固体碱催化戊醛缩合的研究

自制了固体碱催化剂用于催化戊醛缩合反应 ,考察了碱金属、载体、反应温度、反应压力、空速等条件对反应的影响。研究表明 ,以介孔分子筛为载体的催化剂活性尤其是低温活性明显高于以硅胶为载体的催化剂。自制的固体碱催化剂性能稳定 ,在 2 0MPa ,2 60℃ ,1 0h-1条件下连续运转 2 7d,仍能保持转化率高于 90 %、选择性约 80 %的良好效果。     

SO_4~(2-)(S_2O_8~(2-))/Fe_2O_3-SiO_2固体超强酸对乙酸/丁醇酯化反应的催化性能研究

研究了SO2 -4/Fe2 O3 SiO2 固体超强酸对乙酸 /丁醇酯化反应的催化作用 ,得到合适的工艺条件 :复合氧化物中n(Fe)∶n(Si) =1∶2 ,浸渍的H2 SO4浓度 1mol/L ,5 5 0℃预焙烧活化 3h ,催化剂用量 0 .8g ,酯化反应时间 4h ,乙酸的转化率达 96 .3%。在此条件下制得S2 O2 -8/Fe2 O3 SiO2 固体超强酸催化剂 ,并考察了其催化活性 ,实验结果显示该固体超强酸具有更高的催化活性 ,乙酸转化率高达 98.6 %。     

Fe—Ga—O系平衡测定

在钼丝炉内氩气保护下，利用固体电解质定氧探头测定了含镓１．８７％～６．２１％范围内Ｆｅ－Ｇａ－Ｏ三元系平衡时的氧活度，通过处理得到镓在铁液中的标准溶解自由能等热力学参数与温度的关系。     

Intermediate temperature solid oxide fuel cell based on fully integrated plasma-sprayed components

This work addresses the fabrication of membrane-type solid oxide fuel cells (SOFCs) operating at medium temperatures, where all components are fabricated by plasma spray technology, and the evaluation of the performance of the SOFC single unit in a temperature range of 500 to 800 °C. Single cells composed of LaSrMgO₃ cathodes, LaSrGaMgO₃ (LSGM) electrolytes, and Ni/yttria-stabilized zirconia anodes were fabricated in successive atmospheric plasma-spraying processes. Plasma-spraying processes have been optimized and tailored to each layer to achieve highly porous cathode and anode layers as well as high-density electrolyte layers. A major effort has been devoted to the production of the LSGM electrolyte that has a high density and is free of cracks. Electrochemical impedance spectroscopy was used to investigate the conductivity of the electrode layers, and particularly the resistance of the electrolyte layer. It revealed that the heat treatment had a great influence on the specific conductivity of the sprayed electrolyte layers and that the specific conductivity of the heat-treated layers was dramatically increased to the same magnitude as is typical for sintered LSGM pellets. The experimental results have demonstrated that the plasma-spraying process has a great potential for the integrated fabrication of medium-temperature SOFC units. The original version of this article was published as part of the ASM Proceedings, Thermal Spray 2003: Advancing the Science and Applying the Technology, International Thermal Spray Conference (Orlando, FL), May 5–8, 2003, Basil R. Marple and Christian Moreau, Ed., ASM International, 2003.     

A panoramic view of Li7P3S11 solid electrolytes synthesis,structural aspects and practical challenges for all-solid-state lithium batteries

The development of an inorganic electrochemical stable solid-state electrolyte is essentially responsible for future state-of-the-art all-solid-state lithium batteries (ASSLBs). Because of their advantages in safety, working temperature, high energy density, and packaging, ASSLBs can develop an ideal energy storage system for modern electric vehicles (EVs). A solid electrolyte (SE) model must have an economical synthesis approach, exhibit electrochemical and chemical stability, high ionic conductivity, and low interfacial resistance. Owing to its highest conductivity of 17 mS·cm^-1, and deformability, the sulfide-based Li₇P₃S₁₁ solid electrolyte is a promising contender for the high-performance bulk type of ASSLBs. Herein, we present a current glimpse of the progress of synthetic procedures, structural aspects, and ionic conductivity improvement strategies. Structural elucidation and mechanistic approaches have been extensively discussed by using various characterization techniques. The chemical stability of Li₇P₃S₁₁ could be enhanced via oxide doping, and hard and soft acid/base (HSAB) concepts are also discussed. The issues to be undertaken for designing the ideal solid electrolytes, interfacial challenges, and high energy density have been discoursed. This review aims to provide a bird's eye view of the recent development of Li₇P₃S₁₁-based solid-state electrolyte applications and explore the strategies for designing new solid electrolytes with a target-oriented approach to enhance the efficiency of high energy density all-solid-state lithium batteries.     

