TY - JOUR
T1 - Fixation of trace elements – A positive side effect of nitrate removal from contaminated groundwater
AU - Ortmeyer, Felix
AU - Kim, Hyojin
AU - Hansen, Birgitte
AU - Jakobsen, Rasmus
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/10/25
Y1 - 2025/10/25
N2 - This study presents the binding of trace elements, which can be a positive side effect of adding organic C to remediate nitrate (NO3−) contamination in groundwater. The processes responsible for trace element removal are examined via circulation column experiments, with two different types of unconsolidated sandy sediments from aquifers in Denmark (Quaternary) and Germany (Cretaceous). Selected trace elements (As, Co, Ni, V and Zn) were injected into the nitrate-polluted water of the column experiments at a concentration of around 100 μg·L−1. By addition of ethanol as electron donor, a decrease in trace element concentrations (e.g., Ni 50.2 to 76.2 % and Zn 92.2 to 94.0 %) was observed in both sediments together with the expected denitrification. A six-step sequential extraction procedure was carried out to identify the sinks of the trace elements. Results show sorption of trace elements, but also binding by newly formed oxyhydroxides extractable by oxalate. Due to pH differences resulting from the properties of the sediments (Haltern Formation, Germany: pH approx. 5.5 and meltwater deposits, Denmark: pH approx. 7.8), carbonate precipitation was promoted in the meltwater deposits, in which trace elements likewise bind. Saturation indices from reactive transport modeling support these conclusions. The effectivity of denitrification differs between the two sediments, which is presumably likewise due to the pH and the existing microbiology. Sulfate (SO42−) reduction and binding of trace elements by sulfides was not observed. Nevertheless, a number of emerging questions open up the need for further research. As the trace element concentrations do not increase at the end of the experiments, this method seems to be a positive side effect from mitigating NO3− concentrations in groundwater by addition of organic C.
AB - This study presents the binding of trace elements, which can be a positive side effect of adding organic C to remediate nitrate (NO3−) contamination in groundwater. The processes responsible for trace element removal are examined via circulation column experiments, with two different types of unconsolidated sandy sediments from aquifers in Denmark (Quaternary) and Germany (Cretaceous). Selected trace elements (As, Co, Ni, V and Zn) were injected into the nitrate-polluted water of the column experiments at a concentration of around 100 μg·L−1. By addition of ethanol as electron donor, a decrease in trace element concentrations (e.g., Ni 50.2 to 76.2 % and Zn 92.2 to 94.0 %) was observed in both sediments together with the expected denitrification. A six-step sequential extraction procedure was carried out to identify the sinks of the trace elements. Results show sorption of trace elements, but also binding by newly formed oxyhydroxides extractable by oxalate. Due to pH differences resulting from the properties of the sediments (Haltern Formation, Germany: pH approx. 5.5 and meltwater deposits, Denmark: pH approx. 7.8), carbonate precipitation was promoted in the meltwater deposits, in which trace elements likewise bind. Saturation indices from reactive transport modeling support these conclusions. The effectivity of denitrification differs between the two sediments, which is presumably likewise due to the pH and the existing microbiology. Sulfate (SO42−) reduction and binding of trace elements by sulfides was not observed. Nevertheless, a number of emerging questions open up the need for further research. As the trace element concentrations do not increase at the end of the experiments, this method seems to be a positive side effect from mitigating NO3− concentrations in groundwater by addition of organic C.
KW - Drinking water
KW - Enhanced denitrification
KW - Ethanol
KW - Organic carbon
KW - Sources and sinks
KW - Treatment
UR - https://www.scopus.com/pages/publications/105016008893
U2 - 10.1016/j.scitotenv.2025.180480
DO - 10.1016/j.scitotenv.2025.180480
M3 - Article
C2 - 40966813
AN - SCOPUS:105016008893
SN - 0048-9697
VL - 1001
JO - Science of the Total Environment
JF - Science of the Total Environment
M1 - 180480
ER -