US3617277A - Dye developer diffusion transfer systems - Google Patents
Dye developer diffusion transfer systems Download PDFInfo
- Publication number
- US3617277A US3617277A US797282A US3617277DA US3617277A US 3617277 A US3617277 A US 3617277A US 797282 A US797282 A US 797282A US 3617277D A US3617277D A US 3617277DA US 3617277 A US3617277 A US 3617277A
- Authority
- US
- United States
- Prior art keywords
- silver halide
- dye
- catechol
- processing
- alkali
- Prior art date
- 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 - Lifetime
Links
- 238000012546 transfer Methods 0.000 title claims abstract description 35
- 238000009792 diffusion process Methods 0.000 title abstract description 22
- -1 catechol silver halide Chemical class 0.000 claims abstract description 235
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims abstract description 207
- 238000012545 processing Methods 0.000 claims abstract description 149
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 63
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 45
- 239000002738 chelating agent Substances 0.000 claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- 229910052709 silver Inorganic materials 0.000 claims description 180
- 239000004332 silver Substances 0.000 claims description 180
- 239000000839 emulsion Substances 0.000 claims description 98
- 150000003839 salts Chemical class 0.000 claims description 96
- 239000000243 solution Substances 0.000 claims description 53
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 28
- 229920003169 water-soluble polymer Polymers 0.000 claims description 26
- 239000012670 alkaline solution Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 23
- 230000008569 process Effects 0.000 claims description 22
- QDNPCYCBQFHNJC-UHFFFAOYSA-N 1,1'-biphenyl-3,4-diol Chemical compound C1=C(O)C(O)=CC=C1C1=CC=CC=C1 QDNPCYCBQFHNJC-UHFFFAOYSA-N 0.000 claims description 20
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 20
- 230000006872 improvement Effects 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 238000011161 development Methods 0.000 claims description 17
- 230000003100 immobilizing effect Effects 0.000 claims description 16
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 15
- 230000000694 effects Effects 0.000 claims description 13
- 238000001228 spectrum Methods 0.000 claims description 12
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 11
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 11
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical class [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 claims description 7
- 150000002500 ions Chemical class 0.000 claims description 4
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 200
- 239000010410 layer Substances 0.000 description 132
- 239000000203 mixture Substances 0.000 description 14
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 12
- 108010010803 Gelatin Proteins 0.000 description 12
- 229920000159 gelatin Polymers 0.000 description 12
- 239000008273 gelatin Substances 0.000 description 12
- 235000019322 gelatine Nutrition 0.000 description 12
- 235000011852 gelatine desserts Nutrition 0.000 description 12
- 239000000463 material Substances 0.000 description 11
- 238000009835 boiling Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000011248 coating agent Substances 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 239000003352 sequestering agent Substances 0.000 description 7
- 230000002378 acidificating effect Effects 0.000 description 6
- 125000004104 aryloxy group Chemical group 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000000084 colloidal system Substances 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical class 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- 125000005702 oxyalkylene group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 235000010443 alginic acid Nutrition 0.000 description 4
- 229920000615 alginic acid Polymers 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 3
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 229940072056 alginate Drugs 0.000 description 3
- 229910052788 barium Inorganic materials 0.000 description 3
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 235000010410 calcium alginate Nutrition 0.000 description 3
- 239000000648 calcium alginate Substances 0.000 description 3
- 229960002681 calcium alginate Drugs 0.000 description 3
- 229910001424 calcium ion Inorganic materials 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 3
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 3
- 229910052712 strontium Inorganic materials 0.000 description 3
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000013522 chelant Substances 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 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 description 2
- ZWDZJRRQSXLOQR-UHFFFAOYSA-N n-butyl-n-phenylacetamide Chemical compound CCCCN(C(C)=O)C1=CC=CC=C1 ZWDZJRRQSXLOQR-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 125000006850 spacer group Chemical group 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 125000001302 tertiary amino group Chemical group 0.000 description 2
- QAIPRVGONGVQAS-DUXPYHPUSA-N trans-caffeic acid Chemical compound OC(=O)\C=C\C1=CC=C(O)C(O)=C1 QAIPRVGONGVQAS-DUXPYHPUSA-N 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- ACEAELOMUCBPJP-UHFFFAOYSA-N (E)-3,4,5-trihydroxycinnamic acid Natural products OC(=O)C=CC1=CC(O)=C(O)C(O)=C1 ACEAELOMUCBPJP-UHFFFAOYSA-N 0.000 description 1
- LFWGYTIGZICTTE-BTJKTKAUSA-N (z)-but-2-enedioic acid;styrene Chemical compound C=CC1=CC=CC=C1.OC(=O)\C=C/C(O)=O LFWGYTIGZICTTE-BTJKTKAUSA-N 0.000 description 1
- ZXHDVRATSGZISC-UHFFFAOYSA-N 1,2-bis(ethenoxy)ethane Chemical compound C=COCCOC=C ZXHDVRATSGZISC-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N 2,3,4,5-tetrahydroxypentanal Chemical compound OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 description 1
- 125000000143 2-carboxyethyl group Chemical group [H]OC(=O)C([H])([H])C([H])([H])* 0.000 description 1
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
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- 229930194542 Keto Natural products 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
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- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
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- 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 description 1
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- 229910052794 bromium Inorganic materials 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
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 125000005843 halogen group Chemical group 0.000 description 1
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- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
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- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004010 onium ions Chemical class 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- LCLHHZYHLXDRQG-ZNKJPWOQSA-N pectic acid Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)O[C@H](C(O)=O)[C@@H]1OC1[C@H](O)[C@@H](O)[C@@H](OC2[C@@H]([C@@H](O)[C@@H](O)[C@H](O2)C(O)=O)O)[C@@H](C(O)=O)O1 LCLHHZYHLXDRQG-ZNKJPWOQSA-N 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 239000010318 polygalacturonic acid Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229940080236 sodium cetyl sulfate Drugs 0.000 description 1
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 150000004026 tertiary sulfonium compounds Chemical class 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920003176 water-insoluble polymer Polymers 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
Definitions
- Kline ABSTRACT In dye developer diffusion transfer systems in which chelatable metal ions are present during processing, the processing is conducted in the presence of a catechol silver halide developing agent and a compound which is a more effective chelating agent for the chelatable metal ions than catechol.
