3种高电流密度离子膜电解槽的性能对比与介绍

目前离子膜电解槽的发展方向为复极、自然循环、高电流密度、低电耗，伍德诺拉公司BM2．7-Ⅲ型槽、美国西方化学公司ExL^B-65槽、日本氯工程公司BiTAC-858槽即具有这些先进性能。对这3种槽进行了介绍与对比。     

过磷酸钙折流混合器的改进

由于绿原化工有限公司过磷酸钙装置生产能力由 6 70 t/ d(实物量 )提高到 84 0 t/ d,折流混合器负荷增大 ,出现折流环磨损加快等问题。采用若干技改措施 :扩大折流环内径、改变折流混合器喷射方向、采用新材料制作折流环 ,使折流混合器能满足 84 0 t/ d过磷酸钙生产的需要     

如何提高预焙铝电解槽阳极质量

预焙阳极的质量已严重制约铝电解技术的发展，必须予以足够的重视．国外在提高阳极质量方面的有效措施，可以供国内阳极工厂技术改造及科研攻关借鉴．     

PC／PA1010共混物的热行为

利用热失重、微分热失重和显示扫描量热法研究了聚碳酸酯／尼龙１０１０共混物的热行为和解降解过程。结果表明：共混物在６００℃以下分两步降解，降解温度随尼龙１０１０用量增加有下降趋势；共混物的熔点随尼龙１０１０用量增加而升高。     

氯化聚丙烯改性胶粘剂的合成及粘附性能研究

以甲苯为溶剂，过氧化二苯甲酰(BP0)为引发剂，通过自由基聚合，采用甲基丙烯酸羟乙酯(HEMA)和苯乙烯(St)接枝改性氯化聚丙烯(CPP)。研究了不同苯乙烯用量、不同反应温度、不同反应时间、不同引发剂用量对改性氯化聚丙烯胶粘剂粘附性能的影响，得出较佳的工艺条件为反应温度90℃，反应时问2h，原料配比m(CPP)：m(HEMA)：m(St)：m(BPO)=50：0．5：0．6：0．15。     

热熔凝聚法加工农药悬浮剂研究

介绍了采用热熔凝聚法对加工二氯喹磷酸、氟虫睛、乙霉威悬浮剂的试验结果，并测定了制剂的粒度分布、冷贮、热贮稳定性等理化性质。该法工艺简单、加工方便、节省能源、工业上切实可行。     

相转移催化法合成多聚乙二醇二环氧甘油醚

以多聚乙二醇和环氧氯丙烷为原料合成了多聚乙二醇二环氧甘油醚。NaOH为催化剂,季铵盐为相转移催化剂。结论为:作为催化剂NaOH固体效果优于NaOH溶液;四正丁基硫酸氢铵(TBAS)催化醚化反应效果最佳,GC监测表明,二醚的选择性达98％以上;n(多聚乙二醇):n(环氧氯丙烷):n(NaOH):n(TBAS)= 1:10:7:0．08;反应温度55-60℃;反应时间1．5 h;产率83％。     

Poly(3‐chlorothiophene) films prepared by the direct electrochemical oxidation of 3‐chlorothiophene in mixed electrolytes of boron trifluoride diethyl etherate and sulfuric acid

3‐Chlorothiophene (CT) was electrochemically polymerized in mixed electrolytes of a boron trifluoride diethyl etherate solution containing 0–20% (by volume) sulfuric acid. The oxidation potentials of the monomer in these media were measured to be only 1.06–1.31 V (vs Ag/AgCl). These values were much lower than that of CT in acetonitrile and 0.1 mol/L (Bu)₄NBF₄ (1.92 V vs Ag/AgCl). Poly(3‐chlorothiophene) (PCT) films with conductivities of 0.1–2 S cm^?1 were obtained. The structure, morphology, and electrochemical behavior of the PCT films also were investigated. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 502–509, 2003     

Strain-induced crystallization,Part IV: Induction time analysis

The empirical equation, 1/t_i = Ae^Ei/RT, which expresses the exponential dependence of the reciprocal of crystallization induction time, t_i, has been analyzed and shown to be equivalent to the nucleation rate equations derived earlier in Part III (1). Consequently we have used the t_i measurements obtained earlier by Krueger and Yeh to calculate not only the nucleation rate enhancements but also the melting point elevations, the relative crystal thickness changes and molecular coil extension ratios of shear-crystallization polyethylene. It is shown that polyethylene when crystallized between 129 and 131°C at shear rates between 1.56 and 9.70 sec^?1 can have melting point increases of 4.2 to 7.2°C and crystal thickness decreases of 20 to 25 percent, when compared to those crystallized at 130°C in the quiescent state. The predicted “coil” extension in the melt just prior to shear-induced crystallization ranges between 21 and 36 percent. The results of these analyses as well as those on nucleation rates of polyethylene oxide are discussed in detail.