Abstract: Monomeric epoxides are purified by mixing with a hydrocarbyl alkali metal. The requisite amount of hydrocarbyl lithium is readily detectable by a change in color of a suitable indicator. The monomeric epoxide so purified can be rapidly and completely polymerized to yield high molecular weight homopolymers or copolymers.
Abstract: The inactive palladium-containing precipitate formed during the reaction of a carboxylic acid and an olefin to form an ester can be reactivated by the addition of a suitable reducing agent to a slurry of the precipitate in the ester.
Abstract: Certain alkaline earth pyrophosphates, such as Ca, Mg, and Sr pyrophosphates are superior catalysts for oxydehydrogenating alkyl aromatic compounds including nitrogen heterocyclics which have at least one C.sub.2 -C.sub.6 alkyl side chain to form derivatives having side chain unsaturation. The alkyl aromatic compound can have 1-2 rings. The process is carried out at 450.degree.-650.degree.C. and a space velocity of 55-2500.
Abstract: Hydrogen fluoride can be separated from an organic mixture of fluorinated C.sub.1 -C.sub.3 compounds and recovered for reuse by selectively absorbing the HF in a glycol in which the HF is soluble, but the fluorinated organic compound is substantially insoluble. If desired, HF can be obtained in anhydrous form.
Abstract: Alkaline earth-nickel phosphates having from about 61% to about 70% phosphate are superior catalysts for oxydehydrogenating alkyl aromatic compounds including nitrogen heterocyclics which have at least one C.sub.2 -C.sub.6 alkyl side chain to form derivatives having side chain unsaturation. The alkyl aromatic compound can have 1-2 rings. The process is carried out at 450.degree.-650.degree.C. and a space velocity of 55-2500.
Abstract: Lanthanum phosphate, lanthanum pyrophosphate and rare earth phosphates and pyrophosphates containing a major portion of that lanthanum compound are good catalysts for oxydehydrogenating alkyl aromatic compounds, including nitrogen heterocyclics having at least one C.sub.2 -C.sub.6 alkyl side chain to form derivatives having side chain unsaturation. The alkyl aromatic compound can have 1-2 rings. The process is carried out at 450.degree.-640.degree.C. and a space velocity of 55-2500.