DE2425781A1 - Verwendung von aldonamiden zur herstellung photographischer materialien - Google Patents

Verwendung von aldonamiden zur herstellung photographischer materialien

Info

Publication number: DE2425781A1
Authority: DE; Germany
Prior art keywords: aldonamides; alkali; layer; recording materials; silver halide
Prior art date: 1973-05-29
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.): Pending

Application number

DE19742425781

Other languages

German (de)

English (en)

Inventor

Grant Milford Haist

Wilbert Jeptha Humphlett

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.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

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.)

1973-05-29

Filing date

1974-05-28

Publication date

1974-12-19

1974-05-28 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1974-12-19 Publication of DE2425781A1 publication Critical patent/DE2425781A1/de

Status Pending legal-status Critical Current

Links

239000000463 material Substances 0.000 title claims description 92
238000004519 manufacturing process Methods 0.000 title claims description 31
-1 silver halide Chemical class 0.000 claims description 90
150000001875 compounds Chemical class 0.000 claims description 76
239000003513 alkali Substances 0.000 claims description 49
239000002243 precursor Substances 0.000 claims description 41
229910052709 silver Inorganic materials 0.000 claims description 37
239000004332 silver Substances 0.000 claims description 37
230000005855 radiation Effects 0.000 claims description 27
239000003381 stabilizer Substances 0.000 claims description 24
125000004432 carbon atom Chemical group C* 0.000 claims description 20
239000011230 binding agent Substances 0.000 claims description 15
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 12
239000003795 chemical substances by application Substances 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
JCZPMGDSEAFWDY-MGCNEYSASA-N (2r,3s,4s,5r)-2,3,4,5,6-pentahydroxyhexanamide Chemical compound NC(=O)[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO JCZPMGDSEAFWDY-MGCNEYSASA-N 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
125000000623 heterocyclic group Chemical group 0.000 claims description 5
238000002360 preparation method Methods 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 3
125000006413 ring segment Chemical group 0.000 claims description 3
NFFPKRVXIPSSQR-BXXZVTAOSA-N (2r,3r,4r)-2,3,4,5-tetrahydroxypentanamide Chemical compound NC(=O)[C@H](O)[C@H](O)[C@H](O)CO NFFPKRVXIPSSQR-BXXZVTAOSA-N 0.000 claims description 2
JCZPMGDSEAFWDY-SQOUGZDYSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanamide Chemical compound NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO JCZPMGDSEAFWDY-SQOUGZDYSA-N 0.000 claims description 2
NFFPKRVXIPSSQR-UZBSEBFBSA-N (2s,3s,4r)-2,3,4,5-tetrahydroxypentanamide Chemical compound NC(=O)[C@@H](O)[C@@H](O)[C@H](O)CO NFFPKRVXIPSSQR-UZBSEBFBSA-N 0.000 claims description 2
JCZPMGDSEAFWDY-MBMOQRBOSA-N (2s,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanamide Chemical compound NC(=O)[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO JCZPMGDSEAFWDY-MBMOQRBOSA-N 0.000 claims description 2
APCDJAFTHLPEKO-HRFVKAFMSA-N (2s,3s)-2,3,4-trihydroxybutanamide Chemical compound NC(=O)[C@@H](O)[C@@H](O)CO APCDJAFTHLPEKO-HRFVKAFMSA-N 0.000 claims 1
125000003342 alkenyl group Chemical group 0.000 claims 1
INDZTCRIYSRWOH-UHFFFAOYSA-N undec-10-enyl carbamimidothioate;hydroiodide Chemical compound I.NC(=N)SCCCCCCCCCC=C INDZTCRIYSRWOH-UHFFFAOYSA-N 0.000 claims 1
239000000839 emulsion Substances 0.000 description 42
238000011161 development Methods 0.000 description 19
238000000576 coating method Methods 0.000 description 16
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
239000011248 coating agent Substances 0.000 description 15
239000002253 acid Substances 0.000 description 13
239000012190 activator Substances 0.000 description 13
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 12
229920000159 gelatin Polymers 0.000 description 10
235000019322 gelatine Nutrition 0.000 description 10
150000003839 salts Chemical class 0.000 description 10
JCZPMGDSEAFWDY-RSJOWCBRSA-N (2s,3r,4r,5s)-2,3,4,5,6-pentahydroxyhexanamide Chemical compound NC(=O)[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)CO JCZPMGDSEAFWDY-RSJOWCBRSA-N 0.000 description 8
239000004793 Polystyrene Substances 0.000 description 8
238000010438 heat treatment Methods 0.000 description 8
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 8
239000000243 solution Substances 0.000 description 8
108010010803 Gelatin Proteins 0.000 description 7
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 7
235000011852 gelatine desserts Nutrition 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
230000004913 activation Effects 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
