Oxide passivated Ni-supported Ru nanoparticles in silica: A new catalyst for low-temperature carbon dioxide methanation

被引:52
作者
Polanski, Jaroslaw [1 ]
Siudyga, Tomasz [2 ]
Bartczak, Piotr [1 ,5 ]
Kapkowski, Maciej [1 ]
Ambrozkiewicz, Weronika [1 ]
Nobis, Agata [1 ]
Sitko, Rafal [1 ]
Klimontko, Joanna [3 ]
Szade, Jacek [3 ]
Lelatko, Jozef [4 ]
机构
[1] Univ Silesia, Inst Chem, Szkolna 9, PL-40006 Katowice, Poland
[2] Silesian Tech Univ, Dept Chem, PL-44100 Gliwice, Poland
[3] Univ Silesia, Silesian Ctr Educ & Interdisciplinary Res, A Chelkowski Inst Phys, PL-41500 Chorzow, Poland
[4] Univ Silesia, Inst Mat Sci, 75 Pulku Piechoty 1A, PL-41500 Chorzow, Poland
[5] NANO CHEM TECH, Rewolucjonistow 12-22, PL-42500 Bedzin, Poland
关键词
Methanation; Carbon-dioxide conversion; Nanocatalysis; Nano-Ru/Ni catalyst; Nano-Re/Ni catalyst; CO2; METHANATION; NICKEL-CATALYST; HYDROGENATION; SURFACE; MECHANISM; KINETICS; STABILITY; RHENIUM; COPPER;
D O I
10.1016/j.apcatb.2017.01.017
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
We tested the catalytic performance of Ni-supported Ru nanoparticles in silica for the first time. The Method for supporting Ru nanoparticles on Ni included the formation of nano-Ru/nano-SiO2, from which silica was digested in the presence of Ni. This provided a nano-Ru/Ni catalyst with an oxide passivation layer on the surface in which unalloyed metallic Ru and Ni were detected. This system, which was tested as a potential methanation catalyst, appears to be highly productive and efficient at low temperature, e.g. ca. 100% conversion can be achieved at ca. 200 degrees C at a high TOF value of 940 h(-1). The longer reaction duration deactivated the catalyst by carbon deposition; however, it did not destroy the catalyst, which could be fully reactivated by hydrogen treatment. In turn, the highest methane productivity (among nano-Re, Rh, Ir or Pd/Ni) given by TOF value of ca. 13855 h(-1) at higher temperature (460 degrees C) was observed for the nano-Re/Ni catalyst. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:16 / 23
页数:8
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