GB696282A - Process for the dimensional stabilisation of cellulose fabrics - Google Patents

Process for the dimensional stabilisation of cellulose fabrics

Info

Publication number
GB696282A
GB696282A GB2611748A GB2611748A GB696282A GB 696282 A GB696282 A GB 696282A GB 2611748 A GB2611748 A GB 2611748A GB 2611748 A GB2611748 A GB 2611748A GB 696282 A GB696282 A GB 696282A
Authority
GB
United Kingdom
Prior art keywords
glycerol
dichlorhydrin
per
solution
epichlorhydrin
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
Application number
GB2611748A
Inventor
Brindley Jack Brown
Leonard Steger
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fothergill and Harvey Ltd
Original Assignee
Fothergill and Harvey Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to BE491553D priority Critical patent/BE491553A/xx
Application filed by Fothergill and Harvey Ltd filed Critical Fothergill and Harvey Ltd
Priority to GB2611748A priority patent/GB696282A/en
Publication of GB696282A publication Critical patent/GB696282A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/11Compounds containing epoxy groups or precursors thereof

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Natural and regenerated cellulose fabrics are impregnated with epichlorhydrin or a substance which may be hydrolysed by aqueous caustic alkali to release epichlorhydrin, and then treated with aqueous caustic alkali at a temperature above 70 DEG C. whilst under tension. Cross linkages are produced between neighbouring cellulose chains. Suitable reagents which give rise to epichlorhydrin on hydrolysis include glycerol-1,3-dichlorhydrin, glycerol-1,2-dichlorhydrin, 1-chloro-2-bromopropanol-(3) and mixtures of these, particularly a mixture of the glycerol-dichlorhydrins which is commercially available. The selected reagent may be used in solution in water, benzene, acetone, carbon tetrachloride or diethyl ether. Sodium or potassium hydroxide may be used as the alkali, and it is advantageous to have present in the solution one or more alkali metal salts, such as the chloride, bromide, nitrate, carbonate or acetate of sodium or potassium. The conditions for treatment of regenerated cellulose fabrics may be 8.2-15.5 g. of glycerol 1,3 dichlorhydrin or up to 18 g. if the solution is warmed, 0.8-7.5 g. (preferably 2-4 g.) of caustic soda, 1.0-28.2 g. of alkali metal salt, say sodium chloride (preferably 20-25 g.), all per 100 ml. of aqueous treating liquids, reaction temperature 70-107 DEG C. (preferably about 90 DEG C.) and time of treatment 10 seconds to 30 minutes. The conditions for natural cellulose may be 2.1-15.5 g. of glycerol 1 : 3 dichlorhydrin, 0.8-25.2 g. (preferably 10-20 g.) of caustic soda, 1.0-28.2 g. (preferably 15-25 g.) of alkali metal salt, say sodium chloride, all per 100 ml. of aqueous treating liquids, reaction temperature 70-110 DEG C. (preferably about 90 DEG C.) and time of treatment 5 seconds to 60 minutes. Lower concentrations of reagents may be used with higher temperatures and longer reaction times. The treated fabric is proofed against laundry shrinkage and ironing extensions, is insoluble in cuprammonium solutions, and possesses low swelling properties. In an example a plain weave spun viscose rayon fabric is impregnated at room temperature with an aqueous solution containing 15 g. of glycerol-1,3-dichlorhydrin per 100 ml. Excess solution is squeezed out and the fabric passed under tension into a solution containing 3.0 g. of sodium hydroxide and 25 g. of sodium chloride per 100 ml. at 90 DEG C. for 2 minutes. It is washed, soured with 0.5 per cent sulphuric acid, washed again, soaped and dried. The Provisional Specification is not limited to the use of epichlorhydrin and compounds which give rise to it, but p refers to the use of any halogenated compound of the aliphatic or alicyclic series containing at least two halogen atoms, at least two of which are not situated on the same carbon atom and are capable of forming epoxide rings with at least one hydroxyl group which also must be present in the molecule, or alternatively containing at least one halogen atom and at least one epoxide ring either adjacent to it or, if not adjacent, with the additional presence of one or more hydroxyl groups, at least one of which is capable of forming a second epoxide ring with at least one halogen atom. Compounds falling within this definition include, in addition to those listed in the Complete Specification, glycerol - 1,2 - dibromhydrin, glycerol - 1,3-dibromhydrin, 1 - bromo - 3 - chloropropanol - (2), 1 - bromo - 2 - chloropropanol - (3), and epibromhydrin. Natural cellulose may be treated at any temperature between 20 DEG and 110 DEG C. and regenerated cellulose at any temperature between 60 DEG and 107 DEG C.
GB2611748A 1948-10-07 1948-10-07 Process for the dimensional stabilisation of cellulose fabrics Expired GB696282A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
BE491553D BE491553A (en) 1948-10-07
GB2611748A GB696282A (en) 1948-10-07 1948-10-07 Process for the dimensional stabilisation of cellulose fabrics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2611748A GB696282A (en) 1948-10-07 1948-10-07 Process for the dimensional stabilisation of cellulose fabrics

