GB217166A - Cellulose solutions and process for their production - Google Patents
Cellulose solutions and process for their productionInfo
- Publication number
- GB217166A GB217166A GB16963/23A GB1696323A GB217166A GB 217166 A GB217166 A GB 217166A GB 16963/23 A GB16963/23 A GB 16963/23A GB 1696323 A GB1696323 A GB 1696323A GB 217166 A GB217166 A GB 217166A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- products obtained
- acids
- solutions
- ammonium hydroxide
- 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
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent 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)
- Cosmetics (AREA)
Abstract
Cellulose solutions are prepared by treating cellulose or a cellulose conversion product with a strong organic base, for example, a quaternary ammonium base or a base in the aqueous solution of which a highly electrolytically-dissociated hydroxide may be assumed to be present, in the presence or absence of caustic alkali. Suitable bases are tetra-ethyl ammonium hydroxide, tetra-methyl ammonium hydroxide, and phenyl trimethyl ammonium hydroxide. The reaction may be carried out in aqueous solution and at a room temperature or lower, for instance, below 0 DEG C., depending on the character of the original cellulosic material and on the presence or absence of alkali, the temperature being lowered by stages until solution occurs. The initial cellulose material may be bleached or unbleached cellulose products obtained by mechanical comminution of cellulose in the presence of water; products obtained by treating cellulose with oxidizing or reducing agents with or without a preliminary treatment with alkalies, acids, salts, etc.; products obtained by heating cellulose alone or in the presence of water or glycerine; products obtained by treating cellulose with hot or cold alkalies alone or in the presence of salts, with or without subsequent treatment with dilute acid and with or without previous or subsequent or simultaneous treatment with bleaching or oxidizing agents; products separated from solutions of cellulose, cellulose hydrate or hydrocellulose in ammoniacal copper oxide &c., zinc halides, or strong mineral acids such as sulphuric, phosphoric, arsenic or hydrochloric acid, or from viscose solutions; artificial silk, artificial cotton, staple fibre, etc.; products obtained by treating cellulose or its conversion products with these solvents to a point short of dissolution; hydrocelluloses such as are obtained by treating cellulose with dilute acids at ordinary or raised temperature, or by drying in the presence of acids, or by employing strong sulphuric acid at temperatures below 0 DEG C., gaseous hydrochloric acid, or chlorine; oxycelluloses; products obtained by denitrating, saponifying, &c. cellulose esters; the alkali-soluble derivatives of Specification 177,810. The solutions are coagulated by acids, salts, alcohols, water, steam, heat, etc.; and they may be worked up into artificial silk &c., films, artificial hair, plastic masses, coatings, finishings, fillings, sizes, artificial leather, &c. In examples, the starting material is treated with an aqueous or alkaline solution of tetra-ethyl or methyl ammonium hydroxide or phenylmethylammonium hydroxide, and the mixture cooled to \sw8 DEG to \sw11 DEG C. Specification 216,475 is referred to. The Specification as open to inspection under Sect. 91 (3) (a) includes the use of guanidine. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT217166X | 1923-06-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB217166A true GB217166A (en) | 1924-09-29 |
Family
ID=3669779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16963/23A Expired GB217166A (en) | 1923-06-05 | 1923-06-29 | Cellulose solutions and process for their production |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB217166A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4324593A (en) * | 1978-09-01 | 1982-04-13 | Akzona Incorporated | Shapeable tertiary amine N-oxide solution of cellulose, shaped cellulose product made therefrom and process for preparing the shapeable solution and cellulose products |
US4526620A (en) * | 1982-12-08 | 1985-07-02 | Neste Oy | Cellulose carbamate solutions |
-
1923
- 1923-06-29 GB GB16963/23A patent/GB217166A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4324593A (en) * | 1978-09-01 | 1982-04-13 | Akzona Incorporated | Shapeable tertiary amine N-oxide solution of cellulose, shaped cellulose product made therefrom and process for preparing the shapeable solution and cellulose products |
US4526620A (en) * | 1982-12-08 | 1985-07-02 | Neste Oy | Cellulose carbamate solutions |
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