WO1995024367A1 - Conversion du gaz naturel en hydrocarbures superieurs - Google Patents

Conversion du gaz naturel en hydrocarbures superieurs Download PDF

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Publication number
WO1995024367A1
WO1995024367A1 PCT/US1995/003092 US9503092W WO9524367A1 WO 1995024367 A1 WO1995024367 A1 WO 1995024367A1 US 9503092 W US9503092 W US 9503092W WO 9524367 A1 WO9524367 A1 WO 9524367A1
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reactor
water
carbon dioxide
carbon monoxide
hydrocarbons
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PCT/US1995/003092
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Louis De Vries
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Louis De Vries
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/02—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon
    • C07C1/04—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon from carbon monoxide with hydrogen
    • C07C1/0485—Set-up of reactors or accessories; Multi-step processes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/32—Manganese, technetium or rhenium
    • C07C2523/34—Manganese
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74—Iron group metals
    • C07C2523/75—Cobalt
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C07C2523/74—Iron group metals
    • C07C2523/755—Nickel
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry

Definitions

  • the field of this invention is production of higher hydrocarbons from syn gas.
  • Natural gas is an abundant energy source and is the preferred fuel for many uses, including home heating and cooking, electricity generation, various manufacturings, etc. As such, there is a constantly increasing demand for natural gas.
  • the term "natural gas” is used to describe a wide variety of gaseous mixtures. That is, natural gas from different fields varies in composition. In general, it varies from essentially pure methane to mixtures of methane with other gases, such as nitrogen, carbon dioxide, ethane, ethene, propane, hydrogen sulfide, dimethyl sulfide, and the like. In many cases, the chief diluent of the methane is carbon dioxide which may vary from very small amounts to quantities as great as 50% or more. The presence of gases other than methane affects the quality of the gas and in some cases may render the field unfit for commercialization.
  • a more preferred method for the "liquification" of natural gas is the one in which natural gas is converted into higher molecular weight hydrocarbons which are liquids at normal temperatures and pressures. Such products are as easily handled and transported as are any other liquid hydrocarbons. In spite of many years of research and development on this problem, there is still no generally accepted method for making a higher molecular weight liquid hydrocarbon from natural gas. Reviews of this problem are given in: (1) Tecnol. Ciencia Ed., 1_, (1) 25-37 (1991), (2)
  • Direct conversion of syn gas into hydrocarbons involves the hydrogenation of carbon monoxide into paraffins, olefins and oxygen containing products.
  • the Fischer-Tropsch reaction the gaseous mixture of carbon monoxide and hydrogen is reacted in the presence of a promoted transition metal catalyst to produce a hydrocarbon mixture having a broad molecular weight distribution.
  • This product is predominately straight chain, saturated hydrocarbons of low octane value.
  • One big drawback of this process is the conversion of about 40% of the feed gases into methane. Furthermore, the reaction is highly exothermic, requiring heat disposal.
  • the Shell Middle Distillate Synthesis of hydrocarbons involves carrying out the Fischer-Tropsch reaction under conditions that produce a high molecular weight, waxy paraffinic product. This product is then catalytically cracked to yield predominantly fuel in the middle distillate range. Kerosene and gas oil fractions are also obtained. This process suffers from the same drawbacks as the Fischer-Tropsch reaction, plus it requires a second catalytic reactor with its attendant catalyst deactivation and regeneration problems.
  • the third process for converting syn gas into liquid hydrocarbons involves first the catalytic conversion of syn gas into methanol which is then further reacted in the presence of a second catalyst to produce hydrocarbons.
  • This route is known as the Mobil MTG (methanol-to-gasoline) process.
  • Mobil MTG methanol-to-gasoline
  • the process requires two catalytic reactors, each with its own catalyst deactivation and regeneration problems.
  • natural gas is partially oxidized to a syn gas having a 2:1 ratio of hydrogen to carbon monoxide, the ratio preferred for the classical Fischer-Tropsch reaction.
  • the hydrogen is separated from the carbon monoxide to produce two gas streams.
  • the carbon monoxide is reacted with water to produce liquid hydrocarbons and carbon dioxide.
  • the carbon dioxide is separated and reacted with the hydrogen from the syn gas to produce additional carbon monoxide and water.
  • FIG. 1 is a block flow diagram of the subject process
  • Fig. 2 is a block flow diagram of the preferred process
  • Fig. 3 is a detailed flow diagram of the preferred process reacting carbon dioxide and hydrogen in equimolar amounts in a first reactor while feeding methane containing 10% carbon dioxide to the oxidizer.
  • the term "return” shall mean the addition of a reaction product from a subsequent process to the feed of a previous process; and the term “recycle” shall mean the reintroduction of unreacted feed components from the reaction product of a reactor into the feed of said reactor.
  • syn gas preferably obtained by the partial oxidation of natural gas is converted to higher hydrocarbons, particularly C 2 + (two or more carbons per molecule) , in high yield based on the amount of carbon source in the natural gas charged to the system.
