GB520162A - Improvements in or relating to the working up of cellulose derivatives - Google Patents

Improvements in or relating to the working up of cellulose derivatives

Info

Publication number
GB520162A
GB520162A GB29713/38A GB2971338A GB520162A GB 520162 A GB520162 A GB 520162A GB 29713/38 A GB29713/38 A GB 29713/38A GB 2971338 A GB2971338 A GB 2971338A GB 520162 A GB520162 A GB 520162A
Authority
GB
United Kingdom
Prior art keywords
cellulose
sulpho
butyl
methyl
acetate
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
GB29713/38A
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.)
Deutsche Hydrierwerke AG
Original Assignee
Deutsche Hydrierwerke AG
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 Deutsche Hydrierwerke AG filed Critical Deutsche Hydrierwerke AG
Publication of GB520162A publication Critical patent/GB520162A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/43Compounds containing sulfur bound to nitrogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

520,162. Cellulose derivative compositions. DEUTSCHE HYDRIERWERKE AKT.-GESOct. 13, 1938, Nos. 29713 and 29714. Conven. tion dates, Oct. 13, 1937, and Oct. 7, 1938. [Class 2 (ii)] An aliphatic or cycloaliphatic sulphonamide containing at least 3 carbon atoms in the molecule and having at the nitrogen atom at least one substituted or unsubstituted hydrocarbon residue, the chain of which is not interrupted by an oxygen atom, is employed as solvent, softening, gelatinizing or swelling agent in the working up of cellulose derivatives to manufactured or partly manufactured products. The sulphonamide may be substituted at the nitrogen atom by one or more aliphatic, cycloaliphatic, or aliphatic-cycloaliphatic residues. Atoms other than carbon or hydrogen or groups containing such atoms may be present in the hydrocarbon residues. Halogen, oxygen, or sulphur atoms, or groups containing oxygen, sulphur, or nitrogen may be present. The hydrocarbon residue may be a methyl, butyl, octyl, dodecyl, octadecyl, oleyl, cyclohexyl, methylcyclohexyl, decahydronaphthyl, alkyl substituted cycloalkyl, naphthenyl, or abietyl group. Butyl-sulpho-N-octadecylamide, octylsulpho-N-cyclohexylamide, methyl sulpho-N- methyl-N-octadecylamide, methyl sulpho-N- dodecyloxyethylamide, ethoxyethane-sulpho-N- diethylamide, and ethyl-sulpho-N-oleylamide, may be used. The sulphonamides may be used alone or in admixture with one another or with other solvent or softening agents for the production of lacquers, films, and other shaped structures, plastic masses and the like from cellulose ethers such as ethyl or benzyl cellulose, or cellulose esters such as the acetate, formate, or nitrate. In an example, a cellulose nitrate lacquer is obtained by dissolving cellulose nitrate in butyl acetate, butyl alcohol, and xylene mixture, and then adding to the solution butyl-sulpho-N-octadecylamide and cyclohexyl-sulpho-N-dibutylamide. The Specification as open to inspection under Sect. 91 refers also to the use of sulphonamides which are unsubstituted at the nitrogen atom. In an example, cellulose acetate is dissolved in acetone, methyl alcohol, methyl acetate, ethyl acetate, benzene, and methylene chloride and n-butyl sulphonamide is added as plasticiser. The solution is used as a lacquer for cables. In another example, cellulose acetate is dissolved in tetrahydrofurfuryl alcohol, ethyl alcohol, and acetone, and a mixture of n-butyl-, and ndodecyl sulphonamide is added, the solution being used as a painting lacquer. In another example, a cellulose nitrate lacquer containing methylcyclohexyl sulphonamide is obtained. This subject-matter does not appear in the Specification as accepted
GB29713/38A 1937-10-13 1938-10-13 Improvements in or relating to the working up of cellulose derivatives Expired GB520162A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE520162X 1937-10-13

Publications (1)

Publication Number Publication Date
GB520162A true GB520162A (en) 1940-04-16

Family

ID=6550863

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29713/38A Expired GB520162A (en) 1937-10-13 1938-10-13 Improvements in or relating to the working up of cellulose derivatives

Country Status (1)

Country Link
GB (1) GB520162A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2700617A (en) * 1951-04-14 1955-01-25 Henkel & Cie Gmbh Acetyl cellulose plasticized with an alkylbenzol-sulfamide

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2700617A (en) * 1951-04-14 1955-01-25 Henkel & Cie Gmbh Acetyl cellulose plasticized with an alkylbenzol-sulfamide

Similar Documents

Publication Publication Date Title
GB520162A (en) Improvements in or relating to the working up of cellulose derivatives
US3094491A (en) Wax-free paint remover
GB717712A (en) Improvements in photomechanical resist compositions
ES447946A1 (en) Autoxidisable composition
US2316242A (en) Plasticized cellulose derivative composition
GB238485A (en) Solutions of cellulose esters
GB517820A (en) A method of producing soluble benzyl ether of dextran
US2305920A (en) Coating composition
US1480016A (en) Cellulose solvent and resulting cellulosic composition
US1397986A (en) seaton
DE612583C (en) Gelatinizing and softening agents for cellulose derivatives
US1984983A (en) Solvent or plasticizer for compositions with cellulose derivatives
GB158586A (en) Pyroxylin solvent and pyroxylin compositions containing the same
GB164386A (en) Improvements in or relating to the manufacture of products having a basis of cellulose derivatives
GB1000876A (en) Plasticising nitrocellulose
GB765674A (en) Improvements in and relating to fluorescent coating compositions
GB1120418A (en) Process for the manufacture of transparent coloured shaped articles based on regenerated cellulose using phthalocyanine dyestuffs
GB491199A (en) An improved manufacture of cellulose compound compositions
GB441716A (en) Improved manufacture of nitrocellulose lacquers
GB626880A (en) Paint removers
GB566068A (en) Coating compositions
GB318166A (en) Process for producing a liquid-and moisture-proof transparent and flexible material
GB250894A (en) Improvements in varnishes, lacquers, lacquer-enamels and the like
GB307361A (en) Process for the manufacture of cellulose ether oxyn lacquers and application of the products obtained
GB164385A (en) Improvements in or relating to the manufacture of products having a basis of cellulose derivatives