binder remains solvent soluble and thermoplastic. The moieties may form part of the 2~ monomeric units which constitute the polymeric binder or may be grated onto a prepared polymer or interpolymer. The binder of this type may be a homopolymer or it may be an interpolymer of two or more separate monomeric units wherein at least one of the munomeric units contains one of 3 0 the moieties identified above.
Preferred binders for use in the Binder Oriented System include polystyrene, poly (styrene/acrylonitrile), poly (styrene/methyl methacrylate), and polyvinyl benzal as well as 35 admixtures thereof.
WO 92/00555 PCI`/US91/04623 The same photoinitiator system activatable by actinic radiation may be used in either the Monomer Oriented System or the Binder Oriented System. Typically ~he photoinitiator system will contain a photoinitiator and may contain a sensitizer which ex~ends the spectral response into the near U. V. region and the visible spectral regions.
Preferred photoinitiators include CDM-HABI, i.e., 2-(o-1 O chlorophenyl)-4, 5-bis~m.-methoxyphenyl)-imidazole dimer; Q-Ci-HABI, i.e., 1,1'-Biimidazole, 2,2'-bis-(p-chlorophenyl)-4,4', 5,5'-tetraphenyl-; and TCTM-HABI, i.e., 1 H-lrni~azole, 2,5-bis(o-chlorophenyl~-4-3,4-dimethoxypheny!-, dimer each of which is typically used with a hydrogen donor, e.g., 2-1 5 mercapto-benzoxazole.
Preferred sensitizers include the following:
DBC, i.~., Cyclopentanone, 2,5-bis-((4-(diethylamino)-2-methylphenyl)methylene);
DEAW, i.e., Cyclopentanone, 2,5-bis-((4-(diethylamino)-phenyl)methylene); and Dimsthoxy-JDI, i.e., 1 H-lnden-1-one, 2,3-dihydrv-5,6-dimethoxy-2((2,3,6,7-tetrahydro-l H,5H-benzo~i,j]quinolizin-9-yl)-methylene)-.
JAW, i.e., 2,5-bis [2,3,6,7-tetrahydro (1 H, 5H-benzo[i,j,]quinolizin-9-yl~ methylene]-cyclopentanone .
3 0 Ths solid photopolymerizable compositions of this invention may contain a plasticizer. Plasticizers of this invention may be used in amounts varying from about /O to about 20% by weight of the compositions preferably 5~to l~
wt.%.
3~
WO 92/00555 PCT/lJS91/04623 Preferred plasticizers for use in simple cellulose acetate butyrate systems are triethyleneglycol dicaprylate, tetraethyleneglycol diheptanoate, diethyl adipate, Brij~30 and tris-(2-ethylhexyl)phosphate. Similarly, triethyleneglycol 5 dicaprylate, diethyl adipate, Brij~30, and tris-(2-ethylhexyl)phosphate are preferred in "Monomer Oriented Systems" where cellulose acetate butyrate is the binder.
Other components in addition to those described above 10 can be present in the photopolymerizable compositions in varying amounts. such components include: ultraviolet radiation absorbing material, thermal stabili~ers, hydrogen donors, oxygen scavengers and release agents.
Amounts of ingredients in the photopolymerizable compositions will generally be within the following percentage ranges based on total weight of the photopolymerizable layer; monomer, 5-50%, pre~erably 15-35%; initiator 0.1-10%, preferably 1-5%; binder, 25-75%, 2 0 preferably 45-65%; plasticizer, ~-25%, pre~erably 5-15%;
other ingredients 0-5%, pre~erably 1-4%.
~x~eL~
The holographic recording material as used in this example used a coating emulsion that had the ingredients as Iisted in the following Table 1:
TABL~ 1 3 ~n~r~sli~
Cellulose acetate butyrate, 51.90 Eastman type CAB 531-1 Ethoxylated pheno~ acrylate 26.93 3 5(Photomer 4039~
WO 92/0055~ P~/US9l/04623 9-Vinylcarbazole (NVC) 6.00 Ethoxylated bisphenol A diacrylate 9.97 (Sartomer 349) 4-Methyl-4H-1,2,4-triazole-3-thiol 2.52 (MMT) Q-CI HABI (1,1'-Biimidazole, 2,2'-bis- 2.48 (Q-chlorophenyl)-4,4', 5,5'-tetraphenyl; CAS 1707-68-2 Fluorocarbon coating aid, 0.10 Fluorad FC-430 (3M Inc.) JAW dye 2,5-bis [2,3,6,7-tetrahydro 0.10 (1 H, 5H-benzo[i,j,]quinolizin-9-yl) methylene]-cyclopentanone.
Figure 7 shows a holographic recording material comprising a thirty-eight (38j micron photopolymer emulsion 90 ~ingredients given in Table 1) coated onto a 50.8 micron optical grade base 92 formed from a polyester film such as that manufactured and sold by E.l. Du Pont de Nemours and 20 Company under the trademark Mylar~. The coating was cast from solvent (95% methylcne chloride, 5% methanol) and the coatin~ solution was 25% by weight emulsion, 75% solvent.
The emulsion and base were laminated onto a 2" x 2" x 1/8 inch float glass plate 94, forming a glass-photopolymer-base 25 sandwich as shown in Figure 7. The plate was mounted in the plate holder 34 at the film plane with the base facing ~he incident beams. Th~ experiment was performed under red safelight in the nonsensitive spectrum of the photopolymer.
The optical wavelength used for holographic image exposure was 514.5 nanometers generated by an Argon ion laser 12 with an intercavity etalon for single frequency operation. The power density of each of the respective reference an~ o~ject beams 30 and 42 was approximately 3 5 eighty (80) milliWatts per square centimeter.
Table 2 iists the results for nine (9) samples of multiplexing holographic images by temporal interleaving. For each sample, two holographic images (N = 2) were multiplsxed 5 by temporal interleaving with sequence period, imaging, and gap times as indicated in Table 2. The reference and object beams 30 and 42 were each about five (5) millimeters in diameter. The plateholder was translated during the experiment to fit several multiplexed holograms onto the 2" x 10 2" plate. The experiment beam angles: object beam angle 36 -about fifteen (15) degrees; reference beam angle 50 of about 8.25 degrees for image j = 1 (galvanorneter mirror 44 directing the reference beam 42 at Position A in Figure 4) and 21.75 degrees for image j = 2 (Position B in Figure 4).
WO 92/00555 PCr/US91104623 ~L~Z
HOL~GRAM IMAGING G~PSE~JE~:E NUMBER OF DIFFRACTION
SAMPLE TIME TIME PERIODPERIODS EFFICIENCY.
NUMBER ( % ) tjj (msec) tgjj (msec)Tp (sec) M image 1 image 2 5 0 0 1 000 3 5 9.3 1~
2 250 1250 3 10 9.6 22 3 100 1 400 3 20 1~ 27 4 500 1 000 3 10 9.3 16 7 250 750 2 10 9.1 16 9 400 600 2 5 8.4 20 After imaging, the holograms were fixed by turning on room lights and exposing the photopolymer plate to a Hg lamp for approximately ten ~10) minutes. The plate was reinserted 20 into the appara~us identical to exposure. The obj~ct beam 30 was blocked and the dlffraction efficiency was measured by reconstruoting the mllltiplexed holograrns with the reference beam 42 at incident angles corresponding to image j = 1 (Position A) and image j - 2 (Position B). The diffraction 25 efficieney was calculated as the detected power measured in the first-order diffracted reconstruction of the object beam, divided by the sum of the detected first-order and zero-order (undiffracted from reference beam~ powers.
3 0 The diffraction efficiencies reported for the nine (9) samples show that temporal interleaving is effective over a range of exposure parameteYs (imaging time, gap time, sequence, etc.), and that changes in those parameters will affect the resul~s. No optimization of these parameters was performed in the experiments reported here, but it is exp~sted WO 92/005S5 PCI`/US91/04623 J~;~ 7 that optimization is important for achieving the best possible results. Given the maximum possible refractive index modulation for the recording material used, the maximum diffraction efficiencies for the irnages in the samples are 5 expected in the range of 30%-45%. The results obtained could be improved by optimizing the exposure parameters and other aspects of the experiment (in particular, the plate should be mounted such that the glass side of the plate faces the incident beams to eliminate the effect of base birefringence).
The results show that the temporal interleaving method is useful for multiplexing holograms, and works well for dynamic media such as a holographic photopolymeric recording mate rial .
1 ~
Those skilled in the art, having the benafit of the teachings of the present invention may impart numerous modifications thereto, it should be understood that such modifications lie within the contemplation of the present invention, as defined by 20 the appended claims.
IIIL~
~ U 1~ 7~
~ b~n~ This invention relates generally to a method of recording holographic images and, in particular, to a method for recording a plural number of such holo~raphic images into a recording material.
