Abstract: Provided is a methanation catalyst processing method capable of suppressing degradation of a catalyst performance. A methanation catalyst processing method of the present disclosure includes oxidizing nickel through a heat treatment of a methanation catalyst by supplying an oxygen gas containing oxygen to a reactor, the reactor housing the methanation catalyst containing the nickel as a catalyst component. In the oxidizing, the oxygen gas is supplied to the reactor such that the oxygen is supplied to 1 g of the methanation catalyst at a supply rate in a range of from 0.0213 mmol-O2/sec·g-cat. to 0.0638 mmol-O2/sec·g-cat., and a time period of the heat treatment of the methanation catalyst by supplying the oxygen gas to the reactor is set to 30 minutes or more.

Abstract: Herein disclosed is an economical standalone system that replaces conventional monomer purification methods needed to perform chemical reactions that require reactants with a high degree of purity. Chemical reactions, such as anionic polymerization, can produce highly monodisperse homopolymers and block copolymers, however to do so they require very high purity reactants along with a moisture and oxygen free atmosphere. The system and method uses traditional column purification methods, but incorporates them into an economical, standalone, compact, and hazard free system. This method is different in view of safety, cost of cleaning procedure, time commitment, space availability, design and operational ease; helping researchers save time by cutting down the operating commitment by 90% and most importantly making it safer.

Abstract: One exemplary embodiment can be a process for initializing hydroprocessing. Generally, the process can include providing a hydrocarbon feed to a hydrotreating zone within which the hydrotreating temperature is catalytically limited, passing an effluent from the hydrotreating zone to a hydrocracking zone, and adding a gas to the effluent that has a higher temperature than the effluent. Thus, the temperature of the effluent may be raised, facilitating hydrocracking reactions within the hydrocracking zone.

Abstract: Diesel fuel is produced from a feedstock that is at least partially biocomponent in origin. A feedstock is treated in a reactor including one or more hydrotreating zones having a continuous gas phase. The liquid effluent from the hydrotreating zones is then hydroprocessed in a hydroprocessing zone having a continuous liquid phase, such as a hydroprocessing zone in the same reactor. The hydroprocessing zone can be operated under effective catalytic dewaxing conditions.

Abstract: A process for desulphurizing hydrocarbons includes passing a mixture of hydrocarbon and hydrogen over a hydrodesulphurization catalyst to convert organosulphur compounds present in the hydrocarbon to hydrogen sulphide, passing the resulting mixture over a hydrogen sulphide sorbent including zinc oxide to reduce the hydrogen sulphide content of the mixture, and passing the hydrogen sulphide-depleted mixture over a further desulphurization material. The further desulphurization material includes one or more nickel compounds, a zinc oxide support material, and optionally one or more promoter metal compounds of iron, cobalt, copper and precious metals. The desulphurization material has a nickel content in the range 0.3 to 20% by weight and a promoter metal compound content in the range 0 to 10% by weight.

Abstract: Exemplary embodiments of the present invention relate to the processing of hydrocarbon-containing feedstreams in the presence of an interstitial metal hydride containing catalyst comprising a surface, and a Group VI/Group VIII metal sulfide coated onto the surface of the interstitial metal hydride. The catalysts and processes of the present invention can improve overall hydrogenation, product conversion, as well as sulfur reduction in hydrocarbon feedstreams.

Abstract: Provided is a method for reducing the amount of organic acids in a hydrocarbon oil fraction by hydrogenating the organic acids in the hydrocarbon oil fraction under mild conditions. Provided is a new method able to overcome the problem of organic-acid-induced corrosion during the process of distillation, by using hydrogen or a hydrogen-containing mixed gas and a hydrogenation catalyst to subject the organic acids in the hydrocarbon oil fraction to hydrogenation at an appropriate temperature and pressure, thereby converting the same to hydrocarbons and so reducing the amount of organic acids in the hydrocarbon oil fraction.