  • the methane in the natural gas is used as a source for the production of syn gas.
  • the syn gas is reacted in a first reactor with carbon dioxide at elevated temperatures to produce additional carbon monoxide and water.
  • the water and carbon monoxide are separated from the other components of the effluent stream, the remainder of which is recycled to the first reactor.
  • the carbon monoxide and at least a portion of the water are then reacted in the presence of a metal catalyst in a second reactor to produce higher hydrocarbons, C 2 +.
  • These hydrocarbons are removed with the water from the second reactor effluent, leaving the second reactor remainder, all or a portion of which is returned to the first stage of the process.
  • the desired liquid hydrocarbon product is isolated substantially free of non- hydrocarbon components.
  • the only carbon containing substances withdrawn from the cyclic process are the desired higher hydrocarbon products and the only carbon containing substance admitted is the carbon monoxide which is essentially quantitatively produced from the methane in the natural gas. Only sufficient carbon monoxide is charged to the process to produce the amount of hydrocarbons that are withdrawn. Carbon monoxide is never vented and carbon dioxide is vented only to balance any carbon dioxide being charged in the natural gas feed stock. Therefore, the cyclic process of my invention converts the methane in the feed essentially quantitatively into higher hydrocarbons.
  • a very important advantage of my process over the processes of the prior art is that natural gases containing relatively large amounts of carbon dioxide are satisfactory feed stocks. That is, natural gas with as much as 60% or more carbon dioxide will produce liquid hydrocarbons from the methane portion of the gas and at the same time give a separated stream of carbon dioxide. Therefore, the feedstocks will normally comprise at least 25 mole % methane, preferably at least about 35 mole % methane.
  • the total process is in large measure adiabatic, since the heat produced in the exothermic partial oxidation essentially balances the heat needed in the endothermic reaction between carbon dioxide and hydrogen. Accordingly very little, if any, natural gas is burned to supply this heat. This is superior to any of the prior art processes for making liquid hydrocarbons from natural gas, wherein large amounts of extra heat are required.
  • the effect of any inefficiencies in any stage of the process is to slow down the conversion of natural gas but not to diminish the yield of hydrocarbon product based on carbon charged from the natural gas.
  • the movement of gases is efficient, minimizing the energy costs and wastes of moving large volumes of gases and having to heat large volumes of diluent gases which are not involved in the reactions of the different steps.
  • my new invention is a process for the production of higher i.e. multicarbon hydrocarbons from a mixture of hydrogen and carbon monoxide gases, comprising the steps of:
  • This preferred process may be further characterized as a process for the production of multicarbon hydrocarbons from natural gas comprising the steps of: (a) oxidizing said natural gas in a partial oxidizer to produce a syn gas, (b) heating said syn gas at a temperature above 800°C in a first reactor with carbon dioxide (c) separating essentially all of the carbon monoxide and water from the reaction product of said first reactor and recycling the remainder of said first reactor reaction product back to the first reactor, (d) mixing and reacting said separated carbon monoxide and at least 50% of said water in contact with a metal catalyst in a second reactor, (e) removing the hydrocarbons and excess water from the reaction product of the second reactor, (f) returning at least a portion of the remainder of the reaction product from the second reactor back to the oxidizer and (g) separating
  • the multicarbon hydrocarbons prepared by the process of this invention are compounds of carbon and hydrogen having more than one carbon atom per molecule.
  • the preferred hydrocarbons produced by the present process are liquid hydrocarbons having more than four carbon atoms per molecule. These latter compounds have boiling points in excess of 25°C at atmospheric pressure. Hydrocarbons boiling below this value include ethane, propanes, propenes, butenes and butanes which are separated from the higher hydrocarbons.
  • These lower molecular weight compounds have many uses, e.g. polymerization of the olefins to other higher molecular weight hydrocarbons, including high octane polymer gasoline and other products, oxidation to alcohols. etc. They may also be returned to the oxidizer for conversion into syn gas.
  • reaction product is meant all of the material, including product, by-product and unreacted feed stock, passing out of a reactor, normally a gaseous effluent, and into any other piece of equipment as a single stream, usually being separated into at least two streams for further processing, until the final product is obtained.
  • a reactor normally a gaseous effluent
  • the hydrogen of the syn gas mixture is reacted with carbon dioxide, in the absence of a catalyst, to produce more carbon monoxide. It is preferred to carry out this reaction with about an equimolar ratio of hydrogen to carbon monoxide in the reaction zone.
  • about equimolar refers to a molar ratio of hydrogen:carbon dioxide in the range of 1.5:1 to 1:1.5. However, an excess of either hydrogen or carbon dioxide may be employed.
  • excess refers to the relative ratio of the reactants. It is the amount of hydrogen or carbon dioxide in excess of the stoichiometric amount required for the reaction occurring in the first reactor, where stoichiometric is a 1:1 molar ratio.
