Abstract: In a process for the catalytic conversion of lower hydrocarbons to aromatic compounds comprising benzene, toluene and xylenes, a process stream containing lower hydrocarbons is contacted with a zeolitic catalyst having an MFI framework and containing 0.1 to 10 percent by weight of a zinc compound. The process stream further contains one or more sulfur compounds, especially hydrogen sulfide, for improving the selectivity.

Abstract: Methods of converting ethane to ethylene at relatively low temperatures are described. Ir02-based catalysts are used in the conversion. Methods of converting a base gas to a first gas by exposing the base gas to an IrO2-based catalyst and forming the first gas are described. The base gas can be an alkane. The first gas can include an alkene, an alkyne, an alcohol, an aldehyde, or combinations thereof.

Abstract: The invention relates to catalysts and their use in processes for dehydrocyclization of light paraffinic hydrocarbon feedstock to higher-value hydrocarbon, such as aromatic hydrocarbon, to dehydrocyclization catalysts useful in such processes, and to the methods of making such catalysts. One of more of the dehydrocyclization catalysts comprising a crystalline aluminosilicate zeolite having a constraint index of less than or equal to about 12, at least one Group 3 to Group 13 metal of the IUPAC Periodic Table and phosphorous.

Abstract: The oxidative coupling of methane (OCM) and the oxidative dehydrogenation (ODH) of ethane and higher hydrocarbons is described using SO3 and sulfate, sulfite, bisulfite and metabifulfite salts as oxygen transfer agents in the presence of one or more elements selected from Groups 3 to 14 of the periodic table, optionally further in the presence of alkali or alkaline salts and/or sulfur-containing compounds.

Abstract: A catalyst composition, suitable for producing ethylene and other C2+ hydrocarbons from methane. The composition includes a blended product of two distinct catalyst components, blended at such synergistic proportions, that results in a catalyst having high C2+ hydrocarbon selectivity while maintaining an overall sufficient catalyst activity and low ethyne selectivity. Methods for preparing such a catalyst composition and a process for producing C2+ hydrocarbons using such a catalyst composition are provided.

Abstract: Aspects of the invention relate to enhanced oxygen transfer agent systems and methods of use thereof. According to one aspect, a method for producing olefins from a hydrocarbon feed includes the step of contacting a hydrocarbon feed comprised of one or more alkanes with an oxygen transfer agent at a temperature of 350° C. to 1000° C. The oxygen transfer agent comprising an oxygen-donating chalcogen agent comprised of at least one of S, Se, or Te and a reducible metal oxide. The chalcogen having an oxidation state greater than +2. According to another aspect, a method for producing one or more olefins by partial combustion of a hydrocarbon feed includes partially combusting a hydrocarbon feed comprised of one or more alkanes by contacting the hydrocarbon feed with an oxygen transfer agent comprising CaS04 at a temperature of 350° C. to 1000° C. to produce one or more olefins comprising ethylene and coproducing water.

Abstract: Improved methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins, and improved methods of oxidative coupling of methane (OCM) to ethylene and/or ethane, are disclosed. The disclosed methods use boron- or nitride-containing catalysts, and result in improved selectivity and/or byproduct profiles than methods using conventional ODH or OCM catalysts.

Abstract: Process and apparatus ensure high on-stream reliability of a complex that requires a heat pump which is using a compound having a high boiling point, such as xylenes. When the compressor is shutdown, it can be isolated from the distillation column and receiver while the column is allowed to continue to operate with an auxiliary reboiler for constant heat input. The heat pump can be started up and heated to the normal process temperature, so that when the heavy vapor is charged to the heat pump, it does not immediately condense into liquid, causing damage to the compressor.

Abstract: The present invention relates to a process for performing a chemical reaction consisting of at least two sequential reversible steps characterized by being performed in a cycle, and to a reactor for performing such process.

