10 research outputs found
Theoretical study of infrared spectra of iodide molecules on NaCl surfaces
No full textInternational audienceIodine, when released into the environment, contributes to the oxidizing capacity of the atmosphere through the catalytic destruction of ozone [1, 2]. Iodine-131 can be released during a severe nuclear accident and can be carcinogenic for humans [3]. In the literature, there are missing pieces of knowledge about interactions between iodinated compounds and aerosols. In this context, this work consists in investigating the adsorption on sea salt aerosols of gaseous methyl iodide (CH3I), diiodomethane (CH2I2), and water. We have used two different methods: a periodic approach using Quantum ESPRESSO [4, 5] and a cluster QM/QM' approach using the ONIOM method [6] from Gaussian 16 [7]. We have computed the adsorption energies and the shift in vibrational frequencies, due to adsorption. We have shown that the vibrational frequency shifts are small, mainly because there is no strong coupling between the adsorbates and the NaCl (001) surface, as illustrated by the low values of the adsorption energies.(1) Saiz-Lopez, A.; Plane, J. M. C.; Baker, A. R.; Carpenter, L. J.; von Glasow, R.; GĂłmez MartĂn, J. C.; McFiggans, G.; Saunders, R. W. Chem. Rev. 2012, 112, 1773-1804(2) Calvert, J. G.; Lindberg, S. E. Atmospheric Environ. 2004, 38, 5087-5104(3) Dobyns, B. M.; Sheline, G. E.; Workman, J. B.; Tompkins, E. A.; McConahey, W. M.; Becker, D. V. J. Clin. Endocrinol. Metab. 1974, 38, 976(4) Giannozzi, P. et al. J. Phys. Condens. Matter 2009, 21, 395502(5) Giannozzi, P. et al. J. Phys. Condens. Matter 2017, 29, 465901(6) Svensson, M.; Humbel, S.; Froese, R. D.; Matsubara, T.; Sieber, S.; Morokuma, K. J. Phys. Chem. 1996, 100, 19357-19363(7) Frisch, M. J. et al. Gaussian 16 Revision B.01, Gaussian Inc. Wallingford CT, 2016<br
The Atmospheric Oxidation of CH3I by the OH Radical: the Effect of Water Vapor
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Experimental and theoretical study on the capture/desorption of gaseous methyl iodide on sea salt aerosols
No full textInternational audienceIodine-131, when released into the environment during severe nuclear power plant accident can have a high radiological impact on the population at short term [1]. Interaction between gaseous Iodine compounds and aerosols was not considered by the current post-accident management. In this context, this work was focused on investigating the influence of sea salt aerosols on the transport of gaseous methyl iodide (CH3I). The identification of uptake processes as well as the formation of new products at the particle surfaces was the main objectives. We have studied the interaction between NaCl particles as surrogate of sea salt particles and CH3I in various humidity conditions to reproduce the atmospheric conditions. The nature of this interaction was investigated by Infrared Spectroscopy (DRIFTS, Diffuse Reflectance Infrared Fourier Spectroscopy). Solid NaCl was exposed to CH3I (1000 and 500 ppm) with a relative humidity (RH) ranging between 0 and 80%.DRIFTS results clearly evidenced adsorbed CH3I on NaCl particles surface under both dry and humid conditions. The adsorption process can be fitted with First-order Langmuir adsorption isotherm model and exhibited very low uptake coefficients in all the experimental conditions. Additionally, to the CH3I absorption bands, the DRIFT spectrum evidenced typical absorption bands that could be assigned either to the CH2 deformation of CH2I2 or to CH3 degenerate rocking of CH3Cl. The formation of new bands appears only when CH3I is in presence of halogenated salts. However, at RH=80%, the water layer at the particle surface inhibits the interaction between gaseous CH3I and NaCl surface due to the low solubility of CH3I in water.Theoretical calculations are carried out to complement the experimental results. Isolated hydrated clusters of CH3I are characterized by means of electronic structure calculations and ab initio molecular dynamics is used to mimic the CH3I / salt system at various humidities. Although the uptake and accommodation coefficients of CH3I are quite low, a coverage of particle surface with CH3I-derived compounds may affect the reactivity of the particles and in term the cycling life of Iodine in the atmosphere.RĂ©fĂ©rences:[1] Lebel, L. S.; Dickson, R. S.; Glowa, G. A. J. Environ. Radioact. 2016, 151, 82â93
