GB611665A - Improvements in the production of cellulose esters - Google Patents
Improvements in the production of cellulose estersInfo
- Publication number
- GB611665A GB611665A GB13517/46A GB1351746A GB611665A GB 611665 A GB611665 A GB 611665A GB 13517/46 A GB13517/46 A GB 13517/46A GB 1351746 A GB1351746 A GB 1351746A GB 611665 A GB611665 A GB 611665A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cellulose
- acid
- ester
- long chain
- distilled water
- 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
- C08B3/00—Preparation of cellulose esters of organic acids
- C08B3/16—Preparation of mixed organic cellulose esters, e.g. cellulose aceto-formate or cellulose aceto-propionate
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 partially hydrolysed cellulose ester of a lower aliphatic acid is subjected to the washing or leaching action of hot distilled water to render it more reactive, and is then converted into a mixed ester of cellulose by reacting it with a long chain aliphatic acid esterifying agent such as the acid chloride. The long chain esterifying agent may contain 12-20 carbon atoms. The cellulose ester may be treated with 24-60 volumes of distilled water at 80-100 DEG C. A single treatment or several treatments with distilled water may be given. Following the activation treatment, the hydrolysed lower aliphatic ester of cellulose is dried and it is then ready for the further esterification. It may be dissolved in pyridine at a temperature of 50 DEG to 70 DEG C. and may then be heated with the acid chloride of a long chain aliphatic acid at 85 DEG to 100 DEG C. The product may be isolated by diluting the pyridine solution with acetone, methyl acetate, or dioxane, and then streaming the solution into water, whereby the cellulose ester is precipitated. The production of cellulose acetatelaurates is described. These may contain 0.6 to 0.8 free hydroxyl groups, 0.5 to 0.8 lauryl groups, and 1.4 to 1.75 acetyl groups per glucose residue. The products may be moulded at 165 DEG to 200 DEG C. The freshly precipitated cellulose acetate-laurate may be washed with hydrochloric acid, dried, ground, extracted with ether, and then stabilized by heating under pressure with very dilute sulphuric acid. It may then be washed with aqueous alcohol and then with water.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US611665XA | 1945-05-03 | 1945-05-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB611665A true GB611665A (en) | 1948-11-02 |
Family
ID=22034062
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13517/46A Expired GB611665A (en) | 1945-05-03 | 1946-05-03 | Improvements in the production of cellulose esters |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB611665A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2260333A (en) * | 1991-10-11 | 1993-04-14 | John Mark Lawther | Wax-like polysaccharide derivatives |
WO2009102306A1 (en) * | 2008-02-13 | 2009-08-20 | Eastman Chemical Company | Cellulose esters and their production in halogenated ionic liquids |
US7919631B2 (en) | 2007-02-14 | 2011-04-05 | Eastman Chemical Company | Production of ionic liquids |
US8067488B2 (en) | 2009-04-15 | 2011-11-29 | Eastman Chemical Company | Cellulose solutions comprising tetraalkylammonium alkylphosphate and products produced therefrom |
US8188267B2 (en) | 2008-02-13 | 2012-05-29 | Eastman Chemical Company | Treatment of cellulose esters |
US8354525B2 (en) | 2008-02-13 | 2013-01-15 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
US8729253B2 (en) | 2011-04-13 | 2014-05-20 | Eastman Chemical Company | Cellulose ester optical films |
US9777074B2 (en) | 2008-02-13 | 2017-10-03 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
US9834516B2 (en) | 2007-02-14 | 2017-12-05 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
US10174129B2 (en) | 2007-02-14 | 2019-01-08 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
-
1946
- 1946-05-03 GB GB13517/46A patent/GB611665A/en not_active Expired
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2260333A (en) * | 1991-10-11 | 1993-04-14 | John Mark Lawther | Wax-like polysaccharide derivatives |
US10174129B2 (en) | 2007-02-14 | 2019-01-08 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
US7919631B2 (en) | 2007-02-14 | 2011-04-05 | Eastman Chemical Company | Production of ionic liquids |
US9834516B2 (en) | 2007-02-14 | 2017-12-05 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
US8148518B2 (en) | 2007-02-14 | 2012-04-03 | Eastman Chemical Company | Cellulose esters and their production in carboxylated ionic liquids |
US8153782B2 (en) | 2007-02-14 | 2012-04-10 | Eastman Chemical Company | Reformation of ionic liquids |
US8158777B2 (en) | 2008-02-13 | 2012-04-17 | Eastman Chemical Company | Cellulose esters and their production in halogenated ionic liquids |
US9156918B2 (en) | 2008-02-13 | 2015-10-13 | Eastman Chemical Company | Treatment of cellulose esters |
US8273872B2 (en) | 2008-02-13 | 2012-09-25 | Eastman Chemical Company | Cellulose esters and their production in halogenated ionic liquids |
US8354525B2 (en) | 2008-02-13 | 2013-01-15 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
WO2009102306A1 (en) * | 2008-02-13 | 2009-08-20 | Eastman Chemical Company | Cellulose esters and their production in halogenated ionic liquids |
US8188267B2 (en) | 2008-02-13 | 2012-05-29 | Eastman Chemical Company | Treatment of cellulose esters |
US9777074B2 (en) | 2008-02-13 | 2017-10-03 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
US9175096B2 (en) | 2008-02-13 | 2015-11-03 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a halogenated ionic liquid process and products produced therefrom |
US9926384B2 (en) | 2009-04-15 | 2018-03-27 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom |
US8871924B2 (en) | 2009-04-15 | 2014-10-28 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom |
US8067488B2 (en) | 2009-04-15 | 2011-11-29 | Eastman Chemical Company | Cellulose solutions comprising tetraalkylammonium alkylphosphate and products produced therefrom |
US8524887B2 (en) | 2009-04-15 | 2013-09-03 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a tetraalkylammonium alkylphosphate ionic liquid process and products produced therefrom |
US9096691B2 (en) | 2011-04-13 | 2015-08-04 | Eastman Chemical Company | Cellulose ester optical films |
US9796791B2 (en) | 2011-04-13 | 2017-10-24 | Eastman Chemical Company | Cellulose ester optical films |
US8729253B2 (en) | 2011-04-13 | 2014-05-20 | Eastman Chemical Company | Cellulose ester optical films |
US9975967B2 (en) | 2011-04-13 | 2018-05-22 | Eastman Chemical Company | Cellulose ester optical films |
US10494447B2 (en) | 2011-04-13 | 2019-12-03 | Eastman Chemical Company | Cellulose ester optical films |
US10836835B2 (en) | 2011-04-13 | 2020-11-17 | Eastman Chemical Company | Cellulose ester optical films |
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