~ Ib~ Optical holography, often called "wavefront reconstructionn, may be described as the recording of a holographic image within a holographic recording material. Conventional holographic r~cording materials include 20 silver halide emulsiorls, dichromated ~elatin, thermoplastic media and time-dependent diffusion media.
A standard technique of producing a holographic image is by the interference of two coherant bearns of light, respectively 25 termed an "object beam" and a l'reference beam~. Both beams are generated from the same coherent source (typically a laser) to insure sufficient mutual coherence to form a stable interference pattern. To produce the holographic image the object beam is typically spatially modulated, e. g., it is reflected from a three-30 dimensional object. The reference beam is typically a non-spatially modulated coherent beam. The object b~arn and the reference beam are br4ught together (that is, spatially overlapped) at a predetermined position within a holographic recording material. It is the coherent addition of the wavefronts 35 of the obJect beam and the reference beam within the material WO 9~/005~ , PCI'/US91/04623 that constructs a holographic image within the recording material. In a similar manner holographic images may be created with multiple reference and object beams. The holographic image so constructed may also be referred to as the interference 5 pattern, the holographic grating, the hologram, or simply, the image.
The term "multiplexed" holographic image refers to the construction of more than one holographic image within a 10 holographic recording material. A variety of wavefront reconstruction options is permitted using multiplexed holographic images. Multiplexed holographic images in some cases make efficient use of the available area or volume of the recording medium. The holographic images produced by 15 combinations of several reference and object beams may be constructed in the same physical region in the recording material.
Alternatively, each of the holographic images may be constructed in a respective region of the recording material (spatial multiplsxing) . .
Convention~l methods used to multiplex a plural number N of holographic ima~es into the same volume of the holographic recording material use two basic approaches: a simultaneous exposure technique or a sequential exposure technique. These two 25 approaches are discussed in La Macchia and Vincelette, "Comparison of the Diffraction Efficiency of Multiple Exposure and Single Exposure Holograms", Applied Optics, Vol. 7, No. 9, pp.
1857-1858, Septembar 1968) and in R. J. Collier et al., "Optical Holography", Academic press, Inc., 1971 and H. J. Caulfield, Ed., 30 "Handbook of Optical Holography1', Academic Press, Ino., 1979.
These methods are particularly important for volume holography, where multiplexing N holograms at different angles (angle multiplexing) in the holographic recording material optimizes information recording density.
WO 92t0055~ PCl-tUS91/04623 2~ r:-,3';~
Simultaneous exposure requires that the optical bearns constructing all N h~lographic images be generated simultaneously, so that only a single exposure of the holographic recording material is made. Perceived disadvantages of this 5 approach include the difficulty in simultaneously generating beams for the N holographic images when N is large, and the problem of crosstaik between reference beams and object beams when constructing the N holograms.
Holographic exposure of conventional holographic recording materials, such as silver halide emulsions, dichromated gela~in, and thermoplastic media, involves recording a latent holographic image in the material. The final holographic image is obtained by a developing and fixing process. In the course of making 15 multiplexed holographic images by sequential exposure, for example, the recording material may be left in the dark between exposures for extended periods of time while the recording apparatus is being modified. Subsequent exposures will simply add to the latent image that already exists.
Photopolymeric holographic recording materials are now known. Copending application Serial Number 07/144,281, copending application Serial Number 07/144,355, and copending application Serial Number 07!144,840, all filed January 15,1988 25 and all assigned to the assignee of the present invention disclose and claim holographic recording materials. Holographic images are recorded in a photopoiymer recording medium as a resul$ of diffusion of unexposed monomer towards areas exposed with the highest intensity cf incident light, creating a density gradient in 3 0 the material which corresponcls to the optical intensity gradient in the holographic image. After polymerization the higher density areas have a larger index of refraction than the lower density areas, thus forming a dielectric (phase) grating.
WO 92/005~;5 z~r ~ 7 PCI`/US91/04623 Identical serially recorded exposures, using typical exposure energies (ten milliJoules per square centimeter) recorded on the order of several seconds apart, are not recorded with equal strength in the material. This is due to the dynamics 5 of the diffusion mechanism. Furthermore, monorner does not flow as readily to the second exposure as it does to the first, and not as much flows per unit of inoident optical radiation.
When using a photopolymeric holographic recording material 10 based on a time-dependent diffusion mechanism the material should not, in general, be left in the dark for extended periods of time (several seconds or minutes) between sequential exposures if one expects to achieve performance comparable to oonventional holographic materials. Since in the holographic materials the 15 latent image mechanism is replaced by a process involving the dynamic diffusion of molecules in the material the possibility of reciprocity failure exists. Reciprocity failure is due to the fact that the index of refraction change is not only a funçtion of the irradiance-exposure time product, but also is dependent on the 20 magnitude of the irradiance on the exposure time. In addition, the available modulation ran~e (i.e., the possible index of refraction change) of the photopolymerizable holographic material varies with time b~cause the diffusion mechanism and polymerization continues in the dark.
Conventional sequential multiple-exposure angle multiplexing has been demonstrated in current photopolymer formulations. HQwever the resulting diffraction efficiencies are lower than predicted for this type of exposure, possibly due to 3 0 the diffusion mechanism and its reversibility properties.
In view of the foregoing it is believed advantageous to provide a sequential exposure technique for multiplexi~ng N
holograms into a photopolymerizable holographic material which WO 92/00555 PCI`/US91/04623 s can overcome or minimize the dynamic effects of the time-dependent diffusion in the material.
-o -O-o-Conventional apparatus for forming sequential multiplexed holograms typically include a manual or automated (e.g., galvanometer controlled) mirror whereby the location and/or angie of incidence of at ieast either the object beam or the 10 reference beam on the holographic recording ma~erial may be controlled. However, the degree of control over incident beam location and/or angl~ of incidence required in the formation of sequential multiplexed holograms is not a significant factor. So long as the mirror control system is able to place the incident 15 beam within the region of the recording material dedicated to a given holographic image, the control system is sufficient for the purpose of forming sequential multiplexed holograrns. Sirnilarly, the beam positioning requirements placed on conventional apparatus for reading a sequen~ial multiplexed holo~ram are not 20 unduly stringent. So long as tho rcading beam is placed within the range of Bragg angle appropriate for the thickness of the holographic material, the angle between the object and reference beam and the wavelength of the light being used, the signal-to-noise ratio of the hologram is acceptable.
~5 For reasons that become apparent hereinafter it is believed advantageous to provide an apparatus for forming holograms in which the position of either an object or a reference beam may be repeatably and precisely controlled.
~E~
The present invention relates to a method of recording a predetermined number of holographic images into a holographic 35 recording material. The method of the present invention may be w09~00555 ~ 3~~3'7 PCI/U591/046Z3 used both for an~ularly multiplexed and for spatially multiplexed holograrns.
In accordance with the present invention each one of a set 5 of N holographic images is constructed into a predetermined defined region of the recording material in accordance with a first predetermined sequence. Each holographic image is constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the 10 ima~es. Thereafter, in accordance with a subsequent predetermined sequence, each one of a predetermined number of the set of N holographic images is constructed into the same predetermined region. Each holographic image is constructed into the predetermined defined region of the holo~raphic recording 15 material for a predetermined corresponding second imaging tirne.
A predetermined second time gap is defined between each of the images in the second sequence. Preferably, but not necessarily, th~ holographic images constructed during the second sequence includes all of the images constructed in the first sequence.
In accordance with one aspect of the invention all of the images are constructed into the same predetermined defined region of the holographic rscording rnaterial (an angle hologram).
In another aspect of the present invention the predetermined 25 defined region into which each of the N images is constructed is separate from all other regions of the holographic recording material (a spatial hologram). Altarnatively, in accordance with another aspect of the invention some of the N images may be constructed in the same region of the holographic recording 30 material and each one of the others of the N images may be constructed into spatially separate regions of the holographic recording material.
The predetermined first and secsnd imaging times are 35 preferably, but need not be, equal. The predetermined first and WO 92/005~5 PCI`/US91/04623 secand sequences are preferably, but need not be, the same. To remain within the contemplation of the invention the first and the subsequent sequences should each contain at least one common member. The predetermined first and second time gaps 5 are preferably, but need not be, equal.
In the preferred instance the holographic recording material is a photopolymerizable recording material comprising (a) a polymeric binder selected from the group consisting of cellulose 10 esters, polystyrene, stryene copolymers containing at least 60%
by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl aoetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine; (b) a iiquid 15 ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (o) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
The holographic images are recorded by construc~ing hotographic imag~s sequentially with short exposure times so that rapid in~erleaving of multiple holograms occurs. By exposing the photopolymer material in a time-multiplexed manner the recording material "sees" all of the holographic images and, due to the rapid temporal interleaving, responds to each equally with the diffusion process. By temporally interleaving the holographic images at a rate much faster than the diffusion mechanism of the photopolymer, the present invention circumvents, or at least minimizes, the problems associated with monomer flow in response to subsequent exposures and the reduction in monomer flow per unit of incident optical radiation.
