Formation of β‐iPP in isotactic polypropylene/ethylene–propylene rubber blends: Effects of preparation method,composition, and thermal condition

The effects of preparation method, composition, and thermal condition on formation of β‐iPP in isotactic polypropylene/ethylene–propylene rubber (iPP/EPR) blends were studied using modulated differential scanning calorimeter (MDSC), wide angle X‐ray diffraction (WAXD), and phase contrast microscopy (PCM). It was found that the α‐iPP and β‐iPP can simultaneity form in the melt‐blended samples, whereas only α‐iPP exists in the solution‐blended samples. The results show that the formation of β‐iPP in the melt‐blended samples is related to the crystallization temperature and the β‐iPP generally diminishes and finally vanishes when the crystallization temperature moves far from 125 °C. The phenomena that the lower critical temperature of β‐iPP in iPP/EPR obviously increases to 114 °C and the upper critical temperature decreases to 134 °C indicate the narrowing of temperature interval, facilitating the formation of β‐iPP in iPP/EPR. Furthermore, it was found that the amount of β‐iPP in melt‐blended iPP/EPR samples is dependent on the composition and the maximum amount of β‐iPP formed when the composition of iPP/EPR blends is 85:15 in weight. The results through examining the effect of annealing for iPP/EPR samples at melt state indicate that this annealing may eliminate the susceptibility to β‐crystallization of iPP. However, only α‐iPP can be observed in solution‐blended samples subjected to annealing for different time. The PCM images demonstrate that an obvious phase‐separation happens in both melt‐blended and solution‐blended iPP/EPR samples, implying that compared with the disperse degree of EPR in iPP, the preparation method plays a dominant role in formation of β‐iPP. It is suggested that the origin of formation of β‐iPP results from the thermomechanical history of the EPR component in iPP/EPR. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 1704–1712, 2007     

套索冠醚毛细管色谱柱的研制

用套索冠醚N,N′-双(2-甲基吡啶)-二氮杂-18-冠-6作为固定相,涂渍在弹性石英毛细管内,测其柱效、惰性、热稳定性、平均极性及选择性等性质.其结构由元素分析、红外光谱、核磁共振及质谱分析的试验数据所证实.试验表明,它具有良好的色谱性能、中等极性,适用于对醇、卤代烃、芳香烃等各类异构体的分离,并用分子结构观点探讨了保留机理.     

平行双铂丝微电极用于铁氰化钾电流滴定法测定抗坏血酸的研究

平行双柱微电极是一种基于可逆氧化还原物质在电极间反馈扩散使得信噪比进一步增大的新型微电极,作者首次将这种电极应用于电流滴定分析中。结果显示,电极间距很小时,终点突跃变敏锐,使灵敏度进一步提高。该方法不需搅拌溶液,单次测量样品量只需约3μ1,是一种有实用价值的新方法。     

Pulse radiolysis of one-electron oxidation of rare tricyclic nucleoside derivative

~~Pulse radiolysis of one-electron oxidation of rare tricyclic nucleoside derivative@赵红卫$Shanghai Institute of Nuclear Research, Chinese Academy of Sciences! Shanghai 201800,China @江致勤$Department of Chemistry, Tongji Unviersity!Shanghai 200092,China @窦大营$Shanghai Institute of Nuclear Research, Chinese Academy of Sciences! Shanghai 201800,China @吴铁一$Shanghai Institute of Nuclear Research, Chinese Academy of Sciences! Shanghai 201800,China @王文锋$Shanghai…     

Co3O4 Decorated Ti/TiO2 Nanotubes for Photogenerated Cathodic Protection of 304 Stainless Steel

The Co₃O₄ decorated TiO₂ nanotube arrays(NTAs) coatings are fabricated by the combination of anodization and impregna-ting methods. It is found that the introduction of Co₃O₄ can reduce the diffraction intensity of (101) plane of the TiO₂ and accelerate the separation of photogenerated electron/hole pairs. In addition, the open circuit potential(OCP) and the corrosion potential of 304 stainless steel(304SS) with or without Co₃O₄ decorated TiO₂ NTAs were measured under visible light, which indicated the 304SS coupled with Co₃O₄ decorated TiO₂ NTAs had better anticorrosion performance than that of the 304SS or the 304SS coupled with pure TiO₂ NTAs. The enhancement of the cathodic protection performance of the Co₃O₄ decorated TiO₂ NTAs can be ascribed to the matched energy levels and strong interaction between Co₃O₄ and TiO₂ NTAs, and the improvement of light absorption.     