Abstract: A method for producing a catalyst using an additive layer method includes: (i) forming a layer of a powdered catalyst or catalyst support material, (ii) binding or fusing the powder in said layer according to a predetermined pattern, (iii) repeating (i) and (ii) layer upon layer to form a shaped unit, and (iv) optionally applying a catalytic material to said shaped unit.

Abstract: A process is presented for the removal of oxygen from a hydrocarbon stream. The oxygen can react and cause polymerization of the hydrocarbons when the hydrocarbon stream is heated. Controlling the removal of the oxygen from the hydrocarbon stream produces a hydrocarbon stream that is substantially free of oxygen and has a reduced activity for generating undesired compounds.

Abstract: A process is disclosed for recovering hydroprocessing effluent from a hydroprocessing unit utilizing a hot stripper and a cold stripper. Only the hot hydroprocessing effluent is heated in a fired heater prior to product fractionation, resulting in substantial operating and capital savings.

Abstract: A method of preparing a hydroprocessing catalyst that may have a high metals loading and has a particularly high activity for hydrodenitrogenation. The method uses several metal impregnations in combination with different intermediate treatment steps so as to provide a catalyst composition that includes a mix of different types of catalytically active sites. The method of the invention allows for the optimization and control of the relative ratio of the different types of active catalyst sites on the catalyst composition in order to give certain desired results and improved catalytic performance. The catalyst composition comprises a one or more active metals or active metal precursors that are incorporated onto a support material.

Abstract: The invention relates to a bulk catalyst comprising at least 60 wt % metal oxidic particles comprising one or more Group VIII metals and Group VIB metal molybdenum, comprising less than 10 mole % of a second Group VIB metal and comprising a Group V metal in an amount less than 10 mole %, which bulk catalyst has been calcined at a temperature below a temperature where the hexagonal metastable crystal structure changes to an inactive crystalline structure, and which bulk catalyst has a metastable hexagonal phase characterized by an X-ray diffraction pattern having reflections at 33-35 and 58-61 °2?; and to a process for the manufacture of the bulk catalyst, to the corresponding sulphided bulk catalyst and to the use of said bulk catalyst or sulphided bulk catalyst in the hydroprocessing of a hydrocarbon feedstock.

Abstract: A hydrocarbon oil is hydrotreated in a process employing at least a first and a second reactor vessel, which process comprises: (i) contacting the hydrocarbon oil in the first reactor vessel at elevated temperature and pressure with a hydrotreating catalyst in the presence of a hydrogen-containing gas, thereby consuming hydrogen; (ii) separating the effluent of step (i) into partly hydrotreated hydrocarbon oil and contaminated hydrogen containing gas using a stripping column employing used hydrogen-containing gas as stripping gas; (iii) contacting partly hydrotreated hydrocarbon oil obtained in step (ii) in the second reactor vessel at elevated temperature and pressure with a hydrotreating catalyst in the presence of clean hydrogen-containing gas, thereby consuming hydrogen, wherein at least 80% of the hydrogen consumed in steps (i) and (iii) is supplemented by additional clean hydrogen-containing gas fed to the second reactor; (iv) separating the product from step (iii) in the second reactor vessel into a hy

Abstract: A process for purifying an olefin-containing hydrocarbon feedstock comprising the steps of: (a) passing the said hydrocarbon feedstock in the presence of hydrogen over a first catalyst bed material comprising nickel deposited on a support material wherein said nickel is present as both nickel oxide and metallic nickel (b) recovering the feedstock having a substantially reduced acetylenics (in particular methylacetylene) and allenes (in particular propadiene) content.

Abstract: The present invention relates to an improved method for recovering hydrocarbons trapped in hydrate formations.