- the present invention relates to photography, and more particularly to multicolored dye diffusion transfer systems utilizing dye developers.
- Still another object of this invention is to provide dye developer diffusion transfer processes containing a catechol as auxiliary developer, which products exhibit increased activity by the catechol as auxiliary developer.
- a further object of this invention is to provide dye developer diffusion transfer processes and products which yield dye images of good density and color saturation.
- Still another object of this invention is to provide dye developer diffusion transfer processes and products which have high maximum densities and low minimum densities.
- the activity of catechols as auxiliary developers in dye developer diffusion transfer systems is increased by the presence of a compound which is more active chelating agent than the catechol, when processing is conducted in the presence of chelatable metal ions.
- the improvement provided by this invention comprises effecting such processing in the presence of (l) a substantially colorless, alkali-soluble catechol as auxiliary silver halide develop ing agent; and (2) a compound which is more effective chelating agent for said chelatable metal ions than catechol.
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least one lightsensitive layer and a dye-developer which is both a silver halide developing agent and a dye contiguous to the silver halide of the silver halide emulsion layer; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; the photosensitive element and the dye developer reception layer being capable of being superposed on each other; the container being so positioned as to be capable, upon being ruptured, of releasing processing solution for application to the superposed photosensitive element and reception layer; the product containing chelatable metal ions so positioned in said product as to be present in the photosensitive element during development; and, said product containing l) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent, and (2) a compound which is a more effective chelating agent for said chelatable metal ions than catechol, said catechol and
- an improvement in the processing of an imagewise exposed photographic element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, water-insoluble salt stratum positioned between at least two of the dye image-forming units, the dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of the emulsion, and the salt stratum comprising an alkali-permeable, water-insoluble salt of a polyvalent metal and a film-forming alkali-permeable, water-soluble polymer having free carboxylic acid groups, the salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than the water soluble polymer used to prepare said slat stratum; the processing being effected by treating the photographic element with an alkaline processing liquid, developing latent images in the regions of exposure of the silver halide emulsion layers and thereby immobilizing dye
- the improvement provided by this embodiment of this invention comprises effecting said processing in the presence of (l) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent; and (2) a compound which is a more effective chelating agent for said polyvalent metal ions than catechol.
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable,- water-insoluble salt stratum positioned between at least two of the dye image-forming units, the dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of the emulsion, and the salt stratum comprising an alkali-permeable,
- the salt stratum being less permeable to dye developers comprising the dye image-forming units in aqueous alkaline solution than the water-soluble polymer used to prepare the salt stratum; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; the photosensitive element and dye developer recep tion layer being capable of being superposed on each other; the container being so positioned as to be capable, upon being ruptured, of releasing the processing solution for application to said superposed photosensitive element and reception layer; and, said product containing (1.
- a substantially colorless alkali-soluble catechol as auxiliary silver halide developing agent, and (2 a compound which is more effective chelat' ing agent for said polyvalent metal ions than the catechol; the catechol and the compound being so positioned in said product as to be present in the photosensitive element during development.
- Chelatable metal ions can be introduced into dye developer diffusion transfer systems during processing in a variety of ways.
- the emulsions employed in the photo graphic elements utilized in dye developer diffusion transfer systems comprise gelatin which contains varying amounts of alkaline earth ion, generally calcium ion. Calcium ions can' be introduced into the emulsion during washing operations, in the preparation of the photographic silver halide emulsions utilized in the element.
- the emulsion typically would be washed with water containing alkaline earth ions, such as calcium ions, which would be introduced in the gelatin and retained in the emulsion after coating and formation into the photographic elements of the type utilized in dye developer diffusion transfer systems.
- alkaline earth ions such as calcium ions
- Chelatable metal ions can also be present in the dye developer diffusion transfer element in the form of barrier layers or salt strata of the type described by Becker in U.S. Pat. No. 3,384,483 issued May 21, 1968, the disclosure of which is incorporated herein by reference.
- barrier layers can be prepared with a variety of polyvalent metal salts and polymeric carboxylic a acids.
- the subject salt strata can be formed in the element by coating a solution, on a waterpermeable substrate, containing the polyvalent metal in watersoluble form on a polymeric carboxylic acid layer previously coated on the element to form a thin layer of a water-insoluble salt.
- the polyvalent metal in water-soluble form can be coated directly on silver halide emulsion layers if the vehicle for the silver halide is a polymeric carboxylic acid that forms a waterinsoluble salt with the polyvalent metal moiety.
- Interlayers of water-permeable materials can be utilized on either side of the subject water-insoluble salt strata.
- Such salt strata are preferably utilized between the magenta and cyan dye imageforming units to particularly improve red purity and saturation of the transferred dye developer images.
- the subject salt strata can be utilized between the yellow and the magenta dye image-forming units as well as between both the magenta and the cyan dye image-forming units to improve color purity and saturation of the transfer dye developer images.
- a wide variety of film-forming, alkali-permeable, watersoluble polymeric compositions containing free carboxylic acid groups, and including water-soluble salts thereof, can be utilized to form the barrier layer or salt strata with polyvalent metal moieties.
- such polymers typically contain about 5 percent to 60 percent by weight of polymer of free carboxylic acid groups (i.e., available for reaction with the subject polyvalent metal moieties in aqueous alkaline solutions) or the equivalent weight of water-soluble salts thereof.
