浮法硼硅酸盐玻璃下表面渗锡的研究

根据实验样品的成分,制定一定的浮法成型的温度制度,采用自制小型石墨锡槽,模拟硼硅酸盐玻璃的浮法成型过程,用电子探针结合能谱仪,测试浮法硼硅酸盐玻璃在1250~650℃温度范围内不同温度段下表面渗锡的分布情况,研究硼硅酸盐玻璃不同于传统钠钙硅浮法玻璃的渗锡特点。研究结果表明,在特定的浮法工艺制度下,硼硅酸盐玻璃渗锡的深度达到40μm左右,并且高温段锡离子以纵向深度扩散为主,低温下锡离子主要在玻璃的近表面富集。在浮法成型的过程中,渗锡的分布曲线上会出现卫星峰,但是最终在出锡槽的温度下渗锡曲线是单调递减的。     

废弃木粉与短切玻璃纤维组合增强聚丙烯的力学性能

用废弃木粉与短切玻璃纤维作为增强材料，制得了组合增强的聚丙烯复合材料，研究了制备工艺及设备、材料配方及界面改性方法等对材料力学性能的影响。结果表明，用单螺杆挤出机制备组合增强材料，可减少对玻璃纤维的损伤，保持较长的玻璃纤维，有利于其增强作用的发挥；随着玻璃纤维含量的增加，体系的力学性能提高，而木粉含量对材料力学性能的影响与玻璃纤维的含量相关；采用硅烷偶联剂对木粉进行表面处理，在基体中添加接枝极性基团的改性聚丙烯，可改善体系的界面结合，提高力学性能。     

A comparison of concentration-glasses and temperature-hyperquenched glasses: CO2-formed glass versus temperature-formed glass

Prior work from this laboratory has reported anomalous differences in the viscoelastic responses between temperature-jump formed glasses and carbon dioxide pressure-jump or relative humidity formed glasses. In the present work, we investigate the anomalous behaviour further by examining the structural response of an epoxy resin after pre-annealing treatments. In particular, we have measured the volume change of amine-cured diglycidyl ether of bisphenol A after thermal and carbon dioxide pressure (PCO₂) treatments. Our results show that contrary to prior interpretations in the literature, a plasticizer quench is different from a temperature hyperquench. Consistent with our prior work, the CO₂-formed glass is more stable than the temperature-formed glass in spite of the former having a higher excess volume. Our new results show that the stability persists to above the nominal glass temperature, contrary to what happens in a temperature hyperquench.     

影响有机硅热防护涂层的热导率的因素

以硅树脂为基料,配合中空玻璃微球等填料,制备了有机硅热防护涂层;研究了填料的组合、添加量、规格以及溶剂体系等对有机硅热防护涂层热导率的影响。结果表明,采用表面经过处理的中空玻璃微球和气相法白炭黑A380的组合填料、中空玻璃微球的用量选择60份、并使用酮类溶剂和芳香类溶剂的混合溶剂制成的热防护涂层,其热导率≤0·1W/(m·K),密度≤0·55g/cm3,拉伸强度≥2·0MPa。     

Na_2O-TeO_2系统玻璃形成液体脆性的研究

通过测量Na2 O -TeO2 系统玻璃转化区的热容曲线 ,对该系统不同成分玻璃形成液体的热力学和动力学脆性进行研究。结果表明 :该系统玻璃形成液体从热力学和动力学综合看脆性程度介于强弱之间 ,为中性偏脆性。随着氧化钠含量的升高 ,玻璃形成液体的脆性增强。用Kissinger方程和Ritland -Bartanev方程 ,得到的在玻璃转变区的结构松弛激活能十分接近。对该系统玻璃形成液体脆性参数的计算也得到该玻璃形成液体脆性分类的相同结果     

Relation of swelling and Tg depression to the apparent free volume of a particle‐filled,epoxy‐based adhesive

