Photodegradation of the herbicide azimsulfuron using nanocrystalline titania films as photocatalyst and low intensity Black Light radiation or simulated solar radiation as excitation source

Aqueous solutions of the herbicide azimsulfuron have been treated by a photocatalytic process employing titania nanocrystalline films as photocatalyst. Results showed that solutions of this herbicide at maximum possible concentration can be photodegraded in a time of a few hours by using low intensity UVA radiation comparable with that of the UVA of solar noon. Similar results have also been obtained with simulated solar radiation. Thus heterogeneous photocatalysis can be employed for the treatment of waters polluted by this herbicide.     

Performance of Pilot-scale Constructed Floating Wetlands in the Removal of Nutrients and Pesticides

Aiming to evaluate the efficacy of constructed floating wetlands (CFW) in removing agrochemicals (nutrients and pesticides), a series of experiments were run continuously for a 16-week period in pilot-scale CFW systems to study the effect of two aquatic plant species (duckweed and water hyacinth) and climatic parameters. The CFW systems were loaded daily with agricultural polluted water containing a fertilizer and five pesticides, whose concentrations and removal efficiencies were measured in the experiments. Average nutrient and pesticide reductions varied from 27.4% to 83.6% and from 12.4% to 42.7%, respectively. The two plants performed almost equally well. High temperatures and increased solar radiation significantly contributed to increased removal performance. The results suggest the use of CFW systems as effective and low-cost agricultural pollution control technologies.

     

Electrochemical promotion of CO<Subscript>2</Subscript> hydrogenation on Rh/YSZ electrodes

The electrochemical promotion of the CO₂ hydrogenation reaction on porous Rh catalyst–electrodes deposited on Y₂O₃-stabilized-ZrO₂ (or YSZ), an O²⁻ conductor, was investigated under atmospheric total pressure and at temperatures 346–477 °C, combined with kinetic measurements in the temperature range 328–391 °C. Under these conditions CO₂ was transformed to CH₄ and CO. The CH₄ formation rate increased by up to 2.7 times with increasing Rh catalyst potential (electrophobic behavior) while the CO formation rate was increased by up to 1.7 times with decreasing catalyst potential (electrophilic behavior). The observed rate changes were non-faradaic, exceeding the corresponding pumping rate of oxygen ions by up to approximately 210 and 125 times for the CH₄ and CO formation reactions, respectively. The observed electrochemical promotion behavior is attributed to the induced, with increasing catalyst potential, preferential formation on the Rh surface of electron donor hydrogenated carbonylic species leading to formation of CH₄ and to the decreasing coverage of more electron acceptor carbonylic species resulting in CO formation.