Experimental and theoretical study on the capture/desorption of gaseous methyl iodide on sea salt aerosols
No full textInternational audienceIodine-131, when released into the environment during severe nuclear power plant accident can have a high radiological impact on the population at short term [1]. Interaction between gaseous Iodine compounds and aerosols was not considered by the current post-accident management. In this context, this work was focused on investigating the influence of sea salt aerosols on the transport of gaseous methyl iodide (CH3I). The identification of uptake processes as well as the formation of new products at the particle surfaces was the main objectives.We have studied the interaction between NaCl particles as surrogate of sea salt particles and CH3I in various humidity conditions to reproduce the atmospheric conditions.The nature of this interaction was investigated by Infrared Spectroscopy (DRIFTS, Diffuse Reflectance Infrared Fourier Spectroscopy). Solid NaCl was exposed to CH3I (1000 and 500 ppm) with a relative humidity (RH) ranging between 0 and 80%.DRIFTS results clearly evidenced adsorbed CH3I on NaCl particles surface under both dry and humid conditions. The adsorption process can be fitted with First-order Langmuir adsorption isotherm model and exhibited very low uptake coefficients in all the experimental conditions.Additionally, to the CH3I absorption bands, the DRIFT spectrum evidenced typical absorption bands that could be assigned either to the CH2 deformation of CH2I2 or to CH3 degenerate rocking of CH3Cl. The formation of new bands appears only when CH3I is in presence of halogenated salts. However, at RH = 80%, the water layer at the particle surface inhibits the interaction between gaseous CH3I and NaCl surface due to the low solubility of CH3I in water.Theoretical calculations are carried out to complement the experimental results. Isolated hydrated clusters of CH3I are characterized by means of electronic structure calculations and ab initio molecular dynamics is used to mimic the CH3I / salt system at various humidities.Although the uptake and accommodation coefficients of CH3I are quite low, a coverage of particle surface with CH3I-derived compounds may affect the reactivity of the particles and in term the cycling life of Iodine in the atmosphere.Reference[1] Lebel, L. S.; Dickson, R. S.; Glowa, G. A. J. Environ. Radioact. 2016, 151, 82â93.We acknowledge support by the French government through the Program âInvestissement d'avenirâ through the Labex CaPPA (contract ANR-11-LABX-0005-01) and I-SITE ULNE project OVERSEE (contract ANR-16-IDEX-0004), CPER CLIMIBIO (European Regional Development Fund, Hauts de France council, French Ministry of Higher Education and Research) and French national supercomputing facilities (grants DARI x2016081859 and A0050801859)
Experimental and theoretical study on the capture/desorption of gaseous methyl iodide on sea salt aerosols
No full textInternational audienceIodine-131, when released into the environment during severe nuclear power plant accident can have a high radiological impact on the population at short term [1]. Interaction between gaseous Iodine compounds and aerosols was not considered by the current post-accident management. In this context, this work was focused on investigating the influence of sea salt aerosols on the transport of gaseous methyl iodide (CH3I). The identification of uptake processes as well as the formation of new products at the particle surfaces was the main objectives. We have studied the interaction between NaCl particles as surrogate of sea salt particles and CH3I in various humidity conditions to reproduce the atmospheric conditions. The nature of this interaction was investigated by Infrared Spectroscopy (DRIFTS, Diffuse Reflectance Infrared Fourier Spectroscopy). Solid NaCl was exposed to CH3I (1000 and 500 ppm) with a relative humidity (RH) ranging between 0 and 