Enhancement of ferromagnetic properties in In1.99Co0.01O3 by additional Cu doping

This paper reports room-temperature ferromagnetism in Co- and Cu-doped In2O3 samples synthesized by a solid-state reaction method. Structure and composition analyses revealed that Co and Cu were incorporated into the In2O3 lattices. Photoluminescence measurement revealed an additional emission at 520 urn from these doped samples. The magnetic measurement showed that additional Cu doping greatly enhanced the ferromagnetism of In1.99Co0.01O3 bulk samples. The implication of the effects of additional Cu doping is also discussed. (c) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

"85-01"花卉营养土的研究

该营养土是由含氮、磷、钾和含有有机物质的有机质、腐殖泥炭土为基质，以珍珠岩、泡塑粒为填充料再加入其它配料制成的，其含有花卉培植所需养分，含量均比花泥高，具有疏松，透气性好，保水性较强，比重小，无臭味等特点，适于兰花、茶花、菊花、月季等多种花卉及阴生植物，盆景、盆栽柑桔等栽培需要。产品质量达到广东省企业标准报批稿的指标要求。

固定化假单胞菌CTP-01细胞分解对硫磷的研究

用明胶-戊二醛(GGA)和聚丙烯酰胺(PAA)包埋的固定化Pseudomonas sp.CTP-01细胞具有降解对硫磷的特性。GGA固定化细胞水解对硫磷的活力比PAA固定化细胞高5.8倍。当保存在4℃时GGA和PAA固定化细胞分别可以保持活力31.3和70%。GGA和PAA包埋的细胞最适反应温度分别为50℃到70℃和60℃到70℃,然而整细胞在温度超过65℃时活力很快下降。GGA和PAA两种固定化细胞最适pH为8.0,当pH低于7.0时活力开始下降,pH4吋则完全失活。

有机磷农药在水生态系中生物净化机理研究---- ----4. Pseudomonas sp. CTP-01 的对硫磷水解酶诱导合成性质

Pseudomonas sp.CTP-01的对硫磷水解酶具有底物诱导合成性质。停滞生长期的细胞接触底物半小时即产生相应酶的合成,而指数生长期的细胞接触底物48小时后才发生酶的合成。甲基对硫磷及对硝基酚也具有诱导作用,可见合成对硫磷水解酶的诱导特异基团可能与对硝基酚及其苯环上的取代基有密切关系。

Optical properties of alloy states in GaNxAs1-x (x < 0.01)

A set of GaNxAs1-x samples with a small content of nitrogen (N) (< 1%) were investigated by continuous-wave photoluminescence (PL), pulse-wave excitation PL, and photo reflectance technology. Temperature-and excitation-dependence of PL disclosed the intrinsic band gap properties of alloy states in GaNxAs1-x, which was extremely different from the N-related impurity states. At the same time, PR spectra were also studied in this work.

GaNxAs1-x(x＜0.01)中合金态的光学特性

应用多种光谱手段研究了分子束外延生长在半绝缘的(001,GaAs衬底上的低氮含量的GaNAs中三元合金态的光学特性.变温PL谱揭示了合金态的本征特性以及其与氮的杂质态的根本区别,而脉冲激发的光荧光谱则进一步显示了合金态的本征光学特性.最后还研究了GaNAs的吸收光谱特征.

基于ARM920T的HIRFL-CSR前端总线控制器FBC-01

本文论述用于兰州重离子加速器冷却存储环(HIRFL-CSR)控制系统的前端总线系统控制器FBC-01的硬件设计。该控制器是基于0.8mmBGA封装的AT91RM9200(ARM9)处理器,运行嵌入式LINUX操作系统。控制器可以连接标准的VGA显示器、键盘、鼠标,具有通用的10M/100M以太网接口、USB接口、RS-232接口、485接口、CANBUS接口。可以带SD卡、CF卡存储器。该控制器采用现场可编程的FPGA器件设计背板接口,并采用具有64mA高驱动能力的总线驱动器,不仅符合VME规范的电气要求,而且具有灵活的接口信号定义可编程能力,是HIRFL-CSR控制系统的关键部件。

