EP0870623A1 - Recording material for receiving water-based inks - Google Patents
Recording material for receiving water-based inks Download PDFInfo
- Publication number
- EP0870623A1 EP0870623A1 EP98105981A EP98105981A EP0870623A1 EP 0870623 A1 EP0870623 A1 EP 0870623A1 EP 98105981 A EP98105981 A EP 98105981A EP 98105981 A EP98105981 A EP 98105981A EP 0870623 A1 EP0870623 A1 EP 0870623A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- epoxy
- recording material
- water
- receiving layer
- layer
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 20
- 239000000976 ink Substances 0.000 title description 17
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 23
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 21
- 238000001035 drying Methods 0.000 claims abstract description 16
- 238000000576 coating method Methods 0.000 claims abstract description 12
- 239000011248 coating agent Substances 0.000 claims abstract description 11
- 238000000034 method Methods 0.000 claims abstract description 9
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 9
- 229920003118 cationic copolymer Polymers 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- 125000002843 carboxylic acid group Chemical group 0.000 claims abstract description 6
- 239000004593 Epoxy Substances 0.000 claims description 13
- 239000012876 carrier material Substances 0.000 claims description 11
- 239000000178 monomer Substances 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
- 238000007639 printing Methods 0.000 claims description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000002985 plastic film Substances 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000001879 gelation Methods 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 abstract description 12
- 229920000642 polymer Polymers 0.000 abstract description 10
- 238000010521 absorption reaction Methods 0.000 abstract description 5
- 239000000758 substrate Substances 0.000 abstract description 3
- 150000002118 epoxides Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 13
- 239000000975 dye Substances 0.000 description 10
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 6
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 6
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000001828 Gelatine Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229920000058 polyacrylate Polymers 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- -1 silver halide Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 2
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 2
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- MAGFQRLKWCCTQJ-UHFFFAOYSA-N 4-ethenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001541 aziridines Chemical class 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000037237 body shape Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000006855 networking Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920006316 polyvinylpyrrolidine Polymers 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5245—Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5218—Macromolecular coatings characterised by inorganic additives, e.g. pigments, clays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31507—Of polycarbonate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31515—As intermediate layer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
- Y10T428/31779—Next to cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31884—Regenerated or modified cellulose
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31909—Next to second addition polymer from unsaturated monomers
- Y10T428/31928—Ester, halide or nitrile of addition polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31942—Of aldehyde or ketone condensation product
- Y10T428/31949—Next to cellulosic
- Y10T428/31953—Modified or regenerated cellulose
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
Definitions
- the invention relates to a recording material for water-dilutable Inks, especially for use with inkjet printers, and a process for its manufacture.
- Image recording or reproduction using inkjet printers is a common method because it is direct and fast implementation of electronic image data is possible.
- Modern printer technology allows image reproduction with a Resolution, which is the resolution of the image displayed with the corresponds to conventional silver halide photography, below Use of various print media such as paper backing or transparent films.
- the quality of the pictures, in particular The resolution depends on both the possibilities of the used Printer as well as crucial from the properties ds recording material.
- the recording material further determines the further handling and the possible applications of the finished pictures.
- the Recording material meets the following requirements: good Ink absorption to achieve high color densities; low Diffusion of the ink (dye solution) in the recording material, to keep the droplet size small and thus high sharpness of contours and good resolution achieve; fast drying and good smudge resistance after the Ink application; low stickiness even with high air humidity; high transparency of the recording material Training as projection screen; and low sensitivity to water and therefore suitability for outdoor applications.
- ink-receptive layers from water-soluble Polymers, e.g. Polyvinyl alcohol, polyvinyl pyrrolidone, To provide gelatin etc. (US 4,503,111, US 4,680,235, US 4,555,432, DE 4,405,969). These polymers are characterized by a high moisture influence Stickiness and lack of water resistance.
- the stake of cationic polishing as a binder for fixing the Dyes in a color absorption layer and to increase the Wipe resistance is known from DE 3 707 624 or EP 514 633.
- Polymer mixtures of polyvinyl alcohol or polyalkylene oxides can also be used can be used with cationic polymers (EP 379 964, EP 634 284, JP 56-84992, JP 59-20696).
- metal oxide sols as fillers is in the EP 524 626 and DE 4 405 969.
- silane the binder solutions add to form matrix polymers (see EP 583 141, EP 482 837).
- EP 233 703 Polyacrylates and polyvinyl pyrrolidone as a color receiving layer to use.
- the known recording materials meet the above Requirements not. In particular, they are not for Suitable applications where a moisture or Water contact is possible because the swelling or solution Color receiving layer dye extracted from the layer is, so that the color densities achieved and develops poor contour definition.
- the object of the invention is to provide a new recording material, which has improved moisture and water resistance owns, and a process for its preparation specify.
- the recording material is intended in particular to have a wider range of applications and practical drying times after ink application.
- a recording material according to the invention has one Color receiving layer, which contains an epoxy-crosslinkable, carboxylic acid group cationic copolymer, a water-soluble Polymer and an epoxy-containing metal oxide sol contains.
- the weight fractions are preferably each corresponding to 30 to 60% by weight of the copolymer, 30 to 60 % By weight of the metal oxide and 10 to 40% by weight of the water-soluble Polymer.
- the component of the crosslinkable polymer can also be a Composition from different polymers according to the general structural formula included.
- the carboxylic acid-containing monomer unit is acrylic acid, Methacrylic acid or itaconic acid is preferred. In this case the content in the polymer component is preferably 20 to 35 mol%.
- ethyl acrylate as a comonomer component all known vinyl monomers, e.g. Vinyl pyrrolidone, Styrene, acrylamide or vinyl acetate act. The molecular weight this polymer component is usually 10,000 D to 500000 D.
- the hydrolysis and condensation can be carried out in the presence of tetraalkoxysilanes, Alkyltrialkoxysilanes or dialkyldialkoxysilanes is carried out, whereby the epoxy content of the Metal oxide brine can be controlled in a targeted manner.
- metal oxide mixtures can be used by the Sol production alkoxylates of boron, aluminum or titanium as Co building blocks act.
- the epoxy-containing metal oxide sols react with the free carboxylic acid groups of the polymers and thus result a water-insoluble network of metal oxide and cationic Polymer.
- the Composition additional epoxy catalysts may be added.
- epoxy catalysts are triethylamine, dimethylbenzylamine and N-methylimidazole. Based on the epoxy The concentration of metal oxide sol is preferably 1 to 5 % By weight.
- the second, water-soluble polymer component is preferred a nonionic or cationic water soluble polymer. This can be done, for example, with polyvinyl alcohol, polyvinyl pyrrolidone, Polyacrylamide, cationic polyacrylamide, cationic polyacrylic esters or compositions thereof be formed.
