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곽자훈

Kwak, Ja Hun
Molecular Catalysis Lab.
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dc.citation.endPage 2987 -
dc.citation.number 8 -
dc.citation.startPage 2981 -
dc.citation.title JOURNAL OF PHYSICAL CHEMISTRY C -
dc.citation.volume 112 -
dc.contributor.author Kim, Do Heui -
dc.contributor.author Kwak, Jahun -
dc.contributor.author Szanyi, Janos -
dc.contributor.author Cho, Sung June -
dc.contributor.author Peden, Charles H. F. -
dc.date.accessioned 2023-12-22T08:44:56Z -
dc.date.available 2023-12-22T08:44:56Z -
dc.date.created 2015-07-21 -
dc.date.issued 2008-02 -
dc.description.abstract The roles of barium oxide and platinum during the sulfation of Pt-BaO/Al2O3 lean NOx trap catalysts were investigated by S K edge XANES (X-ray absorption near-edge spectroscopy) and Pt L-III XAFS (X-ray absorption fine structure). All of the samples studied [Al2O3, BaO(x; x = 8 or 20 wt %)/Al2O3, Pt(2.5 wt %)/Al2O3, and Pt(2 wt %)-BaO(x; x = 8 or 20 wt %)/Al2O3] were pre-sulfated prior to the X-ray absorption measurements. It was found that barium oxide itself has the ability to directly form barium sulfate even in the absence of Pt and gas-phase oxygen. In the platinum-containing samples, the presence of Pt-O species plays an important role in the formation of sulfate species. For the case of the BaO(8)/Al2O3 sample, where the barium coverage is about 0.26 ML, both baria and alumina phases are available for sulfation. S XANES results show that barium sulfates are formed preferentially over aluminum sulfates. When oxygen is absent from the gas phase, the sulfation route that involves Pt-O is eliminated after the initially present Pt-O species are completely consumed. In this case, formation of sulfates is suppressed unless barium oxide is also present. Pt L-III XAFS results show that the first coordination sphere around the Pt atoms in the Pt particles is dependent upon the gas mixture used during the sulfation process. Sulfation under reducing environments (e.g., SO2/H-2) leads to formation of Pt-S bonds, while oxidizing conditions (e.g., SO2/O-2) continue to show the presence of Pt-O bonds. In addition, a reducing environment was found to cause Pt sintering in greater extent than an oxidizing one. This result explains why samples sulfated under reducing conditions had lower NOx uptakes than those sulfated under oxidizing conditions. Therefore, our results provide needed information for the development of optimum practical operation conditions (e.g., sulfation or desulfation) for lean NOx trap catalysts that minimize deactivation by sulfur -
dc.identifier.bibliographicCitation JOURNAL OF PHYSICAL CHEMISTRY C, v.112, no.8, pp.2981 - 2987 -
dc.identifier.doi 10.1021/jp077563i -
dc.identifier.issn 1932-7447 -
dc.identifier.scopusid 2-s2.0-40549090577 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/12374 -
dc.identifier.url http://pubs.acs.org/doi/abs/10.1021/jp077563i -
dc.identifier.wosid 000253355700027 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title.alternative Roles of Pt and BaO in the sulfation of Pt/BaO/Al2O3 lean NOx trap materials: Sulfur K-edge XANES and Pt L-III XAFS studies -
dc.title Roles of Pt and BaO in the sulfation of Pt/BaO/Al2O3 lean NOx trap materials: Sulfur K-edge XANES and Pt L-III XAFS studies -
dc.type Article -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus RAY-ABSORPTION SPECTRA -
dc.subject.keywordPlus STORAGE CATALYSTS -
dc.subject.keywordPlus EXPOSURE CONDITIONS -
dc.subject.keywordPlus REDUCTION CATALYST -
dc.subject.keywordPlus GAMMA-ALUMINA -
dc.subject.keywordPlus DEACTIVATION -
dc.subject.keywordPlus SO2 -
dc.subject.keywordPlus SPECTROSCOPY -
dc.subject.keywordPlus TOLERANCE -
dc.subject.keywordPlus OXIDATION -

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