US3877947A - Photographic element - Google Patents
Photographic element Download PDFInfo
- Publication number
- US3877947A US3877947A US347523A US34752373A US3877947A US 3877947 A US3877947 A US 3877947A US 347523 A US347523 A US 347523A US 34752373 A US34752373 A US 34752373A US 3877947 A US3877947 A US 3877947A
- Authority
- US
- United States
- Prior art keywords
- light
- photographic element
- phase
- alkyl ester
- maleic acid
- 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
- 239000010410 layer Substances 0.000 claims abstract description 59
- 238000005191 phase separation Methods 0.000 claims abstract description 54
- 239000003112 inhibitor Substances 0.000 claims abstract description 52
- 229920000159 gelatin Polymers 0.000 claims abstract description 51
- 239000008273 gelatin Substances 0.000 claims abstract description 51
- 108010010803 Gelatin Proteins 0.000 claims abstract description 49
- 235000019322 gelatine Nutrition 0.000 claims abstract description 49
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 49
- 239000000839 emulsion Substances 0.000 claims abstract description 30
- 229920003169 water-soluble polymer Polymers 0.000 claims abstract description 29
- 229910052709 silver Inorganic materials 0.000 claims abstract description 25
- 239000004332 silver Substances 0.000 claims abstract description 25
- -1 silver halide Chemical class 0.000 claims abstract description 25
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 20
- 238000012546 transfer Methods 0.000 claims abstract description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- 239000011241 protective layer Substances 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims description 36
- 125000005907 alkyl ester group Chemical group 0.000 claims description 35
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 34
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 34
- 239000011976 maleic acid Substances 0.000 claims description 34
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 34
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 16
- 229920002554 vinyl polymer Polymers 0.000 claims description 10
- 238000009792 diffusion process Methods 0.000 claims description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 8
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 6
- 229920002472 Starch Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 5
- 229920002678 cellulose Polymers 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 claims description 5
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 5
- 239000008107 starch Substances 0.000 claims description 5
- 235000019698 starch Nutrition 0.000 claims description 5
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 claims description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 230000006641 stabilisation Effects 0.000 abstract description 7
- 238000011105 stabilization Methods 0.000 abstract description 7
- 238000012545 processing Methods 0.000 abstract description 3
- 239000000123 paper Substances 0.000 description 22
- 239000000203 mixture Substances 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000007864 aqueous solution Substances 0.000 description 11
- 229920001577 copolymer Polymers 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 7
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 5
- 229910021607 Silver chloride Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 4
- 229920001059 synthetic polymer Polymers 0.000 description 4
- 229940101006 anhydrous sodium sulfite Drugs 0.000 description 3
- 230000002401 inhibitory effect Effects 0.000 description 3
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 3
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 3
- 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 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- 229910001864 baryta Inorganic materials 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229960001755 resorcinol Drugs 0.000 description 2
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- WWNBZGLDODTKEM-UHFFFAOYSA-N sulfanylidenenickel Chemical compound [Ni]=S WWNBZGLDODTKEM-UHFFFAOYSA-N 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 2
- LUMLZKVIXLWTCI-NSCUHMNNSA-N (e)-2,3-dichloro-4-oxobut-2-enoic acid Chemical compound OC(=O)C(\Cl)=C(/Cl)C=O LUMLZKVIXLWTCI-NSCUHMNNSA-N 0.000 description 1
- BDHGFCVQWMDIQX-UHFFFAOYSA-N 1-ethenyl-2-methylimidazole Chemical compound CC1=NC=CN1C=C BDHGFCVQWMDIQX-UHFFFAOYSA-N 0.000 description 1
- LPNSCOVIJFIXTJ-UHFFFAOYSA-N 2-methylidenebutanamide Chemical compound CCC(=C)C(N)=O LPNSCOVIJFIXTJ-UHFFFAOYSA-N 0.000 description 1
- WDGCBNTXZHJTHJ-UHFFFAOYSA-N 2h-1,3-oxazol-2-id-4-one Chemical class O=C1CO[C-]=N1 WDGCBNTXZHJTHJ-UHFFFAOYSA-N 0.000 description 1
- UVRCNEIYXSRHNT-UHFFFAOYSA-N 3-ethylpent-2-enamide Chemical compound CCC(CC)=CC(N)=O UVRCNEIYXSRHNT-UHFFFAOYSA-N 0.000 description 1
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- VMNRZYKMPOZISX-UHFFFAOYSA-M COC(C[Hg]O)Cc1cccc2cc(C(O)=O)c(=O)oc12 Chemical compound COC(C[Hg]O)Cc1cccc2cc(C(O)=O)c(=O)oc12 VMNRZYKMPOZISX-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920001479 Hydroxyethyl methyl cellulose Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- GMEHFXXZSWDEDB-UHFFFAOYSA-N N-ethylthiourea Chemical compound CCNC(N)=S GMEHFXXZSWDEDB-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XCFIVNQHHFZRNR-UHFFFAOYSA-N [Ag].Cl[IH]Br Chemical compound [Ag].Cl[IH]Br XCFIVNQHHFZRNR-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
- 235000015241 bacon Nutrition 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910021538 borax 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
- 230000003197 catalytic effect Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- ZUIVNYGZFPOXFW-UHFFFAOYSA-N chembl1717603 Chemical compound N1=C(C)C=C(O)N2N=CN=C21 ZUIVNYGZFPOXFW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- MQRJBSHKWOFOGF-UHFFFAOYSA-L disodium;carbonate;hydrate Chemical compound O.[Na+].[Na+].[O-]C([O-])=O MQRJBSHKWOFOGF-UHFFFAOYSA-L 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 108010025899 gelatin film Proteins 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000002344 gold compounds Chemical class 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- AGBQKNBQESQNJD-UHFFFAOYSA-N lipoic acid Chemical compound OC(=O)CCCCC1CCSS1 AGBQKNBQESQNJD-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- ZAKLKBFCSHJIRI-UHFFFAOYSA-N mucochloric acid Natural products OC1OC(=O)C(Cl)=C1Cl ZAKLKBFCSHJIRI-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- LSWADWIFYOAQRZ-UHFFFAOYSA-N n-(ethoxymethyl)prop-2-enamide Chemical compound CCOCNC(=O)C=C LSWADWIFYOAQRZ-UHFFFAOYSA-N 0.000 description 1
- ULYOZOPEFCQZHH-UHFFFAOYSA-N n-(methoxymethyl)prop-2-enamide Chemical compound COCNC(=O)C=C ULYOZOPEFCQZHH-UHFFFAOYSA-N 0.000 description 1
- YYMRAHJYANNJQC-UHFFFAOYSA-N n-(morpholin-4-ylmethyl)prop-2-enamide Chemical compound C=CC(=O)NCN1CCOCC1 YYMRAHJYANNJQC-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- FHSAKWZEUVVHFN-UHFFFAOYSA-N n-morpholin-4-ylprop-2-enamide Chemical compound C=CC(=O)NN1CCOCC1 FHSAKWZEUVVHFN-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940076133 sodium carbonate monohydrate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000008053 sultones Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 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
- 229910052718 tin Inorganic materials 0.000 description 1
- 150000003918 triazines Chemical class 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
- G03C1/053—Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/162—Protective or antiabrasion layer
Definitions
- ABSTRACT A photographic element for use in silver halide photography having a silver halide emulsion layer, a protective layer, a subbing layer or a diffusion-transfer image-receiving layer, each using gelatin as the main binding component, in which into one of said layers are incorporated a nonionic water-soluble polymer and a phase separation inhibitor containing the -CH2-CH- ,-CH-CH- 0COCH COOH COOH and - CH CH COOH COOR groups in 50, 50 X and X molar percent proportions, respectively, X being not more than 50 and R being an alkyl group having from 1 to 4 carbon atoms.
