US3155514A - Photographic compositions and elements - Google Patents
Photographic compositions and elements Download PDFInfo
- Publication number
- US3155514A US3155514A US236412A US23641262A US3155514A US 3155514 A US3155514 A US 3155514A US 236412 A US236412 A US 236412A US 23641262 A US23641262 A US 23641262A US 3155514 A US3155514 A US 3155514A
- Authority
- US
- United States
- Prior art keywords
- silver
- silver halide
- sodium thiosulfate
- photographic
- dispersion
- 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
- 239000000203 mixture Substances 0.000 title claims description 20
- 229910052709 silver Inorganic materials 0.000 claims description 120
- 239000004332 silver Substances 0.000 claims description 120
- -1 SILVER HALIDE Chemical class 0.000 claims description 109
- 239000000839 emulsion Substances 0.000 claims description 37
- 239000006185 dispersion Substances 0.000 claims description 35
- 239000013078 crystal Substances 0.000 claims description 30
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 25
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 25
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- UMGDCJDMYOKAJW-UHFFFAOYSA-N aminothiocarboxamide Natural products NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 12
- 108010010803 Gelatin Proteins 0.000 claims description 10
- 229920000159 gelatin Polymers 0.000 claims description 10
- 239000008273 gelatin Substances 0.000 claims description 10
- 235000019322 gelatine Nutrition 0.000 claims description 10
- 235000011852 gelatine desserts Nutrition 0.000 claims description 10
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 9
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 9
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 claims description 7
- 229910021607 Silver chloride Inorganic materials 0.000 claims description 6
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 3
- 238000012360 testing method Methods 0.000 description 39
- 150000002894 organic compounds Chemical class 0.000 description 24
- 239000000243 solution Substances 0.000 description 22
- 150000001875 compounds Chemical class 0.000 description 21
- 238000000034 method Methods 0.000 description 21
- 230000008569 process Effects 0.000 description 12
- CYCKHTAVNBPQDB-UHFFFAOYSA-N 4-phenyl-3H-thiazole-2-thione Chemical compound S1C(S)=NC(C=2C=CC=CC=2)=C1 CYCKHTAVNBPQDB-UHFFFAOYSA-N 0.000 description 9
- 230000008901 benefit Effects 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 8
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- 239000003638 chemical reducing agent Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 150000001241 acetals Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 150000003585 thioureas Chemical class 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- FULZLIGZKMKICU-UHFFFAOYSA-N N-phenylthiourea Chemical compound NC(=S)NC1=CC=CC=C1 FULZLIGZKMKICU-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 230000003381 solubilizing effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- FPZXQVCYHDMIIA-UHFFFAOYSA-N 1,1-diphenylthiourea Chemical compound C=1C=CC=CC=1N(C(=S)N)C1=CC=CC=C1 FPZXQVCYHDMIIA-UHFFFAOYSA-N 0.000 description 1
- WYMLGVPROUZGCI-UHFFFAOYSA-N 1,3-bis(2-ethylphenyl)thiourea Chemical compound CCC1=CC=CC=C1NC(=S)NC1=CC=CC=C1CC WYMLGVPROUZGCI-UHFFFAOYSA-N 0.000 description 1
- LQZPSWMMTICWHD-UHFFFAOYSA-N 1,3-dibenzylthiourea Chemical compound C=1C=CC=CC=1CNC(=S)NCC1=CC=CC=C1 LQZPSWMMTICWHD-UHFFFAOYSA-N 0.000 description 1
- VFCZSWPNOOGGAJ-UHFFFAOYSA-N 1,3-dinaphthalen-1-ylthiourea Chemical compound C1=CC=C2C(NC(NC=3C4=CC=CC=C4C=CC=3)=S)=CC=CC2=C1 VFCZSWPNOOGGAJ-UHFFFAOYSA-N 0.000 description 1
- QRMPKOFEUHIBNM-UHFFFAOYSA-N 1,4-dimethylcyclohexane Chemical group CC1CCC(C)CC1 QRMPKOFEUHIBNM-UHFFFAOYSA-N 0.000 description 1
- ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)CN1C1=CC=CC=C1 ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 0.000 description 1
