Development of microwave-assisted functionalized nanosilicas for instantaneous removal of heavy metals

被引:24
|
作者
Mahmoud, Mohamed E. [1 ]
Hassan, Saad S. M. [2 ]
Kamel, Ayman H. [2 ]
Elserw, Mahmoud I. A. [2 ]
机构
[1] Alexandria Univ, Chem Dept, Fac Sci, POB 426, Alexandria 21321, Egypt
[2] Ain Shams Univ, Chem Dept, Fac Sci, POB 80205, Cairo, Egypt
关键词
MES technique; Immobilized nanosilica; Carboxylic acids; Microwave-assisted technique; Solvent-free reaction; Heavy metals removal; AQUEOUS-SOLUTION; BIOSORPTIVE REMOVAL; SILICON DIOXIDE; WATER-TREATMENT; DRUG RESIDUE; PB(II) IONS; ADSORPTION; ADSORBENT; SURFACE; EQUILIBRIUM;
D O I
10.1016/j.powtec.2017.12.001
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nanosilica (N-Si) sorbent was functionalized by salicylic acid (N-Si-Sa) and succinic acid (N-Si-Su) utilizing mechanochemical blending and microwave-assisted reaction under solvent free conditions. The surface alteration of nanosilica particles was examined utilizing different techniques. N-Si-Sa and N-Si-Su sorbents were employed to remove Cd(II), Hg(II) and Pb(II) from water matrices utilizing microwave-enforced sorption (MES) technique as a powerful, quick and green approach. The MES values of Cd(II), Hg(II) and Pb(II) were characterized as 1100, 750 and 1000 mu mol g(-1), respectively utilizing 10 mg of N-Si-Sa and 15 s of microwave warming as well as 1100, 650 and 1000 mu mol g(-1), respectively by utilizing N-Si-Su under the same conditions. The sorption behaviors of metals by N-Si-Sa and N-Si-Su were described by Langmuir and Freundlich isotherm models. The functionalized nanosilica sorbents were effectively connected for adsorptive treatment of the three analyzed metals from various water samples with superb recovery estimations through the productive utilization of MES technique. The collected data displayed a superior and excellent solid phase extraction procedure for treatment of the three analyzed metals from their matrices in few seconds utilizing the MES strategy. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:454 / 466
页数:13
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