- the photographic element has reduced propensity to curling and to becoming sticky after stabilization processing.
- Field of the invention 7 This invention relates to photographic elements, and more particularly to composition of layers to be provided 'on a photographic element support.
- Photographic elements in general comprise a support material such as paper, a synthetic resin film, a glass or metallic plate, with a subbing layer optionally being provided thereon for the purpose of enhancing the adhesivity between the support and photographic layer adjacent thereto, together with a silver halide emulsion layer, usually with a protective layer provided thereon to prevent damage to said emulsion layer, the latter two layers being applied onto the surface of the foregoing support or subbing layer.
- a support material such as paper, a synthetic resin film, a glass or metallic plate
- a subbing layer optionally being provided thereon for the purpose of enhancing the adhesivity between the support and photographic layer adjacent thereto, together with a silver halide emulsion layer, usually with a protective layer provided thereon to prevent damage to said emulsion layer, the latter two layers being applied onto the surface of the foregoing support or subbing layer.
- an imagereceiving element used in the diffusion transfer photographic process, which element comprises an imagereceiving layer having incorporated therein a catalytic substance, i.e., silver deposits or so-called development nuclei, in a dispersed form for reduction of a soluble silver complex transported by diffusion from a photographic light-sensitive element.
- a catalytic substance i.e., silver deposits or so-called development nuclei
- gelatin As the binding agent for these photographic elements, gelatin has heretofore been used in almost all cases due to its outstanding photographic and physical properties. Since gelatin is a natural substance, however, its use has suffered from the disadvantage that the properties of gelatin largely depend upon the raw materials and manufacturing processes used to form it; and often it is therefore not possible to insure constant quality in the finished product. Besides such a disadvantage, the use of gelatin presents some other problems. For instance, it is sensitive to changes in temperature and humidity and tends to curl. Furthermore, in the stabilization process wherein a photographic element is processed in a stabilizing solution containing ammonium thiocyanate, the surface of a gelatin film which constitutes a photographic layer becomes sticky after stabilization.
- substitutes for gelatin as a binding agent for photographic layers.
- These include, for example, polyvinyl alcohol, polyacrylamide, polyvinyl pyrrolidone, poly-1-vinyl-2-methylimidazole, sodium polyacrylate, an acrylamide-1-vinyl-2-methylimidazole copolymer and an acrylamide-l-vinyl-2-methylimidazole-acrylic acid copolymer.
- These synthetic polymers are not superior gelatin in various other photographic and physical properties, so that in practice gelatin is used.
- a method has been proposed wherein a third substance is added to prevent the phase separation.
- MVE/MA methyl vinyl ether maleic anhydride copolymer
- an amide or ester thereof as a phase-separation inhibitor upon using gelatin with polyvinyl alcohol.
- the compounds disclosed hereinafter are extremely effective as phase-separation inhibitors upon admixing gelatin with nonionic polymers. Furthermore, we have also confirmed the following advantages: the coating composition prepared using such compounds can be applied onto a support more uniformly than in the case of using the prior art phaseseparation inhibitor, i.e., the above-described copolymer (MVE/MA) or an amide or ester thereof; the photographic elements produced have little tendency to curl, and they show little tendency to be sticky after stabilization, if such is used.
- the prior art phaseseparation inhibitor i.e., the above-described copolymer (MVE/MA) or an amide or ester thereof
- the photographic elements produced have little tendency to curl, and they show little tendency to be sticky after stabilization, if such is used.
- the present invention provides a photographic element comprising a support having thereon at least one layer comprising gelatin, a nonionic water-soluble polymer and a polymer, said polymer comprising 50 mole percent of vinyl acetate, (50 x) mole of maleic acid and mole of half alkyl ester of maleic acid, wherein x is 0 2; 50 and the alkyl group has 1 to 4 carbon atoms.
- the polymer of the present invention which can be employed as an inhibitor for phase-separation between gelatin and the nonionic water-soluble polymer, may be characterized by the following chemical units and the specified proportion thereof.
- Atomic groups Proportion contained (50 X) molar COOH COOH Unit No. Atomic groups Proportion contained '3 CH (IIH- Xmo1ar% COOH COOR (X being not more (R being an alkyl than 50) group having from 1 1:0 4 carbon atoms.)
- the nonionic water-soluble polymers which may be S E; y" 2' 047 used in accordance with the present invention include 5 polyvinyl alcohols, polymers Of acrylamlde 01' its derlv- (R n butyl) (R means alkyl group of the half ester of atives such as acrylamide, N-methylacrylamide, N-
- nonionic water-soluble polymer polyvinyl alcohol is the most typical one. Any known polymer which is used together with gelatin in the photographic art may be employed.
- phase-separation inhibitors used according to the present invention may be obtained by synthesizing a l l (polymerization ratio) copolymer of vinyl acetate and maleic anhydride by means of any conventional radical polymerization method, and heat-treating the copolymer in water or an alcohol having from l to 4 carbon atoms to effect hydrolysis or alcoholysis of the same.
- the decomposition reaction may also be par- 40 tially carried out to produce the half ester.
- phase-separation inhibitors Several examples of such phase-separation inhibitors will be given below where the values of the intrinsic viscosity are taken in a methanolic solution of each phaseseparation inhibitor at 300C.
- gelatin and the nonionic water-soluble polymer can be used in admixture with the phase-separation inhibiting polymer in photographic layers.