Abstract: Aspects of the invention relate to producing olefins by oxidative dehydrogenation cocracking of a hydrocarbon feed. In one embodiment, the method includes oxidative cocracking a hydrocarbon feed comprised of at least one alkane having a carbon chain of five or more and at least one alkane having a carbon chain of four or less by contacting the hydrocarbon feed with a metal oxide, such that the cracking of the at least one alkane having a carbon chain of four or less produces olefins and is exothermic, and the cracking of the at least one alkane having a carbon chain of five or more produces olefins and is endothermic. The method further includes utilizing the energy produced from the exothermic cracking of the alkane having a carbon chain of four or less for the endothermic cracking of the alkane having a carbon chain of five or more, and collecting the product.

Abstract: Methods for oxidative coupling of methane using metal oxide catalysts and a sulfur oxidant.

Abstract: The invention relates to catalysts and their use in processes for conversion of hydrocarbon feedstock to a product comprising single-ring aromatic hydrocarbons having six or more carbon atoms, to the methods of making such catalysts, to processes for using such catalysts, and to apparatus and systems for carrying out such processes. One of more of the catalysts comprise a crystalline aluminosilicate having a Constraint Index in the range of 1 to 12, a first metal and/or a second metal, and at least one selectivating agent, such as, for example, an organo-silicate.

Abstract: Improved methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins, and improved methods of oxidative coupling of methane (OCM) to ethylene and/or ethane, are disclosed. The disclosed methods use boron- or nitride-containing catalysts, and result in improved selectivity and/or byproduct profiles than methods using conventional ODH or OCM catalysts.

Abstract: A catalyst for the conversion of methane to higher hydrocarbons including aromatic hydrocarbons comprises molybdenum or a compound thereof dispersed on an aluminosilicate zeolite, wherein the amount of aluminum present as aluminum molybdate in the catalyst is less than 2700 ppm by weight.

Abstract: Improved methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins, and improved methods of oxidative coupling of methane (OCM) to ethylene and/or ethane, are disclosed. The disclosed methods use boron- or nitride-containing catalysts, and result in improved selectivity and/or byproduct profiles than methods using conventional ODH or OCM catalysts.

Abstract: This application provides a catalyst for producing paraxylene by co-conversion of methanol and/or dimethyl ether and C4 liquefied gas, and preparation and application thereof. The catalyst is an aromatization molecular sieve catalyst with a shape-selective function co-modified by bimetal and siloxane compound. Methanol and/or dimethyl ether and C4 liquefied gas are fed in reactor together, wherein aromatization reaction occurring on a modified shape-selective molecular sieve catalyst. The yield of aromatics is effectively improved, in which paraxylene is the main product. In products obtained by co-conversion of methanol and/or dimethyl ether and C4 liquefied gas, the yield of aromatics is greater than 70 wt %, and the content of paraxylene in aromatics is greater than 80 wt %, and the selectivity of paraxylene in xylene is greater than 99 wt %.

Abstract: A method for producing C2+ hydrocarbons and H2 comprising (a) introducing to a reactor a reactant mixture comprising methane, (b) heating the reactant mixture to a preheating temperature to yield a heated mixture, (c) generating free radicals in the heated mixture to form a primary effluent mixture comprising free radicals, C2+ hydrocarbons, H2, and unreacted methane, (d) reacting the primary effluent mixture in a secondary reaction zone to form a secondary effluent mixture comprising C2+ hydrocarbons, H2, free radicals, and unreacted methane, at a secondary reaction zone temperature that is greater than the preheating temperature, wherein a free radicals amount in the primary effluent mixture is greater than a free radicals amount in the secondary effluent mixture, (e) cooling the secondary effluent mixture to a quench temperature lower than the secondary reaction zone temperature to yield a product mixture comprising C2+ hydrocarbons and H2, and (f) recovering the product mixture.