  • the molar excess of hydrogen or carbon dioxide in the first reactor ranges from 0.5 to 4 fold. Preferably there is no excess of either reactant. Nevertheless, the mole ratio of hydrogen:carbon dioxide ranges from 4:1 to 1:4, preferably from 1.5:1 to 1:1.5 and most preferably 1:1.
  • the decision as to which mode to employ in any given situation is determined by weighing the advantages of high conversion in the first reactor versus the sizes of the first reactor and first separator.
  • the desired ratio of the two reactants in the first reactor is maintained by (1) recycling the remainder of the reaction product from the first reactor, after removing carbon monoxide and water, back to the first reactor, (2) determining the amount of carbon dioxide in the syn gas feed stock and (3) adjusting the amount of carbon dioxide returned from the second reactor back to the first reactor to allow for any carbon dioxide in the syn gas feed.
  • the recycle stream from the first separator is mainly hydrogen and carbon dioxide, the relative amounts of each depending on the operating mode selected. When in the equimolar mode, the amounts of hydrogen and carbon dioxide in this recycle stream are essentially equal. In an excess mode, all of the excess gas is present in the recycle stream along with any unreacted species.
  • the remainder of the reaction product from the second reactor after separation of the hydrocarbons and water is a gas, and is essentially carbon dioxide with small amounts of hydrogen and methane.
  • Some or all of this gaseous material is returned to the first reactor, preferably via the oxidizer.
  • the amount returned depends on the amount of carbon dioxide in the natural gas feed stock. As the concentration of carbon dioxide in the natural gas increases, the amount of the gaseous material returned to the first reactor or to the oxidizer, decreases until the two quantities balance at about 66% carbon dioxide in the natural gas.
  • any low molecular weight hydrocarbons are oxidized to syn gas and the carbon dioxide passes through unchanged. It is known that the presence of carbon dioxide in a partial oxidizer limits the formation of soot.
  • the process occurring in the first reactor is the non-catalytic, high temperature Reverse Water Gas Shift reaction, i.e. H 2 + C0 2 ⁇ CO + H 2 0..
  • the reverse water gas reaction is in equilibrium with the water gas shift reaction. Above 800°C the reverse reaction is thermodynamically favored and proceeds without the need for a catalyst. A description of this reaction is given in U.S. Patent No. 3,723,344 and in L'Actualite Chimique, pp 28-30 (Jan. 1982) .
  • the process occurring in the second reactor is the catalytic Koelbel-Engelhardt reaction, i.e.
  • the hydrocarbons produced by this reaction are mixtures of straight chain, branched and cyclic hydrocarbons preferably having at least 5 carbon atoms per molecule (i.e. C 5+) . For each carbon number, there are both saturated and unsaturated isomers.
  • the hydrocarbon fraction in the gasoline boiling range has high octane value and is useful as gasoline.
  • the product may contain small amounts of oxygenated compounds such as alcohols, ketones, etc. Usually the product has less than 5 mole percent of oxygen containing compounds. When operating under the preferred conditions of this process, less than 2 mole percent of oxygen containing compounds are produced.
  • the term liquid hydrocarbons refers to a product that is a major amount of hydrocarbons but may contain from 0 to 5 volume % of oxygen containing compounds.
  • the first step in this process is the conversion of natural gas to syn gas.
  • the preferred method of preparing syn gas feed stock from natural gas or methane is by a partial oxidation process. This partial oxidation process is well described in: Ind. and Eng. Chem. 40 (4) 601-607 (1948).
  • the heat produced by the oxidation of natural gas to syn gas essentially balances the heat required by the reaction occurring in the first reactor.
  • additional higher molecular weight hydrocarbons can be added to the oxidation feed. These higher molecular weight hydrocarbons include ethane, propane, butane and the like.
  • An integral part of the instant invention is control of the relative ratio of hydrogen to carbon dioxide in the first reactor.
  • Hydrogen is charged to the first reactor in the syn gas feed stock in a fixed ratio to carbon monoxide. But the ratio of reactants is determined by the amount of carbon dioxide charged to the first reactor.
  • the carbon dioxide in the first reactor is mainly obtained by (1) recycling the water free and carbon monoxide free remainder of the first reactor product back to the first reactor, and (2) returning from 0 to 100% of the carbon dioxide made in the second reactor back to the first reactor.
  • the amount of carbon dioxide returned from the second reactor depends on the amount of carbon dioxide charged directly or via the syn gas feed stock. It is preferred to operate with about an equal amount of carbon dioxide and hydrogen in the first reaction zone. But in the excess gas mode, the excess hydrogen or carbon dioxide in the reaction product of the first reactor is separated and recycled back to the first reactor, thereby initially creating and then maintaining an excess of cycling hydrogen or carbon dioxide within that reactor.
  • methane (CH 4 ) is used in the chemical equations to exemplify natural gas. These equations are idealized but are not unrealistic.
