WO2009048724A2 - Compositions for catalytic gasification of a petroleum coke and process for their conversion to methane - Google Patents

Compositions for catalytic gasification of a petroleum coke and process for their conversion to methane Download PDF

Info

Publication number
WO2009048724A2
WO2009048724A2 PCT/US2008/076991 US2008076991W WO2009048724A2 WO 2009048724 A2 WO2009048724 A2 WO 2009048724A2 US 2008076991 W US2008076991 W US 2008076991W WO 2009048724 A2 WO2009048724 A2 WO 2009048724A2
Authority
WO
WIPO (PCT)
Prior art keywords
gasification
particulate composition
petroleum coke
calcium
alkali metal
Prior art date
Application number
PCT/US2008/076991
Other languages
French (fr)
Other versions
WO2009048724A3 (en
Inventor
Yasuo Ohtsuka
Original Assignee
Greatpoint Energy, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Greatpoint Energy, Inc. filed Critical Greatpoint Energy, Inc.
Publication of WO2009048724A2 publication Critical patent/WO2009048724A2/en
Publication of WO2009048724A3 publication Critical patent/WO2009048724A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L5/00Solid fuels
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/46Gasification of granular or pulverulent flues in suspension
    • C10J3/463Gasification of granular or pulverulent flues in suspension in stationary fluidised beds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L5/00Solid fuels
    • C10L5/02Solid fuels such as briquettes consisting mainly of carbonaceous materials of mineral or non-mineral origin
    • C10L5/34Other details of the shaped fuels, e.g. briquettes
    • C10L5/36Shape
    • C10L5/366Powders
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L9/00Treating solid fuels to improve their combustion
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0903Feed preparation
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/0943Coke
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0973Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0983Additives
    • C10J2300/0986Catalysts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/1853Steam reforming, i.e. injection of steam only
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Definitions

  • the present invention relates particulate compositions of a crude oil resid-based petroleum coke containing at least two preselected catalytic components, which composition exhibits an efficient, enhanced-yielding gasification to value-added gaseous products, particularly when used in a steady-state integrated gasification process. More particularly, this invention concerns compositions of a petroleum coke loaded with a mixture of (i) an alkali metal component, and (ii) a calcium component.
  • the present invention further relates to processes wherein these particulate compositions, in the presence of steam, exhibit gasification activity, and thereby form value-added gaseous products including methane and one or more of hydrogen, carbon monoxide and other higher hydrocarbons.
  • Petroleum coke is a generally solid carbonaceous residue derived from delayed coking or fluid coking a carbon source such as a crude oil resid. Petroleum coke in general has a poorer gasification reactivity, particularly at moderate temperatures, than does bituminous coal due, for example, to its highly crystalline carbon and elevated levels of organic sulfur derived from heavy-gravity oil. Use of catalysts is necessary for improving the lower reactivity of petroleum cokes.
  • the present invention is directed to the gasification of a petroleum coke derived from a crude oil resid, for example, by coking processes used for upgrading heavy-gravity residual crude oil, which petroleum coke contains ash but as a minor component, typically about 1.0 wt% or less, and more typically about 0.5 wt% of less, based on the weight of the coke.
  • the ash in such lower-ash cokes predominantly comprises metals such as nickel and vanadium.
  • the present invention is directed to particulate compositions of such petroleum coke containing at least two preselected components that exhibit an efficient, enhanced-yielding gasification to value-added gaseous products. More particularly, the present invention is a particulate composition having a particle distribution size suitable for gasification in a fluidized bed zone, comprising an intimate mixture of (A) a petroleum coke derived from crude oil comprising ash in an amount of about 1.0 wt% or less, based on the weight of the petroleum coke, and (B) a gasification catalyst which under suitable conditions of temperature and pressure and in the presence of steam exhibits gasification activity whereby value added gaseous products are formed, wherein:
  • the gasification catalyst comprises (i) a first component which is a source of at least one alkali metal, and (ii) a second component which is a source of calcium; and
  • compositions of the present invention are particularly useful for catalytic gasification of petroleum coke at moderate temperatures, such as disclosed in US2007/0083072A1.
  • compositions and process according to the invention can be readily incorporated into fluidized bed gasification units, and can result in a more cost-effective, high-yielding production of methane gas.
  • the present invention also provides a process for converting petroleum coke to methane, comprising the steps of:
  • the petroleum coke utilized in the present invention is derived from a crude oil, for example, by coking processes used for upgrading heavy-gravity residual crude oil, which petroleum coke contains ash but as a minor component, typically about 1.0 wt% or less, and more typically about 0.5 wt% of less, based on the weight of the coke.
  • the ash in such lower-ash cokes predominantly comprises metals such as nickel and vanadium.
  • the petroleum coke preferably comprises at least about 70 wt% carbon, and alternatively at least about 80 wt% carbon, based on the weight of the petroleum coke.
  • the petroleum coke comprises less than about 20 wt% percent inorganic compounds, based on the weight of the petroleum coke.
  • the petroleum coke is utilized in particulate form as a fine powder having a particle size distribution suitable for gasification in a fluidized bed zone, which size also facilitates efficient catalyst loading.
  • the ground coke (and resulting composition) has a particle size preferably ranging from about 25 microns, or from about 45 microns, to about 2500 microns, or to about 500 microns. Petroleum coke can be ground by any methods known to the art.
  • Particulate compositions according to the present invention are based on the above-described petroleum coke, and contain (i) an amount of an alkali metal component, as alkali metal and/or a compound containing alkali metal, sufficient to provide, in the composition, a ratio of alkali metal atoms to carbon atoms in the range of from about 0.01 to about 0.1 , or in a range from about 0.01 to about 0.08, or in a range from about 0.01 to about 0.05; and (ii) an amount of calcium component, as calcium metal and/or a compound containing calcium, sufficient to provide, in the composition, a ratio of calcium atoms to carbon atoms in the range of from about 0.01 to about 0.1 , or in a range from about 0.01 to about 0.08, or in a range from about 0.01 to about 0.05.
  • an alkali metal component as alkali metal and/or a compound containing alkali metal
  • the alkali metal component is typically loaded to achieve an alkali metal content of from about 3 to about 10 times more than the ash content of the petroleum coke, on a mass basis.
  • the ratio of alkali metal atoms to calcium atoms can range from about
  • Suitable alkali metals are lithium, sodium, potassium, rubidium and cesium, and potassium is preferred.
  • Particulate compositions in accordance with the present invention can be prepared by a process comprising the steps of: (a) grinding a petroleum coke, and (b) soaking the ground coke in a catalyst-containing solution for a contact time and at a temperature so as to provide ample opportunity to achieve substantial and uniform catalyst loading.
  • the soaked catalyst-loaded coke can be recovered and used as such or, more preferably, can be further processed prior to gasification as disclosed in US2007/0083072A1.
  • the finely ground coke is soaked as a slurry in a catalyst-rich solution, preferably of a salt of a catalysts.
  • the solution is in an aqueous medium.
  • other liquids such as ethanol may be used.
  • a slurry mixture is useful, for example, a mixture of an aqueous potassium hydroxide and calcium hydroxide powder.
  • Suitable alkali metal catalyst salts include, but are not limited to, carbonate, hydroxide, acetate, halide and nitrate salts.
  • carbonate or hydroxide salts are used and, more preferably, carbonate salts are used.
  • potassium carbonate is used.
  • Suitable calcium salts include, but are not limited to, hydroxide, acetate, halide and nitrate salts. In preferred embodiments, nitrate and acetate salts are used.
  • the total amount of catalyst loaded is controlled by controlling the concentration of catalyst components in the solution, as well as the contact time, temperature and method, as can be readily determined by those of ordinary skill in the relevant art based on the characteristics of the starting petroleum coke.
  • the particulate compositions of the present invention are particularly useful in integrated gasification processes for converting petroleum coke to combustible gases, such as methane.
  • the particulate compositions of the present invention provide a suitable feedstream of catalyst-containing petroleum coke to any steam gasification process.
  • steam gasification processes provide a means for the introducing of dry particulate feed into a fluidized bed zone in a gasification reactor.
  • Coke and superheated steam are reacted while in contact with the catalyst having steam gasification activity, to form a raw product gas, comprised of unreacted steam, methane, carbon dioxide, hydrogen and carbon monoxide, and a particulate residue, or char having catalyst values incorporated therewith.
  • a purge of the char is withdrawn from the gasification reactor.
  • a raw product effluent stream is cooled to condense unreacted steam to form a sour water stream and a stream of cooled raw product gas from which methane and other components such as syngas are recovered.
  • the particulate compositions of the present invention are particularly useful for gasification at moderate temperatures of at least about 450 0 C, or of at least about 600 0 C or above, to about 900°C, or to about 75O 0 C, or to about 700 0 C; and at pressures of at least about 50 psig, or at least about 200 psig, or at least about 400 psig, to about 1000 psig, or to about 700 psig, or to about 600 psig.
  • Analyses of the petroleum coke samples provided results as follows: 8.9 percent by weight volatile matter and 0.38 percent by weight ash (proximate analysis); metal components in the ash of vanadium 170 mg/kg and nickel 220 mg/kg; carbon 86.3 percent, hydrogen 3.6 percent, nitrogen 1.8 percent, sulfur 6.0 percent and oxygen 2.3 percent (ultimate analysis); and a BET surface area of 2 to 3 m 2 /g.
  • the atomic ratio of hydrogen to carbon was 0.20, and sulfur to carbon 0.026.

