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Nitromethane is used as a fuel in motor racing, particularly drag racing, as well as for radio-controlled model power boats, cars, planes and helicopters. In this context, nitromethane is commonly referred to as "nitro fuel" or simply "nitro", and is the principal ingredient for fuel used in the "Top Fuel" category of drag racing. [14]
Food products and household items commonly handled by humans can be toxic to dogs. The symptoms can range from simple irritation to digestion issues, behavioral changes, and even death. The categories of common items ingested by dogs include food products, human medication, household detergents, indoor and outdoor toxic plants, and rat poison. [1]
TNM is a pale yellow liquid that can be prepared in the laboratory by the nitration of acetic anhydride with anhydrous nitric acid (Chattaway's method). [8] This method was attempted on an industrial scale in the 1950s by Nitroform Products Company in Newark, USA, but the entire plant was destroyed by an explosion in 1953.
Here are some of the most common plants that are toxic to dogs, according to Dr Wismer: Sago Palm This handsome prehistoric-looking palm is the most dangerous houseplant on the list for dogs ...
Chocolate contains theobromine and caffeine, which can speed the heart rate and stimulate the nervous system of dogs, according to the Merck/Merial Manual for Veterinary Health. Just how sick a ...
Water gel explosives are produced by combining nitroparaffins, usually nitromethane, with an aqueous salt solution and a gelling agent. These nitroparaffins typically make up most of the water gel explosive. Different types of gelling agents are used to create the water gel explosive. One agent is insoluble in water, but able to gel with ...
Methyl nitrate is a sensitive explosive.When ignited it burns extremely fiercely with a gray-blue flame. Methyl nitrate is a very strong explosive with a detonation velocity of 6,300 m/s, [8] like nitroglycerin, ethylene glycol dinitrate, and other nitrate esters.
Nitromethane can be produced in the laboratory by treating sodium chloroacetate with sodium nitrite. [7] Oxidation of oximes [8] or primary amines. [9] Reduction of β-nitro alcohols [10] or nitroalkenes. [11] By decarboxylation of α-nitro carboxylic acids formed from nitriles and ethyl nitrate. [12] [13]