SU520560A1 - Фотографический материал - Google Patents

Info

Publication number

SU520560A1

SU520560A1 SU1980013A SU1980013A SU520560A1 SU 520560 A1 SU520560 A1 SU 520560A1 SU 1980013 A SU1980013 A SU 1980013A SU 1980013 A SU1980013 A SU 1980013A SU 520560 A1 SU520560 A1 SU 520560A1

Authority

SU

USSR - Soviet Union

Prior art keywords

fixing agent

compounds

dyes

photographic material

alkyl

Prior art date

1972-12-07

Links

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• 239000000463 material Substances 0.000 title claims description 6
• 239000003795 chemical substances by application Substances 0.000 claims description 11
• 150000001875 compounds Chemical class 0.000 claims description 8
• 125000001424 substituent group Chemical group 0.000 claims description 6
• 239000002253 acid Substances 0.000 claims description 5
• 239000000975 dye Substances 0.000 claims description 5
• 125000000217 alkyl group Chemical group 0.000 claims description 3
• 238000009792 diffusion process Methods 0.000 claims description 3
• 239000000987 azo dye Substances 0.000 claims description 2
• 239000000839 emulsion Substances 0.000 claims description 2
• 230000002378 acidificating effect Effects 0.000 claims 2
• 239000001257 hydrogen Substances 0.000 claims 1
• 229910052739 hydrogen Inorganic materials 0.000 claims 1
• -1 carboxylic acid chlorides Chemical class 0.000 description 5
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• 108010010803 Gelatin Proteins 0.000 description 3
• 229920000159 gelatin Polymers 0.000 description 3
• 239000008273 gelatin Substances 0.000 description 3
• 235000019322 gelatine Nutrition 0.000 description 3
• 235000011852 gelatine desserts Nutrition 0.000 description 3
• 239000000243 solution Substances 0.000 description 3
• 239000007864 aqueous solution Substances 0.000 description 2
• 150000004985 diamines Chemical class 0.000 description 2
• 239000008164 mustard oil Substances 0.000 description 2
• 230000003287 optical effect Effects 0.000 description 2
• 229940105325 3-dimethylaminopropylamine Drugs 0.000 description 1
• YZICFVIUVMCCOC-UHFFFAOYSA-N 3-piperidin-1-ylpropanenitrile Chemical compound N#CCCN1CCCCC1 YZICFVIUVMCCOC-UHFFFAOYSA-N 0.000 description 1
• SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
• VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
• ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 1
• 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 239000004202 carbamide Substances 0.000 description 1
• 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
• 150000001805 chlorine compounds Chemical class 0.000 description 1
• IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
• 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
• WRNOAELBRPKVHC-UHFFFAOYSA-N dodecylurea Chemical compound CCCCCCCCCCCCNC(N)=O WRNOAELBRPKVHC-UHFFFAOYSA-N 0.000 description 1
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
• 239000012948 isocyanate Substances 0.000 description 1
• 150000002513 isocyanates Chemical class 0.000 description 1
• WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1