Monte-Carlo calculation of the primary yields of H2O2 in the 1H+, 2H+, 4He2+, 7Li3+, and 12C6+ radiolysis of liquid water at 25 and 300°C

2002 ◽  
Vol 80 (1) ◽  
pp. 68-75 ◽  
Author(s):  
Jintana Meesungnoen ◽  
Jean-Paul Jay-Gerin ◽  
Abdelali Filali-Mouhim ◽  
Samlee Mankhetkorn

Monte-Carlo simulations are used to calculate the primary yield of hydrogen peroxide (GH2O2) of the radiolysis of pure, deaerated liquid water as a function of linear energy transfer (LET) of the incident radiation over the range ~0.3–100 keV µm–1, at 25 and 300°C. The radiations include 1H+, 2H+, 4He2+, 7Li3+, and 12C6+ ions with energies from 0.17 MeV to 3.6 GeV. At 25°C, it is found that our GH2O2 values, calculated with protons of different initial energies, show a monotonic increase as a function of LET, in agreement with the commonly assumed expectation of an increase in molecular yields with increasing LET. Our calculated H2O2 yields at 300°C increase significantly faster with LET than do their corresponding 25°C values, showing that the temperature dependence of GH2O2 at higher LET is less than for low-LET radiation. We also report our results on the temporal variations of the H2O2 yields, in the interval ~1 × 10–13 – 1 × 10–6 s, at 25 and 300°C and for the different types of radiation considered. Finally, we find that for incident ions of equal LET > 10 keV µm–1, GH2O2 decreases as the ion velocity increases, from protons (or deuterons) to carbon ions. These differences produced in GH2O2 by changing the type of radiation are explained by the greater mean energy of secondary electrons from the higher velocity ions, which penetrate to a greater average distance from the actual particle track, with a corresponding decrease in molecular yields. Our calculated GH2O2 values compare generally well with the experimental data available from the literature and are also in good accord with the predictions of deterministic diffusion-kinetic model calculations reported earlier.Key words: liquid water, radiolysis, primary yields, hydrogen peroxide (H2O2), linear energy transfer (LET), accelerated protons and heavy ions, temperature, Monte-Carlo simulations.

2011 ◽  
Vol 508 (4-6) ◽  
pp. 224-230 ◽  
Author(s):  
S. Sanguanmith ◽  
Y. Muroya ◽  
J. Meesungnoen ◽  
M. Lin ◽  
Y. Katsumura ◽  
...  

2007 ◽  
Vol 85 (3) ◽  
pp. 214-229 ◽  
Author(s):  
Narongchai Autsavapromporn ◽  
Jintana Meesungnoen ◽  
Ianik Plante ◽  
Jean-Paul Jay-Gerin

Monte Carlo simulations are used to investigate the effects of acidity (pH) on the primary yields of various chemical species produced in the radiolysis of de-aerated aqueous sulfuric acid solutions over the range from neutral solution to 0.4 mol/L H2SO4. The effects of the quality of radiation, measured in terms of linear energy transfer (LET), have also been studied for LET varying from ~0.3 to 15 keV/µm at ambient temperature. Our results show that an increase in acidity (1 < pH < 4) leads to an increase in the yield [Formula: see text] of the "reducing" free radicals (hydrated electron and H• atom) and a slight increase in G·OH and [Formula: see text], while there is a slight decrease in [Formula: see text] At pH < 1, •OH radicals react with HSO4- anions to form SO4·– radicals, resulting in a steep decrease in G.OH. By contrast, in the range of pH from ~4 to 7, the calculated yield values are independent of sulfuric acid concentration. In both neutral water and 0.4 mol/L H2SO4 (pH 0.46) solutions, the primary molecular yields increase upon increasing LET to ~15 keV/µm with a concomitant decrease in those of free radicals. As an exception, GH. at first increases with LET, reaching a maximum near 6.5 keV/µm before decreasing steeply at higher LET. The results obtained are generally in good agreement with available experimental data over the whole acidity and LET ranges studied. Finally, as an application, we have simulated the radiation-induced oxidation of ferrous sulfate solutions in aerated aq. 0.4 mol/L H2SO4 (Fricke dosimeter) as a function of time up to ~50 s and addressed the effects of LET on the resulting ferric ion yield at 25 °C. The production of Fe3+ ions is highly sensitive to free-radical yields, especially H• atoms (via formation of HO2•), resulting in a marked decline of G(Fe3+) with increasing LET. The general trend of the observed variation of G(Fe3+) with radiation quality is well reproduced by our computed Fe3+ ion yield values.Key words: liquid water, acidic (H2SO4) aqueous solutions, radiolysis, free-radical and molecular yields, linear energy transfer (LET), Fricke dosimeter, Monte Carlo simulations.


