GB671721A - Improvement in organo-silicon derivatives of cellulose - Google Patents

Improvement in organo-silicon derivatives of cellulose

Info

Publication number
GB671721A
GB671721A GB3042/50A GB304250A GB671721A GB 671721 A GB671721 A GB 671721A GB 3042/50 A GB3042/50 A GB 3042/50A GB 304250 A GB304250 A GB 304250A GB 671721 A GB671721 A GB 671721A
Authority
GB
United Kingdom
Prior art keywords
cellulose
glucose unit
solution
per glucose
groups per
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
GB3042/50A
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.)
Dow Silicones UK Ltd
Original Assignee
Dow Corning 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 Dow Corning Ltd filed Critical Dow Corning Ltd
Publication of GB671721A publication Critical patent/GB671721A/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
    • C08B15/00Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
    • C08B15/05Derivatives containing elements other than carbon, hydrogen, oxygen, halogens or sulfur

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)

Abstract

A chemical product consisting essentially of a triorgano silyl derivative of cellulose in which there is an average of 0.25-2.0 triorgano silyl groups per glucose unit of the cellulose molecules is obtained. The triorgano silyl groups are of the formula (R2R1Si-) where R is an aryl radical and R1 is an aryl or alkyl radical, and each of the silicon atoms is attached through an oxygen atom to a cellulose carbon atom which before the substitution would normally carry a hydroxyl group. As aryl radical there may be used a phenyl, xenyl, tolyl, xylyl, or naphthyl group. The alkyl group may be methyl, ethyl, propyl, butyl, amyl, hexyl, octyl, dodecyl, or octadecyl. A partially esterified or etherified cellulose containing 1-2.75 ester or ether groups per glucose unit of the cellulose may be used in making the silicon derivative. Cellulose nitrate, acetate, or p-toluene sulphonate, or a cellulose methyl, ethyl, propyl, butyl, benzyl, allyl, hydroxy ethyl, triphenyl carbinyl or carboxy methyl ether, may be used. The cellulose ester or ether may be etherified with a triorgano silicon halide preferably in presence of a hydrogen halide acceptor such as pyridine, ammonia, piperidine, or other amino compound. The reaction may be effected at room temperature. Films may be obtained by casting a solution of the organo silicon cellulose derivative in an aromatic hydrocarbon or an ether on to a smooth surface, evaporating the solvent, and stripping the dried film. The films may be used for insulation of electrical equipment, and for packaging. The organo silicon cellulose derivatives may also be used for making articles by moulding or extrusion. Pigments, fillers, and finely-divided dielectric solids may be incorporated. In an example, methyl cellulose containing 1.7 methoxy groups per glucose unit is suspended in pyridine. A solution of triphenyl chloro silane in pyridine is added. Reaction proceeds at once and a clear viscous solution of the methyl cellulose silane reaction product is obtained. The solution is left for 2 days and then poured into dilute hydrochloric acid solution. The viscous mass is washed with water and then dissolved in benzene. The solution is cast to form a transparent film containing 1.3 triphenyl silyl groups per glucose unit of the cellulose. In other examples, ethyl cellulose containing 2.4 ethoxy radicals per glucose unit is reacted with diphenylethyl chloro silane, and cellulose acetate containing 2 acetyl groups per glucose unit is reacted with triphenyl chlorosilane.
GB3042/50A 1949-02-23 1950-02-06 Improvement in organo-silicon derivatives of cellulose Expired GB671721A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US671721XA 1949-02-23 1949-02-23

Publications (1)

Publication Number Publication Date
GB671721A true GB671721A (en) 1952-05-07

Family

ID=22074176

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3042/50A Expired GB671721A (en) 1949-02-23 1950-02-06 Improvement in organo-silicon derivatives of cellulose

Country Status (1)

Country Link
GB (1) GB671721A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2477158A1 (en) * 1980-02-28 1981-09-04 Chemiefaser Lenzing Ag PROCESS FOR PREPARING O-TRIMETHYLSILYL CELLULOSES
FR2477157A1 (en) * 1980-02-28 1981-09-04 Chemiefaser Lenzing Ag PROCESS FOR THE PREPARATION OF O-TRIMETHYLSILYL-CELLULOSES AND NEW PRODUCTS OBTAINED THEREBY
WO2003020770A1 (en) * 2001-08-31 2003-03-13 Unilever Plc Polymers and their use
FR2856073A1 (en) * 2003-06-16 2004-12-17 Rhodia Chimie Sa Water-in-oil emulsion useful in laundry applications comprises a liquid or fusible hydrophobic phase and an aqueous phase containing a silicone-modified polysaccharide ester
US8907026B2 (en) 2004-12-23 2014-12-09 Dow Corning Corporation Crosslinkable saccharide-siloxane compositions, and networks, coatings and articles formed therefrom

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2477158A1 (en) * 1980-02-28 1981-09-04 Chemiefaser Lenzing Ag PROCESS FOR PREPARING O-TRIMETHYLSILYL CELLULOSES
FR2477157A1 (en) * 1980-02-28 1981-09-04 Chemiefaser Lenzing Ag PROCESS FOR THE PREPARATION OF O-TRIMETHYLSILYL-CELLULOSES AND NEW PRODUCTS OBTAINED THEREBY
WO2003020770A1 (en) * 2001-08-31 2003-03-13 Unilever Plc Polymers and their use
US6903208B2 (en) 2001-08-31 2005-06-07 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Polymers and their use
AU2002333459B2 (en) * 2001-08-31 2005-10-27 Unilever Plc Polymers and their use
CN1302011C (en) * 2001-08-31 2007-02-28 荷兰联合利华有限公司 Polymers and their use
FR2856073A1 (en) * 2003-06-16 2004-12-17 Rhodia Chimie Sa Water-in-oil emulsion useful in laundry applications comprises a liquid or fusible hydrophobic phase and an aqueous phase containing a silicone-modified polysaccharide ester
WO2005003270A1 (en) * 2003-06-16 2005-01-13 Rhodia Chimie Inverse or multiple water/oil or water/oil/water emulsion, comprising a hydrophobic phase and a hydrosoluble or hydrodispersable substituted polysaccharide
US8907026B2 (en) 2004-12-23 2014-12-09 Dow Corning Corporation Crosslinkable saccharide-siloxane compositions, and networks, coatings and articles formed therefrom

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