Abstract: Diesel fuel is produced from a feedstock that is at least partially biocomponent in origin. A feedstock is treated in a reactor including one or more hydrotreating zones having a continuous gas phase. The liquid effluent from the hydrotreating zones is then hydroprocessed in a hydroprocessing zone having a continuous liquid phase, such as a hydroprocessing zone in the same reactor. The hydroprocessing zone can be operated under effective catalytic dewaxing conditions.

Abstract: A process is presented for the removal of oxygen from a hydrocarbon stream. The oxygen can react and cause polymerization of the hydrocarbons when the hydrocarbon stream is heated. Controlling the removal of the oxygen from the hydrocarbon stream produces a hydrocarbon stream that is substantially free of oxygen and has a reduced activity for generating undesired compounds.

Abstract: A process for the selective catalytic hydrogenation of alkynes and/or dienes in a hydrocarbon stream in the presence of hydrogen, an alcohol, and a supported catalyst is disclosed. The presence of the alcohol reduces the catalyst deactivation and improves the selectivity of the hydrogenation.

Abstract: Disclosed is a process for removing sulfur from a fuel gas stream that comprises an organic sulfur compound and a light olefin. The process includes introducing a fuel gas stream into an elongated hydrotreating reactor vessel in which it is contacted with a hydrodesulfurization catalyst under hydrodesulfurization process conditions. A quench gas stream is also introduced into the elongated hydrotreating reactor vessel at a location below the point of introduction of the fuel gas stream. A reactor effluent is yielded that contains hydrogen sulfide and a significantly reduced organic sulfur concentration that is below the organic sulfur concentration of the fuel gas stream.

Abstract: Process for obtaining a hydrocarbon fraction that can be used as a feedstock of an etherification unit and that contains a small amount of diene compounds, nitrogen-containing compounds and sulfur-containing compounds, starting from an initial hydrocarbon feedstock that comprises a mixture of olefins, dienes, and nitrites as well as sulfur-containing compounds, whereby said process comprises at least the following successive stages: a) a selective hydrogenation of said initial hydrocarbon feedstock in the presence of a catalyst of group VIII of the periodic table, b) a fractionation by distillation of the effluents that are obtained from stage a) under conditions that make it possible to obtain at least two fractions including said hydrocarbon fraction and that comprises a small amount of diene compounds, nitrogen-containing compounds and sulfur-containing compounds, and a heavy fraction that contains heavy hydrocarbons and the majority of the nitrogen-containing compounds and sulfur-containing compounds

Abstract: Apparatus, methods and systems useful for removing phenylacetylene from crude styrene feedstock are disclosed. Generally the processes and systems comprise the catalytic reduction of phenylacetylene to produce styrene via injection of a phenylacetylene reducing agent, such as hydrogen. A phenylacetylene reduction catalyst preferred Wherein comprises palladium on a calcium aluminate carrier, wherein the catalyst comprises less than 0.3 weight percent palladium.

Abstract: A process for the desulfurization of a light boiling range (C5-350° F.) fluid catalytically cracked naphtha, which may be first subjected to a thioetherification to react the diolefins with mercaptans contained in it to form sulfides, is fed to a high pressure (>250 psig) catalytic distillation hydrodesulfurization step along with hydrogen under conditions to react most of the organic sulfur compounds, including sulfides from the thioetherification to form H2S. The H2S and a light product stream (C5's and C6's) are removed as overheads. The bottoms from the catalytic distillation hydrodesulfurization step is fractionated and the bottoms from the fractionation contacted with hydrogen in a straight pass hydrogenation step in the presence of a hydrodesulfurization catalyst at pressure of >250 and temperature >400° F. to further reduce the sulfur content.

Abstract: A process for the treatment of a feed comprising at least hydrocarbons containing at least 3 to 10 carbon atoms per molecule, including acetylenic and diolefinic hydrocarbons, comprises passing the feed into a distillation zone associated with a selective hydrogenation reaction zone comprising at least one catalytic hydrogenation bed which is internal to or external of the distillation zone, in which hydrogenation of at least a portion of the acetylenic and diolefinic hydrocarbons contained in the feed is carried out in the presence of a gas stream rich in hydrogen. The process is particularly suitable for the treatment of products from catalytic cracking.

