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Influences on the sorption affinity of soil organic matter for non-ionic organic pollutants.Ahangar, Ahmad G. January 2009 (has links)
Sorption of non-ionic organic compounds to organic matter is usually characterized as a partitioning interaction, which is quantified by K [subscript]oc, the organic-C normalized partitioning coefficient. However K [subscript]oc for any single compound varies considerably between soils, often by a factor of 3-10. This study addresses some of the potential causes of this variability. Forty-four soil cores were collected from a 2 ha paddock. Ten of these cores were selected for sorption measurements. The chemical composition of the soil organic matter (SOM) was determined using ¹³C NMR analysis. It was found that K [subscript]oc for diuron was positively correlated with aryl C (r² = 0.59) and negatively correlated with O-alkyl C (r² = 0.84). There were no such correlations for phenanthrene K [subscript]oc. A second set of experiments was carried out to investigate the effects of SOM– mineral interactions on the sorption properties of a selection of the soils. It was found that HF-treatment increased K [subscript]oc for both phenanthrene and diuron. The HF treatment removes mineral matter leaving the organic phase unaffected by the treatment. The increase in K [subscript]oc on HF-treatment soils provides strong evidence that interactions between organic matter and soil minerals block organic matter sorption sites. Furthermore, following HF-treatment, there was a positive correlation between K [subscript]oc for phenanthrene and aryl C and carbonyl C and a negative correlation with O-alkyl C. This suggests that the non-constancy of the relationship between organic matter chemistry and K [subscript]oc, for whole soils in the case of phenanthrene, may be a consequence of variability of the effect of organic matter-mineral interactions on K [subscript]oc. The influence of lipids on the sorption of diuron and phenanthrene to soils was also investigated. Lipids are known to cover the surfaces of organic matter in soil. K [subscript]oc for diuron and phenanthrene were consistently higher for the lipid-extracted soils than for the whole soils (average of 31% for diuron and 29% for phenanthrene), indicating that lipids block sorption sites on the organic matter. Sorption experiments on one pair of HF-treated soils indicated that the blocking effects of minerals and lipids are independent, because lipid extraction and HF-treatment combined increased K [subscript]oc by more than either treatment alone. In the last experiment, the effect of solvent conditioning on the sorption of diuron and phenanthrene was investigated. The K [subscript]oc values for compounds were consistently higher for solvent-treated whole soil and lipid-extracted soil than corresponding soils before solvent treatment. Solid-state ¹³C NMR spectra of the solvent-treated soils indicated that there were no significant changes in the chemical structure of SOM caused by solvent treatment. Solvent treatment changes the physical conformation of the SOM, increasing its sorption affinity. The key findings from the research are: • Variations in sorption affinity for diuron are related to differences in the soil organic matter chemistry. • SOM-mineral interactions can have a substantial influence on K [subscript]oc for non- ionic compounds. • Lipids may block the active sorption sites on the SOM thereby diminishing sorption overall. • Solvent conditioning can change the physical conformation of SOM and lead to enhancement sorption of diuron and phenanthrene. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1372068 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009
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Influences on the sorption affinity of soil organic matter for non-ionic organic pollutants.Ahangar, Ahmad G. January 2009 (has links)
Sorption of non-ionic organic compounds to organic matter is usually characterized as a partitioning interaction, which is quantified by K [subscript]oc, the organic-C normalized partitioning coefficient. However K [subscript]oc for any single compound varies considerably between soils, often by a factor of 3-10. This study addresses some of the potential causes of this variability. Forty-four soil cores were collected from a 2 ha paddock. Ten of these cores were selected for sorption measurements. The chemical composition of the soil organic matter (SOM) was determined using ¹³C NMR analysis. It was found that K [subscript]oc for diuron was positively correlated with aryl C (r² = 0.59) and negatively correlated with O-alkyl C (r² = 0.84). There were no such correlations for phenanthrene K [subscript]oc. A second set of experiments was carried out to investigate the effects of SOM– mineral interactions on the sorption properties of a selection of the soils. It was found that HF-treatment increased K [subscript]oc for both phenanthrene and diuron. The HF treatment removes mineral matter leaving the organic phase unaffected by the treatment. The increase in K [subscript]oc on HF-treatment soils provides strong evidence that interactions between organic matter and soil minerals block organic matter sorption sites. Furthermore, following HF-treatment, there was a positive correlation between K [subscript]oc for phenanthrene and aryl C and carbonyl C and a negative correlation with O-alkyl C. This suggests that the non-constancy of the relationship between organic matter chemistry and K [subscript]oc, for