Isomerizing dehydration of feedstock containing a primary alcohol substituted in position 2 by an alkyl group in which the feedstock is heated to the reaction temperature by indirect heat exchange then vaporization by mixing with a diluent effluent, the diluted and vaporized feedstock being dehydrated in at least one dehydration reactor operating in gas phase at an inlet temperature comprised between 250 and 375° C., at a pressure comprised between 0.2 MPa and 1 MPa and at a WHSV comprised between 1 and 18 h.sup.−1, in the presence of a catalyst comprising a zeolite having at least one series of channels the opening of which is defined by a ring with 8 oxygen atoms (8MR) and a binder, the catalyst being coked beforehand in-situ or ex-situ, so as to produce a dehydration effluent, the latter being treated and separated into a diluent effluent, an alkenes effluent and a heavy hydrocarbons effluent.

Disclosed is a composition useful in the hydrolysis of sulfur compounds that are contained in a gas stream. The composition comprises a calcined co-mulled mixture of psuedoboehmite, a cobalt compound, and a molybdenum compound such that the composition comprises gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt. The composition is made by forming into an agglomerate a co-mulled mixture pseudoboehmite, a cobalt component, and a molybdenum component followed by drying and calcining the agglomerate to provide a catalyst composition comprising gamma-alumina, at least 7.5 wt. % molybdenum, and at least 2.75 wt. % cobalt.

Disclosed are a catalyst system and its use in a process for the conversion of a feedstock containing C.sub.8+ aromatic hydrocarbons to produce light aromatic products, comprising benzene, toluene and xylene. The catalyst system comprises (a) a first catalyst bed comprising a first catalyst composition, said first catalyst composition comprising a zeolite having a constraint index of 3 to 12 combined (i) optionally with at least one first metal of Group 10 of the IUPAC Periodic Table, and (ii) optionally with at least one second metal of Group 11 to 15 of the IUPAC Periodic Table; and (b) a second catalyst bed comprising a second catalyst composition, said second catalyst composition comprising (i) a meso-mordenite zeolite, combined (ii) optionally with at least one first metal of Group 10 of the IUPAC Periodic Table, and (iii) optionally with at least one second metal of Group 11 to 15 of the IUPAC Periodic Table, wherein said meso-mordenite zeolite is synthesized from TEA or MTEA and having a mesopore surface area of greater than 30 m.sup.2/g and said meso-mordenite zeolite comprises agglomerates composed of primary crystallites, wherein said primary crystallites have an average primary crystal size as measured by TEM of less than 80 nm and an aspect ratio of less than 2.

A catalyst fibrous structure having a catalyst metal carried on a fibrous structure, wherein (a) a Log differential micropore volume distribution curve thereof obtained by measurement using a mercury intrusion technique has a peak having a maximum micropore diameter in the range of from 0.1 μm to 100 μm; (b) a Log differential micropore volume at the peak is 0.5 mL/g or more; and (c) an amount of a catalyst metal compound and a binder carried per unit volume is 0.05 g/mL or more. A production method for producing a catalyst fibrous structure having: (1) mixing a catalyst metal compound or a catalyst precursor, and an inorganic binder and a solvent; (2) grinding the mixture to obtain a coating material of the catalyst metal compound or the catalyst precursor having a median particle diameter of 2 μm or less and a viscosity of from 10 mPa.Math.s to 200 mPa.Math.s; (3) impregnating a fibrous structure with the coating material to fill up voids of the fibrous structure with the coating material of the catalyst metal compound or the catalyst precursor; (4) heating and drying the fibrous structure, directly as it is, at a temperature not lower than the boiling point of the solvent; and (5) heating and calcination the dried fibrous structure at a temperature not lower than the dehydration temperature of the inorganic binder to obtain a catalyst fibrous structure.

An ebullated bed process for the hydroconversion of heavy hydrocarbon feedstocks that provides for high conversion of the heavy hydrocarbon with a low sediment yield. The process uses for its catalyst bed small particles of a specifically defined shaped hydroprocessing catalyst which is contacted with the heavy hydrocarbon feedstock under hydroconversion conditions and yields a hydrocarbon conversion having a relatively low sediment content.

An improved method of operating a conventional ebullated bed process for the hydroconversion of heavy hydrocarbon feedstocks so as to provide for low or reduced sediment content in the conversion product without the loss of hydrodesulfurization function.

An ebullated bed process for the hydroconversion of heavy hydrocarbon feedstocks that provides for high conversion of the heavy hydrocarbon with a low sediment yield. The process uses for its catalyst bed an impregnated shaped ebullated bed catalyst having a low macroporosity and a geometry such that its characteristic cross section perimeter-to-cross sectional area is within a specifically defined range.

An alumina support for a catalyst for a gas-phase reaction that increases the catalytic activity and allows a reduction in by-product yield, and a catalyst for a gas-phase reaction that is a metal compound supported on the alumina support are provided. The alumina support for a catalyst for a gas-phase reaction has a tubular shape with at least one hollow through hole and a BET specific surface area of 140 to 280 m.sup.2/g. In this alumina support, a volume (total pore volume) of pores with a diameter of not less than 15 nm and not more than 20000 nm is 0.04 to 0.15 cm.sup.3/g, and a volume of pores with a diameter of not less than 1000 nm and not more than 20000 nm is 0.02 cm.sup.3/g or less, as measured by the mercury intrusion technique, and a tapped bulk density is 620 to 780 g/L.

The invention relates to a method for producing catalysts by the method of combustion in solution, to the catalysts produced by said method, and to the particular use thereof in the reverse water-gas shift reaction and in the partial oxidation of the methane into synthesis gas. Therefore, it is understood that the present invention pertains to the area of the green industry aimed at the reduction of CO.sub.2 on the planet.

A novel MFI zeolite that when used as a catalyst, can be used for a selective catalytic reaction for larger molecules and provides a method for producing the MFI zeolite. The MFI zeolite includes uniform mesopores having a pore distribution curve which a peak-width thereof at half height (hw) is at most 20 nm (hw≦20 nm) and a center value (μ) of a maximum peak is 10 nm or more and 20 nm or less (10 nm≦μ≦20 nm), and having a pore volume (pv) of the uniform mesopores of at least 0.05 mL/g (0.05 mL/g≦pv); the MFI zeolite has no peak in a range of 0.1° to 3° in powder X-ray diffraction measurement with a diffraction angle represented by 2θ; and the MFI zeolite has an average particle diameter (PD) of at most 100 nm (PD≦100 nm).