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dc.contributor.authorChang, YCen_US
dc.contributor.authorKo, FHen_US
dc.contributor.authorKo, CJen_US
dc.contributor.authorChu, TCen_US
dc.date.accessioned2014-12-08T15:37:17Z-
dc.date.available2014-12-08T15:37:17Z-
dc.date.issued2004-11-22en_US
dc.identifier.issn0003-2670en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.aca.2004.09.084en_US
dc.identifier.urihttp://hdl.handle.net/11536/25627-
dc.description.abstractWe have detected the volatile organic species obtained after microwave digestion of poly(hydroxystyrene) with nitric acid in closed vessels at various reaction temperatures by using headspace solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC-MS). We probed the digestion reaction by measuring the response of the detectable species - we detected a total of 20 volatile organic compounds - with respect to the temperature over the range from room temperature to 80 degreesC. These compounds can be classified into alkane, alkanol, and aromatic species. The alkane species decreased monotonically, whereas the alkanol and aromatic compounds first increased and then decreased, as the digestion temperature increased. We have established the degradation mechanisms, which involve bond scission, recombination, adduct formation, and ring opening, on the basis of product analyses and bond length simulations. (C) 2004 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectmicrowave digestionen_US
dc.subjectvolatile organic speciesen_US
dc.subjectdigestion reactionen_US
dc.subjectdegradation mechanismsen_US
dc.titleProbing the microwave degradation mechanism of phenol-containing polymeric compounds by sample pretreatment and GC-MS analysisen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.aca.2004.09.084en_US
dc.identifier.journalANALYTICA CHIMICA ACTAen_US
dc.citation.volume526en_US
dc.citation.issue2en_US
dc.citation.spage121en_US
dc.citation.epage129en_US
dc.contributor.department材料科學與工程學系奈米科技碩博班zh_TW
dc.contributor.departmentGraduate Program of Nanotechnology , Department of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000225340700002-
dc.citation.woscount6-
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