Search results for "Humic"
showing 10 items of 127 documents
Environmentally relevant precursors of carbonyl sulfide in aquatic systems
1997
Seawater solutions of environmentally relevant organosulfur compounds, commercial humic acid (HA), and natural dissolved organic matter (DOM) were incubated with and without UV light in order to determine the carbonyl sulfide (COS) producing capabilities of these compounds. COS dark- and photo-production rate constants were determined for dilute solutions of the organosulfur compounds (μmol l−1) and HA/DOM (mg l−1). Dissolved COS was determined using a purge and cryogenic trap method followed by GC/FPD detection. COS was produced in considerable amounts both non-photochemically and photochemically from the reduced form of free acid of glutathione (GSH) and photochemically from cysteine (CYS…
Interactions between 2-Aminobenzothiazole and Natural Organic Matter as Evidenced by CPMAS Nitrogen-15 NMR Spectroscopy
2009
Cross-polarization magic angle spinning (CPMAS) 15N nuclear magnetic resonance (NMR) spectroscopy was used to study the interactions between 2-aminobenzothiazole (ABT) and natural organic matter in the presence of the natural enzyme laccase and synthetic air. Through the use of synthesized model compounds, we were able to confirm previous findings by CPMAS 13C NMR spectroscopy that showed the formation of covalent amide bonds. We also provide evidence of the presence of two additional H bonds between ABT and the natural organic matter. Both H bonds involved the amino and thiazole groups of ABT.
Transformation of monuron photosensitized by soil extracted humic substances: energy or hydrogen transfer mechanism?
1997
The humic and fulvic acids extracted from a Ranker type soil sensitize the transformation of monuron. When monuron is irradiated at 365 nm in the presence of the fulvic acid, its degradation is faster in deoxygenated medium than in air-saturated solution. Chloride ions are released, and the para-hydroxylated derivative is formed as upon direct photolysis. It is deduced that the consumption of monuron observed in the absence of oxygen is due to an energy transfer from reactive triplet states of the fulvic acid to monuron. Energy transfer reactions also take place when hydroquinone or acetophenone are used as sensitizers, showing that the energy level of the triplet state of monuron is lower …
Copper Isotope Fractionation during Complexation with Insolubilized Humic Acid
2010
The bioavailability, mobility, and toxicity of Cu depend on Cu speciation in solution. In natural systems like soils, sediments, lakes, and river waters, organo-Cu complexes are the dominating species. Organo-complexation of Cu may cause a fractionation of stable Cu isotopes. The knowledge of Cu isotope fractionation during sorption on humic acid may help to better understand Cu isotope fractionation in natural environments and thus facilitate the use of Cu stable isotope ratios (delta(65)Cu) as tracer of the fate of Cu in the environment. We therefore studied Cu isotope fractionation during complexation with insolubilized humic acid (IHA) as a surrogate of humic acid in soil organic matter…
How Humic Substances Dominate Mercury Geochemistry in Contaminated Floodplain Soils and Sediments
1998
The interaction of mercury (Hg) and humic substances (hs) was studied in floodplain topsoils and surface sediments of the contaminated German river Elbe. An intimate coupling exists between the geochemical cycles of Hg and organic carbon (OC) in this ecosystem. Humic substances exert a dominant influence on several important parallel geochemical pathways of Hg, including binding, transformation, and transport processes. Significant differences exist between the Hg-hs associations in floodplains and sediments. Both humic acids (ha) and fulvic acids (fa) contribute to Hg binding in the sediments. In contrast, ultrafiltration experiments proved that Hg in the floodplain soils is almost exclusi…
MODIFICATION OF HUMIC SUBSTANCES FOR DEVELOPMENT OF MATERIALS FOR ENVIRONMENTAL TECHNOLOGIES
2019
Humic substances are high molecular weight refractory polycationites formed during decay of living organic matter and through biosynthesis of low molecular weight organic substances (metabolites or decay products of living organisms). Presence of many functional groups in the structure of humic substances determines their ability to interact with metal ions forming stable complexes and influencing metal ion speciation in the environment and mobility, behaviour and speciation forms in the environment. Presently humic substances are a product of industrial scale and quantities in amounts of hundreds of tons are produced. The aim of this study is to analyse derivatization possibilities of humi…
Remediation of Soil Contamination with Heavy Metals by Using Zeolite and Humic Acid Additives
2012
- Soil remediation at contaminated sites very often needs customized approach, because of the different content of pollutants. Various technologies from simple soil excavation and transporting to hazardous waste landfills to different kinds of remediation by vitrification and the use of additives can be used for the treatment of soil. A series of remediation experiments using zeolites and humic acids were applied to soil contaminated with copper. Remediation can be performed with easily available additive materials of natural origin found near the place of application, in order to diminish the leaching of contaminants. Soils contaminated and spiked with copper were mixed with additives, and…
Chemical speciation of polycyclic aromatic hydrocarbons in sediments: partitioning and extraction of humic substances.
2010
The primary objective of this study was to examine the chemical speciation of polycyclic aromatic hydrocarbons (PAHs) found in sediments endowed with different characteristics. To achieve this purpose and because the nature of the sediments influences the distribution of PAHs, we have analyzed four different types of sediments. To study the role of organic matter in the sequestration of PAHs, we fractionated humic substances into humic acids and humin–mineral fractions. After their separation and purification, the humic components were examined for their sorptive reactivity by extracting them with organic solvents; these extracts were subsequently subjected to GC/MS analysis. Our results sh…
Effect of ramp size and sample spinning speed on CPMAS 13C NMR spectra of soil organic matter
2011
Abstract Cross polarization (CP) magic angle spinning (MAS) 13C NMR spectroscopy is a solid state NMR technique widely applied to study the chemical composition of natural organic matter. In high magnetic fields (>7 T), fast sample spinning is required in order to reduce the influence of spinning sidebands underlying other chemical shift regions. As the spinning speed increases, the Hartmann–Hahn matching profiles break down into a series of narrow matching bands. In order to account for this instability variable amplitude cross polarization techniques (e.g. VACP, ramp-CP) have been developed. In the present study, we experimentally verified the stability of the Hartmann–Hahn condition unde…
O-Alkylation of a lignite humic acid by phase-transfer catalysis
2006
A mild phase-transfer catalytic reaction has been conducted to O-alkylate the acidic functions of a lignite humic acid (HA), using tetrabutylammonium hydroxide as the phase-transfer catalyst. The HA acidic functional groups were made to react, in tetrahydrofuran, by nucleophilic substitution with several alkyl halides-methyl iodide, and ethyl, propyl, and butyl, and benzyl bromide. The occurrence of the O-alkylation reaction was assessed by elemental analysis and 1H NMR, CPMAS 13C NMR, and FTIR spectroscopy. Bonding of alkyl groups increased the carbon and hydrogen content and the H/C ratios of all the humic reaction products. Increased nitrogen in the reaction products suggested incomplete…