GB954275A - Improvements in and relating to the treatment of cellulosic textile materials - Google Patents
Improvements in and relating to the treatment of cellulosic textile materialsInfo
- Publication number
- GB954275A GB954275A GB34521/62A GB3452162A GB954275A GB 954275 A GB954275 A GB 954275A GB 34521/62 A GB34521/62 A GB 34521/62A GB 3452162 A GB3452162 A GB 3452162A GB 954275 A GB954275 A GB 954275A
- Authority
- GB
- United Kingdom
- Prior art keywords
- epihalohydrin
- vapour
- weight
- textile materials
- water
- 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
- D06M13/10—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 oxygen
- D06M13/11—Compounds containing epoxy groups or precursors thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/08—Oxirane
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Cellulosic textile materials are treated in either order with an aqueous caustic solution and with the hot vapour of an epihalohydrin or material which liberates an epihalohydrin when in an alkaline medium. The textile materials may be impregnated with a solution containing 1-25% by weight of sodium or potassium hydroxide by dipping, spraying or padding to a liquid uptake of 40-100% by weight at a temperature from ambient temperature to 80 DEG C. The caustic solution may contain 0.1-25% by weight of a cationic, anionic or nonionic wetting agent, e.g. sodium or potassium myristate, laurate, palmitate, oleate or stearate, ammonium stearate, lauryl amine hydrochloride and stearyl amine hydrochloride. The textile materials may be treated with a reducing agent, e.g. sodium or potassium hydrosulphite, hypophosphite, thiosulphate or borohydride, before or after treatment with the epihalohydrin or material liberating an epihalohydrin or the reducing agent may be added to the caustic solution. Suitable ephialohydrins and materials liberating epihalohydrins are epichlorohydrin, epibromohydrin, 2, 3-epoxy-2-methyl-1-chloro propane, 2, 3 epoxy-1-chlorobutane, 2, 3 epoxy-1-bromobutane, 2, 3 epoxy-l-chloropentane, 1, 3 dichloro-2-hydroxy propane and 1, 3 dibromo-2-hydroxy propane. The epihalohydrin or material liberating an epihalohydrin may be admixed with a diluent, e.g. water, the preferred vapour mixture being the water and epichlorohydrin constant boiling vapour composition at 87.8 DEG C., at 760 mm having a composition of 76% by weight of epichlorochydrin and 24% by weight of water. The temperature of the vapour may range from the reflux temperature of the epihalohydrin or material liberating the epihalohydrin up to 100 DEG C. in excess thereof and the textile materials may be hung in or passed through a chamber filled by the vapour so that the contact time with the vapour is from 15 seconds to 5 minutes. The textile materials may be washed with water or water and detergents and dried at 20 DEG -125 DEG C.ALSO:Cellulosic textile materials are creaseproofed by treating them in either order with an aqueous caustic solution and with the hot vapour of an epihalohydrin or material which liberates an epihalohydrin when in an alkaline medium. The textile materials may be impregnated with a solution containing 1-25% by weight of sodium or potassium hydroxide by dipping, spraying or padding to a liquid uptake of 40-100% by weight at a temperature from ambient temperature to 80 DEG C. The caustic solution may contain 0.1-25% by weight of a cationic, anionic or nonionic wetting agent, e.g. sodium or potassium myristate, laurate, palmitate, oleate or stearate, ammonium stearate, lauryl amine hydrochloride and stearyl amine hydrochloride. The textile materials may be treated with a reducing agent, e.g. sodium or potassium hydrosulphite, hypophosphite, thiosulphate or borohydride, before or after treatment with the epihalohydrin or material liberating an epihalohydrin or the reducing agent may be added to the caustic solution. Suitable epihalohydrins and materials liberating epihalohydrins are epichlorohydrin, epibromohydrin, 2, 3-epoxy-2-methyl-1-chloro propane, 2, 3 epoxy-1-chlorobutane, 2, 3 epoxy-1-bromobutane, 2, 3 epoxy-1-chloropentane, 1, 3 dichloro-2-hydroxy propane and 1, 3 dibromo-2-hydroxy propane. The epihalohydrin or material liberating an epihalohydrin may be admixed with a diluent, e.g. water, the preferred vapour mixture being the water and epichlorohydrin constant boiling vapour composition at 87.8 DEG C. at 760 mm having a