甲醇与乙醇一步合成异丁醛用CuO-ZnO/Al2O3催化剂

在ＣｕＯ－ＺｎＯ／Ａｌ２Ｏ３催化剂上，甲醇与乙醇在常压和２１０￣３６０℃温度下一步反应合成异丁醛。利用正交设计方法，研究了ＣｕＯ－ＺｎＯ／Ａｌ２Ｏ３体系催化剂组成和制备条件等因素对催化剂催化性能的影响。结果表明，催化剂中ＣｕＯ含量对催化剂的催化活性影响最大，而ＺｎＯ含量则主要影响催化剂对异丁醛的选择性。催化剂制备条件，如沉淀温度、陈化时间等，也不同程度也影响催化剂的催化性能。ＸＲＤ和ＢＥＴ表征结果     

Optimization of sucrose ethanol fermentation for K,Na, Ca,and cu metal contents

The effect of the trace metals Cu, K, Na, and Ca, separately or in mixture, on fermentation time, ethanol production rate, and cell growth in the fermentation of synthetic media containing sucrose is discussed. The results are related to the range of contents found in raw materials, molasses and raisins, in order to determine their optimum concentrations for alcohol production.     

分子筛修饰电极的研究（Ⅰ）──氢醌／醌电对在分子筛修饰电极上的电化学行为

考察了中性分子电对Ｈ_２Ｑ／Ｑ在１３Ｘ型分子筛修饰电极上的电化学行为。发现Ｈ_２Ｑ／Ｑ电对在修饰电极上电响应迅速，为双电子可逆反应，不受溶液温度及电极与溶液相对运动的影响，而与溶液的ｐＨ值有关。当ｐＨ≤２．０时，修饰电极对Ｈ_２Ｑ／Ｑ电对的氧化／还原有明显的催化作用．     

Structural and electrochemical studies of annealed LiNiVO4 thin films

We prepared stoichiometric lithium nickel vanadate amorphous thin films by using r.f. magnetron sputtering under controlled oxygen partial pressure. The amorphous films were heated at various temperatures, 300–600 °C, for 8 h. The as‐deposited and annealed thin films were characterized by Rutherford backscattering spectroscopy, nuclear reaction analysis, Auger electron spectroscopy, X‐ray diffraction, scanning electron microscopy and atomic force microscopy. The electrochemical behavior of the various films was studied by the galvanostatic method. The cells were tested in a liquid electrolyte at room temperature, with lithium metal used as the counter and reference electrode. The best electrochemical storage value was obtained with the thin film annealed at 300 °C, which showed superior capacity and small capacity loss during cycling. Copyright © 2007 John Wiley & Sons, Ltd.     

聚合物-Ni(II)膜电极的研究

Ni(Ⅱ)离子可与聚8羟基喹啉、聚邻氨基酚、聚邻苯二胺和聚苯胺络合。聚合物-Ni(Ⅱ)膜电极的循环伏安图有明显的氧化还原蜂, 和彼此相似的电化学特性。聚8羟基喹啉膜(聚邻氨基酚, 聚邻苯二胺)可用以交换Ni(Ⅱ)与H~+离子和分离Ni(Ⅱ)、Co(Ⅱ)和Fe(Ⅱ)离子。     

Application of recoverable nanosized palladium(0) catalyst in Sonogashira reaction

In the absence of ligand, copper and amine, a recoverable nanoparticle palladium(0) catalyzed Sonogashira reaction of aryl iodides and bromides with terminal alkynes was developed. The protocol involved the use of an environmental-friendly reaction system with ethanol as the solvent, potassium carbonate as a base, and poly(vinylpyrrolidone) (PVP) supported nanosized palladium metal colloids as the catalyst. The palladium metal was recovered and recycled by a simple decantation of the reaction solution and used for eight consecutive trials without significant loss of its reactivity.     

碳糊电极阳极溶出法测定中药甘草中桑色素

用碳糊电极阳极溶出法测定桑色素的含量。在0.15mol·L-1NH4Cl 氨水缓冲溶液的介质中富集120s,桑色素在+0.10V(vs.SCE)左右出现阳极溶出峰。其峰电流的大小与桑色素的浓度呈线性关系。线性范围为4.00×10-6～1.40×10-5mol·L-1,相关系数为0.9996,检出限可达1.00×10-6mol·L-1,回收率为99.87%～102.01%。此法不用汞电极,灵敏度高,操作方便、快捷,成功地用于甘草提取物中桑色素的测定。     

香蕉组织膜草酸电极的研究

将香焦组织与氧电极偶合,制成了草酸生物组织电极。在静态和流动条件下,测得电极的线性响应范围分别为8.8×10~(-5)～6.3×10~(-4)mol/L和5.0×10~(-5)～1.8×10~(-3)mol/L,二者的相关系数均为0.9998。研究了介质条件、pH、温度、流速、取样量和固定化等条件的影响。测定了电极的选择性和使用寿命等性能。计算了该实验条件下酶反应的米氏常数。采用静态法和流动注射法测得7份草酸标液的平均回收率分别为98.4％和98.9％。电极已用于一些食品中草酸的测定,所得结果与文献报道基本一致。     

对甲苯磺酸铜的电化学表征

合成了对甲苯磺酸铜,用X光单晶衍射确定了其结构.实验结果表明,该盐容易脱除全部结晶水,在空气中不潮解.分别测定了对甲苯磺酸铜(Cu(p-OTs)2)在H2O、CH3OH和DMF中的电化学参数.实验结果表明Cu(p-OTs)2在不同溶剂中的反应机理各异. Cu(II)的电化学还原在H2O中是分两步进行,而在CH3OH和DMF中的电化学还原是一步两电子过程.对实验结果进行了分析讨论.     

Re-Evaluation of the Activity Coefficients of Aqueous Hydrochloric Acid Solutions up to a Molality of 2.0 Using Two-Parameter Hückel and Pitzer Equations. Part I. Results at 25°C

Simple two-parameter Hückel and Pitzer equations were used for the calculation of the activity coefficients of aqueous hydrochloric acid at 25°C up to a molality of 2.0 mol-kg^–1. The data obtained by Harned and Ehlers^(12,13) from galvanic cells without liquid junction were used in the analysis and the parameters obtained were compared to those obtained from all reliable data presented in the literature for HCl at this temperature. A good agreement between the parameters was always observed. The activity coefficients obtained by the new equations were compared to those suggested by Robinson and Stokes,⁽⁸⁾ Hamer and Wu,⁽¹⁾ and Pitzer and Mayorga,⁽⁹⁾ and good agreement was also found. The data from the most important literature data sets for HCl were also predicted using the new activity coefficient equations, and the magnitude of the resulting errors was close to the precision of the measurements, the errors forming an almost random pattern for all data sets.