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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.accessioned2017-04-21T06:48:23Z-
dc.date.available2017-04-21T06:48:23Z-
dc.date.issued2012en_US
dc.identifier.isbn978-1-4665-6276-9en_US
dc.identifier.urihttp://hdl.handle.net/11536/134781-
dc.description.abstractPhotocatalytic reduction of carbon dioxide (CO2) to form valuable energy source of methane (CH4) in the ethanolamine (MEA) solution is investigated in this study. The TiO2 photocatalysts were prepared by doping with nano-sized metals (Fe, Zn, Mn, Ce) via the co-precipitation method. The photocatalytic reduction process was performed in the MEA solution because the MEA absorption is one of the most popular methods for CO2 greenhouse gas capture from flue gas streams. And it is intended to integrate the CO2 capture and utilization into one process. The tests were performed with the UV light source of 9W and 365 nm. The light intensity of 6.3 mW/cm(2) was measured at the center point between the UV light source and the outer glass of the reactor. The 5 hours test results showed the methane yield followed the order of Ce-TiO2 > Mn-TiO2> Zn-TiO2 > Fe-TiO2. Tests were also evaluated with a solar light concentrator, and it has been proved that it is possible to produce CH4 under solar light without the addition of any external energy source.en_US
dc.language.isoen_USen_US
dc.subjectcarbon dioxideen_US
dc.subjectphotoreductionen_US
dc.subjectethanolamineen_US
dc.subjectphotocatalysten_US
dc.subjectmethaneen_US
dc.titleMetal-doped Photocatalysts to Reduce Carbon Dioxide in Ethanolamine Solution for Methane Productionen_US
dc.typeProceedings Paperen_US
dc.identifier.journalNANOTECHNOLOGY 2012, VOL 3: BIO SENSORS, INSTRUMENTS, MEDICAL, ENVIRONMENT AND ENERGYen_US
dc.citation.spage746en_US
dc.citation.epage748en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000391249300196en_US
dc.citation.woscount0en_US
Appears in Collections:Conferences Paper