退火温度对EB熔炼低成本TC4钛合金宽厚板组织和性能的影响

采用EB炉一次熔炼TC4合金扁锭作为直轧坯料,在4200 mm宽厚板轧机上成功制备出规格46 mm×2650 mm×8700 mm的低成本TC4合金宽厚板,研究了退火温度对低成本TC4合金板材显微组织和力学性能的影响。结果表明:EB熔炼TC4合金扁锭经过两火换向轧制,粗大铸态组织得到充分破碎,热轧态TC4合金板材显微组织中等轴α或条状α含量较高,横纵向室温拉伸性能差异小,横向室温冲击吸收能量小于纵向,横纵向心部强度均高于表层。TC4合金板材经750~900 ℃退火,横纵截面为等轴组织,经950 ℃退火,横纵截面为双态组织,经980 ℃退火,横截面为双态组织,纵截面为魏氏组织。随着退火温度升高,TC4合金板材抗拉强度和规定塑性延伸强度呈下降趋势,伸长率基本不变,室温冲击吸收能量先升高后降低,900 ℃退火后,强度、伸长率和冲击吸收能量达到最佳匹配。     

METCAL 在 Co3O4 制备工艺设计中的应用

采用 METCAL 软件创建计算模型，对沉淀 - 热分解法制备四氧化三钴材料的工艺进行了模拟，并简要介绍了过程模拟的步骤和思路。通过对工艺流程的模拟计算，得到了直观的物流分配走向、金属平衡和热平衡数据等，为四氧化三钴材料制备工艺工程设计提供了基础数据支撑。     

FDM用PETG系列耗材的改性研究

对市售聚对苯二甲酸乙二醇酯-1，4-环己烷二甲醇酯（PETG）丝材及原材料进行研究，选用PETG 2012作为制备熔融堆积成型技术（FDM）用PETG丝材的基体树脂。选用聚碳酸酯（PC）对基体PETG进行增韧增强改性，并制成3D打印高分子丝材进行打印测试，探讨了PC含量对PETG耗材及制件性能的影响。结果表明，在低PC含量下，PETG与PC的相容性较好，PETG与PC制件未出现明显的分层，分布比较均匀；共混物的流动性随着PC含量的增加而降低，且打印件的维卡软化温度和热变形温度随着PC用量的增加而增加；此外，PC材料的加入使得PETG打印件的力学性能得到较大改善：打印件的拉伸强度随着PC用量的增加而增大，缺口冲击强度却随着PC用量的增加呈现先增加后减小的趋势； PETG/PC的配比为1∶1时，可制得力学性能优异的3D打印耗材。     

（S）-噻吗洛尔半水合物的合成及表征

为了开发β受体阻断剂新药（S）-噻吗洛尔半水合物，采用3-吗啉-4-氯-1，2，5-噻二唑为起始原料，经水解反应得到中间体1（3-吗啉-4-羟基-1，2，5-噻二唑）。中间体1与R-环氧氯丙烷发生醚化反应，经后处理及重结晶得到中间体2 {（R）-4-［4-（环氧乙烷-2-基甲氧基）-1，2，5-噻二唑-3-基］吗啉}。中间体2经胺化反应、马来酸成盐及重结晶得到（S）-马来酸噻吗洛尔。（S）-马来酸噻吗洛尔经游离、纯水转晶得到符合药典标准的（S）-噻吗洛尔半水合物，总收率14.05%且e.e.值为99.66%。最终成品经IR、1H-NMR、13C-NMR、MS、TGA、DSC表征，并优化各步反应条件。结果表明:以三乙胺为醚化反应缚酸剂75 ℃反应最佳；以乙醇为胺化反应溶剂46 ℃反应16 h最佳；S-噻吗洛尔的转晶拆分以水作溶剂，比传统不对称合成工艺安全稳定，操作简单，适合工业化生产。     

新型硫酸法C_4烷基化工艺的模拟

提出了一种新型硫酸法C4烷基化生产工艺,丁烯原料在气相状态下进入反应器,与液相异丁烷、浓硫酸混合后,部分丁烯溶于液相,在液相中进行反应;通过控制反应器的压力,部分液相吸收反应热而汽化,使反应温度基本稳定;经气液分离、酸烃分离及产品分馏后,气相丁烯、异丁烷、浓硫酸分别构成循环。采用Aspen Plus过程模拟软件对新工艺过程进行模拟计算的结果表明,在反应器进口压力0.2 MPa、压降4.5 k Pa的条件下,反应器进出口温度均在7.2℃左右,可通过调节反应器压力实现温度的控制;反应器进口液相中烷烯质量比为145∶1,可减少副反应的发生;与传统硫酸法C4烷基化工艺相比,新工艺耗电量可降低30%。     

荧光防水透湿特种防护面料的开发

在聚氨酯胶料中掺杂稀土铝酸锶制备荧光防水透湿薄膜,采用离型纸转移层压工艺,和细旦尼丝纺基布贴合,开发荧光防水透湿特种防护面料。对基布和胶料的选择、制备和贴合工艺进行了详细介绍,并对所开发的产品进行了荧光、防水、透湿和物理性能的检测,结果表明开发的面料能满足防护服用要求。     

Enhanced Stability,Conductance, and Catalytic Activity of Gold Nanoparticles via Oxidative Dissolution by KMnO4

The present paper reports the oxidative etching of Au nanospheres by an oxidant, KMnO₄, which resulted in the formation of new particles of different reduced sizes from single starting nanoparticles. The significant blue-shifting (536 → 527 nm) of the surface plasmon band for Au nanospheres was observed due to their size alterations after oxidative dissolution of Au⁰ to Au⁺³. This was supported by the cyclic voltammetry studies, which revealed an anodic peak at ?0.90 V in agreement with the standard electrode potential of Au⁰/Au⁺³ (?0.96 V). Dynamic light scattering (DLS) analysis showed that the hydrodynamic diameter of Au nanospheres (～41 nm) was decreased from ～26 to 4 nm as a function of KMnO₄ concentration, as further evidenced by TEM. This oxidation-driven process resulted in colloids with higher zeta potential, conductance, and enhanced catalytic activity (～2 times) than their bare nanoparticles for the reduction of p-nitrophenol to p-aminophenol attributed to the higher surface area-to-volume ratio.     

Multi-innovation auto-constructed least squares identification for 4 DOF ship manoeuvring modelling with full-scale trial data

This research is concerned with the problem of 4 degrees of freedom (DOF) ship manoeuvring identification modelling with the full-scale trial data. To avoid the multi-innovation matrix inversion in the conventional multi-innovation least squares (MILS) algorithm, a new transformed multi-innovation least squares (TMILS) algorithm is first developed by virtue of the coupling identification concept. And much effort is made to guarantee the uniformly ultimate convergence. Furthermore, the auto-constructed TMILS scheme is derived for the ship manoeuvring motion identification by combination with a statistic index. Comparing with the existing results, the proposed scheme has the significant computational advantage and is able to estimate the model structure. The illustrative examples demonstrate the effectiveness of the proposed algorithm, especially including the identification application with full-scale trial data.