  • syn gas containing hydrogen and carbon monoxide in a ratio of 1:1 to 3:1, preferably 2:1.
  • gases may be present in the syn gas feed, for example, carbon dioxide, nitrogen, etc.
  • sulfur-containing gases can not be tolerated in the catalyzed second reaction zone and must be removed from the process stream prior to that time. This separation may be effected before or after the oxidizer, or after the first reactor.
  • the syn gas feed preferably from the partial oxidation of natural gas, containing carbon monoxide and hydrogen, is reacted with carbon dioxide to produce water and additional carbon monoxide.
  • the carbon dioxide in the outlet gasses of the first reactor is recycled to the first reactor along with the syn gas, but the carbon dioxide in the off gasses of the second reactor may contain lower hydrocarbons and is preferably returned via the oxidizer. Additional carbon dioxide may have been in the natural gas charged to the oxidizer, or alternatively it may originate from the burning of natural gas with pure oxygen. The carbon dioxide may come from any or all of these sources. In any case the amount charged to the first reactor is regulated so as to maintain the preferred ratio of hydrogen to carbon dioxide as described above. This is preferably done by controlling the amount of carbon dioxide returned from the second reactor.
  • the thermal Reverse Water Gas Shift reaction taking place in the first reactor is carried out at a temperature within the range of 800°C to 1800°C, preferably 800°C to 1300°C, and most preferably about 800°C to 1100°C and at a pressure within the range of 1 to 350 atm. , preferably 40 to 200 atm. Contact times are within the range of 0.05 to 5 seconds, preferably 0.1 to 2 seconds. This reaction is entirely thermal, a catalyst is not needed or used. Under these conditions, the mixture of carbon monoxide, hydrogen and carbon dioxide is largely converted into a mixture of water and carbon monoxide, any excess of cycling hydrogen or carbon dioxide remaining intact. This is shown by the following chemical equations where in equation (2) there is a 1:1 ratio of hydrogen to carbon dioxide, in equation (3) there is a 4:1 excess of hydrogen over carbon dioxide in the first reactor and in equation (4) there is an 4:1 excess of carbon dioxide over hydrogen in the first reactor:
  • High purity carbon monoxide is selectively isolated from a gas mixture by any one of several processes.
  • the Pressure Swing Adsorption process and (2) the COSORB absorption process. Either process is satisfactory for use in the present invention, however, the COSORB process is preferred. In both of these processes the gas feed containing carbon monoxide must be dried to less than about 1 ppm water.
  • the pressure (or vacuum) swing adsorption separation is well known and is described in U.S. patents 4,836,833 and 4,690,695 and in Gas Separation and Purification 5 . , 241 (December 1991) .
  • the COSORB process is also well known.
  • the carbon monoxide containing gas is passed into a toluene solution of a cuprous chloride-aluminum chloride complex at ambient temperatures.
  • the carbon monoxide is bound into the complex and the remaining gasses pass through the solution unchanged.
  • the carbon monoxide is recovered by heating the toluene solution. See for example: Chem. Eng. Prog. 70(5) . (1974) and Chem. economy and Eng. Rev. £(12), 29 (Dec. 1977) .
  • the presence of hydrogen in the feed to the Koelbel- Engelhardt reactor negatively affects the quality and yield of the hydrocarbon product of this process.
  • Any hydrogen present in this reactor reduces half of an equivalent molar amount of carbon monoxide via a Fischer-Tropsch reaction to produce saturated, straight chain hydrocarbons of low molecular weight.
  • about 40% of the product from this Fischer-Tropsch reaction is methane.
  • the feed stock to the second reactor must have a carbon monoxide:hydrogen ratio greater than 4:1, preferably greater than 9:1.
  • Low concentrations of hydrogen in the feed to the second reactor are obtained by having (1) a high conversion of hydrogen in the first reactor and/or (2) an efficient procedure to separate unreacted hydrogen in the first reactor effluent from carbon monoxide.
  • High conversions of hydrogen are obtained by operating in the excess carbon dioxide mode. These high conversions are obtained at the cost of an increase in reactor size and a corresponding increase in the size of the first separator.
  • the preferred method of lowering the hydrogen concentration is through the use of a gas separation procedure such as the COSORB process or other similar processes which produce essentially pure carbon monoxide.
  • High concentrations of carbon dioxide in the feed to the second reactor are also detrimental and are to be avoided.
  • the metal catalysts are converted to the corresponding inactive carbides.
  • cobalt carbide unlike iron carbide, is easily and totally converted to the cobalt metal catalyst by heating in a hydrogen atmosphere.
  • the same separation processes as described above also remove essentially all carbon dioxide from the carbon monoxide feed stock.
  • the water produced in the first reactor and condensed out in the above separation process is essential for the last step of the instant process wherein carbon monoxide and water are converted into liquid hydrocarbons. Since that reaction is a catalytic reaction, all material charged to it must be of high purity. This is especially true of the water, which must be free of any dissolved minerals.
