某1000 MW汽轮机组励磁系统实测建模过程浅析

该机组是上海汽轮发电机有限公司生产的1000 MW汽轮机组,励磁调节器是ABB公司生产的UNITROL-6800型数字励磁调节器。文章论述了该机组励磁系统参数测试结果,给出了电力系统稳定计算用励磁系统的模型和参数。     

不同变截面桩竖向承载特性的数值分析

基于现场试验,采用Abaqus有限元软件对等截面桩及变截面桩单桩竖向承载力测试实验过程进行数值模拟。结果表明:弹性变形阶段,竖向荷载-沉降曲线呈线性变化趋势,等截面桩比变截面桩桩身沉降较小;塑性屈服阶段,等截面桩与变截面桩单桩承载力几乎一致。变截面位置对桩侧摩阻力沿深度的分布有一定影响,最大侧摩阻力位置根据变截面的位置而变化。变截面桩的平均侧摩阻力较等截面桩的平均侧摩阻力大,变截面桩侧摩阻力效果较等截面桩更有优势。在相同承载力条件下,变截面桩所耗费的材料较等截面少,对于竖向承载特性,变截面桩与等截面桩表现基本一致,因此使用变截面桩能节约工程成本。     

丁腈橡胶硫化反应动力学研究

设计了促进剂A 4种不同用量的丁腈橡胶配方;基于配方,先利用密炼机将丁腈橡胶、硬脂酸和ZnO混炼,再利用开炼机加入硫黄、促进剂和防老剂,再利用无转子硫化仪分别测试了160℃、170℃和180℃下胶料硫化曲线;基于硫化曲线计算出了每组配方胶料硫化反应速率常数K和活化能Ea。结果表明,在焦烧期时,NBR硫化反应为非一级反应,真正的一级反应开始于硫化速率达到最大时,即tdis;焦烧期后的反应可分为2个阶段且遵循一级动力学反应规律。     

轴承钢GCr15的恒温相变超塑性

研究了ＧＣｒ１５钢在Ａｃ１相变点附近的恒温超塑性特性与变形温度的关系。结果表明，与一些材料一样，该钢也存在恒温相变超塑性现象。当初始应变速率为２．５×１０＾－４ｓ＾－１时，经预调质处理的ＧＣｒ１５钢试样，在７４８℃进行超塑性拉伸试验获得最大延伸率达８００％，流动应力为２４ＭＰａ。与已有的同类研究结果相比，其延伸率提高了２００％以上。     

Electrochemical injection of organic corrosion inhibitors into carbonated cementitious materials: Part 1. Effects on pore solution chemistry

This series of investigations was intended to clarify phenomena associated with electrochemical injection of the organic base corrosion inhibitors, ethanolamine and guanidine, into carbonated concrete. In Part 1, experiments were conducted with laminated specimens of carbonated cement paste, that were specially designed to facilitate analysis with adequate spatial resolution to assess changes in their pore solution phase chemistry after they had been subjected to constant current electrolysis between embedded cathodes and external anodes. The anolyte solutions provided sources of ethanolamine or guanidine in contact with the exterior specimen surfaces. Effects of variations in the applied current density and duration of electrolysis on the concentration profiles of the two inhibitors and the other main constituents of the pore solution phase were determined. The results have been used to underpin the development of a mathematical model, which is described in Part 2.     

灰铁铸件牌号要求与熔炼配料选择

由于铸件壁厚对其性能有明显影响，牌号要求相同、壁厚不同的灰铁铸件必须采用不同的成分和配料。介绍不同灰铁铸件牌号标准的对照，并用生产实例说明如何根据图纸牌号要求、铸件结构和使用性能要求选择化学成分控制标准和熔炼配料。     

变频器在机床电力拖动中的应用问题

本文分析了机床拖动的特点,变频调速对电动机及变频器的要求,分析了变频器应用中的干扰问题及采取的抑制措施。     

均相催化水合法合成乙二醇动力学研究

在反应温度为45～75℃,NY 健化剂浓度为0.093mol/L,水比为6～10的反应条件下,对均相催化水合法合成乙二醇动力学进行了研究。测定了反应速率常数及反应过程中溶液 pH 值的变化。依据实验结果,提出了反应机理,建立了反应动力学方程,并利用 Levenberg-Marquardt 方法回归了动力学参数。研究结果表明:在 NY 催化剂存在下,均相催化水合法合成乙二醇反应对环氧乙烷浓度是一级反应,其表观活化能为71113.8 J/mol 和指前因子3.05×10~9 min~(-1)。相对直接水合法而言,NY 催化剂降低了反应的活化能,大大提高了反应速度。     

钢管除锈机设计与经验

介绍了钢管除锈机的基本原理及设计过程,实践证明:使用钢管除锈机不仅保证了除锈质量,还提高了工作效率。     

Surface photografting polymerization of vinyl acetate,maleic anhydride,and their charge‐transfer complex. VI. Charge‐transfer complex (2)

The photografting copolymerization of a low‐density polyethylene/vinyl acetate (VAC)–maleic anhydride (MAH) binary monomer system was studied from the perspective of dynamics. The total conversion percentage (CP) and grafting conversion percentage (CG) were measured by gravimetry. On the basis of plots of CP and CG as functions of the polymerization time, the total polymerization rate (RP) and grafting polymerization rate (RG) were calculated. In addition, the apparent activation energy (E_a) and the reaction orders of the photografting polymerization under different reaction conditions, such as the total monomer concentration and the concentration of benzophenone (BP), were determined also. The results showed that, in comparison with the photografting polymerization of the two single monomers (VAC and MAH), RP and RG noticeably increased for the VAC–MAH binary monomer system. When the total monomer concentration was kept at 4M, the apparent E_a's of the three photografting polymerization systems were as follows: for VAC ([MAH]/[VAC] = 0/4), E_a's for the total polymerization and grafting polymerization were 41.00 and 43.90 kJ/mol, respectively; for MAH ([MAH]/[VAC] = 4/0, E_a's were 39.65 and 43.23 kJ/mol, respectively; and for the VAC–MAH binary monomer system, E_a's were 34.35 and 40.32 kJ/mol, respectively. These results suggested that the polymerization of the binary system occurred more readily than the other two. The reaction orders of RP with respect to the total monomer concentration of the monomers and the concentration of BP were 1.34 and 0.81, respectively. According to these investigations, it could be inferred that in the binary monomer system, both the free monomers and charge‐transfer complex took part in the polymerization; to the termination of the propagating chains, two possible pathways, unimolecular termination and bimolecular termination, coexisted in this binary monomer system. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 910–915, 2005