GB1492500A - Photopolymerizable composition - Google Patents

Photopolymerizable composition

Info

Publication number
GB1492500A
GB1492500A GB5089575A GB5089575A GB1492500A GB 1492500 A GB1492500 A GB 1492500A GB 5089575 A GB5089575 A GB 5089575A GB 5089575 A GB5089575 A GB 5089575A GB 1492500 A GB1492500 A GB 1492500A
Authority
GB
United Kingdom
Prior art keywords
unsaturated
per cent
acid
photopolymerizable
anhydride
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
GB5089575A
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.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co 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
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to GB5089575A priority Critical patent/GB1492500A/en
Publication of GB1492500A publication Critical patent/GB1492500A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/027Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/032Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/66Polyesters containing oxygen in the form of ether groups
    • C08G63/668Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/676Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Macromonomer-Based Addition Polymer (AREA)

Abstract

1492500 Photopolymerizable compositions MITSUBISHI RAYON CO Ltd 11 Dec 1975 50895/75 Heading C3R [Also in Division G2] A photopolymerizable composition comprises (a) 30-95 wt. per cent of an unsaturated polyester having an acid value of 5-100 derived from a carboxylic acid component at least 40 mole per cent of which is of the formula in which R 1 is hydrogen or C1-C4 alkyl, and a diol component, at least 30 mole per cent of which is of the formula in which R 2 is C2-C4 alkylene and n is an integer from 2-5; (b) 5-70 wt. per cent of a photopolymerizable unsaturated monomer, and (c) a photosensitizer. The unsaturated polyester of acid value 5-100 may be prepared by first preparing an unsaturated polyester having a hydroxyl value of 5-200 and then reacting this with a polycarboxylic acid or anhydride. The examples describe (a) unsaturated polyesters derived from α-methylene-#-methyl adipic acid with adipic, succinic, phthalic or terephthalic acids, and di-, tri- or tetra-ethylene glycol or dipropylene glycol, optionally with ethylene glycol or 1,4-butanediol, the unsaturated polyesters being optionally modified with phthalic anhydride, succinic anhydride, maleic anhydride or citraconic acid, (b) forming a photopolymerizable composition by mixing the unsaturated polyesters with various unsaturated monomers, e.g. a mixture of hydroxypropylmethacrylate, ethylene glycol dimethacrylate and triethylene glycol diacrylate, and a photosensitizer, and (c) coating the composition on a substrate, e.g. aluminium, polyester or polymethylmethacrylate, imagewise exposing the composition and washing out the uncured areas.
GB5089575A 1975-12-11 1975-12-11 Photopolymerizable composition Expired GB1492500A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB5089575A GB1492500A (en) 1975-12-11 1975-12-11 Photopolymerizable composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB5089575A GB1492500A (en) 1975-12-11 1975-12-11 Photopolymerizable composition

Publications (1)

Publication Number Publication Date
GB1492500A true GB1492500A (en) 1977-11-23

Family

ID=10457812

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5089575A Expired GB1492500A (en) 1975-12-11 1975-12-11 Photopolymerizable composition

Country Status (1)

Country Link
GB (1) GB1492500A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11877848B2 (en) 2021-11-08 2024-01-23 Satio, Inc. Dermal patch for collecting a physiological sample
US11964121B2 (en) 2021-10-13 2024-04-23 Satio, Inc. Mono dose dermal patch for pharmaceutical delivery
US12023156B2 (en) 2021-10-13 2024-07-02 Satio, Inc. Dermal patch for collecting a physiological sample
US12029562B2 (en) 2021-04-14 2024-07-09 Satio, Inc. Dermal patch system
US12048543B2 (en) 2021-11-08 2024-07-30 Satio, Inc. Dermal patch for collecting a physiological sample with removable vial
US12053284B2 (en) 2021-11-08 2024-08-06 Satio, Inc. Dermal patch for collecting a physiological sample

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12029562B2 (en) 2021-04-14 2024-07-09 Satio, Inc. Dermal patch system
US11964121B2 (en) 2021-10-13 2024-04-23 Satio, Inc. Mono dose dermal patch for pharmaceutical delivery
US12023156B2 (en) 2021-10-13 2024-07-02 Satio, Inc. Dermal patch for collecting a physiological sample
US11877848B2 (en) 2021-11-08 2024-01-23 Satio, Inc. Dermal patch for collecting a physiological sample
US12048543B2 (en) 2021-11-08 2024-07-30 Satio, Inc. Dermal patch for collecting a physiological sample with removable vial
US12053284B2 (en) 2021-11-08 2024-08-06 Satio, Inc. Dermal patch for collecting a physiological sample

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee

Effective date: 19921211