CoCrPtNb／CrTi／C多层膜记录介质的制备和性能研究

采用CoCrPtNb四元合金作磁记录介质，并采用多层膜结构（CoCrPt）100-Nbx/CrTi／C／Glass制备玻璃盘基硬盘。实验结果表明：采用适宜厚度的籽晶层与合适组分的底层和磁性层的多层膜结构，即使在室温下溅射，此种薄膜磁记录介质也可得到高达260kA／m的矫顽力；在550℃高温下，经过30min真空退火后，其矫顽力有较大幅度提高，并在Nb含量为2．4％（原子分数）时达到极大值386kA／m，适用于高密度磁记录。同时，也详细分析了磁性层和底层组分、籽晶层厚度以及真空退火对磁记录介质磁性能和微结构的影响。     

Application of an analytical phase transformation model

Employing isothermal and isochronal differential scanning calorimetry, an analytical phase transformation model was used to study the kinetics of crystallization of amorphous Mg82.3Cu17.7 and Pd40Cu30P20Ni10 alloys. The analytical model comprised different combinations of various nucleation and growth mechanisms for a single transformation. Applying different combinations of nucleation and growth mechanisms, the nucleation and growth modes and the corresponding kinetic and thermodynamic parameters, have been determined. The influence of isothermal pre-annealing on subsequent isochronal crystallization kinetics with the increase of pre-annealing can be analyzed. The results show that the changes of the growth exponent, n, and the effective overall activation energy Q, occurring as function of the degree of transformation, do not necessarily imply a change of nucleation and growth mechanisms, i.e. such changes can occur while the transformation is isokinetic.     

竹/玻璃钢复合建筑材料的研制及性能分析

竹/玻璃钢复合建筑材料是一种新型三维复合材料.本文对其进行了结构设计的研究,并通过大量试验对其力学性能进行了分析,结果证明竹/玻璃钢复合建筑材料确实是一种重量轻、性能好、工艺简单、价格便宜的材料,具有广阔的应用前景.     

低翘曲玻纤增强PET复合材料的制备和性能研究

依据降低翘曲的机理，选用不同降低翘曲的方法，制备了系列翘曲玻纤增强PET复合材料，结果表明，具有较高形状对称性的填料，如滑石粉，云母粉和玻璃微珠都能不同程度地降低玻纤增强PET体系的翘曲，非晶聚合物也能有效改进该体系的翘曲性能。     

玻璃微珠改性PP和PE-LLD的加工流变行为

采用玻璃微珠改性两种基体性质显著不同的聚烯烃并对玻璃微珠的含量、粒径和复合材料加工方法对材料的加工流变行为进行了研究。结果表明：加工方法、玻璃微珠含量和粒径对聚丙烯/空心玻璃微珠(PP/GB)复合材料的熔体流动速率和转矩流变性能的影响远大于对PE-LLD/GB复合材料的影响，其中玻璃微珠含量的影响较粒径大。研究认为，无机刚性粒子填充改性热塑性聚合物时，加工方法、填料含量、几何特征等对复合材料流变特性是否发生影响，影响的程度等，更重要的是取决于基体树脂的特性。     

关于海峡两岸的电子玻纤概况

我国玻纤行业2004年生产总量已经突破60万t大关,其中池窑拉丝产量达到40多万t.这意味着我们玻纤行业又迈上了一个新台阶.我们已经成为世界玻纤第2生产大国并正向着技术强国进军,本文介绍了电子玻纤生产工艺特性;电子玻纤市场现状及其发展前景;海峡两岸电子玻纤生产现状及其发展趋势,希望能使大家对电子玻纤有个更全面的认识.     

Adhesion Mechanisms of Polyurethanes to Glass Surfaces I. Structure-Property Relationships in Polyurethanes and Their Effects on Adhesion to Glass

Polyurethanes were prepared from toluene diisocyanate (TDI), 1-4-butane diol (BDO) and polycaprolactone-based triols with varying molecular weights. Among each molecular weight triol-based urethane, hard segment content was varied from 20% to 70%. Differential scanning calorimetry, tensile testing, and Iosipescu shear testing were done on all the various urethanes prepared. Thermal characterization data revealed the dependence of phase separation on hard segment content as well as on the triol molecular weight. Tensile data and Iosipescu shear data further confirmed the observations made from the DSC data. The data further indicated that phase separation can greatly improve the modulus of cross-linked segmented urethanes. Adhesion of these urethanes to glass surface was evaluated using soda-lime float glass plate. Urethane samples were cast on the air side of the glass plates and adhesion was measured in shear mode. Adhesion data indicated that in addition to hard segment content, modulus, cross-link density, and molecular weight of the triols, phase separation seems to be a major factor in controlling adhesion. Surfaces of the failed adhesion samples were also analyzed and the failure mode was found to be cohesive, in varying degree, with the different urethane systems.     

玻璃纤维毡增强热塑性复合片材的研制和应用

本文简要介绍了玻璃纤维毡增强聚丙烯片材的研制，性能和应用。     

硅酸盐激光玻璃的离子交换增强

用离子交换法能使硅酸盐激光玻璃机械强度增加２－３倍，激光强度增加３倍，从而弥补了自身热光系数较大的缺点。虽然玻璃在处理后，阈值稍微升高，效率稍有下降，但因允许输入更大的能量，使输出得到３倍的增加，说明了离子交换增强方法是成功的。     

Synthesis,characterization, and thermal properties of phosphorus‐containing,wholly aromatic thermotropic copolyesters

A series of phosphorus‐containing, wholly aromatic thermotropic copolyesters from acetylated 2‐(6‐oxide‐6H‐dibenz〈c,e〉〈1,2〉oxa phosphorin‐6‐yl)‐1,4‐dihydroxy phenylene, p‐acetoxybenzoic acid, terephthalic acid, and isophthalic acid were prepared by melting polycondensation. The structure and basic properties of the polymers, such as the glass‐transition temperature (T_g), melting temperature (T_m), thermal stability, crystallinity, and liquid crystallinity, were investigated with Fourier transform infrared, elemental analysis, differential scanning calorimetry (DSC), thermogravimetric analysis, wide‐angle X‐ray diffraction, and hot‐stage polarizing optical microscopy. The copolyesters had relatively high T_g values ranging from 183 to 192°C. The T_m values obtained from DSC curves for samples P‐20 and P‐25 were 290 and 287°C, respectively (where the number in the sample name indicates the molar fraction of the phosphorus‐containing monomer in the reactants). The initial flow temperatures of other samples observed with hot‐stage polarizing microscopy were 271–290°C. The 5% degradation temperatures in nitrogen ranged from 431 to 462°C, and the char yields at 640°C were 41–52%. All the copolyesters, except P‐40, were thermotropic and nematic. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1278–1284, 2002