TY - JOUR
T1 - Degradation of landfill leachate compounds by persulfate for groundwater remediation
AU - Zhong, Hua
AU - Tian, Yaling
AU - Yang, Qi
AU - Brusseau, Mark L.
AU - Yang, Lei
AU - Zeng, Guangming
N1 - Funding Information:
This study was funded by the National Natural Science Foundation of China ( 51378192 , 51378190 and 51308200 ). Additional support was provided by the NIEHS Superfund Research Program (P42 ES04940). The data supporting analysis and the conclusion are all included in the figures, tables, and Supporting Information file .
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/1/1
Y1 - 2017/1/1
N2 - In this study, batch and column experiments were conducted to evaluate the feasibility of using persulfate oxidation to treat groundwater contaminated by landfill leachate (CGW). In batch experiments, persulfate was compared with H2O2 and permanganate for oxidation of organic compounds in CGW. Complementary experiments were conducted to evaluate biodegradation (natural attenuation) potential for the system. Persulfate was observed to be superior to H2O2 and permanganate for degradation of total organic carbon (TOC) in the CGW. Conversely, biodegradation caused only partial removal of TOC in CGW. In contrast, persulfate caused complete degradation of the TOC in the CGW or aged CGW, showing no selectivity to the contaminants. Magnetite (Fe3O4) enhanced degradation of leachate compounds in both CGW and aged CGW with limited increase in persulfate consumption and sulfate production. Under dynamic flow condition in 1-D column experiment, both biodegradation and persulfate oxidation of TOC were enhanced by Fe3O4. The enhancement, however, was significantly greater for persulfate oxidation. In both batch and column experiments, Fe3O4 by itself caused minimal consumption of persulfate and production of sulfate, indicating that magnetite is a good persulfate activator for treating CGW in heterogeneous systems The results of the study show that the persulfate-based in-situ chemical oxidation (ISCO) method has great potential to treat the groundwater contaminated by landfill leachate.
AB - In this study, batch and column experiments were conducted to evaluate the feasibility of using persulfate oxidation to treat groundwater contaminated by landfill leachate (CGW). In batch experiments, persulfate was compared with H2O2 and permanganate for oxidation of organic compounds in CGW. Complementary experiments were conducted to evaluate biodegradation (natural attenuation) potential for the system. Persulfate was observed to be superior to H2O2 and permanganate for degradation of total organic carbon (TOC) in the CGW. Conversely, biodegradation caused only partial removal of TOC in CGW. In contrast, persulfate caused complete degradation of the TOC in the CGW or aged CGW, showing no selectivity to the contaminants. Magnetite (Fe3O4) enhanced degradation of leachate compounds in both CGW and aged CGW with limited increase in persulfate consumption and sulfate production. Under dynamic flow condition in 1-D column experiment, both biodegradation and persulfate oxidation of TOC were enhanced by Fe3O4. The enhancement, however, was significantly greater for persulfate oxidation. In both batch and column experiments, Fe3O4 by itself caused minimal consumption of persulfate and production of sulfate, indicating that magnetite is a good persulfate activator for treating CGW in heterogeneous systems The results of the study show that the persulfate-based in-situ chemical oxidation (ISCO) method has great potential to treat the groundwater contaminated by landfill leachate.
KW - Biodegradation
KW - Contaminated groundwater
KW - Landfill leachate
KW - Magnetite
KW - Persulfate oxidation
UR - http://www.scopus.com/inward/record.url?scp=84984852173&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84984852173&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2016.08.069
DO - 10.1016/j.cej.2016.08.069
M3 - Article
AN - SCOPUS:84984852173
SN - 1385-8947
VL - 307
SP - 399
EP - 407
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -