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Facile green synthesis of functional nanoscale zero-valent iron and studies of its activity toward ultrasound-enhanced decolorization of cationic dyes
被引:85
|作者:
Wang, Xiangyu
[1
]
Wang, Anqi
[1
]
Ma, Jun
[2
]
Fu, Minglai
[3
]
机构:
[1] Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Peoples R China
[2] Harbin Inst Technol, Sch Municipal & Environm Engn, State Key Lab Urban Water Resources & Environm, Harbin 150090, Peoples R China
[3] Chinese Acad Sci, Inst Urban Environm, Key Lab Urban Environm & Hlth, Xiamen 361021, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
One-step green synthesis;
Ultrasound;
Functionalization;
Tea polyphenol;
Nanoscale zero-valent iron;
Cationic dye;
INDUCED CATALYTIC-OXIDATION;
AZO-DYE;
AQUEOUS-SOLUTION;
METHYL-ORANGE;
WASTE-WATER;
REMOVAL;
NANOPARTICLES;
DEGRADATION;
PARTICLES;
REDUCTION;
D O I:
10.1016/j.chemosphere.2016.09.056
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
For the first time, an integrated green technology by coupling functional nanoscale zero-valent iron (NZVI) with ultrasound (US) was innovatively developed for the enhanced decolorization of malachite green (MG) and methylene blue (MB). The functional NZVI (TP-Fe) was successfully fabricated via a facile, one-step and environmentally-benign approach by directly introducing high pure tea polyphenol (TP), where TP contenting abundant epicatechin was employed as reductant, dispersant and capping agent. Note that neither additional extraction procedure nor protection gas was needed during the entire synthesis process. Affecting factors (including US frequency, initial pH, dye concentration, and reaction temperature) were investigated. Results show that TP-Fe exhibited enhanced activity, antioxidizability and stability over the reaction course, which could be attributed to the functionalization of TP on NZVI and the invigorating effect of US (i.e., improving the mass transfer rate, breaking up the aggregates of TP-Fe nanoparticles, and maintaining the TP-Fe surface activity). The kinetics for MG and MB decolorization by the TP-Fe/US system could be well described by a two-parameter pseudo-first-order decay model, and the activation energies of MG and MB decolorization in this new system were determined to be 21 kJ mol(-1) and 24 kJ mol(-1), respectively. In addition, according to the identified reaction products, a possible mechanism associated with MG and MB decolorization with the TP-Fe/US system was proposed. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:80 / 88
页数:9
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