林亚男,张冲融,董文浩,张树永.化学通报,2016,79(12):1204-1208.
溶液反应机理与动力学-2:影响因素与动力学方程的一般形式
Kinetics and Mechanism of Solution Reaction-2: Influential Factors and General Form of Kinetic Equation
投稿时间:2016-04-25  修订日期:2016-06-17
DOI:
中文关键词:  溶液反应  溶剂效应  微观黏度  活化能
英文关键词:Solution reaction  Solvent effect  Micro-viscosity  Activation energy
基金项目:
作者单位E-mail
林亚男 山东大学 化学与化工学院 济南 250100 ynlin0506@163.com 
张冲融 山东大学 化学与化工学院 济南 250100  
董文浩 山东大学 化学与化工学院 济南 250100  
张树永* 山东大学 化学与化工学院 济南 250100 syzhang@sdu.edu.cn 
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中文摘要:
      对引起溶液反应与气相反应速率差异的因素进行了分析。指出大量溶剂分子的存在,并不会导致反应物分子之间的碰撞频率大幅度降低。除影响反应物活度和起催化作用之外,溶剂化和微观黏度是影响溶液反应速率的主要因素。微观黏度的影响可正可负,可能存在“负黏度”效应。基于简单碰撞理论和过渡态理论,给出了溶液反应速率公式的一般形式,可以综合活化能和微观黏度的影响。该方法可以比较合理地解释一些实验现象。
英文摘要:
      The influential factors for the rate of reactions occurring in solution which is different from those occurring in gaseous phase are discussed. The perception that the presence of solvent molecules will cause a significant decrease in the collision frequency between reactant molecules is proven incorrect. Except for the changes in activity of reactants and the catalysis due to the presence of solvent, solvent effect and micro-viscosity are found to be the two main factors affecting the rate of the solution reactions. The micro-viscosity is either of positive value due to the interaction between reactants and solvent molecules or of negative value due to the small molar mass of solvent which moves with higher speed. Based on the simple collision theory and transition state theory, a general kinetic equation correlating the change in reaction rate to the changein activation energy and micro-viscosity is proposed. Based on this equation, more satisfactory explanations to the experimental facts can be given.
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