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Explosions temperature of explosion

Theoretical explosion temperature of explosive mixtures can be calculated in the same manner as flame temperature except for the following ... [Pg.39]

Influence Factors and Ways of Explosion Temperature of Explosives... [Pg.133]

Liquid and Solid Acetylene. Both the Hquid and the soHd have the properties of a high explosive when initiated by detonators or by detonation of adjoining gaseous acetylene (85). At temperatures near the freezing point neither form is easily made to explode by heat, impact, or friction, but initiation becomes easier as the temperature of the Hquid is raised. Violent explosions result from exposure to mild thermal sources at temperatures approaching room temperature. [Pg.377]

Diketene is a flammable Hquid with a flash point of 33°C and an autoignition temperature of 275°C. It decomposes rapidly above 98°C with slow decomposition occurring even at RT. The vapors are denser than air (relative density 2.9, air air = 1). The explosive limits in air are 2—11.7 vol % (135). In case of fire, water mist, light and stabilized foam, as well as powder of the potassium or ammonium sulfate-type should be used. Do not use basic extinguisher powders and do not add water to a closed container. [Pg.480]

The purification of Hquid nitro alcohols by distillation should be avoided because violent decompositions and detonation have occurred when distillation was attempted. However, if the distillation of a nitro alcohol cannot be avoided, the utmost caution should be exercised. Reduced pressure should be utilised, ie, ca 0.1 kPa (<1 mm Hg). The temperature of the Hquid should not exceed 100°C hot water should be used as the heating bath. A suitable explosion-proof shield should be placed in front of the apparatus. At any rise in pressure, the distillation should be stopped immediately. The only commercially produced Hquid nitro alcohol, 2-nitro-1-butanol, is not distilled because of the danger of decomposition. Instead, it is isolated as a residue after the low boiling impurities have been removed by vacuum treatment at a relatively low temperature. [Pg.61]

Propylene is a colorless gas under normal conditions, has anesthetic properties at high concentrations, and can cause asphyxiation. It does not irritate the eyes and its odor is characteristic of olefins. Propjiene is a flammable gas under normal atmospheric conditions. Vapor-cloud formation from Hquid or vapor leaks is the main ha2ard that can lead to explosion. The autoignition temperature is 731 K in air and 696 K in oxygen (80). Evaporation of Hquid propylene can cause skin bums. Propylene also reacts vigorously with oxidising materials. Under unusual conditions, eg, 96.8 MPa (995 atm) and 600 K, it explodes. It reacts violentiy with NO2, N2O4, and N2O (81). Explosions have been reported when Hquid propylene contacts water at 315—348 K (82). Table 8 shows the ratio TJTp where is the initial water temperature, and T is the superheat limit temperature of the hydrocarbon. [Pg.128]

At room temperature, Htde reaction occurs between carbon dioxide and sodium, but burning sodium reacts vigorously. Under controUed conditions, sodium formate or oxalate may be obtained (8,16). On impact, sodium is reported to react explosively with soHd carbon dioxide. In addition to the carbide-forrning reaction, carbon monoxide reacts with sodium at 250—340°C to yield sodium carbonyl, (NaCO) (39,40). Above 1100°C, the temperature of the DeviHe process, carbon monoxide and sodium do not react. Sodium reacts with nitrous oxide to form sodium oxide and bums in nitric oxide to form a mixture of nitrite and hyponitrite. At low temperature, Hquid nitrogen pentoxide reacts with sodium to produce nitrogen dioxide and sodium nitrate. [Pg.163]

The explosion-proof enclosure is designed such that an explosion in the interior of the enclosure containing the electronic circuits will be contained. The enclosure will not allow sufficient flame to escape to the exterior to cause an ignition. Also, a surface temperature rating is given to the device. This rating must indicate a lower surface temperature than the ignition temperature of the gas in the hazardous area. [Pg.786]

Various types of rapid, adiabatic compressions have caused explosions. With propane at an initial temperature of 25°C, To = 432°K (I59°C) for compression and specific heat ratios of 25 and I.I3, respectively. Assume that now air enters a compressor to bring propane into the flammable range at 5 percent by volume. The mixture then will be mostly air with k = 1.47. The same compression ratio of 25 will elevate the final temperature T2 to 834°K (56I°C), i.e., above the published autoignition temperature of 450°C for propane and perhaps high enough to cause an explosion. [Pg.2317]

Hot feed Provide and maintain an automated inerting (increases system—oxygen concentration or pressure fire/explosion risk controlled with flammable. Eliminate leakage sources (ftimes/air) solvents). Use alternative solvents (nonflammable or less flammable) Reduce feed temperature and/or monitor temperature of feed and interlock with feed shutdown NFPA 69... [Pg.65]

The lower explosive limit (LEL) is the minimum concentration of a vapor in air that will support a flame when ignited. The flash point is the lowest temperature of a liquid that produces sufficient vapor for an open flame to ignite in air. [Pg.273]

Explosives which ignite or decompose when subjected to a temperature of 75°C for 48 hours. [Pg.478]

