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Sonophotocatalytic degradation of bisphenol A and its intermediates with graphitic carbon nitride

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dc.contributor.authorSunasee, Sharmini-
dc.contributor.authorLeong, Kah Hon-
dc.contributor.authorWong, Kien Tiek-
dc.contributor.authorLee, Gooyong-
dc.contributor.authorPichiah, Saravanan-
dc.contributor.authorNah, InWook-
dc.contributor.authorJeon, Byong Hun-
dc.contributor.authorYoon, Yeomin-
dc.contributor.authorJang, Min-
dc.date.accessioned2022-07-10T14:54:47Z-
dc.date.available2022-07-10T14:54:47Z-
dc.date.created2021-05-12-
dc.date.issued2019-01-
dc.identifier.issn0944-1344-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/148494-
dc.description.abstractSince bisphenol A (BPA) exhibits endocrine disrupting action and high toxicity in aqueous system, there are high demands to remove it completely. In this study, the BPA removal by sonophotocatalysis coupled with nano-structured graphitic carbon nitride (g-C3N4, GCN) was conducted with various batch tests using energy-based advanced oxidation process (AOP) based on ultrasound (US) and visible light (Vis-L). Results of batch tests indicated that GCN-based sonophotocatalysis (Vis-L/US) had higher rate constants than other AOPs and especially two times higher degradation rate than TiO2-based Vis-L/US. This result infers that GCN is effective in the catalytic activity in Vis-L/US since its surface can be activated by Vis-L to transport electrons from valence band (VB) for utilizing holes (h(VB)(+)) in the removal of BPA. In addition, US irradiation exfoliated the GCN effectively. The formation of BPA intermediates was investigated in detail by using high-performance liquid chromatography-mass spectrometry (HPLC/MS). The possible degradation pathway of BPA was proposed.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER HEIDELBERG-
dc.titleSonophotocatalytic degradation of bisphenol A and its intermediates with graphitic carbon nitride-
dc.typeArticle-
dc.contributor.affiliatedAuthorJeon, Byong Hun-
dc.identifier.doi10.1007/s11356-017-8729-7-
dc.identifier.scopusid2-s2.0-85015003882-
dc.identifier.wosid000455814700009-
dc.identifier.bibliographicCitationENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, v.26, no.2, pp.1082 - 1093-
dc.relation.isPartOfENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH-
dc.citation.titleENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH-
dc.citation.volume26-
dc.citation.number2-
dc.citation.startPage1082-
dc.citation.endPage1093-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusLIGHT PHOTOCATALYTIC ACTIVITY-
dc.subject.keywordPlusENVIRONMENTAL REMEDIATION-
dc.subject.keywordPlusDOPED G-C3N4-
dc.subject.keywordPlusRHODAMINE-B-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusWATER-
dc.subject.keywordPlusTIO2-
dc.subject.keywordPlusPHOTODEGRADATION-
dc.subject.keywordPlusMINERALIZATION-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordAuthorSonophotocatalysis-
dc.subject.keywordAuthorBisphenol A-
dc.subject.keywordAuthorGraphitic carbon nitride-
dc.subject.keywordAuthorUltrasound-
dc.subject.keywordAuthorVisible light-
dc.subject.keywordAuthorIntermediates-
dc.identifier.urlhttps://link.springer.com/article/10.1007/s11356-017-8729-7-
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