-o-O-o-WO 92/00555 PCI/I)S91/04623 ~J ~ ~ r ~
In another aspect, the present invention relates to an apparatus for recording plural holographic images using the temporal interleaving method summarized above. The holographic recording apparatus in accordance with the present invention 5 includes a control arrangement whereby the angle of incid~nce of either an object beam or a reference beam on the holo~raphic recording material may be repeatably and precisely controlled.
The recording apparatus comprises means for forming an object beam and a refersnce beam and a ~alvanometer controlled mirror 10 the position of which controls the angle of incidence of at least one of the object beam and a reference bearn onto the holographic recor~ing material. A laser source and associated detector are respectively located to direct a laser beam toward the mirror and to intersect the reflection of the beam therefrom. The detector 15 is responsive to the reflected beam incident thereon to generate first and second electric currents the magnitude of aach of which is functionally related to the position on the detector at which the reflected laser beam is incident and to the power output of the laser source.
~0 The holographic recording apparatus further includes a control system for generating a galvanometer position signal to control the position of the galvanometer driven mirror ~and thereby the angle of incidence of a beam onto the holographic 2 5 recording material). The control system itself comprises means responsive to the first and the second currents for forming the ratio of the sum and difference thereof thereby to form an actual mirror position signal that is independent of the power output of the laser souroe, and an integrator responsive to the error 3 0 between the signal representative of the actual mirror position and a reference signal representative of a predetermined position of the mirror for forming the galvanometer position signal at the output thereof.
.
2~ 7 The invention will be more fully understood from the foilowing detailed description thereof, taken in connection with the accompanying drawings which form a part of this application 5 and in which:
Figures 1, 2, and 3 are highly stylized pictorial representations of various arrangements of rnultiplexed plural holographic images recorded in a predeterminled defined regions 10 of a holographic recording material by temporal interleaving in accordance with the method of the present invention;
Figures lA, 2A, and 3A are side sectional views of the holographic recording media of Figures 1, 2 and 3 taken along the 15 respective section lines therein;
Figure 4 is a schematic iilustration of an apparatus in accordance with another aspect of the present invention useful for recording multiplexed plural holographic images in 20 predetermined defined region(s) of a holographic recording material by ternporal interleaving;
Figures 5A and ~B ar~ a schematic diagram of a ratioing network and of a serYo feedback control network for a 25 galvanometer control system in accordance with the apparatus of the present invention and which are used in an apparatus for implementing the method of the present invention;
Figure 6 is a timing diagram illustration the relationship 30 between a galvanometer reference signal and a shutter timing signal used in the network of Figure 5; and Figure 7 is a schematic illustration of the holo~raphic recording material as mountsd for use in the Example.
3~ :
:
, WO 92/00555 PC~/US91/04623 5~ ~
Throughout the following detailed description sirnilar reference numerals refer to similar elements in all figures of the 5 drawings.
Referring to Figures 1, 2, and 3 shown are highly stylized pictorial representations of various arrangements of multiplexed plural holographic images I recorded in predetermined defined 10 region(s) R of a holographic recording material ~enerally indicated by the reference character H using the temporal interleaving method in accordance with the present invention, while Figures 1A, 2A, and 3A are side sectional views of the holographic recording material H of Figures 1, 2 and 3 taken along 1~ the respective section lines therein. It should be understood that a given holographic recording material H may contain more than the number of region(s) R shown in Figures 1 to 3, and that a given region R of a holographic recording material H may contain more than the number images I shown in Figures 1 to 3. Figures 1 ~0 to 3 are to be construed as being illustrative of the various possible arrangements of holographic images able to be recorded within predetermined defined region(s) of the recordin~ material H using the method of the present invention. Although any holographio recording material may be used with the method of 2 5 the present invention, a photopolymerizable holographic recording material is preferred. The composition of the photopolymerizable holographic recording material preferably used in the method of the present invention will be more fully discussed hereinafter.
Figures 1 and 1A illustrate ~he arrangement of an angularly multiplexed holographic image recorded in accordance with the present invention. An "angularly multiplexed" holographic image (or "angle hologram"), as the term is used herein, denotes the presence of at least two different holographic imag~s 11 and 12 recorded in the same predetermined defined physical region R of J~ .q~ 7 the holo~raphic material H. Forming angle holograms is most useful in volume holography, where the ~rating spacing is small with respect to the thickness af the recording material, as described in Chapter 9, Section 8 of Collier text referenced 5 earlier. For simplicity of illustration the images shown in Figures 1 through 3A are the interference pattern fringe spacing with the first image 11 being indicated in solid lines while the second image 12 is indicated by dashed lines.
Figures 2 and 2A illustrate the arrangement of a spatially multiplexed holographic image recorded in accordance with the present invention. As the term is used herein a "spatially multiplexed" holographic image (or "spatial hologram") denotes the presence of only a single holographic image within a given 15 region R of the holographic material H. Thus, as seen in Figure 2, each of the holographic images 11 and 12 is recorded in a respective predetermined defined physical region R1 and R2 of the holographic material H. The predetermined defin~d region R1 f the recording material H in which the image 11 is constructed is 20 separate from the predetermined defined region R2 of the recording medium H in whioh the image 12 is constructed. By "separate" it is moant that aven though each the predetermined defined region of the material is physlcally integral with all of the other regions in the sense that a continuous sheet of 25 holographio recording material is defined, each such region is distinct from the others on the sheet.
Combinations of angularly multiplexed and spatially multiplexed holographic images are possible. Figures 3 and 3A
3 0 illustrate the combination of angularly multiplexed holographic images 11 and 12 recorded in a predetermined defined region R1 f the recording material H while a spatially multiplexed holographic image 13 iS recorded in a separate region R2 of the holographic recording material H. It lies within the 35 contemplation of this invention to record one or more additional WO 92/0~55S PCI`/US91/04623 ~,r~.~r-r. ~')1-1 image(s) in the region R2, in effect defining angle holograms (as that term is defined herein) in each of the regions R1 and R2. It should be noted that in some instances such an arrangement has been termed in the art as "both a spatially and an anglarly S multiplexed holograml'.
-o-O-o-The method of temporal interleaving of N holographic 10 images 11 to IN into a recording material H in accordance with the present invention may now be set forth.
In accordance with a first predetermined sequence each one of a set of N holographic images is constructed into a 15 predetermined defined region R of the recording material in accordance with a first predetermined sequence. Depending upon whether an angularly or a spatially multiplexed hologram is being recorded, each image may be recorded in the same predetermined defincd rcgion of the recording matcrial (i.e., an angularly 20 multiplexed hologram, e.g., Figure 1) or each image may be recorded in a predetermined defined region that is separate from all other regions of the recording material (i.e., a spatially multiplexed hologram, e.9.t Figure 2). As discussed above, a combination of the angularly multiplexed or spatially multiplexed 25 holograms in the same reccrding material H (Figure 3) lies within ~he contempla~ion of the presen~ invention.
Each holographic image in the set of N images is constructed for a predetermined first imaging time with a 30 predet~rmined first time gap being defined between each of the images. Thereafter, in accordance with a subsequent predetermined sequence, each one of a predetermined number of the set of N holographic images is constructed into the same predetermined location into which it was constructed during the 35 first sequence. During the subsequent sequence each holographic WO 92/00555 PCI`/US91/04623 '7 t3 image is constructed into the predetermined defined region of the holographic recording material for a predetermined corresponding second imaging time. A predetermined second time gap is defined between each cf the images in the subsequent sequence.
It should be understood that the subsequent sequence may be constructed more than twice. Stated alternatively, more than two exposure sequences may be used, if desired. In general, M
number of exposure sequences may be used, where M can have any 10 convenlent value ~including being equal to N).
It lies within the contemplation of the invention that any subsequent sequence(s) of exposures may include any predetermined number (i.e., subset) of the set of N ima~es 15 constructed during the first sequence. The term "sequence" as used herein is meant to denote the order in which the rnernbers of the set of holographic images is constructed into the material. It is preferable, although not necessary, that the same order of imag0 exposure occurs during any subsequent sequence as 20 occurred in the first sequence.
It is expressly noted that in some instances a subsequent set may contain a greater number of i~nages than the first set of images. The present invention is to be construed to cover such 25 situations. Thus, temporal interleaving in accordance with the present invention may be used for the exposure of two predetermined sets of holographic images, each containing some predetermined number of images N1 and N2, respectively, so long as the first and subsequent sets of holographic images have at 30 least one m0mber in common.
In all situations the construction of an image is effected by relatively short exposures. If the recording material is a photopolymerizable recording material the timing of the 35 subsequent sequence with resp0ct to the first is soverned in WO 92J00555 P~/US91/04623 accordance with (i.e., faster than) the diffusion rate of the monomer in the material.
