Illegal dumping sites are usually characterized by complex contamination situations due to the presence of multiple contamination sources. To improve the efficiency of illegal waste dumping site remediation, this study developed a numerical model considering the effects of groundwater levels and hydraulic gradient changes on remediation operations. Using this model, the most likely sources of contamination for 1,4-dioxane at an illegal waste site in Iwate Prefecture, Japan, were successfully identified (including location, amount, and time of occurrence) by reproducing historical monitoring data (from 2010 to 2022) through history matching, and future contaminant migration in groundwater was predicted. In addition, based on quantitative evaluations of the remediation measures, we found that some remediation measures, such as impermeable wall construction, while having some effects on the control of contamination spreading, may accelerate the migration of contaminants off-site due to the change of hydraulic gradient. Therefore, remediation procedures should be more carefully considered for illegal dumping sites based on an understanding of the distribution of contamination sources and hydraulic gradient evolutions.
Hydration, carbonation, and related metasomatism of mantle peridotite play a significant role in the global geochemical cycle. In this study, we combined an analysis of carbonated serpentinite with hydrothermal experiments on carbonation and Ca-metasomatism for samples from the Manlay ophiolite, southern Mongolia to investigate that carbonation mechanism of the serpentinite body after serpentinization. Samples show that the serpentinite was either transected by calcite and dolomite veins or was completely replaced by carbonates (calcite with minor dolomite) and quartz, in which the original mesh texture of serpentinite was preserved. Carbonation occurred after low-temperature serpentinization (lizardite/chrysotile), suggesting that carbonation occurred at temperatures lower than 300 ˚C. Calcite in the serpentinite showed δ13 CVPDB values ranging from -8.83 to -5.11 ‰ and δ18 OVSMOW from + 20.1 to + 24.4 ‰, suggesting that CO2 in the fluids could be derived from the degradation of organic material or methanotrophic processes rather than the origin of seafloor limestone. Three batch-type experiments, i.e., single step experiments (1) Olivine + NaHCO3,aq + CaCl2,aq and (2) Chrysotile + NaHCO3,aq + wollastonite (Ca source), and two steps experiment (3) Olivine carbonation and Ca-metasomatism, were conducted at 275 °C and 5.7 MPa to constrain the mechanism of calcite replacement of serpentinite. We found that calcite precipitated from the solution directly in the first two experiments, but replacement of serpentinite by calcite was not observed. In contrast, the third experiment caused the initial carbonation to form magnesite and then changed to calcite by later alteration. The natural occurrences and experiments revealed the possibility that the carbonation of olivine followed by Ca-rich fluid infiltration produced calcite in the carbonated serpentinite. Such Ca-metasomatism of Mg carbonates could easily occur in the ultramafic bodies and significantly affect the global carbon cycle.
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