USH1020H - Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it - Google Patents
Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it Download PDFInfo
- Publication number
- USH1020H USH1020H US07/586,284 US58628490A USH1020H US H1020 H USH1020 H US H1020H US 58628490 A US58628490 A US 58628490A US H1020 H USH1020 H US H1020H
- Authority
- US
- United States
- Prior art keywords
- group
- silver halide
- developer
- light
- developing
- 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.)
- Abandoned
Links
- -1 silver halide Chemical class 0.000 title claims abstract description 85
- 229910052709 silver Inorganic materials 0.000 title claims abstract description 68
- 239000004332 silver Substances 0.000 title claims abstract description 68
- 239000000463 material Substances 0.000 title claims abstract description 52
- 238000000034 method Methods 0.000 title claims abstract description 43
- 150000001875 compounds Chemical class 0.000 claims abstract description 46
- 229910021607 Silver chloride Inorganic materials 0.000 claims abstract description 6
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 claims abstract description 6
- 125000003396 thiol group Chemical group [H]S* 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000001033 ether group Chemical group 0.000 claims description 6
- 229920001281 polyalkylene Polymers 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 125000006193 alkinyl group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 abstract description 5
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000101 thioether group Chemical group 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 102
- 239000000839 emulsion Substances 0.000 description 45
- 239000000975 dye Substances 0.000 description 44
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 42
- 239000003795 chemical substances by application Substances 0.000 description 26
- 238000005406 washing Methods 0.000 description 25
- 239000010410 layer Substances 0.000 description 23
- 238000012545 processing Methods 0.000 description 20
- 238000000576 coating method Methods 0.000 description 19
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- 239000011248 coating agent Substances 0.000 description 18
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 16
- 108010010803 Gelatin Proteins 0.000 description 15
- 206010070834 Sensitisation Diseases 0.000 description 15
- 239000008273 gelatin Substances 0.000 description 15
- 229920000159 gelatin Polymers 0.000 description 15
- 235000019322 gelatine Nutrition 0.000 description 15
- 235000011852 gelatine desserts Nutrition 0.000 description 15
- 230000008313 sensitization Effects 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- 238000011161 development Methods 0.000 description 13
- 230000000087 stabilizing effect Effects 0.000 description 12
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- 230000001235 sensitizing effect Effects 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- 229910019142 PO4 Inorganic materials 0.000 description 7
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 7
- 235000021317 phosphate Nutrition 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 150000003568 thioethers Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 238000007865 diluting Methods 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 229910052717 sulfur Inorganic materials 0.000 description 6
- 239000011593 sulfur Substances 0.000 description 6
- GGZHVNZHFYCSEV-UHFFFAOYSA-N 1-Phenyl-5-mercaptotetrazole Chemical compound SC1=NN=NN1C1=CC=CC=C1 GGZHVNZHFYCSEV-UHFFFAOYSA-N 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229910052700 potassium Chemical group 0.000 description 5
- 239000011591 potassium Chemical group 0.000 description 5
- 229960003975 potassium Drugs 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000011241 protective layer Substances 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 229920000126 latex Polymers 0.000 description 4
- 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 4
- 229910000510 noble metal Inorganic materials 0.000 description 4
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 239000011780 sodium chloride Substances 0.000 description 4
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 4
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-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
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 239000002738 chelating agent Substances 0.000 description 3
- ZUIVNYGZFPOXFW-UHFFFAOYSA-N chembl1717603 Chemical compound N1=C(C)C=C(O)N2N=CN=C21 ZUIVNYGZFPOXFW-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 229930182490 saponin Natural products 0.000 description 3
- 150000007949 saponins Chemical class 0.000 description 3
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 239000011550 stock solution Substances 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- VJWBUPGLRCFWEZ-UHFFFAOYSA-N 3,5-dichloro-1-hydroxy-2,4-dihydrotriazine;sodium Chemical compound [Na].ON1NN(Cl)CC(Cl)=C1 VJWBUPGLRCFWEZ-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- YTSAIZQULMWART-UHFFFAOYSA-N 5-ethoxy-2h-benzotriazole Chemical compound C1=C(OCC)C=CC2=NNN=C21 YTSAIZQULMWART-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 229910021538 borax Chemical group 0.000 description 2
- 238000005282 brightening Methods 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000011033 desalting Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 230000003641 microbiacidal effect Effects 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 2
- 235000019252 potassium sulphite Nutrition 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 230000002335 preservative effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000005070 ripening Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000004328 sodium tetraborate Chemical group 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 125000005504 styryl group Chemical group 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 2
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- DBCKMJVEAUXWJJ-UHFFFAOYSA-N 2,3-dichlorobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Cl)=C1Cl DBCKMJVEAUXWJJ-UHFFFAOYSA-N 0.000 description 1
- GPASWZHHWPVSRG-UHFFFAOYSA-N 2,5-dimethylbenzene-1,4-diol Chemical compound CC1=CC(O)=C(C)C=C1O GPASWZHHWPVSRG-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- BDKLKNJTMLIAFE-UHFFFAOYSA-N 2-(3-fluorophenyl)-1,3-oxazole-4-carbaldehyde Chemical compound FC1=CC=CC(C=2OC=C(C=O)N=2)=C1 BDKLKNJTMLIAFE-UHFFFAOYSA-N 0.000 description 1
- HIGSPBFIOSHWQG-UHFFFAOYSA-N 2-Isopropyl-1,4-benzenediol Chemical compound CC(C)C1=CC(O)=CC=C1O HIGSPBFIOSHWQG-UHFFFAOYSA-N 0.000 description 1
- NCDBYAPSWOPDRN-UHFFFAOYSA-N 2-[dichloro(fluoro)methyl]sulfanylisoindole-1,3-dione Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)F)C(=O)C2=C1 NCDBYAPSWOPDRN-UHFFFAOYSA-N 0.000 description 1
- NCKMMSIFQUPKCK-UHFFFAOYSA-N 2-benzyl-4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1CC1=CC=CC=C1 NCKMMSIFQUPKCK-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- LLOAINVMNYBDNR-UHFFFAOYSA-N 2-sulfanylidene-1,3-dihydrobenzimidazole-5-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2NC(=S)NC2=C1 LLOAINVMNYBDNR-UHFFFAOYSA-N 0.000 description 1
- CIULAVLZOPPVFP-UHFFFAOYSA-N 2H-benzotriazole-5-thiol Chemical compound SC1=CC=C2NN=NC2=C1 CIULAVLZOPPVFP-UHFFFAOYSA-N 0.000 description 1
- XSFHICWNEBCMNN-UHFFFAOYSA-N 2h-benzotriazol-5-amine Chemical compound NC1=CC=C2NN=NC2=C1 XSFHICWNEBCMNN-UHFFFAOYSA-N 0.000 description 1
- OEBMOZBCDOBXAN-UHFFFAOYSA-N 2h-benzotriazole-5-carbonitrile Chemical compound C1=C(C#N)C=CC2=NNN=C21 OEBMOZBCDOBXAN-UHFFFAOYSA-N 0.000 description 1
- GUOVBFFLXKJFEE-UHFFFAOYSA-N 2h-benzotriazole-5-carboxylic acid Chemical compound C1=C(C(=O)O)C=CC2=NNN=C21 GUOVBFFLXKJFEE-UHFFFAOYSA-N 0.000 description 1
- VFWJHCOPTQCMPO-UHFFFAOYSA-N 2h-benzotriazole-5-sulfonic acid Chemical compound C1=C(S(=O)(=O)O)C=CC2=NNN=C21 VFWJHCOPTQCMPO-UHFFFAOYSA-N 0.000 description 1
- VXLKZBRLFFGAQT-UHFFFAOYSA-N 3h-benzimidazole-5-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2N=CNC2=C1 VXLKZBRLFFGAQT-UHFFFAOYSA-N 0.000 description 1
- SJSJAWHHGDPBOC-UHFFFAOYSA-N 4,4-dimethyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(C)CN1C1=CC=CC=C1 SJSJAWHHGDPBOC-UHFFFAOYSA-N 0.000 description 1
- DSVIHYOAKPVFEH-UHFFFAOYSA-N 4-(hydroxymethyl)-4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)(CO)CN1C1=CC=CC=C1 DSVIHYOAKPVFEH-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- 150000005168 4-hydroxybenzoic acids Chemical class 0.000 description 1
- ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 4-methyl-1-phenylpyrazolidin-3-one Chemical compound N1C(=O)C(C)CN1C1=CC=CC=C1 ZZEYCGJAYIHIAZ-UHFFFAOYSA-N 0.000 description 1
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 1
- PZBQVZFITSVHAW-UHFFFAOYSA-N 5-chloro-2h-benzotriazole Chemical compound C1=C(Cl)C=CC2=NNN=C21 PZBQVZFITSVHAW-UHFFFAOYSA-N 0.000 description 1
- ZWTWLIOPZJFEOO-UHFFFAOYSA-N 5-ethyl-2h-benzotriazole Chemical compound C1=C(CC)C=CC2=NNN=C21 ZWTWLIOPZJFEOO-UHFFFAOYSA-N 0.000 description 1
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 1
- AOCDQWRMYHJTMY-UHFFFAOYSA-N 5-nitro-2h-benzotriazole Chemical compound C1=C([N+](=O)[O-])C=CC2=NNN=C21 AOCDQWRMYHJTMY-UHFFFAOYSA-N 0.000 description 1
- YCPXWRQRBFJBPZ-UHFFFAOYSA-N 5-sulfosalicylic acid Chemical compound OC(=O)C1=CC(S(O)(=O)=O)=CC=C1O YCPXWRQRBFJBPZ-UHFFFAOYSA-N 0.000 description 1
- NKLOLMQJDLMZRE-UHFFFAOYSA-N 6-chloro-1h-benzimidazole Chemical compound ClC1=CC=C2N=CNC2=C1 NKLOLMQJDLMZRE-UHFFFAOYSA-N 0.000 description 1
- ILMHAGCURJPNRZ-UHFFFAOYSA-N 6-methoxy-1h-benzimidazole Chemical compound COC1=CC=C2N=CNC2=C1 ILMHAGCURJPNRZ-UHFFFAOYSA-N 0.000 description 1
- XPAZGLFMMUODDK-UHFFFAOYSA-N 6-nitro-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC=C2N=CNC2=C1 XPAZGLFMMUODDK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- CSGQJHQYWJLPKY-UHFFFAOYSA-N CITRAZINIC ACID Chemical compound OC(=O)C=1C=C(O)NC(=O)C=1 CSGQJHQYWJLPKY-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-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
- 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
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 238000001016 Ostwald ripening Methods 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920000388 Polyphosphate Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 101150108015 STR6 gene Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical group [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-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
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- XCFIVNQHHFZRNR-UHFFFAOYSA-N [Ag].Cl[IH]Br Chemical compound [Ag].Cl[IH]Br XCFIVNQHHFZRNR-UHFFFAOYSA-N 0.000 description 1
- XEIPQVVAVOUIOP-UHFFFAOYSA-N [Au]=S Chemical compound [Au]=S XEIPQVVAVOUIOP-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
- JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000001661 cadmium Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- UVSNFZAOYHOOJO-UHFFFAOYSA-N chembl1343456 Chemical compound OC1=CC=C2N=NNC2=C1 UVSNFZAOYHOOJO-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229960003887 dichlorophen Drugs 0.000 description 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- JGEMYUOFGVHXKV-OWOJBTEDSA-N fumaraldehyde Chemical compound O=C\C=C\C=O JGEMYUOFGVHXKV-OWOJBTEDSA-N 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- DKPHLYCEFBDQKM-UHFFFAOYSA-H hexapotassium;1-phosphonato-n,n-bis(phosphonatomethyl)methanamine Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[O-]P([O-])(=O)CN(CP([O-])([O-])=O)CP([O-])([O-])=O DKPHLYCEFBDQKM-UHFFFAOYSA-H 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 150000002503 iridium Chemical class 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940071264 lithium citrate Drugs 0.000 description 1
- WJSIUCDMWSDDCE-UHFFFAOYSA-K lithium citrate (anhydrous) Chemical compound [Li+].[Li+].[Li+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WJSIUCDMWSDDCE-UHFFFAOYSA-K 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 235000010292 orthophenyl phenol Nutrition 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GNHOJBNSNUXZQA-UHFFFAOYSA-J potassium aluminium sulfate dodecahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.O.O.[Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GNHOJBNSNUXZQA-UHFFFAOYSA-J 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-UHFFFAOYSA-L potassium sodium tartrate Chemical compound [Na+].[K+].[O-]C(=O)C(O)C(O)C([O-])=O LJCNRYVRMXRIQR-UHFFFAOYSA-L 0.000 description 1
- AVTYONGGKAJVTE-UHFFFAOYSA-L potassium tartrate Chemical compound [K+].[K+].[O-]C(=O)C(O)C(O)C([O-])=O AVTYONGGKAJVTE-UHFFFAOYSA-L 0.000 description 1
- 230000000063 preceeding effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000000837 restrainer Substances 0.000 description 1
- 150000003283 rhodium Chemical class 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229940087562 sodium acetate trihydrate Drugs 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229960001790 sodium citrate Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- NVIFVTYDZMXWGX-UHFFFAOYSA-N sodium metaborate Chemical group [Na+].[O-]B=O NVIFVTYDZMXWGX-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- HELHAJAZNSDZJO-UHFFFAOYSA-L sodium tartrate Chemical compound [Na+].[Na+].[O-]C(=O)C(O)C(O)C([O-])=O HELHAJAZNSDZJO-UHFFFAOYSA-L 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 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 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 150000003475 thallium Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- RSPCKAHMRANGJZ-UHFFFAOYSA-N thiohydroxylamine Chemical compound SN RSPCKAHMRANGJZ-UHFFFAOYSA-N 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 1
- POZPMIFKBAEGSS-UHFFFAOYSA-K trisodium;2-hydroxypropane-1,2,3-tricarboxylate;trihydrate Chemical compound O.O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O POZPMIFKBAEGSS-UHFFFAOYSA-K 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/29—Development processes or agents therefor
- G03C5/30—Developers
Definitions
- the present invention relates to a developing solution for a light-sensitive silver halide photographic material. More particularly, it relates to a developing solution capable of accelerating development to increase sensitivity or speed when developing is carried out, and a method of forming a photographic image making use of the developing solution.
