US3294540A - Lith-type emulsions with block co-polymers - Google Patents
Lith-type emulsions with block co-polymers Download PDFInfo
- Publication number
- US3294540A US3294540A US331141A US33114163A US3294540A US 3294540 A US3294540 A US 3294540A US 331141 A US331141 A US 331141A US 33114163 A US33114163 A US 33114163A US 3294540 A US3294540 A US 3294540A
- Authority
- US
- United States
- Prior art keywords
- polymer
- block
- polymers
- lith
- block polymer
- 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
- 239000000839 emulsion Substances 0.000 title claims description 40
- 229920001400 block copolymer Polymers 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 93
- -1 SILVER HALIDE Chemical class 0.000 claims description 89
- 229910052709 silver Inorganic materials 0.000 claims description 35
- 239000004332 silver Substances 0.000 claims description 35
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 17
- 239000000084 colloidal system Substances 0.000 claims description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 12
- 229920001451 polypropylene glycol Polymers 0.000 claims description 6
- 238000011161 development Methods 0.000 description 33
- 230000018109 developmental process Effects 0.000 description 33
- 230000008901 benefit Effects 0.000 description 16
- 239000000243 solution Substances 0.000 description 13
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 12
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 10
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 9
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 9
- 108010010803 Gelatin Proteins 0.000 description 8
- 229920000159 gelatin Polymers 0.000 description 8
- 239000008273 gelatin Substances 0.000 description 8
- 235000019322 gelatine Nutrition 0.000 description 8
- 235000011852 gelatine desserts Nutrition 0.000 description 8
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- 230000033458 reproduction Effects 0.000 description 6
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- JLKXXDAJGKKSNK-UHFFFAOYSA-N perchloric acid;pyridine Chemical compound OCl(=O)(=O)=O.C1=CC=NC=C1 JLKXXDAJGKKSNK-UHFFFAOYSA-N 0.000 description 4
- 150000004714 phosphonium salts Chemical class 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 3
- 125000005129 aryl carbonyl group Chemical group 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 229920001283 Polyalkylene terephthalate Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 125000006353 oxyethylene group Chemical group 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 235000013772 propylene glycol Nutrition 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- QPJVYLQOALFBLJ-DEOSSOPVSA-N (2s)-3-[4-[3-(5-methyl-2-phenyl-1,3-oxazol-4-yl)propyl]phenyl]-2-pyrrol-1-ylpropanoic acid Chemical compound N1([C@H](C(O)=O)CC2=CC=C(C=C2)CCCC=2N=C(OC=2C)C=2C=CC=CC=2)C=CC=C1 QPJVYLQOALFBLJ-DEOSSOPVSA-N 0.000 description 1
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
- YGKHJWTVMIMEPQ-UHFFFAOYSA-N 1,2-propanedithiol Chemical compound CC(S)CS YGKHJWTVMIMEPQ-UHFFFAOYSA-N 0.000 description 1
- ATFBTSVSJAEVMV-UHFFFAOYSA-N 1,3-dihydroisoindol-2-yl-(6-hydroxy-3,3-dimethyl-1,2-dihydroindol-5-yl)methanone Chemical compound C1C2=CC=CC=C2CN1C(=O)C1=C(O)C=C2NCC(C)(C)C2=C1 ATFBTSVSJAEVMV-UHFFFAOYSA-N 0.000 description 1
- HLHOHTNONYACFD-UHFFFAOYSA-N 1-[4-[4-morpholin-4-yl-1-[1-(pyridine-3-carbonyl)piperidin-4-yl]pyrazolo[3,4-d]pyrimidin-6-yl]phenyl]-3-pyridin-4-ylurea Chemical compound C=1C=C(C=2N=C3N(C4CCN(CC4)C(=O)C=4C=NC=CC=4)N=CC3=C(N3CCOCC3)N=2)C=CC=1NC(=O)NC1=CC=NC=C1 HLHOHTNONYACFD-UHFFFAOYSA-N 0.000 description 1
- ZRFHYAAIQWWRCP-UHFFFAOYSA-M 1-nonylpyridin-1-ium perchlorate Chemical compound Cl(=O)(=O)(=O)[O-].C(CCCCCCCC)[N+]1=CC=CC=C1 ZRFHYAAIQWWRCP-UHFFFAOYSA-M 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- KNUBCZHIBGZRJT-UHFFFAOYSA-N 6-methyl-5-[3-(2,4,5-trichlorophenoxy)propoxy]pyrimidine-2,4-diamine Chemical compound CC1=NC(N)=NC(N)=C1OCCCOC1=CC(Cl)=C(Cl)C=C1Cl KNUBCZHIBGZRJT-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- JJEVXNCIHOTENL-UHFFFAOYSA-N C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)[SH+]C Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C(CCCCCCCCCCC)[SH+]C JJEVXNCIHOTENL-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- NUDUVDNPDDMHCO-UHFFFAOYSA-M Cl(=O)(=O)(=O)[O-].C(CCCCC)OC[N+]1=CC=CC=C1 Chemical compound Cl(=O)(=O)(=O)[O-].C(CCCCC)OC[N+]1=CC=CC=C1 NUDUVDNPDDMHCO-UHFFFAOYSA-M 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 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
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 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
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- BPOZNMOEPOHHSC-UHFFFAOYSA-N butyl prop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCCCOC(=O)C=C BPOZNMOEPOHHSC-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920003090 carboxymethyl hydroxyethyl cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- LKBMPSMLBVPIKO-UHFFFAOYSA-M decyl(dimethyl)sulfanium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.CCCCCCCCCC[S+](C)C LKBMPSMLBVPIKO-UHFFFAOYSA-M 0.000 description 1
- FQRPXALREFKNJX-UHFFFAOYSA-M dimethyl(nonyl)sulfanium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.CCCCCCCCC[S+](C)C FQRPXALREFKNJX-UHFFFAOYSA-M 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- CBURDXCEXJBUAJ-UHFFFAOYSA-M dodecyl(triethyl)phosphanium;bromide Chemical compound [Br-].CCCCCCCCCCCC[P+](CC)(CC)CC CBURDXCEXJBUAJ-UHFFFAOYSA-M 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- ISXSFOPKZQZDAO-UHFFFAOYSA-N formaldehyde;sodium Chemical compound [Na].O=C ISXSFOPKZQZDAO-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 244000145841 kine Species 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- QBIAZVPERXOGAL-UHFFFAOYSA-N prop-1-ene-1,3-diamine Chemical group NCC=CN QBIAZVPERXOGAL-UHFFFAOYSA-N 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
Images
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
- G03C1/043—Polyalkylene oxides; Polyalkylene sulfides; Polyalkylene selenides; Polyalkylene tellurides
-
- 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
- Y10S430/15—Lithographic emulsion
Definitions
- This invention relates to photography and particularly to improved photographic silver halide emulsions of the lith-type.
- Photographic films used in the graphic arts for making half-tone or line images should be capable of producing extremely high contrast and good image sharpness. These factors contribute in the case of half-tone images to high dot quality, that is, to the production of half-tone dots of high density and sharpness.
- the photographic elements of the lith-type that is, elements that have a fine grain high contrast silver halide emulsion containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about mole percent iodide, require the use of pure hydroquinone developer solutions having very low free sulfite ion concentration in the alkaline solution in order to produce the high contrast and high dot quality required for good quality half-tone reproduction.
