我国超细粉碎与超细分级技术的现状及问题

近年来 ,我国的超细粉碎与超细分级技术有很大的发展 ,但在发展过程中存在着一些问题。超细粉体涉及的行业众多 ,但对其粒度的分类至今国内尚无定论。通过调研 ,分析了目前国内超细粉碎设备的现状。对超细粉体分级技术中的干法分级和湿法分级作了比较全面的介绍 ,并对我国超细粉碎与超细分级技术的发展提出了建议     

醇-水法制备纳米NiO粉末的正交实验研究

纳米NiO粉末具有良好的催化性能、热敏性能及在各种材料中的加工性能,因而被广泛地应用在催化剂、磁性材料、电子元件材料等方面,是一种很有前途的新型功能材料。选用Ni(NO3)2.6H2O为原料,以NH4HCO3为沉淀剂,在醇-水介质中制得了纳米NiO粉末。通过扫描电子显微镜(SEM)对NiO粉末进行了表征。实验过程中,按正交表L8(27)安排了正交实验,通过方差分析确定了醇-水制备纳米NiO粉末的最佳煅烧时间、煅烧温度和醇-水比,并确定了各因素对制备过程的影响程度。     

Low-Thermal-Conductivity Rare-Earth Zirconates for Potential Thermal-Barrier-Coating Applications

Rare-earth zirconates have been identified as a class of low-thermal-conductivity ceramics for possible use in thermal barrier coatings (TBCs) for gas-turbine engine applications. To document and compare the thermal conductivities of important rare-earth zirconates, we have measured the thermal conductivities of the following hot-pressed ceramics: (i) Gd₂Zr₂O₇ (pyrochlore phase), (ii) Gd₂Zr₂O₇ (fluorite phase), (iii) Gd_2.58Zr_1.57O₇ (fluorite phase), (iv) Nd₂Zr₂O₇ (pyrochlore phase), and (v) Sm₂Zr₂O₇ (pyrochlore phase). We have also measured the thermal conductivity of pressureless-sintered 7 wt% yttria-stabilized zirconia (7YSZ)—the commonly used composition in current TBCs. All rare-earth zirconates investigated here showed nearly identical thermal conductivities, all of which were ∼30% lower than the thermal conductivity of 7YSZ in the temperature range 25°–700°C. This finding is discussed qualitatively with reference to thermal-conductivity theory.     

激光诱导二甲基二乙氧基硅烷气相合成碳化硅超细粉

本工作首次采用有机硅试剂二甲基二乙氧基硅烷为反应物，进行了激光导气相反应，制备出平均粒径为４０ｎｍ的非晶ＳｉＣ粉末，粉末中Ｃ／Ｓｉ比随反应气流量的变化而变化。非晶ＳｉＣ粉末在１８７３Ｋ，氮气中退火１ｈ后转变为β－ＳｉＣ及α－ＳｉＣ，同时，粉末中部分氧杂质及自由碳脱出粉末。     

超长余辉蓄能发光涂料的制备

通过选用透明度高、太阳能吸收率高的丙烯酸树脂和高亮度、长余辉时间的镝和铕稀土离子共掺杂的稀土硅酸盐光致发光粉末材料aCaO·bZnO·cBaO·dMgO·nSiO2:Eu,Dy,制备出了具有较强的蓄光能力和较长发光时间的夜光涂料,并论述了其制备方法和特性。     

Soft and Hard Adhesion

The force needed to pull a cylindrical stud from a soft elastomeric film depends on their elastic and geometric properties. For a rigid stud and a thick elastomeric film, the pull-off stress (σ) depends on the elastic modulus (E) of the film and the radius (a) of the stud as σ ∼ (E/a)^1/2 (soft adhesion). However, when the film is very thin, the pull-off stress is significantly higher than the case with thick films, and its value depends on the elastic modulus and the thickness (h) of the film as σ ∼ (E/h)^1/2 (hard adhesion). Here, we study the pull-off behavior of a soft cylindrical stud, one flat end of which is coated with a high modulus thin baseplate. As the flexural rigidity of this baseplate is varied, we observe the transition between the two types of adhesion. We present a simple physical interpretation of the problem, which could be of value in understanding various biofouling and adhesive situations.     

用聚丙烯粉料代粒料制塑料扁丝的探讨

概述了以聚丙烯粉料部分代替传统的聚丙烯粒料来生产塑料编织袋扁丝的新工艺，分析了捏合速度、挤出温度、弓板加热温度等因素对扁丝性能的影响。     

三聚氰胺粉料后处理工艺技术改造

经过技改后的三聚氰胺粉料后处理工艺，克服了以往采用螺旋输送机冷却和正压输送工艺所带来的工作环境恶劣、产品因温度较高而不易包装、机械故障频繁等许多难以解决的问题。改用吸送式气力输送后处理工艺后，既能输送，又能冷却、提纯三聚氰胺，实现自动化包装，并彻底改善工作环境。     

A Semi‐Batch Process for Nitroxide Mediated Radical Polymerization

Summary: A semi‐batch process using nitroxide mediated polymerization, was explored for the design of low molecular weight solvent‐borne coatings, typical of those used in the automotive industry. While living radical polymerization (LRP) offers many advantages in the control of polymer chain microstructure that may confer important physical and chemical property benefits to coatings, adapting LRP to a semi‐batch process poses significant challenges in the design and operation of the process. Using styrene monomer, various two‐component initiating systems (free radical initiator, 4‐hydroxy‐TEMPO) were studied to understand the effects of different initiators on the course of polymerization. In addition, an alkoxyamine was synthesized and used as the initiating source. The initiators Luperox 7M75 and Luperox 231 give higher polymerization rates and reasonable control over polymerization, while benzoyl peroxide (BPO), Vazo 67, and the alkoxyamine are less effective. The number of polymer chains in the final product is always less than the theoretical value, reflecting poor initiation efficiency, probably resulting from undesirable termination reactions that become important due to the nature of the semi‐batch process. Adding camphorsulfonic acid (CSA) or charging initiator concurrently with monomer during semi‐batch feed, can increase the polymerization rate while maintaining the living character of the polymerization. The copolymerization of styrene and butyl acrylate is also shown to exhibit living character.

Schematic representation of the exchange reaction to produce N‐TEMPO capped polymer chains.