The Effect of Time of Exposure to Elevated Temperatures on the Flammability Limits of Some Common Gaseous Fuels in Air

1999 ◽  
Vol 121 (1) ◽  
pp. 74-79 ◽  
Author(s):  
I. Wierzba ◽  
B. B. Ale

The flammability limits of methane, ethylene, propane, and hydrogen were experimentally determined at elevated initial mixture temperatures up to 350°C at atmospheric pressure for upward flame propagation in a steel test tube apparatus. The existence of preignition reactions at these levels of temperatures that may influence the value of the flammability limits was also investigated. The fuel-air mixtures were exposed to elevated temperatures over different periods of time before spark ignition (up to 2 h). It was shown that the flammability limits for methane widened approximately linearly with an increase in the initial mixture temperature over the entire range of temperatures tested and were not affected by the length of the exposure time to these temperatures before spark ignition. However, different behaviour was observed for the flammability limits of the other tested fuels—ethylene, propane, and hydrogen. At higher temperatures the flammability limits narrowed and were very significantly affected by the exposure time. The longer was the exposure time of fuel-air mixtures to the elevated temperatures, the narrower were their flammability limits.

Author(s):  
B. B. Ale ◽  
L. Wierzba

The flammability limits of methane, ethylene, propane and hydrogen were determined experimentally at elevated initial mixture temperatures up to 350°C at atmospheric pressure for upward flame propagation in a steel test tube apparatus. The existence of preignition reactions at these levels of temperatures that may influence the value of the flammability limits was also investigated. The fuel-air mixtures were exposed to elevated temperatures over different periods of time before spark ignition (up to 2 hours). It was shown that the flammability limits for methane widened approximately linearly with an increase in the initial mixture temperature over the entire range of temperatures tested and were not affected by the length of the exposure time to these temperatures before spark ignition. However, different behaviour was observed for the flammability limits of the other tested fuels — ethylene, propane and hydrogen. At higher temperatures the flammability limits narrowed and were very significantly affected by the exposure time. The longer was the exposure time of fuel-air mixtures to the elevated temperatures, the narrower were their flammability limits.


Author(s):  
B. B. Ale ◽  
I. Wierzba

The flammability limits of hydrogen and methane in air were determined experimentally at elevated initial mixture temperatures up to 350°C at atmospheric pressure for upward flame propagation in a conventional steel test tube apparatus. Additionally the extent to which a prolonged exposure (i.e., residence time) of the mixture to elevated temperatures before spark ignition and, consequently, the existence of pre-ignition reactions that may influence the value of the lean and rich flammability limits was also investigated. It was shown that the flammability limits for methane widened approximately linearly with an increase in the initial mixture temperature over the whole range of temperatures tested. These limits were not affected by the length of the residence time before spark ignition. Different behaviour was observed for flammability limits of hydrogen. They were also widened with an increase in the initial temperature but only up to 200°C. In this initial temperature range the limits were not affected by the length of the residence time. However, at initial temperature exceeding 200°C the flammability limits, especially, the rich limits narrowed with an increase in the temperature and were significantly affected by the residence time before spark ignition. The results of detailed chemical kinetic simulation showed that the gas phase reactions of hydrogen oxidation could not be responsible for the substantial drop in the value of the rich limit. It was therefore, suggested that this drop in the value of the rich limit with the increase in the residence time was caused by the relatively low temperature catalytic reactions on the stainless steel surface of the flame tube. Simple method for calculating the hydrogen conversion to water was proposed. The results of calculations are in fair agreement with the experimental evidence.


2003 ◽  
Vol 125 (2) ◽  
pp. 500-504 ◽  
Author(s):  
A. A. Attar ◽  
G. A. Karim

The knock tendency in spark ignition engines of binary mixtures of hydrogen, ethane, propane and n-butane is examined in a CFR engine for a range of mixture composition, compression ratio, spark timing, and equivalence ratio. It is shown that changes in the knock characteristics of binary mixtures of hydrogen with methane are sufficiently different from those of the binary mixtures of the other gaseous fuels with methane that renders the use of the methane number of limited utility. However, binary mixtures of n-butane with methane may offer a better alternative. Small changes in the concentration of butane produce almost linearly significant changes in both the values of the knock limited compression ratio for fixed spark timing and the knock limited spark timing for a fixed compression ratio.