- suitable acid polymers include:
- carboxylic acid group-containing polysaccharides and derivatives thereof such as alginic acid, pectic acid, tragacanthic acid, carboxymethyl cellulose, and the like, and
- Polyvalent metal moieties are utilized to form the present salts as such moieties can be used to cross-link carboxylic acid moieties of the polymeric carboxylic acid to form the present strata which have the proper degree of alkali permeability and water-insolubility to serve as barrier layers to prevent color contamination and interdevelopment between dye imageforming units.
- a wide variety of polyvalent metal moieties can be utilized in preparing the subject salt strata. Suitable polyvalent metals with which slat strata can be prepared include alkaline earth metals, such as calcium, barium and strontium, and the like polyvalent metals that form alkalipermeable, water-insoluble salts with the above-described polymeric materials containing carboxylicacid groups.
- the amount of polymeric salt utilized in the subject salt strata can be widely varied, the amount varying with the effect desired and the nature of the polyvalent metal and the polymeric carboxylic acid. More generally, the amount of coverage of the polyvalent metal-polymeric carboxylic acid salt stratum utilized is that which is substantially equivalent in permeability to dye developers in aqueous alkaline solution to the calcium alginate formed when a stratumconsisting essentially of sodium alginate is reacted with calcium chloride coated thereover at a coverage of about 5 to mg. per square foot.
- Typical alkali-permeable water-insoluble salts comprising the barrier layers of the light-sensitive photographic elements used in the invention include:
- catechol which is a silver halide developing agent can be used in the practice of this invention.
- Such catechols chelate chelatable metal ions.
- the catechol is substantially colorless and is soluble in alkaline solution.
- the word catechol is used generically herein to include 1,2- dihydroxybenzenes, which can contain additional hydroxyl groups such as a l,2,3,-trihydroxybenzene, a l,2,4,-trihydroxybenzene or a l,2,4,S-tetrahydroxybenzene.
- Suitable catechols include those having the structural formula:
- R,, R R and R can be hydrogen an alkyl radical, preferably of about one to eight carbon atoms (e.g., methyl, ethyl, propyl, butyl, amyl, hexyl, heptyl, octyl, etc.), an aryl radical (etc., phenyl, tolyl, naphthyl, etc.), hydroxyl, aryloxy such as phenoxy, halogen such as chlorine or bromine, carboxy or R and R or R and R when taken together with the carbon atoms to which they are attached, represent the atoms to complete a cycloalkyl group containing from four to six carbon atoms (e.g., cyclohexyl, cyclopentyl, etc.) which can contain an endomethylene group (e.g., methanocyclohexyl, methanocyclopentyl, etc.). Salts and esters of these catechols can also be
- a preferred class of catechols having the aforesaid structural formula are those in which R R R and R, are either hydrogen or an alkyl radical of from one to eight carbon atoms.
- Suitable catechols include:
- catechol a compound which is a more effective chelating or sequestering agent than catechol for the chelatable metal ions present in the element.
- An especially preferred class of compound for this purpose is the nonpolymeric tertiary amino compounds having at least three carboxyalkyl groups. The most useful tertiary amino
- R and R each represents a carboxyalkyl group such as carboxymethyl, 2-carboxyethyl, Z-carboxypropyl, 3-carboxypropyl, 2-carboxybutyl or 4-carboxybutyl; and, Y represents a carboxyalkyl group, such as one described above, or a group having the formula:
- R represents an alkylene group, such as methylene, ethylene, propylene or butylene or, R, can represent an alkylenebis(oxyalkylene) group such as methylenebis(oxymethylene), ethylenebis(oxyethylene), ethylenebis(oxypropylene), propylenebis(oxybutylene) and the like;
- R represents a carboxyalkyl group, such as one of those referred to above; and and R represents a carboxyalkyl group, such as one of those referred to above, or a hydroxyalkyl group such as hydroxymethyl, Z-hydroxyethyl, 2-hydroxypropyl, 3- hydroxypropyl, 2-hydroxybutyl or 4-hydroxybutyl.
- nitrilotriacetic acid disodium salt
- ethylenediamine tetraacetic acid [ethylenebis-(oxyethylenenitrilo]tetraacetic acid or N-(2-hydroxyethyl)- ethylenedinitrilo triacetic acid, which have the following formulas:
- chelatable metal ions can be present during processing at widely varying concentrations. Accordingly, the optimum concentrations for the catechol and more effective chelating compound will vary considerably depending on the concentration of chelatable metal ions present during processing and the effects (particularly auxiliary development activity) desired. Generally speaking, when the. chelatable metal ions are present primarily in the gelatin as a resultof washing the material with water, or as a salt stratum, good results are achieved when about 1 to about 150 mg. of catechol are are employed per square foot when the catechol is used in the light sensitive element; about 50 to 200 mg. of catechol per square foot are used when the catechol is incorporated in the -image receiving sheet or layer for dye developers; and, at
- the chelatable metal ions can be introduced during processing from sources within the element.
- the chelatable metal ions can also be introduced from the receiving sheet or the processing material.
- the invention can be practiced when the catechol and the more effective chelating or sequestering agent are present in the alkaline processing solution, the receiving sheet or in the element itself.
- the catechol and the more effective chelating agent do not need to be together in the product.
- the catechol can be present in the alkaline processing solution and the more effective chelating compound can be incorporated in the photographic element.
- both the chelating agent and the more active sequestering agent are incorporated in th alkaline proceging solution.
- Dye developers are well known in the photographic art. Such compounds function both as a silver halide developing agent and as a dye in photographic diffusion transfer systems.
- Dye developers are characterized as being relatively nondiffusible in colloid layers such as the hydrophilic organic colloids used in photographic emulsions at neutral pH, but diffusible in the photographic elements in the presence of alkaline processing solutions.
