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Improved activity of Ni-Mo/SiO_(2) bimetallic catalyst synthesized via sol-gel method for methylcyclohexane cracking
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作者 Jun Zhang Ting Chen +5 位作者 Yi Jiao Mei Cheng lin-lin Wang Jian-li Wang xiang-yuan li Yao-Qiang Chen 《Petroleum Science》 SCIE CAS CSCD 2021年第5期1530-1542,共13页
To improve the cracking behavior of hydrocarbon,Ni-Mo/SiO_(2) bimetallic catalysts were synthesized by different preparation methods(sol-gel,co-impregnation and single-impregnation) and added the additives(citric acid... To improve the cracking behavior of hydrocarbon,Ni-Mo/SiO_(2) bimetallic catalysts were synthesized by different preparation methods(sol-gel,co-impregnation and single-impregnation) and added the additives(citric acid,polyethylene glycol and cetyltrimethylammonium bromide) based on the most suitable method above.The cracking reaction of methylcyclohexane under supercritical conditions was performed as the probe reaction to estimate the catalytic performance,and the properties of Ni-Mo/SiO_(2) catalyst were characterized by N_(2) absorption-desorption,XRD,XPS,H_(2)-TPR,NH_(3)-TPD,in-situ IR of NH_(3) desorption,HRTEM and STEM-mapping so as to study the structure-activity relationship.The catalyst synthesized via sol-gel method showed the best conversion and heat sink,being 81.8% and 3.81 MJ/kg,which was closely related to strong mutual effect between active components and SiO_(2) as well as strong acid sites.Besides,the introduction of additives by sol-gel method has an affirmative influence on properties of Ni-Mo/SiO_(2) catalysts,being that the acidity(more L and B acid sites) was modulated and organic groups interact with metal to suppress the aggregation of metal species(Ni and Mo),thereby enhancing the catalytic activity.At 750℃,the conversion(89.3%) as well as heat sink(3.99 MJ/kg) of MCH cracking obtained an optimum over Ni-Mo/SiO_(2) catalyst with addition of citric acid. 展开更多
关键词 Ni dispersion Ni-Mo/SiO_(2) Catalytic cracking Citric acid Sol-gel method Acidity modulation
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Solvent Reorganization Energy and Electronic Coupling for Intramolecular Electron Transfer in BiphenyI-Acceptor Anion Radicals
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作者 Jing-bo Wang Jian-yi Ma +2 位作者 xiang-yuan li Fu-cheng He Ke-xiang Fu 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 北大核心 2008年第1期45-54,共10页
关键词 非平衡溶剂化 电子转移 溶剂重组能 连续介质模型 电子偶合 联苯
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Shock tube study of n-decane ignition at low pressures 被引量:2
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作者 Xiao-Fei Nie Ping li +3 位作者 Chang-Hua Zhang Wei Xie Cong-Shan li xiang-yuan li 《Acta Mechanica Sinica》 SCIE EI CAS CSCD 2012年第1期79-82,共4页
Ignition delay times for n-decane/O2/Ar mixtures were measured behind reflected shock waves using endwall pressure and CH* emission measurements in a heated shock tube. The initial postshock conditions cover pressure... Ignition delay times for n-decane/O2/Ar mixtures were measured behind reflected shock waves using endwall pressure and CH* emission measurements in a heated shock tube. The initial postshock conditions cover pressures of 0.09-0.26 MPa, temperatures of 1 227-1 536 K, and oxygen mole fractions of 3.9%-20.7% with an equivalence ratio of 1.0. The correlation formula of ignition delay dependence on pressure, temperature, and oxygen mole fraction was obtained. The current data are in good agreement with available low-pressure experimental data, and they are then compared with the prediction of a kinetic mechanism. The current measurements extend the kinetic modeling targets for the n-decane combustion at low pressures. 展开更多
关键词 Ignition delay time n-Decane Heated shock tube
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