- PIVQQUNOTICCSA-UHFFFAOYSA-N ANTU Chemical compound C1=CC=C2C(NC(=S)N)=CC=CC2=C1 PIVQQUNOTICCSA-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 229920002307 Dextran Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- FCSHMCFRCYZTRQ-UHFFFAOYSA-N N,N'-diphenylthiourea Chemical compound C=1C=CC=CC=1NC(=S)NC1=CC=CC=C1 FCSHMCFRCYZTRQ-UHFFFAOYSA-N 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- WDLUEZJSSHTKAP-UHFFFAOYSA-N acetaldehyde;1,1-diethoxyethane Chemical compound CC=O.CCOC(C)OCC WDLUEZJSSHTKAP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000005234 chemical deposition Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013098 chemical test method Methods 0.000 description 1
- OIDPCXKPHYRNKH-UHFFFAOYSA-J chrome alum Chemical compound [K]OS(=O)(=O)O[Cr]1OS(=O)(=O)O1 OIDPCXKPHYRNKH-UHFFFAOYSA-J 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- VYXSBFYARXAAKO-UHFFFAOYSA-N ethyl 2-[3-(ethylamino)-6-ethylimino-2,7-dimethylxanthen-9-yl]benzoate;hydron;chloride Chemical compound [Cl-].C1=2C=C(C)C(NCC)=CC=2OC2=CC(=[NH+]CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920001480 hydrophilic copolymer Polymers 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- BOQKCADLPNLYCZ-UHFFFAOYSA-N n-phenylbenzenecarbothioamide Chemical compound C=1C=CC=CC=1C(=S)NC1=CC=CC=C1 BOQKCADLPNLYCZ-UHFFFAOYSA-N 0.000 description 1
- 239000010956 nickel silver Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- VPQBLCVGUWPDHV-UHFFFAOYSA-N sodium selenide Chemical compound [Na+].[Na+].[Se-2] VPQBLCVGUWPDHV-UHFFFAOYSA-N 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C391/00—Compounds containing selenium
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D293/00—Heterocyclic compounds containing rings having nitrogen and selenium or nitrogen and tellurium, with or without oxygen or sulfur atoms, as the ring hetero atoms
- C07D293/10—Heterocyclic compounds containing rings having nitrogen and selenium or nitrogen and tellurium, with or without oxygen or sulfur atoms, as the ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D293/12—Selenazoles; Hydrogenated selenazoles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/492—Photosoluble emulsions
Definitions
- novel photographic emulsion layers and elements of this invention comprise, before exposure to actinic light, silver halide crystals having associated therewith, in substantially greater than fog-inhibiting amounts, a silver mercaptide of a substituted thiourea having at least one SH group in one of its tautomeric forms, the latter compouind being characterized in that when admixed with an aqueous silver halide dispersion it protects the silver halide crystals to such an extent that when a silver halide dispersion protected by said compound is treated with 10%, by weight, aqueous sodium thiosulfate at least three times the amount of silver halide remains undissolved as in a similar dispersion successively treated with aqueous sodium hypochlorite and sodium thiosulfate, after vigorous agitation of the dispersions for 30 seconds at C.
- the silver halide dispersion insolubility is determined by taking a 0.5-ml. portion of the silver halide dispersion (after each incremental addition of the candidate organic compound), adding about 0.1 to 0.2 ml. of 10% aqueous sodium thiosulfate solution and observing the turbidity after seconds.
- Water-permeable organic colloid binding agents can be used and in some cases such binders can be used alone.
- Such agents include water-permeable or watersoluble polyvinyl alcohol and its derivatives, e.g., partially hydrolyzed polyvinyl acetates, polyvinyl ethers and acetals containing a large number of intralinear groups, hydrolyzed interpolymers of vinyl acetate and unsaturated addition polymerizable compounds such as maleic anhydride, acrylic and methacrylic acid esters and styrene.
- Suitable such colloids of the last-mentioned type were disclosed in US. Patents 2,276,322; 2,276,323 and 2,397,866.
- a particularly preferred organic compound is 2- mercapto-4-phenylthiazole (hereinafter to be referred to as MPT).
- MPT 2- mercapto-4-phenylthiazole
- This compound is disclosed and claimed in my copending application Ser. No. 317,824, filed October 21, 1963, entitled Photographic Compositions, Layers and Elements which is a continuation-in-part of this application. Assuming that a single molecule of MPT could occupy an area of 28 square angstroms, it would require 1.5 10 molecules to occupy a molar surface area of silver halide. With a molecular weight of 193, this would require of MPT to insolubilize one mole of the silver halide.