- a first object of the present invention is to provide a novel developing solution for a light-sensitive silver halide photographic material, that may cause less increase in fog, can increase the rate of development and can achieve an increase of speed, and a method of forming a photographic image making use of such a developing solution.
- a second object of the present invention is to provide a developing solution for a light-sensitive silver halide photographic material, that can give a superior running stability and can achieve an increase in effective speed, and a method of forming a photographic image making use of such a developing solution.
- a developing solution for a light-sensitive silver halide photographic material comprising a developing agent, a thioether compound and a compound represented by the following Formula I or II. ##STR2##
- Y, Y 1 and Y 2 each represent a hydrogen atom or a mercapto group
- R and R 1 each represent a hydrogen atom, a halogen atom, a nitro group, an amino group, a cyano group, a hydroxyl group, a mercapto group, a sulfo group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkoxy group, a hydroxycarbonyl group, an alkyl carbonyl group or an alkoxy carbonyl group.
- the light-sensitive silver halide photographic material used in the method of forming a photographic image making use of the above developing solution comprises a silver halide grain having an area ratio of (100) face to (111) face of not less than 5.
- These compounds are known as antifoggants in the field of photography, and can be synthesized by known synthesis methods. Some of the compounds are commercially available as chemical reagents.
- the compound represented by Formula I or II may preferably be added in an amount of from 0.0001 to 2 g per liter of the developing solution.
- the thioether compound used in the present invention may be any of the thioether compounds disclosed in the patent publications previously set out, but may preferably be a compound represented by the following Formula III. ##STR3## wherein A represents an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group which is a group represented by --(CH 2 CH 2 O) p --, --(CH 2 CH 2 O) p --CH 2 CH 2 -- or ##STR4## and not linked to B through an oxygen atom.
- A' represents an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group represented by --(CH 2 CH 2 ) p --CH 2 CH 2 -- or ##STR5## provided that A and A' are not polyalkylene ether groups at the same time.
- the letter symbol p is an integer of 2 to 30.
- B and B' each represent --NH-- or --O--, provided that B and B' are not --O--'s at the same time.
- R 2 represents an alkyl group having 1 to 3 carbon atoms, a phenyl group, an aralkyl group or --(CH 2 ) q --COOR', where q represents an integer of 1 to 3.
- R' represents an alkyl group having 1 to 3 carbon atoms.
- X represents a divalent group selected from --S--, --O--, --CH 2 --, ##STR6## where R N represents an alkyl group having 1 to 3 carbon atoms.
- the compound of Formula III when added in the developing solution, it may preferably be added in an amount of from 0.0001 to 2 g, and particularly from 0.001 to 1 g, per liter of the developing solution.
- the developing agent according to the present invention is used as a liquid developer, i.e., a developing solution.
- a black and white developing agent used in the developing solution includes dihydroxybenzenes as exemplified by hydroquinone, chlorohydroquinone, isopropylhydroquinone, 2,3-dichlorohydroquinone and 2,5-dimethylhydroquinone, 3-pyrasolidones as exemplified by 1-phenyl-3-pyrazolidone, 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone and 1-phenyl 4-methyl-3-pyrazolidone, aminophenols as exemplified by o-aminophenol, p-aminophenol and N-methyl-p-aminophenol, pyrogalol, ascorbic acid, 1-aryl-3-pyrazolidones as exemplified by 1-(p-hydroxyphenyl)-3-aminopyrazolidone, which may be used alone or in combination.
- a black and white developing solution according to the present invention may contain an alkali agent usually used in the developing solution of the above black and white developing agent, which alkali agent is as exemplified by sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium carbonate, potassium carbonate, tertiary phosphate, secondary phosphate, sodium sulfate, sodium metaborate, and borax.
- alkali agent is as exemplified by sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium carbonate, potassium carbonate, tertiary phosphate, secondary phosphate, sodium sulfate, sodium metaborate, and borax.
- an alkali halide as exemplified by potassium bromide, or citrazinic acid or the like as a development regulator, a sulfite or the like as a preservative, and, as a chelating agent, a phosphate such as polyphosphate, an aminopolycarbox
- the black and white developing solution may also contain a developer hardening agent as exemplified by glutaldehyde, ⁇ -methylglutaldehyde, maleicdialdehyde, succinicaldehyde, methylmaleicaldehyde, ⁇ , ⁇ -dimethylglutaldehyde, and an addition compound of any of these with sodium bisulfite. It may further contain a conventionally known development accelerator.
- any of silver halides such as silver bromide, silver chloride, silver iodobromide, silver chlorobromide and silver chloroiodobromide can be used, which are used in usual silver halide emulsions.
- the silver halide may preferably contain 50 mol % or more of silver chloride, and may preferably have a grain size of 0.2 ⁇ m or more and 0.5 ⁇ m or less.
- gelatin On the side of the emulsion layer, gelatin may be contained in an amount of not more than 2.8 g/m 2 , and preferably not more than 2.5 g/m 2 .
- Silver halide grains may be any of those obtained by the acidic method, the neutral method or the ammoniacal method.
- the silver halide grains may be those having a uniform distribution of silver halide composition in a grain, or core/shell grains having different composition between the inner part and surface layer of a grain. They may be grains in which a latent image is mainly formed on the surface of a grain, or those in which a latent image is mainly formed in the inner part of a grain.
- the silver halide grains according to the present invention may have any form. They may preferably contain a silver halide grain having an area ratio of (100) face to (111) face of not less than 5 at the surface thereof.
- the silver halide photographic emulsion grains with an area ratio of (100) face to (111) face of not less than 5 can be prepared by various methods. In general, they can be preferably prepared by what is called controlled double-jet precipitation, which is a method in which an aqueous silver nitrate solution and an aqueous alkali halide solution are simultaneously added at a rate so selected as to be higher than the rate of dissolution of grains and also achieve little renucleation, while keeping the pAg value to a given value of not more than 8.10 during the formation of grains.
- the pAg value is more preferably controlled to be not more than 7.80.
- the formation of silver halide grains is divided into two processes, the formation of nuclei and the growth of nuclei, there are no particular limitations on the pAg value at the time Of the formation of nuclei, and the pAg value at the time of the growth of nuclei may preferably be controlled to be not more than 8.10, and more preferably not more than 7.80.
- the face area ratios can also be controlled by Ostwald ripening. It is also possible to use various restrainers or dyes for regulating crystal habits when grains are formed.
- the reaction between a soluble silver salt and a soluble halide salt may be carried out in the form of single jet precipitation. Double jet precipitation is preferred in order to obtain a good monodispersibility.
- the area ratio of (100) face to (111) face of a silver halide grain can be measured by Kubelka-Munk's dye adsorption method.
- used is a dye that is preferentially adsorbed either on the (100) face or on the (111) face and gives a spectrometrically different state of aggregation between the dye adsorbed on the (100) face and the dye adsorbed on the (III) face.
- the area ratio of (100) face to (111) face can be determined by detailed spectrometry with respect to the amounts of dyes added.
- the silver halide grains relating to the present invention may comprise grains having a single form, or may comprise a mixture of grains having various forms.
- Emulsions having any grain size distribution may be used.
- An emulsion having a broad grain size distribution called a polydisperse emulsion
- an emulsion having a narrow grain size distribution called a monodisperse emulsion
- the polydisperse emulsion and the monodisperse emulsion may be used in a mixed form.
- the silver halide emulsion may be used in the form of a mixture of two or more silver halide emulsions separately formed.
- a monodisperse emulsion is preferred.
- Silver halide grains monodispersed in the monodisperse emulsion may preferably be those in which the weight of silver halide grains included within the grain size range of ⁇ 20% around the average grain size r holds not less than 60%. particularly preferably not less than 70%, and more preferably not less than 80%, based on the total weight of silver halide grains.
- the average grain size r is defined to be a grain size ri determined when ni ⁇ ri 3 , the product of frequencies ni and ri 3 of grains having a grain size ri, comes to be maximum.
- the effective number is three figures, and a minimum figure number is round off.
- the grain size is based on based on the diameters of grains in the case of spherical silver halide grains, and, in the case of grains with shapes other than the spherical shape, the diameters obtained when a projected image of the grain is calculated into a circular image having the same area.
- the grain size can be obtained, for example, by photographing the grains under 10,000 to 50,000 magnifications by means of an electron microscope, and actually measuring the diameters or projected areas of grains on the print. Number of grains to be measured should be not less than 1,000 at random.
- a highly monodisperse emulsion particularly preferred in the method of the present invention, has a degree of monodispersion of not more than 20, and more preferably not more than 15, when it is defined by the expression: ##EQU1##
- the monodisperse emulsion can be obtained by making reference to, for example, Japanese Patent O.P.I. Publications No. 48521/1979, No. 49938/1983 and No. 122935/1985.
- a light-sensitive silver halide emulsion may not be chemically sensitized and can be used as it stands as what is called a primitive emulsion. In usual instances, it is chemically sensitized. In order to carry out chemical sensitization, it is possible to use the method as disclosed in Glafkides, or Zelikman et al's writings, or H. Frieser, Die Gundlagen der Photographischen mit Silberhalogeniden, Akademische Verlagsgesellschaft, 1968.
- sulfur sensitization in which a compound containing sulfur capable of reacting with silver ions or an active gelatin is used, reduction sensitization in which a reducing substance is used, and noble metal sensitization in which gold or other noble metal is used.
- the pH value may preferably be 4 to 9, and particularly 5 to 8.
- the pAg value may preferably be kept at 5 to 11, and particularly 7 to 9.
- the temperature may preferably be 40° to 90° C., and particularly 45° to 75° C.
- the above sulfur sensitization, the gold-sulfur sensitization, as well as the reduction sensitization that uses a reducing substance and the noble metal sensitization that uses a noble metal compound can be used in combination.
- a single kind of emulsion may be used alone, or two or more kinds of emulsions may be mixed. At least one of them may preferably contain the grain having an area ratio of (100) face to (111) face of not less than 5.
- stabilizers can be used after completion of the chemical sensitization described above, which stabilizers include, for example, 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, 5-mercapto-1-phenyltetrazole, and 2-mercaptobenzothiazole. It is also possible to optionally further use a silver halide solvent such as thioether, or a crystal habit modifier such as a mercapto group-containing compound or a sensitizing dye.
- a silver halide solvent such as thioether
- crystal habit modifier such as a mercapto group-containing compound or a sensitizing dye.
- metal ions may be added using a cadmium salt, a zinc salt, a lead salt, a thallium salt, an iridium salt or its complex salt, a rhodium salt or its complex salt, or an iron salt or its complex salt in the course of the formation of grains and/or in the course of the growth of grains so that the metal ions can be incorporated in the inner part and/or the surface of a grain.
- Excess soluble salts may be removed from the emulsion of the present invention after completion of the growth of silver halide grains, or may remain unremoved. When the salts are removed, they can be removed according to the method as disclosed in Research Disclosure No. 17643.
- a sensitizing dye may further be added and used in combination.
- Usable dyes include cyanine dyes, merocyanine dyes, composite cyanine dyes, composite merocyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes, and hemioxanol dyes.
- the sensitizing dye may be used in substantially the same concentration as used in usual negative silver halides.
- the sensitizing dye can be advantageously used in such a concentration that may not substantially lower the inherent sensitivity of a silver halide emulsion.
- the sensitizing dye may preferably be used in a concentration of from about 1.0 ⁇ 10 -5 mol to about 5 ⁇ 10 -4 mol per mol of silver halide, and particularly preferably be used in a concentration of from about 4.0 ⁇ 10 -5 mol to about 2 ⁇ 10 -4 mol per mol of silver halide.
- the sensitizing dye of the present invention can be used alone or in combination of two or more kinds. When the sensitizing dyes are used in combination, they are often used for the purpose of super sensitization.
- the light-sensitive silver halide photographic material relating to the present invention may contain in its hydrophilic colloidal layer a water-soluble dye as a filter dye or for the purposes of anti-irradiation, antihalation and others.
- a water-soluble dye includes oxonol dyes, hemioxonol dyes, styryl dyes, merocyanine dyes, cyanine dyes, and azo dyes.
- oxonol dyes, hemioxanol dyes and merocyanine dyes are useful.
