Geochemical modeling of chromium oxidation and treatment of polluted waters by RO/NF membrane processes

Author(s):  
Ilaria Fuoco ◽  
Alberto Figoli ◽  
Alessandra Criscuoli ◽  
Rosanna De Rosa ◽  
Bartolo Gabriele ◽  
...  

<p>Geogenic Cr(VI) contamination is a worldwide environmental issue which mainly occurs in areas where ophiolitic rocks crop out. In these areas Cr (VI) can reach high concentrations into groundwaters becoming highly dangerous for human health. Indeed Cr(VI) is recognized as highly toxic element with high mobility and bioavailability [1]. Due to these features, starting from July 2017, Italian government has lowered the Cr(VI) limit value for drinking water to 10 µg/L. To improve the living standards in contaminated areas, it is needed (i) to understand the release and fate of contaminant during the water-rock interaction and (ii) to develop efficient remediation systems for natural polluted waters. In this regard, a complementary study on genesis and treatment of a Cr-rich groundwater coming from Italian ophiolitic aquifers was conducted. Reaction path modelling is a proven geochemical tool to understand the release of Cr and its oxidation from Cr(III) to Cr(VI) during the water-rock interaction. The generally accepted hypothesis of scientific community is that geogenic Cr(III) oxidation  is driven by the reduction of trivalent and tetravalent manganese (Mn(III); Mn (IV)) [2] whereas in this work the role of trivalent Fe hosted in serpentine minerals was re-evaluated. Unlike Mn, Fe is the main oxidant present in suitable amount in these rocks. Literature data confirmed the presence of Fe(III) into serpentine minerals hence reaction path modelling was performed varying the Fe (III)/Fe(tot) ratio ranging  from 0.60 to 1.00. The theoretical paths, reproduce the analytical concentrations of relevant solutes, including Cr(VI), in the Mg-HCO<sub>3</sub> water type hosted in the ophiolitic aquifers of Italy [3]. With increasing of Fe(III)/Fe(tot) ratio in serpentine minerals, high Cr(VI) concentration hold into solution until high alkalinity values. In addition, the spring with the highest Cr(VI) content (75 µg/L) was treated to lower its concentration below the threshold values.  In this work membrane technologies were used as  innovative method considering their many benefits, like the improvement of product quality without using chemicals [4]. A laboratory-scale set-up was used to carry out both Nanofiltration (NF) and Reverse Osmosis (RO) experiments. The experiments were conducted on different commercial membranes: one NF membrane module named DK (polyamide) and two RO membrane modules named AD (polyamide) and CD (cellulose).Tests were performed varying the operating pressures, and high Cr(VI) rejections (around 95%) were reached for all tested membranes, leading to a water containing Cr(VI) in concentrations below the threshold limits. The high flux, obtained already at lower operating pressures (27 L/m<sup>2</sup>h-10bar), combined with high selectivity towards Cr(VI) makes NF a favorable remediation option. The results obtained in this work are in line with the few data available in the literature for natural contaminated waters and there are quite promising for future scientific developments and application.</p><p> </p><p> </p><p>References</p><p>[1]Marinho B. A. et al., 2019. Environ Sci Pollut Res, 26(3), 2203-2227</p><p>[2]Oze C. et al., 2007. Proc. Natl. Acad. Sci. 104, 6544–6549</p><p>[3]Apollaro C. et al., 2019. Sci. Total Environ. 660, 1459-1471</p><p>[4]Figoli  A. & Criscuoli  A., 2017. Springer (Singapore); ISBN:9789811056215</p>

Geofluids ◽  
2021 ◽  
Vol 2021 ◽  
pp. 1-17
Author(s):  
C. Apollaro ◽  
I. Fuoco ◽  
L. Bloise ◽  
E. Calabrese ◽  
L. Marini ◽  
...  

This work is aimed at reconstructing the water-rock interaction processes controlling the geochemical characteristics of the shallow or relatively shallow groundwaters of the Pollino National Park, based on the data acquired for 105 water samples from local springs. Reaction path modeling of rock dissolution was carried out in a purely stoichiometric mode for the main lithotypes cropping out in the study area, that is, limestone, Mg-limestone, dolomite, serpentinite, Al-silicate fraction of calcschist, and carbonate fraction of calcschist. Reaction path modeling was carried out in a purely stoichiometric mode, considering the rocks of interest as materials of known stoichiometry and unknown thermodynamic properties. Calculations were carried out assuming a closed system for secondary solid phases whereas an open system was assumed for gases, O2(g) and CO2(g). Comparison of the results of geochemical modeling and the analytical data acquired for the groundwaters of the Pollino National Park shows that concentrations of major solutes, SiO2, Li, Al, and Fe of the different chemical types of waters, are explained by the dissolution of pertinent lithotypes. Moreover, the detected concentrations of Al, Cl, F, NO3, and SO4 are within the threshold values recommended by WHO.