Abstract

The present invention relates to particulate compositions of a lower ash type petroleum coke containing at least two preselected components (alkali metal and calcium) that exhibit an efficient, enhanced-yielding gasification to value added gaseous products, particularly when used in a steady-state integrated gasification process. The compositions of the present invention are particularly useful for catalytic gasification of petroleum coke at moderate temperatures ranging from about 450°C to about 900°C. Advantageously, the compositions can be readily incorporated into fluidized bed gasification units, and can result in a cost-effective, high-yielding production of methane gas from petroleum coke.

Description

TITLE
COMPOSITIONS FOR CATALYTIC GASIFICATION OF A PETROLEUM
COKE
FIELD OF THE INVENTION
[0001 ] The present invention relates particulate compositions of a crude oil resid-based petroleum coke containing at least two preselected catalytic components, which composition exhibits an efficient, enhanced-yielding gasification to value-added gaseous products, particularly when used in a steady-state integrated gasification process. More particularly, this invention concerns compositions of a petroleum coke loaded with a mixture of (i) an alkali metal component, and (ii) a calcium component.
[0002] The present invention further relates to processes wherein these particulate compositions, in the presence of steam, exhibit gasification activity, and thereby form value-added gaseous products including methane and one or more of hydrogen, carbon monoxide and other higher hydrocarbons.
BACKRGOUND OF THE INVENTION
[0003] In view of numerous factors such as higher energy prices and environmental concerns, the production of value-added gaseous products from lower- fuel-value carbon sources, such as petroleum coke and coal, is receiving renewed attention. The catalytic gasification of such materials to produce methane and other value-added gases is disclosed, for example, in US3828474, US3958957, US3998607, US4057512, US4092125, US4094650, US4204843, US4468231 and GB1599932.
[0004] More recent developments to such technology directed specifically to methane as a predominant gaseous product are disclosed in commonly owned US2007/0000177A1 , US2007/0083072A1 , U.S. Application Serial No. 11/421511 (filed
1 June 2006 and entitled "Catalytic Steam Gasification Process with Recovery and Recycle of Alkali Metal Compounds"), and U.S. Application Serial No. 11/832809 (filed
2 August 2007 and entitled "Catalyst-Loaded Coal Compositions, Processes for Preparing Same, and Integrated Processes for Preparation of Methane from Coal").
[0005] Petroleum coke is a generally solid carbonaceous residue derived from delayed coking or fluid coking a carbon source such as a crude oil resid. Petroleum coke in general has a poorer gasification reactivity, particularly at moderate temperatures, than does bituminous coal due, for example, to its highly crystalline carbon and elevated levels of organic sulfur derived from heavy-gravity oil. Use of catalysts is necessary for improving the lower reactivity of petroleum cokes.
[0006] One advantageous catalytic process for gasifying petroleum cokes to methane and other value-added gaseous products is disclosed in the above- mentioned US2007/0083072A1. This publication discloses the use of alkali metals to catalyze the gasification reaction. While the process disclosed in this publication is generally quite effective, it would be desirable to find alternative catalyst systems with potentially improved gasification activity.
SUMMARY OF THE INVENTION
[0007] The present invention is directed to the gasification of a petroleum coke derived from a crude oil resid, for example, by coking processes used for upgrading heavy-gravity residual crude oil, which petroleum coke contains ash but as a minor component, typically about 1.0 wt% or less, and more typically about 0.5 wt% of less, based on the weight of the coke. Typically the ash in such lower-ash cokes predominantly comprises metals such as nickel and vanadium.
[0008] In this context, the present invention is directed to particulate compositions of such petroleum coke containing at least two preselected components that exhibit an efficient, enhanced-yielding gasification to value-added gaseous products. More particularly, the present invention is a particulate composition having a particle distribution size suitable for gasification in a fluidized bed zone, comprising an intimate mixture of (A) a petroleum coke derived from crude oil comprising ash in an amount of about 1.0 wt% or less, based on the weight of the petroleum coke, and (B) a gasification catalyst which under suitable conditions of temperature and pressure and in the presence of steam exhibits gasification activity whereby value added gaseous products are formed, wherein:
[0009] (a) the gasification catalyst comprises (i) a first component which is a source of at least one alkali metal, and (ii) a second component which is a source of calcium; and
[001 0] (b) the gasification catalyst is present in an amount sufficient to provide, in the particulate composition, a ratio of alkali metal atoms to carbon atoms in the range of from about 0.01 to about 0.1 , and a ratio of calcium atoms to carbon atoms in the range of from about 0.01 to about 0.1. [001 1 ] The compositions of the present invention are particularly useful for catalytic gasification of petroleum coke at moderate temperatures, such as disclosed in US2007/0083072A1. Advantageously, compositions and process according to the invention can be readily incorporated into fluidized bed gasification units, and can result in a more cost-effective, high-yielding production of methane gas.
[001 2] In this context, the present invention also provides a process for converting petroleum coke to methane, comprising the steps of:
[001 3] (1 ) combining a petroleum coke and a catalyst having steam gasification activity to produce a particulate composition having a particle distribution size suitable for gasification in a fluidized bed zone,
[001 4] (2) reacting the particulate composition in a fluidized bed zone in the presence of steam to form gaseous products including methane and one or more of hydrogen, carbon monoxide and other higher hydrocarbons, and
[001 5] (3) recovering methane from the gaseous products,
[001 6] wherein the particulate composition is as set forth herein.
DETALED DESCRIPTION THE PREFERRED EMBODIMENTS
[001 7] All publications, patent applications, patents and other references mentioned herein, if not otherwise indicated, are explicitly incorporated by reference herein in their entirety for all purposes as if fully set forth.
[001 8] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. In case of conflict, the present specification, including definitions, will control.
[001 9] Except where expressly noted, trademarks are shown in upper case.
[0020] Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described herein.
[0021 ] Unless stated otherwise, all percentages, parts, ratios, etc., are by weight. [0022] When an amount, concentration, or other value or parameter is given as either a range, preferred range or a list of upper preferable values and lower preferable values, this is to be understood as specifically disclosing all ranges formed from any pair of any upper range limit or preferred value and any lower range limit or preferred value, regardless of whether ranges are separately disclosed. Where a range of numerical values is recited herein, unless otherwise stated, the range is intended to include the endpoints thereof, and all integers and fractions within the range. It is not intended that the scope of the invention be limited to the specific values recited when defining a range.
[0023] When the term "about" is used in describing a value or an end-point of a range, the disclosure should be understood to include the specific value or end-point referred to.
[0024] As used herein, the terms "comprises," "comprising," "includes,"
"including," "has," "having" or any other variation thereof, are intended to cover a non- exclusive inclusion. For example, a process, method, article, or apparatus that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Further, unless expressly stated to the contrary, "or" refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
[0025] Use of "a" or "an" are employed to describe elements and components of the invention. This is done merely for convenience and to give a general sense of the invention. This description should be read to include one or at least one and the singular also includes the plural unless it is obvious that it is meant otherwise.
[0026] The materials, methods, and examples herein are illustrative only and, except as specifically stated, are not intended to be limiting.
Petroleum Coke
[0027] As indicated previously, the petroleum coke utilized in the present invention is derived from a crude oil, for example, by coking processes used for upgrading heavy-gravity residual crude oil, which petroleum coke contains ash but as a minor component, typically about 1.0 wt% or less, and more typically about 0.5 wt% of less, based on the weight of the coke. Typically the ash in such lower-ash cokes predominantly comprises metals such as nickel and vanadium. The petroleum coke preferably comprises at least about 70 wt% carbon, and alternatively at least about 80 wt% carbon, based on the weight of the petroleum coke. Typically, the petroleum coke comprises less than about 20 wt% percent inorganic compounds, based on the weight of the petroleum coke.
