Preparation, Characterisation and Catalytic Behaviour of a New TeVMoO Crystalline Phase

TeM_xMo_1.7O mixed oxides (M = V and/or Nb; x = 0-1.7) have been prepared by calcination of the corresponding salts at 600 °C in an atmosphere of N₂. A new crystalline phase, with a Te/V/Mo atomic ratio of 1/0.2-1.5/1.7, has been isolated and characterised by XRD and IR spectroscopy. This phase is observed in the TeVMo or TeVNbMo mixed oxide but not in the TeNbMo mixed oxide. The new crystalline phase shows an XRD pattern similar to Sb₄Mo₁₀O₃₁ and probably corresponds to the M1 phase recently proposed by Aouine et al. (Chem. Commun. 1180, 2001) to be present in the active and selective MoVTeNbO catalysts. Although these catalysts present a very low activity in the propane oxidation, they are active and selective in the oxidation of propene to acrolein and/or acrylic acid. However, the product distribution depends on the catalyst composition. Acrolein or acrylic acid can be selectively obtained from propene on Nb-free or Nb-containing TeVMo catalysts, respectively. The presence of both V and Nb, in addition to Mo and Te, appears to be important in the formation of acrylic acid from propene.     

MIP-CGP工艺专用催化剂CGP-1的开发与应用

阐述了生产汽油组分满足欧Ⅲ排放标准并多产丙烯的催化裂化工艺（简称MIP-CGP）专用催化剂（简称CGP-1）的研究开发与工业应用结果。CGP-1催化剂的基质具有良好的容炭性能，使活性组元受到良好保护，其优势作用在第二反应区得以充分发挥，具有更高的氢转移活性和强的汽油小分子烯烃裂化活性。中国石化九江分公司和镇海炼化公司的MIP-CGP工业试验标定结果表明，与常规FCC相比，采用CGP-1催化剂的MIP-CGP技术在生产烯烃体积分数小于18％的汽油组分的同时，丙烯产率达到8％以上。此外，汽油诱导期大幅提高，抗爆指数增加；总液体收率有所提高，干气产率下降，焦炭选择性良好。     

大功率CO_2激光器非平衡态合成WO_3／Fe_2O_3新型陶瓷催化剂──Ⅱ．WO_3／Fe_2O_3烯烃歧化反应催化剂的催化活性

用大功率ＣＯ２激光器熔制ＷＯ３／Ｆｅ２Ｏ３新型烯烃歧化反应催化剂。考查了催化剂组成、激光功率及熔炼时间与丙烯歧化反应催化活性之间的关系。     

Ni-Mo-O催化剂中协同作用对丙烷氧化脱氢的影响

在 Ni-Mo-O体系中 ,加入 Mo O3 能极大地提高丙烷氧化脱氢制丙烯的反应活性。选用固混法、沉淀法、柠檬酸法制备了 Mo O3 过量 1 5 % (摩尔分数 )的α -Ni Mo O4催化剂 ,其中用沉淀法制得催化剂在 5 0 0℃ ,V( C3 H8) /V ( O2 ) /V ( N2 ) =1 0 /1 0 /5 0 ,反应气流量为 70 m L/min的条件下丙烷转化率可达 38.7% ,丙烯选择性达 70 .1 4 %。经 XRD,XPS,TPR表征说明 ,在含有过量 Mo O3 的催化剂中 ,α -Ni Mo O4与 Mo O3 两种晶体之间可产生微小的相互吸引 ;从而发挥协同作用 ,是提高催化剂活性     

Hysys软件在分析精丙烯硫化物来源中的应用

气体分馏装置原料液化石油气 (LPG)中有机硫化物形态复杂 ,考察分析工业装置精丙烯硫化物含量变化难度大。利用Hysys模拟 ,分析判断LPG中小分子有机硫化物在气体分馏产品的分布并提出了控制措施。考虑操作条件对精丙烯硫含量的影响 ,并对工业装置精丙烯总硫超标原因进行了分析。     

Oxidative dimerisation of propene to 1,5-hexadiene on Bi-Zn-O catalysts

The oxidative dimerisation of propene to 1,5-hexadiene has been investigated on Bi-Zn-O catalysts. The Bi₄₈ZnO₇₃ phase, observed in the catalysts calcined at 700 ° C is an active and selective catalyst for the formation of 1,5-hexadiene. The best catalytic performance (1,5-hexadiene selectivity 64%) has been obtained at 525 ° C, with a propene to oxygen ratio of 26, on a catalyst formed by Bi₄₈ZnO₇₃ with a small excess of ZnO.     

铂系低碳烷烃脱氢催化剂研究进展

综述了近年来国内外铂系低碳烷烃脱氢催化剂的技术现状与研究进展。首先从热力学角度论述了低碳烷烃脱氢反应与相关副反应的反应机理,随后分别从活性位点性能与催化脱氢的关系,氧化铝、分子筛等载体的作用,以及锡、碱金属、碱土金属、过渡金属等助剂改性对催化剂的影响等3个方面分析了铂系低碳烷烃脱氢催化剂的优势与存在的问题,进而探究了铂系脱氢催化剂的失活原因。最后对铂系脱氢催化剂的研究前景做了展望,提出该系列催化剂的主要发展方向包括降低贵金属铂的负载量、提高催化剂的稳定性、减少积炭副反应等。     

Chemisorption of alkenes on copper-exchanged ZSM-5 zeolite

On Cu-ZSM-5 zeolite at room temperature, propane is physisorbed, while propene shows characteristics of chemisorption. The chemisorption mode has certain advantages for the catalytic control of automotive emissions. Alkane and alkene adsorption equilibria and kinetics are compared on Cu-ZSM-5 and on ZSM-5 free of alumina. The results are discussed in terms of the Langmuir adsorption isotherm.     

碳四烃催化裂解制丙烯反应过程中尾气分析

采用2阀2柱HP6890气相色谱运行系统,通过HPPLOT/Al2O3"S"毛细管柱分析有机烃类,并用FID检测,13 X分子筛填充柱分析氢气,用TCD检测,建立了碳四烃催化裂解制丙烯反应尾气分析方法。结果表明:标准样品的分析结果标准偏差不大于4%,实际样品测试结果可保障物料平衡在98%以上。     

Mechanism for the reduction of NOx on Rh/sulfated titanias

Titanias of different surface areas have been sulfated and used as supports of Rh oxide for the selective catalytic reduction of nitrogen oxides. Only the sulfation of TiO₂ of large surface areas gives strong Br?nsted acid sites, retaining pyridine up to 773 K. Low surface area anatase is unable to retain sulfates. The catalytic activities measured at 523 K, increase with the number of acid sites, and then reach a plateau, showing the intervention of acidity in the SCR. This is true only for Rh but not for Pt. The investigation of the elemental steps on Rh/sulfated TiO₂ by in situ diffuse reflectance spectroscopy permits to clarify a few points: the oxidation of propene, presumably to acetaldehyde, occurs by the reaction with nitrates adsorbed on the support. The further oxidation of this intermediate by NO₂ yields an isocyanate, which can be hydrolysed to ammonia.