用碳化养护电弧熔炉钢渣制备集料和混凝土

将电弧熔炉(electric arc furnace,EAF)钢渣和石灰混和制成球状集料,置于密闭容器当中,并通入100%的CO2气体进行碳化,在0.506 6MPa保持2h.通过质量法测定添加质量分数为11.94%石灰的EAF钢渣(下同)集料CO2的吸收率为5%,通过红外光谱(infrared,IR)分析测定CO2的吸收率为13.88%.用碳化的钢渣集料制备混凝土再进行碳化养护,同时利用碎石和河砂为集料制备碳化混凝土作为参比样.用质量法测定2种混凝土的碳化率分别为21.14%和10.57%;用IR法的为13.81%和16.97%.碳化后电弧熔炉钢渣集料内生长着大量簇生的犬牙状碳酸钙晶体.     

水分对高碱值硫化烷基酚钙结构和清净性的影响

采用傅立叶红外光谱仪，分析了水分对清净剂高碱值硫化烷基酚钙结构组成的影响；采用热管氧化试验法和曲轴箱模拟试验法，考察了高碱值硫化烷基酚钙在加水前后清净性能的变化；采用四球试验机和高频往复试验机，分析了水分对高碱值硫化烷基酚钙润滑性能的影响。结果表明，油中的水含量对高碱值硫化烷基酚钙的水解安定性能影响较大，并且随着水含量的增加，油品的清净性能和抗磨性能变差。     

Pu(OH)4(am)与碳酸根的配位行为研究

为了解在惰气环境Pu(OH)_4(am)与碳酸盐溶液中HCO^-₃，CO^2-₃的配位行为，考察了放置时间对Pu总浓度的影响；同时也考察了pH值、碳酸根总浓度变化对碳酸盐溶液中Pu的主要存在形态及溶解总浓度的影响。实验结果表明，HCO^-₃离子与Pu(OH)_4(am)生成[Pu(OH)₄(HCO₃)₂]^2-（lg K=-2.61±0.18, lgβ=54.25±0.18）或[Pu(OH)₂(CO₃)₂]^2-（lgK=-2.61±0.18, lgβ=46.91±0.18）；CO^2-₃离子与Pu(OH)_4(am）生成[Pu(OH)₄(CO₃)₂]^4-（lgK=-3.52±0.11, lgβ=53.33±0.11）。可能的配位反应方程式为： Pu(OH)_4(am)+2HCO^-₃ = [Pu(OH)₄(HCO₃)₂]^2-, Pu(OH)_4(am)+2HCO^-₃ =[Pu(OH)₂(CO₃)₂]^2-+2H₂O, Pu(OH)_4(am)+2CO^2-₃=[Pu(OH)₄(CO₃)₂]^4-。     

中碱值硫化烷基水杨酸钙的制备及性能研究

介绍了一种碱值达170mgKOH／g以上、硫含量大于3．0％、钙含量大于6．0％的硫化烷基水杨酸钙盐润滑油添加剂的制备过程及其性能。实验中重点考察了促进剂及硫磺加入量对产品碱值及硫含量的影响；通过冷冻蚀刻电镜法观察了含碳酸盐的胶体粒子结构及粒度分布情况；应用凸轮挺校、四球试验机等考察了硫化烷基水杨酸钙盐产品的极压抗磨性能。结果表明，硫化烷基水杨酸钙产品不但具有良好的高温洁净性、抗氧化安定性、胶体稳定性，而且具有突出的极压抗磨性及热稳定性。     

真空钙热还原炉渣的综合利用研究

研究了从真空钙热还原炉渣中回收稀土的工艺条件；采用本工艺得到的合格稀土溶液，其回收率达65．41％；副产品氟化钙用作炼硅铁合金的助熔剂，使钙热还原炉渣得到综合利用。     

