DE1188944B - Verfahren zur Herstellung einer Farbstoffentwicklersubstanz-Dispersion fuer farbphotographische Materialien - Google Patents

Verfahren zur Herstellung einer Farbstoffentwicklersubstanz-Dispersion fuer farbphotographische Materialien

Info

Publication number: DE1188944B
Authority: DE; Germany
Prior art keywords: dye; water; developing agent; dispersion; sulfite
Prior art date: 1963-03-01
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

DEE26451A

Other languages

German (de)

English (en)

Inventor

Carl James Williams Jun

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.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

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.)

1963-03-01

Filing date

1964-02-21

Publication date

1965-03-11

1964-02-21 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1965-03-11 Publication of DE1188944B publication Critical patent/DE1188944B/de

Status Pending legal-status Critical Current

Links

239000006185 dispersion Substances 0.000 title claims description 91
239000000463 material Substances 0.000 title claims description 25
238000000034 method Methods 0.000 title claims description 20
238000002360 preparation method Methods 0.000 title claims description 13
239000000975 dye Substances 0.000 claims description 93
239000003795 chemical substances by application Substances 0.000 claims description 59
239000000126 substance Substances 0.000 claims description 29
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
239000002904 solvent Substances 0.000 claims description 25
239000000203 mixture Substances 0.000 claims description 22
108010010803 Gelatin Proteins 0.000 claims description 21
239000008273 gelatin Substances 0.000 claims description 21
229920000159 gelatin Polymers 0.000 claims description 21
235000019322 gelatine Nutrition 0.000 claims description 21
235000011852 gelatine desserts Nutrition 0.000 claims description 21
238000009835 boiling Methods 0.000 claims description 19
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical group [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 19
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 18
150000004056 anthraquinones Chemical class 0.000 claims description 18
239000000084 colloidal system Substances 0.000 claims description 18
235000010265 sodium sulphite Nutrition 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 9
229910052709 silver Inorganic materials 0.000 claims description 9
239000004332 silver Substances 0.000 claims description 9
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 8
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239000010410 layer Substances 0.000 description 50
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OIPQUBBCOVJSNS-UHFFFAOYSA-L bromo(iodo)silver Chemical compound Br[Ag]I OIPQUBBCOVJSNS-UHFFFAOYSA-L 0.000 description 3
238000009792 diffusion process Methods 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
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OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
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QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
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239000002253 acid Substances 0.000 description 2
125000003282 alkyl amino group Chemical group 0.000 description 2
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125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
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SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 2
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239000000543 intermediate Substances 0.000 description 1
125000000468 ketone group Chemical group 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
QRWZCJXEAOZAAW-UHFFFAOYSA-N n,n,2-trimethylprop-2-enamide Chemical compound CN(C)C(=O)C(C)=C QRWZCJXEAOZAAW-UHFFFAOYSA-N 0.000 description 1
ZWDZJRRQSXLOQR-UHFFFAOYSA-N n-butyl-n-phenylacetamide Chemical compound CCCCN(C(C)=O)C1=CC=CC=C1 ZWDZJRRQSXLOQR-UHFFFAOYSA-N 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
235000019252 potassium sulphite Nutrition 0.000 description 1
238000003825 pressing Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000004023 quaternary phosphonium compounds Chemical class 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-M sodium 2-anthraquinonesulfonate Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)[O-])=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-M 0.000 description 1
DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000003860 storage Methods 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
229940104261 taurate Drugs 0.000 description 1
150000004026 tertiary sulfonium compounds Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 description 1
239000001069 triethyl citrate Substances 0.000 description 1
VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
235000013769 triethyl citrate Nutrition 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
238000009827 uniform distribution Methods 0.000 description 1
239000003021 water soluble solvent 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
- G03C8/12—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors characterised by the releasing mechanism
- G03C8/14—Oxidation of the chromogenic substances
- G03C8/16—Oxidation of the chromogenic substances initially diffusible in alkaline environment
- G03C8/18—Dye developers
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
- G03C8/12—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors characterised by the releasing mechanism
- G03C8/14—Oxidation of the chromogenic substances
- G03C8/16—Oxidation of the chromogenic substances initially diffusible in alkaline environment

Landscapes

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

DEE26451A 1963-03-01 1964-02-21 Verfahren zur Herstellung einer Farbstoffentwicklersubstanz-Dispersion fuer farbphotographische Materialien Pending DE1188944B (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US262167A US3287133A (en)	1963-03-01	1963-03-01	Photographic dye developer dispersions utilizing water-soluble sulfites

Publications (1)

Publication Number	Publication Date
DE1188944B true DE1188944B (de)	1965-03-11

Family

ID=22996440

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DEE26451A Pending DE1188944B (de)	1963-03-01	1964-02-21	Verfahren zur Herstellung einer Farbstoffentwicklersubstanz-Dispersion fuer farbphotographische Materialien

Country Status (4)

