Featured Application The results of such studies will enable researchers to gain insight into the behavior of metals in wet depositions, which is fundamental knowledge to carry out atmospheric photochemistry studies and to model biogeochemical cycles of metal cations. Both inorganic and organic complexation of metal cations in clouds or rainwater is essential to describe the global biogeochemical cycles of metals, because complexation can increase metal solubility and stabilize some of their oxidation states. Within a Project of the National Research Program in the Antarctica, atmospheric depositions were collected during the Antarctic summer 2017-2018 in eight sampling sites. The main ionic components occurring in water extracts of these atmospheric depositions were quantified, and a chemical model was applied, in order to identify the main species occurring in the samples. The speciation study showed that most cations were present as aquoions, except for Fe, which occurred predominantly in hydrolytic forms. The model allowed us to foresee the effect of an increase in the concentration levels of all the solution components, by simulating what could happen when the original particles act as cloud condensation nuclei. The role of inorganic anions as complexing agents becomes important when increasing total concentrations of all the solutes by a factor >100 compared to the water extracts, while the presence of organic acids acquires significance for samples having organic acid concentration higher than 10(-5) mol L-1. Moreover, it was possible to pinpoint the formation constants that mostly affect the chemical system, and to gain insight into the behavior of metals in wet depositions, which is fundamental knowledge in atmospheric photochemistry studies and in the modeling of the biogeochemical cycles of metal cations.

Chemical Speciation of Antarctic Atmospheric Depositions / Bertinetti, S; Berto, S; Malandrino, M; Vione, D; Abollino, O; Conca, E; Marafante, M; Annibaldi, A; Truzzi, C; Illuminati, S. - In: APPLIED SCIENCES. - ISSN 2076-3417. - STAMPA. - 12:9(2022), p. 4438. [10.3390/app12094438]

Chemical Speciation of Antarctic Atmospheric Depositions

Annibaldi, A;Truzzi, C;Illuminati, S
2022-01-01

Abstract

Featured Application The results of such studies will enable researchers to gain insight into the behavior of metals in wet depositions, which is fundamental knowledge to carry out atmospheric photochemistry studies and to model biogeochemical cycles of metal cations. Both inorganic and organic complexation of metal cations in clouds or rainwater is essential to describe the global biogeochemical cycles of metals, because complexation can increase metal solubility and stabilize some of their oxidation states. Within a Project of the National Research Program in the Antarctica, atmospheric depositions were collected during the Antarctic summer 2017-2018 in eight sampling sites. The main ionic components occurring in water extracts of these atmospheric depositions were quantified, and a chemical model was applied, in order to identify the main species occurring in the samples. The speciation study showed that most cations were present as aquoions, except for Fe, which occurred predominantly in hydrolytic forms. The model allowed us to foresee the effect of an increase in the concentration levels of all the solution components, by simulating what could happen when the original particles act as cloud condensation nuclei. The role of inorganic anions as complexing agents becomes important when increasing total concentrations of all the solutes by a factor >100 compared to the water extracts, while the presence of organic acids acquires significance for samples having organic acid concentration higher than 10(-5) mol L-1. Moreover, it was possible to pinpoint the formation constants that mostly affect the chemical system, and to gain insight into the behavior of metals in wet depositions, which is fundamental knowledge in atmospheric photochemistry studies and in the modeling of the biogeochemical cycles of metal cations.
2022
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/309121
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