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DC Field | Value | Language |
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dc.contributor.author | Kwanjira Suwannarat | en_US |
dc.contributor.author | Kontee Thongthai | en_US |
dc.contributor.author | Supon Ananta | en_US |
dc.contributor.author | Laongnuan Srisombat | en_US |
dc.date.accessioned | 2018-09-05T04:23:40Z | - |
dc.date.available | 2018-09-05T04:23:40Z | - |
dc.date.issued | 2018-03-05 | en_US |
dc.identifier.issn | 18734359 | en_US |
dc.identifier.issn | 09277757 | en_US |
dc.identifier.other | 2-s2.0-85039862992 | en_US |
dc.identifier.other | 10.1016/j.colsurfa.2017.12.046 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85039862992&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/58403 | - |
dc.description.abstract | © 2017 Elsevier B.V. The hollow trimetallic Ag/Au/Pd nanoparticles with controllable Ag:Au:Pd ratio were successfully prepared by using a successive reduction method. Their optical properties, morphologies, structures, chemical compositions and electronic properties were carefully characterized by UV-vis, TEM, WDS, XRD and XPS techniques. The synthesized nanoparticles were also employed as catalysts for reduction of 4-nitrophenol. The results show that the trimetallic Ag/Au/Pd nanoparticles provided better catalytic activity than those obtained from bimetallic Ag/Au nanoparticles and monometallic counterparts. This study demonstrated that both atomic ratio of constituent metal and hollow interior structure strongly affect the catalytic activities of the synthesized Ag/Au/Pd nanocatalysts. | en_US |
dc.subject | Chemical Engineering | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Physics and Astronomy | en_US |
dc.title | Synthesis of hollow trimetallic Ag/Au/Pd nanoparticles for reduction of 4-nitrophenol | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Colloids and Surfaces A: Physicochemical and Engineering Aspects | en_US |
article.volume | 540 | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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