scholarly journals Far Wing Asymmetry of Rotational Raman Lines in Hydrogen

2010 ◽  
Vol 2010 ◽  
pp. 1-5 ◽  
Author(s):  
Magnus Gustafsson

Depolarized Raman spectra of compressed hydrogen gas have been computed rigorously previously for 36 K and 50 K (Gustafsson et al. (2009)). The far wings of the rotational lines show asymmetry that goes beyond that expected from the theory for intracollisional interference and Fano line shapes. Here we analyze the (0) line for pure hydrogen at 36 K in detail. The added asymmetry stems partly from a shape resonance which adds significant intensity to the higher frequency side of the line profile. The influence of the threshold energy for the rotational transition accounts for the remainder.

From the fact that no carbonic acid gas is given out by venous blood when that fluid is subjected to the action of the air-pump, former experimentalists had inferred that this blood contains no carbonic acid. The author of the present paper contends that this is an erroneous inference; first, by showing that serum, which had been made to absorb a considerable quantity of this gas, does not yield it upon the removal of the atmospheric pressure; and next, by adducing several experiments in proof of the strong attraction exerted on carbonic acid both by hydrogen and by oxygen gases, which were found to absorb it readily through the medium of moistened membrane. By means of a peculiar apparatus, consisting of a double-necked bottle, to which a set of bent tubes were adapted, he ascertained that venous blood, agitated with pure hydrogen gas, and allowed to remain for an hour in contact with it, imparts to that gas a considerable quantity of carbonic acid. The same result had, indeed, been obtained, in a former experiment, by the simple application of heat to venous blood confined under hydrogen gas; but on account of the possible chemical agency of heat, the inference drawn from that experiment is less conclusive than from experiments in which the air-pump alone is employed. The author found that, in like manner, atmospheric air, by remaining, for a sufficient time, in contact with venous blood, on the application of the air-pump, acquires carbonic acid. The hypothesis that the carbon of the blood attracts the oxygen of the air into the fluid, and there combines with it, and that the carbonic acid thus formed is afterwards exhaled, appears to be inconsistent with the fact that all acids, and carbonic acid more especially, impart to the blood a black colour; whereas the immediate effect of exposing venous blood to atmospheric air, or to oxygen gas, is a change of colour from a dark to a bright scarlet, implying its conversion from the venous to the arterial character: hence the author infers that the acid is not formed during the experiment in question, but already exists in the venous blood, and is extracted from it by the atmospheric air. Similar experiments made with oxygen gas, in place of atmospheric air, were attended with the like results, but in a more striking degree and tend therefore to corroborate the views entertained by the author of the theory of respiration. According to these views, it is neither in the lungs, nor generally in the course of the circulation, but only during its passage through the capillary system of vessels, that the blood undergoes the change from arterial to venous; a change consisting in the formation of carbonic acid, by the addition of particles of carbon derived from the solid textures of the body, and which had combined with the oxygen supplied by the arterial blood: and it is by this combination that heat is evolved, as well as a dark colour imparted to the blood. The author ascribes, however, the bright red colour of arterial blood, not to the action of oxygen, which is of itself completely inert as a colouring agent, but to that of the saline ingredients naturally contained in healthy blood. On arriving at the lungs, the first change induced on the blood is effected by the oxygen of the atmospheric air, and consists in the removal of the carbonic acid, which had been the source of the dark colour of the venous blood; and the second consists in the attraction by the blood of a portion of oxygen, which it absorbs from the air, and which takes the place of the carbonic acid. The peculiar texture of the lungs, and the elevation of temperature in warm-blooded animals, concur in promoting the rapid production of these changes.


2014 ◽  
Vol 86 (12) ◽  
pp. 1931-1943 ◽  
Author(s):  
Jonathan Tennyson ◽  
Peter F. Bernath ◽  
Alain Campargue ◽  
Attila G. Császár ◽  
Ludovic Daumont ◽  
...  

Abstract The report of an IUPAC Task Group, formed in 2011 on “Intensities and line shapes in high-resolution spectra of water isotopologues from experiment and theory” (Project No. 2011-022-2-100), on line profiles of isolated high-resolution rotational-vibrational transitions perturbed by neutral gas-phase molecules is presented. The well-documented inadequacies of the Voigt profile (VP), used almost universally by databases and radiative-transfer codes, to represent pressure effects and Doppler broadening in isolated vibrational-rotational and pure rotational transitions of the water molecule have resulted in the development of a variety of alternative line-profile models. These models capture more of the physics of the influence of pressure on line shapes but, in general, at the price of greater complexity. The Task Group recommends that the partially Correlated quadratic-Speed-Dependent Hard-Collision profile (pCqSD-HCP) should be adopted as the appropriate model for high-resolution spectroscopy. For simplicity this should be called the Hartmann–Tran profile (HTP). The HTP is sophisticated enough to capture the various collisional contributions to the isolated line shape, can be computed in a straightforward and rapid manner, and reduces to simpler profiles, including the Voigt profile, under certain simplifying assumptions.