Ti_(0.17)Zr_(0.08)V_(0.34)Nb_(0.01)Cr_(0.1)Ni_(0.3)氢化物电极合金微观结构及电化学性能研究

采用XRD、FESEM-EDS、ICP及EIS等方法研究了Ti0.17Zr0.08V0.34Nb0.01Cr0.1Ni0.3氢化物电极合金微观结构和电化学性能。X射线衍射分析表明:该合金由体心立方结构(bcc)的V基固溶体主相和少量六方结构的C14型Laves相组成;FESEM及EDS分析表明:V基固溶体主相形成树枝晶,C14型Laves相呈网格状围绕着树枝晶的晶界,元素在两相中的分布呈现镜像关系。电化学性能测试结果表明:该合金的氢化物电极在303￣343K较宽的温度区间内,表现出较高的电化学容量,在303K和343K时,电化学容量分别为337.0mAh·g-1和327.9mAh·g-1。在303K循环100周后,容量为282.7mAh·g-1。ICP分析结果表明,氢化物电极在充放电循环过程中,V及Zr元素向KOH电解质中的溶出较为严重。EIS研究表明,金属氢化物电极表面电化学反应的电荷转移电阻(RT)随循环次数的增加而增加,相应的交换电流密度则随循环次数的增加而降低。氢化物电极循环过程中RT的增大以及V和Zr元素的溶解,可能是导致电极容量衰减的主要原因。

GH-01超低温胶粘剂的性能

介绍了GH -0 1双组分、室温固化环氧树脂超低温胶粘剂的某些性能 ,说明这种胶粘剂能粘接多种材料 ,尤其是在液氮温度下仍有良好的粘接性能 ,并且真空放气量小 ,是在超低温环境下使用的良好胶粘剂

EA-01电应力疏散胶的研制

本文报导了用于热缩电缆附件中间连接的一种新型填充段电应力疏散胶的配方，研究了电性能调节剂，增粘剂，填料，氨酸橡胶等对产品性能的影响．

Cys-92, Cys-95, and the C-terminal 12 residues of the Vibrio harveyi ferric uptake regulator (Fur) are functionally inessential

Ferric uptake regulator (Fur) is a global regulator involved in multiple aspects of bacterial life. The gene encoding the Vibrio harveyi Fur (Fur(vh)) was cloned from a pathogenic V. harveyi strain isolated from diseased fish. Furvh shares 77% overall sequence identity with the Escherichia coli Fur (Fur(Ec)) and could complement a mutant of Fur(Ec). Like Fur(Ec), Fur(Vh), possesses two cysteine residues at positions 92 and 95, yet unlike Fur(Ec), in which these cysteine residues constitute part of the metal ion coordination site and hence are vital to the repressor activity, C92 and C95 of Fur(Vh) proved to be functionally inessential. Further study identified a Vibrio Fur signature sequence, which is preserved in all the ten Vibrio Fur proteins that have been discovered to date but in none of the non-vibrio Fur proteins. Site-directed and random mutation analyses of the signature residues, the cysteine residues, and seven highly charged amino acid residues indicated that D9, H32, C137, and K138 of Fur(vh) are functionally important but D9, C137, and K138 can be replaced by more than one functional substitutes. Systematic deletion analysis demonstrated that the C-terminal 12 residues of Fur(Vh) are functionally inessential. These results (i) indicated that the activation mechanism, or certain aspects of which, of Fur(Vh) is possibly different from that of Fur(Ec); and (ii) suggested that it is not very likely that the C-terminal 12 residues play any significant role in the activation or stability of Fur(Vh); and (iii) provided insights into the potential function of the local structure involving C137 and K138.