Key Laboratory of Functional Polymer Materials, Ministry of Education, Institute of Polymer Chemistry, Nankai University, Tianjin 300071, China.
J Colloid Interface Sci. 2011 Feb 1;354(1):353-8. doi: 10.1016/j.jcis.2010.10.032. Epub 2010 Oct 21.
In this paper a post-crosslinked polymeric adsorbent PDHT-2 with high specific surface area was prepared by Friedel-Crafts reaction of the pendant vinyl groups without an externally added crosslinking agent. It was obvious that both the specific surface area and the pore volume of starting copolymer PDHT-1 increased significantly after post-crosslinking. Batch adsorption runs of phenol from aqueous solution onto adsorbent PDHT-1 and PDHT-2 were researched, and commercial macroporous resin XAD-4 was chosen for comparison purpose. Experimental results showed that the adsorption isotherms could be fitted by Langmuir model and Freundlich model and the adsorption capacity onto PDHT-2 was much larger than that onto PDHT-1 and XAD-4 with respect to phenol and phenolic compound, which possibly resulted from its larger specific surface area. The adsorption process for phenol onto the three adsorbents was proved to be exothermic and spontaneous in nature. The thermodynamic parameters such as Gibb's free energy (ΔG), change in enthalpy (ΔH) and change in entropy (ΔS) had been calculated. The adsorption kinetic curves obeyed the pseudo-second order model and the intraparticle diffusion process was the rate-controlling step.
本文采用无外加交联剂的芳基侧基Friedel-Crafts 反应,制备了比表面积高的后交联聚合物吸附剂 PDHT-2。很明显,起始共聚物 PDHT-1 的比表面积和孔体积在后交联后都显著增加。研究了从水溶液中吸附酚到吸附剂 PDHT-1 和 PDHT-2 的批量吸附实验,并选择商业大孔树脂 XAD-4 进行比较。实验结果表明,吸附等温线可以用 Langmuir 模型和 Freundlich 模型拟合,与 PDHT-1 和 XAD-4 相比,PDHT-2 对酚和酚类化合物的吸附容量要大得多,这可能是由于其较大的比表面积所致。酚在三种吸附剂上的吸附过程是放热和自发的。计算了吉布斯自由能(ΔG)、焓变(ΔH)和熵变(ΔS)等热力学参数。吸附动力学曲线符合准二级动力学模型,颗粒内扩散过程是速率控制步骤。