热传导对气-液射流界面不稳定性的作用机理研究

研究了平面分层气-液射流在非线性温度分布条件下的界面不稳定性性质.考虑了气体的可压缩性、液体的粘性、以及气体热导率和密度随温度变化等事实.并应用正则模态方法将问题转化为四阶变系数常微分方程,用数值积分和多重打靶法对模型的空间模式进行了计算,研究了不稳定模态随各物理参量的变化趋势.计算表明模型所体现的不稳定性特征与其它模型的计算结果是一致的.同时计算还得出气体和液体的温差越小、雷诺数越大、热导率变大均将有利于液体射流有效雾化的结果.该结论与HJE.Co.Inc(Glens Falls,NY,USA)的实验数据是定性吻合的.     

苯对N,N-二甲基甲酰胺化合物1H NMR的影响研究

本文研究了N,N-二甲基甲酰胺(DMF)在四氯化碳和苯混合溶剂中的¹H NMR。观察到N,N-二甲基甲酰胺(DMF)分子中两个甲基和混合溶剂中苯的共振吸收峰的化学位移随苯的摩尔分数增加而逐渐移向高场,而且两个甲基共振吸收峰向高场移动的程度不同,α甲基较β甲基为甚。DMF分子中两个甲基和混合溶剂中苯的化学位移可以用线性方程表示(δ=A+Bx),这里x是混合溶剂中苯的摩尔分数。相关系数R接近于-1。     

苯对N,N-二甲基甲酰胺化合物~1H NMR的影响研究

本文研究了N,N-二甲基甲酰胺(DMF)在四氯化碳和苯混合溶剂中的~1H NMR。观察到N,N-二甲基甲酰胺(DMF)分子中两个甲基和混合溶剂中苯的共振吸收峰的化学位移随苯的摩尔分数增加而逐渐移向高场,而且两个甲基共振吸收峰向高场移动的程度不同,α甲基较β甲基为甚。DMF分子中两个甲基和混合溶剂中苯的化学位移可以用线性方程表示(δ=A+Bx),这里x是混合溶剂中苯的摩尔分数。相关系数R接近于-1。     

F−(H2O)+CH3I配体交换反应动力学

本文介绍F^?(H₂O)+CH₃I→[FCH₃I]^?+H₂O在交叉分子束碰撞能量0.3∽2.6 eV的配体交换动力学成像结果. 产物的动能受到弱键结合配合物的稳定性的影响,大量水分子的内部激发不利于中间物有效的能量重新分配,随着碰撞增加,低动能受到抑制. 在0.3 eV时,内部亲核取代非常重要,为形成I^?和I^?(H₂O)的竞争性亲核取代途径提供了依据.     

Edge-enriched graphene with boron and nitrogen co-doping for enhanced oxygen reduction reaction

Carbon-based electrocatalysts for oxygen reduction reaction (ORR), especially in anion exchange membrane fuel cells (AEMFCs), have received a lot of attention because they exhibit excellent stability and are comparable to commercial Pt/C catalysts. Currently, to maximize the catalytic activity of carbon-based electrocatalysts, there are two major strategies: heteroatom doping or exposing active edge sites. However, the approach of increasing heteroatomic dopants of active edge sites has been rarely addressed. In this study, we present a simple strategy to prepare edge-enriched graphene catalysts with an increased ratio of heteroatomic dopants suitable for ORR of AEMFCs. The catalysts were prepared under harsh oxidation conditions, followed by a simple co-doping process with boron and nitrogen. The ORR activity of the catalysts was observed to be related to an increase of edge sites with heteroatomic dopants. We believe that the edge-enriched structure leads to accelerated electron transfer with enhanced oxygen adsorption.     

Addition,elimination, exchange,and epimerization in nitro sulfones

Three reactions were studied in the diastereomers of 1‐(benzenesulfonyl)‐2‐nitro‐1‐phenylpropane ( 1A and 1B ) and briefly in related compounds: elimination of the benzenesulfonyl group, epimerization of one diastereomer to the other, and deuterium/hydrogen exchange at the methine group next to nitro in starting material. The two diastereomers showed quite different reactivity. The high melting diasteromer showed rapid elimination and some exchange. The low melting diastereomer (at approximately a half‐life) showed extensive epimerization, and elimination to the alkene, but little exchange. There is little effect of aromatic substituents on reaction course. The situation is complicated by re‐addition of benzenesulfinate to the alkene. The addition reaction was similar to elimination in agreement with the Principle of Microscopic Reversibility expectations. An electron transfer mechanism for addition is calculated to be comparatively favorable. Copyright © 2007 John Wiley & Sons, Ltd.     

圆筒内氢等离子体非定常化学反应羽流场DSMC分析

利用直接模拟Monte Carlo方法研究圆筒侧壁注入氢等离子体羽流场在8×10^-6s内的非定常流动特性.根据Bird的化学反应模型考虑离解-复合反应模型和电荷转移反应模型.在流场中注入H₂、H、金属原子X、H₂⁺和H⁺五种组分,研究离解-复合反应对流场中粒子分布和密度的影响,结果表明离解-复合反应使H₂数密度降低,H数密度增加,说明在流场中H₂的离解反应速率大于H的复合反应速率.加入电荷转移反应后H₂⁺数密度降低,H⁺数密度增加,对其他组分数密度没有显著影响.     

Triangular arbitrage as an interaction among foreign exchange rates

We first show that there are in fact triangular arbitrage opportunities in the spot foreign exchange markets, analyzing the time dependence of the yen–dollar rate, the dollar–euro rate and the yen–euro rate. Next, we propose a model of foreign exchange rates with an interaction. The model includes effects of triangular arbitrage transactions as an interaction among three rates. The model explains the actual data of the multiple foreign exchange rates well.     

Untersuchungen zum Verhalten der Pt-Metalle gegenüber festen und flüssigen Kationenaustauschern mit Hilfe der Radiotracermethode

Mit Hilfe radioaktiver Nuklide wurde die Aufnahme der Pt-Metalle aus chloridhaltigen Lösungen sowoht durch feste (Wofatit KPS) als auch durch flüssige Kationenaustauscher (Bis-2-äthylhexylphosphorsäure) bei Variation des pH-Wertes, der Vorbehandlung sowie der Edelmetallkonzentration bestimmt. Pt und Ir wurden nur geringfügig, Pd und Rh dagegen deutlich stärker adsorbiert. Beide Austauschertypen zeigten qualitativ das gleiche Verhalten. Die gefundenen Abhängigkeiten der Adsorption wurden auf das komplexchemische Verhalten der Pt-Metalle zurückgeführt. Es werden Verfahren zur schnellen radiochemischen Reinigung der benutzten Nuklide angegeben.     

A Repaid Procedure for Preparing Oxyen-18 Determination in Water Samples

An equipment for the speed δ¹⁸O analysis of water samples is described. It used the equilibrium isotopic exchange reaction between water and CO₂ gas. Outgasing of samples through capillary without freezing down the samples, together with shaking during the equilibrium time, reduced considerably time for sample preparation.

Apparatus is air termostated with hand valves. Measured δ values are not very sensitive to precision of preparation work and reaction conditions, except of temperature. With good temperature control the standard reproducibility of single measurement is better than 0,1‰