[0028] The petroleum coke is utilized in particulate form as a fine powder having a particle size distribution suitable for gasification in a fluidized bed zone, which size also facilitates efficient catalyst loading. The ground coke (and resulting composition) has a particle size preferably ranging from about 25 microns, or from about 45 microns, to about 2500 microns, or to about 500 microns. Petroleum coke can be ground by any methods known to the art.
Catalyst Component
[0029] Particulate compositions according to the present invention are based on the above-described petroleum coke, and contain (i) an amount of an alkali metal component, as alkali metal and/or a compound containing alkali metal, sufficient to provide, in the composition, a ratio of alkali metal atoms to carbon atoms in the range of from about 0.01 to about 0.1 , or in a range from about 0.01 to about 0.08, or in a range from about 0.01 to about 0.05; and (ii) an amount of calcium component, as calcium metal and/or a compound containing calcium, sufficient to provide, in the composition, a ratio of calcium atoms to carbon atoms in the range of from about 0.01 to about 0.1 , or in a range from about 0.01 to about 0.08, or in a range from about 0.01 to about 0.05.
[0030] The alkali metal component is typically loaded to achieve an alkali metal content of from about 3 to about 10 times more than the ash content of the petroleum coke, on a mass basis.
[0031 ] The ratio of alkali metal atoms to calcium atoms can range from about
1 :5, or about 1 :3, or about 1 :2, to about 5:1 , or about 3:1 , or about 2:1.
[0032] Suitable alkali metals are lithium, sodium, potassium, rubidium and cesium, and potassium is preferred.
Methods of Making the Particulate Compositions
[0033] Particulate compositions in accordance with the present invention can be prepared by a process comprising the steps of: (a) grinding a petroleum coke, and (b) soaking the ground coke in a catalyst-containing solution for a contact time and at a temperature so as to provide ample opportunity to achieve substantial and uniform catalyst loading. The soaked catalyst-loaded coke can be recovered and used as such or, more preferably, can be further processed prior to gasification as disclosed in US2007/0083072A1.
[0034] The finely ground coke is soaked as a slurry in a catalyst-rich solution, preferably of a salt of a catalysts. The solution is in an aqueous medium. Depending upon the solubility of the source compounds, other liquids such as ethanol may be used. Where the desired source is insoluble in water and alcohols, a slurry mixture is useful, for example, a mixture of an aqueous potassium hydroxide and calcium hydroxide powder.
[0035] Suitable alkali metal catalyst salts include, but are not limited to, carbonate, hydroxide, acetate, halide and nitrate salts. In preferred embodiments, carbonate or hydroxide salts are used and, more preferably, carbonate salts are used. In a particularly preferred embodiment, potassium carbonate is used.
[0036] Suitable calcium salts include, but are not limited to, hydroxide, acetate, halide and nitrate salts. In preferred embodiments, nitrate and acetate salts are used.
[0037] The total amount of catalyst loaded is controlled by controlling the concentration of catalyst components in the solution, as well as the contact time, temperature and method, as can be readily determined by those of ordinary skill in the relevant art based on the characteristics of the starting petroleum coke.
Catalytic Gasification
[0038] The particulate compositions of the present invention are particularly useful in integrated gasification processes for converting petroleum coke to combustible gases, such as methane.
[0039] Generally, the particulate compositions of the present invention provide a suitable feedstream of catalyst-containing petroleum coke to any steam gasification process. Generally, such steam gasification processes provide a means for the introducing of dry particulate feed into a fluidized bed zone in a gasification reactor. Coke and superheated steam are reacted while in contact with the catalyst having steam gasification activity, to form a raw product gas, comprised of unreacted steam, methane, carbon dioxide, hydrogen and carbon monoxide, and a particulate residue, or char having catalyst values incorporated therewith. A purge of the char is withdrawn from the gasification reactor. A raw product effluent stream is cooled to condense unreacted steam to form a sour water stream and a stream of cooled raw product gas from which methane and other components such as syngas are recovered.
[0040] The particulate compositions of the present invention are particularly useful for gasification at moderate temperatures of at least about 4500C, or of at least about 6000C or above, to about 900°C, or to about 75O0C, or to about 7000C; and at pressures of at least about 50 psig, or at least about 200 psig, or at least about 400 psig, to about 1000 psig, or to about 700 psig, or to about 600 psig.
[0041 ] A preferred process is described in US2007/0083072A1 , and reference can be had to that publication for further process details.
EXAMPLES
Petroleum Coke Sample Preparation
[0042] Where the as-received petroleum coke was found to be too damp (i.e. not free-flowing) to be jaw-crushed, it was necessary to first air-dry it in a mechanical- convection oven at 35°C for an extended period of time. Stage-crushing was performed carefully so as not to generate excessive fines and to maximize the amount of material having particle sizes ranging from about 0.85 to about 1.4 mm.
[0043] Analyses of the petroleum coke samples provided results as follows: 8.9 percent by weight volatile matter and 0.38 percent by weight ash (proximate analysis); metal components in the ash of vanadium 170 mg/kg and nickel 220 mg/kg; carbon 86.3 percent, hydrogen 3.6 percent, nitrogen 1.8 percent, sulfur 6.0 percent and oxygen 2.3 percent (ultimate analysis); and a BET surface area of 2 to 3 m2/g. The atomic ratio of hydrogen to carbon was 0.20, and sulfur to carbon 0.026.
[0044] Compounds of potassium (nitrate, acetate, hydroxide and carbonate) and calcium (nitrate, acetate and hydroxide) were used as catalyst precursors in a liquid medium. Preselected amounts were contacted with the petroleum coke by mixing with a rotary evaporator at room temperature or at 0°C if a water/ethanol solution was used. After separation from the liquid, the wet solid particles were subjected to reduced pressure thereby drying them for gasification. [0045] Catalysts of about 1 and about 5 mass % of potassium were made, as well as catalysts of 3 mass % calcium. Binary catalysts of combinations of the above were also made.
Petroleum Coke Gasification
[0046] Gasification was carried out in a high-pressure apparatus that included a quartz reactor. About 100 mg of the sample was first charged into a platinum cell held in the reactor and then gasified. Typical gasification conditions were as follows: total pressure, 1.0 MPa; partial pressure of H2O, 0.21 MPa, in an atmosphere of high purity argon; temperatures, 75O0C to 9000C; and reaction times, 2 to 3 hr. Product gas after the removal of H2O and H2S was analyzed on-line with a high-speed micro GC attached with a thermal conductivity detector. In order to determine the amount of H2 produced precisely, argon gas was used as the carrier gas of GC. Coke conversion was estimated by using the weight change before and after gasification and expressed in percent by weight on a catalyst-free basis.
[0047] The conversion of petroleum coke without any catalyst was only about
25 percent at 7500C; however, it increased with increased temperature and reached about 95 percent at 9000C. Petroleum coke treated with a calcium salt (3%) exhibited almost no catalytic effects, irrespective of the temperature. By contrast, potassium compounds promoted the steam gasification even at low loading of 1 percent by weight and the conversion was about 40 percent at 75O0C and about 95 percent at 85O0C.
[0048] Gasification of petroleum coke using binary combinations of calcium and potassium compounds (1 % K/3% Ca) was also studied. Conversions of petroleum coke at 75O0C with these binary catalysts was higher than that with only potassium compounds alone - about 55% versus about 40%.
[0049] In a second test, petroleum coke overall conversion, after 2 hours at
75O0C, without any catalysts was only about 15 percent, which was almost unchanged with calcium compounds alone (3%), whereas conversion increased up to about 40-45 percent when a potassium-containing catalyst (5%) was used. An increase in conversion to more than 95% was observed with the use of binary compositions (5% K/3% Ca). A temperature of about 9000C was required to obtain a conversion that high for uncatalyzed coke, meaning that the binary catalysts demonstrated a lowering of more than 15O0C in gasification temperature. [0050] The rates of methane formation for the binary catalysts at 7500C were found to be high (and highest) under the conditions at the start of the gasification (where the molar ratio of coke/H2O was highest), but decreased rapidly as the time increased (and the molar ratio of coke/H2O decreased).