- photographic layers include not only a light-insensitive layer such as a protective or uppermost layer, a subbing or under-coated layer, an image receiving layer for diffusion-transfer process, which layer may also contain nuclei for precipitating silver, such as colloidal silver or heavy metal sulfides, but also a light-sensitive layer such as a light-sensitive silver halide emulsion layer.
- the phase-separation inhibiting polymer of the present invention may be added to a mixture to be coated at any stage before coating.
- the polymer may also be added to a silver halide emulsion during preparation thereof.
- the proportions of gelatin, nonionic water-soluble polymer and phase-separation inhibiting polymer may be varied depending upon the specific requirement of the photographic layers being produced and the specific compound to be used. ln general, the preferred proportions are set out below.
- phase-separation inhibitors used according to the present invention may be of any molecular weight, although it is most preferred to use those having an intrinsic viscosity [1 as measured in a methanolic solution at 30C., of about 0.05 to about 5.0, preferably about 0.3 to about 2.0.
- Suitable support material include any of those used in photography such as cellulose acetate, synthetic resins such as polyesters, polystyrenes or polycarbonates, paper, or resin coated paper such as polyethylene coated paper.
- copolymers used according to the present invention remarkedly improve the compatibility between gelatin and nonionic water-soluble polymers, and are extremely effective for the prevention of phaseseparation which often takes place.
- the present invention can be applied to varied silver halide emulsions using silver chloride, silver bromide, silver chlorobromide, silver iodobromide and/or silver chloroiodobromide, and mixtures thereof.
- the emulsions to which the present invention may be applied may be chemically sensitized by any conventional method, for example using labile-sulfur containing compounds such as ammonium thiosulfate or ethylthiourea (see, for example, P. Glafkindes, Chimie Photographique; 2 eme Edition Photocinema, Paul Montel, Paris, 1957, pages 297299); gold compounds such as complexes of monovalent gold and thiocyanic acid (see lbid., page 301) or any combination of these compounds.
- labile-sulfur containing compounds such as ammonium thiosulfate or ethylthiourea
- gold compounds such as complexes of monovalent gold and thiocyanic acid (see lbid., page 301) or any combination of these compounds.
- the emulsions may be optically sensitized by incorporating thereinto spectral sensitizers such as cyanine or merocyanine dyes (see, for example, Shinichi Kikuchi, et a], Kagaku-Shashin Binran, Maruzen Co., Ltd.. 1959, pages -24). Furthermore, they may be stabilized by any stabilizers well known in the art, for example, heterocyclic compounds such as benzotriazole, l-phenyl-5-mercaptotetrazole, 4-hydroxy-6- methyl-1,3,3a, 7-tetrazaindene or 6-thioctic acid, mercury compounds such as mercumallylic acid (see Japanese Patent Publication No.
- the emulsions may be hardened using hardening agents such as formaldehyde, mucochloric acid, chromium alum or triazine derivatives (see, for example, Belgian Pat. No. 641,044), or a combination of these hardeners with hardening adjuvants such as resorcin or resorcin aldehyde.
- hardening agents such as formaldehyde, mucochloric acid, chromium alum or triazine derivatives (see, for example, Belgian Pat. No. 641,044), or a combination of these hardeners with hardening adjuvants such as resorcin or resorcin aldehyde.
- surface active agents such as saponin, sodium alkylbenzene sulfonate or an addition polymer of an alkylphenol and sultone (see British Pat. No. 1,024,808) in order to facilitate the application of said emulsions
- the emulsions prepared in accordance with the present invention can be used, after the addition of couplers, in the manufacture of natural color photographic films or papers. Furthermore, by increasing the ratio of the water-soluble polymer to gelatin, the developed film can be removed by means of rinsing, so that it may be used as a negative layer for use in the so-called multi-layer diffusion transfer process (C.E. Neblette, Photography, its Materials and Processes, 6th Edition, D. Van Nostrand Co., Princeton, New Jersey, 1962, pages 371-373) The present invention will now be further illustrated by the following non-limitative examples.
- a silver halide photographic emulsion thickness (4 microns) was prepared which contained g. silver chloride and 10 g. gelatin, and was divided into three equal portions A, B and C. lnto each portion there was Composition of the developer:
- the curling value was determined by measuring across the center of the circular form the distance (.r em) between the tips which were closest upon the curling, and the value (10 x) cm was taken as the curling value. The results of the measurement are shown in Table 1.
- EXAMPLE 2 A silver halide-gelatin emulsion (thickness: 4 microns) was preparedwhich contained 20 g. silver chloride and 10 g. gelatin, and, after addition of 10 g. hydroquinone as a developing agent, was divided into two equal portions A and B, into which were added the following solutions, respectively:
- Emulsion B 180 c.c. of a 10 weight percent aqueous solution of polyvinyl alcohol plus 20 c.c. of a 10 weight percent aqueous solution of a phaseseparation inhibitor (1).
- Emulsions A and B were each thoroughly agitated and applied onto a photographic base paper of g./m.'- to give photographic papers A and B, respectively, for use in a stabilization process. These photographic papers were each developed in an activator having the composition shown below, after which they were processed in a stabilizing solution containing Composition of the activator:
- EXAMPLE 3 A silver chlorobromide emulsion was prepared which contained 30 molar percent of silver bromide and 60 g. of gelatin and, after addition of 10 g. of hydroquinone as a developing agent, applied onto a photographic baryta-coated paper of 135 g./m On top of the coating layer there was further applied a thin protective layer of the following composition, thereby giving a photographic paper for use in the stabilization process.
- EXAMPLE 4 Colloidal nickel sulfide nuclei were incorporated into an aqueous solution having the composition as shown below and applied onto a photographic base paper of 85 g./m On top of the coating layer there was further applied a stripping layer mainly containing sodium alginate to give an image-receiving paper for use in the silver salt diffusion transfer process.
- the image-receiving paper was dipped for several seconds in a developer (composition is shown below) for use in the silver salt diffusion transfer process while held in tight surface contact with a negative paper having a silver halide emulsion layer for use in the diffusion transfer process, which negative paper had been exposed to light.
- the image-receiving paper after being separated from the negative paper after seconds showed an extremely low curling tendency and was satisfactory.
- Amount of nickel sulfide in the layer was 0.6 mg/m
- Amount of sodium alginate in the layer was 0.2 g/m.
- composition of the developer for use in the silver salt diffusion transfer process is a composition of the developer for use in the silver salt diffusion transfer process:
- EXAMPLE 5 A silver halide-gelatin emulsion was prepared which contained 20 g. AgCl and 10 g. gelatin; and was divided into four equal portions, into which the following compounds were added, respectively:
- Sample Substances added 200 c.c. of a 1071 aqueous solution of gelatin
- a mixture of I c.c. of a l0 /r aqueous solution of hydroxycthyl cellulose and 20 c.c. of a 10% aqueous solution of phaseseparation inhibitor (ll) (Substances according to the invention).
