Abstract: A method and apparatus for removing peroxides from an exposed naphtha stream is shown and described. The process includes the catalytic reactive oxygen stripping of peroxides thereby generating hydrocarbons and oxygen. Numerous conventional catalysts may be employed. The catalytic stripping reaction can be carried out at substantially lower temperatures than conventional reboiled oxygen strippers thereby resulting in substantial energy savings. Further, the disclosed reactor vessels are substantially smaller and less expensive to build than conventional oxygen stripper columns The disclosed energy efficient reactive oxygen stripping process and equipment is intended to be utilized upstream of a naphtha hydrotreating unit.

Abstract: Process for reduction of bromine index in aromatics, comprising the steps of feeding an aromatics feed stream which contains olefin impurities to a distillation column; withdrawing an overhead stream from the distillation column; subjecting at least a portion of the overhead stream to a treatment for the alkylation or polymerization of olefin in a clay treater to provide a purified overhead stream which is then injected to the aromatics feed stream.

Abstract: Carbonyl compound contaminants are removed from hydrocarbon streams containing olefins for use, for example, in the process for the skeletal isomerization of olefins by pretreating the hydrocarbon stream by passing it over an acidic catalyst at elevated temperatures in the range of 100-400° C. under conditions to react the carbonyls to form reaction products which are deposited onto the catalyst.

Abstract: A process for the removal of hydrocarbon contaminants, such as dienes and olefins, from an aromatics reformate by contacting an aromatics reformate stream with a hydrotreating catalyst and/or a molecular sieve. The hydrotreating catalyst substantially converts all dienes to oligomers and partially converts olefins to alkylaromatics. The molecular sieve converts the olefins to alkylaromatics. The process provides an olefin depleted product which can be passed through a clay treater to substantially convert the remaining olefins to alkylaromatics. The hydrotreating catalyst has a metal component of nickel, cobalt, chromium, vanadium, molybdenum, tungsten, nickel-molybdenum, cobalt-nickel-molybdenum, nickel-tungsten, cobalt-molybdenum or nickel-tungsten-titanium, with a nickel molybdenum/alumina catalyst being preferred. The molecular sieve is an intermediate pore size zeolite, preferably MCM-22. The clay treatment can be carried out with any clay suitable for treating hydrocarbons.

Abstract: Hydrocarbon feeds are upgraded by contacting same, at elevated temperature and in the presence of hydrogen, with a self-promoted catalyst prepared by heating one or more water soluble catalyst precursors in a non-oxidizing atmosphere in the presence of sulfur at a temperature of at least about 200.degree. C. The precursors will be one or more compounds of the formula ML(Mo.sub.y W.sub.1-y O.sub.4) wherein M is one or more promoter metals selected from the group consisting essentially of Mn, Fe, Co, Ni, Cu, Zn and mixtures thereof, wherein O.ltoreq.y.ltoreq.1 and wherein L is a nitrogen containing, neutral multidentate, chelating ligand. In a preferred embodiment the ligand L will comprise one or more chelating alkyl di or triamines and the non-oxidizing atmosphere and to form the catalyst will comprise H.sub.2 S.

Abstract: This invention relates to the preparation and use of supported, manganese sulfide promoted molybdenum and tungsten sulfide catalysts useful for hydroprocessing processes, particularly hydrotreating. These catalysts are prepared by heating a composite of support material and precursor salt under oxygen-free conditions and in the presence of sulfur, wherein said precursor salt contains a thiometallate anion of Mo, W or mixture thereof and a cation comprising one or more promoter metals which are chelated by at least one neutral, nitrogen-containing polydentate ligand, and wherein said promoter metal comprises Mn alone or a mixture of Mn with Co, Ni, Zn, Cu or mixture thereof.

Abstract: Hydrocarbon feeds are upgraded by contacting same, at elevated temperature and in the presence of hydrogen, with a self-promoted catalyst prepared by heating one or more water soluble catalyst precursors in a non-oxidizing atmosphere in the presence of sulfur at a temperature of at least about 200.degree. C. The precursors will be one or more compounds of the formula ML(Mo.sub.y W.sub.1-y O.sub.4) wherein M is one or more promoter metals selected from the group consisting essentially of Mn, Fe, Co, Ni, Cu, Zn and mixtures thereof, wherein O.ltoreq.y.ltoreq.1 and wherein L is a nitrogen containing, neutral multidentate, chelating ligand. In a preferred embodiment the ligand L will comprise one or more chelating alkyl di or triamines and the non-oxidizing atmosphere and to form the catalyst will comprise H.sub.2 S.

Abstract: Hydrocarbon feeds are upgraded by contacting a feed, at elevated temperature and in the presence of hydrogen, with a self-promoted catalyst prepared by heating one or more catalyst precursors under oxygen-free conditions in the presence of sulfur at a temperature of at least about 150.degree. C. The catalyst precursors will be one or more compounds of the formula (ML)(Mo.sub.y W.sub.1-y S.sub.4) wherein M comprises one or more divalent promoter metals selected from the group consisting of Ni, Co, Zn, Cu and mixtures thereof, wherein y is any value ranging from 0 to 1 and wherein L is one or more neutral, nitrogen-containing ligands at least one of which is a chelating, polydentate ligand.

Abstract: A method for reducing the pour point of a hydrocarbon oil which comprises contacting said oil under dewaxing conditions with a zeolite dewaxing catalyst thereby forming a dewaxed oil that contains olefins, and contacting said dewaxed oil and said contained olefins with a solid acidic catalyst under conditions effective to increase the stability of said oil.

Abstract: This invention provides a method of processing thermal cracked by-product oil which comprises reacting a distillate from a thermal cracked by-product oil principally containing components of a boiling range between 75.degree. C. and 198.degree. C. said distillate being one of the distillates from the cracking of petroleum hydrocarbons at a cracking temperature of 700.degree. C. or higher, and containing a ratio of 5-100 molar percent aromatic olefins to non-olefinic aromatic hydrocarbons, in liquid phase in the presence of an acid catalyst under such conditions that the reaction temperature is 0.degree. C.-200.degree. C., the liquid residence time is 0.1 hour-5 hours and wherein the content of aromatic olefins in the reaction system are 5% by weight or less at the end of the reaction, to yield a processed distillate containing non-condensed di- and tricyclic aromatic compounds which are reaction products of aromatic olefins with other aromatic hydrocarbons but no substantial amount of unsaturated components.