Atoms ◽  
2019 ◽  
Vol 7 (3) ◽  
pp. 63 ◽  
Author(s):  
Christian G. Parigger ◽  
Christopher M. Helstern ◽  
Ghaneshwar Gautam

This work discusses laboratory measurements of atomic and diatomic molecular species in laser-plasma generated in gases. Noticeable self-absorption of the Balmer series hydrogen alpha line occurs for electron densities of the order of one tenth of standard ambient temperature and pressure density. Emission spectra of selected diatomic molecules in air or specific gaseous mixtures at or near atmospheric pressure reveal minimal plasma re-absorption. Abel inversion of the plasma in selected gases and gas mixtures confirm expansion dynamics that unravel regions of atomic and molecular species of different electron temperature and density. Time resolved spectroscopy diagnoses self-absorption of hydrogen alpha and hydrogen beta lines in ultra-high pure hydrogen gas. Radiation from a Nd:YAG laser device induces micro-plasma for pulse widths in the range of 6–14 ns, energies in the range of 100–800 mJ, and peak irradiances of the order 1–10 TW/cm 2 . Atomic line profiles yield electron density and temperature from fitting of line profiles to wavelength and sensitivity corrected spectral radiance data. Analysis of measured diatomic emission data yields excitation temperature of primarily molecular recombination spectra. Applications of the laboratory experiments extend to investigations of stellar astrophysics white dwarf spectra.


2006 ◽  
Vol 986 ◽  
Author(s):  
Marilyn E. Hawley ◽  
Mary Ann Hill ◽  
Yongqiang Wang ◽  
Roland K. Schulze

AbstractUranium is an extremely important material for commercial and military applications (i.e. nuclear power, nuclear weapons, conventional weapons, and armor systems) and, like a number of other materials, is vulnerable to corrosion by environmental gases that affect their properties, leading to component degradation, shortened lifetimes and materials failure. For uranium this is particularly true in the case of corrosion by hydrogen. A fundamental understanding of the corrosion process at the nucleation stage is of critical importance. The goal of this work is to study the role of common chemical impurities in uranium with initiation sites for the formation of destructive hydride blisters. Samples were implanted with various ions, annealed under vacuum at 200°C, than exposed to one atm of ultra-pure hydrogen. Scanning force microscopy surface potential imaging was used to characterize the structure and corresponding electrical properties of polycrystalline uranium surfaces that resulted from the implantation of different suspect atoms after exposure to hydrogen gas. Surface potential images revealed features related to different oxide structures and hydride spots/blisters as well as other features not obvious in the corresponding topograph. In the surface potential images, blisters appear as bright (higher potential) features in sharp contrast to the uranium oxide background. Often a possible inclusion was observed in the center of a blister. Blister formation did not appear to correlate with implantation of any specific specie, however, distinct differences were seen between implanted and non implanted sides of the same sample.


2018 ◽  
Vol 115 (20) ◽  
pp. 5072-5076 ◽  
Author(s):  
Christian Schröter ◽  
Jong Chan Lee ◽  
Thomas Schultz

We present mass-correlated rotational alignment spectroscopy, based on the optical excitation of a coherent rotational quantum wave and the observation of temporal wave interferences in a mass spectrometer. Combined electronic and opto-mechanical delays increased the observation time and energy resolution by an order of magnitude compared with preceding time-domain measurements. Rotational transition frequencies were referenced to an external clock for accurate absolute frequency measurements. Rotational Raman spectra for six naturally occurring carbon disulfide isotopologues were resolved with 3 MHz resolution over a spectral range of 500 GHz. Rotational constants were determined with single-kilohertz accuracy, competitive with state-of-the-art frequency domain measurements.


Author(s):  
Clinten D. Lingel

Storing hydrogen gas under pressure to provide an energy source for fuel cells or internal combustion engines is a real issue that must be addressed. Diatomic hydrogen does not occur naturally and therefore, must be made through electrolysis, methane reforming or some other process. From the production of pure hydrogen to the final end user, the entire cycle must be considered. Once formed, hydrogen will need to be compressed to a storage container. A hydrogen based transportation system will be both an economic and engineering challenge.