- a mixture of Hi0 cc. of a 10% aqueous solution of P. ⁇ '.A. and 20 c.c. of a l0'7r aqueous solution of phase-separation inhibitor (lV) (Substances according to the invention).
- Emulsions A to D were each thoroughly agitated and.
- a light-sensitive photographic element comprising a support having thereon at least one silver halide emulsion layer which consists essentially of silver halide, gelatin, a nonionic water-soluble polymer which is photographically compatible with said gelatin and a polymer which is a phase-separation inhibitor for said gelatin and said nonionic water-soluble polymer, said polymer comprising 50 mole percent of vinyl acetate (50 X) mole percent of maleic acid and X mole percent of a half alkyl ester of maleic acid, wherein X is 0 X 50 and the alkyl group in said half alkyl ester has 1 to 4 carbon atoms, wherein the proportion of said gelatin, said nonionic water-soluble polymer and said polymer is about 5 to about 70 percent by weight, about to about 15 percent by weight and about 5 to about 15 percent by weight, respectively.
- a light-sensitive photographic element comprising a support having thereon at least two layers, at least one of said layers being a silver halide emulsion layer and at least one of said layers containing gelatin, a nonionic water-soluble polymer which is photographically compatible with said gelatin and a polymer which is a phase-separation inhibitor for said gelatin and said nonionic water-soluble polymer, said polymer comprising 50 mole percent of vinyl acetate, (50 X) mole percent of maleic acid and X mole percent of a half alkyl ester of maleic acid, wherein X is 2 X 50 and said alkyl group in said half alkyl ester has 1 to 4 carbon atoms, wherein the proportion of said gelatin, said nonionic water-soluble polymer and said polymer is about 5 to about 70 percent by weight, about 90 to about percent by weight and about 5 to about 15 percent by weight, respectively, said at least one of said layers which contains gelatin, a nonionic water-soluble polymer and a
- a light-sensitive photographic element as claimed in claim 1 wherein 50 mole percent, (50 X) mole percent and X mole percent total 100 mole percent.
- nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
- phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.73.
- phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.2.
- phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phaseseparation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.52.
- phase-separation inhibitor has an intrinsic viscosity measured in a methanolic solution at 30C in the range of from 0.3 to 2.0.
- a light-sensitive photographic element as claimed in claim 2 wherein said nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
- phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid, in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.73.
- phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and 20 molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, 0.2.
- phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phaseseparation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.52.
- phase-separation inhibitor has an intrinsic viscosity measured in a methanolic solution at 30C in the range of from 0.3 to 2.0.
- a light-sensitive photographic element as claimed in claim 2 wherein 50 mole percent, 50 X mole percent and X mole percent total 100 mole percent.
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Abstract
GROUPS IN 50, 50 - X and X molar percent proportions, respectively, X being not more than 50 and R being an alkyl group having from 1 to 4 carbon atoms. The photographic element has reduced propensity to curling and to becoming sticky after stabilization processing.
A photographic element for use in silver halide photography having a silver halide emulsion layer, a protective layer, a subbing layer or a diffusion-transfer image-receiving layer, each using gelatin as the main binding component, in which into one of said layers are incorporated a nonionic water-soluble polymer and a phase separation inhibitor containing the
A photographic element for use in silver halide photography having a silver halide emulsion layer, a protective layer, a subbing layer or a diffusion-transfer image-receiving layer, each using gelatin as the main binding component, in which into one of said layers are incorporated a nonionic water-soluble polymer and a phase separation inhibitor containing the
Description
United States Patent 1 Tsuji et al.
[ 1 Apr. 15, 1975 [30] Foreign Application Priority Data Jan. 19,1971 Japan 46-13211 [52] US. Cl 96/87 R; 96/85; 96/67;
96/114; 96/ll4.4; 96/114.5; 96/114.7; 117/161 R; 117/161 UC; 117/161 C [51] Int. Cl G03c H78 [58] Field of Search 96/85, 67, 114, 114.4, 96/114.5, 114.7, 87 R; 117/16] R, 161 UC, 161 C [56] References Cited UNITED STATES PATENTS 2,964,403 12/1960 Beekman et al. 96/85 2,980,534 4/1961 Printy et al. 96/85 3,085,897 4/1963 Priest et al.... 96/114 3,161,519 12/1964 Alsup 96/85 3,165,412 1/1965 Minsk et al. 96/114 3,369,901 2/1968 Fogg et al. 96/85 3,397,988 8/1968 Van Paesschen.... 96/85 3,425,857 2/1969 Bacon et a1 96/85 Grabhofer et al. 96/1 14 Yano et al. 96/1 14 Primary Examiner-Norman G. Torchin Assistant Examiner-Edward C. Kimlin Attorney, Agent, or FirmSughrue, Rothwell, Mion, Zinn & Macpeak [57] ABSTRACT A photographic element for use in silver halide photography having a silver halide emulsion layer, a protective layer, a subbing layer or a diffusion-transfer image-receiving layer, each using gelatin as the main binding component, in which into one of said layers are incorporated a nonionic water-soluble polymer and a phase separation inhibitor containing the -CH2-CH- ,-CH-CH- 0COCH COOH COOH and - CH CH COOH COOR groups in 50, 50 X and X molar percent proportions, respectively, X being not more than 50 and R being an alkyl group having from 1 to 4 carbon atoms.
The photographic element has reduced propensity to curling and to becoming sticky after stabilization processing.
21 Claims, No Drawings PHOTOGRAPHIC ELEMENT CROSS-REFERENCE TO RELATED APPLICATIONS The present application is a divisional application of 5 our earlier co-pending application Ser. No. 219,179 filed on Jan. 19, 1972, and claims priority from Jan. 19, 1971 based on Japanese Patent Application No. 1321/71.
BACKGROUND OF THE INVENTION 1. Field of the invention 7 This invention relates to photographic elements, and more particularly to composition of layers to be provided 'on a photographic element support.
2. Description of the Prior Art Photographic elements in general comprise a support material such as paper, a synthetic resin film, a glass or metallic plate, with a subbing layer optionally being provided thereon for the purpose of enhancing the adhesivity between the support and photographic layer adjacent thereto, together with a silver halide emulsion layer, usually with a protective layer provided thereon to prevent damage to said emulsion layer, the latter two layers being applied onto the surface of the foregoing support or subbing layer. Furthermore, as one special kind of photographic material there is an imagereceiving element used in the diffusion transfer photographic process, which element comprises an imagereceiving layer having incorporated therein a catalytic substance, i.e., silver deposits or so-called development nuclei, in a dispersed form for reduction of a soluble silver complex transported by diffusion from a photographic light-sensitive element.
