BE898482A - Procédé de stabilisation et de prévention contre le voile de matérielsphotographiques en couleurs à halogénure d'argent. - Google Patents

Procédé de stabilisation et de prévention contre le voile de matérielsphotographiques en couleurs à halogénure d'argent. Download PDF

Info

Publication number: BE898482A
Authority: BE; Belgium
Prior art keywords: sep; compounds; silver halide; formula; haze
Prior art date: 1982-12-17

Application number

BE0/212060A

Other languages

English (en)

French (fr)

Inventor

G Fischer

G Bach

H Bohm

S Wilschek

J Tamm

G Hanisch

Original Assignee

Wolfen Filmfab Veb

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.)

1982-12-17

Filing date

1983-12-16

Publication date

1984-04-16

1983-12-16 Application filed by Wolfen Filmfab Veb filed Critical Wolfen Filmfab Veb

1984-04-16 Publication of BE898482A publication Critical patent/BE898482A/fr

Links

238000000034 method Methods 0.000 title claims abstract description 17
-1 silver halide Chemical class 0.000 title claims description 31
229910052709 silver Inorganic materials 0.000 title claims description 25
239000004332 silver Substances 0.000 title claims description 25
239000000463 material Substances 0.000 title claims description 17
230000000087 stabilizing effect Effects 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 37
230000002265 prevention Effects 0.000 claims abstract description 9
230000006641 stabilisation Effects 0.000 claims abstract description 9
238000011105 stabilization Methods 0.000 claims abstract description 9
125000000217 alkyl group Chemical group 0.000 claims abstract description 7
150000001450 anions Chemical class 0.000 claims abstract description 3
125000003118 aryl group Chemical group 0.000 claims abstract description 3
239000000839 emulsion Substances 0.000 claims description 24
108010010803 Gelatin Proteins 0.000 claims description 16
239000006185 dispersion Substances 0.000 claims description 16
229920000159 gelatin Polymers 0.000 claims description 16
239000008273 gelatin Substances 0.000 claims description 16
235000019322 gelatine Nutrition 0.000 claims description 16
235000011852 gelatine desserts Nutrition 0.000 claims description 16
125000004432 carbon atom Chemical group C* 0.000 claims description 4
239000003086 colorant Substances 0.000 claims description 3
230000008569 process Effects 0.000 claims description 3
INVVMIXYILXINW-UHFFFAOYSA-N 5-methyl-1h-[1,2,4]triazolo[1,5-a]pyrimidin-7-one Chemical compound CC1=CC(=O)N2NC=NC2=N1 INVVMIXYILXINW-UHFFFAOYSA-N 0.000 claims description 2
KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
229960003237 betaine Drugs 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
150000007522 mineralic acids Chemical class 0.000 claims description 2
150000007524 organic acids Chemical class 0.000 claims description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical class C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 claims 1
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
239000002253 acid Substances 0.000 abstract description 2
239000000654 additive Substances 0.000 description 24
239000000126 substance Substances 0.000 description 19
239000003795 chemical substances by application Substances 0.000 description 13
230000035945 sensitivity Effects 0.000 description 11
230000000694 effects Effects 0.000 description 6
230000009467 reduction Effects 0.000 description 6
150000003839 salts Chemical group 0.000 description 6
230000000996 additive effect Effects 0.000 description 5
238000005266 casting Methods 0.000 description 5
230000003595 spectral effect Effects 0.000 description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
230000009471 action Effects 0.000 description 4
238000000586 desensitisation Methods 0.000 description 4
238000011161 development Methods 0.000 description 4
