LiCoO2中锂离子固相扩散系数随循环次数的变化

The solid diffusion coefficient of lithium-ion in LiCoO₂ cathode material has been investigated by the capacity intermittent titration technique (CITT) at different voltages and at different charge/discharge cycles. By SEM, XRD and FTIR techniques, the structure of LiCoO₂ was studied before and after charge-discharge cycles, and the relationship between solid diffusion coefficient and crystal structure was further discussed. CITT results show that the value of Li⁺ solid diffusion coefficient of LiCoO₂ is about 10^-12 cm²·s^-1. During the whole charge-discharge cycles, the Li⁺ solid diffusion coefficient decreased within the voltage of 4.0～4.3 V, which is attributed to the change of the structure of LiCoO₂.     

密度泛函理论研究DMSO溶剂中邻-二(吡咯-2-甲酰胺基)亚苯与卤素阴离子间的超分子作用

采用混合密度泛函B3LYP方法, 在LANL2DZ水平上优化DMSO溶剂中邻-二(吡咯-2-甲酰胺基)亚苯(PFP)及其卤素阴离子复合物的几何构型, 从几何结构参数、电荷布居、前线轨道、结合能以及热力学参数等角度探讨复合物形成过程中主体分子的构象变化以及主客体间的超分子作用. 研究结果表明, 邻-二(吡咯-2-甲酰胺基)亚苯识别卤素阴离子是一个自发过程. 复合阴离子过程中, 两者的前线轨道发生作用, 电子容易从卤素阴离子的HOMO向主体分子的LUMO转移. 在所形成的四种复合物PFP:X^－(X^－＝F^－, Cl^－, Br^－, I^－)中, 以PFP:F^－最稳定, 与文献报道邻-二(吡咯-2-甲酰胺基)亚苯识别卤素阴离子能力的实验结果相一致. 设计合成含多个吡咯酰胺基团、并能形成合适“杯口”大小的主体化合物, 将增强对卤素阴离子的识别能力.     

火焰原子吸收法测定鸡尾木中无机元素的含量

鸡尾木(ExcoecariaVenenataS.LeeetF.N.Wei)属大戟科,海漆属,为民间药用珍贵植物,用于治疗牛皮癣、慢性湿疹等,疗效颇佳[1]。鸡尾木中无机元素,尤其是医学微量元素的测定对其药理效的研究有重要的参考价值。1　实验部分1 1　仪器及试剂TAS 986原子吸收分光光度计(北京普析通用仪器有限责任公司);空心阴极灯:Fe、Cu、Ni、Cr、Cd、Zn、Co、Ba、Ca(北京瑞利普光电器厂);Mg、Pb(北京真空电子技术总公司);Mn(北京市朝阳天宫电器厂);AdventurerTM电子天平(奥豪斯国际贸易〈上海〉有限公司)。标准储备液:配制Zn2+、Mg2+、Fe3+、Mn2…     

Investigation of 2-[(<Emphasis Type="Italic">E</Emphasis>)-2-(4-diethylaminophenyl)-1-ethenyl]-1,3,3-trimethyl-3H-indolium as a new highly sensitive reagent for the spectrophotometric determination of nitrophenols

A new, simple, rapid, and sensitive spectrophotometric method has been developed for the determination of nitrophenols [picric acid (PA); dinitrophenols (DNP)] in wastewater samples. The method is based on the reaction of nitrophenols with 2-[(E)-2-(4-diethylaminophenyl)-1-ethenyl]-1,3,3-trimethyl-3 H-indolium chloride reagent to form the colored ion associates, which are extracted by organic solvents. The molar absorptivity of the ion associates of PA with the investigated reagent ranges from 8.3×10⁴ to 11.3×10⁴ L mol^–1 cm^–1, depending on the extractant. Because only PA is extracted in an acidic medium with the investigated reagent, but both PA and DNP are extracted in an alkaline medium, it is possible to determine both substances in a mixture. Appropriate reaction conditions have been established. The absorbance of the colored extracts obeys Beers law in the range of 0.04–4.58 mg L^–1 PA, 1.0–18.4 mg L^–1 2,4-DNP and 1.2–14.7 mg L^–1 2,6-DNP, respectively. The limit of detections, calculated from a blank test (n=10; P=0.95), are 0.05 mg L^–1 PA, 0.9 mg L^–1 (2,4-DNP), and 1.1 mg L^–1 (2,6-DNP), respectively.     

