FR1234357A - Films photographiques d'halogénure d'argent comportant une couche d'adhérence - Google Patents

Films photographiques d'halogénure d'argent comportant une couche d'adhérence

Info

Publication number: FR1234357A
Authority: FR; France
Prior art keywords: groups; group; epoxypropyl; replaced; aldehyde
Prior art date: 1958-07-09
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

FR799628A

Other languages

English (en)

Inventor

Helfried Klockgether

Wolfgang Himmelmann

Ottmar Wahl

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 AG

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.)

1958-07-09

Filing date

1959-07-08

Publication date

1960-10-17

1959-07-08 Application filed by Agfa AG filed Critical Agfa AG

1960-10-17 Application granted granted Critical

1960-10-17 Publication of FR1234357A publication Critical patent/FR1234357A/fr

Status Expired legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 title abstract 7
229910052709 silver Inorganic materials 0.000 title abstract 2
239000004332 silver Substances 0.000 title abstract 2
239000002253 acid Substances 0.000 abstract 4
150000001299 aldehydes Chemical class 0.000 abstract 4
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 abstract 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
125000003282 alkyl amino group Chemical group 0.000 abstract 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
150000001875 compounds Chemical class 0.000 abstract 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
230000007062 hydrolysis Effects 0.000 abstract 2
238000006460 hydrolysis reaction Methods 0.000 abstract 2
229920002451 polyvinyl alcohol Polymers 0.000 abstract 2
SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 abstract 2
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical class CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 abstract 1
IVIDDMGBRCPGLJ-UHFFFAOYSA-N 2,3-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(CO)COCC1CO1 IVIDDMGBRCPGLJ-UHFFFAOYSA-N 0.000 abstract 1
QECCQGLIYMMHCR-UHFFFAOYSA-N 2-({2,2-Bis[(2-oxiranylmethoxy)methyl]butoxy}methyl)oxirane Chemical compound C1OC1COCC(COCC1OC1)(CC)COCC1CO1 QECCQGLIYMMHCR-UHFFFAOYSA-N 0.000 abstract 1
SYEWHONLFGZGLK-UHFFFAOYSA-N 2-[1,3-bis(oxiran-2-ylmethoxy)propan-2-yloxymethyl]oxirane Chemical compound C1OC1COCC(OCC1OC1)COCC1CO1 SYEWHONLFGZGLK-UHFFFAOYSA-N 0.000 abstract 1
AOBIOSPNXBMOAT-UHFFFAOYSA-N 2-[2-(oxiran-2-ylmethoxy)ethoxymethyl]oxirane Chemical compound C1OC1COCCOCC1CO1 AOBIOSPNXBMOAT-UHFFFAOYSA-N 0.000 abstract 1
SHKUUQIDMUMQQK-UHFFFAOYSA-N 2-[4-(oxiran-2-ylmethoxy)butoxymethyl]oxirane Chemical compound C1OC1COCCCCOCC1CO1 SHKUUQIDMUMQQK-UHFFFAOYSA-N 0.000 abstract 1
PLDLPVSQYMQDBL-UHFFFAOYSA-N 2-[[3-(oxiran-2-ylmethoxy)-2,2-bis(oxiran-2-ylmethoxymethyl)propoxy]methyl]oxirane Chemical compound C1OC1COCC(COCC1OC1)(COCC1OC1)COCC1CO1 PLDLPVSQYMQDBL-UHFFFAOYSA-N 0.000 abstract 1
AKCRQHGQIJBRMN-UHFFFAOYSA-N 2-chloroaniline Chemical compound NC1=CC=CC=C1Cl AKCRQHGQIJBRMN-UHFFFAOYSA-N 0.000 abstract 1
IBMUHJIDXFMZPI-UHFFFAOYSA-N 2-chlorobenzaldehyde Chemical compound ClC1=CC=CC=C1C=O.ClC1=CC=CC=C1C=O IBMUHJIDXFMZPI-UHFFFAOYSA-N 0.000 abstract 1
UUODQIKUTGWMPT-UHFFFAOYSA-N 2-fluoro-5-(trifluoromethyl)pyridine Chemical compound FC1=CC=C(C(F)(F)F)C=N1 UUODQIKUTGWMPT-UHFFFAOYSA-N 0.000 abstract 1
QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 abstract 1
AVPYQKSLYISFPO-UHFFFAOYSA-N 4-chlorobenzaldehyde Chemical compound ClC1=CC=C(C=O)C=C1 AVPYQKSLYISFPO-UHFFFAOYSA-N 0.000 abstract 1
241001479434 Agfa Species 0.000 abstract 1
239000004593 Epoxy Substances 0.000 abstract 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
239000005977 Ethylene Substances 0.000 abstract 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 abstract 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 1
125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
150000007513 acids Chemical class 0.000 abstract 1
150000001279 adipic acids Chemical class 0.000 abstract 1
125000003277 amino group Chemical group 0.000 abstract 1
150000004982 aromatic amines Chemical class 0.000 abstract 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract 1
239000007795 chemical reaction product Substances 0.000 abstract 1
239000011248 coating agent Substances 0.000 abstract 1
238000000576 coating method Methods 0.000 abstract 1
229920001577 copolymer Polymers 0.000 abstract 1
238000004132 cross linking Methods 0.000 abstract 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract 1
230000000694 effects Effects 0.000 abstract 1
239000000839 emulsion Substances 0.000 abstract 1
230000002209 hydrophobic effect Effects 0.000 abstract 1
125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
150000002691 malonic acids Chemical class 0.000 abstract 1
229910052757 nitrogen Inorganic materials 0.000 abstract 1
RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 abstract 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 abstract 1
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 abstract 1
125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
150000003022 phthalic acids Chemical class 0.000 abstract 1
229920000768 polyamine Polymers 0.000 abstract 1
229920000642 polymer Polymers 0.000 abstract 1
229920001290 polyvinyl ester Polymers 0.000 abstract 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
230000003381 solubilizing effect Effects 0.000 abstract 1
150000003444 succinic acids Chemical class 0.000 abstract 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
150000003504 terephthalic acids Chemical class 0.000 abstract 1
229920001567 vinyl ester resin Polymers 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/91—Photosensitive materials characterised by the base or auxiliary layers characterised by subbing layers or subbing means
- G03C1/93—Macromolecular substances therefor
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/48—Isomerisation; Cyclisation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2810/00—Chemical modification of a polymer
- C08F2810/20—Chemical modification of a polymer leading to a crosslinking, either explicitly or inherently
- 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
- Y10S430/136—Coating process making radiation sensitive element

