JPH07117721B2 - ハロゲン化銀カラー写真感光材料の処理方法 - Google Patents

ハロゲン化銀カラー写真感光材料の処理方法

Info

Publication number: JPH07117721B2
Authority: JP; Japan
Prior art keywords: group; layer; washing; color; amount
Prior art date: 1988-01-21
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related

Application number

JP63011300A

Other languages

English (en)

Japanese (ja)

Other versions

JPH01187557A (ja

Inventor

伸二上田

隆利石川

央藤本

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date (The priority date 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 date listed.)

1988-01-21

Filing date

1988-01-21

Publication date

1995-12-18

1988-01-21 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1988-01-21 Priority to JP63011300A priority Critical patent/JPH07117721B2/ja

1989-01-18 Priority to AU28592/89A priority patent/AU615021B2/en

1989-01-20 Priority to DE1989626579 priority patent/DE68926579T2/de

1989-01-20 Priority to EP19890100968 priority patent/EP0326030B1/de

1989-07-26 Publication of JPH01187557A publication Critical patent/JPH01187557A/ja

1992-09-30 Priority to US07/954,411 priority patent/US5250396A/en

1995-12-18 Publication of JPH07117721B2 publication Critical patent/JPH07117721B2/ja

2010-12-18 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 title claims description 100
229910052709 silver Inorganic materials 0.000 title claims description 43
239000004332 silver Substances 0.000 title claims description 43
239000000463 material Substances 0.000 title claims description 39
238000003672 processing method Methods 0.000 title claims description 8
238000005406 washing Methods 0.000 claims description 74
238000012545 processing Methods 0.000 claims description 60
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 57
230000000087 stabilizing effect Effects 0.000 claims description 29
238000000034 method Methods 0.000 claims description 28
239000003755 preservative agent Substances 0.000 claims description 26
239000003381 stabilizer Substances 0.000 claims description 21
230000002335 preservative effect Effects 0.000 claims description 18
239000010410 layer Substances 0.000 description 104
239000000243 solution Substances 0.000 description 77
239000000839 emulsion Substances 0.000 description 60
125000000217 alkyl group Chemical group 0.000 description 46
108010010803 Gelatin Proteins 0.000 description 40
239000008273 gelatin Substances 0.000 description 40
229920000159 gelatin Polymers 0.000 description 40
235000019322 gelatine Nutrition 0.000 description 40
235000011852 gelatine desserts Nutrition 0.000 description 40
125000004435 hydrogen atom Chemical group [H]* 0.000 description 39
150000001875 compounds Chemical class 0.000 description 36
239000003795 chemical substances by application Substances 0.000 description 30
125000003118 aryl group Chemical group 0.000 description 24
238000000576 coating method Methods 0.000 description 23
239000011248 coating agent Substances 0.000 description 22
125000000623 heterocyclic group Chemical group 0.000 description 22
239000007788 liquid Substances 0.000 description 22
238000011282 treatment Methods 0.000 description 22
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 20
229910021612 Silver iodide Inorganic materials 0.000 description 18
125000003545 alkoxy group Chemical group 0.000 description 17
230000001235 sensitizing effect Effects 0.000 description 17
125000003277 amino group Chemical group 0.000 description 16
125000004432 carbon atom Chemical group C* 0.000 description 16
239000002245 particle Substances 0.000 description 16
239000002904 solvent Substances 0.000 description 16
239000002253 acid Substances 0.000 description 15
239000013078 crystal Substances 0.000 description 15
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 14
235000002639 sodium chloride Nutrition 0.000 description 14
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 13
238000001704 evaporation Methods 0.000 description 13
230000008020 evaporation Effects 0.000 description 13
239000000203 mixture Substances 0.000 description 13
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 13
230000008859 change Effects 0.000 description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 description 12
150000003839 salts Chemical class 0.000 description 12
125000001424 substituent group Chemical group 0.000 description 12
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
238000009826 distribution Methods 0.000 description 11
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 10
230000000694 effects Effects 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 10
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 10
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 9
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
239000002738 chelating agent Substances 0.000 description 9
125000005843 halogen group Chemical group 0.000 description 9
239000003112 inhibitor Substances 0.000 description 9
238000002156 mixing Methods 0.000 description 9
239000011734 sodium Substances 0.000 description 9