150000002344 gold compounds Chemical class 0.000 description 4
238000012545 processing Methods 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 3
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000003860 storage Methods 0.000 description 3
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 2
230000008901 benefit Effects 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
235000010265 sodium sulphite Nutrition 0.000 description 2
239000000979 synthetic dye Substances 0.000 description 2
238000005406 washing Methods 0.000 description 2
FMCAFXHLMUOIGG-JTJHWIPRSA-N (2s)-2-[[(2r)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-JTJHWIPRSA-N 0.000 description 1
FMCAFXHLMUOIGG-IWFBPKFRSA-N (2s)-2-[[(2s)-2-[[(2s)-2-[[(2r)-2-formamido-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,5-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoic acid Chemical compound O=CN[C@@H](CS)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(O)=O)CC1=CC(C)=C(O)C=C1C FMCAFXHLMUOIGG-IWFBPKFRSA-N 0.000 description 1
OKBJVIVEFXPEOU-UHFFFAOYSA-N 1,2,3-trichloro-4-(2,3,6-trichlorophenyl)benzene Chemical compound ClC1=C(Cl)C(Cl)=CC=C1C1=C(Cl)C=CC(Cl)=C1Cl OKBJVIVEFXPEOU-UHFFFAOYSA-N 0.000 description 1
GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 1
FLSYUUDKLRRXAO-UHFFFAOYSA-M 2,3-dimethyl-1,3-benzothiazol-3-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C1=CC=C2[N+](C)=C(C)SC2=C1 FLSYUUDKLRRXAO-UHFFFAOYSA-M 0.000 description 1
CLDZVCMRASJQFO-UHFFFAOYSA-N 2,5-bis(2,4,4-trimethylpentan-2-yl)benzene-1,4-diol Chemical compound CC(C)(C)CC(C)(C)C1=CC(O)=C(C(C)(C)CC(C)(C)C)C=C1O CLDZVCMRASJQFO-UHFFFAOYSA-N 0.000 description 1
WZTIODSAMDFHIB-UHFFFAOYSA-N 2,5-bis(3-methylpentan-3-yl)benzene-1,4-diol Chemical compound CCC(C)(CC)C1=CC(O)=C(C(C)(CC)CC)C=C1O WZTIODSAMDFHIB-UHFFFAOYSA-N 0.000 description 1
CEZVGLHZVYEJBR-UHFFFAOYSA-N 2,5-didodecylbenzene-1,4-diol Chemical compound CCCCCCCCCCCCC1=CC(O)=C(CCCCCCCCCCCC)C=C1O CEZVGLHZVYEJBR-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
SGYIRNXZLWJMCR-UHFFFAOYSA-M 3-methyl-1,3-benzothiazol-3-ium;iodide Chemical compound [I-].C1=CC=C2[N+](C)=CSC2=C1 SGYIRNXZLWJMCR-UHFFFAOYSA-M 0.000 description 1
ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 1
FCSKOFQQCWLGMV-UHFFFAOYSA-N 5-{5-[2-chloro-4-(4,5-dihydro-1,3-oxazol-2-yl)phenoxy]pentyl}-3-methylisoxazole Chemical compound O1N=C(C)C=C1CCCCCOC1=CC=C(C=2OCCN=2)C=C1Cl FCSKOFQQCWLGMV-UHFFFAOYSA-N 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical class [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 1
238000007171 acid catalysis Methods 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000010933 acylation Effects 0.000 description 1
238000005917 acylation reaction Methods 0.000 description 1
230000002411 adverse Effects 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
239000002168 alkylating agent Substances 0.000 description 1
229940100198 alkylating agent Drugs 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
230000006399 behavior Effects 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
239000007822 coupling agent Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000000975 dye Substances 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
230000035800 maturation Effects 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
AGJSNMGHAVDLRQ-IWFBPKFRSA-N methyl (2s)-2-[[(2s)-2-[[(2s)-2-[[(2r)-2-amino-3-sulfanylpropanoyl]amino]-3-methylbutanoyl]amino]-3-(4-hydroxy-2,3-dimethylphenyl)propanoyl]amino]-4-methylsulfanylbutanoate Chemical compound SC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C(=O)N[C@@H](CCSC)C(=O)OC)CC1=CC=C(O)C(C)=C1C AGJSNMGHAVDLRQ-IWFBPKFRSA-N 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
150000003557 thiazoles Chemical class 0.000 description 1
239000000080 wetting agent Substances 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
- G03C7/39296—Combination of additives