Country	Link
US (1)	US3287133A (fr)
BE (1)	BE644383A (fr)
DE (1)	DE1188944B (fr)
GB (1)	GB1060241A (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1099416A (en) *	1965-01-25	1968-01-17	Agfa Gevaert Nv	Method of incorporating photographic ingredients into a photographic colloid
US3630730A (en) *	1970-06-01	1971-12-28	Eastman Kodak Co	Diffusion transfer processes and elements comprising dye developers and bis-sulfonyl alkane speed-increasing agents

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA606417A (en) *		1960-10-04	R. Blout Elkan	Photographic products
US2360290A (en) *	1941-07-31	1944-10-10	Eastman Kodak Co	Preventing formation of color fog in emulsions
DE1066092B (fr) *	1954-03-09
US2983606A (en) *	1958-07-14	1961-05-09	Polaroid Corp	Processes and products for forming photographic images in color

1963
- 1963-03-01 US US262167A patent/US3287133A/en not_active Expired - Lifetime
1964
- 1964-02-21 DE DEE26451A patent/DE1188944B/de active Pending
- 1964-02-26 BE BE644383A patent/BE644383A/xx unknown
- 1964-03-02 GB GB8808/64A patent/GB1060241A/en not_active Expired

Also Published As

Publication number	Publication date
GB1060241A (en)	1967-03-01
US3287133A (en)	1966-11-22
BE644383A (fr)	1964-06-15

Publication	Publication Date	Title
DE1772192C2 (de)	1983-03-17	Verfahren zur Herstellung von lichtempfindlichen und nicht lichtempfindlichen Schichten für photographische Aufzeichnungsmaterialien
DE2628043C3 (de)	1980-10-16	Photographisches Aufzeichnungsmaterial
DE1965042A1 (de)	1971-07-15	Lichtempfindliches,farbfotographisches Aufzeichnungsmaterial
DE3686458T2 (de)	1993-01-28	3-aminoallylidenmalononitrile als uv-absorbierende verbindungen und sie enthaltende photographische materialien.
DE1157479B (de)	1963-11-14	Photographisches, Farbstoffentwickler verwendendes Mehrfarben-Diffusionsuebertragungsverfahren und Material zur Durchfuehrung des Verfahrens
DE1285882B (de)	1968-12-19	Verfahren zum Schutze von photographischem Material vor der Einwirkung ultravioletter Strahlung
DE3048165A1 (de)	1981-09-17	Xanthenverbindungen und photographische produkte und verfahren
DE2515771A1 (de)	1975-10-23	Verfahren zur erzeugung eines farbphotographischen bildes
DE1138630B (de)	1962-10-25	Verfahren zur Herstellung von ein- oder mehrfarbigen UEbertragungsbildern mit Hilfe von Farbstoffentwicklersubstanzen
DE2043271A1 (de)	1971-03-11	Lichtempfindliches Farbfotomatenal
DE1002625B (de)	1957-02-14	Gegen Einwirkung der Ultraviolettstrahlung geschuetztes photographisches Material
DE1188944B (de)	1965-03-11	Verfahren zur Herstellung einer Farbstoffentwicklersubstanz-Dispersion fuer farbphotographische Materialien
EP0032699B1 (fr)	1982-11-10	Matériau d'enregistrement pour la photographie en couleurs contenant un composé formateur de colorant émulsionné et hydrophile
DE1797198A1 (de)	1970-12-03	Bildempfangsmaterial fuer das Farbstoffdiffusionsuebertragungsverfahren
DE2149789B2 (de)	1975-05-22	Farbfotografisches Aufzeichnungsmaterial
DE2058545A1 (de)	1971-06-09	Photographisches Aufzeichnungsmaterial fuer mehrfarbige Bilder
DE1116533B (de)	1961-11-02	Verfahren zum Einverleiben von diffusionsfesten eine wasserloeslich machende Gruppe enthaltenden Farbkupplern in photographische Halogensilber-Gelatine-Emulsionen
EP0035685B1 (fr)	1984-02-22	Matériaux photographiques d'enregistrement pour des procédés de diffusion et composés de sulfilimine non-diffusants appropriés pour ces procédés
DE2005300A1 (de)	1970-09-03	Photographisches Verfahren zur Herstellung von Farbbildern nach dem Farbdiffus ions üb ertragungs verfahren
DE3620824A1 (de)	1987-12-23	Farbfotografisches aufzeichnungsmaterial mit einem farbabspalter fuer blaugruene farbstoffe und ein mit diesen farbstoffen erzeugtes farbbild
DE3025080A1 (de)	1981-01-08	Photographisches aufzeichnungsmaterial fuer das farbdiffusionsuebertragungsverfahren
DE2415125A1 (de)	1974-10-10	Farbstoffe fuer photographische zwecke, die einen diffusionsfaehigen farbstoff abspalten, und damit durchfuehrbares photographisches verfahren
CH505405A (de)	1971-03-31	Photographisches Diffusionsübertragungsverfahren
DE2129684A1 (de)	1972-02-17	Nach dem Dispergierverfahren mit wasserunloeslichen,schwerfluechtigen organischen Loesungsmitteln hergestelltes,Farbkuppler enthaltendes photographisches Material
DE2724488A1 (de)	1977-12-15	Antifarbschleiermittel und sie enthaltende photoempfindliche farbelemente