- the recording material according to the invention can in the color receiving layer furthermore means for controlling the layer uniformity and surface tension included.
- the layer uniformity and surface tension included are particularly suitable nonionic or cationic surfactants. Hexadecyltrimethylammonium bromide is particularly preferred.
- the recording material according to the invention can be used as a carrier material contain a flexible support for printing is suitable in an inkjet printer.
- a flexible support for printing is suitable in an inkjet printer.
- a carrier material rigid or non-flexible materials such as Use glass or plastic sheets.
- the carrier material can be essentially flat or any Have body shape, with the application of the color receiving layer possible on any surface of the carrier material is. Finally, it is possible to use the color receiving layer to produce such a thickness that a self-supporting Recording material is formed.
- the production of a recording material according to the invention is done by applying a coating solution for formation an ink receiving layer on a substrate.
- the approach the coating solution is made by preparing a Metal oxide sol according to the above composition and addition of the polymer components.
- the approach is preferably carried out in aqueous-organic solvents, e.g. in one Water-ethanol mixture.
- the application of the coating solution on the carrier material is done by a casting process like this for example of photochemical coating processes is known.
- the carrier material can also be used Diving, spraying or a similar application process be coated. Subsequently, the Coating solution on the carrier material, which by a Heat can be accelerated.
- the recording material according to the invention has the following advantages.
- the recording material contains one novel ink receiving layer, which is insoluble in water, at Moisture contact does not form a sticky surface and one practical drying time.
- the ink receiving layer is transparent and therefore for both paper and Suitable film carrier.
- the ink receiving layer can be with known layers of conventional recording materials combine by using the new color receiving layer as Top layer is used. After a site-specific order from Ink (dye solution) the ink dyes become solid in the crosslinked polymer composition of the ink receiving layer anchored and will not be washed out in contact with water.
- the use of the recording material is not limited to printing material for inkjet printers, but also possible for outdoor or outdoor use. A bleeding from smallest ink stains do not occur, so that the recording material according to the invention for recording operations (Printing processes) with resolution requirements is suitable for use with modern printing devices Production of overhead projector foils or color prints be made from photographs.
- the layer is not waterproof.
- the dye is washed out and also diffuses in the layer.
- the layer is not waterproof.
- the dye diffuses in the layer and is washed out considerably.
- the layer is waterproof. In the case of water contact, none noticeable bleaching of the dye. After drying sharp images will be obtained again.
- the layer is waterproof. There is no watering significant washout of the dye. After drying sharp images will be obtained again.
- the layer is waterproof. There is no contact with water significant washout of the dye. After drying sharp images will be obtained.
- the examples show compared to the conventional comparative examples a high density, constant after contact with water, dry, non-sticky surfaces and high transparency too after contact with water and drying again.
- the ink receiving layer has a largely non-toxic composition.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Laminated Bodies (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Pens And Brushes (AREA)
- Paints Or Removers (AREA)
- Duplication Or Marking (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
Die Erfindung betrifft ein Aufzeichnungsmaterial für wasserverdünnbare Tinten, insbesondere zur Verwendung von Tintenstrahldruckern, und ein Verfahren zu dessen Herstellung.The invention relates to a recording material for water-dilutable Inks, especially for use with inkjet printers, and a process for its manufacture.
Die Bildaufzeichnung oder -wiedergabe mittels Tintenstrahldruckern ist ein verbreitetes Verfahren, da eine direkte und schnelle Umsetzung elektronischer Bilddaten möglich ist. Die moderne Druckertechnik erlaubt Bildwiedergabe mit einer Auflösung, die der Auflösung bei der Bildwiedergabe mit der herkömmlichen Silberhalogenidphotographie entspricht, unter Verwendung verschiedenster Druckmedien wie Papierträger oder transparenten Folien. Die Qualität der Bilder, insbesondere der Auflösung, hängt sowohl von den Möglichkeiten des eingesetzten Druckers als auch entscheidend von den Eigenschaften ds Aufzeichnungsmaterials ab. Das Aufzeichnungsmaterial bestimmt ferner die weitere Handhabung und die Anwendungsmöglichkeiten der fertigen Bilder. Es wird angestrebt, daß das Aufzeichnungsmaterial den folgenden Anforderungen genügt: gute Tintenaufnahme zur Erzielung hoher Farbdichten; geringe Diffusion der Tinte (Farbstofflösung) im Aufzeichnungsmaterial, um die Tröpfchengröße gering zu halten und somit eine hohe Konturenschärfe und ein gutes Auflösungsvermögen zu erzielen; schnelle Trocknung und gute Wischfestigkeit nach dem Tintenauftrag; geringe Klebrigkeit selbst bei hohen Luftfeuchten; hohe Transparenz des Aufzeichnungsmaterials bei Ausbildung als Projektionsfolie; und geringe Wasserempfindlichkeit und somit Eignung für Anwendungen im Außenbereich.Image recording or reproduction using inkjet printers is a common method because it is direct and fast implementation of electronic image data is possible. Modern printer technology allows image reproduction with a Resolution, which is the resolution of the image displayed with the corresponds to conventional silver halide photography, below Use of various print media such as paper backing or transparent films. The quality of the pictures, in particular The resolution depends on both the possibilities of the used Printer as well as crucial from the properties ds recording material. The recording material further determines the further handling and the possible applications of the finished pictures. The aim is that the Recording material meets the following requirements: good Ink absorption to achieve high color densities; low Diffusion of the ink (dye solution) in the recording material, to keep the droplet size small and thus high sharpness of contours and good resolution achieve; fast drying and good smudge resistance after the Ink application; low stickiness even with high air humidity; high transparency of the recording material Training as projection screen; and low sensitivity to water and therefore suitability for outdoor applications.
Herkömmliche Aufzeichnungsmaterialien realisieren diese Anforderungen nicht und sind daher in ihrer Anwendung beschränkt. Conventional recording materials realize this Requirements are not and are therefore in their application limited.