The method of the present invention may be more clearly 5 understood from the following typical activity schedule for its practice. A temporally interleaved exposure schedule for N
images follows, with the interleaving period T denoting the time required to expose each of the N images in the sequence.
it is assumed that each sequence of exposures contains all N
10 images. If some subset of the N images are contained within a given sequence then the periods Tp of such sequences varies (assuming uniform exposure times and gap times).
WO 92/00555 P~IUS91/04623 $Ç~lE~I~
PERIOD Tl, SEQUENCE 1 expose image 1 for imaging time t gap tg1 1 expose image 2 for imaging time t12 gap tg1 2 expose image N for imaging time t1N
gap tg 1 N
PERIOD T2, SEQUENCE
expose irnage 1 for imaging time t gap tg21 expose image 2 for imaging time t22 ~ap tg22 . . .
expose image N for imaging time ~2N
gap tg2N
~0 . ~ .
PERIOD T3, SEQUENCE 3 through PERIOD T~l, SEQUENC:E M-1 PERIOD TM- SEQUEN~E M
expose image 1 for imaging time t gap tgM1 expose image 2 for imaging time tM2 gap tgM2 expose image N for imaging time tMN
3ap tgMN
WO 92~00555 PCI'/US91/04~i23 It is understood that during the second and subsequent sequences (if any) each one of a predetermined number of the set of N holographis images is constructed into the same predetermined location into which it was constructed during 5 the first sequence.
The total imaging time for a single image k is given by M
i O ~ (tjk)-i = 1 As noted earlier, it lies within the contemplation of the invention that the imaging times for each image need not be 15 equal, the time gaps need not be equal, and/or that each sequence need not contain all of the N images in the set of holographic images. It should also be understood that either an angularly multiplexed hologram (i.e., two or more images) or an spatially multiplexed hologram (i.e., one image) may be 20 constructed in a given region R of the recording material.
-o-O-o-With reference now to Figure 4 shown is a 2 5 schematic illustration of an apparatus generally indicated by reference character 10 suitable for use in accordance with the method of the present invention for recording a plural number N of two-beam holographic images on a recording material H.
Although any holographic recording material may be used, in 30 the preferred instance the recording material H is a photopolymerizable film the details of which are fully set forth hereinafter. The apparatus 10 is able to be used to form -`
both spatially multiplexed holographic images and angularly multiplexed holographic images.
wo 92/00s5~ Pcr/US9l/o4623 . .
~?`~ 7 The apparatus 10 includes a laser source 12 which produces a beam 14. The beam 14 passes thrnugh a beam attenuator 16 and a controllable shutter 18 and is incident 5 upon a variable beam splitter 20. The beam splitter 20 bifurcates the beam 14 into an object beam path generally indicated by the chàracter 24 ancl a reference beam path generaily indicated by the character 26. Suitable for use as the source 10 is a twenty (20) Watt argon laser such as that 10 manufactured by Spectra-Physics, Inc. of Mo~ntain View, California and sold as model 2045. The attenuator is preferably implemented using a device manufactured by Newport Research Corporation, Fountain Valley, California and sold as model 935-5 Attenuator. The controllable shutter 18 15 is preferably implemented using a device manufactured by Vincent Associates, Rochester, New York, and sold as model 225L2AOZ5.
The portion of the beam turned ninety degrees by the 20 action of the beam splitter 20 propagates along the object beam path 24 through a spatial filter/collimator assembly 28A
to produce a collimated object beam indicated by the reference oharacter 30. The spatial filter/collimàtor assembly 28A is preferably implemented using a 40x microscope objective and 25 a ten micron pinhole mounted in a model 910-B spatial filter and a 63.5 mm focal length achromatic lens. These devices are all available from Newport Research Corporation.
The object bearn 30 is directed by a mirror 32 onto the 3 0 holographic recording material H. The material H is itself mechanically secured by a plateholdar schematically indicated at reference character 34 in any convenient manner. The mirror 32 is arranged such that the object beam 30 deflected from the mirror impinges on the holographic recording 35 rnaterial H at a predetermined object beam angle 36. The Wo 92~00S5~ PCl'/US91/04623 surface of the recording material H is termed herein as "the film plane~'. The object beam angle 36 is measured with respect to a normal to the ~ilm plane. To form spatially multiplexed holograms the plateholder must be able to be 5 translated in mutually orthogonal directions in the film plane.
To effect such translation an actuator generally indicated by the reference character 38 is operatively associated with the plateholder 34. The actuator 38 may be implemented in any convenient fashion, such as by manual or motorized translator 10 stages, as should be apparent to those skilled in the art.
The portion of the b0am 14 that continues through the beam splitter 20 along the reference beam path 26 is turned ninety degrees by a mirror 40 toward a spatial 15 filter/collimator assembly 28B. The spatial filter/collimator assembly 28B is similar to the assembly 28A described earlier. The collimated reference beam 42 emanating from the assembly 28B is turned by a double-sided mirror 44 mounted on a galvanometer 46. Suitable for USB as the galvanome~er 46 20 is a device manufactured by General Scanning Inc., Watsrtown, Massachusetts, and sold as model G120PD Galvo.
The reference beam 42 passes throu~h a unity angular magnification Keplerian afocal telescopic ima~ing system 48 25 that directs the reference beam 42 towards the film plane at a predetermined reference beam angle 50, also measured with respect to the normal from the film plane. The sum of the object beam angle 36 and the reference beam angle 50 defines an interbeam angle 52.
The object beam 30 and the reference beam 42 are coincident at the film plane. Since both beams 30, 42 are sufficiently coherent they produce an interference pattern, or holographic image, at the film plane. The holo~raphic image is 35 recorded in the recording material H. The cornbined action of WO 92~00S5~ $, j;, PCl`tUS91/~4623 the attenuator 16 and the variable beam splitter 20 controls the intensities of the object beam and the reference bearns 30 and 42, respectively.
Rotation the mirror 44 under control of the galvanometer 46 changes the angle at which the reference beam 42 is input to the telescopic imaging system 48. Since the reflection of the reference beam 42 from the mirror 44 is irnaged by telescopic imaging system 48 at the plane of the holographic recording material H any change in the position of the mirror 44 produces a corresponding equal change in the reference beam angle 50, assuming that the reference beam 42 remains in the aperture of the imaging system 48. The reference beam 42 remains coincident with the object beam 30 for any rotation of the mirror 44. The position of the mirror 44 under control of the galvanometer 46 thereby varies and controls the reference beam angle 50, and thus the interbeam angle 52.
An interfersnce pattern (image) suitable for recording as a holographic image is constructed at the filrn plane (the surface of the holo~raphic material H) when the shutter 18 is open. The properties of the holographic image (namely the interference fringe spacing and fringe slant) are determined by the reference beam angle 50 and the object beam angle 36.
Thus a different holographic image may be recorded in the material H by changing the reference beam angle 50.
The actual position of the mirror 44 is derived from a mirror position sensing system generally indicated at reference character 56. The mirror position. sensing system 56 includes a laser source 58 and an associated detector 60.
The source 58 and the detector 60 are respectively located to direct a laser beam 58B toward the undersurface of the mirror 44 and to intersect the reflected beam 58R therefrom. The 3 5 suitable biased detector 60 is responsive to the reflected WO 92/005~i~ PCI'/US91/04623 $~
beam 58R incident thereon to generate first and second electric currents (i1 and i2, respectively) on lines 62A, 62B.
The magnitude of the signals on the lines 62A, 62B is functionally related to the position on the detector 60 at 5 which the reflected laser beam 58R is incident and also to the power output of the laser source. Suitable for use as the laser 58 is the HeNe laser device formerly manufactured by Hughes Aircraft Corporation, of Carlsbad, California and sold as 3221H-C 5 mW. Equivalent equipment is now believed 10 available from Melles Griot of Irvine, California. The detector 60 is preferably implemented by a linear position sensor such as that manufactured and sold by Quantrad Incorporated of Los Angeles, California as model PS-100-50.
Rotation of the galvanometer 46 is controlled by a galvanometer drive signal carried on a line 64 from a galvanometer position controller generally indicated by the reference character 66. The controller 66 is shown in more detail in Figures 5A and 5B. The controller 66 is responsive to 20 the signals applied thareto on the lines 62A, 62B (which eontain information as to the actual position of the mirror 44) and to a reference signal carried on a line 58 to generate the ~alvanometer drive signal on the line 64. As will be developed, the controller 66 permits the repeatable and accurate 2 5 positioning of the mirror 44 whereby temporal interleaving of holographic images in accordance with the present method may be effected.
The controller 66 itself includes means generally indicated 30 at reference character 70 (shown in Figure 5A) responsive to the first and the second currents i1 and i2 for forming the ratio of the sum and difference thereof. The ratio is implemented using a - ratio module such as that sold by Burr-Brown Inc. of Tucson, Arizona as model number DIV100. This ratio action forms on a 35 line 72 an actual mirror position signal that is independent of the WO 92/00555 ~2lr~ ~rli(r~7 PC~/US91/04623 power output.of the laser source 58. It is noted that the signal on the line 72 is also independent of any thermal responses of the detector 60.