Claims

What is claimed:
1. A particulate composition having a particle distribution size suitable for gasification in a fluidized bed zone, comprising an intimate mixture of (A) a petroleum coke derived from crude oil comprising ash in an amount of about 1.0 wt% or less, based on the weight of the petroleum coke, and (B) a gasification catalyst which under suitable conditions of temperature and pressure and in the presence of steam exhibits gasification activity whereby value added gaseous products are formed, wherein:
(a) the gasification catalyst comprises (i) a first component which is a source of at least one alkali metal, and (ii) a second component which is a source of calcium; and
(b) the gasification catalyst is present in an amount sufficient to provide, in the particulate composition, a ratio of alkali metal atoms to carbon atoms in the range of from about 0.01 to about 0.1 , and a ratio of calcium atoms to carbon atoms in the range of from about 0.01 to about 0.1.
2. The particulate composition according to claim 1 , wherein the alkali metal is potassium.
3. The particulate composition according to claim 1 or claim 2, wherein the source of alkali metal is an alkali metal salt selected from the group consisting of carbonate, hydroxide, acetate, halide and nitrate salts.
4. The particulate composition according to claim 1 , wherein the source of alkali metal is potassium carbonate.
5. The particulate composition according to any of claims 1-4, wherein the source of calcium is a calcium salt selected from the group consisting of hydroxide, acetate, halide and nitrate salts.
6. The particulate composition according to any of claims 1-5, wherein the source of calcium is calcium nitrate or calcium acetate.
7. The particulate composition according to any of claims 1-6, wherein the gasification catalyst is present in an amount sufficient to provide in the particulate composition a molar ratio of alkali metal atoms to carbon atoms in the range of from about 0.01 to about 0.08.
8. The particulate composition according to any of claims 1-7, wherein the gasification catalyst is present in an amount sufficient to provide in the particulate composition a molar ratio of calcium atoms to carbon atoms in the range of from about 0.01 to about 0.08.
9. The particulate composition according to any of claims 1-8, having a particle size ranging from about 25 microns to about 2500 microns.
10. A process for converting petroleum coke to methane, comprising the steps of:
(1 ) combining a petroleum coke and a catalyst having steam gasification activity to produce a particulate composition having a particle distribution size suitable for gasification in a fluidized bed zone,
(2) reacting the particulate composition in a fluidized bed zone in the presence of steam to form gaseous products including methane and one or more of hydrogen, carbon monoxide and other higher hydrocarbons, and
(3) recovering methane from the gaseous products,
wherein the particulate composition is as set forth in any one of claims 1-9.
PCT/US2008/076991 2007-10-09 2008-09-19 Compositions for catalytic gasification of a petroleum coke and process for their conversion to methane WO2009048724A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97858807P 2007-10-09 2007-10-09
US60/978,588 2007-10-09

Publications (2)

Publication Number Publication Date
WO2009048724A2 true WO2009048724A2 (en) 2009-04-16
WO2009048724A3 WO2009048724A3 (en) 2009-06-25

Family

ID=40445646

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2008/076991 WO2009048724A2 (en) 2007-10-09 2008-09-19 Compositions for catalytic gasification of a petroleum coke and process for their conversion to methane

Country Status (2)

