Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/61206
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dc.contributor.authorZikant Saenkasaen_US
dc.contributor.authorChaiyavat Chaiyasuten_US
dc.contributor.authorRoongnapa Srichanaen_US
dc.contributor.authorSirivipa Piyamongkolen_US
dc.date.accessioned2018-09-10T04:06:34Z-
dc.date.available2018-09-10T04:06:34Z-
dc.date.issued2007-02-15en_US
dc.identifier.issn10974628en_US
dc.identifier.issn00218995en_US
dc.identifier.other2-s2.0-33846255341en_US
dc.identifier.other10.1002/app.24741en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33846255341&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61206-
dc.description.abstractThe target of this study was to synthesize the molecularly imprinted polymers (MIPs) of L-phenylalanine as the solid phases for characterization of molecular adsorption by molecularly imprinted solid phase extraction (MISPE). These MIPs, in microscale, were synthesized using thermal (40°C)-compared with thermal (65°C)-initiated polymerization process. Itaconic acid was chosen as the functional monomers, and either ethylene glycol dimethacrylate or trimethylolpropane trimethacrylate (TRIM) was used as the cross linker and was compared together. The influences of several parameters on the properties of the MIPs were investigated, especially physical robustness from the percentage yields and molecular adsorption from the percentage recovery by MISPE. The best yields were obtained from polymers made using TRIM and thermal (65°C)-initiated polymerization. However, there were no significant differences in molecular adsorption. It was concluded that these parameters can be considered to synthesize MIPs for chiral separation in advance steps such as other related Chromatographic techniques. © 2006 Wiley Periodicals, Inc.en_US
dc.subjectMaterials Scienceen_US
dc.titleComparison of molecular adsorption ability of the molecularly imprinted polymers prepared by ethylene glycol dimethacrylate and trimethylolpropane trimethacrylate as cross linkersen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Applied Polymer Scienceen_US
article.volume103en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsPrince of Songkla Universityen_US
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