- Such developer solutions are unstable, having very short tray or tank life after exposure to air, so that the solutions must be mixed fresh just before they are to be used for processing and then discarded.
- the films and processes available do not produce the desired latitude and have the desired ease in exposing and processing the film to produce the required quality. This has resulted from the contrast of the image reproduction in the photographic elements being overly sensitive to development time, and from a nonlinearity in the relationship between the film speed and development time, causing unequal increases in film speed from equal increases in development time.
- a photographic light sensitive element comprising a support, at least one hydrophilic colloid layer containing a very fine grain photographic silver halide emulsion having at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide, and at least one hydrophilic colloid layer containing certain water-soluble block polymers of polyoxypropylene and polyoxyethylene such that the block polymer is contiguous with the silver halide.
- the water-soluble block polymers used in photographic elements according to my invention include those block polymers in which the polyoxypropylene chain (or moiety) has an average molecular weight between 800 and 3,000 and in which the polyoxyethylene units consti- "ice tute from about 10 to about percent by weight of the polymer.
- the image reproductions produced in my lith-type emulsion layers are of excellent quality.
- the conventional alkaline, pure hydroquinone, low free-sulfite developer may be used to develop my exposed elements, it is also advantageous to use a developer having from 10 to about 30 grams of an alkali sulfite per liter of the developer solution.
- Y represents an organic radical having a valence of x, said radical being the residue of an organic compound containing atoms selected from the class consisting of carbon, hydrogen, oxygen, nitrogen and sulfur with x active hydrogen atoms, such as, the residue of polyhydroxy compounds, e.g., ethylene glycol, 1,2-propanediol, 1,5-pentanediol, 1,2,3-propanetriol, sucrose, etc., the residue of a polybasic acid, e.g., oxalic acid, malonic acid, succinic acid, maleic acid, citric acid, etc., the residue of a polyamine, e.g., ethylenediamine, 1,3- diaminopropylene, etc., the residue of a polyamide, e.g., malonamide, succinamide, etc., the residue of a polythiol, e.g., 1,2 ethylenedithiol, 1,3 -.propylenedithiol
- b represents an integer of from 14 to 52; a and c are each integers such that the sum of a-i-c has a total of from 4 to 48 and the polyoxyethylene groups constitute between 10 and 70 percent by weight of the block polymer.
- the block polymers of Formula II and of Formula I where R represents the hydrogen atom are described in Lundsted U.S. Patent 2,674,619, issued April 6, 1954, and Lundsted U.S. Patent 3,022,335, issued February 20, 1962.
- the block polymers of Formula I in which R is hydrogen are readily converted to compounds where R represents an organic residue by reaction with the appropriate reagent in a suitable inert organic solvent that is preferably anhydrous.
- alkyl halides such as alkyl chlorides, alkyl bromides, etc., are used to advantage to replace the terminal hydrogen atom of the block polymer with an alkyl group.
- Alkylp-toluenesulfonates are also used to advantage to place an alkyl group on the end of the block polymers.
- the appropriate acid chloride or acid anhydride such as, acetyl chloride, propionyl chloride, stearoyl chloride, benzoyl chloride, acetic anhydride, etc., are used to advantage to prepare block polymers of Formula I in which R is an alkyl carbonyl or an aryl carbonyl group. These reactions are well known to those skilled in the'art. Many of the block polymers of Formulas I and II are available commercially.
- My photographic elements coated with a lith-type emulsion containing my block polymers of polyoxypropylene and polyoxyethylene are valuable for use in graphic art reproduction.
- My elements are particularly valuable when developed with a dihydroxybenzene developer with a high free sulfite ion concentration in an alkaline solution.
- My elements provide the following advantages:
- the quality of the silver images produced in lithtype emulsion layers is conveniently measured in terms of contrast (i.e., 'y) and dot quality.
- Photographic image contrast is the slope of the straight line portion of a graph of optical density of the image vs. log of exposure.
- Dot quality is a measure of the quality of the reproduction of a half-tone image. Lith-type photographic elements exposed to a half-tone image, and developed, produce areas commonly referred to as shadow dots and areas known as highlight areas. Intermediate between these two extremes are areas of varying size.
- the dot quality used herein is a measure of the areas referred to as 50% dots (i.e., /2 clear and /2 developed density) and is expressed -in a progressive scale Where 9 is excellent and "1 is extremely poor. A 50% dot quality below "6 is generally not acceptable.
- block polymers used to advantage according to my invention are the following typical polymers used for illustrative purposes.
- Block polymer 1 Average Percent poly- Block Polymer Y Group derived Value of 'n in oxyethylene No. Irom- Formula I by weight of Block polymer 1 1,2-propanediol 30 2 d0 30 20 3 .do 22 40 4 .do 30 50 5. d0 30 40 6- d0 47 20 7 do 39 10 8. 1,5-pentauediol 24 50 9 1,2,3,-propanetriol 36 48 10 Ethyleuediamine- 32 50 These block polymers are available commercially under the tradename Pluronic. Block polymers 1 through 7 are sold under the trade name Pluronic L61, L62, L44, P65, L64, L92 and L81, respectively.
- the block polymers used according to my invention are water soluble and are advantageously added in a water solution to the aqueous hydrophilic colloid (either with or without the silver halide) before it is coated.
- the block polymers are used to advantage over a wide range of concentrations.
- the operable range of concentrations is from .001 to 1.00 gram of block polymer per mole of silver, while the preferred range is from 0.010 to 0.200 gram per mole of silver.
- the optimum concentration of a given block polymer used in my elements depends upon the results desired, the particular silver halide emulsion, the developer solution, etc., and is readily determined by methods well known in the art.
- the determination of the optimum concentration is preferably made by employing the block polymer in the silver halide emulsion layer or in an adjacent hydrophilic colloid layer according to the element that is desired.
- the fine grain silver halide emulsions used to advantage have silver halide crystals preferably containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide.
- the emulsions can be prepared as described by MacWilliam U.S. 2,756,148, issued July 24, 1956. These emulsions may be used without being sensitized, however, it is advanageous to spectrally sensitize them according to methods well known in the art to make them orthosensitized or panchromatically-sensitized.
- the silver halide is dispersed in hydrophilic colloid materials used as binders, including gelatin, collodion, gum arabic, cellulose ester derivatives, such as, alkyl esters of carboxylated cellulose, hydroxy ethyl cellulose, carboxy methyl hydroxy ethyl cellulose, synthetic resins, such as the amphoteric copolymers described by Clavier et al. in U.S. Patent 2,949,442, issued August 16, 1960, polyvinyl alcohol, and others well known in the art.
- hydrophilic colloid materials used as binders including gelatin, collodion, gum arabic, cellulose ester derivatives, such as, alkyl esters of carboxylated cellulose, hydroxy ethyl cellulose, carboxy methyl hydroxy ethyl cellulose, synthetic resins, such as the amphoteric copolymers described by Clavier et al. in U.S. Patent 2,949,442, issued August 16, 1960, poly
- polymeric gelatin substitutes examples include copolymers of allylamine and methacrylic acid; copolymers of allylamine, acrylic acid and acrylamide; hydrolyzed copolymers of allylamine, methacrylic acid and vinyl acetate; the copolymers of allylamine, acrylic acid and styrene; the copolymers of allylamine, methacrylic acid and acrylonitrile; alkyl acrylateacrylic acid copolymers, e.g., copolymers of butyl acrylateacrylic acid, etc.
- any of the hydrophilic colloids described hereinbefore may be used to advantage as a binder for coating my polymers.
