The oxidation state of copper in bimetallic (Pt-Cu, Pd-Cu) catalysts during water denitration

被引:28
作者
Sa, Jacinto [1 ,2 ]
Barrabes, Noelia [3 ]
Kleymenov, Evgeny [1 ]
Lin, Chen [1 ]
Foettinger, Karin [3 ]
Safonova, Olga V. [1 ]
Szlachetko, Jakub [1 ,4 ]
van Bokhoven, Jeroen A. [1 ,2 ]
Nachtegaal, Maarten [1 ]
Urakawa, Atsushi [5 ]
Crespo, Gaston A. [6 ]
Rupprechter, Guenther [3 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
[2] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[3] Vienna Univ Technol, Inst Mat Chem, A-1060 Vienna, Austria
[4] Univ Kielce, Inst Phys, Kielce, Poland
[5] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
[6] Univ Geneva, Dep Inorgan Analyt & Appl Chem, CH-1211 Geneva, Switzerland
关键词
X-RAY SPECTROSCOPY; ENERGY-RESOLUTION FLUORESCENCE; NITRATE REDUCTION; DRINKING-WATER; REMOVAL; NITRITE; OXYGEN;
D O I
10.1039/c2cy00461e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Catalytic denitration of water with bimetallic systems has emerged as a viable solution for removal of nitrates from drinking water. Despite the progress in process development during the last two decades, only a few studies were performed to determine catalyst structure under working conditions. Herein, we determined the relative population of Cu oxidation states in Pt-Cu and Pd-Cu bimetallic catalysts by in situ high resolution X-ray absorption spectroscopy in combination with principal component analysis. The initial state of the catalyst was a Pt-Cu or Pd-Cu alloy. Segregation of the metal components occurred under reaction conditions especially for a Pt-Cu system. The active oxidation states of copper were metallic and alloy, and their concentration was highly dependent on the amount of hydrogen in the feed. Initial alloy phase of the catalysts ensures close proximity between Cu and the noble metals after segregation, essential to maintain catalysts activity.
引用
收藏
页码:794 / 799
页数:6
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