80%.DRIFTS results clearly evidenced adsorbed CH3I on NaCl particles surface under both dry and humid conditions. The adsorption process can be fitted with First-order Langmuir adsorption isotherm model and exhibited very low uptake coefficients in all the experimental conditions. Additionally, to the CH3I absorption bands, the DRIFT spectrum evidenced typical absorption bands that could be assigned either to the CH2 deformation of CH2I2 or to CH3 degenerate rocking of CH3Cl. The formation of new bands appears only when CH3I is in presence of halogenated salts. However, at RH=80%, the water layer at the particle surface inhibits the interaction between gaseous CH3I and NaCl surface due to the low solubility of CH3I in water.Theoretical calculations are carried out to complement the experimental results. Isolated hydrated clusters of CH3I are characterized by means of electronic structure calculations and ab initio molecular dynamics is used to mimic the CH3I / salt system at various humidities. Although the uptake and accommodation coefficients of CH3I are quite low, a coverage of particle surface with CH3I-derived compounds may affect the reactivity of the particles and in term the cycling life of Iodine in the atmosphere.RĂ©fĂ©rences:[1] Lebel, L. S.; Dickson, R. S.; Glowa, G. A. J. Environ. Radioact. 2016, 151, 82â93
Experimental and theoretical study on the capture/desorption of gaseous methyl iodide on sea salt aerosols
No full textInternational audienceIodine-131, when released into the environment during severe nuclear power plant accident can have a high radiological impact on the population at short term [1]. Interaction between gaseous Iodine compounds and aerosols was not considered by the current post-accident management. In this context, this work was focused on investigating the influence of sea salt aerosols on the transport of gaseous methyl iodide (CH3I). The identification of uptake processes as well as the formation of new products at the particle surfaces was the main objectives.We have studied the interaction between NaCl particles as surrogate of sea salt particles and CH3I in various humidity conditions to reproduce the atmospheric conditions.The nature of this interaction was investigated by Infrared Spectroscopy (DRIFTS, Diffuse Reflectance Infrared Fourier Spectroscopy). Solid NaCl was exposed to CH3I (1000 and 500 ppm) with a relative humidity (RH) ranging between 0 and 80%.DRIFTS results clearly evidenced adsorbed CH3I on NaCl particles surface under both dry and humid conditions. The adsorption process can be fitted with First-order Langmuir adsorption isotherm model and exhibited very low uptake coefficients in all the experimental conditions.Additionally, to the CH3I absorption bands, the DRIFT spectrum evidenced typical absorption bands that could be assigned either to the CH2 deformation of CH2I2 or to CH3 degenerate rocking of CH3Cl. The formation of new bands appears only when CH3I is in presence of halogenated salts. However, at RH = 80%, the water layer at the particle surface inhibits the interaction between gaseous CH3I and NaCl surface due to the low solubility of CH3I in water.Theoretical calculations are carried out to complement the experimental results. Isolated hydrated clusters of CH3I are characterized by means of electronic structure calculations and ab initio molecular dynamics is used to mimic the CH3I / salt system at various humidities.Although the uptake and accommodation coefficients of CH3I are quite low, a coverage of particle surface with CH3I-derived compounds may affect the reactivity of the particles and in term the cycling life of Iodine in the atmosphere.Reference[1] Lebel, L. S.; Dickson, R. S.; Glowa, G. A. J. Environ. Radioact. 2016, 151, 82â93.We acknowledge support by the French government through the Program âInvestissement d'avenirâ through the Labex CaPPA (contract ANR-11-LABX-0005-01) and I-SITE ULNE project OVERSEE (contract ANR-16-IDEX-0004), CPER CLIMIBIO (European Regional Development Fund, Hauts de France council, French Ministry of Higher Education and Research) and French national supercomputing facilities (grants DARI x2016081859 and A0050801859)