' As the binding agent for these photographic elements, gelatin has heretofore been used in almost all cases due to its outstanding photographic and physical properties. Since gelatin is a natural substance, however, its use has suffered from the disadvantage that the properties of gelatin largely depend upon the raw materials and manufacturing processes used to form it; and often it is therefore not possible to insure constant quality in the finished product. Besides such a disadvantage, the use of gelatin presents some other problems. For instance, it is sensitive to changes in temperature and humidity and tends to curl. Furthermore, in the stabilization process wherein a photographic element is processed in a stabilizing solution containing ammonium thiocyanate, the surface of a gelatin film which constitutes a photographic layer becomes sticky after stabilization.
Recently, in an attempt to eliminate these defects, various kinds of synthetic polymers have been pro- Unit No.
posed as substitutes for gelatin as a binding agent for photographic layers. These include, for example, polyvinyl alcohol, polyacrylamide, polyvinyl pyrrolidone, poly-1-vinyl-2-methylimidazole, sodium polyacrylate, an acrylamide-1-vinyl-2-methylimidazole copolymer and an acrylamide-l-vinyl-2-methylimidazole-acrylic acid copolymer. These synthetic polymers, however, are not superior gelatin in various other photographic and physical properties, so that in practice gelatin is used.
It has been attempted to employ gelatin with such synthetic polymers, thereby maintaining the superior properties of the gelatin and compensating for the defects of the same by means of the properties of the synthetic polymers. However, when a portion of the gelatin is replaced by a nonionic water-soluble polymer, complete mixing of both components is optional proportions cannot be effected and phase-separation takes place.
To attempt to overcome this effect, a method has been proposed wherein a third substance is added to prevent the phase separation. For example, in Japanese Patent Publication No. 4,272/64 there is described the use of a methyl vinyl ether maleic anhydride copolymer (hereinafter referred to as MVE/MA) or an amide or ester thereof as a phase-separation inhibitor upon using gelatin with polyvinyl alcohol.
SUMMARY OF THE INVENTION We have found that the compounds disclosed hereinafter are extremely effective as phase-separation inhibitors upon admixing gelatin with nonionic polymers. Furthermore, we have also confirmed the following advantages: the coating composition prepared using such compounds can be applied onto a support more uniformly than in the case of using the prior art phaseseparation inhibitor, i.e., the above-described copolymer (MVE/MA) or an amide or ester thereof; the photographic elements produced have little tendency to curl, and they show little tendency to be sticky after stabilization, if such is used.
Thus, the present invention provides a photographic element comprising a support having thereon at least one layer comprising gelatin, a nonionic water-soluble polymer and a polymer, said polymer comprising 50 mole percent of vinyl acetate, (50 x) mole of maleic acid and mole of half alkyl ester of maleic acid, wherein x is 0 2; 50 and the alkyl group has 1 to 4 carbon atoms.
The polymer of the present invention, which can be employed as an inhibitor for phase-separation between gelatin and the nonionic water-soluble polymer, may be characterized by the following chemical units and the specified proportion thereof.
Atomic groups Proportion contained (50 X) molar COOH COOH Unit No. Atomic groups Proportion contained '3 CH (IIH- Xmo1ar% COOH COOR (X being not more (R being an alkyl than 50) group having from 1 1:0 4 carbon atoms.)
The nonionic water-soluble polymers which may be S E; y" 2' 047 used in accordance with the present invention include 5 polyvinyl alcohols, polymers Of acrylamlde 01' its derlv- (R n butyl) (R means alkyl group of the half ester of atives such as acrylamide, N-methylacrylamide, N-
()See Page relmeso ethylacrylamide, N, N-dimethylacrylamide, N, N- W Unit I 50 niolar 7! diethylacrylamide, N-methoxymethylacrylamide, 8"}: g molar?! 0.52 N-ethoxymethylacrylamide, N-morpholinoacrylamide, 20 mo or N-morpholinomethylacrylamide, the corresponding polymers of methyacrylamide or its derivatives, polyvinyl methyl ethers, polyvinyl pyrrolidones, polyvinyl oxazolidones, polyvinyl caprolactams, soluble starch and cellulosic derivatives such as hydroxyethyl cellulose or methyl cellulose. Besides these homopolymers, there may also be used water-soluble copolymers consisting of the monomer units mentioned above.
Among the nonionic water-soluble polymer polyvinyl alcohol is the most typical one. Any known polymer which is used together with gelatin in the photographic art may be employed.
The phase-separation inhibitors used according to the present invention may be obtained by synthesizing a l l (polymerization ratio) copolymer of vinyl acetate and maleic anhydride by means of any conventional radical polymerization method, and heat-treating the copolymer in water or an alcohol having from l to 4 carbon atoms to effect hydrolysis or alcoholysis of the same. The decomposition reaction may also be par- 40 tially carried out to produce the half ester. By the procedure, the
- CH CH i l COOH COOH group which initially occupies molar percent of the copolymer is converted into the CH CH 50 coon COOR group by X molar percent. In the present invention, the above-described decomposition reaction can be eliminated, so that the range of X is 0 g X 50. The properties of the polymer are substantially not affected on the proportion of X.
Several examples of such phase-separation inhibitors will be given below where the values of the intrinsic viscosity are taken in a methanolic solution of each phaseseparation inhibitor at 300C.
Intrinsic viscosity l Unit I 50 molar 0.64
Unit 2 50 molar "/1 ll Unit 1 50 molar 7: 0.73
Unit 3 50 molar '71 (R ethyl) According to the present invention, gelatin and the nonionic water-soluble polymer can be used in admixture with the phase-separation inhibiting polymer in photographic layers. These photographic layers include not only a light-insensitive layer such as a protective or uppermost layer, a subbing or under-coated layer, an image receiving layer for diffusion-transfer process, which layer may also contain nuclei for precipitating silver, such as colloidal silver or heavy metal sulfides, but also a light-sensitive layer such as a light-sensitive silver halide emulsion layer. The phase-separation inhibiting polymer of the present invention may be added to a mixture to be coated at any stage before coating. The polymer may also be added to a silver halide emulsion during preparation thereof.
The proportions of gelatin, nonionic water-soluble polymer and phase-separation inhibiting polymer may be varied depending upon the specific requirement of the photographic layers being produced and the specific compound to be used. ln general, the preferred proportions are set out below.
gelatin about 5 about by weight nonionic water-soluble about about 1571 by weight polymer phase-separation about 5 about [5'71 by weight inhibitor The phase-separation inhibitors used according to the present invention may be of any molecular weight, although it is most preferred to use those having an intrinsic viscosity [1 as measured in a methanolic solution at 30C., of about 0.05 to about 5.0, preferably about 0.3 to about 2.0.
