Gry Lyngsie

Deposition of Nutrients From Harmattan Dust in Ghana, West Africa

In order to measure dusts nutrient input on farmland in different agro-ecological zones, Harmattan dust was sampled by mats with plastic straw in Ghana between 2002-2006. The inputs of total nutrients by Harmattan dust in Ghana per Harmattan period were about 1-2 kg Ca ha-1, 0.5-2 kg K ha-1, 0.5-1.5 kg Mg ha-1 and less than 0.5 kg P ha-1. Compared with the annual input of nutrients by precipitation, the dust accounted for 10% or less of Ca, Mg and K but approximately 20%-40% of P. The input of nutrients by dust was only valid for areas with vegetation, because in areas with none or sparse vegetation, loss of soil due to wind erosion and hereby loss of nutrients might be significant. In farmland areas with bare and vegetated fields there seemed to be an internal redistribution of the nutrients and not a net gain of nutrients from outside the area (long-range transported dust). The input of P by dust might be of some importance in the traditional shifting cultivation systems, while the inputs of other three nutrients of Ca, Mg and K were so low that they must be considered insignificant. In the intensive agriculture systems with huge inputs of manures and fertilizers the nutrient input by dust is insignificant and could be neglected. (Less)

Oxidation of a Dimethoxyhydroquinone by Ferrihydrite and Goethite Nanoparticles : Iron Reduction versus Surface Catalysis

Hydroquinones are important mediators of electron transfer reactions in soils with a capability to reduce Fe(III) minerals and molecular oxygen, and thereby generating Fenton chemistry reagents. This study focused on 2,6-dimethoxy hydroquinone (2,6-DMHQ), an analogue to a common fungal metabolite, and its reaction with ferrihydrite and goethite under variable pH and oxygen concentrations. Combined wet-chemical and spectroscopic analyses showed that both minerals effectively oxidized 2,6-DMHQ in the presence of oxygen. Under anaerobic conditions the first-order oxidation rate constants decreased by one to several orders of magnitude depending on pH and mineral. Comparison between aerobic and anaerobic results showed that ferrihydrite promoted 2,6-DMHQ oxidation both via reductive dissolution and heterogeneous catalysis while goethite mainly caused catalytic oxidation. These results were in agreement with changes in the reduction potential (EH) of the Fe(III) oxide/Fe(II)aq redox couple as a function of dissolved Fe(II) where EH of goethite was lower than ferrihydrite at any given Fe(II) concentration, which makes ferrihydrite more prone to reductive dissolution by the 2,6-DMBQ/2,6-DMHQ redox couple. This study showed that reactions between hydroquinones and iron oxides could produce favorable conditions for formation of reactive oxygen species, which are required for nonenzymatic Fenton-based decomposition of soil organic matter.

Generation of hydroxyl radicals from reactions between a dimethoxyhydroquinone and iron oxide nanoparticles

The hydroxyl radical (·OH) is a powerful oxidant that is produced in a wide range of environments via the Fenton reaction (Fe2+  + H2O2 → Fe3+  + ·OH + OH-). The reactants are formed from the reduction of Fe3+ and O2, which may be promoted by organic reductants, such as hydroquinones. The aim of this study was to investigate the extent of ·OH formation in reactions between 2,6-dimethoxyhydroquinone (2,6-DMHQ) and iron oxide nanoparticles. We further compared the reactivities of ferrihydrite and goethite and investigated the effects of the O2 concentration and pH on the generation of ·OH. The main finding was that the reactions between 2,6-DMHQ and iron oxide nanoparticles generated substantial amounts of ·OH under certain conditions via parallel reductive dissolution and catalytic oxidation reactions. The presence of O2 was essential for the catalytic oxidation of 2,6-DMHQ and the generation of H2O2. Moreover, the higher reduction potential of ferrihydrite relative to that of goethite made the former species more susceptible to reductive dissolution, which favored the production of ·OH. The results highlighted the effects of surface charge and ligand competition on the 2,6-DMHQ oxidation processes and showed that the co-adsorption of anions can promote the generation of ·OH.