Supported Vanadia Catalysts for Dehydrogenation of Ethylbenzene with CO2

Alumina supported vanadia catalysts (V/Al) for selective oxidehydrogenation of ethylbenzene with CO₂ were prepared by impregnation method. During preparation the effect of promoters and calcined temperature was investigated, it was found these two items had a strong influence on the activity of V/Al catalysts. Dehydrogenation reaction with CO₂ was happened in the fixed-bed reactor at 450 °C. Results showed that 15.2% ethylbenzene conversion and 99.2% styrene selectivity were acquired when V₂K/Al catalyst was used.     

甲缩醛空气氧化制甲醛催化剂的研制和工艺条件探讨

考察了铁钼催化剂对甲缩醛空气氧化制甲醛的催化性能。制备了多种不同钼铁比和第三、第四组分的催化剂,进行了活性评价和筛选,探讨了适宜的工艺条件范围。对于所选定的催化剂(钼铁比为1.82～1.88;铬铁比为0.1～0.38)在适宜的工艺条件(甲缩醛进料浓度4.5～5.5％;甲缩醛和氧气进料比1:2.0±0.2;空速12000～22000h~(-1);热点温度370～390℃)下,甲醛收率可达85％左右。     

湿浸法制备活性组分非均匀分布负载型催化剂过程的计算机模拟

对活性组分非均匀分布的负载型催化剂的湿浸法制备过程进行了计算机模拟,其模拟程度可适用于任意多个活性组分的浸渍。发现单组分浸渍时,通过控制浸渍时间可获得活性组分由薄到厚的蛋壳型分布和均匀分布,但通过预浸渍吸附至一定分布后,再在空白溶液中浸渍洗脱,控制洗脱条件也可获得蛋黄、蛋白型的分布;加入竞争吸附剂,进行双组分及多组分浸渍,通过控制浸渍溶液性质及浸渍时间可获得各种类型的活性组分分布,诸如蛋壳型、蛋白型、蛋黄型和均匀型。通过对制备过程参数(如竞争吸附剂的选择、各组分有效扩散系数、初始浓度、吸脱附速率常数等)与活性组分分布形式之间关系的分析,可实现对任一分布形式的催化剂的制备过程参数的优化。这对实际制备催化剂具有指导意义。     

酯对钼系Ziegler-Natta催化剂引发丁二烯聚合的影响

以MoCl_4(Mo)为主催化剂,甲苯氧基二异丁基铝(Al)为助催化剂,在加氢汽油溶剂中,研究了8种酯对丁二烯(Bd)聚合的影响。结果表明,凡是能够溶解在酯中的Mo与Al所组成的二元催化体系,大多能很好地引发Bd聚合,并有较高的催化活性。酯的主要作用是增加Mo在加氢汽油中的溶解性,对聚合物的分子量影响不大,对微观结构几乎无影响。     

One-step formation of ethyl methyl ketone from 1-butene and water on ultrastable Y-type zeolite catalyst

Proton exchanged ultrastable Y-type zeolite with silica/alumina = 40 showed a pronounced catalytic activity for the formation of ethyl methyl ketone directly from 1-butene and water. The formation rate of ethyl methyl ketone was much higher than those on MoO₃-based catalysts in the oxidation of 1-butene by oxygen. It was suggested that the basic site necessary for the formation of ethyl ketone directly from 1-butene and water would be the pentacoordinated Al.     

负载型Au催化剂的研究进展

金一直被认为是一种相对惰性的化学元素，但是近年来的研究发现，金催化剂对于CO及VOCs的低温氧化表现出很高的催化活性。本文综述了近年来金催化剂研究的进展情况，系统介绍了金催化剂的制备方法，以及金催化剂在不同反应中的催化活性和反应的机理。     

Synthesis, characterization, and catalytic properties of polysiloxanes with pendant 4-(3-pyridinyl)butyl and 4-(1-oxypyridin-3-yl)butyl groups