  • the water produced by the Reverse Water Gas Shift reaction meets this criterion.
  • One of the advantages of the present invention is that the water produced in the first reactor is more than enough for reaction in the second reactor.
  • the carbon dioxide produced in the second reactor is the stoichiometric amount needed in the first reactor. In the second reactor the water and carbon monoxide feed are converted into a mixture of carbon dioxide and hydrocarbons as shown in the following chemical equation:
  • the feed mixture to this reaction carbon monoxide and water
  • iron based catalysts require a carbon monoxide:water mole ratio of at least 2:1, preferably 3:1 whereas with cobalt based catalysts the preferred ratio is 3:2. This adjustment is made when revaporizing water in the previous step of the process.
  • the process occurring in the second reactor known as the Koelbel-Engelhardt reaction is carried out over a metallic catalyst.
  • Those catalysts known for catalyzing the Fischer-Tropsch reaction are useful in this reaction.
  • These catalysts are primarily the transition metals of the eighth sub-group of the periodic table of elements, namely, iron, nickel, and cobalt.
  • Other metals which can be used include ruthenium, manganese and thorium. Alloys of these metals are also satisfactory catalysts.
  • the catalysts may be supported on any suitable support such as talc, diatomaceous earth, silica gel, alumina, activated carbon, bauxite, kieselguhr and the like.
  • Catalysts may also contain promoters, such as the oxides, hydroxides and salts of the alkali and alkaline earth metals such as sodium, potassium, rubidium, etc.
  • promoters are the difficult to reduce metal oxides, such as alumina, potassium oxide, calcium oxide and magnesium oxide.
  • Compounds of vanadium, boron, copper and silver may also be used as promoters.
  • the preferred catalysts are based on cobalt or iron.
  • Cobalt has advantages such as its oxidation resistance and ease of regeneration upon carbiding, as occurs when the gas feed to the reaction has more than a 3:1 ratio of carbon monoxide:water.
  • carbiding of cobalt catalysts it is preferred to operate with a feed stock having a 0.3:1 to 2.8:1, preferably about 1.5:1 mole ratio of carbon monoxide to water.
  • the cobalt based catalysts are much more tolerant of carbon dioxide in the feed than are the iron based catalysts.
  • cobalt catalysts produce hydrocarbons having a high degree of unsaturation, thereby producing feed stocks for a variety of processes and products, e.g. polymerization or detergent manufacture.
  • Iron based catalysts are superior to the cobalt based catalysts in some respects, i.e. under identical conditions the reaction rate is higher for the iron catalyst.
  • the iron catalyst is easily oxidized by excess water and the ratio of carbon monoxide:water must be 2:1 or greater. Iron catalysts are much more sensitive to carbon dioxide contamination because they are oxidized by carbon dioxide.
  • the metal catalyst must be activated. Activation is accomplished by heating the metal under reducing conditions.
  • One way to activate the iron catalyst is by contacting it with a 1:2 carbon monoxide:hydrogen gas mixture by volume at a space velocity of 100/hour and at 230°C for 70 hours.
  • a cobalt catalyst may be activated by contact with a gas mixture of 20% carbon monoxide and 80% nitrogen at 170°C for 55 hours.
  • Other metal catalysts are activated under similar conditions as described in the prior art.
  • the reactor may contain a fixed bed of the metallic catalyst or employ a fluidized bed.
  • a liquid phase reactor may also be utilized.
  • Reaction temperatures are within the range of 150°C to 400°C, preferably from 180°C to 300°C and most preferably about 230°C.
  • Pressures in the reactor range from 1 atm. to 100 atm. , preferably from 5 atm. to 50 atm. and most preferably about 10 atm.
  • the gases are passed through the reactor at a space velocity dependent upon the catalyst.
  • useful space velocities are from 10 to 200/hr, preferably 10 to 100/hr and most preferably, 20 to 50/hr.
  • the space velocity must be such that a single pass over the catalyst gives over 50% preferably over 95% conversion of carbon monoxide.
  • the corresponding range of space velocities is from about 10 to 1000/hr.
  • the reaction product stream from the second reactor comprising a mixture of hydrocarbons, carbon dioxide, some hydrogen and excess water, is passed into a separator wherein the multicarbon hydrocarbons and water are separated from the gaseous carbon dioxide and volatile hydrocarbons. This separation may be carried out by cooling and condensing out the water and the higher hydrocarbons, leaving carbon dioxide and volatile hydrocarbons.
  • the carbon dioxide may then be separated from the low boiling hydrocarbons such as ethane, ethene, propanes, propenes, butanes, butenes etc. by scrubbing with an aqueous solution containing a carbon dioxide absorbant, e.g. 10 to 20% monoethanolamine. Carbon dioxide absorption is at relatively low temperatures where it is converted into a carbonate.
  • carbon dioxide is regenerated by heating the carbonate containing solution to about 100°C (Chem. Eng. Progr. October 1986 pp. 38-46) .