- dyes or ultraviolet absorbents are contained in the hydrophilic colloid layer of the light-sensitive silver halide photographic material, they may be mordanted with a cationic polymer or the like.
- the above photographic emulsion may be incorporated with various compounds for the purpose of preventing a lowering of sensitivity or generation of fog in the course of preparation, during storage or in the course of processing, of light-sensitive materials.
- the light-sensitive silver halide photographic material may also contain in its photographic component layer the alkyl acrylate latex as disclosed in U.S. Pat. Nos. 3,411,911 and 3,411,912, Japanese Patent Examined Publication No. 5331/1970, etc.
- the light-sensitive material may be comprised of, for example, emulsion layers and other photographic component layers coated on one side or both sides of a flexible support usually used in light sensitive materials.
- a flexible support usually used in light sensitive materials.
- a film comprising a semi-synthetic or synthetic polymer such as cellulose nitrate, cellulose acetate, cellulose acetate butyrate, polystyrene, polyvinyl chloride, polyethylene terephthalate, or polycarbonate, and a paper coated or laminated with a baryta layer or an ⁇ -olefin polymer as exemplified by polyethylene, polypropylene or an ethylene/butene copolymer.
- the support may be colored using a dye or pigment.
- the surface of such a support may usually be under-coated so that its adhesion to an emulsion layer can be improved.
- the under coating may preferably be carried out by the treatment as disclosed in Japanese Patent O.P.I. Publications No. 104913/1977, No. 18949/1984, No. 19940/1984 and No. 11941/1984.
- the surface of the support may be subjected to corona discharging, ultraviolet irradiation, flame treating, etc. before or after the under coating.
- an emulsion layer or other hydrophilic colloid layer can be coated on the support or other layer by various coating methods such as dip coating, roller coating, curtain coating and extrusion coating.
- the developing in the present invention is carried out in a development time of 20 seconds or less, and preferably 15 seconds or less.
- the pH of the developing solution of the present invention may preferably be in the range of from 9 to 13, and more preferably in the range of from 9.5 to 12.
- An alkali agent for setting the pH includes pH adjustors such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium tertiary phosphate, and potassium tertiary phosphate.
- a buffer may also be used, including those disclosed in Japanese Patent O.P.I. Publication No. 28708/1986 (borates), Japanese Patent O.P.I. Publication No. 3439/1985, for example, sucrose, acetoxime, and 5-sulfosalicylic acid, phosphates, and carbonates.
- developer time and “fixing time” refer to the time from which a light-sensitive material to be processed is immersed in a developing tank of an automatic processor and before which it is immersed in the next fixing solution, and the time from which it is immersed in a fixing tank and before which it is immersed in the next washing tank or a stabilizing solution, respectively.
- washing time refers to the time during which the light-sensitive photographic material to be processed is immersed in a washing tank.
- drying time refers to the time during which the light sensitive material to be processed is held in a drying zone, which is provided in the automatic processor and in which a hot wind of usually from 35° C. to 100° C., and preferably from 40° C. to 80° C., is blown to the light-sensitive material.
- the developing may preferably be carried out at a temperature of from about 25° C. to about 50° C. and for a period of time of not more than 15 seconds, and more preferably from 30° C. to 40° C. and 6 seconds to 15 seconds.
- the fixing solution may preferably be an aqueous solution containing a thiosulfate and having a pH of 3.8 or more, and more preferably 4.2 to 5.5.
- the fixing solution contains a fixing agent including sodium thiosulfate and ammonium thiosulfate, and commonly contains thiosulfate ions and ammonium ions. Ammonium thiosulfate is particularly preferred from the viewpoint of a fixing speed.
- the amount of the fixing agent used may be appropriately varied, and may commonly range from 0.1 to 0.6 mol/l in approximation.
- the fixing solution may contain a water-soluble aluminum compound that acts as a hardening agent.
- a water-soluble aluminum compound that acts as a hardening agent.
- a compound includes, for example, aluminum chloride, aluminum nitrate, and potassium alum.
- the fixing solution may also contain tartaric acid, citric acid or a derivative of each of them, which may be used alone or in combination of two or more kinds. These compounds ma be effective when contained in an amount of not less than 0.005 mol per liter of the fixing solution, and particularly effective when contained in an amount of from 0.01 mol/l to 0.03 mol/l.
- tartaric acid potassium tartarate, sodium tartarate, sodium potassium tartarate, citric acid, sodium citrate, potassium citrate, lithium citrate, and ammonium citrate.
- the fixing solution may optionally contain a preservative as exemplified by a sulfite and a bisulfite, a pH buffer as exemplified by acetic acid and nitric acid, a pH adjuster as exemplified by sulfuric acid, a chelating agent having a water softening ability.
- Fixing may preferably be carried out ar a temperature of from about 20° C. to about 50° C. and for a period of time of from 6 seconds to 1 minute, more preferably from 30° C. to 40° C. and 6 seconds to 30 seconds, and still more preferably from 30° C. to 40° C. and 6 seconds to 15 seconds.
- the concentrated fixing solution is most preferably comprised of one agent, like the case of the developing solution.
- a fixing stock solution comprised of one agent can be stable when its pH is not less than 4.5, and more preferably not less than 4.65.
- a solution of pH less than 4.5 tends to cause decomposition of a thiosulfate, which finally results in precipitation of sulfur or a sulfide, particularly when the solution is left to stand for a long period of time before it is actually used as a fixing solution.
- sulfite gas can be less generated and also work environment can be improved.
- the upper limit of the pH is not so strict. However, once the fixing is carried out at an excessively high pH, the film pH may increase even if washing is carried out thereafter, resulting in a large film swell and hence a large drying burden. Thus, the upper limit should be about pH 7.
- the upper limit of the pH is 5.5 for the purpose of preventing deposition and precipitation of the aluminum salt.
- the developing solution or fixing solution may be what is called a tank solution, which requires no diluting water as described above, in other words, can be replenished in the form of a stock solution as it is.
- each concentrated solution to a processing tank solution and the mixing proportion thereof to diluting water can be variously changed depending on the composition of a concentrated solution.
- the concentrated solution and the diluting water may be in a proportion of 1:0 to 8, and the total amount of each of these developing solution and fixing solution may preferably be in the range of from 50 ml to 1,500 ml per 1 m 2 of a light-sensitive material.
- the light-sensitive material having been subjected to developing and fixing, is further subjected to washing or stabilizing.
- the washing or stabilizing can be carried out by the application of all methods known in the present field.
- Water that contains various additives known in the present field can also be used as washing water or stabilizing solution.
- Water to which a mildew proofing means has been applied may be used as the washing water or stabilizing solution.
- This not only makes it possible to carry out water-saving processing such that water may be replenished in an amount of not more than 3 l per 1 m 2 of a light-sensitive material, but also makes it unnecessary to provide piping for the installation of an automatic processor and further makes it possible to reduce stock tanks. More specifically, diluting water for preparing a developing solution and a fixing solution and the washing water or the stabilizing solution can be fed from one stock tank used in common, so that the automatic processor can be made more compact.
- the water to which a mildew proofing means has been applied may be used in combination with the washing water or stabilizing solution. This enables effective prevention of fur from being formed. Hence, it is possible to carry out water saving processing in which water is used in an amount of from 0 to 3 l, and preferably from 0 to 1 l, per 1 m 2 of a light-sensitive material.
- the instance in which water is replenished in an amount of zero l refers to an instance in which no water is replenished at all except that water is appropriately replenished only in the amount corresponding to the decrease due to natural evaporation or the like of the washing water in a washing tank, in other words, an instance in which what is called "standing water” processing, where substantially no watter is replenished, is carried out.
- a cascaded or multiple stage counter-current system for example, two stages or three stages is known in the art from old times.
- Application of this multiple stage counter-current system to the present invention facilitates more efficient washing, because a light-sensitive material in the fixing solution can be processed in successive contact with processing solutions in the direction where they are kept cleaner, i.e., with processing solutions not contaminated by the fixing solution.
- This makes it possible to appropriately remove unstable thiosulfates or the like to cause less color change or fading, so that more remarkable stabilization effect can be obtained.
- the washing water can also be made very small in quantity, compared with a conventional method.
- the mildew proofing means that can be used includes the ultraviolet irradiation method as disclosed in Japanese Patent O.P.I. Publication No. 263939/1985, the method in which a magnetic field is used, as disclosed in Japanese Patent O.P.I. Publication No. 263940/1985, the method in which water is purified using an ion exchange resin, as disclosed in Japanese Patent O.P.I. Publication No. 131632/1986, and the method in which a mildew proofing agent is used, as disclosed in Japanese Patent O.P.I Publications No. 115154/1987, No. 153952/1987, No. 220951/1987 and No. 209532/1987.
- the isothiazoline compound as disclosed in R. T. Kreiman, J. Image. Tech., 10, (6) 242 (1984), the isothiazoline compound as disclosed in Research Disclosure, Vol. 205, Item 20526 (May, 1981), the isothiazoline compound as disclosed in the ditto, Vol. 228, Item 22845 (April, 1983), and the compound as disclosed in Japanese Patent O.P.I. Publication No. 209532/1987.
- mildew proofing agent examples include phenol, 4-chlorophenol, pentachlorophenol, cresol, o-phenylphenol, chlorophene, dichlorophene, formaldehyde, glutaldehyde, chloroacetamide, p-hydroxybenzoic acid esters, 2-(4-thiazoline)-benzimidazole, benzoisothiazolin-3-one, dodecyl-benzyl-dimethylammonium chloride, N-(fluorodichloromethylthio)-phthalimide, and 2,4,4'-trichloro-2'-hydroxydiphenyl ether.
- the water to which a mildew proofing means has been applied and held in a water stock tank is added as the diluting water for the processing stock solutions such as the developing solution and the fixing solution, and may preferably be added in an amount of from 0.01 to 10 g/l, and more preferably from 0.1 to 5 g/l.
- Various surface active agents can also be added in the washing water in addition to a silver image stabilizing agent, for the purpose of preventing a wetting non-uniformity.
- a silver image stabilizing agent for the purpose of preventing a wetting non-uniformity.
- Any of cationic, anionic, nonionic or amphoteric types can be used as the surface active agents.
- the surface active agents are the compounds as disclosed, for example, in "KAIMENKASSEIZAI HANDOBUKKU (Surfactant Handbook)", published by Kogaku Tosho K.K.
- various compounds can be added for the purpose of stabilizing an image. They typically include, for example, various buffers used for adjustment of pH in the photographic layers of the light-sensitive material, e.g., pH 3 to 8, such as a borate, a metaborate, borax, phosphate, a carbonate, a potassium hydroxide, sodium hydroxide, ammonia water, monocarboxylic acid, a dicarboxylic acid, a polycarboxylic acid, which are used in suitable combination, and aldehydes such as formalin.
- various buffers used for adjustment of pH in the photographic layers of the light-sensitive material, e.g., pH 3 to 8, such as a borate, a metaborate, borax, phosphate, a carbonate, a potassium hydroxide, sodium hydroxide, ammonia water, monocarboxylic acid, a dicarboxylic acid, a polycarboxylic acid, which are used in suitable combination, and aldehydes such as formalin.
- a chelating agent such as a thiazole type, an isothiazole type, a halogenated phenol, sulfanylamide or benzotriazole, a surface active agent, a fluorescent brightening agent, and a hardening agent may be used.
- a chelating agent such as a thiazole type, an isothiazole type, a halogenated phenol, sulfanylamide or benzotriazole, a surface active agent, a fluorescent brightening agent, and a hardening agent may be used.
- an ammonium salt of various types such as ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium phosphate, ammonium sulfite or ammonium thiosulfate to control the pH in the processed photographic layers of a light-sensitive material.
- the washing or stabilizing according to the above method may preferably be carried out at a temperature of from 0° C. to 50° C. and for a period of time of from 6 seconds to 1 minute, more preferably from 15° C. to 40° C. and from 6 seconds to 30 seconds, and still more preferably from 15° C. to 40° C. and from 6 seconds to 15 seconds.
- a photographic material having been subjected to development, fixing and washing is preferably dried after complete removal of washing water, i.e., after roller squeegeeing.
- the drying can be carried out at about 40° C. to about 100° C. Drying time may be appropriately varied depending on the condition of surroundings. In usual instances, the drying may be carried out for about 5 seconds to 1 minute, and preferably at 40° C. to 80° C. for about 5 seconds to 30 seconds.
- a more desirable effect can be obtained such that the drying time can be shortened with a decrease in the swelling percentage of a light-sensitive photographic material.
- the processing time what is called a dry-to-dry time, ranging from the developing to the fixing, the washing and the drying, may preferably be not longer than 100 seconds, more preferably not longer than 60 seconds, and still more preferably not longer than 50 seconds.
- dry-to-dry time refers to the time from the instant at which the head of a light-sensitive material to be processed enters a film inlet of an automatic processor, to the instant at which the head of the light sensitive material having been processed emerges from the automatic processor.
- Black and white light-sensitive materials to which the developing solution containing the compound of the present invention may be any of commonly available light-sensitive silver halide photographic materials such as black and white light-sensitive photographic materials for ordinary photographying, light-sensitive photographic materials for X-rays, light-sensitive photographic materials for graphic art, light-sensitive photographic materials for medical use, light-sensitive photographic material for motion pictures, light-sensitive photographic materials for aerial photography, and light-sensitive photographic materials for TV.
