Patent classifications
B01J27/055
Oxidative conversion of hydrocarbons using sulfur oxides as oxygen carriers
The oxidative coupling of methane (OCM) and the oxidative dehydrogenation (ODH) of ethane and higher hydrocarbons is described using SO.sub.3 and sulfate, sulfite, bisulfite and metabifulfite salts as oxygen transfer agents in the presence of one or more elements selected from Groups 3 to 14 of the periodic table, optionally further in the presence of alkali or alkaline salts and/or sulfur-containing compounds.
SHAPED CATALYST BODY IN THE FORM OF TETRALOBES OF UNIFORM WALL THICKNESS
The invention relates to a shaped catalyst body in the form of a tetralobe having four circular through-passages, with the midpoints of the through-passages forming a square and the spacings between in each case two adjacent through-passages being from 0.8 to 1.2 times the thickness of the outer walls of the through-passages. The shaped catalyst body is used for the oxidation of S02 to S03.
SHAPED CATALYST BODY IN THE FORM OF TETRALOBES OF UNIFORM WALL THICKNESS
The invention relates to a shaped catalyst body in the form of a tetralobe having four circular through-passages, with the midpoints of the through-passages forming a square and the spacings between in each case two adjacent through-passages being from 0.8 to 1.2 times the thickness of the outer walls of the through-passages. The shaped catalyst body is used for the oxidation of S02 to S03.
ENHANCED OXYGEN TRANSFER AGENT SYSTEMS FOR OXIDATIVE DEHYDROGENATION OF HYDROCARBONS
Enhanced oxygen transfer agent systems and methods of use thereof are provided. According to one aspect, a method for producing olefins from a hydrocarbon feed includes the step of contacting a hydrocarbon feed comprised of one or more alkanes with an oxygen transfer agent at a temperature of 350° C. to 1000° C. The oxygen transfer agent includes an oxygen-donating chalcogen agent including at least one of S, Se, or Te and a reducible metal oxide. The chalcogen has an oxidation state greater than +2. A method for producing one or more olefins by partial combustion of a hydrocarbon feed is provided. The method includes partially combusting a hydrocarbon feed comprised of one or more alkanes by contacting the hydrocarbon feed with an oxygen transfer agent comprising CaSO.sub.4 at a temperature of 350° C. to 1000° C. to produce one or more olefins comprising ethylene and coproducing water.
ENHANCED OXYGEN TRANSFER AGENT SYSTEMS FOR OXIDATIVE DEHYDROGENATION OF HYDROCARBONS
Enhanced oxygen transfer agent systems and methods of use thereof are provided. According to one aspect, a method for producing olefins from a hydrocarbon feed includes the step of contacting a hydrocarbon feed comprised of one or more alkanes with an oxygen transfer agent at a temperature of 350° C. to 1000° C. The oxygen transfer agent includes an oxygen-donating chalcogen agent including at least one of S, Se, or Te and a reducible metal oxide. The chalcogen has an oxidation state greater than +2. A method for producing one or more olefins by partial combustion of a hydrocarbon feed is provided. The method includes partially combusting a hydrocarbon feed comprised of one or more alkanes by contacting the hydrocarbon feed with an oxygen transfer agent comprising CaSO.sub.4 at a temperature of 350° C. to 1000° C. to produce one or more olefins comprising ethylene and coproducing water.
Oxygen transfer agent conditioning systems and methods
Improvements in the commercial viability of oxygen transfer agents (OTAs) and/or catalysts associated with the OCM and the ODH of hydrocarbons to olefins through enhancement of one or more of the selectivity, yield, rate and lifetime of the OTA and/or catalyst is described by one or more of (i) exposing the OTA or the catalyst to a sulfur-containing compound at a site or at a time that is different from where and when the saturated hydrocarbon is converted by the OTA or the catalyst to an unsaturated hydrocarbon; (ii) increasing the particle density of the OTA or the catalyst by treating the OTA or the catalyst with a reducing agent at a site different from where the saturated hydrocarbon is converted by the OTA or by the catalyst to an unsaturated hydrocarbon; and (iii) removing non-selective redox oxygen (NSRO) present on the OTA by subjecting the OTA to a gas that is substantially free of any molecular oxygen.