Abstract: Provided are zeolite catalysts that allow reactions to proceed at temperatures as low as possible when lower olefins are produced from hydrocarbon feedstocks with low boiling points such as light naphtha, make it possible to make propylene yield higher than ethylene yield in the production of lower olefins, and have long lifetime. The zeolite catalysts are used in the production of lower olefins from hydrocarbon feedstocks with low boiling points such as light naphtha. The zeolite catalysts are MFI-type crystalline aluminosilicates containing iron atoms and have molar ratios of iron atoms to total moles of iron atoms and aluminum atoms in the range from 0.4 to 0.7. The use of the zeolite catalysts make it possible to increase propylene yield, to lower reaction temperatures, and to extend catalyst lifetime.

Abstract: Natural gas and petrochemical processing systems including oxidative coupling of methane reactor systems that integrate process inputs and outputs to cooperatively utilize different inputs and outputs of the various systems in the production of higher hydrocarbons from natural gas and other hydrocarbon feedstocks.

Abstract: This invention is for a catalyst for conversion of hydrocarbons. The catalyst is a non-acidic germanium zeolite, such as Ge-ZSM-5, on which at least two metals, platinum and at least one other metal selected from Group 7, Group 8, Group 9, Group 10 and tin, are deposited on the germanium zeolite. Examples of the other metal are iridium, rhenium, palladium, ruthenium, rhodium, iron, cobalt and tin. The catalyst is prepared by synthesizing a germanium zeolite; depositing platinum and at least one other metal on the germanium zeolite; and calcining after preparation of the zeolite, before depositing the metals or after depositing the metals. The catalyst may be used in a process for the conversion of hydrocarbons, such as propane to aromatics, by contacting the catalyst with a hydrocarbon stream containing alkanes, olefins and mixtures thereof having 2 to 12 carbon atoms per molecule and recovering the product.

Abstract: Form ethylene via a method that includes vaporizing elemental sulfur, providing a metal sulfide catalyst, and contacting the metal sulfide catalyst with a mixture of methane and the vaporized elemental sulfur to form ethylene. The mixture has a methane to sulfur molar ratio greater than 1.2:1.0.

Abstract: A method for the oxidative coupling of hydrocarbons, such as the oxidative coupling of methane to toluene, includes providing an oxidative catalyst inside a reactor, and carrying out the oxidative coupling reaction under a set of reaction conditions. The oxidative catalyst includes (A) at least one element selected from the group consisting of the Lanthanoid group, Mg, Ca, and the elements of Group 4 of the periodic table (Ti, Zr, and Hf); (B) at least one element selected from the group consisting of the Group 1 elements of Li, Na, K, Rb, Cs, and the elements of Group 3 (including La and Ac) and Groups 5-15 of the periodic table; (C) at least one element selected from the group consisting of the Group 1 elements of Li, Na, K, Rb, Cs, and the elements Ca, Sr, and Ba; and (D) oxygen.

Abstract: The invention relates to a process for production of propylene from a C4/C5 olefin cut (for example from steam cracking and/or catalytic cracking), this process comprising an optional selective hydrogenation, a selective oligomerization of the isobutenes and an oligocracking of the n-butenes. The invention makes it possible to obtain a high conversion rate with a good propylene yield and to maximize the production of good-quality gasoline.

Abstract: The present invention provides a process for forming a refined hydrocarbon that includes providing a feed including methanol, dimethyl ether or a mixture thereof, and contacting the feed with a methanol conversion catalyst under suitable conditions to yield an intermediate composition including olefins having at least two carbon atoms. The intermediate composition is introduced to an oligomerization catalyst under suitable conditions to yield gasoline boiling range components and distillate boiling range components.

Abstract: A process is disclosed for removing hydrogen gas that is produced during a DHA (dehydroaromatization) reaction that is used to produce benzene from methane. The hydrogen gas is reacted with a quantity of an alkali metal to produce an alkali metal hydride, which may be separated out from the benzene and any unreacted methane. This removal of the hydrogen gas “drives” the reaction to produce more benzene, thereby increasing the theoretical yield of the DHA reaction.

