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Adsorptive removal of Pb(II) by magnetic activated carbon incorporated with amino groups from aqueous solutions

机译:结合氨基的磁性活性炭从水溶液中吸附去除Pb(II)

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摘要

A novel adsorbent (AC/Fe3O4@SiO2-NH2) was synthesized via a co-condensation process for the enhanced removal of Pb(II) from aqueous solutions. Characterization analyses including SEM, TEM, BET and XRD confirmed the successful integration of magnetic nanoparticles and amino groups with carbon matrix. Results demonstrated that AC/Fe3O4@SiO2-NH2 (mass ratio of AC to Fe3O4 was 1:0.25) with specific surface area (48.9 m(2)/g) showed higher adsorption capacity for Pb(II) as compared to other mass ratios. Kinetics study revealed that the adsorption reach equilibrium within 20 h and the maximum adsorption capacity of 104.2 mg/g was achieved with increasing the initial concentration from 20 to 250 mg/L using AC/Fe3O4@SiO2-NH2. Maximum removal efficiency was recorded at pH 5.2 and the removal capacities toward four divalent metal ions calculated by the Langmuir model were found to be in the order of Pb(II) > Cu(II) > Ni(II) > Cd(II). Furthermore, Delta G(0) decreased from -1.6 to -3.1 kJ/mol with increase in temperature from 293 to 333 K illustrating that the adsorption was spontaneous and an endothermic process. Complexation adsorption mechanism was found prominent in FTIR and XPS analyses between Pb(II) and AC/Fe3O4@SiO2-NH2 due to the presence of amino groups. (C) 2016 Taiwan Institute of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
机译:通过共缩合工艺合成了一种新型吸附剂(AC / Fe3O4 @ SiO2-NH2),以提高水溶液中Pb(II)的去除率。包括SEM,TEM,BET和XRD在内的表征分析证实了磁性纳米颗粒和氨基与碳基质的成功整合。结果表明,比表面积(48.9 m(2)/ g)的AC / Fe3O4 @ SiO2-NH2(AC与Fe3O4的质量比为1:0.25)与其他质量比相比,对Pb(II)的吸附能力更高。动力学研究表明,使用AC / Fe3O4 @ SiO2-NH2将初始浓度从20 mg / L增加到20 mg / L时,吸附在20 h内达到平衡,最大吸附容量为104.2 mg / g。在pH值为5.2时记录了最大去除效率,并且通过Langmuir模型计算得出的对四种二价金属离子的去除能力为Pb(II)> Cu(II)> Ni(II)> Cd(II)。此外,随着温度从293 K增加到333 K,Delta G(0)从-1.6降低到-3.1 kJ / mol,这表明吸附是自发的并且是吸热过程。由于氨基的存在,在Pb(II)和AC / Fe3O4 @ SiO2-NH2之间的FTIR和XPS分析中发现了络合吸附机理。 (C)2016台湾化学工程师学会。由Elsevier B.V.发布。保留所有权利。

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