- light-sensitive silver halide photographic materials such as black and white light-sensitive photographic materials for ordinary photographying, light-sensitive photographic materials for X-rays, light-sensitive photographic materials for graphic art, light-sensitive photographic materials for medical use, light-sensitive photographic material for motion pictures, light-sensitive photographic materials for aerial photography, and light-sensitive photographic materials for TV.
- a graphic art film comprising a support coated with a silver chlorobromide emulsion was exposed to light through a contact screen according to usual sensitometry.
- the exposed film was developed at 38° C. for 13 seconds using a developing solution 1 having the following composition and to which the compound represented by Formula I as shown in Table 1 was added.
- the emulsion used in the film was comprised of silver chlorobromide grains containing 75 mol % of silver chloride and the grain had an area ratio of (100) face to (111) face of 98:2.
- a developing solution was prepared by adding in the developing solution 1 the thioether compound of Formula III as shown in Table 1.
- the developing solutions thus prepared all had a pH ranging from 10.7 to 10.8.
- Fixing was carried out using the following fixing solution.
- Results obtained by sensitometry are shown in Table 1.
- the sensitivity or speed is expressed as a relative speed regarding as 100 the speed obtained using the developing solution No. 1-2 shown in Table 1.
- Running stability was evaluated by processing 50 sheets per day of exposed films of 508 mm ⁇ 610 mm in size and measuring photographic performance at the time the processing was started, on 7th day, and on 14th day.
- Halftone dot quality was visually evaluated according to five grades, where "5" indicates the best, and "1", the worst in quality. As halftone dots for lithography, the grades “5" and “4" are feasible for practical use; “3”, a lower limit for practical use; and “2" and "1”, infeasible for practical use.
- a graphic art film coated with a silver chlorobromide emulsion was exposed to light in the same manner as in Example 1.
- the exposed film was developed at 38° C. for 13 seconds using a developing solution 2 having the following composition and to which the compound represented by Formula I as shown in Table 2 was added. Fixing was carried out in the same manner as in Example 1.
- the emulsion used in the graphic art film was comprised of silver chlorobromide grains containing 90 mol % of silver chloride and the grain had a area ratio of (100) face to (111) face of 100:0.
- the following antihalation dyes (A), (B) and (C) were added so that the coating weights of the dyes were 80 mg/m 2 , 50 mg/m 2 and 100 mg/m 2 , respectively.
- an aqueous solution of silver nitrate and an aqueous mixed solution comprising potassium bromide and sodium chloride to which 5 ⁇ 10 -7 mol of potassium hexachloroiridate and 6 ⁇ 10 -8 of potassium hexabromorhodate were added were added by double-jet precipitation.
- Silver chlorobromide grains containing 35 mol % of silver bromide were thus prepared while maintaining the pH to 3.0 and the pAg to 7.7. After the pH was returned to 5 9, desalting was carried out by a conventional method.
- the silver halide grains thus obtained were comprised of cubic grains with a degree of monodispersion of 9% and an average grain size of 0.25 ⁇ m, and the grain had an area ratio of (100) face to (111) face of 98:2.
- the emulsion thus obtained was subjected to gold sensitization and sulfur sensitization, a sensitizing dye (a) was thereafter added in an amount of 60 mg per mole of silver halide, and then 70 mg of 1-phenyl-5-mercaptotetrazole per mol of silver halide, 1.2 g of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene per mol of silver halide, and gelatin were added to stop the chemical ripening.
- a sensitizing dye (a) was thereafter added in an amount of 60 mg per mole of silver halide, and then 70 mg of 1-phenyl-5-mercaptotetrazole per mol of silver halide, 1.2 g of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene per mol of silver halide, and gelatin were added to stop the chemical ripening.
- a 100 ⁇ m thick polyethylene terephthalate film base was provided with a back-surface under layer and a back-surface upper layer by simultaneous multilayer coating, and subsequently, on its opposite side to the back-surface layers, provided with an emulsion layer and a protective layer by simultaneous multilayer coating.
- the coating weight of silver was 3.8 g/m 2 and the gelatin was in an amount of 1.8 g/m 2 for the emulsion layer and 1.0 g g/m 2 for the protective layer.
- Samples thus obtained were exposed to light through a contact screen in the same manner as Example 1, and processed by means of a usual roller-type automatic processor under the following conditions.
- Processing was carried out using the same developing solution as the developing solution 1 as in Example 1 to which the compound of Formula I was added.
- the compound of Formula I was added as shown in Table I, in an amount as also shown in Table 1. Further, developing solutions each having various pH values as shown in Table 3 were prepared by controlling the amount of potassium hydroxide.
- Results obtained by sensitometry are shown in Table 3.
- the speed is expressed as a relative speed regarding as 100 the speed obtained using the developing solution No. 3-1 shown in Table 3.
- Example 3 Three kinds of emulsions were prepared in the same manner as in Example 3 except that they were each varied in the area ratio of (110) to (111) as shown in Table 4 by control of pAg value and use of a grain growing controlling agent. Samples were prepared each using thus obtained emulsions and processed in the same manner as in Example 3. In the processing, developing solution 3-3 of Example 3 was used which contained 150 mg/l of compound I-2 and 25 mg/l of compound III-5 and had a pH value of 10.78. Development was carried out for 12.4 seconds.
- an aqueous solution of silver nitrate and an aqueous mixed solution comprising potassium bromide and sodium chloride to which 5 ⁇ 10 -7 mol of potassium hexachloroiridate and 6 ⁇ 10 -8 of potassium hexabromorhodate were added were added by double-jet precipitation.
- Silver chlorobromide grains containing 35 mol % of silver bromide were thus prepared while maintaining the pH to 3.0 and the pAg to 7.7. After the pH was returned to 5.9, desalting was carried out by a conventional method.
- the silver halide grains thus obtained were comprised of cubic grains with a degree of monodispersion of 9% and an average grain size of 0.25 ⁇ m.
- the emulsion thus obtained was subjected to gold sensitization and sulfur sensitization, a sensitizing dye (a) was thereafter added in an amount of 240 mg per mole of silver halide, and then 70 mg of 1-phenyl-5-mercaptotetrazole per mol of silver halide, 1.2 g of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, and gelatin were added to stop the chemical ripening. Thereafter.
- the resulting emulsion was coated on a subbed polyethylene terephthalate film base so as to give a silver weight of 4.3 g/m 2 and a gelatin weight of 2.5 g/m 2 , and the same protective layer coating solution as the one prepared in Example 3 was further coated so as to give a gelatin weight of 1.0 g/m 2 .
- An emulsion layer and a protective layer was thus provided by simultaneous coating.
- Example 5 Samples thus obtained were processed and evaluated in the same manner as in Example 3 except that in the developing solution the compound of Formula I used in Example 3 was replaced with the compound of Formula II.
- the composition of each developing solution and the results of evaluation are shown in Table 5.
- the developing solutions all had a pH ranging from 10.7 to 10.8.
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Abstract
A developer for developing a silver halide light-sensitive material and an image forming method using the developer are disclosed. The developer contains a compound represented by the following formula I or II and a compound containing a thioether group. ##STR1## wherein Y, Y1 and Y2 are each a hydrogen atom or a mercapto group, and R and R1 are each a substituent. A silver halide light-sensitive material containing silver halide grains comprising not less than 50 mol % of silver chloride and have a ratio of (100) surface and (111) surface of not less than 5 is preferably used in the image forming method. Developing speed and sensitivity of light-sensitive material can be rised by use of the developer.
Description
The present invention relates to a developing solution for a light-sensitive silver halide photographic material. More particularly, it relates to a developing solution capable of accelerating development to increase sensitivity or speed when developing is carried out, and a method of forming a photographic image making use of the developing solution.
In the development of light-sensitive silver halide photographic materials, it is desired to accelerate the rate of development and to increase speed without degrading anti fogging properties or graininess of the light-sensitive silver halide photographic materials. For such purposes, methods for the acceleration of development have been hitherto proposed in a large number. Well known as compounds capable of accelerating development by their addition in developing solutions are polyalkylene oxide compounds as exemplified by the compounds as disclosed in U.S. Pat. Nos. 2,531,832, 2,950,970, 3,291,607, 3,495,981, 3,671,247, 3,915,710 and 3,996,054, etc.; thioether compounds as exemplified by the compounds as disclosed in U.S. Pat. Nos. 3,046,129, 3,201,242 and 3,271,157, British Patents No. 1,129,085 and No. 1,129,086, Japanese Patent Publication Open to Public Inspection (hereinafter referred to as Japanese Patent O.P.I. Publication) No. 207045/1983, etc.; and also onium and polyonium compounds of an ammonium, phosphonium or sulfonium type. Most of these development accelerators, however, tend to increase fog of a light-sensitive photographic material and even to make its graininess rough. In addition, some of them have the disadvantage that they bring about a poor running stability of developer. Under such existing circumstances, they have been little put into practical use.
On the other hand, there is a method in which these development accelerators are incorporated into light sensitive silver halide photographic materials so that the speed can be increased. In such an instance, however, the storage stability of light-sensitive silver halide photographic materials may be deteriorated, causing, in particular, the problem of an increase in fog with time.
To cope with the above problems, a first object of the present invention is to provide a novel developing solution for a light-sensitive silver halide photographic material, that may cause less increase in fog, can increase the rate of development and can achieve an increase of speed, and a method of forming a photographic image making use of such a developing solution.
A second object of the present invention is to provide a developing solution for a light-sensitive silver halide photographic material, that can give a superior running stability and can achieve an increase in effective speed, and a method of forming a photographic image making use of such a developing solution.
The above objects can be achieved by a developing solution for a light-sensitive silver halide photographic material, comprising a developing agent, a thioether compound and a compound represented by the following Formula I or II. ##STR2##
In Formulas I and II, Y, Y1 and Y2 each represent a hydrogen atom or a mercapto group; R and R1 each represent a hydrogen atom, a halogen atom, a nitro group, an amino group, a cyano group, a hydroxyl group, a mercapto group, a sulfo group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkoxy group, a hydroxycarbonyl group, an alkyl carbonyl group or an alkoxy carbonyl group.
The light-sensitive silver halide photographic material used in the method of forming a photographic image making use of the above developing solution comprises a silver halide grain having an area ratio of (100) face to (111) face of not less than 5.
Typical examples of the compound represented by Formula I or II are shown below, but by no means limited to these.
I-1: Benzotriazole
I-2: 5-Methylbenzotriazole
I-3: 5-Chlorobenzotriazole
I-4: 5-Nitrobenzotriazole
I-5: 5-Ethylbenzotriazole
I-6: 5-Carboxybenzotriazole
I-7: 5-Hydroxybenzotriazole
I-8: 5-Aminobenzotriazole
I-9: 5-Sulfobenzotriazole
I-10: 5-Cyanobenzotriazole
I-11: 5-Ethoxybenzotriazole
I-12: 5-Ethoxybenzotriazole
I-13: 5-Mercaptobenzotriazole
II-1: 5-Benzimidazole
II-2: 5-Sulfobenzimidazole
II-3: 5-Methoxybenzimidazole
II-4: 5-Chlorobenzimidazole
II-5: 5-Nitrobenzimidazole
II-6: 2-Mercapto-5-sulfobenzimidazole
These compounds are known as antifoggants in the field of photography, and can be synthesized by known synthesis methods. Some of the compounds are commercially available as chemical reagents.
The compound represented by Formula I or II may preferably be added in an amount of from 0.0001 to 2 g per liter of the developing solution.
The thioether compound used in the present invention may be any of the thioether compounds disclosed in the patent publications previously set out, but may preferably be a compound represented by the following Formula III. ##STR3## wherein A represents an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group which is a group represented by --(CH2 CH2 O)p --, --(CH2 CH2 O)p --CH2 CH2 -- or ##STR4## and not linked to B through an oxygen atom. A' represents an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group represented by --(CH2 CH2)p --CH2 CH2 -- or ##STR5## provided that A and A' are not polyalkylene ether groups at the same time. The letter symbol p is an integer of 2 to 30.
B and B' each represent --NH-- or --O--, provided that B and B' are not --O--'s at the same time.
R2 represents an alkyl group having 1 to 3 carbon atoms, a phenyl group, an aralkyl group or --(CH2)q --COOR', where q represents an integer of 1 to 3.
R' represents an alkyl group having 1 to 3 carbon atoms.
X represents a divalent group selected from --S--, --O--, --CH2 --, ##STR6## where RN represents an alkyl group having 1 to 3 carbon atoms.
Typical examples of the compound of the present invention are shown below. The compound of the present invention is by no means limited to these. ##STR7##
In the present invention, when the compound of Formula III is added in the developing solution, it may preferably be added in an amount of from 0.0001 to 2 g, and particularly from 0.001 to 1 g, per liter of the developing solution.
The developing agent according to the present invention is used as a liquid developer, i.e., a developing solution. A black and white developing agent used in the developing solution includes dihydroxybenzenes as exemplified by hydroquinone, chlorohydroquinone, isopropylhydroquinone, 2,3-dichlorohydroquinone and 2,5-dimethylhydroquinone, 3-pyrasolidones as exemplified by 1-phenyl-3-pyrazolidone, 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone and 1-phenyl 4-methyl-3-pyrazolidone, aminophenols as exemplified by o-aminophenol, p-aminophenol and N-methyl-p-aminophenol, pyrogalol, ascorbic acid, 1-aryl-3-pyrazolidones as exemplified by 1-(p-hydroxyphenyl)-3-aminopyrazolidone, which may be used alone or in combination.