239000008273 gelatin Substances 0.000 description 6
238000000034 method Methods 0.000 description 6
229920002554 vinyl polymer Polymers 0.000 description 6
229920002678 cellulose Polymers 0.000 description 5
CZLCEPVHPYKDPJ-UHFFFAOYSA-N guanidine;2,2,2-trichloroacetic acid Chemical compound NC(N)=N.OC(=O)C(Cl)(Cl)Cl CZLCEPVHPYKDPJ-UHFFFAOYSA-N 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000000758 substrate Substances 0.000 description 5
239000004372 Polyvinyl alcohol Substances 0.000 description 4
MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 4
150000005840 aryl radicals Chemical class 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
FBSFWRHWHYMIOG-UHFFFAOYSA-N methyl 3,4,5-trihydroxybenzoate Chemical compound COC(=O)C1=CC(O)=C(O)C(O)=C1 FBSFWRHWHYMIOG-UHFFFAOYSA-N 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 description 4
229920002451 polyvinyl alcohol Polymers 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
150000005208 1,4-dihydroxybenzenes Chemical group 0.000 description 3
GJOWSEBTWQNKPC-UHFFFAOYSA-N 3-methyloxiran-2-ol Chemical compound CC1OC1O GJOWSEBTWQNKPC-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
239000001828 Gelatine Substances 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
229910021607 Silver chloride Inorganic materials 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 3
239000001913 cellulose Substances 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
239000000123 paper Substances 0.000 description 3
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WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical group OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 3
238000007789 sealing Methods 0.000 description 3
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
229940066528 trichloroacetate Drugs 0.000 description 3
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
LAQYHRQFABOIFD-UHFFFAOYSA-N 2-methoxyhydroquinone Chemical compound COC1=CC(O)=CC=C1O LAQYHRQFABOIFD-UHFFFAOYSA-N 0.000 description 2
XCZKKZXWDBOGPA-UHFFFAOYSA-N 2-phenylbenzene-1,4-diol Chemical compound OC1=CC=C(O)C(C=2C=CC=CC=2)=C1 XCZKKZXWDBOGPA-UHFFFAOYSA-N 0.000 description 2
LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
238000007792 addition Methods 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001450 anions Chemical group 0.000 description 2
235000010323 ascorbic acid Nutrition 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical group OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
229920002301 cellulose acetate Polymers 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
150000001989 diazonium salts Chemical class 0.000 description 2
230000000694 effects Effects 0.000 description 2
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
239000007789 gas Substances 0.000 description 2
229940093915 gynecological organic acid Drugs 0.000 description 2
IGMNYECMUMZDDF-UHFFFAOYSA-N homogentisic acid Chemical compound OC(=O)CC1=CC(O)=CC=C1O IGMNYECMUMZDDF-UHFFFAOYSA-N 0.000 description 2
IBKQQKPQRYUGBJ-UHFFFAOYSA-N methyl gallate Natural products CC(=O)C1=CC(O)=C(O)C(O)=C1 IBKQQKPQRYUGBJ-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
235000005985 organic acids Nutrition 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 2
229920002223 polystyrene Polymers 0.000 description 2
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239000004800 polyvinyl chloride Substances 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
239000001267 polyvinylpyrrolidone Substances 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
230000002028 premature Effects 0.000 description 2
150000003254 radicals Chemical class 0.000 description 2
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230000000087 stabilizing effect Effects 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
125000003107 substituted aryl group Chemical group 0.000 description 2
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
CPEONABTMRSIKA-UHFFFAOYSA-N 1,4$l^{2}-oxazinane Chemical compound C1COCC[N]1 CPEONABTMRSIKA-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
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 1
LTHWZZOUNJCHES-YZRHJBSPSA-N 2-(c-aminocarbonimidoyl)sulfanylethanesulfonic acid Chemical compound N[14C](=N)SCCS(O)(=O)=O LTHWZZOUNJCHES-YZRHJBSPSA-N 0.000 description 1
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UEGFKFNFTYLWMM-UHFFFAOYSA-N 3-azaniumylbutan-2-ylazanium;dichloride Chemical compound Cl.Cl.CC(N)C(C)N UEGFKFNFTYLWMM-UHFFFAOYSA-N 0.000 description 1
OWRVXIRUFQIGJV-UHFFFAOYSA-N 5-methyl-2h-benzotriazole;1-phenylpyrazolidin-3-one Chemical compound C1=C(C)C=CC2=NNN=C21.N1C(=O)CCN1C1=CC=CC=C1 OWRVXIRUFQIGJV-UHFFFAOYSA-N 0.000 description 1
