Ji Biyan, Shao Fei, Hu Guanjiu, Zheng Shourong, Zhang Qingmei, Xu Zhaoyi
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210093, China.
J Hazard Mater. 2009 Jan 15;161(1):81-7. doi: 10.1016/j.jhazmat.2008.03.052. Epub 2008 Mar 20.
MTBE has emerged as an important water pollutant because of its high mobility, persistence, and toxicity. In this study, a postcrosslinked polymeric adsorbent was prepared by postcrosslinking of a commercial chloromethylated polymer, and a nonpolar porous polymer with comparable surface area and micropore volume to the postcrosslinked polymer was prepared by suspended polymerization. The postcrosslinked polymer, nonpolar porous polymer and chloromethylated polymer were characterized by N2 adsorption, FTIR and XPS analysis. Results showed that postcrosslinking reaction led to the generation of a microporous postcrosslinked polymer with BET surface area 782m2g(-1), average pore width 3.0nm and micropore volume 0.33cm3g(-1). FTIR and XPS analysis indicated the formation of surface oxygen-containing groups on the postcrosslinked polymer. The three polymers were used as adsorbents to remove aqueous methyl tert-butyl ether (MTBE). Adsorption of MTBE over the postcrosslinked polymeric adsorbent was found to follow the linear adsorption isotherm, whereas MTBE adsorption onto the nonpolar porous polymer and chloromethylated polymer followed Langmuir adsorption model. Comparison of adsorption capacities of the postcrosslinked polymer, chloromethylated polymer and nonpolar porous polymer revealed that the adsorption of MTBE from aqueous solution is dependent on both pore structure and surface chemistry of polymeric adsorbents, and the high adsorption efficiency of the postcrosslinked polymer towards MTBE is attributed to its high surface area, large micropore volume and moderate hydrophility. The process of MTBE adsorption onto the adsorbents can be well described by pseudo-second-order kinetics, and the rate of adsorption decreased at higher MTBE initial concentration.
由于甲基叔丁基醚(MTBE)具有高迁移率、持久性和毒性,它已成为一种重要的水污染物。在本研究中,通过对一种商业氯甲基化聚合物进行后交联制备了一种后交联聚合物吸附剂,并通过悬浮聚合制备了一种比表面积和微孔体积与后交联聚合物相当的非极性多孔聚合物。通过N2吸附、傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)分析对后交联聚合物、非极性多孔聚合物和氯甲基化聚合物进行了表征。结果表明,后交联反应导致生成了一种微孔后交联聚合物,其BET比表面积为782m2g(-1),平均孔径为3.0nm,微孔体积为0.33cm3g(-1)。FTIR和XPS分析表明后交联聚合物表面形成了含氧基团。将这三种聚合物用作吸附剂以去除水中的甲基叔丁基醚(MTBE)。发现MTBE在后交联聚合物吸附剂上的吸附遵循线性吸附等温线,而MTBE在非极性多孔聚合物和氯甲基化聚合物上的吸附遵循朗缪尔吸附模型。后交联聚合物、氯甲基化聚合物和非极性多孔聚合物吸附容量的比较表明,从水溶液中吸附MTBE既取决于聚合物吸附剂的孔结构又取决于其表面化学性质,后交联聚合物对MTBE的高吸附效率归因于其高比表面积、大微孔体积和适度的亲水性。MTBE在吸附剂上的吸附过程可用准二级动力学很好地描述,并且在较高的MTBE初始浓度下吸附速率降低。