Thermal evolution of ferromagnetic metallic glasses

A traditional TG apparatus was modified by placing two permanent magnets producing a controlled magnetic field (TG(M): Magneto Thermogravimetry). This technique proved to be useful to study both structural relaxation and crystallisation of ferromagnetic metallic glasses. Results obtained for the amorphous alloys Fe₄₀Ni₄₀P₁₄B₆ and Fe_62.5Co₆Ni_7.5Zr₆Nb₂Cu₁B₁₅, are reported in this paper. Structural relaxation can be evaluated by measuring changes in Curie temperature induced by thermal treatments. Crystallisation in TG(M) is detected through a change in the measured apparent mass (difference between the sample mass and magnetic force driving it upward). These results were confirmed by DSC analysis. Whether the obtained crystalline phase is ferromagnetic, it can be identified through its Curie temperature, measured by TG(M). In fact the value of 770°C measured as Curie temperature of crystallised Fe_62.5Co₆Ni_7.5Zr₆Nb₂Cu₁B₁₅led to conclude that the only ferromagnetic crystalline phase is a-Fe. These hypothesis was confirmed by XRD analysis, showing that the first crystallisation yields to a-Fe nanocrystals. This revised version was published online in July 2006 with corrections to the Cover Date.     

WS2 超细粉体的固相法合成

WS2 超细粉体的固相法合成;WS2;固相反应;过硫系数;高能球磨;粒度     

四（五氟化苯基）卟啉氯化铁选择催化氧化超临界丙烷的反应机理

 以BHT为自由基捕捉剂，研究了四（五氟化苯基）卟啉氯化铁（Ⅲ）将超临界丙烷高选择性催化氧化为丙醇的反应机理．通过GC－MS分析发现，反应产物中有PBHT，故可认为在超临界丙烷氧化反应过程中有丙基自由基存在，初步推断反应涉及自由基机理．同时发现高浓度BHT抑制反应，低浓度BHT促进反应的现象，而以戊烷为底物时没有促进作用．这是由于BHT的位阻效应所致．并对BHT存在时超临界丙烷氧化反应机理进行了初步的推断．     

可溶导电聚苯胺的合成及其性能研究

以十二烷基苯磺酸（ＤＢＳＡ）为乳化剂和掺杂剂，采用水一油二相乳液聚合物方法对苯胺进行合成，制备出高溶解性和高电导率的ＰＡｎ，通过ｘ－射线，电镜分析和热重分析对产物的结构和性能进行了研究。结果表明，该法合成的导电性ＰＡｎ具有较高的特性粘度，溶解性，耐热性及结晶度，与非极性溶剂－表面活性剂－水三相体系聚合产物结果相似，透射电镜显示水乳液聚合产物呈较规则的纤维状取向排列。     

两种荧光LB膜的制备和光谱性能

制取了４－二氰基亚甲基－２－甲基－６－对二甲胺基苯乙烯基－４Ｈ－吡喃（ＤＣＭ）和１，２－双（５－甲基苯并恶唑）基乙烯（ＤＴ）两种荧光分子的ＬＢ膜以及两者的混合膜，以吸收光谱和荧光光谱探讨了膜中分子的构型，微环境，发光性能等特征，发现在ＬＢ膜的缀密排布环境中ＤＣＭ顺式构型的含量较之在溶液中大为增加。