成都奥力公司率53人考察团赴德国埃森国际焊接与切割展会

九月，秋高气爽的日子，同时也是“第十六届德国埃森国际焊接与切割展览会”盛大举办的日子。这个极负盛名的国际展会每四年举行一次，享誉全球，吸引着来自世界知名的焊接与切割生产厂商、用户集聚德国埃森，共同分享世界先进的焊接与切割技术。本届德国埃森国际焊接展于9月12—17日在德国埃森市举办。     

LiFePO4基正极材料容量的温度敏感特性及交流阻抗谱研究

采用原位碳包覆法制备了锂离子二次电池用LiFePO4／C复合正极材料。考察了环境温度对LiFePO4/C电池容量的影响，得到容量与绝对温度之间符合Arrhenius关系。运用交流阻抗谱分析了温度与电池电化学特性的关系，并对电极基于电荷和质量传递控制过程给出了一种新的模拟等效电路，通过Zview拟合软件得到了各个模拟元件的数值及变化趋势，从而定量地解释LiFePO4／C复合电极容量与温度的关系。     

粉煤灰基混凝剂的制备及在大麻废水中的应用

采用酸溶法以粉煤灰为基础原料 ,通过添加一定量的硫铁矿烧渣 ,制备成粉煤灰基复合混凝剂 ,确定了最佳工艺条件 .实验结果表明 ,影响混凝剂制备的主要因素是粉煤灰与硫铁矿渣的质量比、酸用量、浸取时间和温度 .此混凝剂对大麻废水中 CODcr去除率达 88% ,色度去除率可达 96.6%以上 ,具有沉淀快和污泥体积小等优点 .     

磁化水配料对TiO2压敏陶瓷电性能和微观结构的影响

研究了使用磁化水配料对TiO2压敏陶瓷电性能和微观结构的影响。电性能测量及SEM和XRD微观结构分析结果表明：磁化水配料制备的TiO2压敏电阻具有较低的压敏电压和较高的非线性指数α。材料的主晶相为金红石相，由Ce,Si,Ti组成的Perrierite第二相均匀分布在晶界区域。因此，采用磁化水配料可以改善材料的工艺性能和陶瓷烧结体的微观结构，从而提高元件的电性能。     

环戊烯催化氧化合成戊二醛及其动力学

对在非水溶剂存在下过氧化氢一步催化氧化环戊烯制备戊二醛过程中的催化体系进行了研究。考察了具有脱水功能的Ｂ２Ｏ３的作用及用量，确立了具有优良催化性能的催化体系ＷＯ３－Ｂ２Ｏ３；实验测定了反应动力学数据，采用非线性回归Ｐｏｗｅｌ共扼法求得了反应动力学方程。在推荐的催化剂体系和工艺条件下，环戊烯转化率６７％，戊二醛收率６３％，选择性９１％。     

锂离子电池固态聚合物电解质研究进展

电解质是制备高功率密度和高能量密度、长循环寿命的锂离子电池的重要材料之一,而聚合物电解质是实现全固态锂离子电池的关键技术.总结近几年来为提高聚合物电解质电导率所作研究的新进展,并提出了今后的研究方向.     

Characteristics of electrical responsive chitosan/polyallylamine interpenetrating polymer network hydrogel

An interpenetrating polymer network (IPN) hydrogel composed of chitosan and polyallylamine exhibited electric‐sensitive behavior. The chitosan/polyallylamine IPN hydrogel was synthesized by radical polymerization using 2,2‐dimethoxy‐2‐phenylacetophenone (DMPAP) and methylene bisacrylicamide (MBAAm) as initiator and crosslinker, respectively. The swelling behavior of the IPN was studied by immersion of the gel samples in aqueous NaCl solutions at various concentrations and pHs. The swelling ratio decreased with increasing concentration and pH of electrolyte solution. The stimuli response of the IPN hydrogel in electric fields was also investigated. When a swollen the IPN was placed between a pair of electrodes, the IPN exhibited bending behavior in response to the applied electric field. The IPN also showed stepwise bending behavior depending on the electric stimulus. In addition, thermal properties of the IPN were investigated by differential scanning calorimetry (DSC) and dielectric analysis (DEA). © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2290–2295, 2002     

Pb2+ binding by polyaspartyl polymers and their application to Pb2+ removal from glycyrrhizin

Polyaspartate is an excellent Pb²⁺‐binding agent in comparison with some polyaspartamide derivatives with different side chains, in that it possesses a higher Pb²⁺ uptake and a lower Pb²⁺ equilibrium concentration. Equilibrium sorption data for Pb²⁺ on polyaspartate can be well fitted with the Freundlich and Langmuir models. Experimental results show that a crosslinked polyaspartate hydrogel is superior to poly(acrylic acid)‐based resins and polystyrene‐based chelating resins. IR spectra and X‐ray photoelectron spectra reveal that the polyaspartate hydrogel binds Pb²⁺ by both an ion‐exchange mechanism and a chelating mechanism. The polyaspartate hydrogel is also an effective agent for the removal of Pb²⁺ from glycyrrhizin. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 2215–2220, 2005     

Miscibility and morphology in crystalline/amorphous blends of poly(caprolactone)/poly(4-vinylphenol) as studied by DSC, FTIR, and C solid state NMR

The miscibility and morphology of poly(caprolactone) (PCL) and poly (4-vinylphenol) (PVPh) blends were investigated by using differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy and ¹³C solid state nuclear magnetic resonance (NMR) spectroscopy. The DSC results indicate that PCL is miscible with PVPh. FTIR studies reveal that hydrogen bonding exists between the hydroxyl groups of PVPh and the carbonyl groups of PCL. ¹³C cross polarization (CP)/magic angle spinning (MAS)/dipolar decoupling (DD) spectra of the blends show a 1 ppm downfield shifting of ¹³C resonance of PVPh hydroxyl-substituted carbons and PCL carbonyl carbons with increasing PCL content. Both FTIR and NMR give evidence of inter-molecular hydrogen bonding within the blends. The proton spin-lattice relaxation in the laboratory frame, T₁(H), and in the rotating frame, T_1ρ(H), were studied as a function of the blend composition. The T₁(H) results are in good agreement with thermal analysis; i.e. the blends are completely homogeneous on the scale of 50-80 nm. The T_1ρ(H) results indicate that PCL in the blends has both crystalline and amorphous phases. The amorphous PCL phase is miscible with PVPh, but the PCL crystal domain size is probably larger than the spin-diffusion path length within the T_1ρ(H) time-frame, i.e. larger than 2-4 nm. The mobility differences between the crystalline and amorphous phases of PCL are clearly visible from the T_1ρ(H) data.