- Example II Example I was repeated except that other thiourea compounds, in the same amounts by weight, were examined in place of MPT. After photographic processing as described in Procedure A, the optical densities of completely unexposed areas and heavily exposed areas of the film were determined using a Western Electric RA-lOO-C Densitometer.
- silver chlorooromide dispersion is treated with 10%, by weight, aqueous sodium thiosulfate (so that the resulting mixture contains 0.29 mg. of silver and 1 mg. of sodium thiosulfate), at least three times the amount of silver chlorobromide remains undissolved as compared with similar dispersion successively treated with a 5%, by weight, aqueous sodium hypochlorite and by weight, aqueous sodium thiosulfate (so that the resulting mixture contains 0.29 mg. of silver, 25 mg. of sodium hypochlorite and 100 mg. of sodium thiosulfate), after vigorous agitation of the dispersions for 30 seconds at 25 C.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Priority Applications (26)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL134365D NL134365C (en, 2012) | 1961-12-08 | ||
FR88737D FR88737E (en, 2012) | 1961-12-08 | ||
FR89467D FR89467E (en, 2012) | 1961-12-08 | ||
US236418A US3155516A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236412A US3155514A (en) | 1961-12-08 | 1962-11-08 | Photographic compositions and elements |
US236417A US3155515A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236420A US3155507A (en) | 1961-12-08 | 1962-11-08 | Photographic processes |
GB46344/62A GB1031902A (en) | 1961-12-08 | 1962-12-07 | Improvements in silver halide photography |
DEP30721A DE1261397B (de) | 1961-12-08 | 1962-12-07 | Photographisches Verfahren zur Herstellung positiver Bilder |
GB46345/62A GB1031903A (en) | 1961-12-08 | 1962-12-07 | Photographic silver halide materials and processes |
DEP30723A DE1226877B (de) | 1961-12-08 | 1962-12-07 | Photographische Silberhalogenidemulsion |
US317824A US3155519A (en) | 1961-12-08 | 1963-10-21 | Photographic compositions, layers and elements |
NL6408533A NL6408533A (en, 2012) | 1961-12-08 | 1964-07-24 | |
US388919A US3418124A (en) | 1961-12-08 | 1964-08-11 | High contrast direct positive by using active cations in silver halide solvent |
DK395464A DK119392B (da) | 1961-12-08 | 1964-08-11 | Fotografisk sølvhalogenidmateriale til kopiering. |
BE651688A BE651688A (en, 2012) | 1961-12-08 | 1964-08-11 | |
US390460A US3384485A (en) | 1961-12-08 | 1964-08-18 | Silver halide emulsions photosolubilized with optical sensitizing dyes and silver mercaptides |
CH1270464A CH486719A (de) | 1961-12-08 | 1964-09-30 | Photographische Halogensilberemulsion und ihre Verwendung |
US403661A US3284206A (en) | 1961-12-08 | 1964-10-13 | Image yielding layers |
DEP37430A DE1294186B (de) | 1961-12-08 | 1965-08-10 | Photographisches Verfahren zur Herstellung positiver Bilder |
GB34231/65A GB1111226A (en) | 1961-12-08 | 1965-08-10 | Improvements relating to the production of images |
BE668111D BE668111A (en, 2012) | 1961-12-08 | 1965-08-10 | |
DEP37479A DE1293581B (de) | 1961-12-08 | 1965-08-18 | Photographische Silberhalogenidemulsion |
GB43289/65A GB1124772A (en) | 1961-12-08 | 1965-10-12 | Improvements in silver halide photography |
BE670823D BE670823A (en, 2012) | 1961-12-08 | 1965-10-12 | |
DEP37856A DE1293582B (de) | 1961-12-08 | 1965-10-13 | Photographische Silberhalogenidemulsion |
Applications Claiming Priority (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15813261A | 1961-12-08 | 1961-12-08 | |
US236417A US3155515A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236418A US3155516A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236420A US3155507A (en) | 1961-12-08 | 1962-11-08 | Photographic processes |
