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氨基改性MCM-41对水中1,2-二氯乙烷的吸附
引用本文:魏晨军, 孟宪荣, 许伟, 周佳伟, 吴建生, 施维林. 氨基改性MCM-41对水中1,2-二氯乙烷的吸附[J]. 环境工程学报, 2023, 17(1): 13-23. doi: 10.12030/j.cjee.202209074
作者姓名:魏晨军  孟宪荣  许伟  周佳伟  吴建生  施维林
作者单位:1.苏州科技大学环境科学与工程学院,苏州 215009; 2.苏州市环境科学研究所,苏州 215009
基金项目:苏州市科技局项目(SS202036, SS2019005);2020年度第五期“333高层次人才培养工程”项目(BRA2020130)
摘    要:
为治理地下水中氯代烃污染,以3-氨丙基三乙氧基硅烷(APTES)为改性试剂,采用共聚法制备NH2-MCM-41。利用XRD、SEM、TEM、BET和FT-IR对材料结构进行表征,并研究材料对水中1,2-二氯乙烷(1,2-DCA)的吸附行为。结果表明:氨基取代部分硅羟基,造成孔道毛糙,未改变材料的六方堆积结构;改性后材料比表面积、孔容、孔径分别减小了约10%、25%和26%。
氨基的引入增强了材料对1,2-DCA的亲和力和吸附能力,吸附容量由11.75 mg·g−1增加到15.59 mg·g−1,提升32.68%;NH2-MCM-41对1,2-DCA吸附初始阶段受物理吸附控制,后续过程主要受化学吸附控制;颗粒内扩散拟合表明颗粒内扩散过程是主要控速步骤;等温吸附拟合说明材料吸附位点分布均匀,吸附过程中单层与多层吸附共存;在温度为20 ℃,pH为7时NH2-MCM-41对1,2-DCA的吸附效果最佳;腐殖酸(HA)和共存阴离子对 NH2-MCM-41吸附1,2-DCA起抑制作用。由此可知,NH2-MCM-41能够有效地吸附水中1,2-DCA。该研究成果可为地下水氯代烃污染治理提供相关参考。


关 键 词:MCM-41   氨基   功能化   吸附   1  2-二氯乙烷
收稿时间:2022-09-14

Adsorption of 1,2-dichloroethane in water by amino modified MCM-41
WEI Chenjun, MENG Xianrong, XU Wei, ZHOU Jiawei, WU Jiansheng, SHI Weilin. Adsorption of 1,2-dichloroethane in water by amino modified MCM-41[J]. Chinese Journal of Environmental Engineering, 2023, 17(1): 13-23. doi: 10.12030/j.cjee.202209074
Authors:WEI Chenjun  MENG Xianrong  XU Wei  ZHOU Jiawei  WU Jiansheng  SHI Weilin
Affiliation:1.College of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou 215009, China; 2.Suzhou Institute of Environmental Sciences, Suzhou 215009, China
Abstract:
In order to control the pollution of chlorinated hydrocarbons in groundwater, NH2-MCM-41 was prepared by copolymerization with 3-aminopropyltriethoxysilane (APTES) as the modifier. The structure of NH2-MCM-41 was characterized by XRD, SEM, TEM, BET and FT-IR, and its adsorption behavior towards 1,2-DCA in water was studied. The results showed that amino groups substituted part of silicon hydroxyl groups, resulting in the rough pores, while slight change on the hexagonal stacking structure of NH2-MCM-41 occurred. After modification, the specific surface area, pore volume and pore diameter decreased by about 10%, 25% and 26%, respectively. The introduction of amino groups enhanced the affinity and adsorption capacity of NH2-MCM-41 toward 1,2-DCA, and the adsorption capacity increased from 11.75 mg·g−1 to 15.59 mg·g−1 with an increase rate of 32.68%.
The kinetic fitting showed that at the initial stage, NH2-MCM-41 adsorbing 1,2-DCA was controlled by physical adsorption, and it was mainly controlled by chemical adsorption during the subsequent process. The fitting of particle internal diffusion showed that the particle internal diffusion process was the main speed control step. Isothermal adsorption fitting showed that the adsorption sites of NH2-MCM-41 were evenly distributed, and monolayer and multilayer adsorption coexisted in the adsorption process. At 20 ℃ and pH 7, NH2-MCM-41 presented the best adsorption toward 1,2-DCA. Humic acid (HA) and coexisting anions inhibited the adsorption of 1,2-DCA on NH2-MCM-41. Thus, NH2-MCM-41 could effectively adsorb 1,2-DCA in water. The research results can provide a relevant reference for the treatment of polluted groundwater by chlorinated hydrocarbon.
Keywords:MCM-41  amino  functionalization  adsorption  1,2- dichloroethane
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