Suitable support material include any of those used in photography such as cellulose acetate, synthetic resins such as polyesters, polystyrenes or polycarbonates, paper, or resin coated paper such as polyethylene coated paper.
The copolymers used according to the present invention remarkedly improve the compatibility between gelatin and nonionic water-soluble polymers, and are extremely effective for the prevention of phaseseparation which often takes place.
The present invention can be applied to varied silver halide emulsions using silver chloride, silver bromide, silver chlorobromide, silver iodobromide and/or silver chloroiodobromide, and mixtures thereof.
The emulsions to which the present invention may be applied may be chemically sensitized by any conventional method, for example using labile-sulfur containing compounds such as ammonium thiosulfate or ethylthiourea (see, for example, P. Glafkindes, Chimie Photographique; 2 eme Edition Photocinema, Paul Montel, Paris, 1957, pages 297299); gold compounds such as complexes of monovalent gold and thiocyanic acid (see lbid., page 301) or any combination of these compounds. The emulsions may be optically sensitized by incorporating thereinto spectral sensitizers such as cyanine or merocyanine dyes (see, for example, Shinichi Kikuchi, et a], Kagaku-Shashin Binran, Maruzen Co., Ltd.. 1959, pages -24). Furthermore, they may be stabilized by any stabilizers well known in the art, for example, heterocyclic compounds such as benzotriazole, l-phenyl-5-mercaptotetrazole, 4-hydroxy-6- methyl-1,3,3a, 7-tetrazaindene or 6-thioctic acid, mercury compounds such as mercumallylic acid (see Japanese Patent Publication No. 22, 063/64), or benzenesulfonic acid. In addition, the emulsions may be hardened using hardening agents such as formaldehyde, mucochloric acid, chromium alum or triazine derivatives (see, for example, Belgian Pat. No. 641,044), or a combination of these hardeners with hardening adjuvants such as resorcin or resorcin aldehyde. Into the emulsions there may be incorporated surface active agents such as saponin, sodium alkylbenzene sulfonate or an addition polymer of an alkylphenol and sultone (see British Pat. No. 1,024,808) in order to facilitate the application of said emulsions. Furthermore, the emulsions may be sensitized using polyalkylene oxide derivatives such as condensation products of an alkylphenol and polyethylene oxide.
The emulsions prepared in accordance with the present invention can be used, after the addition of couplers, in the manufacture of natural color photographic films or papers. Furthermore, by increasing the ratio of the water-soluble polymer to gelatin, the developed film can be removed by means of rinsing, so that it may be used as a negative layer for use in the so-called multi-layer diffusion transfer process (C.E. Neblette, Photography, its Materials and Processes, 6th Edition, D. Van Nostrand Co., Princeton, New Jersey, 1962, pages 371-373) The present invention will now be further illustrated by the following non-limitative examples.
EXAMPLE 1 A silver halide photographic emulsion thickness (4 microns) was prepared which contained g. silver chloride and 10 g. gelatin, and was divided into three equal portions A, B and C. lnto each portion there was Composition of the developer:
Metol 1 Anhydrous sodium sulfite 15 Hydroquinone 4 Sodium carbonate monohydrate 27 Potassium bromide 1 Water to make 1,000 c.c. Composition of the fixing solution:
C rystalline sodium thiosulfate 240 g.
Anhydrous sodium sulfite 15 g Glacial acetic acid 13.3 g Borax 7.5 g. Potash alum powder 15 g.
Water to make 1.000 c.c.
After drying each specimen under the conditions mentioned above, the curling value was determined by measuring across the center of the circular form the distance (.r em) between the tips which were closest upon the curling, and the value (10 x) cm was taken as the curling value. The results of the measurement are shown in Table 1.
Table 1 Specimens Condition 1 Condition 2 A 5.2 cm. 9.8 cm. B (Separation took place in the emulsion phase and uniform application was impossible.) C 0.4 cm. 1.2 cm.
As is evident from Table 1, the photographic paper using the compounds according to the invention (Specimen A) showed extremely low curling values as compared with the photographic paper using gelatin alone (Specimen A). No changes were found in the photographic properties between Specimens A and C.
EXAMPLE 2 A silver halide-gelatin emulsion (thickness: 4 microns) was preparedwhich contained 20 g. silver chloride and 10 g. gelatin, and, after addition of 10 g. hydroquinone as a developing agent, was divided into two equal portions A and B, into which were added the following solutions, respectively:
Emulsion A 200 c.c. ofa 10 weight percent aqueous solution of gelatin.
Emulsion B 180 c.c. of a 10 weight percent aqueous solution of polyvinyl alcohol plus 20 c.c. of a 10 weight percent aqueous solution of a phaseseparation inhibitor (1).
Emulsions A and B were each thoroughly agitated and applied onto a photographic base paper of g./m.'- to give photographic papers A and B, respectively, for use in a stabilization process. These photographic papers were each developed in an activator having the composition shown below, after which they were processed in a stabilizing solution containing Composition of the activator:
Anhydrous sodium sulfite Sodium hydroxide Potassium bromide Water to make 1,000 c.c.
EXAMPLE 3 A silver chlorobromide emulsion was prepared which contained 30 molar percent of silver bromide and 60 g. of gelatin and, after addition of 10 g. of hydroquinone as a developing agent, applied onto a photographic baryta-coated paper of 135 g./m On top of the coating layer there was further applied a thin protective layer of the following composition, thereby giving a photographic paper for use in the stabilization process.
Formulation of the protective layer composition:
Gelatin 5 g. P.V.A. l5 g.
Phase-separation inhibitor (ll) 1.5 g.
Water to make L000 c.c.
EXAMPLE 4 Colloidal nickel sulfide nuclei were incorporated into an aqueous solution having the composition as shown below and applied onto a photographic base paper of 85 g./m On top of the coating layer there was further applied a stripping layer mainly containing sodium alginate to give an image-receiving paper for use in the silver salt diffusion transfer process. The image-receiving paper was dipped for several seconds in a developer (composition is shown below) for use in the silver salt diffusion transfer process while held in tight surface contact with a negative paper having a silver halide emulsion layer for use in the diffusion transfer process, which negative paper had been exposed to light. The image-receiving paper, after being separated from the negative paper after seconds showed an extremely low curling tendency and was satisfactory.
Amount of nickel sulfide in the layer was 0.6 mg/m Amount of sodium alginate in the layer was 0.2 g/m".
20g. 30 g. 4 g.
