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作者:

Zhan, Zongcheng (Zhan, Zongcheng.) | Song, Liyun (Song, Liyun.) | Liu, Xiaojun (Liu, Xiaojun.) | Jiao, Jiao (Jiao, Jiao.) | Li, Jinzhou (Li, Jinzhou.) | He, Hong (He, Hong.) (学者:何洪)

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摘要:

The 0.7 wt% Pt + 0.3 wt% Rh/Ce0.6Zr0.4O2 catalysts were fabricated via different methods, including ultrasonic-assisted membrane reduction (UAMR) co-precipitation, UAMR separation precipitation, co-impregnation, and sequential impregnation. The catalysts were physico-chemically characterized by N-2 adsorption, XRD, TEM, and H-2-TPR techniques, and evaluated for three-way catalytic activities with simulated automobile exhaust. UAMR co-precipitation- and UAMR separation precipitation-prepared catalysts exhibited a high surface area and metal dispersion, wide lambda window and excellent conversion for NOx reduction under lean conditions. Both fresh and aged catalysts from UAMR-precipitation showed the high surface areas of ca. 60-67 m(2)/g and 18-22 m(2)/g, respectively, high metal dispersion of 41%-55%, and small active particle diameters of 2.1-2.7 nm. When these catalysts were aged, the catalysts prepared by the UAMR method exhibited a wider working window (Delta lambda = 0.284-0.287) than impregnated ones (Delta lambda = 0.065-0.115) as well as excellent three-way catalytic performance, and showed lower T-50 (169 degrees C) and T-90 (195 degrees C) for NO reduction than the aged catalysts from impregnation processes, which were at 265 and 309 degrees C, respectively. This implied that the UAMR-separation precipitation has important potential for industrial applications to improve catalytic performance and thermal stability. The fresh and aged 0.7 wt% Pt + 0.3 wt% Rh/Ce0.6Zr0.4O2 catalysts prepared by the UAMR-separation precipitation method exhibited better catalytic performance than the corresponding catalysts prepared by conventional impregnation routes.

关键词:

precipitation Pt and Rh nanoparticles thermal stability three way catalyst UAMR

作者机构:

  • [ 1 ] [Zhan, Zongcheng]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
  • [ 2 ] [Song, Liyun]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
  • [ 3 ] [Liu, Xiaojun]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
  • [ 4 ] [Jiao, Jiao]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
  • [ 5 ] [Li, Jinzhou]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China
  • [ 6 ] [He, Hong]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China

通讯作者信息:

  • 何洪

    [He, Hong]Beijing Univ Technol, Coll Environm & Energy Engn, Dept Chem & Chem Engn, Lab Catalysis Chem & Nanosci, Beijing 100124, Peoples R China

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来源 :

JOURNAL OF ENVIRONMENTAL SCIENCES

ISSN: 1001-0742

年份: 2014

期: 3

卷: 26

页码: 683-693

6 . 9 0 0

JCR@2022

ESI学科: ENVIRONMENT/ECOLOGY;

ESI高被引阀值:211

JCR分区:2

中科院分区:4

被引次数:

WoS核心集被引频次: 15

SCOPUS被引频次: 15

ESI高被引论文在榜: 0 展开所有

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