US236412A US3155514A (en) | 1961-12-08 | 1962-11-08 | Photographic compositions and elements |
US317824A US3155519A (en) | 1961-12-08 | 1963-10-21 | Photographic compositions, layers and elements |
NL6408533A NL6408533A (en, 2012) | 1961-12-08 | 1964-07-24 | |
US388919A US3418124A (en) | 1961-12-08 | 1964-08-11 | High contrast direct positive by using active cations in silver halide solvent |
US390460A US3384485A (en) | 1961-12-08 | 1964-08-18 | Silver halide emulsions photosolubilized with optical sensitizing dyes and silver mercaptides |
US403661A US3284206A (en) | 1961-12-08 | 1964-10-13 | Image yielding layers |
Publications (1)
Publication Number | Publication Date |
---|---|
US3155514A true US3155514A (en) | 1964-11-03 |
Family
ID=27580572
Family Applications (8)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US236412A Expired - Lifetime US3155514A (en) | 1961-12-08 | 1962-11-08 | Photographic compositions and elements |
US236417A Expired - Lifetime US3155515A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236420A Expired - Lifetime US3155507A (en) | 1961-12-08 | 1962-11-08 | Photographic processes |
US236418A Expired - Lifetime US3155516A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US317824A Expired - Lifetime US3155519A (en) | 1961-12-08 | 1963-10-21 | Photographic compositions, layers and elements |
US388919A Expired - Lifetime US3418124A (en) | 1961-12-08 | 1964-08-11 | High contrast direct positive by using active cations in silver halide solvent |
US390460A Expired - Lifetime US3384485A (en) | 1961-12-08 | 1964-08-18 | Silver halide emulsions photosolubilized with optical sensitizing dyes and silver mercaptides |
US403661A Expired - Lifetime US3284206A (en) | 1961-12-08 | 1964-10-13 | Image yielding layers |
Family Applications After (7)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US236417A Expired - Lifetime US3155515A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US236420A Expired - Lifetime US3155507A (en) | 1961-12-08 | 1962-11-08 | Photographic processes |
US236418A Expired - Lifetime US3155516A (en) | 1961-12-08 | 1962-11-08 | Photographic products |
US317824A Expired - Lifetime US3155519A (en) | 1961-12-08 | 1963-10-21 | Photographic compositions, layers and elements |
US388919A Expired - Lifetime US3418124A (en) | 1961-12-08 | 1964-08-11 | High contrast direct positive by using active cations in silver halide solvent |
US390460A Expired - Lifetime US3384485A (en) | 1961-12-08 | 1964-08-18 | Silver halide emulsions photosolubilized with optical sensitizing dyes and silver mercaptides |
US403661A Expired - Lifetime US3284206A (en) | 1961-12-08 | 1964-10-13 | Image yielding layers |
Country Status (5)
Country | Link |
---|---|
US (8) | US3155514A (en, 2012) |
BE (1) | BE670823A (en, 2012) |
DE (5) | DE1226877B (en, 2012) |
FR (1) | FR89467E (en, 2012) |
GB (4) | GB1031902A (en, 2012) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3368899A (en) * | 1964-10-13 | 1968-02-13 | Du Pont | Emulsion layers and elements |
US3458318A (en) * | 1965-08-02 | 1969-07-29 | Eastman Kodak Co | Supersensitized silver halide emulsions |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR89467E (en, 2012) * | 1961-12-08 | |||
US3379529A (en) * | 1963-02-28 | 1968-04-23 | Eastman Kodak Co | Photographic inhibitor-releasing developers |
US3368898A (en) * | 1963-10-17 | 1968-02-13 | Gen Aniline & Film Corp | Autopositive film and paper and emulsions therefor |
DE1281842B (de) * | 1964-06-22 | 1968-10-31 | Du Pont | Fotografisches Aufzeichnungsmaterial mit einer fotoloeslichen Schicht |
US3341574A (en) * | 1964-09-18 | 1967-09-12 | Celanese Corp | Di-(neopentylglycol mononeoheptanoate)azelate |
US3407067A (en) * | 1964-10-13 | 1968-10-22 | Du Pont | Photosolubilization with mercaptooxazoles |
