强酸性阳离子交换树脂催化合成氯乙酸异辛酯的研究

对采用７３２强酸性苯乙烯系阳离子交换树脂作催化剂合成氯乙酸异辛酯进行了实验研究，提出了适宜的反应条件。实验结果表明，该法酯化率高、过程简便、产物颜色浅，优于浓硫酸作催化剂。     

金属离子掺杂二氧化钛及水体光催化脱氮研究

采用溶胶-凝胶法制备了掺杂Ce^3＋、La^3＋、Ag^＋、Fe^3＋的TiO2光催化剂，以考察其薄膜和粉体形式对水中无机氮的光催化去除效果和活性．用所制备的催化剂对含氨氮-亚硝酸氮的混合液进行了光催化脱氮研究．本文利用UV—Vis吸收光谱、XRD和TEM对催化剂进行了表征．同时，对影响TiO2光催化效率的因素：如掺杂金属离子的种类、浓度、涂膜层数、反应液中有无Fe^2＋、不锈钢和玻璃载体、反应器的构型等进行了探讨，并对今后的研究进行展望．经过2h紫外光照射反应，实验最佳脱氮效果：金属离子掺杂TiO2薄膜型催化剂总氮去除率在30％左右，金属离子掺杂粉末型催化剂光催化最高总氮去除率可达41．7％．     

核壳型二氧化钛复合纳米材料研究进展

核壳材料由中心核和外部壳层组成，因其组成、大小、结构的不同，性能优于普通材料。二氧化钛具有优异的光、电和化学等特性可作为理想的核壳材料。从二氧化钛作为核壳型复合纳米材料的核、壳及核壳结构的载体3个方面出发，介绍了核壳型结构的二氧化钛复合纳米材料的分类、制备、性质及应用概况，并对其发展前景及存在问题进行了简要概述。     

Chemistry of hydrogen sulphide under coal liquefaction conditions: 1. Modelling hydrogen transfer catalysis

The work reported here represents initial attempts to develop a complete kinetic and mechanistic understanding of the reaction chemistry of H₂S under coal liquefaction conditions, using both model systems and coal. Hydrogen sulphide was found to promote/catalyse the transfer of hydrogen from tetralin to 2-hydroxyquinoline (2-HOQ). The presence of H₂S can increase the rate of hydrogen transfer from tetralin to 2-HOQ by a factor of 10 compared with the same reaction run in the absence of H₂S. The energy of activation for hydrogen transfer was found to decrease by ≈5 kcal mol⁻¹ in the presence of H₂S. The presence of H₂S was also found to promote loss of oxygen from 2-HOQ to form small amounts of quinoline. No evidence of CC or CN bond cleavage in 2-HOQ was noted under any of the reaction conditions studied. These results suggest that the presence of H₂S reduces the temperatures necessary to promote effective hydrogen transfer from tetralin by 50–75 °C. Moreover, they imply that similar effects occur in H₂S-promoted coal liquefaction.     

甲基-酰基-萘在庚烷、辛烷和十二烷中溶解度的测定与关联

The solubilities of 2-methyl-6-acetylnaphthalene (2,6-MAN) and 2-methyl-7-acetylnaphthalene (2,7-MAN) in n-heptane, n-octane, and n-dodecane were measured, respectively, from 273.15 to 319.15 K using an analytical method. On the basis of the thermodynamics theory of solid-liquid equilibrium, a model was derived to relate the solubilities with temperature. Using the least square method, the parameters of the model, the fusion enthalpies △fusH and the Margules equation coefficients A12 and A21 of 2,6-MAN and 2,7-MAN in n-heptane, n-octane, and n-dodecane-were obtained by regressing the experimental data. The average deviation of the model was 1.70%.     