The effect of hygrothermal aging on a particle‐filled, epoxy‐based adhesive was studied using a gravimetric sorption technique. This study has explored moisture sorption characteristics as well as the associated behaviors of swelling and the depression of the glass transition temperature (T_g). We observed that the diffusion of water in this adhesive has a non‐Fickian behavior, and the depression of T_g proceeds to a definite value that is independent of the final equilibrium water content of the system. Our observations suggest that water diffuses into the polymer in a dual‐sorption mode, in which water resides in two populations. In one population, water is considered to occupy apparent free volume of the adhesive, and the second population water infiltrates polymer structure and forms hydrogen‐bonded clusters. Our results show that hygrothermal aging temperature and swelling do not alter the apparent free volume of this adhesive. We conclude that the constant value of T_g depression at saturation implies that only water in the apparent free volume is responsible for the T_g depression, whereas the swelling proceeds through the formation of hydrogen bonds in the adhesive. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 1436–1444, 2003     

不同氧磷比对磷酸盐包边玻璃性质的影响规律

包边技术是提高大尺寸激光玻璃饱和增益系数的关键技术.采用传统的方法熔制玻璃,研究了P2O5含量对P2O5-Al2O3-B2O3-CuCl-Na2O-ZnO磷酸盐包边玻璃的折射率、热膨胀系数、玻璃转变温度、膨胀软化温度以及化学稳定性的影响.结果表明:当P2O5的摩尔分数为60%左右,玻璃样品具有最高的折射率(1.5220)、最低的玻璃转变温度(352.4℃)、较好的化学稳定性[0.52mg/(cm2·d)]和适宜的热膨胀系数(128.427×10-7/℃),是用作钕磷酸盐激光玻璃硬包边的理想材料.     

制造泡沫玻璃的方法与模具

将泡沫玻璃配合料制备成块状物,将配合料块按规定间隙在模具中平铺码放并烧成,使配合料块熔为一体,形成较小变形的平板状泡沫玻璃.其制造模具是由底板、上盖及L型围板构成的箱型结构,模具各部位通过V字沟相互联结,保证各部位能自由地附着和脱离.模具多层码放烧制,模具间必须设置间隙.在模具上设置通孔可以有效地抑制膨胀过量问题.     

Fully aliphatic polyimides from adamantane‐based diamines for enhanced thermal stability,solubility, transparency,and low dielectric constant

We have synthesized a series of fully aliphatic polyimides (APIs) from bicyclo[2,2,2]oct‐7‐ene‐2,3,5,6‐tetracarboxylic dianhydride (BOCA) and various aliphatic diamines, including linear aliphatic, flexible alicyclic, and rigid adamantyl diamines. We performed the polymerization reactions using one‐step syntheses in m‐cresol at elevated temperatures without the isolation of poly(amic) acid. The chemical composition and structure of the polymers were characterized by nuclear magnetic resonance (NMR) and infrared (IR) spectrometry. The characterization data are reported from analyses using gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimeter (DSC), and wide‐angle X‐ray diffraction (WXAD) measurements. The polyimides are also subjected to solubility, solution viscosity, tensile strength, transparency, and dielectric constant measurements. The resultant polyimides possess well‐controlled molecular weight, reasonable intrinsic viscosity, good transparency, enhanced solubility, low dielectric constants, and high glass transition temperature, together with marginal thermal and mechanical stability. These properties were enhanced in copolyimides containing equimolar amounts of rigid and flexible moieties. These rigid‐rod APIs derived from the alicyclic dianhydride and aliphatic diamines are promising candidates as advanced materials for future applications in micro‐ and photoelectronic devices. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3316–3326, 2006     

Copper ⇌ Alkali Ion Exchange of Alkali Aluminosillcate Glasses in Copper-Containing Molten Salt: I, Monovalent Copper Salt, CuCl

Cu⁺⇌ R⁺ (R = Li, Na, and K) ion exchange experiments were conducted for 20R₂O·10Al₂O₃·70SiO₂ glasses in molten CuCl at 550°C in air and nitrogen atmospheres. The depth profiles of the copper incorporated into glasses were determined with an electron microprobe X-ray analyzer. The total amount of diffusing copper, M _t, strongly depended on the type of alkali ion in the glass and the ion-exchange atmosphere; i.e., M _t increased with increasing cationic size in the order Li < Na < K and M _t was greater in air than in nitrogen. The Cu ⇌ R⁺ ion exchange kinetics are discussed in detail.