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- Chaoquan, Hu, 1981, et al.
(författare)
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Selectivity and kinetics of methyl crotonate hydrogenation over Pt/Al2O3
- 2015
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Ingår i: Catalysis Science and Technology. - 2044-4753 .- 2044-4761. ; 5:3, s. 1716-1730
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Tidskriftsartikel (refereegranskat)abstract
- The hydrogenation of gas-phase methyl crotonate (MC) over Pt/Al2O3 was investigated with the aim to understand C=C hydrogenation in unsaturated methyl esters. Three Pt/Al2O3 catalysts with different Pt dispersions were prepared by varying calcination temperature and evaluated for MC hydrogenation. The main products were found to be methyl butyrate (MB) and methyl 3-butenoate (M3B), resulting from hydrogenation and shift of the C=C bond in MC, respectively. The measured activity for both hydrogenation and shift of the C=C in MC was found to depend on the Pt dispersion where higher Pt dispersion favors the C=C hydrogenation reaction. The effect of reactant concentrations on the activity and selectivity for MC hydrogenation over the Pt/Al2O3 catalyst was examined in detail. Under the investigated conditions, the C=C hydrogenation was found to have a negative reaction order with respect to MC concentration but a positive H2 order. Further understanding of the MC hydrogenation was provided from H2 chemisorption experiments over the catalyst with and without pre-adsorbed MC and from transient experiments using alternating MC and H2 feeds. Based on the present experimental results, a reaction pathway was proposed to describe gas-phase MC hydrogenation over Pt/Al2O3. In order to gain more insight into the reaction, a kinetic analysis of MC hydrogenation was performed by fitting a power-law model to the kinetic data, moreover, dissociative H2 adsorption on the catalyst was found to be the rate-determining step by comparing the power-law model with the overall rate expressions derived from mechanistic considerations.
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| 2. |
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| 3. |
- Ojagh, Houman, 1976, et al.
(författare)
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Effect of Thermal Treatment on Hydrogen Uptake and Characteristics of Ni-, Co-, and Mo-Containing Catalysts
- 2015
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Ingår i: Industrial & Engineering Chemistry Research. - : American Chemical Society (ACS). - 1520-5045 .- 0888-5885. ; 54:46, s. 11511-11524
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Tidskriftsartikel (refereegranskat)abstract
- Nonsulfided alumina supported Ni, Co, Mo, NiMo, and CoMo hydrotreating catalysts were synthesize. The TEM results indicated low dispersions of the active metals for Mo, NiMo, and CoMo, samples but significantly higher dispersion for the Ni sample. The effect of calcination and reduction on the hydrogen uptake capacity of the samples was investigated. The H-2-chemisorption and XPS results together showed that the precalcination step had a detrimental effect on the hydrogen absorption of the Ni sample formation of stable metal oxides. The XPS results revealed that the metal oxides of all calcined samples reached with the alumina support to form very stable spinels. Futher, the positive effects of a hydrogen atmosphere during the reduction, on the hyderogen uptake of the samples were cinfirmed by H-2-chemisorption measurements. Finally, the heats of adsorption (Delta H) of hydrogen for the Ni and Co samples were calculated to be 140 and 98 kJ mol(-1), respectively.
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| 4. |
- Xiao, Y., et al.
(författare)
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NiCo2O4 3 dimensional nanosheet as effective and robust catalyst for oxygen evolution reaction
- 2015
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Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 5:76, s. 61900-61905
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Tidskriftsartikel (refereegranskat)abstract
- Water electrolysis plays a fundamental role in the development of a sustainable energy system. In practice the efficiency of water electrolysis is severely limited by the sluggish kinetics of the oxygen evolution reaction. We reported a kind of integrated 3 dimensional oxygen evolution reactions (OER) catalyst by growing NiCo2O4 nanosheet arrays directly on conductive substrates. Such self-supported NiCo2O4 nanosheet electrodes exhibit high catalytic activity, good durability and nearly 100% faradic efficiency (FE) in alkaline electrolyte due to the enlarged electrochemical surface area and reduced electron transference resistance.
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