Abstract: A system for radial flow contact of a reactant stream with catalyst particles includes a reactor vessel and a catalyst retainer in the reactor vessel. The catalyst retainer includes an inner particle retention device and an outer particle retention device. The inner particle retention device and the outer particle retention device are spaced apart to define a catalyst retaining space. The inner particle retention device defines an axial flow path of the reactor vessel, and the outer particle retention device and an inner surface of a wall of the reactor vessel define an annular flow path of the reactor vessel. The system includes an inlet nozzle having an exit opening in fluid communication with the axial flow path, and an outlet nozzle in fluid communication with the annular flow path. The system can further include a fluid displacement device in the axial flow path of the reactor vessel.

Abstract: A process for the pre-treatment of Mo/ZSM-5 and Mo/MCM-22 catalysts is provided, which process comprises heating the catalyst at 500° C. in the presence of propane. The treated catalyst, when used in the non-oxidative dehydrogenation of methane demonstrates improved benzene yield and catalyst stability as compared to catalysts pre-treated with He, methane or H2.

Abstract: The present invention is related to the preparation of a metal lattice-doping catalyst in an amorphous molten state, and the process of catalyzing methane to make olefins, aromatics, and hydrogen using the catalyst under oxygen-free, continuous flowing conditions. Such a process has little coke deposition and realizes atom-economic conversion. Under the conditions encountered in a fixed bed reactor (i.e. reaction temperature: 750˜1200° C.; reaction pressure: atmospheric pressure; the weight hourly space velocity of feed gas: 1000˜30000 ml/g/h; and fixed bed), conversion of methane is 8-50%. The selectivity of olefins is 30˜90%. And selectivity of aromatics is 10˜70%. There is no coking. The reaction process has many advantages, including a long catalyst life (>100 hrs), high stability of redox and hydrothermal properties under high temperature, high selectivity towards target products, zero coke deposition, easy separation of products, good reproducibility, safe and reliable operation, etc.

Abstract: A process for producing aromatic hydrocarbons which comprises (a) contacting ethane with a dehyroaromatization aromatic catalyst which is comprised of about 0.005 to about 0.1% wt platinum, an amount of an attenuating metal which is no more than about 0.02% wt less than the amount of platinum, from about 10 to about 99.9% wt of an aluminosilicate, and a binder, and (b) separating methane, hydrogen, and C2-5 hydrocarbons from the reaction products of step (a) to produce aromatic reaction products including benzene.

Abstract: In a process for the regeneration of a coked metal-containing catalyst, the coked catalyst is contacted in a regeneration zone with an atmosphere which contains carbon dioxide and carbon monoxide at a temperature of at least 400° C.

Abstract: A process for producing aromatic hydrocarbons which comprises (a) contacting one or more lower alkanes with a dehydroaromatization aromatic catalyst which is comprised of 0.005 to 0.1% wt platinum, not more than 0.2% wt of an amount of an attenuating metal wherein the amount of platinum is not more than about 0.02% wt more than the amount of the attenuating metal, from about 10 to about 99.9% wt of an aluminosilicate, and a binder, and (b) separating methane, hydrogen, and C2-5 hydrocarbons from the reaction products of step (a) to produce aromatic reaction products including benzene.

Abstract: The present invention relates to a process for nonoxidatively dehydroaromatizing a reactant stream comprising C1-C4-aliphatics, comprising the steps of I. feeding reactant stream E into a reaction zone 1, converting reactant stream E under nonoxidative conditions in the presence of a particulate catalyst to a product stream P comprising aromatic hydrocarbons and discharging product stream P from reaction zone 1, II. transferring the catalyst with reduced activity as a result of deposited coke into a reaction zone 2, III. at least partly regenerating the catalyst with supply of a hydrogen-comprising gas stream H in a reaction zone 2, at least some of the coke deposited being converted to methane to form a methane-comprising gas stream M which is fed at least partly to reaction zone 1, IV. discharging the catalyst from reaction zone 2 and V.

Abstract: The present invention relates to a process for nonoxidatively dehydroaromatizing a reactant stream comprising C1-C4-aliphatics by converting the reactant stream in the presence of a catalyst in a reaction zone 1 to a product stream P comprising aromatic hydrocarbons, and regenerating the catalyst whose activity has been reduced by deposited coke with a hydrogen-comprising mixture H in a reaction zone 2, wherein at least a portion of the deposited coke is converted to methane and at least a portion of the methane formed is fed to reaction zone 1.