As seen in Figure 5B, a module 74 within the controller 66 subtracts the actual mirror position signal 72 from the reference position signal on the line 68 to produce an error signal at a summing junction J. An integrator oircuit 75 ~Fi~ure 5B) produces a galvanometer position control signal at the output point K thereof. After dynamic response compensation in an amplifier 76 the galvanometer position control signal is inpu~ to the galvanometer servo amplifier 77 which produces the galvanometer drive signal on the line 64.
The integrator 75 serves to maintain at least some drive voltage level to the amplifier 76 during those times when the galvanometer error signal (point J) is zero, thus maintaining the galvanometer 46 in the position that generates the zero positlon error.
2 0 The shutt~r 18 is controlled eiectronically by a shutter control signal applied on a line 79 from a shutter controller 78. Suitable for use as the shutter eontroller 7~ is the device manufactured by Vincent Associates and sold as Model SD-10 Shutter Drive/Timer. The input timing signal to the shutter controller 78 is a timing pa~tern applied over a line 80 (typically at a standard logic level of five Volts) which controls the stat~ of ~he shutter 18, i.e., whether the shutter 18 is open or closed.
If the number of holographic images N is two the galvanometer reference signat 68 and the timing signal 80 may be generated using a square wave generator 84 and a pulse 3enerator 86. Suitable for use as the square wave ge~nerator 84 is the device manufactured by Textronix, Beaverton, Oregon 35 and sold as model FG502 while the pulse generator 86 may be WO 92/~0555 o'~ PCI`/US91tO4623 implemented using a device manufactured by Hewlett-Packard, Palo Alto, California and sold as model 811~A Pulse Generator.
The square wave output is applied as the galvanometer 5 reference signal on the line 68 and moves the galvanometer 46 ~and thus the mirror 44), as described earlier. The square wave signal from the generator 84 is also used as the pulse generator trigger applied over a line 88 to the pulse generator 86. The pulse generator 86 triggers on both the positive and 10 negative transitions of the square wave trigger signal 88, triggering one pulse during each image position (one half of the square wave). The output of the pulse generator 86 forms the shutter timing signal 80. The assertion of the shutter control signal on the iine 79 in response to the input timing signal on 15 the line 80 serves to open the normally closed shutter 18, thereby causing an image exposure to occur in the holographic recording material H. The duration of each pulse on the line 79 is equal to tjj. The relationship of the waveforms of a galvanometor reference signal 68 and a shutter timin~ signal 20 80 is shown in Figure 6 for an N equals 2 image embodiment.
It shouid be readily apparen$ to those skilled in the ar~
that the galvanometer re~erence signal on the line 68 and the shutter timing signal on the 80 may be generated by a 25 computer system, other conventional instrumentation, or any other convenient arrangement. For example, if N is greater than two, a microprocessor based system could drive, under program control, a plurality of digital-to-analog converters to provicle the N shutter timing signals on the line 80. The 30 microprocessor based system also can be used to expeditiously provide the galvanome$er reference signal on the line 68.
Moreover, if a spatially multiplexed hologram is being prep~red, the microprocessor based system could also be used to provide appropriate indexing signals to the actuator~s) 38 3 5 associated with the plateholder 34.
WO 92/00555 PCl/US91/04623 ~r~~3);j~
It should thus be appreciated from the foregoing that by providing the appropriate electronic galvanometer reference signal on the line 68 and the appropriate shutter timing signal 5 80 any sequence of holographic exposures, exposure times, an gap times between exposures may be implemented using the apparatus 10. The apparatus 10 described above is suitable for practicing the method of the pres~nt invention whereby a predetermined number N of spatially and/or angularly 10 multiplexed holographic images may be recorded into the holographic recording material H. The N difFerent angularly multiplexed holographic images may be formed at the film plane when the mirror 44 is rotated by the action of the galvanometer 46 to each of N different positions. Spatially 15 multiplexed holograms are recorded in separate regions of the material H in accordance with the translations effected by the actuator 38.
I~, as preferred, a photopolymeric holographic recording 20 material H is usad to record the N multipiexed holographic images, temporal interleaving in accordance with the present invention overcomes the dynamic effects of the grating formation time-dependent diffusion process in the film, ~nd records N hologram images in a repetitive sequential fashion.
25 The sequence periods Tp are made shorter than the diffusion mechanism in the material, thus minimizing undesired effects obtained with conventional sequential exposure of N
holograms. This method avoids crosstalk effeots of simultaneous exposure and the difficulty of generating N
3 0 reference beams sirnultaneously.
Alternate embodiments of the apparatus 10 which one skilled in the art may easily implement include, among others:
1) spatial madulation of the object beam 30 and/or reference 35 beam 42; 2) nonplanar wavefronts in the object beam path 30 WO 92/00555 PCT/US91/0~S623 f . ~.-~C..9~ 4 and/or the reference beam path 42, (e.g. the object beam 30 is a converging spherical wavefront focusing at the film plane forming a Fourier transform hologram); 3) angle adjustment for the object beam 30,as for example, using the controller 66 5 as shown in Figures 5A and 5B; 4) angle adjustment for the film plane; and 5) non-unity angular magnification in imaging system 48.
-o-O-o-The photopolymerizable materials used herein are thermoplastic compositions that upon exposure to aotinic radiation form crosslinks or polymers of high molecular weight to change the refractive index and rheological character of the composition (s). Preferred 15 photopolymerizable materials are photopolymerizable compositions, such as disclosed in United States Patent 3,658,526 (Haugh) and more preferred materials are described copending application Serial Numbers 07/144,355, 07/144,281 and 07/144,840, all filed January 15, 1988 and all assigned to Z0 E. I. du Pont de Nemours and Company, Incorporated. In these - materials, free radical addition polymerization and crosslinking sf a compound containing one or more ethylenically unsaturated groups, usually in a lerminal position, hardens and insolubilizes the cornposition. The 25 sensitivity of the photopolymerizable composition is enhanced by the photoinitiating system which may contain a component which sensitizes the composition to predetermined radiation sources, e.g., visible light. Conventionally a binder is the most significant component of a substantially dry 30 photopolymerizable base or layer in terms of what physical properties the base or layer will have while being used in the invention. The binder serves as a containing medium for the monomer and photoinitiator prior to exposure, provides the base line refractive index, and after exposure contributes to 3 5 the physical and refraGtive index characteristics needed for .
WO 92/00555 PCI'/US91/04623 '7 the base layer or buffer layer. Cohesion, adhesion, flexibility, diffusibility, tensile strength and index of refraction are some of the many properties which determine if the binder is suitable for use in the base layer.
Photopolymerizabie materials contemplated to be equivalent are photodimerizable or photocrs)sslinkable compositions such as disclosed in United States Patent 3,526,504 ~Celeste) or those compositions in which hardening 10 is achieved by a mechanism other than the free radicai initiated type identified above.
The photopolymerizable material is composed of three rnajor components, a solid solvent-soluble preformed 15 polymeric material, at least one liquid ethylenically unsaturated monomer capable of addition polymerization to produce a polymeric material with a refractive index substantially different from that of the preformed polymeric material, or binder, and a photoinitiator system activatable by 20 actinic radiation. Although the base or layer is a solid composition, components interdiffuse before, during and after imaging exposure until they are fixed or destroyed by a ~inal uniform treatment usually by a further uniform exposure to actinic radiation. Interdiffusion may be further promoted by 2 6 incorporation into the composition of an otherwise inactive plasticizer.
In addition to the liquid rnonomer, the composition may contain solid monomer components capable of interdiffusing in 30 solid composition and reacting with the liquid monomer to form a copolymer with a refractive index shifted from that of the binder.
In the preferred compositions for use in this invention, 35 the preformed polymeric material and the liquid monomer are WO 92/00555 PCS/US91/046~3 r~ ~~ r~ r- . t ~t selected so that either the preformed polymeric material or the monomer contains one or more moieties taken frorn the group consisting essentially of substituted or unsubstituted phenyl, phenoxy, naphthyl, naphthyloxy, heteroaromatic grcups 5 containing one to three aromatic rings, chlorine, and bromine and wherein the remaining component is substantially free of the specified moieties. in the instance when the monomer contains these moieties, the photopolymerizable system hereinafter is identified as a"Monomer Oriented System" and 10 when the polymeric material contains these moieties, the photopolymerizable system hereinafter is identified as a "Binder Oriented System."
The stable, solid, photopolymerizable compositions 15 preferred for this invention will be more fully described by reference to the "Monomer Oriented System" and "Binder Oriented System."