云母钛珠光颜料的研究

综述了云母钛珠光颜料的发展概况，介绍了它的三种类型：银白色型、虹彩型、着色型，着重论述了它的生产工艺和制备方法(气相包覆法和液相沉积法)，并比较了各类方法的优缺点，分析了它的晶型类别(板钛型、锐钛型、金红石型)、包膜的复合机理和虹彩效应形成的原因，并指出国内产品的发展方向。     

Investigation of bio-ethanol steam reforming over cobalt-based catalysts

The catalytic performance of cobalt catalysts supported on γ-Al₂O₃, TiO₂, ZrO₂ were studied for bio-ethanol steam reforming (BESR) reaction. The supported catalysts (10 wt%Co) were prepared by impregnation and characterized through Thermogravimetric analysis (TGA), H₂ chemisorption, laser Raman Spectroscopy, Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS), and temperature-programmed reaction (TPRxn). The metallic cobalt sites were found to correlate with the BESR reaction activity. The reaction and H₂ chemisorption showed that ZrO₂ supported catalyst showed the best dispersion and best catalytic activity. Over the 10% Co/ZrO₂ catalyst, using a H₂O:EtOH:inert molar ratio of 10:1:75 and a GHSV = 5000 h⁻¹, 100% ethanol conversion and a yield of 5.5 mol H₂/mol EtOH were obtained at 550 °C and atmospheric pressure.     

阳离子香豆胶的合成及结构表征

以3-氯-2-羟丙基三甲基氯化铵(HAT)为阳离子醚化剂,天然香豆胶为原料,异丙醇为分散剂制得季铵盐型阳离子香豆胶。研究了HAT、催化剂NaOH、反应温度和反应时间对合成阳离子香豆胶(CFG)的影响,用凯氏定氮法测定了CFG的取代度。合成CFG的优化实验条件为:m(香豆胶)∶m(异丙醇)∶m(HAT)∶m(NaOH)=1∶(1.6~2)∶(0.15~0.3)(∶4~8),反应温度40~50℃,反应时间2~3 h,制得的产品能满足工业应用要求的黏度及取代度范围(500~800 mPa.s,DS=0.86~1.32)。用FTIR和13CNMR对CFG的结构进行了表征。     

The effects of Cl-induced alloying in Pt–Sn/Al2O3 catalysts on butane/H2 reactions

The effects of oxidation/reduction regeneration treatments, with and without 1,2-dichloropropane present as a chlorinating agent, on the structure of Pt(3%)–Sn(4.5%)/Al₂O₃ catalysts have been correlated with selectivities for butane/H₂ reactions. Particles of Pt⁰ fin Cl-free catalysts were partly covered by Sn⁰, but retained exposed ensembles of Pt atoms which were active for isomerisation, hydrogenolysis and dehydrogenation reactions, the latter becoming dominant at high reaction temperatures. Coking reduced Pt ensemble size and, hence, also favoured high selectivities for dehydrogenation as hydrogenolysis and isomerisation sites became poisoned. In contrast, the addition of 1,2-dichloropropane in an oxychlorination step before reduction promoted 1:1 Pt⁰–Sn⁰ alloy formation after reduction, the proportion of the total Pt in alloy being enhanced by increasing 1,2-dichloropropane concentration and oxychlorination temperature. The alloy surfaces were inactive for isomerisation and hydrogenolysis reactions, giving dehydrogenation as the sole catalytic reaction.     

低(等)压合成氨的最佳H2/N2与催化活性的关系

采用高压催化剂性能评价实验装置，在压力分别为7.0,10.0和15.0MPa，温度分别为350,400和450℃条件下，在H2／N2为1.6-3.0范围内研究了H2／N2对A301，ZA－5和A110－2型催化剂的活性和合成塔出口氨浓度的影响。在压力和空速一定的条件下，最佳H2／N2随反应温度而异。在350，400和450℃下，最佳H2／N2分别为1.8-2.2,2.2-2.5和2.5-3.0。由此可见，合成氨反应的速率达到最大值时的最佳H2／N2值与反应的进程有关。为此提出了催化剂效率K（Catalysis efficiency)的概念来表征在催化剂作用下反应器出口氨浓度趋近平衡的程度，即K＝CNH3／C^*NH3。根据实验结果，得到了最佳H2／N2与催化剂效率的定量关系：（H2／N2）m=1.5(1 CNH3/C^*NH3)=1.5(1 K)。由此可以根据催化剂在不同反应条件下的催化剂效率来确定最佳H2／N2。凡是会降低催化剂效率的因素，都会使最佳H2／N2降低。各种影响因素对最佳H2／N2的影响中，反应温度的影响最大，其次是空速和催化剂的活性，而压力和惰性气体含量的影响相对较小。在低温（低压）下合成氨，宜采用较低的H2／N2。