RUMEN GAS ANALYSIS BY GAS-SOLID CHROMATOGRAPHY

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.

2008 ◽  
Vol 53 (No. 4) ◽  
pp. 126-133 ◽  
Author(s):  
A. Jelínek ◽  
M. Dědina ◽  
R. Kraus

The reduction of ammonia and greenhouse gases emissions resulting from the livestock breeding is conditioned by the performance of many experiments for the reducing technologies verification. The utilisation of biotechnological agents in the livestock breeding enables to reduce not only ammonia but in many cases also the principal greenhouse gases. In the paper is presented the system and methodology of the measurements, the choice of more than eighty authorised measurements, and the determination of the emission factors for methane, carbon dioxide, hydrogen sulphide, and nitrogen oxide from pig and poultry breeding.


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.


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


1976 ◽  
Vol 22 (8) ◽  
pp. 1314-1318 ◽  
Author(s):  
L D Bowers ◽  
L M Canning ◽  
C N Sayers ◽  
P W Carr

Abstract We used a differential thermal detector in conjunction with an immobilized urease reactor to determine urea in serum. Samples (120 mul) are introduced into a flow stream and passed through an "adiabatic" column, which is packed with enough insolubilized urease to completely convert urea to ammonia and carbon dioxide. Measured temperature changes are directly proportional to the serum urea concentration. Urea in the presence of protein, bilirubin, and hemoglobin can thus be rapidly, simply, and inexpensively measured. Results correlate well with those obtained by the manual diacetyl monoxime and urease/indophenol methods.


Author(s):  
G J Van Stekelenburg ◽  
C Valk ◽  
M J G Van Wijngaarden-Penterman

For those clinical laboratories equipped with a microprocessor-controlled gas analyser, an extremely simple method is described for the determination of the total carbon dioxide content in various biological fluids. Since this method needs only 20 μL of blood plasma or is less dependent on the original total carbon dioxide content, it is especially suited for paediatric purposes. With our procedure the time necessary for one determination equals the time for one capillary blood gas analysis.


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