GB953171A - Process for finishing cellulosic textile materials - Google Patents

Process for finishing cellulosic textile materials

Info

Publication number
GB953171A
GB953171A GB1814760A GB1814760A GB953171A GB 953171 A GB953171 A GB 953171A GB 1814760 A GB1814760 A GB 1814760A GB 1814760 A GB1814760 A GB 1814760A GB 953171 A GB953171 A GB 953171A
Authority
GB
United Kingdom
Prior art keywords
sodium
compounds
radical
groups
group
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
GB1814760A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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
Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB953171A publication Critical patent/GB953171A/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
    • D06M13/322Treating 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
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/41Amides derived from unsaturated carboxylic acids, e.g. acrylamide

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

Textile materials comprising a major proportion of natural or regenerated cellulose are reacted in an alkalized condition with a compound containing more than one CH2=CH-CO-N< group in such a manner that there is no substantial loss of water from the material under treatment. Suitable compounds containing more than one CH2=CH-CO-N< group are those of the general formula: <FORM:0953171/C3/1> in which R2 and R3 each represent hydrogen or a methyl or ethyl group, X is a radical of the constitution CH2=CH-CO-, R1 is a alkylene radical containing 1-6 carbon atoms which may be interrupted by -O- or -NCH3- or a radical of the constitution: <FORM:0953171/C3/2> in which X has the meaning given above and m and n are 1, 2 or 3 and when m and n=1, R2 and R3 together represent a methylene radical, the compounds being cyclic substances, e.g. derivatives of perhydrotriazine. Compounds which under the conditions of reaction form CH2-CH-CO-N< groups, e.g. N:N1-bis b -chloropropionyl methylene diamide and 1:3:5-tris-b -chloropropionyl-s-perhydrotriazine, the corresponding esters of alkyl and aryl sulphonic acids and the partial esters of sulphuric and phosphoric acids, may also be used. The alkalization of the cellulose may be carried out at room temperature using sodium or potassium hydroxide, sodium silicate, sodium aluminate, sodium zincate, sodium borate, tertiary sodium phosphate or the corresponding potassium or lithium salts, trimethyl benzyl ammonium hydroxide or tetra ethyl- or tetra methyl ammonium hydroxide or their hydrolysable salts. The alkalizing agent and the compound containing CH2=CH-CO-N< groups may be applied to the textile material in either order or simultaneously. The compounds containing CH2=CH-CO-N< groups may be applied as an aqueous solution, suspension, dispersion or paste or from solution in an inert organic solvent, e.g. acetane or dioxane. After treatment the textile material may be rolled up, if desired covered with a waterproof foil and left at a temperature of 180-150 DEG C. while the reaction takes place. Heating may be effected by steaming. Specification 664,795 is referred to.ALSO:Textile materials, e.g. yarns and fabrics, comprising a major proportion of natural cellulose, e.g. cotton, or regenerated cellulose are crease proofed by reacting them in an alkalised condition with a compound containing more than one CH2 = CH-CO-N< group in such a manner that there is no substantial loss of water from the material under treatment. Suitable compounds containing more than one CH2 = CH-CO-N< group are those of the general formula <FORM:0953171/D1-D2/1> in which R2 and R3 each represent hydrogen or a methyl or ethyl group, X is a radical of the constitution CH2 = CH-CO-, R1 is an alkylene radical containing 1-6 carbon atoms which may be interrupted by -O- or -NCH3- or a radical of the constitution <FORM:0953171/D1-D2/2> in which X has the meaning given above and m and n are 1, 2 or 3 and when m and n = 1, R2 and R3 together represent a methylene radical, the compounds being cyclic substances, e.g. derivatives of perhydrotriazine. Compounds which under the conditions of reaction form CH2-CH-CO-N< groups, e.g. N:N1-bis b chloropropianyl methylene diamide and 1:3:5-tris-b -chloropropionyl-s-perhydro triazine, the corresponding esters of alkyl and aryl sulphonic acids and the partial esters of sulphuric and phosphoric acids may also be used. The alkalization of the cellulose may be carried out at room temperature using sodium or potassium hydroxide, sodium silicate, sodium aluminate, sodium zincate, sodium borate, tertiary sodium phosphate or the corresponding potassium or lithium salts, trimethyl benzyl ammonium hydroxide or tetraethyl-or tetramethyl p ammonium hydroxide or their hydrolysable salts. The alkalioning agent and the compound containing CH2 = CH-CO-N< groups may be applied to the textile material in either order or simultaneously. The compound containing CH2 = CH-CO-N< groups may be applied as an aqueous solution, suspension dispersion or paste or from solution in an inert organic solvent, e.g. aceton or dioxane. After treatment the textile material may be rolled up, if desired covered with a water proof foil and left at a temperature of 18 DEG -150 DEG C. while the reaction take place. Heating may be effected by steaming. The process may be combined with other textile finishing processes, e.g. treatment with divinyl sulphone, 1:3-dichloropropanol, urea-or melamine-formaldehyde compounds or their ethers, compounds containing only one CH2 = CH-CO-N< group acrylic acid and esters thereof, acrylonitrile and maleic acid or the esters or nitrile thereof. Specification 664,795 is referred to.
GB1814760A 1959-05-23 1960-05-23 Process for finishing cellulosic textile materials Expired GB953171A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF28500A DE1109135B (en) 1959-05-23 1959-05-23 Textile finishing process