A black and white developing solution according to the present invention may contain an alkali agent usually used in the developing solution of the above black and white developing agent, which alkali agent is as exemplified by sodium hydroxide, potassium hydroxide, ammonium hydroxide, sodium carbonate, potassium carbonate, tertiary phosphate, secondary phosphate, sodium sulfate, sodium metaborate, and borax. It may further contain an alkali halide as exemplified by potassium bromide, or citrazinic acid or the like as a development regulator, a sulfite or the like as a preservative, and, as a chelating agent, a phosphate such as polyphosphate, an aminopolycarboxylic acid such as nitrilotriacetic acid or 1,3-diamino 2-propanoltetraacetic acid, an oxycarboxylic acid such as citric acid or gluconic acid or an organic phosphonic acid such as 1-hydroxyethylidiene-1,1-disulfonic acid or aminotri(methylenephosphonio acid).
The black and white developing solution may also contain a developer hardening agent as exemplified by glutaldehyde, α-methylglutaldehyde, maleicdialdehyde, succinicaldehyde, methylmaleicaldehyde, α,α-dimethylglutaldehyde, and an addition compound of any of these with sodium bisulfite. It may further contain a conventionally known development accelerator.
As a silver halide contained in a silver halide emulsion layer of the light-sensitive material to be developed with the developing solution of the present invention, any of silver halides such as silver bromide, silver chloride, silver iodobromide, silver chlorobromide and silver chloroiodobromide can be used, which are used in usual silver halide emulsions. The silver halide may preferably contain 50 mol % or more of silver chloride, and may preferably have a grain size of 0.2 μm or more and 0.5 μm or less. On the side of the emulsion layer, gelatin may be contained in an amount of not more than 2.8 g/m2, and preferably not more than 2.5 g/m2.
Silver halide grains may be any of those obtained by the acidic method, the neutral method or the ammoniacal method.
The silver halide grains may be those having a uniform distribution of silver halide composition in a grain, or core/shell grains having different composition between the inner part and surface layer of a grain. They may be grains in which a latent image is mainly formed on the surface of a grain, or those in which a latent image is mainly formed in the inner part of a grain.
The silver halide grains according to the present invention may have any form. They may preferably contain a silver halide grain having an area ratio of (100) face to (111) face of not less than 5 at the surface thereof.
The silver halide photographic emulsion grains with an area ratio of (100) face to (111) face of not less than 5 can be prepared by various methods. In general, they can be preferably prepared by what is called controlled double-jet precipitation, which is a method in which an aqueous silver nitrate solution and an aqueous alkali halide solution are simultaneously added at a rate so selected as to be higher than the rate of dissolution of grains and also achieve little renucleation, while keeping the pAg value to a given value of not more than 8.10 during the formation of grains. The pAg value is more preferably controlled to be not more than 7.80. When the formation of silver halide grains is divided into two processes, the formation of nuclei and the growth of nuclei, there are no particular limitations on the pAg value at the time Of the formation of nuclei, and the pAg value at the time of the growth of nuclei may preferably be controlled to be not more than 8.10, and more preferably not more than 7.80. The face area ratios can also be controlled by Ostwald ripening. It is also possible to use various restrainers or dyes for regulating crystal habits when grains are formed. The reaction between a soluble silver salt and a soluble halide salt may be carried out in the form of single jet precipitation. Double jet precipitation is preferred in order to obtain a good monodispersibility.
It is also possible to prepare grains having a crystal form such as an octahedron, a tetradecahedron or a dodecahedron, using the methods as described in U.S. Pat. Nos. 4,183,756 and 4,225,666, Japanese Patent Publication Open to Public Inspection (hereinafter referred to as Japanese Patent O.P.I. Publication) No. 26589/1980, Japanese Patent Examined Publication No. 42737/1980, and The Journal of Photographic Science (J. Photgr. Sci.) 21, 39(1973), and use the resulting grains. Grains having a twin plane may also be used.
The area ratio of (100) face to (111) face of a silver halide grain can be measured by Kubelka-Munk's dye adsorption method. In this method, used is a dye that is preferentially adsorbed either on the (100) face or on the (111) face and gives a spectrometrically different state of aggregation between the dye adsorbed on the (100) face and the dye adsorbed on the (III) face. The area ratio of (100) face to (111) face can be determined by detailed spectrometry with respect to the amounts of dyes added.
Detailed proportions of the (100) face on the surface of a silver halide grain can be determined by the method as disclosed in Tadaaki Tani, "Identification of Crystal Phases of Silver Halide Grains in Photographic Emulsions That Utilizes Adsorption of Dyes", Journal of Chemical Society of Japan, 6, 942-946 (1984).
The silver halide grains relating to the present invention may comprise grains having a single form, or may comprise a mixture of grains having various forms.
Emulsions having any grain size distribution may be used. An emulsion having a broad grain size distribution, called a polydisperse emulsion, may be used, or an emulsion having a narrow grain size distribution, called a monodisperse emulsion, may be used alone or in the form of a mixture of several kinds. Alternatively, the polydisperse emulsion and the monodisperse emulsion may be used in a mixed form.
The silver halide emulsion may be used in the form of a mixture of two or more silver halide emulsions separately formed.
In the method of the present invention, a monodisperse emulsion is preferred. Silver halide grains monodispersed in the monodisperse emulsion may preferably be those in which the weight of silver halide grains included within the grain size range of ±20% around the average grain size r holds not less than 60%. particularly preferably not less than 70%, and more preferably not less than 80%, based on the total weight of silver halide grains.
Here, the average grain size r is defined to be a grain size ri determined when ni×ri3, the product of frequencies ni and ri3 of grains having a grain size ri, comes to be maximum. The effective number is three figures, and a minimum figure number is round off.
In the present specification, the grain size is based on based on the diameters of grains in the case of spherical silver halide grains, and, in the case of grains with shapes other than the spherical shape, the diameters obtained when a projected image of the grain is calculated into a circular image having the same area.
The grain size can be obtained, for example, by photographing the grains under 10,000 to 50,000 magnifications by means of an electron microscope, and actually measuring the diameters or projected areas of grains on the print. Number of grains to be measured should be not less than 1,000 at random.
A highly monodisperse emulsion, particularly preferred in the method of the present invention, has a degree of monodispersion of not more than 20, and more preferably not more than 15, when it is defined by the expression: ##EQU1##
Here, the average grain size and the grain size standard deviation is determined from the above definition. The monodisperse emulsion can be obtained by making reference to, for example, Japanese Patent O.P.I. Publications No. 48521/1979, No. 49938/1983 and No. 122935/1985.
A light-sensitive silver halide emulsion may not be chemically sensitized and can be used as it stands as what is called a primitive emulsion. In usual instances, it is chemically sensitized. In order to carry out chemical sensitization, it is possible to use the method as disclosed in Glafkides, or Zelikman et al's writings, or H. Frieser, Die Gundlagen der Photographischen Prozesse mit Silberhalogeniden, Akademische Verlagsgesellschaft, 1968.
More specifically, it is possible to use sulfur sensitization in which a compound containing sulfur capable of reacting with silver ions or an active gelatin is used, reduction sensitization in which a reducing substance is used, and noble metal sensitization in which gold or other noble metal is used.
There are no particular limitations on the conditions such as pH, pAg and temperature when chemical sensitization is carried out. The pH value may preferably be 4 to 9, and particularly 5 to 8. The pAg value may preferably be kept at 5 to 11, and particularly 7 to 9. The temperature may preferably be 40° to 90° C., and particularly 45° to 75° C.
In the silver halide emulsion used in the present invention, the above sulfur sensitization, the gold-sulfur sensitization, as well as the reduction sensitization that uses a reducing substance and the noble metal sensitization that uses a noble metal compound can be used in combination.
As a light sensitive emulsion, a single kind of emulsion may be used alone, or two or more kinds of emulsions may be mixed. At least one of them may preferably contain the grain having an area ratio of (100) face to (111) face of not less than 5.
Various stabilizers can be used after completion of the chemical sensitization described above, which stabilizers include, for example, 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, 5-mercapto-1-phenyltetrazole, and 2-mercaptobenzothiazole. It is also possible to optionally further use a silver halide solvent such as thioether, or a crystal habit modifier such as a mercapto group-containing compound or a sensitizing dye.
To the silver halide grains used in the emulsion, metal ions may be added using a cadmium salt, a zinc salt, a lead salt, a thallium salt, an iridium salt or its complex salt, a rhodium salt or its complex salt, or an iron salt or its complex salt in the course of the formation of grains and/or in the course of the growth of grains so that the metal ions can be incorporated in the inner part and/or the surface of a grain.
Excess soluble salts may be removed from the emulsion of the present invention after completion of the growth of silver halide grains, or may remain unremoved. When the salts are removed, they can be removed according to the method as disclosed in Research Disclosure No. 17643.
In the emulsion, a sensitizing dye may further be added and used in combination. Usable dyes include cyanine dyes, merocyanine dyes, composite cyanine dyes, composite merocyanine dyes, holopolar cyanine dyes, hemicyanine dyes, styryl dyes, and hemioxanol dyes.
The sensitizing dye may be used in substantially the same concentration as used in usual negative silver halides. In particular, the sensitizing dye can be advantageously used in such a concentration that may not substantially lower the inherent sensitivity of a silver halide emulsion. The sensitizing dye may preferably be used in a concentration of from about 1.0×10-5 mol to about 5×10-4 mol per mol of silver halide, and particularly preferably be used in a concentration of from about 4.0×10-5 mol to about 2×10-4 mol per mol of silver halide.
The sensitizing dye of the present invention can be used alone or in combination of two or more kinds. When the sensitizing dyes are used in combination, they are often used for the purpose of super sensitization.
The light-sensitive silver halide photographic material relating to the present invention may contain in its hydrophilic colloidal layer a water-soluble dye as a filter dye or for the purposes of anti-irradiation, antihalation and others. Such a dye includes oxonol dyes, hemioxonol dyes, styryl dyes, merocyanine dyes, cyanine dyes, and azo dyes. In particular, oxonol dyes, hemioxanol dyes and merocyanine dyes are useful.
In instances in which dyes or ultraviolet absorbents are contained in the hydrophilic colloid layer of the light-sensitive silver halide photographic material, they may be mordanted with a cationic polymer or the like.
The above photographic emulsion may be incorporated with various compounds for the purpose of preventing a lowering of sensitivity or generation of fog in the course of preparation, during storage or in the course of processing, of light-sensitive materials.
The light-sensitive silver halide photographic material may also contain in its photographic component layer the alkyl acrylate latex as disclosed in U.S. Pat. Nos. 3,411,911 and 3,411,912, Japanese Patent Examined Publication No. 5331/1970, etc.
In the light-sensitive material, various additives can be further used depending on the purpose. These additives are more detailed in Research Disclosures Vol 176, Item 17643 (December, 1978) and Vol. 187, Item 18716 (November, 1976). Corresponding passages thereof are summarized in the following table.
______________________________________
Type of additives
RD 17643 RD 18716
______________________________________
1. Chemical sensitizer
p.23 p.648, right col.
2. Speed-increasing agent p.648, right col.
3. Spectral sensitizer
pp.23-24 p.648, right
Supersensitizer col. to p.649,
right col.
4. Brightening agent
p.24
5. Antifoggant and
pp.24-25 p.649, right col.
stabilizer
6. Light-absorbent
pp.25-26 p.649, right
Filter dye col. to p.650,
Ultraviolet absorbent left col.
7. Anti-stain agent
p.25, p.650, left col.
right col.
to right col.
8. Dye-image stabilizer
p.25
9. Hardening agent
p.26 p.651, left col.
10. Binder p.26 p.651, left col.
11. Plasticizer, lubricant
p.27 p.650, right col.
12. Coating aid pp.26-27 p.650, right col.
Surfactant
13. Antistatic agent
p.27 p.650, right col.
______________________________________
The light-sensitive material may be comprised of, for example, emulsion layers and other photographic component layers coated on one side or both sides of a flexible support usually used in light sensitive materials. Useful as the flexible support are a film comprising a semi-synthetic or synthetic polymer such as cellulose nitrate, cellulose acetate, cellulose acetate butyrate, polystyrene, polyvinyl chloride, polyethylene terephthalate, or polycarbonate, and a paper coated or laminated with a baryta layer or an α-olefin polymer as exemplified by polyethylene, polypropylene or an ethylene/butene copolymer. The support may be colored using a dye or pigment. It may be black for the purpose of light shading. The surface of such a support may usually be under-coated so that its adhesion to an emulsion layer can be improved. The under coating may preferably be carried out by the treatment as disclosed in Japanese Patent O.P.I. Publications No. 104913/1977, No. 18949/1984, No. 19940/1984 and No. 11941/1984.
The surface of the support may be subjected to corona discharging, ultraviolet irradiation, flame treating, etc. before or after the under coating.
