TY - JOUR
T1 - Enhanced degradation of herbicides in groundwater using sulfur-containing reductants and spinel zinc ferrite activated persulfate
AU - Chokejaroenrat, Chanat
AU - Sakulthaew, Chainarong
AU - Chantakulvanich, Sirimon
AU - Angkaew, Athaphon
AU - Teingtham, Kanokwan
AU - Phansak, Piyaporn
AU - Poompoung, Thapanee
AU - Snow, Daniel D.
AU - Harris, Clifford E.
AU - Comfort, Steve D.
N1 - Funding Information:
This work was financially supported by the Office of the Ministry of Higher Education, Science, Research and Innovation; and the Thailand Science Research and Innovation through the Kasetsart University Reinventing University Program 2021. We also appreciate Professor Dr. Roch E. Gaussoin, Department of Agronomy and Horticulture, University of Nebraska-Lincoln, for providing soils for providing topsoil for our mineralization study.
Funding Information:
This work was financially supported by the Office of the Ministry of Higher Education, Science, Research and Innovation ; and the Thailand Science Research and Innovation through the Kasetsart University Reinventing University Program 2021. We also appreciate Professor Dr. Roch E. Gaussoin, Department of Agronomy and Horticulture, University of Nebraska-Lincoln, for providing soils for providing topsoil for our mineralization study.
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/9/20
Y1 - 2023/9/20
N2 - A challenge to successfully implementing an injection-based remedial treatment in aquifers is to ensure that the oxidative reaction is efficient and lasts long enough to contact the contaminated plume. Our objective was to determine the efficacy of zinc ferrite nanocomposites (ZnFe2O4) and sulfur-containing reductants (SCR) (i.e., dithionite; DTN and bisulfite; BS) to co-activate persulfate (S2O82−; PS) and treat herbicide-contaminated water. We also evaluated the ecotoxicity of the treated water. While both SCRs delivered excellent PS activation in a 1:0.4 ratio (PS:SCR), the reaction was relatively short-lived. By including ZnFe2O4 in the PS/BS or PS/DTN activations, herbicide degradation rates dramatically increased by factors of 2.5 to 11.3. This was due to the SO4[rad]− and [rad]OH reactive radical species that formed. Radical scavenging experiments and ZnFe2O4 XPS spectra results revealed that SO4[rad]− was the dominant reactive species that originated from S(IV)/PS activation in solution and from the Fe(II)/PS activation that occurred on the ZnFe2O4 surface. Based on liquid chromatography mass spectrometry (LC–MS), atrazine and alachlor degradation pathways are proposed that involve both dehydration and hydroxylation. In 1-D column experiments, five different treatment scenarios were run using 14C-labeled and unlabeled atrazine, and 3H2O to quantify changes in breakthrough curves. Our results confirmed that ZnFe2O4 successfully prolonged the PS oxidative treatment despite the SCR being completely dissociated. Toxicity testing showed treated 14C-atrazine was more biodegradable than the parent compound in soil microcosms. Post-treatment water (25 %, v/v) also had less impact on both Zea Mays L. and Vigna radiata L. seedling growth, but more impact on root anatomies, while ≤4 % of the treated water started to exert cytotoxicity (<80 % viability) on ELT3 cell lines. Overall, the findings confirm that ZnFe2O4/SCR/PS reaction is efficient and relatively longer lasting in treating herbicide-contaminated groundwater.
AB - A challenge to successfully implementing an injection-based remedial treatment in aquifers is to ensure that the oxidative reaction is efficient and lasts long enough to contact the contaminated plume. Our objective was to determine the efficacy of zinc ferrite nanocomposites (ZnFe2O4) and sulfur-containing reductants (SCR) (i.e., dithionite; DTN and bisulfite; BS) to co-activate persulfate (S2O82−; PS) and treat herbicide-contaminated water. We also evaluated the ecotoxicity of the treated water. While both SCRs delivered excellent PS activation in a 1:0.4 ratio (PS:SCR), the reaction was relatively short-lived. By including ZnFe2O4 in the PS/BS or PS/DTN activations, herbicide degradation rates dramatically increased by factors of 2.5 to 11.3. This was due to the SO4[rad]− and [rad]OH reactive radical species that formed. Radical scavenging experiments and ZnFe2O4 XPS spectra results revealed that SO4[rad]− was the dominant reactive species that originated from S(IV)/PS activation in solution and from the Fe(II)/PS activation that occurred on the ZnFe2O4 surface. Based on liquid chromatography mass spectrometry (LC–MS), atrazine and alachlor degradation pathways are proposed that involve both dehydration and hydroxylation. In 1-D column experiments, five different treatment scenarios were run using 14C-labeled and unlabeled atrazine, and 3H2O to quantify changes in breakthrough curves. Our results confirmed that ZnFe2O4 successfully prolonged the PS oxidative treatment despite the SCR being completely dissociated. Toxicity testing showed treated 14C-atrazine was more biodegradable than the parent compound in soil microcosms. Post-treatment water (25 %, v/v) also had less impact on both Zea Mays L. and Vigna radiata L. seedling growth, but more impact on root anatomies, while ≤4 % of the treated water started to exert cytotoxicity (<80 % viability) on ELT3 cell lines. Overall, the findings confirm that ZnFe2O4/SCR/PS reaction is efficient and relatively longer lasting in treating herbicide-contaminated groundwater.
KW - Ferrite nanocomposites
KW - Groundwater remediation
KW - Herbicide degradation
KW - Mineralization
KW - Persulfate activator
KW - Sulfur-containing reductant
UR - http://www.scopus.com/inward/record.url?scp=85161655287&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85161655287&partnerID=8YFLogxK
U2 - 10.1016/j.scitotenv.2023.164652
DO - 10.1016/j.scitotenv.2023.164652
M3 - Article
C2 - 37295514
AN - SCOPUS:85161655287
SN - 0048-9697
VL - 892
JO - Science of the Total Environment
JF - Science of the Total Environment
M1 - 164652
ER -