GB231809A - Manufacture of new cellulose derivatives - Google Patents

Manufacture of new cellulose derivatives

Info

Publication number
GB231809A
GB231809A GB13357/24A GB1335724A GB231809A GB 231809 A GB231809 A GB 231809A GB 13357/24 A GB13357/24 A GB 13357/24A GB 1335724 A GB1335724 A GB 1335724A GB 231809 A GB231809 A GB 231809A
Authority
GB
United Kingdom
Prior art keywords
alkali
acid
lye
molecular
fatty acid
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
GB13357/24A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of GB231809A publication Critical patent/GB231809A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B11/00Preparation of cellulose ethers
    • C08B11/02Alkyl or cycloalkyl ethers
    • C08B11/04Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
    • C08B11/10Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals
    • C08B11/12Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals substituted with acid radicals substituted with carboxylic radicals, e.g. carboxymethylcellulose [CMC]

Abstract

Cellulose derivatives soluble in aqueous alkalies, and which are precipitated as products insoluble in water by the addition of alcohol to the solutions in aqueous alkalies, are prepared by carrying out the treatment of cellulose or a cellulose conversion product insoluble in alkali, with a monohalogen fatty acid, or a salt or ester of such acid, and alkali, in the absence of alcohol or in the presence of not more than 20 parts of alcohol for each 100 parts of water present; the process is conducted so that the maximum quantity of halogen fatty acid &c. is inversely proportional to the strength of the alkali solution. Other conditions are:-the halogen fatty acid should not be used in more than 18/a molecular proportions to each molecular proportion of caustic alkali, where a represents the percentage strength of the alkali lye; for each molecular proportion of caustic alkali, if this is used as a solution of not more than 25 per cent strength, there should be used not more than 180 (n + 1)/a molecular proportions of halogen fatty acid (a being the percentage strength of the alkali lye, and n the number of parts of alkali lye used to each part of cellulose), or, if the alkali lye is of more than 25 per cent strength, not more than 60/a (n + 1) molecular equivalents of halogen fatty acid, or generally, with lye up to 25 per cent strength, not more than 0.75-1 molecular proportions of halogen fatty acid, and with stronger lye, not more than 0.5-0.6 molecular equivalents, although smaller amounts than these are usually sufficient; and there should be used not more than one molecular equivalent of halogen fatty acid to one molecular proportion of cellulose. The cellulose &c. to be treated may be soaked in an excess of alkali lye, the surplus being subsequently removed, or it may be mixed or kneaded with the required quantity of lye, or with solid caustic alkali, or with a mixture of solid caustic alkali and saturated lye; the reaction is carried out at room temperature or below, or with the application of heat; and contact substances such as copper, iron, silver, and benzoyl superoxide may be added. Suitable halogen fatty acids &c. are:-monochloracetic acid, methyl or ethyl chloracetate, a-bromopropionic acid, bromosuccinic acid, a-bromo-isobutyric acid and their salts and esters. The products are isolated from the reaction mixtures by the addition of an acid, an acid salt, &c., or by treating with alcohol. When precipitated in the form of threads and films from their solutions, they give solid, flexible, and transparent products. The cellulose derivatives may be employed in the manufacture of artificial fibres, films, plastic compositions, coatings, dressings for fabrics, sizes, thickening-agents for textile printing, agents for fixing pigments, &c. Specifications 138,116, 177,810, 203,346, and 203,347 are referred to.
GB13357/24A 1924-04-04 1924-05-30 Manufacture of new cellulose derivatives Expired GB231809A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AT231809X 1924-04-04

Publications (1)

Publication Number Publication Date
GB231809A true GB231809A (en) 1925-09-30

Family

ID=3669955

Family Applications (1)

Application Number Title Priority Date Filing Date
GB13357/24A Expired GB231809A (en) 1924-04-04 1924-05-30 Manufacture of new cellulose derivatives

Country Status (1)

Country Link
GB (1) GB231809A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003010206A1 (en) * 2001-07-20 2003-02-06 Unilever Plc Polymers and their synthesis

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003010206A1 (en) * 2001-07-20 2003-02-06 Unilever Plc Polymers and their synthesis
US7041730B2 (en) 2001-07-20 2006-05-09 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Polymers and their synthesis

Similar Documents

Publication Publication Date Title
US2759925A (en) Process for preparing cellulose dicarboxylic acid esters
GB356277A (en) Improved manufacture of paper
GB231809A (en) Manufacture of new cellulose derivatives
JPH0582841B2 (en)
US1543310A (en) Process for the preliminary treatment of cellulose prior to esterification
GB260650A (en) Manufacture of cellulose formate and of materials therefrom
US3057852A (en) Method of preparing heat stable cellulose acetate sulfates
US2652340A (en) Stabilized cellulose lower alkanoates
US2059619A (en) Treatment of benzyl cellulose
US1938044A (en) Process of preparing esters of the carbohydrates
GB231810A (en) Manufacture of cellulose derivatives
US1682292A (en) Leon lilienfeld
US1962828A (en) Process for the manufacture of cellulose derivatives containing phosphorus
US2512983A (en) Mixed cellulose esters and process of making same
GB317117A (en) Process for dressing artificial silk yarn
SU8817A1 (en) The way sex students xanthogen cellulose derivatives
US2592305A (en) Method of lowering the viscosity of hydrolyzed cellulose esters and product
US1739210A (en) Process of making unsaturated acyl cellulose esters
GB231802A (en) A process for making cellulose combinations
US1379699A (en) Cellulose composition
US2358064A (en) Method of preparing oxidized cellulose esters
US1655870A (en) Process for the manufacture of cellulose acetate
GB496354A (en) A process for the preparation of size solutions and size compositions containing salts of cellulose ether carboxylic acids as their essential constituent
AT86129B (en) Process for the production of cellulosic compounds.
GB203599A (en) Process for the manufacture of acetose, that is, acetylated cellulose and products derived therefrom, such as artificial silk, horsehair, films and the like