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1.
Chemosphere ; 44(4): 613-9, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11482648

ABSTRACT

The redox process between iron(III) (in dissolved form and as the mineral phase ferrihydrite) and phenolic substances has been examined. We investigated the relationship between the structure and reactivity for the dihydrobenzene reductants catechol, hydroquinone and resorcine, and for the 2-methoxyphenol guaiacol with iron(III), by determining the rate of the Fe(III) reduction as well as the production of CO2. This work demonstrates that catechol and guaiacol will be effectively oxidized to CO2 by reducing iron(III). Hydroquinone shows a reduction of iron(III), but no accompanying mineralization could be determined. In contrast, resorcine showed no reaction with Fe(II). The deciding factor on whether or not mineralization occurs were controlled by the position of the hydroxy groups. It is shown that phenolic substances with two hydroxy groups in the orthoposition or at least one hydroxy group and a methoxy group can be oxidized to CO2 while iron(III) is reduced.


Subject(s)
Ferric Compounds/chemistry , Phenols/chemistry , Soil Pollutants , Carbon Dioxide/analysis , Carbon Dioxide/chemistry , Oxidation-Reduction , Structure-Activity Relationship
2.
Nature ; 403(6767): 298-301, 2000 Jan 20.
Article in English | MEDLINE | ID: mdl-10659846

ABSTRACT

Volatile halogenated organic compounds (VHOC) play an important role in atmospheric chemical processes-contributing, for example, to stratospheric ozone depletion. For anthropogenic VHOC whose sources are well known, the global atmospheric input can be estimated from industrial production data. Halogenated compounds of natural origin can also contribute significantly to the levels of VHOC in the atmosphere. The oceans have been implicated as one of the main natural sources, where organisms such as macroalgae and microalgae can release large quantities of VHOC to the atmosphere. Some terrestrial sources have also been identified, such as wood-rotting fungi, biomass burning and volcanic emissions. Here we report the identification of a different terrestrial source of naturally occurring VHOC. We find that, in soils and sediments, halide ions can be alkylated during the oxidation of organic matter by an electron acceptor such as Fe(III): sunlight or microbial mediation are not required for these reactions. When the available halide ion is chloride, the reaction products are CH3Cl, C2H5Cl, C3H7Cl and C4H9Cl. (The corresponding alkyl bromides or alkyl iodides are produced when bromide or iodide are present.) Such abiotic processes could make a significant contribution to the budget of the important atmospheric compounds CH3Cl, CH3Br and CH3I.


Subject(s)
Atmosphere/chemistry , Geologic Sediments , Hydrocarbons, Halogenated/analysis , Soil , Ferric Compounds/chemistry , Geologic Sediments/analysis , Hydrocarbons, Halogenated/chemistry , Organic Chemicals/analysis , Organic Chemicals/chemistry , Oxidation-Reduction , Soil/analysis
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