Bei Aufzeichnungsmaterialien mit Papierträgern wird eine schnelle Tintenaufnahme und eine Wischfestigkeit durch eine Modifizierung einer Farbaufnahmeschicht mit hohen Pigmentmengen realisiert (DE 3 024 205, EP 379 964) . Dabei tritt jedoch eine starke Trübung auf, so daß derartig modifizierte Aufzeichnungsmaterialien nicht als Projektionsfolien geeignet sind. Es ist bekannt, Farbaufnahmeschichten aus wasserlöslichen Polymeren, wie z.B. Polyvinylalkohol, Polyvinylpyrrolidon, Gelatine etc. vorzusehen (US 4 503 111, US 4 680 235, US 4 555 432, DE 4 405 969) . Diese Polymere zeichnen sich jedoch bei Feuchtigkeitseinfluß durch eine hohe Klebrigkeit und fehlende Wasserbeständigkeit aus. Der Einsatz von kationischen Polieren als Bindemittel zur Fixierung der Farbstoffe in einer Farbaufnahmeschicht und zur Erhöhung der Wischfestigkeit ist aus DE 3 707 624 oder EP 514 633 bekannt. Es können auch Polymergemische aus Polyvinylalkohol oder Polyalkylenoxiden mit kationischen Polymeren eingesetzt werden (EP 379 964, EP 634 284, JP 56-84992, JP 59-20696).In the case of recording materials with paper substrates, a fast ink absorption and smudge resistance thanks to Modification of a color absorption layer with high pigment quantities realized (DE 3 024 205, EP 379 964). This occurs however, a strong cloudiness, so that modified in such a way Recording materials are not suitable as projection foils are. It is known to make ink-receptive layers from water-soluble Polymers, e.g. Polyvinyl alcohol, polyvinyl pyrrolidone, To provide gelatin etc. (US 4,503,111, US 4,680,235, US 4,555,432, DE 4,405,969). These polymers are characterized by a high moisture influence Stickiness and lack of water resistance. The stake of cationic polishing as a binder for fixing the Dyes in a color absorption layer and to increase the Wipe resistance is known from DE 3 707 624 or EP 514 633. Polymer mixtures of polyvinyl alcohol or polyalkylene oxides can also be used can be used with cationic polymers (EP 379 964, EP 634 284, JP 56-84992, JP 59-20696).
Der Einsatz von Metalloxidsolen als Füllstoffe ist in den EP 524 626 und DE 4 405 969 beschrieben. Zur Verbesserung der Wischfestigkeit ist es bekannt, Silane den Bindemittellösungen zuzusetzen, um Matrixpolymere zu bilden (siehe EP 583 141, EP 482 837). Zur Verminderung der Wasserempfindlichkeit wird in EP 233 703 vorgeschlagene, säurehaltige, wasserunlösliche Polyacrylate und Polyvinylpyrrolidon als Farbempfangsschicht zu verwenden.The use of metal oxide sols as fillers is in the EP 524 626 and DE 4 405 969. To improve the Smudge resistance is known to silane the binder solutions add to form matrix polymers (see EP 583 141, EP 482 837). To reduce water sensitivity proposed acidic, water-insoluble in EP 233 703 Polyacrylates and polyvinyl pyrrolidone as a color receiving layer to use.
Es ist auch bekannt, 2-Schicht-Systeme herzustellen, die eine mikroporöse Polyvinylacetat-Deckschicht zur Verbesserung der Wischfestigkeit aufweisen. Dadurch wird jedoch die Transparenz vermindert, so daß eine Anwendung als Projektionsfolie unmöglich ist. Für Folienträger wird deshalb vorgeschlagen, wasserlösliche Mischpolymerisate auf der Basis von Acrylsäure oder p-Styrensulfonsäure mit polyfunktionellen Aziridinen zu vernetzen (EP 482 838). Durch diese Vernetzung wird jedoch die Trocknungszeit der aufgebrachten Tinte negativ beeinflußt. It is also known to manufacture 2-layer systems, one microporous polyvinyl acetate top layer to improve the Have smudge resistance. However, this will increase transparency reduced, so that an application as a projection film is impossible. It is therefore proposed for film carriers water-soluble copolymers based on acrylic acid or p-styrene sulfonic acid with polyfunctional aziridines network (EP 482 838). Through this networking, however Drying time of the applied ink is negatively affected.
Die bekannten Aufzeichnungsmaterialien erfüllen die obengenannten Anforderungen nicht. Sie sind insbesondere nicht für Anwendungen geeignet, bei denen ein Feuchtigkeits- oder Wasserkontakt möglich ist, da unter Quellung oder Lösung der Farbempfangsschicht Farbstoff aus der Schicht extrahiert wird, so daß sich die erzielten Farbdichten verringern und eine mangelhafte Konturenschärfe ausbildet.The known recording materials meet the above Requirements not. In particular, they are not for Suitable applications where a moisture or Water contact is possible because the swelling or solution Color receiving layer dye extracted from the layer is, so that the color densities achieved and develops poor contour definition.
Die Aufgabe der Erfindung ist es, ein neues Aufzeichnungsmaterial, das eine verbesserte Feuchtigkeits- und Wasserbeständigkeit besitzt, und ein Verfahren zu dessen Herstellung anzugeben. Das Aufzeichnungsmaterial soll insbesondere einen erweiteren Anwendungsbereich besitzen und praktikable Trocknungszeiten nach Tintenauftrag aufweisen.The object of the invention is to provide a new recording material, which has improved moisture and water resistance owns, and a process for its preparation specify. The recording material is intended in particular to have a wider range of applications and practical drying times after ink application.
Diese Aufgabe wird durch ein Material gemäß Anspruch 1 und ein Verfahren gemäß Anspruch 8 gelöst. Vorteilhafte Ausführungsformen ergeben sich aus den Unteransprüchen.This object is achieved by a material according to claim 1 and Method according to claim 8 solved. Advantageous embodiments result from the subclaims.
Ein erfindungsgemäßes Aufzeichnungsmaterial besitzt eine Farbempfangsschicht, die ein epoxidvernetzbares, carbonsäuregruppenhaltiges kationisches Mischpolymerisat, ein wasserlösliches Polymerisat und ein epoxidhaltiges Metalloxidsol enthält. Die Gewichtsanteile betragen vorzugsweise jeweils entsprechend 30 bis 60 Gew.-% des Mischpolymerisats, 30 bis 60 Gew.-% des Metalloxids und 10 bis 40 Gew.-% des wasserlöslichen Polymerisats.A recording material according to the invention has one Color receiving layer, which contains an epoxy-crosslinkable, carboxylic acid group cationic copolymer, a water-soluble Polymer and an epoxy-containing metal oxide sol contains. The weight fractions are preferably each corresponding to 30 to 60% by weight of the copolymer, 30 to 60 % By weight of the metal oxide and 10 to 40% by weight of the water-soluble Polymer.
