Phosphine oxide combustion

If RX is methyl iodide, bromide, or chloride, it may cool the flame and, consequently, reduce combustion. Further, the phosphine can be oxidized readily to the phosphine oxide. The latter reaction may lead to self-extinguishing properties either by absorption of energy to complete the reaction and/or more likely by formation of the polyphosphates and the subsequent shielding of the polymer by this thermally stable glass (19). 

MERCURIC NITRATE (10045-94-0) A powerful oxidizer. Violent reaction with reducing agents, combustibles, phosphinic acid, hypophosphoric acid, petroleum hydrocarbons. Forms heat- and/or shock-sensitive compounds with acetylene (forms mercury acetylide), ethanol (forms mercury fulminate), ferrocene, isobutene, phosphine, potassium cyanide, sulfur. Incompatible with strong acids, acetic anhydride, ammonia, ammonium hexacyanofer-rate(II), organic azides, citric acid, hydrazinium perchlorate, isopropyl chlorocarbonate, nitrosyl perchlorate, sodium thiosulfate, sulfamic acid, thiocyanates, hydrozoic acid, methyl isocyanoacetate, sodium peroxyborate, trinitrobenzoic acid, urea nitrate. Aqueous solution corrodes metals. 

Purification by vacuum distillation (102—103 °C, 13 Torr). Handling, Storage, and Precautions the pure material is pyrophoric and must be handled under an oxygen-free atmosphere to avoid spontaneous combustion. In the absence of oxygen, it is indefinitely stable. Solutions (ca. 10%) of tri-tert-butylphosphine are not pyrophoric, but should be handled under an inert atmosphere in order to avoid oxidation to the phosphine oxide. The HBF4 salt is air-stable. Tri-tert-butylphosphine is corrosive and causes burns on contact with skin. It is incompatible with oxidizing agents. 

All phosphoms oxides are obtained by direct oxidation of phosphoms, but only phosphoms(V) oxide is produced commercially. This is in part because of the stabiUty of phosphoms pentoxide and the tendency for the intermediate oxidation states to undergo disproportionation to mixtures. Besides the oxides mentioned above, other lower oxides of phosphoms can be formed but which are poorly understood. These are commonly termed lower oxides of phosphoms (LOOPs) and are mixtures of usually water-insoluble, yeUow-to-orange, and poorly characteri2ed polymers (58). LOOPs are often formed as a disproportionation by-product in a number of reactions, eg, in combustion of phosphoms with an inadequate air supply, in hydrolysis of a phosphoms trihahde with less than a stoichiometric amount of water, and in various reactions of phosphoms haUdes or phosphonic acid. LOOPs appear to have a backbone of phosphoms atoms having —OH, =0, and —H pendent groups and is often represented by an approximate formula, (P OH). LOOPs may either hydroly2e slowly, be pyrophoric, or pyroly2e rapidly and yield diphosphine-contaminated phosphine. LOOP can also decompose explosively in the presence of moisture and air near 150° C. 

Phosphine combusts spontaneously in contact with nitrogen oxides. 

Chlorine dioxide Copper Fluorine Hydrazine Hydrocarbons (benzene, butane, propane, gasoline, turpentine, etc) Hydrocyanic acid Hydrofluoric acid, anhydrous (hydrogen fluoride) Hydrogen peroxide Ammonia, methane, phosphine or hydrogen sulphide Acetylene, hydrogen peroxide Isolate from everything Hydrogen peroxide, nitric acid, or any other oxidant Fluorine, chlorine, bromine, chromic acid, peroxide Nitric acid, alkalis Ammonia, aqueous or anhydrous Copper, chromium, iron, most metals or their salts, any flammable liquid, combustible materials, aniline, nitromethane... 

White phosphorus has an autoignition temperature only shghtly above ambient, dispersed it will soon heat itself to that by the slow oxidation responsible for its glow. Red is not spontaneously combustible, however if it does catch fire white will be produced, so that the fire, once extinguished, may spontaneously re-ignite. Both can produce phosphine, among other products, by slow reaction with water. Sealed containers of damp phosphorus (white is often stored under water) may pressurise with highly toxic, pyrophoric, gas mixtures [1]. 

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