Abstract: A process for the removal of vinylacetylene, ethylacetylene and 1,2-butadiene from C.sub.4 aliphatic hydrocarbon streams comprising, concurrently: (1) feeding hydrogen and a hydrocarbon stream comprising C.sub.4 hydrocarbons including butanes, butenes, butadienes and vinylacetylene to a distillation column reactor containing a bed comprising a hydrogenation catalyst of the type characterized by platinum, palladium or rhodium which is prepared as a distillation structure to selectively hydrogenate a portion of the vinylacetylene and the 1,2-butadiene and (2) fractionally distilling the reaction mixture to remove a heavier fraction and removing a fraction overhead comprising substantially all of the C.sub.4.

Abstract: A process for purifying an alkylate feedstream is disclosed. The feedstream contains hydrogen, hydrogen chloride, C.sub.2 -C.sub.7+ alkanes, C.sub.2 -C.sub.6 alkenes and C.sub.2 -C.sub.6 alkyl halides. The process involves flowing the alkylate through a series of separation zones and a reaction zone to provide a halide free alkylate stream.

Abstract: A process for treating a light cracked naphtha to be used as an etherification or alkylation feedstock in which the mercaptans and diolefins are removed simultaneously in a distillation column reactor using a Pd catalyst. The mercaptans are reacted with the diolefins to form sulfides which are higher boiling than that portion of the naphtha which is used as feed to the etherification or alkylation unit. H.sub.2 S reacts in the same manner as the mercaptans to for the sulfides and is similarly removed from streams. The higher boiling sulfides are removed as bottoms along with any C.sub.6 and heavier materials. Any diolefins not converted to sulfides are selectively hydrogenated to mono-olefins for use in the etherification process. Certain C.sub.5 olefins, for example pentene-1 and 3-methyl butene-1 are isomerized during the process to more beneficial isomers.

Abstract: A method and operating technique for treating diene-containing aliphatic streams by introducing the light hydrocarbon stream at a top portion of a vertical stripping tower having an upper catalytic contact zone containing a bed of solid hydrogenation catalyst particles and a lower contact zone, and introducing a light gas stream containing hydrogen at a lower portion of said stripping tower. Selective hydrogenation is effected by flowing the light hydrocarbon stream and light gas stream countercurrently in contact with the solid hydrogenation catalyst particles under hydrogenation and stripping conditions, thereby converting said diene to mono-alkene in the upper contact zone.

Abstract: A novel catalyst has been provided for the selective hydrogenation of benzene in gasoline. The catalyst mixture comprises a water-soluble, organo-metallic, selective benzene hydrogenation catalyst comprising catalytically-active mixture of (A) M[L].sub.x [X].sub.y wherein M is a metal selected from the group consisting of Cr, Fe, Co, Ni, Mo, Ru, Rh, Pd, Ta, W, Re, Os, Ir, Pt, La and Ce; L is an aromatic hydrocarbon, e.g., benzene, diphenyl, etc., or a diaromatic hydrocarbon, e.g., naphthalene; X is a halogen; x is an integer from 1 to 10 inclusive; and y is an integer from 1 to 10 inclusive; and (B) tris(triphenylphosphine)rhodium(I)halide or tris(triphenylphosphine)ruthenium(I)halide. In use the process comprises admixing the gasoline with water. The above-identified water-soluble, organo-metallic selective benzene hydrogenation catalyst mixture is then added. A catalytic hydrogenation is then carried out in a hydrogenation zone at a temperature of about 150.degree. to about 245.degree. C.

Abstract: An improved method for the dechlorination of polychlorinated biphenyls that are dissolved in an organic solvent, which comprises the incremental additions of a hydrogen transfer agent, such as potassium formate, in the presence of a catalytic amount of a hydrogenation catalyst, such as palladium supported on carbon, and water.

