Sorption of Polycyclic Aromatic Hydrocarbons (PAHs) to Lignin: Effects of Hydrophobicity and Temperature

被引:36
|
作者
Zhang, Ming [1 ,2 ,3 ]
Ahmad, Mahtab [2 ,3 ,4 ]
Lee, Sang Soo [2 ,3 ]
Xu, Li Heng [1 ]
Ok, Yong Sik [1 ,2 ,3 ]
机构
[1] China Jiliang Univ, Dept Environm Engn, Hangzhou 310018, Zhejiang, Peoples R China
[2] Kangwon Natl Univ, Korea Biochar Res Ctr, Chunchon 200701, South Korea
[3] Kangwon Natl Univ, Dept Biol Environm, Chunchon 200701, South Korea
[4] King Saud Univ, Coll Food Sci & Agr, Dept Soil Sci, Riyadh 11362, Saudi Arabia
基金
中国国家自然科学基金;
关键词
Adsorbent; Hydrophobic organic compounds (HOCs); Biopolymer; Distribution coefficient; Soil organic matter; Biosorption; ADSORPTION; SOIL; PHENANTHRENE; WATER;
D O I
10.1007/s00128-014-1290-x
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The study of the sorption of contaminants to lignin is significant for understanding the migration of contaminants in the environment as well as developing low cost sorbent. In this study, sorption of three polycyclic aromatic hydrocarbons (PAHs), naphthalene, acenaphthene and phenanthrene, to lignin was investigated. Sorption isotherms were well described by both linear and Freundlich sorption models. Sorption coefficients of PAHs to lignin from water obtained from regression of both linear model (K (d)) and Freundlich model (K (f)) were highly positively correlated with hydrophobicity of PAHs. The amorphous structure of lignin provided sufficient sorption domain for partitioning of PAHs, and the attraction between PAHs molecules and aromatic fractions in lignin via pi-pi electron-donor-acceptor (pi-pi EDA) interaction is hypothesized to provide a strong sorption force. Thermodynamic modeling revealed that sorption of PAHs to lignin was a spontaneous and exothermic process.
引用
收藏
页码:84 / 88
页数:5
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