SU93645A1 - Suspension method of dyeing with insoluble azo dyes formed on the fiber - Google Patents
Suspension method of dyeing with insoluble azo dyes formed on the fiberInfo
- Publication number
- SU93645A1 SU93645A1 SU400488A SU400488A SU93645A1 SU 93645 A1 SU93645 A1 SU 93645A1 SU 400488 A SU400488 A SU 400488A SU 400488 A SU400488 A SU 400488A SU 93645 A1 SU93645 A1 SU 93645A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- dyeing
- fiber
- azo dyes
- suspension method
- insoluble azo
- Prior art date
Links
- 238000004043 dyeing Methods 0.000 title description 9
- 239000000725 suspension Substances 0.000 title description 8
- 239000000835 fiber Substances 0.000 title description 7
- 238000000034 method Methods 0.000 title description 7
- 239000000987 azo dye Substances 0.000 title 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- QZIQJVCYUQZDIR-UHFFFAOYSA-N mechlorethamine hydrochloride Chemical compound Cl.ClCCN(C)CCCl QZIQJVCYUQZDIR-UHFFFAOYSA-N 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- NIPDVSLAMPAWTP-UHFFFAOYSA-N 2-methoxy-5-nitroaniline Chemical compound COC1=CC=C([N+]([O-])=O)C=C1N NIPDVSLAMPAWTP-UHFFFAOYSA-N 0.000 description 1
- QGZGJNPVHADCFM-UHFFFAOYSA-N 3-hydroxy-n-naphthalen-1-ylnaphthalene-2-carboxamide Chemical compound C1=CC=C2C(NC(=O)C3=CC4=CC=CC=C4C=C3O)=CC=CC2=C1 QGZGJNPVHADCFM-UHFFFAOYSA-N 0.000 description 1
- 241000060350 Citronella moorei Species 0.000 description 1
- 241000234295 Musa Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
Landscapes
- Coloring (AREA)
Description
Обычный способ крашени расиительных волокнистых материалов нерастворимыми образуемыми на волокне азоюрааител лщ (так (назыBiaeMoe лед иое крашение) состоит -в пропитке окрашиваемого материала сначала раствором азотол та, а затем раствором диазосост1авл юш;ей.The usual way of dyeing fibrous materials insoluble with azo-based fibers (so-called ice dyeing) formed on the fiber consists in impregnating the material to be painted, first with a solution of nitrogen, and then with a solution of diazo-composites;
Известен также суспензионный способ лдд ного крашени , при котором окрашиваемый матер иал обрабатывают водной суспензией азотола, полученной меха|нически1м путем, а затем азотол сочетают на волокне с да,азосоставл юш..ей. HeiaacTaTKOiM этого способа вл етс непрочность получаемых окрасок к мылу.Also known is the suspension method of dye dyeing, in which the material being painted is treated with an aqueous suspension of azotole, obtained mechanically by the first route, and then the azotole is combined on the fiber with yes, azo composition of y. HeiaacTaTKOiM of this method is the fragility of the resulting stains to soap.
Предлагаемый способ лед ного крашени также Езл етс суспензионным и основное отличие его от ужазаннаго заключаетс в том, ч го за нанесением на волокно суспензии азотола (азосоставллющей) следует обработка ш;елочью с целью перевода на волокне азотола в азотол т. В результате того с диазосоставл юш,ей сочетаетс не азотол, а азотол т.The proposed method of ice dyeing is also Suspended, and its main difference from the Uzzanine is that a suspension of Nitol (azo-compositing) is applied to the fiber using an alkaline solution in order to convert Nitol to Nitol on the fiber. As a result, Yush, it combines not nitrogen, but nitrogen.
ПрвИ(Муш1ест Вом предлаг.а1вмото способа вл етс то, что он:PrVI (Mush1est Vom proposes a1moto the method is that he:
а)позвол ет осуш:е1ствить глубокое проникновение суспемзии азотола в 1волок1но и образование азотол та в толше волокна/а ие только на его поверхности;a) allows drying: it allows deep penetration of the suspension of azototal into volokolno and the formation of azototal in the thickness of the fiber / ae only on its surface;
б)обеспечивает возможность получени широкой гаммы расцветок (синих, оранжевых, розовых, красных) с высокими прочност м,и к трению и мыловка1М при температуре 100°; по прочности к ррению и мыловкам окр.аокм, получаемые по предлагаемому способу, вполие конкурируют с окрасками лучшими мар«ам1и .нтреновых красителей, что позвол ет 1вести работы по замане крашени вышивальных ниток (ирис, мулине) ализарином красным по алюми-н-иевой протраве лед ны-м крашением .b) provides the possibility of obtaining a wide range of colors (blue, orange, pink, red) with high strengths, and friction and soaping 1M at a temperature of 100 °; on strength to rrenia and soap boxes of the arakm, obtained by the proposed method, completely compete with the colors of the best martins and dyes, which allows one to work on the luring of the dyeing of embroidery threads (iris, muline) alizarin red on aluminum and ice stained with dyeing.