  • the unsaturated hydrocarbons from this low boiling fraction may then be polymerized by contact with an appropriate catalyst to produce additional liquid hydrocarbons of more than 4 carbon atoms per molecule.
  • the low boiling hydrocarbons may not be separated from the carbon dioxide, but rather remain in the gaseous carbon dioxide stream.
  • the gaseous by-product material remaining after separation of the liquid hydrocarbons and excess water is a mixture of carbon dioxide, a small amount of hydrogen, and low molecular weight hydrocarbons. From 0 to 100% of this material is returned to the first reactor, preferably via the oxidizer. The quantity returned depends on the concentration of carbon dioxide in the natural gas fed to the oxidizer. Thus, when the natural gas is essentially free of carbon dioxide, all of the by-product material is returned because all of the carbon dioxide is needed in the first reactor.
  • the amount of carbon dioxide in the natural gas increases, the amount of by-product material returned is decreased so that the total carbon dioxide concentration in the first reactor is constant. Excess carbon dioxide vented from the second reactor may be collected for other uses such as enhanced oil recovery, carbonation, etc. Because of carbon dioxide return, the yield of hydrocarbons is effectively 100% based on the methane in the natural gas fed to the process.
  • the liquid hydrocarbons are readily separated from the excess water by decanting or other similar phase separation techniques. These hydrocarbons have an atmospheric pressure boiling point from about 25°C to about 300°C. This range of boiling points indicates a hydrocarbon product having from 5 to 20 carbons per molecule, which are for the most part aliphatic and may be saturated or unsaturated.
  • FIG. 1 This figure is a block flow diagram of the basic process of the instant invention.
  • a syn gas feed stock comprising carbon monoxide in line 1 and hydrogen in line 2 is charged to reactor 4.
  • carbon dioxide is charged to reactor 4 via line 17 optionally comprising fresh carbon dioxide from line 3, and return as well as recycle carbon dioxide from line 15 and 16.
  • Reactor 4 is a Reverse Water Gas Shift Reactor maintained at a temperature in excess of 800°C.
  • the reaction product from reactor 4 is passed to separator 6 via line 5.
  • separator 6 carbon monoxide and water are separated from the remainder of the reaction product. Unreacted gases, are recycled to reactor 4 via lines 7, 16 and 17. Any excess water is removed through line 8.
  • the remaining water and carbon monoxide are fed into reactor 10 through line 9.
  • Reactor 10 is a Koelbel-Englehardt reactor containing a metallic catalyst and operating at elevated temperatures in the range of 150°C to 400°C.
  • the reaction product from reactor 10 is passed to separator 12 via line 11.
  • separator 12 any excess water is removed via line 14.
  • Multicarbon hydrocarbon product is removed via line 13 and the carbon dioxide by-product is returned to reactor 4 via lines 15, 16 and 17. Excess carbon dioxide is vented through line 18.
  • Figure 2 This figure is a block flow diagram showing in a simplified manner how the steps of the present preferred process, operating with equal amounts of carbon dioxide and hydrogen in the first reactor, are coordinated with recycle of unreacted feed components and return of by-product streams to achieve essentially complete conversion of the carbon in the natural gas feed into a mixture of liquid hydrocarbons.
  • the natural gas feed stock to the cyclic process of the present invention is essentially 100% methane.
  • This natural gas is fed to oxidizer 1 via line 7 while oxygen is fed to it via line 8.
  • oxygen is fed to it via line 8.
  • oxidizer 1 under conditions of full return carbon dioxide and optionally low molecular weight hydrocarbons from condenser 6 are charged into oxidizer 1, via line 10.
  • oxidizer 1 the natural gas and the returned low boiling hydrocarbons are partially oxidized to syn gas.
  • the syn gas product of oxidizer 1 and carbon dioxide from the sources mentioned above are then passed via line 9 to the Reverse Water Gas Shift reactor, 2. Hydrogen and carbon dioxide from condenser 4 are recycled to reactor 2 via line 11.
  • the reaction product mixture from reactor 2 is passed via line 12 to a separator 3.
  • the gaseous carbon monoxide is removed from separator 3 via line 13.
  • the water, hydrogen and carbon dioxide from separator 3 are removed via line 14 and charged to condenser 4.
  • the liquid water formed within this condenser is removed via line 15, and after revaporization in vaporizer 22, it is removed through line 19 and is combined with the carbon monoxide in line 13 and then charged to reactor 5 via line 16.
  • an iron catalyst is used in reactor 5
  • half of the water remains in vaporizer 22.
  • a cobalt catalyst is used therein, all of the water is removed and charged to reactor 5 via line 19. Any excess water remaining in vaporizer 22 is removed via line 21.
  • the hydrogen and carbon dioxide remaining after water separation in condenser 4 are removed and recycled to reactor 2 via line 11.
  • the reaction product from reactor 5 is passed into condenser 6 via line 17.
