Al2O3—TiB2陶瓷刀具材料的研制及其耐磨性能研究

本文研制成功了一种新型陶瓷刀具材料即Al_2O_3-Ti B_2陶瓷刀具材料。文中讨论了该材料的研制方法,力学性能和微观结构特点,并对该材料的磨损行为和磨损机理进行了研究。结果表明:Ti B_2粒子的弥散可以明显提高该材料的耐磨性。加工淬火钢时该材料的抗磨损能力明显优于Al_2O_3-TiC陶瓷刀具材料。Al_2O_3-Ti B_2陶瓷刀具材料的磨损过程主要受粘着、耕犁和微破损机制的控制。     

聚苯硫醚／聚砜共混物的动态黏弹行为及相容性研究

研究了聚苯硫醚／聚砜熔融共混物的的加工流变行为以及共混物在不同温度下的动态黏弹响应；并对其相容性作出判断。结果表明，聚苯硫醚的加入显著改善了共混物的流动性，使其可在较低温度下成型；熔融态共混体系的相容性较差，固态条件下的相分离程度及损耗因子峰值大小依赖于组成变化。     

Possible use of methylbenzenes as electrolyte additives for improving the overcharge tolerances of Li-ion batteries

Based on the voltammetric behaviour of a series of methyl-substituted benzenes in 1M LiPF₆/EC-DMC electrolyte, xylene was selected and tested as an electrolyte additive for overcharge protection of Li-ion batteries. From the overcharge curves, CV behaviour and SEM observations of the cells in the presence of xylene, it was found that the additive can polymerize at the overcharged voltage to form a dense layer of isolating polymer film at the cathode surface, which blocks off further oxidation of the electroactive material and electrolyte and, therefore, improves the overcharge tolerance of the Li-ion battery. In addition, the xylene additive has shown only a slight influence on the cycling behaviour.     

白色纯聚酯粉末涂料的性能研究

简要介绍了粉末涂料的特点 ,并从涂膜性能的优化角度论述了粉末涂料原料的选择和使用情况。从羧基聚酯树脂 -TGIC体系纯聚酯粉末涂料配方设计入手 ,研究了基料、填料、助剂对其涂膜性能 (主要物理机械性能 :涂膜之耐冲击力、柔韧性、倾斜流动性、硬度、附着力、抗UV老化等 )的影响 ,得到了一个在给出原料中涂膜综合性能最好的配比     

循环冷却水零排污运行方案的研究

对循环冷却水系统零排污的技术可行性、经济性等进行了讨论，并针对大庆炼化公司循环冷却水系统零排污方案的实施加以详细描述，对实施过程中存在的问题予以了详细说明。     

基于数据密度的半监督自训练分类算法

在实际的分类任务中,无标记样本数量充足而有标记样本数量稀少的情况经常出现,目前处理这种情况的常用方法是半监督自训练分类算法。提出了一种基于数据密度的半监督自训练分类算法,该算法首先依据数据的密度对数据集进行划分,从而确定数据的空间结构;然后再按照数据的空间结构对分类器进行自训练的迭代,最终得到一个新的分类器。在UCI中6个数据集上的实验结果表明,与三种监督学习算法以及其分别对应的自训练版本相比,提出的算法分类效果更好。     

不同粒径可膨胀石墨无卤阻燃高密度硬质聚氨酯泡沫塑料研究

采用高速混合破碎机对可膨胀石墨（EG）进行处理，制得不同粒径的EG。考察了不同粒径EG填充的硬质聚氨酯泡沫塑料（RPUF）的微观形态，研究了EG对于RPUF燃烧行为的影响。结果表明：EG的粒径越小，其在聚氨酯体系中的分散就越困难；20％未经处理的EG粒子（EG0）填充的RPUF氧指数为39．5％，比未填充的RPUF氧指数提高了近一倍，而经过13min破碎的EG粒子（EG13）其氧指数仅为23．5％，与纯RPUF的氧指数在同一水平；水平垂直燃烧结果可进一步验证氧指数结果，当EGO填充量超过10％时，RPUF燃烧已经达到了V-0级，而RPUF／EG13因其阻燃性能较差只能用水平燃烧分级。由此可见，EGO可有效提高RPUF的阻燃性能，而EG13对RPUF的燃烧性能几乎没有影响；研究同时提出了不同粒径EG无卤阻燃高密度硬质聚氨酯泡沫塑料的阻燃机理。     

PA-1010/ABS合金的性能研究

研究了以自制的马来酸酐 (MAH)接枝改性ABS(MABS)作为PA 10 10 /ABS增容剂所形成的PA 10 10 /ABS合金的性能。研究结果表明 ,随ABS中马来酸酐接枝量的上升 ,PA 10 10 /ABS合金的冲击强度提高 ,保持PA 10 10与ABS用量在某一恰当配比范围内 ,可得到冲击强度高 ,维卡软化温度较高的合金。     

Imaging and probing catalytic surface reactions on the nanoscale: Field Ion Microscopy and atom-probe studies of O2–H2/Rh and NO–H2/Pt

We present dynamic studies of surface reactions using video-Field Ion Microscopy (FIM) along with Pulsed Field Desorption Mass Spectrometry (PFDMS). Catalytic water formation is followed using rhodium and platinum 3D field emitter crystals for the oxidation of hydrogen with either oxygen (Rh) or NO (Pt). Strongly non-linear dynamics are observed with nanoscale spacial resolution. For both reactions quasi-oscillatory behaviour exists under certain conditions of temperatures and partial pressures. An influence of the probing electric field is observed and possibly essential in establishing oscillatory behaviour. Local chemical probing of selected surface areas with up to 400 atomic surface sites proves catalytic water formation to take place. Since water ions (H₂O⁺/H₃O⁺) cause image formation of the O₂–H₂ reaction on Rh, respective videos provide space-time resolved information on the catalytically active sites. Atom-probe data also reveal that the surface of the Rh sample reversibly switches from a metallic to an oxidized state during oscillations. As to the NO–H₂ reaction on Pt, fast ignition phenomena are observed to precede wave fronts. After catalytic water formation, NO molecules diffuse into emptied areas and cause high image brightness. Depending on the size of the Pt crystal, the reaction may ignite in planes or kinked ledges along the <100> zone lines. Thus FIM provides clear experimental evidence that kinks are more reactive than steps in the catalytic NO + H₂ reaction. Pt surface oxidation occurs and has probably been underestimated in previous FIM studies.     

O,O -二甲基硫代磷酰胺异构反应动力学与绿色集成工艺

研究了硫酸二甲酯浓度和反应温度对O,O-二甲基硫代磷酰胺异构化反应的影响,建立了O,O-二甲基硫代磷酰胺异构化反应的动力学模型.拟合得到了O,O-二甲基硫代磷酰胺在硫酸二甲酯催化作用下的反应动力学模型参数.结果表明,主副反应均为二级反应,主反应的活化能为104 kJ/mol,副反应的活化能为111～116 kJ/mol,降低反应温度可减少副反应的发生.提出了采用硫酸二甲酯为催化剂,O,O-二甲基硫代磷酰胺异构合成O,S-二甲基硫代磷酰胺的绿色集成工艺.