GB796384A - Production of articles of cellulose triesters by wet spinning - Google Patents

Production of articles of cellulose triesters by wet spinning

Info

Publication number
GB796384A
GB796384A GB17790/56A GB1779056A GB796384A GB 796384 A GB796384 A GB 796384A GB 17790/56 A GB17790/56 A GB 17790/56A GB 1779056 A GB1779056 A GB 1779056A GB 796384 A GB796384 A GB 796384A
Authority
GB
United Kingdom
Prior art keywords
acetate
ester
per cent
cellulose
coagulant
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
GB17790/56A
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.)
Celanese Corp
Original Assignee
Celanese Corp
Celanese Corp of America
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 Celanese Corp, Celanese Corp of America filed Critical Celanese Corp
Publication of GB796384A publication Critical patent/GB796384A/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
    • D01F2/24Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
    • D01F2/28Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Artificial Filaments (AREA)

Abstract

Shaped articles having a basis of a monocarboxylic acid ester of cellulose of a degree of substitution of at least 2.7, preferably 2.85 or more, are made by extruding a solution of the cellulose ester in an organic solvent through one or more shaping orifices into a coagulant consisting essentially of water and an organic ester which will form with water a homogeneous mixture containing at least 0.5 per cent of the ester at a temperature between 0 DEG and 100 DEG C. The cellulose ester may be a propionate, butyrate, acetate formate, acetate pripionate, acetate butyrate, or particularly a cellulose triacetate of acetyl value (as acetic acid) above 58.8 and preferably about 61.0 per cent or higher. The solvent for the cellulose ester may be acetic acid, acetone, ethylene chlorohydrin, dimethyl-sulphoxide or dimethyl-formamide. Chlorinated hydrocarbon, e.g. methylene chloride, ethylene chloride or chloroform, either alone or in admixture with a small proportion of an auxiliary solvent, are preferred, particularly methylene chloride, either alone or in a mixture containing also up to about 20 per cent by weight of a lower aliphatic alcohol such as methanol, ethanol, n-propanol, isopropanol or a butanol. The organic ester present in the coagulant is preferably a lower aliphatic ester, e.g. ethyl acetate, isopropyl acetate, isobutyl acetate or secondary butyl acetate, or ethylene glycol or diethylene glycol diacetate. Ether esters may also be used, especially 2-methoxyethyl acetate, 2 - ethoxyethyl acetate, 2 - (2 - methoxyethoxy)-ethyl acetate and 2-(2-ethoxyethoxy)-ethyl acetate. The proportion of organic ester in the coagulant may be 0.5-25 per cent by weight and the temperature of the coagulant may be between 0 DEG and 100 DEG C. In an example, a solution of cellulose acetate of acetyl value 61.2 per cent (as acetic acid) in a 90/10 by weight methylene chloride/methanol solution is spun into an aqueous solution of 2-methoxyethyl acetate of 4.6 per cent by weight concentration at 24 DEG C. contained in an open trough. The filaments are drawn through the trough for a distance of 90 cm. and withdrawn as a yarn at a rate of 50 metres per minute, washed with water and dried.
GB17790/56A 1955-06-10 1956-06-08 Production of articles of cellulose triesters by wet spinning Expired GB796384A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US796384XA 1955-06-10 1955-06-10

Publications (1)

Publication Number Publication Date
GB796384A true GB796384A (en) 1958-06-11

Family

ID=22151823

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17790/56A Expired GB796384A (en) 1955-06-10 1956-06-08 Production of articles of cellulose triesters by wet spinning

Country Status (1)

Country Link
GB (1) GB796384A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3081145A (en) * 1961-03-08 1963-03-12 Celanese Corp Process for manufacturing fibers and threads from cellulose triacetate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3081145A (en) * 1961-03-08 1963-03-12 Celanese Corp Process for manufacturing fibers and threads from cellulose triacetate

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