GB1006727A - Preparation of cross-linked cellulose products - Google Patents

Preparation of cross-linked cellulose products

Info

Publication number
GB1006727A
GB1006727A GB4523162A GB4523162A GB1006727A GB 1006727 A GB1006727 A GB 1006727A GB 4523162 A GB4523162 A GB 4523162A GB 4523162 A GB4523162 A GB 4523162A GB 1006727 A GB1006727 A GB 1006727A
Authority
GB
United Kingdom
Prior art keywords
amide
cellulose
product
cross
weight
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
GB4523162A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
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 claimed from US230985A external-priority patent/US3093446A/en
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB1006727A publication Critical patent/GB1006727A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F2/00Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
    • D01F2/06Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from viscose
    • D01F2/08Composition of the spinning solution or the bath
    • D01F2/10Addition to the spinning solution or spinning bath of substances which exert their effect equally well in either
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00Chemical after-treatment of artificial filaments or the like during manufacture
    • D01F11/02Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

1,006,727. Cross-linked regenerated cellulose filamentary materials. ROHM & HAAS CO. Nov. 29, 1962 [Dec. 5, 1961; Oct. 16, 1962], No. 45231/62. Heading B5B. Cross-linked regenerated cellulose films and filaments are made by (A) adding at least one amide selected from the group consisting of N - methylolacrylamide N - methylolmethacrylamide and the (C 1 -C 4 ) alkyl ethers thereof to an alkaline solution of viscose or cuprammonium cellulose to form therein a modified cellulosic compound; (B) extruding the solution containing the modified cellulosic compound into a coagulating bath to form a film or filamentary product; (C) regenerating the modified cellulosic compound to a modified regenerated cellulose; (D) stretching the regenerated product at least in a longitudinal direction; and (E) heating the stretched product in the presence of an acidic catalyst so that the substituted amido groups therein undergo reaction and a cross-linked product is formed. The modified cellulosic compound may be formed by adding 0À15 to 0À60 mols. of amide per glucose unit in the viscose or cuprammonium cellulose. N-alkoxymethylacrylamides specified include N-methoxymethyl-, N-ethoxymethyl - N - isopropoxymethyl-, and N - tert.- butoxymethylacrylamides. From 1-25% by weight of N-substituted amide monomer, based on the weight of cellulose in the spinning solution, may be used, especially 5-10% by weight, and the amide is preferably added shortly before spinning so as to minimize hydrolysis. Coagulating baths of conventional compositions are used. Thus the amide-treated viscose having a sodium chloride salt test of 3-6, containing 6-9% caustic soda and having a ball fall viscosity of 35 secs. at 18‹ C., may be extruded into a coagulating bath containing 7-13.5% sulphuric acid, 18-28% anhydrous sodium sulphate and if desired, 0À1-5% anhydrous zinc sulphate, or an amide treated cuprammonium cellulose solution containing 3À8% cellulose and 30 gms. ammonia per litre may be extruded into an aqueous 4% caustic soda bath. Stretching may be effected immediately after the product leaves the coagulating and/or regenerating bath while the films or filaments are submerged in or sprayed with hot water or other heated aqueous baths which may contain acids or salts, and may amount to 70-100% of the original length of the products. After stretching, the product is purified in known manner, e.g. viscose products are washed, desulphurized, bleached and lubricated and before drying, the stretched product is heated in the presence of an acid catalyst or a substance yielding an acidic catalyst to effect cross-linking by reaction of methylol or alkoxymethyl groups with the hydroxyl groups of the cellulose, e.g. at least 220‹ F. for at least 30 sees., preferably at 220-350‹ F. for 30 secs.- 5 mins. The catalyst may be applied as a bath or spray of an aqueous solution of ¢-3% by weight concentration. Specified catalysts include ammonium chloride, monobasic and dibasic ammonium phosphates, oxalic, lactic, citric, tartaric, formic, acetic, propionic, boric and succinic acids, and salts of amines, e.g. 2-amino-2-methyl-propanol-1, with acids, e.g. hydrochloric and sulphuric acids. Products containing only 1% of amide show reduced water-retention and reduced swelling or shrinking on exposure to water, while products containing 5-10% by weight of amide show greatly improved resistance to shrinkage and creasing or wrinkling. U.S.A. Specifications 2,173,005 and 2,858,185 are referred to.
GB4523162A 1961-12-05 1962-11-29 Preparation of cross-linked cellulose products Expired GB1006727A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US15726761A 1961-12-05 1961-12-05
US230985A US3093446A (en) 1962-10-16 1962-10-16 Modified spinning solutions, methods for producing fibers and films, and filmy products produced therefrom

Publications (1)

Publication Number Publication Date
GB1006727A true GB1006727A (en) 1965-10-06

Family

ID=26853961

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4523162A Expired GB1006727A (en) 1961-12-05 1962-11-29 Preparation of cross-linked cellulose products

Country Status (1)

Country Link
GB (1) GB1006727A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2358830A (en) * 1999-12-13 2001-08-08 Fuji Spinning Co Ltd Regenerated cellulose fibre

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2358830A (en) * 1999-12-13 2001-08-08 Fuji Spinning Co Ltd Regenerated cellulose fibre
GB2358830B (en) * 1999-12-13 2003-10-08 Fuji Spinning Co Ltd A method for manufacturing improved regenerated cellulose fiber

Similar Documents

Publication Publication Date Title
GB715915A (en) Improvements in or relating to the production of shaped products from acrylonitrile polymerization products
GB298548A (en) Manufacture of artificial threads
US2796656A (en) Modified regenerated cellulose articles and method for making the same
DE69228861T2 (en) Process for the production of fibers from regenerated collagen
GB1006727A (en) Preparation of cross-linked cellulose products
GB1248840A (en) Wet fixation of resins in fiber systems for durable press products
GB915356A (en) Regenerated cellulose fibres and their production
GB743742A (en) N-methylol polypyrrolidones
US4777249A (en) Crosslinked cellulose aminomethanate
US1857263A (en) Process of strengthening cotton, artificial silk, artificial foils of cellulose, viscose, or the like and material prepared by this process
GB1438831A (en) Process for the manufacture of consolidated shaped structures of cellulose hydrate
US3093446A (en) Modified spinning solutions, methods for producing fibers and films, and filmy products produced therefrom
US3329519A (en) Methylolated ureidopyrimidone modified regenerated cellulose product and process forpreparing same
US3102112A (en) Modification of cellulose with epoxypropyl amine compounds
US2552079A (en) Production of zein fibers
US3956539A (en) Imidazolines in preparing fibrous artificial sausage casings
GB847431A (en) "shaped structures of amylose and a process for the manufacture thereof"
US2727836A (en) Anti-sticking cellulose pellicles and method of making
US1961268A (en) Method of treating cellulose
US2283809A (en) Method of coagulating cellulosic solutions
US2699406A (en) Coating cellophane and the like
ES234979A1 (en) Process of creaseproofing linen fabric by applying resin, mercerizing and reapplyingresin and product produced thereby
US2445333A (en) Process of making regenerated cellulose films
US2234016A (en) Cellulosic structure and process for producing same
US2897044A (en) Production of artificial protein threads, fibres, filaments and the like