2020 ◽  
Vol 22 (14) ◽  
pp. 7430-7439
Author(s):  
Abida Sultana ◽  
Jintana Meesungnoen ◽  
Jean-Paul Jay-Gerin

Monte Carlo track chemistry simulations were used to calculate the yields (G values) for the radical (eaq−, H˙, ˙OH) and molecular (H2, H2O2) species formed in low-LET water radiolysis from ∼1 ps to 1 ms between 25 and 700 °C, at 25 MPa pressure.


2001 ◽  
Vol 341 (1-2) ◽  
pp. 135-143 ◽  
Author(s):  
Marie-Anne Hervé du Penhoat ◽  
Jintana Meesungnoen ◽  
Thomas Goulet ◽  
Abdelali Filali-Mouhim ◽  
Samlee Mankhetkorn ◽  
...  

2019 ◽  
Vol 47 (2) ◽  
pp. 745-752 ◽  
Author(s):  
Wei Deng ◽  
Xiaoning Ding ◽  
James E. Younkin ◽  
Jiajian Shen ◽  
Martin Bues ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (94) ◽  
pp. 76813-76824 ◽  
Author(s):  
Jintana Meesungnoen ◽  
Sunuchakan Sanguanmith ◽  
Jean-Paul Jay-Gerin

The effect of temperature on the yields of H2 and hydrated electrons in the low linear energy transfer radiolysis of water has been modeled by Monte Carlo track chemistry simulations using phenol/N2O aqueous solutions from 25 up to 350 °C.


2002 ◽  
Vol 80 (10) ◽  
pp. 1367-1374 ◽  
Author(s):  
Yusa Muroya ◽  
Jintana Meesungnoen ◽  
Jean-Paul Jay-Gerin ◽  
Abdelali Filali-Mouhim ◽  
Thomas Goulet ◽  
...  

A re-examination of our Monte-Carlo modeling of the radiolysis of liquid water by low linear-energy-transfer (LET ~ 0.3 keV µm–1) radiation is undertaken herein in an attempt to reconcile the results of our simulation code with recently revised experimental hydrated electron (e–aq) yield data at early times. The thermalization distance of subexcitation electrons, the recombination cross section of the electrons with their water parent cations prior to thermalization, and the branching ratios of the different competing mechanisms in the dissociative decay of vibrationally excited states of water molecules were taken as adjustable parameters in our simulations. Using a global-fit procedure, we have been unable to find a set of values for those parameters to simultaneously reproduce (i) the revised e–aq yield of 4.0 ± 0.2 molecules per 100 eV at "time zero" (that is, a reduction of ~20% over the hitherto accepted value of 4.8 molecules per 100 eV), (ii) the newly measured e–aq decay kinetic profile from 100 ps to 10 ns, and (iii) the time-dependent yields of the other radiolytic species H•, •OH, H2, and H2O2 (up to ~1 µs). The lowest possible limiting "time-zero" yield of e–aq that we could in fact obtain, while ensuring an acceptable agreement between all computed and experimental yields, was ~4.4 to 4.5 molecules per 100 eV. Under these conditions, the mean values of the electron thermalization distance and of the geminate electron–cation recombination probability, averaged over the subexcitation electron "entry spectrum," are found to be equal to ~139 Å and ~18%, respectively. These values are to be compared with those obtained in our previous simulations of liquid water radiolysis, namely ~88 Å and ~5.5%, respectively. Our average electron thermalization distance is also to be compared with the typical size (~64–80 Å) of the initial hydrated electron distributions estimated in current deterministic models of "spur" chemistry. Finally, our average probability for geminate electron–cation recombination agrees well with an estimated value of ~15% recently reported in the literature. In conclusion, this work shows that an adaptation of our calculations to a lower hydrated electron yield at early times is possible, but also suggests that the topic is not closed. Further measurements of the e–aq yields at very short times are needed. Key words: liquid water, radiolysis, electron–cation geminate recombination, electron thermalization distance, hydrated electron (e–aq), e–aq decay kinetics, time-dependent molecular and radical yields, Monte-Carlo simulations.


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