Mimura Naoki, Okamoto Masaki, Yamashita Hiromi, Oyama S Ted, Murata Kazuhisa
Research Institute for Innovation in Sustainable Chemistry, National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan.
J Phys Chem B. 2006 Nov 2;110(43):21764-70. doi: 10.1021/jp061966l.
Highly active catalysts for oxidative dehydrogenation of ethane with CO2 were characterized by temperature-programmed reduction (TPR), temperature-programmed oxidation (TPO), Fourier transform infrared (FTIR) spectroscopy, and X-ray absorption fine-structure (XAFS) analysis. In the active catalysts, Cr/H-ZSM-5 (SiO2/Al2O3 > 190), Cr6+ = O, or possibly Cr5+ = O was the catalytic species on the zeolite support. In contrast, little Cr6+ (or Cr5+) was detected in the less-active catalysts. The Cr6+ (or Cr5+) species was reduced to an octahedral Cr3+ species by treatment with ethane at 773 K, and the reduced Cr species was reoxidized to the Cr6+ (or Cr5+) species by treatment with CO2 at 673-773 K. The Cr redox cycle played an important role in the catalyst's high activity.
采用程序升温还原(TPR)、程序升温氧化(TPO)、傅里叶变换红外(FTIR)光谱和X射线吸收精细结构(XAFS)分析对用于乙烷与二氧化碳氧化脱氢反应的高活性催化剂进行了表征。在活性催化剂中,Cr/H-ZSM-5(SiO2/Al2O3 > 190)、Cr6+ = O或可能的Cr5+ = O是沸石载体上的催化物种。相比之下,在活性较低的催化剂中几乎检测不到Cr6+(或Cr5+)。通过在773 K下用乙烷处理,Cr6+(或Cr5+)物种被还原为八面体Cr3+物种,并且通过在673 - 773 K下用二氧化碳处理,还原后的Cr物种被重新氧化为Cr6+(或Cr5+)物种。Cr氧化还原循环在催化剂的高活性中起重要作用。