SU63000A1 - Method for increasing the strength of dyes with substantive and acid dyes - Google Patents
Method for increasing the strength of dyes with substantive and acid dyesInfo
- Publication number
- SU63000A1 SU63000A1 SU44515A SU307471A SU63000A1 SU 63000 A1 SU63000 A1 SU 63000A1 SU 44515 A SU44515 A SU 44515A SU 307471 A SU307471 A SU 307471A SU 63000 A1 SU63000 A1 SU 63000A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dyes
- substantive
- strength
- increasing
- acid
- Prior art date
Links
- 239000000982 direct dye Substances 0.000 title description 5
- 239000000975 dye Substances 0.000 title description 4
- 238000000034 method Methods 0.000 title description 3
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 title description 2
- 239000000980 acid dye Substances 0.000 title description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- HTYFFCPFVMJTKM-UHFFFAOYSA-N 2-(4-chlorophenyl)-1-(diaminomethylidene)guanidine Chemical compound NC(N)=NC(N)=NC1=CC=C(Cl)C=C1 HTYFFCPFVMJTKM-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical group NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 229940123208 Biguanide Drugs 0.000 description 1
- 125000000218 acetic acid group Chemical class C(C)(=O)* 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- CUQCMXFWIMOWRP-UHFFFAOYSA-N phenyl biguanide Chemical compound NC(N)=NC(N)=NC1=CC=CC=C1 CUQCMXFWIMOWRP-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- ORFSSYGWXNGVFB-UHFFFAOYSA-N sodium 4-amino-6-[[4-[4-[(8-amino-1-hydroxy-5,7-disulfonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-5-hydroxynaphthalene-1,3-disulfonic acid Chemical compound COC1=C(C=CC(=C1)C2=CC(=C(C=C2)N=NC3=C(C4=C(C=C3)C(=CC(=C4N)S(=O)(=O)O)S(=O)(=O)O)O)OC)N=NC5=C(C6=C(C=C5)C(=CC(=C6N)S(=O)(=O)O)S(=O)(=O)O)O.[Na+] ORFSSYGWXNGVFB-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Coloring (AREA)
Description
Насто щее изобретение относитс к спо-собу повышени прочности окрасок субстантивными и кислотными красител ми.The present invention relates to a process for increasing the strength of dyes with substantive and acidic dyes.
Авторами найдено, что продукты глубокой конденсации фенил- и п-хлорфе;нилби1гуанида, будучи переводимыми в водный раствор добавлением эквивалентного количества уксусной кислоты, осаждают некоторые пр мые красители из кип щего водного раствора 1 : 200.The authors found that the products of deep condensation of phenyl and p-chlorof; nilbi guanide, being converted into an aqueous solution by adding an equivalent amount of acetic acid, precipitate some direct dyes from a boiling aqueous solution of 1: 200.
Способность к осаждению пр мых и кислотных красителей у этих препаратов чрезвычайно вели:ка в сравнении с другими препаратами.The ability to precipitate direct and acid dyes with these drugs is extremely high: ka in comparison with other drugs.
Продукты конденсации фенил- и п-хлорфенилбигуанида с формалином провер лись :на многих субстантивных красител х.The condensation products of phenyl and p-chlorophenylbiguanide with formalin were tested: on many substantive dyes.
После обработки миткал , окрашенного пр мым: чистоголубыад или диаминовым красным F, плюсовани 5-процентнъш раствором конденсата , приготовленного из фенилбигуанида , сушки и глажени (температура утюга 140°), окраска становитс прочной к воде, слабой к стирке и не измен етс на свету. Продукт, полученный из п-хлорфенилбигуанида и формалина, уступает указанHOiMy выше.After processing the nitrated, colored straight: pure blue or diamine red F, plus 5% condensate solution prepared from phenylbiguanide, drying and ironing (iron temperature 140 °), the color becomes durable to water, weak to washing and does not change in the light . The product obtained from p-chlorophenylbiguanide and formalin is inferior to that indicated above.
Оба конденсата дают упрочнение окрасо К светлыми тонами красителей , не мен их оттенка. При упрочнении окрасок тёмными прочность незначительна.Both condensates give hardening of the color K to light tones of dyes, not changing their shade. When hardening dark color strength is negligible.
Пример. Смешивают 17,7 г фе«илбигуаеида , 20 мл воды и 17 г 36,5процентного фОрмалина; при этом происходит растворение и разогревание массы. Через 3 часа на- дне сосуда выдел етс масло. После двух часов нагревани на кип щей вод ной бане масло застывает. Его отдел ют от водного раствора, раствор ют в 30-процентной уксусной кислоте и осаждают аммиаком или 40- процентны1М раствором едкого натри .Example. 17.7 g of feblossalloid are mixed with 20 ml of water and 17 g of 36.5 per cent of formalin; when this occurs, the dissolution and heating of the mass. After 3 hours, oil is released at the bottom of the vessel. After two hours of heating in a boiling water bath, the oil solidifies. It is separated from the aqueous solution, dissolved in 30% acetic acid, and precipitated with ammonia or 40% IM sodium hydroxide solution.
Выделившийс белый творожистый осадок отфильтровывают, промыыают водой и высушивают. Полученный белый или слегка кремовый пыл щий порошок раствор ют в эквивалентном ) количестве уксусной кислоты, предварительно разбавленной водой до желаемой концентрации . Дл осаждени субстантивных красителей из кип щего водного раствора 1 : 200 можно применить 0,5- 1-процентные растворы препарата в виде уксуснокислой или другой соли. Приготовление препарата просто в аппаратурном отнюш-внии и может быть выполнено полностью из отечественного сырь .The white, cheesy precipitate that formed was filtered off, washed with water and dried. The white or slightly creamy powder obtained is dissolved in an equivalent amount of acetic acid previously diluted with water to the desired concentration. For the deposition of substantive dyes from a boiling aqueous solution of 1: 200, 0.5-1 percent solutions of the preparation in the form of an acetic acid or other salt can be used. Preparation of the drug is simple in hardware otnush-vnii and can be made entirely from domestic raw materials.
Предмет изобретени Способ повышени прочности окрасок субстантивными и кислотными кра1сител ми путём об.рабютки водным раствором продуктов конденсации форм1альдегида с соединением группы бигуанида, отличающийс тем, что дл упрочнени окрасок примен ют раствор солей продуктов конденсации бигуанида, например, фенил- или п-хлорфенилбигуанида .The subject of the invention is a method of enhancing the strength of colorings by substantive and acidic colors by using an aqueous solution of formaldehyde condensation products with a compound of the biguanide group, characterized in that a solution of the biguanide condensation products, for example, phenyl or p-chlorophenylbiguanide, is used to harden the colors.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU44515A SU63000A1 (en) | 1941-06-06 | 1941-06-06 | Method for increasing the strength of dyes with substantive and acid dyes |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU44515A SU63000A1 (en) | 1941-06-06 | 1941-06-06 | Method for increasing the strength of dyes with substantive and acid dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU63000A1 true SU63000A1 (en) | 1943-11-30 |
Family
ID=48244025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU44515A SU63000A1 (en) | 1941-06-06 | 1941-06-06 | Method for increasing the strength of dyes with substantive and acid dyes |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU63000A1 (en) |
-
1941
- 1941-06-06 SU SU44515A patent/SU63000A1/en active
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