A Method for the Determination of Carbon Monoxide, Carbon Dioxide, Nitrous Oxide and Sulphur Dioxide in Air by Gas Chromatography Using an Emissive Helium Plasma Detector

1973 ◽  
Vol 6 (2) ◽  
pp. 87-95 ◽  
Author(s):  
R. M. Dagnall ◽  
D. J. Johnson ◽  
T. S. West
Author(s):  
G.P. Morie ◽  
C.H. Sloan

AbstractA gas chromatographic method for the determination of carbon monoxide and carbon dioxide in cigarette smoke was developed. A column containing Porapak Q packing and a cryogenic temperature programmer which employed liquid nitrogen to cool the column to subambient temperatures was used. The separation of N


Author(s):  
Gyula Nyerges ◽  
Dénes Szieberth ◽  
Judit Mátyási ◽  
József Balla

Gas chromatography (GC) is a frequently used analytical method for the determination of permanent and organic air components. The analysis usually needs two different columns in practice. The molecular sieve stationary phase can separate oxygen, nitrogen and carbon monoxide, but irreversibly adsorbs carbon dioxide and water. Porapak type columns are applicable for the measurement of carbon dioxide, however oxygen, argon, nitrogen and carbon monoxide are co-eluted. Usually these two types of columns are used in parallel for the determination. Carboxen stationary phase can separate carbon monoxide and carbon dioxide, but argon, oxygen and nitrogen are co-eluted. Thermal conductivity detector (TCD) and flame ionization detector (FID) are used commonly together for the determination of the separated components. TCD is applied for permanent gas analysis whereas FID – combined with a methanizer – is used for the detection of carbon monoxide, carbon dioxide and light hydrocarbons. Mass spectrometer (MS) is also a potential detector, because the properly chosen fragment ions can increase the selectivity.We developed a method for the determination of air components, using only one column and one detector. This method is suitable for the measurements by combining the advantages of the carboxen column with mass spectrometry. The validation parameters of the method were in the acceptable interval, so this method is able to determine the air components. The application of this technique to the analysis of cave air provided valuable information to the exploration of the Molnár János cave system.


2003 ◽  
Vol 989 (2) ◽  
pp. 277-283 ◽  
Author(s):  
Marian Kamiński ◽  
Rafał Kartanowicz ◽  
Daniel Jastrzębski ◽  
Marcin M. Kamiński

1961 ◽  
Vol 41 (2) ◽  
pp. 187-196 ◽  
Author(s):  
J. M. McArthur ◽  
J. E. Miltimore

Methods are described for sampling and analysing rumen gases. The analysis requires less than 15 minutes for the determination of hydrogen, oxygen, nitrogen, methane, carbon monoxide, carbon dioxide, and hydrogen sulphide, i.e., for all gases occurring in the rumen. The method is sensitive and requires only a small quantity of sample, and the sample volume need not be known. The presence of water or other vapours in the sample does not influence the results. Relative thermal detector responses have been determined for gases which occur in the rumen. These eliminate the necessity for the calibration of gas chromatographs using thermal detection. The first complete analysis of rumen gas is presented.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Leonard Nitzsche ◽  
Jens Goldschmidt ◽  
Armin Lambrecht ◽  
Jürgen Wöllenstein

Abstract A dual comb spectrometer is used as gas sensor for the parallel detection of nitrous oxide (N2O) and carbon monoxide (CO). These gases have overlapping absorption features in the mid-infrared (MIR) at a wavelength of 4.6 µm. With a spectra acquisition rate of 10 Hz, concentrations of 50 ppm N2O and 30 ppm CO are monitored with a relative precision of 6 × 10 − 3 6\times {10^{-3}} and 3 × 10 − 3 3\times {10^{-3}} respectively. The limit of detections are 91 ppb for N2O and 50 ppb for CO for an integration time of 25 s. The system exhibits a linear sensitivity from 2 ppm to 100 ppm with coefficients of determination of 0.99998 for N2O and 0.99996 for CO.


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