GB815277A - Photo sensitive addition polymerisable compositions and products made therefrom - Google Patents

Photo sensitive addition polymerisable compositions and products made therefrom

Info

Publication number
GB815277A
GB815277A GB3955656A GB3955656A GB815277A GB 815277 A GB815277 A GB 815277A GB 3955656 A GB3955656 A GB 3955656A GB 3955656 A GB3955656 A GB 3955656A GB 815277 A GB815277 A GB 815277A
Authority
GB
United Kingdom
Prior art keywords
vinyl
groups
acetal
polyvinyl
acetate
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
GB3955656A
Inventor
Elmore Louis Martin
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 to US461291A priority Critical patent/US2929710A/en
Priority claimed from US461291A external-priority patent/US2929710A/en
Priority to GB27394/55A priority patent/GB786119A/en
Priority to FR1168153D priority patent/FR1168153A/en
Priority to DEP17620A priority patent/DE1104825B/en
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB815277A publication Critical patent/GB815277A/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
    • G03F7/038Macromolecular compounds which are rendered insoluble or differentially wettable
    • G03F7/0388Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the side chains of the photopolymer
    • 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
    • C08F2/00Processes of polymerisation
    • C08F2/46Polymerisation initiated by wave energy or particle radiation
    • 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
    • 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
    • G03F7/033Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with binders the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

An addition photopolymerizable composition comprises more than 50 per cent by weight of (1) a solid polyester, polyacetal or mixed polyester/polyacetal of a polyvinyl alcohol having 0-15 per cent of free hydroxyl groups and 5-80 per cent of ester or acetal groups which contain non-terminal addition polymerizable ethylenic unsaturation, 5.35 per cent of (2) a compatible polymerizable monomer boiling above 100 DEG C. at atm. pressure and (3) a small amount of a free radical-generating polymerization initiator activatable by actinic light and inactive thermally below 80 DEG C. The polyvinyl alcohol from which the polyester, polyacetal or mixed polyester/polyacetal is formed may be a partially or completely hydrolysed polymer of a vinyl carboxylate or copolymer of a vinyl carboxylate with other polymerizable vinyl monomers. Suitable polyvinyl alcohols of the hydrolysed olefine/vinyl ester copolymers are described in U.S.A. Specification 2,386,347 and Specification 600,023. In addition to the unsaturated ester or acetal groups, saturated ester, acetal or ether groups may be introduced into the polyvinyl alcohol. The mixed polyesters/polyacetals may be prepared by simultaneous or separate conventional reactions. Some specified polyesters, polyacetals or mixed polyester/polyacetals are poly (vinyl alcohol co vinyl crotonate co vinyl butyral); poly (vinyl alcohol co vinyl acetate co vinyl crotonal); poly (vinyl acetate co vinyl butyral co vinyl crotonate); poly (vinyl acetate co vinyl crotonate co vinyl butyral); poly (vinyl alcohol co vinyl acetate co vinyl butyrate co vinyl butyral co vinyl crotonal); poly (vinyl alcohol co vinyl acetate co vinyl crotonate co vinyl acetal co vinyl butyral). Others include the following groups in various combinations p-sorboyloxylbenzal; o- or p-crotonoyloxybenzal; p-cinnamoyloxybenzal; m-sorbamido-benzal; cinnamal; sorbate; cinnamate; and as saturated groups benzal; benzoyloxybenzal; chloroacetal; o- or p-chlorobenzal; propionate; benzoate; sulphonic acid ester groups. Some specified monomers are acrylic or methacrylic acid; bis-acrylates or methacrylates of polyols, e.g. diethylene glycol diacrylate; glycerol triacrylate; pentaerythritol tetramethacrylate; acrylamide; methacrylamide; methylene-bis-acrylamide; the tris-methacrylamide of diethylenetetramine; vinyl benzoate; divinyl succinate; divinyl terephthalate; divinyl sulphonates; acrylamidoacetaldehyde; b -(methacrylamido) propionaldehyde; m-(a -ethylacrylamido) - benzaldehyde; p - (2 - methacryloyl - oxyethoxy) benzaldehyde; a -vinylcrotonaldehyde; a -phenylacrolein; 4-vinyl-41-formylbiphenol; 1 - vinyl - 4 - naphthaldehyde. Suitable polymerization initiators are diacetyl; benzil; benzoin; pivalin; benzoin methyl or ethyl ether; a -methyl-, a -allyl, or a -phenyl-benzoin. The compositions may include stabilizers, e.g. hydroquinone or p-tertiary-butyl catechol. The compositions are especially useful for making photopolymerizable elements consisting of a layer of the composition on a support. By exposing them to light under an image-bearing transparency and dissolving away unpolymerized composition relief printing elements can be made. They are also suitable for coatings, pellicles, sheets, cast objects or in the preparation of phosphor patterns in colour television screens. Suitable solvents for unpolymerized composition are methanol; ethanol; ethyl acetate/ethanol mixtures; acetone; methyl ethyl ketone. In the examples: I. An 86-89 per cent hydrolysed polyvinyl acetate, p-sorboyloxybenzaldehyde, glacial acetic acid, trifluoracetic and hydroquinone were heated at 60-65 DEG C., and the resultant p-sorboyloxybenzaldehyde polyvinyl acetal was precipitated with ether-petroleum ether, and purified by repeated solution in acetone and precipitation with ether. The bis-methacrylate of a polyethylene glycol (mol. wt. 200) and a little benzoin methyl ether were added to an acetone solution of the p-sorboyloxybenzaldehyde polyvinyl acetal and the solution cast on to glass at room temperature in subdued light. The film was then exposed to ultra-violet light under a line negative, and the unexposed parts removed by working with acetone to give a relief image suitable for printing. II and III were similar but used a polyvinyl acetal containing in addition to the acetoxy and hydroxy groups, either p-crotonoyloxybenzal groups, or o-crotonoyloxybenzal groups. IV. The polyvinyl alcohol was esterified with sorbic acid and acetic anhydride to form a polyvinyl acetate/sorbate free of hydroxyl groups which was used as in Example I to form a relief image in conjunction with the bis-methacrylate of polyethylene glycol. V. The poly-vinylacetal used in this example contained acetate, hydroxyl, p-sorboyloxybenzal, and p-benzoyloxybenzal groups. VI. Polyvinylacetate/cinnamate substantially free of OH groups was used as before. VII. The polyvinyl acetal used contained acetoxy, hydroxy, p-benzoyloxybenzal and p-cinnamoyloxybenzal groups. VIII. The relief printing image was prepared from a copolymer of a polyvinyl acetal containing acetate, benzal and crotonal groups with triethylene glycol dimethacrylate, again using benzoin methyl ether as catalyst. IX and X were similar to VIII but used a polyvinyl acetal containing acetoxy, butyral and crotonal groups. XI was similar to I but uses a polyvinyl acetal containing acetoxy and m-sorbamidobenzal groups. Specification 638,895 also is referred to.ALSO:p-Sorboyloxybenzaldehyde is prepared by reacting sorboyl chloride with p-hydroxybenzaldehyde in methylene chloride in the presence of triethylamine, at 15-20 DEG C. o- and p-Crotonoyloxybenzaldehydes and p-cinnamoyloxybenzaldehyde are similarly prepared. In Example XI m-sorbamidobenzaldehyde ethylene glycol acetal is prepared by reacting m-aminobenzaldehyde ethylene glycol acetal (see Specification 638,895) in acetone with a dioxane solution of sorboyl chloride at 0-5 DEG C. and pH 7-9.
GB3955656A 1954-10-08 1956-12-28 Photo sensitive addition polymerisable compositions and products made therefrom Expired GB815277A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US461291A US2929710A (en) 1954-10-08 1954-10-08 Polyvinyl acetal with terminal vinylidene groups
GB27394/55A GB786119A (en) 1954-10-08 1955-09-26 Improvements in or relating to polymers and their uses
FR1168153D FR1168153A (en) 1954-10-08 1956-12-14 Improvements to polymers and their uses
DEP17620A DE1104825B (en) 1954-10-08 1956-12-15 Photopolymerizable films for the production of printing forms