Das epoxidvernetzbare, carbonsäuregruppenhaltige kationische Mischpolymerisat besitzt die Strukturformel: wobei
- M:
- carbonsäurehaltiges Monomer
- Z:
- Vinylmonomer
- A:
- Sauerstoff oder Stickstoff
- R1:
- H, CH3
- R2:
- Alkylengruppe von C2 bis C8
- R3:
- CH3, C2H5, C3H7, C4H9
- X:
- Chlorid, Bromid, und
- a:
- 10 bis 50 Mol-%, b: 0 bis 20 Mol.-%, c: 50 bis 90 Mol.-%
- M:
- monomer containing carboxylic acid
- Z:
- Vinyl monomer
- A:
- Oxygen or nitrogen
- R 1 :
- H, CH 3
- R 2 :
- Alkylene group from C 2 to C 8
- R 3 :
- CH 3 , C 2 H 5 , C 3 H 7 , C 4 H 9
- X:
- Chloride, bromide, and
- a:
- 10 to 50 mol%, b: 0 to 20 mol%, c: 50 to 90 mol%
Beispiele für derartige, vernetzbare Polymere der angegebenen
allgemeinen Strukturformel sind:
Die Komponente des vernetzbaren Polymers kann auch eine Zusammensetzung aus verschiedenen Polymeren entsprechend der allgemeinen Strukturformel enthalten. The component of the crosslinkable polymer can also be a Composition from different polymers according to the general structural formula included.
Als carbonsäurehaltiger Monomerbaustein wird Acrylsäure, Methacrylsäure oder Itaconsäure bevorzugt. In diesem Fall beträgt der Gehalt in der Polymerkomponente vorzugsweise 20 bis 35 Mol-%. Neben Ethylacrylat als Comonomerbaustein können alle bekannten Vinylmonomere, z.B. Vinylpyrrolidon, Styrol, Acrylamid oder Vinylacetat fungieren. Das Molekulargewicht dieser Polymerkomponent beträgt gewöhnlich 10000 D bis 500000 D.The carboxylic acid-containing monomer unit is acrylic acid, Methacrylic acid or itaconic acid is preferred. In this case the content in the polymer component is preferably 20 to 35 mol%. In addition to ethyl acrylate as a comonomer component all known vinyl monomers, e.g. Vinyl pyrrolidone, Styrene, acrylamide or vinyl acetate act. The molecular weight this polymer component is usually 10,000 D to 500000 D.
Die Metalloxidsolkomponente wird in bekannter Weise durch durch Sol/Gel-Technologien aus epoxidhaltigen Metalloxidsolen mit einem organischen Lösungsmittel (z.B. Methanol, Ethanol) hergestellt (siehe US 3 955 035, H.I. Schmidt et al. Non-Cryst. Solids 80 (1989) 557) . Es werden vorzugsweise Hydrolysate von Epoxidsilanen eingesetzt. Beispiele der epoxidhaltigen, hydrolysierbaren Silane sind:
- Glycidoxypropyltrimethoxysilan,
- Glycidoxypropyltriethoxysilan, und
- (3,4-Epoxycyclohexylethyltrimethoxysilan).
- Glycidoxypropyltrimethoxysilane,
- Glycidoxypropyltriethoxysilane, and
- (3,4-epoxycyclohexylethyltrimethoxysilane).
Die Hydrolyse und Kondensation kann in Gegenwart von Tetraalkoxysilanen, Alkyltrialkoxysilanen oder Dialkyldialkoxysilanen durchgeführt wird, wodurch der Epoxidgehalt der Metalloxidsole gezielt steuerbar ist. Erfindungsgemäß können auch Metalloxidgemische eingesetzt werden, indem bei der Solherstellung Alkoxylate von Bor, Aluminium oder Titan als Cobausteine fungieren.The hydrolysis and condensation can be carried out in the presence of tetraalkoxysilanes, Alkyltrialkoxysilanes or dialkyldialkoxysilanes is carried out, whereby the epoxy content of the Metal oxide brine can be controlled in a targeted manner. According to the invention also metal oxide mixtures can be used by the Sol production alkoxylates of boron, aluminum or titanium as Co building blocks act.
Bei der Vernetzung der Epoxidgruppen bzw. Gelbildung (während der Trocknung) reagieren die epoxidhaltigen Metalloxidsole mit den freien Carbonsäuregruppen der Polymeren und ergeben somit ein wasserunlösliches Netzwerk aus Metalloxid und kationischem Polymerisat. Um diese Reaktion zu beschleunigen, können der Zusammensetzung zusätzlich Epoxidkatalysatoren zugesetzt sein. When crosslinking the epoxy groups or gel formation (during drying) the epoxy-containing metal oxide sols react with the free carboxylic acid groups of the polymers and thus result a water-insoluble network of metal oxide and cationic Polymer. To accelerate this reaction, the Composition additional epoxy catalysts may be added.
Beispiele für Epoxidkatalysatoren sind Triethylamin, Dimethylbenzylamin und N-Methylimidazol. Bezogen auf das epoxidhaltige Metalloxidsol beträgt ihre Konzentration vorzugsweise 1 bis 5 Gew.-%.Examples of epoxy catalysts are triethylamine, dimethylbenzylamine and N-methylimidazole. Based on the epoxy The concentration of metal oxide sol is preferably 1 to 5 % By weight.
Die zweite, wasserlösliche Polymerkomponente ist vorzugsweise ein nichtionisches oder kationisches wasserlösliches Polymer. Dies kann beispielsweise durch Polyvinylalkohol, Polyvinylpyrrolidon, Polyacrylamid, kationisches Polyacrylamide, kationische Polyacrylester oder Zusammensetzungen aus diesen gebildet werden.The second, water-soluble polymer component is preferred a nonionic or cationic water soluble polymer. This can be done, for example, with polyvinyl alcohol, polyvinyl pyrrolidone, Polyacrylamide, cationic polyacrylamide, cationic polyacrylic esters or compositions thereof be formed.
Das erfindungsgemäße Aufzeichnungsmaterial kann in der Farbempfangsschicht ferner Mittel zur Steuerung der Schichtgleichmäßigkeit und Oberflächenspannung enthalten. Hierfür sind insbesondere nichtionische oder kationische Tenside geeignet. Besonders wird Hexadecyltrimethylammoniumbromid bevorzugt.The recording material according to the invention can in the color receiving layer furthermore means for controlling the layer uniformity and surface tension included. For this are particularly suitable nonionic or cationic surfactants. Hexadecyltrimethylammonium bromide is particularly preferred.
Das erfindungsgemäße Aufzeichnungsmaterial kann als Trägermaterial einen flexiblen Träger enthalten, der zum Bedrucken in einem Tintenstrahldrucker geeignet ist. Hierbei werden vorzugsweise Papier oder transparente Kunststoff-Folien verwendet. Es ist Jedoch auch möglich, als Trägermaterial starre oder nicht-flexible Materialien wie beispielsweise Glas- oder Kunststofftafeln zu verwenden. Das Trägermaterial kann im wesentlichen flächig sein oder auch eine beliebige Körperform besitzen, wobei die Auftragung der Farbempfangsschicht auf beliebigen Oberflächen des Trägermaterial möglich ist. Schließlich ist es möglich, die Farbempfangsschicht mit einer derartigen Dicke herzustellen, daß ein freitragendes Aufzeichnungsmaterial gebildet wird.The recording material according to the invention can be used as a carrier material contain a flexible support for printing is suitable in an inkjet printer. Here are preferably paper or transparent plastic films used. However, it is also possible as a carrier material rigid or non-flexible materials such as Use glass or plastic sheets. The carrier material can be essentially flat or any Have body shape, with the application of the color receiving layer possible on any surface of the carrier material is. Finally, it is possible to use the color receiving layer to produce such a thickness that a self-supporting Recording material is formed.
