Abstract

以硝酸钙和硅酸钠为原料,十六烷基三甲溴化铵为模板剂,(3-巯基丙基)三甲氧基硅烷为改性剂,采用后接枝法制备巯基化介孔硅酸钙(MCS-SH),并对其结构进行了表征。考察了其对Pb2+的吸附性能,探讨了吸附热力学特征。结果表明,MCS-SH在改性后仍维持较稳定的介孔结构,为夹缝孔,比表面积和孔径范围分别为129.32 m2∙g−1和5~49 nm,接入的−SH量为0.4594 mmol∙g−1;MCS-SH对Pb2+的吸附符合Langmuir模型,更符合Redlich-Peterson模型;MCS-SH对Pb2+吸附是一个熵增自发进行的过程,为吸热反应,存在物理吸附和化学吸附。根据Langmuir吸附模型,在293 K下MCS-SH对Pb2+的最大吸附容量为618.09 mg∙g−1,远大于文献报道的吸附剂。MCS-SH在pH 5.0~7.5的范围内对Pb2+具有优异的吸附性能。 Thiol-functionalized mesoporous calcium silicate (MCS-SH) was synthesized by post-grafting method using calcium nitrate tetrahydrate and sodium metasilicate nonahydrate as raw materials, cetyl trimethyl ammonium bromide as template, and (3-mercaptopropyl) trimethoxysilane as modifying agent, and its structures were characterized. The adsorption performance of MCS-SH for Pb2+ was investigated, and the adsorptive thermodynamics were explored. The results show that MCS-SH has still maintained mesoporous slit-pore structure in the modification process, with a specific surface area of 129.32 m2∙g−1 and pore size mainly distributed in 5-49 nm. The amount of substance of −SH grafted to MCS-SH is calculated to be 0.4594 mmol∙g−1 according to the sulfur content determined. The equilibrium adsorption data of MCS-SH for Pb2+ fitted to Langmuir model, and fitted better to Redlich-Peterson model. The adsorption of MCS-SH towards Pb2+ is an endothermic reaction and spontaneous process driven by an increase in entropy, and there exists both physical and chemical adsorption. The maximum adsorption capacity for Pb2+ deduced from the Langmuir model was 618.09 mg∙g−1, which is much higher than those of adsorbents in the literature. MCS-SH exhibited an excellent adsorption performance for Pb2+ in the pH range of 5.0-7.5.

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