GB671721A - Improvement in organo-silicon derivatives of cellulose - Google Patents
Improvement in organo-silicon derivatives of celluloseInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/05—Derivatives 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.
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2477157A1 (en) * | 1980-02-28 | 1981-09-04 | Chemiefaser Lenzing Ag | PROCESS FOR THE PREPARATION OF O-TRIMETHYLSILYL-CELLULOSES AND NEW PRODUCTS OBTAINED THEREBY |
FR2477158A1 (en) * | 1980-02-28 | 1981-09-04 | Chemiefaser Lenzing Ag | PROCESS FOR PREPARING O-TRIMETHYLSILYL CELLULOSES |
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 |
-
1950
- 1950-02-06 GB GB3042/50A patent/GB671721A/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2477157A1 (en) * | 1980-02-28 | 1981-09-04 | Chemiefaser Lenzing Ag | PROCESS FOR THE PREPARATION OF O-TRIMETHYLSILYL-CELLULOSES AND NEW PRODUCTS OBTAINED THEREBY |
FR2477158A1 (en) * | 1980-02-28 | 1981-09-04 | Chemiefaser Lenzing Ag | PROCESS FOR PREPARING O-TRIMETHYLSILYL CELLULOSES |
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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