- dye developers are substantially insoluble in water, which property usually necessitates the use of organic solvents to incorporate the dye developers into the organic colloid layers of the photoelements.
- the dye developers are particularly characterized as containing both a chromophoric or dye moiety and at least one moiety having a silver halide developing agent function.
- Particularly useful dye developers are those wherein the chromophoric moiety is an azo or anthraquinone dye moiety and the silver halide developing moiety is a benzenoid moiety such as a hydroquinonyl moiety.
- M is an aromatic or heterocyclic ring or ring systems such as a benzene, naphthalate, tetralin, anthracene, anthraquinone, pyrazole, quinoline, etc., ring which can be substituted with such groups as hydroxyl, amine, keto, nitro, alkoxy, aryl
- D represents a silver halide developing agent moiety imparting the developing agent function to the dye developer such as a hydroquinonyl group which can be substituted with amino, alkylamino, alkyl, hydroxyl, alkoxyl or halogen groups.
- Typical useful dye developers are described in columns 9-13 of U.S. Pat. No. 3,146,102, as well as elsewhere in the patent literature, including: Australian 220,279; German 1036,640; British 804,971 and 804,973-5; Belgian 554,935; French 1,168,292; and Canadian 577,021 and 579,038.
- the dye developers are preferably incorporated in hydrophilic organic colloidal vehicles or carries comprising the layers of the photographic element dissolved in high-boiling or crystalloidal solvents and dispersed in finely divided droplets.
- high-boiling or substantially water-immiscible organic liquids having boiling points above about 175 C. are utilized.
- the high-boiling solvent can be used along in dissolving the dye developer and in forming the dispersion or it can be mixed with a low-boiling organic solvent (e.g., boiling at least 25' C. below the boiling point of the higher boiling solvent), or a water-soluble organic solvent, as an auxiliary solvent to facilitate solution of the dye developer.
- a preferred range of proportions of high-boiling solvent to auxiliary is 1/0 to l/l0 on a weight basis.
- auxiliary solvents can be readily removed from the high-boiling solvent, for example, by air-drying a chilled, noodled dispersion or by continuous water washing.
- highboiling solvents and auxiliary solvents utilized for incorporating dye developers are described in French Pat. No. 1,313,765.
- the dye developers can also be incorporated into vehicles soluble in organic solvents which are also solvents for the dye developer.
- other incorporating techniques for the dye developer such as ball-milling can be utilized.
- the photographic elements of the invention desirably contain auxiliary developing agents, in addition to catechols, such as colorless substantially water-insoluble hydroquinone derivatives, e.g., those disclosed in French Pat. No. 1,313,086.
- auxiliary developing agents can be incorporated in the silver halide emulsion layers, in overcoat layers, in interlayers or in other layers of the element.
- the silver halide emulsions utilized in preparing the photographic elements of the invention are more generally the conventional negative-type, developing-out emulsions, positive transfer images resulting from such emulsions.
- reversal emulsions such as solarized emulsions and emulsions that form latent images predominantly internal to the silver halide grains as described in U.S. Pat. No. 2,592,250, can also be used, negative transfer images resulting from such emulsions.
- Typical suitable silver halides include silver chloride, silver bromide, silver bromoiodine, silver chloroiodide, silver chlorobromoiodide, etc.
- Useful sensitizers are those in Kennard Ser. No. 377,792, filed Jan.
- hydrophilic organic colloids can be utilized as the vehicle or carrier.
- gelatin as the hydrophilic colloid or carrier material although such material as polyvinyl alcohol and its water-soluble derivatives and copolymers, water-soluble copolymers such as polyacrylamide, imidized polyacrylamide, etc., or polymerized vinyl compounds such as those disclosed in U.S. Pat. Nos.
- the dye developers are disposed integral with the element and contiguous to silver halide of each of the light-sensitive silver halide emulsion layers. Such dye developers can be incorporated directly in the light-sensitive silver halide emulsion layers or in separate layers contiguous to the layers containing the silver halide.
- the present photographic elements contain at least two dye image-forming units, each unit comprising a light-sensitive silver halide emulsion and a dye developer contiguous to silver halide in the unit. Each dye image-forming unit is preferably spectrally sensitized to record light that is substantially complementary to the color of the dye developer in the unit.
- Typical supports include cellulose nitrate film, cellulose acetate film, polyvinyl acetal film polystyrene film polyethylene terephthalate film, polyethylene film, polypropylene film, paper, polyethylenecoated paper, glass.
- a wide variety of receiving sheets can be utilized to receive the dye developer images from the present light-sensitive photographic elements.
- the sequestering agents used in the invention can be positioned in any of the layers of the receiving sheet.
- Typical reception layers for dye developer receiving sheets which are, or include, mordants for dye developers, are such materials as linear polyamides, proteins such as gelatin, polyvinyl pyrrolidones, poly-4-vinyl pyridine, polyvinyl alcohol, polyvinyl salicylal, partially hydrolyzed polyvinyl acetate, methyl cellulose, regenerated cellulose, carboxymethyl cellulose and hydroxyethyl cellulose, or mixtures of such.
- reception layers can be coated on a suitable support of the type described above for the light-sensitive elements of the invention and including transparent as well as opaque supports.
- receiving sheets that release acidic material such as that derived from an acidic polymer or other acidic compound at a controlled rate are as described in U.S. Pat. No. 2,584,030 are particularly useful.
- acidic materials are typically positioned in layers on the receiving sheet below the dye developer reception layer, there suitably being a spacer layer between the acid layer and the mordanting layer to control the release of acidic material.
- Such acidic materials serve to neutralize residual portions of the alkaline activator on the receiving sheet.
- nondiffusible cationic or basic dye-mordanting compounds can be used in liquid permeable reception layers including amines such as polymeric amines, quaternary ammonium compounds, quaternary phosphonium compounds and tertiary sulfonium compounds.