Country Link
US (1) US20090090056A1 (en)
WO (1) WO2009048724A2 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8999020B2 (en) 2008-04-01 2015-04-07 Greatpoint Energy, Inc. Processes for the separation of methane from a gas stream
US10344231B1 (en) 2018-10-26 2019-07-09 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with improved carbon utilization
US10435637B1 (en) 2018-12-18 2019-10-08 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with improved carbon utilization and power generation
US10464872B1 (en) 2018-07-31 2019-11-05 Greatpoint Energy, Inc. Catalytic gasification to produce methanol
US10618818B1 (en) 2019-03-22 2020-04-14 Sure Champion Investment Limited Catalytic gasification to produce ammonia and urea
CN111676079A (en) * 2020-06-11 2020-09-18 大冶市都鑫摩擦粉体有限公司 Preparation system and process of petroleum coke composition for catalytic gasification

Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8114176B2 (en) * 2005-10-12 2012-02-14 Great Point Energy, Inc. Catalytic steam gasification of petroleum coke to methane
US7922782B2 (en) * 2006-06-01 2011-04-12 Greatpoint Energy, Inc. Catalytic steam gasification process with recovery and recycle of alkali metal compounds
KR101138096B1 (en) * 2007-08-02 2012-04-25 그레이트포인트 에너지, 인크. Catalyst-loaded coal compositions, methods of making and use
WO2009048723A2 (en) * 2007-10-09 2009-04-16 Greatpoint Energy, Inc. Compositions for catalytic gasification of a petroleum coke and process for conversion thereof to methane
WO2009086370A2 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Processes for making syngas-derived products
JP2011508066A (en) * 2007-12-28 2011-03-10 グレイトポイント・エナジー・インコーポレイテッド Petroleum coke composition for catalytic gasification
WO2009086361A2 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Catalytic gasification process with recovery of alkali metal from char
US7897126B2 (en) * 2007-12-28 2011-03-01 Greatpoint Energy, Inc. Catalytic gasification process with recovery of alkali metal from char
CA2713642A1 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Catalytic gasification process with recovery of alkali metal from char
CA2713656C (en) 2007-12-28 2014-07-08 Greatpoint Energy, Inc. Steam generating slurry gasifier for the catalytic gasification of a carbonaceous feedstock
WO2009086363A1 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Coal compositions for catalytic gasification and process for its preparation
US20090165361A1 (en) * 2007-12-28 2009-07-02 Greatpoint Energy, Inc. Carbonaceous Fuels and Processes for Making and Using Them
WO2009086367A1 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Petroleum coke compositions for catalytic gasification and preparation process thereof
US8297542B2 (en) * 2008-02-29 2012-10-30 Greatpoint Energy, Inc. Coal compositions for catalytic gasification
US8114177B2 (en) 2008-02-29 2012-02-14 Greatpoint Energy, Inc. Co-feed of biomass as source of makeup catalysts for catalytic coal gasification
US20090217575A1 (en) 2008-02-29 2009-09-03 Greatpoint Energy, Inc. Biomass Char Compositions for Catalytic Gasification
US20090260287A1 (en) * 2008-02-29 2009-10-22 Greatpoint Energy, Inc. Process and Apparatus for the Separation of Methane from a Gas Stream
US8286901B2 (en) * 2008-02-29 2012-10-16 Greatpoint Energy, Inc. Coal compositions for catalytic gasification
US20090220406A1 (en) * 2008-02-29 2009-09-03 Greatpoint Energy, Inc. Selective Removal and Recovery of Acid Gases from Gasification Products
WO2009111345A2 (en) 2008-02-29 2009-09-11 Greatpoint Energy, Inc. Catalytic gasification particulate compositions
CN101959996B (en) * 2008-02-29 2013-10-30 格雷特波因特能源公司 Particulate composition for gasification, preparation and continuous conversion thereof
US7926750B2 (en) * 2008-02-29 2011-04-19 Greatpoint Energy, Inc. Compactor feeder
US8361428B2 (en) * 2008-02-29 2013-01-29 Greatpoint Energy, Inc. Reduced carbon footprint steam generation processes
US20090217582A1 (en) * 2008-02-29 2009-09-03 Greatpoint Energy, Inc. Processes for Making Adsorbents and Processes for Removing Contaminants from Fluids Using Them
US8709113B2 (en) 2008-02-29 2014-04-29 Greatpoint Energy, Inc. Steam generation processes utilizing biomass feedstocks
CA2718536C (en) 2008-04-01 2014-06-03 Greatpoint Energy, Inc. Sour shift process for the removal of carbon monoxide from a gas stream
CN102076828A (en) * 2008-06-27 2011-05-25 格雷特波因特能源公司 Four-train catalytic gasification systems
CA2729003C (en) * 2008-06-27 2014-08-12 Francis S. Lau Two-train catalytic gasification systems
US20090324462A1 (en) * 2008-06-27 2009-12-31 Greatpoint Energy, Inc. Four-Train Catalytic Gasification Systems
WO2010033850A2 (en) 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
WO2010033848A2 (en) * 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
WO2010033846A2 (en) * 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Char methanation catalyst and its use in gasification processes
WO2010033852A2 (en) 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
WO2010048493A2 (en) * 2008-10-23 2010-04-29 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
WO2010078298A1 (en) 2008-12-30 2010-07-08 Greatpoint Energy, Inc. Processes for preparing a catalyzed coal particulate
KR101290453B1 (en) * 2008-12-30 2013-07-29 그레이트포인트 에너지, 인크. Processes for preparing a catalyzed carbonaceous particulate
EP2430126A2 (en) * 2009-05-13 2012-03-21 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
WO2010132551A2 (en) * 2009-05-13 2010-11-18 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
US8268899B2 (en) 2009-05-13 2012-09-18 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
WO2011017630A1 (en) 2009-08-06 2011-02-10 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
WO2011034891A1 (en) 2009-09-16 2011-03-24 Greatpoint Energy, Inc. Two-mode process for hydrogen production
CN102575181B (en) 2009-09-16 2016-02-10 格雷特波因特能源公司 Integrated hydromethanation combined cycle process
EP2478071A1 (en) 2009-09-16 2012-07-25 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
CN102549121B (en) * 2009-09-16 2015-03-25 格雷特波因特能源公司 Integrated hydromethanation combined cycle process
CA2773845C (en) 2009-10-19 2014-06-03 Greatpoint Energy, Inc. Integrated enhanced oil recovery process
AU2010310846B2 (en) 2009-10-19 2013-05-30 Greatpoint Energy, Inc. Integrated enhanced oil recovery process
CA2780375A1 (en) * 2009-12-17 2011-07-14 Greatpoint Energy, Inc. Integrated enhanced oil recovery process
WO2011084581A1 (en) 2009-12-17 2011-07-14 Greatpoint Energy, Inc. Integrated enhanced oil recovery process injecting nitrogen
WO2011106285A1 (en) 2010-02-23 2011-09-01 Greatpoint Energy, Inc. Integrated hydromethanation fuel cell power generation
US8652696B2 (en) * 2010-03-08 2014-02-18 Greatpoint Energy, Inc. Integrated hydromethanation fuel cell power generation
WO2011139694A1 (en) 2010-04-26 2011-11-10 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with vanadium recovery
US8653149B2 (en) 2010-05-28 2014-02-18 Greatpoint Energy, Inc. Conversion of liquid heavy hydrocarbon feedstocks to gaseous products
CN103154213B (en) 2010-08-18 2015-06-17 格雷特波因特能源公司 Hydromethanation of carbonaceous feedstock
JP2013537248A (en) 2010-09-10 2013-09-30 グレイトポイント・エナジー・インコーポレイテッド Hydrogenation methanation of carbonaceous feedstock.
JP2013541622A (en) 2010-11-01 2013-11-14 グレイトポイント・エナジー・インコーポレイテッド Hydrogenation methanation of carbonaceous feedstock.
CN103210068B (en) 2010-11-01 2015-07-08 格雷特波因特能源公司 Hydromethanation of a carbonaceous feedstock
US8648121B2 (en) 2011-02-23 2014-02-11 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with nickel recovery
EP2865735B1 (en) 2011-03-29 2018-02-21 Fuelina Technologies, LLC Method and apparatus for making a hybrid fuel
CN103492537A (en) 2011-04-22 2014-01-01 格雷特波因特能源公司 Hydromethanation of a carbonaceous feedstock with char beneficiation
US9127221B2 (en) 2011-06-03 2015-09-08 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock
CN103890147A (en) 2011-08-17 2014-06-25 格雷特波因特能源公司 Hydromethanation of a carbonaceous feedstock
WO2013025808A1 (en) 2011-08-17 2013-02-21 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock
US9012524B2 (en) 2011-10-06 2015-04-21 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock
CN104685039B (en) 2012-10-01 2016-09-07 格雷特波因特能源公司 Graininess low rank coal raw material of agglomeration and application thereof
CN104704089B (en) 2012-10-01 2017-08-15 格雷特波因特能源公司 Graininess low rank coal raw material of agglomeration and application thereof
KR101576781B1 (en) 2012-10-01 2015-12-10 그레이트포인트 에너지, 인크. Agglomerated particulate low-rank coal feedstock and uses thereof
KR101717863B1 (en) 2012-10-01 2017-03-17 그레이트포인트 에너지, 인크. Use of contaminated low-rank coal for combustion
US10308885B2 (en) 2014-12-03 2019-06-04 Drexel University Direct incorporation of natural gas into hydrocarbon liquid fuels
CA3015050C (en) 2016-02-18 2024-01-02 8 Rivers Capital, Llc System and method for power production including methanation
HU231341B1 (en) 2019-03-29 2023-01-28 Mol Magyar Olaj- És Gázipari Nyilvánosan Működő Részvénytársaság Method for producing hydrogen rich gaseous mixture