- onium salts such as, quaternary ammonium salts, sulfonium salts and phosphonium salts
- onium salts such as, quaternary ammonium salts, sulfonium salts and phosphonium salts
- quaternary ammonium salts include nonyl pyridinium perchlorate, hexoxymethyl pyridinium perchlorate, ethylene bis-dioxymethyl pyridinium perchlorate and others described by Carroll U.S.
- 2,288,226, issued June 30, 1942 such as bis(lauryl methyl sulfonium p-toluene sulfonate) 1,2-ethane, N,N-trimethylene dioxymethyl pyridinium perchlorate etc., the sulfonium salts of Carroll et al. U.S. 2,275,727, issued March 10, 1942, such as, n-decyl dimethyl sulfonium p-toluene sulfonate, n-nonyl dimethyl sulfonium p-toluene sulfonate, etc., and the phosphonium salts of Carroll et al. U.S. 2,271,622, issued February 3, 1942, such as, tetramethylene bis-triethyl phosphonium bromide, lauryltriethylphosphonium bromide, etc.
- My light-sensitive emulsions can be coated to advantage on any of the conventional photographic supports, including glass, cellulose acetate, polystyrene, polyalkyleneterephthalate, etc.
- the block polymers can be coated advantageously in the silver halide emulsion layer, or in a hydrophilic colloid layer that is either under or over the silver halide emulsion layer so that the block polymer the development time, the slope of the resultant curve will approach as K approaches a constant value.
- Evenness of development is the slope of the plot of K against time. In the above table, evenness of development is exis contiguous to the silver halide. pressed in this way. The smaller the number, the more My invention is still further illustrated by the following even the development. This value indicates the even examples. spacing between the sensitometric curves for eqaul differ- Example 1 ences in development time.
- FIG. 3 snows curves 1 through 4 for a lith element outside my invention containing block polymer A de- Hydroquinone 15 scnbed previously Sodium formaldehyde bi lfit 501)
- IG. 4 shows curves 1 through 4 for my lith element s i carbonate 3 containing my block polymer No. 3.
- FIG. 5 shows curves 1 hrough 4 for my lith elesodiu lfit 2,5 ment containing my block polymer No. 5. Potassium bromide 0.75
- FIG. 6 shows curves 1 through 4 for my lith ele- Water to make 1.0 liter. ment containing my block polymer No. 7.
- the polymer PEO is the oleyl ether of polyethylene oxide shown by FIG. 4 when a lith emulsion contains one having an average molecular weight of 1500.
- Example 3 A.very fine grain high contrast gelatino silver chlorobromide emulsion in which 70 percent of the halide was the chloride was prepared and divided into three equal portions. One portion wa used as a control. Oleyl ether of polyoxyethylene (molecular weight 1540) was .added to the second portion and stock polymer No. 2
- My lith elements coated with fine grain high contrast silver halide emulsions containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide contain certain water-soluble block polymers of polyoxypropylenc and polyoxyethylene.
- the block polymer is incorporated in the light-sensitive layer or in a layer adjacent to the lightsensitive layer so that the polymer and silver halide are contiguous.
- the block polymers used to advantage according to my invention include those in which the polyoxypropylene chain has an average molecular weight between 800 and 3000, and in which the polyoxyethylene units constitute from about 10 to about 70 percent ,by weight of the block polymer.
- My elements give high contrast images with high dot quality and good evenness of development with lith developer solutions. My elements are particularly valuable because they produce these high quality image reproductions even when stable high free-sulfite developer solutions are used. Since lith" elements containing simple polyoxyethylene and certain block polymers of polyoxy-propylene and polyoxyethylene that are outside my invention produce low contrast and poor dot quality, it is unexepected that my elements containing my block polymers produce the high quality images that characterize them, especially with the stable high free-sulfite developer solutions.
- a light-sensitive photographic element comprising a support coated with at least one hydrophilic colloid layer containing a silver halide emulsion in which the chloride comprises at least 6,0 mole percent of the halide, and at least one hydrophilic colloid layer containing a watersoluble block polymer of polyoxypropylene and poly oxyethylene in which the polyoxypropylene moiety has an average molecular weight between 800 and 3,000 and the polyoxyethylene units constitute from about 10 to about 70 percent by weight of said polymers, such that the said block polymer is contiguous to the said silver halide.
- Y represents an organic radical having a valence of X
- n is an integer
- x is an integer greater than 1, so that the values of n and x are such that the molecular weight of the said polymer exclusive of Y, E and R is between 800 and 3,000
- E represents a polyoxyethylene chain constituting from about 10 to about 70 percent by weight of said polymer
- R is a member selected from the class consisting of the hydrogen atom, an alkyl group, an alkyl carbonyl group, and an aryl carbonyl group.
- b represents an integer of from 14 to 52
- a and each represent integers such that the sum of a+c represents an integer of from 4 to 48 and the polyoxyethylene groups constitute between and 70 percent by weight of said polymer
- a photographic element of claim 1 in which the water-soluble block polymer and the silver halide emulsion are in the same hydrophilic colloid layer.
- a photographic element of claim 1 in which the water-soluble block polymer is in a hydrophilic colloid layer coated over the hydrophilic colloid layer containing the silver halide emulsion.
- a photographic element of claim 1 in which the Water-soluble block polymer is in a hydrophilic colloid layer coated under the hydrophilic colloid layer containing the silver halide emulsion.
- a photographic element comprising a transparent support coated with alight-sensitive layer comprising:
- a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 10 percent by weight of said copolymer.
- a photographic element comprising a transparent support coated with a light-sensitive layer comprising:
- a silver chlorobromoiodide emulsion containing (c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 20 percent by weight of said polymer.
- a photographic element comprising a transparent support coated with a light-sensitive layer comprising:
- a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1200 and the polyoxyethylene groups constitute 40 percent by weight of said polymer.
- a photographic element comprising a transparent support coated with a light-sensitive layer comprising:
- a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 40 percent by weight of said polymer.
- a photographic element comprising a transparent support coated with a light-sensitive layer comprising:
- a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 2750 and the polyoxyethylene groups constitute 20 percent by weight of the said polymer.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Polyethers (AREA)
Description
Dec. 27, 1966 GOFFE 3,294,540
LITE-TYPE EMULSIONS WITH BLOCK CO-POLYMERS Filed Dec. 17, 1963 2 Sheets-Sheet 1 SPEED FIG. 3
Al/SW30 CHARLES A. GOFFE I NV-EN TOR.
-- HIS/V30 ATTORNEY a AGE/VT Dec. 27, 1966 c. A. GOFFE LITH-TYPE EMULSIONS WITH BLOCK (JO-POLYMERS 2 Sheets-Sheet 2 Filed Dec. 17, 1965 E F T T A N A W 1 8 m m L n M M M 6 74% ,m a W .QGR m 6R v QFm @mmm Ewan Emmw w G U 3 3 N m m V m M M M 1. H J w n w w n v United States Patent 3,294,540 LITH-TYPE EMULSIONS WITH BLOCK CO-POLYMERS Charles A. Golfe, Rochester, N.Y., assignor to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey Filed Dec. 17, 1963, Ser. No. 331,141 12 Claims. (Cl. 9687) This invention relates to photography and particularly to improved photographic silver halide emulsions of the lith-type.
Photographic films used in the graphic arts for making half-tone or line images should be capable of producing extremely high contrast and good image sharpness. These factors contribute in the case of half-tone images to high dot quality, that is, to the production of half-tone dots of high density and sharpness.
