Assessing a Large-Scale Sequential In Situ Chloroethene Bioremediation System Using Compound-Specific Isotope Analysis (CSIA) and Geochemical Modeling

Abstract

Compound-specific isotopic analysis (CSIA) and geochemical modeling were applied to evaluate the effectiveness of an 800 m-long sequential in situ bioremediation (ISB) system in Northern Italy. The system was created for the clean-up of a polluted aquifer affected by chloroethenes. A hydraulically upgradient anaerobic (AN)-biobarrier-stimulated reductive dichlorination (RD) of higher chloroethenes (PCE, TCE) and a downgradient aerobic (AE)-biobarrier-stimulated oxidation (OX) of lower chloroethenes (DCE, VC) were proposed. Carbon CSIA and concentration data were collected for PCE, TCE, cis-DCE and VC and interpreted using a reactive transport model that was able to simulate isotopic fractionation. The analysis suggested that the combination of CSIA and modeling was critical to evaluate the efficiency of sequential ISBs for the remediation of chloroethenes. It was found that the sequential ISB could reduce the PCE, TCE and cis-DCE concentrations by >99% and VC concentrations by >84% along the flow path. First-order RD degradation rate constants (kRD) increased by 30 times (from kRD = 0.2–0.3 y−1 up to kRD = 6.5 y−1) downgradient of the AN barrier. For cis-DCE and VC, the AE barrier had a fundamental role to enhance OX. First-order OX degradation rate constants (kOX) ranged between kOX = 0.7–155 y−1 for cis-DCE and kOX = 1.7–12.6 y−1 for VC.