Abstract: A method for refining a methylnaphthalene-containing oil includes the steps of azeotropically distilling the methylnaphthalene-containing oil with ethylene glycol to produce a methylnaphthalene fraction having a reduced content of nitrogen compounds; and hydrodesulfurizing the methylnaphthalene fraction in the presence of a catalyst having loaded thereto at least one member selected from molybdenum, cobalt and nickel.

Abstract: A novel process is provided for the selective hydrogenation of benzene in a solution of gasoline and other aromatic organic compounds. The process includes the steps of carrying out the catalytic hydrogenation in a hydrogenation zone at a temperature of about 45.degree. to about 250.degree. C. at a pressure of about 200 psi to about 500 psi in a biphasic system of aqueous and organic liquids the hydrogenation catalyst being water-soluble. The organic liquid is removed from the hydrogenation zone. At least a catalytic amount of the catalyst is retained in the hydrogenation zone. The catalyst above described is also a facet of this invention.

Abstract: A process for the selective hydrogenation of butadiene to butenes in the liquid phase or trickle phase in contact with a fixed-bed supported noble metal catalyst, wherein a high-butadiene C.sub.4 stream having a butadiene content of from 20 to 80% w/w, based on the weight of the C.sub.4 stream, is hydrogenated in a cascade of two reaction zones such that the hydrogenation product from the first reaction zone has a butadiene content of from 0.1 to 20% w/w and the hydrogenation product from the second reaction zone has a butadiene content of from 0.005 to 1% w/w, based in both cases on the weight of the C.sub.4 stream, provided that the butadiene content of the hydrogenation product from the second reaction zone is at least 5 times smaller than that of the hydrogenation product from the first reaction zone.

Abstract: A method for the separation of benzene from a hydrocarbon stream, such as a gasoline boiling range stream, which comprises contacting the hydrocarbon stream with an adsorbent capable of selectively adsorbing the benzene from the stream, hydrogenating the adsorbed benzene to cyclohexane, and desorbing the cyclohexane from the adsorbent. The hydrogenation of the benzene to cyclohexane facilitates the removal of the benzene from the adsorbent.

Abstract: A method for refining liquified petroleum gases so that gases can be treated to reduce odor, olefins, moisture and wherein side reactions are minimized to produce stable aerosol by multistage liquid-liquid extraction of the aerosol using electrolyte solutions at controlled pH, chemically treating, drying and finishing by using molecular sieves and metal sulfides.

Abstract: A process for the preparation of hydrogenated deodorized polybutene polymers, wherein the polybutene polymer is hydrogenated, distilled to substantially remove low boiling odorous compounds, and treated with silica gel to substantially remove the remaining odorous compounds thereby providing an improved hydrogenated, distilled, silica gel-treated polybutene polymer substantially free of odorous compounds.

Abstract: A non-catalytic process for the conversion of a hydrocarbonaceous stream containing less than about 5 weight percent halogenated organic compounds which process comprises: (a) reacting the hydrocarbonaceous stream in the presence of hydrogen in a reaction zone at reaction conditions including an elevated temperature selected to convert at least a portion of the halogenated organic compounds to more highly hydrogenated organic compounds; and (b) recovering a hydrocarbonaceous product stream containing lower halogen content.

Abstract: A process is disclosed for hydrotreating olefin-containing hydrocarbon streams for the purpose of producing very low olefin concentrations without the use of high pressure hydrotreating. The process is useful in preparing feeds to adsorptive separation zones. In the process the effluent of a hydrotreating reaction zone is passed into a stripping column. Preferably, substantially all liquid flowing downward through the lower section of the column is withdrawn and then passed through a hydrogenation reactor. The hydrogenation reactor effluent is passed into the bottom of the column to allow removal of dissolved hydrogen.

