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Kinetic and adsorption mechanism of Cu(II) and Pb(II) on prepared nanoparticle layered double hydroxide intercalated with EDTA

机译:Cu(II)和Pb(II)在制备的EDTA嵌入的纳米颗粒层状双氢氧化物中的动力学和吸附机理

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MgFe-LDH-EDTA was obtained by the anion exchange method, with the aim of adsorpting Cu(II) and Pb(II) from the aqueous solutions by chelating process between EDTA and metal cations. The prepared LDH was characterized by XRD, TG-DTA and FTR spectroscopy. Low-Vacuum Scanning Electron Microscope (LV-SEM) revealed that the particle size of the prepared MgFe-LDH-EDTA mainly in the range 100-150 nm. The adsorption was studied at different contact time, pH and metal concentrations. The results indicate the relatively fast adsorption of the metal cations Cu(II) and Pb(II) by MgFe-LDH-EDTA reaching the equilibrium of the uptake reaction in 2 h. The shape of the adsorption isotherm suggests specific interaction and high affinity. The batch kinetics of Cu(II) adsorption onto MgFe-EDTA were carried out and thermodynamic parameters calculated. The adsorption equilibrium constant, K-c, has been calculated at different temperatures between 306 and 323 degrees K. The values of Delta H, Delta G and Delta S were 83.4 kJ/mol, 65.0 kJ/mol and 62 J/mol K, respectively. The positive Delta H value obtained for the adsorption indicates that it is endothermic and dehydration seems to be more significant than complexation in the adsorption system.
机译:MgFe-LDH-EDTA是通过阴离子交换法制得的,其目的是通过EDTA与金属阳离子之间的螯合工艺从水溶液中吸附Cu(II)和Pb(II)。通过XRD,TG-DTA和FTR光谱对所制备的LDH进行表征。低真空扫描电子显微镜(LV-SEM)显示,制备的MgFe-LDH-EDTA的粒径主要在100-150nm范围内。在不同的接触时间,pH和金属浓度下研究了吸附。结果表明,MgFe-LDH-EDTA相对较快地吸附了金属阳离子Cu(II)和Pb(II),在2小时内达到了吸收反应的平衡。吸附等温线的形状表明特定的相互作用和高亲和力。进行了Cu(II)在MgFe-EDTA上吸附的间歇动力学,并计算了热力学参数。已在306至323度之间的不同温度下计算了吸附平衡常数K-c。ΔH,Delta G和Delta S的值分别为83.4 kJ / mol,65.0 kJ / mol和62 J / molK。从吸附获得的正Delta H值表明它是吸热的,并且脱水似乎比吸附系统中的络合更为重要。

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