Direct dehydrogenation of propane over Co@silicalite-1 zeolite: Steaming-induced restructuring of Co2+active sites

被引:17
|
作者
Long, Jiangping [1 ]
Tian, Suyang [1 ]
Wei, Sheng [1 ]
Lin, Hongqiao [2 ]
Shi, Guiwen [1 ]
Zong, Xupeng [3 ]
Yang, Yanhui [1 ,4 ]
Yang, Dan [1 ]
Tang, Yu [2 ]
Dai, Yihu [1 ]
机构
[1] Nanjing Tech Univ, Inst Adv Synth, Sch Chem & Mol Engn, Nanjing 211816, Peoples R China
[2] Fuzhou Univ, Inst Mol Catalysis & In Situ Operando Studies, Coll Chem, Fuzhou 350108, Peoples R China
[3] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[4] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 73000, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Propane dehydrogenation; Propylene; Co2+catalyst; Silicalite-1; zeolite; Steaming; C-H ACTIVATION; CATALYTIC DEHYDROGENATION; COBALT; NANOPARTICLES; SPECTROSCOPY; PERFORMANCE; STABILITY; CO-MCM-41; EVOLUTION; CLUSTERS;
D O I
10.1016/j.apsusc.2022.156238
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
The chemical state of the Co-relevant active site determines the catalytic performance of the Co-containing zeolite catalysts in non-oxidative propane dehydrogenation (PDH) reaction. Herein, we demonstrate that the moderate steaming pre-treatment is an available strategy to enhance catalytic activity of silicalite-1 zeolite-supported Co catalyst through tuning the Co state. The steaming-treated Co@S-1-steam catalyst exhibits sevenfold increased specific reaction rate (0.44 s-1) than the untreated Co@S-1 catalyst and maintains 95 % propylene selectivity in the PDH reaction at 590 degrees C. By comprehensive characterizations on the structural properties of the catalysts, multiple roles of steaming treatment are discovered. Steaming treatment can induce the reductive restructuring of the Co catalytic sites in zeolite micropores to form tetrahedral Co2+ species with enhanced dispersion and unsaturation degree, and significantly accelerate the selective activation of propane C-H bonds. Furthermore, it also reduces the surface acidity and consequently promotes the desorption of propylene intermediates for enhancing the catalytic reaction rate and anti-coke stability.
引用
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页数:11
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