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2852710A1 (en) * 1978-12-06 1980-06-12 Didier Eng Steam gasification of coal or coke - with injection of gaseous ammonia or aq. metal oxide as catalyst
US4336034A (en) * 1980-03-10 1982-06-22 Exxon Research & Engineering Co. Process for the catalytic gasification of coal
US4551155A (en) * 1983-07-07 1985-11-05 Sri International In situ formation of coal gasification catalysts from low cost alkali metal salts
US5435940A (en) * 1993-11-12 1995-07-25 Shell Oil Company Gasification process
US20070000177A1 (en) * 2005-07-01 2007-01-04 Hippo Edwin J Mild catalytic steam gasification process
US20070083072A1 (en) * 2005-10-12 2007-04-12 Nahas Nicholas C Catalytic steam gasification of petroleum coke to methane

Family Cites Families (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US383327A (en) * 1888-05-22 Envelope for protecting grapes while maturing
US2886405A (en) * 1956-02-24 1959-05-12 Benson Homer Edwin Method for separating co2 and h2s from gas mixtures
US3034848A (en) * 1959-04-14 1962-05-15 Du Pont Compaction of dyes
DE1403859A1 (en) * 1960-09-06 1968-10-31 Neidl Dipl Ing Georg Circulation pump
US3435590A (en) * 1967-09-01 1969-04-01 Chevron Res Co2 and h2s removal
US3647567A (en) * 1969-11-28 1972-03-07 Celanese Coatings Co Post-dipping of acidic deposition coatings
US3985519A (en) * 1972-03-28 1976-10-12 Exxon Research And Engineering Company Hydrogasification process
US4094650A (en) * 1972-09-08 1978-06-13 Exxon Research & Engineering Co. Integrated catalytic gasification process
JPS5323777B2 (en) * 1972-12-04 1978-07-17
US4021370A (en) * 1973-07-24 1977-05-03 Davy Powergas Limited Fuel gas production
US3958957A (en) * 1974-07-01 1976-05-25 Exxon Research And Engineering Company Methane production
DE2501376A1 (en) * 1975-01-15 1976-07-22 Metallgesellschaft Ag METHOD FOR REMOVING MONOPHENOLS, DIPHENOLS AND THE LIKE FROM WASTEWATERS
DE2503507C2 (en) * 1975-01-29 1981-11-19 Metallgesellschaft Ag, 6000 Frankfurt Process for the purification of gases produced by gasifying solid fossil fuels using water vapor and oxygen under pressure
GB1508712A (en) * 1975-03-31 1978-04-26 Battelle Memorial Institute Treating solid fuel
US4091073A (en) * 1975-08-29 1978-05-23 Shell Oil Company Process for the removal of H2 S and CO2 from gaseous streams
US4005996A (en) * 1975-09-04 1977-02-01 El Paso Natural Gas Company Methanation process for the production of an alternate fuel for natural gas
US4077778A (en) * 1975-09-29 1978-03-07 Exxon Research & Engineering Co. Process for the catalytic gasification of coal
US4322222A (en) * 1975-11-10 1982-03-30 Occidental Petroleum Corporation Process for the gasification of carbonaceous materials
US4069304A (en) * 1975-12-31 1978-01-17 Trw Hydrogen production by catalytic coal gasification
US4330305A (en) * 1976-03-19 1982-05-18 Basf Aktiengesellschaft Removal of CO2 and/or H2 S from gases
IT1075397B (en) * 1977-04-15 1985-04-22 Snam Progetti METHANATION REACTOR
US4152119A (en) * 1977-08-01 1979-05-01 Dynecology Incorporated Briquette comprising caking coal and municipal solid waste
US4204843A (en) * 1977-12-19 1980-05-27 Exxon Research & Engineering Co. Gasification process
US4200439A (en) * 1977-12-19 1980-04-29 Exxon Research & Engineering Co. Gasification process using ion-exchanged coal
US4265868A (en) * 1978-02-08 1981-05-05 Koppers Company, Inc. Production of carbon monoxide by the gasification of carbonaceous materials
US4193771A (en) * 1978-05-08 1980-03-18 Exxon Research & Engineering Co. Alkali metal recovery from carbonaceous material conversion process
US4193772A (en) * 1978-06-05 1980-03-18 Exxon Research & Engineering Co. Process for carbonaceous material conversion and recovery of alkali metal catalyst constituents held by ion exchange sites in conversion residue
US4189307A (en) * 1978-06-26 1980-02-19 Texaco Development Corporation Production of clean HCN-free synthesis gas
US4318712A (en) * 1978-07-17 1982-03-09 Exxon Research & Engineering Co. Catalytic coal gasification process
US4372755A (en) * 1978-07-27 1983-02-08 Enrecon, Inc. Production of a fuel gas with a stabilized metal carbide catalyst
GB2027444B (en) * 1978-07-28 1983-03-02 Exxon Research Engineering Co Gasification of ash-containing solid fuels
US4249471A (en) * 1979-01-29 1981-02-10 Gunnerman Rudolf W Method and apparatus for burning pelletized organic fibrous fuel
US4243639A (en) * 1979-05-10 1981-01-06 Tosco Corporation Method for recovering vanadium from petroleum coke
US4260421A (en) * 1979-05-18 1981-04-07 Exxon Research & Engineering Co. Cement production from coal conversion residues
US4315758A (en) * 1979-10-15 1982-02-16 Institute Of Gas Technology Process for the production of fuel gas from coal
US4331451A (en) * 1980-02-04 1982-05-25 Mitsui Toatsu Chemicals, Inc. Catalytic gasification
EP0061326B1 (en) * 1981-03-24 1985-06-19 Exxon Research And Engineering Company Apparatus for converting a fuel into combustible gas
NL8101447A (en) * 1981-03-24 1982-10-18 Shell Int Research METHOD FOR PREPARING HYDROCARBONS FROM CARBON-CONTAINING MATERIAL
DE3113993A1 (en) * 1981-04-07 1982-11-11 Metallgesellschaft Ag, 6000 Frankfurt METHOD FOR THE SIMULTANEOUS PRODUCTION OF COMBUSTION GAS AND PROCESS HEAT FROM CARBON-MATERIAL MATERIALS
US4428535A (en) * 1981-07-06 1984-01-31 Liquid Carbonic Corporation Apparatus to cool particulate matter for grinding
US4500323A (en) * 1981-08-26 1985-02-19 Kraftwerk Union Aktiengesellschaft Process for the gasification of raw carboniferous materials
US4432773A (en) * 1981-09-14 1984-02-21 Euker Jr Charles A Fluidized bed catalytic coal gasification process
US4439210A (en) * 1981-09-25 1984-03-27 Conoco Inc. Method of catalytic gasification with increased ash fusion temperature
EP0093501B1 (en) * 1982-03-29 1988-07-13 Asahi Kasei Kogyo Kabushiki Kaisha Process for thermal cracking of carbonaceous substances which increases gasoline fraction and light oil conversions
DE3217366A1 (en) * 1982-05-08 1983-11-10 Metallgesellschaft Ag, 6000 Frankfurt METHOD FOR PRODUCING A MOST INERT-FREE GAS FOR SYNTHESIS
US4436028A (en) * 1982-05-10 1984-03-13 Wilder David M Roll mill for reduction of moisture content in waste material
DE3229396C2 (en) * 1982-08-06 1985-10-31 Bergwerksverband Gmbh, 4300 Essen Process for the production of carbonaceous adsorbents impregnated with elemental sulfur
US4436531A (en) * 1982-08-27 1984-03-13 Texaco Development Corporation Synthesis gas from slurries of solid carbonaceous fuels
