scholarly journals High-resolution absorption cross sections of C2H6 at elevated temperatures

2015 ◽  
Vol 1 ◽  
pp. 20-25 ◽  
Author(s):  
Robert J. Hargreaves ◽  
Eric Buzan ◽  
Michael Dulick ◽  
Peter F. Bernath
2021 ◽  
pp. 000370282199044
Author(s):  
Wubin Weng ◽  
Shen Li ◽  
Marcus Aldén ◽  
Zhongshan Li

Ammonia (NH3) is regarded as an important nitrogen oxides (NOx) precursor and also as an effective reductant for NOx removal in energy utilization through combustion, and it has recently become an attractive non-carbon alternative fuel. To have a better understanding of thermochemical properties of NH3, accurate in situ detection of NH3 in high temperature environments is desirable. Ultraviolet (UV) absorption spectroscopy is a feasible technique. To achieve quantitative measurements, spectrally resolved UV absorption cross-sections of NH3 in hot gas environments at different temperatures from 295 K to 590 K were experimentally measured for the first time. Based on the experimental results, vibrational constants of NH3 were determined and used for the calculation of the absorption cross-section of NH3 at high temperatures above 590 K using the PGOPHER software. The investigated UV spectra covered the range of wavelengths from 190 nm to 230 nm, where spectral structures of the [Formula: see text] transition of NH3 in the umbrella bending mode, v2, were recognized. The absorption cross-section was found to decrease at higher temperatures. For example, the absorption cross-section peak of the (6, 0) vibrational band of NH3 decreases from ∼2 × 10−17 to ∼0.5 × 10−17 cm2/molecule with the increase of temperature from 295 K to 1570 K. Using the obtained absorption cross-section, in situ nonintrusive quantification of NH3 in different hot gas environments was achieved with a detection limit varying from below 10 parts per million (ppm) to around 200 ppm as temperature increased from 295 K to 1570 K. The quantitative measurement was applied to an experimental investigation of NH3 combustion process. The concentrations of NH3 and nitric oxide (NO) in the post flame zone of NH3–methane (CH4)–air premixed flames at different equivalence ratios were measured.


Author(s):  
Brion Jean ◽  
A. Chakir ◽  
B. Coquart ◽  
D. Daumont ◽  
A. Jenouvrier ◽  
...  

1994 ◽  
Author(s):  
D. Malmasson ◽  
A. Vient ◽  
J. L. Lemaire ◽  
A. Le Floch ◽  
F. Rostas

1977 ◽  
Vol 50 (1) ◽  
pp. 101-106 ◽  
Author(s):  
P.H. Wine ◽  
A.R. Ravishankara ◽  
D.L. Philen ◽  
D.D. Davis ◽  
R.T. Watson

2005 ◽  
Vol 7 (1) ◽  
pp. 79 ◽  
Author(s):  
Francis D. Pope ◽  
Carina A. Smith ◽  
Michael N. R. Ashfold ◽  
Andrew J. Orr-Ewing

2016 ◽  
Vol 9 (6) ◽  
pp. 2593-2601 ◽  
Author(s):  
Jeremy J. Harrison

Abstract. The most widely used hydrochlorofluorocarbon (HCFC) commercially since the 1930s has been chloro-difluoromethane, or HCFC-22, which has the undesirable effect of depleting stratospheric ozone. As this molecule is currently being phased out under the Montreal Protocol, monitoring its concentration profiles using infrared sounders crucially requires accurate laboratory spectroscopic data. This work describes new high-resolution infrared absorption cross sections of chlorodifluoromethane over the spectral range 730–1380 cm−1, determined from spectra recorded using a high-resolution Fourier transform spectrometer (Bruker IFS 125HR) and a 26 cm pathlength cell. Spectra of chlorodifluoromethane/dry synthetic air mixtures were recorded at resolutions between 0.01 and 0.03 cm−1 (calculated as 0.9/MOPD; MOPD denotes the maximum optical path difference) over a range of temperatures and pressures (7.5–762 Torr and 191–295 K) appropriate for atmospheric conditions. This new cross-section dataset improves upon the one currently available in the HITRAN (HIgh-resolution TRANsmission) and GEISA (Gestion et Etude des Informations Spectroscopiques Atmosphériques) databases; in particular it provides coverage over a wider range of pressures and temperatures, has more accurate wavenumber scales, more consistent integrated band intensities, improved signal-to-noise, is free of channel fringing, and additionally covers the ν2 and ν7 bands.


1997 ◽  
Vol 51 (9) ◽  
pp. 1311-1315 ◽  
Author(s):  
J. Vattulainen ◽  
L. Wallenius ◽  
J. Stenberg ◽  
R. Hernberg ◽  
V. Linna

A heated and pressurized quartz cell with 150.5-mm pathlength was used to experimentally determine UV absorption spectra and further absorption cross sections of SO2, C2H2, and O2 in the wavelength range between 200 and 400 nm. Spectra were recorded at room temperature, and at 600 and 800 °C and at absolute pressures between 1 and 6 bar. A 30-W deuterium lamp was used as a light source, and the light was detected with a photomultiplier tube through a 0.4-m Czerny–Turner monochromator. Slit widths of the monochromator were adjusted to achieve a 5 Å measurement bandwidth, and the scan through the wavelength range was made in 5 Å steps. For each individual temperature and pressure level, a reference spectrum was first recorded with the cell filled with nitrogen. After this, the cell was filled with the selected species mixed with nitrogen, and the absorption spectra were recorded in similar conditions. The studied gas mixtures were calibrated to 3% accuracy.


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