Evolution of the chemistry of Fe bearing waters during CO 2 degassing

J.N. Geroni; C.A. Cravotta; D.J. Sapsford

doi:10.1016/j.apgeochem.2012.07.017

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Evolution of the chemistry of Fe bearing waters during CO 2 degassing

J.N. Geroni·C.A. Cravotta·D.J. Sapsford

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Abstract

The rates of Fe(II) oxidation and precipitation from groundwater are highly pH dependent. Elevated levels of dissolved CO 2 can depress pH and cause difficulty in removing dissolved Fe and associated metals during treatment of ferruginous water. This paper demonstrates interdependent changes in pH, dissolved inorganic C species, and Fe(II) oxidation rates that occur as a result of the removal (degassing) of CO 2 during aeration of waters discharged from abandoned coal mines. The results of field monitoring of aeration cascades at a treatment facility as well as batchwise aeration experiments conducted using net alkaline and net acidic waters in the UK are combined with geochemical modelling to demonstrate the spatial and temporal evolution of the discharge water chemistry. The aeration cascades removed approximately 67% of the dissolved CO 2 initially present but varying the design did not affect the concentration of Fe(II) leaving the treatment ponds. Continued removal of the residual CO 2 by mechanical aeration increased pH by as much as 2 units and resulted in large increases in the rates of Fe(II) oxidation and precipitation. Effective exsolution of CO 2 led to a reduction in the required lime dose for removal of remaining Fe(II), a very important factor with regard to increasing the sustainability of treatment practices. An important ancillary finding for passive treatment is that varying the design of the cascades had little impact on the rate of CO 2 removal at the flow rates measured.

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J.N. Geroni, C.A. Cravotta, D.J. Sapsford. 2012. Evolution of the chemistry of Fe bearing waters during CO 2 degassing. https://doi.org/10.1016/j.apgeochem.2012.07.017

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