TY - JOUR
T1 - Are We There Yet? A Critical Experimental Assessment of the Application of Induced Polarization for Monitoring Geochemical Processes
AU - Strobel, C.
AU - Störiko, A.
AU - Cirpka, O. A.
AU - Mellage, A.
PY - 2025
Y1 - 2025
N2 - Spectral induced polarization (SIP) can provide valuable information about (bio)geochemical processes taking place in the poorly accessible subsurface. The method is sensitive to reactions that alter the solid-water interface. Here, we critically evaluate the effectiveness of SIP to monitor geochemical processes by focusing on a model-supported analysis of cation exchange dynamics in sediments containing organic matter. Organic matter is a crucial substrate for contaminant immobilization that exhibits a strong SIP response. We compare the SIP response of columns during the injection of cations (Na+, Ca2+ and Zn2+) with different sorption strengths. We assess whether a change in surface ion mobility due to cation exchange is reflected by an increasing (Na+, high surface mobility) or decreasing (Zn2+, low surface mobility) imaginary conductivity. Our work demonstrates how we can qualitatively monitor reactive solute fronts using (S)IP, thus, helping to target sampling events. Furthermore, we explore the quantitative value of SIP data sets in constraining reactive transport models. We use the imaginary conductivity as a proxy for sorbed concentrations by separating the contributions of ion exchange and bulk electrical conductivity to changes in imaginary conductivity. By integrating a Bayesian parameter-estimation scheme, we test whether the use of SIP can replace geochemical sampling and improve reaction-parameter estimates. While inverting SIP-data alone does not yield better results than breakthrough samples, their integration reduces the uncertainty of some parameters, highlighting their potential value. Finally, we discuss opportunities and limitations for reaction monitoring using SIP and provide an outlook for its successful application by non-geophysicists.
AB - Spectral induced polarization (SIP) can provide valuable information about (bio)geochemical processes taking place in the poorly accessible subsurface. The method is sensitive to reactions that alter the solid-water interface. Here, we critically evaluate the effectiveness of SIP to monitor geochemical processes by focusing on a model-supported analysis of cation exchange dynamics in sediments containing organic matter. Organic matter is a crucial substrate for contaminant immobilization that exhibits a strong SIP response. We compare the SIP response of columns during the injection of cations (Na+, Ca2+ and Zn2+) with different sorption strengths. We assess whether a change in surface ion mobility due to cation exchange is reflected by an increasing (Na+, high surface mobility) or decreasing (Zn2+, low surface mobility) imaginary conductivity. Our work demonstrates how we can qualitatively monitor reactive solute fronts using (S)IP, thus, helping to target sampling events. Furthermore, we explore the quantitative value of SIP data sets in constraining reactive transport models. We use the imaginary conductivity as a proxy for sorbed concentrations by separating the contributions of ion exchange and bulk electrical conductivity to changes in imaginary conductivity. By integrating a Bayesian parameter-estimation scheme, we test whether the use of SIP can replace geochemical sampling and improve reaction-parameter estimates. While inverting SIP-data alone does not yield better results than breakthrough samples, their integration reduces the uncertainty of some parameters, highlighting their potential value. Finally, we discuss opportunities and limitations for reaction monitoring using SIP and provide an outlook for its successful application by non-geophysicists.
KW - cation exchange
KW - organic matter
KW - reactive transport modeling
KW - spectral induced polarization
UR - http://www.scopus.com/inward/record.url?scp=85219521880&partnerID=8YFLogxK
U2 - 10.1029/2024WR038567
DO - 10.1029/2024WR038567
M3 - Article
AN - SCOPUS:85219521880
SN - 0043-1397
VL - 61
JO - Water Resources Research
JF - Water Resources Research
IS - 2
M1 - e2024WR038567
ER -