Selective Hydrogenation of Methyl Palmitate to Cetyl Alcohol via Ternary Synergistic Catalysis of Ni, Oxygen Vacancies, and Lewis Acid Sites under Mild Reaction Conditions

Author(s):  
Xincheng Cao ◽  
Feng Long ◽  
Gaoyue Zhang ◽  
Junming Xu ◽  
Jianchun Jiang
2011 ◽  
Vol 236-238 ◽  
pp. 958-963 ◽  
Author(s):  
Bin Wang ◽  
Ying Zhang ◽  
Guang Sheng Guo

The reaction process of methanol to hydrocarbons was studied by means of in situ FTIR spectroscopic technique. The interaction between methanol and HZSM-5 surface was determined under different reaction conditions. It was found that the Lewis acid sites on the HZSM-5 surface played an important role in the conversion of methanol to hydrocarbons. During the catalysis process, methanol was adsorbed on the Lewis acid sites through chemical bond which was stronger than the interaction between methanol and the Brønsted acid sites. The dehydration of methanol took place on the Lewis acid sites to form the intermediate, dimethyl ether. According to the experimental results, the elaborate mechanism of methanol to hydrocarbons conversion was discussed.


2018 ◽  
Vol 238 ◽  
pp. 03004
Author(s):  
Wenzhi Jia ◽  
Xia Cai ◽  
Yong Zhang ◽  
Xiaohua Zuo ◽  
Juanjuan Yuan ◽  
...  

The hydrofluoric acid-resisting aluminum compounds (AlF3, AlPO4, AlN) supported with Ni catalyst were prepared by the wetness impregnation and tested for dehydrofluorination of hydrofluoroalkane to synthesize fluoroolefins. It is found that Ni/AlF3 catalyst has the best catalytic performance, CF3CFH2 conversion of 29.3% after the reaction at 430 °C for 30 h, CF2HCH3 conversion of 31.8% after the reaction at 250 °C for 30 h, respectively. Comparatively, dehydrofluorination temperature of CF3CFH2 is higher than CF2HCH3 over the aluminum compounds catalyst, and the activity of catalysts is related with Lewis acidity. For the aluminum compounds catalyst, addition of Ni had promoted the activity and stability of Lewis acidic catalysts, it is attributed to synergistic catalysis of Lewis acid sites and Ni.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 887
Author(s):  
Rujeeluk Khumho ◽  
Satit Yousatit ◽  
Chawalit Ngamcharussrivichai

5-Hydroxymethylfurfural (HMF) is one of the most important lignocellulosic biomass-derived platform molecules for production of renewable fuel additives, liquid hydrocarbon fuels, and value-added chemicals. The present work developed niobium oxides (Nb2O5) supported on mesoporous carbon/silica nanocomposite (MCS), as novel solid base catalyst for synthesis of HMF via one-pot glucose conversion in a biphasic solvent. The MCS material was prepared via carbonization using natural rubber dispersed in hexagonal mesoporous silica (HMS) as a precursor. The Nb2O5 supported on MCS (Nb/MCS) catalyst with an niobium (Nb) loading amount of 10 wt.% (10-Nb/MCS) was characterized by high dispersion, and so tiny crystallites of Nb2O5, on the MCS surface, good textural properties, and the presence of Bronsted and Lewis acid sites with weak-to-medium strength. By varying the Nb loading amount, the crystallite size of Nb2O5 and molar ratio of Bronsted/Lewis acidity could be tuned. When compared to the pure silica HMS-supported Nb catalyst, the Nb/MCS material showed a superior glucose conversion and HMF yield. The highest HMF yield of 57.5% was achieved at 93.2% glucose conversion when using 10-Nb/MCS as catalyst (5 wt.% loading with respect to the mass of glucose) at 190 °C for 1 h. Furthermore, 10-Nb/MCS had excellent catalytic stability, being reused in the reaction for five consecutive cycles during which both the glucose conversion and HMF yield were insignificantly changed. Its superior performance was ascribed to the suitable ratio of Brønsted/Lewis acid sites, and the hydrophobic properties generated from the carbon moieties dispersed in the MCS nanocomposite.


Zeolites ◽  
1997 ◽  
Vol 19 (4) ◽  
pp. 288-296 ◽  
Author(s):  
G.L. Woolery ◽  
G.H. Kuehl ◽  
H.C. Timken ◽  
A.W. Chester ◽  
J.C. Vartuli

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