- amines such as polymeric amines, quaternary ammonium compounds, quaternary phosphonium compounds and tertiary sulfonium compounds.
- Such mordants are nondiffusible in the alkaline processing composition and contain at least one hydrophobic ballast group.
- the receiving sheet can be prepared by superficially hardening with a nondiffusing hardener and a surfactant.
- a dye developer image receiving layer on a receiving sheet containing poly-4- vinyl pyridine mordant in polyvinyl alcohol can be efficaciously treated with an oxyguar gum hardener solution containing a surfactant such as sodium cetyl sulfate or sodium N- methyl-N-oleoyl taurate.
- integral reception layers for dye developer images can also be utilized.
- Such integral reception layers can be coated beneath the emulsion and dye developer layers near the support.
- a stripping layer coated over the integral reception layer can be used to facilitate the removal of the overcoated layers after the diffusion of the dye developer images to the reception layer.
- the processing compositions or activators used to initiate development of the exposed light-sensitive elements of the invention are strongly alkaline.
- Such processing compositions generally have a pH of at least about 12 or contain a least 0.01 N hydroxyl ion.
- Alkali metal hydroxides such as sodium hydroxide, and potassium hydroxide, are advantageously used in the composition for imparting such high alkalinity.
- volatile amines such as diethyl amine can also be used, such amines having the advantage of being volatilized from the prints to leave no residue of alkali.
- Such processing compositions are generally aqueous liquids or solutions, and when utilized in rupturable pods for in-camera processing, generally contain thickening agents such as hydroxyethyl cellulose, particularly as described in U.S. Pat. No. 3,266,894, or carboxymethyl cellulose.
- thickening agents such as hydroxyethyl cellulose, particularly as described in U.S. Pat. No. 3,266,894, or carboxymethyl cellulose.
- Onium compounds such as are disclosed in U.S. Pat. No. 3,146,102 are preferably utilized in the alkaline processing composition.
- the described sequestering agents can also be utilized in the alkaline processing compositions used in the processes of the invention.
- Camera apparatus of the type useful for exposing and processing the sensitive elements of the invention have been described, for example, in U.S. Pat. No. 2,435,717.
- the processing of the subject photographic elements can also be effected outside of camera apparatus by imbibing either the receiving element or the negative element or both in the alkaline processing composition, and thereafter sandwiching together the two element to allow the dye developer images to diffuse to the receiving element.
- the positioning of the dye image-forming units of the photographic elements of the invention can be varied. In three-color systems, it is preferred to utilize the cyan dye image-forming unit most proximate to the support, the yellow dye-forming unit furthest from the support, and the magenta dye image-forming unit between the cyan and yellow dye image-forming units. lt is also preferred to utilize the dye developers in the respective dye image-forming units in a separate underlying layer contiguous to the silver halide emulsion layer. Likewise, it is preferred to utilize in each dye image-forming unit a dye developer that is substantially complementary in color to the color oflight recorded by the silver halide in the unit.
- Examples 1-4 A photographic element, element 1, is prepared by coating successively the following layers on a subbed cellulose acetate film support:
- Cyan Dye Developer Layer A coating of the cyan dye developer, 5,8,-dihydroxy-l,4- bis[ (13 -hydroquinonyl-a-methyl)ethylamino]- anthraquninone, dissolved in N-n-butylacetanilide, dispersed in gelatin and coated on the support.
- Red-Sensitive Emulsion Layer A coating of a developing-out negative gelatino-silver bromoiodide emulsion sensitized to red light coated at a coverage of about mg. of silver per square foot.
- a gelatin layer is coated over the red-sensitive emulsion layer.
- Magenta Dye Developer Layer A coating of the magenta dyedeveloper, 4-isopropox y5-[p- (B -hydroquinonylethyl)-phenylazo]-l-naphthol, dissolved in N-n-butylacetanilide dispersed in gelatin.
- Green-Sensitive Emulsion Layer A coating of a developing-out negative gelatino-silver bromoiodide emulsion sensitized to green light is then coated A developing-out negative gelatino-silver bromoiodide emulsion that is inherently sensitive to blue light is coated at a coverage of about 70 mg. of silver per square foot.
- Overcoat Layer A gelatin layer is coated over layer 10.
- the gelatin layers of the above photographic element contains calcium ions as a result of washing the emulsion with water.
- the photographic element obtained is exposed through a 0.3 density increment color step wedge in an intensity scale sensitometer 1/50 inch to a 500-watt positive lamp using a blue colored filter that absorbs some red light to convert the tungsten exposure to daylight color balance. Separate samples of the exposed element are treated with a solution of acetonitrile and others with a solution of acetonitrile containing a catechol.
- the acetonitrile solution is spread evenly over the surface of the element, and solutions containing catechol (4- methylphenyl catechol) are treated'to providea coverage of about 0.64 millimoles catechol per square foot.
- the samples are then processed with a processing solution disposed in a processing pod and having a composition like that described by Land in example 7 of US. Pat. No. 3,362,821 issued Jan. 9, 1968.
- Certain processing solutions contain 3.65 grams of ethylenediaminetetraacetic acid (EDTA) per kilogram of processing solution.
- EDTA ethylenediaminetetraacetic acid
- the exposed film' is processed at a gap of 0.004 inch (corresponding to the thickness of the activator layer) for a period of 60 seconds in contact with a color receiving sheet.
- the receiving sheet is a cellulose acetate butyrate subbed paper support carrying in the following order:
- a polyvinyl alcohol spacer layer 3.