Abstract: A process for producing aromatic hydrocarbons which comprises (a) contacting ethane with a dehyroaromatization aromatic catalyst which is comprised of about 0.005 to about 0.1 wt % platinum, an amount of gallium which is equal to or greater than the amount of the platinum, from about 10 to about 99.9 wt % of an aluminosilicate, and a binder, and (b) separating methane, hydrogen, and C2-5 hydrocarbons from the reaction products of step (a) to produce aromatic reaction products including benzene.

Abstract: A process is provided for producing aromatic hydrocarbons which comprises: (a) contacting a lower alkane feed with a solid particulate aromatic hydrocarbon conversion catalyst in a fixed bed reaction zone to produce aromatic hydrocarbons and other products, whereby the catalyst is at least partially deactivated by the formation of undesirable coke deposits, (b) periodically regenerating the catalyst under regeneration conditions, (c) separating aromatic hydrocarbons from the other products and unreacted lower alkanes, and (d) optionally recycling unreacted lower alkanes to the reaction zone wherein the fixed bed reaction zone additionally comprises a volume of a catalytically inactive solid.

Abstract: The present invention relates to a catalyst for dehydroaromatizing C1-C4-aliphatics, said catalyst being obtainable by twice treating a zeolite from the group of MFI and MWW with NH4-containing mixtures, in each case with subsequent drying and calcination. The catalyst comprises molybdenum and, if appropriate, as further elements, Cu, Ni, Fe, Co, Mn, Cr, Nb, Ta, Zr, V, Zn and/or Ga. The present invention further provides a process for dehydroaromatizing a mixture comprising C1-C4-aliphatics by conversion in the presence of the catalyst.

Abstract: A process is disclosed for treating a hydrocarbon stream including flowing the hydrocarbon stream through a hydrocarbon treating vessel, heating a portion of the hydrocarbon treating vessel to a predetermined temperature and for a predetermined amount of time and controlling sensitization of the portion of the interior surface of the hydrocarbon treating vessel.

Abstract: Process for obtaining aromatic hydrocarbons from a stream containing at least one light hydrocarbon selected from the list comprising methane, ethane, ethylene, propane, propene, propylene, butane, butene or butadiene, which comprises putting said stream into contact with a catalyst, which comprises a catalytic material and a binder, in a fluidized bed reactor. Said reactor may have two reaction zones, an oxidizing zone and a reducing zone.

Abstract: A process for producing aromatic hydrocarbons which comprises (a) contacting ethane with a dehyroaromatization aromatic catalyst which is comprised of 0.005 to 0.1% wt platinum, an amount of iron which is equal to or greater than the amount of the platinum, from 10 to 99.9% wt of an aluminosilicate, and a binder, and (b) separating methane, hydrogen, and C2-5 hydrocarbons from the reaction products of step (a) to produce aromatic reaction products including benzene.

Abstract: A process for regenerating a used acidic catalyst which has been deactivated by conjunct polymers by removing the conjunct polymers so as to increase the activity of the catalyst is disclosed. Methods for removing the conjunct polymers include addition of a basic reagent and alkylation. The methods are applicable to all acidic catalysts and are described with reference to certain ionic liquid catalysts.

Abstract: A heated reaction gas comprising methane is contacted with first and second catalysts to catalyze production of an aromatic hydrocarbon. The first catalyst is more active than the second catalyst for catalyzing aromatization of methane, and the second catalyst is more active than the first catalyst for catalyzing aromatization of ethane. A reactor for producing aromatic hydrocarbons from the reaction gas may have a conduit defining a reaction zone for the reaction gas to react therein, and the first and second catalysts may be disposed in the reaction zone.

Abstract: A crystalline molecular sieve of MFS framework type manufactured by the method disclosed herein. A hydrocarbon conversion process using the crystalline molecular sieve is disclosed.

