Ethylene Epoxidation Activity Over Ag-Based Catalysts on Different Nanocrystalline Perovskite Titanate Supports

被引:16
作者
Chongterdtoonskul, Atiporn [1 ]
Schwank, Johannes W. [2 ]
Chavadej, Sumaeth [1 ,3 ]
机构
[1] Chulalongkorn Univ, Petr & Petrochem Coll, Bangkok 10330, Thailand
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Chulalongkorn Univ, Ctr Excellence Petrochem & Mat Technol, Bangkok 10330, Thailand
关键词
Perovskite supports; SrTiO3; Nanocrystalline TiO2; Sol-gel; Ethylene epoxidation; SOL-GEL PROCESS; PHOTOCATALYTIC HYDROGEN EVOLUTION; VISIBLE-LIGHT IRRADIATION; ULTRASTABLE Y-ZEOLITE; SURFACTANT TEMPLATE; ALPHA-ALUMINA; BIMETALLIC CATALYSTS; SILVER CATALYSTS; H-2; PRODUCTION; TIO2;
D O I
10.1007/s10562-012-0848-7
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
Ag-based catalysts on different nanocrystalline perovskite supports (MgTiO3, CaTiO3, SrTiO3, and BaTiO3), and nanocrystalline TiO2 support prepared by a sol-gel method and on a commercial alpha-Al2O3 support were comparatively studied for catalytic activity of the ethylene epoxidation reaction. The dependence of ethylene oxide production performance on calcination temperature of the support, type of titanate nanocrystal supports, Ag loading, and reaction temperature was systematically investigated. The catalysts were analytically characterized by a Brunauer-Emmett-Teller (BET) surface area, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), temperature programmed desorption (TPD), and X-ray photoelectron spectroscopy (XPS). Among studied catalysts, the 17.2 wt% Ag/SrTiO3 catalyst exhibited the highest catalytic activity towards ethylene epoxidation reaction. The long-term stability of the dominant catalysts (which exhibited a high catalytic activity to produce ethylene oxide) was studied at 48 h of time on stream. As shown in the figure, the 17.2 wt% Ag/SrTiO3 catalyst with the support calcination temperature of 923 K is the most effective catalyst for the ethylene epoxidation reaction, giving not only the highest EO selectivity but also providing the highest long-term stability.
引用
收藏
页码:991 / 1002
页数:12
相关论文
共 48 条
  • [1] Epoxidation of ethylene over silver catalysts supported on α-alumina crystal carriers
    Ayame, A
    Uchida, Y
    Ono, H
    Miyamoto, M
    Sato, T
    Hayasaka, H
    [J]. APPLIED CATALYSIS A-GENERAL, 2003, 244 (01) : 59 - 70
  • [2] Bharthwaj A, 2002, THESIS MIT US
  • [3] Bomben K.D, 1995, PHYS ELECT EDEN PRAI
  • [4] Deactivation studies during catalytic cracking of C8 aliphatic hydrocarbons over ultrastable Y-zeolite.: Conversion and product yield profiles with time onstream
    Brillis, AA
    Manos, G
    [J]. CATALYSIS LETTERS, 2003, 91 (3-4) : 185 - 191
  • [5] In situ thermogravimetric study of coke formation during catalytic cracking of normal hexane and 1-hexene over ultrastable Y zeolite
    Chen, S
    Manos, G
    [J]. JOURNAL OF CATALYSIS, 2004, 226 (02) : 343 - 350
  • [6] Effects of oxide supports on ethylene epoxidation activity over Ag-based catalysts
    Chongterdtoonskul, Atiporn
    Schwank, Johannes W.
    Chavadej, Sumaeth
    [J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2012, 358 : 58 - 66
  • [7] Cullity B. D., 1978, ELEMENTS XRAY DIFFRA
  • [8] Daniel T, 2008, J CATAL, V260, P380
  • [9] Rhenium promotion of Ag and Cu-Ag bimetallic catalysts for ethylene epoxidation
    Dellamorte, J. C.
    Lauterbach, J.
    Barteau, M. A.
    [J]. CATALYSIS TODAY, 2007, 120 (02) : 182 - 185
  • [10] Eldridge JM, 2009, US Patent, Patent No. [2:1-35, 2135]