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The “111” type Li x FeAs (x ranges from 0.8 to 1.2) with Cu2Sb type tetragonal structure was synthesized with T c 18 K. The isostructure NaFeAs was further studied, which shows superconductivity with T c up to 26 K. The effect of pressure on superconductivity was investigated. 相似文献
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应用n级等摩尔浓度反应的热动力学理论,在30℃和40℃下研究了丙烯酰胺在水溶液中和CTAB胶束溶液中由亚硫酸钠引发的聚合反应动力学.讨论了引发剂和CTAB的浓度对聚丙烯酰胺分子量的影响。 相似文献
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用分光光度法研究了两种不对称Salen-Mn(Ⅲ)配合物催化α-吡啶甲酸对硝基苯酚酯(PNPP)的水解动力学.提出了相应的PNPP催化水解机理,讨论了底物浓度、体系的酸碱度、温度以及配合物结构对PNPP催化水解反应的影响.结果表明:此两种Schiff碱锰(Ⅲ)配合物在催化PNPP水解中均表现出较好的催化活性,PNPP水解速率随着底物浓度、体系pH值的增大而增大;在15~55℃温度范围内,未观察到催化剂失活现象;其中,带有苯并氮杂-15-冠-5侧基的不对称Salen-Mn(Ⅲ)配合物比带有吗啉基的另一配合物拥有更高的催化活性,这可能主要由这两种模拟水解酶之间较大的疏水微环境差异所引起. 相似文献
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When the red-black subdivisions are satisfied, an iterative substructuring method is proposed to solve the algebraic system of equations arising from the discretization of symmetric elliptic problems via nonconforming finite elements which are only continuous at the quasi-uniform mesh nodes. Theoretical analysis is given and the results of numerical experiments are reported. 相似文献
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分析了不同光窗口位置和不同光窗口面积对SiGe/Si异质结光电晶体管(HPT)光响应特性的影响.光窗口位于发射区时,HPTs吸收路径长,会产生较多的光生载流子,在发射结界面产生较大的发射结光生电压,有利于发射结的电子注入,因此获得较大的集电极输出电流和光增益.当入射光波长为650 nm,集电极电压为2.0 V,光窗口面积为10μm×10μm时,SiGe/SiHPT的光增益最大可以达到9.24.光窗口位于基区时,在较大的入射光功率下,HPTs吸收区的光生载流子密度大,光生空穴发生快速驰豫的可能性增加,一定程度上缓解了空穴迁移率低对器件工作速度的限制,提高了光特征频率.当入射光波长650 nm,集电极电压2.0 V,光窗口面积为10μm×10μm时,SiGe/SiHPT的光特征频率可达16.75 GHz.对于能够获得更高光增益光特征频率优值的发射区光窗口SiGe/SiHPTs,当光窗口面积从3μm×10μm到50μm×10μm逐渐增加时,电子在发射结界面的有效注入面积增加从而光增益逐渐增大;同时发射结和集电结的结电容也随之增大,RC延迟时间增长,光特征频率却逐渐减小.光增益·光特征频率优值随着光窗口面积的增加而逐渐提高,但随着面积的增加,光增益·光特征频率优值提高的速率变慢,并有逐渐趋于饱和的趋势. 相似文献
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A Kinetic Study of Phenolic Oxidation by H2O2 Using the Schiff Base Complexes As Mimetic Peroxidases
Xie Jia-qing Li Jian-zhang Meng Xiang-guang Hu Chang-wei Zeng Xian-cheng Li Shen-xin 《Transition Metal Chemistry》2004,29(4):388-393
The Schiff base complexes containing a transition metal ion, CoII and CuII, were used as mimetic peroxidase in the catalytic oxidation of phenol by H2O2. The characteristic spectra of the Schiff base complexes in H2O2-buffered solution were recorded and analyzed, respectively. The mechanism and the kinetic mathematic model of the phenol catalytic oxidation were studied. The results showed that the Schiff base complexes containing the transition metal ion, CoII and CuII, as peroxidase mimics exhibited good catalytic activity and the character of the peroxidase in the catalytic oxidation of phenol by H2O2 under different conditions. 相似文献
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