whole soils in the case of phenanthrene, may be a consequence of variability of the effect of organic matter-mineral interactions on K [subscript]oc. The influence of lipids on the sorption of diuron and phenanthrene to soils was also investigated. Lipids are known to cover the surfaces of organic matter in soil. K [subscript]oc for diuron and phenanthrene were consistently higher for the lipid-extracted soils than for the whole soils (average of 31% for diuron and 29% for phenanthrene), indicating that lipids block sorption sites on the organic matter. Sorption experiments on one pair of HF-treated soils indicated that the blocking effects of minerals and lipids are independent, because lipid extraction and HF-treatment combined increased K [subscript]oc by more than either treatment alone. In the last experiment, the effect of solvent conditioning on the sorption of diuron and phenanthrene was investigated. The K [subscript]oc values for compounds were consistently higher for solvent-treated whole soil and lipid-extracted soil than corresponding soils before solvent treatment. Solid-state ¹³C NMR spectra of the solvent-treated soils indicated that there were no significant changes in the chemical structure of SOM caused by solvent treatment. Solvent treatment changes the physical conformation of the SOM, increasing its sorption affinity. The key findings from the research are: • Variations in sorption affinity for diuron are related to differences in the soil organic matter chemistry. • SOM-mineral interactions can have a substantial influence on K [subscript]oc for non- ionic compounds. • Lipids may block the active sorption sites on the SOM thereby diminishing sorption overall. • Solvent conditioning can change the physical conformation of SOM and lead to enhancement sorption of diuron and phenanthrene. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1372068 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009
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Influences on the sorption affinity of soil organic matter for non-ionic organic pollutants.Ahangar, Ahmad G. January 2009 (has links)
Sorption of non-ionic organic compounds to organic matter is usually characterized as a partitioning interaction, which is quantified by K [subscript]oc, the organic-C normalized partitioning coefficient. However K [subscript]oc for any single compound varies considerably between soils, often by a factor of 3-10. This study addresses some of the potential causes of this variability. Forty-four soil cores were collected from a 2 ha paddock. Ten of these cores were selected for sorption measurements. The chemical composition of the soil organic matter (SOM) was determined using ¹³C NMR analysis. It was found that K [subscript]oc for diuron was positively correlated with aryl C (r² = 0.59) and negatively correlated with O-alkyl C (r² = 0.84). There were no such correlations for phenanthrene K [subscript]oc. A second set of experiments was carried out to investigate the effects of SOM– mineral interactions on the sorption properties of a selection of the soils. It was found that HF-treatment increased K [subscript]oc for both phenanthrene and diuron. The HF treatment removes mineral matter leaving the organic phase unaffected by the treatment. The increase in K [subscript]oc on HF-treatment soils provides strong evidence that interactions between organic matter and soil minerals block organic matter sorption sites. Furthermore, following HF-treatment, there was a positive correlation between K [subscript]oc for phenanthrene and aryl C and carbonyl C and a negative correlation with O-alkyl C. This suggests that the non-constancy of the relationship between organic matter chemistry and K [subscript]oc, for whole soils in the case of phenanthrene, may be a consequence of variability of the effect of organic matter-mineral interactions on K [subscript]oc. The influence of lipids on the sorption of diuron and phenanthrene to soils was also investigated. Lipids are known to cover the surfaces of organic matter in soil. K [subscript]oc for diuron and phenanthrene were consistently higher for the lipid-extracted soils than for the whole soils (average of 31% for diuron and 29% for phenanthrene), indicating that lipids block sorption sites on the organic matter. Sorption experiments on one pair of HF-treated soils indicated that the blocking effects of minerals and lipids are independent, because lipid extraction and HF-treatment combined increased K [subscript]oc by more than either treatment alone. In the last experiment, the effect of solvent conditioning on the sorption of diuron and phenanthrene was investigated. The K [subscript]oc values for compounds were consistently higher for solvent-treated whole soil and lipid-extracted soil than corresponding soils before solvent treatment. Solid-state ¹³C NMR spectra of the solvent-treated soils indicated that there were no significant changes in the chemical structure of SOM caused by solvent treatment. Solvent treatment changes the physical conformation of the SOM, increasing its sorption affinity. The key findings from the research are: • Variations in sorption affinity for diuron are related to differences in the soil organic matter chemistry. • SOM-mineral interactions can have a substantial influence on K [subscript]oc for non- ionic compounds. • Lipids may block the active sorption sites on the SOM thereby diminishing sorption overall. • Solvent conditioning can change the physical conformation of SOM and lead to enhancement sorption of diuron and phenanthrene. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1372068 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009
