Chemical extractions affect the structure and phenanthrene sorption of soil humin. 2005

Kaijun Wang, and Baoshan Xing
Department of Plant, Soil and Insect Sciences, University of Massachusetts, Amherst, Massachusetts 01003, USA.

Humin is a major fraction of soil organic matter and strongly affects the sorption behavior and fate of organic contaminants in soils and sediments. This study evaluated four different extraction methods for soil humins in terms of their organic carbon structural changes and the consequent effects on phenanthrene sorption. Solid-state 13C NMR demonstrated that 0.1 M NaOH exhaustively extracted humin and humin extracted with 6 M HF/HCl at 60 degrees C had a relatively high amount of aliphatic components as compared with 1 M HF-extracted humin. The treatment of 6 M HF/HCl at 60 degrees C greatly reduced carbohydrate components (50-108 ppm) from humin samples, i.e., more than 50% reduction. In addition, the humin from this 6 M HF/HCl treatment contained relatively more amorphous poly(methylene) domains than the humins extracted by other methods. With the respect to phenanthrene sorption, the linearity of sorption isotherm (N) and sorption affinity (Koc) varied markedly among the humin samples extracted by different methods. The NaOH exhaustively extracted humin had the most nonlinear sorption isotherm and the HF-extracted humin had the lowest Koc. It is concluded that humin samples from different extraction procedures exhibited substantial differences in their organic carbon structure and sorption characteristics, even though they were from the same soil. Therefore, one needs to be cautious when comparing the structural and sorption features of soil humins, especially when they are extracted differently. The 6 M HCl/HF extraction at elevated temperature is not encouraged, due to the modifications of chemical structure and physical conformation of organic matter.

UI MeSH Term Description Entries
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D010616 Phenanthrenes POLYCYCLIC AROMATIC HYDROCARBONS composed of three fused BENZENE rings.
D006812 Humic Substances Organic matter in a state of advanced decay, after passing through the stages of COMPOST and PEAT and before becoming lignite (COAL). It is composed of a heterogenous mixture of compounds including phenolic radicals and acids that polymerize and are not easily separated nor analyzed. (E.A. Ghabbour & G. Davies, eds. Humic Substances, 2001). Humic Acid,Humic Acids,Humic Substance,Sodium Huminate,Acid, Humic,Acids, Humic,Huminate, Sodium,Substance, Humic,Substances, Humic
D006851 Hydrochloric Acid A strong corrosive acid that is commonly used as a laboratory reagent. It is formed by dissolving hydrogen chloride in water. GASTRIC ACID is the hydrochloric acid component of GASTRIC JUICE. Hydrogen Chloride,Muriatic Acid,Acid, Hydrochloric,Acid, Muriatic,Chloride, Hydrogen
D006858 Hydrofluoric Acid Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns. Hydrogen Fluoride,Fluohydric Acid,Fluorhydric Acid,Acid, Fluohydric,Acid, Fluorhydric,Acid, Hydrofluoric,Fluoride, Hydrogen
D012972 Sodium Hydroxide A highly caustic substance that is used to neutralize acids and make sodium salts. (From Merck Index, 11th ed) Caustic Soda,Hydroxide, Sodium,Soda, Caustic
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular

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