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US461291A US2929710A (en) 1954-10-08 1954-10-08 Polyvinyl acetal with terminal vinylidene groups

Publications (1)

Publication Number Publication Date
GB815277A true GB815277A (en) 1959-06-24

Family

ID=23831976

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3955656A Expired GB815277A (en) 1954-10-08 1956-12-28 Photo sensitive addition polymerisable compositions and products made therefrom

Country Status (1)

Country Link
GB (1) GB815277A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0224164A2 (en) * 1985-11-21 1987-06-03 BASF Aktiengesellschaft Photosensitive registration materials with elastomeric graft copolymer binders, and relief forms prepared therefrom
EP0295545A2 (en) * 1987-06-13 1988-12-21 BASF Aktiengesellschaft Heat relief stamping plates hardened by photopolymerisation
CN115785553A (en) * 2022-12-23 2023-03-14 湖北力生电缆有限公司 Crosslinked polyethylene insulated cable

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0224164A2 (en) * 1985-11-21 1987-06-03 BASF Aktiengesellschaft Photosensitive registration materials with elastomeric graft copolymer binders, and relief forms prepared therefrom
EP0224164A3 (en) * 1985-11-21 1988-08-24 Basf Aktiengesellschaft Photosensitive registration materials with elastomeric graft copolymer binders, and relief forms prepared therefrom
US4849307A (en) * 1985-11-21 1989-07-18 Basf Aktiengesellschaft Photosensitive recording materials having a novel graft copolymer binder
EP0295545A2 (en) * 1987-06-13 1988-12-21 BASF Aktiengesellschaft Heat relief stamping plates hardened by photopolymerisation
EP0295545A3 (en) * 1987-06-13 1989-07-26 Basf Aktiengesellschaft Heat relief stamping plates hardened by photopolymerisation
US4957852A (en) * 1987-06-13 1990-09-18 Basf Aktiengesellschaft Hot embossing plates crosslinkable by photopolymerization
CN115785553A (en) * 2022-12-23 2023-03-14 湖北力生电缆有限公司 Crosslinked polyethylene insulated cable

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