Publications (1)

Publication Number Publication Date
GB953171A true GB953171A (en) 1964-03-25

Family

ID=7092904

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1814760A Expired GB953171A (en) 1959-05-23 1960-05-23 Process for finishing cellulosic textile materials

Country Status (5)

Country Link
BE (1) BE591132A (en)
CH (1) CH582860A4 (en)
DE (1) DE1109135B (en)
GB (1) GB953171A (en)
NL (1) NL251910A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994009191A1 (en) * 1992-10-21 1994-04-28 Courtaulds Fibres (Holdings) Limited Fibre treatment
WO1995028516A1 (en) * 1994-04-15 1995-10-26 Courtaulds Fibres (Holdings) Limited Fibre treatment
US5562739A (en) 1994-06-01 1996-10-08 Courtaulds Fibres (Holdings) Limited Lyocell fiber treatment method
US5580356A (en) 1993-03-10 1996-12-03 Courtaulds Fibres (Holdings) Limited Fibre treatment method
US5759210A (en) * 1994-05-03 1998-06-02 Courtaulds Fibres (Holdings) Limited Lyocell fabric treatment to reduce fibrillation tendency
US5882356A (en) * 1992-10-21 1999-03-16 Courtaulds Fibres (Holdings) Limited Fibre treatment

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2357079C2 (en) * 1973-11-15 1982-07-29 Hoechst Ag, 6000 Frankfurt Process for the production of cellulose ethers which absorb water but are more than 50% insoluble therein

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE521282A (en) * 1952-07-11

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994009191A1 (en) * 1992-10-21 1994-04-28 Courtaulds Fibres (Holdings) Limited Fibre treatment
US5882356A (en) * 1992-10-21 1999-03-16 Courtaulds Fibres (Holdings) Limited Fibre treatment
US5580356A (en) 1993-03-10 1996-12-03 Courtaulds Fibres (Holdings) Limited Fibre treatment method
WO1995028516A1 (en) * 1994-04-15 1995-10-26 Courtaulds Fibres (Holdings) Limited Fibre treatment
US5779737A (en) * 1994-04-15 1998-07-14 Courtaulds Fibres Holdings Limited Fibre treatment
US5759210A (en) * 1994-05-03 1998-06-02 Courtaulds Fibres (Holdings) Limited Lyocell fabric treatment to reduce fibrillation tendency
US5562739A (en) 1994-06-01 1996-10-08 Courtaulds Fibres (Holdings) Limited Lyocell fiber treatment method

Also Published As

Publication number Publication date
NL251910A (en)
BE591132A (en)
CH582860A4 (en) 1964-07-31
DE1109135B (en) 1961-06-22

Similar Documents

Publication Publication Date Title
GB939902A (en) Process for imparting oil-repellency to solid materials and materials thus produced
GB953171A (en) Process for finishing cellulosic textile materials
US2837512A (en) Activated cellulose ethers and process of preparing same
GB781489A (en) Method for the coating of fibrous materials such as glass threads with synthetic resin
EP0259251B1 (en) Cationic compounds from the reaction of carbamides with epihalogen hydrines
GB1374869A (en) Phosphonic compounds containing tertiary amine groups
GB587572A (en) Improvements relating to the finishing of textiles
GB947634A (en) Process for the production of phosphorus compounds and their use in fire-proofing
US3212842A (en) Cellulose textile treatment with alkoxy or phenoxy ethyl sulfonium salts
GB1055367A (en) Process for the antistatic finishing of fibrous materials
GB804745A (en) Improvements relating to compositions for flame-proofing cellulosic material, their use, and material treated therewith
US3414367A (en) Process for making n-substituted aminoethylsulfonylethyl ethers of cellulose
GB941044A (en) Ethers of polysaccharides
GB841189A (en) Bis-triazinylamino-stilbene compounds
GB811632A (en) Improvements in or relating to the preparation of steroid compounds
GB887876A (en) New anthraquinone dyestuffs and process for their manufacture
GB891447A (en) Light and heat stable cellulose fibrous products and process for making them
GB929451A (en) Process for fixing pigments on fibrous materials and flat structures
GB846533A (en) A process for the production of filaments and films from viscose solutions
GB929053A (en) Dyeing, fluorescent brightening and/or printing textile materials
GB824598A (en) Improvements in or relating to new phenthiazine derivatives and processes for their preparation
GB1012093A (en) Improvements in the treatment of cotton linen and viscose rayon fabrics
AT221469B (en) Process for making yarns or textile structures wet crease-proof
GB927533A (en) Derivatives of ªÐ-[coumarinyl-(3)]-phenyl carbamic acid
GB951061A (en) Substituted í¸-pyrrolines and í¸-tetrahydropyridines and process for their manufacture