JPS63136038A - カラー写真ハロゲン化銀材料 - Google Patents

カラー写真ハロゲン化銀材料

Info

Publication number: JPS63136038A
Authority: JP; Japan
Prior art keywords: silver halide; color photographic; sensitive; layer; blue
Prior art date: 1986-11-14
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.): Pending

Application number

JP62282286A

Other languages

English (en)

Japanese (ja)

Inventor

ヘルムート・ロイス

ブルーノ・ミユツケ

ヘルムート・メダー

マルセル・カレル・バン・ドールセレール

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 AG

Original Assignee

Agfa Gevaert 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.)

1986-11-14

Filing date

1987-11-10

Publication date

1988-06-08

1987-11-10 Application filed by Agfa Gevaert AG filed Critical Agfa Gevaert AG

1988-06-08 Publication of JPS63136038A publication Critical patent/JPS63136038A/ja

Status Pending legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 title claims description 44
229910052709 silver Inorganic materials 0.000 title claims description 31
239000004332 silver Substances 0.000 title claims description 31
239000000463 material Substances 0.000 title claims description 28
239000000839 emulsion Substances 0.000 claims description 26
125000000217 alkyl group Chemical group 0.000 claims description 14
125000003118 aryl group Chemical group 0.000 claims description 13
229910052736 halogen Inorganic materials 0.000 claims description 13
150000002367 halogens Chemical class 0.000 claims description 13
125000003710 aryl alkyl group Chemical group 0.000 claims description 9
239000003795 chemical substances by application Substances 0.000 claims description 8
125000000623 heterocyclic group Chemical group 0.000 claims description 7
239000004848 polyfunctional curative Substances 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 4
239000000975 dye Substances 0.000 claims description 4
239000001043 yellow dye Substances 0.000 claims description 3
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
UGZVCHWAXABBHR-UHFFFAOYSA-O pyridin-1-ium-1-carboxamide Chemical group NC(=O)[N+]1=CC=CC=C1 UGZVCHWAXABBHR-UHFFFAOYSA-O 0.000 claims 1
CZJWRCGMJPIJSJ-UHFFFAOYSA-O pyridin-1-ium-1-yl carbamate Chemical class NC(=O)O[N+]1=CC=CC=C1 CZJWRCGMJPIJSJ-UHFFFAOYSA-O 0.000 claims 1
239000010410 layer Substances 0.000 description 40
150000001875 compounds Chemical class 0.000 description 27
238000002844 melting Methods 0.000 description 20
230000008018 melting Effects 0.000 description 20
108010010803 Gelatin Proteins 0.000 description 14
238000001723 curing Methods 0.000 description 14
229920000159 gelatin Polymers 0.000 description 14
239000008273 gelatin Substances 0.000 description 14
235000019322 gelatine Nutrition 0.000 description 14
235000011852 gelatine desserts Nutrition 0.000 description 14
229910052739 hydrogen Inorganic materials 0.000 description 14
239000001257 hydrogen Substances 0.000 description 11
238000000034 method Methods 0.000 description 11
150000002431 hydrogen Chemical group 0.000 description 9
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 8
230000005070 ripening Effects 0.000 description 8
238000003860 storage Methods 0.000 description 8
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
229910052757 nitrogen Inorganic materials 0.000 description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 6
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
206010034972 Photosensitivity reaction Diseases 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
239000011230 binding agent Substances 0.000 description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 4
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
125000004433 nitrogen atom Chemical group N* 0.000 description 4
230000036211 photosensitivity Effects 0.000 description 4
230000002194 synthesizing effect Effects 0.000 description 4
239000006188 syrup Substances 0.000 description 4
235000020357 syrup Nutrition 0.000 description 4
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 3
239000006096 absorbing agent Substances 0.000 description 3
239000000654 additive Substances 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000005266 casting Methods 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