In the light-sensitive material, an emulsion layer or other hydrophilic colloid layer can be coated on the support or other layer by various coating methods such as dip coating, roller coating, curtain coating and extrusion coating.
The developing in the present invention is carried out in a development time of 20 seconds or less, and preferably 15 seconds or less.
The pH of the developing solution of the present invention may preferably be in the range of from 9 to 13, and more preferably in the range of from 9.5 to 12.
An alkali agent for setting the pH includes pH adjustors such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium tertiary phosphate, and potassium tertiary phosphate.
A buffer may also be used, including those disclosed in Japanese Patent O.P.I. Publication No. 28708/1986 (borates), Japanese Patent O.P.I. Publication No. 3439/1985, for example, sucrose, acetoxime, and 5-sulfosalicylic acid, phosphates, and carbonates.
In the present invention, the terms "developing time" and "fixing time" refer to the time from which a light-sensitive material to be processed is immersed in a developing tank of an automatic processor and before which it is immersed in the next fixing solution, and the time from which it is immersed in a fixing tank and before which it is immersed in the next washing tank or a stabilizing solution, respectively.
The term "washing time" refers to the time during which the light-sensitive photographic material to be processed is immersed in a washing tank.
The term "drying time" refers to the time during which the light sensitive material to be processed is held in a drying zone, which is provided in the automatic processor and in which a hot wind of usually from 35° C. to 100° C., and preferably from 40° C. to 80° C., is blown to the light-sensitive material.
The developing may preferably be carried out at a temperature of from about 25° C. to about 50° C. and for a period of time of not more than 15 seconds, and more preferably from 30° C. to 40° C. and 6 seconds to 15 seconds.
The fixing solution may preferably be an aqueous solution containing a thiosulfate and having a pH of 3.8 or more, and more preferably 4.2 to 5.5.
The fixing solution contains a fixing agent including sodium thiosulfate and ammonium thiosulfate, and commonly contains thiosulfate ions and ammonium ions. Ammonium thiosulfate is particularly preferred from the viewpoint of a fixing speed. The amount of the fixing agent used may be appropriately varied, and may commonly range from 0.1 to 0.6 mol/l in approximation.
The fixing solution may contain a water-soluble aluminum compound that acts as a hardening agent. Such a compound includes, for example, aluminum chloride, aluminum nitrate, and potassium alum.
The fixing solution may also contain tartaric acid, citric acid or a derivative of each of them, which may be used alone or in combination of two or more kinds. These compounds ma be effective when contained in an amount of not less than 0.005 mol per liter of the fixing solution, and particularly effective when contained in an amount of from 0.01 mol/l to 0.03 mol/l.
They specifically include tartaric acid, potassium tartarate, sodium tartarate, sodium potassium tartarate, citric acid, sodium citrate, potassium citrate, lithium citrate, and ammonium citrate.
The fixing solution may optionally contain a preservative as exemplified by a sulfite and a bisulfite, a pH buffer as exemplified by acetic acid and nitric acid, a pH adjuster as exemplified by sulfuric acid, a chelating agent having a water softening ability.
Fixing may preferably be carried out ar a temperature of from about 20° C. to about 50° C. and for a period of time of from 6 seconds to 1 minute, more preferably from 30° C. to 40° C. and 6 seconds to 30 seconds, and still more preferably from 30° C. to 40° C. and 6 seconds to 15 seconds.
In an instance in which a concentrated fixing solution is replenished together with its diluting water with progress of the processing of a light-sensitive photographic material in an automatic processor, the concentrated fixing solution is most preferably comprised of one agent, like the case of the developing solution.
A fixing stock solution comprised of one agent can be stable when its pH is not less than 4.5, and more preferably not less than 4.65. A solution of pH less than 4.5 tends to cause decomposition of a thiosulfate, which finally results in precipitation of sulfur or a sulfide, particularly when the solution is left to stand for a long period of time before it is actually used as a fixing solution. Hence, in the pH range of not less than pH 4.5, sulfite gas can be less generated and also work environment can be improved. The upper limit of the pH is not so strict. However, once the fixing is carried out at an excessively high pH, the film pH may increase even if washing is carried out thereafter, resulting in a large film swell and hence a large drying burden. Thus, the upper limit should be about pH 7. In the case when an aluminum salt is used in the fixing solution and a gelatin layer is thereby hardened, the upper limit of the pH is 5.5 for the purpose of preventing deposition and precipitation of the aluminum salt.
In the present invention, the developing solution or fixing solution may be what is called a tank solution, which requires no diluting water as described above, in other words, can be replenished in the form of a stock solution as it is.
The feed of each concentrated solution to a processing tank solution and the mixing proportion thereof to diluting water can be variously changed depending on the composition of a concentrated solution. In general, the concentrated solution and the diluting water may be in a proportion of 1:0 to 8, and the total amount of each of these developing solution and fixing solution may preferably be in the range of from 50 ml to 1,500 ml per 1 m2 of a light-sensitive material.
In the present invention the light-sensitive material, having been subjected to developing and fixing, is further subjected to washing or stabilizing.
The washing or stabilizing can be carried out by the application of all methods known in the present field. Water that contains various additives known in the present field can also be used as washing water or stabilizing solution. Water to which a mildew proofing means has been applied may be used as the washing water or stabilizing solution. This not only makes it possible to carry out water-saving processing such that water may be replenished in an amount of not more than 3 l per 1 m2 of a light-sensitive material, but also makes it unnecessary to provide piping for the installation of an automatic processor and further makes it possible to reduce stock tanks. More specifically, diluting water for preparing a developing solution and a fixing solution and the washing water or the stabilizing solution can be fed from one stock tank used in common, so that the automatic processor can be made more compact.
The water to which a mildew proofing means has been applied may be used in combination with the washing water or stabilizing solution. This enables effective prevention of fur from being formed. Hence, it is possible to carry out water saving processing in which water is used in an amount of from 0 to 3 l, and preferably from 0 to 1 l, per 1 m2 of a light-sensitive material.
Here, the instance in which water is replenished in an amount of zero l refers to an instance in which no water is replenished at all except that water is appropriately replenished only in the amount corresponding to the decrease due to natural evaporation or the like of the washing water in a washing tank, in other words, an instance in which what is called "standing water" processing, where substantially no watter is replenished, is carried out.
As a method by which the amount of replenishment is saved, a cascaded or multiple stage counter-current system, for example, two stages or three stages is known in the art from old times. Application of this multiple stage counter-current system to the present invention facilitates more efficient washing, because a light-sensitive material in the fixing solution can be processed in successive contact with processing solutions in the direction where they are kept cleaner, i.e., with processing solutions not contaminated by the fixing solution. This makes it possible to appropriately remove unstable thiosulfates or the like to cause less color change or fading, so that more remarkable stabilization effect can be obtained. The washing water can also be made very small in quantity, compared with a conventional method.
When washing is carried out using a small amount of water, it is more preferred to provide the squeesee roller washing tank as disclosed in Japanese Patent O.P.I. Publication No. 32460/1987.
Part or the whole of a solution resultingly overflowed from a washing or stabilizing bath when the washing or stabilizing bath is replenished as processing proceeds, with the water to which a mildew proofing means has been applied, can be utilized as a processing solution having a fixing ability, used in the preceeding processing step, as disclosed in Japanese Patent O.P.I. Publication No. 235133/1985. Thus, the above stock water can be saved and moreover waste liquor can be more decreased. This is hence more preferred.
The mildew proofing means that can be used includes the ultraviolet irradiation method as disclosed in Japanese Patent O.P.I. Publication No. 263939/1985, the method in which a magnetic field is used, as disclosed in Japanese Patent O.P.I. Publication No. 263940/1985, the method in which water is purified using an ion exchange resin, as disclosed in Japanese Patent O.P.I. Publication No. 131632/1986, and the method in which a mildew proofing agent is used, as disclosed in Japanese Patent O.P.I Publications No. 115154/1987, No. 153952/1987, No. 220951/1987 and No. 209532/1987.
It is possible to use in combination, the microbiocide, mildew proofing agent, surface active agent, etc. as disclosed in L. E. West, Water Quality Criteria, Photo Sci. & Eng., Vol. 9, No. 6 (1965); M. W. Beach, Miorobiological Growth in Motion-Picture Processing, SMPTE Journal, Vol. 85 (1976); R. O. Deegan, Photo Processing Wash Water Biocides, J. Imaging Tech., Vol. 10, No. 6 (1984); and Japanese Patent O.P.I. Publications No. 8542/1982, No. 58143/1982, No 105145/1983, No. 132146/1982, No. 18631/1983, No. 97530/1982 and No. 157214/1982.
In the washing bath, it is also possible to use as a microbiocide in combination, the isothiazoline compound as disclosed in R. T. Kreiman, J. Image. Tech., 10, (6) 242 (1984), the isothiazoline compound as disclosed in Research Disclosure, Vol. 205, Item 20526 (May, 1981), the isothiazoline compound as disclosed in the ditto, Vol. 228, Item 22845 (April, 1983), and the compound as disclosed in Japanese Patent O.P.I. Publication No. 209532/1987.
Examples of the mildew proofing agent are phenol, 4-chlorophenol, pentachlorophenol, cresol, o-phenylphenol, chlorophene, dichlorophene, formaldehyde, glutaldehyde, chloroacetamide, p-hydroxybenzoic acid esters, 2-(4-thiazoline)-benzimidazole, benzoisothiazolin-3-one, dodecyl-benzyl-dimethylammonium chloride, N-(fluorodichloromethylthio)-phthalimide, and 2,4,4'-trichloro-2'-hydroxydiphenyl ether.
The water to which a mildew proofing means has been applied and held in a water stock tank is added as the diluting water for the processing stock solutions such as the developing solution and the fixing solution, and may preferably be added in an amount of from 0.01 to 10 g/l, and more preferably from 0.1 to 5 g/l.
Various surface active agents can also be added in the washing water in addition to a silver image stabilizing agent, for the purpose of preventing a wetting non-uniformity. Any of cationic, anionic, nonionic or amphoteric types can be used as the surface active agents. Examples of the surface active agents are the compounds as disclosed, for example, in "KAIMENKASSEIZAI HANDOBUKKU (Surfactant Handbook)", published by Kogaku Tosho K.K.
In the above stabilizing bath, various compounds can be added for the purpose of stabilizing an image. They typically include, for example, various buffers used for adjustment of pH in the photographic layers of the light-sensitive material, e.g., pH 3 to 8, such as a borate, a metaborate, borax, phosphate, a carbonate, a potassium hydroxide, sodium hydroxide, ammonia water, monocarboxylic acid, a dicarboxylic acid, a polycarboxylic acid, which are used in suitable combination, and aldehydes such as formalin. Besides, various additives such as a chelating agent, a fungicide such as a thiazole type, an isothiazole type, a halogenated phenol, sulfanylamide or benzotriazole, a surface active agent, a fluorescent brightening agent, and a hardening agent may be used. Compounds of the same or different objects may also be used in combination of two or more kinds.
In order to improve an image storage stability, it is preferred to add as a pH adjustor of processing solutions an ammonium salt of various types, such as ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium phosphate, ammonium sulfite or ammonium thiosulfate to control the pH in the processed photographic layers of a light-sensitive material.
The washing or stabilizing according to the above method may preferably be carried out at a temperature of from 0° C. to 50° C. and for a period of time of from 6 seconds to 1 minute, more preferably from 15° C. to 40° C. and from 6 seconds to 30 seconds, and still more preferably from 15° C. to 40° C. and from 6 seconds to 15 seconds.
In the method of the present invention, a photographic material having been subjected to development, fixing and washing is preferably dried after complete removal of washing water, i.e., after roller squeegeeing. The drying can be carried out at about 40° C. to about 100° C. Drying time may be appropriately varied depending on the condition of surroundings. In usual instances, the drying may be carried out for about 5 seconds to 1 minute, and preferably at 40° C. to 80° C. for about 5 seconds to 30 seconds.
In the present invention, a more desirable effect can be obtained such that the drying time can be shortened with a decrease in the swelling percentage of a light-sensitive photographic material.
According to the present invention, the processing time, what is called a dry-to-dry time, ranging from the developing to the fixing, the washing and the drying, may preferably be not longer than 100 seconds, more preferably not longer than 60 seconds, and still more preferably not longer than 50 seconds.
Here, the "dry-to-dry" time refers to the time from the instant at which the head of a light-sensitive material to be processed enters a film inlet of an automatic processor, to the instant at which the head of the light sensitive material having been processed emerges from the automatic processor.
Black and white light-sensitive materials to which the developing solution containing the compound of the present invention may be any of commonly available light-sensitive silver halide photographic materials such as black and white light-sensitive photographic materials for ordinary photographying, light-sensitive photographic materials for X-rays, light-sensitive photographic materials for graphic art, light-sensitive photographic materials for medical use, light-sensitive photographic material for motion pictures, light-sensitive photographic materials for aerial photography, and light-sensitive photographic materials for TV.
The effect of the present invention will be exemplified below by giving Examples.
A graphic art film comprising a support coated with a silver chlorobromide emulsion was exposed to light through a contact screen according to usual sensitometry. The exposed film was developed at 38° C. for 13 seconds using a developing solution 1 having the following composition and to which the compound represented by Formula I as shown in Table 1 was added.