composition of 76% by weight of epichlorohydrin and 24% by weight of water. The temperature of the vapour may range from the reflux temperature of the epihalohydrin or material liberating the epihalohydrin up to 100 DEG C. in excess thereof and the textile materials may be hung in or passed through a chamber filled by the vapour so that the contact time with the vapour is from 15 seconds to 5 minutes. The textile materials may be washed with water and detergents and dried at 20 DEG -125 DEG C. Woven and non woven fabrics threads, gauze, yarn, cord, string or netting comprising cotton, linen or regenerated cellulose fibres alone or in admixture with wool, polyacrylonitrile, polyvinylidene cyanide, polyamide, polyester-polyamide, polyethylene, polypropylene, polyurethane, corn protein-formaldehyde polymer, mineral or alginate rayon fibres may be treated. The treated materials may be used for making dresses, drapes, upholsteries, shoes, carpets, coats, shirts or towels.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13700561A | 1961-09-11 | 1961-09-11 | |
US137024A US3271101A (en) | 1961-09-11 | 1961-09-11 | Process for treating fibrous materials and resulting products |
US137025A US3234043A (en) | 1961-09-11 | 1961-09-11 | Process for treating fibrous materials and resulting products |
Publications (1)
Publication Number | Publication Date |
---|---|
GB954275A true GB954275A (en) | 1964-04-02 |
Family
ID=27384939
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB34521/62A Expired GB954275A (en) | 1961-09-11 | 1962-09-10 | Improvements in and relating to the treatment of cellulosic textile materials |
Country Status (7)
Country | Link |
---|---|
US (2) | US3271101A (en) |
BE (1) | BE622324A (en) |
CH (1) | CH394111A (en) |
DE (1) | DE1184729B (en) |
FR (1) | FR1333398A (en) |
GB (1) | GB954275A (en) |
NL (1) | NL283032A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3647353A (en) * | 1966-08-26 | 1972-03-07 | Triatex International | Method and apparatus for processing cellulose-containing textiles with the vapors from an azeotropic liquid comprising an acidic catalyst |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH1795665D (en) * | 1964-12-30 | |||
US20100032617A1 (en) * | 2007-02-20 | 2010-02-11 | Solvay (Societe Anonyme) | Process for manufacturing epichlorohydrin |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1594532A (en) * | 1922-10-18 | 1926-08-03 | American Carbonic Machinery Company | Refrigerator |
US1914172A (en) * | 1930-08-14 | 1933-06-13 | Burgess Lab Inc C F | Manufacture of ether derivatives of carbohydrates like cellulose |
US1959406A (en) * | 1932-11-12 | 1934-05-22 | Brcoks Emanuel | Treatment of textile |
NL40955C (en) * | 1934-05-17 | |||
GB644213A (en) * | 1948-03-17 | 1950-10-04 | Wolsey Ltd | A process for the treatment of textile fibres |
BE491553A (en) * | 1948-10-07 | |||
GB724096A (en) * | 1951-09-01 | 1955-02-16 | Fothergill & Harvey Ltd | Process for the dimensional stabilisation of cellulose fabrics |
NL175776A (en) * | 1952-02-25 | |||
BE556279A (en) * | 1956-04-03 | |||
FR1178919A (en) * | 1957-07-15 | 1959-05-19 | Traitements Chimiques Des Text | Process for the treatment of cellulosic fibers |
US2967787A (en) * | 1958-08-21 | 1961-01-10 | Joseph Barcroft & Sons Company | Fabric finishing with heat hardenable resin |
-
0
- BE BE622324D patent/BE622324A/xx unknown
- NL NL283032D patent/NL283032A/xx unknown
-
1961
- 1961-09-11 US US137024A patent/US3271101A/en not_active Expired - Lifetime
- 1961-09-11 US US137025A patent/US3234043A/en not_active Expired - Lifetime
-
1962
- 1962-09-10 DE DES81388A patent/DE1184729B/en active Pending
- 1962-09-10 CH CH1070562A patent/CH394111A/en unknown
- 1962-09-10 GB GB34521/62A patent/GB954275A/en not_active Expired
- 1962-09-10 FR FR909027A patent/FR1333398A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3647353A (en) * | 1966-08-26 | 1972-03-07 | Triatex International | Method and apparatus for processing cellulose-containing textiles with the vapors from an azeotropic liquid comprising an acidic catalyst |
Also Published As
Publication number | Publication date |
---|---|
US3271101A (en) | 1966-09-06 |
FR1333398A (en) | 1963-07-26 |
NL283032A (en) | |
US3234043A (en) | 1966-02-08 |
CH394111A (en) | 1965-11-30 |
DE1184729B (en) | 1965-01-07 |
BE622324A (en) | |
CH1070562A4 (en) | 1965-02-15 |
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