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Adsorption Kinetics and Thermodynamics Characteristics of Expanded Graphite for Poly(vinyl alcohol)

机译:膨胀石墨对聚乙烯醇的吸附动力学和热力学特征

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摘要

In the present study, expanded graphite processing of an expanded volume of 400 mL/g is prepared through chemical oxidation intercalation and its adsorption kinetics and thermodynamics characteristics for poly(vinyl alcohol) with polymerization degree of 1750 in aqueous solution is investigated. We studied the influence of initial poly(vinyl alcohol) concentration, temperature and ionic strength on adsorption capacity. Langmuir constants and Gibbs free energy change (ΔG°) are calculated according to the experimental data. Kinetic studies are carried out with a series of poly(vinyl alcohol) concentration under different temperatures and the data are simulated with pseudo first-order and second-order kinetic model, respectively. Thermodynamic study indicates that ionic strength has no obvious influence on the equilibrium adsorbance. Adsorption isotherm of expanded graphite for poly(vinyl alcohol) with a polymerization degree of 1750 is type I; Adsorption processes are all spontaneous. Kinetic studies show that the kinetic data can be delineated by pseudo second-order kinetic model. Second-order rate constants and the initial adsorption rate increase with the increasing of temperature. Adsorption activation energy of expanded graphite for poly(vinyl alcohol) with a polymerization degree of 1750 is less than 20 kJ·mol~-(1), physical adsorption is the major mode of the overall adsorption process.
机译:在本研究中,通过化学氧化插层法制备了膨胀体积为400 mL / g的膨胀石墨工艺,并研究了其在水溶液中的聚合度为1750时对聚乙烯醇的吸附动力学和热力学特征。我们研究了聚乙烯醇的初始浓度,温度和离子强度对吸附容量的影响。根据实验数据计算Langmuir常数和吉布斯自由能变化(ΔG°)。在不同温度下对一系列聚乙烯醇浓度进行动力学研究,并分别用伪一级动力学模型和二级动力学模型模拟数据。热力学研究表明,离子强度对平衡吸附没有明显影响。膨胀度为1750的膨胀石墨对聚乙烯醇的吸附等温线为I型;吸附过程都是自发的。动力学研究表明,动力学数据可以用伪二级动力学模型来描述。随着温度的升高,二阶速率常数和初始吸附速率增加。膨胀度为1750的聚乙烯醇膨胀石墨的吸附活化能小于20 kJ·mol〜-(1),物理吸附是整个吸附过程的主要方式。

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