959results about "Hydrocarbon by isomerisation" patented technology

Fuels and other valuable compositions and compounds can be made from oil extracted from microbial biomass and from oil-bearing microbial biomass via hydroprocessing and/or other chemical treatments, including the alkaline hydrolysis of glycerolipids and fatty acid esters to fatty acid salts.

The present invention provides a process for producing a monoalkylated aromatic compound, particularly cumene, comprising the step of contacting a polyalkylated aromatic compound with an alkylatable aromatic compound under at least partial liquid phase conditions and in the presence of a transalkylation catalyst to produce the monoalkylated aromatic compound, wherein the transalkylation catalyst comprises a mixture of at least two different crystalline molecular sieves, wherein each of said molecular sieves is selected from zeolite beta, zeolite Y, mordenite and a material having an X-ray diffraction pattern including d-spacing maxima at 12.4±0.25, 6.9±0.15, 3.57±0.07 and 3.42±0.07 Angstrom.

The present invention provides a process for producing a monoalkylated aromatic compound, particularly ethylbenzene or cumene, in which a polyalkylated aromatic compound is contacted with an alkylatable aromatic compound in the liquid phase and in the presence of a transalkylation catalyst comprising TEA-mordenite having an average crystal size of less than 0.5 micron.

A catalyst for the selective oxidation of hydrogen has been developed. It comprises an inert core such as cordierite and an outer layer comprising a lithium aluminate support. The support has dispersed thereon a platinum group metal and a promoter metal, e.g. platinum and tin respectively. This catalyst is particularly effective in the selective oxidation of hydrogen in a dehydrogenation process.

A liquid or partially liquid phase process for isomerizing a non-equilibrium mixture of xylenes and ethylbenzene uses a zeolitic catalyst system preferably based on zeolite beta and on pentasil-type zeolite. The invention obtains an improved yield of para-xylene from the mixture relative to prior art processes in a more economical manner. A preferred beta zeolite is a surface-modified zeolite beta resulting from acid washing of a templated native zeolite at conditions insufficient to effect bulk dealumination. A preferred pentasil zeolite is a MTW-type with a silica-to-alumnina ratio between 20 and 45.

Compositions including carbide-containing nanorods and/or oxycarbide-containing nanorods and/or carbon nanotubes bearing carbides and oxycarbides and methods of making the same are provided. Rigid porous structures including oxycarbide-containing nanorods and/or carbide containing nanorods and/or carbon nanotubes bearing carbides and oxycarbides and methods of making the same are also provided. The compositions and rigid porous structures of the invention can be used either as catalyst and/or catalyst supports in fluid phase catalytic chemical reactions. Processes for making supported catalyst for selected fluid phase catalytic reactions are also provided.

An olefin isomerization process employs a basic metal oxide catalyst, such as magnesium oxide, which retains at least about 85 percent of its initial activity for at least about 168 hours of on-stream time. The catalyst is preferably a high purity magnesium oxide. The olefin isomerization process and catalyst described herein are advantageously used for the production of a terminal olefin such as 1-butene from an internal olefin such as 2-butene.

This invention is drawn to a process for isomerizing a non-equilibrium mixture of xylenes and ethylbenzene using an oil-dropped catalyst comprising a zeolite, a platinum-group metal and an aluminophosphate binder, resulting in a greater yield of para-xylene at favorable conditions compared to processes of the known art.

The present invention relates to compositions and rigid porous structures that contain nanorods having carbides and/or oxycarbides and methods of making and using such compositions and such rigid porous structures. The compositions and rigid porous structures can be used either as catalysts and/or catalyst supports in fluid phase catalytic chemical reactions. Processes for making supported catalyst for selected fluid phase catalytic reactions are also provided. The fluid phase catalytic reactions catalyzed include hydrogenation hydrodesulfuriaation, hydrodenitrogenation, hydrodemetallization, hydrodeoxygenation, hydrodearomatization, dehydrogenation, hydrogenolyis, isomerization, alkylation, dealkylation, oxidation and transalkylation.

A process for producing cumene is provided which comprises the step of contacting benzene and propylene under at least partial liquid phase alkylating conditions with a particulate molecular sieve alkylation catalyst, wherein the particles of said alkylation catalyst have a surface to volume ratio of about 80 to less than 200 inch⁻¹.