Composition of the developer for use in the silver salt diffusion transfer process:
Anhydrous sodium thiosulfate Potassium sulfite potassium bromide Hydroquinonc Phenidone Sodium hydroxide Water to make 1.000 c.c.
EXAMPLE 5 A silver halide-gelatin emulsion was prepared which contained 20 g. AgCl and 10 g. gelatin; and was divided into four equal portions, into which the following compounds were added, respectively:
Sample Substances added 200 c.c. of a 1071 aqueous solution of gelatin A mixture of I c.c. of a l0 /r aqueous solution of hydroxycthyl cellulose and 20 c.c. of a 10% aqueous solution of phaseseparation inhibitor (ll) (Substances according to the invention). A mixture of 180 c.c. of a l0/1 aqueous solution of acrylamide and 20 c.c. of a l0/( aqueous solution of phase-separation inhibitor (lll). (Substances according to the invention) A mixture of Hi0 cc. of a 10% aqueous solution of P.\'.A. and 20 c.c. of a l0'7r aqueous solution of phase-separation inhibitor (lV) (Substances according to the invention).
Emulsions A to D were each thoroughly agitated and.
then applied onto a photographic baryta-coated paper of 95 g./m to give corresponding photographic papers. These photographic papers were subjected to the same processing as in Example 1 and examined for their curling properties to find that the samples B to D using the substances of the invention showed little curling tendency and were satisfactory as compared with sample A using gelatin alone.
The invention has been described in detail with particular reference to preferred embodiments thereof but it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
What we claim is:
1. A light-sensitive photographic element comprising a support having thereon at least one silver halide emulsion layer which consists essentially of silver halide, gelatin, a nonionic water-soluble polymer which is photographically compatible with said gelatin and a polymer which is a phase-separation inhibitor for said gelatin and said nonionic water-soluble polymer, said polymer comprising 50 mole percent of vinyl acetate (50 X) mole percent of maleic acid and X mole percent of a half alkyl ester of maleic acid, wherein X is 0 X 50 and the alkyl group in said half alkyl ester has 1 to 4 carbon atoms, wherein the proportion of said gelatin, said nonionic water-soluble polymer and said polymer is about 5 to about 70 percent by weight, about to about 15 percent by weight and about 5 to about 15 percent by weight, respectively.
2. A light-sensitive photographic element comprising a support having thereon at least two layers, at least one of said layers being a silver halide emulsion layer and at least one of said layers containing gelatin, a nonionic water-soluble polymer which is photographically compatible with said gelatin and a polymer which is a phase-separation inhibitor for said gelatin and said nonionic water-soluble polymer, said polymer comprising 50 mole percent of vinyl acetate, (50 X) mole percent of maleic acid and X mole percent of a half alkyl ester of maleic acid, wherein X is 2 X 50 and said alkyl group in said half alkyl ester has 1 to 4 carbon atoms, wherein the proportion of said gelatin, said nonionic water-soluble polymer and said polymer is about 5 to about 70 percent by weight, about 90 to about percent by weight and about 5 to about 15 percent by weight, respectively, said at least one of said layers which contains gelatin, a nonionic water-soluble polymer and a polymer consisting essentially of said components, with the proviso that when said components are in a silver halide emulsion layer silver halide is further present.
3. A light-sensitive photographic element as claimed in claim 1 wherein 50 mole percent, (50 X) mole percent and X mole percent total 100 mole percent.
4. A light-sensitive photographic element as claimed in claim 1 wherein said nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
5. A light-sensitive photographic element as claimed in claim 1 wherein X is 50 and said phase-separation inhibitor has an intrinsic viscosity. measured in a methanolic solution at 30C, of 0.64.
6. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.73.
7. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.2.
8. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phaseseparation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.52.
9. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor has an intrinsic viscosity measured in a methanolic solution at 30C in the range of from 0.3 to 2.0.
10. A light-sensitive photographic element as claimed in claim 1 wherein said polymer contains said 7 half alkyl ester of maleic acid.
11. A light-sensitive photographic element as claimed in claim 2 wherein said nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
12. A light-sensitive photgraphic element as claimed in claim 2 wherein X is 50 and said phase-separation inhibitor has an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.64.
13. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid, in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.73.
14. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and 20 molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, 0.2.
15. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phaseseparation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30C, of 0.52.
16. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor has an intrinsic viscosity measured in a methanolic solution at 30C in the range of from 0.3 to 2.0.
17. A light sensitive photographic element as claimed in claim 2 wherein said polymer contains said half alkyl ester of maleic acid.
18. A light-sensitive photographic element as claimed in claim 2 wherein 50 mole percent, 50 X mole percent and X mole percent total 100 mole percent.
19. A light-sensitive photographic element as claimed in claim 2 wherein said at least one layer is a protective layer.
20. A light-sensitive photographic element as claimed in claim 2 wherein said at least one layer is a subbing layer.
21. A light-sensitive photographic element as claimed in claim 2 wherein at least one layer is an image-receiving layer for a diffusion transfer process.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION PATENT N0. 3, 877, 947
DATED 1 April 15, 1975 INVENTOR(S) I Nobuo TSUJI et: a1
It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
IN THE HEA DING:
Foreign Application Priority Data De1ete-- 46-1321l-- insert 1321/71 Signed and sealed this 10th day of June 1975.
(SEAL) Attest:
C. MARSHALL DANNV Commissioner of Patents and Trademarks RUTH C. MASON Attesting Officer
Claims (21)
1. A LIGHT-SENSITIVE PHOTOGRAPHIC ELEMENT COMPRISING A SUPPORT HAVING THEREON AT LEAST ONE SILVER HALIDE EMULSION LAYER WHICH CONSISTS ESSENTIALLY OF SILVER HALIDE, GELATIN, A NONIONIC WATER-SOLUBLE POLYMER WHICH IS PHOTOGRAPHICALLY COMPATIBLE WITH SAID GELATIN AND A POLYMER WHICH IS A PHASESEPARATION INHIBITOR FOR SAID GELATIN AND SAID NONIONIC WATERSOLUBLE POLYMER, SAID POLYMER COMPRISING 50 MOLE PERCENT OF VINYL ACETATE (50 - X) MOLE PERCENT OF MALEIC ACID AND X MOLE PERCENT OF A HALF ALKYL ESTER OF MALEIC ACID, WHEREIN X IS 0 X 50 AND THE ALKYL GROUP IN SAID HALF ALKYL ESTER HAS 1 TO 4 CARBON ATOMS, WHEREIN THE PROPORTION OF SAID GELATIN, SAID NONIONIC WATER-SOLUBLE POLYMER AND SAID POLYMER IS ABOUT 5 TO ABOUT 70 PERCENT BY WEIGHT, ABOUT 90 TO ABOUT 15 PERCENT BY WEIGHT AND ABOUT 5 TO ABOUT 15 PERCENT BY WEIGHT, RESPECTIVELY.
