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M Mazet

Publications and source records attributed to M Mazet.

4 recordsLinked to original sources

Cathodic dissolution in the electrocoagulation process using aluminium electrodes.

All the authors working with aluminium electrodes in the electrocoagulation process have shown that a dissolution occurs at the cathode. This result cannot be explained by the electrochemical process in which only the anodes should be dissolved. The most probable reaction is a chemical attack by hydroxyl ions (generated during water reduction) on the aluminium cathode but nobody has proved it in the framework of the electrocoagulation process. So we are interested in determining what kind of reactions occurs at the cathode. For that, we have elaborated a batch pilot apparatus divided into two compartments, allowing measurement of gas formation taking place only in one compartment. The gases measurements were performed by mass spectrometry with helium as carrier gas. To validate our experimental protocol, the first experiments have been done with a stainless steel cathode: in this case, the results have indicated that the amount of created hydrogen is in good agreement with the values calculated using the second Faraday's law. The experiments realised with an aluminium cathode have shown that the hydrogen formation, in these conditions, was higher than those observed with the stainless steel cathode. All our investigations enable us to propose that with an aluminium cathode, hydrogen formation can be separated into two phenomena. The first one is due to an electrochemical reaction (water reduction), and the second one arises from a chemical reaction explaining the dissolution observed at the cathode.

Aluminum↗

Organic compounds adsorption onto activated carbon: the effect of association between dissolved humic substances and pesticides.

The quantitative determination of pesticide binding to dissolved humic substances is relevant to both water treatment operation using activated carbon adsorption process and the application of transport models that predict the environmental distribution patterns of a given hydrophobic contaminant. In this study and in a first set of experiments, the extent of binding between (i) three pesticides of environmental concern, aldicarb, lindane and pentachlorophenol, and (ii) dissolved commercial humic acid and soil extracted fulvic acid, was determined using dialysis experiments and water solubility enhancement tests. In a second set of experiments, the influence of dissolved humic substances or pesticide on the retention of the other co-adsorbate onto activated carbon was investigated in binary systems. It was found that association was negligible for aldicarb and that the pesticide sorption onto activated carbon was not affected by humic acid (8.5 mg liter(-1) DOC). The association constants K for lindane and pentachlorophenol were identical in the presence of fulvic acid (logK=4.1) but lower than that observed with humic acid. In the presence of humic acid, binding affinity for pentachlorophenol (logK=4.6) was higher than the one observed for lindane (logK=4.4), despite its much higher water solubility. This observation suggests that the aromatic character of the pentachlorophenol molecule contributes to association interactions with humic acid. From co-adsorption experiments onto activated carbon it was found that fulvic acid (7.7 mg litre(-1) DOC) slightly enhances sorption kinetics of pentachlorophenol. Lindane (1 mg litre(-1)) does not affect sorption kinetics for fulvic acid but markedly enhances both the sorption kinetics and adsorptive capacity for humic acid. Activated carbon retention of dissolved humic substances or pesticide appears to be enhanced by the association potential that exists between these co-adsorbates in some binary systems.

Journal Article↗