KH-Fh的制备及其对Cd(Ⅱ)的吸附性能OA
KH-Fh preparation and its adsorption ability for Cd(Ⅱ)
采用硅烷偶联剂3-氨丙基三乙氧基硅烷(KH550)对水铁矿(Fh)进行改性,制备了KH-Fh,并进行了表征,考察了KH-Fh对溶液中Cd(Ⅱ)的吸附性能及机理.表征结果显示:通过KH550改性,在Fh表面成功引入了—Si—OH和—NH2官能团.KH-Fh对Cd(Ⅱ)的吸附过程是自发的吸热过程;其等温吸附特征符合Langmuir模型与Freundlich模型,25℃时,KH-Fh对Cd(Ⅱ)的饱和吸附量为25.77 mg/g,为Fh(11.10 mg/g)的2.32倍;其吸附动力学特征符合准二级动力学模型.随离子强度的增大、pH的升高,KH-Fh对Cd(Ⅱ)的吸附量增加;K+对Cd(Ⅱ)吸附量的影响较小,Na+的加入使Cd(Ⅱ)吸附量明显增加,而Ca2+的加入使Cd(Ⅱ)吸附量有所降低.在KH-Fh吸附Cd(Ⅱ)的过程中,Cd(Ⅱ)能与Fe—OH、Si—OH和—NH2发生络合,形成稳定的络合物.
The silane coupling agent 3-aminopropyltriethoxysilane(KH550)was employed to modify ferrihydrite(Fh).KH550-modified ferrihydrite(KH-Fh)was prepared and characterized.The adsorption ability and mechanism of KH-Fh for Cd(Ⅱ)in solution were investigated.The characterization results show that—Si—OH and—NH2 functional groups are successfully introduced onto the Fh surface after KH550 modification.Cd(Ⅱ)adsorption onto KH-Fh is a spontaneous and endothermic process.The adsorption isotherms are well fitted by both the Langmuir and Freundlich models.At 25℃,the saturated adsorption capacity of KH-Fh for Cd(Ⅱ)reaches 25.77 mg/g,2.32 times that of Fh(11.10 mg/g).The adsorption kinetics are well described by the pseudo-second-order kinetic model.Cd(Ⅱ)adsorption capacity increases with high NaNO3 concentration and pH.K+shows little effect on Cd(Ⅱ)adsorption capacity.The addition of Na+significantly promotes Cd(Ⅱ)adsorption,while Ca2+slightly decreases the Cd(Ⅱ)adsorption capacity.During the process of KH-Fh-Cd(Ⅱ)adsorption,Cd(Ⅱ)can complex with Fe—OH,Si—OH,and—NH2 to form stable complexes.
蔡琳;涂书新;李杨;熊双莲;郑倩
华中农业大学 资源与环境学院,湖北 武汉 430070华中农业大学 资源与环境学院,湖北 武汉 430070山东华汇达工程技术服务有限公司,山东 济南 250000华中农业大学 资源与环境学院,湖北 武汉 430070华中农业大学 资源与环境学院,湖北 武汉 430070
资源环境
有机硅改性水铁矿界面调控Cd(Ⅱ)吸附机制
organosilicon modificationferrihydriteinterface regulationCd(Ⅱ)adsorption mechanism
《化工环保》 2026 (3)
361-370,10
国家自然科学基金面上项目(42277392,42507039).
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