Reactions of electrons and hydrogen atoms with oxygen and methyl bromide in .gamma.-irradiated water vapor

1967 ◽  
Vol 71 (9) ◽  
pp. 2775-2780 ◽  
Author(s):  
George R. A. Johnson ◽  
Miomir Simic
Keyword(s):  
Water Vapor ◽  
Methyl Bromide ◽  
Hydrogen Atoms ◽  
Gamma Irradiated

Preparation and Characterization of the High Molecular Weight [3H]Hyaluronic Acid

1992 ◽  
Vol 57 (10) ◽  
pp. 2151-2156 ◽  
Author(s):  
Peter Chabreček ◽  
Ladislav Šoltés ◽  
Hynek Hradec ◽  
Jiří Filip ◽  
Eduard Orviský
Keyword(s):  
Molecular Weight ◽  
Hyaluronic Acid ◽  
High Molecular Weight ◽  
Methyl Bromide ◽  
High Performance ◽  
Hydrogen Atoms ◽  
Isolation And Characterization ◽  
Labelling Procedure ◽  
Enzymatic Depolymerization

Two methods for the preparation of high molecular weight [3H]hyaluronic acid were investigated. In the first one, hydrogen atoms in the molecule were replaced by tritium. This isotopic substitution was performed in aqueous solution using Pd/CaCO3 as the catalyst. In the second method, the high molecular weight hyaluronic acid was alkylated with [3H]methyl bromide in liquid ammonia at a temperature of -33.5 °C. High-performance gel permeation chromatographic separation method was used for the isolation and characterization of the high molecular weight [3H]hyaluronic acid. Molecular weight parameters for the labelled biopolymers were Mw = 128 kDa, Mw/Mn = 1.88 (first method) and Mw = 268 kDa, Mw/Mn = 1.55 (second method). The high molecular weight [3H]hyaluronic acid having Mw = 268 kDa was degraded further by specific hyaluronidase. Products of the enzymatic depolymerization were observed to be identical for both, labelled and cold biopolymer. This finding indicates that the described labelling procedure using [3H]methyl bromide does not induce any major structural rearrangements in the molecule.

Fluorescence Emission of Excited Hydrogen Atoms after Core Excitation of Water Vapor

2006 ◽  
Vol 96 (6) ◽  
Author(s):  
E. Melero García ◽  
A. Kivimäki ◽  
L. G. M. Pettersson ◽  
J. Álvarez Ruiz ◽  
M. Coreno ◽  
...  
Keyword(s):  
Water Vapor ◽  
Fluorescence Emission ◽  
Hydrogen Atoms ◽  
Core Excitation

Long-Term Corrosion Behavior of Copper-Base Materials in a Gamma-Irradiated Environment

1986 ◽  
Vol 84 ◽  
Author(s):  
Wlyne H. Yunker ◽  
Robert S. Glass
Keyword(s):  
Water Vapor ◽  
Gamma Radiation ◽  
Nuclear Waste ◽  
Pure Copper ◽  
Department Of Energy ◽  
High Dose ◽  
Uniform Corrosion ◽  
Copper Base ◽  
Base Materials ◽  
Gamma Irradiated

AbstractThe U. S. Department of Energy is currently evaluating the feasibility of using copper-base materials for the manufacture of nuclear waste con- tainers. One site under consideration for geologic disposal of nuclear waste is at Yucca Mountain, Nevada. One feature of this waste repository will be the initial presence of ionizing gamma radiation at high dose rates, which may alter the corrosive medium. To evaluate such effects, three copper-base materials (pure copper, 7% aluminum-copper and 30% nickel-copper) have been exposed (presgntly up to 14 months) to a gamma radiation field of approxi- mately 1 × 104 roentgens/hr. The exposure environments have been: 1) both groundwater (regional to the repository site, although taken from a lower elevation) at 95°C; 2) the water-vapor saturated air phase above it; and 3) air/water vapor at 150°C. In addition to uniform corrosion, both pitting and crevice corrosion have been observed. Characterization of the corrosion layers by X-ray diffraction has shown the presence of mixed copper(I) and copper(II) oxides. Studies by Auger Electron Spectroscopy (AES) have also been conducted in order to further characterize the compositions and structures of these corrosion products.