US4497784A (en) * 1983-11-29 1985-02-05 Shell Oil Company Solution removal of HCN from gaseous streams, with hydrolysis of thiocyanate formed
US4505881A (en) * 1983-11-29 1985-03-19 Shell Oil Company Ammonium polysulfide removal of HCN from gaseous streams, with subsequent production of NH3, H2 S, and CO2
US4508693A (en) * 1983-11-29 1985-04-02 Shell Oil Co. Solution removal of HCN from gaseous streams, with pH adjustment of reacted solution and hydrolysis of thiocyanate formed
US4808194A (en) * 1984-11-26 1989-02-28 Texaco Inc. Stable aqueous suspensions of slag, fly-ash and char
US4572826A (en) * 1984-12-24 1986-02-25 Shell Oil Company Two stage process for HCN removal from gaseous streams
US4720289A (en) * 1985-07-05 1988-01-19 Exxon Research And Engineering Company Process for gasifying solid carbonaceous materials
CA1300885C (en) * 1986-08-26 1992-05-19 Donald S. Scott Hydrogasification of biomass to produce high yields of methane
US4803061A (en) * 1986-12-29 1989-02-07 Texaco Inc. Partial oxidation process with magnetic separation of the ground slag
US4810475A (en) * 1987-08-18 1989-03-07 Shell Oil Company Removal of HCN, and HCN and COS, from a substantially chloride-free gaseous stream
US4892567A (en) * 1988-08-15 1990-01-09 Mobil Oil Corporation Simultaneous removal of mercury and water from fluids
US5093094A (en) * 1989-05-05 1992-03-03 Shell Oil Company Solution removal of H2 S from gas streams
JPH075895B2 (en) * 1989-09-29 1995-01-25 宇部興産株式会社 Method to prevent ash from adhering to gasification furnace wall
US5094737A (en) * 1990-10-01 1992-03-10 Exxon Research & Engineering Company Integrated coking-gasification process with mitigation of bogging and slagging
US5277884A (en) * 1992-03-02 1994-01-11 Reuel Shinnar Solvents for the selective removal of H2 S from gases containing both H2 S and CO2
NZ253874A (en) * 1992-06-05 1996-04-26 Battelle Memorial Institute Catalytic conversion of liquid organic materials into a product gas of methane, carbon dioxide and hydrogen
US5865898A (en) * 1992-08-06 1999-02-02 The Texas A&M University System Methods of biomass pretreatment
US5733515A (en) * 1993-01-21 1998-03-31 Calgon Carbon Corporation Purification of air in enclosed spaces
US5720785A (en) * 1993-04-30 1998-02-24 Shell Oil Company Method of reducing hydrogen cyanide and ammonia in synthesis gas
US5964985A (en) * 1994-02-02 1999-10-12 Wootten; William A. Method and apparatus for converting coal to liquid hydrocarbons
US6506349B1 (en) * 1994-11-03 2003-01-14 Tofik K. Khanmamedov Process for removal of contaminants from a gas stream
US5855631A (en) * 1994-12-02 1999-01-05 Leas; Arnold M. Catalytic gasification process and system
US6028234A (en) * 1996-12-17 2000-02-22 Mobil Oil Corporation Process for making gas hydrates
US6180843B1 (en) * 1997-10-14 2001-01-30 Mobil Oil Corporation Method for producing gas hydrates utilizing a fluidized bed
US6187465B1 (en) * 1997-11-07 2001-02-13 Terry R. Galloway Process and system for converting carbonaceous feedstocks into energy without greenhouse gas emissions
US6168768B1 (en) * 1998-01-23 2001-01-02 Exxon Research And Engineering Company Production of low sulfer syngas from natural gas with C4+/C5+ hydrocarbon recovery
US6015104A (en) * 1998-03-20 2000-01-18 Rich, Jr.; John W. Process and apparatus for preparing feedstock for a coal gasification plant
AUPQ118899A0 (en) * 1999-06-24 1999-07-22 Woodside Energy Limited Natural gas hydrate and method for producing same
US6379645B1 (en) * 1999-10-14 2002-04-30 Air Products And Chemicals, Inc. Production of hydrogen using methanation and pressure swing adsorption
FR2808223B1 (en) * 2000-04-27 2002-11-22 Inst Francais Du Petrole PROCESS FOR THE PURIFICATION OF AN EFFLUENT CONTAINING CARBON GAS AND HYDROCARBONS BY COMBUSTION
US6506361B1 (en) * 2000-05-18 2003-01-14 Air Products And Chemicals, Inc. Gas-liquid reaction process including ejector and monolith catalyst
JP5019683B2 (en) * 2001-08-31 2012-09-05 三菱重工業株式会社 Gas hydrate slurry dewatering apparatus and method
US6878358B2 (en) * 2002-07-22 2005-04-12 Bayer Aktiengesellschaft Process for removing mercury from flue gases
US7205448B2 (en) * 2003-12-19 2007-04-17 Uop Llc Process for the removal of nitrogen compounds from a fluid stream
DE202005021662U1 (en) * 2005-09-07 2009-03-05 Siemens Aktiengesellschaft Apparatus for producing synthesis gases by partial oxidation of slurries produced from ash-containing fuels with partial quenching and waste heat recovery
US7922782B2 (en) * 2006-06-01 2011-04-12 Greatpoint Energy, Inc. Catalytic steam gasification process with recovery and recycle of alkali metal compounds
US20080141591A1 (en) * 2006-12-19 2008-06-19 Simulent Inc. Gasification of sulfur-containing carbonaceous fuels
KR101138096B1 (en) * 2007-08-02 2012-04-25 그레이트포인트 에너지, 인크. Catalyst-loaded coal compositions, methods of making and use
WO2009048723A2 (en) * 2007-10-09 2009-04-16 Greatpoint Energy, Inc. Compositions for catalytic gasification of a petroleum coke and process for conversion thereof to methane
CA2713642A1 (en) * 2007-12-28 2009-07-09 Greatpoint Energy, Inc. Catalytic gasification process with recovery of alkali metal from char
US7897126B2 (en) * 2007-12-28 2011-03-01 Greatpoint Energy, Inc. Catalytic gasification process with recovery of alkali metal from char
US7926750B2 (en) * 2008-02-29 2011-04-19 Greatpoint Energy, Inc. Compactor feeder
WO2010033852A2 (en) * 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
WO2010033850A2 (en) * 2008-09-19 2010-03-25 Greatpoint Energy, Inc. Processes for gasification of a carbonaceous feedstock
CN201288266Y (en) * 2008-09-22 2009-08-12 厦门灿坤实业股份有限公司 Heat insulation cover of electric iron
WO2011017630A1 (en) * 2009-08-06 2011-02-10 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
CN102549121B (en) * 2009-09-16 2015-03-25 格雷特波因特能源公司 Integrated hydromethanation combined cycle process
CN102575181B (en) * 2009-09-16 2016-02-10 格雷特波因特能源公司 Integrated hydromethanation combined cycle process
EP2478071A1 (en) * 2009-09-16 2012-07-25 Greatpoint Energy, Inc. Processes for hydromethanation of a carbonaceous feedstock
WO2011034891A1 (en) * 2009-09-16 2011-03-24 Greatpoint Energy, Inc. Two-mode process for hydrogen production
AU2010310846B2 (en) * 2009-10-19 2013-05-30 Greatpoint Energy, Inc. Integrated enhanced oil recovery process
CA2773845C (en) * 2009-10-19 2014-06-03 Greatpoint Energy, Inc. Integrated enhanced oil recovery process