2019 ◽  
Vol 109 ◽  
pp. 104391
Author(s):  
Carmen Zwahlen ◽  
Roy Wogelius ◽  
Cathy Hollis ◽  
Greg Holland

Water ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1162
Author(s):  
Florian Heine ◽  
Kai Zosseder ◽  
Florian Einsiedl

A comprehensive hydrogeological understanding of the deep Upper Jurassic carbonate aquifer, which represents an important geothermal reservoir in the South German Molasse Basin (SGMB), is crucial for improved and sustainable groundwater resource management. Water chemical data and environmental isotope analyses of D, 18O and 87Sr/86Sr were obtained from groundwater of 24 deep Upper Jurassic geothermal wells and coupled with a few analyses of noble gases (3He/4He, 40Ar/36Ar) and noble gas infiltration temperatures. Hierarchical cluster analysis revealed three major water types and allowed a hydrochemical zoning of the SGMB, while exploratory factor analyses identified the hydrogeological processes affecting the water chemical composition of the thermal water. Water types 1 and 2 are of Na-[Ca]-HCO3-Cl type, lowly mineralised and have been recharged under meteoric cold climate conditions. Both water types show 87Sr/86Sr signatures, stable water isotopes values and calculated apparent mean residence times, which suggest minor water-rock interaction within a hydraulically active flow system of the Northeastern and Southeastern Central Molasse Basin. This thermal groundwater have been most likely subglacially recharged in the south of the SGMB in close proximity to the Bavarian Alps with a delineated northwards flow direction. Highly mineralised groundwater of water type 3 (Na-Cl-HCO3 and Na-Cl) occurs in the Eastern Central Molasse Basin. In contrast to water types 1 and 2, this water type shows substantial water-rock interaction with terrestrial sediments and increasing 40Ar/36Ar ratios, which may also imply a hydraulic exchange with fossil formation waters of overlying Tertiary sediments.


2015 ◽  
Vol 61 (230) ◽  
pp. 1061-1078 ◽  
Author(s):  
Jeff W. Crompton ◽  
Gwenn E. Flowers ◽  
Dirk Kirste ◽  
Birgit Hagedorn ◽  
Martin J. Sharp

AbstractThe subglacial chemical weathering environment is largely controlled by low temperatures and the presence of freshly comminuted minerals with a high surface area. These characteristics are believed to promote dissolution processes that give rise to low silica and high Ca2+fluxes emanating from glacierized basins. We test an alternative hypothesis, that mineral precipitation reactions in the subglacial environment play an equally important role in controlling the water chemistry in glacierized basins. We analyze borehole and proglacial water chemistry from a subarctic polythermal glacier, complemented by mineral XRD analysis of suspended sediment, till and bedrock samples. In conjunction with a thermodynamic analysis of the water and mineral chemistry, we use reaction-path modelling to study the chemical enrichment of water through the glacier system. We find that the high pH of the subglacial environment is conducive to secondary mineral precipitation, and that it is not possible to balance the water chemistry using dissolution reactions alone. We show that low silica can be explained by standard weathering reactions without having to invoke mineral-leaching reactions. Our results suggest that subglacial weathering intensity may be significantly underestimated if the production of secondary minerals is not considered.


2008 ◽  
Vol 39 (3) ◽  
pp. 209-222 ◽  
Author(s):  
N. O. Jørgensen ◽  
J. Heinemeier

A multi-isotope approach in combination with hydrochemical data and borehole logging is applied to identify the source of brackish groundwater in a borehole in the well field of Neksø Municipal Waterworks in Bornholm, Denmark. The aquifer lithology consists of fractured Lower Cambrian sandstones resting on Proterozoic crystalline basement. The water body in the studied borehole is significantly stratified with respect to the hydrochemical and isotopic signatures and reveal a Na–Ca–Cl–HCO3 water type and TDS values >1,000 mg/L below a halocline at 40–55 m below measurement point (bmp). The occurrence of brackish groundwater is remarkable for this aquifer, which otherwise yields potable groundwater of good quality. The stable isotope (18O and 2H) compositions indicate a meteoric origin of the brackish groundwater, which rules out seawater intrusion into the aquifer. 14C activities show apparent 14C ages of the brackish groundwater in the range 2200–4300 yr (BP), whereas the freshwater samples above the halocline indicate modern age. Hydrochemical (Cl/Br and Sr) and isotopic studies (18O, 2H and 87Sr/86Sr) of the brackish groundwater point to a well-mixed and homogeneous water body reflecting long water–rock interaction and suggest a contribution of palaeowater from the fractured crystalline basement which has intruded into the Lower Cambrian sandstone aquifer.


2003 ◽  
Vol 18 (9) ◽  
pp. 1325-1345 ◽  
Author(s):  
James S Cleverley ◽  
Liane G Benning ◽  
Bruce W Mountain

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