Bi_2O_3对堇青石陶瓷的烧结行为、相变和热膨胀性能的影响

采用X射线衍射仪、差热分析仪和热膨胀仪等手段研究了由氧化物粉末 (MgO、Al2 O3 和SiO2 )制备堇青石陶瓷时 ,添加Bi2 O3 对堇青石陶瓷相变和性能的影响 ,分析了Bi2 O3 在烧结过程中的作用机理是低温产生液相促进烧结。试验表明 ,Bi2 O3 能明显降低烧结温度 ,在 12 5 0℃烧成 3h后的陶瓷是由α堇青石和少量的 μ堇青石组成。随着Bi2 O3 含量增加 ,陶瓷的致密度和热膨胀系数逐渐升高。Bi2 O3 的添加量 (质量分数 )为 0 .0 4 ,原料相石英消失。Bi-O膨胀系数较Si-O的大和Bi3 + 离子进入堇青石晶格中是引起堇青石陶瓷热膨胀系数升高的主要原因。     

Bi2O3对堇青石陶瓷的烧结行为、相变和热膨胀性能的影响

采用X射线衍射仪、差热分析仪和热膨胀仪等手段研究了由氧化物粉末(MgO、Al2O3和SiO2)制备堇青石陶瓷时，添加Bi2O3对堇青石陶瓷相变和性能的影响，分析了Bi2O3在饶结过程中的作用机理是低温产生液相促进烧结。试验表明，Bi2O3能明显降低饶结温度，在1250℃烧成3h后的陶瓷是由α堇青石和少量的μ堇青石组成。随着Bi2O3含量增加，陶瓷的致密度和热膨胀系数逐渐升高。Bi2O3的添加量(质量分数)为0．04，原料相石英消失。Bi—O膨胀系数较Si—O的大和Bi^3 离子进入堇青石晶格中是引起堇青石陶瓷热膨胀系数升高的主要原因。     

镍渣制备多孔堇青石陶瓷的研究

以镍渣、Al_2O_3和SiO_2为原料,按偏镁铝方案确定堇青石的组成,无需添加额外的烧结助剂和造孔剂,成功制备出多孔堇青石陶瓷。测定了试样的显气孔率、抗弯强度和热膨胀系数,用XRD分析了试样在烧结过程中的物相变化,并用SEM观察其断面的显微结构。结果表明:在1200~1380℃保温4 h,制备的多孔陶瓷的显气孔率为38.13~31.39%,抗弯强度为25.53~32.54 MPa,热膨胀系数为3.17×10~(-6)~1.43×10~(-6)/℃,且其主晶相为堇青石。SEM图谱显示多孔堇青石陶瓷中堇青石晶体呈六方棱柱状,还存在大量孔洞。     

高能球磨作用对合成堇青石基陶瓷的相组成和相变机理的影响

采用XRD分析研究了由分析纯的氧化物粉末制备堇青石基陶瓷时,高能球磨作用及热处理温度对堇青石陶瓷相组成和相变过程的影响,并分析了高能球磨在堇青石陶瓷烧成过程中的作用.结果表明经高能球磨处理的试样在低温烧成(900℃)时,首先出现中间相镁铝尖晶石(MgAl2O4),但1100℃时中间相又消失;与未球磨的试样比较,高能球磨不仅能够降低堇青石的相变温度,而且可大大加快中间相和原料相向α-堇青石转变的速度;同时发现提高烧成温度有利于中间相向堇青石的转变.此外,还研究了粉末的状态(即是否经成型处理)对堇青石陶瓷相组成的影响.结果表明,加压成型使Si4+、Mg2+和Al3+易于扩散,能促进早期的固相烧结和后期的液相烧结,有利于主晶相α-堇青石的合成,但对相组成没有太大影响.     

晶化处理对堇青石微晶玻璃晶相及其性能影响的研究

以堇青石的理论化学组成为基础玻璃配方,采用熔融法制备堇青石微晶玻璃。利用DSC-TG、XRD、SEM研究堇青石微晶玻璃的析晶特性和微观形貌,并对其热膨胀性能以及烧结性能进行测试。结果表明:微晶玻璃初晶相为亚稳MgAl_2Si_3O_(10)相,终晶相为α-堇青石相,随着热处理温度升高,亚稳MgAl_2Si_3O_(10)相向α-堇青石相转变。在1000～1200℃的温度范围内,堇青石微晶玻璃的结构和性能较为稳定。     

珍珠岩制备单一α-堇青石微晶玻璃及其性能

以珍珠岩为主要原料制备了单相α-堇青石微晶玻璃.采用DSC、XRD及FESEM分别研究了微晶玻璃的烧结和晶化行为、晶相组成及显微结构.探讨了烧结温度和SiO2含量对微晶玻璃晶相、显微结构及性能的影响.结果表明,随着烧结温度升高,微晶玻璃中μ-堇青石逐渐减少并转变成α-堇青石,微晶玻璃的孔隙率减少.随着SiO2含量升高,α-堇青石晶相析出温度先降低后增高,微晶玻璃的密度及抗折强度先增大后减小,介电性能变差.当Mg∶Al∶Si=2∶2∶5.95时经900 ℃烧结6 h制得单一α-堇青石微晶玻璃,并具有高抗折强度(116 MPa),低介电常数(5.72,10 MHz),低介电损耗(0.0059,10 MHz),与Si相匹配的热膨胀系数(2.91×10-6 K-1),可以用作低温共烧陶瓷材料.     

