C07C2523/84

PROCESS FOR PRODUCING COMPOUNDS, INCLUDING TRIPTANE BY AN ALCOHOL COUPLING REACTION

The present invention relates to a method for the production of molecules with seven carbons constituted by a chain of four carbons with three methyl branches, primarily triptane (2,2,3-trimethylbutane), by alcohol coupling reaction (Guerbet reaction), resulting in an alcohol with a four-carbon chain with three methyl branches, which is transformed into triptane. The importance of this method stems from the fact that triptane is the hydrocarbon with the greatest capacity to resist compression without ignition and can be used in unleaded aviation gasolines and in the formulation of high-octane automotive gasolines.

CATALYST, METHOD FOR PRODUCING COMPOUND USING SAME, AND COMPOUND

A catalyst containing, as an essential component, molybdenum; bismuth; and cobalt, in which, with respect to a peak intensity at 2θ=25.3°±0.2° in an X-ray diffraction pattern obtained by using CuKα rays as an X-ray source, a changing rate (Q1) per 1000 hours of reaction time represented by the following formulae (1) to (4) is 16 or less.


Q1={(U1/F1−1)×100}/T×1000  (1)


F1=(peak intensity of catalyst before oxidation reaction at 2θ=25.3°±)0.2°/(peak intensity of catalyst before oxidation reaction at 2θ=26.5°±0.2°)×100  (2)


U1=(peak intensity of catalyst after oxidation reaction at 2θ=25.3°±0.2°)/(peak intensity of catalyst after oxidation reaction at 2θ=26.5°±0.2°)×100  (3)


T=time (hr) during which oxidation reaction is carried out  (4)

Multimetallic catalysts for methanation of carbon dioxide and dry reforming of methane

Processes for forming multimetallic catalysts by grafting nickel precursors to metal oxide supports. Dry reforming reaction catalysts having nickel and promotors grafted to metal oxides supports. Methanation reaction catalysts having nickel and promotors grafted to metal oxides supports.

OXYGEN TRANSFER AGENTS FOR THE OXIDATIVE DEHYDROGENATION OF HYDROCARBONS AND SYSTEMS AND PROCESSES USING THE SAME

A oxygen transfer agent useful for the oxidative dehydrogenation of saturated hydrocarbons includes at least one mixed oxide derived from manganese or compounds thereof, as well as a promoter, such as tungsten and/or phosphorus. The oxygen transfer agent may also include an alkali metal or compounds thereof, boron or compounds thereof, an oxide of an alkaline earth metal, and an oxide containing one or more of one or more of manganese, lithium, boron, and magnesium. A reactor is at least partially filled with the oxygen transfer agent in the form of a fixed or circulating bed and provides an unsaturated hydrocarbon product, such as ethylene and/or propylene. The oxygen transfer agent may be regenerated using oxygen.

MULTIMETALLIC CATALYSTS FOR METHANATION OF CARBON DIOXIDE AND DRY REFORMING OF METHANE

Processes for forming multimetallic catalysts by grafting nickel precusors to metal oxide supports. Dry reforming reaction catalysts having nickel and promotors grafted to metal oxides supports. Methanation reaction catalysts having nickel and promotors grafted to metal oxides supports.

Supported Nanoparticle Compositions and Precursors, Processes for Making the Same and Syngas Conversion Processes

Disclosed are novel supported nanoparticle compositions, precursors, processes for making supported nanoparticle compositions, processes for making catalyst compositions, and processes for converting syngas. The catalyst composition can comprise nanoparticles comprising metal oxide(s), such as manganese cobalt oxide. This disclosure is particularly useful for converting syngas via the Fischer-Tropsch reactions to make olefins and/or alcohols.

TUNGSTEN-CONTAINING BULK CATALYSTS, METHOD OF MAKING THE SAME, AND THEIR USE IN LOW PRESSURE DIESEL HYDROPROCESSING

Compositions can include compounds having a formula: Co.sub.yW.sub.1-xMx0.sub.4 (I), wherein M is Mo, V, or Nb; 0.5≥x≥0; and 1<y≤4; and wherein the compound has an X-ray powder diffraction pattern including characteristic diffraction peaks having d-spacing values of about 2.90 Å, 2.56 Å, and 1.73 Å. Methods can include making a bulk catalyst composition including (i) combining tungstic acid and cobalt carbonate and (ii) reacting the tungstic acid and cobalt carbonate to form a catalyst composition, wherein the cobalt carbonate has an X-ray powder diffraction pattern including characteristic diffraction peaks having d-spacing values of about 10.03 Å, 5.91 Å, 4.35 Å, and 4.21 Å.

Reactor for oxidative conversion of hydrocarbon feeds

A system for oxidative conversion of a mixed hydrocarbon feed stream to a product stream containing at least one olefin is provided. The system includes a plurality of reactors each capable of oxidatively dehydrogenating at least a portion of a hydrocarbon in the mixed hydrocarbon feed, and each reactor able to operate at different set of reaction conditions from other reactors in the plurality of reactors. All of the reactors use the same oxygen transfer agent to produce at least one olefin. In some embodiments, at least one reactor is optimized to oxidatively couple methane to produce ethylene, while other reactors are optimized to oxidatively dehydrogenate ethane to ethylene or to oxidatively dehydrogenate propane to ethylene and/or propylene. All of the reactors feed into a single regeneration unit for the oxygen transfer agent. A method of oxidatively converting the mixed hydrocarbon feed to an olefin is also provided.

Supported nanoparticle compositions and precursors, processes for making the same and syngas conversion processes

Disclosed are novel supported nanoparticle compositions, precursors, processes for making supported nanoparticle compositions, processes for making catalyst compositions, and processes for converting syngas. The catalyst composition can comprise nanoparticles comprising metal oxide(s), such as manganese cobalt oxide. This disclosure is particularly useful for converting syngas via the Fischer-Tropsch reactions to make olefins and/or alcohols.

PROCESS FOR TRANSALKYLATING BENZENE
20200407290 · 2020-12-31 ·

Benzene is transalkylated with existing aromatic alkyl groups in a hydrocracking reactor by feeding a benzene stream and alkylated aromatic compounds to a hydrocracking unit. Alkyl groups migrate from heavier alkylated aromatic compounds to the benzene compounds during transalkylation in the hydrocracking unit. The hydrocracking conditions do not prevent the alkyl groups from transferring from one benzene ring to another benzene ring.