scholarly journals Catalyst Particle Density Controls Hydrocarbon Product Selectivity in CO2 Electroreduction on CuO x

ChemSusChem ◽  
2017 ◽  
Vol 10 (22) ◽  
pp. 4642-4649 ◽  
Author(s):  
Xingli Wang ◽  
Ana Sofia Varela ◽  
Arno Bergmann ◽  
Stefanie Kühl ◽  
Peter Strasser
Author(s):  
Shahram Sharifnia ◽  
A. Khodadadi ◽  
Y. Mortazavi

The present study examines the effect of hydrogen distribution (HD) along a Co/SiO2 catalyst bed on Fischer-Tropsch (FT) synthesis. The synthesis is performed under two pressures of 1.0 and 9.0 atm and different H2/CO ratios. The results are compared to those of the usual co-feed, in which both CO and H2 are introduced to the bed inlet. By HD strategy, the methane selectivity is suppressed by as much as 25% and the C11+ selectivity is enhanced up to 26%. CO conversion and product selectivity exhibited a strong dependence on the operating pressure and H2/CO ratio, when hydrogen is distributed.


2016 ◽  
Vol 41 (4) ◽  
pp. 371-384 ◽  
Author(s):  
Ali Nakhaei Pour ◽  
Fatemeh Dolati

The influence of the catalyst particle size in determining Fischer–Tropsch synthesis (FTS) performance for nano-structured iron catalysts was investigated. The catalysts were prepared by a microemulsion method and to achieve a series of catalysts with different iron particle size, the water-to-surfactant molar ratio (W/S) in the microemulsion system varied from 4 to 12. The results demonstrate that by decreasing the levels of active phase of the iron catalyst, the termination rates for chain growth are increased compared to the propagation rates. In addition, the activation energy for chain propagation is lower than for chain termination, and this difference (Et – Ep) for the hydrocarbon product distributions which is characterised by α1, is lower than the hydrocarbon product distribution which is characterised by α2 The results indicate the H2 concentration on the catalyst surface is decreased by increasing the catalyst particle size. Thus, the dependence of α (α1, and/or α2) on H2 partial pressures is increased by decreasing of catalyst particle size and the dependence of α2 on H2 partial pressures is weaker than for α1.


2016 ◽  
Vol 18 (14) ◽  
pp. 9652-9657 ◽  
Author(s):  
Seoin Back ◽  
Jun-Hyuk Kim ◽  
Yong-Tae Kim ◽  
Yousung Jung

To understand a high selectivity for HCOOH on the Pb electrode during the CO2 reduction reaction, we suggest a proton-assisted-electron-transfer mechanism, and validate the new mechanism by experimentally measuring onset potentials for CO2 reduction vs. H2 production. We find that the origin of this high selectivity lies in the strong O-affinitive and weak C-, H-affinitive characteristics of Pb.


Author(s):  
Xing Zhi ◽  
Yan Jiao ◽  
Yao Zheng ◽  
Kenneth Davey ◽  
Shi-Zhang Qiao

Understanding the late stages of C2 pathways provides great opportunities for fully achieving a selective CO2 electroreduction. The C2 product selectivity can be directed by the active site's oxygen affinity on a range of non-metal doped Cu surfaces.


Author(s):  
Carmen Castro-Castillo ◽  
Kamala Kanta Nanda ◽  
Elías Mardones-Herrera ◽  
Valeria Gazzano ◽  
Domingo Ruiz-León ◽  
...  

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