锡负载量对PtSn/Al2O3催化丙烷脱氢性能的影响

采用羰基合成-浸渍法制备了不同Pt/Sn摩尔比(3:1, 1:1, 1:2和1:3)的PtSn/Al₂O₃催化剂, 利用N₂吸附-脱附实验、 X射线衍射(XRD)、 透射电子显微镜(TEM)、 吡啶吸附红外光谱(Py-IR)和热重-差热分析(TG-DTA)等手段对其进行了表征, 研究了Sn负载量对PtSn/Al₂O₃的结构性质及催化丙烷脱氢性能的影响. 结果表明, 制备的PtSn/Al₂O₃具有较高的丙烯选择性和稳定性. 当Pt/Sn摩尔比为3:1和1:1时, 铂和锡在催化剂上主要以Pt₃Sn和PtSn合金形式存在, 合金的形成明显改善了催化剂的脱氢性能, 可抑制金属颗粒的高温烧结; 当Pt/Sn摩尔比为1:2和1:3时, 铂主要以金属形式存在. 随着Sn负载量的增加, 催化剂上L酸性位逐渐减少, 丙烷转化率降低, 丙烯选择性增加, 同时促使反应积炭从金属表面向载体迁移, 改善了催化剂的稳定性.     

A survey of surface tension,molar volume and density for Sn–Ag–Cu–Bi–Sb quinary alloys as lead-free solders

ABSTRACT

By applying the geometric models and the theoretical equation, the surface tension, the molar volume and the density were studied. The empirical calculations were carried out in temperature range 623?K?≤?T?≤?1123?K. Only few thermophysical properties were estimated for eight quinary alloys: Sn3.55Ag0.5Cu3Bi3Sb, Sn3.48Ag0.5Cu3Bi5Sb, Sn3.48 Ag0.5Cu5Bi3Sb, Sn3.40 Ag0.5Cu5Bi5Sb, Sn3.53Ag1Cu3Bi3Sb, Sn3.46Ag1Cu3Bi5Sb, Sn3.46Ag1Cu5Bi3Sb, Sn3.38Ag1Cu5Bi5Sb. The results show that surface tension and density have a linear appearance for all temperatures. We have also studied the influence of the composition and temperature in the studied alloys. The obtained theoretical results are compared with the experimental ones and with the conventional Pb–Sn welds.     

New Transition Metal Oxo‐Thiostannate: Synthesis,Characterization, and Investigation of its Photocatalytic Properties

The new transition metal oxo‐thiostannate {[Ni(cyclen)]₆[Sn₆S₁₂O₂(OH)₆]} · 2(ClO₄) · 19H₂O ( 1 ) was prepared under hydrothermal conditions using Na₄SnS₄ · 14H₂O and [Ni(cyclen)](ClO₄)₂ as reactants. In the crystal structure the rare [Sn₆S₁₂O₂(OH)₆]^10– anion is observed, which is composed of SnS₂O(OH)₃ and SnS₄O₂ octahedra, and SnS₄ tetrahedra sharing edges and corners. The anion is expanded by six Ni²⁺ centered complexes via Ni–S and Ni–OH bonds. The photocatalytic properties for the visible light driven hydrogen evolution reaction shows that 26.6 mmol · g^–1 H₂ were evolved after 3 h.     

Remarkably improved cycling stability of 3D porous Cu–Sn anode for lithium-ion full cells by adjusting working voltage range

Numerous studies confirm that three dimensional porous Cu–Sn (3DP Cu–Sn) anode possesses good application prospect in light of its desirable electrochemical performance on lithium ion half cells, but there are a few related systematic researches on lithium ion full cells until now, which is indispensable before its commercialization. Herein, the effects of galvanostatic charge-discharge voltage range on the cycling stability of 3DP Cu–Sn anode for lithium ion full cells are investigated systematically. The results show that the suitable charge-discharge voltage range plays a key role in improving the reversible capacity and cycling stability of the 3DP Cu–Sn||LiCoO₂ full cell, which is closely related to maintaining the electrode structure stable by controlling the amount of Li⁺ extracted and inserted. Especially, in the voltage range of 1.2–3.9 ​V, the full cell exhibits remarkably improved electrochemical properties with the high initial reversible capacity of 2.71 ​mAh cm⁻² and 71.95% capacity retention upon 80 cycles. We believe that this work can provide a significant reference for the practical application of porous Sn-based anodes.     