The emulsion used in the film was comprised of silver chlorobromide grains containing 75 mol % of silver chloride and the grain had an area ratio of (100) face to (111) face of 98:2.
______________________________________
Developing solution 1
______________________________________
Potassium sulfite 60 g
Sodium ethylenediaminetetraacetate
2 g
Potassium hydroxide 10.5 g
Diethylene glycol 25 g
1-Phenyl-4,4-dimethyl-3-pyrazolidinone
0.3 g
1-Phenyl-5-mercaptotetrazole
0.06 g
Potassium bromide 3.5 g
Hydroquinone 20 g
Potassium carbonate 15 g
Compound of Formula I as shown in Table 1
______________________________________
Made up to 1 l by adding pure water (ion-exchanged water).
Subsequently, a developing solution was prepared by adding in the developing solution 1 the thioether compound of Formula III as shown in Table 1. The developing solutions thus prepared all had a pH ranging from 10.7 to 10.8.
Fixing was carried out using the following fixing solution.
______________________________________
Formulation of fixing solution
______________________________________
(Composition A)
Ammonium thiosulfate (an aqueous 72.5% w/v
240 mΩ
solution)
Sodium sulfite 17 g
Sodium acetate trihydrate 6.5 g
Boric acid 6 g
Sodium citrate trihydrate 8 g
Acetic acid (an aqueous 90% w/v solution)
13.6 mΩ
(Composition B)
Pure water (ion-exchanged water)
17 mΩ
Sulfuric acid (an aqueous 50% w/v solution)
4.7 g
Aluminum sulfate (an aqueous 8.1% w/v solution
26.5 g
in terms of Al.sub.2 O.sub.3)
______________________________________
In use of the fixing solutions, the above Composition A and Composition B were dissolved in this order in 500 ml of water, and made up to 1 l. This fixing solution had a pH of about 4.3.
Results obtained by sensitometry are shown in Table 1. The sensitivity or speed is expressed as a relative speed regarding as 100 the speed obtained using the developing solution No. 1-2 shown in Table 1.
Running stability was evaluated by processing 50 sheets per day of exposed films of 508 mm×610 mm in size and measuring photographic performance at the time the processing was started, on 7th day, and on 14th day.
Halftone dot quality was visually evaluated according to five grades, where "5" indicates the best, and "1", the worst in quality. As halftone dots for lithography, the grades "5" and "4" are feasible for practical use; "3", a lower limit for practical use; and "2" and "1", infeasible for practical use.
TABLE 1
__________________________________________________________________________
Devel-
Compound of
Compound of
oping
Formula I
Formula III
Speed Fog Dot quality
solu- Amount Amount
Start
7th
14th
Start
7th
14th
Start
7th
14th
Re-
tion
No.
mg/Ω
No.
mg/Ω
day
day
day
day
day
day
day
day
day
marks
__________________________________________________________________________
1-1 -- -- -- -- 110
110
110
0.11
0.11
0.11
4 4 4 X
1-2 I-1
150 -- -- 100
102
103
0.05
0.05
0.06
3 3 4 X
1-3 " " III-2
25 119
119
119
0.05
0.05
0.05
4 4 4 Y
1-4 " " III-5
" 119
119
120
0.05
0.05
0.05
4 4 4 Y
1-5 I-2
" -- -- 101
104
105
0.06
0.07
0.07
3 3 2 X
1-6 " " III-2
25 117
117
117
0.06
0.06
0.06
4 4 4 Y
1-7 " " III-5
" 116
117
117
0.06
0.06
0.06
4 4 4 Y
1-8 I-5
" -- -- 100
102
102
0.04
0.06
0.07
3 3 3 X
1-9 " " III-1
25 120
119
119
0.04
0.05
0.05
4 4 4 Y
1-10
" " III-2
" 119
119
119
0.04
0.04
0.04
4 4 4 Y
1-11
" " III-5
" 119
119
118
0.04
0.04
0.04
5 4 4 Y
1-12
I-6
" -- -- 104
101
102
0.06
0.07
0.08
4 3 3 X
1-13
" " III-1
25 119
119
120
0.06
0.06
0.06
4 4 4 Y
1-14
" " III-2
" 120
120
120
0.06
0.06
0.06
5 5 4 Y
1-15
" " III-5
" 120
120
120
0.06
0.06
0.06
4 4 4 Y
__________________________________________________________________________
X: Comparative Example,
Y: Present Invention
A graphic art film coated with a silver chlorobromide emulsion was exposed to light in the same manner as in Example 1. The exposed film was developed at 38° C. for 13 seconds using a developing solution 2 having the following composition and to which the compound represented by Formula I as shown in Table 2 was added. Fixing was carried out in the same manner as in Example 1.
The emulsion used in the graphic art film was comprised of silver chlorobromide grains containing 90 mol % of silver chloride and the grain had a area ratio of (100) face to (111) face of 100:0.
______________________________________
Developing solution 2
______________________________________
Potassium sulfite 49.5 g
Sodium ethylenediaminetetraacetate
2 g
Potassium hydroxide 3 g
Diethylene glycol 100 g
Phenidone 0.2 g
1-Phenyl-5-mercaptotetrazole
0.02 g
Potassium bromide 2.5 g
Hydroquinone 15 g
Potassium carbonate 66 g
Compound of Formula I as shown in Table 2
Compound of Formula II
as shown in Table 2
90% acetic aid 0.3 mΩ
______________________________________
Made up to 1 l by adding pure water (ion-exchanged water).
All the resulting developing solutions had a pH ranging from 10.5 to 10.7.
Evaluation was made in the same manner as in Example 1.
Results obtained are shown in Table 2.
TABLE 2
__________________________________________________________________________
Devel-
Compound of
Compound of
oping
Formula I
Formula III
Speed Fog Dot quality
solu- Amount Amount
Start
7th
14th
Start
7th
14th
Start
7th
14th
Re-
tion
No.
mg/Ω
No. mg/Ω
day
day
day
day
day
day
day
day
day
marks
__________________________________________________________________________
2-1 -- -- -- -- 112
110
109
0.10
0.10
0.10
4 4 4 X
2-2 I-1
200 -- -- 100
98
96
0.05
0.05
0.06
3 3 4 X
2-3 " " III-3
30 120
120
120
0.05
0.05
0.05
4 4 4 Y
2-4 " " III-5
" 120
119
119
0.05
0.05
0.05
4 4 4 Y
2-5 " " III-8
-- 121
121
120
0.05
0.05
0.05
4 4 4 Y
2-6 " " III-10
" 119
119
119
0.05
0.05
0.05
4 4 4 Y
2-7 " " III-12
" 119
119
119
0.05
0.05
0.06
4 4 4 Y
2-8 " " III-14
-- 119
119
119
0.05
0.05
0.06
4 4 3 Y
2-9 I-2
150 -- -- 96
93
90
0.04
0.04
0.05
3 3 3 X
2-10
" " III-3
20 116
116
116
0.04
0.04
0.04
4 4 3 Y
2-11
" " III-5
" 115
115
114
0.04
0.04
0.04
4 4 4 Y
2-12
" " III-8
-- 115
115
115
0.04
0.04
0.04
4 4 4 Y
2-13
" " III-10
-- 116
115
115
0.04
0.04
0.04
4 4 4 Y
2-14
" " III-12
" 114
114
114
0.04
0.04
0.04
4 4 4 Y
2-15
" " III-14
" 114
114
114
0.04
0.04
0.05
4 4 3 Y
2-16
I-3
150 -- -- 97
96
95
0.04
0.04
0.04
3 3 3 X
2-17
" " III-3
20 117
117
117
0.04
0.04
0.05
4 3 3 Y
2-18
" " III-5
" 117
117
117
0.04
0.04
0.05
4 3 3 Y
2-19
" " III-8
" 116
115
115
0.04
0.04
0.04
4 4 3 Y
2-20
" " III-10
" 116
115
115
0.04
0.04
0.04
4 4 3 Y
2-21
" " III-12
" 115
115
115
0.04
0.04
0.04
4 4 3 Y
2-22
" " III-14
" 115
115
115
0.04
0.04
0.04
4 4 4 Y
2-23
I-4
200 -- -- 101
100
95
0.05
0.05
0.06
3 3 3 X
2-24
" " III-10
25 120
120
120
0.05
0.05
0.05
4 4 3 Y
2-25
" " III-12
" 118
118
117
0.05
0.05
0.05
4 4 3 Y
2-26
" " III-14
" 118
118
118
0.05
0.05
0.05
4 4 3 Y
2-27
I-5
" -- -- 98
95
93
0.04
0.04
0.05
3 3 3 X
2-28
" " III-10
25 114
114
114
0.04
0.04
0.04
4 4 3 Y
2-29
" " III-12
" 114
114
114
0.04
0.04
0.05
4 4 3 Y
2-30
" " III-14
" 115
115
115
0.04
0.05
0.04
4 4 3 Y
__________________________________________________________________________
X: Comparative Example,
Y: Present Invention
Film samples were obtained in the following manner.
After 500 g of gelatin was dissolved in 8 l of water, the following antihalation dyes (A), (B) and (C) were added so that the coating weights of the dyes were 80 mg/m2, 50 mg/m2 and 100 mg/m2, respectively. Further added were 20 g of saponin and 1 g of sodium salt of bis-(2-ethylhexyl)sulfosuccinic acid ester as surface active agents, 20 g of a butyl acrylate/vinylidene chloride copolymer as a polymer latex, 2.5 g of a styrene/maleic anhydride copolymer as a thickening agent, and 2 g of glyoxal as a hardening agent. The coating solution was thus prepared. ##STR8##
After 400 g of gelatin was dissolved in 600 ml of water, 20 g of polymethyl methacrylate with an average particle diameter of 5.5 μm as a matting agent and 3 g of sodium salt of bis-(2-ethylhexyl)sulfosuccinic acid ester as a surface active agent were added. The coating solution was thus prepared.
In a container containing gelatin and sodium chloride and heated to 40° C., an aqueous solution of silver nitrate and an aqueous mixed solution comprising potassium bromide and sodium chloride to which 5×10-7 mol of potassium hexachloroiridate and 6×10-8 of potassium hexabromorhodate were added, were added by double-jet precipitation. Silver chlorobromide grains containing 35 mol % of silver bromide were thus prepared while maintaining the pH to 3.0 and the pAg to 7.7. After the pH was returned to 5 9, desalting was carried out by a conventional method. The silver halide grains thus obtained were comprised of cubic grains with a degree of monodispersion of 9% and an average grain size of 0.25 μm, and the grain had an area ratio of (100) face to (111) face of 98:2.
The emulsion thus obtained was subjected to gold sensitization and sulfur sensitization, a sensitizing dye (a) was thereafter added in an amount of 60 mg per mole of silver halide, and then 70 mg of 1-phenyl-5-mercaptotetrazole per mol of silver halide, 1.2 g of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene per mol of silver halide, and gelatin were added to stop the chemical ripening. Thereafter, 4 g of hydroquinone, 3 g of potassium bromide, 5 g of saponin, 2 g of a styrene/maleic acid copolymer and 3 g of a high-molecular polymer latex of ethyl acrylate were further added, and then sodium 1-hydroxy-3,5-dichlorotriazine was added as a hardening agent. The desired coating solution was thus prepared. ##STR9##
In an aqueous solution of 500 g of gelatin, 10 g of potassium bromide and 4 g of sodium 1-decyl 2-(3-isopentyl)succinato-2-sulfonate were added, and then 100 g of amorphous silica having an average particle diameter of 5 μm was added and dispersed. The coating solution thus prepared.
Using the above coating solutions, a 100 μm thick polyethylene terephthalate film base was provided with a back-surface under layer and a back-surface upper layer by simultaneous multilayer coating, and subsequently, on its opposite side to the back-surface layers, provided with an emulsion layer and a protective layer by simultaneous multilayer coating.
The coating weight of silver was 3.8 g/m2 and the gelatin was in an amount of 1.8 g/m2 for the emulsion layer and 1.0 g g/m2 for the protective layer.
Samples thus obtained were exposed to light through a contact screen in the same manner as Example 1, and processed by means of a usual roller-type automatic processor under the following conditions.
______________________________________
(Developing conditions)
Step Temperature Time
______________________________________
Developing
38° C. 12.4 to 20
seconds
Fixing 34° C. 9.9 seconds
Washing room temperature 10.6 seconds
Drying 50° C. 13.9 seconds
______________________________________
Processing was carried out using the same developing solution as the developing solution 1 as in Example 1 to which the compound of Formula I was added. The compound of Formula I was added as shown in Table I, in an amount as also shown in Table 1. Further, developing solutions each having various pH values as shown in Table 3 were prepared by controlling the amount of potassium hydroxide.
Subsequently, a developing solution was prepared by adding in the developing solution 1 the thioether compound of Formula III as shown in Table 3.
Results obtained by sensitometry are shown in Table 3. The speed is expressed as a relative speed regarding as 100 the speed obtained using the developing solution No. 3-1 shown in Table 3.
Running stability was evaluated in the same manner as in Example 1.
