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Trinitrotoluene (/ ˌ t r aɪ ˌ n aɪ t r oʊ ˈ t ɒ lj u iː n /), [5] [6] more commonly known as TNT (and more specifically 2,4,6-trinitrotoluene, and by its preferred IUPAC name 2-methyl-1,3,5-trinitrobenzene), [1] is a chemical compound with the formula C 6 H 2 (NO 2) 3 CH 3. TNT is occasionally used as a reagent in chemical synthesis ...
2,4,6-Trinitrobenzoic acid is prepared by oxidation of 2,4,6-trinitrotoluene (TNT). It is formed by oxidation of TNT and nitric acid with chlorate [2] and with dichromate. [3] Upon heating, 2,4,6-trinitrobenzoic acid undergoes decarboxylation to give 1,3,5-trinitrobenzene. [4]
TNT is added to create T-ammonal which improves properties such as brisance. The mixture is often referred to as Tannerite, which is a brand of ammonal. The ammonium nitrate functions as an oxidizer and the aluminium as fuel. The use of the relatively cheap ammonium nitrate and aluminium makes it a replacement for pure TNT.
Log–log plot comparing the yield (in kilotonnes) and mass (in kilograms) of various nuclear weapons developed by the United States.. The explosive yield of a nuclear weapon is the amount of energy released such as blast, thermal, and nuclear radiation, when that particular nuclear weapon is detonated, usually expressed as a TNT equivalent (the standardized equivalent mass of trinitrotoluene ...
A molecule is said to have a positive oxygen balance if it contains more oxygen than is needed and a negative oxygen balance if it contains less oxygen than is needed. [2] An explosive with a negative oxygen balance will lead to incomplete combustion, which commonly produces carbon monoxide, which is a toxic gas. Explosives with negative or ...
Six positional isomers are possible for dinitrotoluene. The most common one is 2,4-dinitrotoluene. The nitration of toluene gives sequentially mononitrotoluene, DNT, and finally TNT. 2,4-DNT is the principal product from dinitration, the other main product being about 30% 1,3-DN2-T.
Hexanitrostilbene (HNS), also called JD-X, is an organic compound with the formula [(O 2 N) 3 C 6 H 2 CH] 2. It is a yellow-orange solid. [1] It is used as a heat-resistant high explosive. It is slightly soluble (0.1 - 5 g/100 mL) in butyrolactone, DMF, DMSO, and N-methylpyrrolidone.
Dunnite can be used as a precursor to the highly stable explosive TATB (1,3,5-triamino-2,4,6-trinitrobenzene), by first dehydrating it to form picramide (attaching the ammonia as an amine group instead of an ion) and then further aminating it, using 1,1,1-trimethylhydrazinium iodide (TMHI) made from unsymmetrical dimethylhydrazine rocket fuel ...
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