GB469476A - Improvements in the treatment of cellulosic material - Google Patents
Improvements in the treatment of cellulosic materialInfo
- Publication number
- GB469476A GB469476A GB3577935A GB3577935A GB469476A GB 469476 A GB469476 A GB 469476A GB 3577935 A GB3577935 A GB 3577935A GB 3577935 A GB3577935 A GB 3577935A GB 469476 A GB469476 A GB 469476A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ether
- fabric
- dried
- cotton
- chloromethyl
- 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
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Cellulosic materials are treated with a halogeno-methyl ether of the general formula R--O--CH2--Hal, in which R is a normal or branched chain aliphatic hydrocarbon radical, saturated or unsaturated, of not less than 8 carbon atoms, and Hal is a halogen atom, the treatment being carried out at a raised temperature in an inert organic diluent or solvent for the reagents, and preferably in the presence of an acid-binding agent. As an alternative, there may be used a quaternary ammonium salt formed from the halogeno methyl ether and a tertiary organic amine. The cellulosic material may consist wholly or in part of natural or regenerated cellulose or cellulose esters, e.g. cotton, viscose or other artificial silk including cellulose acetate material, linen, jute or mixtures of these fibres. Paper or films, threads, yarns, woven or knitted fabrics may be treated. The materials may be dyed. The chlormethyl ethers used are obtained by treating the respective alcohol with formaldehyde and hydrogen halide. Chloro methyl dodecyl, sec-dodecyl, cetyl, or octodecyl ether, or a chloromethyl ether of the mixture of alcohols from sperm oil may be used. The treatment renders the material waterproof and gives it a soft handle and these effects are resistant to laundering and dry cleaning. Toluene, benzene, acetone, carbon tetrachloride, trichlorethylene, and other hydrocarbons or chlorinated hydrocarbons may be used as organic diluent or solvent. Pyridine, aniline, N-alkylaniline or dialkyl aniline, di- or triethylamine, piperidine, alkyl piperidines, sodium or potassium carbonate, potassium acetate, or calcium hydroxide may be used as acid binding agent. The treatment is carried out at raised temperature, preferably at or near the boiling point of the diluent. In an example, a -chloromethyl octadecyl ether is dissolved in dry toluene and pyridine is added. Undyed boiled out cotton limbric is immersed in this solution which is heated at 90 DEG C. The fabric is removed, pressed, washed with alcohol, and dried. In other examples, cotton-wool union fabric, gaberdine and limbric are treated. Cotton fabric is impregnated with a solution of octadecoxymethyl pyridinium chloride in trichloroethylene, squeezed, and dried in a current of warm air. It is then baked at 105 DEG C. Limbric is padded with chloromethyl octadecyl ether, diethylaniline, and benzene mixture. It is dried in warm air and then heated at 120 DEG C. on a drying cylinder. Knitted cellulose acetate fabric is immersed in a solution of toluene containing a chloromethyl ether of sperm-oil alcohols, and pyridine. The solution is heated for 30 minutes and the fabric is then rinsed in alcohol and dried. Specifications 340,555, 390,553, 396,992, and 426,482 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3577935A GB469476A (en) | 1935-12-24 | 1935-12-24 | Improvements in the treatment of cellulosic material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3577935A GB469476A (en) | 1935-12-24 | 1935-12-24 | Improvements in the treatment of cellulosic material |
Publications (1)
Publication Number | Publication Date |
---|---|
GB469476A true GB469476A (en) | 1937-07-26 |
Family
ID=10381459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3577935A Expired GB469476A (en) | 1935-12-24 | 1935-12-24 | Improvements in the treatment of cellulosic material |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB469476A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE918982C (en) * | 1939-04-25 | 1954-10-11 | Dehydag Gmbh | Process for the production of quaternary nitrogen compounds |
CN112829395A (en) * | 2021-02-05 | 2021-05-25 | 义乌市皓祺服饰有限公司 | Preparation method of waterproof breathable outdoor jacket fabric |
-
1935
- 1935-12-24 GB GB3577935A patent/GB469476A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE918982C (en) * | 1939-04-25 | 1954-10-11 | Dehydag Gmbh | Process for the production of quaternary nitrogen compounds |
CN112829395A (en) * | 2021-02-05 | 2021-05-25 | 义乌市皓祺服饰有限公司 | Preparation method of waterproof breathable outdoor jacket fabric |
CN112829395B (en) * | 2021-02-05 | 2023-07-04 | 义乌市皓祺服饰有限公司 | Preparation method of waterproof breathable jacket fabric |
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