Production of isobutene from n-butane over Pd modified SAPOs and MeAPOs

Pd modified AlPO-11 and SAPO-5, 11, 34 were used in the direct transformation of n-butane to isobutene. The effect of acidity and porous structure on the supported Pd and the catalytic perfori-nance were discussed. For higher isobutene selectivity, some metals, such as Ti, Fe, Mg, Co and Mn, was incorporated into AlPO-11 framework and isobutene selectivity of 34.86% can be obtained over Pd/MnAPO-11. A combined catalyst system was used for a further improvement of the isobutene selectivity.

长白山北坡河岸带群落植物区系分析

对吉林省二道白河河岸带植物区系的研究结果表明,河岸带植被中共有维管束植物68科169属288种,其中包括蕨类植物11科16属26种,种子植物57科153属262种种子植物中,裸子植物3科6属9种,被子植物54科147属253种;被子植物中,双子叶植物45科118属212种,单子叶植物9科29属41种,由此可见二道白河河岸带的植物种类较为丰富,对其中被子植物分布区类型的分析表明,二道白河流域河岸带种子植物区系科、属的分布类型较为丰富,在科级水平上有6个分布类型2个变型,在属级水平上有9个分布类型7个变型,河岸带植物区系呈温带特性,各类温带分布类型117属,占河岸带种子植物153属的76.5％。二道白河流域河岸带植物区系地理联系广泛,与热带植物区系和东亚区系具有一定的联系,但与地中海植物区系的联系甚少。表明河岸带在生物多样性保护中的重要作用。

The role of coke in the deactivation of Mo/MCM-22 catalyst for methane dehydroaromatization with CO2

The effect of space velocity on reaction performance and coke deposition over 6Mo/MCM-22 catalyst in methane dehydro-aromatization (MDA) with CO2 were studied. The characterization of catalysts reacted at different space velocity after the same amount of methane feed by TG, TPO and Benzene/NH3-TPD techniques suggested that the inert coke maybe responsible for the deactivation of catalyst because of its blockage effect for pore system.

Catalytic alcohols synthesis from CO and H2O on TiO2 catalysts calcined at various temperatures

The reaction performance for CO hydration on a TiO2 catalyst under different calcination temperatures was investigated. Under reaction conditions of T = 573 K, P = 0.5 MPa, CO flow rate of 30 ml min(-1), TOS = 12 h, and CO/H2O (g) = 3/2 (mol), the TiO2 catalyst with a futile content of 18% shows a maximum alcohols STY of 1.81 Mg m(-2) h(-1). In addition, the catalyst deactivation and regeneration were discussed.

Effect of support on chromium based catalysts for the oxidative dehydrogenation of C2H6 with CO2 to C2H4

The oxidative dehydrogenation of ethane (ODE) with CO2 to C2H4 has been studied over a series of Cr-based catalysts using SiO2, Al2O3, (MCM-41 zeolite) MCM-41, MgO and Silicate-2 (Si-2) as the supports. TPR, NH3-TPD, and EPR characterizations of catalysts were carried out to investigate the reduction property of Cr species on different supports, the acidities of catalysts and Cr species of 6Cr/SiO2 catalysts, respectively.

低分子量有机酸对大豆根系形态和磷素吸收积累的影响

采用砂培试验研究了几种低分子量有机酸(柠檬酸、草酸、苹果酸和三种酸的混合)对根系形态和磷素吸收积累的影响。结果表明:不同有机酸处理均显著降低了大豆根系生物量和根冠比,同时使根长、根表面积和根体积均显著降低,而且随着有机酸浓度的增加抑制作用加强,几种有机酸混合后,抑制作用也相对增强,表明不同有机酸处理均抑制了大豆根系的生长,同时使大豆根系的竞争能力降低。几种有机酸处理均降低了大豆对磷素的吸收积累,从而降低了大豆对磷素的吸收效率,但磷利用效率增加。

东北阔叶红松林群落类型划分及物种多样性

运用TWINSPAN分类方法,对我国东北阔叶红松林群落类型进行划分,对乔木层树种进行聚类,并对东北地区长白山、大秃顶子山、平顶山和丰林保护区4个样点的物种多样性进行对比研究.结果表明:24个样地中共记录到维管束植物264种,隶属于64科147属.经过聚类,将阔叶红松林划分为3个群落类型组和7个群落类型;同时,将33个乔木树种间的关联性划分为8组.阔叶红松林群落的物种丰富度和多样性为草本层>灌木层>乔木层.在4个样点中,长白山的样地平均物种丰富度最高,为63.长白山和大秃顶子山乔木层和灌木层的物种多样性略高于平顶山和丰林保护区;丰林保护区草本层的物种多样性为2.83,高于其它3个样点.平顶山灌木层和长白山草本层的均匀度最低,分别为0.71和0.80.

分散型流域农业非点源污染模型研究

本文以探讨农业非点源污染形成的主要机制和预测流域农业非点源污染为目标 ,从研究方法和实践应用两方面进行了深入的研究。以辽西地区典型农业小流域非点源污染形成的特点为基础 ,将机理与建模理论相结合 ,通过建立一个包含流域水文模型、产污模型、汇污模型等子模型的模型系统 ,进行农业非点源污染的预测。建模中针对流域内非点源污染现象的空间差异 ,采用分散参数结构的建模思想 ,运用一种以等级为基础 ,兼顾尺度效应的流域空间单元划分方法 ,同时还探讨了 GIS与模型相结合的途径 ,包括利用 GIS进行空间分析 ,建立和管理模型所需的数据库等。应用结果显示了该模型系统具有良好的适用性和灵活性。

SbOx/SiO2 catalysts for the selective oxidation of methane to formaldehyde using molecular oxygen as oxidant

SbOx and SbOx/SiO2 catalysts were prepared and investigated for methane selective oxidation to HCHO. HCHO selectivity up to 41% can be obtained on Sb2O5/SiO2 catalyst at 873 K and just drop gently to 18% with temperature up to 923 K. HCHO selectivity for SbOx/SiO2 catalysts decreases gently with reaction temperature, so considerable value of HCHO selectivity can still be obtained at high temperatures.

Analysis of aromatic amines by high-performance liquid chromatography with pre-column derivatization by 2-(9-carbazole)-ethyl-chloroformate

2-(9-Carbazole)-ethyl-chloroformate (CEOC), a novel pre-column fluorescence derivatization reagent, has been developed for the analysis of aromatic amines. Taking five monocyclic aromatic amines (o-toluidine, aniline, 3,4-dimethylaniline, N-ethyl-p-toluidine, and p-phenylenediamine) as testing compounds, derivatization conditions such as pH of borate buffer, reaction time and fluorescent tagging reagent concentration have been investigated. By a one-step procedure, CEOC reacts readily with the aromatic amines to form stable derivatives with excitation and emission wavelengths, respectively, at 293 and 360 nm. This derivatization reaction could be finished within 20 min even at room temperature. The peak shapes of the derivatized aromatic amines can be improved greatly without any addition of competition amines into the mobile phase. Furthermore, this method can offer excellent quantitative precision with high tolerance of the matrix of samples. (C) 2003 Elsevier B.V. All rights reserved.