JP3544245B2

JP3544245B2 - ハロゲン化銀カラー写真感光材料の処理方法

ハロゲン化銀カラー写真感光材料の処理方法 Download PDF

Info

Publication number: JP3544245B2
Authority: JP; Japan
Prior art keywords: group; carbon atoms; processing; solution; acid
Prior art date: 1995-06-09
Legal status : Expired - Fee Related

Application number

JP16710095A

Other languages

English (en)

Japanese (ja)

Other versions

JPH08339063A (ja

Inventor

尉浩勝岡

裕之関

久岡田

Current Assignee

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date

1995-06-09

Filing date

1995-06-09

Publication date

2004-07-21

1995-06-09 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1995-06-09 Priority to JP16710095A priority Critical patent/JP3544245B2/ja

1996-06-07 Priority to DE69636681T priority patent/DE69636681T2/de

1996-06-07 Priority to EP03014550A priority patent/EP1365285B1/fr

1996-06-07 Priority to DE69630419T priority patent/DE69630419T2/de

1996-06-07 Priority to EP96109200A priority patent/EP0750226B1/fr

1996-12-24 Publication of JPH08339063A publication Critical patent/JPH08339063A/ja

2004-07-21 Application granted granted Critical

2004-07-21 Publication of JP3544245B2 publication Critical patent/JP3544245B2/ja

2019-07-21 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

-1 silver halide Chemical class 0.000 title claims description 246
239000000463 material Substances 0.000 title claims description 84
229910052709 silver Inorganic materials 0.000 title claims description 40
239000004332 silver Substances 0.000 title claims description 40
238000003672 processing method Methods 0.000 title claims description 6
238000012545 processing Methods 0.000 claims description 118
150000001875 compounds Chemical class 0.000 claims description 75
238000004061 bleaching Methods 0.000 claims description 59
238000000034 method Methods 0.000 claims description 57
230000000087 stabilizing effect Effects 0.000 claims description 43
125000000217 alkyl group Chemical group 0.000 claims description 37
230000005291 magnetic effect Effects 0.000 claims description 36
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 30
229910001868 water Inorganic materials 0.000 claims description 30
238000005406 washing Methods 0.000 claims description 26
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 24
125000003118 aryl group Chemical group 0.000 claims description 18
125000005843 halogen group Chemical group 0.000 claims description 18
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 15
238000011161 development Methods 0.000 claims description 14
125000000623 heterocyclic group Chemical group 0.000 claims description 14
125000003545 alkoxy group Chemical group 0.000 claims description 13
125000002947 alkylene group Chemical group 0.000 claims description 13
150000003839 salts Chemical class 0.000 claims description 12
125000004429 atom Chemical group 0.000 claims description 11
150000001768 cations Chemical class 0.000 claims description 10
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
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PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 claims description 3
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125000000732 arylene group Chemical group 0.000 claims description 3
CEAZRRDELHUEMR-URQXQFDESA-N Gentamicin Chemical compound O1[C@H](C(C)NC)CC[C@@H](N)[C@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](NC)[C@@](C)(O)CO2)O)[C@H](N)C[C@@H]1N CEAZRRDELHUEMR-URQXQFDESA-N 0.000 claims description 2
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125000001424 substituent group Chemical group 0.000 description 19
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VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 10
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238000003756 stirring Methods 0.000 description 10
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NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
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150000007513 acids Chemical class 0.000 description 6
229910052783 alkali metal Inorganic materials 0.000 description 6
239000002216 antistatic agent Substances 0.000 description 6
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239000000986 disperse dye Substances 0.000 description 6
238000005562 fading Methods 0.000 description 6
VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 6
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AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 6
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GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
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UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 4
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125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 3
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IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
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238000003786 synthesis reaction Methods 0.000 description 3
CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 3
238000004804 winding Methods 0.000 description 3
125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 description 2
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