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Physics & Mathematics (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Engineering & Computer Science (AREA)
Spectroscopy & Molecular Physics (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Epoxy Resins (AREA)

FR799628A 1958-07-09 1959-07-08 Films photographiques d'halogénure d'argent comportant une couche d'adhérence Expired FR1234357A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEA29865A DE1086998B (de)	1958-07-09	1958-07-09	Verfahren zur Vorbehandlung von hydrophoben photographischen Schichttraegern fuer den Beguss mit hydrophilen Kolloidschichten

Publications (1)

Publication Number	Publication Date
FR1234357A true FR1234357A (fr)	1960-10-17

Family

ID=6927038

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FR799628A Expired FR1234357A (fr)	1958-07-09	1959-07-08	Films photographiques d'halogénure d'argent comportant une couche d'adhérence

Country Status (5)

Country	Link
US (1)	US3071466A (fr)
CH (1)	CH386837A (fr)
DE (1)	DE1086998B (fr)
FR (1)	FR1234357A (fr)
GB (1)	GB894590A (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE630170A (fr) *	1962-03-27
CA939183A (en) *	1969-01-16	1974-01-01	Teppei Ikeda	Photographic silver halide light-sensitive element
IT1170997B (it)	1981-05-26	1987-06-03	Minnesota Mining & Mfg	Miglioramento nel sottostratare supporti di polietilentereftalato e pellicole fotografiche comprendenti detti supporti migliorati
JPS59155800A (ja) *	1983-02-24	1984-09-04	富士写真フイルム株式会社	蓄積性蛍光体シ−ト
US4999078A (en) *	1988-11-07	1991-03-12	Monsanto Company	Reducing blocking and increasing flow of plasticized polyvinyl butyral sheet
US4999253A (en) *	1988-11-07	1991-03-12	Monsanto Company	Polyvinyl butyral sheet
US4968745A (en) *	1988-11-07	1990-11-06	Monsanto Company	Method of producing ionomeric polyvinyl butyral
US4968743A (en) *	1988-11-07	1990-11-06	Monsanto Company	Process for preparing polyinyl butyral sheet
US4968744A (en) *	1988-11-07	1990-11-06	Monsanto Company	Polyvinyl butyral polyblend
US5030688A (en) *	1988-11-07	1991-07-09	Monsanto Company	Ionomeric polyvinyl butyral
US5324573A (en) *	1992-12-18	1994-06-28	Rexham Industries Corp.	Antifogging plastic lens material
EP0704755A1 (fr) *	1994-09-28	1996-04-03	Minnesota Mining And Manufacturing Company	Eléments photographiques comprenant des couches antistatiques

