离子交换增强玻璃表面化学稳定性的研究

系统研究了化学钢化及盐溶液后处理对Na2O-CaO-SiO2玻璃表面化学稳定性的影响。详细考察了用熔融KNO3化学钢化的玻璃以及用适当盐溶液后处理的化学钢化玻璃,在受水侵蚀后R2O的沥滤量和失重以及受碱侵蚀后SiO2的溶出量和失重。结果表明,用熔融KNO3对玻璃进行钢化处理后,玻璃的耐水性和耐碱性均有明显下降。而将化学钢化的玻璃利用适当盐溶液处理后,可以改善钢化玻璃的化学稳定性,因而可以进一步提高化学钢化玻璃的使用性能和拓展其使用范围。     

Co-LsX催化苯乙烯生成环氧苯乙烷绿色合成工艺研究

采用离子交换法制备Co-LsX催化剂,分子筛经Co2+离子交换后,其骨架结构没有发生变化。考察了反应温度、反应时间、催化剂用量、溶剂加入量及氧气通入速率等因素对苯乙烯环氧化反应的影响。得出最佳工艺条件:反应温度100℃,反应时间6 h,Co-LsX与苯乙烯质量比为0.16,混合溶剂与苯乙烯体积比为5;V(O2)∶V(苯乙烯)=1.3 min-1。在此条件下苯乙烯转化率达到62.5%,环氧苯乙烷的选择性达到57.1%。催化剂经6次循环使用后活性和稳定性都比较好。     

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.     

Composite polymer electrolytes based on the low crosslinked copolymer of linear and hyperbranched polyurethanes

Low crosslinked copolymer of linear and hyperbranched polyurethane (CHPU) was prepared, and the ionic conductivities and thermal properties of the composite polymer electrolytes composed of CHPU and LiClO₄ were investigated. The FTIR and Raman spectra analysis indicated that the polyurethane copolymer could dissolve more lithium salt than the corresponding polymer electrolytes of the non crosslinked hyperbranched polyurethane, and showed higher conductivities. At salt concentration EO/Li = 4, the electrolyte CHPU30‐LiClO₄ reached its maximum conductivity, 1.51 × 10^?5 S cm^?1 at 25°C. DSC measurement was also used for the analysis of the thermal properties of polymer electrolytes. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3607–3613, 2007     

Thermodynamic assessment of MCl–YCl3 (M=Na,K, Rb,Cs) systems

Thermodynamic properties and phase diagrams of the MCl–YCl₃ (M=Na, K, Rb, Cs) systems were reassessed by using the CALPHAD method with the latest phase diagram data. A two-sublattice ionic solution model (M⁺)_P(Cl⁻, ${\mathrm{YCL}}_6^{3-}$, YCl₃)_Q reflecting the ionic behavior of the components was adopted to describe the liquid phase in the systems. A new set of optimized model parameters was found, and the calculated phase diagrams and enthalpies of mixing have good agreement with experimental data. The calculated liquidus near to YCl₃ side agrees much better with experimental data compared with previous work. In consideration of high and low temperature modifications as well as stability of intermediate compounds, Gibbs energies of formation of these compounds evaluated in the present work are more reasonable.     

D301树脂分离衣康酸的工艺研究

采用弱碱性阴离子交换树脂Ｄ３０１对发酵法生产的衣康酸进行了分离研究。通过静态交换实验，研究了Ｄ３０１树脂对衣康酸的静态交换动力学，确定了传质机制和影响因素；通过动态交换实验，研究了以硫酸为洗脱剂，以氨水为再生剂的工艺过程，确定了主要工艺参数。     

离子膜使用过程中起泡的原因及危害

分析并列举了离子交换膜在使用过程中鼓泡的原因，阳极液质量浓度；pH值；阴极液质量浓度；电流密度；开停车及盐水质量等因素都可以造成膜鼓泡，形成针孔。提出了相应的预防措施。     

配位离子液体［3（CH3CH2）4N+Cl-·（NH2）2CO］的合成及表征

采用尿素和氯化四乙基铵为原料，合成了一种新型的配位离子液体，并通过红外和X－射线粉末衍射对其结构进行了表征。结果表明，尿素和氯化四乙基铵发生反应，使得原来尿素羰基峰由1690.72cm－1转移到了1619.10cm－1。由X－射线粉末衍射图可以看出，在2θ = 30.37°处有新的衍射峰。通过差热－热重分析，配位离子液体在室温到250℃可以稳定存在，与其他有机溶剂相比具有良好的稳定性。     

Experimental and theoretical analysis of the operation of a natural gas cogeneration system using a polymer exchange membrane fuel cell

This paper reports experimental and numerical results of an investigation of five identical cogeneration systems using PEM (Polymer Exchange Membrane) fuel cells and running on natural gas. The natural gas is reformed locally to produce hydrogen. The accuracy of numerical results is validated by comparison with experimental data and the system performances are analysed in terms of electrical, thermal and total efficiencies. It appears that the energetic performances are low, particularly at low current. Simple solutions for enhancing the system electrical performances by modifying control laws are proposed.     

Preparation of nanosize Pt clusters using ion exchange of Pt(NH3) 4 2+ inside mesoporous channel of MCM-41

Mesoporous molecular sieve MCM-41 with a Si/Al ratio of 35 was obtained by hydrothermal synthesis using a gel mixture with a molar composition of 6 SiO₂0.1 Al₂O₃1 hexadecyltrimethylammonium chloride 0.25 dodecyltrimethylammonium bromide 0.25 tetrapropylammonium bromide0.15 (NH₄)₂O1.5 Na₂O300 H₂O. The MCM-41 sample was calcined in O₂ flow at 813 K and subsequently ion exchanged with Ca²⁺. A small Pt cluster has been supported on the MCM-41 sample following a procedure using ion exchange of Pt(NH₃) ₄ ²⁺ . The Pt(NH₃) ₄ ²⁺ ion supported on MCM-41 has been activated in O₂ flow at 593 K and subsequently reduced with Fh flow at 573 K, in the same way used for the preparation of a Pt cluster entrapped inside the supercage of zeolite NaY. The resulting Pt cluster supported on the MCM-41 shows hydrogen chemisorption oftotal two H atoms per Pt at 296 K (based on the total amount of Pt) and high catalytic activity for hydrogenolysis of ethane. The chemical shift in¹²⁹Xe NMR spectroscopy of adsorbed xenon indicates that the Pt cluster is located inside the mesoporous molecular sieve.