Требуемую дл крашеви по предлагаемому способу суспеизию азотола рекомеадуетс получать осаж1дением раствора азотол та кислотой , например уксусной, в юрисутствии ализаринового ;мас,та. № 93645- 2 - Пример 1. Крашение алым К,аз и азоамином алым Ж по азотолу АНФ. 1.Приготовление суспензии азотола АНФ: Азотол АНФ Ализариновое масло, 70%-мое, иейтралы-юе Едкий натр уд. в. 1,26 Вода гор ча (98-95°) Продолжительность растворени Вода гор ча Уксусна кислота-до нейтральной реакции по ла 2.Пронитка Cbiipiofi МарсеризОВанной прЯ:Ж;и,от Влажность нр жи перед ироииткой Концентраци азотола Температура пропитки Модуль ванны Продолжительность пропитки Привес пр жи после пропитки 3.Обработка раствором ещкого натра: Модуль ваины Едкий натр уд. в. 1,26 Температура Продолжительность Отжим на центрифуге Влажность пр жи перед сочетанием 4. Приготовлеиие диазорасгворов аз-оамина алого вого 0,1азоамина алого Ж и сочетатие их с азотол рецептам, рекомендуемым в л итератлре 1дл .данного 5.Две промывки по 20 мни. кажда : перва нри 6.Мыловка раствором слабон1;елоч1юго Мыло 50%-ное Температура Модуль ванны Продолжительность 7.Промывка 1на воде: Температура Продолжительность 8.Втора мыловка: 50%-ное Температура Модуль ванны Продолжительность , 9. Две теплые промывки на вqдe при 35° ио 20 10. Отж1км на центрифуге и сушка. Пример 2. Крашение азоамином красным О п 1. Приготовление суспелзаи азотола О: Азотол О Ализариновое масло, 70%-ное, нейтральное Едкий натр уд. в. 1,308 Вода гор ча (98-95°) Продолжительность растворени Вода гор ча Уксусна кислота-до слабокислой реакции по лак ином розовым О 1 кг 0,5 л 1,45 л 30 л 20 мин. 23 л мусу. ренной на воде: 50-55% 18 е/л 55-50° 1:20 55 сек. 55-50% 1:25 35 л(л/л 40-35° 20 мип. 55-50% К, азоа М1ина розоми проводитс по ви,да KpamieiHHiH. 5°, втора нри 35. 5 г/уг 65-60° 1:25 30 мин. 35° 20 мин. 5 65-60° 1:25 30 мин. ин. кажда . азотолу О. кг 0,83 кг л 30 л 20 мин. 23 л су.The required suspension of nitrosol for the proposed method of suspension is recommended to be obtained by precipitating a solution of azotoil with an acid, for example, acetic acid, in the presence of alizarin; No. 93645- 2 - Example 1. Dyeing with scarlet K, az and azoamine scarlet Zh on azotool ANF. 1. Preparation of a suspension of Nitol ANF: Azotol ANF Alizarin oil, 70% mine, and neutrals Acid soda beats. at. 1.26 Hot water (98-95 °) Duration of dissolution Water hot Acetic acid — until neutral: 2. Cbiipiofi impurity Marserized yarn: F; and, from Humidity in front of the ionizer Nitrogen concentration Impregnation temperature Bath module Impregnation duration Yarn weight gain after impregnation 3. Processing with a further soda solution: Vaina module Caustic soda beats. at. 1.26 Temperature Duration Spin on the centrifuge Humidity of the yarn before the combination 4. Prepare the diazores of az-oamine scarlet 0.1azamine scarlet G and combine them with azo-tol recipes recommended in 1 liter of 1 dl. each: the first nri 6. Mosing with a solution of weakly1; firmer Soap 50% Temperature Bath module Duration 7. Wash 1 in water: Temperature Duration 8. Second soap: 50% Temperature Bath module Duration 9. Two warm rinses on high water 35 ° Io 20 10. Otszh1km in a centrifuge and drying. Example 2. Dyeing with azoamine red. O p 1. Preparation of suspensions and azo-tols. A: Nitotol-O Alizarin oil, 70%, neutral Caustic soda beats. at. 1.308 Hot water (98-95 °) Duration of dissolution Water Hot acetic acid — until slightly acidic reaction in a varnish of pink O 1 kg 0.5 l 1.45 l 30 l 20 min. 23 l musa. rented on water: 50-55% 18 e / l 55-50 ° 1:20 55 sec. 55-50% 1:25 35 l (l / l 40-35 ° 20 mip. 55-50% K, azoa m1ina roseomi is carried out by type, yes KpamieiHHiH. 5 °, the second is 35. 5 g / ug 65-60 ° 1:25 30 minutes 35 ° 20 minutes 5 65-60 ° 1:25 30 minutes in. Each. Nitrogen O. kg 0.83 kg l 30 l 20 min 23 l sou.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU400488A SU93645A1 (en) | 1949-12-19 | 1949-12-19 | Suspension method of dyeing with insoluble azo dyes formed on the fiber |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU400488A SU93645A1 (en) | 1949-12-19 | 1949-12-19 | Suspension method of dyeing with insoluble azo dyes formed on the fiber |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU93645A1 true SU93645A1 (en) | 1951-11-30 |
Family
ID=48369042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU400488A SU93645A1 (en) | 1949-12-19 | 1949-12-19 | Suspension method of dyeing with insoluble azo dyes formed on the fiber |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU93645A1 (en) |
-
1949
- 1949-12-19 SU SU400488A patent/SU93645A1/en active
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