- a mordant layer comprising poly-4-vinyl pyridine and polyvinyl alcohol, and
- a process for producing a photographic transfer image in color which comprises processing an imagewise exposed photosensitive element comprising at least one light-sensitive silver halide emulsion layer and a dye developer, which is both a silver halide developing agent and a dye, contiguous to the silver halide of said silver halide emulsion layer; said processing being effected by treating said photographic element with an alkaline solution, developing latent images in the regions of exposure of said silver halide layer and thereby immobilizing dye developer in said regions of exposure, dye developer in undeveloped regions diffusing imagewise in register to a dye developer reception layer, and said processing being conducted in the presence of chelatable metal ions: the improvement which comprises effecting said processing in the presence of l) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent; and (2) a compound which is more effective chelating agent for said chelatable metal ions than catechol.
- a process for producing a photographic transfer image in color which comprises processing an imagewise exposed photosensitive element comprising a plurality of light-sensitive silver halide emulsion layers sensitive to light of different regions of the spectrum, and a dye developer, which is both a silver halide developing agent and a dye, contiguous to the silver halide of said silver halide emulsion layers; said processing being effected by treating said photographic element with an alkaline solution, developing latent images in the regions of exposure of said silver halide layers and thereby immobilizing dye developer in said regions of exposure, dye developer in undeveloped regions diffusing imagewise in register to a dye developer reception layer, and said processing being conducted in-the presence of chelatable metal ions: the improvement which comprises effecting said processing in the presence of (1) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent; and (2) a nonpolymeric tertiary amino compound having at least three carboxyalkyl groups and salts thereof, which tertiary amino
- a process for producing a photographic transfer image in color which comprises processing an imagewise exposed photosensitive element comprising a plurality of lightsensitive silver halide emulsion layers sensitive to light of different regions of the spectrum, and a dye developer, which is both a silver halide developing agent and a dye, contiguous to the silver halide of said silver halide emulsion layers; said processing being effected by treating said photographic element with an alkaline solution, developing latent images in the regions of exposure of said silver halide layers and thereby immobilizing dye developer in said regions of exposure, dye developer in undeveloped regions diffusing imagewise in register to a dye developer reception layer, and said processing being conducted in the presence of chelatable metal ions: the improvement which comprises effecting said processing in the presence of (l) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent, said catechol having the formula:
- R,, R R and R are each selected from the group consisting of hydrogen, hydroxyl, halogen, carboxy, aryloxy, alkyl, aryl and R and R or R and R when taken together with the carbon atoms to which they are attached, represent the atoms to complete a cycloalkyl group; and (2) a tertiary amino compound which has the following formula:
- R and R each represents a carboxyalkyl group; and, Y represents a member selected from the group consisting of a carboxyalkyl group and a group having the formula Rs -R7-N ⁇ wherein R represents a member selected from the group consisting of an alkylene group and an alkylenebis(oxyalkylene) group; R represents a carboxyalkyl group; and, R represents a member selected from the group consisting of a carboxyalkyl group and a hydroxy-substituted alkyl group.
- a process for producing a photographic transfer image in color which comprises processing an imagewise exposed photosensitive element comprising a plurality of light-sensitive silver halide emulsion layers sensitive to light of different regions of the spectrum, and a dye developer, which is both a silver halide developing agent and a dye, contiguous to the :silver halide of said silver halide emulsion layers; said processing being effected by treating said photographic element with an alkaline solution, developing latent images in the regions of exposure of said silver halide layers and thereby im- -mobilizing dye developer in said regions of exposure, dye
- the improvement which comprises effecting said processing in the ,present of (l) 4-phenylcatechol as auxiliary silver halide developing agent; and, (2) a sufficient amount of ethylenediamine tetraacetic acid to effectively increase the silver halide developing activity ofthe 4-phenylcatechol.
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least one light-sensitive layer and a dye-developer which is both a silver halide developing agent and a dye contiguous to the silver halide of said silver halide emulsion layer; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be capable, upon being ruptured, of releasing said processing solution or application to said superposed photosensitive element and reception layer; said product containing chelatable metal ions so positioned in said product as to be present in the photosensitive element during development; and, said product containing (1) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent, and (2) a compound which is a more effective chelating agent for said chelatable metal ions than catechol, said catechol and said compound being so positioned in said product as
- a photographic product comprising: a photosensitive element comprising a support having coated thereon a plurality of light-sensitive layers sensitive to light of different regions of the spectrum, and a dye developer which is both a silver halide developing agent and a dye contiguous to the silver halide of said silver halide emulsion layers; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be capable, upon being ruptured, of releasing said processing solution for application to said superposed photosensitive element and reception layer; said product containing chelatable metal ions so positioned in said product as to be present in the photosensitive element during development; and, said product containing l a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent; and (2) a nonpolymeric tertiary amino compound having at least three carboxyalkyl groups, and salts thereof,
- a photographic product comprising: a photosensitive element comprising a plurality of light-sensitive layers sensitive to light of different regions of the spectrum, and a dye developer which is both a silver halide developing agent and a dye contiguous to the silver halide of said silver halide emulsion layers; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be capable, upon being ruptured, of releasing said processing solution for application to said superposed photosensitive element and reception layer; said product containing chelatable metal ions so positioned in said product as to be present in the photosensitive element during development; and, said product containing (1) a substantially colorless, alkali-soluble catechol as auxiliary silver halide developing agent, said catechol having the formula:
- R,, R R and R are each selected from the group consisting of hydrogen, hydroxyl, halogen, carboxy, aryloxy, alkyl, aryl and R and R or R and R when taken together with the carbon atoms to which they are attached, represent the atoms to complete a cycloalkyl group; and, (2) a tertiary amino compound which has the following formula:
- R and R each represents a carboxylakyl group
- Y represents a member selected from the group consisting of a carboxyalkyl group and a group having the formula wherein R, represents a member selected from the group consisting of an alkylene group and an alkylenebis(oxyalkylene) group; R represents a carboxyalkyl group; and, R represents a member selected from the group consisting of a carboxyalkyl group and a hydroxy-substituted alkyl group, said catechol and said tertiary amino compound being so positioned in said product as to be present in the photosensitive element during processing.