The photographic elements of the lith-type, that is, elements that have a fine grain high contrast silver halide emulsion containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about mole percent iodide, require the use of pure hydroquinone developer solutions having very low free sulfite ion concentration in the alkaline solution in order to produce the high contrast and high dot quality required for good quality half-tone reproduction. Such developer solutions are unstable, having very short tray or tank life after exposure to air, so that the solutions must be mixed fresh just before they are to be used for processing and then discarded.
In many instances the films and processes available do not produce the desired latitude and have the desired ease in exposing and processing the film to produce the required quality. This has resulted from the contrast of the image reproduction in the photographic elements being overly sensitive to development time, and from a nonlinearity in the relationship between the film speed and development time, causing unequal increases in film speed from equal increases in development time.
It is therefore an object of my invention to provide a photographic film which produces high contrast and high quality images even when developed with a developer solution having relatively high free-sulfite content that has good stability upon prolonged exposure to air in tray or tank. Another object is to provide a photographic element which is capable of producing high contrast, high quality half-tone images over a relatively broad range of film exposure and development times. Another object is to provide a photographic element which has good evenness of development. Still other objects will become apparent from the following specification and claims.
These and other objects are accomplished according to my invention by use of a photographic light sensitive element comprising a support, at least one hydrophilic colloid layer containing a very fine grain photographic silver halide emulsion having at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide, and at least one hydrophilic colloid layer containing certain water-soluble block polymers of polyoxypropylene and polyoxyethylene such that the block polymer is contiguous with the silver halide. The water-soluble block polymers used in photographic elements according to my invention include those block polymers in which the polyoxypropylene chain (or moiety) has an average molecular weight between 800 and 3,000 and in which the polyoxyethylene units consti- "ice tute from about 10 to about percent by weight of the polymer. The image reproductions produced in my lith-type emulsion layers are of excellent quality. Although the conventional alkaline, pure hydroquinone, low free-sulfite developer may be used to develop my exposed elements, it is also advantageous to use a developer having from 10 to about 30 grams of an alkali sulfite per liter of the developer solution. When my elements are developed in the preferred developer solutions not only is the image contrast high and the dot quality excellent but this excellent quality is produced over a wide range of exposures and development times.
The water-soluble block polymers of polyoxypropylene and polyoxyethylene used to advantage according to my invention include those represented by the formula:
wherein Y represents an organic radical having a valence of x, said radical being the residue of an organic compound containing atoms selected from the class consisting of carbon, hydrogen, oxygen, nitrogen and sulfur with x active hydrogen atoms, such as, the residue of polyhydroxy compounds, e.g., ethylene glycol, 1,2-propanediol, 1,5-pentanediol, 1,2,3-propanetriol, sucrose, etc., the residue of a polybasic acid, e.g., oxalic acid, malonic acid, succinic acid, maleic acid, citric acid, etc., the residue of a polyamine, e.g., ethylenediamine, 1,3- diaminopropylene, etc., the residue of a polyamide, e.g., malonamide, succinamide, etc., the residue of a polythiol, e.g., 1,2 ethylenedithiol, 1,3 -.propylenedithiol, etc.; n is an integer greater than 1; x is an integer greater than 1, so that the values of n and x are such that the molecular weight of the said polymer exclusive of Y, E and R is between 800 and 3,000; E represents a polyoxyethylene chain constituting from about 10 to about 70 percent by weight of said block polymer; and R represents the hydrogen atom, an alkyl group having from 1 to 20 carbon atoms (such as methyl, propyl, decyl, dodecyl, octadecyl, etc.), an alkyl carbonyl group in which the alkyl group has from 1 to 20 carbon atoms as described above, an aryl carbonyl group, such as, benzoyl, p-methyl benzoyl, etc.
Included among the preferred block polymers are those having the formula:
in which b represents an integer of from 14 to 52; a and c are each integers such that the sum of a-i-c has a total of from 4 to 48 and the polyoxyethylene groups constitute between 10 and 70 percent by weight of the block polymer.
The block polymers of Formula II and of Formula I where R represents the hydrogen atom are described in Lundsted U.S. Patent 2,674,619, issued April 6, 1954, and Lundsted U.S. Patent 3,022,335, issued February 20, 1962. The block polymers of Formula I in which R is hydrogen are readily converted to compounds where R represents an organic residue by reaction with the appropriate reagent in a suitable inert organic solvent that is preferably anhydrous. For example, alkyl halides, such as alkyl chlorides, alkyl bromides, etc., are used to advantage to replace the terminal hydrogen atom of the block polymer with an alkyl group. Alkylp-toluenesulfonates are also used to advantage to place an alkyl group on the end of the block polymers. The appropriate acid chloride or acid anhydride, such as, acetyl chloride, propionyl chloride, stearoyl chloride, benzoyl chloride, acetic anhydride, etc., are used to advantage to prepare block polymers of Formula I in which R is an alkyl carbonyl or an aryl carbonyl group. These reactions are well known to those skilled in the'art. Many of the block polymers of Formulas I and II are available commercially.
My photographic elements coated with a lith-type emulsion containing my block polymers of polyoxypropylene and polyoxyethylene are valuable for use in graphic art reproduction. My elements are particularly valuable when developed with a dihydroxybenzene developer with a high free sulfite ion concentration in an alkaline solution. My elements provide the following advantages:
(1) More even rate of speed change with changes in development time which allows varying the development time systematically to control speed without sacrificing quality;
(2) Better dot quality over a Wider range of development times and temperatures;
(3) Elimination of or reduction in development defeets, such as, drag lines when the materials are developed in automatic roller transport processing equipment;
(4) High contrast and much better dot quality when stable developer solutions containing a high free-sulfite concentration, e.g., 10 to 30 grams of an alkali metal sulfite per liter of solution are used;
(5) Increased speed without loss of dot quality when an onium salt is incorporated in my light-sensitive emulsion layer, and still further advantages will be apparent from the specification and claims.
It is unexpected that the immediate block polymers would produce these advantages since closely related block polymers of polyoxypropylene and polyoxyethylene that are outside my invention produce images having low contrast, low dot quality and unevenness of development.
The quality of the silver images produced in lithtype emulsion layers is conveniently measured in terms of contrast (i.e., 'y) and dot quality. Photographic image contrast is the slope of the straight line portion of a graph of optical density of the image vs. log of exposure. Dot quality is a measure of the quality of the reproduction of a half-tone image. Lith-type photographic elements exposed to a half-tone image, and developed, produce areas commonly referred to as shadow dots and areas known as highlight areas. Intermediate between these two extremes are areas of varying size. The dot quality used herein is a measure of the areas referred to as 50% dots (i.e., /2 clear and /2 developed density) and is expressed -in a progressive scale Where 9 is excellent and "1 is extremely poor. A 50% dot quality below "6 is generally not acceptable.
The factor evenness of development is explained in connection with Example 1 later in the specification.
Included among the block polymers used to advantage according to my invention are the following typical polymers used for illustrative purposes.
Average Percent poly- Block Polymer Y Group derived Value of 'n in oxyethylene No. Irom- Formula I by weight of Block polymer 1 1,2-propanediol 30 2 d0 30 20 3 .do 22 40 4 .do 30 50 5. d0 30 40 6- d0 47 20 7 do 39 10 8. 1,5-pentauediol 24 50 9 1,2,3,-propanetriol 36 48 10 Ethyleuediamine- 32 50 These block polymers are available commercially under the tradename Pluronic. Block polymers 1 through 7 are sold under the trade name Pluronic L61, L62, L44, P65, L64, L92 and L81, respectively.
