Remediation of 2,4-dichlorophenol-contaminated groundwater using nano-sized CaO₂ in a two-dimensional scale tank

Highlights

• Nano CaO₂ is evaluated as a remediation agent for 2,4-DCP contaminated groundwater.

• 2,4-DCP degradation mechanism by different Fe²⁺ concentration was proposed.

• 2,4-DCP was not degraded in the system for solution pH>10.

• The 2,4-DCP degradation area is inconsistent with the nano CaO₂ distribution area.

Abstract

This study evaluates the applicability of nano-sized calcium peroxide (CaO₂) as a source of H₂O₂ to remediate 2,4-dichlorophenol (2,4-DCP) contaminated groundwater via the advanced oxidation process (AOP). First, the effect and mechanism of 2,4-DCP degradation by CaO₂ at different Fe concentrations were studied (Fenton reaction). We found that at high Fe concentrations, 2,4-DCP almost completely degrades via primarily the oxidation of •OH within 5 h. At low Fe concentrations, the degradation rate of 2,4-DCP decreased rapidly. The main mechanism was the combined action of •OH and O₂^•−. Without Fe, the 2,4-DCP degradation reached 13.6% in 213 h, primarily via the heterogeneous reaction on the surface of CaO₂. Besides, 2,4-DCP degradation was significantly affected by solution pH. When the solution pH was>10, the degradation was almost completely inhibited. Thus, we adopted a two-dimensional water tank experiment to study the remediation efficiency CaO₂ on the water sample. We noticed that the degradation took place mainly in regions of pH<10 (i.e., CaO₂ distribution area), both upstream and downstream of the tank. After 28 days of treatment, the average 2,4-DCP degradation level was ≈36.5%. Given the inadequacy of the results, we recommend that groundwater remediation using nano CaO₂: (1) a buffer solution should be added to retard the rapid increase in pH, and (2) the nano CaO₂ should be injected copiously in batches to reduce CaO₂ deposition.

Graphical abstract

Keywords

Calcium peroxide / 2,4-DCP / Reaction zone / Fenton reaction

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Acknowledgements

This work was financially supported by the National Key R&D Program of China (No. 2018YFC1802500).

Electronic Supplementary Material

Supplementary material is available in the online version of this article at https://doi.org/10.1007/s11783-020-1381-3 and is accessible for authorized users.

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