US3394005A (en) * | 1964-10-16 | 1968-07-23 | Du Pont | Increased development rate of photosoluble silver halide emulsions by the action of water-soluble iodide |
US3377169A (en) * | 1965-03-30 | 1968-04-09 | Du Pont | Copper thallium and lead halide and pseudohalides photosoluble crystals |
US3451819A (en) * | 1965-08-09 | 1969-06-24 | Du Pont | Photosoluble silver halide emulsion made spontaneously developable with amine boranes |
US3464822A (en) * | 1965-09-13 | 1969-09-02 | Du Pont | Process for making electrically conductive images |
GB1178800A (en) * | 1966-03-01 | 1970-01-21 | Minnesota Mining & Mfg | Improvements in or relating to Copying Materials |
US3486895A (en) * | 1966-04-29 | 1969-12-30 | Du Pont | Process for obtaining artistic effects in photosoluble direct positive silver halide emulsions |
US3495983A (en) * | 1967-06-23 | 1970-02-17 | Du Pont | Photosolubilization process using phenols as dmax maintainers |
US3628956A (en) * | 1967-12-08 | 1971-12-21 | Du Pont | Process for preparing direct positive images by photosolubilization |
US3862352A (en) * | 1968-04-16 | 1975-01-21 | Itek Corp | Photographically prepared electrical circuits wherein the photosensitive material is a photoconductor |
US3647439A (en) * | 1968-10-01 | 1972-03-07 | Eastman Kodak Co | Photographic element, composition and process |
US3649289A (en) * | 1968-10-21 | 1972-03-14 | Eastman Kodak Co | Photographic materials |
US3653899A (en) * | 1968-11-12 | 1972-04-04 | Eastman Kodak Co | Photographic materials and processes |
US3640717A (en) * | 1969-06-05 | 1972-02-08 | Itek Corp | Photographic reversal process employing organic mercaptan compounds |
US3652279A (en) * | 1969-07-18 | 1972-03-28 | Du Pont | Nitrogen-containing dmax maintainers for use in photosoluble emulsions |
US4014699A (en) * | 1973-05-17 | 1977-03-29 | Ciba-Geigy Ag | Preparation for the processing of photographic materials |
GB1548395A (en) * | 1975-05-29 | 1979-07-11 | Eastman Kodak Co | Photographic materials |
GB1580212A (en) * | 1976-03-29 | 1980-11-26 | Agfa Gevaert | Antifogging and/or stabilizing compounds for silver halide photography |
JPS53134430A (en) * | 1977-04-27 | 1978-11-24 | Mitsubishi Paper Mills Ltd | Silver halide photosensitive materials for multiilayer color photograph |
DE2931690A1 (de) * | 1979-08-04 | 1981-02-19 | Agfa Gevaert Ag | Photographische emulsion, verfahren zur herstellung sowie photographische materialien |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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US2214446A (en) * | 1938-05-10 | 1940-09-10 | Gen Aniline & Film Corp | Photographic development of silver halide layers |
US3008829A (en) * | 1960-04-11 | 1961-11-14 | Gen Aniline & Film Corp | Photographic materials and method of producing the same |
US3046130A (en) * | 1960-05-12 | 1962-07-24 | Gen Aniline & Film Corp | Photographic materials containing a chemical sensitizer |
US3063837A (en) * | 1958-11-07 | 1962-11-13 | Agfa Ag | Photographic diffusion transfer process for planographic printing |
US3080230A (en) * | 1956-02-18 | 1963-03-05 | Agfa Ag | Photographic stratum transfer process and element therefor |
Family Cites Families (15)
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BE388620A (en, 2012) * | 1926-05-21 | |||
DE548323C (de) * | 1929-02-25 | 1932-04-09 | Kodak Akt Ges | Verfahren zum Stabilisieren einer Silberhalogenemulsion |
US2025876A (en) * | 1931-04-11 | 1935-12-31 | Du Pont | Preparation of aryl-amines |
US2131038A (en) * | 1932-05-26 | 1938-09-27 | Eastman Kodak Co | Photographic emulsion containing alkyl quaternary salts of thiazoles and the like asantifoggants |
GB477628A (en) * | 1936-08-14 | 1938-01-04 | Albert Steigmann | Method of preventing yellow stain in photographs |
