Dihydrogen H2 steady state in α-radiolysis of water adsorbed on PuO2 surface
Radiolysis of water adsorbed on PuO2 surface has been the subject of several studies but still remains poorly understood. The present study brings new experimental results helping to further understand the phenomena occurring at PuO2 surface. Radiolysis of adsorbed water on PuO2 surface leads to the...
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Published in | Radiation physics and chemistry (Oxford, England : 1993) Vol. 162; pp. 136 - 145 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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01.09.2019
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Abstract | Radiolysis of water adsorbed on PuO2 surface has been the subject of several studies but still remains poorly understood. The present study brings new experimental results helping to further understand the phenomena occurring at PuO2 surface. Radiolysis of adsorbed water on PuO2 surface leads to the reach of a steady state in hydrogen content when relative humidity is kept constant implying an equilibrium between generation and consumption of hydrogen. The influences of specific surface area, relative humidity, PuO2 dose rate and composition of the atmosphere (Ar vs air) on hydrogen generation were investigated. A significant evolution of the hydrogen generation kinetics was observed upon PuO2 surface aging. This result might be related to an evolution of the surface physicochemical state induced by a long-term storage in H2O/H2/O2 atmosphere. The surface evolution modifies the equilibrium between generation and consumption of hydrogen. Several annealing thermal treatment were necessary to retrieve H2 accumulations kinetics similar to the ones obtained with the same sample as freshly prepared. This indicates an important evolution of PuO2 surface and subsurface. A mechanism is described to explain the surface evolution and its effect on H2 accumulation through radiolysis of adsorbed water.
•H2 formed under α-radiolysis of water sorbed on PuO2 surface reaches a steady state after several days.•The initial rate R0 increases with dose rate, relative humidity and specific surface area.•H2 steady-state concentration increases with dose rate, relative humidity and specific surface area.•Hydrogen accumulation and consumption reach the same steady state and conduct to a kinetic model.•The rates of hydrogen accumulation increase with long term storage and is restored by annealing treatments. |
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AbstractList | Radiolysis of water adsorbed on PuO2 surface has been the subject of several studies but still remains poorly understood. The present study brings new experimental results helping to further understand the phenomena occurring at PuO2 surface. Radiolysis of adsorbed water on PuO2 surface leads to the reach of a steady state in hydrogen content when relative humidity is kept constant implying an equilibrium between generation and consumption of hydrogen. The influences of specific surface area, relative humidity, PuO2 dose rate and composition of the atmosphere (Ar vs air) on hydrogen generation were investigated. A significant evolution of the hydrogen generation kinetics was observed upon PuO2 surface aging. This result might be related to an evolution of the surface physicochemical state induced by a long-term storage in H2O/H2/O2 atmosphere. The surface evolution modifies the equilibrium between generation and consumption of hydrogen. Several annealing thermal treatment were necessary to retrieve H2 accumulations kinetics similar to the ones obtained with the same sample as freshly prepared. This indicates an important evolution of PuO2 surface and subsurface. A mechanism is described to explain the surface evolution and its effect on H2 accumulation through radiolysis of adsorbed water. Radiolysis of water adsorbed on PuO2 surface has been the subject of several studies but still remains poorly understood. The present study brings new experimental results helping to further understand the phenomena occurring at PuO2 surface. Radiolysis of adsorbed water on PuO2 surface leads to the reach of a steady state in hydrogen content when relative humidity is kept constant implying an equilibrium between generation and consumption of hydrogen. The influences of specific surface area, relative humidity, PuO2 dose rate and composition of the atmosphere (Ar vs air) on hydrogen generation were investigated. A significant evolution of the hydrogen generation kinetics was observed upon PuO2 surface aging. This result might be related to an evolution of the surface physicochemical state induced by a long-term storage in H2O/H2/O2 atmosphere. The surface evolution modifies the equilibrium between generation and consumption of hydrogen. Several annealing thermal treatment were necessary to retrieve H2 accumulations kinetics similar to the ones obtained with the same sample as freshly prepared. This indicates an important evolution of PuO2 surface and subsurface. A mechanism is described to explain the surface evolution and its effect on H2 accumulation through radiolysis of adsorbed water. •H2 formed under α-radiolysis of water sorbed on PuO2 surface reaches a steady state after several days.•The initial rate R0 increases with dose rate, relative humidity and specific surface area.•H2 steady-state concentration increases with dose rate, relative humidity and specific surface area.•Hydrogen accumulation and consumption reach the same steady state and conduct to a kinetic model.•The rates of hydrogen accumulation increase with long term storage and is restored by annealing treatments. |
Author | Gaillard, Jérémy Vigier, Nicolas Maurin, Jérôme Deroche, Arnaud Moisy, Philippe Lemaire, Olivier Vermeulen, Jackie Venault, Laurent Budanova, Natalia |
Author_xml | – sequence: 1 givenname: Laurent surname: Venault fullname: Venault, Laurent email: laurent.venault@cea.fr organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 2 givenname: Arnaud surname: Deroche fullname: Deroche, Arnaud organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 3 givenname: Jérémy surname: Gaillard fullname: Gaillard, Jérémy organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 4 givenname: Olivier surname: Lemaire fullname: Lemaire, Olivier organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 5 givenname: Natalia surname: Budanova fullname: Budanova, Natalia organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 6 givenname: Jackie surname: Vermeulen fullname: Vermeulen, Jackie organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 7 givenname: Jérôme surname: Maurin fullname: Maurin, Jérôme organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France – sequence: 8 givenname: Nicolas surname: Vigier fullname: Vigier, Nicolas organization: ORANO, 1 place Jean Millier, 90084 Paris La Défense, France – sequence: 9 givenname: Philippe surname: Moisy fullname: Moisy, Philippe organization: CEA, Nuclear Energy Division, Research Department on Mining and Fuel Recycling Processes, BP 17171, F-30207 Bagnols-sur-Cèze, France |
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SubjectTerms | Alpha radiolysis Dosage Evolution Heat treatment Humidity Hydrogen Hydrogen production Plutonium dioxide Radiolysis Reaction kinetics Relative humidity Steady state Surface Water |
Title | Dihydrogen H2 steady state in α-radiolysis of water adsorbed on PuO2 surface |
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