GB406686A - Improvements in or relating to the treatment of textile and other materials - Google Patents
Improvements in or relating to the treatment of textile and other materialsInfo
- Publication number
- GB406686A GB406686A GB2118832A GB2118832A GB406686A GB 406686 A GB406686 A GB 406686A GB 2118832 A GB2118832 A GB 2118832A GB 2118832 A GB2118832 A GB 2118832A GB 406686 A GB406686 A GB 406686A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyeing
- phenylenediamine
- bases
- cellulose
- diethylaminoacetyl
- Prior art date
- 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.)
- Expired
Links
- 239000000463 material Substances 0.000 title abstract 2
- 239000004753 textile Substances 0.000 title abstract 2
- 238000004043 dyeing Methods 0.000 abstract 6
- 239000002253 acid Substances 0.000 abstract 4
- 239000000243 solution Substances 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 229920002678 cellulose Polymers 0.000 abstract 3
- 229920002301 cellulose acetate Polymers 0.000 abstract 3
- 229920003086 cellulose ether Polymers 0.000 abstract 3
- 239000004744 fabric Substances 0.000 abstract 3
- 239000003517 fume Substances 0.000 abstract 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 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 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 229910021538 borax Inorganic materials 0.000 abstract 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 2
- 239000006185 dispersion Substances 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- 239000000344 soap Substances 0.000 abstract 2
- 239000004328 sodium tetraborate Substances 0.000 abstract 2
- 235000010339 sodium tetraborate Nutrition 0.000 abstract 2
- 238000009987 spinning Methods 0.000 abstract 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 abstract 1
- FCWBHVZCSYIWHX-UHFFFAOYSA-N 1-(dimethylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N(C)C FCWBHVZCSYIWHX-UHFFFAOYSA-N 0.000 abstract 1
- ICVRBKCRXNVOJC-UHFFFAOYSA-N 1-amino-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2NC ICVRBKCRXNVOJC-UHFFFAOYSA-N 0.000 abstract 1
- YVGKCZBJWCNRSO-UHFFFAOYSA-N 4-(diethylaminomethyl)benzamide Chemical compound CCN(CC)CC1=CC=C(C(N)=O)C=C1 YVGKCZBJWCNRSO-UHFFFAOYSA-N 0.000 abstract 1
- XWEVWZCUWKFEBQ-UHFFFAOYSA-N C(C)(=O)NC1=CC=C(CN(CC)CC)C=C1 Chemical compound C(C)(=O)NC1=CC=C(CN(CC)CC)C=C1 XWEVWZCUWKFEBQ-UHFFFAOYSA-N 0.000 abstract 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 abstract 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 abstract 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 abstract 1
- 230000000397 acetylating effect Effects 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000012237 artificial material Substances 0.000 abstract 1
- 150000007942 carboxylates Chemical class 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 238000012505 colouration Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 239000007859 condensation product Substances 0.000 abstract 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 238000005562 fading Methods 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- 150000002484 inorganic compounds Chemical class 0.000 abstract 1
- 229910010272 inorganic material Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- TZHYFNJRLMHJCM-UHFFFAOYSA-N n-(3-phenylpropyl)aniline Chemical compound C=1C=CC=CC=1CCCNC1=CC=CC=C1 TZHYFNJRLMHJCM-UHFFFAOYSA-N 0.000 abstract 1
- OAXCYNSIHXILCT-UHFFFAOYSA-N n-[2-(diethylamino)phenyl]acetamide Chemical compound CCN(CC)C1=CC=CC=C1NC(C)=O OAXCYNSIHXILCT-UHFFFAOYSA-N 0.000 abstract 1
- HSYWKISLWCMZKJ-UHFFFAOYSA-N n-[4-(diethylaminomethyl)phenyl]benzamide Chemical class C1=CC(CN(CC)CC)=CC=C1NC(=O)C1=CC=CC=C1 HSYWKISLWCMZKJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- -1 p - acetylaminobenzyldiethylamine p - benzoylamino - benzyldiethylamine Chemical compound 0.000 abstract 1
- KGCNHWXDPDPSBV-UHFFFAOYSA-N p-nitrobenzyl chloride Chemical compound [O-][N+](=O)C1=CC=C(CCl)C=C1 KGCNHWXDPDPSBV-UHFFFAOYSA-N 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- 235000017281 sodium acetate Nutrition 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 229940045870 sodium palmitate Drugs 0.000 abstract 1
- GGXKEBACDBNFAF-UHFFFAOYSA-M sodium;hexadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCC([O-])=O GGXKEBACDBNFAF-UHFFFAOYSA-M 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
Landscapes
- Coloring (AREA)
- Artificial Filaments (AREA)
Abstract