Die Herstellung eines erfindungsgemäßen Aufzeichnungsmaterials erfolgt durch Auftragung einer Beschichtungslösung zur Bildung einer Farbempfangsschicht auf einem Trägermaterial. Der Ansatz der Beschichtungslösung erfolgt durch Zubereitung eines Metalloxidsols entsprechend der obengenannten Zusammensetzung und Zusatz der Polymerkomponenten. Der Ansatz erfolgt vorzugsweise in wässrig-organischen Lösungsmitteln, z.B. in einem Wasser-Ethanol-Gemisch. Die Auftragung der Beschichtungslösung auf das Trägermaterial erfolgt durch ein Begußverfahren wie es beispielsweise von photochemischen Beschichtungsverfahren bekannt ist. Alternativ kann das Trägermaterial auch durch Tauchen, Besprühen oder ein ähnliches Antragsverfahren beschichtet werden. Anschließend erfolgt eine Gelierung der Beschichtungslösung auf dem Trägermaterial, die durch eine Wärmezufuhr beschleunigt sein kann.The production of a recording material according to the invention is done by applying a coating solution for formation an ink receiving layer on a substrate. The approach the coating solution is made by preparing a Metal oxide sol according to the above composition and addition of the polymer components. The approach is preferably carried out in aqueous-organic solvents, e.g. in one Water-ethanol mixture. The application of the coating solution on the carrier material is done by a casting process like this for example of photochemical coating processes is known. Alternatively, the carrier material can also be used Diving, spraying or a similar application process be coated. Subsequently, the Coating solution on the carrier material, which by a Heat can be accelerated.
Das erfindungsgemäße Aufzeichnungsmaterial besitzt die folgenden Vorteile. Das Aufzeichnungsmaterial enthält eine neuartige Farbempfangsschicht, die wasserunslöslich ist, bei Feuchtigkeitskontakt keine klebrige Oberfläche bildet und eine praktikable Trocknungszeit aufweist. Die Farbempfangsschicht ist transparent und somit sowohl für Papier- als auch für Folienträger geeignet. Die Farbempfangsschicht läßt sich mit bekannten Schichten herkömmlicher Aufzeichnungsmaterialien kombinieren, indem die neue Farbempfangsschicht als Deckschicht verwendet wird. Nach ortsselektivem Auftrag der Tinte (Farbstofflösung) werden die Tintenfarbstoffe fest in der vernetzten Polymerzusammensetzung der Farbempfangsschicht verankert und werden bei Wasserkontakt nicht ausgewaschen. Dadurch ist die Verwendung des Aufzeichnungsmaterials nicht auf Druckmaterial für Tintenstrahldrucker beschränkt, sondern auch im Außen- oder Freilufteinsatz möglich. Ein Verlaufen von kleinsten Tintenflecken erfolgt nicht, so daß sich das erfindungsgemäße Aufzeichnungsmaterial für Aufzeichnungsvorgänge (Druckvorgänge) mit Anforderungen an das Auflösungsvermögen eignet, wie sie an moderne Druckvorrichtungen zur Herstellung von Overhead-Projektorfolien oder von Farb-Prints von Photographien gestellt werden. The recording material according to the invention has the following advantages. The recording material contains one novel ink receiving layer, which is insoluble in water, at Moisture contact does not form a sticky surface and one practical drying time. The ink receiving layer is transparent and therefore for both paper and Suitable film carrier. The ink receiving layer can be with known layers of conventional recording materials combine by using the new color receiving layer as Top layer is used. After a site-specific order from Ink (dye solution) the ink dyes become solid in the crosslinked polymer composition of the ink receiving layer anchored and will not be washed out in contact with water. As a result, the use of the recording material is not limited to printing material for inkjet printers, but also possible for outdoor or outdoor use. A bleeding from smallest ink stains do not occur, so that the recording material according to the invention for recording operations (Printing processes) with resolution requirements is suitable for use with modern printing devices Production of overhead projector foils or color prints be made from photographs.
Mit einer 10 Gew.-%igen Wasser/Alkohollösung (40/60) wird auf eine 100 µm starke Polyesterunterlage in bekannter Weise mittels Abstreichgießers eine 7,8 µm starke Schicht folgender Zusammensetzung aufgebracht:
- 45 Gew.-%
- Gelatine (alkalisch aufgeschlossene Knochengelatine)
- 35 Gew.-%
- Polyvinylpyrrolidon (K 90)
- 20 Gew.-%
- epoxidfunktionelles Metalloxidsol, hergestellt aus 80 Gew.-% Tetraethoxysilan und 20 Gew.-% Glycidooxypropyltrimethoxysilan.
- 45% by weight
- Gelatine (alkaline digested bone gelatine)
- 35% by weight
- Polyvinyl pyrrolidone (K 90)
- 20% by weight
- epoxy-functional metal oxide sol, made from 80% by weight tetraethoxysilane and 20% by weight glycidooxypropyltrimethoxysilane.
Nach Trocknung der Schicht bei 85°C wird die Folie mittels eines Tintenstrahldruckers, Typ HP Desjet 690C bedruckt. Zur Charakterisierung der Eigenschaften wird die Farbdichte bestimmt, visuell die Konturenschärfe beurteilt und die Transparenz sowie die Klebrigkeit der Oberfläche ermittelt. Die Folie wird weiterhin zur Prüfung der Wasserfestigkeit 30 min bei 25°C mit fließendem Wasser in Kontakt gebracht und danach die Farbdichte und Schichtbeschaffenheit geprüft. Folgende Eigenschaften werden erhalten:
- Konturenschärfe:
- gut, nach Wässerung unscharfe Abbildung
- Trocknungszeit:
- 7,5 min
- Oberflächenbeschaffenheit (85% RF):
- leicht klebrig, bei Wasserkontakt starkes Quellen
- Transparenz:
- klare Folie.
- Contour sharpness:
- good, blurred image after watering
- Drying time:
- 7.5 min
- Surface quality (85% RH):
- slightly sticky, strong swelling when in contact with water
- Transparency:
- clear film.
