4.7 Article

Toxicity mechanisms and synergies of silver nanoparticles in 2,4-dichlorophenol degradation by Phanerochaete chrysosporium

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 321, Issue -, Pages 37-46

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2016.08.075

Keywords

Silver nanoparticles; 2,4-Dichlorophenol; Phanerochaete chrysosporium; Synergies; Biodegradation

Funding

  1. National Natural Science Foundation of China [51579099, 51521006, 51508186]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT-13R17]
  3. Hunan Provincial Innovation Foundation [CX2016B134]

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Mechanisms of silver nanoparticles-mediated toxicity to Phanerochaete chrysosporium and the influence of silver nanoparticles (AgNPs) on the biodegradation of 2,4-dichlorophenol (2,4-DCP) have been systematically investigated. AgNPs at low doses (0-60 mu M) have greatly enhanced the degradation ability of P. chrysosporium to 2,4-DCP with the maximum degradation rates of more than 94%, exhibiting excellent synergies between AgNPs and P. chrysosporium in the degradation of 2,4-DCP. Meanwhile, removal of total Ag was also at high levels and highly pH dependent. However, significant inhibition was highlighted on 2,4-DCP biodegradation and Ag removal upon treatment with AgNPs at high doses and AgNO3 at low-level exposure. Results also suggested that AgNPs-induced cytotoxicity could arise from the Trojan-horse mechanism executing particle effects, ion effects, or both, ruling out extracellularly released Ag+. Moreover, under relatively low concentrations of AgNPs exposure, 2,4-DCP was broken into linear chain organics, and eventually turned into CO2 and H2O through reductive dechlorination and reaction with hydroxyl radicals. FTIR analysis showed that amino, carboxyl, carbonyl, and sulfur containing functional groups played crucial roles in Ag transportation and the reduction of Ag+ to Ag-0. (C) 2016 Elsevier B.V. All rights reserved.

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