scholarly journals Effect of Carbon Supported Pt Catalysts on Selective Hydrogenation of Cinnamaldehyde

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Qing Han ◽  
Yunfei Liu ◽  
Dong Wang ◽  
Fulong Yuan ◽  
Xiaoyu Niu ◽  
...  

Selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL) is of both fundamental and industrial interest. It is of great significance to evaluate the possible differences between different supports arising from metal dispersion and electronic effects, in terms of activity and selectivity. Herein, Pt catalysts on different carbon supports including carbon nanotubes (CNTs) and reduced graphene oxides (RGO) were developed by a simple wet impregnation method. The resultant catalysts were well characterized by XRD, Raman, N2physisorption, TEM, and XPS analysis. Applied in the hydrogenation of cinnamaldehyde, 3.5 wt% Pt/CNT shows much higher selectivity towards cinnamyl alcohol (62%) than 3.5 wt% Pt/RGO@SiO2(48%). The enhanced activity can be ascribed to the high graphitization degree of CNTs and high density of dispersed Pt electron cloud.

2019 ◽  
Vol 578 ◽  
pp. 105-115 ◽  
Author(s):  
Zhang Cao ◽  
Jiahao Bu ◽  
Zeqin Zhong ◽  
Changyong Sun ◽  
Qingsong Zhang ◽  
...  

2022 ◽  
Author(s):  
Haiyu Shen ◽  
Huahua Zhao ◽  
Jian Yang ◽  
Jun Zhao ◽  
Liang Yan ◽  
...  

Metal organic frameworks (MOFs) have been applied to stabilize metal nanoparticles due to their excellent properties, but there are many different viewpoints about the interaction between MOF and nanoparticles, which...


2013 ◽  
Vol 2013 ◽  
pp. 1-8
Author(s):  
Carolina P. Betti ◽  
Juan M. Badano ◽  
Ivana L. Rivas ◽  
Vanina A. Mazzieri ◽  
M. Juliana Maccarrone ◽  
...  

The sulfur resistance of low-loaded monometallic Pt catalysts and bimetallic Pt-W catalysts during the partial selective hydrogenation of styrene, a model compound of Pygas streams, was studied. The effect of metal impregnation sequence on the activity and selectivity was also evaluated. Catalysts were characterized by ICP, TPR, XRD, and XPS techniques. Catalytic tests with sulfur-free and sulfur-doped feeds were performed. All catalysts showed high selectivities (>98%) to ethylbenzene. Activity differences between the catalysts were mainly attributed to electronic effects due to the presence of different electron-rich species of Pt0and electron-deficient species ofPtδ+. Pt0promotes the cleavage of H2whilePtδ+the adsorption of styrene. The catalyst successively impregnated with W and Pt (WPt/Al) was more active and sulfur resistant than the catalyst prepared with an inverse impregnation order (PtW/Al). The higher poison resistance of WPt/Al was attributed to both steric and electronic effects.


Catalysts ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. 87 ◽  
Author(s):  
Sasithorn Kuhaudomlap ◽  
Okorn Mekasuwandumrong ◽  
Piyasan Praserthdam ◽  
Shin-Ichiro Fujita ◽  
Masahiko Arai ◽  
...  

2016 ◽  
Vol 180 ◽  
pp. 607-613 ◽  
Author(s):  
Renfeng Nie ◽  
Meng Miao ◽  
Weichen Du ◽  
Juanjuan Shi ◽  
Yingchun Liu ◽  
...  

2010 ◽  
Vol 26 (12) ◽  
pp. 3273-3277 ◽  
Author(s):  
ZHENG Hai-Ying ◽  
◽  
XIE Guan-Qun ◽  
WANG Xiao-Xia ◽  
JIN Ling-Yun ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Dong Wang ◽  
Yujun Zhu

The bimetal catalyst Pt-Cu/SiO2 was prepared by the impregnation method. Its catalytic performance was investigated by the selective hydrogenation of cinnamaldehyde. Pt-Cu/SiO2 exhibited much higher selectivity (64.1%) to cinnamyl alcohol than Pt/SiO2 (3.7%), while they showed similar conversion of cinnamaldehyde. This enhancement was attributed to the increase in the amount of the Pt0 species on the Pt-Cu/SiO2 surface, which is derived from the interaction between Pt and Cu revealed by XRD and XPS.


RSC Advances ◽  
2016 ◽  
Vol 6 (113) ◽  
pp. 112477-112485 ◽  
Author(s):  
Chu-Bai Chen ◽  
Meng-Yuan Chen ◽  
Bakht Zada ◽  
Ying-Jie Ma ◽  
Long Yan ◽  
...  

Selective hydrogenation of biomass-derived ethyl levulinate into γ-valerolactone over commercial zeolite supported catalysts was performed, and high yield was obtained.


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