The block polymers used according to my invention are water soluble and are advantageously added in a water solution to the aqueous hydrophilic colloid (either with or without the silver halide) before it is coated. The block polymers are used to advantage over a wide range of concentrations. The operable range of concentrations is from .001 to 1.00 gram of block polymer per mole of silver, while the preferred range is from 0.010 to 0.200 gram per mole of silver. The optimum concentration of a given block polymer used in my elements depends upon the results desired, the particular silver halide emulsion, the developer solution, etc., and is readily determined by methods well known in the art. The determination of the optimum concentration is preferably made by employing the block polymer in the silver halide emulsion layer or in an adjacent hydrophilic colloid layer according to the element that is desired.
The fine grain silver halide emulsions used to advantage have silver halide crystals preferably containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide. The emulsions can be prepared as described by MacWilliam U.S. 2,756,148, issued July 24, 1956. These emulsions may be used without being sensitized, however, it is advanageous to spectrally sensitize them according to methods well known in the art to make them orthosensitized or panchromatically-sensitized.
The silver halide is dispersed in hydrophilic colloid materials used as binders, including gelatin, collodion, gum arabic, cellulose ester derivatives, such as, alkyl esters of carboxylated cellulose, hydroxy ethyl cellulose, carboxy methyl hydroxy ethyl cellulose, synthetic resins, such as the amphoteric copolymers described by Clavier et al. in U.S. Patent 2,949,442, issued August 16, 1960, polyvinyl alcohol, and others well known in the art. Examples of these polymeric gelatin substitutes are copolymers of allylamine and methacrylic acid; copolymers of allylamine, acrylic acid and acrylamide; hydrolyzed copolymers of allylamine, methacrylic acid and vinyl acetate; the copolymers of allylamine, acrylic acid and styrene; the copolymers of allylamine, methacrylic acid and acrylonitrile; alkyl acrylateacrylic acid copolymers, e.g., copolymers of butyl acrylateacrylic acid, etc.
When my block polymers are incorporated in a layer adjacent to the silver halide emulsion layer instead of in the light-sensitive layer, any of the hydrophilic colloids described hereinbefore may be used to advantage as a binder for coating my polymers.
It is advantageous to add certain onium salts, such as, quaternary ammonium salts, sulfonium salts and phosphonium salts to my light-sensitive emulsions in order to increase the photographic speed without adversely affecting the improved dot quality, contrast and evenness of development. Examples of quaternary ammonium salts include nonyl pyridinium perchlorate, hexoxymethyl pyridinium perchlorate, ethylene bis-dioxymethyl pyridinium perchlorate and others described by Carroll U.S. 2,271,623, issued February 3, 1942, hexadecamethylene- 1,16-bis(pyridinium perchlorate), 9,16-diaza-7,18-dioxa- 8,17 dioxotetracosane-l,24-bis(pyridinium perchlorate), and others of Beavers et al. U.S. 2,944,898, issued July 12, 1960. Other examples include the onium salts of polyoxyalkylenes of Carroll et al. U.S. 2,944,902, issued July 12, 1960, the polyonium salts of Carroll et al. U.S. 2,288,226, issued June 30, 1942, such as bis(lauryl methyl sulfonium p-toluene sulfonate) 1,2-ethane, N,N-trimethylene dioxymethyl pyridinium perchlorate etc., the sulfonium salts of Carroll et al. U.S. 2,275,727, issued March 10, 1942, such as, n-decyl dimethyl sulfonium p-toluene sulfonate, n-nonyl dimethyl sulfonium p-toluene sulfonate, etc., and the phosphonium salts of Carroll et al. U.S. 2,271,622, issued February 3, 1942, such as, tetramethylene bis-triethyl phosphonium bromide, lauryltriethylphosphonium bromide, etc.
My light-sensitive emulsions can be coated to advantage on any of the conventional photographic supports, including glass, cellulose acetate, polystyrene, polyalkyleneterephthalate, etc. The block polymers can be coated advantageously in the silver halide emulsion layer, or in a hydrophilic colloid layer that is either under or over the silver halide emulsion layer so that the block polymer the development time, the slope of the resultant curve will approach as K approaches a constant value. Evenness of development is the slope of the plot of K against time. In the above table, evenness of development is exis contiguous to the silver halide. pressed in this way. The smaller the number, the more My invention is still further illustrated by the following even the development. This value indicates the even examples. spacing between the sensitometric curves for eqaul differ- Example 1 ences in development time.
A gelatino silver chlorobromoiodide emulsion containaccompanymg .irawmgs 5 and ing approximately 90 mole percent chloride, 9 mole 10 wh1ch show plots of image density vs. speed Will further cent bromide, and 1 mole percent iodide was divided into Illustrate mvfintlon' Each gur Sh ws 4 3curves, separate portions and the polymer or copolymer indicated curve 1 for mmute developmeant W 2 for 2 A in Table I was added to the individual portions. The reute developmentacurvfa' 3 for 3 A mmute development sulting compositions were coated on separate pieces of a and curve 4 for 4A mmute development polyalkyleneterephthalate film support at a coverage of 1 shows curves 1 through 4 for a Control 11th 455 mg. of silver and 450 mg. of gelatin per square foot. element g Samples of each coating were exposed on an intensity H 2 9 carves 1 F P 4 for a 11th element scale sensitometer and processed in a developer of the Outslde Invention contalmng polyoxyethylenecomposition: FIG. 3 snows curves 1 through 4 for a lith element outside my invention containing block polymer A de- Hydroquinone 15 scnbed previously Sodium formaldehyde bi lfit 501) IG. 4 shows curves 1 through 4 for my lith element s i carbonate 3 containing my block polymer No. 3. s di bicarbonate 225 FIG. 5 shows curves 1 hrough 4 for my lith elesodiu lfit 2,5 ment containing my block polymer No. 5. Potassium bromide 0.75 FIG. 6 shows curves 1 through 4 for my lith ele- Water to make 1.0 liter. ment containing my block polymer No. 7. for 4 /4 minutes, fixed in a conventional sodium thiosul- The Curves 9? F 2 h thfat Whfin polyoxyethylene fate fixing bath, Washed and dried The polymer or is added to a 11th emulsion to increase the contrast and polymer composition, concentration in each coating are improve dot P Y h l P g -s evenness of listed with the relative speed, contrast (i.e., dot quality dfivelopment) eTrat1C- slmllafly, 3 ShOWS t of the developed coating and the evenness of development a 611111151011 Contalning block Polymer A Outside that were obtained are summarized in Table I. my invention has erratic curve spacing. However, as
TABLE I Molecular Grams of Photographic weight of Percent polymer Relative Dot Evenness of element Polymer polyoxypolyoxyper mole speed 7 quality development propylene ethylene of silver block P130 =Oleylether of polyethylene oxide, average M.W.=1,500.
