Gas phase radiolysis of hydrogen chloride, hydrogen bromide, and nitrous oxide with intense electron pulses

1969 ◽  
Vol 47 (20) ◽  
pp. 3783-3791 ◽  
Author(s):  
C. Willis ◽  
A. W. Boyd ◽  
D. A. Armstrong

Hydrogen chloride and hydrogen bromide have been irradiated with single electron pulses at a very high intensity (1027 eV g−1 s−1) with a Febetron 705. At room temperature the yields of hydrogen from hydrogen chloride and hydrogen bromide, for pressures between 700 and 1200 Torr, are G(H2) = 8.1 ± 0.2 and G(H2) = 9.9 ± 0.3, respectively. These are the same as the yields observed at low dose rates. Detailed lifetime calculations, however, show that the mechanism is significantly different at the higher dose rate. Scavenger experiments with chlorine in hydrogen chloride show that the negative ion intermediates form thermal hydrogen atoms.The value of G(N2) = 12.4 ± 0.2 from nitrous oxide at a dose rate of 1027 eV g−1 s−1 is confirmed and the use of nitrous oxide as a dosimeter for pulsed electron beams is discussed. The higher nitrogen yield at Febetron dose rates appears to be due to changes in the reactions of electrons.

1971 ◽  
Vol 49 (10) ◽  
pp. 1677-1682 ◽  
Author(s):  
C. Willis ◽  
A. W. Boyd ◽  
O. A. Miller

Gaseous H2S has been irradiated with electron pulses from a Febetron 705 at a dose rate of ~2 × 1027 eV g−1 s−1. For single pulse experiments, the yield of hydrogen is G(H2) = 12.0 ± 0.5, independent of pressure from at least 350 to 1600 Torr. Addition of SF6 reduces the yield to G(H2) = 7.9 ± 0.3 which is fairly close to that observed for pure H2S at low dose rates. The reduction, ΔG(H2) = 4.1 ± 0.3, agrees very well with the ion pair yield based on a W value of 25.3 eV.In multi-pulse irradiations, for pure H2S, the yield falls off with dose giving a limiting yield close to G(H2) = 8.0. No similar fall-off is observed for H2S–SF6 mixtures. It is proposed that at high absorbed doses and at low dose rates, there is no contribution to the hydrogen yield from neutralization processes; and that this is due to neutralization of H3S+ by an ion of the type Sn− rather than a free electron.


Metabolites ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 270
Author(s):  
Heng-Hong Li ◽  
Yun-Tien Lin ◽  
Evagelia C. Laiakis ◽  
Maryam Goudarzi ◽  
Waylon Weber ◽  
...  

Our laboratory and others have use radiation metabolomics to assess responses in order to develop biomarkers reflecting exposure and level of injury. To expand the types of exposure and compare to previously published results, metabolomic analysis has been carried out using serum samples from mice exposed to 137Cs internal emitters. Animals were injected intraperitoneally with 137CsCl solutions of varying radioactivity, and the absorbed doses were calculated. To determine the dose rate effect, serum samples were collected at 2, 3, 5, 7, and 14 days after injection. Based on the time for each group receiving the cumulative dose of 4 Gy, the dose rate for each group was determined. The dose rates analyzed were 0.16 Gy/day (low), 0.69 Gy/day (medium), and 1.25 Gy/day (high). The results indicated that at a cumulative dose of 4 Gy, the low dose rate group had the least number of statistically significantly differential spectral features. Some identified metabolites showed common changes for different dose rates. For example, significantly altered levels of oleamide and sphingosine 1-phosphate were seen in all three groups. On the other hand, the intensity of three amino acids, Isoleucine, Phenylalanine and Arginine, significantly decreased only in the medium dose rate group. These findings have the potential to be used in assessing the exposure and the biological effects of internal emitters.


1970 ◽  
Vol 48 (4) ◽  
pp. 598-602 ◽  
Author(s):  
D. E. Wilson ◽  
D. A. Armstrong

Rates of ion neutralization have been measured in hydrogen chloride, hydrogen bromide, and nitrous oxide by collecting the ions remaining in a defined volume at various times after ionization by a pulse of 120 k.v.p. X-rays. Values of the total homogeneous ion-ion recombination coefficient, a, have been obtained for each gas over a range of pressures in the region 50 to 650 Torr. From a study of the effects of pressure and ion density, the relative rates of wall diffusion, mutual neutralization, and three-body neutralization have been deduced.