The cure reaction of structural acrylic adhesives can be started by any of a great number of redox reactions. One commonly used redox couple is the reaction of benzoyl peroxide (BPO) with tertiary aromatic amines. Pure BPO is hazardous when dry [39]. It is susceptible to explosion from shock, friction or heat, and has an autoignition temperature of 79°C. Water is a very effective stabilizer for BPO, and so the initiator is often available as a paste or a moist solid [40], The... [Pg.832]

The next simplest ether is the ether with the simplest alkane as one of the hydrocarbon backbones and the next alkane, which is methyl ethyl ether. Its molecular formula is CH3OC2H5. It is a colorless gas with the characteristic ether odor. It has a flash point of 31 °F, and an ignition temperature of only 374°F. This property, of course, makes it an extreme fire and explosion hazard. [Pg.200]

Temperature of no-return Temperature of a system at which the rate of heat generation of a reactant or decomposition slightly exceeds the rate of heat loss and possibly results in a runaway reaction or thermal explosion. [Pg.1017]

Shock-synthesis experiments were carried out over a range of peak shock pressures and a range of mean-bulk temperatures. The shock conditions are summarized in Fig. 8.1, in which a marker is indicated at each pressure-temperature pair at which an experiment has been conducted with the Sandia shock-recovery system. In each case the driving explosive is indicated, as the initial incident pressure depends upon explosive. It should be observed that pressures were varied from 7.5 to 27 GPa with the use of different fixtures and different driving explosives. Mean-bulk temperatures were varied from 50 to 700 °C with the use of powder compact densities of from 35% to 65% of solid density. In furnace-synthesis experiments, reaction is incipient at about 550 °C. The melt temperatures of zinc oxide and hematite are >1800 and 1.565 °C, respectively. Under high pressure conditions, it is expected that the melt temperatures will substantially Increase. Thus, the shock conditions are not expected to result in reactant melting phenomena, but overlap the furnace synthesis conditions. [Pg.181]

The surface temperature of explosion-proof enclosures cannot exceed that of high-temperature devices, Equipment can be tested by nationally recognized testing laboratories and given one of 14 T ratings, as indicated in Table 17-2. This equipment may exceed the 80 percent rule."... [Pg.521]

Originally the classification of materials was derived from tests of proprietary explosion-proof (flameproof) enclosures. There were no published criteria. Equipment was approved relative to the lowest ignition temperature of any material in the group (Magison 1987). In about 1965 the U.S. Coast Guard asked the National Academy of Sciences (NAS) to form a panel to classify 200 materials of commerce. The Electrical Hazards Panel of the Committee on Hazardous Materials was formed by the NAS. The Panel studied many ways to estimate the hazard classification of materials. The Panel finally reported to die U.S. Coast Guard in 1970 that no workable, predicdve scheme could be defined, and it then proceeded to assign tentative classifications to the 200 materials. [Pg.99]

Use of Figure 9.2 requires that the temperature of the liquid be compared to its boiling point and its superheat-limit temperature. Table 6.1 provides these temperatures T), = 231 K, and 7, = 326 K. It is obvious that the liquid s temperature can easily rise above the superheat limit temperature when the vessel is exposed to a lire. Therefore, the explosively flashing-liquid method must be selected. This method is described schematically in Figure 9.5 (equal to Figure 6.29), and described in Section 6.3.3.3. [Pg.298]

The calculation method can be selected by application of the decision tree in Figure 9.2. The liquid temperature is believed to be about 339 K, which is the temperature equivalent to the relief valve set pressure. The superheat limit temperatures of propane and butane, the constituents of LPG, can be found in Table 6.1. For propane, T, = 326 K, and for butane, T i = 377 K. The figure specifies that, if the liquid is above its critical superheat limit temperature, the explosively flashing liquid method must be chosen. However, because the temperature of the LPG is below the superheat limit temperature (T i) for butane and above it for propane, it is uncertain whether the liquid will flash. Therefore, the calculation will first be performed with the inclusion of vapor energy only, then with the combined energy of vapor and liquid. [Pg.308]

Superheat limit temperature The temperature of a liquid above which flash vaporization can proceed explosively. [Pg.399]


See other pages where Explosions temperature of explosion is mentioned: [Pg.442]    [Pg.384]    [Pg.442]    [Pg.320]    [Pg.127]    [Pg.127]    [Pg.45]    [Pg.598]    [Pg.279]    [Pg.35]    [Pg.187]    [Pg.151]    [Pg.64]    [Pg.369]    [Pg.286]    [Pg.508]    [Pg.461]    [Pg.27]    [Pg.459]    [Pg.515]    [Pg.39]    [Pg.179]    [Pg.84]    [Pg.135]    [Pg.200]    [Pg.431]    [Pg.193]    [Pg.521]    [Pg.207]    [Pg.295]    [Pg.347]    [Pg.364]    [Pg.18]    [Pg.52]    [Pg.199]    [Pg.6]    [Pg.428]    [Pg.639]   


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