GB447530A - Improvements in or relating to the production of cellulose esters - Google Patents

Improvements in or relating to the production of cellulose esters

Info

Publication number
GB447530A
GB447530A GB26403/35A GB2640335A GB447530A GB 447530 A GB447530 A GB 447530A GB 26403/35 A GB26403/35 A GB 26403/35A GB 2640335 A GB2640335 A GB 2640335A GB 447530 A GB447530 A GB 447530A
Authority
GB
United Kingdom
Prior art keywords
acetate
solution
cellulose
sodium
salt
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
GB26403/35A
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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 British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB447530A publication Critical patent/GB447530A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A47FURNITURE; DOMESTIC ARTICLES OR APPLIANCES; COFFEE MILLS; SPICE MILLS; SUCTION CLEANERS IN GENERAL
    • A47JKITCHEN EQUIPMENT; COFFEE MILLS; SPICE MILLS; APPARATUS FOR MAKING BEVERAGES
    • A47J41/00Thermally-insulated vessels, e.g. flasks, jugs, jars
    • A47J41/0055Constructional details of the elements forming the thermal insulation
    • A47J41/0072Double walled vessels comprising a single insulating layer between inner and outer walls
    • A47J41/0077Double walled vessels comprising a single insulating layer between inner and outer walls made of two vessels inserted in each other
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B3/00Preparation of cellulose esters of organic acids
    • C08B3/22Post-esterification treatments, including purification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Polymers & Plastics (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Food Science & Technology (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)

Abstract

Cellulose is esterified in presence of a polybasic inorganic acid or acid derivative thereof as catalyst, the ester is ripened in the esterification solution, a salt of basic character containing a metal of Groups 2--4 of the Periodic Table, or two or more substances which react to form such a salt, is added in amount at least sufficient to neutralize inorganic acid present, and the cellulose ester is precipitated from the solution by means of a non-solvent. The catalyst may be sulphuric acid, sodium bisulphate, methyl sulphate or a mixture of these with each other, or with any other catalyst such as zinc chloride. The basic salt may be basic aluminium acetate, sodium aluminate, sodium stannate, calcium acetate, barium acetate, zinc acetate, or mixtures of aluminium chloride and sodium acetate, or aluminium acetate, lime, acetic acid, and aluminium sulphate, or zinc chloride and sodium acetate. The solution may be heated after addition of the salt and before precipitation of the ester. The process is applicable to the production of cellulose formate, acetate, propionate, or butyrate. The products are free from sulphur compounds and have high stability to light and heat. They may be used for the production of artificial filaments. The ripening may be effected in the presence of metal halides. The catalyst may be neutralized by an ammonium salt of an organic acid or by an alkali metal carbonate. In an example, ripened cellulose acetate solution is mixed with basic aluminium acetate, the solution is heated for several hours, and the cellulose acetate is then precipitated. In another example, sodium acetate is added to a ripened cellulose acetate solution to neutralize the sulphuric acid present. The solution is heated and zinc chloride dissolved in glacial acetic acid is added. After several hours the solution is cooled and the cellulose acetate is precipitated. Specification 446,723 is referred to.
GB26403/35A 1934-09-29 1935-09-24 Improvements in or relating to the production of cellulose esters Expired GB447530A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US447530XA 1934-09-29 1934-09-29

Publications (1)

Publication Number Publication Date
GB447530A true GB447530A (en) 1936-05-20

Family

ID=21934143

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26403/35A Expired GB447530A (en) 1934-09-29 1935-09-24 Improvements in or relating to the production of cellulose esters

Country Status (2)

Country Link
FR (1) FR447530A (en)
GB (1) GB447530A (en)

Also Published As

Publication number Publication date
FR447530A (en) 1913-01-08

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