Intevep, S.a.

Ciemat

Ethz

Alfredo L Morales

Roberto E Galiasso

Angel R Carrasquel

Jose A Salazar

Domingo P Rodriguez

Aldo Steinfeld

Cesar Ovalles

Manuel Romero

Julian Blanco

Luis A Rivas

Nora Urbano

Philipp Haueter

Juan Carlos De Jesus

Dominic Trommer

Andreas Z'Graggen

Nelson P Martinez

Juan Jose Garcia

Jose A Salazar Guillen

Roberto E Galiasso Tailleur

Donald Huskey

Luig G Aquino

Maria M Agudelo

Jose A Guillen

Antonia Hamana

Magdalena M De Agudelo

Rafael Bolivar

Maria M Agudelu

An apparatus for thermochemical conversion of solid carbonaceous materials into fluid fuels using a fluid source of oxygen and an external source of concentrated radiation includes a reactor having a wall defining a cavity; a radiation inlet positioned in the wall for passing concentrated radiation into the cavity; and at least one inlet for introducing a fluid reactant flow of a source of oxygen and particles of carbonaceous material into direct exposure to the concentrated radiation in the cavity so as to heat and thermochemically convert the particles into fluid fuel. A process and system are also provided. The fluid source of oxygen is preferably steam and the carbonaceous material is preferably particles of petcoke.

Method for gasification of carbonaceous solid materials

Apparatus and gasification of carbonaceous solid materials

A process for thermochemical conversion of heavy oil and petroleum coke to fluid fuels includes the steps of: providing a fossil fuel selected from the group consisting of heavy oil, petroleum coke and mixtures thereof; and exposing the fossil fuel to an external source of concentrated radiation so as to increase the temperature of the fossil fuel, supply high-temperature heat required for the desired endothermic conversion process, and convert the fossil fuel to a product selected from the group consisting of hydrogen, carbon monoxide, gaseous hydrocarbons and mixtures thereof.

Process for converting heavy crude oils and petroleum coke to syngas using external source of radiation

A process comprises providing a catalyst comprising a support, a microwave absorption material, and a catalytically active phase; heating the catalyst with a source of microwave energy which is absorbed by said microwave absorption material to increase the temperature of the catalyst to a desired temperature; and contacting said heated catalyst with a hydrocarbon feedstock for upgrading same.

Microwave heated catalyst and process

Process obtains improved viscosity and improved distillates proportion in heavy hydrocarbons, as heavy crude oil, by providing a feedstock of heavy hydrocarbons containing a water content of greater than or equal to 1% with respect to the weight of the hydrocarbons and reacting said hydrocarbons with a gas containing methane under pressure and at an elevated temperature.

Process for treating heavy crude oil

The present invention relates to a hydrocatalytic process for treating vacuum gas oils, residual feedstocks or mixtures thereof in the presence of up to 100 ppm of V and Ni at moderate hydrogen partial pressures. The process consists of two or more stages: (a) demetallization of feedstock to levels below 10 ppm of V and Ni, and (b) hydrodenitrogenation and hydroconversion of catalysts using a combined bed, and catalytic cracking of the 370.degree. C..+-. fraction to obtain gasolines. This process applies also to vacuum gas oils obtained from other processes, such as FCC, Flexicoque, etc.

Hydrocracking high residual contained in vacuum gas oil

A cobalt-molybdenum catalyst and a method for preparing same, said catalyst useful for the hydrodesulfurization (HDS) and hydrodenitrogenation (HDN) of distillates of petroleum. The catalyst is supported by aluminum phosphate or an aluminum borate. In a preferred embodiment the catalyst has a low cobalt content, between 0.5% and 2.0% by weight calculated as CoO, and a molybdenum content of between 10% and 20% by weight, calculated as MoO.sub.3. The phosphorus or boron compounds added to the aluminum before the impregnation of the active metals prevents the formation of undesirable compounds of the CoAl.sub.2 O.sub.4 type, which is inactive in HDS. It is for that reason that the catalyst has a formulation with 70% less cobalt than the previous state-of-the-art catalysts. Very small crystals, highly dispersed on the surface of the catalyst, whose formula is CoMoO.sub.4, are responsible for the stability and the high level of activity in HDS and HDN which results.

Catalyst for hydrotreatment of distillates of petroleum and method for

A catalyst for the hydrotreatment of heavy crudes and their residues, and a method of preparing same, is disclosed, which has significant simultaneous hydrodemetallizing and hydrodesulfurizing activity. The catalyst is prepared by successively impregnating an extruded refractory support with a Group VIb and a Group VIII metal, calcining the pellet thus produced, and presulfurizing same. Pore volume of the catalyst ranges between 0.50 and 1.2 ml/g, total surface area ranges between 120 and 140 m.sup.2 /g, at least 60% of said pore volume consists of pores having diameters greater than 100 .ANG., and x-ray photoelectron spectroscopy signal band strength ratios are as follows: I(Me VIb)/I(refractory metal) is between 5 and 8, and I(Me VIII)/I(refractory metal) is between 1 and 5. The novel catalyst has a useful life greater than conventional catalysts for the simultaneous hydrodemetallization and hydrodesulfurization of continuous feeds of heavy hydrocarbons, as shown by the fact that it exhibits no substantial reduction in catalytic activity over an 80 day period.

