Abstract: Provided herein is an alkane dehydrogenation catalyst, a method of manufacturing an alkane dehydrogenation catalyst, and a method of converting alkanes to alkenes.

Abstract: Provided herein is an alkane dehydrogenation catalyst, a method of manufacturing an alkane dehydrogenation catalyst, and a method of converting alkanes to alkenes.

Abstract: A high-temperature plastic pyrolysis process that can produce high yields of ethylene, propylene and other light olefins from waste plastics is disclosed. The plastic feed is pyrolyzed at a high temperature of about 600 to about 900° C. directly to monomers, such as ethylene and propylene. During pyrolysis, the plastic feed is contacted with a diluent gas stream at a mole ratio of carbon feed to diluent gas of 0.6 to 20.

Abstract: A plastic pyrolysis process that can produce high yields of ethylene, propylene and other light olefins from waste plastics is disclosed. The plastic feed is pyrolyzed at a low-temperature pyrolysis process and subsequently pyrolyzed in a high-temperature pyrolysis process directly to monomers, such as ethylene and propylene. Insufficiently pyrolyzed product from the low-temperature pyrolysis process can be fed to the high-temperature pyrolysis process while preserving the desired low-temperature product monomers.

Abstract: Provided herein is an alkane dehydrogenation catalyst, a method of manufacturing an alkane dehydrogenation catalyst, and a method of converting alkanes to alkenes.

Abstract: A method is provided for synthesizing an aromatic carboxylic acid compound comprising providing an aromatic compound or an aromatic compound with at least one carboxylic group; providing a metal hydroxide and at least one carboxylate to produce a mixture; and adding carbon dioxide to the mixture under pressures from about atmospheric to 1000 psig and sufficient heat for a time sufficient to produce aromatic carboxylic acid compounds. The aromatic carboxylic acid compounds may include terephthalic acid, naphthalic acid, thiophene dicarboxylic acid, pyridine dicarboxylic acid, carbazole dicarboxylic acid, and dibenzothiophene dicarboxylic acid.

Abstract: A method is provided for synthesizing an aromatic carboxylic acid compound comprising providing an aromatic compound or an aromatic compound with at least one carboxylic group; providing a metal hydroxide and at least one carboxylate to produce a mixture; and adding carbon dioxide to the mixture under pressures from about atmospheric to 1000 psig and sufficient heat for a time sufficient to produce aromatic carboxylic acid compounds. The aromatic carboxylic acid compounds may include terephthalic acid, naphthalic acid, thiophene dicarboxylic acid, pyridine dicarboxylic acid, carbazole dicarboxylic acid, and dibenzothiophene dicarboxylic acid.

Abstract: An alkylation process utilizing less than 10 vol % of a halometallate based ionic liquid catalyst is described. By decreasing the catalyst volume fraction, the level of subsequent undesirable reactions may be minimized. The total residence time is typically in the range of about 1 min to about 30 min. The alkylate typically has a research octane number of at least about 93, and the olefin conversion is typically at least about 96%.

Abstract: Processes for the production of transportation fuel from a renewable feedstock. A gaseous mixture of carbon monoxide and hydrogen is used to deoxygenate and hydrogenate the glycerides to produce long chain hydrocarbons. Water is also introduced into the reaction zone to increase the amount of hydrogen and to increase the utilization of carbon monoxide within the reaction zone. Synthesis gas may also be used to supply at least a portion of the gaseous mixture of carbon monoxide and hydrogen. The amount of hydrogen equivalents in the reaction zone is at least 100% of a stoichiometric hydrogen demand within the reaction zone.

Abstract: An alkylation process utilizing less than 10 vol % of a halometallate based ionic liquid catalyst is described. By decreasing the catalyst volume fraction, the level of subsequent undesirable reactions may be minimized. The total residence time is typically in the range of about 1 min to about 30 min. The alkylate typically has a research octane number of at least about 93, and the olefin conversion is typically at least about 96%.

Abstract: A hydrocarbon disproportionation process is described. The process includes contacting a hydrocarbon feed in a disproportionation reaction zone with a disproportionation catalyst in the presence of hydrogen and an added chloride promoter under disproportionation conditions including to obtain disproportionation products, wherein the disproportionation catalyst comprises a solid catalyst comprising a refractory inorganic oxide having a metal halide dispersed thereon.