TABLE 3
__________________________________________________________________________
Devel-
Compound of
Compound of ph of
Proc-
oping
Formula I
Formula III
Speed Fog devel-
essing
solu- Amount Amount
Start
7th
14th
Start
7th
14th
oping
time
Re-
tion
No.
mg/Ω
No.
mg/Ω
day
day
day
day
day
day
solution
(sec)
marks
__________________________________________________________________________
3-1 I-2
300 -- -- 100
100
107
0.05
0.05
0.06
10.77
20 X
3-2 " 150 -- -- 103
104
105
0.05
0.06
0.07
" 12.4
X
3-3 " " III-2
25 116
116
116
0.05
0.05
0.05
10.78
" Y
3-4 " " III-5
" 115
115
115
0.05
0.05
0.06
" " Y
3-5 " " III-7
" 117
117
117
0.05
0.05
0.05
" " Y
3-6 I-5
300 -- -- 101
104
109
0.05
0.05
0.06
10.77
20 X
3-7 " 150 -- -- 104
106
110
0.06
0.06
0.08
" 12.4
X
3-8 " " III-2
25 117
117
117
0.06
0.06
0.06
10.78
" Y
3-9 " " III-5
" 117
117
117
0.06
0.06
0.06
" " Y
3-10
" " III-7
" 116
116
116
0.06
0.06
0.06
" " Y
3-11
I-6
300 -- -- 104
106
109
0.05
0.05
0.07
10.77
20 X
3-12
" 150 -- -- 107
110
113
0.05
0.06
0.07
" 12.4
X
3-13
" " III-2
25 121
121
121
0.05
0.05
0.05
10.79
" Y
3-14
" " III-5
" 120
120
120
0.05
0.05
0.06
" " Y
3-15
" " III-7
" 120
120
120
0.05
0.05
0.05
" " Y
__________________________________________________________________________
X: Comparative Example,
Y: Present Invention
Three kinds of emulsions were prepared in the same manner as in Example 3 except that they were each varied in the area ratio of (110) to (111) as shown in Table 4 by control of pAg value and use of a grain growing controlling agent. Samples were prepared each using thus obtained emulsions and processed in the same manner as in Example 3. In the processing, developing solution 3-3 of Example 3 was used which contained 150 mg/l of compound I-2 and 25 mg/l of compound III-5 and had a pH value of 10.78. Development was carried out for 12.4 seconds.
TABLE 4
______________________________________
Speed Fog
Area ratio
Start 7th 14th Start 7th 14th
(100)/(111)
day day day day day day
______________________________________
100/0 121 122 121 0.04 0.04 0.04
90/10 110 112 108 0.05 0.05 0.05
80/20 82 75 73 0.07 0.08 0.06
______________________________________
In a container containing gelatin and sodium chloride and heated to 40° C., an aqueous solution of silver nitrate and an aqueous mixed solution comprising potassium bromide and sodium chloride to which 5×10-7 mol of potassium hexachloroiridate and 6×10-8 of potassium hexabromorhodate were added, were added by double-jet precipitation. Silver chlorobromide grains containing 35 mol % of silver bromide were thus prepared while maintaining the pH to 3.0 and the pAg to 7.7. After the pH was returned to 5.9, desalting was carried out by a conventional method. The silver halide grains thus obtained were comprised of cubic grains with a degree of monodispersion of 9% and an average grain size of 0.25 μm.
The emulsion thus obtained was subjected to gold sensitization and sulfur sensitization, a sensitizing dye (a) was thereafter added in an amount of 240 mg per mole of silver halide, and then 70 mg of 1-phenyl-5-mercaptotetrazole per mol of silver halide, 1.2 g of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene, and gelatin were added to stop the chemical ripening. Thereafter. 4 g of hydroquinone, 3 g of potassium bromide, 5 g of saponin, 2 g of a styrene/maleic acid copolymer and 3 g of a high-molecular polymer latex of ethyl acrylate, all per mol of silver halide, were further added, and then sodium 1-hydroxy-3,5-dichlorotriazine and formalin were added as a hardening agent.
The resulting emulsion was coated on a subbed polyethylene terephthalate film base so as to give a silver weight of 4.3 g/m2 and a gelatin weight of 2.5 g/m2, and the same protective layer coating solution as the one prepared in Example 3 was further coated so as to give a gelatin weight of 1.0 g/m2. An emulsion layer and a protective layer was thus provided by simultaneous coating.
On the opposite side to the surface on which the above solutions were coated, a gelatin solution containing dyes (b) and (c) had been previously coated so as to give a gelatin weight of 3.3 g/m2 ; dye (b), 180 mg/m2 ; and dye (c), 50 mg/m2. ##STR10##
Samples thus obtained were processed and evaluated in the same manner as in Example 3 except that in the developing solution the compound of Formula I used in Example 3 was replaced with the compound of Formula II. The composition of each developing solution and the results of evaluation are shown in Table 5. The developing solutions all had a pH ranging from 10.7 to 10.8.
TABLE 5
__________________________________________________________________________
Devel-
Compound of
Compound of
oping
Formula I
Formula III
Speed Fog Dot quality
solu- Amount Amount
Start
7th
14th
Start
7th
14th
Start
7th
14th
Re-
tion
No.
mg/Ω
No. mg/Ω
day
day
day
day
day
day
day
day
day
marks
__________________________________________________________________________
4-1 -- -- -- -- 110
110
110
0.11
0.11
0.11
4 4 4 X
4-2 II-2
170 -- -- 100
103
105
0.04
0.05
0.05
4 4 3 X
4-3 II-2
170 III-5
30 136
135
135
0.04
0.04
0.04
5 5 5 Y
4-4 II-2
170 III-9
30 140
140
140
0.04
0.05
0.05
5 5 5 Y
4-5 II-2
170 III-13
30 140
140
140
0.04
0.04
0.04
5 5 5 Y
4-6 II-4
150 -- -- 98
103
106
0.04
0.06
0.07
3 3 2 X
4-7 II-4
150 III-3
25 142
142
142
0.04
0.04
0.05
4 4 4 Y
4-8 II-4
150 III-5
25 140
140
140
0.04
0.04
0.04
4 4 4 Y
4-9 II-4
150 III-9
30 144
144
143
0.04
0.04
0.04
4 4 4 Y
4-10
II-4
150 III-13
30 145
144
144
0.04
0.04
0.04
4 4 4 Y
4-11
II-5
120 -- -- 101
106
109
0.04
0.06
0.07
4 4 3 X
4-12
II-5
120 III-3
25 145
145
145
0.04
0.04
0.04
5 5 5 Y
4-13
II-5
120 III-5
25 145
145
145
0.04
0.04
0.04
5 5 5 Y
4-14
II-5
120 III-9
30 146
146
146
0.04
0.04
0.04
5 5 5 Y
4-15
II-5
120 III-13
30 149
149
149
0.04
0.04
0.04
5 5 3 Y
__________________________________________________________________________
X: Comparative Example,
Y: Present Invention
Claims (12)
1. An image forming method comprising steps of
imagewise exposing a silver halide photographic light-sensitive material comprising silver halide grains having a ratio of (100) surface to (111) surface of not less than 5 to light, and
developing said silver halide photographic light-sensitive material with a developer comprising a compound represented by the following formula I or II: ##STR11## wherein Y, Y1 and Y2 are each a hydrogen atom or a mercapto group, R and R1 are each a hydrogen atom, a halogen atom, a nitro group, an amino group, a cyano group, a hydroxyl group, a mercapto group, a sulfo group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkinyl group, a substituted or unsubstituted aryl group, a substituted or unsubstituted alkoxy group, a hydroxycarbonyl group, an alkylcarbonyl group or an alkoxycarbonyl group, and
a compound represented by the following formula III: ##STR12## wherein A is an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group represented by --(CH2 CH2 O)p--, --(CH2 CH2 O)p--CH2 --CH2 -- or ##STR13## which is linked through the carbon atom thereof with B; A' is an alkylene group having 1 to 3 carbon atoms, or a polyalkylene ether group represented by --(CH2 CH2 O)p--CH2 --CH2 -- or ##STR14## provided that both of A and A' are not a polyalkylene ether group at the same time and p is an integer of 2 to 30; B and B' are independently --NH-- or --O--, provided that both of B and B' are not --O-- at the same time; R is an alkyl group having 1 to 3 carbon atoms, a phenyl group, an aralkyl group or a --(CH2)q-COOR' group, in which q is an integer of 1 to 3 and R' is an alkyl group having 1 to 3 carbon atoms; X is --S--, --O--, --CH2 --, ##STR15## in which --Rn is an alkyl group having 1 to 3 carbon atoms.
2. A method of claim 1, wherein said compound represented by Formula I or II is contained in said developer in an amount of from 0.0001 g to 2 g per liter of the developer.
3. A method of claim 1, wherein said comound represented by Formula III is contained in said developer in an amount of from 0.0001 g to 2 g per liter of the developer.
4. A method of claim 3, wherein said compound represented by Formula III is contained in said developer in an amount of from 0.001 g to 1 g per liter.
5. A method of claim 1, wherein the pH value of said developer is within the range of from 9 to 13.
6. A method of claim 5, wherein the pH value of said developer is within the range of from 9.5 to 12.
7. A method of claim 1, wherein said silver halide photographic light-sensitive material comprises a silver halide grains containing not less than 50 mol % of silver chloride.
8. A method of claim 1, wherein said silver halide photographic light-sensitive material comprises a silver halide grains having a size of from 0.2 μm to 0.5 μm.
9. A method of claim 1, wherein said developing step is performed for a time of not more than 20 seconds.
10. A method of claim 9, wherein said developing step is performed for a time of not more than 15 seconds.
11. The method of claim 1, wherein said developing is performed for a time of 20 seconds or less.
12. The method of claim 11, wherein said developing is performed for a time of from 6 seconds to 15 seconds.
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1-249578 | 1989-09-25 | ||
| JP24957789A JPH03110547A (en) | 1989-09-25 | 1989-09-25 | Method for processing silver halide photographic sensitive material |
| JP24957889A JPH03110548A (en) | 1989-09-25 | 1989-09-25 | Developer for silver halide photographic sensitive material |
| JP1-249577 | 1989-09-25 | ||
| JP1-282469 | 1989-10-30 | ||
| JP28246989A JPH03144440A (en) | 1989-10-30 | 1989-10-30 | Developer for silver halide photographic sensitive material |
| JP28309589A JPH03145643A (en) | 1989-11-01 | 1989-11-01 | Method for processing silver halide photographic sensitive material |
| JP1-283095 | 1989-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH1020H true USH1020H (en) | 1992-02-04 |
Family
ID=27478164
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/586,284 Abandoned USH1020H (en) | 1989-09-25 | 1990-09-21 | Developing solution for light-sensitive silver halide photographic material and method of forming photographic image making use of it |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH1020H (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5318881A (en) * | 1992-03-06 | 1994-06-07 | Minnesota Mining And Manufacturing Company | Method of processing a silver halide radiographic material |
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| US2531832A (en) | 1947-06-12 | 1950-11-28 | Du Pont | Silver halide developers containing polyethylene glycols |
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| US3046129A (en) | 1958-12-12 | 1962-07-24 | Eastman Kodak Co | Sensitization of photographic silver halide emulsions containing colorforming compounds with polymeric thioethers |
| US3201242A (en) | 1961-09-11 | 1965-08-17 | Eastman Kodak Co | Accelerators for reversal color development |
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| US3495981A (en) | 1965-06-17 | 1970-02-17 | Fuji Photo Film Co Ltd | Color developing process |
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| US3671247A (en) | 1969-10-22 | 1972-06-20 | Fuji Photo Film Co Ltd | Development of silver halide photographic materials |
| US3915710A (en) | 1973-06-28 | 1975-10-28 | Konishiroku Photo Ind | Light-sensitive silver halide photographic material |
| US3996054A (en) | 1971-09-24 | 1976-12-07 | Minnesota Mining And Manufacturing Company | Color photographic developing solution |
| US4063951A (en) | 1974-12-19 | 1977-12-20 | Ciba-Geigy Ag | Manufacture of tabular habit silver halide crystals for photographic emulsions |
| US4414305A (en) | 1981-07-28 | 1983-11-08 | Fuji Photo Film Co., Ltd. | Image-forming method |
| US4435500A (en) | 1981-08-31 | 1984-03-06 | Fuji Photo Film Co., Ltd. | Method for developing silver halide photographic light-sensitive material |
| US4672025A (en) | 1984-07-30 | 1987-06-09 | Fuji Photo Film Co., Ltd. | Method for processing silver halide photographic material |
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| US4946772A (en) | 1987-04-30 | 1990-08-07 | Fuji Photo Film Co., Ltd. | Silver halide emulsions and photographic materials |
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1990
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| US2531832A (en) | 1947-06-12 | 1950-11-28 | Du Pont | Silver halide developers containing polyethylene glycols |
| US2950970A (en) | 1957-03-08 | 1960-08-30 | Eastman Kodak Co | Color developers containing polyethylene glycols |
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| US3201242A (en) | 1961-09-11 | 1965-08-17 | Eastman Kodak Co | Accelerators for reversal color development |
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| US3291607A (en) | 1965-05-28 | 1966-12-13 | Gen Aniline & Film Corp | Water-soluble polyoxyalkylenated butyne-2-diol-1, 4 development accelerators |
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| US5318881A (en) * | 1992-03-06 | 1994-06-07 | Minnesota Mining And Manufacturing Company | Method of processing a silver halide radiographic material |
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