An integrated process for maximizing recovery of hydrogen is provided. The process comprises: providing a hydrocarbonaceous feed comprising naphtha, and a hydrogen stream to a reforming zone, wherein the hydrogen stream is obtained from at least one of a hydrocracking zone, a transalkylation zone, and an isomerization zone. The hydrocarbonaceous feed is reformed in the reforming zone in the presence of the hydrogen stream and a reforming catalyst to provide a reformate effluent stream. At least a portion of the reformate effluent stream is passed to a debutanizer column of the reforming zone to provide a net hydrogen stream and a fraction comprising liquid petroleum gas (LPG). At least a portion of the net hydrogen stream is recycled to the reforming zone as the hydrogen stream.

The invention relates to a reforming catalyst. The reforming catalyst comprises a reforming metal, such as Pt, a support, such as an alumina support, and a USY zeolite, which has had part of its aluminum framework substituted with Zr and Ti. The amount of USY zeolite does not exceed 5 wt %, and most preferably, contains 2-3 wt % USY zeolite.

The group of inventions relates to a process of co-converting hydrocarbon feedstock with a high content of unsaturated hydrocarbons and aliphatic alcohols into components of high octane gasolines or aromatic hydrocarbons, as well as to catalysts of such a co-conversion. The method of co-converting hydrocarbon fractions and oxygenates into high octane components of fuels or aromatic hydrocarbons including contacting a hydrocarbon stream mixed with oxygenates with a catalyst under a reduced pressure and with heating. The process is carried under using a catalyst that contains the HZSM-5 zeolite that passed thermal and steam treatment.

The invention relates to the field of gas chemistry and, more specifically, to methods and devices for producing aromatic hydrocarbons from natural gas, which involve producing synthesis gas, converting same into methanol producing, from the methanol, in the presence of a catalyst, a concentrate of aromatic hydrocarbons and water, separating the water, air stripping hydrocarbon residues from the water, and separating-out the resultant concentrate of aromatic hydrocarbons and hydrogen-containing gas, the latter being at least partially used in the production of synthesis gas to adjust the ratio therein of H.sub.2:CO 1.8-2.3:1, and can be used for producing aromatic hydrocarbons. According to the invention, the production of aromatic hydrocarbons from methanol in the presence of a catalyst is carried out in two consecutively-connected reactors for synthesizing aromatic hydrocarbons: in a first, low-temperature isothermal reactor for synthesizing aromatic and aliphatic hydrocarbons, and in a second, high-temperature adiabatic reactor for synthesizing aromatic and aliphatic hydrocarbons from aliphatic hydrocarbons formed in the first reactor, and the subsequent stabilization thereof in an aromatic hydrocarbon concentrate stabilization unit. At least a portion of the hydrogen-containing gas is fed to a synthesis gas production unit and is used for producing synthesis gas using autothermal reforming technology. The installation carries out the method. The achieved technical result consists in increasing the efficiency of producing concentrates of aromatic hydrocarbons.

A hydrocarbon conversion catalyst composition which comprises dealuminated ZSM-48 and/or EU-2 zeolite and a refractory oxide binder essentially free of alumina, processes for preparing such composition and processes for converting hydrocarbon feedstock with the help of such compositions.

A method of making a multifunctional catalyst for upgrading pyrolysis oil includes contacting a zeolite support with a solution including at least a first metal catalyst precursor and a second metal catalyst precursor, the first metal catalyst precursor, the second metal catalyst precursor, or both, including a heteropolyacid. Contacting the zeolite support with the solution deposits or adsorbs the first metal catalyst precursor and the second catalyst precursor onto outer surfaces and pore surfaces of the zeolite support to produce a multifunctional catalyst precursor. The method further includes removing excess solution from the multifunctional catalyst precursor and calcining the multifunctional catalyst precursor to produce the multifunctional catalyst comprising at least a first metal catalyst and a second metal catalyst deposited on the outer surfaces and pore surfaces of the zeolite support.

A process for the production of middle distillates by the catalytically promoted hydration of olefinic compounds having a carbon number ranging from 7 to 14 to convert the olefins to the corresponding mixed alcohols having a higher boiling point that is in the diesel range, the process being conducted in a continuous stirred tank reactor, e.g., an ebullated-bed reactor, utilizing catalysts that include soluble homogeneous acidic compounds and solid heterogeneous compounds such as resins, and amorphous or structured metal oxides containing elements selected from IUPAC Groups 4-10, 13 and 14, and having Lewis or Bronsted acid sites.

A process for the production of middle distillates by the catalytically promoted hydration of olefinic compounds having a carbon number ranging from 7 to 14 to convert the olefins to the corresponding mixed alcohols having a higher boiling point that is in the diesel range, the process being conducted in a continuous stirred tank reactor, e.g., an ebullated-bed reactor, utilizing catalysts that include soluble homogeneous acidic compounds and solid heterogeneous compounds such as resins, and amorphous or structured metal oxides containing elements selected from IUPAC Groups 4-10, 13 and 14, and having Lewis or Bronsted acid sites.

Systems for reforming a feedstock comprising paraffins and naphthenes. A first reactor containing a first reforming catalyst is operable to maintain a temperature and pressure that facilitates conversion of naphthenes in the feedstock to aromatics while facilitating conversion of less than 50 wt. % of paraffins in the feedstock to olefins. A first separator receives and separates the first effluent that is produced in the first reactor to produce a first fraction enriched in aromatics and a second fraction enriched in paraffins. A second reactor containing a second reforming catalyst is operable to maintain a temperature and pressure that facilitates conversion of at least 50 wt. % of paraffins in the second fraction to olefins. The system is operable to produce a liquid hydrocarbon product suitable for use as a blend component of a liquid transportation fuel.

Systems for reforming a feedstock comprising paraffins and naphthenes. A first reactor containing a first reforming catalyst is operable to maintain a temperature and pressure that facilitates conversion of naphthenes in the feedstock to aromatics while facilitating conversion of less than 50 wt. % of paraffins in the feedstock to olefins. A first separator receives and separates the first effluent that is produced in the first reactor to produce a first fraction enriched in aromatics and a second fraction enriched in paraffins. A second reactor containing a second reforming catalyst is operable to maintain a temperature and pressure that facilitates conversion of at least 50 wt. % of paraffins in the second fraction to olefins. The system is operable to produce a liquid hydrocarbon product suitable for use as a blend component of a liquid transportation fuel.