New silane monomers with the pendant 4-(3-pyridine)butyl group have been synthesized by hydrosilation of 3-(3-butenyl)pyridine with Me _n Si(OEt)_3-n H (n=0, 1) using a platinum catalyst. Only -addition products were observed. The products were characterized by elemental analysis, infrared,¹H- and¹³C-NMR spectroscopy, and gas chromatography-mass spectrometry. Hydrolysis-polycondensation of the difunctional monomer with a basic catalyst, Me₄NOH, gave a mixture of cyclic oligomers, principally cyclic tetramer, and linear homopolymer. Under similar reaction conditions, the trifunctional monomer gave crosslinked material which was soluble in common organic solvents. The linear homopolymer and crosslinked polymer were trimethylsilyl end-blocked with hexamethyldisilazane. The cyclic and end-blocked polymers were characterized by elemental analysis and spectroscopic methods. Molecular weights of the polymers were obtained by end-group analysis using¹H-NMR spectral data, size exclusion chromatography, and direct insertion-probe mass spectrometry. The cyclic, linear, and crosslinked materials were N-oxidized withm-chloroperoxybenzoic acid and characterized by spectroscopic methods. The polymeric N-oxide derivatives were shown to be effective transacylation catalysts in the synthesis of mixed carboxylic acid anhydrides in immiscible solvents (H₂O/CH₂Cl₂) under phase-transfer conditions. The implications of the results on the mechanism of catalysis are discussed.     

Production of agrochemical from waste polyesters

In this study, agrochemical was produced from waste polyesters. Reactions of waste polyesters [poly (ethylene terephthalate) (PET) and poly (butylene terephthalate) (PBT)] powder with ethylene glycol (EG) in the presence of tetrahydrofurane (THF) using 0.003 mol lead acetate as a catalyst were carried out in a batch reactor at 470 K and at atmospheric pressure conditions. Reactions were undertaken with various particle size ranges from 50 to 512.5 μm, and reaction time from 30 to 70 min for reactions of polyesters. Low molecular weight product of polyester was obtained during this process. In the next stage, hydroxylamine hydrochloride (HAHC), cyclohexylamine (CHA), and potasium hydroxide (KOH) solution were introduced to convert low molecular weight product of polyester into terephthalohydroxamic acid (TPHA) by introduction of HCl (Hydrochloric Acid) as per stoichiometric requirement. TPHA can be used as an agrochemical (insecticide) with appreciable efficiency. To increase the polyester conversion rate, external catalyst (0.003 mol lead acetate) was introduced during the reaction. The product was deposited on the surface of unreacted polyester, which was removed from the surface by introducing dimethyl sulfoxide (DMSO). To accelerate the reaction rate, DMSO, CHA, and THF were introduced during the reaction, which has an industrial significance. Depolymerization of polyester was proportional to the reaction time. Depolymerization of polyester was inversely proportional to the particle size of polyester. Analyses of value‐added product (TPHA) and byproducts [EG and BD (1,4‐butanediol)] as well as polyesters were undertaken. A kinetic model is developed, and experimental data simulated with it, which was consistent with the model. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2504–2510, 2006     

Effects of main factors on remedying northern landscaping water by hybrid ecological filter

Natural zeolite and coal cinder were layered as main packing medium of the ecological filter instead of traditional filling to remedy the static lake water in Northern China.The ecological filter was running in a combined upward and downward flow mode.Dynamic experiments were carried out to study the effects of retention time and ambient temperature on pollutants’ removal efficiency of the hybrid ecological filter.The function of plant was also studied by contrast test.It is showed that the removal efficiencies of NH4+-N and TP are increased when the retention time is changed from 1 h to 2 h and 4 h,but the removal efficiency of TN is decreased,the removal efficiency of NH4+-N is increased from 91.5% to 98% and that of TP is increased from 31.8% to 52.5%.When the temperature declines,the temporal removal efficiency of NH4+-N is reduced,but the removal efficiency of 24 h and 48 h is remained.The removal efficiency of TP after 24 h and 48 h is decreased when the temperature declines evidently.The retention time plays an important role in NH4+-N and TP removal,and the ambient temperature is significant for TP removal.The plant favors for TP and organic matter removal but has little effect on TN removal.     

含给电子Z-N催化剂催化乙烯/1-丁烯共聚的研究

研究了两种含有给电子体分别为对硝基苯胺、乙二醇二甲醚的Ziegler-Natta催化剂催化乙烯与1-丁烯高压的共聚反应性能,主要考察了反应条件对聚合活性、聚合物物理性质的影响,同时采用红外光谱法测定了聚合物的支化度.研究表明,给电子体为乙二醇二甲醚的催化剂催化活性高于对硝基苯胺.反应条件如反应压力、温度、铝钛比对聚合活性、丁烯的插入率以及聚合物性质都有明显影响.高的反应压力有利于1-丁烯插入和聚合物堆密度的提高;反应温度在50℃时的聚合活性最大,聚合物的支化度较高,聚合物熔点较低;铝钛比为500时聚合活性高于低铝钛比的聚合活性.