GB562581A - Alkali-soluble carboxyethyl cellulose ether - Google Patents

Alkali-soluble carboxyethyl cellulose ether

Info

Publication number
GB562581A
GB562581A GB15423/42A GB1542342A GB562581A GB 562581 A GB562581 A GB 562581A GB 15423/42 A GB15423/42 A GB 15423/42A GB 1542342 A GB1542342 A GB 1542342A GB 562581 A GB562581 A GB 562581A
Authority
GB
United Kingdom
Prior art keywords
cellulose
solution
per cent
caustic soda
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
Application number
GB15423/42A
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
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB562581A publication Critical patent/GB562581A/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]

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

A water-insoluble, alkali-soluble carboxyethyl cellulose ether is produced by mixing cellulose with a solution containing about 15-40 per cent of a strongly basic, water-soluble hydroxide in an amount at least molecularly proportional to the glucose units of the cellulose, and about 0.2-0.5 molecular proportions of acrylonitrile per glucose unit of the cellulose, and allowing the reaction to proceed within the temperature range of 5-35 DEG C. The reaction is continued until the reaction mixture is dispersible in a 5-10 per cent solution of a strongly basic hydroxide to form a substantially homogeneous solution or paste. The cellulosic material may be cotton, regenerated cellulose, cellulose bast fibre, or wood pulp from which resin, lignin, and other impurities have been removed. The alkali may be caustic soda or potash or a strongly basic quaternary ammonium hydroxide, e.g. benzyl trimethyl or dibenzyl dimethyl or fetraethyl ammonium hydroxide. In an example, wood pulp is treated with a solution of 30 per cent caustic soda in a mechanical mixer. Acrylo-nitrile is added and mixing is continued for several hours. The product is dissolved in 5 per cent caustic soda solution. The cellulose ether is precipitated by adding acid. It is washed and then redissolved in p caustic soda solution. The cellulose ether may be dissolved in a solution of trimethyl benzyl ammonium hydroxide and sodium hydroxide and used to impregnate a piece of cotton sheeting which is then squeezed, acidified with a solution of sulphuric acid and sodium sulphate, rinsed and dried. The cloth is stiffened and the effect is retained after laundering with soap and soda solutions. The cellulose ethers obtained by the process may be used as thickening agents, protective colloids, sizing and finishing agents for textiles, and their solutions may be extruded to form filaments and films, coagulation being effected in acid media.
GB15423/42A 1942-01-17 1942-11-02 Alkali-soluble carboxyethyl cellulose ether Expired GB562581A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US562581XA 1942-01-17 1942-01-17

Publications (1)

Publication Number Publication Date
GB562581A true GB562581A (en) 1944-07-07

Family

ID=22003228

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15423/42A Expired GB562581A (en) 1942-01-17 1942-11-02 Alkali-soluble carboxyethyl cellulose ether

Country Status (1)

Country Link
GB (1) GB562581A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2539417A (en) * 1948-06-18 1951-01-30 Hercules Powder Co Ltd Preparation of cellulose derivative

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2539417A (en) * 1948-06-18 1951-01-30 Hercules Powder Co Ltd Preparation of cellulose derivative

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