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dc.contributor.authorWu, Hung-Yuen_US
dc.contributor.authorBai, Hsunlingen_US
dc.contributor.authorWu, Jeffrey C. S.en_US
dc.date.accessioned2019-04-02T06:00:44Z-
dc.date.available2019-04-02T06:00:44Z-
dc.date.issued2014-07-16en_US
dc.identifier.issn0888-5885en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ie403742jen_US
dc.identifier.urihttp://hdl.handle.net/11536/147748-
dc.description.abstractPhotocatalytic reduction of carbon dioxide (CO2) to form a valuable energy source of methane (CH4) in monoethanolamine (MEA) solution is first investigated by mesoporous photocatalysts of Ti-MCM-41 in this study. The MEA solution was chosen as the absorbent and reductant because amine absorption is one of the most popular methods for CO2 capture from flue gas streams. Also, it is intended to integrate the CO2 capture and utilization into one process. The photocatalytic results of methane yields indicated that MEA served as a better reductant than water and NaOH which have been commonly used for CO2 reduction. For the best photocatalyst of Ti-MCM-41(50) manufactured at a Si/Ti molar ratio of 50, its methane yield (62.42 mu mol/g of cat.) was much higher than that of commercial P25 photocatalyst after 8 h of UV illumination. A photoreduction quantum efficiency (PQE) of 9.18% was achieved.en_US
dc.language.isoen_USen_US
dc.titlePhotocatalytic Reduction of CO2 Using Ti-MCM-41 Photocatalysts in Monoethanolamine Solution for Methane Productionen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ie403742jen_US
dc.identifier.journalINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCHen_US
dc.citation.volume53en_US
dc.citation.spage11221en_US
dc.citation.epage11227en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000339227700002en_US
dc.citation.woscount18en_US
Appears in Collections:Articles