GB942188A - Polymers of use in photography - Google Patents

Polymers of use in photography

Info

Publication number
GB942188A
GB942188A GB3799659A GB3799659A GB942188A GB 942188 A GB942188 A GB 942188A GB 3799659 A GB3799659 A GB 3799659A GB 3799659 A GB3799659 A GB 3799659A GB 942188 A GB942188 A GB 942188A
Authority
GB
United Kingdom
Prior art keywords
acid
polymers
drying
water
ester
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
GB3799659A
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.)
Kodak Ltd
Original Assignee
Kodak Ltd
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
Priority claimed from US772725A external-priority patent/US3007901A/en
Application filed by Kodak Ltd filed Critical Kodak Ltd
Publication of GB942188A publication Critical patent/GB942188A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/825Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
    • G03C1/835Macromolecular substances therefor, e.g. mordants
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F22/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
    • C08F22/04Anhydrides, e.g. cyclic anhydrides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/14Esterification
    • C08F8/16Lactonisation
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
    • G03C1/053Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polyesters Or Polycarbonates (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)

Abstract

Polymers comprise recurring units of four kinds represented by formulae A, B, C, D: <FORM:0942188/C3/1> wherein n is an integer from 1 to 5; R is H, a C1- 12 alkyl group or a phenyl- or tolyl-substituted C1- 4 alkyl group; and R1 is H or CH3. The invention relates to such polymers which neutralise 4 to 6 ml. N NaOH per gm. They may be prepared by heating, in the presence of a strong acid catalyst and water, a fluid mixture comprising (i) 15 to 30% of a copolymer of vinyl alcohol or a carboxylic acid ester thereof with maleic, citraconic, dimethylmaleic, fumaric, mesaconic or dimethylfumaric acid, anhydride or C1- 4 alkyl ester; (ii) 35 to 65% of a monohydroxy carboxylic acid (CnH2n) (OH) (COOH) or (CnH2n- 1)(OH)(COOH)2; and (iii) 10 to 45% of an alcohol ROH, the percentages being by weight of the total of (i), (ii) and (iii) and R and n being as defined above. The vinyl ester in (i) may be the acetate, propionate or benzoate. The strong acid may be sulphuric or hydrochloric. The reaction can take place at 60 to 100 DEG C. in an organic media. The copolymer may be reacted with a hydroxylated material which has another hydrophilic group e.g. amide or sulphonic acid. Modifying agents such as drying, non-drying, and semi-drying oils; natural or synthetic resins, waxes and cellulose derivatives may be added to the products. Details are given of the preparation of vinyl acetate-maleic anhydride copolymers using benzoyl peroxide as catalyst, (a) in bulk followed by purification by dissolution in acetone and precipitation in water, and (b) in benzene. The copolymers are heated in the presence of sulphuric acid with lactic or glycolic acid and a variety of alcohols, including benzylalcohol. The presence of water is achieved either by using aqueous glycolic acid or moist polymer. Applications. The products can be dissolved in organic solvents e.g. dioxane; mixtures thereof with ethanol, methanol and butanol; ketones such as acetone; ethylene chloride; and alkyl ethers of ethylene glycol- and cast into films on a glass or metal plate or smooth revolving drum, or used to form coatings. The polymers are particularly useful for photographic materials and may be used as the carrier for light-sensitive materials, as a support for light sensitive coatings, as a stripping interlayer or as an antihalation backing layer, in which case they may contain a dye or pigment such as carbon black. Specification 537,709 is referred to.
GB3799659A 1958-11-10 1959-11-10 Polymers of use in photography Expired GB942188A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US772725A US3007901A (en) 1953-11-12 1958-11-10 Resinous mixed alkyl ester and carboxy ester lactones and preparation process therefor

Publications (1)

Publication Number Publication Date
GB942188A true GB942188A (en) 1963-11-20

Family

ID=25096025

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3799659A Expired GB942188A (en) 1958-11-10 1959-11-10 Polymers of use in photography

Country Status (1)

Country Link
GB (1) GB942188A (en)

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