Catalyst for removing sulfur and metal contaminants from heavy crudes

A catalyst for use in the mild hydrocracking (MHC) of heavy vacuum gas oils to produce middle distillates and a method for the preparation of the catalyst and a process for treating the heavy vacuum gas oils with the catalyst. The catalyst comprises molybdenum, nickel and phosphorus supported on gamma alumina. The catalyst of the invention possesses a P/Mo+Ni ratio between 0.7 and 1.1, which endows it with a high capacity for hydrodesulfurization (HDS), hydrodenitrogenation (HDN) and hydroconversion of the fraction which can be distilled at 370.degree. C.+ to middle distillates, when the catalyst is used under MHC conditions, that is, T=variable, P=750 psig, LHSV=0.70 m.sup.3 /m.sup.3 h and the ratio H.sub.2 /VGO=300 Nm.sup.3 /m.sup.3. The new catalyst can operate for more than 26 months, maintaining a consistent conversion of 20% and achieving the sulfur and nitrogen requirements in the product obtained.

Catalyst for the hydrocracking of heavy vacuum gas oils, method of

Heavy crudes or vacuum residues are treated in a thermal hydroconversion process in the presence of a metal catalyst from Groups IVb, Vb, VIb, VIIb and VIII of the Periodic Table of Elements and water. Fresh catalyst is introduced into the process as a soluble, metallic catalyst precursor which is then decomposed while feedstock admixed with water is preheated to a temperature of at least about 230.degree. C. but no more than about 420.degree. C.

Hydroconversion of heavy crudes with high metal and asphaltene content

A catalyst for the hydrotreatment of heavy crudes and their residues, and a method of preparing same, is disclosed, which has significant simultaneous hydrodemetallizing and hydrodesulfurizing activity. The catalyst is prepared by successively impregnating an extruded refractory support with a Group VIb and a Group VIII metal, calcining the pellet thus produced, and presulfurizing same. Pore volume of the catalyst ranges between 0.50 and 1.2 ml/g, total surface area ranges between 120 and 400 m.sup.2 /g, at least 60% of said pore volume consists of pores having diameters greater than 100 .ANG., and X-ray photoelectron spectroscopy signal band strength ratios are as follows: I(Me VIb)/I(refractory metal) is between 5 and 8, and I(Me VIII)/I(refractory metal) is between 1 and 5. The novel catalyst has a useful life greater than conventional catalysts for the simultaneous hydrodemetallization and hydrodesulfurization of continuous feeds of heavy hydrocarbons, as shown by the fact that it exhibits no substantial reduction in catalytic activity over an 80 day period.

A new active stable catalyst for use in the removal of sulphur, nitrogen, contaminating metals, asphaltenes and Conradson carbon from heavy crudes and residues and, in particular, a method for the preparation of the catalyst and a process for the treatment of heavy crudes and residues with the catalyst. The catalyst comprises a hydrogenation component selected from Group VIB of the Periodic Table, a hydrogenation component selected from Group VIII of the Periodic Table and a phosphorus oxide component as active components all supported on an alumina carrier. The catalyst is made up of a dispersion of the above metals on the surface of the alumina carrier such that, when the catalyst is sulphided under specific conditions, catalytic activities such as hydrodesulphurization (HDS), hydrodenitrogenation (HDN) and hydrodemetallization (HDM) and the conversion of asphaltenes and Conradson carbon are improved. In addition, due to the phosphorus oxide, the catalyst does not contain aluminum oxides of the Group VIII and Group VIB metals which are undesirable compounds generally present in known catalysts.

Process for demetallization of heavy crudes using a catalyst having high

A catalyst for the hydrotreatment of heavy crudes and residues and a method for the preparation thereof are claimed, specifying an amount of Group VIb metallic hydrogenation compound irreversibly absorbed by the silica or alumina extruded support structure surface to be between 0.5 and 3% of the dried and calcined catalyst by weight. The percentage limit on the hydrogenation compound can be achieved by either obtaining a dense alumina support structure having a novel pore diameter distribution, or treating a prior art support with an absorption site restricter such as MgO prior to hydrogenation compound impregnation. Subsequent fabrication steps comprise washing, drying, calcining and presulfurizing. The resultant catalyst has a monolayer of hydrogenating compound deposited on the reaction surface, and interfering compounds such as massive MoO.sub.3, Al(MoO.sub.4).sub.3 or polymolybdates are not formed. The unimetallic catalyst is demonstrated to be comparable or superior to a bimetallic catalyst employing five times as much hydrogenating metal, and has superior service life due to uniform metal contaminant deposition throughout the catalyst interior.

Process for catalyst preparation for the hydrodemetallization of heavy

A new active stable catalyst for use in the removal of sulphur, nitrogen, contaminating metals, asphaltenes and Conradson carbon from heavy crudes and residues and, in particular, a method for the preparation of the catalyst and a process for the treatment of heavy crudes and residues with the catalyst. The catalyst comprises a hydrogenation component selected from Group VIB of the Periodic Table, a hydrogenation component selected from Group VIII of the Periodic Table and a phosphorus oxide component as active components all supported on an alumina carrier. The catalyst is made up of a dispersion of the above metals on the surface of the alumina carrier such that, when the catalyst is sulphided under specific conditions, catalytic activities such as hydrodesulphurization (HDS), hydrodenitrogenation (HDN) and hydrodemetallization (HDM) and the conversion of asphaltenes and Conradson carbon are improved.

Growing community of inventors

San Antonio de Los Altos, Venezuela

Alfredo L Morales