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Synthesis and characterization of long-chain fatty acid cellulose ester (FACE)
Long‐chain fatty acid cellulose esters (FACE) were synthesized by the acid chloride‐pyridine reaction with different degrees of substitution (DS). The hydrolyzed soybean oil was used as unsaturated fatty acids, its unsaturation degree, and composition were analyzed by 1H and 13C NMR methods. The che...
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Published in: | Journal of applied polymer science 1994-05, Vol.52 (6), p.755-761 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Long‐chain fatty acid cellulose esters (FACE) were synthesized by the acid chloride‐pyridine reaction with different degrees of substitution (DS). The hydrolyzed soybean oil was used as unsaturated fatty acids, its unsaturation degree, and composition were analyzed by 1H and 13C NMR methods. The chemical structures of FACE were confirmed by solid‐state 13C NMR, and substitution reaction of fatty acid chloride on cellulose were analyzed by IR spectroscopy. FACE(s) are insoluble in common organic solvents, such as benzene, toluene, THF, etc., at refluxing temperature. As the DS increased, the tensile strength of extruded FACE films decreased, but elongation increased. © 1994 John Wiley & Sons, Inc. |
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ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/app.1994.070520605 |