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Grant: NSERC/NRCan/AECL Generation IV Energy Technologies Program

Simon Fraser University

$100,660.00

Reaction Kinetics In Supercritical Water as Probed with Muonium

FY 2010-11

Summary
We propose to make measurements of muonium reaction rates in supercritical water to provide unique data necessary for the development of a supercritical-water-cooled nuclear reactor. Muonium (Mu) behaves as a light isotope of atomic hydrogen (H). TRIUMF, in Vancouver, B.C. is one of only four locations in the world with intense muon beams suitable for such work. We have already made measurements as high as 470?°C, but for this new project it will be necessary to engineer new apparatus capable of higher temperatures, ideally up to 650?°C. A common feature of our measurements to date is that muonium rate constants initially increase with temperature (the expected behaviour) but then go through a maximum. For one reaction (Mu + methanol) the rate constant was found to go through a minimum close to the critical point (374?°C) and then rise again. It is our belief that the key factor is the solvent-driven dynamics, in particular the number of collisions per encounter of a pair of reactants. Recent work on H, OH and hydrated electrons by other authors shows similar behaviour, thus supporting our model. Therefore Mu reaction data can be used to simulate the behaviour of H and other radiolysis transients under such conditions, or at the very least provide data which can be used to model the behaviour of the solvent. It is relatively easy to carry out Mu kinetics experiments on samples under extreme conditions. This is because muon spin spectroscopy is sensitive only to the transient species under study and is unaffected by environmental effects. It is possible to produce a beam of muons with sufficient energy to penetrate a thick metal window of a pressure vessel, avoiding the problems associated with optical windows needed for competing methods. Muon spin spectroscopy operates on the microsecond timescale, so optimal Mu decay rates can be achieved with reactant concentrations of 0.01-100 mM for the fast rate constants expected. The choice of reactions to be studied will be made with the guidance of AECL scientists and will include key products of the radiolysis of water (hydrogen and oxygen) as well as studies as a function of pH and ionic strength.
Program
NSERC/NRCan/AECL Generation IV Energy Technologies Program
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
376313-2008
Name nom
Percival, Paul
Department département
Chemistry
Organization id
5
Institution établissement
Simon Fraser University
Province en
British Columbia
Province fr
Colombie-Britannique
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2008
Award amount
100660
Program id
NNAPJ
Program name en
NSERC/NRCan/AECL Generation IV Energy Technologies Program
Program name fr
Programme des technologies énergétiques de quatrième génération CRSNG RNCan EACL
Group en
Research partnerships programs
Group fr
Programmes de partenariat
Committee code
96
Committee name en
RPP Internal Decision Cttee
Committee name fr
Cté de décision interne - PPR
Area of application code
302
Area of application group en
Energy resources
Area of application group fr
Ressources d'énergie
Area of application en
Nuclear energy
Area of application fr
Énergie nucléaire
Research subject code
3405
Research subject group en
Physical chemistry
Research subject group fr
Chimie physique
Research subject en
Catalysis, kinetics
Research subject fr
Catalyse et cinétique
Partie
2 & 3
Nb partie
3
Application title
Reaction Kinetics In Supercritical Water as Probed with Muonium
Keyword
NSERC
Application summary
We propose to make measurements of muonium reaction rates in supercritical water to provide unique data necessary for the development of a supercritical-water-cooled nuclear reactor. Muonium (Mu) behaves as a light isotope of atomic hydrogen (H). TRIUMF, in Vancouver, B.C. is one of only four locations in the world with intense muon beams suitable for such work. We have already made measurements as high as 470?°C, but for this new project it will be necessary to engineer new apparatus capable of higher temperatures, ideally up to 650?°C. A common feature of our measurements to date is that muonium rate constants initially increase with temperature (the expected behaviour) but then go through a maximum. For one reaction (Mu + methanol) the rate constant was found to go through a minimum close to the critical point (374?°C) and then rise again. It is our belief that the key factor is the solvent-driven dynamics, in particular the number of collisions per encounter of a pair of reactants. Recent work on H, OH and hydrated electrons by other authors shows similar behaviour, thus supporting our model. Therefore Mu reaction data can be used to simulate the behaviour of H and other radiolysis transients under such conditions, or at the very least provide data which can be used to model the behaviour of the solvent. It is relatively easy to carry out Mu kinetics experiments on samples under extreme conditions. This is because muon spin spectroscopy is sensitive only to the transient species under study and is unaffected by environmental effects. It is possible to produce a beam of muons with sufficient energy to penetrate a thick metal window of a pressure vessel, avoiding the problems associated with optical windows needed for competing methods. Muon spin spectroscopy operates on the microsecond timescale, so optimal Mu decay rates can be achieved with reactant concentrations of 0.01-100 mM for the fast rate constants expected. The choice of reactions to be studied will be made with the guidance of AECL scientists and will include key products of the radiolysis of water (hydrogen and oxygen) as well as studies as a function of pH and ionic strength.
Simon Fraser University - $100,660 Grant (2010-11) | Canada Spends