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2133110A (en) *	1937-12-10	1938-10-11	Eastman Kodak Co	Manufacture of photographic film
US2310943A (en) *	1938-10-05	1943-02-16	Du Pont	Polyvinyl acetals
BE519171A (fr) *	1952-04-14
US2713567A (en) *	1952-04-14	1955-07-19	Shell Dev	Composition containing glycidyl polyether and a polyvinyl acetal resin
US2734825A (en) *	1953-06-16	1956-02-14		morgan
DE960334C (de) *	1954-11-19	1957-03-21	Agfa Ag Fuer Photofabrikation	Verfahren zur Vorbehandlung von Folien aus Polyvinylchlorid oder vinylchloridhaltigen Mischpolymerisaten fuer den Auftrag von hydrophilen Kolloidschichten
BE541244A (fr)	1955-09-13
US2844571A (en) *	1956-05-09	1958-07-22	Union Carbide Corp	Production of highly hydroxyalkylated polyvinyl alcohols

1958
- 1958-07-09 DE DEA29865A patent/DE1086998B/de active Pending
1959
- 1959-07-06 CH CH7534059A patent/CH386837A/de unknown
- 1959-07-07 US US825426A patent/US3071466A/en not_active Expired - Lifetime
- 1959-07-08 FR FR799628A patent/FR1234357A/fr not_active Expired
- 1959-07-08 GB GB23493/59A patent/GB894590A/en not_active Expired

Also Published As

Publication number	Publication date
DE1086998B (de)	1960-08-11
GB894590A (en)	1962-04-26
CH386837A (de)	1965-01-15
US3071466A (en)	1963-01-01

Publication	Publication Date	Title
FR1234357A (fr)	1960-10-17	Films photographiques d'halogénure d'argent comportant une couche d'adhérence
US3642908A (en)	1972-02-15	Vinyl and ether containing sulfones
US3271345A (en)	1966-09-06	Adhering layers to polyester film
US2990281A (en)	1961-06-27	Photosensitive resinous compositions and photographic elements
US3091537A (en)	1963-05-28	Hardening of photographic layers
US2874046A (en)	1959-02-17	Process for the retreatment of foils consisting of highly polymeric substances for the application of hydrophilic colloids
US3501301A (en)	1970-03-17	Coating compositions for polyester sheeting and polyester sheeting coated therewith
US3271178A (en)	1966-09-06	Adhering layer to polyester film
GB1048393A (en)	1966-11-16	Photographic materials containing antistatic polymers
US3415649A (en)	1968-12-10	Process for the production of light-sensitive material containing coating aids
US3201251A (en)	1965-08-17	Composite film element
US2805173A (en)	1957-09-03	Photographic film base and process for the manufacture thereof
US3589905A (en)	1971-06-29	Inking properties of matte-surfaced polyester sheeting
US3042524A (en)	1962-07-03	Plasticized gelatin and related proteinaceous colloids
US2725295A (en)	1955-11-29	Hardening of gelatin with organic acid chlorides
US4175970A (en)	1979-11-27	Process for sensitizing photographic silver halide emulsions
US3701680A (en)	1972-10-31	Polyester film with phenoxy resin coating
US3255000A (en)	1966-06-07	Activated hardening of photographic emulsions
US3442654A (en)	1969-05-06	Gelatin coating composition containing purified polyoxyalkylene glycol ether
GB988759A (en)	1965-04-14	Improvements in the treatment of polyester articles
US3317344A (en)	1967-05-02	Antistatic photographic film
US3271175A (en)	1966-09-06	Aziridinyl phosphonitrile gelatin hardening agent
US3161511A (en)	1964-12-15	Methacrylonitrile vehicle for vesicular photography and method of using same
US3600217A (en)	1971-08-17	Process for pretreating polyester film support for the coating with photographic emulsions
US2263015A (en)	1941-11-18	Sheeting