Detection of trapped electrons in organic glasses after gamma irradiation at 4.2 °K by electron spin resonance spectroscopy

1967 ◽  
Vol 45 (22) ◽  
pp. 2723-2727 ◽  
Author(s):  
D. R. Smith ◽  
J. J. Pieroni
Keyword(s):  
Electron Spin Resonance ◽  
Electron Spin ◽  
Dipole Interaction ◽  
Necessary Condition ◽  
Resonance Spectroscopy ◽  
Hydrogen Atoms ◽  
Trapped Electrons ◽  
Organic Glasses ◽  
Spin Resonance ◽  
Gamma Irradiated

Several organic glasses which are known to form trapped electrons when gamma irradiated at 77 °K have been irradiated at 4.2 °K and examined by electron spin resonance (e.s.r.) at the same temperature. In each case an absorption is observed which is probably due to trapped electrons. In three cases, the yield of trapped electrons at 4.2 °K seems to be as great as at 77 °K. In one case, a glassy alkane, the yield is enhanced at 4.2 °K. Trapped electrons in ethanol give a narrower e.s.r. line at 4.2 °K than at 77 °K, suggesting less orientation in the solvent cage.Trapped hydrogen atoms are not detected after irradiation at 4.2 °K. Contrary to prediction, hydrogen atoms are also not detected after post-irradiation photolysis of the trapped electrons.The results suggest that electron traps exist prior to irradiation and that molecular orientation via electronic dipole interaction is not a necessary condition for electron trapping. The results do not distinguish between trapping in solvent defects or trapping via electron-induced polarization of molecular orbitals.

An Overview of Aeronomic Processes in the Stratosphere and Mesosphere

1974 ◽  
Vol 52 (8) ◽  
pp. 1381-1396 ◽  
Author(s):  
M. Nicolet
Keyword(s):  
Nitric Oxide ◽  
Water Vapor ◽  
Nitric Acid ◽  
Oxygen Atom ◽  
Eddy Diffusion ◽  
Atmospheric Conditions ◽  
Hydrogen Atoms ◽  
Electronically Excited ◽  
The Vertical Distribution ◽  
Excited Oxygen

The discrepancy noted between theoretical and observational concentrations of O3 in the mesosphere and stratosphere can be explained by an effect of hydrogen compounds and of nitrogen oxides. Solar radiation dissociates water vapor and methane in the thermosphere and upper mesosphere. In the stratosphere the reaction of the excited oxygen atom O(1D) with methane and nitrous oxide leads to a destruction of these two molecules in the stratosphere which corresponds to a production of carbon monoxide with water vapor and of nitric oxide, respectively. Hydrogen and water vapor molecules also react with the electronically excited oxygen atom O(1D) leading to hydroxyl radicals. Insitu sources of H2 exist in the stratosphere and mesosphere: reaction of OH with CH1, photodissociation of formaldehyde, and also reaction between hydroperoxyl radicals and hydrogen atoms. The vertical distribution of water vapor is not affected by its dissociation in the stratosphere and mesosphere since its reformation is rapid.The ratio of the hydroxyl and hydroperoxyl radical concentrations cannot be determined with adequate precision and complicates the calculation of the destruction of ozone which occurs through reactions of OH and HO2 not only with atomic oxygen at the stratopause but also directly in the middle stratosphere and with CO and NO in the lower stratosphere.In addition to the various reactions involving nitric oxide and nitrogen dioxide, the reactions leading to the production and destruction of nitric acid and nitrous acid must be considered. Nitric acid molecules are involved in an eddy diffusion transport from the lower stratosphere into the troposphere and are, therefore, responsible for the removal of nitric oxide which is produced in the stratosphere. Atmospheric conditions must be known at the tropopause.

The X-radiolysis of water vapor containing methanol. Effects of some electron and hydrogen atom scavengers

1968 ◽  
Vol 46 (12) ◽  
pp. 1957-1964 ◽  
Author(s):  
R. S. Dixon ◽  
M. G. Bailey
Keyword(s):  
Nitrous Oxide ◽  
Water Vapor ◽  
Carbon Tetrachloride ◽  
Hydrogen Atom ◽  
Sulfur Hexafluoride ◽  
Hydrogen Yield ◽  
Hydrogen Atoms ◽  
A Value ◽  
Ion Recombination ◽  
Positive Ion

The X-radiolysis of water vapor containing methanol at 125 °C and 1 atm pressure has been studied alone and in the presence of some electron and hydrogen atom scavengers. In water vapor containing methanol only, a plateau value G(H2) = 7.9 ± 0.3 is obtained at all methanol concentrations above 0.5 mole %. Addition of propylene drastically reduces this yield due to efficient scavenging of hydrogen atoms, and values for the total number of H atoms from all precursors g(H)t = 7,5 ± 0.2 and [Formula: see text] are deduced from the competition. An unscavengeable hydrogen yield g(H2) ~ 0.5 is also indicated in mixtures containing propylene. Nitrous oxide and sulfur hexafluoride are found to scavenge electrons efficiently in water vapor containing methanol and the number of hydrogen atoms arising from electron–positive ion recombination is estimated to have a value G = 2.2 ± 0.6. The number of hydrogen atoms arising from processes not involving electrons is g(H) = 5.2 ± 0.3. Carbon tetrachloride reacts efficiently with both electrons and hydrogen atoms, with k(H + CH3OH)/k(H + CCl4) = 0.085. Values of g(H) = 4.9 ± 0.5 and g(H2) = 0.8 ± 0.2 are deduced from mixtures containing carbon tetrachloride.

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