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PIBQGZLFBAQMLH-UHFFFAOYSA-N [amino(sulfanyl)methylidene]-(2-hydroxyethyl)azanium;2,2,2-trichloroacetate Chemical compound NC(S)=[NH+]CCO.[O-]C(=O)C(Cl)(Cl)Cl PIBQGZLFBAQMLH-UHFFFAOYSA-N 0.000 description 1
SDWGJGRDMAKEFT-UHFFFAOYSA-N [amino(sulfanyl)methylidene]-(2-hydroxypropyl)azanium;2,2,2-trichloroacetate Chemical compound [O-]C(=O)C(Cl)(Cl)Cl.CC(O)C[NH+]=C(N)S SDWGJGRDMAKEFT-UHFFFAOYSA-N 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000001785 acacia senegal l. willd gum Substances 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
230000002411 adverse Effects 0.000 description 1
229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
150000008041 alkali metal carbonates Chemical class 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical class NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229960002684 aminocaproic acid Drugs 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
235000006708 antioxidants Nutrition 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
229910052601 baryte Inorganic materials 0.000 description 1
239000010428 baryte Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000006172 buffering agent Substances 0.000 description 1
QDHFHIQKOVNCNC-UHFFFAOYSA-M butane-1-sulfonate Chemical compound CCCCS([O-])(=O)=O QDHFHIQKOVNCNC-UHFFFAOYSA-M 0.000 description 1
125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
229920006217 cellulose acetate butyrate Polymers 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 description 1
229940089960 chloroacetate Drugs 0.000 description 1
AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
ZHGASCUQXLPSDT-UHFFFAOYSA-N cyclohexanesulfonic acid Chemical compound OS(=O)(=O)C1CCCCC1 ZHGASCUQXLPSDT-UHFFFAOYSA-N 0.000 description 1
238000012217 deletion Methods 0.000 description 1
230000037430 deletion Effects 0.000 description 1
235000019425 dextrin Nutrition 0.000 description 1
150000008049 diazo compounds Chemical class 0.000 description 1
230000029087 digestion Effects 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
235000010350 erythorbic acid Nutrition 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
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239000006260 foam Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
229940074391 gallic acid Drugs 0.000 description 1
235000004515 gallic acid Nutrition 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical compound [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 description 1
150000002443 hydroxylamines Chemical class 0.000 description 1
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002541 isothioureas Chemical class 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000007788 liquid Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
ORTFAQDWJHRMNX-UHFFFAOYSA-M oxidooxomethyl Chemical compound [O-][C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-M 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
229960003540 oxyquinoline Drugs 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000728 polyester Polymers 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
229920001155 polypropylene Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
239000010970 precious metal Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
VKDBLXQITPBAAG-UHFFFAOYSA-N propanenitrile;hydrochloride Chemical compound Cl.CCC#N VKDBLXQITPBAAG-UHFFFAOYSA-N 0.000 description 1
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
238000000746 purification Methods 0.000 description 1
NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical compound O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
229940079877 pyrogallol Drugs 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
230000033458 reproduction Effects 0.000 description 1
238000011160 research Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000000837 restrainer Substances 0.000 description 1
239000005060 rubber Substances 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
150000003378 silver Chemical class 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
DINKXUCRJBUQAZ-UHFFFAOYSA-N tert-butyl 5-bromopyridine-3-carboxylate Chemical compound CC(C)(C)OC(=O)C1=CN=CC(Br)=C1 DINKXUCRJBUQAZ-UHFFFAOYSA-N 0.000 description 1
125000001302 tertiary amino group Chemical group 0.000 description 1
RXMRGBVLCSYIBO-UHFFFAOYSA-M tetramethylazanium;iodide Chemical compound [I-].C[N+](C)(C)C RXMRGBVLCSYIBO-UHFFFAOYSA-M 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920003176 water-insoluble polymer Polymers 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/61—Compositions containing diazo compounds as photosensitive substances with non-macromolecular additives
- G03C1/615—Substances generating bases
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/43—Processing agents or their precursors, not covered by groups G03C1/07 - G03C1/42