Cellulose esters or ethers, dyeing; unspecified types of dyes, dyeing with; dye preparations; cellulose carboxylates; cellulose ethers.--The fastness of colourations on textile or other materials, especially the fastness to the combined action of light and of acid fumes, is improved by incorporating therein compounds which contain an acidylamino or an acid amide group as a substituent in an aryl nucleus and which contain also (a) an additional substituent in the aryl nucleus, said substituent bearing a non-aromatically linked basic amino group or (b) a non-aromatically linked basic amino group as a substituent in the acidyl group of the said acidylamino group. Specified bases are o -diethylaminoacetanilide, di-(o -diethylaminoacetyl) - p - phenylenediamine, p - acetylaminobenzyldiethylamine p - benzoylamino - benzyldiethylamine and 4 - (diethylaminomethyl) benzamide. Other substances capable of improving the fastness, such as those of Specifications 243,841, [Class 15 (ii)], 340,541, 340,572, 355,726, 361,362, 361,381, 373,628, or 378,473, with or without inorganic compounds having an alkaline reaction, such as sodium carbonate, borax, disodium hydrogen phosphate, sodium acetate, sodium palmitate or sodium oleate, may be used in conjunction with the bases. The bases may in some cases be absorbed from aqueous solutions of their salts; they may also be applied as aqueous dispersions produced, for example, by the methods of Specifications 219,349, 224,925, 242,393, 242,711, 269,960, 273,819, 273,820, 322,737, or 323,788, [all in Class 15 (ii)]. Compositions containing the bases and the dyestuffs in dispersed form may be prepared for use in dyeing. In the application to cellulose ester or ether artificial materials the bases may be incorporated in the spinning solutions used. The following examples are specified: (1) a cellulose acetate fabric, dyed with 1 : 4-dimethylaminoanthraquinone, is treated in an aqueous bath containing p-acetylaminobenzyldiethylamine dispersed with turkey red oil and soap, the temperature being raised from 15 to 50 DEG C. during \ba3/4\be hour and thereafter maintained at about 80 DEG C. for a further \ba3/4\be hour; the treatment improves the resistance of the dyeing to the combined action of light and acid fumes; (2) a scoured cellulose acetate fabric is entered into a cold or luke warm aqueous bath containing 1-amino-4-methylaminoanthraquinone and di-(o -diethylaminoacetyl)-p-phenylenediamine dispersed with turkey red oil and soap and the temperature is slowly raised to 80 DEG C and there maintained for about \ba3/4\be hour; the dyeing has improved fastness to the combined action of light and acid fumes; (3) a solution of cellulose acetate containing di-(o -diethylaminoacetyl-p-phenylenediamine is dry spun to form filaments and a fabric made therefrom is dyed in a bath containing a dispersion of 1 : 4-diethanolaminoanthraquinone and benzylethylaniline and thereafter washed, hydroextracted, treated with a dilute solution of borax and dried; the incorporation of the base in the spinning solution gives the dyeing improved resistance to fading under acid conditions. The invention is applicable also to wool, cotton, silk and other fibres. p-Acetylamino- and p-benzoylamino-benzyl-diethylamines are obtained by acetylating and benzoylating respectively the products obtained by reducing the nitro group of the condensation product of p-nitrobenzyl chloride with diethylamine. Di-(o -diethylaminoacetyl)-p-phenylenediamine is obtained by condensing diethylamine with the product of condensation of p-phenylenediamine (1 mol.) with chloracetyl chloride (2 mols.).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2118832A GB406686A (en) | 1932-07-27 | 1932-07-27 | Improvements in or relating to the treatment of textile and other materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2118832A GB406686A (en) | 1932-07-27 | 1932-07-27 | Improvements in or relating to the treatment of textile and other materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB406686A true GB406686A (en) | 1934-02-27 |
Family
ID=10158661
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2118832A Expired GB406686A (en) | 1932-07-27 | 1932-07-27 | Improvements in or relating to the treatment of textile and other materials |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB406686A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE740983C (en) * | 1939-02-15 | 1943-11-02 | Ig Farbenindustrie Ag | Process for improving the fastness of dyeings with acetate artificial silk dyes, which are poorly soluble or insoluble in water, on artificial silk made from cellulose esters |
| CN108120834A (en) * | 2017-12-08 | 2018-06-05 | 上海君联医疗设备有限公司 | A kind of reagent composition for being aggregated mutant |
| CN111751557A (en) * | 2020-07-16 | 2020-10-09 | 上海君联医疗设备有限公司 | Sugar chain protein and calcium-histone detection reagent composition and use thereof |
-
1932
- 1932-07-27 GB GB2118832A patent/GB406686A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE740983C (en) * | 1939-02-15 | 1943-11-02 | Ig Farbenindustrie Ag | Process for improving the fastness of dyeings with acetate artificial silk dyes, which are poorly soluble or insoluble in water, on artificial silk made from cellulose esters |
| CN108120834A (en) * | 2017-12-08 | 2018-06-05 | 上海君联医疗设备有限公司 | A kind of reagent composition for being aggregated mutant |
| CN108120834B (en) * | 2017-12-08 | 2020-04-24 | 上海君联医疗设备有限公司 | Reagent composition for agglutinating variant cells |
| CN111751557A (en) * | 2020-07-16 | 2020-10-09 | 上海君联医疗设备有限公司 | Sugar chain protein and calcium-histone detection reagent composition and use thereof |
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