A series of mixed oxides Sr4Fe6?xCoxO13?δ (x=0, 1, 2, 3, or 4) were prepared by sol‐gel method and used for catalytic combustion of methane. The structural properties of oxides were characterized by XRD, TGA, and XPS. The layered intergrowth perovskite‐like oxide Sr4Fe5CoO13?δ exhibits the highest catalytic activity for methane combustion under the experimental conditions. The enhanced catalytic activity of Sr4Fe5CoO13?δ for methane combustion could be attributed to the increased amount of oxygen vacancy caused by the partial substitution of cobalt for iron in the Sr4Fe6O13, which was confirmed by TGA and XPS. 相似文献
A two-step method has been used to fabricate nano-particles of layer-structured bismuth chalcogenide compounds, including
Bi2Te3, Bi2Se3, and Bi2Se0.3Te2.7, through a nano-scaled top-down route. In the first step, lithium (Li) atoms are intercalated between the van der Waals bonded
quintuple layers of bismuth chalcogenide compounds by controllable electrochemical process inside self-designed lithium ion
batteries. And in the second step, the Li intercalated bismuth chalcogenides are subsequently exposed to ethanol, in which
process the intercalated Li atoms would explode like atom-scaled bombs to exfoliate original microscaled powder into nano-scaled
particles with size around 10 nm. The influence of lithium intercalation speed and amount to three types of bismuth chalcogenide
compounds are compared and the optimized intercalation conditions are explored. As to maintain the phase purity of the final
nano-particle product, the intercalation lithium amount should be well controlled in Se contained bismuth chalcogenide compounds.
Besides, compared with binary bismuth chalcogenide compound, lower lithium intercalation speed should be applied in ternary
bismuth chalcogenide compound. 相似文献
This paper aims to evaluate the influence of three kinds of sulfates from the green production of cement on its sintering and hydration. The properties of clinker and hydration were monitored by thermogravimetric and differential thermal analysis (TG–DTA), X-ray diffraction, X-ray fluorescence and isothermal conduction calorimeter. Results indicate that gypsum lowers the decomposition temperature of CaCO3 and all these Sulfates will enhance the solid-phase reaction but increase melting temperature. Sulfates reduce the content of C3S, but K2SO4 and 2CaSO4·K2SO4 is conducive to the formation of β-C2S. The hydration induction period is shortened by the sulfates. K2SO4 and 2CaSO4·K2SO4 improve the early hydration of clinker, but gypsum may lightly reduce the hydration reactivity of clinker in acceleration period. 2CaSO4·K2SO and K2SO can significantly accelerate the compressive strength development of cement clinker before 3 d; by contrast, gypsum is detrimental for that. The precipitation of hydration products (CH and C–S–H) in clinker with sulfates is more than that of clinker without sulfates at 9 h. K2SO4 can accelerate the hydration of clinker without forming ettringite.
We study the complementary design problem, which is to express the uniformity pattern of a q-level design in terms of that of its complementary design. Here, a pair of complementary designs form a design in which all the Hamming distances of any two distinct runs are the same, and the uniformity pattern proposed by H. Qin, Z. Wang, and K. Chatterjee [J. Statist. Plann. Inference, 2012, 142: 1170–1177] comes from discrete discrepancy for q-level designs. Based on relationships of the uniformity pattern between a pair of complementary designs, we propose a minimum projection uniformity rule to assess and compare q-level factorials. 相似文献