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GB615890A - Improvements in cross-linked crystalline films - Google Patents

Improvements in cross-linked crystalline films

Info

Publication number
GB615890A
GB615890A GB21876/44A GB2187644A GB615890A GB 615890 A GB615890 A GB 615890A GB 21876/44 A GB21876/44 A GB 21876/44A GB 2187644 A GB2187644 A GB 2187644A GB 615890 A GB615890 A GB 615890A
Authority
GB
United Kingdom
Prior art keywords
film
treatment
polyvinyl
tank
films
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.)
Expired
Application number
GB21876/44A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of GB615890A publication Critical patent/GB615890A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/12Chemical modification
    • C08J7/126Halogenation
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3025Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

<PICT:0615890/IV(a)/1> A light-polarizing film is obtained by stretching a film of an organic polymer and then treating the film in the stretched microcrystalline state with a halogen compound which intensifies the polarizing effect and with an alkyl silicate so as to render the extended or stretched film substantially non-retractive. The treatment of the stretched film may be carried out as a continuous process on a long length of film. The treatment of polyvinyl acetal films is restricted to this continuous form of the process. The film may be treated simultaneously or separately with the halogen compound and the alkyl silicate. For the stretching step, the film may be brought into a rubbery-elastic state by means of heat or swelling agents. Heat may be supplied by infra-red rays. The organic polymer from which the film is obtained may be a polymethylene, polyvinylidene chloride, polyvinyl alcohol, polyvinyl ether, polyvinyl ester, polyamide, rubber or rubber homologue, amylose, keratin, or silk fibroin. Iodine, bromine, chlorine, fluorine, hydrochloric acid, or hydrofluoric acid may be employed as the intensifying compound, and the alkyl silicate may be ethyl orthosilicate. The treatment appears to form p cross-linkages between the long chains of atoms in the molecules of the film substance. The colour of the film produced may be neutral gray or blue-green according to the intensity of the chemical treatment. As shown, the film 10, which has previously been submitted to a stretching operation, is unwound from a roll and passed through the treatment tanks 4, 5, 6, and drying chamber 19. The film may be of polyvinyl butyral, and tank 4 may contain an aqueous solution of iodine, n-propyl alcohol, hydriodic acid and a sulphonated alcohol wetting agent. The tank 5 may contain a solution of ethyl silicate in n-propyl alcohol. Tank 6 contains a liquid such as isopropyl or butyl ether for removing excess of reagents. The treatment may be effected at 30 DEG C. If desired, the tank 4 may contain a solution of iodine in n-propyl alcohol and ethyl silicate. When the treatment is carried out at 20 DEG C., the polarizing film obtained may be of a neutral gray colour, but when the temperature is 30-40 DEG C., the film obtained may be of a blue-green tint. For making light-polarizers, the films may be treated with plasticisers and laminated. Specification 591,943 is referred to. The Specification as open to inspection under Sect. 91, comprises also the treatment of films of other polymeric substances, e.g. phosphonitrilic chloride or fluoride, polymerized sulphur or selenium, sulphur trioxide polymers, and silicates. It also comprises the use of other cross-linking agents or agents for permeation of the crystal lattice, e.g. oxygen, cyanogen, ethylene, acetylene, iron carbonyl, magnesium ethyl, sulphur chloride, carbon disulphide, sulphuric acid, zinc chloride, ammonia, amines, and caustic alkalis. This subject-matter does not appear in the Specification as accepted.
GB21876/44A 1943-12-24 1944-11-07 Improvements in cross-linked crystalline films Expired GB615890A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US615890XA 1943-12-24 1943-12-24

Publications (1)

Publication Number Publication Date
GB615890A true GB615890A (en) 1949-01-13

Family

ID=22036766

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21876/44A Expired GB615890A (en) 1943-12-24 1944-11-07 Improvements in cross-linked crystalline films

Country Status (1)

Country Link
GB (1) GB615890A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004094510A1 (en) * 2003-03-31 2004-11-04 3M Innovative Properties Company Process for making an intrinsic polarizer
EP2634611A1 (en) * 2009-05-01 2013-09-04 Nitto Denko Corporation Poly-Vinyl-Alcohol polarizer based on adsorbed iodine

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004094510A1 (en) * 2003-03-31 2004-11-04 3M Innovative Properties Company Process for making an intrinsic polarizer
EP2634611A1 (en) * 2009-05-01 2013-09-04 Nitto Denko Corporation Poly-Vinyl-Alcohol polarizer based on adsorbed iodine
EP2637048A1 (en) * 2009-05-01 2013-09-11 Nitto Denko Corporation Poly-Vinyl-Alcohol polarizer based on adsorbed iodine
US9291744B2 (en) 2009-05-01 2016-03-22 Nitto Denko Corporation Method for producing polarizer
US9329307B2 (en) 2009-05-01 2016-05-03 Nitto Denko Corporation Method for producing polarizer
US9575214B2 (en) 2009-05-01 2017-02-21 Nitto Denko Corporation Method for producing polarizer

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