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Oxidant Concentration (oxidant + concentration)

Distribution by Scientific Domains

Engineering	50%
Life Sciences	33%

Selected Abstracts

Optimization of Full-Scale Permanganate ISCO System Operation: Laboratory and Numerical Studies

GROUND WATER MONITORING & REMEDIATION, Issue 4 2008
Jeffrey L. Heiderscheidt
Laboratory characterization studies, one-dimensional flow-through studies, and numerical model simulations were conducted to examine site conditions and system features that may have adversely affected in situ chemical oxidation (ISCO) performance at the Naval Training Center's (NTC) Operable Unit 4 located in Orlando, Florida, and to identify potential ISCO system modifications to achieve the desired remediation performance. At the NTC site, ISCO was implemented using vertical injection wells to deliver potassium permanganate into a ground water zone for treatment of tetrachloroethylene and its breakdown products. However, oxidant distribution was much more limited than anticipated. Characterization studies revealed that the ground water zone being treated by ISCO was very fine sand with a small effective particle size and low uniformity coefficient, along with a high organic carbon content, high natural oxidant demand (NOD), and a high ground water dissolved solids concentration, all of which contributed to full-scale ISCO application difficulties. These site conditions contributed to injection well permeability loss and an inability to achieve the design oxidant injection flow rate, limiting the actual oxidant distribution at the site. Flow-through experiments demonstrated that more favorable oxidant delivery and distribution conditions are enabled by applying a lower oxidant concentration at a faster delivery rate for a greater number of pore volumes. Numerical simulations, run for a variety of conditions (injection/extraction well flow rates, injected oxidant concentration, amount of NOD present, and NOD oxidation rate), also revealed that low,oxidant concentration injection at a high flow rate is a more effective method to deliver the required mass of oxidant to the target treatment zone. [source]

On the effect of the local turbulence scales on the mixing rate of diffusion flames: assessment of two different combustion models

INTERNATIONAL JOURNAL OF ENERGY RESEARCH, Issue 10 2002
Jose Lopes
Abstract A mathematical model for the prediction of the turbulent flow, diffusion combustion process, heat transfer including thermal radiation and pollutants formation inside combustion chambers is described. In order to validate the model the results are compared herein against experimental data available in the open literature. The model comprises differential transport equations governing the above-mentioned phenomena, resulting from the mathematical and physical modelling, which are solved by the control volume formulation technique. The results yielded by the two different turbulent-mixing physical models used for combustion, the simple chemical reacting system (SCRS) and the eddy break-up (EBU), are analysed so that the need to make recourse to local turbulent scales to evaluate the reactants' mixing rate is assessed. Predictions are performed for a gaseous-fuelled combustor fired with two different burners that induce different aerodynamic conditions inside the combustion chamber. One of the burners has a typical geometry of that used in gaseous fired boilers,fuel firing in the centre surrounded by concentric oxidant firing,while the other burner introduces the air into the combustor through two different swirling concentric streams. Generally, the results exhibit a good agreement with the experimental values. Also, NO predictions are performed by a prompt-NO formation model used as a post-processor together with a thermal-NO formation model, the results being generally in good agreement with the experimental values. The predictions revealed that the mixture between the reactants occurred very close to the burner and almost instantaneously, that is, immediately after the fuel-containing eddies came into contact with the oxidant-containing eddies. As a result, away from the burner, the SCRS model, that assumes an infinitely fast mixing rate, appeared to be as accurate as the EBU model for the present predictions. Closer to the burner, the EBU model, that establishes the reactants mixing rate as a function of the local turbulent scales, yielded slightly slower rates of mixture, the fuel and oxidant concentrations which are slightly higher than those obtained with the SCRS model. As a consequence, the NO concentration predictions with the EBU combustion model are generally higher than those obtained with the SCRS model. This is due to the existence of higher concentrations of fuel and oxygen closer to the burner when predictions were performed taking into account the local turbulent scales in the mixing process of the reactants. The SCRS, being faster and as accurate as the EBU model in the predictions of combustion properties appears to be more appropriate. However, should NO be a variable that is predicted, then the EBU model becomes more appropriate. This is due to the better results of oxygen concentration yielded by that model, since it solves a transport equation for the oxidant concentration, which plays a dominant role in the prompt-NO formation rate. Copyright © 2002 John Wiley & Sons, Ltd. [source]

