نتایج جستجو برای: ni co catalyst
تعداد نتایج: 412488 فیلتر نتایج به سال:
The atomic structure of an electrodeposited Ni catalyst film is dominated by extensive di-μ-oxido bridging between Ni(III/IV) ions, as revealed by X-ray absorption spectroscopy. The structure is surprisingly similar to that of an analogous Co-based film and colloidal Mn-based catalysts. Structural requirements for water oxidation are discussed.
The nanoparticles of Ni–Si mixed oxides were prepared by co-precipitation method using nickel nitrate; Ni(NO3)2 6H2O and tetraethylorthosilicate (TEOS). The products were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and hydrogen temperature program reduction (H2-TPR). The results revealed that Ni–Si mixed oxides particles were obtained with average particle ...
Fe, Co, and Ni are catalytically effective for growing single-walled carbon nanotubes (SWNTs). On substrates, however, Ni tends to yield only multi-walled carbon nanotubes. Because enhanced surface diffusion at the elevated growth temperature required for deposition might cause coarsening of Ni catalyst nanoparticles, adjusting the nominal Ni thickness should be crucial for controlling the part...
Kinetic comparison of Ni/Al2O3 and Ni/MgO-Al2O3 nano structure catalysts in CO2 reforming of methane
The kinetic characteristics of the Ni/Al2O3 and Ni/MgO-Al2O3 catalysts were investigated in CO2 reforming of methane (CRM). The reaction orders (α and β) and the rate constant (k) were calculated using the non-linear regression analysis, in which the sum of the squared differences of calculated and experimental CO2 reforming of m...
The electrocatalytic proton reduction activity of a Ni bis(diphosphine) (NiP) and a cobaloxime (CoP) catalyst has been studied in water in the presence of the gaseous inhibitors O2 and CO. CoP shows an appreciable tolerance towards O2, but its activity suffers severely in the presence of CO. In contrast, NiP is strongly inhibited by O2, but produces H2 under high CO concentrations.
The partial oxidation of methane to syngas was studied in this work over Ni-containing ceria catalysts with nickel content of 5, 10 and 20 at.% at atmospheric pressure. All catalysts, in the as prepared state, showed similar activity and CO selectivity at T ≥ 550◦C. Catalyst pre-reduction was not required. Reaction mixtures were dilute, containing 3 mol% CH4 and 1.5 mol% O2. Methane conversion ...
The Al, Zr, and Ti modified MCM-41 materials were prepared by the post-synthesis method, and then the Ni-W species were introduced on them by using the co-impregnation method in order to obtain high-performance hydrodenitrogenation (HDN) catalysts. The activity of the catalysts was evaluated by the HDN reaction of quinoline. The optimum HDN activity was observed on the catalyst sup...
In this research effect of synthesis method of magnesium aluminate as support of Ni catalysts at the reverse water gas shift (RWGS) reaction was evaluated. The RWGS reaction is applied in Carbon Dioxide Hydrogenation to Form Methanol via a Reverse Water-Gas Shift Reaction (CAMERE) process for the transformation of CO2 into methanol. The MgAl2O4 supports were prepared by sol-gel (M1), surfactant...
It has been demonstrated both thermodynamically and experimentally that fuel-cell grade hydrogen can be produced by a one-step sorption enhanced water gas shift (SEWGS) process at about 500 oC, where the water gas shift (WGS) catalyst and the CO2 sorbent are highly integrated. A synthetic CaO-based mixed oxide sorbent was also assessed, which showed a good CO2 capture capacity and stability in ...
Mesoporous Ni–alumina catalysts (Ni–alumina-pre and Ni–alumina-post) were synthesized by one-step sol–gel method using micelle complex comprising lauric acid and nickel ion as a template with metal source and using aluminum sec-butoxide as an aluminum source. The Ni–alumina catalysts showed relatively high surface areas (303 m/g for Ni–alumina-pre and 331 m/g for Ni–alumina-post) and narrow por...
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