The polymer PEO is the oleyl ether of polyethylene oxide shown by FIG. 4 when a lith emulsion contains one having an average molecular weight of 1500. Block 55 of my block polymers such asNo. 3 the curve spacing is polymers A and B have polyoxypropylene units and polymore regular indicating good evenness of development oxyethylene units but are outside of the invention. Cowhich is a distinct advantage, since it allows one to vary polymers 1, 2, 3, 4, 5 and 6 have been described prevthe speed of the material at a constant rate by varying the iously. development time without sacrificing contrast or dot The data in Table I show that my lith elements conq ytaining block polymers 1, 2, 3, 4, 5 and 6 produced good By varying the concentration of my block polymer or by image contrasts of from 10 to 12, good dot quality rangusing block polymers having polyoxypropylene chains ing from 7 to 8 and good evenness of development i dihaving relatively hlgh molecular weights it is also poscated by a value from .02 to .13. The elements-outside my sible to make lith elements giving relatively small invention containing PEO produced very poor to unacceptchanges in speed with development time. This characterable' dot quality and very poor evenness of development. istic is particularly advantageous in automatic processing Similarly elements containing block polymers A or B equipment where the activity of the developer may vary produced very low contrast images, very poor dot quality with aging, or other variables may be present which affect and poor eveness of development. the development rate. The following will serve to illus- Ideally, the rate of change in the log of the speed with 7 trate this advantage. change in development time should equal a constant; Example 2 that 1S Coatmgs were made and processed as in Example 1 for log Speed at tune Speed at tZK the polymer indicated in Table II. Development times When the rate of change in the speed is plotted against of 1%, 2%, 3% and 4% minutes were used.. The changes in relative speed over 3 minutes development were determined and listed below.
This effect can be more clearly seen by noting the closer spacing of curves 1 through 4 in FIG. 6 than in FIG. 5.
Example 3 A.very fine grain high contrast gelatino silver chlorobromide emulsion in which 70 percent of the halide was the chloride was prepared and divided into three equal portions. One portion wa used as a control. Oleyl ether of polyoxyethylene (molecular weight 1540) was .added to the second portion and stock polymer No. 2
was added to the third portion of the emulsion as indicated in Table III. These emulsions were coated, exposed and developed as described in Example 1 but using a very low free-sulfite developer having the composition:
G. Sodium sulfite, desiccated 30.0 Paraformaldehyde 7.5 Sodium bisulfite 2.2 Boric acid, crystals 7.5 Hydroquinone 22.5 Potassium bromide 1.6 Water to make 1.0 liter.
The results are summarized in the following table.
TABLE III Gm. poly- Relative Dot Polymer mer per speed 1 Fog quality mole Ag None 100 5.1 .01 1 Oleyl ether of PEG 1540 0. 72 9. 1 .01 5 Block Polymer N o. 2-- 0.125 49 9. 5 01 9 The results clearly show that my block polymer No. 2 produces excellent dot quality at a high contrast while the oleyl ether of PEG 1540 produces poor dot quality.
Example 4 Hydroquinone g 15.0
Boric acid g 5.5 Potassium bromide g 2.7 Potassium carbonate g 90.0 Potassium sulfite g 20.0 Diethylene glycol ec 30.0
Water to make 1000.0 cc.
The results summarized in Table IV show the better quality obtained with my polymers No. 3 and No. 2
compared to a simple PEO having a molecular weight of 1540.
TABLE V Gm. polymer Relative Dot Polymer per mole of speed 7 quality silver PEO 120 7. 0 5 N o. 3 03 42 13+ 8 N0. 2 045 12. 5 7
The following example will serve to illustrate that the speed of my lith emulsions can be increased by adding an onium salt to the emulsion without adversely affecting the improved dot quality and contrast obtained from the addition of a preferred block polymer.
Example 5 TABLE v Onium Salt Grams per Relative 1 Dot mole silver speed quality None. 100 6. 1 9 N ,N -ethylenedioxymethyl pyridinium perchlorate- 066 151 7. 9 9
Similarly, other quaternary ammonium salts, sulfonium salts and phosphonium salts as disclosed previously can be used to advantage with other block polymers of my invention.
My lith elements coated with fine grain high contrast silver halide emulsions containing at least 60 mole percent chloride, less than 40 mole percent bromide and less than about 5 mole percent iodide contain certain water-soluble block polymers of polyoxypropylenc and polyoxyethylene. The block polymer is incorporated in the light-sensitive layer or in a layer adjacent to the lightsensitive layer so that the polymer and silver halide are contiguous. The block polymers used to advantage according to my invention include those in which the polyoxypropylene chain has an average molecular weight between 800 and 3000, and in which the polyoxyethylene units constitute from about 10 to about 70 percent ,by weight of the block polymer. My elements give high contrast images with high dot quality and good evenness of development with lith developer solutions. My elements are particularly valuable because they produce these high quality image reproductions even when stable high free-sulfite developer solutions are used. Since lith" elements containing simple polyoxyethylene and certain block polymers of polyoxy-propylene and polyoxyethylene that are outside my invention produce low contrast and poor dot quality, it is unexepected that my elements containing my block polymers produce the high quality images that characterize them, especially with the stable high free-sulfite developer solutions.
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 elfected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
I claim:
1. A light-sensitive photographic element comprising a support coated with at least one hydrophilic colloid layer containing a silver halide emulsion in which the chloride comprises at least 6,0 mole percent of the halide, and at least one hydrophilic colloid layer containing a watersoluble block polymer of polyoxypropylene and poly oxyethylene in which the polyoxypropylene moiety has an average molecular weight between 800 and 3,000 and the polyoxyethylene units constitute from about 10 to about 70 percent by weight of said polymers, such that the said block polymer is contiguous to the said silver halide.
2. A photographic element of claim 1 in which the water-soluble block polymer has the formula:
wherein Y represents an organic radical having a valence of X; n is an integer; x is an integer greater than 1, so that the values of n and x are such that the molecular weight of the said polymer exclusive of Y, E and R is between 800 and 3,000; E represents a polyoxyethylene chain constituting from about 10 to about 70 percent by weight of said polymer; and R is a member selected from the class consisting of the hydrogen atom, an alkyl group, an alkyl carbonyl group, and an aryl carbonyl group.
3. A photographic element of claim 1 in which the water-soluble block polymer has the formula:
IIO(OH2CH20) CIIOII20](CH2CI{20)H wherein b represents an integer of from 14 to 52; and a and each represent integers such that the sum of a+c represents an integer of from 4 to 48 and the polyoxyethylene groups constitute between and 70 percent by weight of said polymer;
4. A photographic element of claim 1 in which the water-soluble block polymer and the silver halide emulsion are in the same hydrophilic colloid layer.
5. A photographic element of claim 1 in which the water-soluble block polymer is in a hydrophilic colloid layer coated over the hydrophilic colloid layer containing the silver halide emulsion.
6. A photographic element of claim 1 in which the Water-soluble block polymer is in a hydrophilic colloid layer coated under the hydrophilic colloid layer containing the silver halide emulsion.
7. A photographic element of claim 1 in which the light-sensitive layer contains an oniurn salt selected from the class consisting of a quaternary ammonium salt, a sulfonium salt and a phosphonium salt.
8. A photographic element comprising a transparent support coated with alight-sensitive layer comprising:
(a) gelatin;
(b) a silver chlorobromoiodide emulsion containing approximately 90 mole percent chloride, approximately 9 mole percent bromide and approximately 1 mole percent iodide; and
(c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 10 percent by weight of said copolymer.
9. A photographic element comprising a transparent support coated with a light-sensitive layer comprising:
(a) gelatin;
(b) a silver chlorobromoiodide emulsion containing (c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 20 percent by weight of said polymer.