Activation of the redox sensor Pap1 by hydrogen peroxide requires modulation of the intracellular oxidant concentration

MOLECULAR MICROBIOLOGY, Issue 5 2004
Ana P. Vivancos
Summary The transcription factor Pap1 and the MAP kinase Sty1 are key regulators of hydrogen peroxide-induced responses in Schizosaccharomyces pombe. Pap1 can be activated quickly at low, but not high, hydrogen peroxide concentrations. The MAP kinase Sty1 has been reported to participate in Pap1 activation by the oxidant. Here, we provide biochemical and genetic evidence for the in vivo formation of a hydrogen peroxide-induced disulphide bond in Pap1, which precedes the rapid and reversible nuclear accumulation of the transcription factor. We show that activation of the Sty1 cascade before the oxidative insult, or overexpression of the Sty1-regulated genes ctt1 (encoding catalase) or gpx1 (encoding glutathione peroxidase), can accelerate Pap1 entry even at high doses of hydrogen peroxide. In fact, the lack of Sty1 impedes Pap1 nuclear localization, but only at high doses of the oxidant. We propose that, whereas low doses of hydrogen peroxide lead directly to Pap1 oxidation-activation, high concentrations of the oxidant initially activate the Sty1 pathway, with the consequent increase in scavenging enzymes, which in turn helps to decompose the excess of hydrogen peroxide and achieve an appropriate concentration for the subsequent activation of Pap1. Our results also suggest that activation of Sty1 at high doses of hydrogen peroxide may also be required to trigger other antioxidant activities such as those reverting the overoxidation of cysteine residues at the Pap1 pathway. [source]

Atmospheric Pressure Barrier Discharge Deposition of Silica-Like Films on Polymeric Substrates

PLASMA PROCESSES AND POLYMERS, Issue S1 2007
Sergei Starostine
Abstract Silica-like coatings were deposited on polymer foils in APG discharge in a roll-to-roll configuration. The dependence of film structure and chemical composition on the conditions during deposition process was studied by means of SEM, ATR-FTIR, and XPS analysis. The influence of oxidant concentration on the deposited film properties is analyzed and discussed. It was observed that pulsing of the APG discharge suppresses dust formation in atmospheric plasma and, therefore, provides uniform coatings. [source]

Empirical and modeling evidence of regional atmospheric transport of current-use pesticides

ENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 10 2004
Derek C. G. Muir
Abstract Water samples from 30 lakes in Canada and the northeastern United States were analyzed for the occurrence of 27 current-use pesticides (CUPs). Eleven CUPs were frequently detected in lakes receiving agricultural inputs as well as in remote lakes hundreds of kilometers from known application areas. These included the triazine herbicide atrazine and its desethylated degradation product; the herbicides alachlor, metolachlor, and dacthal; the organophosphate insecticides chlorpyrifos, diazinon, and disulfoton; the organochlorine insecticides ,-endosulfan and lindane; and the fungicides chlorothalonil and flutriafol. For six of the pesticides, empirical half-distances on the order of 560 to 1,820 km were estimated from the water-concentration gradient with latitude. For most of the pesticides, a suite of assessment models failed to predict such atmospheric long-range transport behavior, unless the effect of periods of lower hydroxyl radical concentrations and dry weather were taken into account. Observations and model results suggest that under the conditions prevailing in south-central Canada (relatively high latitude, low precipitation rates), many CUPs will be able to undergo regional-scale atmospheric transport and reach lakes outside areas of agricultural application. When assessing the potential of fairly reactive and water-soluble substances to undergo long-range transport, it is imperative to account for periods of no precipitation, to assure that degradation rate constants are correct, and to apply oxidant concentrations that are valid for the region and time period of interest. [source]