Origin of nickel in water solution of the chalk aquifer in the north of France and influence of geochemical factors |
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Authors: | Daniel Bernard Jamal El Khattabi Emilie Lefevre Hani Serhal Sabine Bastin-Lacherez Isam Shahrour |
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Institution: | (1) Laboratoire de Mécanique de Lille (CNRS UMR 8107), Université des Sciences et Technologies de Lille (USTL), Polytech-Lille, Avenue Paul Langevin, 59655 Villeneuve d’Ascq Cedex, France |
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Abstract: | In the north of France, high registers of nickel are sometimes recorded within the chalk aquifer. In a confined context, the
presence of pyrite in the covering clays or in the marcasite nodules encrusted in the clay may constitute a natural source
of trace metals. With an objective of sanitary control, the limits of chemical contents regulating the quality of water destined
for human consumption have been lowered by the European Framework Directive in the field of water policy (2000/60/EC). As
a result, nickel limits have been reduced from 50 to 20 μg/l. The analyses, carried out on three water catchment fields in
our area of study, were centred on variable parameters (Eh, O2(d), pH, Conductivity, T°), major elements (SO4, NO3) and metals (Fe, Ni, Mn, Co). The acquired data enabled us to identify from one hand, the conditions which are presented
within the site, special thanks to the evolution of nitrate and iron contents and on the other hand, the natural origin (geological)
of nickel for two of the three sites studied based essentially on the evaluation of the Nickel/Cobalt ratio. Thus, on the
first site, the evolution of nickel content and nitrate content showed the influence of the phenomenon of denitrification
on the re-mobilisation of the nickel. Whereas on the second site, a high variation of total iron content and oxygen dissolved
in solution highlighted a particular phenomenon of oxidation of the pyrite through molecular oxygen. Finally, the correlation
with the sulphates clearly showed behaviour of the nickel, once released, that was entirely dependent on the phenomenon of
adsorption on the iron and manganese hydroxides. |
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