Landscapes

Physics & Mathematics (AREA)
Chemical & Material Sciences (AREA)
Spectroscopy & Molecular Physics (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
General Physics & Mathematics (AREA)
Chemical Kinetics & Catalysis (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Heat Sensitive Colour Forming Recording (AREA)

DE19742425781 1973-05-29 1974-05-28 Verwendung von aldonamiden zur herstellung photographischer materialien Pending DE2425781A1 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US36458173A	1973-05-29	1973-05-29

Publications (1)

Publication Number	Publication Date
DE2425781A1 true DE2425781A1 (de)	1974-12-19

Family

ID=23435154

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE19742425781 Pending DE2425781A1 (de)	1973-05-29	1974-05-28	Verwendung von aldonamiden zur herstellung photographischer materialien

Country Status (6)

Country	Link
JP (1)	JPS5022625A (fr)
BE (1)	BE815695A (fr)
CA (1)	CA1010702A (fr)
DE (1)	DE2425781A1 (fr)
FR (1)	FR2231983B1 (fr)
GB (1)	GB1470451A (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS59174830A (ja) *	1983-03-25	1984-10-03	Fuji Photo Film Co Ltd	熱現像感光材料
EP0143424B1 (fr)	1983-11-25	1990-06-27	Fuji Photo Film Co., Ltd.	Matériel photosensible développable à chaud
US4710631A (en) *	1984-08-28	1987-12-01	Fuji Photo Film Co., Ltd.	Temperature compensation for a semiconductor light source used for exposure of light sensitive material
US4775613A (en)	1985-03-30	1988-10-04	Fuji Photo Film Co., Ltd.	Heat-developable light-sensitive material
JPH083621B2 (ja)	1985-07-31	1996-01-17	富士写真フイルム株式会社	画像形成方法
JPH0619553B2 (ja) *	1986-03-11	1994-03-16	富士写真フイルム株式会社	熱現像用感光材料
JPS6332536A (ja) *	1986-07-25	1988-02-12	Fuji Photo Film Co Ltd	感光材料
US11401370B2 (en)	2018-02-26	2022-08-02	Nippon Kayaku Kabushiki Kaisha	Base proliferating agent, and base-reactive resin composition containing said base proliferating agent

