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dc.contributor.authorBülow, Leifde
dc.contributor.authorIsarankura-Na-Ayudhya, Chartchalermde
dc.contributor.authorNantasenamat, Chaninde
dc.contributor.authorPrachayasittikul, Virapongde
dc.contributor.authorYe, Leide
dc.date.accessioned2008-06-17T14:05:35Z-
dc.date.available2008-06-17T14:05:35Z-
dc.date.issued2006-09-26de
dc.identifier.issn1611-2156de
dc.identifier.urihttp://hdl.handle.net/2003/25668-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-8284-
dc.description.abstractBisphenol A (BPA), a ubiquitous chemical used in industries, has attracted great attention due to its widespread leakage to the environment and foodstuff. This has spurred great interest in the preparation of synthetic polymers capable of selectively sequestering BPA. In this study, theoretical calculation was utilized to confirm the selection of suitable functional monomer capable of strong interaction with BPA. It was found that 4-vinylpyridine was the optimal functional monomer as demonstrated in the literature. A series of molecularly imprinted polymers (MIPs) were prepared by varying the functional monomer, cross-linker, and porogen. After template removal, rebinding with the original template molecule was carried out in acetonitrile, acetonitrile/water (50/50 - 20/80, v/v). 4-vinylpyridine co-polymerized with ethylene glycol dimethacrylate (4VPY-co-EDMA) and 4-vinylpyridine co-polymerized with trimethylolpropane trimethacrylate (4VPY-co-TRIM) were found to exhibit good binding performance towards bisphenol A in acetonitrile. However, only 4VPY-co-EDMA was able to maintain its imprinting effect in acetonitrile/water (50/50 v/v) whereas 4VPY-co-TRIM totally lost its imprinting effect.en
dc.language.isoende
dc.relation.ispartofseriesEXCLI Journal ; Vol. 5, 2006en
dc.subjectBisphenol Aen
dc.subjectestrogen disruptoren
dc.subjectmicrospheresen
dc.subjectmolecular imprintingen
dc.subjectprecipitation polymerizationen
dc.subject.ddc610-
dc.titleIn silico design for synthesis of molecularly imprinted microspheres specific towards bisphenol A by precipitation polymerizationen
dc.typeTextde
dc.type.publicationtypearticlede
dcterms.accessRightsopen access-
eldorado.dnb.zdberstkatid2132560-1-
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