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The long-term performance of the permeable reactive barriers in remediating contaminated groundwater may diminish as a result of oxidation, precipitation on the particle surfaces, and pore space clogging. Evaluating its performance through monitoring could address this dilemma. We investigate the spectral induced polarization (SIP) response of zero valent iron (ZVI)-activated carbon (AC)-sand mixtures.The chargeablity exhibits a perfect linear relation to the volumetric concentration of ZVI (2.5-50%) and AC (2.5%-75%) with r = 0.99. However, the low-frequency electrical conductivity shows low sensitivity to the volumetric content of ZVI and AC. The relaxation time increases with the particle sizes. When these two particles are mixed, chargeablity is approximated as a superposition of their individual values. In terms of phase values and frequencies of the phase peaks, it also exhibits this superposition effect. Furthermore, we conducted 720-hour SIP measurements on ZVI-AC-sand columns flushed with NaCl or NaNO3 solutions. It suggests that precipitation of 0.06 mm thick sedimentation onto the ZVI surface induced by changes in redox chemistry observed in micromorphology images, resulting an increase in the normalized chargeability by 44.05%, the scaled relaxation time and Cole–Cole model exponent by 1098.99% and 23.11%. Compared to flow-through by NaCl solution, changes in these parameters are more pronounced for columns saturated with NaNO3 solution, indicating the corrosion of ZVI. Our findings illustrate that induced polarization parameters vary in response to the chemical alteration of ZVI-AC-sand mixed media, showing the potential for noninvasive long-term monitoring of the reactive barriers.
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Mao et al. (2024) studied this question.
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