Abstract: A process for the conversion of mixed lower alkanes into aromatics which comprises first reacting a mixed lower alkane feed comprising at least propane and ethane in the presence of an aromatization catalyst under reaction conditions which maximize the conversion of propane into first stage aromatic reaction products, separating ethane from the first stage aromatic reaction products, reacting ethane in the presence of an aromatization catalyst under reaction conditions which maximize the conversion of ethane into second stage aromatic reaction products, and optionally separating ethane from the second stage aromatic reaction products.

Abstract: The present invention is for a catalyst, a process for making the catalyst and a process for using the catalyst in aromatization of alkanes having three to five carbon atoms per molecule, such as propane, to aromatics, such as benzene, toluene and xylene. The catalyst is an aluminum-silicon zeolite having a silicon to aluminum atomic ratio (Si:Al) greater than 15:1, such as MFI or ZSM-5, on which germanium, aluminum and a noble metal, such as platinum, have been deposited. The catalyst may be bound with magnesia, alumina, titania, zirconia, thoria, silica, boria or mixtures thereof. The aluminum and germanium may be deposited simultaneously on the zeolite.

Abstract: A process for producing a supported mesoporous and microporous material, comprises contacting a support with a template to produce a supported template, and contacting the supported template with one or more microporous material precursor to produce a supported microporous material-template composite, and subsequently removing the template from the supported microporous material-template composite to produce the supported mesoprous and microporous material. A composition comprising a supported mesoprous and microporous material produced by this process can be used for methane dehydroaromatization.

Abstract: In a process for the regeneration of a coked metal-containing catalyst, the coked catalyst is contacted in a regeneration zone with an atmosphere which contains carbon dioxide and carbon monoxide at a temperature of at least 400° C.

Abstract: In a process for converting methane to alkylated aromatic hydrocarbons, a feed containing methane is contacted with a dehydrocyclization catalyst under conditions effective to convert said methane to aromatic hydrocarbons and produce a first effluent stream comprising aromatic hydrocarbons and hydrogen. At least a portion of said aromatic hydrocarbon from said first effluent stream is then contacted with an alkylating agent under conditions effective to alkylate said aromatic hydrocarbon and produce an alkylated aromatic hydrocarbon having more alkyl side chains than said aromatic hydrocarbon prior to the alkylating.

Abstract: [Object] To produce aromatic hydrocarbon stably for a long time maintaining a high aromatic hydrocarbon yield when the aromatic hydrocarbon is produced upon making a contact reaction between lower hydrocarbon and a catalyst. [Solving Means] In a method of producing aromatic hydrocarbon, including repeating a reaction step for obtaining aromatic hydrocarbon upon making a contact reaction between lower hydrocarbon and a catalyst and a regeneration step for regenerating the catalyst used in the reaction step, carbon dioxide in an amount of 0.33 to 1.6% by volume relative to an amount of the lower hydrocarbon is added to the lower hydrocarbon, in the reaction step.

Abstract: The present invention relates to a process for carrying out endothermic, heterogeneously catalyzed reactions in which the reaction of the starting materials is carried out in the presence of a mixture of inert heat transfer particles and catalyst particles, where the catalyst particles are regenerated in a nonoxidative atmosphere at regular intervals and the heat of reaction required is introduced by separating off the inert heat transfer particles, heating the heat transfer particles in a heating zone and recirculating the heated heat transfer particles to the reaction zone. The process of the invention is particularly suitable for the nonoxidative dehydroaromatization of C1-C4-aliphatics in the presence of zeolite-comprising catalysts.

Abstract: The present invention relates to a pillared silicate compound comprising a layered silicate structure, and bridging metal atoms located between adjacent silicate layers of the silicate structure, wherein said bridging metal atoms form at least one covalent bond to each of the adjacent silicate layers, as well as a process for the preparation of a pillared silicate compound, and further includes a pillared silicate compound obtainable and or obtained according to said process, as well as a method of catalyzing a chemical reaction comprising the step of contacting one or more chemical compounds with the any of the aforementioned pillared silicate compounds.