常压烧结莫来石／氧化锆／碳化硅复相陶瓷的研究

本文对莫来石／氧化锆／碳化硅复相陶瓷进行了Ｎ２气氛中常压烧结的研究。实验结果表明：ＳｉＣ粒子添加量≤２０ｖｏｌ％，材料均可致密烧结并可获得均匀的微观结构。ＳｉＣ粒子的加入使材料人力学性能较莫来石／氧化锆陶瓷有明显的提高，并在ＳｉＣ含量为１０ｖｏｌ％时达到峰值，室温强度和断裂韧性分别为６０１ＭＰａ和５．８ＭＰａ＾Ｃ２，接近热压材料。     

短切碳纤维增强LAS玻璃—陶瓷的研究

研究了短切碳纤维增强ＬＡＳ玻璃－陶瓷基复合材料的制备工艺及纤维含量，热压工艺对其强韧性的影响，获得了短切碳纤维均匀分散并单向排列的复合材料，当纤维体积分数为１％左右时，材料强度和断裂韧性分别达到４３０ＭＰａ和８．８ＭＰａ．ｍ＾１／２。用光学显微镜和扫描电子显微镜观察了复合材料中短切碳纤维的分布状态和断口形貌。     

SiC—Al2O3基复相陶瓷的N2—HIP研究

通过对热压ＳｉＣ－Ａｌ２Ｏ３复合材料进行了Ｎ２－ＨＩＰ后处理，制备得到Ｓｉ３Ｎ４－ＡｌＮ＝ＳｉＣ－Ａｌ２Ｏ３梯度材料，经Ｎ２－ＨＩＰ处理后，材料抗弯强度提高３５％－９５％，并得到经强度达１０３０ＭＰａ的ＳｉｅＮ４－ＡｌＮ／ＳｉＣｐ－ＳｉＣＷ－Ａｌ２Ｏ３复合材料。     

残余应力对TiCp—AIN复合材料的影响

本工作采用热压工艺，以Ｙ２Ｏ３为烧结添加剂，在１８５０℃下制备ＴｉＣｐ－ＡＩＮ复合材料。结果表明：复合材料的密度、抗折强度、断裂韧性受第二相ＴｉＣｐ的影响，通过合理工艺因素选择，可以使复合材料的抗折强度和断裂韧性比基体ＡＩＮ材料分别提高４０％，８０％，达到４３８ＭＰａ，５．５９ＭＰａ·ｍ＾１／２。由ＸＲＤ内应力分析和ＴＥＭ显微结构测试结果可知，复合材料性能改善原因在于高弹性模型的ＴｉＣ引入以及ＡＩ     

湿化学法制备微晶（Y,Mg）—PSZ／MgAl2O4陶瓷的研究

研究了用湿化学法制备Ｙ２Ｏ３－ＭｇＯ－ＺｒＯ２－Ａｌ２Ｏ３四元系超细粉的工艺技术，探讨了包裹沉和包裹沉淀－乙酸镁混合两种制备工艺组成对微晶ＰＳＺ材料结构、性能的影响。经１１００℃适当时间的热处理获得了在ｃ－ＺｒＯ２中具有ｔ－ＺｒＯ２梭形析出体的微晶ＰＳＺ复相陶瓷，其室温强度达８００ＭＰａ，断裂韧笥在１４ＭＰａ，Ｍ＾１／２左右，１０００℃下高温强度可达４５８ＭＰａ。     

A1对热压烧结C—B4C—SiC复合材料性能的影响

本文对在２５ＭＰａ压力下，２０００℃处理０．５小时的热压Ｃ－Ｂ４Ｃ－ＳｉＣ复合材料添加和不添加Ａｌ粉进行了研究，发现添加Ａｌ能使复合材料的密度、强度提高，电阻率下降，材料的各项性能优于石墨。     

Y2O3改性的MgO—ZrO2共析陶瓷

共析ＭｇＯ－ＺｒＯ２陶瓷添加Ｙ２Ｏ３可以获得高温热稳定性和较佳的力学性能，添加２％Ｙ２Ｏ３时断裂韧性为７．６ＭＰａ．ｍ＾１／２，弯曲强度为６１８ＭＰａ，用透射电子显微镜详细研究和讨论了上述材料的时效显微组织和韧化的原因。     

