Partial Oxidation of Methane to Syngas over Calcined Ni–Mg/Al Layered Double Hydroxides

The catalytic partial oxidation of CH₄ to syngas was carried out over an Ni–Mg/Al mixed-oxide catalyst prepared from layered double hydroxide-type precursors. The catalysts were characterized by XRD, TPR, UV-DRS, XRF, BET and CHNS analysis. The effects of the catalyst composition and the calcination temperature on the catalytic performance and the extent of catalyst deactivation were investigated. Ni–Mg/Al oxide catalysts converted CH₄ into syngas efficiently with high selectivity. The catalyst performance was strongly related to the Ni particle size and the calcination temperature. The catalysts that were calcined at higher temperature exhibited a better catalytic performance. In conclusion, the NiAl₂O₄ spinel phase had a positive effect on the stability of the catalyst.     

利用微波介电加热和微波干燥水解法制备TiO2微粒

利用微波介电加热和微波干燥条件下TiCl4直接水解的方法制备出平均尺寸为40m，粒径分布窄，均为球形且形态均一，团聚较少，金红石型的TiO2纳米粒子，其内部品粒平均大小为17nm。而传统加热和干燥条件下形成的纳米微粒平均为60nm，粒经大小不均一，形态较不规则，团聚严重。微波加热和干燥方法具有清洁、快速均匀高效、环境友好的优点，推广前景良好。TiCl4水解法经济便利，适于工业化生产。     

Nile blue adsorbed onto silica gel modified with niobium oxide for electrocatalytic oxidation of NADH

A study of modified carbon paste electrode employing Nile blue (NB) adsorbed on silica gel modified with niobium oxide (SN) for electrocatalytic oxidation of reduced nicotinamide adenine dinucleotide (NADH) is described. The adsorbed organic dye on SN was used to prepare a modified carbon paste electrode to investigate its electrochemical properties. The formal potential (E°′) of the adsorbed NB (−230 mV vs. saturated calomel electrode, SCE) showed a shift of 70 mV towards a more positive potential value, compared to NB dissolved in aqueous solution. In solutions with pH between 6.0 and 8.0 did stability and E°′ remained almost constant. However, for a solution pH lower than 6.0 the E°′ was affected by the acidity of the contacting solution, shifting the E°′ towards more positive values. For the solution pHs between 6.0 and 8.0 the electrocatalytic activity remained almost constant. A linear response range for NADH between 1.0×10⁻⁵ and 5.2×10⁻⁴ mol l⁻¹, at pH 7.0, was observed for the electrode, with an applied potential of −200 mV versus SCE. The formation of an intermediate charge transfer (CT) complex was proposed to the CT reaction between NADH and adsorbed NB. The heterogeneous electron transfer rate, k_obs, was 1400 M⁻¹ s⁻¹ and the apparent Michaelis-Menten constant, was 0.21 mM at pH 7.0 evaluated from rotating disk electrode (RDE) experiments with an electrode coverage of about 5.2×10⁻⁹ mol cm⁻². The increase in the reaction rate between NADH and the immobilized NB compared to those obtained with dissolved NB was assigned to the shift of the E°′ towards more positive values.     

自粘聚合物改性沥青防水卷材胶粘剂

在SBS改性沥青防水卷材表面涂敷一层自粘性胶粘剂并以隔离纸覆盖，使用时撕掉隔离纸直接粘贴于屋面即可粘接密封牢，不但施工方便而且消除了熔融法施工造成的污染。该胶粘剂由沥青40％～65％，SBS 5％～30％，增粘剂2％～25％和助剂5％～25％构成。胶层具有可塑性、延展性，可自行填补屋面出现的裂缝，保证防水卷材的防水密封效果。     

High solids content emulsions. III. Synthesis of concentrated latices by classic emulsion polymerization

