影响聚丙烯β晶型形成的外部因素

简单介绍形成β晶型聚丙烯的几种常见途径及影响β晶型的各种因素，重点介绍了温度、应力、填料、成核剂及工艺条件等外部因素对β晶型形成的影响。     

聚丙烯的晶型及常用成核剂

介绍了α,β这两种最重要的聚丙烯的结晶形态及性能特点,阐述了常用的α晶型成核剂(包括无机成核剂、有机成核机和高分子成核剂)及β晶型成核剂的结构特点和使用性能,并结合当前的工作展望了成核剂的发展方向。     

农药中间体3,5,6-三氯吡啶-2-醇钠研究进展

在调研国内外农药中间体3,5,6-三氯吡啶-2-醇钠研究文献的基础上,综述了三氯吡啶醇钠的合成方法,重点介绍了三氯乙酰氯路线,并比较了各种路线的利弊。提出三氯乙酰氯路线和吡啶路线是目前较适合我国国情的两种方法。     

The development of vehicle recycling in Europe: Sorting,shredding, and separation

The large scale mechanical processing of end-of-life vehicles (ELVs) started in the United States and was improved in Europe. In the United States, ELV recycling focused on high volumes while in Europe, optimization of processing plants was directed at high grades and recoveries. Legislation by the European Commission (EC) and the fast-growing consumption of metals in China has created an uneven playing field and new markets, which influences the technological developments in the United States and the European Union. In the Netherlands, the EC legislation has been implemented by car dismantling and in the future, mechanical auto shredder residue processing will be added to reduce cost.     

喷丸对23Co14Ni12Cr3Mo超高强度钢 表面性能的影响

针对23Co14Ni12Cr3Mo超高强度钢材料，研究喷丸强化对其表面性能的影响。采用扫描电镜、白光干涉仪等设备，分析喷丸强化对试样表面形貌、粗糙度、硬度、残余应力、元素含量等的影响。结果表明:喷丸强化后，试样表面留有大量弹坑，产生明显塑性变形；表面粗糙度增大，算术平均粗糙度为1.33 μm；硬度显著增大，最表层硬度由喷丸前的HV 476增加至HV 497，硬化层深度约150 μm；试样表层的残余压应力值由375 MPa增加至475 MPa，最大残余压应力值约518 MPa，位于距表面50 μm深度处，喷丸形成的残余压应力层深度约为134 μm；喷丸后试样中C、Si、Cr等各元素的质量分数均略有增加。喷丸在一定程度上改善了23Co14Ni12Cr3Mo钢材料的表面性能，有利于提高其疲劳抗力和耐腐蚀性。     

电弧喷涂铝青铜涂层的力学性能

铝青铜是一种重要的电弧喷涂涂层材料.为了使其得到更大范围的应用,对电弧喷涂铝青铜涂层的某些力学性能(涂层与钢基体的抗拉结合强度、涂层与钢基体的剪切强度、涂层自身结合强度、涂层的硬度、涂层的摩擦磨损性能)进行了测试与研究.结果表明,该涂层具有很好的综合力学性能,可以胜任多种机械零部件的使用要求.铝青铜涂层特有的微观组织结构使其具有优良的抗摩擦磨损性能,适合用作钢铁机件的对偶摩擦材料.     

Phase Stability of Fine-Grained (Mg,Y)-PSZ

A fine-grained zirconia, which has been costabilized with yttria and magnesia, has been prepared. Its stability during subeutectoid annealing at 1100^deg;C, and its hydrothermal stability during hydrothermal treatment at 180^deg;C, have been determined and they are compared to those of Y-TZP and Mg-PSZ materials .     

Elastomer–carbon black interaction: Influence of elastomer chemical structure and carbon black surface chemistry on bound rubber formation

The contribution of elastomer polarity and reactivity to bound rubber formation has been investigated. In this study, a number of elastomers of different chemical nature have been tested. The surface of the carbon black (N110) has also been modified by nitric acid oxidation in order to increase the concentration of surface functional groups. The experimental results have shown that the bound rubber formation is barely related to the polarity of the polymers. It is the reactive sites in both the elastomer and carbon black which are mainly responsible for bound rubber formation. It therefore appears that the elastomer/carbon black interaction leading to the formation of bound rubber is essentially a chemical process involving primary bond formation between elastomer and carbon black. The oxidized carbon black exhibits a higher surface activity which may be due to an increased concentration of oxygen-containing reactive surface sites, namely, phenolic hydroxyl, carboxyl, lactone, and quinone groups. © 1995 John Wiley & Sons, Inc.     

Fabrication and characterization of planar and channel polymer wave guides. I. Plasma-polymerized HMDS films

Plasma-polymerized hexamethyldisiloxane (HMDS) films have been prepared as both planar and channel wave guides. The optical attenuation results measured in both the planar and channel HMDS wave guides were found to be similar, thus demonstrating that the inherent solvent resistance and chemical inertness of the plasma polymerized films allows the use of common photoresist techniques, including application of the photoresist, photomasking, and subsequent etching. This may be contrasted with wave guides made from conventional polymers, where careful consideration must be given to photoresist/polymer compatibility, because the photoresist solvents may adversely affect the underlying polymer and lead to degradation of the material during processing. © 1995 John Wiley & Sons, Inc.