热压工艺参数对新型陶瓷刀具材料JX—2—I力学性能的影响

ＪＸ－２－Ｉ是最新研制成功的新型陶瓷刀具材料，热压工艺参数对材料的力学性能有较在的影响，本文重点研究了压力、热压温度和保温时间对材料的抗弯强度（σｂｂ）、断理解韧性（ＩＣ）和硬度（ＨＲＡ）的影响，结果表明，对于ＪＸ－２－Ｉ，在压力为３０－４０ＭＰａ，热压温度为１７００－１８５０℃，保温时间为３０－６０ｍｉｎ，材料的性能最好。     

高性能细晶粒刚玉瓷的研制

本文对商用γ－ Ａｌ２ Ｏ３ 粉预处理后，采用热压工艺制备了高性能细晶粒刚玉瓷，１５００ ℃／３０ｍｉｎ 热压获得晶粒尺寸为０ ．６μｍ ，抗弯强度为４８０ Ｍ Ｐａ ，１６００ ℃／３０ｍｉｎ 获得断裂韧性为５ ．３ Ｍ Ｐａ·ｍ １／２ 的刚玉瓷材料，并探讨了添加剂 Ｍｇ Ｏ 在刚玉瓷中的不同作用机理。     

反应结合Al2O3—ZrO2—SiC复合陶瓷的制备工艺与性能

采用反应结合技术研究了Ａｌ２Ｏ３－ＺｒＯ２－ＳｉＣ复合陶瓷的制备工艺与材料性能，比较孙同的原料来源对致密化行为及材料性能的影响，含细Ａｌ２Ｏ３和粗ＳｉＣ的配方获得了最快的致密化速率及最高的烧结密度，该材料经１５５０℃烧结３０ｍｉｎ后再热等静压获得了近１００％的致密度和７６０ＭＰａ的弯曲强度。     

骑式摩托车油箱喷涂工艺的改进

面对日益激烈的市场竞争,摩托车油箱外观质量越来越成为影响销售的因素之一。文章介绍了改进工艺后的油箱涂装,该涂装体系提高了油箱外观的丰满度,降低了油箱涂装的生产成本。     

茶多酚提取方法进展

本文综述了国内外现有茶多酚提取方法的现状以及近期的研究进展，并对其优缺点进行了评价。这将有助于中低档茶的综合利用和茶多酚的进一步开发应用。     

SEDIMENTATION OF BINARY MIXTURES OF PARTICLES OF UNEQUAL DENSITIES AND OF DIFFERENT SIZES

A model is developed for the sedimentation from a suspension of two particle species of unequal densities and of different sizes. The composition and the thickness of various layers in the sediments are predicted using graphical and analytical methods. The model predictions were in excellent agreement with experimental results, when the particle size ratio was ≥ 108. When size ratio of the particles was 2.60 and 4.31 the agreement occurred in about 50 percent of the cases.     

氢气纯度分析方法准确性的探讨

ONACCURACYOFANALYSISOFOFHYDROGEN1前言我公司目前应用的氢气纯度分析方法有两种,一种是爆炸反应法,另一种是焦性没食子酸吸收法。几年来,人们对两种分析方法的准确性曾有过褒贬不一的评论。这里我们也谈谈自己粗浅的观点。2爆炸法测定氢气纯度一定量的氢气样品与适量的空气之均匀混合物因反应后生成液体水而引起气体体积减少,减少的体积等于参加反应气体体积之和。其中l／3为氧气,2／3为氢气。根据氢气取样量和反应前后混气体体积之差,以及氢气在反应中的体积比例关系,可计算出样品的氢气纯度。计算公式式中：A一混…     

HEASUREHENT OF INSTANTANEOUS RATES OF LOSS OF VOIATILE COMPOUNDS DURING DRYING OF DROPS

A novel technique serves to monitor instantaneous rates of loss of a volatile solute from a suspended drop during drying. A highly sensitive electron capture detector is used to monitor concentrations of SF6 released into a flowing gas stream from a suspended, drying drop. Simultaneously, the appearance and morphological development of the drop are monitored with a video camera. This provides the wherewithal of relating instantaneous rates of loss of the volatile solute to particular events during the development of particle morphology.

Initial experiments have been carried out with drops of aqueous solutions of glucose, sucrose, maltodextrin and coffee extract. The results clearly display the onset of the volatiles-retentive selective diffusion phenomenon. There is also substantial loss of the volatile component later in the drying process, when the drops undergo repeated ex ansion, bursting and cratering due to the formation of internaf bubbles. These experiments appear to be the first quantitative demonstration of major losses accompanying changes in drop morphology.     