229910021607 Silver chloride Inorganic materials 0.000 description 8
125000004104 aryloxy group Chemical group 0.000 description 8
238000004061 bleaching Methods 0.000 description 8
239000007844 bleaching agent Substances 0.000 description 8
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 8
229910052799 carbon Inorganic materials 0.000 description 8
239000011777 magnesium Substances 0.000 description 8
229910052749 magnesium Inorganic materials 0.000 description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 8
238000011160 research Methods 0.000 description 8
238000001223 reverse osmosis Methods 0.000 description 8
230000035945 sensitivity Effects 0.000 description 8
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 8
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 8
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 7
239000011575 calcium Substances 0.000 description 7
229910052791 calcium Inorganic materials 0.000 description 7
239000002612 dispersion medium Substances 0.000 description 7
239000012528 membrane Substances 0.000 description 7
239000000126 substance Substances 0.000 description 7
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 7
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 6
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 6
VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 6
125000002947 alkylene group Chemical group 0.000 description 6
239000003729 cation exchange resin Substances 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
238000005562 fading Methods 0.000 description 6
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 5
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 5
101100221809 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cpd-7 gene Proteins 0.000 description 5
239000004698 Polyethylene Substances 0.000 description 5
150000007513 acids Chemical class 0.000 description 5
125000003368 amide group Chemical group 0.000 description 5
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 5
239000003957 anion exchange resin Substances 0.000 description 5
230000000844 anti-bacterial effect Effects 0.000 description 5
229940121375 antifungal agent Drugs 0.000 description 5
239000000872 buffer Substances 0.000 description 5
238000011161 development Methods 0.000 description 5
239000006185 dispersion Substances 0.000 description 5
150000002429 hydrazines Chemical class 0.000 description 5
239000003456 ion exchange resin Substances 0.000 description 5
229920003303 ion-exchange polymer Polymers 0.000 description 5
125000004433 nitrogen atom Chemical group N* 0.000 description 5
125000000962 organic group Chemical group 0.000 description 5
150000002989 phenols Chemical class 0.000 description 5
ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical class OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 5
229920000573 polyethylene Polymers 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
230000002829 reductive effect Effects 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 4
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 4
239000006096 absorbing agent Substances 0.000 description 4
229960000583 acetic acid Drugs 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
125000003342 alkenyl group Chemical group 0.000 description 4
125000004414 alkyl thio group Chemical group 0.000 description 4
235000011114 ammonium hydroxide Nutrition 0.000 description 4
230000000843 anti-fungal effect Effects 0.000 description 4
125000000732 arylene group Chemical group 0.000 description 4
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 4
229910021538 borax Inorganic materials 0.000 description 4
229920001577 copolymer Polymers 0.000 description 4
125000004093 cyano group Chemical group *C#N 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
230000002349 favourable effect Effects 0.000 description 4
239000006081 fluorescent whitening agent Substances 0.000 description 4
229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 4
239000004816 latex Substances 0.000 description 4
229920000126 latex Polymers 0.000 description 4
150000002772 monosaccharides Chemical class 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
229920000768 polyamine Polymers 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000011241 protective layer Substances 0.000 description 4
150000003242 quaternary ammonium salts Chemical class 0.000 description 4
235000010265 sodium sulphite Nutrition 0.000 description 4
235000010339 sodium tetraborate Nutrition 0.000 description 4
235000000346 sugar Nutrition 0.000 description 4
125000000565 sulfonamide group Chemical group 0.000 description 4
238000003786 synthesis reaction Methods 0.000 description 4
NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical class C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 3
229910019142 PO4 Inorganic materials 0.000 description 3
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 3
235000011054 acetic acid Nutrition 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000000654 additive Substances 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 3