Publications (1)

Publication Number Publication Date
GB696282A true GB696282A (en) 1953-08-26

Family

ID=10238642

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2611748A Expired GB696282A (en) 1948-10-07 1948-10-07 Process for the dimensional stabilisation of cellulose fabrics

Country Status (2)

Country Link
BE (1) BE491553A (en)
GB (1) GB696282A (en)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3044843A (en) * 1959-05-13 1962-07-17 Du Pont Fiber dyeing process
US3061399A (en) * 1959-02-09 1962-10-30 Stevens & Co Inc J P Treating cotton to improve wet and dry crease recovery in one operation
US3066005A (en) * 1958-02-01 1962-11-27 Bayer Ag Process for the treatment of hydroxyl group-containing textile materials
US3082052A (en) * 1958-05-19 1963-03-19 Ici Ltd Process for the coloration of cellulose textile materials with reactive dyestuffs
DE1184729B (en) * 1961-09-11 1965-01-07 Shell Int Research Process for improving the wash resistance and abrasion resistance of fibrous cellulose-containing textiles
US3194627A (en) * 1956-04-03 1965-07-13 Deering Milliken Res Corp Processes for producing modified cellulosic textile materials
DE1221188B (en) * 1956-04-03 1966-07-21 Deering Milliken Research Corporation, Spartanburg, S. C. (V. St. A.) Process for improving the smooth drying capacity of cellulosic yarns or fabrics
US3382029A (en) * 1963-07-02 1968-05-07 Agriculture Usa Alkaline catalyzed cellulose-epichlorohydrin reactions wherein cellulose is pretreated with aqueous salt solutions
US3445177A (en) * 1963-06-20 1969-05-20 Deering Milliken Res Corp Discharge printing a direct-dye dyed haloalkanol crosslinked cellulose fabric and creaseproofing with an aminoplast
US3451763A (en) * 1963-03-08 1969-06-24 Heberlein Patent Corp Cellulose-containing fabrics and process therefor
US3489503A (en) * 1967-09-25 1970-01-13 Us Agriculture Cellulosic fabric reacted in wet state with ethylene chlorohydrin and thereafter with dimethylol ethyleneurea under dehydrating conditions
US3506391A (en) * 1962-02-15 1970-04-14 Deering Milliken Res Corp Cross-linking cellulosics with epichlorohydrin vapors

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3194627A (en) * 1956-04-03 1965-07-13 Deering Milliken Res Corp Processes for producing modified cellulosic textile materials
DE1221188B (en) * 1956-04-03 1966-07-21 Deering Milliken Research Corporation, Spartanburg, S. C. (V. St. A.) Process for improving the smooth drying capacity of cellulosic yarns or fabrics
US3066005A (en) * 1958-02-01 1962-11-27 Bayer Ag Process for the treatment of hydroxyl group-containing textile materials
US3082052A (en) * 1958-05-19 1963-03-19 Ici Ltd Process for the coloration of cellulose textile materials with reactive dyestuffs
US3061399A (en) * 1959-02-09 1962-10-30 Stevens & Co Inc J P Treating cotton to improve wet and dry crease recovery in one operation
US3044843A (en) * 1959-05-13 1962-07-17 Du Pont Fiber dyeing process
DE1184729B (en) * 1961-09-11 1965-01-07 Shell Int Research Process for improving the wash resistance and abrasion resistance of fibrous cellulose-containing textiles
US3506391A (en) * 1962-02-15 1970-04-14 Deering Milliken Res Corp Cross-linking cellulosics with epichlorohydrin vapors
US3451763A (en) * 1963-03-08 1969-06-24 Heberlein Patent Corp Cellulose-containing fabrics and process therefor
US3445177A (en) * 1963-06-20 1969-05-20 Deering Milliken Res Corp Discharge printing a direct-dye dyed haloalkanol crosslinked cellulose fabric and creaseproofing with an aminoplast
US3382029A (en) * 1963-07-02 1968-05-07 Agriculture Usa Alkaline catalyzed cellulose-epichlorohydrin reactions wherein cellulose is pretreated with aqueous salt solutions
US3489503A (en) * 1967-09-25 1970-01-13 Us Agriculture Cellulosic fabric reacted in wet state with ethylene chlorohydrin and thereafter with dimethylol ethyleneurea under dehydrating conditions

Also Published As

Publication number Publication date
BE491553A (en)

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