吸湿介质对碳纤维增强铸型尼龙复合材料的吸湿行为及力学性能的影响

本文对碳纤维增强铸型尼龙(CF／MC 尼龙)复合材料在不同吸湿介质中的吸湿行为进行了研究。结果表明，对于纤维体积分数为10％的碳纤维增强铸型尼龙复合材料(10％CF／MC尼龙复合材料)，随着吸湿介质的PH值减小，它的吸湿率增大。同时，经过吸湿后，10％CF／MC尼龙复合材料的弯曲强度有明显的下降。随着吸湿介质的PH值减小，试样的弯曲强度下降。使用环境扫描电子显微镜观察在10％HCl溶液中吸湿的试样的剪切断口形貌，得到的结果与吸湿实验的结果一致。     

Template synthesis of novel porous carbons using various types of zeolites

As previously reported, high surface area microporous carbons with long-range order can be synthesized by using zeolite Y as a template. In this work, an attempt is made to synthesize porous carbon using several other types of zeolites (zeolite β, ZSM-5, mordenite and zeolite L). Special attention is paid to whether the structural regularity of each zeolite can be transferred to the carbon structure as well as with the case of zeolite Y. The carbon filling method was then examined to see which gives the highest regularity to the carbon structure. It has been found that the optimum carbon filling method for zeolite Y is not an optimum one for the other zeolites and the degree of the regularity of long-range ordering in the carbons strongly depends on zeolite type. The order of the regularity in the resultant carbons is zeolite β>>zeolite L>mordenite>ZSM-5. The effect of zeolite type on the regularity is discussed in relation to the size and the shape of the zeolite channels.     

Polymer reaction engineering: From reaction kinetics to polymer reactor control

Polymer reaction engineering is a relatively “young”, very broad, multidisciplinary, rapidly developing field. It is the combination of polymer science, chemistry and technology with process engineering principles. The outcome of this high degree of synergism has evolved over the last fifteen or so years towards an area that includes any or all of the following: polymerization and post-polymerization (chemical modification) reaction kinetics; mathematical modelling and process simulation; polymer reactor design and scale-up; sensor development and process monitoring; and polymer reactor optimization, state estimation and computer control. This article will attempt to give an overview of the results obtained in our laboratory over the last seven years from systematic studies of polymer reaction engineering and polymer production technology problems. These problems cover all aspects of polymer reaction engineering mentioned above. Going from fundamentals to practice, the basic premise of the article is that only by adopting a holistic approach can one devise effective strategies in order to achieve the final objective of more efficient polymer reactor design and control, and hence improved production systems of polymeric materials.     

Effect of polymer density on polyethylene hollow fiber membrane formation via thermally induced phase separation

Microporous high‐density polyethylene (HDPE) and low‐density polyethylene (LDPE) hollow fiber membranes were prepared from polyethylene–diisodecyl phthalate solution via thermally induced phase separation. Effect of the polyethylene density on the membrane structure and performance was investigated. The HDPE membrane showed about five times higher water permeability than the LDPE membrane because it had the larger pore and the higher porosity at the outer membrane surface. The formation of the larger pore was owing to both the initial larger structure formed by spinodal decomposition and the suppression of the diluent evaporation from the outer membrane surface due to the higher solution viscosity. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 471–474, 2004     

臭氧生物活性炭工艺处理饮用水时各阶段的特点

论述了臭氧生物活性炭工艺中的臭氧发生系统、臭氧尾气处理系统、臭氧预氧化及后氧化、生物活性炭滤池各阶段的应用现状及特点。指出：臭氧发生系统采用氧气为原料来提高臭氧浓度，臭氧质量分数可达6％左右；由于电加热分解臭氧尾气反应速度快，可在1．5～2s内完全分解，应是今后自来水厂臭氧尾气处理技术应用的重点；臭氧预氧化一般采用静态混合器或水射器单点投加，投加量为1～2mg／L，接触时间为1～4min；臭氧后氧化一般采用微孔曝气盘以微气泡的形式多点投加，水中臭氧余量控制在0．2～0．4mg／L，接触时间大于10min；生物活性炭滤池对苯类化合物和相对分子质量在500～1000范围内的腐殖质去除率达70％～86．7％。     

