GB1365730A - Creación de Inventos y Patentes con Inteligencia Artificial

GB1365730A – Photopolymerizable copying compositions
– Google Patents

GB1365730A – Photopolymerizable copying compositions
– Google Patents
Photopolymerizable copying compositions

Info

Publication number
GB1365730A

GB1365730A
GB5674671A
GB5674671A
GB1365730A
GB 1365730 A
GB1365730 A
GB 1365730A
GB 5674671 A
GB5674671 A
GB 5674671A
GB 5674671 A
GB5674671 A
GB 5674671A
GB 1365730 A
GB1365730 A
GB 1365730A
Authority
GB
United Kingdom
Prior art keywords
binder
radical
dec
monomer
substituted
Prior art date
1970-12-09
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
GB5674671A
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.)

Kalle GmbH and Co KG

Original Assignee
Kalle GmbH and Co KG
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.)
1970-12-09
Filing date
1971-12-07
Publication date
1974-09-04

1971-12-07
Application filed by Kalle GmbH and Co KG
filed
Critical
Kalle GmbH and Co KG

1974-09-04
Publication of GB1365730A
publication
Critical
patent/GB1365730A/en

Status
Expired
legal-status
Critical
Current

Links

Espacenet

Global Dossier

Discuss

239000000203
mixture
Substances

0.000
title
abstract
5

-1
vinylidene compound
Chemical class

0.000
abstract
5

239000011230
binding agent
Substances

0.000
abstract
3

ZWEHNKRNPOVVGH-UHFFFAOYSA-N
2-Butanone
Chemical compound

CCC(C)=O
ZWEHNKRNPOVVGH-UHFFFAOYSA-N
0.000
abstract
2

YXFVVABEGXRONW-UHFFFAOYSA-N
Toluene
Natural products

CC1=CC=CC=C1
YXFVVABEGXRONW-UHFFFAOYSA-N
0.000
abstract
2

150000005840
aryl radicals
Chemical class

0.000
abstract
2

239000003795
chemical substances by application
Substances

0.000
abstract
2

239000003112
inhibitor
Substances

0.000
abstract
2

239000000178
monomer
Substances

0.000
abstract
2

PYSRRFNXTXNWCD-UHFFFAOYSA-N
3-(2-phenylethenyl)furan-2,5-dione
Chemical group

O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1
PYSRRFNXTXNWCD-UHFFFAOYSA-N
0.000
abstract
1

NIXOWILDQLNWCW-UHFFFAOYSA-M
Acrylate
Chemical compound

[O-]C(=O)C=C
NIXOWILDQLNWCW-UHFFFAOYSA-M
0.000
abstract
1

229920000147
Styrene maleic anhydride
Polymers

0.000
abstract
1

DAKWPKUUDNSNPN-UHFFFAOYSA-N
Trimethylolpropane triacrylate
Chemical group

C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C
DAKWPKUUDNSNPN-UHFFFAOYSA-N
0.000
abstract
1

239000000654
additive
Substances

0.000
abstract
1

125000003545
alkoxy group
Chemical group

0.000
abstract
1

229920006217
cellulose acetate butyrate
Polymers

0.000
abstract
1

229920001577
copolymer
Polymers

0.000
abstract
1

239000013078
crystal
Substances

0.000
abstract
1

239000000852
hydrogen donor
Substances

0.000
abstract
1

AFAIELJLZYUNPW-UHFFFAOYSA-N
pararosaniline free base
Chemical compound

C1=CC(N)=CC=C1C(C=1C=CC(N)=CC=1)=C1C=CC(=N)C=C1
AFAIELJLZYUNPW-UHFFFAOYSA-N
0.000
abstract
1

ISWSIDIOOBJBQZ-UHFFFAOYSA-N
phenol group
Chemical group

C1(=CC=CC=C1)O
ISWSIDIOOBJBQZ-UHFFFAOYSA-N
0.000
abstract
1

229920003229
poly(methyl methacrylate)
Polymers

0.000
abstract
1

229920002037
poly(vinyl butyral) polymer
Polymers

0.000
abstract
1

229920000151
polyglycol
Polymers

0.000
abstract
1

239000010695
polyglycol
Substances

0.000
abstract
1

239000004926
polymethyl methacrylate
Substances

0.000
abstract
1

229920002689
polyvinyl acetate
Polymers

0.000
abstract
1

239000011118
polyvinyl acetate
Substances

0.000
abstract
1

150000003254
radicals
Chemical class

0.000
abstract
1

229920005989
resin
Polymers

0.000
abstract
1

239000011347
resin
Substances

0.000
abstract
1

239000001488
sodium phosphate
Substances

0.000
abstract
1

229910000162
sodium phosphate
Inorganic materials

0.000
abstract
1

150000005846
sugar alcohols
Polymers

0.000
abstract
1

RYFMWSXOAZQYPI-UHFFFAOYSA-K
trisodium phosphate
Chemical compound

[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O
RYFMWSXOAZQYPI-UHFFFAOYSA-K
0.000
abstract
1

125000000391
vinyl group
Chemical group

[H]C([*])=C([H])[H]

0.000
abstract
1

229920002554
vinyl polymer
Polymers

0.000
abstract
1

229910052724
xenon
Inorganic materials

0.000
abstract
1

FHNFHKCVQCLJFQ-UHFFFAOYSA-N
xenon atom
Chemical compound

[Xe]
FHNFHKCVQCLJFQ-UHFFFAOYSA-N
0.000
abstract
1

Classifications

G—PHYSICS

G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY

G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR

G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor

G03F7/004—Photosensitive materials

G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds

G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators

G03F7/031—Organic compounds not covered by group G03F7/029

Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof

Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface – process, composition, or product: radiation sensitive composition or product or process of making binder containing