  • condenser 6 the hydrocarbons having a boiling point above 25°C as well as excess water are separated from the more volatile components of the reaction product by cooling the reaction product mixture to about 10°C.
  • the liquified material comprising water and all hydrocarbons having 5 or more carbon atoms per molecule, is removed via line 18 and sent to phase separator 23.
  • phase separator 23 In this separator, the upper hydrocarbon phase is removed via line 24 and the aqueous phase is removed via line 25.
  • the remainder of the reaction product mixture in condenser 16, consisting mainly of carbon dioxide, with some hydrogen and low boiling hydrocarbons is returned to reactor 1 via line 10. This procedure is preferred when the process is producing a negligible quantity of volatile hydrocarbons.
  • the return gas from condenser 6 be first passed into an aqueous solution of monoethanolamine wherein the carbon dioxide is absorbed and the volatile hydrocarbon gases are easily removed via line 26. Carbon dioxide is then recovered by heating the absorbant solution to the boiling point. The resulting vapor is cooled to condense the water. The thereby liberated carbon dioxide is then returned to the oxidizer. Under some conditions of operation, excess carbon dioxide is removed through line 20.
  • the oxygen and heated natural gas in volumetric ratio of about 0.5 are introduced into noncatalytic partial combustion reactor 2 operating at a temperature of 1100°C under a pressure of 10 atmospheres. At the same time, carbon dioxide from condenser 15 via line 5 and through multiple heat exchanger 6, is charged to the oxidizer 2.
  • One method of utilizing the heat generated during oxidation for heating the subsequent carbon dioxide/hydrogen reaction is by the use of two concentric reactors.
  • the outer reactor being the partial oxidation zone and the inner reactor being the Reverse Water Gas Shift Reaction zone as shown in Figure 3, vessels 2 and 7.
  • the carbon monoxide containing solution in separator 11 is heated to regenerate carbon monoxide which is removed via line 21.
  • the gaseous carbon dioxide and hydrogen in line 9 are passed through the multiple heat exchanger 6 wherein the temperature is raised to about 900°C, and is then recycled to the noncatalystic converter 7.
  • the water from line 18 is vaporized by heating to 100°C in vaporizer 12. All of the steam generated in vaporizer 12 is added through line 13 to the carbon monoxide stream in line 21 to give a combined mixture having a 3:2 carbon monoxide:water ratio which is preferred for cobalt catalysts.
  • This mixture is charged through line 22 to the Koelbel-Engelhardt reactor, 14 at a space velocity of about 30 per hour.
  • Reactor 14 is maintained at 230°C and 10 atmospheres. Reactor 14 is kept at the desired temperature by boiling water under pressure in a reactor jacket. Reactor 14 is charged with a cobalt-thorium oxide-magnesium oxide-silicon dioxide catalyst containing 100 parts of cobalt, 5 parts of thorium, 10 parts of magnesium and 100 parts of silica. The catalyst is activated by heating for two hours at 450°C, with hydrogen gas passing over it at a space velocity of 1000/hr.
  • the reaction product stream from reactor 14 is passed into condenser 15 via line 19.
  • the temperature of the reaction product is lowered to 5°C, causing the hydrocarbons having more than 4 carbon atoms and the water present to condense and pass out of the condenser through line 20.
  • This condensate amounts to about 30% of the reaction product stream from reactor 14.
  • the uncondensed gases, about 70% of the rection product stream, comprising about 95% carbon dioxide, 3% lower hydrocarbons (i.e. less than 5 carbon atoms per molecule) and 2% hydrogen are passed through line 26 to the extractive carbon dioxide- volatile hydrocarbon separator, 27.
  • separator 27 the carbon dioxide is first separated from the volatile hydrocarbons by absorption in aqueous monoethanolamine.
  • the unabsorbed volatile hydrocarbons are removed via line 28.
  • the carbon dioxide is regenerated by heating the absorbant solution to the boiling point and passing the resulting vapors through a condenser in separator 27 to liquify the water which is returned to the monoethanolamine solution.
  • the resulting relatively dry carbon dioxide in line 5 is then returned to the oxidizer 2 via the multiple heat exchanger 6, after removal of excess carbon dioxide via line 30.
  • phase separator 23 a hydrocarbon product having more than 4 carbon atoms in about 30% yield based on carbon monoxide entering reactor 14, is removed via line 24. Any excess water is removed through line 25.
  • the catalyst is an iron-copper catalyst, alkalized with potassium carbonate and containing 100 parts of iron, 0.1 part of copper and 0.25 parts of potassium carbonate. This catalyst is activated by heating to 270°C and passing carbon monoxide over it for 24 hours at ' atmospheric pressure and a space velocity of 100/hr. Then hydrogen is passed over it under the same conditions and for the same amount of time.
  • the subject process provides for many advantages in the utilization of natural gas for the production of liquid hydrocarbons, which are liquid at room temperature and may serve as a mobile fuel, and may be further processed to provide gasoline or other fuel or feedstock for the production of high value chemicals.