The monomer of the Monomer Oriented System is a liquid, 2 0 ethylenically unsaturated compound capable of addition polymerization and having a boiling point above 100C. The monomer contains either a phenyl, phenoxy, naphthyl, naphthoxy, heteroaromatic group containing one to thr~e aromatic rings, chlorine or bromine. The monomer contains at 25 least one such moiety and rnay contain two or more of the same or different moieties of the group, provided the monomer remains liquid. Contemplated as equivalent to the groups are substituted groups where the substitution may be lower alkyl, alkoxy, hydroxy, carboxy, carbonyl, amino, amido, imido or 30 combinations thereof provided the monomer remains liquid and diffusable in the photopolymerizable layer.
Preferred liquid monomers for use in the Monomer Oriented System of this invention are 2-phenoxyethyl acrylate, 3 5 2-ph~noxyethyl methacrylate, phenol ethoxylate acrylate, 1-WO 92/005~5 PCI/US91/0~623 27(p-chlorophenoxy) ethyl, p-chlorophenyl acrylate, phenyl acrylate, 1-phenylethyl acrylate, di(2-acryloxyethyl) either of bisphenol-A, and 2-(2-naphthyioxy) ethyl acrylate.
While rnonomers useful in this invention are liquids, they may be used in admixture with a second solid monomer of the same type, e.g., N-vinyl-carbzole, ethylenically unsaturated carbazole monomers such as disclosed in ~Q~naLQ~Q~m~
__ , Vol.. 18, pp. 9-18 (1979) 10 by H. Kamagawa et al., 2-naphthyl acrylate, penta-ohlorophenyl acrylate, 2,4,6-tribromophenyl acrylate, and bisphenol A
diacrylate, 2-(2-naphthyloxy) ethyl acrylate, and N-phenyl maleimide.
.
The solvent soluble polymeric material or binder of the Monomer Oriented System is substantially free of phenyl, phenoxy, naphthyl, naphthyloxy, heteroaromatic group containing one to three aromatic rings, chlorine and bromine.
Preferred binders for use in the Monomer Oriented System of this invention are cellulosa acetate butyrate polymers; acrylic polymers and inter polyrners including polymethyi m~thacrylate, methyl methacrylate/methacrylic aoid and methyl methacrylate/acrylio acid copolymers, terpolymers of methylmethacrylate/C2-C~ alkyl acrylate or methacrylate/acrylic or methacrylic acid; polyvinyl-acetate;
polyvinyi acetal, polyvinyl butyral, polyvinyl formal; and as well as mixtures thereof.
The monomer of the Binder Oriented System is a liquid ethylenically unsaturated compound capable of addition polymerization and having a boiling point above 100C. The monomer is substantially free of moieties taken from~the group consistin~ essentially of phenyl, phenoxy, naphthyl, WO 92/û0555 PCI/US91/04623 '7 naphthyloxy, heteroaromatic group containing one to three arornatic rings chlorine and bromine.
Preferred liquid monomers for use in Binder Oriented 5 Systems of this invention include decanediol diacrylate, iso-bornyl acrylate, triethylene glycol diacrylate, diethyleneglycol diacrylate, triethylene glycol dimethacrylate, ethoxyethoxyethyl acrylate, triacrylate ester of ethoxylated trimethylolpropane, and 1-vinyl-2-pyrrolidinone.
While monomers used in Binder Oriented Systems are liquids, they may be used in admixture with a second solid - monomer of the same type, e.g., N-vinyl-caprolactam.
The solvent soluble polymeric material or binder of the Binder Oriented System contains in its polymeric structure rnoieties taken from the group consisting essentially of phenyl, phenoxy, naphthyl naphthyloxy or heteroaromatic group containing one to three aromatic rings as well as chloro or 20 bromo atoms. Contemplated as equivalent to the groups are substituted groups where the substitution may be lower alkyl, alkoxy, hydroxy, carboxy, carbonyl, amido, imido or combinations thereof provid~d the binder remains solvent soluble and thermoplastic. The moieties may form part of the 2~ monomeric units which constitute the polymeric binder or may be grated onto a prepared polymer or interpolymer. The binder of this type may be a homopolymer or it may be an interpolymer of two or more separate monomeric units wherein at least one of the munomeric units contains one of 3 0 the moieties identified above.
Preferred binders for use in the Binder Oriented System include polystyrene, poly (styrene/acrylonitrile), poly (styrene/methyl methacrylate), and polyvinyl benzal as well as 35 admixtures thereof.
WO 92/00555 PCI`/US91/04623 The same photoinitiator system activatable by actinic radiation may be used in either the Monomer Oriented System or the Binder Oriented System. Typically ~he photoinitiator system will contain a photoinitiator and may contain a sensitizer which ex~ends the spectral response into the near U. V. region and the visible spectral regions.
Preferred photoinitiators include CDM-HABI, i.e., 2-(o-1 O chlorophenyl)-4, 5-bis~m.-methoxyphenyl)-imidazole dimer; Q-Ci-HABI, i.e., 1,1'-Biimidazole, 2,2'-bis-(p-chlorophenyl)-4,4', 5,5'-tetraphenyl-; and TCTM-HABI, i.e., 1 H-lrni~azole, 2,5-bis(o-chlorophenyl~-4-3,4-dimethoxypheny!-, dimer each of which is typically used with a hydrogen donor, e.g., 2-1 5 mercapto-benzoxazole.
Preferred sensitizers include the following:
DBC, i.~., Cyclopentanone, 2,5-bis-((4-(diethylamino)-2-methylphenyl)methylene);
DEAW, i.e., Cyclopentanone, 2,5-bis-((4-(diethylamino)-phenyl)methylene); and Dimsthoxy-JDI, i.e., 1 H-lnden-1-one, 2,3-dihydrv-5,6-dimethoxy-2((2,3,6,7-tetrahydro-l H,5H-benzo~i,j]quinolizin-9-yl)-methylene)-.
JAW, i.e., 2,5-bis [2,3,6,7-tetrahydro (1 H, 5H-benzo[i,j,]quinolizin-9-yl~ methylene]-cyclopentanone .
3 0 Ths solid photopolymerizable compositions of this invention may contain a plasticizer. Plasticizers of this invention may be used in amounts varying from about /O to about 20% by weight of the compositions preferably 5~to l~
wt.%.
3~
WO 92/00555 PCT/lJS91/04623 Preferred plasticizers for use in simple cellulose acetate butyrate systems are triethyleneglycol dicaprylate, tetraethyleneglycol diheptanoate, diethyl adipate, Brij~30 and tris-(2-ethylhexyl)phosphate. Similarly, triethyleneglycol 5 dicaprylate, diethyl adipate, Brij~30, and tris-(2-ethylhexyl)phosphate are preferred in "Monomer Oriented Systems" where cellulose acetate butyrate is the binder.
Other components in addition to those described above 10 can be present in the photopolymerizable compositions in varying amounts. such components include: ultraviolet radiation absorbing material, thermal stabili~ers, hydrogen donors, oxygen scavengers and release agents.
Amounts of ingredients in the photopolymerizable compositions will generally be within the following percentage ranges based on total weight of the photopolymerizable layer; monomer, 5-50%, pre~erably 15-35%; initiator 0.1-10%, preferably 1-5%; binder, 25-75%, 2 0 preferably 45-65%; plasticizer, ~-25%, pre~erably 5-15%;
other ingredients 0-5%, pre~erably 1-4%.
~x~eL~
The holographic recording material as used in this example used a coating emulsion that had the ingredients as Iisted in the following Table 1:
TABL~ 1 3 ~n~r~sli~
Cellulose acetate butyrate, 51.90 Eastman type CAB 531-1 Ethoxylated pheno~ acrylate 26.93 3 5(Photomer 4039~
WO 92/0055~ P~/US9l/04623 9-Vinylcarbazole (NVC) 6.00 Ethoxylated bisphenol A diacrylate 9.97 (Sartomer 349) 4-Methyl-4H-1,2,4-triazole-3-thiol 2.52 (MMT) Q-CI HABI (1,1'-Biimidazole, 2,2'-bis- 2.48 (Q-chlorophenyl)-4,4', 5,5'-tetraphenyl; CAS 1707-68-2 Fluorocarbon coating aid, 0.10 Fluorad FC-430 (3M Inc.) JAW dye 2,5-bis [2,3,6,7-tetrahydro 0.10 (1 H, 5H-benzo[i,j,]quinolizin-9-yl) methylene]-cyclopentanone.
Figure 7 shows a holographic recording material comprising a thirty-eight (38j micron photopolymer emulsion 90 ~ingredients given in Table 1) coated onto a 50.8 micron optical grade base 92 formed from a polyester film such as that manufactured and sold by E.l. Du Pont de Nemours and 20 Company under the trademark Mylar~. The coating was cast from solvent (95% methylcne chloride, 5% methanol) and the coatin~ solution was 25% by weight emulsion, 75% solvent.