239000003242 anti bacterial agent Substances 0.000 description 3
239000003429 antifungal agent Substances 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
125000003710 aryl alkyl group Chemical group 0.000 description 3
125000005110 aryl thio group Chemical group 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
239000002585 base Substances 0.000 description 3
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical group C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
150000001720 carbohydrates Chemical class 0.000 description 3
238000005859 coupling reaction Methods 0.000 description 3
230000006866 deterioration Effects 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
239000010946 fine silver Substances 0.000 description 3
125000000717 hydrazino group Chemical group [H]N([*])N([H])[H] 0.000 description 3
150000002443 hydroxylamines Chemical class 0.000 description 3
230000001678 irradiating effect Effects 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
150000002923 oximes Chemical class 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229960003330 pentetic acid Drugs 0.000 description 3
235000021317 phosphate Nutrition 0.000 description 3
ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 3
229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
239000004926 polymethyl methacrylate Substances 0.000 description 3
239000011591 potassium Substances 0.000 description 3
229910052700 potassium Inorganic materials 0.000 description 3
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 3
235000019252 potassium sulphite Nutrition 0.000 description 3
230000002265 prevention Effects 0.000 description 3
230000008569 process Effects 0.000 description 3
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical class N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 3
230000009467 reduction Effects 0.000 description 3
239000001488 sodium phosphate Substances 0.000 description 3
239000004328 sodium tetraborate Substances 0.000 description 3
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 3
235000019345 sodium thiosulphate Nutrition 0.000 description 3
238000010186 staining Methods 0.000 description 3
150000008163 sugars Chemical class 0.000 description 3
LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 3
239000002699 waste material Substances 0.000 description 3
WQZGKKKJIJFFOK-SVZMEOIVSA-N (+)-Galactose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-SVZMEOIVSA-N 0.000 description 2
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 2
XNCSCQSQSGDGES-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]propyl-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)C(C)CN(CC(O)=O)CC(O)=O XNCSCQSQSGDGES-UHFFFAOYSA-N 0.000 description 2
RNMCCPMYXUKHAZ-UHFFFAOYSA-N 2-[3,3-diamino-1,2,2-tris(carboxymethyl)cyclohexyl]acetic acid Chemical compound NC1(N)CCCC(CC(O)=O)(CC(O)=O)C1(CC(O)=O)CC(O)=O RNMCCPMYXUKHAZ-UHFFFAOYSA-N 0.000 description 2
XWSGEVNYFYKXCP-UHFFFAOYSA-N 2-[carboxymethyl(methyl)amino]acetic acid Chemical compound OC(=O)CN(C)CC(O)=O XWSGEVNYFYKXCP-UHFFFAOYSA-N 0.000 description 2
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 2
GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 description 2
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-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
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 2
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
241000220317 Rosa Species 0.000 description 2
206010070834 Sensitisation Diseases 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
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RGQFFQXJSCXIJX-UHFFFAOYSA-N n-[2-[2-amino-5-(diethylamino)phenyl]ethyl]methanesulfonamide Chemical compound CCN(CC)C1=CC=C(N)C(CCNS(C)(=O)=O)=C1 RGQFFQXJSCXIJX-UHFFFAOYSA-N 0.000 description 1
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125000003107 substituted aryl group Chemical group 0.000 description 1
125000005649 substituted arylene group Chemical group 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002344 surface layer Substances 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
239000008399 tap water Substances 0.000 description 1
235000020679 tap water Nutrition 0.000 description 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
230000008719 thickening Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003567 thiocyanates Chemical class 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
235000019798 tripotassium phosphate Nutrition 0.000 description 1
229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
235000019801 trisodium phosphate Nutrition 0.000 description 1
229910000406 trisodium phosphate Inorganic materials 0.000 description 1
125000002987 valine group Chemical class [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000012463 white pigment Substances 0.000 description 1
239000011787 zinc oxide 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/44—Regeneration; Replenishers

