Literature DB >> 30384050

Adsorption behavior and mechanism of Mg/Fe layered double hydroxide with Fe3O4-carbon spheres on the removal of Pb(II) and Cu(II).

Yuanyuan Xie1, Xingzhong Yuan2, Zhibin Wu3, Guangming Zeng1, Longbo Jiang1, Xin Peng4, Hui Li5.   

Abstract

Mg/Fe layered double hydroxide loaded with Magnetic(Fe3O4) carbon spheres (MCs@Mg/Fe-LDHs) was firstly synthesized by a facile in-situ co-precipitation method to remove Pb(II) and Cu(II) pollution. To search the adsorption mechanism, MCs@Mg/Fe-LDHs was characterized by XRD, FTIR, XPS, TEM, and BET. There may exist surface complexation, precipitation, isomorphic substitution and physical adsorption in MCs@Mg/Fe-LDHs. The combination of those four types of reactions/interactions of metal ions with composite could improve the removal of Pb(II) and Cu(II). And the surface complexation was the main factor leading to the difference maximum adsorption capacity of Pb(II) (3.66 mmol/g) and Cu(II) (5.33 mmol/g). The adsorption kinetics and adsorption thermodynamics of MCs@Mg/Fe-LDHs for Pb(II) and Cu(II) could be better described by pseudo-second-order model and Langmuir model, respectively. The adsorption reaction was a spontaneous and endothermic process. Moreover, there existed competitive effect between Pb(II) and Cu(II) on the co-adsorption by MCs@Mg/Fe-LDHs. And the selectivity adsorption order of MCs@Mg/Fe-LDHs is as follows: Cu(II) > Pb(II) > Zn(II) > Ni(II) > Cd(II). Besides, in the real river water, the MCs@Mg/Fe-LDHs also exhibited stable adsorption capacity for Pb(II). In general, the MCs@Mg/Fe-LDHs has the potential for purification of water contaminated by Pb(II) and Cu(II).
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Heavy metal pollution; Magnetic carbon spheres; Mg/Fe LDHs; Selective adsorption

Year:  2018        PMID: 30384050     DOI: 10.1016/j.jcis.2018.10.066

Source DB:  PubMed          Journal:  J Colloid Interface Sci        ISSN: 0021-9797            Impact factor:   8.128


  7 in total

1.  Transport and numerical simulation of Cu2+ in saturated porous medium in the presence of magnetic nanoparticles.

Authors:  Shihui Song; Yinghao Song; Mengdi Shi; Zheng Hu; Tianyu Li; Shanshan Lin
Journal:  Environ Sci Pollut Res Int       Date:  2019-11-08       Impact factor: 4.223

Review 2.  Covalent and Non-covalent Functionalized Nanomaterials for Environmental Restoration.

Authors:  Shizhong Zhang; Sumeet Malik; Nisar Ali; Adnan Khan; Muhammad Bilal; Kashif Rasool
Journal:  Top Curr Chem (Cham)       Date:  2022-08-11

3.  APTMS-BCAD modified magnetic iron oxide for magnetic solid-phase extraction of Cu(II) from aqueous solutions.

Authors:  Ali Bilgiç; Hacer Sibel Karapınar
Journal:  Heliyon       Date:  2022-06-05

4.  In Situ Copolymerized Polyacrylamide Cellulose Supported Fe3O4 Magnetic Nanocomposites for Adsorptive Removal of Pb(II): Artificial Neural Network Modeling and Experimental Studies.

Authors:  Imran Hasan; Rais Ahmad Khan; Walaa Alharbi; Khadijah H Alharbi; Ali Alsalme
Journal:  Nanomaterials (Basel)       Date:  2019-11-25       Impact factor: 5.076

5.  The Performance and Mechanism of a Mg-Al Double-Layer Oxide in Chloride ion Removal from an Aqueous Solution.

Authors:  Xueqin Xu; Peng Li; Shichong Yang; Tong Zhang; Xiangke Han; Guoli Zhou; Yijun Cao; Daoguang Teng
Journal:  Nanomaterials (Basel)       Date:  2022-03-02       Impact factor: 5.076

6.  Adsorption of Cu(II) and Zn(II) Ions from Aqueous Solution by Gel/PVA-Modified Super-Paramagnetic Iron Oxide Nanoparticles.

Authors:  Anudari Dolgormaa; Chang-Jiang Lv; Yin Li; Jian Yang; Jun-Xing Yang; Peng Chen; Hong-Peng Wang; Jun Huang
Journal:  Molecules       Date:  2018-11-15       Impact factor: 4.411

7.  In Situ Synthesis of MIL-100(Fe) at the Surface of Fe3O4@AC as Highly Efficient Dye Adsorbing Nanocomposite.

Authors:  Asma Hamedi; Francesco Trotta; Mahmood Borhani Zarandi; Marco Zanetti; Fabrizio Caldera; Anastasia Anceschi; Mohammad Reza Nateghi
Journal:  Int J Mol Sci       Date:  2019-11-09       Impact factor: 5.923

  7 in total

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