Ming Zhang W, Long Chen J, Cai Pan B, Xing Zhang Q, Zhang B
State Key Laboratory of Pollution Control and Resources Reuse, School of the Environment, Nanjing University, Nanjing 210093, PR China.
J Hazard Mater. 2006 Feb 6;128(2-3):123-9. doi: 10.1016/j.jhazmat.2005.03.036. Epub 2006 Feb 2.
Adsorption of phenol from aqueous solution onto a nonpolar adsorbent, aminated adsorbent and weak base adsorbent (Amberlite XAD4, NDA103 and Amberlite IRA96C, respectively) at temperatures from 293 to 313K was studied for the weak interactions between the phenol molecules and the polymeric adsorbents. Isotherms of Langmuir and Freundlich equation with characteristic parameters for different adsorbents were well fitted to the batch equilibrium adsorption data. The adsorption capacity on NDA103 driven by hydrogen bonding and van der Waals interaction together is higher than that on IRA96C driven by hydrogen bonding interaction only and on XAD4 driven by van der Waals interaction only. For evaluating synergistic adsorption for phenol-water systems onto polymeric adsorbents, the adsorption capacity is normalized to the amounts of specific surface area and amino groups of adsorbents. The synergistic effect with other weak interactions would contribute more to the adsorption as acting simultaneously than that of acting individually.
研究了在293至313K温度下,酚从水溶液中吸附到非极性吸附剂、胺化吸附剂和弱碱吸附剂(分别为Amberlite XAD4、NDA103和Amberlite IRA96C)上的情况,以研究酚分子与聚合物吸附剂之间的弱相互作用。不同吸附剂的具有特征参数的Langmuir和Freundlich方程等温线与间歇平衡吸附数据拟合良好。由氢键和范德华相互作用共同驱动的NDA103上的吸附容量高于仅由氢键相互作用驱动的IRA96C上的吸附容量以及仅由范德华相互作用驱动的XAD4上的吸附容量。为了评估聚合物吸附剂对酚 - 水体系的协同吸附,将吸附容量归一化为吸附剂的比表面积和氨基量。与其他弱相互作用同时起作用时的协同效应比单独起作用时对吸附的贡献更大。