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Weak ignition

The results in Tables 4. la and 4. lb demonstrate that in the absence of obstacles, the highest flame speed observed was 84 m/s, and it was accompanied by an overpressure of 60 mbar for hydrogen-air in a 10-m radius balloon (Schneider and Pfortner 1981). For all other fuels, flame speeds were below 40 m/s and corresponding overpressures were below 35 mbar. Hence, weak ignition of an unconfined... [Pg.74]

Figure 8.4.5 presents the streak, direct photograph illustrating the stages of transition to detonation after a weak ignition and flame acceleration phase. Four main regions may be identified ... [Pg.199]

H.Wells, "Coal, Coke and Coal Chemicals," McGraw-Hill, NY (1950) 4)Kirk St Othmer 6, (1951), 899 (Coke as a fuel) 5)H.Gesner St H.R.Zbinden, SchweizVerGas - und Wasser-fachMonatsBull 32, 45-52 (1952) St CA 47, 7196 (1953) (Tests with coke dusts have shown that it is practically impossible to ignite their mixts with air. A weak ignition was observed only once in 15 tests) 6)W.Gluud, "Handbuch der ICokerei, K.Knapp, Diisseldorf (1953) 7)0. [Pg.175]

When long induction periods are necessary, weak ignition sources can initiate the explosion, such as light, wall effects, tar deposits, catalyst deposits on the wall, NC13 decomposition flame (refs. 5,9). [Pg.436]

The explosion of an unconfined hydrogen gas doud in the presence of a weak ignition source was never observed to have turned into a detonation [45]. The ignition energy required for a direct detonation can only be provided by either an intensive turbulent hot gas jet or by an explosive. For a stoichiometric mixture, the minimum energy was experimentally determined to be 4.7 kJ ( 1 g TNT). A methane-air mixture even requires... [Pg.215]

For special purposes (e.g., highchemcialresistance), materials of Group 1 can be lined with substances which by tiiemselves are not suitable for ceramic manufacture (for example, MgO, CaO). For example, according to Goehrens [3], one can apply to the vessel a paste made of a mixture of finely ground, weakly ignited and... [Pg.12]

Formula weight 277.52. Yellow material the lower the ignition temperature, the more soluble in water hygroscopic when weakly ignited, nonhygroscopic when strongly ignited. M.p. about 2000°C d 7.04. C sesquioxide structure type. [Pg.863]

Procedure. Alloys rich in tin. A few fine filings are treated in a micro crucible with several drops of nitric acid, evaporated, and then weakly ignited. The cold residue is treated with 1 drop buffer solution and 1 drop sodium rhodizonate. Red lead rhodizonate appears. [Pg.565]

The experiments [26] conducted for various combustion regimes of H2 + N2 + O2 mixtures in water-mechanical foams at water concentration of 10 kg/m have shown that even weak ignition of 2H2 + O2 contained in the foam cells initiates blast propagation with a 2,500 m/s velocity and a front pressure of 1.0-1.5 MPa. When the mixture is diluted to 2H2 + O2 + N2, the explosive front velocity reduces to 800-500 m/s. The velocity reduction has been recorded with the same mixture composition but with reduced the bubble size, i.e. with an increase of the heat transfer surface. [Pg.110]

Indirect initiation by a weak ignition, flame acceleration and DDT. [Pg.114]

Processes resulting from combustion initiated by a weak igniter contain complicated interactions between turbulent flows and chemical reactions. Simulation of such processes requires detailed calculations of non-stationary turbulent compressible reactive flows in three-dimensional space. [Pg.115]


See other pages where Weak ignition is mentioned: [Pg.2316]    [Pg.546]    [Pg.2071]    [Pg.175]    [Pg.341]    [Pg.216]    [Pg.319]    [Pg.2320]    [Pg.341]    [Pg.116]    [Pg.116]    [Pg.117]    [Pg.118]   
See also in sourсe #XX -- [ Pg.110 , Pg.114 ]




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