固体酸的酸性和结构对苯与乙烯烷基化的影响

在搅拌高压釜中,研究了纯磷钨酸、负载磷钨酸、工业Y-分子筛、工业β-分子筛和纳米β-分子筛5种固体酸催化剂进行苯与乙烯的液相烷基化反应的催化活性和反应选择性。实验结果表明,固体酸催化剂的烷基化反应活性高低主要取决于表面酸强度和酸量;乙苯的选择性主要取决于催化剂的孔道结构;乙基化的选择性则与催化剂的表面酸强度、酸性中心位置和孔道结构等因素有关。     

溶胶-凝胶生物玻璃多孔材料显微结构和生物活性的扫描电镜及红外光谱分析

本文利用溶胶．凝胶法制备了CaO-P2O5-SiO，系统生物活性玻璃，并以其为原料制备了用于骨修复及骨组织工程支架的块状生物活性材料。利用体外实验方法(invitro)结合x射线衍射(XRD)、扫描电子显微镜(SEM)和傅立叶变换红外光谱分析(FTIR)技术对不同烧结工艺制备的材料结构、晶相和生物活性的影响进行了分析研究。研究表明，经800℃和1100℃烧结5min的两种材料均有硅磷酸钙Ca5(PO4)2SjO4微晶相析出。烧结温度越高，析出微晶相的体积比例越大，材料的生物活性则越低。在模拟生理溶液中碳酸羟基磷灰石(HCA)只在烧结体中的玻璃颗粒表面形成，而在其硅磷酸钙Ca5(PO4)2SiO4微晶相表面未发现HCA形成。     

The flame retardant mechanism of polyolefins modified with chalk and silicone elastomer

This paper presents the current understanding of the flame retardant mechanism of Casico?. The study includes the flame retardant effect of each individual component: ethylene–acrylate copolymer, chalk and silicone elastomer, as well as the formation of an intumescent structure during heating. The flame retardant properties were investigated by cone calorimetry and oxygen index tests. To obtain insight into the flame retardant mechanism, heat treatment under different conditions has also been performed. The results indicate that the flame retardant mechanism of Casico is complex and is related to a number of reactions, e.g. ester pyrolysis of acrylate groups, formation of carbon dioxide by reaction between carboxylic acid and chalk, ionomer formation and formation of an intumescent structure stabilized by a protecting char. Special emphasis is given to the formation of the intumescent structure and its molecular structure as evaluated from ¹³C MAS‐NMR and ²⁹Si MAS‐NMR, ESCA and XRD analysis. After treatment at 500°C the intumescent structure consists mainly of silicon oxides and calcium carbonate and after treatment at 1000°C the intumescent structure consists of calcium silicate, calcium oxide and calcium hydroxide. Copyright © 2003 John Wiley & Sons, Ltd.     

In situ polymerization and characterization of polyester‐based polyurethane/nano‐silica composites

Polyester‐based polyurethane/nano‐silica composites were obtained via in situ polymerization and investigated by Fourier‐transform infrared spectroscopy (FTIR), or FTIR coupled with attenuated total reflectance (FTIR‐ATR), Transmission electron microscopy (TEM), atomic force microscopy (AFM), an Instron testing machine, dynamic mechanical analysis (DMA) and ultraviolet‐visible spectrophotometry (UV‐vis). FTIR analysis showed that in situ polymerization provoked some chemical reactions between polyester molecules and nano‐silica particles. FTIR‐ATR, TEM and AFM analyses showed that both surface and interface contained nano‐silica particles. Instron testing and DMA data showed that introducing nano‐silica particles into polyurethane enhanced the hardness, glass temperature and adhesion strength of polyurethane to the substrate, but also increased the resin viscosity. UV‐vis spectrophotometry showed that nano‐silica obtained by the fumed method did not shield UV radiation in polyurethane films. Copyright © 2003 Society of Chemical Industry     

基于SPM技术的纳米信息存储薄膜的研究进展

扫描探针显微技术SPM可以在原子或分子尺度上对表面进行表征和修饰，应用SPM技术可以在薄膜表面形成纳米级的信息点阵，特别适合发展超高密度的信息存储，是一种非常有希望代替传统磁存储，光存储的纳米级存储技术，本文介绍了纳米信息存储薄膜的研究进展，并对其制备技术和读写机制进行了初步的探讨。