10. A photographic element comprising a transparent support coated with a light-sensitive layer comprising:
(a) gelatin;
(b) a silver chlorobromoiodide emulsion containing approximately mole percent chloride, approximately 9 mole percent bromide and approximately 1 mole percent iodide; and
(c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1200 and the polyoxyethylene groups constitute 40 percent by weight of said polymer.
11. A photographic element comprising a transparent support coated with a light-sensitive layer comprising:
(a) gelatin;
(b) a siliver chlorobromoiodide emulsion containing approximately 90 mole percent chloride, approximately 9 mole percent bromide and approximately 1 mole percent iodide; and
(c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 1750 and the polyoxyethylene groups constitute 40 percent by weight of said polymer.
12. A photographic element comprising a transparent support coated with a light-sensitive layer comprising:
(a) gelatin;
(b) a silver chlorobromoiodide emulsion containing approximately 90 mole percent chloride, approximately 9 mole percent bromide and approximately 1 mole percent iodide; and
(c) a water-soluble block polymer comprising a waterinsoluble polyoxypropylene chain having water-soluble polyoxyethylene groups at each end of said polyoxypropylene chain in which the molecular weight of the polyoxypropylene chain is 2750 and the polyoxyethylene groups constitute 20 percent by weight of the said polymer.
References Cited by the Examiner UNITED STATES PATENTS 2,423,549 7/1947 Blake 96107 2,674,619 4/1954 Lunsted 26030.8 X 3,022,335 2/1962 Lunsted 252-351 X 3,030,209 4/1962 Henn et al 9694 X 3,084,044 4/1963 Dersch et al. 9666 3,193,386 7/1965 White 9666 OTHER REFERENCES Churayeva et al.: Zh. Nauch. Prikl. Fot. Kine. 6, 139- 40 (#2, 1961); translation in Ansco Abstracts, vol. 21, p. 421, April 1962.
NORMAN G. TORCHIN, Primary Examiner.
J. RAUBITSCHEK, Assistant Examiner.
Claims (1)
1. A LIGHT-SENSITIVE PHOTOGRAPHIC ELEMENT COMPRISING A SUPPORT COATED WITH AT LEAST ONE HYDROPHILLIC COLLOID LAYER CONTAINING A SILVER HALIDE EMULSION IN WHICH THE CHLORIDE COMPRISES AT LEAST 60 MOLE PERCENT OF THE HALIDE, AND AT LEAST ONE HYDROPHILIC COLLOID LAYER CONTAINING A WATERSOLUBLE BLOCK POLYMER OF POLYOXYPROPYLENE AND POLYOXYETHYLENE IN WHICH THE POLYOXYPROPYLENE MOIETY HAS AN AVERAGE MOLECULAR WEIGHT BETWEEN 800 AND 3,000 AND THE POLYOXYETHYLENE UNITS CONSTITUTE FROM ABOUT 10 TO ABOUT 70 PERCENT BY WEIGHT OF SAID POLYMERS, SUCH THAT THE SAID BLOCK POLYMER IS CONTIGUOUS TO THE SAID SILVER HALIDE.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US331141A US3294540A (en) | 1963-12-17 | 1963-12-17 | Lith-type emulsions with block co-polymers |
| DE19641447659 DE1447659A1 (en) | 1963-12-17 | 1964-11-26 | Photographic material |
| FR997778A FR1416850A (en) | 1963-12-17 | 1964-12-08 | New photosensitive product for photomechanical reproduction |
| GB51378/64A GB1092814A (en) | 1963-12-17 | 1964-12-17 | Sensitive silver halide photographic materials and emulsions therefor |
| US596043A US3433639A (en) | 1963-12-17 | 1966-11-07 | Photographic emulsion containing a block polymer sensitized with saponin |
| GB49903/67A GB1199988A (en) | 1963-12-17 | 1967-11-02 | Photographic Silver Halide Emulsions and Sensitive Materials Prepared Therefrom |
| DE19671597553 DE1597553A1 (en) | 1963-12-17 | 1967-11-06 | Photosensitive photographic material |
| FR127164A FR93238E (en) | 1963-12-17 | 1967-11-07 | New photosensitive product for reproduction. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US331141A US3294540A (en) | 1963-12-17 | 1963-12-17 | Lith-type emulsions with block co-polymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3294540A true US3294540A (en) | 1966-12-27 |
Family
ID=23292769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US331141A Expired - Lifetime US3294540A (en) | 1963-12-17 | 1963-12-17 | Lith-type emulsions with block co-polymers |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3294540A (en) |
| DE (1) | DE1447659A1 (en) |
| FR (1) | FR1416850A (en) |
| GB (1) | GB1092814A (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3433639A (en) * | 1963-12-17 | 1969-03-18 | Eastman Kodak Co | Photographic emulsion containing a block polymer sensitized with saponin |
| US3516830A (en) * | 1965-09-17 | 1970-06-23 | Eastman Kodak Co | Photographic silver halide emulsions and elements |
| US3518085A (en) * | 1965-09-23 | 1970-06-30 | Eastman Kodak Co | Lith-type emulsions containing a polyalkyleneoxy polymer and a 3-pyrazolidone developing agent |
| US3632340A (en) * | 1968-09-09 | 1972-01-04 | Eastman Kodak Co | Cored direct positive silver halide emulsion developed with polyhydroxybenzene |
| US3650759A (en) * | 1968-07-09 | 1972-03-21 | Fuji Photo Film Co Ltd | Silver halide emulsion containing 1.2-glycol as sensitizer and antifoggant |
| US3709689A (en) * | 1969-04-02 | 1973-01-09 | Agfa Gevaert | Surface development of an imagewise exposed emulsion containing silver halide grains with cores chemically ripened in two stages |
| US3895948A (en) * | 1971-12-28 | 1975-07-22 | Fuji Photo Film Co Ltd | Silver halide light-sensitive material containing a heterocyclic thione and a polyalkylene oxide |
| DE2525320A1 (en) * | 1974-06-06 | 1975-12-18 | Fuji Photo Film Co Ltd | PHOTOGRAPHIC SILVER HALOGENIDE RECORDING MATERIAL |
| DE2710026A1 (en) * | 1976-03-08 | 1977-09-15 | Fuji Photo Film Co Ltd | IMAGE GENERATION PROCESS |
| EP0112162A2 (en) | 1982-12-13 | 1984-06-27 | Konica Corporation | Light-sensitive silver halide photographic material |
| EP0124795A2 (en) | 1983-04-11 | 1984-11-14 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsion |
| US5310633A (en) * | 1992-05-13 | 1994-05-10 | Fuji Photo Film Co., Ltd. | Bleach-fixing composition for color photographic material and method for processing a color photographic material with the same |
| US6071688A (en) * | 1998-07-29 | 2000-06-06 | Eastman Kodak Company | Providing additives to a coating composition by vaporization |
| US20060165625A1 (en) * | 2005-01-22 | 2006-07-27 | Verrall Andrew P | Water-soluble film article having salt layer, and method of making the same |
| US7250202B1 (en) | 1998-06-18 | 2007-07-31 | Ilford Imaging Ch Gmbh | Recording sheets for ink jet printing |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58190943A (en) * | 1982-04-30 | 1983-11-08 | Fuji Photo Film Co Ltd | Silver halide photosensitive material and its developing method |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2423549A (en) * | 1945-01-10 | 1947-07-08 | Du Pont | Silver halide photographic emulsions sensitized by polyalkylene glycols |
| US2674619A (en) * | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US3022335A (en) * | 1955-03-30 | 1962-02-20 | Wyandotte Chemicals Corp | Surface active polyoxyalkylene compounds having a plurality of heteric polyoxypropylene-polyoxyethylene chains |