A process for the double-bond isomerization of olefins is disclosed. The process may include contacting a fluid stream comprising olefins with a fixed bed comprising an activated basic metal oxide isomerization catalyst to convert at least a portion of the olefin to its isomer. The isomerization catalysts disclosed herein may have a reduced cycle to cycle deactivation as compared to conventional catalysts, thus maintaining higher activity over the complete catalyst life cycle.

A process for treating organic compounds includes providing a composition which includes a substantially mesoporous structure of silica containing at least 97% by volume of pores having a pore size ranging from about 15 Å to about 30 Å and having a micropore volume of at least about 0.01 cc/g, wherein the mesoporous structure has incorporated therewith at least about 0.02% by weight of at least one catalytically and/or chemically active heteroatom selected from the group consisting of Al, Ti, V, Cr, Zn, Fe, Sn, Mo, Ga, Ni, Co, In, Zr, Mn, Cu, Mg, Pd, Pt and W, and the catalyst has an X-ray diffraction pattern with one peak at 0.3° to about 3.5° at 2θ. The catalyst is contacted with an organic feed under reaction conditions wherein the treating process is selected from alkylation, acylation, oligomerization, selective oxidation, hydrotreating, isomerization, demetalation, catalytic dewaxing, hydroxylation, hydrogenation, ammoximation, isomerization, dehydrogenation, cracking and adsorption.

Hydrocarbon or oxygenate conversion process in which a feedstock is contacted with a non zeolitic molecular sieve which has been treated to remove most, if not all, of the halogen contained in the catalyst. The halogen may be removed by one of several methods. One method includes heating the catalyst in a low moisture environment, followed by contacting the heated catalyst with air and/or steam. Another method includes steam-treating the catalyst at a temperature from 400° C. to 1000° C. The hydrocarbon or oxygenate conversion processes include the conversion of oxygenates to olefins, the conversion of oxygenates and ammonia to alkylamines, the conversion of oxygenates and aromatic compounds to alkylated aromatic compounds, cracking and dewaxing.

The invention belongs to the field of craft processes of arene production devices, and particularly relates to a system and method of preparing paraxylene by alcohol/ether conversion. The system provided by the invention mainly consists of an alcohol/ether aromatization reaction device, a gas-liquid-liquid three phase separating device, a benzene fractional device, a paraxylene fractional device, an olefin-removing device, a paraxylene separating device and a paraxylene product tower. The yield of the paraxylene is increased by means of aromatization reaction of non-arene, alkylation reaction of benzene and disproportionated reaction of xylene and arene with more than 9 carbon atoms. By adopting an unclear separation technology of a product with less than 7 carbon atoms, an arene extraction system is canceled, the investment and energy consumption are greatly reduced, and gaseous phase hydrocarbon with more than 2 carbon atoms is fully utilized as a raw material of an alcohol/ether aromatization system. Hydrogen generated is used for disproportionation of C9 methyl arene and C10 methyl arene and isomerization reaction of C8 arene. The system and method have the advantages of self supply of raw materials, less investment, low energy consumption, short flow and high yield of paraxylene.

A process for the conversion of paraffin hydrocarbon feed stock via skeletal isomerisation by contacting this feed with a catalyst comprised of an ionic liquid formed from an N-containing heterocyclic and/or N-containing aliphatic organic cation and an inorganic anion derived from metal halides.

A process for producing propylene and 1-butene is disclosed. The process comprises dimerizing ethylene in the presence of a dimerization catalyst to produce a dimerization mixture comprising 1-butene and 2-butenes. The dimerization mixture is distilled to produce a 1-butene stream containing 1-butene and ethylene, a 2-butenes stream, and a heavy stream. The 2-butenes stream is reacted with ethylene in the presence of a metathesis catalyst to produce a metathesis mixture comprising propylene, ethylene, and 2-butenes. Propylene is separated from the metathesis mixture.

The invention relates to a process for carrying out metathesis reactions, wherein the process is carried out continuously and a ruthenium-containing catalyst is used.