US2195150A (en) * | 1938-06-16 | 1940-03-26 | Ilford Ltd | Stabilization of photographic emulsions |
US2520358A (en) * | 1948-09-04 | 1950-08-29 | Eastman Kodak Co | Heterocyclic bis acetones, thioacetones, and selenoacetones |
US2710256A (en) * | 1951-04-25 | 1955-06-07 | Gen Aniline & Film Corp | Photographic print-out process |
BE511060A (en, 2012) * | 1951-04-30 | |||
US2985661A (en) * | 1956-02-06 | 1961-05-23 | American Cyanamid Co | Preparation of 2(omicron-aminophenyl)-benzimidazole |
BE557661A (en, 2012) * | 1956-05-23 | |||
US3038800A (en) * | 1957-12-19 | 1962-06-12 | Eastman Kodak Co | Photopolymerization of olefinicallyunsaturated monomers by silver halides |
BE582161A (en, 2012) * | 1958-08-29 | |||
US3155518A (en) * | 1963-10-21 | 1964-11-03 | Du Pont | Silver halide compositions, layers and elements |
FR89467E (en, 2012) * | 1961-12-08 |
-
0
- FR FR89467D patent/FR89467E/fr active Active
-
1962
- 1962-11-08 US US236412A patent/US3155514A/en not_active Expired - Lifetime
- 1962-11-08 US US236417A patent/US3155515A/en not_active Expired - Lifetime
- 1962-11-08 US US236420A patent/US3155507A/en not_active Expired - Lifetime
- 1962-11-08 US US236418A patent/US3155516A/en not_active Expired - Lifetime
- 1962-12-07 GB GB46344/62A patent/GB1031902A/en not_active Expired
- 1962-12-07 DE DEP30723A patent/DE1226877B/de active Pending
- 1962-12-07 GB GB46345/62A patent/GB1031903A/en not_active Expired
- 1962-12-07 DE DEP30721A patent/DE1261397B/de active Pending
-
1963
- 1963-10-21 US US317824A patent/US3155519A/en not_active Expired - Lifetime
-
1964
- 1964-08-11 US US388919A patent/US3418124A/en not_active Expired - Lifetime
- 1964-08-18 US US390460A patent/US3384485A/en not_active Expired - Lifetime
- 1964-10-13 US US403661A patent/US3284206A/en not_active Expired - Lifetime
-
1965
- 1965-08-10 GB GB34231/65A patent/GB1111226A/en not_active Expired
- 1965-08-10 DE DEP37430A patent/DE1294186B/de active Pending
- 1965-08-18 DE DEP37479A patent/DE1293581B/de active Pending
- 1965-10-12 GB GB43289/65A patent/GB1124772A/en not_active Expired
- 1965-10-12 BE BE670823D patent/BE670823A/xx unknown
- 1965-10-13 DE DEP37856A patent/DE1293582B/de active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2214446A (en) * | 1938-05-10 | 1940-09-10 | Gen Aniline & Film Corp | Photographic development of silver halide layers |
US3080230A (en) * | 1956-02-18 | 1963-03-05 | Agfa Ag | Photographic stratum transfer process and element therefor |
US3063837A (en) * | 1958-11-07 | 1962-11-13 | Agfa Ag | Photographic diffusion transfer process for planographic printing |
US3008829A (en) * | 1960-04-11 | 1961-11-14 | Gen Aniline & Film Corp | Photographic materials and method of producing the same |
US3046130A (en) * | 1960-05-12 | 1962-07-24 | Gen Aniline & Film Corp | Photographic materials containing a chemical sensitizer |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3368899A (en) * | 1964-10-13 | 1968-02-13 | Du Pont | Emulsion layers and elements |
US3458318A (en) * | 1965-08-02 | 1969-07-29 | Eastman Kodak Co | Supersensitized silver halide emulsions |
Also Published As
Publication number | Publication date |
---|---|
DE1293581B (de) | 1969-04-24 |
US3418124A (en) | 1968-12-24 |
FR89467E (en, 2012) | |
GB1124772A (en) | 1968-08-21 |
US3155519A (en) | 1964-11-03 |
DE1261397B (de) | 1968-02-15 |
DE1294186B (de) | 1969-09-11 |
US3155515A (en) | 1964-11-03 |
BE670823A (en, 2012) | 1966-04-12 |
GB1111226A (en) | 1968-04-24 |
DE1226877B (de) | 1966-10-13 |
US3155507A (en) | 1964-11-03 |
US3284206A (en) | 1966-11-08 |
DE1293582B (de) | 1969-04-24 |
GB1031902A (en) | 1966-06-02 |
US3155516A (en) | 1964-11-03 |
US3384485A (en) | 1968-05-21 |
GB1031903A (en) | 1966-06-02 |
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