- a photographic product comprising: a photosensitive element comprising a plurality of light-sensitive layers sensitive to light of different regions of the spectrum, and a dye developer which is both a silver halide developing agent and a dye contiguous to the silver halide of said silver halide emulsion layers; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be capable, upon being ruptured, of releasing said processing solution for application to said superposed photosensitive element and reception layer; said product containing chelatable metal ions so positioned in said product as to be presen t i n the photosensitive element during development; and, said element containing l) 4-phenylcatechol as auxiliary silver halide developing agent; and, (2) a sufficient amount of ethylenediamine tetraacetic acid to effectively increase the silver halide developing activity of the 4-phenylcatechol
- an imagewise exposed photographic element comprising a support having coated thereon at least' two dye image-forming units with an alkali-permeable, waterinsoluble salt stratum positioned between at least two of said dye image-forming units, said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of a polyvalent metal and a film-forming alkali-permeable, watersoluble polymer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer sued to prepare said salt stratum; said processing being effected by treating the photographic element with an alkaline processing liquid, developing latent images in the regions of exposure of the silver halide emulsion layers and thereby immobilizing dye developers in said regions of exposure, dye developers in undeveloped regions diff
- an imagewise exposed photographic element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, waterinsoluble salt stratum positioned between at least two of said dye image-forming units, said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of an alkaline earth metal and a film-forming alkali-permeable, watersoluble polymer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer used to prepare said salt stratum; said processing being effected by treating the photographic element with an alkaline processing liquid, developing latent images in the regions of exposure of the silver halide emulsion layers and thereby immobilizing dye developers in said regions of exposure, dye developers in undeveloped regions diff
- an imagewise exposed photographic element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable waterinsoluble salt stratum positioned between at least two of said dye image-forming units, said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of an alkaline earth metal and a film-forming alkali-permeable, watersoluble polymer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer used to prepare said salt stratum; said processing being effected by treating the photographic element with an alkaline processing liquid, developing latent images in the regions of exposure of the silver halide emulsion layers and thereby immobilizing dye developers in said regions of exposure, dye developers in undeveloped regions diffusing
- R,, R R and R are each selected from the group consisting of hydrogen, hydroxyl, halogen, carboxy, aryloxy, alkyl, aryl and R and R or R and R when taken together with the carbon atoms to which they are attached, represent the atoms to complete a cycloalkyl group; and (2) a tertiary amino compound which has the following formula:
- R and R each represents a carboxyalkyl group; and, Y represents a member selected from the group consisting of a carboxyalkyl group and a group having the formula wherein R represents a member selected from the group consisting of an alkylene group and an alkylenebis(oxyalkylene) group; R represents a carboxyalkyl group; and, R, represents a member selected from the group consisting of a carboxyalkyl group and a hydroxy-substituted alkyl group.
- an imagewise exposed photographic element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, waterinsoluble calcium alginate salt stratum positioned between at least two of said dye image-forming units, said dye imageforming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion; said processing being effected by treating the photographic element with an alkaline processing liquid, developing latent images in the regions of exposure of the silver halide emulsion layers and thereby immobilizing dye developers in said regions of exposure, dye developers in undeveloped regions diffusing imagewise in register to a reception layer for dye developer images: the improvement which comprises effecting said processing in the presence of l) 4-phenylcatechol as auxiliary silver halide developing agent; and, (2) a sufficient amount of ethylenediamine tetraacetic acid to effectively increase the silver halide developing activity of the 4-phenylcatechol; said 4-phenylcatechol and said
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, waterinsoluble salt stratum positioned between at least two of said dye image-forming units, said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide to said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of a polyvalent metal and a film-forming, alkali-permeable, watersoluble polmyer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer used to prepare said salt stratum; a dye developer reception layer; and, a rupturable c ontainer holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, waterinsoluble salt stratum positioned between at least two of said dye image-forming units, said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of an alkaline earth metal and a film-forming, alkali-permeable, water-soluble polymer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer used to prepare said salt stratum; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution, said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable waterinsoluble salt stratum positioned between at least two of said dye image-forming units said dye image-forming units comprising a silver halide emulsion layer and a dye developer contiguous to silver halide of said emulsion, and said salt stratum comprising an alkali-permeable, water-insoluble salt of an alkaline earth metal and a film-forming, alkali-permeable water-soluble polymer having free carboxylic acid groups, said salt stratum being less permeable to dye developers comprising said dye image-forming units in aqueous alkaline solution than said water-soluble polymer used to prepare said salt stratum; a dye developer reception layer; and, a rupturable container holding an aqueous alkaline processing solution; said photosensitive element and said dye developer reception layer being capable of being superposed on each other; said container being so positioned as to be capable, upon
- R,, R R and R are each selected from the group consisting of hydrogen, hydroxyl, halogen, carboxy, aryloxy, alkyl, aryl and R and R or R and R when taken together with the carbon atoms to which they are attached, represent the atoms to complete a cycloalkyl group; and, (2) a tertiary amino compound which has the following formula:
- R and R each represents a carboxyalkyl group; and, Y represents a member selected from the group consisting or a carboxyalkyl group and a group having the formula Rs -R7N wherein R represents a member selected from the group consisting of an alkylene group and an alkylenebis(oxyalkylene) group; R represents a carboxyalkyl group; and, R represents a member selected from the group consisting of a carboxyalkyl group and, a hydroxy-substituted alkyl group, said catechol and said tertiary amino compound being so positioned in said product as to be present in the photosensitive element during development.
