STUDY ON 1-HEXENE POLYMERIZATION BASED ON ZIEGLER-NATTA CATALYSTS WITH DOPED SUPPORT

A series of Ti/Mg supported catalysts are prepared by using ball-milled mixtures of MgCl2-ethanol adducts and NaCl as supports, and 1-hexene polymerizations catalyzed by the novel catalysts are studied. It is found that the molecular weight distribution of poly(1-hexene) becomes apparently narrower when catalysts with doped supports are used, indicating that changing the structure of the support is an effective way to regulate the active center distribution of heterogeneous Ziegler-Natta catalyst.     

Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions performed in dioxane. The effects of halide and acid impurities on the reactions were also investigated. Recycling experiments on catalysts were carried out in order to evaluate Ti leaching and its effect on activity and selectivity.     

聚丙烯纤维辐射接枝进展

本文对聚丙烯纤维的辐射接枝方法、特征和机理、以及其研究进展和表征进行了扼要综述。     

醋酸乙烯酯在硅橡胶上的辐射接枝研究

研究了不同溶剂中的醋酸乙烯酯在硅橡胶上的辐射接技状况及接枝后硅橡胶表面结构情况．结果表明：（１）在硅橡胶－乙酸乙酯－醋酸乙烯酯体系中，接枝有自加速效应；（２）适量加入对苯二酚，接枝诱导期延长，接枝速率下降，凝胶效应消失，辐射接技经验关联式为ＲＰ＝０．２７×［Ｄ］（－０．５６０）×［Ｉ］（０．４９０）×［Ｃ］（０．９２０），接核反应为扩散控制反应；（３）不同的溶剂对硅橡胶接枝有不同的影响，如甲醇发生敏化作用，提高接枝速率，而苯发生惰化作用，降低接枝速率；（４）在合适的甲醇和苯配比时，接枝反应几乎恒速进行，用扫描电镜（ＳＥＭ）观察断面，接枝区比较均一，出现微相分离．     

多相催化反应原位红外系统及其应用

设计和建立了一套能耐高温的用于多相催化反应研究的原位红外系统，反应温度从室温到１１５０Ｋ，系统真空为１．０＊１０＾５－１．０－１０＾－４Ｐａ，红外光谱检测范围为４８００－２００ｃｍ＾－１。此系统扩展了原仪器的功能，提高了仪器利用率和效率。     

基于异质预期的量子伯川德博弈复杂动力机制分析

针对伯川德双寡头垄断博弈经济系统中出现的混沌现象,利用量子博弈论,构建了基于有限理性与天真预期行为的量子伯川德动态博弈模型,分析了量子纠缠度对纳什均衡点稳定性及复杂动力行为的影响。结果表明:量子纠缠度能增强该系统的稳定性,企业价格调整速度达到某一程度时会导致该系统的复杂混沌特性,纠缠度可以有效控制混沌状态。最后利用数值模拟从分岔、最大李雅普诺夫指数、奇怪吸引子、初始条件敏感性及分数维数方面验证了理论准确性。     

Carbocyclic and nitrogen-containing fused CH-acids with an annelated indenyl fragment. Thermogravimetric and X-ray structural analysis of 6H-indeno[1,2-b]quinoline

Based on thermogravimetric characteristics first obtained for the model 6H-indeno [1,2-b]quinoline, the scheme of thermal conversions of this compound in the temperature range 20–700 °C has been proposed, and the limit of its thermal stability (300 °C) has been determined. This temperature is recommended as the optimum for synthesizing fused benzoaza(diaza)fluorenes. Based on the results of X-ray structural analysis, the molecules of the studied indenoquinoline form centrosymmetric pairs, which are arranged in (110) layers. The molecules are orientationally disordered. The observed self-association of these molecules is similar to the - association of fused heterocyclic systems with-excessive and ****- deficient fragments. It has been suggested that interferon-inducing and antitumor compounds with an annelated indenyl fragment have a common mechanism of action according to the intercalation model of stacking structures.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 703–709, April, 1995.     

Radiation grafting from binary monomer mixtures. I. Vinyl ether of monoethanolamine and vinyl ether of ethyleneglycol

Gamma-radiation grafting of vinyl ether of monoethanolamine and vinyl ether of ethyleneglycol (VEEG) on polyethylene films has been studied from binary monomer mixtures. The effect of co-monomer composition and total exposure radiation dose on the grafting process is investigated. A combination of potentiometric and gravimetric techniques is applied to determine the grafting degree of each monomer in the final graft copolymer. The presence of more active monomer VEEG in the mixture was found to enhance the grafting of both monomers because the increasing of copolymerization rate which in turn increases the total grafting degree. The modification of the hydrophilic properties of the graft copolymer is studied by examining the grafted films for water- and copper (II) ions uptake.