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多壁碳纳米管上吸附的菲矿化作用。

Mineralization of phenanthrene sorbed on multiwalled carbon nanotubes.

机构信息

State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing, China.

出版信息

Environ Toxicol Chem. 2013 Apr;32(4):894-901. doi: 10.1002/etc.2125. Epub 2013 Feb 22.

Abstract

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, (14) C-labeled and unlabeled phenanthrene was spiked onto four kinds of multiwalled carbon nanotubes (MWCNTs) and aged for 60 d, 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 35 d, 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 35 d, 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.

摘要

碳纳米管因其对疏水性有机化合物(HOCs)的高吸附能力而受到全球关注;然而,被碳纳米管吸附的 HOCs 对细菌的生物可利用性尚不清楚。在本研究中,(14)C 标记和未标记的菲被添加到四种多壁碳纳米管(MWCNTs)上,并老化 60d,研究了 MWCNTs 上吸附的菲的矿化作用。在孵育 35d 后,吸附在四种 MWCNTs 上的菲的矿化效率分别为 2.38%、8.84%、23.88%和 31.47%,与菲的快速和慢速解吸分数之和呈正相关(p<0.05)。作者发现,矿化效率与 MWCNT 的性质相符;MWCNTs 的比表面积和中孔及微孔体积的增加导致菲的矿化效率显著降低(p<0.05)。在孵育 35d 后,细菌的密度与解吸和矿化效率均呈显著正相关。作者推断,尽管 MWCNTs 可能对细菌具有毒性作用,但在低表面积 MWCNTs 的影响下,细菌的生物降解能力可能不会显著下降。

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