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141.
Nickel electrodes were prepared by electrodeposition in electrolytes of various anionic compositions. The deposition conditions and bath types were evaluated with special emphasis on the electrocatalytic properties for the oxygen evolution reaction (OER). Electrochemical characterizations in a 5 mol/L KOH solution at 25°C showed that the electrode deposited from the chloride bath, having a low Tafel slope of 50 mV/dec and an overpotential of 396 mV at 100 mA/cm2, is the most catalytically active among electrodes prepared in electrolytes of various anionic compositions. The electrode activity for the OER is related to the real surface areas, which depend on the anion compositions in the deposition bath and the deposition conditions. 相似文献
142.
目的 分析甲肝病毒基因型,为确定我国甲肝的分子流行病学及疫苗的安全性和免疫原性奠定基础。方法 采用抗原捕获聚合酶链反应(AC/PCR),依据国际上甲肝病毒分型标准,扩增VP1/2A结合处的168个核苦酸(nt2909~3264)。结果 经生物信息学软件分析,得出L-A-1株病毒属于甲肝病毒基因IB亚型。结论 在我国有IA和IB两个亚型甲肝病毒流行。 相似文献
143.
144.
145.
聚酯酰胺热熔胶的合成及其性能研究 总被引:2,自引:1,他引:2
研究了以聚酯胶和聚酰胺胶为原料在催化剂作用下加热共熔,通过大分子链交换反应制备织物用聚酯酰胺热熔胶的方法。用聚酯胶的溶剂对所得产品进行溶取试验并且通过红外光谱分析都证明了链交换反应的存在。用该法所得产品粘接强度大,既耐水洗又耐干洗,适用于粘合衬生产。 相似文献
146.
147.
《Expert systems with applications》2014,41(5):2134-2143
In this paper, a hybrid method for optimization is proposed, which combines the two local search operators in chemical reaction optimization with global search ability of for global optimum. This hybrid technique incorporates concepts from chemical reaction optimization and particle swarm optimization, it creates new molecules (particles) either operations as found in chemical reaction optimization or mechanisms of particle swarm optimization. Moreover, some technical bound constraint handling has combined when the particle update in particle swarm optimization. The effects of model parameters like InterRate, γ, Inertia weight and others parameters on performance are investigated in this paper. The experimental results tested on a set of twenty-three benchmark functions show that a hybrid algorithm based on particle swarm and chemical reaction optimization can outperform chemical reaction optimization algorithm in most of the experiments. Experimental results also indicate average improvement and deviate over chemical reaction optimization in the most of experiments. 相似文献
148.
149.
The selective oxidation of n-butane to maleic anhydride(MA) on a vanadium-phosphorus oxide (VPO) catalyst was studied using on-line gas-chromatography combined with mass spectrometry(GC-MS) and transient response technique.The reaction intermediates,butene and furan,were found in the reaction effuent under near industrial feed condition (3% butane 15% O2),while dihydrofuran was detected at high butane concentration (12% butane,5%O2).Some intermediates of MA decomposition were also identified.Detection of these intermediates shows that the vanadium phosphorus oxides are able to dehydrogenate butane to butene,and butene further to form MA.Based on these observations,a modified scheme of reaction network is proposed.The transient experiments show that butane in the gas phase may directly react with oxygen both on the surface and from the metal oxide lattice,without a proceeding adsorption step.Gas phase oxygen can be adsorbed and transformed to surface lattice oxygen but it can not participate in selective oxidation.Adsorbed oxygen leads to deep oxidation,while lattice oxygen leads to selective oxidation. 相似文献
150.
The electrochemical reduction of nitrate ion was studied by cyclic voltammetry on Pt(1 1 1) and [n(1 1 1) × (1 1 1)] stepped Pt surfaces, where n (=14, 10, 7, 6, 5, 4, 3, 2) is the number of terrace atoms, in 0.1 M HClO4 + 10 mM KNO3. The electrocatalytic nitrate reduction was found to hardly proceed on Pt(1 1 1) in the hydrogen adsorption region, while the electrocatalytic activity was improved with the increase in the step density. Inactivation was observed in the presence of adsorbed hydrogen or nitrate-derived reduced adsorbate, i.e. adsorbed NO, on (1 1 1) step sites. It was, therefore, concluded that the electrocatalytically active NO3− species does not adsorb on the (1 1 1) terraces but on the (1 1 1) monoatomic steps. The nitrate reduction current increased with the step density in a non-linear relationship. The overall current density at 0.21 V (RHE) corresponding to the peak potential of the main electrocatalytic nitrate reduction wave which was maximum at n = 2, abruptly increased with short terraces, i.e. n < 5, where the current wave of adsorbed hydrogen on the Pt stepped surface with comparatively narrow (1 1 1) terraces, denoted as Hnt, also appeared unmodified for n < 5 on voltammograms recorded in 0.1 M HClO4 in the absence of nitrate. 相似文献