Abstract:
Aromatic hydrocarbons are separated from non-aromatic hydrocarbons or different aromatic hydrocarbons by complex formation with hydrogen fluoride and a copper fluoride under anhydrous conditions. Aromatic hydrocarbons form the complex and non-aromatics do not; one molecule of cuprous fluoride complexes two hydrocarbon molecules while one molecule of cupric fluoride complexes one hydrocarbon molecule, and the complex dissolves in the hydrogen fluoride. In separating aromatics from non-aromatics preferably at least sufficient copper fluoride is used to complex all the aromatic hydrocarbon and 3-15 mols. of hydrogen fluoride are used per mol. of hydrocarbon (30-150 volume per cent based on hydrocarbon). Temperatures of -40 DEG to 150 DEG C. are used under sufficient pressure to maintain the liquid phase. The feed is preferably free of olefinic hydrocarbons and sulphur compounds. The resulting mixture may be distilled without separation; the non-aromatic hydrocarbons, possibly with hydrogen fluoride, are recovered first followed by the aromatic hydrocarbons and hydrogen fluoride at a higher temperature. Solid copper fluoride remains. The separation of ethylbenzene and xylenes may also be effected, several stages being necessary to effect complete separation. The "extract" phase containing the complex contains a higher proportion of xylenes and the "raffinate" a higher proportion of ethyl benzene. Cuprous fluoride is added in amounts of 0.1-0.6 mol. per mol. of xylene and cupric fluoride in amounts of 0.2-1.2 mol. per mol. Hydrogen fluoride is used in amounts of 3-30 mols. per mol. of aromatic hydrocarbon. Non-aromatic hydrocarbons may be present but olefinic and sulphur compounds are preferably excluded. In a multi-stage operation the "extract" phase may be contacted with a xylene "reflux". Continuous operation may be effected by passing the mixed feed and complexing agents to a distillation zone maintained at a temperature which will distil off the uncomplexed material while maintaining the hydrogen fluoride in a liquid condition, the complex being recovered at the base of the column.
Abstract:
An improved process for alkylating at least one alkylatable isoparaffin with at least one alkylating agent selected from the class consisting of an olefin and an alkyl sulfate ester in the presence of a catalyst comprising a major amount of hydrofluoric acid and a minor amount of fluorosulfuric acid.
Abstract:
ALUMINA. THE SECOND CATALYST MAY CONTAIN ALSO A SMALL AMOUNT OF RHENIUM. THE FIRST REFORMATE SHOULD POSSESS A PARAFFINS-TO-NAPHTHENES RATIO OF AT LEAST 5 TO 1. A PETROLEUM HYDROCARBON FRACTION IS CONTACTED IN A FIRST REFORMING ZONE WITH A FIRST CATALYST COMPRISING A GROUP VIII NOBLE METAL, A HALIDE, AND ALUMINA TO PRODUCE A FIRST REFORMATE, WHICH IS SUBSEQUENTLY CONTACTED IN A SECOND REFORMING ZONE WITH A SECOND CATALYST COMPRISING THE OXIDES OF CHROMIUM, A MEMBER SELECTED FROM THE GROUP CONSISTING OF AN OXIDE, OF AN ALKALI METAL, AN OXIDE OF AN ALKALINE EARTH METAL, AND MIXTURES THEREOF, AND