Advanced Sn/C composite anodes for lithium ion batteries

Metallic tin was deposited in fine particulate form on the surface of carbonaceous mesophase spherules (CMS) and in the pores of porous carbon by the decomposition and reduction of tin(II) 2-ethylhexanoate at 450 °C. The Sn/C composite powders obtained were used as anode materials for lithium ion cells. Electrochemical cycling tests of coin cells show that the dispersion of tin into the carbonaceous materials enhances the reversible capacity of the electrodes. The capacity retention at the 50th cycle is 91 % for Sn/CMS composite containing 22% tin, against 428 mAh g^–1 at the first cycle. With further increase in tin content, the capacity fade upon cycling is more rapid.     

Order Distance Estimation in Porous Glasses via Transformed Correlation Function of Small-Angle Scattering

A mesoporous two-phase system, consisting of colloidal silica in the cavities of the main silica frame work of a macroporous glass, was investigated by use of Small-Angle X-ray scattering. The transformed correlation function _T(r) was determined for this material for distances r<40 nm. The application of the intrinsic properties of _T(r) yields estimations for two fundamental order distances L ₁=11 nm and L ₂=120 nm of the~porous glass possessing a clear geometric interpretation: L ₁, a short-order-range, is the mean chord length of the mesopores plus the mean chord length in the secondary particles. L ₂, a long-order-range, is an estimation of the mean diameter of a macropore plus the mean free distance in the silica framework which separates two nearly parallel segments of two adjacent macropores.     

地下水多孔介质中胶体与污染物协同运移规律研究进展

在总结国内外地下水中污染物运移规律研究的基础上,阐述了地下水多孔介质中胶体与污染物协同运移的研究进展。讨论了胶体运移的基本过程、相关机理,探究污染物-胶体-微生物(生物胶体)协同运移的作用方式、影响因素、实验分析、模型构造,并指出该领域目前研究存在的主要问题,以及对该领域研究趋势的展望。     

多孔陶瓷材料的制备技术及应用

本文综述了近年来多孔陶瓷材料制备技术的研究现状及应用，多孔陶瓷性能特殊，应用广泛，并为生物医学等相关行业带来进步。     

多孔淀粉在内墙涂料中的应用

本用多孔淀粉和淀粉吸附天然除虫菊酯后加入内墙涂料，通过对两解吸附量、释放时间的比较，说明在内墙涂料中加入杀虫剂的可行性，同时也表明多孔淀粉作为一种新型的吸附和缓释剂，有着广泛的用途。     

Polyimides containing 4,4′‐bipyridinium units

New polyimides containing 4,4′‐bipyridinium units were synthesized by the reaction of bis(dichloromaleimide)arylene derivatives with 4,4′‐bipyridine in meta‐cresol. IR and ¹H‐NMR spectroscopy and elemental analysis as well confirmed their structures. The polymers were characterized by viscometric measurements, softening points, and thermogravimetric data. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2091–2100, 2004     

Porous mullite ceramics through diphasic gels of large boehmite and small silica particles

Mullite formation process has been studied in stoichiometric mullite (3Al₂O₃·2SiO₂) diphasic gel containing large boehmite (1 m) and small silica (10 nm) particles. It has been found that initial mullitization did not take place inside the silica phase (cristobalite), but took place in the defect -alumina phase. -alumina was stabilized by silica when the temperature was below 1350°C. At temperatures above 1350°C, mullite crystallized directly. It was suggested that silica diffused into the pores (<1.8 nm) of -alumina and prevented the collapse of -alumina pore structure. On the other hand, when silica was not present, the pore structure of -alumina collapsed and -alumina crystallized at 1100°C. Porous mullite ceramics were obtained by using special diphasic gels containing large boehmite and small silica particles.     

纳米二氧化硅模板的制备

以微乳液法制备纳米二氧化硅（SiO2）粒子，经压制、烧结制备SiO2模板。通过红外（IR）、热分析（TGDTA）、扫描电镜（SEM）等方法对SiO2模板进行表征，结果表明所得SiO2粒度在100nm左右．烧结温度在800℃时，SiO2粒子之间将实现颈长，有利于有机／无机杂化多孔材料的制备。     

硅灰石制多孔二氧化硅在硅橡胶中的应用研究

研究了硅灰石制得多孔二氧化硅在硅橡胶中的应用,重点考察了粒径和比表面积的影响,实验结果表明:粒径越小,比表面积越大,增强效果越好,其中比表面积起主导作用。文章和其他几种填料比较了增强效果,提出了多孔二氧化硅的再加工和应用方向。     

CO2 hydrogenation over micro‐ and mesoporous oxides supported Ru catalysts

We prepared relatively uniform supported Ru catalysts by ion‐exchange and CVD methods, using an NaY zeolite and a mesoporous FSM‐16 as substrates, and carried out CO₂ hydrogenation. They showed high activity for CO₂ hydrogenation. A Ru‐ion‐exchanged catalyst showed high activity for methanol production. Co addition promoted methanol formation. This revised version was published online in July 2006 with corrections to the Cover Date.