Y10S430/1055—Radiation sensitive composition or product or process of making

Y10S430/106—Binder containing

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof

Y10S430/1055—Radiation sensitive composition or product or process of making

Y10S430/106—Binder containing

Y10S430/111—Polymer of unsaturated acid or ester

Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC

Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS

Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof

Y10S430/1055—Radiation sensitive composition or product or process of making

Y10S430/106—Binder containing

Y10S430/112—Cellulosic

Abstract

1365730 Photoinitiators KALLE AG 7 Dec 1971 [9 Dec 1970] 56746/71 Heading C3P [Also in Division G2] A photopolymerizable composition comprises a binder, a polymerizable vinyl or vinylidene compound and a photoinitiator of the formula R-C#C-CO-R1 where R is a C 1 to C 8 alkyl radical or C 6 to C 10 ) aryl radical, either of which may be substituted, and R1 is a C 6 to C 10 ) aryl radical or C 8 to C 12 aralkenyl radical, which may also be substituted. Preferably R and R1 are mononuclear aromatic radicals, at least one having an alkoxy or alkylenedioxy substituent. The binder is preferably an alkali-soluble or -softenable resin so that non-polymerized parts of the composition can be removed or softened by an alkaline developing agent, such as a sodium phosphate. The monomer may be an acrylate or methacrylate ester, preferably of a polyhydric alcohol. Other additives may also be present, e.g. hydrogen donors, sensitizers, inhibitors and conventional photoinitiators. Examples describe compositions in which the binder is a styrene-maleic anhydride copolymer mixed with one or more of: α-methylstyrenevinyl toluene copolymer, cellulose acetate butyrate, polyvinyl acetate, polyvinyl butyral and polymethyl methacrylate; the monomer is trimethylolpropane triacrylate; and a phenolic inhibitor and/or a dye (Crystal Violet or Pararosaniline) or a polyglycol are included in some cases. The compositions are coated on to plates or films from butanone solution and exposed in a copying device using a xenon lamp.

GB5674671A
1970-12-09
1971-12-07
Photopolymerizable copying compositions

Expired

GB1365730A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

DE2060576A

DE2060576C3
(en)

1970-12-09
1970-12-09

Photosensitive mixture

Publications (1)

Publication Number
Publication Date

GB1365730A
true

GB1365730A
(en)

1974-09-04

Family
ID=5790448
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB5674671A
Expired

GB1365730A
(en)

1970-12-09
1971-12-07
Photopolymerizable copying compositions

Country Status (14)

Country
Link

US
(1)

US3737320A
(en)

JP
(1)

JPS5418567B1
(en)

AT
(1)

AT324833B
(en)

AU
(1)

AU451135B2
(en)

BE
(1)

BE776325A
(en)

CA
(1)

CA962507A
(en)

DE
(1)

DE2060576C3
(en)

ES
(1)

ES397769A1
(en)

FR
(1)

FR2117572A5
(en)

GB
(1)

GB1365730A
(en)

IT
(1)

IT945317B
(en)

NL
(1)

NL7116374A
(en)

SE
(1)

SE366846B
(en)

ZA
(1)

ZA718227B
(en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

CA2128991A1
(en)

1993-08-02
1995-02-03
Hisao Takayanagi
Benzoylacetylene derivatives

AT412346B
(en)

2003-09-12
2005-01-25
Robert Liska
Photopolymerizable mixtures based on ethylenically unsaturated photopolymerizable compounds, useful e.g. in lacquers or printing inks, containing penta-1,4-diyn-3-one derivative as high reactivity photoinitiator

US8092984B2
(en)

2008-09-02
2012-01-10
Gary Ganghui Teng
Lithographic printing plate having specific polymeric binders

1970

1970-12-09
DE
DE2060576A
patent/DE2060576C3/en
not_active
Expired

1971

1971-11-29
NL
NL7116374A
patent/NL7116374A/xx
unknown

1971-12-06
BE
BE776325A
patent/BE776325A/en
unknown

1971-12-06
CA
CA129,353A
patent/CA962507A/en
not_active
Expired

1971-12-06
AT
AT1049271A
patent/AT324833B/en
not_active
IP Right Cessation

1971-12-07
ES
ES397769A
patent/ES397769A1/en
not_active
Expired

1971-12-07
IT
IT54585/71A
patent/IT945317B/en
active

1971-12-07
US
US00205701A
patent/US3737320A/en
not_active
Expired – Lifetime

1971-12-07
GB
GB5674671A
patent/GB1365730A/en
not_active
Expired

1971-12-08
SE
SE15743/71A
patent/SE366846B/xx
unknown

1971-12-08
ZA
ZA718227A
patent/ZA718227B/en
unknown

1971-12-09
JP
JP9982171A
patent/JPS5418567B1/ja
active
Pending

1971-12-09
AU
AU36686/71A
patent/AU451135B2/en
not_active
Expired

1971-12-09
FR
FR7144186A
patent/FR2117572A5/fr
not_active
Expired

Also Published As

Publication number
Publication date

IT945317B
(en)

1973-05-10

SU437316A3
(en)

1974-07-25

AU3668671A
(en)

1973-06-14

DE2060576C3
(en)

1978-08-03

FR2117572A5
(en)

1972-07-21

DE2060576A1
(en)

1972-06-15

SE366846B
(en)

1974-05-06

AU451135B2
(en)

1974-07-25

AT324833B
(en)

1975-09-25

DE2060576B2
(en)

1977-11-17

JPS5418567B1
(en)

1979-07-09

ES397769A1
(en)

1975-05-01

NL7116374A
(en)

1972-06-13

BE776325A
(en)

1972-06-06

CA962507A
(en)

1975-02-11

US3737320A
(en)

1973-06-05

ZA718227B
(en)

1972-10-25

Información de contacto