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2852710A1 (en) * 1978-12-06 1980-06-12 Didier Eng Steam gasification of coal or coke - with injection of gaseous ammonia or aq. metal oxide as catalyst
US4336034A (en) * 1980-03-10 1982-06-22 Exxon Research & Engineering Co. Process for the catalytic gasification of coal
US4551155A (en) * 1983-07-07 1985-11-05 Sri International In situ formation of coal gasification catalysts from low cost alkali metal salts
US5435940A (en) * 1993-11-12 1995-07-25 Shell Oil Company Gasification process
US20070000177A1 (en) * 2005-07-01 2007-01-04 Hippo Edwin J Mild catalytic steam gasification process
US20070083072A1 (en) * 2005-10-12 2007-04-12 Nahas Nicholas C Catalytic steam gasification of petroleum coke to methane

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8999020B2 (en) 2008-04-01 2015-04-07 Greatpoint Energy, Inc. Processes for the separation of methane from a gas stream
US10464872B1 (en) 2018-07-31 2019-11-05 Greatpoint Energy, Inc. Catalytic gasification to produce methanol
US10344231B1 (en) 2018-10-26 2019-07-09 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with improved carbon utilization
US10435637B1 (en) 2018-12-18 2019-10-08 Greatpoint Energy, Inc. Hydromethanation of a carbonaceous feedstock with improved carbon utilization and power generation
US10618818B1 (en) 2019-03-22 2020-04-14 Sure Champion Investment Limited Catalytic gasification to produce ammonia and urea
CN111676079A (en) * 2020-06-11 2020-09-18 大冶市都鑫摩擦粉体有限公司 Preparation system and process of petroleum coke composition for catalytic gasification

Also Published As

Publication number Publication date
WO2009048724A3 (en) 2009-06-25
US20090090056A1 (en) 2009-04-09

Similar Documents

Publication Publication Date Title
US20090090056A1 (en) Compositions for Catalytic Gasification of a Petroleum Coke
US20090090055A1 (en) Compositions for Catalytic Gasification of a Petroleum Coke
AU2011248701B2 (en) Hydromethanation of a carbonaceous feedstock with vanadium recovery
AU2008345189B2 (en) Petroleum coke compositions for catalytic gasification
Waheed et al. Hydrogen production from high temperature steam catalytic gasification of bio-char
Onwudili et al. Reaction of different carbonaceous materials in alkaline hydrothermal media for hydrogen gas production
AU2017307385A1 (en) A process and a system for producing synthesis gas
JP2021134328A (en) Biomass gasification method
DeGroot et al. The effects of ion-exchanged cobalt catalysts on the gasification of wood chars in carbon dioxide
Ross et al. Catalytic conversion of wood barks to fuel gases
JP3975271B2 (en) Biomass gasification method and catalyst used therefor
WO2020201785A2 (en) Improved process for production of hydrogen rich gaseous mixture
KR20140074025A (en) Method for Gasification Using Spent Catalyst Discharged from Refinery Process
US11697107B2 (en) Process for gasification of a carbonaceous raw material of low value as a fuel using a nanocatalyst
CN109923061B (en) Hydrothermal stable catalyst formula and preparation process thereof
Minowa et al. Hydrogen Production from Lignocellulosic Materials by Steam Gasification Using a Reduced Nickel Catalyst: Hydrogen production from biomass
CN115279866B (en) Catalytic gasification process, catalyst, use of a catalyst and process for preparing a catalyst
WO2013154910A1 (en) Catalytical gasifier configuration for biomass pyrolysis
Tewari et al. Unlocking Syngas Synthesis from Lignocellulose Pinewood Without Gasifying Agent: Catalytic and Pressure Insights
CN117884125A (en) Catalytic gasification process, catalyst, use of a catalyst and process for preparing a catalyst
Tomishige et al. Catalyst development for the synthesis gas and hydrogen production from biomass by gasification, pyrogasification, and steam reforming
Huttinger et al. Inhibition of hydrogasification of brown coals by moisture: influence of heating rate, temperature and pressure
Tristantini et al. Utilization of CaO coal char Prepared through Ion Exchange of CaCl2 for Partial Oxidation of Methane
Diniyati et al. Catalytic Activity of Coal Char on Water–Gas Shift Reaction

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08838207

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 08838207

Country of ref document: EP

Kind code of ref document: A2