2018 ◽  
Vol 47 (3-4) ◽  
pp. 97-112 ◽  
Author(s):  
M.P. Little

For stochastic effects such as cancer, linear-quadratic models of dose are often used to extrapolate from the experience of the Japanese atomic bomb survivors to estimate risks from low doses and low dose rates. The low dose extrapolation factor (LDEF), which consists of the ratio of the low dose slope (as derived via fitting a linear-quadratic model) to the slope of the straight line fitted to a specific dose range, is used to derive the degree of overestimation (if LDEF > 1) or underestimation (if LDEF < 1) of low dose risk by linear extrapolation from effects at higher doses. Likewise, a dose rate extrapolation factor (DREF) can be defined, consisting of the ratio of the low dose slopes at high and low dose rates. This paper reviews a variety of human and animal data for cancer and non-cancer endpoints to assess evidence for curvature in the dose response (i.e. LDEF) and modifications of the dose response by dose rate (i.e. DREF). The JANUS mouse data imply that LDEF is approximately 0.2–0.8 and DREF is approximately 1.2–2.3 for many tumours following gamma exposure, with corresponding figures of approximately 0.1–0.9 and 0.0–0.2 following neutron exposure. This paper also cursorily reviews human data which allow direct estimates of low dose and low dose rate risk.


1960 ◽  
Vol 38 (1) ◽  
pp. 559-567 ◽  
Author(s):  
J. E. Watkin ◽  
A. C. Neish

The effect on the conversion of carbon14 to quercetin by a buckwheat plant caused by variation in the dose rate of a carbon 14-labelled precursor in μmoles over a 100-fold range has been studied. The results expressed as dilution of carbon14 varied over a 200-fold range for the same precursor with most of the variation being found at low dose rates. When expressed as the percentage of administered carbon14 converted to quercetin the results for acetate, D-glucose, and L-phenyllactic acid were mostly constant over this range but L-phenylalanine had a maximum percentage conversion or an optimal dose rate. An explanation of the results in metabolic terms has been attempted.It is recommended that the "percentage of C14 converted" be used to express results in plant biosynthetic work.


1970 ◽  
Vol 48 (19) ◽  
pp. 3029-3033 ◽  
Author(s):  
C. Willis ◽  
O. A. Miller

Carbon monoxide has been irradiated with single intense pulses from an electron accelerator at a dose rate of ~ 2 × 1027 eV g−1 s−1. The yield of carbon dioxide obtained was G(CO2) = 0.7 ± 0.1 with a very small yield of carbon suboxide, G(C3O2) ≤ 0.02.Addition of propene reduces the carbon dioxide yield to almost zero while addition of propane has no effect. This suggests that propene is acting as an oxygen atom scavenger rather than as a quencher of an excited state of carbon monoxide. However, rate constant data do not support this suggestion and it is concluded that the residual yield of carbon dioxide observed at high dose rates arises from reaction 9[Formula: see text]where CO+ is in an A2Π or B2Σ+ state.


2014 ◽  
Vol 54 (11) ◽  
pp. 2360-2363 ◽  
Author(s):  
V.S. Pershenkov ◽  
M. Ullán ◽  
M. Wilder ◽  
H. Spieler ◽  
E. Spencer ◽  
...  

1990 ◽  
Vol 201 ◽  
Author(s):  
E. Cortesi ◽  
F. Namavar ◽  
R. F. Pinizzotto ◽  
H. Yang

AbstractWe have studied Separation by IMplantation of OXygen (SIMOX) processes using very high dose rates (40–60 μA/cm2). For a dose of 4 × 1017 O+/cm2 at 160 keV, the structure formed by implantation at 50 μA/cm2 is very similar to that associated with lower dose rates. The same dose implanted at a dose rate of 60 μA/cm2, however, results in the formation of pits in the silicon surface as well as a somewhat different oxide structure. Implantation through a surface oxide layer appears to result in a structure similar to that associated with lower dose rate implantation. These and higher dose samples suggest that the threshold for pit formation is related to both dose rate and dose.


1976 ◽  
Vol 54 (17) ◽  
pp. 2767-2772
Author(s):  
Robert D. McAlpine ◽  
O. A. Miller ◽  
A. W. Boyd

Gas phase radiolysis studies have been carried out on mixtures of H2S and D2S using as irradiation sources, either a Gammacell or a Febetron 705 pulsed electron accelerator. Separation factors (α = (H/D)prod ÷ (H/D)react) were obtained for various values of xD (the mole fraction of D2S), dose rate and temperature, as well as with the addition of SF6. All of the observed α values, for 0.2 ≤ xD ≤ 0.8, fall on the following empirical straight line.[Formula: see text]The addition of neon to a D2S/H2S mixture gives a value of α which decreases as the partial pressure of neon increases. For a 70% D2S/30% H2S mixture, &([a-z]+); = 1.9 ± 0.1 for the pure mixture and 1.28 ± 0.08 when 90 kPa of neon has been added to 10 kPa of the mixture. The &([a-z]+); values described by eq. 1 are interpreted as arising from kinetic isotope effects in the reactions of (translationally) hot H or D atoms with H2S, HDS, or D2S to form H2, HD or D2.Hydrogen yields from the gas phase radiolysis of pure H2S and pure D2S have been determined for dose rates from 4 × 1016 to 2 × 1028 eV g−1 s−1. Using dose rates of up to 2 × 1027 eV g−1 s−1, ΔG = G(H2) − G(D2) = 0.5. For the highest dose rate used (2 × 1028 eV g−1 s−1), ΔG = 1.5. The larger value of ΔG at very high dose rates is thought to arise from the dissociative neutralization processes. A possible mechanism is discussed.


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