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Peroxydisulfate Persistence in ISCO for Groundwater Remediation: Temperature Dependence, Batch/Column Comparison, and Sulfate Fate.

Authors :
McGachy, Lenka
Škarohlíd, Radek
Kostrakiewicz, Richard
Kühnl, Karel
Těšínská, Pavlína
Müllerová, Barbora
Šír, Marek
Martinec, Marek
Source :
Water (20734441); Dec2024, Vol. 16 Issue 24, p3552, 18p
Publication Year :
2024

Abstract

The persistence of peroxydisulfate anion (S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript>) in soil is a key factor influencing the effectiveness of in situ chemical oxidation (ISCO) treatments, which use S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> (S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> based ISCO) to remediate contaminated groundwater. However, only a few studies have addressed aspects of S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> persistence, such as the effect of temperature and the fate of sulfates (SO<subscript>4</subscript><superscript>2−</superscript>) generated by S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition in real soil and/or aquifer materials. Additionally, there are no studies comparing batch and dynamic column tests. To address these knowledge gaps, we conducted batch tests with varying temperatures (30–50 °C) and initial S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> concentrations (2.7 g/L and 16.1 g/L) along with dynamic column experiments (40 °C, 16.1 g/L) with comprehensively characterized real soil/aquifer materials. Furthermore, the principal component analysis (PCA) method was employed to investigate correlations between S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition and soil material parameters. We found that S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition followed the pseudo-first-order rate law in all experiments. In all tested soil materials, thermal dependence of S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition followed the Arrhenius law with the activation energies in the interval 65.2–109.1 kJ/mol. Decreasing S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> concentration from 16.1 g/L to 2.7 g/L led to a several-fold increase (factor 2–11) in bulk S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition rate coefficients (k′) in individual soil/aquifer materials. Although k′ in the dynamic column tests showed higher values compared to the batch tests (factor 1–3), the normalized S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition rate coefficients to the total BET surface were much lower, indicating the inevitable formation of preferential pathways in the columns. Furthermore, mass balance analysis of S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> decomposition and SO<subscript>4</subscript><superscript>2−</superscript> generation suggests the ability of some systems to partially accumulate the produced SO<subscript>4</subscript><superscript>2−</superscript>. Principal Component Analysis (PCA) identified total organic carbon (TOC), Ni, Mo, Co, and Mn as key factors influencing the decomposition rate under varying soil conditions. These findings provide valuable insights into how S<subscript>2</subscript>O<subscript>8</subscript><superscript>2−</superscript> behaves in real soil and aquifer materials, which can improve the design and operation of ISCO treatability studies for groundwater remediation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20734441
Volume :
16
Issue :
24
Database :
Complementary Index
Journal :
Water (20734441)
Publication Type :
Academic Journal
Accession number :
181912934
Full Text :
https://doi.org/10.3390/w16243552