压力容器无损检测 --长管拖车气瓶的无损检测技术

长管拖车是新类型的压力容器,作为一种高效运输工具,在许多领域应用广泛。综述了国内外拖车气瓶在制造和使用过程采用的各种无损检测方法及标准。方法包括超声、磁粉、渗透和声发射检测等。并介绍了各种无损检测方法的特点。     

铁精矿粒度对球团强度的影响

以大红山、曼南坎和滇滩等精矿的粒度以及膨润土用量和润磨时间为因子,以生球落下强度、生球爆裂温度、预热球抗压强度和焙烧球抗压强度为评价指标,进行了五因子二次回归组合实验研究。结果表明:随着铁精矿小于0.074mm粒级含量的增加,生球爆裂温度下降,预热球和焙烧球抗压强度提高;当铁精矿小于0.074mm粒级含量小于75%(质量分数)时,生球落下强度逐渐上升,当小于0.074mm粒级含量为75%时,生球落下强度达到最大值,之后有下降趋势。并不是铁精矿粒度越细球团强度就会越好,铁精矿粒度还应该满足一个合适的粒度组成。     

Cu-Al-Be形状记忆合金的应力腐蚀性能

用恒载荷法和慢应变速率法及SEM研究了Cu-Al-Be形 状记忆合金在甘油、海水和氨介质中的应力腐蚀性能.结果表明，Cu-Al-Be合金具有良 好的抗海水应力腐蚀性能和较低的氨介质应力腐蚀倾向.单相马氏体有较 好的耐海水腐蚀能力，可减少腐蚀引起的裂纹源；外应力下马氏体的孪晶变形和变体间的界 面迁移，则有利于松弛应力集中，阻碍和延缓腐蚀裂纹源的扩展，从而提高Cu-Al-Be合金的 应力腐蚀能力.     

微细粒技术在洁净煤技术中的作用和地位

从煤加工利用对颗粒粒度及其分布的要求，解离度对超纯煤的制备以及煤炭组分工业化分离的影响等方面论述了微细粒技术在洁净煤技术中的作用和地位。研究表明煤的粒度及其分布对水煤浆制备及其利用，燃烧等有极其重要的影响；     

环形截面提升管内颗粒的运动行为

采用PDPA(phase Doppler particle analyzer system)及磷光颗粒示踪技术对环形截面提升管中颗粒的运动行为进行了研究。与传统提升管相比，环形截面提升管中颗粒速度分布的均匀性有所改善，其最高速度与最低速度之差变小。环形截面提升管最大速度值出现在相对径向位置φ=0.3-0．4处。与传统提升管相似，环形截面提升管内颗粒的轴向返混较严重，停留时间分布曲线存在较明显的拖尾，其中颗粒的轴向Peclet数与传统提升管也处于同一数量级范围。提升管床结构的改变并未显著改变其中气固流动的微观相结构，稀相与密相颗粒团微观两相仍然存在，这种微观相结构是造成颗粒严重返混的决定性原因：稀相中的颗粒与密相颗粒团中的颗粒分别造成了颗粒停留时间分布曲线的前峰与拖尾峰。     

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。     

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     

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.