2018 ◽  
Vol 48 (1) ◽  
pp. 191-222
Author(s):  
Anna Turlej ◽  
Marta Skolniak

Abstract The development of the commercial air carriers market causes an increase in the aviation fuel consumption and the air pollution. There are intensive works in order to invent the possibility of supplying the aviation engines with biofuels. The hydrogen gas is needed for technological processes to obtain the synthetic biocomponents from biomass, which met the quality standards for fuels and aviation fuels. Pure hydrogen gas is scarce in the Earth’s atmosphere and has to be derived from petroleum products. Its acquisition currently requires the processing of petroleum-based matter. The whole world is looking for easy, cheap and safe ways of producing hydrogen from a variety of renewable raw materials, that are an alternative to fossil fuels. The article shows the technological potential of experimental methods for hydrogen production from ethanol produced from biodegradable waste, which is widely considered as a renewable and environmentally friendly resource.


2021 ◽  
Author(s):  
◽  
Sigit Prabowo

<p>Titanomagnetite (TTM) ironsand has been used to produce steel in New Zealand (NZ) for about 40 years. However, the current steelmaking process in NZ produces high emissions of CO2 because it uses coal as a primary reducing agent. The fluidised bed (FB) process allows the use of pure hydrogen gas to reduce ironsand, and as a result, does not produce CO2 gas. However, for conventional hematite ores, reduction in a FB system is usually limited by the onset of particle sticking at temperatures ≳ 800°C. This thesis investigates the reduction of NZ TTM ironsand by hydrogen gas in the FB system with a key focus on ore sticking behaviour.  Initially, this thesis reports preliminary fluidisation tests by nitrogen and helium gases at room temperature, carried out to determine key fluidisation parameters for ironsand powder. From these results, a laboratory-scale experimental FB reactor has been designed and built for the hydrogen reduction study at high temperatures. A key feature of the reactor is a novel in-situ sampling system, which enables extraction of multiple samples during a single experimental run without interrupting operation of the FB.  Quantitative X-ray diffraction (q-XRD) has been used to determine the metallisation degree of partially reduced samples. Phase evolution during the reaction has also been analysed using q-XRD alongside scanning electron microscopy/energy dispersed spectroscopy (SEM/EDS). Additionally, the water vapour compositions in the exhaust gas were calculated from the q-XRD data and also measured in real-time using a high-temperature humidity sensor.   The effect of various parameters has been investigated within the FB reduction experiments: hydrogen gas concentrations, hydrogen gas flow rate, bed mass, particle size, and temperature. The results indicate that across the entire range of controlled studied, the FB reduction rate of TTM ironsand is simply controlled by the rate of hydrogen gas supply. Interestingly, there were no occurrences of the sticking phenomenon at any point during the reduction by hydrogen gas at high temperatures of up to 1000°C. Sticking appears to be prevented by the formation of a protective titanium-rich oxide shell around each particle during the initial reduction stage. Importantly, this shell remains present throughout the reduction process, and as a result, the reduction reaction proceeds rapidly to completion with a metallisation degree of ~93%.  The influence of temperature on the reaction progress has also been investigated. The reduction pathway appears to vary within different temperature regimes. At low temperatures (750°C-800°C), TTM is directly reduced to metallic iron and ilmenite without any evidence of wüstite phase. At ‘intermediate temperatures’ (850°C-900°C) small amount of short-lived wüstite is observed. Some of the amount of TTM appears to be reduced to wüstite, and some is directly reduced to metallic iron. At high temperatures (≥ 950°C), approximately half of the initial TTM phase is quickly reduced to wüstite. After that point, wüstite is then reduced to metallic iron whilst the reduction of TTM stops. This is due to the enrichment of Ti species in TTM phase, which stabilises TTM crystal. Once wüstite has been fully reduced, the reduction of TTM then resumes.   Throughout the entire experimental program for this thesis, particle sticking was observed to occur only under two specific sets of experimental conditions. These were: reduction by 100% H2 gas at 1050°C (case A) and reduction by 7.5 mol.% H2O – 92.5 mol.% H2 at 950°C (case B). In both cases, sticking occurred as a sinter which nucleated at the reactor wall surface, while most particles remained fluidised as loose powder. The mechanism of these sticking cases has been analysed by XRD and SEM. The results suggest that silica from the quartz reactor wall reacted and bonded with Fe from particles to nucleate the initial sinter.   In summary, the findings in this thesis show that the hydrogen-FB process is highly effective in reducing NZ ironsand to a direct reduced iron (DRI) product. These findings open up the possibility of developing a new industrial FB technology for the direct reduction of NZ TTM ironsand, with extremely low CO2 emissions.</p>


2022 ◽  
pp. 100043
Author(s):  
Wenxu Zhang ◽  
Travis J.A. Craddock ◽  
Yajuan Li ◽  
Mira Swartzlander ◽  
Robert R. Alfano ◽  
...  

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