The invention relates to a catalyst for a normal paraffin hydroisomerization reaction and a preparation method as well as an application thereof. The catalyst has the characteristics that the activity is high in an n-hexane hydroisomerization reaction, and the selectivity and stability are good for a double-branched-chain product. The catalyst comprises modified zeolite molecular sieve ZSM-12 treated by alkaline solution and noble metal of family VIII, wherein the zeolite molecular sieve ZSM-12 adopts zeolite molecular sieve ZSM-12 containing organic amine template. The preparation method of the catalyst comprises the following steps of: desilication of zeolite molecular sieve ZSM-12 containing template after being treated with alkaline solution to obtain zeolite molecular sieve ZSM-12 with high content of mesoporous, and preparing isomerized catalyst by loading Pt. The catalyst is applied in the normal paraffin hydroisomerization reaction, when the catalyst is applied, the n-hexane hydroisomerization reaction is carried out on a fixed bed miniature reactor, the reacting raw material n-hexane is fed into the reactor by a force pump, and is contacted with the catalyst to react in the reactor after being mixed with hydrogen in a mixer.

Compositions including modified carbide-containing nanorods and/or modified oxycarbide-containing nanorods and/or modified carbon nanotubes bearing carbides and oxycarbides and methods of making the same are provided. Rigid porous structures including modified oxycarbide-containing nanorods and/or modified carbide containing nanorods and/or modified carbon nanotubes bearing modified carbides and oxycarbides and methods of making the same are also provided. The compositions and rigid porous structures of the invention can be used either as catalyst and/or catalyst supports in fluid phase catalytic chemical reactions. Processes for making supported catalyst for selected fluid phase catalytic reactions are also provided.

Disclosed herein is a process for producing a selected butene, comprising obtaining a C4 feed stream comprising C4 paraffins and C4 olefins, splitting the C4 feed stream to form a first stream comprising a first butene and a second stream comprising a second butene, isomerizing at least a part of the second stream to convert a portion of the second butene to the first butene, and recycling at least some of the isomerized part of the second steam to the splitting step, wherein a portion of at least one of the C4 feed stream and the second stream is passed through a facilitated transport membrane to remove butanes, forming at least one purge stream comprising butanes. A process for the conversion of C4 olefins, comprising obtaining a C4 feed stream comprising C4 paraffins and C4 olefins, including 1-butene and 2-butene, and reacting the C4 feed stream in a metathesis reactor to form a second stream is also disclosed. The second stream is fractionated to form one or more product streams and a recycle stream primarily containing C4 olefins and C4 paraffins. The recycle stream and/or the C4 feed stream is passed through a facilitated transport membrane to remove butanes, forming at least one purge stream.

The invention provides a method for preparing isobutylene by comprehensively using mixed C4 and mainly solves the problems of low overall utilization efficiency and low additional value of the mixed C4 byproduct of a refinery or a steam cracking device. An aim is fulfilled by adopting a technical scheme which comprises the following steps of: (1) selectively hydrogenating to remove butadiene in the mixed C4; (2) isomerizing butylenes-1 in the mixed C4 obtained in the first step into butylenes-2 by using catalytic distillation technology, and simultaneously dividing the mixed C4 into two strands of materials, namely the first material comprising isobutylene and iso-butane, and the second material comprising n-butane and butylenes-2; (3) separating the first material through an etherifying device to obtain high-purity isobutylene and high-concentration iso-butane; (4) dehydrogenating the iso-butane to obtain the high-purity isobutylene; and (5) isomerizing the butylenes-2 of the second material into the isobutylene by using isomerizing technology, and simultaneously separating to obtain higher-purity n-butane. The method can be applied to the industrial field of producing the high-purity isobutylene.

A process for increasing the production of benzene from a hydrocarbon mixture. A process for producing an aromatic hydrocarbon mixture and liquefied petroleum gas (LPG) from a hydrocarbon mixture, and a solvent extraction process for separating and recovering polar hydrocarbons from a hydrocarbon mixture containing polar hydrocarbons (that is, aromatic hydrocarbons) and nonpolar hydrocarbons (that is, non-aromatic hydrocarbons) are integrated, thereby it is possible to increase the production of benzene.