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Influences on the sorption affinity of soil organic matter for non-ionic organic pollutants.Ahangar, Ahmad G. January 2009 (has links)
Sorption of non-ionic organic compounds to organic matter is usually characterized as a partitioning interaction, which is quantified by K [subscript]oc, the organic-C normalized partitioning coefficient. However K [subscript]oc for any single compound varies considerably between soils, often by a factor of 3-10. This study addresses some of the potential causes of this variability. Forty-four soil cores were collected from a 2 ha paddock. Ten of these cores were selected for sorption measurements. The chemical composition of the soil organic matter (SOM) was determined using ¹³C NMR analysis. It was found that K [subscript]oc for diuron was positively correlated with aryl C (r² = 0.59) and negatively correlated with O-alkyl C (r² = 0.84). There were no such correlations for phenanthrene K [subscript]oc. A second set of experiments was carried out to investigate the effects of SOM– mineral interactions on the sorption properties of a selection of the soils. It was found that HF-treatment increased K [subscript]oc for both phenanthrene and diuron. The HF treatment removes mineral matter leaving the organic phase unaffected by the treatment. The increase in K [subscript]oc on HF-treatment soils provides strong evidence that interactions between organic matter and soil minerals block organic matter sorption sites. Furthermore, following HF-treatment, there was a positive correlation between K [subscript]oc for phenanthrene and aryl C and carbonyl C and a negative correlation with O-alkyl C. This suggests that the non-constancy of the relationship between organic matter chemistry and K [subscript]oc, for whole soils in the case of phenanthrene, may be a consequence of variability of the effect of organic matter-mineral interactions on K [subscript]oc. The influence of lipids on the sorption of diuron and phenanthrene to soils was also investigated. Lipids are known to cover the surfaces of organic matter in soil. K [subscript]oc for diuron and phenanthrene were consistently higher for the lipid-extracted soils than for the whole soils (average of 31% for diuron and 29% for phenanthrene), indicating that lipids block sorption sites on the organic matter. Sorption experiments on one pair of HF-treated soils indicated that the blocking effects of minerals and lipids are independent, because lipid extraction and HF-treatment combined increased K [subscript]oc by more than either treatment alone. In the last experiment, the effect of solvent conditioning on the sorption of diuron and phenanthrene was investigated. The K [subscript]oc values for compounds were consistently higher for solvent-treated whole soil and lipid-extracted soil than corresponding soils before solvent treatment. Solid-state ¹³C NMR spectra of the solvent-treated soils indicated that there were no significant changes in the chemical structure of SOM caused by solvent treatment. Solvent treatment changes the physical conformation of the SOM, increasing its sorption affinity. The key findings from the research are: • Variations in sorption affinity for diuron are related to differences in the soil organic matter chemistry. • SOM-mineral interactions can have a substantial influence on K [subscript]oc for non- ionic compounds. • Lipids may block the active sorption sites on the SOM thereby diminishing sorption overall. • Solvent conditioning can change the physical conformation of SOM and lead to enhancement sorption of diuron and phenanthrene. / http://proxy.library.adelaide.edu.au/login?url= http://library.adelaide.edu.au/cgi-bin/Pwebrecon.cgi?BBID=1372068 / Thesis (Ph.D.) - University of Adelaide, School of Earth and Environmental Sciences, 2009
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Influence of soil properties and organic pesticides om soil microbial metabolism /Schnürer, Ylva, January 2006 (has links) (PDF)
Diss. (sammanfattning) Umeå : Sveriges lantbruksuniv., 2007. / Härtill 3 uppsatser.
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Nutrient management in smallholder peri-urban farming systems : a case study in southern Vietnam /Hedlund, Anna, January 2003 (has links) (PDF)
Lic.-avh. Uppsala : Sveriges lantbruksuniv. / Härtill 2 uppsatser.
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The influence of sorption on transport of organic compounds in soil /Brücher, Jörg, January 1900 (has links) (PDF)
Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv. / Härtill 4 uppsatser.
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Mechanisms controlling the solubility of aluminium in B horizons of podzolized soils /Simonsson, Magnus, January 1900 (has links) (PDF)
Diss. (sammanfattning) Uppsala : Sveriges lantbruksuniv. / Härtill 4 uppsatser.
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Retention and mobilisation of trinitrotoluene, aniline, nitrobenzene and toluene by soil organic matter /Eriksson, Johan, January 2003 (has links) (PDF)
Diss. (sammanfattning) Umeå : Sveriges lantbruksuniv., 2003. / Härtill 4 uppsatser.
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The Sorption and Transformation of Tylosin and Progesterone by SoilsKreinberg, Allison J. 14 August 2012 (has links)
No description available.
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