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 ◽  
...  
2016 ◽  
Vol 2016 ◽  
pp. 1-6
Author(s):  
Pu-Reun Choi ◽  
Hyun Chul Kim ◽  
Sun Min Kim ◽  
Eunhae Koo

The most critical issue on flexible electronics such as organic solar-cell, OLEDs, and flexible display is the protection of the core active materials from the degradation by water and oxygen. The defect of barrier film is the main channel for the transmission of water and oxygen molecules. Herein, in order to monitor the defects of barrier films, we have developed anthracene boronic acid pinacol ester (ABAPE) sensor which is very sensitive to water vapor. When ABAPE film is exposed to water, it gives off fluorescence emission at 389 and 408 nm under excitation peak at 366 nm. Based on the fluorescence microscopy and SEM images, the optical method using the ABAPE sensor film can monitor the defects of barrier film smaller than 1 μm. This result suggests that ABAPE can be utilized to monitor the defect and water vapor transmission rate (WVTR) in the barrier film.


1974 ◽  
Vol 52 (8) ◽  
pp. 1381-1396 ◽  
Author(s):  
M. Nicolet

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.


1968 ◽  
Vol 46 (12) ◽  
pp. 1957-1964 ◽  
Author(s):  
R. S. Dixon ◽  
M. G. Bailey

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.


2020 ◽  
Author(s):  
Anna Fedorova ◽  
Franck Montmessin ◽  
Oleg Korablev ◽  
Mikhail Luginin ◽  
Alexander Trokhimovskiy ◽  
...  

<p>The water vapour vertical distribution is an eloquent gauge of the relative roles of the various sources, sinks and processes that control the Martian water cycle. However, its behaviour is still poorly studied while it is instrument for our understanding of the loss of water from Mars to space, which results from the transport of water to the upper atmosphere where it is disassociated to hydrogen atoms that later escape. We use the Atmospheric Chemistry Suite on the ExoMars Trace Gas Orbiter to characterize the water distribution with altitude. Here we present results of the Atmospheric Chemistry Suite (ACS) instrument NIR channel for the first year of TGO observations covering the almost full year from Ls 160° of the Martian year 34 (April 2018) to Ls 130° of the Martian year 35 (January 2020). Simultaneous measurements of the water vapour mixing ratio, temperature and dust vertical distribution and formation of water ice clouds allow us to constrain the complex water behaviour and estimate the saturation state of H2O. Water profiles during the 2018-2019 southern spring and summer stormy seasons show that high altitude water is preferentially supplied close to perihelion and that large supersaturation occurs even when clouds are present. Here we attempt to complete the story by studying water vapor during the northern spring and summer to explore whether saturation impacts water transport between hemispheres in this season. The data analysis of MY35 was supported by RSF (project No. 20-42-09035).</p>


2004 ◽  
Vol 842 ◽  
Author(s):  
T. Takasugi ◽  
Y. Hotta ◽  
S. Shibuya ◽  
Y. Kaneno ◽  
H. Inoue ◽  
...  

ABSTRACTThermomechanically processed TiAl-based intermetallic alloys with various alloy compositions and microstructures were tensile tested in various environmental media including air, water vapor and a mixture gas of 5vol.%H2+Ar as a function of temperature. All the TiAl-based intermetallic alloys showed reduced tensile fracture stress (or elongation) in air, water vapor and a mixture gas of 5vol.%H2+Ar not only at ambient temperature (RT∼600K) but also at high temperature mostly from 600K to 1000K (sometimes higher temperature than 1000K). The high-temperature environmental embrittlement of TiAl-based intermetallic alloy depended upon the microstructure. The possible species causing the high-temperature environmental embrittlement are hydrogen atoms decomposed from water vapor (H2O) or hydrogen gas (H2), similar to those causing the low-temperature environmental embrittlement.


1967 ◽  
Vol 71 (4) ◽  
pp. 1118-1123 ◽  
Author(s):  
George R. A. Johnson ◽  
Miomir Simic
Keyword(s):  

1966 ◽  
Vol 44 (8) ◽  
pp. 869-876 ◽  
Author(s):  
Norisuke H Ata ◽  
Paul A. Glguère

Hydrogen gas partly dissociated in an electrodeless discharge was mixed downstream with hydrogen peroxide vapor at low pressure (0.1 mm Hg) in a liquid nitrogen trap. The reaction products condensed readily on the wall as a clear, yellowish glass resembling that from dissociated water vapor and other related systems. A manometric study of the warming-up process has revealed four distinct steps. The first two, in which only traces of gas are given off, look like the recombination of trapped free radicals. The major evolution of oxygen upon crystallization of the glassy deposit at 160 °K is ascribed to the decomposition of hydrogen peroxide under the influence of some unidentified species generated in the electric discharge through hydrogen. Experimental evidence for this is presented. In any case the stoichiometry cannot be reconciled with the formation of a metastable intermediate, such as the hypothetical polyoxide H2O4.In the last step beginning around 215 °K more peroxide is decomposed during the eutectic melting of the solid. Qualitatively these phenomena are similar to those shown by the condensate from dissociated water vapor.


1973 ◽  
Vol 51 (24) ◽  
pp. 4056-4061 ◽  
Author(s):  
A. W. Boyd ◽  
C. Willis ◽  
O. A. Miller

The isotope effect in the formation of hydrogen has been measured for H2O–D2O mixtures (10–90% H2O, 0.5–1.0 mg ml−1, 412–138 °C) with and without 1 mol% SF6 at 2 × 1027 eV g−1 s−1. The values of α ((H/D) radiolytic hydrogen/(H/D) H2O–D2O) for the reactions of hydrogen atoms are in the range 3–6 varying with H/D ratio of the substrate. Consideration of possible mechanisms for these large α values leads to the conclusions that reaction of the hydrogen atoms to form hydrogen involves the substrate and that the species H3O may be formed as an intermediate.


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