铅酸电池管式正极添加四碱式硫酸铅晶种的研究

在铅酸电池正极铅粉中加入一定量的四碱式硫酸铅（4BS）,按照工业化的操作工艺,制备出原料中4BS含量不同的正极板,并与常规负极板组装成小电池。对正极的初始容量和循环寿命等电化学性能做了测试,结果表明,在添加粒径为1.5 μm的4BS质量分数达1%时,65 ℃固化后,正极初始容量和循环寿命分别为未加4BS正极的1.02倍和1.06倍,4BS的加入提升了电池容量和电池寿命等的综合性能;XRD结果显示,原料中加4BS的正极中β-PbO₂含量稍高于未加4BS的正极;SEM结果显示,加4BS的正极活性物质更细小,大小更均匀。     

无隔膜电解槽制备铁氰化钾的研究

在无隔膜电解槽中采用钛阳极、铜阴极电解制备铁氰化钾。本文探索了影响此过程电流效率及能耗的各种因素，分析确立了实际应用的电解条件     

二水硫酸钙结晶过程研究进展

综述了二水硫酸钙结晶过程的最新研究进展,从各个角度介绍了外部条件对硫酸钙结晶的影响,以达到对二水硫酸钙结晶的各种技术有一种比较客观综合的理解和认识,对未来二水硫酸钙结晶过程的研究方向作了探讨。     

准同型相界附近(Na1-xKx)0.5Bi0.5TiO3的制备及性能研究

利用固相法制备了（Na1-xKx）0.5Bi0.5TiO3系压电陶瓷，XRD分析表明所得陶瓷样品为纯的钙钛矿结构，其准同型相界在x=0．18～0．22之间；电子探针显微分析显示所做陶瓷样品晶粒发育良好，具有规则的外形和明显的晶界；实验所得陶瓷样品损耗tanδ最大不超过5％，最好的压电常数d33=153 pC／N，平面机电耦合系数kp=0．299，它们分别出现在x=0．22和0．20处。     

Perkin反应合成肉桂酸

以无水碳酸钾为催化荆，PEG-400为相转移催化剂，对苯二酚为阻聚剂．通过Perkin反应合成肉桂酸，研究了物料比、催化刺用量、PEG-400用量、对苯二酚用量、回流时间对产品产率的影响。最佳反应条件是n(苯甲醛)：n(乙酸酐)：n(碳酸钾)：n(PEG-400)：n(对苯二酚)=1：3：1．1：0．03：0．02．回流溢度180℃时．回流时间1．5h，肉桂酸产率呵达82.4％。     

从钛白的副产品生产硫酸钾肥的新工艺研究

通过对钛白生产中的副产品硫酸亚铁的综合利用进行深入研究，提出了萃取法生产硫酸钾的新工艺，分别对萃取铁离子和萃取氯离子的体系进行了系统研究。优化了工艺流程，通过对工业副产品硫酸亚铁的综合利用，可获得较大的经济效益和社会效益。     

歧化松香钾皂制备方法的改进与性能研究

以歧化松香为主要原料,在较低的温度(75~95℃)下,溶入KOH水溶液,并进行皂化反应,制备固体份质量分数45%的歧化松香钾皂。研究了反应温度、皂化时间、pH值、添加复合助剂TX-A对反应速度、去氢枞酸钾含量,以及黏度、结晶、胶凝等产品性能的影响。得出歧化松香钾皂化的较佳制备条件为:pH值为10.36,皂化时间分别为120 min(未加TX-A)、98 min(加TX-A),反应温度85℃,TX-A加入量为反应物质量的0.2%。制备出的歧化松香钾皂产品,在性能上完全符合行业标准ZBB 72003-84的要求,并且结晶、胶凝性质有所改善,加纳色号标准降低两个等级。     

Microstructures and Dielectric Properties of Pure and Doped KNbO3 Ceramics

Regions consisting of grains of pronounced cubic develpment exist in pure KNbO₃ ceramics which exhibit a temperature dependence of dielectric constant very similar to that of KNbO₃ crystals. KNbO₃ ceramics doped with GeO₂-K₂O additives have small grains, semiconducting resistance, and a different curve of dielectric constant versus temperature. As the average grain size decreases, the shape of the curve differs increasingly from that of KNbO₃ crystals.     

Application of K2CO3 catalysts in the coal gasification process using nuclear heat

Conventional gasification processes use coal not only as feedstock to be gasified but also for supply of energy for reaction heat, steam production, and other purposes. With a nuclear high temperature reactor (HTR) as a source for process heat, it is possible to transform the whole of the coal feed into gas. This concept offers advantages over existing gasification processes: saving of coal, as more gas can be produced from coal; less emission of pollutants, as the HTR is used for the production of steam and electricity instead of a coal-fired boiler; and a lower production cost for the gas. However, the process has the disadvantage that the temperature is limited to the outlet temperature (950 °C max) of the helium cooling gas of the HTR. Therefore the possibility of catalytic steam gasification was examined. Model calculations based on experimental results show that use of 3–4 wt% relative to coal of K²CO³ catalyst increases the throughput of a large scale nuclear gasification plant by ≈65%, while gas production costs decrease by ≈15%. Corrosion by catalysts is not significant at low concentration (< 5 wt%) and low temperature (< 900 °C).     

Electrochemical behaviour of heat-treated AlZnMg alloys in chloride solutions containing sulphate

The electrochemical corrosion and passivation of Al5Zn1.7Mg0.23Cu0.053Nb alloys, submitted to different heat treatments (cold-rolled, annealed, quenched and aged, and quenched in two steps and aged), in sulphate-containing chloride solutions, has been studied by means of cyclic polarization, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), energy-dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS). The cyclic polarization curves showed that sulphate addition to the chloride solution produced a poor reproducible shift of the breakdown potential to more positive potentials. The repassivation potentials, much more reproducible, and practically separating the passive from the pitting potential region, were slightly displaced in the negative direction with that addition. When the alloys were potentiodynamically polarized in the passive potential region, sulphate was incorporated in the oxide film, thus precluding chloride ingress. In addition, Zn depletion was favoured, whereas Mg losses were avoided. Different equivalent circuits corresponding to different alloys and potentials in the passive and pitting regions were employed to account for the electrochemical processes taking place in each condition. This work shows that sulphate makes these alloys more sensitive to corrosion, increasing the fracture properties of the surface layer and favouring the pitting attack over greater areas than chloride alone.