125000001072 heteroaryl group Chemical group 0.000 description 3
239000011229 interlayer Substances 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
125000003860 C1-C20 alkoxy group Chemical group 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
239000012790 adhesive layer Substances 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
125000000732 arylene group Chemical group 0.000 description 2
238000004132 cross linking Methods 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
230000008961 swelling Effects 0.000 description 2
PTUCPHGSAFOJAU-MGONOCMRSA-N (4s)-5-amino-4-[[(2s)-2-[[(2s)-2-[[(4-bromophenyl)-hydroxyphosphoryl]methyl]-3-[3-[4-(3-chlorophenyl)phenyl]-1,2-oxazol-5-yl]propanoyl]amino]-4-carboxybutanoyl]amino]-5-oxopentanoic acid Chemical compound C([C@@H](C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N)CP(O)(=O)C=1C=CC(Br)=CC=1)C(ON=1)=CC=1C(C=C1)=CC=C1C1=CC=CC(Cl)=C1 PTUCPHGSAFOJAU-MGONOCMRSA-N 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
PMWJOLLLHRDHNP-UHFFFAOYSA-N 2,3-dioctylbenzene-1,4-diol Chemical compound CCCCCCCCC1=C(O)C=CC(O)=C1CCCCCCCC PMWJOLLLHRDHNP-UHFFFAOYSA-N 0.000 description 1
QVLXDGDLLZYJAM-UHFFFAOYSA-N 2,5-dioctylbenzene-1,4-diol Chemical compound CCCCCCCCC1=CC(O)=C(CCCCCCCC)C=C1O QVLXDGDLLZYJAM-UHFFFAOYSA-N 0.000 description 1
CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
102100040996 Cochlin Human genes 0.000 description 1
101000748988 Homo sapiens Cochlin Proteins 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
208000035480 Ring chromosome 8 syndrome Diseases 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
229910052785 arsenic Inorganic materials 0.000 description 1
RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000005605 benzo group Chemical group 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
ZEUDGVUWMXAXEF-UHFFFAOYSA-L bromo(chloro)silver Chemical compound Cl[Ag]Br ZEUDGVUWMXAXEF-UHFFFAOYSA-L 0.000 description 1
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001805 chlorine compounds Chemical group 0.000 description 1
RCTYPNKXASFOBE-UHFFFAOYSA-M chloromercury Chemical compound [Hg]Cl RCTYPNKXASFOBE-UHFFFAOYSA-M 0.000 description 1
OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical group FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
USQBFMHVASTQGU-UHFFFAOYSA-N ethyl 2-(3-tert-butyl-4-hydroxyphenoxy)tetradecanoate Chemical compound CCCCCCCCCCCCC(C(=O)OCC)OC1=CC=C(O)C(C(C)(C)C)=C1 USQBFMHVASTQGU-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
150000002730 mercury Chemical class 0.000 description 1
229940100892 mercury compound Drugs 0.000 description 1
150000002731 mercury compounds Chemical class 0.000 description 1
LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
BQPIGGFYSBELGY-UHFFFAOYSA-N mercury(2+) Chemical class [Hg+2] BQPIGGFYSBELGY-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000012038 nucleophile Substances 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
125000004043 oxo group Chemical group O=* 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
125000003386 piperidinyl group Chemical group 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
238000011417 postcuring Methods 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
125000006839 xylylene group Chemical group 0.000 description 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/392—Additives
- G03C7/39204—Inorganic compounds
- 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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/30—Hardeners

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
General Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Inorganic Chemistry (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP62282286A 1986-11-14 1987-11-10 カラー写真ハロゲン化銀材料 Pending JPS63136038A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3638930.7		1986-11-14
DE19863638930 DE3638930A1 (de)	1986-11-14	1986-11-14	Farbfotografisches silberhalogenidmaterial

Publications (1)

Publication Number	Publication Date
JPS63136038A true JPS63136038A (ja)	1988-06-08

Family

ID=6313943

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62282286A Pending JPS63136038A (ja)	1986-11-14	1987-11-10	カラー写真ハロゲン化銀材料