The emulsion and base were laminated onto a 2" x 2" x 1/8 inch float glass plate 94, forming a glass-photopolymer-base 25 sandwich as shown in Figure 7. The plate was mounted in the plate holder 34 at the film plane with the base facing ~he incident beams. Th~ experiment was performed under red safelight in the nonsensitive spectrum of the photopolymer.
The optical wavelength used for holographic image exposure was 514.5 nanometers generated by an Argon ion laser 12 with an intercavity etalon for single frequency operation. The power density of each of the respective reference an~ o~ject beams 30 and 42 was approximately 3 5 eighty (80) milliWatts per square centimeter.
Table 2 iists the results for nine (9) samples of multiplexing holographic images by temporal interleaving. For each sample, two holographic images (N = 2) were multiplsxed 5 by temporal interleaving with sequence period, imaging, and gap times as indicated in Table 2. The reference and object beams 30 and 42 were each about five (5) millimeters in diameter. The plateholder was translated during the experiment to fit several multiplexed holograms onto the 2" x 10 2" plate. The experiment beam angles: object beam angle 36 -about fifteen (15) degrees; reference beam angle 50 of about 8.25 degrees for image j = 1 (galvanorneter mirror 44 directing the reference beam 42 at Position A in Figure 4) and 21.75 degrees for image j = 2 (Position B in Figure 4).
WO 92/00555 PCr/US91104623 ~L~Z
HOL~GRAM IMAGING G~PSE~JE~:E NUMBER OF DIFFRACTION
SAMPLE TIME TIME PERIODPERIODS EFFICIENCY.
NUMBER ( % ) tjj (msec) tgjj (msec)Tp (sec) M image 1 image 2 5 0 0 1 000 3 5 9.3 1~
2 250 1250 3 10 9.6 22 3 100 1 400 3 20 1~ 27 4 500 1 000 3 10 9.3 16 7 250 750 2 10 9.1 16 9 400 600 2 5 8.4 20 After imaging, the holograms were fixed by turning on room lights and exposing the photopolymer plate to a Hg lamp for approximately ten ~10) minutes. The plate was reinserted 20 into the appara~us identical to exposure. The obj~ct beam 30 was blocked and the dlffraction efficiency was measured by reconstruoting the mllltiplexed holograrns with the reference beam 42 at incident angles corresponding to image j = 1 (Position A) and image j - 2 (Position B). The diffraction 25 efficieney was calculated as the detected power measured in the first-order diffracted reconstruction of the object beam, divided by the sum of the detected first-order and zero-order (undiffracted from reference beam~ powers.
3 0 The diffraction efficiencies reported for the nine (9) samples show that temporal interleaving is effective over a range of exposure parameteYs (imaging time, gap time, sequence, etc.), and that changes in those parameters will affect the resul~s. No optimization of these parameters was performed in the experiments reported here, but it is exp~sted WO 92/005S5 PCI`/US91/04623 J~;~ 7 that optimization is important for achieving the best possible results. Given the maximum possible refractive index modulation for the recording material used, the maximum diffraction efficiencies for the irnages in the samples are 5 expected in the range of 30%-45%. The results obtained could be improved by optimizing the exposure parameters and other aspects of the experiment (in particular, the plate should be mounted such that the glass side of the plate faces the incident beams to eliminate the effect of base birefringence).
The results show that the temporal interleaving method is useful for multiplexing holograms, and works well for dynamic media such as a holographic photopolymeric recording mate rial .
1 ~
Those skilled in the art, having the benafit of the teachings of the present invention may impart numerous modifications thereto, it should be understood that such modifications lie within the contemplation of the present invention, as defined by 20 the appended claims.
Claims (89)
1. A method of recording a predetermined number N of holographic images into a holographic recording material, the method comprising the steps of:
(a) constructing each one of a first set of holographic images into a predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, constructing each one of a subsequent set of holographic images into the predetermined defined region of the holographic recording material, each holographic image in the subsequent set being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images, the first and subsequent sets of holographic images having at least one member in common.
(a) constructing each one of a first set of holographic images into a predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, constructing each one of a subsequent set of holographic images into the predetermined defined region of the holographic recording material, each holographic image in the subsequent set being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images, the first and subsequent sets of holographic images having at least one member in common.
2. The method of claim 1 wherein all of the images are constructed into the same predetermined defined region of the holographic recording material.
3. The method of claim 1 wherein the predetermined defined region into which each of the N images is constructed is separate from all other regions of the holographic recording material.
4. The method of claim 1 wherein some of the N images are constructed in the same physical region of the holographic recording material and each one of the others of the N images are constructed in spatially separate regions of holographic recording material.
5. The method of claim 4 wherein all of the holographic images in the first set are included in the subsequent set.
6. The method of claim 3 wherein all of the holographic images in the first set are included in the subsequent set.
7. The method of claim 2 wherein all of the holographic images in the first set are included in the subsequent set.
8. The method of claim 1 wherein all of the holographic images in the first set are included in the subsequent set.
9. The method of claim 8 wherein the sequence of the images in the first set is identical to the sequence of the images in the subsequent set.
10. The method of claim 7 wherein the sequence of the images in the first set is identical to the sequence of the images in the subsequent set.
11. The method of claim 6 wherein the sequence of the images in the first set is identical to the sequence of the images in the subsequent set.
12. The method of claim 5 wherein the sequence of the images in the first set is identical to the sequence of the images in the subsequent set.
13. The method of claim 4 wherein the predetermined first and second gap times are equal.
14. The method of claim 3 wherein the predetermined first and second time gaps are equal.
15. The method of claim 2 wherein the predetermined first and second time gaps are equal.
16. The method of claim 1 wherein the predetermined first and second time gaps are equal.
17. The method of claim 4 wherein the predetermined first and second imaging times are equal.
18. The method of claim 3 wherein the predetermined first and second imaging times are equal.
19. The method of claim 2 wherein the predetermined first and second imaging times are equal.
20. The method of claim 1 wherein the predetermined first and second imaging times are equal.
21. The method of claim 4 further comprising the step of repeating step (b) a predetermined number of times.
22. The method of claim 3 further comprising the step of repeating step (b) a predetermined number of times.
23. The method of claim 2 further comprising the step of repeating step (b) a predetermined number of times.
24. The method of claim 1 further comprising the step of repeating step (b) a predetermined number of times.
25. The method of claim 4 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
26. The method of claim 4 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
27. The method of claim 3 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
28. The method of claim 3 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
29. The method of claim 2 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
30. The method of claim 2 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
31. The method of claim 1 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
32. The method of claim 1 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
33. The product of the process of claim 24.
34. The product of the process of claim 23.
35. The product of the process of claim 22.
36. The product of the process of claim 21.
37. The product of the process of claim 4.
38. The product of the process of claim 3.
39. The product of the process of claim 2.
40. The product of the process of claim 1.
41. A method of recording a predetermined number N of holographic images into a holographic recording material, the method comprising the steps of.
(a) in accordance with a first predetermined sequence, constructing each one of a set of N holographic images into a predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, in accordance with a subsequent predetermined sequence, constructing each one of a predetermined number of the set of N holographic images into the predetermined defined region of the holographic recording material, each holographic image in the subsequent sequence being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
(a) in accordance with a first predetermined sequence, constructing each one of a set of N holographic images into a predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, in accordance with a subsequent predetermined sequence, constructing each one of a predetermined number of the set of N holographic images into the predetermined defined region of the holographic recording material, each holographic image in the subsequent sequence being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
42. The method of claim 41 wherein all of the images are constructed into the same predetermined defined region of the holographic recording material.
43. The method of claim 41 wherein the predetermined defined region into which each of the N images is constructed is separate from all other regions of the holographic recording material.
44. The method of claim 41 wherein some of the N images are constructed in the same physical region of the holographic recording material and each one of the others of the N images are constructed in spatially separate regions of holographic recording material.
45. The method of claim 44 wherein the predetermined number of the set of N holographic images constructed during the subsequent sequence is equal to N.
46. The method of claim 43 wherein the predetermined number of the set of N holographic images constructed during the subsequent sequence is equal to N.
47. The method of claim 42 wherein the predetermined number of the set of N holographic images constructed during the subsequent sequence is equal to N.
48. The method of claim 41 wherein the predetermined number of the set of N holographic images constructed during the subsequent sequence is equal to N.
