Origine du manganèse de la nappe alluviale de Beaucaire (Gard, France) Essai de démanganisation in situ (procédé Vyredox)

L'origine et le mécanisme de l'augmentation de la concentration en manganèse dans l'eau de la nappe phréatique de Beaucaire ont été recherchés afin d'orienter le choix d'un procédé de démanganisation adapté aux conditions du site.L'aquifère est caractérisé par son déficit en oxygène et par la présence de dépôts d'oxyde de manganèse (Mn(IV)) sur les sédiments. Dans ces conditions la microflore utilise les oxydes de manganèse conne accepteur final d'électrons (démontré dans les expériences in vitro) et le manganèse réduit passe alors en solution.Lors des essais d'application du procédé Vyredox le potentiel d'oxydoréduction de la nappe augmente et la concentration en manganèse dissous diminue. Rien n'indique une précipitation du manganèse et donc un colmatage à la périphérie de la partie oxygénée de la nappe.The origin and the mechanism of the increase of the dissolved manganese concentrations have been investigated to choose a system of demanganization well fitted b the site conditions.The aquifer characteristics are a depletion of the dissolved oxygen amount and deposits of manganese oxides (Mn(IV)) on the detriments. Under these conditions the microflora utilizes these manganese oxides as a final electron acceptor (as demonstrated by in vitro experiments) and the solubilization of manganese takes place.The field application of the Vyredox system increases the redox potential of the groundwater and the manganese concentration decreases. Nothing indicates that manganese precipitation and consequently warping of the water table takes place at the periphery of the oxygenated part of the aquifer

PET waste as organic linker source for the sustainable preparation of MOF-derived methane dry reforming catalysts

A catalyst made of Ni0 nanoparticles highly dispersed on a lamellar alumina support was prepared by an environmentally-friendly route. The latter involved the synthesis of an aluminum-containing metalorganic framework (MOF) MIL-53(Al) in which the linkers were derived from the depolymerization of polyethylene terephthalate (PET) originating from plastic wastes. After demonstrating the purity and structure integrity of the PET-derived MIL-53(Al), this MOF was impregnated with nickel nitrate salt and then calcined to form a lamellar Ni-Al2O3 mixed metal oxide with a high surface area (SBET = 1276 m2 g-1, N2 sorption). This mixed oxide consisted of nickel aluminate nanodomains dispersed within amorphous alumina, as revealed by PXRD and TPR analyses. Subsequent reduction under H2 resulted in the formation of well-dispersed 5 nm Ni0 nanoparticles homogeneously occluded within the interlamellar porosity of the γ-alumina matrix, as attested by electron microscopy. This waste-derived catalyst displayed catalytic performances in the reaction of dry reforming of methane (DRM) as good as its counterpart made from a MOF obtained from commercial benzene-1,4-dicarboxylic acid (BDC). Thus, under similar steady state conditions, at 650 °C and 1 bar, the PET-derived catalyst led to CH4 and CO2 conversions as high as those on the BDC-derived catalyst, and its catalytic stability and selectivity towards DRM were excellent as well (no loss of activity after 13 h and H2:CO products ratio remaining at 1). Moreover, both catalysts were much better than those of a reference nickel alumina catalyst prepared by conventional impregnation route. This work therefore demonstrates the possibility of using plastic wastes instead of commercial chemicals to prepare efficient porous nickel-alumina DRM catalysts from MOFs, fostering the concept of circular economy