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首页> 外文期刊>Journal of Colloid and Interface Science >Adsorption characteristics of poly(styrene-co-divinylbenzene) resin functionalized with methoxy and phenoxy groups for phenol
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Adsorption characteristics of poly(styrene-co-divinylbenzene) resin functionalized with methoxy and phenoxy groups for phenol

机译:甲氧基和苯氧基官能化的聚(苯乙烯-共二乙烯基苯)树脂​​对苯酚的吸附特性

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Two macroporous crosslinked poly(styrene-co-divinylbenzene) resins functionalized with methoxy and phenoxy groups, PVBME and PVBPE were prepared and their adsorption characteristics for phenol were studied in hexane as well as in aqueous solution. It was shown that the equilibrium adsorption capacity of phenol onto PVBPE was a little larger than that onto PVBME at the same temperature and equilibrium concentration. The adsorption onto PVBME in hexame can be correlated to Langmuir isotherm model, whereas the semi-empirical Freundlich isotherm model characterized the adsorption onto PVBPE better. The adsorption thermodynamic parameters were calculated and it was found that the adsorption enthalpy, adsorption free energy, and adsorption entropy were all negative, and the adsorption thermodynamic parameters onto PVBPE were more negative than the corresponding ones onto PVBME. The relationship of the adsorption capacity with the equilibrium concentration was linear in aqueous solution. The adsorption was hypersensitive to the solution pH in aqueous solution, and the optimum pH was determined to be 6.0. The adsorption dynamics of phenol onto PVBPE in aqueous solution was investigated and it was seen that the adsorption can be well fitted by the pseudo-first-order rate equation. (C) 2008 Elsevier Inc. All rights reserved.
机译:制备了两种用甲氧基和苯氧基官能化的大孔交联聚(苯乙烯-共二乙烯基苯)树脂​​PVBME和PVBPE,并研究了它们在己烷和水溶液中对苯酚的吸附特性。结果表明,在相同的温度和平衡浓度下,苯酚在PVBPE上的平衡吸附容量略大于在PVBME上的吸附量。六边形对PVBME的吸附与Langmuir等温线模型相关,而半经验Freundlich等温线模型对PVBPE的吸附效果更好。计算了吸附热力学参数,发现吸附焓,吸附自由能和吸附熵均为负,PVBPE上的吸附热力学参数比PVBME上的吸附热力学参数更负。水溶液中吸附容量与平衡浓度的关系呈线性关系。吸附对水溶液中的溶液pH敏感,确定最佳pH为6.0。研究了苯酚在水溶液中对PVBPE的吸附动力学,发现该吸附可以很好地拟合拟一级反应速率方程。 (C)2008 Elsevier Inc.保留所有权利。

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