Carbon explosive

C2H3N. Colourless liquid with strong ammoniacal smell b.p. 56 C. Miscible with water and strongly basic. Prepared commercially from 2-aminoelhanol. Pure dry aziridine is comparatively stable but it polymerizes explosively in the presence of traces of water. Carbon dioxide is sufficiently acidic to promote polymerization. 

Explosives based on liquid oxygen and a fuel, generally carbon black. 

Certain types of equipment are specifically excluded from the scope of the directive. It is self-evident that equipment which is already regulated at Union level with respect to the pressure risk by other directives had to be excluded. That is the case with simple pressure vessels, transportable pressure equipment, aerosols and motor vehicles. Other equipment, such as carbonated drink containers or radiators and piping for hot water systems are excluded from the scope because of the limited risk involved. Also excluded are products which are subject to a minor pressure risk which are covered by the directives on machinery, lifts, low voltage, medical devices, gas appliances and on explosive atmospheres. A further and last group of exclusions refers to equipment which presents a significant pressure risk, but for which neither the free circulation aspect nor the safety aspect necessitated their inclusion. 

Halogen derivatives of silanes can be obtained but direct halogena-tion often occurs with explosive violence the halogen derivatives are usually prepared by reacting the silane at low temperature with a carbon compound such as tetrachloromethane, in the presence of the corresponding aluminium halide which acts as a catalyst. 

Carbon disulphide is a volatile, evil-smelling liquid, although if carefully purified, the unpleasant smell is removed, as it is due to impurity. The vapour is inflammable and can form explosive mixtures in air ... 

The solid readily dissolves chemically in concentrated hydrochloric acid, forming a complex, and in ammonia as the colourless, linear, complex cation [H3N -> Cu <- NHj] (cf AgCl) if air is absent (in the presence of air, this is oxidis to a blue ammino-copper(II) complex). This solution of ammoniacal copper(I) chloride is a good solvent or carbon monoxide, forming an addition compound CuCl. CO. H2O, and as such is used in gas analysis. On passing ethyne through the ammoniacal solution, a red-brown precipitate of hydrated copper(I) dicarbide (explosive when dry) is obtained ... 

Carbon disulphide should never be used if any alternative solvent is available, as it has a dangerously low flash-point, and its vapours form exceedingly explosive mixtures with air. Ether as a solvent for recrystallisation is much safer than carbon disulphide, but again should be avoided whenever possible, partly on account of the danger of fires, and partly because the filtered solution tends to creep up the walls of the containing vessel and there deposit solid matter by complete evaporation instead of preferential crystallisation. 

Chloroform and carbon tetrachloride must not be heated with metallic sodium as an explosive reaction is likely to take place (see footnote, p. 321). 

The chief danger and main source of error in a combustion is that of moving the Bunsen forward a little too rapidly and so causing much of the substance to burn very rapidly, so that a flash-back occurs. This usually causes an explosion wave to travel back along the tube towards the purification train, some carbon dioxide and water vapour being carried with it. If these reach the packing of the purification train they will, of course, be absorbed there and the results of the estimation will necessarily be low. 

The second indication is a faint smoke-like cloudiness in the zone of the tube which is being heated by the Bunsen this is readily visible as the interior of the tube is normally quite clear and bright. This is a later stage of development of the flash-back than the rise of pressure, already mentioned, and should be counteracted by moving the Bunsen immediately to the point of the combustion tube where heating was commenced. In either case the Bunsen should then be moved slowly forwards as before. A flash-back is attended by the deposition of carbon particles, carried back by the explosion wave, on the cold walls of the tube. Care should be taken that these are completely burnt off as the Bunsen is slowly moved forward again. 

Carbon tetrachloride must not be dried with sodium as an explosion may result. Fire extinguishers containing this solvent (e.g., Pyrene ) cannot therefore be applied to a fire originating from sodium. 

CARBON - DIAMOND,NATURAL] (Vol 4) pXPLOSIVES AND PROPELLANTS - EXPLOSIVES] (Vol 10)... 

Flash points and autoignition temperatures are given in Table 11. The vapor can travel along the ground to an ignition source. In the event of fire, foam, carbon dioxide, and dry chemical are preferred extinguishers. The lower and upper explosion limits are 1% and 7%. 

Acrylonitrile is combustible and ignites readily, producing toxic combustion products such as hydrogen cyanide, nitrogen oxides, and carbon monoxide. It forms explosive mixtures with air and must be handled in weU-ventilated areas and kept away from any source of ignition, since the vapor can spread to distant ignition sources and flash back. 

The removal of volatile organic compounds (VOC) from air is most often accompHshed by TSA. Air streams needing treatment can be found in most chemical and manufacturing plants, especially those using solvents. At concentrations from 500 to 15,000 ppm, recovery of the VOC from steam used to regenerate activated carbon adsorbent thermally is economically justified. Concentrations above 15,000 ppm ate typically in the explosive range and... 

Pentaerythritol may be nitrated by a batch process at 15.25°C using concentrated nitric acid in a stainless steel vessel equipped with an agitator and cooling coils to keep the reaction temperature at 15—25°C. The PETN is precipitated in a jacketed diluter by adding sufficient water to the solution to reduce the acid concentration to about 30%. The crystals are vacuum filtered and washed with water followed by washes with water containing a small amount of sodium carbonate and then cold water. The water-wet PETN is dissolved in acetone containing a small amount of sodium carbonate at 50°C and reprecipitated with water the yield is about 95%. Impurities include pentaerythritol trinitrate, dipentaerythritol hexanitrate, and tripentaerythritol acetonitrate. Pentaerythritol tetranitrate is shipped wet in water—alcohol in packing similar to that used for primary explosives. 

This reaction has often reached explosive proportions in the laboratory. Several methods were devised for controlling it between 1940 and 1965. For fluorination of hydrocarbons of low (1—6 carbon atoms) molecular weight at room temperature or below by these methods, yields as high as 80% of perfluorinated products were reported together with partially fluorinated species (9—11). However, fluorination reactions in that eta involving elemental fluorine with complex hydrocarbons at elevated temperatures led to appreciable cleavage of the carbon—carbon bonds and the yields invariably were only a few percent. 

Tetrafluoroethylene undergoes addition reactions typical of an olefin. It bums in air to form carbon tetrafluoride, carbonyl fluoride, and carbon dioxide (24). Under controlled conditions, oxygenation produces an epoxide (25) or an explosive polymeric peroxide (24). Trifluorovinyl ethers,... 

In the absence of air, TEE disproportionates violently to give carbon and carbon tetrafluoride the same amount of energy is generated as in black powder explosions. This type of decomposition is initiated thermally and equipment hot spots must be avoided. The flammability limits of TEE are 14—43% it bums when mixed with air and forms explosive mixtures with air and oxygen. It can be stored in steel cylinders under controlled conditions inhibited with a suitable stabilizer. The oxygen content of the vapor phase should not exceed 10 ppm. Although TEE is nontoxic, it may be contaminated by highly toxic fluorocarbon compounds. 

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