TY - JOUR
T1 - Hematite as a natural mineral in activating persulfate to degrade chlorinated compounds
T2 - combined effects of soluble iron release and surface activation
AU - Li, Yan
AU - Zhou, Lian
AU - Zhang, Juntao
AU - Wang, Yake
AU - Liu, Guansheng
AU - He, Jingping
AU - Zhong, Hua
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/4
Y1 - 2024/4
N2 - In this study, six naturally occurring iron-containing minerals (pyrite (FeS2), magnetite (Fe3O4), ilmenite (FeTiO3), hematite (Fe2O3), limonite (FeO(OH)·nH2O), siderite (FeCO3)) were examined on activation of persulfate for degradation of 1,1,2-TCA in groundwater. Hematite was selected for further study due to its abundance in subsurface porous media, low persulfate consumption, and efficient 1,1,2-TCA removal. Through ferric ion-activated persulfate experiments and model simulations, we found that hematite activates persulfate through a combination of surface reactions (40%) and dissolved ferric ion activation (60%). High persulfate concentration and lower pH resulted in an increase in the degradation rate. Column experiments revealed a notable improvement in 1,1,2-TCA degradation when natural hematite was employed as the activator. Dissolution-advection-reaction model well described the dissolution process of hematite and degradation process of 1,1,2-TCA in the column. A decrease in efficiency of hematite activation was observed and model simulation showed that this was primarily due to a decrease in ferric ion release. This study underscores the potential of natural hematite minerals in activating persulfate for chlorinated solvent degradation, which should be considered in application of persulfate-based ISCO technologies to reduce cost.
AB - In this study, six naturally occurring iron-containing minerals (pyrite (FeS2), magnetite (Fe3O4), ilmenite (FeTiO3), hematite (Fe2O3), limonite (FeO(OH)·nH2O), siderite (FeCO3)) were examined on activation of persulfate for degradation of 1,1,2-TCA in groundwater. Hematite was selected for further study due to its abundance in subsurface porous media, low persulfate consumption, and efficient 1,1,2-TCA removal. Through ferric ion-activated persulfate experiments and model simulations, we found that hematite activates persulfate through a combination of surface reactions (40%) and dissolved ferric ion activation (60%). High persulfate concentration and lower pH resulted in an increase in the degradation rate. Column experiments revealed a notable improvement in 1,1,2-TCA degradation when natural hematite was employed as the activator. Dissolution-advection-reaction model well described the dissolution process of hematite and degradation process of 1,1,2-TCA in the column. A decrease in efficiency of hematite activation was observed and model simulation showed that this was primarily due to a decrease in ferric ion release. This study underscores the potential of natural hematite minerals in activating persulfate for chlorinated solvent degradation, which should be considered in application of persulfate-based ISCO technologies to reduce cost.
KW - 1,1,2-TCA
KW - Activation mechanism
KW - Hematite
KW - Naturally occurring minerals
KW - Persulfate
UR - https://www.scopus.com/pages/publications/85185399799
U2 - 10.1016/j.jece.2024.112184
DO - 10.1016/j.jece.2024.112184
M3 - Article
AN - SCOPUS:85185399799
SN - 2213-2929
VL - 12
JO - Journal of Environmental Chemical Engineering
JF - Journal of Environmental Chemical Engineering
IS - 2
M1 - 112184
ER -