苯二甲酰基桥联铁硫配合物［（μ－RS）Fe_2（CO）_6］_2（μ－OCC_6

通过由Ｆｅ３（ＣＯ）１２、ＲＳＨ和Ｅｔ３Ｎ所形成的［（μ－ＣＯ）（μ－ＲＳ）Ｆｅ２（ＣＯ）６］Ｅｔ３ＮＨ于室温下分别与对或间苯二甲酰氯的原位反应，首次合成６个结构新颖的苯二甲酰基桥联铁硫配合物［（μ－ＲＳ）·Ｆｅ２（ＣＯ）６］２（μ－ｐ－ＯＣＣ６Ｈ４ＣＯ－ｐ－μ）（Ｒ＝Ｅｔ，ｎ－Ｂｕ，ｔ－Ｂｕ）以及［（μ－ＲＳ）Ｆｅ２（ＣＯ）６］２（μ－ｍ－ＯＣＣ６Ｈ４ＣＯ－ｍ－μ）（Ｒ＝ｎ－Ｐｒ，ｎ－Ｂｕ，ｔ－Ｂｕ）。经元素分析、ＩＲ光谱及１ＨＮＭＲ表征了它们的结构，并讨论了产物的生成过程。此外，还提出了合成对苯二甲酰氯的一种新方法。     

Application of thermal analysis to carbon black-elastomer systems

In this study a relationship between the surface and textural properties of carbon blacks and the gasification process induced thermally in air is noted. A temperature jump method was used to follow the gasification in air and to establish the relevant Arrhenius parameters. This can be associated with the activity of ‘basal’ plane carbon atoms as well as ‘edge’ carbon atoms at the surface. This is based on a model of carbon black structure consisting of the irregular packing of small graphite carbon structures. The carbon black surface was measured using a single measurement of adsorption based essentially on the BET volumetric method. The carbon black surface had a rate of oxidation per unit are which clearly indicated that the lower area carbon blacks had a predominately active area of ‘edge’ atoms at the surface while the surface of the higher area carbon blacks had a predominate amount of ‘basal’ plane graphite carbon atoms.     

吲哚衍生物与花生酸混合LB膜的制备及结构研究

本文将3-三氰基乙烯基-N-十六烷基吲哚与花生酸混合制成单分子膜。不同摩尔比混合膜的π-A曲线均出现平台,表明膜压缩过程中分子排列相态发生变化。混合LB膜的紫外吸收光谱证明吲哚分子形成聚集体,X-射线衍射结果说明这种聚集体被夹带在花生酸的框架结构中。     

冠醚B15C5萃取分离锂同位素的阴离子效应

本文研究了B15C5冠醚萃取锂盐时,不同阴离子对体系的同位素分离效应的影响。结果表明,阴离子在冠醚萃取过程中不仅对萃取络合物的稳定性有显著影响,而且阴离子半径及软度越大时,萃取体系的锂同位素分离系数(α_(LI))也越大。     

An electrochemical investigation on (MoO<Subscript>3</Subscript>+PVP+PVA) nanobelts for lithium batteries

Molybdenum trioxide (MoO₃) xerogel films modified with poly(vinyl alcohol)+poly(vinyl pyrrolidone) (PVP+PVA) polyblends were obtained by ion-exchange method with sol-gel technique. Investigations were conducted using X-ray “diffractometry”, Fourier transform infrared spectroscopy, and cyclic voltammetry. The results show that the H atoms in polyblend are H-bonded with the O atoms in the Mo=O bonds of MoO₃ xerogel, which effectively shield the electrostatic interaction between MoO₃ interlayer and Li⁺ ions when MoO₃ xerogel is modified by the intercalation of (PVP+PVA). The reversibility of the insertion/extraction of Li⁺ ions is greatly improved by the modification with polyblend of MoO₃ nanocomposite films. MoO₃ and (PVP+PVA) _x MoO₃ (x = 0, 0.5) nanobelts were obtained by a simple hydrothermal process from MoO₃ sol. The electrochemical cells with configuration Li/(LiPF₆+EC+DMC)/MoO₃ modified by (PVP+PVA) were fabricated and their discharge profiles studied.     

Immobilization of Glucose Oxidase on Cellulose／Cellulose Acetate Membrane and its Detection by Scanning Electrochemical Microscope （SECM）

Cellulose/cellulose acetate membranes were prepared and functionalized by introducingamino group on it, and then immobilized the glucose oxidase (Gox) on the functionalizd membrane.SECM was applied for the detection of enzyme activity immobilized on the membrane.Immobilized biomolecules on such membranes was combined with analysis apparatus and can beused in bioassays.     

超声雾化进样微波诱导等离子体原子吸收光谱法测定银的某些影响因素研究

本文将超声雾化技术与MIP-AAS联用,以“L”型吸收管代替“T”型吸收管作为AAS测量的吸收池,采用水冷凝和浓H_2SO_4吸收相结合去溶,研究TUSN-MIP-AAS方法测银时的某些影响因素,讨论了微波前向功率,载气流速、去溶系统、溶液酸度、共存离子及易也离元素等对吸收信号的影响,本法所得的测银的特征浓度为0.01μg/ml(328.1nm)和0.03μg/ml(338.3nm),相对标准偏差为7.5％.     

Self-assembly of lanthanide mixed-carboxylates coordination polymers

Two new mixed-ligands lanthanide coordination polymers, [Ln(Ac)(ip)(H₂O)₂]·0.5H₂O (Ln=La (1); Ln=Eu (2); Ac=acetate; ip=isophthalate) have been synthesized under hydrothermal condition. Single-crystal X-ray analyses show that complexes 1 and 2 are three-dimensional structure in which lanthanide ions are bridged by monocarboxylate ligand, acetate or dicarboxylate ligand, isophthalate. And the central lanthanide ions, La³⁺ and Eu³⁺, are both nine-coordinate with oxygen atoms. The thermogravimetric analysis was carried out to examine the thermal stability of the title complexes. And the photoluminescence property of complex 2 was also investigated.     

Synthesis of silk-like FeS2/NiS2 hybrid nanocrystals with improved reversible oxygen catalytic performance in a Zn-air battery

The development of highly active and stable reversible oxygen electrocatalysts is crucial for improving the efficiency of metal-air battery devices. Herein, an efficient liquid exfoliation strategy was designed for producing silk-like FeS₂/NiS₂ hybrid nanocrystals with enhanced reversible oxygen catalytic performance that displayed excellent properties for Zn-air batteries. Because of the unique silk-like morphology and interface nanocrystal structure, they can catalyze the oxygen evolution reaction (OER) efficiently with a low overpotential of 233 mV at j = 10 mA cm^?2. This is an improvement from the recently reported catalysts in 1.0 M KOH. Meanwhile, the oxygen reduction reaction (ORR) activity of the silk-like FeS₂/NiS₂ hybrid nanocrystals showed an onset potential of 911 mV and a half-wave potential of 640 mV. In addition, the reversible oxygen electrode activity of the silk-like FeS₂/NiS₂ hybrid nanocrystals was calculated to be 0.823 V, based on the potential of the OER and ORR. Further, the homemade rechargeable Zn-air batteries using FeS₂/NiS₂ hybrid nanocrystals as the air-cathode displayed a high open-circuit voltage of 1.25 V for more than 17 h and an excellent rechargeable performance for 25 h. The solid Zn-air batteries exhibited an excellent rechargeable performance for 15 h. This study provided a new method for designing interface nanocrystals with a unique morphology for efficient multifunctional electrocatalysts in electrochemical reactions and renewable energy devices.