Comparison of degradation mechanisms of microcystin-LR using nanoscale zero-valent iron (nZVI) and bimetallic Fe/Ni and Fe/Pd nanoparticles

被引:79
作者
Gao, Ying [1 ]
Wang, Feifeng [1 ]
Wu, Yan [1 ]
Naidu, Ravendra [2 ]
Chen, Zuliang [1 ,2 ]
机构
[1] Fujian Normal Univ, Sch Environm Sci & Engn, Fuzhou 350007, Fujian Province, Peoples R China
[2] Univ Newcastle, Global Ctr Environm Remediat, Callaghan, NSW 2308, Australia
关键词
Iron-based nanoparticles; Degradation; MC-LR; Characterization; Mechanism; AQUEOUS-SOLUTION; WATER-TREATMENT; DECHLORINATION; KINETICS; HYDRODECHLORINATION; TRICHLOROETHYLENE; OXIDATION; PATHWAYS; REMOVAL;
D O I
10.1016/j.cej.2015.09.078
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Microcystin-LR (MC-LR) as a drinking water contaminant was degraded using iron-based nanoparticles such as nZVI, Fe/Ni and Fe/Pd. Batch experiments showed that 28.0% of MC-LR with the initial concentration of 5 mg L-1 was removed using nZVI, while more than 90% of MC-LR was removed using either bimetallic Fe/Ni or Fe/Pd after degrading for 120 min. In addition, the results indicated that Fe was oxided to iron oxide or hydroxide after reacting with MC-LR, while Ni or Pd acted as the catalysis to prevent Fe corrosion and generating hydrogen via water reduction. Degradation of MC-LR by iron-based nanoparticles fitted well to the pseudo-first order kinetic model and the degradation was a diffusion-controlled reaction with low activation energies (8-21 kJ mol(-1)). Finally, the degradation mechanisms of MC-LR using iron-based nanoparticles were proposed according to the LC-MS analysis. In nZVI case, when the MC-LR was quickly adsorbed on nanoparticles, electron transfer and H-2 generated from iron corrosion were generated and broke down the Adda composition of MC-LR. Based on corrosion in the Fe-0-H2O system, bimetallic Fe/Ni and Fe/Pd further utilized the abundant hydrogen radical decomposed from H-2 under the catalysis of Ni or Pd, and destroyed the Adda to form small molecules. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:459 / 466
页数:8
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