Die Schicht ist nicht wasserfest. Der Farbstoff wird ausgewaschen und diffundiert auch in der Schicht.The layer is not waterproof. The dye is washed out and also diffuses in the layer.
Analog zu Beispiel 1 wird eine 8,5 µm starke Schicht folgende Zusammensetzung aufgetragen:
- 33 Gew.-%
- Na-Polyacrylat
- 59 Gew.-%
- Polyacylsäure (vernetzt in Gegenwart von Silanen gemäß EP 583 141)
- 8 Gew.-%
- Metalloxidsole aus Tetraethoxysilan
- 33% by weight
- Na polyacrylate
- 59% by weight
- Polyacrylic acid (crosslinked in the presence of silanes according to EP 583 141)
- 8% by weight
- Metal oxide sols made from tetraethoxysilane
Es werden folgende Eigenschaften erhalten:
- Konturenschärfe:
- gut, nach Wässerung unscharfe Abbildung
- Trocknungszeit:
- 6,5 min
- Oberflächenbeschaffenheit (85% RF):
- nicht klebrig, Schicht quillt stark bei Wasserkontakt
- Transparenz:
- klare Folie
- Contour sharpness:
- good, blurred image after watering
- Drying time:
- 6.5 min
- Surface quality (85% RH):
- not sticky, layer swells strongly when in contact with water
- Transparency:
- clear film
Die Schicht ist nicht wasserfest. Der Farbstoff diffundiert in der Schicht und wird beträchtlich ausgewaschen.The layer is not waterproof. The dye diffuses in the layer and is washed out considerably.
Analog zu Beispiel 1 wird eine 11,5 µm starke Schicht folgender Zusammensetzung aufgetragen:
- 45 Gew.-%
- Copolymeres aus Acrylsäure und Methacryloxyethyltrimethylammoniumchlorid (20/80), Molekulargewicht 130000 D,
- 45 Gew.-%
- Metalloxidsol, hergestellt aus 75 Gew.-% Tetraethoxysilan und 25 Gew.-% Glycidopropyltrimethoxysilan
- 10 Gew.-%
- Polyvinylalkohol (voll verseift, Molekulargewicht 95000 D)
- 45% by weight
- Copolymer of acrylic acid and methacryloxyethyltrimethylammonium chloride (20/80), molecular weight 130,000 D,
- 45% by weight
- Metal oxide sol made from 75% by weight tetraethoxysilane and 25% by weight glycidopropyltrimethoxysilane
- 10% by weight
- Polyvinyl alcohol (fully saponified, molecular weight 95000 D)
Es werden folgende Eigenschaften erhalten.
- Konturenschärfe:
- gut, auch nach Wässerung scharfe Abbildungen
- Trocknungszeit:
- 7,0 min
- Oberflächenbeschaffenheit:
- nicht klebrig, bei Wasserkontakt klebefreie unlösliche Schicht
- Transparenz:
- klare Folie.
- Contour sharpness:
- good, sharp images even after watering
- Drying time:
- 7.0 min
- Surface quality:
- not sticky, non-sticky layer on contact with water
- Transparency:
- clear film.
Die Schicht ist wasserfest. Bei Wasserkonakt erfolgt keine nennenswerte Ausbleiching des Farbstoffes. Nach der Trocknung werden wieder scharfe Abbildungen erhalten.The layer is waterproof. In the case of water contact, none noticeable bleaching of the dye. After drying sharp images will be obtained again.
Analog zu Beispiel 1 wird eine 12,5 µm starke Schicht folgender Zusammensetzung aufgetragen:
- 55 Gew.-%
- Mischpolymerisat aus Acrylsäure/Ethylacrylat/Methacryloxyethyltrimethylammoniumchlorid (28/12/60), Molekulargewicht 140000 D.
- 35 Gew.-%
- Metalloxidsol aus 50 Gew.-% Glycidoxypropyltriethoxysilan und 50 Gew.-% Tetraethoxysilan
- 10 Gew.-%
- Polyvinylpyrrolidon, Molekulargewicht 320000 D.
- 55% by weight
- Copolymers of acrylic acid / ethyl acrylate / methacryloxyethyltrimethylammonium chloride (28/12/60), molecular weight 140,000 D.
- 35% by weight
- Metal oxide sol composed of 50% by weight glycidoxypropyltriethoxysilane and 50% by weight tetraethoxysilane
- 10% by weight
- Polyvinyl pyrrolidone, molecular weight 320,000 D.
Es werden folgende Eigenschaften erhalten:
- Konturenschärfe:
- gut, auch nach Wässerung scharfe Abbildungen
- Trocknungszeit:
- 7,0 min
- Oberflächenbeschaffenheit (85% RF):
- nicht klebrig, bei Wasserkontakt klare nichtklebrige Schicht
- Transparenz:
- klare Schicht
- Contour sharpness:
- good, sharp images even after watering
- Drying time:
- 7.0 min
- Surface quality (85% RH):
- not sticky, clear non-sticky layer on contact with water
- Transparency:
- clear layer
Die Schicht ist wasserfest. Bei der Wässerung erfolgt keine nennenswerte Auswaschung des Farbstoffes. Nach der Trocknung werden wieder scharfe Abbildungen erhalten.The layer is waterproof. There is no watering significant washout of the dye. After drying sharp images will be obtained again.
Analog zu Beispiel 1 wird eine 10,5 µm starke Schicht folgender Zusammensetzung aufgetragen:
- 48,5 Gew.-%
- Copolymer aus Acrylsäure und Acrylamidopropyltrimethylammoniumchlorid (35/65), Molekulargewicht 195000 D.
- 40 Gew.-%
- Metalloxidsol, hergestellt aus 80 Gew.-% Tetraethoxysilan und 20 Gew.-% Glycidoxypropyltrimethoxysilan
- 10 Gew.-%
- Poly-methacrylamidopropyltrimethylammoniumchlorid, Molekulargewicht 85000 D.
- 1,5 Gew.-%
- Hexadecyltrimethylammoniumbromid.
- 48.5% by weight
- Copolymer of acrylic acid and acrylamidopropyltrimethylammonium chloride (35/65), molecular weight 195000 D.
- 40% by weight
- Metal oxide sol made from 80% by weight tetraethoxysilane and 20% by weight glycidoxypropyltrimethoxysilane
- 10% by weight
- Poly-methacrylamidopropyltrimethylammonium chloride, molecular weight 85000 D.
- 1.5% by weight
- Hexadecyltrimethylammonium bromide.
