GB899902A - Process for treating cellulosic textile materials - Google Patents
Process for treating cellulosic textile materialsInfo
- Publication number
- GB899902A GB899902A GB1400761A GB1400761A GB899902A GB 899902 A GB899902 A GB 899902A GB 1400761 A GB1400761 A GB 1400761A GB 1400761 A GB1400761 A GB 1400761A GB 899902 A GB899902 A GB 899902A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphoxide
- catalyst
- treated
- alkali metal
- textile material
- 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
- D06M13/244—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 sulfur or phosphorus
- D06M13/248—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 sulfur or phosphorus with compounds containing sulfur
- D06M13/272—Unsaturated compounds containing sulfur atoms
- D06M13/278—Vinylsulfonium compounds; Vinylsulfone or vinylsulfoxide compounds
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
Abstract
The dimensional stability and wash and wear characteristics of textile materials containing cellulosic fibres are improved by reacting the textile material with a compound of the formula <FORM:0899902/IV (a)/1> in which each R may be the same or different and represents hydrogen or a hydrocarbon radical containing 1-8 carbon atoms, inclusive, e.g. divinyl, dipropenyl, diisopropenyl and diisobutenyl sulphoxides, in the presence of an alkaline catalyst, e.g. alkali metal hydroxides and carbonates, quaternary ammonium hydroxides, alkali metal salts which in the reaction mixtures hydrolyse to form alkaline solutions, such as alkali metal sulphides, and strongly alkaline organic acid-alkali metal salts. The textile material may be treated with the sulphoxide and then passed into an aqueous solution of the catalyst containing inorganic or organic salts, e.g. sodium chloride, acetate or sulphate or trisodium phosphate. Alternatively the textile material may be treated with the catalyst and then with the sulphoxide, or the sulphoxide and catalyst may be applied simultaneously. The sulphoxide and catalyst may be applied from aqueous solutions or from solutions in water-miscible organic solvents, e.g. acetone, tertiary butanol and tetrahydrofuran. From 1 to 100% of the sulphoxide, calculated on the dry weight of the textile material, may be applied. The reaction is preferably carried out at room temperature for 1/2 -4 hours, although temperatures of up to 100 DEG C. and higher may be employed. Woven and knitted fabrics, yarns, threads and separate fibres in the form of a sliver made from cotton, jute, hemp, flax, viscose rayon or partially esterified or etherified cellulose, alone or in admixture with non-cellulosic materials, e.g. nylon and polyesters, may be treated.ALSO:Compounds having the formula <FORM:0899902/IV (b)/1> in which each R may be the same or different and represents hydrogen or a hydrocarbon radical containing 1-8 carbon atoms, inclusive, are prepared by <FORM:0899902/IV (b)/2> <FORM:0899902/IV (b)/3> <FORM:0899902/IV (b)/4> wherein R has the value defined. Specified compounds are divinyl sulphoxide, dipropenyl sulphoxide, diisopropenyl sulphoxide and diisobutenyl sulphoxide.ALSO:The dimensional stability and wash and wear characteristics of textile materials containing cellulosic fibres are improved by reacting the textile material with a compound of the formula <FORM:0899902/IV (c)/1> in which each R may be the same or different and represents hydrogen or a hydrocarbon radical containing 1-8 carbon atoms, inclusive, e.g. divinyl, dipropenyl, diisopropenyl and diisobutenyl sulphoxides, in the presence of an alkaline catalyst, e.g. alkali metal hydroxides and carbonates, quaternary ammonium hydroxides, alkali metal salts which in the reaction mixtures hydrolyze to form alkaline solutions, such as alkali metal sulphides, and strongly alkaline organic acid-alkali metal salts. The textile material may be treated with the sulphoxide and then passed into an aqueous solution of the catalyst containing inorganic or organic salts, e.g. sodium chloride, acetate or sulphate or trisodium phosphate. Alternatively the textile material may be treated with the catalyst and then with the sulphoxide, or the sulphoxide and catalyst may be applied simultaneously. The sulphoxide and catalyst may be applied from aqueous solutions or from solutions in water miscible organic solvents, e.g. acetone, tertiary butanol and tetrahydrofuran. From 1 to 100% of the sulphoxide, calculated on the dry weight of the textile material, may be applied. The reaction is preferably carried out at room temperature for 1/2 -4 hours, although temperatures of up to 100 DEG C. and higher may be employed. Cellulosic fabrics treated may have previously been treated with 2%-6% by weight of a resin, or the fabric may be treated with a resin to improve its flat drying properties and dry crease resistance after treatment with the sulphoxide. Woven and knitted fabrics, yarns, threads and separate fibres in the form of a sliver made from cotton, jute, hemp, flax, viscose rayon or partially esterified or etherified cellulose, alone or in admixture with non cellulosic materials, e.g. nylon and polyesters, may be treated.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2553460A | 1960-04-29 | 1960-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB899902A true GB899902A (en) | 1962-06-27 |
Family
ID=21826641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1400761A Expired GB899902A (en) | 1960-04-29 | 1961-04-18 | Process for treating cellulosic textile materials |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1139465B (en) |
FR (1) | FR1289717A (en) |
GB (1) | GB899902A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL267024A (en) * | 1960-08-25 | 1900-01-01 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2524399A (en) * | 1948-07-07 | 1950-10-03 | Us Rubber Co | Cellulose treated with di-vinyl sulfone to shrinkproof |
-
1961
- 1961-04-18 GB GB1400761A patent/GB899902A/en not_active Expired
- 1961-04-20 FR FR859285A patent/FR1289717A/en not_active Expired
- 1961-04-28 DE DED35956A patent/DE1139465B/en active Pending
Also Published As
Publication number | Publication date |
---|---|
DE1139465B (en) | 1962-11-15 |
FR1289717A (en) | 1962-04-06 |
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