1996 ◽  
Vol 118 (2) ◽  
pp. 159-163 ◽  
Author(s):  
O. A. Badr ◽  
N. Elsayed ◽  
G. A. Karim

Examination is made of the operational limits in two variable compression-ratio single-cylinder engines when operating on the gaseous fuels methane, propane, LPG, and hydrogen under a wide range of conditions. Two definitions for the limits were employed. The first was associated with the first detectable misfire on leaning the mixture, while the second was the first detectable firing under motoring condition in the presence of a spark when the mixture was being enriched slowly. Attempts were also made to relate these limits to the corresponding values for quiescent conditions reckoned on the basis of the flammability limits evaluated at the mean temperature and pressure prevailing within the cylinder charge at the time of the spark. The measured limits in the engine were always higher than the corresponding flammability limit values for the three fuels. Both of these limits appear to correlate reasonably well with the calculated mean temperature of the mixture at the time of passing the spark.


1994 ◽  
Vol 116 (3) ◽  
pp. 181-185 ◽  
Author(s):  
I. Wierzba ◽  
S. O. Bade Shrestha ◽  
G. A. Karim

A procedure is described for calculating the lean flammability limits of fuel-diluent mixtures in air over a wide range of fuel-diluent combinations and for different initial mixture temperatures. Good agreement is shown to exist between the predicted values of the limits with the corresponding experimental values for some common gaseous fuels that include CH4, C2H6, C2H4, C3H8, C4H10, H2, and CO and the diluents CO2, N2, He, and Ar over the temperature range of −60°C up to 400°C.


2008 ◽  
Vol 59 (1) ◽  
pp. 45-48
Author(s):  
Oana Ciocirlan ◽  
Olga Iulian

This paper reports the viscosities measurements for the binary system dimethyl sulfoxide + 1,4-dimethylbenzene over the entire range of mole fraction at 298.15, 303.15, 313.15 and 323.15 K and atmospheric pressure. The experimental viscosities were correlated with the equations of Grunberg-Nissan, Katti-Chaudhri, Hind, Soliman and McAllister; the adjustable binary parameters have been obtained. The excess Gibbs energy of activation of viscous flow (G*E) has been calculated from the experimental measurements and the results were fitted to Redlich-Kister polynomial equation. The obtained negative excess Gibbs free energy of activation and negative Grunberg-Nissan interaction parameter are discussed in structural and interactional terms.


Author(s):  
Seung Wan Hong ◽  
Tae Won Kim ◽  
Jae Hun Kim

Abstract Physicians and nurses stand with their back towards the C-arm fluoroscope when using the computer, taking things out of closets and preparing drugs for injection or instruments for intervention. This study was conducted to investigate the relationship between the type of lead apron and radiation exposure to the backs of physicians and nurses while using C-arm fluoroscopy. We compared radiation exposure to the back in the three groups: no lead apron (group C), front coverage type (group F) and wrap-around type (group W). The other wrap-around type apron was put on the bed instead of on a patient. We ran C-arm fluoroscopy 40 times for each measurement. We collected the air kerma (AK), exposure time (ET) and effective dose (ED) of the bedside table, upper part and lower part of apron. We measured these variables 30 times for each location. In group F, ED of the upper part was the highest (p < 0.001). ED of the lower part in group C and F was higher than that in group W (p = 0.012). The radiation exposure with a front coverage type apron is higher than that of the wrap-around type and even no apron at the neck or thyroid. For reducing radiation exposure to the back of physician or nurse, the wrap-around type apron is recommended. This type of apron can reduce radiation to the back when the physician turns away from the patient or C-arm fluoroscopy.


2008 ◽  
Vol 580-582 ◽  
pp. 319-322 ◽  
Author(s):  
Manabu Tanaka ◽  
Kentaro Yamamoto ◽  
Tashiro Shinichi ◽  
John J. Lowke

Study of current attachment at thermionic cathode for TIG arc at atmospheric pressure is attempted from numerical calculations of arc-electrodes unified model. The calculations show that the maximum temperature of arc plasma close to the cathode tip for W-2% ThO2 reaches 19,000 K and it is the highest value in comparison with the other temperatures for W-2% La2O3 and W-2% CeO2, because the current attachment at the cathode tip is constricted by a centralized limitation of liquid area of ThO2 due to its higher melting point. The calculations also show that, in cases of W- 2% La2O3 and W-2% CeO2, the liquid areas of La2O3 and Ce2O3 are widely expanded at the cathode tip due to their lower melting points and then produce uniform current attachments at the cathode. It is concluded that the current attachment at thermionic cathode is strongly dependent on work function, melting point and Richardson constant of emitter materials.


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