Equilibrium sorption of phenanthrene by soil humic acids

被引:39
|
作者
Liang, Chongshan
Dang, Zhi [1 ]
Mao, Baohua
Huang, Weilin
Liu, Congqiang
机构
[1] S China Univ Technol, Coll Environm Sci & Engn, Guangzhou 510641, Peoples R China
[2] Chinese Acad Sci, Inst Geochem, State Key Lab Environm Geochem, Guiyang 55002, Peoples R China
[3] Rutgers State Univ, Dept Environm Sci, New Brunswick, NJ 08901 USA
基金
中国国家自然科学基金;
关键词
phenanthrene; humic acid; sorption;
D O I
10.1016/j.chemosphere.2005.09.065
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigated the effect of chemical heterogeneity of humic acids (HAs) on the equilibrium sorption of phenanthrene by HA extracts. Six HA samples were extracted from three different soils with 0.5 M NaOH and 0.1 M Na4P2O7 and were characterized with elemental analysis, infrared spectrometry, and solid-state C-13 nuclear magnetic resonance (NMR) spectrometry. The equilibrium sorption measurements were carried out with a batch technique and using the six HA solids as the sorbents and phenanthrene as the sorbate. The measured sorption isotherm data were fitted to the Freundlich equation. The results showed that, for the same soil, (i) the total HA mass extracted with Na4P2O7 was 13.7-22.6% less than that extracted with NaOH, (ii) the Na4P2O7-extracted HA had higher O/C atomic ratio, greater content of polar organic carbons (POC), and lower aliphatic carbon content than the NaOH-extracted HA, and (iii) the Na4P2O7-extracted HA exhibited greater sorption isotherm linearity and but not dramatic difference in sorption capacities than the NaOH extracted HA. The differences in the HA properties resulting from the two different extraction methods may be because NaOH can hydrolyze insoluble HA fractions such as fatty acid like macromolecules bound on soils whereas Na4P2O7 could not. As a result, the HAs extracted with the two different methods had different polarity and functionality which affected their sorption property for phenanthrene. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1961 / 1968
页数:8
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