TEM喇叭馈源与共面馈源脉冲辐射天线性能比较

在反射面尺寸一定的情况下,优化设计了 TEM喇叭馈源与共面馈源脉冲辐射天线,并对比了两种天线的辐射性能。分析了反射面型脉冲辐射天线的工作机理,通过准静态近似,分别得到了两种天线的远区辐射场解析解。通过理论求解,得到了两种馈源在反射面口径造成的场分布,为天线结构设计提供参考。通过分析不同脉冲宽度时两种天线的辐射情况,比较了这两种馈源性能的优劣。完成了上述两种GW级高功率高效率馈源的研制,并开展了对比实验,实验结果与理论分析相吻合。     

全固态高重复频率磁脉冲压缩发生器

设计制作了全固态高重复频率磁脉冲压缩发生器,最高重复频率5 kHz,脉宽70 ns,通过调节初始储能电容上的电压可在500 阻性负载上获得4~40 kV连续可调的输出电压。通过分析简化的磁压缩末级回路,分析了预脉冲产生的过程,得出了预脉冲的电压表达式,选取适当的磁芯相对磁导率,经过求解,得出在磁开关未饱和电感一定时预脉冲随负载阻值变化的曲线簇,从曲线中可以看出：随着负载的阻值的增大,预脉冲的峰值绝对值也增大;在负载恒定的情况下,增大磁开关未饱和电感的大小可以显著地减小负载两端预脉冲的峰值绝对值,这要求磁开关磁芯有更高的相对磁导率。     

Pipette vial dispersive liquid–liquid microextraction combined with high‐performance liquid chromatography for the determination of benzoylurea insecticide in fruit juice

A simple, sensitive, and efficient method of using a pipette vial to perform dispersive liquid–liquid microextraction based on the solidification of floating organic droplets was coupled with high‐performance liquid chromatography (HPLC) and a diode array detector for the preconcentration and analysis of four benzoylurea insecticides in fruit juice. In this method, 1‐dodecanol was used as an extractant, and a snipped pipette was used as an experimental vial to simplify the procedure of collecting and separating solidified extractant. The experimental parameters were optimized using a Plackett–Burman design and one‐factor‐at‐a‐time method. Under the optimal conditions in the water model, the limits of detection for analytes varied from 0.03 to 0.28 μg/L, and the enrichment factors ranged from 147 to 206. Linearity was achieved for diflubenzuron and flufenoxuron in a range of 0.5–500 μg/L, for hexaflumuron in a range of 1–500 μg/L, and for triflumuron in a range of 5–500 μg/L. The correlation coefficients for the analytes ranged from 0.9986 to 0.9994 with recoveries of 91.4–110.9%. Finally, the developed technique was successfully applied to fruit juice samples with acceptable results. The relative standard deviations of the analytes at two spiking levels (50 and 200 μg/L) varied between 0.2 and 4.5%.     

三粒子纠缠W态隐形传态的正交完备基展开与算符变换

先是对利用单个两粒子及单个三粒子纠缠态作为量子信道实现三粒子纠缠W态的隐形传态方案进行讨论.然后由波函数的叠加原理与算符变换出发,将体系的总量子量按照Bell基展开实现量子隐形传态,给出了变换算符与实际操作算符之间的联系.进一步验证出变换算符可逆是成功实现三粒子纠缠W态隐形传态的必要条件的结论. 关键词： 三粒子纠缠W态 Bell基展开 变换算符 隐形传态     

酚醛型氰酸酯与双酚A型环氧共固化反应的FTIR研究

在恒温固化条件下,通过FTIR跟踪方法,研究了酚醛型氰酸酯与双酚A型环氧共固化反应的路径及其反应机理.共固化体系的反应过程包括在150℃及其以下温度,主要发生的是氰酸酯的三嗪环化固化反应,其中三嗪环化固化反应由于环氧的加入,反应速率被极大地提高了;同时,酚醛型氰酸酯中的氨基甲酸酯类杂质与环氧发生开环聚合反应,引起环氧官能团产生弱而持续的消耗.但在此阶段,酚醛型氰酸酯与环氧之间没有化学反应发生;在180℃及其以上温度,三嗪环和环氧发生反应,异构为异氰脲酸环结构,并进一步反应生成唑啉酮环结构,由于该反应的发生,促进了环氧官能团的消耗速度,在环氧官能团的转化率-时间图中,出现倒S曲线;在三嗪环的转化率图中,出现一个极大值后再降落的曲线.反应温度的提高有利于促进酚醛型氰酸酯与环氧之间的共固化反应,特别是当反应温度为220℃时,氰酸酯官能团和环氧官能团的消耗、三嗪环和唑啉酮环的生成均以较快的速率进行,—OCN生成三嗪环的转化率可以较容易地达到1,而唑啉酮环的转化率不超过0.5.