Country Status (3)

Country	Link
EP (1)	EP0267523B1 (de)
JP (1)	JPS63136038A (de)
DE (2)	DE3638930A1 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0850342A (ja) *	1994-05-30	1996-02-20	Konica Corp	写真用塗布液

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2728664A (en) *	1952-11-08	1955-12-27	Eastman Kodak Co	Photographic emulsions containing mercury salts
FR2084668A5 (en) *	1970-03-20	1971-12-17	Eastman Kodak Co	Mercury salts as antifoggants incoverted silver halide emul
DE2924035A1 (de) *	1979-06-13	1981-01-08	Agfa Gevaert Ag	Verfahren zur kettenverlaengerung von gelatine durch partielle haertung

1986
- 1986-11-14 DE DE19863638930 patent/DE3638930A1/de not_active Withdrawn
1987
- 1987-11-03 DE DE8787116144T patent/DE3777335D1/de not_active Expired - Fee Related
- 1987-11-03 EP EP87116144A patent/EP0267523B1/de not_active Expired - Lifetime
- 1987-11-10 JP JP62282286A patent/JPS63136038A/ja active Pending

Also Published As

Publication number	Publication date
EP0267523B1 (de)	1992-03-11
DE3638930A1 (de)	1988-05-26
EP0267523A3 (en)	1989-03-15
DE3777335D1 (de)	1992-04-16
EP0267523A2 (de)	1988-05-18

Publication	Publication Date	Title
US3926869A (en)	1975-12-16	Process for hardening gelatin in photographic layers which contain a thickener and hardener by utilizing acrylic acid-acrylamide copolymers
JPS63136038A (ja)	1988-06-08	カラー写真ハロゲン化銀材料
US5009990A (en)	1991-04-23	Photographic recording material
JP3191191B2 (ja)	2001-07-23	ハロゲン化銀写真感光材料
US3969117A (en)	1976-07-13	Lithographic developing process utilizing a silver halide photographic material containing hydroimidazo-s-triazine and polyalkylene oxide derivative
JP2835633B2 (ja)	1998-12-14	ハロゲン化銀写真感光材料
JPS63264572A (ja)	1988-11-01	プロテインのための硬化剤、それで硬化されたバインダー層及びそのような層を含む写真記録材料
US5021336A (en)	1991-06-04	Color photographic material
DE3819082A1 (de)	1989-12-14	Farbfotografisches silberhalogenidmaterial
US4544628A (en)	1985-10-01	Silver halide photographic emulsion
US4845024A (en)	1989-07-04	Hardeners for proteins, a binder layer hardened therewith and a photographic recording material containing such a layer
JP3282045B2 (ja)	2002-05-13	ハロゲン化銀写真感光材料
JP2791816B2 (ja)	1998-08-27	ハロゲン化銀写真感光材料
JP3544732B2 (ja)	2004-07-21	硬化ハロゲン化銀写真成分
JP2662235B2 (ja)	1997-10-08	ゼラチンを硬化する方法及び組成物
JPS606940A (ja)	1985-01-14	ハロゲン化銀写真感光材料
US4810627A (en)	1989-03-07	Photographic recording material
JP2743202B2 (ja)	1998-04-22	ハロゲン化銀写真感光材料
JPH01155334A (ja)	1989-06-19	カラー写真記録材料
JPH04157452A (ja)	1992-05-29	ハロゲン化銀写真感光材料
JPH0627579A (ja)	1994-02-04	ハロゲン化銀写真感光材料
JPH06337495A (ja)	1994-12-06	ハロゲン化銀写真感光材料
JPH04306644A (ja)	1992-10-29	ハロゲン化銀写真感光材料
JPH01252955A (ja)	1989-10-09	カラー像の製造方法及びそのために適するカラー写真記録材料
JPH03226734A (ja)	1991-10-07	ハロゲン化銀写真感光材料