File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

정상호

Chung, Sang-Ho
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Catalytic reduction of nitrate in water over Pd-Cu/TiO2 catalyst: Effect of the strong metal-support interaction (SMSI) on the catalytic activity

Author(s)
Kim, Min-SungChung, Sang-HoYoo, Chun-JaeLee, Myung SukCho, Il-HyoungLee, Dae-WonLee, Kwan-Young
Issued Date
2013-10
DOI
10.1016/j.apcatb.2013.05.033
URI
https://scholarworks.unist.ac.kr/handle/201301/87322
Citation
APPLIED CATALYSIS B-ENVIRONMENTAL, v.142, pp.354 - 361
Abstract
In this study, we prepared TiO2-supported Pd-Cu catalysts of different anatase/rutile phase compositions, which were used in a nitrate reduction in water. It was shown that the catalysts containing a greater anatase phase composition had higher catalytic performance. Through characterization studies using H-2-temperature programmed reduction (H-2-TPR) and X-ray photoelectron spectroscopy (XPS), the observed trend of the catalytic activity was correlated to the degree of the strong metal-support interaction (SMSI) over the catalysts. The SMSI occurred through pre-treatment of the catalysts by H-2 reduction (at 200 degrees C), which resulted in increased partially reduced TiO2-x, and electron-rich active metal (Pd and Cu) states at the catalyst of higher composition of anatase phase. The relationships between the changes in the properties and activities of the catalysts as a result of the anatase phase composition are discussed. (c) 2013 Elsevier B.V. All rights reserved.
Publisher
ELSEVIER SCIENCE BV
ISSN
0926-3373
Keyword (Author)
SMSIPd-Cu/TiO2H-2-TPRXPSNitrate reduction
Keyword
LIQUID-PHASE HYDROGENATIONPALLADIUM-BASED CATALYSTSPD-CU CATALYSTSPT-CUSELECTIVE HYDROGENATIONAQUEOUS NITRATEDRINKING-WATERREMOVALNITRITECARBON

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.