Es werden folgende Eigenschaften erhalten:
- Konturenschärfe:
- gut, auch nach Wässerung scharfe Abbildungen
- Trocknungszeit:
- 7,5 min
- Oberflächenbeschaffenheit (85% RF):
- nicht klebrig, auch bei Wasserkontakt
- Transparenz:
- klare Schicht
- Contour sharpness:
- good, sharp images even after watering
- Drying time:
- 7.5 min
- Surface quality (85% RH):
- not sticky, even when in contact with water
- Transparency:
- clear layer
Die Schicht ist wasserfest. Bei Wasserkontakt erfolgt keine nennenswerte Auswaschung des Farbstoffes. Nach der Trocknung werden scharfe Abbildungen erhalten.The layer is waterproof. There is no contact with water significant washout of the dye. After drying sharp images will be obtained.
Die Beispiele zeigen gegenüber den herkömmlichen Vergleichsbeispielen eine hohe, nach Wasserkontakt konstante Dichte, trockene, nicht-klebende Oberflächen und hohe Transparenz auch nach Wasserkontakt und erneuter Trocknung. Die Farbempfangsschicht besitzt eine weitgehend ungiftige Zusammensetzung.The examples show compared to the conventional comparative examples a high density, constant after contact with water, dry, non-sticky surfaces and high transparency too after contact with water and drying again. The ink receiving layer has a largely non-toxic composition.
Claims (10)
dadurch gekennzeichnet, daß
die Farbempfangsschicht ein epoxidvernetzbares, carbonsäuregruppenhaltiges kationisches Mischpolymerisat, ein epoxidhaltiges Metalloxid und ein wasserlösliches Polymer enthält.Recording material which has at least one ink receiving layer which is provided for receiving a water-soluble dye solution,
characterized in that
the ink-receiving layer contains an epoxy-crosslinkable, carboxylic acid-containing cationic copolymer, an epoxy-containing metal oxide and a water-soluble polymer.
- M:
- carbonsäurehaltiges Monomer
- Z:
- Vinylmonomer
- A:
- Sauerstoff oder Stickstoff
- R1:
- H, CH3
- R2:
- Alkylengruppe von C2 bis C8
- R3:
- CH3, C2H5, C3H7, C4H9
- X:
- Chlorid, Bromid
- a:
- 10 bis 50 Mol-%
- b:
- 0 bis 20 Mol-%
- c:
- 50 bis 90 Mol-%
- M:
- monomer containing carboxylic acid
- Z:
- Vinyl monomer
- A:
- Oxygen or nitrogen
- R 1 :
- H, CH 3
- R 2 :
- Alkylene group from C 2 to C 8
- R 3 :
- CH 3 , C 2 H 5 , C 3 H 7 , C 4 H 9
- X:
- Chloride, bromide
- a:
- 10 to 50 mol%
- b:
- 0 to 20 mol%
- c:
- 50 to 90 mol%
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19715187A DE19715187C2 (en) | 1997-04-11 | 1997-04-11 | Recording material for water-dilutable inks |
DE19715187 | 1997-04-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0870623A1 true EP0870623A1 (en) | 1998-10-14 |
EP0870623B1 EP0870623B1 (en) | 2001-01-03 |
Family
ID=7826245
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98105981A Expired - Lifetime EP0870623B1 (en) | 1997-04-11 | 1998-04-01 | Recording material for receiving water-based inks |
Country Status (9)
Country | Link |
---|---|
US (1) | US6136448A (en) |
EP (1) | EP0870623B1 (en) |
JP (1) | JPH1134485A (en) |
KR (1) | KR19980081115A (en) |
AT (1) | ATE198448T1 (en) |
DE (2) | DE19715187C2 (en) |
DK (1) | DK0870623T3 (en) |
ES (1) | ES2154918T3 (en) |
PT (1) | PT870623E (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1422071A1 (en) * | 2002-11-19 | 2004-05-26 | Fuji Photo Film Co., Ltd. | Ink jet recording sheet |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1229186C (en) * | 1999-11-09 | 2005-11-30 | 皇家菲利浦电子有限公司 | Method of providing a marking on a substrate |
US8158221B2 (en) * | 2006-11-22 | 2012-04-17 | Hewlett-Packard Development Company, L.P. | Reactive ink and ink-media system for reduced air fade on porous media |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4830911A (en) * | 1986-11-04 | 1989-05-16 | Jujo Paper Co., Ltd. | Recording sheet for ink jet printers |
EP0627324A1 (en) * | 1993-06-03 | 1994-12-07 | Mitsubishi Paper Mills, Ltd. | Ink jet recording medium |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3024205C2 (en) * | 1980-06-27 | 1990-11-15 | Felix Schoeller jr. GmbH & Co KG, 4500 Osnabrück | Recording paper for ink jet recording processes |
US4503111A (en) * | 1983-05-09 | 1985-03-05 | Tektronix, Inc. | Hydrophobic substrate with coating receptive to inks |
JPS60198285A (en) * | 1984-03-23 | 1985-10-07 | Ricoh Co Ltd | Ink jet recording material |
US4555437A (en) * | 1984-07-16 | 1985-11-26 | Xidex Corporation | Transparent ink jet recording medium |
GB8602593D0 (en) * | 1986-02-03 | 1986-03-12 | Ici Plc | Inkable sheet |
JP2633671B2 (en) * | 1989-01-18 | 1997-07-23 | 日本製紙 株式会社 | Inkjet recording sheet |
US5219928A (en) * | 1990-10-24 | 1993-06-15 | Minnesota Mining And Manufacturing Company | Transparent liquid absorbent materials |
US5208092A (en) * | 1990-10-24 | 1993-05-04 | Minnesota Mining And Manufacturing Company | Transparent liquid absorbent materials for use as ink-receptive layers |
DE4116595A1 (en) * | 1991-05-22 | 1992-11-26 | Schoeller Felix Jun Papier | RECORDING MATERIAL FOR THE INK HEAD RECORDING METHOD |
DE69215781T2 (en) * | 1991-07-26 | 1997-04-03 | Asahi Glass Co Ltd | Recording strips for inkjet printers |
JPH06135124A (en) * | 1992-08-13 | 1994-05-17 | Canon Inc | Recording material for business machine and its production |
JP3302792B2 (en) * | 1993-07-06 | 2002-07-15 | キヤノン株式会社 | Recording medium and ink jet recording method using the same |
JP3287706B2 (en) * | 1993-10-20 | 2002-06-04 | キヤノン株式会社 | Recording medium, image forming method using the same, and method for manufacturing printed matter |
DE4405969C2 (en) * | 1994-02-24 | 1997-06-12 | Wolfen Filmfab Gmbh | Information recording material for ink jet printers |
-
1997
- 1997-04-11 DE DE19715187A patent/DE19715187C2/en not_active Expired - Fee Related
-
1998
- 1998-04-01 PT PT98105981T patent/PT870623E/en unknown
- 1998-04-01 DK DK98105981T patent/DK0870623T3/en active
- 1998-04-01 EP EP98105981A patent/EP0870623B1/en not_active Expired - Lifetime
- 1998-04-01 DE DE59800412T patent/DE59800412D1/en not_active Expired - Fee Related
- 1998-04-01 ES ES98105981T patent/ES2154918T3/en not_active Expired - Lifetime
- 1998-04-01 AT AT98105981T patent/ATE198448T1/en not_active IP Right Cessation
- 1998-04-03 US US09/054,853 patent/US6136448A/en not_active Expired - Fee Related
- 1998-04-06 KR KR1019980012020A patent/KR19980081115A/en not_active Application Discontinuation
- 1998-04-13 JP JP10101414A patent/JPH1134485A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4830911A (en) * | 1986-11-04 | 1989-05-16 | Jujo Paper Co., Ltd. | Recording sheet for ink jet printers |