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP63011300A 1988-01-21 1988-01-21 ハロゲン化銀カラー写真感光材料の処理方法 Expired - Fee Related JPH07117721B2 (ja)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
JP63011300A JPH07117721B2 (ja)	1988-01-21	1988-01-21	ハロゲン化銀カラー写真感光材料の処理方法
AU28592/89A AU615021B2 (en)	1988-01-21	1989-01-18	Method for processing silver halide color photographic material
DE1989626579 DE68926579T2 (de)	1988-01-21	1989-01-20	Verfahren zur Behandlung eines farbphotographischen Silberhalogenidmaterials
EP19890100968 EP0326030B1 (de)	1988-01-21	1989-01-20	Verfahren zur Behandlung eines farbphotographischen Silberhalogenidmaterials
US07/954,411 US5250396A (en)	1988-01-21	1992-09-30	Method for processing silver halide color photographic material

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP63011300A JPH07117721B2 (ja)	1988-01-21	1988-01-21	ハロゲン化銀カラー写真感光材料の処理方法

Publications (2)

Publication Number	Publication Date
JPH01187557A JPH01187557A (ja)	1989-07-26
JPH07117721B2 true JPH07117721B2 (ja)	1995-12-18

Family

ID=11774145

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP63011300A Expired - Fee Related JPH07117721B2 (ja)	1988-01-21	1988-01-21	ハロゲン化銀カラー写真感光材料の処理方法

Country Status (4)

Country	Link
EP (1)	EP0326030B1 (de)
JP (1)	JPH07117721B2 (de)
AU (1)	AU615021B2 (de)
DE (1)	DE68926579T2 (de)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0285010A3 (en) *	1987-03-25	1989-11-08	Fuji Photo Film Co., Ltd.	Method for forming a direct positive color image
JP3010361B2 (ja) *	1988-05-07	2000-02-21	コニカ株式会社	ハロゲン化銀写真感光材料の現像処理方法
JPH07122736B2 (ja) *	1988-09-28	1995-12-25	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法
JP2684224B2 (ja) *	1989-07-31	1997-12-03	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法
JP2684444B2 (ja) *	1989-08-11	1997-12-03	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法
US5206121A (en) *	1989-11-30	1993-04-27	Fuji Photo Film Co., Ltd.	Method of replenishing photographic processing apparatus with processing solution
US5124239A (en) *	1989-11-30	1992-06-23	Fuji Photo Film Co., Ltd.	Method of replenishing photographic processing apparatus with processing solution
JP2961170B2 (ja) *	1990-03-29	1999-10-12	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法および自動現像機
JP2866951B2 (ja) *	1990-11-28	1999-03-08	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法
JP3372994B2 (ja)	1993-06-11	2003-02-04	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料の処理方法
US5534395A (en)	1994-06-09	1996-07-09	Fuji Photo Film Co., Ltd.	Method of processing silver halide color photographic materials
GB9422109D0 (en)	1994-11-02	1994-12-21	Minnesota Mining & Mfg	Black and white photographic elements

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE613239A (de) *	1961-02-01
JPS5818632A (ja) *	1981-07-28	1983-02-03	Konishiroku Photo Ind Co Ltd	ハロゲン化銀カラ−写真感光材料の処理方法
JPS60252350A (ja) *	1984-05-30	1985-12-13	Konishiroku Photo Ind Co Ltd	ヨウ臭化銀含有撮影用感光材料の処理方法
DE3431860A1 (de) *	1984-08-30	1986-03-06	Agfa-Gevaert Ag, 5090 Leverkusen	Verfahren zur herstellung farbfotografischer bilder
JPS6161160A (ja) *	1984-08-31	1986-03-28	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料の処理方法
JPH0679143B2 (ja) *	1986-01-21	1994-10-05	コニカ株式会社	ハロゲン化銀カラ−写真感光材料の処理方法
CA1314424C (en) *	1986-01-24	1993-03-16	Sheridan E. Vincent	Photographic color developing compositions which are especially useful with high chloride photographic elements
JPS62234158A (ja) *	1986-04-04	1987-10-14	Konika Corp	色素画像の形成方法
JPH0746217B2 (ja) *	1986-04-15	1995-05-17	コニカ株式会社	最大発色濃度の高い色素画像が得られるハロゲン化銀写真感光材料の処理方法
JPH0658521B2 (ja) *	1986-06-24	1994-08-03	富士写真フイルム株式会社	カラ−現像液組成物
EP0269227B1 (de) *	1986-10-07	1992-12-30	Konica Corporation	Verfahren zur gemeinsamen Entwicklungsbehandlung zweier Arten von lichtempfindlichem photographischen Silberhalogenidmaterial
JPS63129341A (ja) *	1986-11-19	1988-06-01	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−反転写真感光材料の処理方法