49. The method of claim 48 wherein the subsequent sequence is identical to the first sequence.
50. The method of claim 47 wherein the subsequent sequence is identical to the first sequence.
51. The method of claim 46 wherein the subsequent sequence is identical to the first sequence.
52. The method of claim 45 wherein the subsequent sequence is identical to the first sequence.
53. The method of claim 44 wherein the predetermined first and second gap times are equal.
54. The method of claim 43 wherein the predetermined first and second time gaps are equal.
55. The method of claim 42 wherein the predetermined first and second time gaps are equal.
56. The method of claim 41 wherein the predetermined first and second time gaps are equal.
57. The method of claim 44 wherein the predetermined first and second imaging times are equal.
58. The method of claim 43 wherein the predetermined first and second imaging times are equal.
59. The method of claim 42 wherein the predetermined first and second imaging times are equal.
60. The method of claim 41 wherein the predetermined first and second imaging times are equal.
61. The method of claim 44 further comprising the step of repeating step (b) a predetermined number of times.
62. The method of claim 43 further comprising the step of repeating step (b) a predetermined number of times.
63. The method of claim 42 further comprising the step of repeating step (b) a predetermined number of times.
64. The method of claim 41 further comprising the step of repeating step (b) a predetermined number of times.
65. The method of claim 44 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
66. The method of claim 44 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing a least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing a least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
67. The method of claim 43 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
68. The method of claim 43 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
69. The method of claim 42 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
70. The method of claim 42 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
71. The method of claim 41 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
72. The method of claim 41 wherein the holographic recording material is a photopolymerizable holographic recording material comprising:
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
(a) a polymeric binder selected from the group consisting of cellulose esters, polystyrene, stryene copolymers containing at least 60% by weight styrene, polymethyl methacrylate, polyvinylbutryal, polyvinylformal, polyvinyl acetate and copolymers of vinyl acetate with tetrafluoroethylene and hexafluoropropylene containing up to about 25% by weight fluorine;
(b) a liquid ethylenically unsaturated monomer, the monomer being capable of free-radical initiated addition polymerization; and (c) a photoinitiator system that activates polymerization of said unsaturated monomer on exposure to actinic radiation.
73. The product of the process of claim 64.
74. The product of the process of claim 63.
75. The product of the process of claim 62.
76. The product of the process of claim 61.
77. The product of the process of claim 44.
78. The product of the process of claim 43.
79. The product of the process of claim 42.
80. The product of the process of claim 41.
81. A method of recording a predetermined number N of holographic images into a predetermined region of a holographic recording material, the method comprising the steps of:
(a) in accordance with a first predetermined sequence, constructing each one of a set of N holographic images into the same predetermined defined region of the holographic recording material, each holographic image being constructed into the predetermined region for a predetermined corresponding first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, in accordance with a second predetermined sequence, constructing each one of the set of N holographic images into the same predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
(a) in accordance with a first predetermined sequence, constructing each one of a set of N holographic images into the same predetermined defined region of the holographic recording material, each holographic image being constructed into the predetermined region for a predetermined corresponding first imaging time with a predetermined first time gap being defined between each of the images; and (b) thereafter, in accordance with a second predetermined sequence, constructing each one of the set of N holographic images into the same predetermined defined region of the holographic recording material, each holographic image being constructed for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
82. The method of claim 81 wherein the predetermined first and second imaging times are equal.
83. The method of claim 81 wherein the predetermined first and second time gaps are equal.
84. The method of claim 81 further comprising the step of repeating step (b) a predetermined number of times.
85. A method of recording a predetermined number N of holographic images into a holographic recording material, the holographic recording material having a corresponding number N
of regions, the method comprising the steps of:
(a) in accordance with a first predetermined sequence, constructing each one of the set of N holographic images into a respective region of the recording material, each image being constructed for a predetermined corresponding first imaging time with a predetermined first time gap being defined between each of the images, and (b) thereafter, in accordance with a second predetermined sequence, constructing each one of the set of N holographic images into the holographic material, each image being constructed into the respective region into which it was constructed during the first sequence for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
of regions, the method comprising the steps of:
(a) in accordance with a first predetermined sequence, constructing each one of the set of N holographic images into a respective region of the recording material, each image being constructed for a predetermined corresponding first imaging time with a predetermined first time gap being defined between each of the images, and (b) thereafter, in accordance with a second predetermined sequence, constructing each one of the set of N holographic images into the holographic material, each image being constructed into the respective region into which it was constructed during the first sequence for a predetermined corresponding second imaging time with a predetermined second time gap being defined between each of the images.
86. The method of claim 85 wherein the predetermined first and second imaging times are equal.
87. The method of claim 85 wherein the predetermined first and second time gaps are equal.
88. The method of claim 85 further comprising the step of repeating step (b) a predetermined number of times.
89. Apparatus for recording a predetermined number N of holographic images into a predetermined region of a holographic recording material, the apparatus comprising:
means for forming an object beam and a reference beam;
a galvanometer controlled mirror for controlling the position of incidence of at least one of the object beam and a reference beam onto the holographic recording material;
a laser source and associated detector respectively located to direct a laser beam toward the mirror and to intersect the reflection of the beam therefrom, the detector being responsive to the reflected beam incident thereon to generate first and second electric currents the magnitude of each of which is functionally related to the position on the detector at which the reflected laser beam is incident and to the power output of the laser source; and a control system for generating a galvanometer position signal to control the position of the galvanometer driven mirror, the control system itself comprising:
means responsive to the first and the second currents for forming the ratio of the sum and difference thereof thereby to form an actual mirror position signal that is independent of the power output of the laser source, and an integrator responsive to the error between the signal representative of the actual mirror position and a reference signal representative of a predetermined position of the mirror for forming a galvanometer position control signal at the output thereof.
means for forming an object beam and a reference beam;
a galvanometer controlled mirror for controlling the position of incidence of at least one of the object beam and a reference beam onto the holographic recording material;
a laser source and associated detector respectively located to direct a laser beam toward the mirror and to intersect the reflection of the beam therefrom, the detector being responsive to the reflected beam incident thereon to generate first and second electric currents the magnitude of each of which is functionally related to the position on the detector at which the reflected laser beam is incident and to the power output of the laser source; and a control system for generating a galvanometer position signal to control the position of the galvanometer driven mirror, the control system itself comprising:
means responsive to the first and the second currents for forming the ratio of the sum and difference thereof thereby to form an actual mirror position signal that is independent of the power output of the laser source, and an integrator responsive to the error between the signal representative of the actual mirror position and a reference signal representative of a predetermined position of the mirror for forming a galvanometer position control signal at the output thereof.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/546,179 | 1990-06-29 | ||
US07/546,179 US5543251A (en) | 1990-06-29 | 1990-06-29 | Method of recording plural holographic images into a holographic recording material by temporal interleaving |
US07/546,180 US5098176A (en) | 1990-06-29 | 1990-06-29 | Apparatus for recording plural holographic images into a holographic recording material by temporal interleaving |
US07/546,180 | 1990-06-29 |
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Publication Number | Publication Date |
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CA2085587A1 true CA2085587A1 (en) | 1991-12-30 |
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ID=27068141
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA 2085587 Abandoned CA2085587A1 (en) | 1990-06-29 | 1991-06-28 | Method of recording plural holographic images into a holographic recording material by temporal interleaving |
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Country | Link |
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EP (1) | EP0536314A4 (en) |
JP (1) | JPH05509418A (en) |
CA (1) | CA2085587A1 (en) |
WO (1) | WO1992000555A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2130632C1 (en) * | 1992-11-27 | 1999-05-20 | Фоксел | Method and device for manufacturing holograms |
US5672448A (en) * | 1992-12-29 | 1997-09-30 | Nippondenso Co., Ltd. | Multi-exposure system for hologram |
JP4534516B2 (en) * | 2004-02-18 | 2010-09-01 | ソニー株式会社 | Hologram recording / reproducing device |
WO2024005139A1 (en) * | 2022-06-30 | 2024-01-04 | 三菱ケミカル株式会社 | Method for producing optical element |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE755251A (en) * | 1969-08-25 | 1971-02-25 | Du Pont | HOLOGRAPHIC RECORDING IN PHOTOPOLY-MERISABLE LAYERS |
US3572882A (en) * | 1969-11-28 | 1971-03-30 | Us Air Force | Variable reference phase holocamera to compensate for object motion |
US4859548A (en) * | 1985-11-04 | 1989-08-22 | Gerhard Heise | Method for generating a lattice structure with a phase shift on the surface of a substrate |
US4942112A (en) * | 1988-01-15 | 1990-07-17 | E. I. Du Pont De Nemours And Company | Photopolymerizable compositions and elements for refractive index imaging |
US4889780A (en) * | 1988-03-14 | 1989-12-26 | Hughes Aircraft Company | Multiple exposure hologram for minimizing crosstalk |
-
1991
- 1991-06-28 CA CA 2085587 patent/CA2085587A1/en not_active Abandoned
- 1991-06-28 JP JP3512303A patent/JPH05509418A/en active Pending
- 1991-06-28 EP EP19910913478 patent/EP0536314A4/en not_active Withdrawn
- 1991-06-28 WO PCT/US1991/004623 patent/WO1992000555A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO1992000555A1 (en) | 1992-01-09 |
EP0536314A4 (en) | 1993-12-08 |
EP0536314A1 (en) | 1993-04-14 |
JPH05509418A (en) | 1993-12-22 |
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