- a photographic product comprising: a photosensitive element comprising a support having coated thereon at least two dye image-forming units with an alkali-permeable, waterinsoluble calcium alginate salt stratum positioned between at least two of said dye image-forming units, said dye imageforming units comprising a silver halide emulsion layer and a said superposed photosensitive element and reception layer; and, said product containing (1) 4-phenylcatechol as auxiliary silver halide developing agent; and, (2) a sufficient amount of ethylenediamine tetraacetic acid to effectively increase the silver halide developing activity of the 4-phenylcatechol said 4-phenylcatechol and said ethylenediamine tetraacetic acid being present in said rupturable container.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79728269A | 1969-02-06 | 1969-02-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3617277A true US3617277A (en) | 1971-11-02 |
Family
ID=25170395
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US797282A Expired - Lifetime US3617277A (en) | 1969-02-06 | 1969-02-06 | Dye developer diffusion transfer systems |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3617277A (fr) |
| JP (1) | JPS494329B1 (fr) |
| BE (1) | BE745488A (fr) |
| CA (1) | CA927170A (fr) |
| CH (1) | CH523521A (fr) |
| DE (1) | DE2005300B2 (fr) |
| FR (1) | FR2033883A5 (fr) |
| GB (1) | GB1292358A (fr) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3930862A (en) * | 1973-05-16 | 1976-01-06 | Fuji Photo Film Co., Ltd. | Dye developer transfer photosensitive material with substituted catechol auxiliary developer |
| USRE29148E (en) * | 1972-08-17 | 1977-03-08 | Fuji Photo Film Co., Ltd. | Color photographic diffusion transfer process |
| US4365072A (en) * | 1981-10-22 | 1982-12-21 | Polaroid Corporation | Biphenyl aldehydes |
| US4417064A (en) * | 1981-01-05 | 1983-11-22 | Polaroid Corporation | Biphenyl compounds and method of preparing same |
| US4551411A (en) * | 1984-12-28 | 1985-11-05 | Eastman Kodak Company | Sequestrants used in diffusion transfer elements with metallizable dyes |
| US4559291A (en) * | 1984-12-28 | 1985-12-17 | Eastman Kodak Company | Ligands for metallizable dyes |
| CN117886966A (zh) * | 2024-01-17 | 2024-04-16 | 山东京博石油化工有限公司 | 一种5-氨基-8-羟基喹啉-海藻酸聚烯烃材料灰分脱除剂及其制备方法和应用 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3196015A (en) * | 1962-01-31 | 1965-07-20 | Polaroid Corp | Diffusion transfer process |
| US3262781A (en) * | 1962-07-05 | 1966-07-26 | Polaroid Corp | Photographic products |
| US3345163A (en) * | 1956-02-13 | 1967-10-03 | Polaroid Corp | Photographic diffusion transfer color processes |
| US3477849A (en) * | 1964-03-23 | 1969-11-11 | Eastman Kodak Co | Multi-color dye developer systems |
-
1969
- 1969-02-06 US US797282A patent/US3617277A/en not_active Expired - Lifetime
-
1970
- 1970-01-13 CA CA072004A patent/CA927170A/en not_active Expired
- 1970-01-30 JP JP45007782A patent/JPS494329B1/ja active Pending
- 1970-02-03 FR FR7003691A patent/FR2033883A5/fr not_active Expired
- 1970-02-04 BE BE745488D patent/BE745488A/fr unknown
- 1970-02-05 DE DE19702005300 patent/DE2005300B2/de active Granted
- 1970-02-06 GB GB5770/70A patent/GB1292358A/en not_active Expired
- 1970-02-06 CH CH174070A patent/CH523521A/fr not_active IP Right Cessation
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3345163A (en) * | 1956-02-13 | 1967-10-03 | Polaroid Corp | Photographic diffusion transfer color processes |
| US3196015A (en) * | 1962-01-31 | 1965-07-20 | Polaroid Corp | Diffusion transfer process |
| US3262781A (en) * | 1962-07-05 | 1966-07-26 | Polaroid Corp | Photographic products |
| US3477849A (en) * | 1964-03-23 | 1969-11-11 | Eastman Kodak Co | Multi-color dye developer systems |
Non-Patent Citations (1)
| Title |
|---|
| Martell, A. E. and Calvin, M. Chemistry of the Metal Chelate Compounds; Third Printing (1956). Prentice-Hall, Engelwood Cliffs, N.J. * |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE29148E (en) * | 1972-08-17 | 1977-03-08 | Fuji Photo Film Co., Ltd. | Color photographic diffusion transfer process |
| US3930862A (en) * | 1973-05-16 | 1976-01-06 | Fuji Photo Film Co., Ltd. | Dye developer transfer photosensitive material with substituted catechol auxiliary developer |
| US4417064A (en) * | 1981-01-05 | 1983-11-22 | Polaroid Corporation | Biphenyl compounds and method of preparing same |
| US4365072A (en) * | 1981-10-22 | 1982-12-21 | Polaroid Corporation | Biphenyl aldehydes |
| US4551411A (en) * | 1984-12-28 | 1985-11-05 | Eastman Kodak Company | Sequestrants used in diffusion transfer elements with metallizable dyes |
| US4559291A (en) * | 1984-12-28 | 1985-12-17 | Eastman Kodak Company | Ligands for metallizable dyes |
| CN117886966A (zh) * | 2024-01-17 | 2024-04-16 | 山东京博石油化工有限公司 | 一种5-氨基-8-羟基喹啉-海藻酸聚烯烃材料灰分脱除剂及其制备方法和应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2005300A1 (de) | 1970-09-03 |
| JPS494329B1 (fr) | 1974-01-31 |
| FR2033883A5 (fr) | 1970-12-04 |
| CH523521A (fr) | 1972-05-31 |
| BE745488A (fr) | 1970-07-16 |
| DE2005300B2 (de) | 1973-02-01 |
| GB1292358A (en) | 1972-10-11 |
| CA927170A (en) | 1973-05-29 |
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