4.2 Article

Simulation of the Environmental Fate and Transformation of Nano Copper Oxide in a Freshwater Environment

Journal

ACS ES&T WATER
Volume 2, Issue 9, Pages 1532-1543

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsestwater.2c00157

Keywords

WASP; environmental modeling; nanocopper; nanomaterials; freshwater

Funding

  1. U.S. Environmental Protection Agencys Chemical Safety for Sustainability program in the Office of Research and Development
  2. CSS 3.1.6: Emerging Contaminants
  3. Model Fate and Transport of Nanomaterials in Surface Waters

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This study investigates the behavior of nano copper oxide in a lake environment and finds that the highest concentrations of nano copper oxide and its dissolved product are found in the surface sediments. Simulation results show that increasing attachment efficiency leads to higher concentrations of nano copper oxide in the water column and sediments, while the opposite trend is observed for the dissolved product. The results highlight the importance of heteroaggregation in the behavior of nano copper oxide inputs and suggest the potential for legacy contamination in sediments.
Production of engineered nanomaterials (ENMs) has rapidly increased, yet uncertainty exists regarding the full extent of their environmental implications. This study investigates the fate, transformation, and speciation of nano copper oxide (nanoCuO) released into Lake Waccamaw, North Carolina, over 101 years. Using the Advanced Toxicant module of the Water Quality Analysis Simulation Program (WASP8), we assessed the accumulation and mass proportions of nanoCuO and Cu2+ (the product of nanoCuO's dissolution) in the water column and sediments. Our simulations suggest that when nanoCuO is released into Lake Waccamaw, the highest concentrations of both nanoCuO and Cu2+ are found in the surface sediments, followed by the subsurface sediments and the water column. Simulating different heteroaggregation attachment efficiencies of nanoCuO suggested that increases in attachment efficiency increased nanoCuO concentrations and mass proportions in the water column and sediments, while Cu2+ exhibited the opposite trends. After 101 years, most nanoCuO in the sediments was attached to particulate organic matter and clay particles at all attachment efficiencies, while low attachment efficiency slowed aggregate formation in the water column. Our results highlight the influence that heteroaggregation has on the behavior of nanoCuO inputs and suggest the potential for legacy contamination of nanoCuO and Cu2+ in sediments.

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