Deep oxidation of aqueous organics over a silicon carbide-activated carbon supported platinum–ruthenium bimetallic catalyst

In previous work, we developed a highly active bimetallic platinum–ruthenium catalyst supported on a very high surface area activated carbon substrate. In fixed bed reactors, this catalyst proved capable of the continuous long-term deep oxidation of a variety of aqueous organic contaminants associated with spacecraft wastewater streams at 121 °C. This work was extended to the mineralization of more typical environmental contaminants, including halocarbons and aromatics. The primary weakness of this catalyst was the tendency toward relatively high rates of chemical decomposition. To overcome this limitation, methods were developed for the production of a silicon carbide coating over the surface of the activated carbon, yielding a reasonable trade-off between increasing resilience and decreasing surface area. Here we report the catalytic decomposition of dissolved organic contaminants at 130 °C using this silicon carbide/activated carbon supported bimetallic catalyst.     

Resins containing amino and carboxylic acid groups. Synthesis,characterization, and metal ion retention properties

The crosslinked poly[3‐(methacryloylamino)propyl]dimethyl(3‐sulfopropyl)ammonium hydroxide], P(MAPDSA), and poly[3‐(methacryloylamino)propyl]dimethyl(3‐sulfopropyl)ammonium hydroxide‐co‐acrylic acid], P(MAPDSA‐co‐AA), were synthesized by radical polymerization. The resins were completely insoluble in water. Due to the lower metal ion retention of P(MAPDSA), the metal ions investigated under competitive and noncompetitive conditions for Cu(II), Cd(II), Hg(II), Zn(II), Pb(II), and Cr(III) ions by batch and column equilibrium procedures were carried out only for P(MAPDA‐co‐AA), particularly for Hg(II). The resin–Hg(II) ion equilibrium was achieved before 15 min. The resin showed a maximum retention capacity value for Hg(II) at pH 2 of 1.89 meq/g. The resin showed a high selectivity to Hg(II) ions. The recovery of the resin was investigated at 25°C with different concentrations of HNO₃ and HClO₄. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 525–530, 2005     

Electrochemical capacitance of well-coated single-walled carbon nanotube with polyaniline composites

Well-coated single-walled carbon nanotube (SWNT) with polyaniline (PANI) composite electrodes with good uniformity for electrochemical capacitors are prepared by the polymerization of aniline containing well-dissolved SWNTs. The capacitance properties are investigated with cyclic voltammetry, charge-discharge tests and ac impedance spectroscopy. The composite electrode shows much higher specific capacitance, better power characteristics and is more promising for application in capacitor than pure PANI electrode. The effect and role of SWNT in the composite electrode are also discussed in detail.     

Structure and conductivity of multi-walled carbon nanotube/poly(3-hexylthiophene) composite films

This work reports a structure-property investigation of a conjugated polymer nanocomposite with enhanced conductivity. Regioregular poly(3-hexylthiophene) (rrP3HT) was used to prepare composites with thin, short, multi-walled carbon nanotube (MWNT) addition over a wide range of concentrations. Scanning and transmission electron microscopies demonstrated an excellent dispersion and good wetting properties within the carbon nanotube composites. Coated MWNTs showed superstructures of P3HT self-organized on nanotube surfaces. Changes in the long range order and on the self-ordered mesophase of the bulk material were investigated by infrared and Raman spectroscopies, differential scanning calorimetry and X-ray diffraction. Interplay between charge transport through the semiconducting polymer and carbon nanotube network increased the composite's conductivity after percolation to values close to 10⁻² S cm⁻¹.     

农作物秸秆增强氟石膏复合材料的微观结构研究

将玉米秸秆加入改性后的氟石膏中，研究改性剂、玉米秸秆对氟石膏复合材料结构性能的影响；并用苯丙乳液对玉米秸秆纤维进行表面处理，用以改善基体材料和增强材料的界面结合状况，由此显著提高制品性能。