Electrodeposition and characterization of Zn–Sn alloy coatings from a deep eutectic solvent based on choline chloride for corrosion protection

With the aim of obtaining high corrosion resistant Zn–Sn alloy coatings from an ionic liquid, the effects of electrodeposition potential and electrolyte composition on the electrodeposition behavior, film composition, morphology and corrosion performance were investigated. Cyclic voltammograms indicate that Zn and Sn were co‐deposited at distinct reduction potentials as pure Zn and Sn elements. In addition, the phase composition analysis also showed that the obtained Zn–Sn alloy deposits (8 wt.%–45 wt.% Zn) consist of a two‐phase mechanical mixture of small aggregates of Zn and Sn metals. The Zn content of the alloy significantly increases as the electrodeposition potential and electrolyte Zn (II)/Sn (II) ratio increase. The corrosion performance study of the obtained Zn–Sn coatings showed that they have a passivation behavior and their corrosion resistance increases as the alloy‐Sn content increases. To improve their morphological properties, ethylene diamine tetraacetic acid additive was introduced into the electrolyte and greatly improved the morphology and corrosion resistance of the deposits. For the first time, it was shown that high corrosion resistance Zn–Sn coatings can be obtained from ionic liquids. Copyright © 2014 John Wiley & Sons, Ltd.     

双功能[Sn,Al]-Beta分子筛一步催化葡萄糖生成5-羟甲基糠醛

以部分脱铝的Beta分子筛为母体,采用同晶置换法将Sn植入骨架制备双功能[Sn,Al]-Beta分子筛,并应用于葡萄糖一步催化生成5-羟甲基糠醛(5-HMF)反应中.样品中Sn与Al的含量通过酸洗的浓度和酸洗的时间以及SnCl4处理的时间来控制.由于骨架中有与Al相关为B酸位,和Sn相关的L酸位,[Sn,Al]-Beta可作为一种双功能的固体酸催化剂.优化了[Sn,Al]-Beta催化葡萄糖一步催化生成5-HMF的反应参数,在最优Sn/Al比条件下,葡萄糖转化率为60.0%,5-HMF选择性为62.1%.     

Surface tension modelling of liquid Cd–Sn–Zn alloys

The thermodynamic model in conjunction with Butler equation and the geometric models were used for the surface tension calculation of Cd–Sn–Zn liquid alloys. Good agreement was found between the experimental data for limiting binaries and model calculations performed with Butler model. In the case of ternary alloys, the surface tension variation with Cd content is better reproduced in the case of alloys lying on vertical sections defined by high Sn to Zn molar fraction ratio. The calculated surface tension is in relatively good agreement with the available experimental data. In addition, the surface segregation of liquid ternary Cd–Sn–Zn and constituent binaries has also been calculated.     

Sn Mössbauer spectroscopy of Gd0.8L0.2Mn6Sn6 and Tb0.8L0.2Mn6Sn6 compounds (L=Sc,Y, Lu)

The HfFe₆Ge₆-type compounds Gd_0.8L_0.2Mn₆Sn₆ and Tb_0.8L_0.2Mn₆Sn₆ (L = Sc, Y, Lu) have been studied by ¹¹⁹Sn Mössbauer spectroscopy. The values of the apparent quadrupolar splitting clearly evidence the easy plane magnetization of the gadolinium compounds and the easy axis one in the terbium compounds. The three tin sites behave differently with the nature and size of the substituting L element. For a given series, the hyperfine field of the Sn_2d site is almost unchanged whatever the size of the L element. The hyperfine field of the Sn_2e site strongly varies with the L size in relation with atomic displacements. The hyperfine field of the Sn_2c site exhibits a more complicated behavior. The field difference in the easy plane and easy axis compounds confirms the angle-dependent anisotropic contribution of the Mn moment to the hyperfine field. The analysis of the results also suggests the play of angle-dependent contributions arising from the rare earth moment.     

Solid–state diffusion–controlled growth of the phases in the Au–Sn system

The solid state diffusion-controlled growth of the phases is studied for the Au–Sn system in the range of room temperature to 200 °C using bulk and electroplated diffusion couples. The number of product phases in the interdiffusion zone decreases with the decrease in annealing temperature. These phases grow with significantly high rates even at the room temperature. The growth rate of the AuSn₄ phase is observed to be higher in the case of electroplated diffusion couple because of the relatively small grains and hence high contribution of the grain boundary diffusion when compared to the bulk diffusion couple. The diffraction pattern analysis indicates the same equilibrium crystal structure of the phases in these two types of diffusion couples. The analysis in the AuSn₄ phase relating the estimated tracer diffusion coefficients with grain size, crystal structure, the homologous temperature of experiments and the concept of the sublattice diffusion mechanism in the intermetallic compounds indicate that Au diffuses mainly via the grain boundaries, whereas Sn diffuses via both the grain boundaries and the lattice.