1988
- 1988-01-21 JP JP63011300A patent/JPH07117721B2/ja not_active Expired - Fee Related
1989
- 1989-01-18 AU AU28592/89A patent/AU615021B2/en not_active Expired
- 1989-01-20 EP EP19890100968 patent/EP0326030B1/de not_active Expired - Lifetime
- 1989-01-20 DE DE1989626579 patent/DE68926579T2/de not_active Expired - Lifetime

Also Published As

Publication number	Publication date
AU2859289A (en)	1989-07-27
EP0326030A3 (en)	1990-08-08
AU615021B2 (en)	1991-09-19
EP0326030B1 (de)	1996-06-05
DE68926579D1 (de)	1996-07-11
DE68926579T2 (de)	1996-10-17
JPH01187557A (ja)	1989-07-26
EP0326030A2 (de)	1989-08-02

Legal Events

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2007-06-20	FPAY	Renewal fee payment (event date is renewal date of database)	Free format text: PAYMENT UNTIL: 20071218 Year of fee payment: 12
2007-06-20	R350	Written notification of registration of transfer	Free format text: JAPANESE INTERMEDIATE CODE: R350
2007-12-18	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
JPH07117721B2 (ja)	1995-12-18	ハロゲン化銀カラー写真感光材料の処理方法
JP2520634B2 (ja)	1996-07-31	ハロゲン化銀カラ−写真感光材料の処理方法
JP2889999B2 (ja)	1999-05-10	写真用処理組成物及び処理方法
EP0675406A1 (de)	1995-10-04	Entwicklungsverfahren mit einem niedrigvolumen Dünntank-Entwicklungssystem
US5071734A (en)	1991-12-10	Method for processing silver halide color photographic materials
JPH0711696B2 (ja)	1995-02-08	ハロゲン化銀カラ−写真感光材料の処理方法
EP0381183B1 (de)	1995-10-04	Farbphotographisches Silberhalogenidmaterial mit einem Pyrazolo(1,5-b)-1,2,4-triazol-Purpurkuppler
JP2670887B2 (ja)	1997-10-29	ハロゲン化銀カラー写真感光材料の処理方法
US5534394A (en)	1996-07-09	Method for processing silver halide color photographic materials
US5252439A (en)	1993-10-12	Method of replenishing developing solution with replenisher
US5250396A (en)	1993-10-05	Method for processing silver halide color photographic material
JPH07122735B2 (ja)	1995-12-25	ハロゲン化銀カラー写真感光材料の処理方法
JP2829445B2 (ja)	1998-11-25	写真用処理組成物及び処理方法
US5288597A (en)	1994-02-22	Method for forming a color image
JPH0789210B2 (ja)	1995-09-27	ハロゲン化銀カラ−写真感光材料の処理方法
JP2890361B2 (ja)	1999-05-10	ハロゲン化銀写真感光材料の処理方法
JP2543720B2 (ja)	1996-10-16	ハロゲン化銀カラ―写真感光材料の処理方法
JPH087410B2 (ja)	1996-01-29	ハロゲン化銀カラー写真感光材料の処理方法
JPH0760258B2 (ja)	1995-06-28	ハロゲン化銀カラー写真感光材料の処理方法
JPH06100806B2 (ja)	1994-12-12	ハロゲン化銀カラ−写真感光材料の処理方法
JP2909492B2 (ja)	1999-06-23	カラー画像形成方法
JP2543722B2 (ja)	1996-10-16	ハロゲン化銀カラ―写真感光材料の処理方法
JP2896403B2 (ja)	1999-05-31	カラー現像組成物およびそれを用いた処理方法
JPH05127330A (ja)	1993-05-25	ハロゲン化銀カラー写真感光材料の処理方法
JPH06130604A (ja)	1994-05-13	直接ポジ型ハロゲン化銀カラー写真感光材料の処理方法