Two different methods of producing bi‐ and trimodal latices of a mixture of methyl methacrylate, butyl acrylate, and small amounts of acrylic acid were tested. It is shown that a combination of concentrating blends of seed particles by semibatch reaction, followed by a nucleation of small particles plus a second semibatch phase allowed us to obtain stable latices with solids contents over 65% and viscosities of below 2500 mPa s^?1 with little coagulum formation. The key parameter in determining latex stability, coagulum formation, and viscosity appears to be the the particle size distribution, and especially its modification attributed to secondary nucleation. Because it is not possible to eliminate water‐soluble monomers from the polymerization recipe, secondary (homogeneous) nucleation must be minimized by careful addition of the free‐radical initiator and choice of monomer feed flow rates. The nucleation of the third population in the trimodal latices is best accomplished with a mixed surfactant system because renucleation by anionic surfactant alone leads to detrimental changes in the particle size distribution (PSD) resulting from excessive flocculation of particles. In addition, it was found that the viscosity of the final products was not sensitive to small changes in the ionic strength of the latex, although neutralization to a pH of 6 effectively doubles the final latex viscosity. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 1916–1934, 2002; DOI 10.1002/app.10513     

淀粉丙烯酸接枝共聚吸水性树脂的研究进展

基于淀粉丙烯酸接枝共聚作为吸水性树脂具有环保和可生物降解的优良特性 ,目前 ,人们普遍关注的是如何提高其吸水性 ,抗温性 ,控制水份释放 ,压力下保水 ,以及电解液的吸收等。这些特性的改进将使产品的用途更为广泛 ,可以预见 ,淀粉丙烯酸接枝共聚作为吸水性树脂具有广阔的应用和发展前景。     

大颗粒煤燃烧传递动力学破碎理论模型

研究了大颗粒煤燃烧中的颗粒破碎现象，理论分析了大颗粒煤的着火过程和颗粒破碎过程，建立了大颗粒煤燃烧传递动力学破碎模型，对褐煤、烟煤和无烟煤三个典型煤种进行了燃烧初期数值模拟，指出了大颗粒煤燃烧时着火和颗粒破碎的内在联系。     

Interaction of inositol phosphate with calcite

The interaction of myo-inositol hexaphosphate with calcite was studied to evaluate the adsorption mechanisms and the electrochemical modifications induced by interaction of a molecule at such a high-charge density. In addition to quantitative information through the construction of adsorption isotherms, FT-IR and Laser Doppler Velocimetry - Photon Correlation Spectroscopy (LDV-PCS) were employed to investigate the nature of the adsorbent-adsorbate bonds and to determine the electrophoretic mobility and size of the particles before and after sorption. The experiments were also run with orthophosphate (Pi) for comparison. The amount of sorbed P increased to reach a plateau at 17.8 mol m^-2 for inositol hexaphosphate (IHP) while for Pi rose 1.4 mol m^-2 but at C_e > 610^-4 M it had a sharp increase reaching 155 mol m^-2. As expected, for Pi, adsorption predominated up Ce 610^-4 M by covering about 20% of total surface. The adsorption occurred at sites that behaved as nucleus of formation of the clustering of Ca- and PO₄-ions with the ending formation of calcium phosphate precipitates at C_e higher than 610^-4 M. The reaction of inositol hexaphosphate with calcite involves, besides adsorption, precipitation of Ca salts and hence calcite dissolution also at the lowest added IHP concentrations, accounting for the large amount retained by calcite. Sorption of IHP on calcite caused aggregation of particles at low concentrations followed by an increase of their negative charge and hence re-dispersion at higher concentrations. These results indicate a great IHP-fixing capacity of calcite that can affect its accumulation in soils and P bioavailability, and a considerable change of calcite electrochemical properties and particle size distribution that can modify aggregate stability.     

流行性出血热病毒在地鼠肾细胞中增殖动态的形态学及形态发生学研究

用普通电镜及免疫电镜对流行性出血热病毒(EHFV)不同毒株感染地鼠肾细胞(GHKC)的形态及形态发生学特点、其特征性包含体的形态及感染细胞超微结构的改变,以及感染后不同天数的病毒增殖动态进行了观察。     

增容树脂对SBS改性沥青性能的影响

采用光学显微镜、熔体流动速率仪、动态力学分析仪和沥青基本性能测试，研究了增容树脂（T）对SBS分散及改性效果的影响。结果表明：SBS/沥青共混物加入增容树脂（T）后，光学显微镜相片中SBS颗料消失；动态粘弹谱中低温侧（PB链段）的玻璃化温度从-55℃升至-43.8℃，这些表明加入增容树脂（T）能改善SBS在沥青中的分散，树脂与PB链段有较好的相互作用。在改性沥青中加入增容树脂（T）后对软化点、针入度影响不大，而延度显著增大。