Abstract: The invention disclosed herein is a method of treating middle distillate hydrocarbons to selectively convert tricyclic hydrocarbons to hydrocarbons of better cetane value by means of hydrogenation and cracking. The process is performed in the presence of an intercalated clay catalyst having high temperature stable pillars intermediate layers of the clay. This process achieves a diesel fuel having a higher cetane value than is currently obtainable utilizing molecular sieve catalysts such as a metal impregnated Y zeolite. The tricyclic aromatics are selectively hydrogenated and cracked in preference to accompanying paraffins, isoparaffins, tetralins and decalins.

Abstract: Hydrocarbon feedstocks such as distillate fuel oils and gas oils are dewaxed by isomerizing the waxy components over a zeolite beta catalyst. The process may be carried out in the presence or absence of added hydrogen. Preferred catalysts have a zeolite silica:alumina ratio over 100:1.

Abstract: This invention consists essentially in a method of removing oxygen from a gas containing an unsaturated hydrocarbon, which comprises contacting a gas containing an unsaturated hydrocarbon and oxygen with silver and/or gold, or a catalyst containing at least one of them, in the presence of hydrogen.

Abstract: A process for producing benzene is provided which comprises the steps of subjecting a charge rich in alkylaromatic hydrocarbons and containing 2-20% by weight paraffinic and/or naphthenic hydrocarbons, in a first catalytic zone, to a hydrotreatment in the presence of a catalyst mixture containing a selective mordenite catalyst and a reforming catalyst, then subjecting at least a portion of the resultant effluent to thermal or catalytic hydrodealkylation in a second zone, and separating and recovering benzene from the effluent from the second zone.

Abstract: Waxy distillate lubricating oil stocks suitable for the preparation, by conventional unit processes, of high V.I., low pour point lubricating oils, are advantageously catalytically dewaxed with macrocrystalline ZSM-5 (crystallites larger than 2 microns) preferably associated with a hydrogenation metal such as platinum or palladium.

Abstract: A process for hydrotreating (hydroprocessing) hydrocarbons and mixtures of hydrocarbons utilizing a catalytic composite comprising a combination of a nickel component, a molybdenum component and a platinum component with a zeolitic carrier material wherein said platinum component is present in an amount sufficient to result in the composite containing, on an elemental basis, about 0.2 to about 0.5 percent by weight platinum, in which process there is effected a chemical consumption of hydrogen. Hydrocarbon hydroprocesses are hydrocracking, the hydrogenation of aromatic nuclei, the ring-opening of cyclic hydrocarbons, desulfurization, denitrification, hydrogenation, etc.

Abstract: A cyclohexylbenzene-cyclohexanone-phenol-containing mixture, for example as obtained by the cleavage of cyclohexylbenzene hydroperoxide, is separated by first catalytically hydrogenating selectively the phenol in the mixture, resulting in a mixture of cyclohexylbenzene, which is unchanged, and cyclohexanone; the thus obtained mixture is subjected to fractional distillation to obtain cyclohexylbenzene which can be returned as to a process for the production of cyclohexylbenzene hydroperoxide, and cyclohexanone.

Abstract: A method of preparing benzene and xylenes from catalysates of reforming of gasoline fractions comprising a mixture of aromatic C.sub.6 -C.sub.10 hydrocarbons and non-aromatic hydrocarbons which involves separation of a low-boiling fraction boiling out at a temperature of 90.degree.-108.degree. C. from a reforming catalysate by rectification. The remaining high-boiling fraction is processed in the presence of a hydrogen-containing gas at a temperature within the range of from 450.degree. to 600.degree. C. under a pressure of from 10 to 60 atm on a catalyst. The catalyst consists of 1 to 85% by weight of H-mordenite, 0.1 to 10% by weight of a hydrogenating component as which use might be made of oxides of metals of Group VI of the periodic system, sulphides of these metals, metals of Group VIII of the periodic system, sulphides thereof; the balance being a binder.