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

BE0/212060A 1982-12-17 1983-12-16 Procédé de stabilisation et de prévention contre le voile de matérielsphotographiques en couleurs à halogénure d'argent. BE898482A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD24614682A DD213528B5 (de)	1982-12-17	1982-12-17	Verfahren zur Stabilisierung und Schleierverhuetung bei farbfotografischen Halogensilbermaterialien

Publications (1)

Publication Number	Publication Date
BE898482A true BE898482A (fr)	1984-04-16

Family

ID=5543475

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE0/212060A BE898482A (fr)	1982-12-17	1983-12-16	Procédé de stabilisation et de prévention contre le voile de matérielsphotographiques en couleurs à halogénure d'argent.

Country Status (5)

Country	Link
BE (1)	BE898482A (de)
DD (1)	DD213528B5 (de)
DE (1)	DE3320483A1 (de)
FR (1)	FR2538135B1 (de)
GB (1)	GB2135069B (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3603099C2 (de) *	1986-02-01	1994-11-10	Agfa Gevaert Ag	Farbfotografisches Aufzeichnungsmaterial und Verfahren zur Herstellung fotografischer Bilder
FR2721117B1 (fr) *	1994-06-09	1998-07-10	Kodak Pathe	Procédé de préparation d'une émulsion photographique aux halogénures d'argent sensibilisée en présence de dérivés de l'hydroquinone.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2034064A (en) *	1929-11-12	1936-03-17	Western Union Telegraph Co	Stock selecting and indicating system
DE1472774C3 (de) *	1965-08-07	1974-01-31	Agfa-Gevaert Ag, 5090 Leverkusen	Stabilisierte photographische Silberhalogenidemul sion
JPS4834170B1 (de) *	1969-07-10	1973-10-19
JPS5023813B1 (de) *	1970-10-07	1975-08-11
JPS5952815B2 (ja) *	1976-12-21	1984-12-21	富士写真フイルム株式会社	硬調な画像を形成する方法

1982
- 1982-12-17 DD DD24614682A patent/DD213528B5/de not_active IP Right Cessation
1983
- 1983-06-07 DE DE19833320483 patent/DE3320483A1/de not_active Ceased
- 1983-09-29 FR FR8315542A patent/FR2538135B1/fr not_active Expired
- 1983-11-30 GB GB08331935A patent/GB2135069B/en not_active Expired
- 1983-12-16 BE BE0/212060A patent/BE898482A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
FR2538135A1 (fr)	1984-06-22
FR2538135B1 (fr)	1985-12-06
GB2135069A (en)	1984-08-22
GB8331935D0 (en)	1984-01-04
GB2135069B (en)	1986-04-09
DD213528A1 (de)	1984-09-12
DE3320483A1 (de)	1984-06-20
DD213528B5 (de)	1994-04-14

Legal Events

Date

Code

Title

Description

1991-06-30

RE

Patent lapsed

Owner name: VEB FILMFABRIK WOLFEN

Effective date: 19901231

Publication	Publication Date	Title
DE2901468A1 (de)	1979-08-16	Verfahren zum entwickeln eines lichtempfindlichen farbphotographischen silberhalogenidmaterials mit einer farbentwicklerloesung und anschliessenden bleichfixieren mit einer bleichfixierloesung
DE2629148A1 (de)	1977-02-03	Photographisches lichtempfindliches silberhalogenidmaterial
DE2034064C3 (de)	1979-04-12	Farbfotografisches Aufzeichnungsmaterial
FR2485758A1 (fr)	1981-12-31	Emulsion photosensible a l'halogenure d'argent sensibilisee au vert
JPH0314168B2 (de)	1991-02-26
BE898482A (fr)	1984-04-16	Procédé de stabilisation et de prévention contre le voile de matérielsphotographiques en couleurs à halogénure d'argent.
DE3337882A1 (de)	1984-04-19	Verfahren zum entwickeln von belichteten photographischen silberhalogenidmaterialien
US4322492A (en)	1982-03-30	Process for the development of color photographic images with p-dialkylaminoaniline color developers
WO1987006360A1 (fr)	1987-10-22	Revelateur couleur pour papier photographique couleur a base d'halogenure d'argent et procede pour traiter ledit papier photographique a l'aide d'un tel revelateur
US3667956A (en)	1972-06-06	Light-sensitive silver halide color photographic materials containing cyan couplers
US5747230A (en)	1998-05-05	Photographic silver halide colour material having improved granularity and dye hue
JPH06194780A (ja)	1994-07-15	ハロゲン化銀写真乳剤
CA1156503A (en)	1983-11-08	Photographic material containing a 1-halo-3-aryl-1- propyne derivative as stabilizing agent
US4299913A (en)	1981-11-10	Photographic reversal process without second exposure
US3619156A (en)	1971-11-09	Competing color developer composition
US2292306A (en)	1942-08-04	Method of color-forming development
JPH0128375B2 (de)	1989-06-02
US3471295A (en)	1969-10-07	Production of colored direct-positive images
GB2111234A (en)	1983-06-29	Light-sensitive silver halide photographic material
EP0745898A1 (de)	1996-12-04	Verfahren zur Herstellung eines chromogen entwickelten farbfotografischen Bildes unter Verwendung einer Verbindung die mit primären aromatischen Aminen zu reagieren vermag
DE2112728B2 (de)	1977-03-24	Photographisches aufzeichnungsmaterial
US3520693A (en)	1970-07-14	Merocyanine dye-sensitized photographic materials comprising silver halide emulsion layers containing azo-dyes
DE10221125B3 (de)	2004-02-05	Farbfotografisches Kopiermaterial
DE10230980A1 (de)	2004-01-29	Farbfotografisches Silberhalogenidmaterial
DE3402311A1 (de)	1984-07-26	Photographisches lichtempfindliches silberhalogenidmaterial