In situ chemical oxidation (ISCO) with persulfate (S2O82-) or hydrogen peroxide (H2O2) are being employed increasingly for hazardous waste site remediation due its potential to quickly and inexpensively remediate recalcitrant Superfund contaminants. Similarly, advanced oxidation processes (AOPs) and electrochemical treatment technologies are promising alternatives to physical treatment processes for the ex situ treatment of waters containing low concentrations of contaminants. Although these techniques are being employed for site remediation, the mechanisms through which contaminants are degraded are not well understood. In particular, available evidence suggests that oxidation of contaminants may result in the formation of toxic transformation products. The overall goal of this research project is to assess the formation, fate and toxicity of transformation products produced by oxidative remediation with existing ISCO approaches and emerging remediation technologies, such as electrochemical treatment, and develop approaches for reducing potential exposure to oxidative transformation products. Through rigorous research on reaction mechanisms, contaminant fate and toxicity we will provide engineers with the ability to predict when oxidative treatment will be effective and to determine under which conditions potentially toxic transformation products will be formed. The latter may lead to the development of additional treatment steps that could be used in concert with oxidative remediation technologies. We will focus our efforts on the identification of oxidative transformation products of substituted aromatic compounds, including amino-, chloro-, nitro- and alkyl-benzenes. This knowledge will be used to identify reaction mechanisms and predict the reaction mechanisms of structurally similar compounds. To assess the stability of transformation products, we will conduct laboratory experiments with groundwater and aquifer sediments to determine if transformation products can be degraded further by microorganisms or by reactions with minerals or natural organic matter. To determine the potential health effects arising from the exposure to transformation products, we will use state-of-the-art bioanalytical strategies that allow for the determination of the interactions of reactive transformation products with biomolecules at the molecular level. This framework will substantially increase our understanding of mechanisms that lead to the removal of contaminants and formation of stable transformation products during oxidative treatment. It will also allow us to better predict under which conditions oxidative treatment technologies are appropriate and steps that can be taken to advance their adoption in situations where the production of toxic transformation products is possible.

Public Health Relevance

Chemical oxidation is increasingly being employed to clean-up hazardous waste sites as it is relatively quick and inexpensive, but oxidation of contaminants may result in the formation of toxic transformation products. The overall goal of this research project is to assess the formation, fate and toxicity of transformation products produced by oxidative remediation and to develop approaches for reducing exposure to these potentially toxic transformation products, thereby protecting public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES004705-32
Application #
9919587
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
32
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California Berkeley
Department
Type
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94710
Bruton, Thomas A; Sedlak, David L (2018) Treatment of perfluoroalkyl acids by heat-activated persulfate under conditions representative of in situ chemical oxidation. Chemosphere 206:457-464
Schiffman, Courtney; McHale, Cliona M; Hubbard, Alan E et al. (2018) Identification of gene expression predictors of occupational benzene exposure. PLoS One 13:e0205427
Wiemels, Joseph L; Walsh, Kyle M; de Smith, Adam J et al. (2018) GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Nat Commun 9:286
Prasse, Carsten; Ford, Breanna; Nomura, Daniel K et al. (2018) Unexpected transformation of dissolved phenols to toxic dicarbonyls by hydroxyl radicals and UV light. Proc Natl Acad Sci U S A 115:2311-2316
Smith, Allan H; Marshall, Guillermo; Roh, Taehyun et al. (2018) Lung, Bladder, and Kidney Cancer Mortality 40?Years After Arsenic Exposure Reduction. J Natl Cancer Inst 110:241-249
Castriota, Felicia; Acevedo, Johanna; Ferreccio, Catterina et al. (2018) Obesity and increased susceptibility to arsenic-related type 2 diabetes in Northern Chile. Environ Res 167:248-254
Rothman, Nathaniel; Zhang, Luoping; Smith, Martyn T et al. (2018) Formaldehyde, Hematotoxicity, and Chromosomal Changes-Response. Cancer Epidemiol Biomarkers Prev 27:120-121
Yik-Sham Chung, Clive; Timblin, Greg A; Saijo, Kaoru et al. (2018) Versatile Histochemical Approach to Detection of Hydrogen Peroxide in Cells and Tissues Based on Puromycin Staining. J Am Chem Soc 140:6109-6121
Rappaport, Stephen M (2018) Redefining environmental exposure for disease etiology. NPJ Syst Biol Appl 4:30
Tachachartvanich, Phum; Sangsuwan, Rapeepat; Ruiz, Heather S et al. (2018) Assessment of the Endocrine-Disrupting Effects of Trichloroethylene and Its Metabolites Using in Vitro and in Silico Approaches. Environ Sci Technol 52:1542-1550

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