Effects of NaCl on Pt/ZrO2 catalysts for selective hydrogenation of crotonaldehyde

被引:21
|
作者
Wang, Xiao-Xia [1 ]
Zheng, Hai-Ying [1 ]
Liu, Xi-Jing [1 ]
Xie, Guan-Qun [1 ]
Lu, Ji-Qing [1 ]
Jin, Ling-Yun [1 ]
Luo, Meng-Fei [1 ]
机构
[1] Zhejiang Normal Univ, Inst Phys Chem, Minist Educ Adv Catalysis Mat, Key Lab, Jinhua 321004, Peoples R China
关键词
Pt/NaCl/ZrO2; catalyst; NaCl; Crotonaldehyde hydrogenation; Crotyl alcohol; VAPOR-PHASE HYDROGENATION; PARTICLE-SIZE; PT/CEO2; CATALYSTS; FT-IR; ADSORPTION; SUPPORT; ACETALDEHYDE; PERFORMANCE; OXIDATION; ALDEHYDES;
D O I
10.1016/j.apcata.2010.08.044
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
A series of NaCl-modified Pt/ZrO2 catalysts were prepared and tested for vapor phase selective hydrogenation of crotonaldehyde. It was found that the reactivities of the catalysts increased with NaCl contents, with the highest selectivity to crotyl alcohol (60%) at a NaCl content of 1%. Ammonia temperature programmed desorption and Fourier transmission infrared spectra of pyridine adsorption results indicated that the strengths of surface Lewis acids of the catalysts were weakened with increasing NaCl contents, such weakening was responsible for the enhancement of the reactivity. Diffuse reflectance infrared transform spectra of CO adsorption and X-ray photoelectron spectrometer results suggested that increased electron density on Pt species with the NaCl modification was responsible for the enhanced selectivity. However, high NaCl content (>3%) in the catalyst resulted in the growth of Pt particles and fewer interfacial Pt sites contacting with the surface Lewis acid sites, such changes were unfavorable for the selectivity. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:134 / 140
页数:7
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