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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/16816
DC FieldValueLanguage
dc.contributor.authorMin-Lang Tsaien_US
dc.contributor.authorRong Huei Chenen_US
dc.date.accessioned2021-05-05T08:35:39Z-
dc.date.available2021-05-05T08:35:39Z-
dc.date.issued2003-12-20-
dc.identifier.issn0021-8995-
dc.identifier.urihttp://scholars.ntou.edu.tw/handle/123456789/16816-
dc.description.abstractThe objective of the study was to explore the effect of the degree of deacetylation (DD) of the chitosan used on the degradation rate and rate constant during ultrasonic degradation. Chitin was extracted from red shrimp process waste. Four different DD chitosans were prepared from chitin by alkali deacetylation. Those chitosans were degraded by ultrasonic radiation to different molecular weights. Changes of the molecular weight were determined by light scattering, and data of molecular weight changes were used to calculate the degradation rate and rate constant. The results were as follows: The molecular weight of chitosans decreased with an increasing ultrasonication time. The curves of the molecular weight versus the ultrasonication time were broken at 1‐h treatment. The degradation rate and rate constant of sonolysis decreased with an increasing ultrasonication time. This may be because the chances of being attacked by the cavitation energy increased with an increasing molecular weight species and may be because smaller molecular weight species have shorter relaxation times and, thus, can alleviate the sonication stress easier. However, the degradation rate and rate constant of sonolysis increased with an increasing DD of the chitosan used. This may be because the flexibilitier molecules of higher DD chitosans are more susceptible to the shear force of elongation flow generated by the cavitation field or due to the bond energy difference of acetamido and β‐1,4‐glucoside linkage or hydrogen bonds. Breakage of the β‐1,4‐glucoside linkage will result in lower molecular weight and an increasing reaction rate and rate constant.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.relation.ispartofJournal of Applied Polymer Scienceen_US
dc.subjectchitosanen_US
dc.subjectultrasonic degradationen_US
dc.subjectdegree of deacetylationen_US
dc.titleThe effect of degree of deacetylation of chitosan on the kinetics of ultrasonic degradation of chitosanen_US
dc.typejournal articleen_US
dc.identifier.doi10.1002/app.13027-
dc.identifier.isi000186374600010-
dc.relation.journalvolume90en_US
dc.relation.journalissue13en_US
dc.relation.pages3526-3531en_US
item.openairetypejournal article-
item.fulltextno fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.languageiso639-1en-
crisitem.author.deptCollege of Life Sciences-
crisitem.author.deptDepartment of Food Science-
crisitem.author.deptNational Taiwan Ocean University,NTOU-
crisitem.author.orcid0000-0003-4619-208x-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgCollege of Life Sciences-
Appears in Collections:食品科學系
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