Oxygen transfer agent conditioning systems and methods
Improvements in the commercial viability of oxygen transfer agents (OTAs) and/or catalysts associated with the OCM and the ODH of hydrocarbons to olefins through enhancement of one or more of the selectivity, yield, rate and lifetime of the OTA and/or catalyst is described by one or more of (i) exposing the OTA or the catalyst to a sulfur-containing compound at a site or at a time that is different from where and when the saturated hydrocarbon is converted by the OTA or the catalyst to an unsaturated hydrocarbon; (ii) increasing the particle density of the OTA or the catalyst by treating the OTA or the catalyst with a reducing agent at a site different from where the saturated hydrocarbon is converted by the OTA or by the catalyst to an unsaturated hydrocarbon; and (iii) removing non-selective redox oxygen (NSRO) present on the OTA by subjecting the OTA to a gas that is substantially free of any molecular oxygen.
Enhanced oxygen transfer agent systems for oxidative dehydrogenation of hydrocarbons
Aspects of the invention relate to enhanced oxygen transfer agent systems and methods of use thereof. According to one aspect, a method for producing olefins from a hydrocarbon feed includes the step of contacting a hydrocarbon feed comprised of one or more alkanes with an oxygen transfer agent at a temperature of 350° C. to 1000° C. The oxygen transfer agent comprising an oxygen-donating chalcogen agent comprised of at least one of S, Se, or Te and a reducible metal oxide. The chalcogen having an oxidation state greater than +2. According to another aspect, a method for producing one or more olefins by partial combustion of a hydrocarbon feed includes partially combusting a hydrocarbon feed comprised of one or more alkanes by contacting the hydrocarbon feed with an oxygen transfer agent comprising CaS0.sub.4 at a temperature of 350° C. to 1000° C. to produce one or more olefins comprising ethylene and coproducing water.
Enhanced oxygen transfer agent systems for oxidative dehydrogenation of hydrocarbons
Aspects of the invention relate to enhanced oxygen transfer agent systems and methods of use thereof. According to one aspect, a method for producing olefins from a hydrocarbon feed includes the step of contacting a hydrocarbon feed comprised of one or more alkanes with an oxygen transfer agent at a temperature of 350° C. to 1000° C. The oxygen transfer agent comprising an oxygen-donating chalcogen agent comprised of at least one of S, Se, or Te and a reducible metal oxide. The chalcogen having an oxidation state greater than +2. According to another aspect, a method for producing one or more olefins by partial combustion of a hydrocarbon feed includes partially combusting a hydrocarbon feed comprised of one or more alkanes by contacting the hydrocarbon feed with an oxygen transfer agent comprising CaS0.sub.4 at a temperature of 350° C. to 1000° C. to produce one or more olefins comprising ethylene and coproducing water.
Vanadium-based catalyst and preparation method therefor
A vanadium-based catalyst comprises an active phase carried on a carrier. The active phase comprises vanadium oxide, potassium sulfate, sodium sulfate, and assistants. The carrier comprises ultra-large-pore silicon dioxide and diatomite, the average pore size of the ultra-large-pore silicon dioxide ranges from 100 nm to 500 nm, and the diatomite is a refined diatomite having a silicon dioxide content of higher than 85% after refinement. The preparation method for the vanadium-based catalyst comprises: 1) mixing potassium vanadium and potassium hydroxide, and allowing a prepared mixed solution and sulfuric acid to carry out a neutralization reaction; and 2) mixing a neutralization reaction product in step 1) with the carrier and sodium sulfate, and carrying out rolling, band extrusion, drying and roasting to prepare the vanadium-based catalyst, assistant compounds being added in step 1) and/or step 2).