Mineralization of phenanthrene sorbed on multiwalled carbon nanotubes

被引:13
作者
Xia, Xinghui [1 ]
Zhou, Chuanhui [1 ]
Huang, Jianhua [2 ]
Wang, Ran [1 ]
Xia, Na [1 ]
机构
[1] Beijing Normal Univ, Sch Environm, State Key Lab Water Environm Simulat, Beijing 100875, Peoples R China
[2] Beijing Normal Univ, Analyt & Testing Ctr, Beijing 100875, Peoples R China
基金
美国国家科学基金会;
关键词
Carbon nanotubes; PAHs; Biodegradation; Bioavailability; Toxic effects of CNTs; POLYCYCLIC AROMATIC-HYDROCARBONS; ORGANIC CONTAMINANTS; BLACK CARBON; SEDIMENT; ADSORPTION; SORPTION; BIOACCUMULATION; NANOMATERIALS; WATER; SIZE;
D O I
10.1002/etc.2125
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon nanotubes have attracted attention around the world because of their high sorption capacity for hydrophobic organic compounds (HOCs); however, the bioavailability of HOCs sorbed on carbon nanotubes to bacteria is not well known. In the present study, 14C-labeled and unlabeled phenanthrene was spiked onto four kinds of multiwalled carbon nanotubes (MWCNTs) and aged for 60d, and the mineralization of phenanthrene sorbed on MWCNTs was studied. The mineralization efficiencies of phenanthrene sorbed on the four kinds of MWCNTs were 2.38, 8.84, 23.88, and 31.47%, respectively, after incubation for 35d, which were positively correlated with the sum of fast and slow desorption fractions of phenanthrene (p<0.05). The authors found that the mineralization efficiencies agreed well with the MWCNT properties; the increasing specific surface area and mesopore and micropore volume of MWCNTs caused a significant decrease in the mineralization efficiency of phenanthrene (p<0.05). After incubation for 35d, the density of bacteria had a significant positive correlation with both the desorption and the mineralization efficiencies. The authors inferred that, although MWCNTs might have toxic effects on the bacteria, the biodegrading ability of bacteria might not decrease significantly under the influence of MWCNTs with low surface area. Environ. Toxicol. Chem. 2013;32:894901. (c) 2013 SETAC
引用
收藏
页码:894 / 901
页数:8
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