2. A light-sensitive photographic element comprising a support having thereon at least two layers, at least one of said layers being a silver halide emulsion layer and at least one of said layers containing gelatin, a nonionic water-soluble polymer which is photographically compatible with said gelatin and a polymer which is a phase-separation inhibitor for said gelatin and said nonionic water-soluble polymer, said polymer comprising 50 mole percent of vinyl acetate, (50 - X) mole percent of maleic acid and X mole percent of a half alkyl ester of maleic acid, wherein X is 0 < or = X < or = 50 and said alkyl group in said half alkyl ester has 1 to 4 carbon atoms, wherein the proportion of said gelatin, said nonionic water-soluble polymer and said polymer is about 5 to about 70 percent by weight, about 90 to about 15 percent by weight and about 5 to about 15 percent by weight, respectively, said at least one of said layers which contains gelatin, a nonionic water-soluble polymer and a polymer consisting essentially of said components, with the proviso that when said components are in a silver halide emulsion layer silver halide is further present.
3. A light-sensitive photographic element as claimed in claim 1 wherein 50 mole percent, (50 - X) mole percent and X mole percent total 100 mole percent.
4. A light-sensitive photographic element as claimed in claim 1 wherein said nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
5. A light-sensitive photographic element as claimed in claim 1 wherein X is 50 and said phase-separation inhibitor has an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.64.
6. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.73.
7. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and 20 molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.2.
8. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.52.
9. A light-sensitive photographic element as claimed in claim 1 wherein said phase-separation inhibitor has an intrinsic viscoSity measured in a methanolic solution at 30*C in the range of from 0.3 to 2.0.
10. A light-sensitive photographic element as claimed in claim 1 wherein said polymer contains said half alkyl ester of maleic acid.
11. A light-sensitive photographic element as claimed in claim 2 wherein said nonionic water-soluble polymer is selected from the group consisting of polyvinyl alcohol; polymers of an acrylamide or methacrylamide, polyvinyl methyl ether, polyvinyl pyrrolidone, polyvinyl oxazolidone, polyvinyl caprolactams, soluble starch and cellulose derivatives.
12. A light-sensitive photgraphic element as claimed in claim 2 wherein X is 50 and said phase-separation inhibitor has an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.64.
13. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate and said half alkyl ester of maleic acid, in which the alkyl group of said half alkyl ester is an ethyl group, in 50 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.73.
14. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being an n-butyl group, in 50, 30 and 20 molar percent proportions, respectively, said inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, 0.2.
15. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor contains said vinyl acetate, said maleic acid and said half alkyl ester of maleic acid, the alkyl group of said half alkyl ester being a methyl group, in 50, 20 and 30 molar percent proportions, respectively, said phase-separation inhibitor having an intrinsic viscosity, measured in a methanolic solution at 30*C, of 0.52.
16. A light-sensitive photographic element as claimed in claim 2 wherein said phase-separation inhibitor has an intrinsic viscosity measured in a methanolic solution at 30*C in the range of from 0.3 to 2.0.
17. A light sensitive photographic element as claimed in claim 2 wherein said polymer contains said half alkyl ester of maleic acid.
18. A light-sensitive photographic element as claimed in claim 2 wherein 50 mole percent, 50 - X mole percent and X mole percent total 100 mole percent.
19. A light-sensitive photographic element as claimed in claim 2 wherein said at least one layer is a protective layer.
20. A light-sensitive photographic element as claimed in claim 2 wherein said at least one layer is a subbing layer.
21. A light-sensitive photographic element as claimed in claim 2 wherein at least one layer is an image-receiving layer for a diffusion transfer process.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US347523A US3877947A (en) | 1971-01-19 | 1973-04-03 | Photographic element |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP46001321A JPS5027375B1 (en) | 1971-01-19 | 1971-01-19 | |
| US219179A US3877946A (en) | 1971-01-19 | 1972-01-19 | Photographic element |
| US347523A US3877947A (en) | 1971-01-19 | 1973-04-03 | Photographic element |
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| Publication Number | Publication Date |
|---|---|
| US3877947A true US3877947A (en) | 1975-04-15 |
Family
ID=34437580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US347523A Expired - Lifetime US3877947A (en) | 1971-01-19 | 1973-04-03 | Photographic element |
Country Status (1)
| Country | Link |
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| US (1) | US3877947A (en) |
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|---|---|---|---|---|
| US4008087A (en) * | 1974-08-05 | 1977-02-15 | Fuji Photo Film Co., Ltd. | Photographic light-sensitive material |
| US4033772A (en) * | 1975-12-09 | 1977-07-05 | Gaf Corporation | Amphoteric maleic anhydride copolymers and photographic emulsions employing the same |
| US4056396A (en) * | 1973-02-12 | 1977-11-01 | Fuji Photo Film Co., Ltd. | Layers used to prevent reticulation in photographic elements |
| US4296195A (en) * | 1980-08-01 | 1981-10-20 | Eastman Kodak Company | Two-sheet diffusion transfer assemblages and photographic elements |
| US4450230A (en) * | 1981-10-23 | 1984-05-22 | Minnesota Mining And Manufacturing Company | Photographic elements with improved surface characteristics |
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| US2980534A (en) * | 1956-12-17 | 1961-04-18 | Monsanto Chemicals | Photographic compositions and photographic elements |
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| US3397988A (en) * | 1963-01-25 | 1968-08-20 | Gevaert Photo Prod Nv | Photographic material |
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| US3635715A (en) * | 1968-11-07 | 1972-01-18 | Agfa Gevaert Ag | Gelatine-containing photographic layers which have improved physical properties |
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| US2964403A (en) * | 1955-09-01 | 1960-12-13 | Reheis Company Inc | Surface-sizing of fibrous void-containing sheets with hydrous zirconium compounds |
| US2980534A (en) * | 1956-12-17 | 1961-04-18 | Monsanto Chemicals | Photographic compositions and photographic elements |
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| US4056396A (en) * | 1973-02-12 | 1977-11-01 | Fuji Photo Film Co., Ltd. | Layers used to prevent reticulation in photographic elements |
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| US4033772A (en) * | 1975-12-09 | 1977-07-05 | Gaf Corporation | Amphoteric maleic anhydride copolymers and photographic emulsions employing the same |
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| US4450230A (en) * | 1981-10-23 | 1984-05-22 | Minnesota Mining And Manufacturing Company | Photographic elements with improved surface characteristics |
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