用两个形状指数表征粉煤灰颗粒形貌的研究

引用两个形状指数表征颗粒形状的概念,即先将颗粒形状近似为椭圆,再将椭圆图像分离:以圆为基准的颗粒宏观形状指数δ;以光滑椭圆为基准的颗粒轮廓凹凸度,即微观形状指数ζ。分析和发展了近似椭圆模型。并运用图像分析仪对粉煤灰、水泥样品进行实验。结果表明,粉煤灰颗粒的两个形状指数δ和ζ都大于水泥颗粒。证明粉煤灰颗粒的球形度、表面光滑度优于水泥,而且,随着粒径增大,δ和ζ呈下降趋势,表明磨制颗粒越粗。(?)粒形状越不规则。文中还运用近似椭圆模型再现了颗粒的模拟图像。     

典型煤碳燃烧特性研究和数值模拟

本文以三种典型煤的碳燃烧为研究对象，分别采用简单一维沉降燃烧方式和等温加热燃烧方式，实验研究了煤在快速加热条件下，其碳的初期和中，后期燃烧过程。以实验为基础，建立了煤的碳燃烧模型，变工况数值模拟了煤的碳燃烧过程，揭示了煤不同条件下的单颗粒碳燃烧特性。     

剪力对梁变形影响的分析

本文用材料力学的分析方法,导出了一个计入剪力时梁的挠曲线的微分方程式。为了估计剪力对梁变形的影响,在集中力作用下梁内剪力用一个单值连续的反三角函数表示。由能量法确定了截面因子数值之后,定量地给出计入剪力时梁变形的分析结果。其结果和弹性力学的结来是一致的。     

酚醛树脂热降解动力学研究

用热失重非等温法对不同甲醛,苯酚魔鬼洋比的酚树脂进行了热降解动力学研究。结果表明,甲醛,苯酚摩尔比为１．５时,酚醛树旨的热发活化能最高。耐热性最好。     

ANALYSIS OF RECENT MEASUREMENTS OF THE VISCOSITY OF GLASSES

Viscosity of Simple Soda-Silicate 500° to 1400°C Comparison of the results given by English with those of Washburn, Shelton and Libman, indicates a discrepancy in the absolute values of log₁₀ viscosity amounting to 0.6, those of Washburn et al., being relatively too high. If correction for this is made, the isothermal curves of log₁₀ viscosity as a function of soda content are smooth up to 50% Na₂O, showing no inflection. The observations as a function of temperature T are all represented within accidental error by an equation of the type where all three constants vary regularly with the composition. Change of Viscosity of Glass (6SiO₂, 2Na₂O) due to Molecular Substitution of CaO, MgO and Al₂O₃ for Na₂O The effect is clearly brought out by plotting (from the results of English) the change of log₁₀η due to the substitution as a function of temperature. The curves each show a sharp bend at a temperature between 840° and 1050°C, which is designated the aggregation temperature T_a. If we divide these curves by the corresponding percentage substituted, we get curves for each oxide which are straight and parallel below the aggregation temperatures, the slopes (increase of change of log₁₀η per 100°C) being −0.056 (CaO), −0.055 (MgO), −0.018 (A1₂O₃) per per cent oxide substituted. For substitution of 1/2 molecule the slopes are −0.325 (CaO), −0.23 (MgO) and −0.18 (Al₂O₃) per 100°. At the aggregation temperature the change of log₁₀η per per cent is a minimum, 0.03 to 0.06 for CaO, 0.12 for MgO, 0.07 for Al₂O₃. Evidence of Aggregation in Glasses, from viscosity Measurements The sharp bends in the plots of change of log₁₀η due to substitution of an oxide for Na₂O, suggest the beginning of molecular aggregation at these temperatures. These aggregation temperatures are close to the devitrification temperatures, but the effect on the viscosity curves cannot be due to actual devitrification since it does not change with time. Taking the aggregation temperatures as equal to devitrification temperatures, additional isotherms are roughly sketched into the equilibrium triangle of the system Na₂O-CaO-SiO₂. Change of Viscosity of Glass (4SiO₂, 2Na₂O) due to of Substitution of B₂O₃ for SiO₂ The change of log₁₀η (from the results of English) is plotted as a function of temperature, and also the change of log₁₀η per per cent B₂O₃. The curves are more complex than for the substitution for Na₂O.