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dc.contributor.authorHo, Kuo-Lingen_US
dc.contributor.authorChung, Ying-Chienen_US
dc.contributor.authorLin, Yueh-Hsienen_US
dc.contributor.authorTseng, Ching-Pingen_US
dc.date.accessioned2014-12-08T15:12:12Z-
dc.date.available2014-12-08T15:12:12Z-
dc.date.issued2008-05-01en_US
dc.identifier.issn0045-6535en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.chemosphere.2008.01.044en_US
dc.identifier.urihttp://hdl.handle.net/11536/9364-
dc.description.abstractA biofilter using granular activated carbon with immobilized Paracoccus sp. CP2 was applied to the elimination of 10-250 ppm of trimethylamine (TMA), dimethylamine (DMA), and methylamine (MA). The results indicated that the system effectively treated MA (>93%), DMA (>90%), and TMA (>85%) under high loading conditions, and the maximum degradation rates were 1.4, 1.2, and 0.9 g-N kg(-1) GAC d(-1). Among the three different amines treated, TMA was the most difficult to degrade and resulted in ammonia accumulation. Further study on TMA removal showed that the optimal pH was near neutral (6.0-8.0). The supply of high glucose (>0.1%) inhibited TMA removal, maybe due to substrate competition. However, complete TMA degradation was achieved under the co-immobilization of Paracoccus sp. CP2 and Arthrobacter sp. CP1 (similar to 96%). Metabolite analysis results demonstrated that the metabolite NH(4)(+) concentrations decreased by a relatively small 27% while the metabolite NO(2)(-) apparently increased by heterotrophic nitrification of Arthrobacter sp. CP1 in the co-immobilization biofilter. (C) 2008 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectactivated carbonen_US
dc.subjectammoniaen_US
dc.subjectdegradationen_US
dc.subjectimmobilizationen_US
dc.subjectnitrificationen_US
dc.titleBiofiltration of trimethylamine, dimethylamine, and methylamine by immobilized Paracoccus sp CP2 and Arthrobacter sp CP1en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.chemosphere.2008.01.044en_US
dc.identifier.journalCHEMOSPHEREen_US
dc.citation.volume72en_US
dc.citation.issue2en_US
dc.citation.spage250en_US
dc.citation.epage256en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000256737900015-
dc.citation.woscount17-
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