豆油脚脂肪酸制备松香改性醇酸树脂的配方研究

利用豆油脚脂肪酸-松香-甘油-苯酐，采用脂肪酸法制备松香改性醇酸树脂。通过实验得到较佳工艺条件，确定经济合理的配方和各种原料用量，制备出符合标准的醇酸树脂产品，为加工成各色醇酸调合磁漆和脂肪酸调合磁漆奠定基础。此方法有效利用了废弃的大豆下脚料以代替市场紧缺的天然桐油和亚麻油，为豆油脚在涂料工业上的开发和利用开辟了新途径。     

SBR/LDPE复合改性沥青高温性能研究

研究了SBR／LDPE熔融共混物改性沥青的高温贮存稳定性及其粘温特性和动态力学性能，并利用光学显微镜观察了各种改性沥青在高温下随时间的变化。结果表明：采用预先制备的SBR／LDPE共混物所得到的改性沥青能够在高温下稳定贮存。同时，相形态观察也表明。这种共混物改性沥青的高温相形态也不随时间变化。而聚合物的加入在一定程度上降低了沥青的温度敏感性，提高了沥青的高温使用等级。     

纳米碳酸钙的表面活化改性研究

本文主要介绍通过加入特定的表面改性剂,制得了表面改性的活性碳酸钙.并对活化过程中的一系列影响因素,如活化温度、活化时间、碳酸钙悬浊液浓度、表面改性剂用量进行了研究.     

离子化对SBS/聚(苯乙烯-甲基丙烯酸甲酯)热塑性互穿聚合物网络结构与力学性能影响的研究

采用原子转移自由基聚合（ATRP）法合成了聚（苯乙烯一甲基丙烯酸甲酯）[P（St—MMA）]，采用两步法制备了SBS／P（St—MMA）热塑性互穿聚合物网络（TIPN）。在双螺杆挤出机上通过熔融挤出方法对SBS／P（St—MMA）直接进行水解，制备了含有离子键的SBS／P（St—MMA）TIPN。离子化后TIPN的拉伸强度明显增加，在离子化程度为25％时达到最大，断裂伸长率明显下降。TIPN的中PB和PS嵌段的Tg均明显增加，PS嵌段增加更加明显，提高20℃；弹性模量E’均明显提高。     

In situ impedance study of the Y-Ni thin film under electrochemical hydrogenation

A thin film of yttrium Y (150 nm) protected by a 6 nm coating of nickel Ni on a glass substrate was completely hydrogenated in a 1 M NaOH electrolyte at a constant negative current until the transparent Y tri-hydride phase was achieved and hydrogen gas evolution from the electrode began. A series of impedance measurements were performed in situ during the electrochemical experiment to study the properties of the system as dependent on hydrogenation degree and time of relaxation. The equivalent electrical circuit (EEC) simulations were performed with a Randles-like scheme R₀[R₁CPE₁], where R₀ is the thin film electrode resistance, R₁ the charge transfer resistance and CPE₁ is the capacitive constant phase element. The behavior of all the components of the EEC undergoes a clear transition when the hydrogenation degree of the electrode is approximated to its maximum value (H to Y ratio 2.7) and electrochemical process changes from hydrogen uptake to hydrogen evolution.     

新型碳纤维复合芯导线在输电线路中的应用分析

新型碳纤维复合芯导线具有良好的力学性能和电气特性,与等径钢芯铝绞线相比,其主要有芯线强度高、导电率高、载流量大、质量轻、耐腐蚀、弧垂小等优点;与普通碳纤维导线相比,新型碳纤维复合芯导线采用铝包覆技术,在配套金具、导线压接和施工工艺等方面都有较大改进。以110～500 kV新建线路为例,对185～800 mm~2截面的新型碳纤维复合芯导线进行了全面的经济性比较。研究结果得到:对于500 kV新建双回线路,推荐采用JLRX1/F2A-710/50、JLRX1/F2A-800/50导线;对于220 kV新建双回线路,推荐采用JLRX1/F2A-400/50、JLRX1/F2A-450/50导线;对于110 kV新建双回线路,推荐采用JLRX1/F2A-300/40、JLRX1/F2A-360/40导线。     

关于我国精细磷化工发展的几点建议

介绍了国内外精细磷化工的生产现状，分析了我国发展磷酸盐的产品领域和市场前景，对基础产品、市场营销、技术创新、大型企业进入磷酸盐行业提出了建议。     

Methane activation without using oxidants over Mo/HZSM-5 zeolite catalysts

The effect of Mo loading, calcination temperature, reaction temperature and space velocity on the catalytic performance of methane dehydrogenation and aromatization without using oxidants over Mo/HZSM-5 has been studied. The XRD and BET measurements show that Mo species are highly dispersed in the channels of the HZSM-5 zeolite, resulting from the interaction between the Mo species and the zeolite, which also leads to a decrease in its crystallinity. The Brønsted acidity, the channel structure and the state and location of Mo species in the zeolite seem to be crucial factors for its catalytic performance. It was found that 2% Mo/HZSM-5 calcined at 773 K showed the best aromatization activity among the tested catalysts, the methane conversion being 9% at 1013 K with the selectivity to aromatics higher than 90%. The experimental results obtained from the variation of space velocity gave evidence that ethylene is an initial product. On the basis of these results a possible mechanism for methane dehydrogenation and aromatization has been proposed in which both the heterolytic splitting of methane in a solid acid environment and a molybdenum carbene-like complex as an intermediate are of significance.     

有色丙纶细旦棉型短纤维生产及纺纱技术研究

定性地分析和讨论有色PP细且棉型短纤维生产及其纺纱过程的主要因素,着重探讨有色母粒对成品纤维性能及纺纱过程的影响,确定最佳纺丝工艺条件,控制 PP 有色细且短纤维物理性能,以满足纺纱工艺要求.     

A vibrational study of the activation sequence of C–H and C–C bonds of isobutene and 1-butene on Mo(110) and (4 × 4)-C/Mo(110) surfaces

The thermal decomposition pathways of isobutene and 1-butene on both Mo(110) and 4 × 4-C/Mo(110) surfaces have been studied using high-resolution electron energy loss spectroscopy (HREELS) in order to highlight the substantially different activities of these two surfaces towards the cleavage of C–H and C–C bonds. On clean Mo(110), the CH₂ group of isobutene decomposes upon heating to 150 K, producing either a /-bonded isobutenylidene [(CH₃)₂CCH] species or a 1,1-di-/-bonded isobutenyl [(CH₃)₂CC] species. Upon further heating, extensive C–H bond scission occurs to form hydrocarbon fragments which do not contain CH₃ or CH₂ groups, but appear to have largely intact carbon skeletons. By contrast, isobutene is molecularly adsorbed on the carbide-modified surface at 150 K. Further heating produces isobutylidyne [(CH₃)₂HCC] by 300 K, which subsequently decomposes via C–C bond scission to generate surface methyl groups. The different activation sequence of the C–H and C–C bonds of isobutene on clean and carbide-modified Mo(110) surfaces is also qualitatively confirmed by comparative studies of 1-butene on the two surfaces.