The invention relates to a method for improving reaction selectivity of isomerization of double bonds of butylene. The method mainly solves the problem of poor reaction selectivity in the prior art. Through a technical proposal that butylenes-1, butylenes-2 or a mixture which contains the butylenes-1 and butylenes-2 and does not meet a thermodynamic equilibrium value is used as a raw material; carbon-predeposited aluminosilicate is used as a catalyst, wherein the amount of predeposited carbon is 0.01 to 5 percent counted by the weight of the catalyst; and under the conditions of reaction temperature of between 50 and 480 DEG C, reaction pressure of between -0.08 and 10MPa and weight space velocity of between 0.1 and 100 hours<-1>, the raw material and the catalyst contact and have the isomerization reaction of the double bonds of the butylene to generate an effluent substance with the molar ratio of butylenes-1 to butylenes-2 close to the thermodynamic equilibrium value, and the method well solves the problems and can be applied to industrial production of isomerization of double bonds of butylene.

Catalytic complexes including a metal atom having anionic ligands, at least one nucleophilic carbene ligand, and an alkylidene, vinylidene, or allenylidene ligand. The complexes are highly stable to air, moisture and thermal degradation. The complexes are designed to efficiently carry out a variety of olefin metathesis reactions.

A process for the production of at least one xylene isomer, paraxylene, metaxylene or orthoxylene from an aromatic feedstock that has 7 to 10 carbon atoms per molecule. The process comprises a stage for transalkylation of C7- and C9-aromatic compounds, a stage for separation of xylenes and a stage for isomerization of xylenes. The isomerization catalyst used in the process comprises at least one EUO zeolite composition whose crystals are grouped in aggregates that have a grain size with a value of Dv,90 less than or equal to 500 microns and at least one element of group VIII.

The present invention provides a process for natural gas in the form, e.g., of stranded gas or associated gas to transportable liquids. More particularly, the present invention provides a process in which the gas is non-oxidatively converted to aromatic liquid, preferably in proximity to the welihead, which may be onshore or offshore. In one aspect, the present invention provides integration of separation of wellhead fluids into associated gas and crude with blending of the aromatic liquid derived from the gas with the crude. Alternatively, or in combination, in another aspect, the present invention provides integration of conversion of byproduct hydrogen to power with non-oxidative conversion of gas to aromatic liquid.

Enabling a transalkylation process to handle both C₁₀ alkylaromatics and unextracted toluene permits the following improvements to be realized. No longer extracting toluene allows a reformate-splitter column to be eliminated. The extraction unit can be moved to the overhead of a benzene column and integrated together with the transalkylation unit to reduce costs. No longer requiring a rigorous split between C₉ and C₁₀ alkylaromatics allows a heavy aromatics column to be eliminated. Such an enabled transalkylation process requires stabilization of a transalkylation catalyst through the introduction of a metal function. These improvements result in an aromatics complex apparatus with savings on inside battery limits curve costs and an improvement on the return on investment in such a complex.

A process for transalkylating aromatic hydrocarbon compounds, the process comprising introducing an aromatic hydrocarbon feed stream and a water source to a transalkylation zone. The feed stream contacts a catalyst in the transalkylation zone in the presence of water, and produces a reaction product stream comprising benzene and xylene. The invention includes methods to control the transalkylation process.

A layered composition which can be used in various processes has been developed. The composition comprises an inner core such as a cordierite core and an outer layer comprising a refractory inorganic oxide, a fibrous component and an inorganic binder. The refractory inorganic oxide layer can be alumina, zirconia, titania, etc. while the fibrous component can be titania fibers, silica fibers, carbon fibers, etc. The inorganic oxide binder can be alumina, silica, zirconia, etc. The layer can also contain catalytic metals such as gold and platinum plus other modifiers. The layered composition is prepared by coating the inner core with a slurry comprising the refractory inorganic oxide, fibrous component, an inorganic binder precursor and an organic binding agent such as polyvinyl alcohol. The composition can be used in various hydrocarbon conversion processes.

The present invention relates to an olefin isomerization catalyst and a preparation method of the catalyst. The present invention mainly solves the problem that the former similar catalyst has the disadvantages of low specific surface area, little active sites and bad stability. The present invention solves the problem well by adopting a technical proposal that a proper hydroxyl polar solvent is selected; an alkaline earth oxide is hydrated, dried and calcined; the temperature and time are controlled during the course of preparation, and an olefin double-bond isomerization catalyst with larger specific surface area and more active sites is obtained, and which can be used for industrial productions of a dismutation of ethylene and butylene for producing propylene and a butylene double-bond isomerization.