添加氧化铈对堇青石基微晶玻璃的烧结和性能的影响

采用X射线衍射、扫描电镜和差热分析等手段研究了稀土氧化铈对由熔融淬冷法制备的非化学计量组成的堇青石基微晶玻璃的相变、烧结特性和性能的影响。研究结果表明：添加氧化铈能够明显抑制μ-堇青石相的形成和促进μ-堇青石向α-堇青石的转变。氧化铈的加入降低了微晶玻璃的烧结活化能和堇青石微晶玻璃的烧结温度,添加氧化铈质量分数为4％的微晶玻璃的μ-堇青石转变为α-堇青石的最低温度约为900℃,此时烧结样品几乎完全致密化,但氧化铈加入量太多将会阻止微晶玻璃的烧结和晶化。微晶玻璃的抗折强度随氧化铈含量的增加而增加,当氧化铈为4％时样品的抗折强度达到最大值。微晶玻璃的热膨胀系数随着氧化铈含量的增加变化不大。该微晶玻璃可望应用于微电子封装领域,能够与高导电率、低成本的金属如铜、银／钯低温共烧制成电子基板材料。     

烧成温度对溶胶-凝胶法制备堇青石陶瓷性能的影响

为解决工业生产堇青石烧结温度高的问题,首先以结晶氯化镁MgCl_2·6H_2O、结晶氯化铝AlCl_3·6H_2O和正硅酸乙酯(C_2H_5O)_4Si为原料,按照堇青石的化学计量配比,以溶胶-凝胶法并经600℃煅烧制备堇青石先驱体粉体;然后采用半干压成型法将该粉体压制成Φ20 mm×20 mm的圆柱状试样,分别在950、1 000、1 050、1 100、1 150、1 200和1 250℃保温2 h烧成,检测试样的基本物理性能,并利用XRD和SEM分析物相组成和显微结构。结果表明:溶胶-凝胶法制备堇青石陶瓷,可以降低堇青石的合成温度。在1 250℃的烧成温度下,不添加任何烧结助剂,就可以获得纯度较高的α-堇青石相,试样的体积密度为2.25 g·cm~(-3),达到α-堇青石理论密度的90%,基本达到了致密化烧结。     

SiO_2—Al_2O_3—MgO—K_2O—MgF_2系玻璃陶瓷析晶机理及断裂机制

以SiO2—Al2O3—MgO—K2O—MgF2体系玻璃为基础,采用整体析晶法,在高温条件下制备出堇青石/氟金云母玻璃陶瓷。借助于综合热分析仪、X射线衍射仪和扫描电子显微镜等分析手段,研究了玻璃陶瓷的析晶机制、显微形貌和断裂机制。结果表明:所制备的玻璃陶瓷主晶相为板条状氟金云母和β-堇青石,经1 000℃保温3h热处理后,主晶相转变为镁橄榄石;以堇青石和氟金云母为主晶相的玻璃陶瓷断裂机理为穿晶断裂,以镁橄榄石为主晶相的玻璃陶瓷为沿晶断裂。在基础玻璃中添加5%B2O3,可抑制氟金云母相的析出,并提高玻璃陶瓷的致密度。     

低热膨胀系数堇青石材料的合成研究

以高岭土、烧滑石和氧化镁为原料合成堇青石,研究了烧成温度、镁铝硅含量及高岭土种类对合成堇青石热膨胀系数的影响。实验结果表明:合成堇青石的最佳配方1#高岭土82.4 wt%、滑石9.3 wt%、氧化镁8.4 wt%,试样热膨胀系数为1.24×10-6℃-1。适当的提高烧成温度可得到热膨胀系数低的堇青石材料,但合成温度过高则会因为形成过多的玻璃相而使其热膨胀系数增大。过多或过少的引入Si O2、Al2O3、Mg O均会由于形成高热膨胀系数的晶相而导致所合成堇青石的热膨胀系数增大。     

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.     

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。     

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…     

COMPARISON OF METHODS OF ANALYSIS OF GYPSUM1

The different analytical methods proposed for the evaluation of gypsum have been subjected to an experimental test. A combination method, consisting of a fusion with KHCO₃ and determination of CaO by KMnO₄ titration, the SO₃ by Andrews method of titration of BaCrO₄ has been found to give very reliable results with the least consumption of time.     

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。     

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。     

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.     

环氧树脂羟基值测定方法的研究

利用乙酸酐、吡啶和浓硫酸混合的乙酰化试剂测定环氧树脂中羟基值含量的方法具有操作简便、滴定终点明显和分析结果误差小等优点。