1974
- 1974-04-10 CA CA197,317A patent/CA1010702A/en not_active Expired
- 1974-05-17 GB GB2214774A patent/GB1470451A/en not_active Expired
- 1974-05-27 FR FR7418171A patent/FR2231983B1/fr not_active Expired
- 1974-05-28 DE DE19742425781 patent/DE2425781A1/de active Pending
- 1974-05-29 BE BE144886A patent/BE815695A/fr unknown
- 1974-05-29 JP JP5981774A patent/JPS5022625A/ja active Pending

Also Published As

Publication number	Publication date
GB1470451A (en)	1977-04-14
JPS5022625A (fr)	1975-03-11
CA1010702A (en)	1977-05-24
FR2231983B1 (fr)	1977-10-14
BE815695A (fr)	1974-11-29
FR2231983A1 (fr)	1974-12-27

Legal Events

Date	Code	Title	Description
1980-04-03	OHN	Withdrawal

Publication	Publication Date	Title
DE2736229C2 (fr)	1991-01-17
DE69121965T2 (de)	1997-04-10	Photographisches Hochkontrastelement, das ein eine Alkylpyridiniumgruppe enthaltendes Arylsulphonamidophenylhydrazid einschliesst
DE1547704A1 (de)	1969-11-20	Verfahren zum Entwickeln belichteter photographischer Silberhalogenidschichten auf trockenem Wege
DE1447737A1 (de)	1969-01-09	Durch Waerme entwickelbares Reproduktionsmaterial fuer die Diazotypie
DE2302462B2 (de)	1979-05-03	Thermophotographisches Aufzeichnungsmaterial
DE2119093A1 (de)	1971-11-04	Photographisches Arbeitsblatt oder -band für die Verarbeitung belichteter photographischer Aufzeichnungsmaterialien
DE2020939A1 (de)	1972-02-24	Lichtempfindliches photographisches Material
DE1100464B (de)	1961-02-23	Kopierschichten zur Herstellung von Bildern durch Einwirkung von Waerme
DE2425781A1 (de)	1974-12-19	Verwendung von aldonamiden zur herstellung photographischer materialien
DE2336379A1 (de)	1974-01-31	Strahlungsempfindliches aufzeichnungsmaterial
DE1547655B2 (de)	1977-06-23	Diazotypiematerial
DE1622268A1 (de)	1971-12-30	Verfahren zum Stabilisieren eines photographischen Materials
DE1572103C3 (de)	1973-10-31	Warmeentwickelbares Diazotypie material
DE864657C (de)	1953-01-26	Material fuer die Herstellung von Diazotypien
DE1572072A1 (de)	1970-02-26	Waermeentwickelbares Diazotypiematerial
DE2322873C3 (de)	1978-06-08	Photographisches Aufzeichnungsmaterial sowie Verfahren zur Herstellung photographischer Bilder
DE2609565C2 (de)	1986-07-24	Aufzeichnungsverfahren zur Erzeugung eines positiven Bildes
DE2421069A1 (de)	1974-12-05	Photoempfindliche hitze-entwickelbare materialien
DE1942400U (de)	1966-07-14	Diazolichtpausbahn.
DE2404202A1 (de)	1974-08-01	Photographisches aufzeichnungsmaterial
DE2300772A1 (de)	1973-07-12	Farbuebertragendes farbfotografisches material
DE2237760B2 (de)	1974-03-14	Photographisches Aufzeichnungsmaterial mit einer ein Organoazid enthaltenden Schicht sowie Verfahren zur Herstellung photographischer Bilder
DE2123282A1 (de)	1971-11-25	Wärmeempfindliches Kopiermaterial
DE1522448B2 (de)	1977-04-14	Diazoverbindungen, verfahren zu deren herstellung und diese enthaltende diazotypiematerialien
DE1693191A1 (de)	1971-06-24	Diazotypiematerial