低温反应制备高纯度纳米BN包覆Al2O3和ZrO2粉体

硼酸和尿素在氮气中于650℃反应,生成t-BN-Al2O3和t-BN-ZrO2纳米包覆粉.IR分析表明,反应产物中含CH2和CN基团的杂质属尿素缩聚的复杂产物,经450℃煅烧即可除去.硼酸和尿素完全反应,得到纯净的纳米复合粉体.BN产率大于99%,在复合粉中的含量与计算值吻合.     

含氧膦结构的可溶性感光聚酰亚胺合成与表征

聚酰亚胺(PI)是一类综合性能优异的功能性材料,广泛应用于航天、航空及电子工业等领域[1].感光聚酰亚胺可以采用光刻工艺,大大简化了其应用加工程序[2,3],因而备受人们所青睐.含查尔酮结构的聚合物对UV辐射敏感度高和化学稳定性好,最近被广泛的研究和应用[4～7].主链含查尔酮结     

Direct Synthesis, Crystal Structure and Thermal Kinetics of Supramolecular Complex [Co（H2O）6]·（Hnip）2·（H2nip）2·（DMA）2·（H2O）8 （nip=5-nitroisophthalate, DMA=CH3NHCH3）

The crystal of [Co（H2O）6]·（Hnip）2·（H2nip）2·（OMA）2·（H2O）8 has been cultured using direct method and characterized by X-ray single crystal diffractometry, elemental analysis and FTIR spectroscopy. It crystallizes in triclinic system, P-1 space group with the cell parameters of a=0.7012（1） nm, b=1.1378（2） nm, c=1.6612（3） nm, α= 84.92（3）°, β=85.19（3）°, γ=85.91（3）°, V= 1.3128（5） nm^3, Z=1, Dc= 1.573 g·cm^-3. Final R indices [1〉2σ（I）] are： R1 =0.0279, wR2=0.0765 while R indices for all data are： R1 =0.0327, wR2=0.0806. The Co coordination octahadra are each surrounded by two Hnip, two H2nip, two DMA and eight water molecules that are linked by hydrogen bonds and π-π stacking interactions. Thermal analyses of DSC and TG-DTG have been performed on the complex to predict its thermal decomposition mechanism and determine the most probable kinetic model function using Kissinger, Ozawa, integral and differential methods.     

SNAP-tag蛋白标签技术与荧光分析法在蛋白原位分析中的联合应用

为将生物体内微观的蛋白行为可视化并以宏观信号呈现出来对蛋白进行实时、动态分析，借助SNAP-tag蛋白标签技术与有机小分子荧光染料，构建了一系列用于活细胞内实时监测目标蛋白的免洗荧光探针。标签蛋白SNAP-tag能够特异性识别探针中的苄基鸟嘌呤，从而使目标蛋白共价连接上荧光团（萘酰亚胺），携带上荧光信使。此外，由于萘酰亚胺从水环境中被牵引至SNAP-tag蛋白的疏水空腔，其荧光信号呈现出2~13倍的增强。通过SNAP-tag标签蛋白与目标蛋白的融合，该荧光探针实现了对活细胞内线粒体蛋白CoX8A及核内蛋白H2B特异性识别，在免洗条件下完成了对目标蛋白的实时追踪及原位分析。     

Electrochemical Characteristics of Mg0.9Ti0.1-xZrxNi （x=0.02, 0.04, 0.06） Alloys

Mg-based hydrogen storage alloys Mg0.9Ti0.1-xZrxNi (x=0.02, 0.04, 0.06) were successfully prepared by means of mechanical alloying (MA). The effects of Zr addition on the discharge capacity and the cycle performance of the Mg-based electrodes were also studied. It was found that the discharge capacities were improved with addition of a small amount of Zr and the cycle performances of the alloy were stabilized with the addition of Ti. The effects of surface modification or coating on the properties of Mg0.9Ti0.06Zr0.04Ni were also studied. The results indicated that coating with graphite improved both the discharge capacity and cycle life of the amorphous Mg0.9Ti0.06Zr0.04Ni electrode.     

Ni添加对0.4Zr0.1V1.1Mn0.5Cr0.1合金的相结构和电化学性能的影响

本文通过XRD、SEM、EDS研究了Ti_0.4Zr_0.1V_1.1Mn_0.5Cr_0.1Ni_x(x=0，0.2，0.4，0.6，0.8)合金的相结构和电化学性能。该合金系由BCC结构的V基固溶体主相和六方结构的C14 Laves第二相组成，Ni能够促进第二相的生成，Ni含量的增加导致了各相中的化学组成和晶格参数的变化，并通过电化学方法研究了Ni含量对_0.4Zr_0.1V_1.1Mn_0.5Cr_0.1合金电极的最大放电容量、自放电性能、高倍率放电性能、循环稳定性能等的影响。     

纳米硫化镉修饰玻碳电极对血红蛋白的直接电化学和生物电催化

0IntroductionStudies of direct electrochemistry of proteins orenzymes at electrodes can serve as a basis for build-ing electrochemical biosensors,enzymatic bioreactors,and biomedical devices[1].This approach simplifiessuch devices without using mediators and is of partic-ular significance for fabricating the third generationbiosensors[2].For example,if a protein or enzyme im-mobilized on electrode surface is capable of directelectron transfer without loss of bioactivities,it can beused in the …     

高中有机化学教材“烃类化合物”的国际比较研究

基于闫春更等建立的二维度四指标教材难度微观评价模型，重点对中国、美国、新加坡、澳大利亚、日本、英国的高中化学教材中"烃类化合物"内容的整合广度、表征深度进行测评和比较。研究发现6国教材内容的整合广度整体上差异不大，但其表征深度差异明显；美国教材注重学生认识物质的思路和方法的渗透，日本教材注重基本知识与技能的掌握，中国教材将概念诠释与样例分析相融合；英国、新加坡、美国教材注重情境推理或比较等信息处理策略的运用，对学习者学习的引导性较强。     

再谈磷的同素异形体(1)——块体磷的同素异形体

结合最新研究进展，全面介绍了块体状磷的同素异形体——白磷、红磷、黑磷等，包括存在、组成、性质、结构、制备、应用等，同时明确了紫磷、希拖夫磷、灰磷、褐磷等概念，提出了大学本科化学教学的建议。     

Vibrational Spectroscopic Study on Ion Solvation and Association of Lithium Perchlorate in 4-Methoxymethyl-ethylene Carbonate

Solvation interaction and ion association in solutions of lithium perchlorate/4-methoxymethyl-ethylene carbonate （MEC） have been studied by using Infrared and Raman spectra as a function of concentration of lithium perchlorate. The splitting of ring deformation band and ring ether asymmetric stretching band, and the change of carbonyl stretching band suggest that there should be a strong interaction between Li^＋ and the solvent molecules, and the site of solvation should be the oxygen atom of carbonyl group. The apparent solvation number of Li^＋ was calculated by using band fitting technique. The solvation number was decreased from 3.3 to 1.1 with increasing the concentration of LiClO4/MEC solutions. On the other hand, the band fitting for the ClO4^- band revealed the presence of contact ion pair, and free ClO4^- anion in the concentrated solutions.