Abstract: A process for producing dimethylhexanes (DMH) is provided. The DMH can be used to produce p-xylene. The process involves the alkylation of isobutane and 1-butene using an ionic liquid to produce naphtha that is rich in DMH. The DMH is then converted in high selectivity to xylene, including p-xylene, by dehydrocyclization.

Abstract: A process for a liquid phase selective hydrogenation of acetylene to ethylene in a reaction zone. In order to decrease the selectivity to C4+ hydrocarbons, the concentration of acetylene in solvent is lowered by recycling solvent, using a split feed injection, or both. The streams can be split in to equal or unequal portions. A hot separator may be used to separate solvent from the reactor effluent, and the solvent may be recovered and used to decrease the concentration of acetylene in the solvent.

Abstract: A process for a liquid phase selective hydrogenation of acetylene to ethylene in a reaction zone in which acetylene is contacted with hydrogen under hydrogenation conditions and a molar ratio of hydrogen to acetylene in the reaction zone is at least 5, preferably at least 9. A molar ratio of hydrogen to carbon monoxide is preferably approximately 10. The acetylene is preferably absorbed in a solvent.

Abstract: A process for providing aromatics from a coal tar stream. A coal tar stream is provided, and the coal tar stream is fractionated into at least a naphtha range stream. The naphtha range stream is hydrotreated, and the hydrotreated naphtha range stream is separated to provide at least a naphthene rich stream. The naphthene rich stream is reformed or dehydrogenated to convert the naphthene. The dehydrogenated naphthene rich stream may be combined with a portion of a reformed crude oil hydrocarbon stream.

Abstract: A process for selectively dealkylating aromatic compounds includes providing a coal tar stream comprising aromatic compounds and hydrotreating the coal tar stream to reduce a concentration of one or more of organic sulfur, nitrogen, and oxygen in the coal tar stream, and to hydrogenate at least a portion of the aromatic compounds in the coal tar stream. The process further includes hydrocracking the hydrotreated coal tar stream to further hydrogenate the aromatic compounds and to crack at least one ring of multi-ring aromatic compounds to form single-ring aromatic compounds. The single-ring aromatic compounds present in the hydrocracked stream are then dealkylated to remove alkyl groups containing two or more carbon atoms.

Abstract: A process for transalkylating a coal tar stream is described. A coal tar stream is provided, and is fractionated to provide at least one hydrocarbon stream having polycyclic aromatics. The hydrocarbon stream is hydrotreated in a hydrotreating zone, and then hydrocracked in a hydrocracking zone. A light aromatics stream is added to the hydrocracking zone. The light aromatics stream comprises one or more light aromatics having a ratio of methyl/aromatic available position that is lower than a ratio of methyl/aromatic available position for the hydrotreated stream. The hydrocracked stream is transalkylated in the hydrocracking zone.

Abstract: One exemplary embodiment can be a process for increasing a mole ratio of methyl to phenyl of one or more aromatic compounds in a feed. The process can include reacting an effective amount of one or more aromatic compounds and an effective amount of one or more aromatic methylating agents to form a product having a mole ratio of methyl to phenyl of at least about 0.1:1 greater than the feed.

Abstract: A process for pyrolyzing a coal feed is described. A coal feed is pyrolyzed into a coal tar stream and a coke stream in a pyrolysis zone. The coal tar stream is separated into at least a pitch stream comprising aromatic hydrocarbons. The pitch stream is reacted in a reaction zone to add at least one functional group to an aromatic ring of the aromatic hydrocarbons in the pitch stream. The functionalized pitch stream is recycled to the pyrolysis zone.

Abstract: A process for transalkylating a coal tar stream is described. A coal tar stream is provided, and is fractionated to provide at least one hydrocarbon stream having polycyclic aromatics. The hydrocarbon stream is hydrotreated in a hydrotreating zone, and then hydrocracked in a hydrocracking zone. A light aromatics stream is added to the hydrocracking zone. The light aromatics stream comprises one or more light aromatics having a ratio of methyl/aromatic available position that is lower than a ratio of methyl/aromatic available position for the hydrotreated stream. The hydrocracked stream is transalkylated in the hydrocracking zone.