  • the subject process is highly efficient in the transformation of methane to higher aliphatics, in its utilization of thermal energy and its adaptability to a wide variety of natural gas compositions as a feedstock.
  • the subject process combines well known processes in a novel way, so that the individual steps may utilize the technology which has been developed in association with these individual stages to optimize the process.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Un procédé de conversion du gaz naturel en hydrocarbures comprend une nouvelle combinaison de phases de traitement qui consistent à d'abord convertir le gaz naturel (7) en gaz synthétique (9) dont l'hydrogène est mis en réaction avec du dioxyde de carbone dans un convertisseur gaz-eau inverse (2) pour produire un mélange d'eau et de monoxyde de carbone qui est ensuite mis en contact avec un catalyseur métallique dans un réacteur (5) pour produire un mélange d'hydrocarbures.
PCT/US1995/003092 1994-03-11 1995-03-09 Conversion du gaz naturel en hydrocarbures superieurs WO1995024367A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU19906/95A AU1990695A (en) 1994-03-11 1995-03-09 Natural gas conversion to higher hydrocarbons

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US21216794A 1994-03-11 1994-03-11
US08/212,167 1994-03-11
US36878995A 1995-01-04 1995-01-04
US08/368,789 1995-01-04

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002090467A1 (fr) * 2001-05-03 2002-11-14 Institut Neftekhimicheskogo Sinteza Imeni. A.V. Topchieva Procede de fabrication d'essence a partir de matieres premieres a base d'hydrocarbures gazeux
WO2010136980A1 (fr) * 2009-05-26 2010-12-02 University Of The Witwatersrand Système absorbant du carbone utilisé dans la production de gaz de synthèse
US8946308B2 (en) 2008-12-17 2015-02-03 Saudi Basic Industries Corporation Process for increasing the carbon monoxide content of a syngas mixture
EP3031884A1 (fr) 2014-12-08 2016-06-15 Commissariat A L'energie Atomique Et Aux Energies Alternatives Procédé de gazéification de charge de matière carbonée à rendement matière et coût de production optimisés
RU2638853C1 (ru) * 2017-02-28 2017-12-18 Олег Петрович Андреев Блок конверсии синтез-газа в жидкие углеводороды установки для переработки природного газа

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US2579663A (en) * 1948-12-15 1951-12-25 Gulf Research Development Co Process of synthesizing hydrocarbons
US4595702A (en) * 1984-01-20 1986-06-17 Mobil Oil Corporation Conversion of synthesis gas to liquid hydrocarbons

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US2579663A (en) * 1948-12-15 1951-12-25 Gulf Research Development Co Process of synthesizing hydrocarbons
US4595702A (en) * 1984-01-20 1986-06-17 Mobil Oil Corporation Conversion of synthesis gas to liquid hydrocarbons

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Title
GREEN et al., "Conversion of Naturel Gas to Transport Fuels", TECHNOL. CIENCIA ED., (1991), 7:25-37. Pacific Area Chemical Engineering Congress, Energy-Alternative Sources, October 19-22, 1088, Acalpulco Mexico. *
INDUSTRIAL AND ENGINEERING CHEMISTRY, April (1948), Vol. 40, No. 4, April, MONTGOMERY et al., "Thermodynamics and Stoichiometry of Synthesis Gas Production", pages 601-607. *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002090467A1 (fr) * 2001-05-03 2002-11-14 Institut Neftekhimicheskogo Sinteza Imeni. A.V. Topchieva Procede de fabrication d'essence a partir de matieres premieres a base d'hydrocarbures gazeux
US8946308B2 (en) 2008-12-17 2015-02-03 Saudi Basic Industries Corporation Process for increasing the carbon monoxide content of a syngas mixture
US9249079B2 (en) 2008-12-17 2016-02-02 Saudi Basic Industries Corporation Process for increasing the carbon monoxide content of a syngas mixture
WO2010136980A1 (fr) * 2009-05-26 2010-12-02 University Of The Witwatersrand Système absorbant du carbone utilisé dans la production de gaz de synthèse
CN102482080A (zh) * 2009-05-26 2012-05-30 约翰内斯堡金山大学 用于生产合成气的碳吸收系统
US8940188B2 (en) 2009-05-26 2015-01-27 University of the Witwartersrand Johannesburg Carbon absorbing system used in the production of synthesis gas
AP3348A (en) * 2009-05-26 2015-07-31 Univ Witwatersrand Jhb A carbon absorbing system used in the production of synthesis gas
EP3031884A1 (fr) 2014-12-08 2016-06-15 Commissariat A L'energie Atomique Et Aux Energies Alternatives Procédé de gazéification de charge de matière carbonée à rendement matière et coût de production optimisés
RU2638853C1 (ru) * 2017-02-28 2017-12-18 Олег Петрович Андреев Блок конверсии синтез-газа в жидкие углеводороды установки для переработки природного газа

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