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The main objective of this work was to investigate the different effects of transition metals (TiO2, VCl3, HfCl4) on the hydrogen desorption/absorption of NaAlH4. The HfCl4 doped NaAlH4 showed the lowest temperature of the first desorption at 85 °C, while the one doped with VCl3 or TiO2 desorbed at 135 °C and 155 °C, respectively. Interestingly, the temperature of desorption in subsequent cycles of the NaAlH4 doped with TiO2 reduced to 140 °C. On the contrary, in the case of NaAlH4 doped with HfCl4 or VCl3, the temperature of desorption increased to 150 °C and 175 °C, respectively. This may be because Ti can disperse in NaAlH4 better than Hf and V; therefore, this affected segregation of the sample after the desorption. The maximum hydrogen absorption capacity can be restored up to 3.5 wt% by doping with TiO2, while the amount of restored hydrogen was lower for HfCl4 and VCl3 doped samples. XRD analysis demonstrated that no Ti-compound was observed for the TiO2 doped samples. In contrast, there was evidence of Al–V alloy in the VCl3 doped sample and Al–Hf alloy in the HfCl4 doped sample after subsequent desorption/absorption. As a result, the V- or Hf-doped NaAlH4 showed the lower ability to reabsorb hydrogen and required higher temperature in the subsequent desorptions.  相似文献   
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Two sized fractions (<75 μm and 150–250 μm) of Ban Pu lignite A and Lampang subbituminous B coals were pyrolyzed in a drop tube fixed bed reactor under nitrogen atmosphere at 500–900 °C. Gasification of coal chars with excess carbon dioxide was then performed at 900–1,100 °C. The result was analyzed in terms of reactivity index, reaction rate and activation energy. It was found that chars at lower pyrolysis temperature had highest carbon conversion, and for chars of the same sized fraction and at the same pyrolysis temperature, reactivity indices increased with gasification temperature. The lower rank Ban Pu lignite A had higher R s values than higher rank Lampang subbituminous B coals. Smaller chars from both coals had higher R s values, due to the higher ash content. At present, it can be concluded that, within the gasification temperature range studied, gasification rates of chars obtained at various pyrolysis temperatures showed a linear correlation with temperature. However, additional experiment is needed to verify the correlation.  相似文献   
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This work presents the synthesis and characterization of multi-walled carbon nanotubes (multi-walled CNTs) deposited with Pd or V and their hydrogen storage capacity measured by Sievert's volumetric apparatus. The CNTs were grown by the CVD method using LPG and LaNi5 as the carbon source and catalyst, respectively. Pd was impregnated on the CNTs by the reflux method with hydrogen gas as a reducing agent, while V was embedded on the CNTs by the vapor deposition method. The average metal particle size deposited on the CNTs was around 5.8 nm for Pd and 3.6 nm for V. Hydrogen adsorption experiments were performed at room temperature and at −196 °C under a hydrogen pressure of 65 bar. At −196 °C, the treated CNTs had a maximum hydrogen uptake of 1.21 wt%, while the CNTs deposited with Pd (Pd-CNTs) and CNTs deposited with V (V-CNTs) possessed lower surface areas, inducing lower hydrogen adsorption capacities of 0.37 and 0.4 wt%, respectively. For hydrogen sorption at room temperature, the CNTs decorated with the metal nanoparticles had a higher hydrogen uptake compared to the treated CNTs. Hydrogen adsorption capacity was 0.125 and 0.1 wt% for the Pd-CNTs and V-CNTs, respectively, while the hydrogen uptake of the treated CNTs was <0.01 wt%. For the second cycle, only half of the first hydrogen uptake was obtained, and this was attributed to the re-crystallization of the defect sites on the carbon substrate after the first hydrogen desorption.  相似文献   
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Freshly H2-reduced catalyst samples and FTS catalyst samples (i.e., freshly reduced and immediately exposed to the onset of FTS conditions corresponding to 50 % CO conversion) were prepared. Each sample was coated in situ using molten polywax and solidified so that an air-protected sample was obtained, which was stored in inert gas. XAS was utilized to investigate the oxidation state of cobalt. A fraction of cobalt crystallites in the freshly reduced research catalysts having lower-than-commercial loading and smaller crystallites undergoes a degree of oxidation to CoO at the onset of FTS conditions simulating 50 % CO conversion (i.e., the H2O partial pressure is high enough to induce some oxidation). Therefore, by decreasing Co content with the aim of improving the dispersion of cobalt and Co efficiency, very small Co crystallites are obtained. Their reoxidation at the onset of FTS is an unintended consequence. Thus, catalysts should be designed to have an optimum narrow cluster size range—small enough to increase Co surface site densities, but large enough to avoid reoxidation, and the stability problems that arise from having unreduced Co in the working catalyst (e.g., a complex coalescence and reduction mechanism).  相似文献   
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