GB1118213A - Light-sensitive modified epoxy resins - Google Patents

Light-sensitive modified epoxy resins

Info

Publication number
GB1118213A
GB1118213A GB2339265A GB2339265A GB1118213A GB 1118213 A GB1118213 A GB 1118213A GB 2339265 A GB2339265 A GB 2339265A GB 2339265 A GB2339265 A GB 2339265A GB 1118213 A GB1118213 A GB 1118213A
Authority
GB
United Kingdom
Prior art keywords
aqueous
acid
light
epoxy resins
so2cl2
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
GB2339265A
Inventor
Urbain Leopold Laridon
Gerard Albert Delzenne
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.)
Agfa Gevaert NV
Original Assignee
Agfa Gevaert NV
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 Agfa Gevaert NV filed Critical Agfa Gevaert NV
Priority to GB2339265A priority Critical patent/GB1118213A/en
Priority to DE1966A0052579 priority patent/DE1522382A1/en
Priority to FR63184A priority patent/FR1481459A/en
Priority to NL6607506A priority patent/NL6607506A/xx
Priority to BE681794A priority patent/BE681794A/xx
Priority to CH790666A priority patent/CH466703A/en
Priority to AT517366A priority patent/AT272071B/en
Publication of GB1118213A publication Critical patent/GB1118213A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1477Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing nitrogen
    • 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
    • C08G59/00Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/14Polycondensates modified by chemical after-treatment
    • C08G59/1433Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds
    • C08G59/1483Polycondensates modified by chemical after-treatment with organic low-molecular-weight compounds containing sulfur

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Epoxy Resins (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)

Abstract

Light-sensitive compositions comprise soluble modified epoxy resins obtained by reacting a chlorosulphonyl or chlorocarbonyl substituted azidoaryl compound with a polycondensate of a bisphenol with epichlorohydrin. The modification is performed in the presence of pyridine and, optionally, of methylene dichloride as a solvent. After dilution of the reaction mixture with methylene dichloride the product is recovered by precipitation with methanol. The compositions preferably contain organic solvents and photosensitizers. The compositions are photochemically cross-linked on exposure to actinic light.ALSO:p-Azidobenzoic acid is prepared by adding aqueous NaNO2 and NaN3 successively to a cold solution of p-aminobenzoic acid in strong hydrochloric acid and filtering off the precipitate p-Azidobenzoyl chloride is obtained by reacting the acid with SO2Cl2. Sodium p-azidobenzenesulphonate is prepared by dissolving sulphanilic acid in aqueous Na2CO3, cooling, and adding successively aqueous NaNO2, aqueous HCl and aqueous NaN3. The product is precipitated by the addition of NaCl. p-Azidobenzenesulphonyl chloride is obtained from the sodium salt by reaction with SO2Cl2.
GB2339265A 1965-06-01 1965-06-01 Light-sensitive modified epoxy resins Expired GB1118213A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
GB2339265A GB1118213A (en) 1965-06-01 1965-06-01 Light-sensitive modified epoxy resins
DE1966A0052579 DE1522382A1 (en) 1965-06-01 1966-05-25 Recording method
FR63184A FR1481459A (en) 1965-06-01 1966-05-26 Process for the photochemical crosslinking of polymers
NL6607506A NL6607506A (en) 1965-06-01 1966-05-31
BE681794A BE681794A (en) 1965-06-01 1966-05-31
CH790666A CH466703A (en) 1965-06-01 1966-06-01 Process for the production of photographic resist images or printing plates
AT517366A AT272071B (en) 1965-06-01 1966-06-01 Recording material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2339265A GB1118213A (en) 1965-06-01 1965-06-01 Light-sensitive modified epoxy resins

Publications (1)

Publication Number Publication Date
GB1118213A true GB1118213A (en) 1968-06-26

Family

ID=10194878

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2339265A Expired GB1118213A (en) 1965-06-01 1965-06-01 Light-sensitive modified epoxy resins

Country Status (6)

Country Link
AT (1) AT272071B (en)
BE (1) BE681794A (en)
CH (1) CH466703A (en)
DE (1) DE1522382A1 (en)
GB (1) GB1118213A (en)
NL (1) NL6607506A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4735891A (en) * 1984-06-29 1988-04-05 Siemens Aktiengesellschaft Thermally stable, irradiation cross-linkable polymer systems based on bisphenols and epichlorohydrin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4735891A (en) * 1984-06-29 1988-04-05 Siemens Aktiengesellschaft Thermally stable, irradiation cross-linkable polymer systems based on bisphenols and epichlorohydrin

Also Published As

Publication number Publication date
NL6607506A (en) 1966-08-25
CH466703A (en) 1968-12-15
BE681794A (en) 1966-10-31
AT272071B (en) 1969-06-25
DE1522382A1 (en) 1969-11-06

Similar Documents

Publication Publication Date Title
Danielson et al. Photochemically induced charge separation at the molecular level. A chromophore-quencher complex containing both an electron donor and an acceptor
US4760013A (en) Sulfonium salt photoinitiators
Harpp et al. Organic sulfur chemistry. III. Chemistry of small-ring sulfur compounds. Thietanes and 1, 2-dithiolanes
KR850003146A (en) Water-soluble polyimide manufacturing method
GB1118213A (en) Light-sensitive modified epoxy resins
KR900018737A (en) Radioactive Sensitivity Mixture and Embossing Pattern
US3542558A (en) Hardeners for photographic gelatin emulsions
Agrawal et al. Potential Antitumor Agents III: Sodium Salts of α-[N]-Heterocyclic Carboxaldehyde Thiosemicarbazones
GB1377659A (en) Process for producing cephalosporin derivatives
US3853943A (en) Cyclopentadienes in which at least four of the ring carbons carry cyano substituents and methods for their preparation
Pan et al. Derivatives of fluorene. XXIV. 1 Synthesis and antitumor activities of some imidazolidine-2, 5-diones
US2786871A (en) Process for the preparation of aminomethyl-(monohydroxyphenyl)-ketones
Dewey et al. The Identification of Organic Acids by the Use of p-Bromobenzyl Pseudothiuronium Bromide
SE7609237L (en) WAY TO EXTRACT ZEARALENONE FROM A MIXTURE
US2269893A (en) Insecticide
US3578656A (en) Method of making allantoin polygalacturonic acid compounds
FR2384000A1 (en) PROCESS FOR PACKAGING PHTHALOCYANIN PIGMENTS
US1799068A (en) Process for manufacturing concentrated diazo solutions from solid aryldiazonium-fluoborates
GB605444A (en) Improvements in or relating to the resolution of racemic ª‡-hydroxy-ª‰-ª‰-dimethyl-ª†-butyrolactone
Taylor LVIII.—Constitution of the salts of s-alkylthiocarbamides
Witucki et al. Preparation and properties of 2-fluoro-2, 2-dinitroethyl pentafluorothioacetate
Thomas Recovering silver nitrate from silver chloride residues in about thirty minutes
Taylor II.—The chloroacetates of S-alkylthiocarbamides
Komppa et al. Some new Monosubstitution Derivatives of Retene
CN112114495A (en) Fluorine-free photoacid generator and preparation method thereof