EP0627324A1 (en) * | 1993-06-03 | 1994-12-07 | Mitsubishi Paper Mills, Ltd. | Ink jet recording medium |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1422071A1 (en) * | 2002-11-19 | 2004-05-26 | Fuji Photo Film Co., Ltd. | Ink jet recording sheet |
US7754297B2 (en) | 2002-11-19 | 2010-07-13 | Fujifilm Corporation | Ink jet recording sheet |
Also Published As
Publication number | Publication date |
---|---|
JPH1134485A (en) | 1999-02-09 |
DE19715187C2 (en) | 2000-06-29 |
ES2154918T3 (en) | 2001-04-16 |
ATE198448T1 (en) | 2001-01-15 |
DE59800412D1 (en) | 2001-02-08 |
PT870623E (en) | 2001-06-29 |
EP0870623B1 (en) | 2001-01-03 |
US6136448A (en) | 2000-10-24 |
DK0870623T3 (en) | 2001-04-09 |
KR19980081115A (en) | 1998-11-25 |
DE19715187A1 (en) | 1998-10-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE69107953T2 (en) | Transparent materials absorbing liquids. | |
DE69504384T2 (en) | Reactive substrate and ink system for inkjet printing processes | |
US4564560A (en) | Recording sheets for water base ink and process for making the same | |
DE69401305T2 (en) | Inkjet recording layer | |
DE69620782T2 (en) | IMAGE RECEPTION COATING | |
DE69809606T2 (en) | Recording material, method for producing the same and ink jet printed images using this material | |
DE10020346C5 (en) | Ink-jet recording sheet | |
DE19505295C2 (en) | Ink jet recording sheet | |
DE60213768T2 (en) | POLYVINYL ACETAL, POLYVINYL ACETAL COMPOSITION, INK OR PRINTING COLOR, COATING MATERIAL, DISPERSIBLE, HEAT-RELATABLE LIGHT-SENSITIVE MATERIAL, CERAMIC GREEN FILM, PLASTIC LENS PRIMER, WATER BASE INK OR PRINTING INK AND ADHESIVE FOR METAL FILM | |
DE4446551C1 (en) | Water-resistant recording material for ink-jet printing | |
DE60104727T2 (en) | IMAGE RECEIVING SHEET | |
DE69703773T2 (en) | Transparent phase change ink printing materials containing silica | |
DE19952356A1 (en) | Ink-jet printing sheets with ink-accepting coating containing fine inorganic particles and binder resin has coating containing tetraalkoxy-titanium monomer, oligomer or polymer | |
DE69904425T2 (en) | Ink jet recording sheet containing silica particles and method of using the same | |
DE69519392T2 (en) | AQUEOUS INK RECORDING INK JET RECEIVING MEDIUM, WHICH GIVES A WATER RESISTANT INK JET PRINT | |
DE69811453T2 (en) | Waterproof ink-absorbing material | |
DE69523240T2 (en) | Non-stick, clear color acceptor sheet | |
DE69700228T2 (en) | Recording sheet for the ink jet printing process | |
DE69709063T2 (en) | AQUEOUS INK RECORDING INK JET RECEIVING MEDIUM THAT GENERATES A WATER RESISTANT INK JET PRINT | |
DE60012869T2 (en) | Recording material, production method of the same and imaging method | |
DE60310499T2 (en) | Process for the preparation of ink jet recording materials | |
DE69606357T2 (en) | Multicolored ink jet recording layer | |
EP0870623B1 (en) | Recording material for receiving water-based inks | |
DE60009240T2 (en) | Recording material, manufacturing method thereof, recording method and product recorded therewith | |
DE60108335T2 (en) | A coating liquid for producing a recording medium for use in ink-jet printing |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB IT LI NL PT |
|
AX | Request for extension of the european patent |
Free format text: AL;LT;LV;MK;RO;SI |
|
17P | Request for examination filed |
Effective date: 19990324 |
|
AKX | Designation fees paid |
Free format text: AT BE CH DE DK ES FI FR GB IT LI NL PT |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
17Q | First examination report despatched |
Effective date: 20000518 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: EMTEC MAGNETICS GMBH Owner name: FEW CHEMICALS GMBH |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: EMTEC MAGNETICS GMBH Owner name: FEW CHEMICALS GMBH |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FI FR GB IT LI NL PT |
|
REF | Corresponds to: |
Ref document number: 198448 Country of ref document: AT Date of ref document: 20010115 Kind code of ref document: T |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
ITF | It: translation for a ep patent filed | ||
REF | Corresponds to: |
Ref document number: 59800412 Country of ref document: DE Date of ref document: 20010208 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: DIPL.-ING. ETH H. R. WERFFELI PATENTANWALT |
|
ET | Fr: translation filed | ||
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 20010308 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2154918 Country of ref document: ES Kind code of ref document: T3 |
|
REG | Reference to a national code |
Ref country code: PT Ref legal event code: SC4A Free format text: AVAILABILITY OF NATIONAL TRANSLATION Effective date: 20010327 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20020319 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 20020327 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 20020328 Year of fee payment: 5 Ref country code: NL Payment date: 20020328 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20020402 Year of fee payment: 5 Ref country code: FI Payment date: 20020402 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: PT Payment date: 20020404 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20020415 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20020416 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20020418 Year of fee payment: 5 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030401 Ref country code: FI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030401 Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030401 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030402 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030430 Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030430 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030430 Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20030430 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20030521 Year of fee payment: 6 |
|
BERE | Be: lapsed |
Owner name: *EMTEC MAGNETICS G.M.B.H. Effective date: 20030430 Owner name: *FEW CHEMICALS G.M.B.H. Effective date: 20030430 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031031 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031101 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20030401 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 20031101 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20031231 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Ref country code: PT Ref legal event code: MM4A Free format text: LAPSE DUE TO NON-PAYMENT OF FEES Effective date: 20031031 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20030402 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20041103 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20050401 |