| US3030209A (en) * | 1958-07-02 | 1962-04-17 | Eastman Kodak Co | High-contrast photographic silver chloride emulsions and method of processing |
| US3084044A (en) * | 1960-12-09 | 1963-04-02 | Gen Aniline & Film Corp | Nitrogenous heterocyclic carboxyal-kylmercapto polyoxyalkylene ester photographic sensitizer |
| US3193386A (en) * | 1961-11-29 | 1965-07-06 | Du Pont | Silver halide emulsions and elements containing antifoggants |
-
1963
- 1963-12-17 US US331141A patent/US3294540A/en not_active Expired - Lifetime
-
1964
- 1964-11-26 DE DE19641447659 patent/DE1447659A1/en active Pending
- 1964-12-08 FR FR997778A patent/FR1416850A/en not_active Expired
- 1964-12-17 GB GB51378/64A patent/GB1092814A/en not_active Expired
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2423549A (en) * | 1945-01-10 | 1947-07-08 | Du Pont | Silver halide photographic emulsions sensitized by polyalkylene glycols |
| US2674619A (en) * | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US3022335A (en) * | 1955-03-30 | 1962-02-20 | Wyandotte Chemicals Corp | Surface active polyoxyalkylene compounds having a plurality of heteric polyoxypropylene-polyoxyethylene chains |
| US3030209A (en) * | 1958-07-02 | 1962-04-17 | Eastman Kodak Co | High-contrast photographic silver chloride emulsions and method of processing |
| US3084044A (en) * | 1960-12-09 | 1963-04-02 | Gen Aniline & Film Corp | Nitrogenous heterocyclic carboxyal-kylmercapto polyoxyalkylene ester photographic sensitizer |
| US3193386A (en) * | 1961-11-29 | 1965-07-06 | Du Pont | Silver halide emulsions and elements containing antifoggants |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3433639A (en) * | 1963-12-17 | 1969-03-18 | Eastman Kodak Co | Photographic emulsion containing a block polymer sensitized with saponin |
| US3516830A (en) * | 1965-09-17 | 1970-06-23 | Eastman Kodak Co | Photographic silver halide emulsions and elements |
| US3518085A (en) * | 1965-09-23 | 1970-06-30 | Eastman Kodak Co | Lith-type emulsions containing a polyalkyleneoxy polymer and a 3-pyrazolidone developing agent |
| US3650759A (en) * | 1968-07-09 | 1972-03-21 | Fuji Photo Film Co Ltd | Silver halide emulsion containing 1.2-glycol as sensitizer and antifoggant |
| US3632340A (en) * | 1968-09-09 | 1972-01-04 | Eastman Kodak Co | Cored direct positive silver halide emulsion developed with polyhydroxybenzene |
| US3709689A (en) * | 1969-04-02 | 1973-01-09 | Agfa Gevaert | Surface development of an imagewise exposed emulsion containing silver halide grains with cores chemically ripened in two stages |
| US3895948A (en) * | 1971-12-28 | 1975-07-22 | Fuji Photo Film Co Ltd | Silver halide light-sensitive material containing a heterocyclic thione and a polyalkylene oxide |
| DE2525320A1 (en) * | 1974-06-06 | 1975-12-18 | Fuji Photo Film Co Ltd | PHOTOGRAPHIC SILVER HALOGENIDE RECORDING MATERIAL |
| DE2710026A1 (en) * | 1976-03-08 | 1977-09-15 | Fuji Photo Film Co Ltd | IMAGE GENERATION PROCESS |
| US4144069A (en) * | 1976-03-08 | 1979-03-13 | Fuji Photo Film Co., Ltd. | Method of image formation |
| EP0112162A2 (en) | 1982-12-13 | 1984-06-27 | Konica Corporation | Light-sensitive silver halide photographic material |
| EP0124795A2 (en) | 1983-04-11 | 1984-11-14 | Fuji Photo Film Co., Ltd. | Silver halide photographic emulsion |
| US5310633A (en) * | 1992-05-13 | 1994-05-10 | Fuji Photo Film Co., Ltd. | Bleach-fixing composition for color photographic material and method for processing a color photographic material with the same |
| US7250202B1 (en) | 1998-06-18 | 2007-07-31 | Ilford Imaging Ch Gmbh | Recording sheets for ink jet printing |
| US6071688A (en) * | 1998-07-29 | 2000-06-06 | Eastman Kodak Company | Providing additives to a coating composition by vaporization |
| US20060165625A1 (en) * | 2005-01-22 | 2006-07-27 | Verrall Andrew P | Water-soluble film article having salt layer, and method of making the same |
| US8728449B2 (en) * | 2005-01-22 | 2014-05-20 | Monosol Llc | Water-soluble film article having salt layer, and method of making the same |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1092814A (en) | 1967-11-29 |
| DE1447659A1 (en) | 1969-02-20 |
| FR1416850A (en) | 1965-11-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3294540A (en) | Lith-type emulsions with block co-polymers | |
| US3150977A (en) | Light-sensitive photographic materials | |
| US3708303A (en) | Photographic elements and processes lithographic silver halide element containing a 1-(amidophenyl)-5-mercaptotetrazole sensitizing agent and development process of using same | |
| US3532501A (en) | Water-soluble acid esters of polyoxyalkylenated pentaerythritol in silver halide emulsions | |
| US3518085A (en) | Lith-type emulsions containing a polyalkyleneoxy polymer and a 3-pyrazolidone developing agent | |
| US3849146A (en) | Direct-print light-developable silver halide emulsion containing cyclic dioxide or selenone as sensitizer | |
| US3325286A (en) | Photographic emulsions and elements | |
| US3361564A (en) | Amine borane as fogging agent in direct positive | |
| US3271158A (en) | Photographic silver halide emulsions having high wet density retention | |
| GB1591640A (en) | Sensitive silver salt photothermographic material | |
| US4126472A (en) | Process of making a lithographic photosensitive silver halide emulsion having reduced susceptibility to pressure containing an iridium compound, a hydroxytetrazaindene and a polyoxyethylene | |
| US3516830A (en) | Photographic silver halide emulsions and elements | |
| US4070190A (en) | Process for producing photographic silver halide emulsions having a core/shell structure | |
| US3567458A (en) | Photographic emulsion containing a water-soluble alkylene oxide block copolymer and a merocyanine dye | |
| US3671247A (en) | Development of silver halide photographic materials | |
| US2757089A (en) | Phytic acid sensitizer for silver halide emulsions | |
| US3294537A (en) | Lith-type emulsions with organosilicone block copolymers | |
| US3272631A (en) | Haze reduction of photographic emulsions containing a covering power agent | |
| US3655390A (en) | Direct positive emulsions containing amine boranes and bismuth salts | |
| US3433639A (en) | Photographic emulsion containing a block polymer sensitized with saponin | |
| US3647455A (en) | Direct positive emulsions containing iodide ions and a sensitizing dye | |
| US3607278A (en) | Photographic elements containing fogged and unfogged silver halide grains and a slow silver halide emulsion layer | |
| US3650759A (en) | Silver halide emulsion containing 1.2-glycol as sensitizer and antifoggant | |
| US4022621A (en) | Photographic developer composition | |
| US3178293A (en) | Radiation-sensitive elements and their preparation |