脱硫废水旋转喷雾蒸发特性实验研究

脱硫废水旋转喷雾干燥技术是一种利用热烟气蒸发脱硫废水的零排放技术。开展了不同悬浮物（SS）含量的脱硫废水原水以及经浓缩的高盐废水的蒸发实验,采用可视化手段观察了脱硫废水在干燥塔内的蒸发特性,考察了脱硫废水喷雾蒸发过程中停留时间、进口烟气温度、气液比对蒸发特性的影响。结果表明,旋转喷雾蒸发工艺对高盐、高SS含量等复杂脱硫废水组分具有较佳的适应性;脱硫废水从旋转雾化器喷出后迅速蒸发,主蒸发区在雾化盘下方0.75~1.00 m区域内;随后是蒸发析出的未干盐分及未完全蒸发的废水液滴进一步蒸干至含水率低于2 %;烟气在喷雾干燥塔内的停留时间需要维持在20 s以上才能保证塔出口灰分含水率低于2 %;入口烟气温度越高,其塔底及塔出口的灰分含水率越低,在气液比为12 000 m³/m³（标准状态）的废水工况下,入口烟温为280 ℃时已经难以保证废水液滴良好蒸发;在入口烟气温度为340 ℃、气液比大于10 000 m³/m³（标准状态）时,塔底灰分含水率小于2%,蒸发效果良好。     

Room-Temperature Solid-State Lithium Metal Batteries Using Metal Organic Framework Composited Comb-Like Methoxy Poly(ethylene glycol) Acrylate Solid Polymer Electrolytes

Solid polymer electrolyte with good thermal stability and flexibility is an excellent candidate for solid-state lithium metal batteries, while its low ionic conductivity caused by high crystallinity limits its application at ambient temperature. Here a metal organic framework (zeolitic imidazolate framework-8, ZIF-8) composited comb-like methoxy poly(ethylene glycol) acrylate polymer electrolyte (MCPE) with high ionic conductivity (9.96 × 10⁻⁵ S cm⁻¹ at 30 °C) is prepared by an in situ UV polymerization method. The as-prepared MCPE exhibits improved mechanical property due to the introduction of porous ZIF-8 nanofillers, which is beneficial to suppress the growth of lithium dendrites. Consequently, the LiFePO₄||MCPE||Li cells show a high capacity of 116 mAh g⁻¹ at 30 °C and 0.5 C, and maintain 89.4% of initial capacity after 150 cycles with the average Coulombic efficiency of 99.9%. These results demonstrate that the MCPE shows great potential in solid-state lithium metal batteries near room temperature.     

我国压力铸造技术的现状与发展

概述了压力铸造技术的特点,总结了目前中国压铸技术与国外的差距,分析了我国压铸业面临的机遇和挑战,论述了压力铸造技术的新工艺以及今后压力铸造的研发方向.     

ECAP制备的亚微米7050铝合金的力学性能和微观结构

采用等通道角挤压法 (ECAP法 )制备亚微米 70 5 0铝合金。为了提高合金的力学性能 ,在挤压过程中增加了固溶时效处理工艺 ,并对 70 5 0铝合金在不同处理工艺条件下的显微组织和力学性能的变化进行了研究。结果表明 :ECAP挤压后进行固溶和时效处理能明显提高合金的力学性能。退火态合金经过ECAP后 ,晶粒尺寸明显细化到亚微米级。将挤压一次的试样进行固溶处理和时效处理 ,合金的强度在 5 75MPa左右 ,而延伸率能达到2 5 .5 %左右 ;若经等通道角挤压过的试样在固溶处理后立即进行再次挤压 ,并配合时效处理 ,合金强度能迅速达到 6 16MPa ,延伸率为 16 .9%。     

Zr替代Ti对Ti19．5V40Mn16．2Cr9．8Ni14．5合金的影响Ⅱ：电化学性能

在对合金微观结构和储氢性能研究的基础上，详细考察了少量Zr取代Ti对Ti19．5V40Mn16．2Cr9．8Ni14．5合金电化学性能的影响。通过观察电极的充放电行为，并结合EIS及多种极化曲线的分析结果，发现少量Zr对Ti的取代能够显著提高合金电极的实际电化学容量和循环稳定性，而且还能在一定程度上改善合金的电极动力学性能。对于这些性能的改善，从合金微观结构方面进行了解释。