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Synthesis and characterization of chitosan alkyl carbamates
The synthesis of chitosan methylcarbamate (ChMC) and ethylcarbamate (ChEC) is described by using a new methodology. Polymers with substitution degrees up to 63% for ChEC and 68.5% for ChMC were obtained. Derivatives with lower substitutions were acid soluble but those with higher ones were completel...
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Published in: | Journal of applied polymer science 2002-12, Vol.86 (11), p.2742-2747 |
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container_title | Journal of applied polymer science |
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creator | Cárdenas, Galo Paredes, Juan C. Cabrera, Gustavo Casals, Pedro |
description | The synthesis of chitosan methylcarbamate (ChMC) and ethylcarbamate (ChEC) is described by using a new methodology. Polymers with substitution degrees up to 63% for ChEC and 68.5% for ChMC were obtained. Derivatives with lower substitutions were acid soluble but those with higher ones were completely insoluble. This could be due to the loss in hydrophilic sites when the substitution degree increases. The reaction conditions and degree of substitution obtained for both derivatives were also described. A complete chemical characterization was carried out by spectroscopic techniques. The thermal degradation of chitosan and derivatives were studied in the range 25–500°C and both derivatives were shown to be thermally less stable than chitosan. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2742–2747, 2002 |
doi_str_mv | 10.1002/app.11252 |
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Polymers with substitution degrees up to 63% for ChEC and 68.5% for ChMC were obtained. Derivatives with lower substitutions were acid soluble but those with higher ones were completely insoluble. This could be due to the loss in hydrophilic sites when the substitution degree increases. The reaction conditions and degree of substitution obtained for both derivatives were also described. A complete chemical characterization was carried out by spectroscopic techniques. The thermal degradation of chitosan and derivatives were studied in the range 25–500°C and both derivatives were shown to be thermally less stable than chitosan. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2742–2747, 2002</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.11252</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; biopolymer ; chitosan ; chitosan derivative ; Exact sciences and technology ; Natural polymers ; NMR ; Physicochemistry of polymers ; Starch and polysaccharides ; thermogravimetric analysis</subject><ispartof>Journal of applied polymer science, 2002-12, Vol.86 (11), p.2742-2747</ispartof><rights>Copyright © 2002 Wiley Periodicals, Inc.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3762-be49cd49db17492056165b7884300d9293c62ec48069529ceee61b5c545b30893</citedby><cites>FETCH-LOGICAL-c3762-be49cd49db17492056165b7884300d9293c62ec48069529ceee61b5c545b30893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13966219$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Cárdenas, Galo</creatorcontrib><creatorcontrib>Paredes, Juan C.</creatorcontrib><creatorcontrib>Cabrera, Gustavo</creatorcontrib><creatorcontrib>Casals, Pedro</creatorcontrib><title>Synthesis and characterization of chitosan alkyl carbamates</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>The synthesis of chitosan methylcarbamate (ChMC) and ethylcarbamate (ChEC) is described by using a new methodology. Polymers with substitution degrees up to 63% for ChEC and 68.5% for ChMC were obtained. Derivatives with lower substitutions were acid soluble but those with higher ones were completely insoluble. This could be due to the loss in hydrophilic sites when the substitution degree increases. The reaction conditions and degree of substitution obtained for both derivatives were also described. A complete chemical characterization was carried out by spectroscopic techniques. The thermal degradation of chitosan and derivatives were studied in the range 25–500°C and both derivatives were shown to be thermally less stable than chitosan. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2742–2747, 2002</description><subject>Applied sciences</subject><subject>biopolymer</subject><subject>chitosan</subject><subject>chitosan derivative</subject><subject>Exact sciences and technology</subject><subject>Natural polymers</subject><subject>NMR</subject><subject>Physicochemistry of polymers</subject><subject>Starch and polysaccharides</subject><subject>thermogravimetric analysis</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1jztPwzAUhS0EEqUw8A-yMDCk9SN2YjFVpRRQBUU8Olo3jqOapklkR4Lw60kJj4npSud-55MOQqcEjwjGdAx1PSKEcrqHBgTLOIwETfbRoPuRMJGSH6Ij718xJoRjMUAXj23ZrI23PoAyC_QaHOjGOPsBja3KoMq7zDaVhzKAYtMWgQaXwhYa44_RQQ6FNyffd4ier2ZP0-twcT-_mU4WoWaxoGFqIqmzSGYpiSNJMRdE8DROkohhnEkqmRbU6CjBQnIqtTFGkJRrHvGU4USyITrvvdpV3juTq9rZLbhWEax2q1W3Wn2t7tiznq3BayhyB6W2_q_ApBCU7JzjnnuzhWn_F6rJcvljDvuG9Y15_22A2ygRs5ir1d1cvawub6fiAasl-wQnyXQX</recordid><startdate>20021209</startdate><enddate>20021209</enddate><creator>Cárdenas, Galo</creator><creator>Paredes, Juan C.</creator><creator>Cabrera, Gustavo</creator><creator>Casals, Pedro</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20021209</creationdate><title>Synthesis and characterization of chitosan alkyl carbamates</title><author>Cárdenas, Galo ; Paredes, Juan C. ; Cabrera, Gustavo ; Casals, Pedro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3762-be49cd49db17492056165b7884300d9293c62ec48069529ceee61b5c545b30893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Applied sciences</topic><topic>biopolymer</topic><topic>chitosan</topic><topic>chitosan derivative</topic><topic>Exact sciences and technology</topic><topic>Natural polymers</topic><topic>NMR</topic><topic>Physicochemistry of polymers</topic><topic>Starch and polysaccharides</topic><topic>thermogravimetric analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cárdenas, Galo</creatorcontrib><creatorcontrib>Paredes, Juan C.</creatorcontrib><creatorcontrib>Cabrera, Gustavo</creatorcontrib><creatorcontrib>Casals, Pedro</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cárdenas, Galo</au><au>Paredes, Juan C.</au><au>Cabrera, Gustavo</au><au>Casals, Pedro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of chitosan alkyl carbamates</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. 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subjects | Applied sciences biopolymer chitosan chitosan derivative Exact sciences and technology Natural polymers NMR Physicochemistry of polymers Starch and polysaccharides thermogravimetric analysis |
title | Synthesis and characterization of chitosan alkyl carbamates |
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