Methane oxidative coupling with La—Ce catalysts

Abstract

A metal oxide catalyst capable of catalyzing an oxidative coupling of methane reaction is described. The metal oxide catalyst includes a lanthanum (La) cerium (Ce) metal oxide and further including a lanthanum hydroxide (La(OH).sub.3) crystalline phase. The catalyst is capable of catalyzing the production of C.sub.2+ hydrocarbons from methane and oxygen. Methods and systems of using the metal oxide catalyst to produce C.sub.2+ hydrocarbons from a reactant gas are also described.

Claims

1. A metal oxide catalyst capable of catalyzing an oxidative coupling of methane reaction, the metal oxide catalyst comprising a lanthanum (La) cerium (Ce) metal oxide and further including a lanthanum hydroxide (La(OH).sub.3) crystalline phase in the crystal lattice of the metal oxide catalyst, wherein the molar ratio of La:Ce is 5<La:Ce<30, and wherein the catalyst is capable of catalyzing the production of C.sub.2+ hydrocarbons from methane and oxygen.

2. The metal oxide catalyst of claim 1, wherein the La:Ce is 5<La:Ce<15.

3. The metal oxide catalyst of claim 1, wherein the metal oxide catalyst is a bulk metal oxide catalyst.

4. The metal oxide catalyst of claim 1, wherein the LaCe metal oxide is incorporated into the crystal lattice of the metal oxide catalyst.

5. The metal oxide catalyst claim 1, wherein the metal oxide catalyst is catalyzes the production of C.sub.2+ hydrocarbons from methane and oxygen at an average temperature of 400 C. to 550 C.

6. The metal oxide catalyst of claim 5, wherein the metal oxide catalyst has a C.sub.2+ hydrocarbon selectivity of at least 60%.

7. The metal oxide catalyst of claim 5, wherein the metal oxide catalyst has an O.sub.2 conversion of at least 90%.

8. The metal oxide catalyst of claim 1, wherein the metal oxide catalyst is in contact with a reactant feed that includes methane and an oxygen source.

9. The metal oxide catalyst of claim 8, wherein the reactant feed has an average temperature of less than 1000 C.

10. The metal oxide catalyst of claim 9, wherein at least a portion of the methane in the reactant feed has ignited or has formed into a C.sub.2+ hydrocarbon.

11. A method of producing C.sub.2+ hydrocarbons from an oxidative coupling of methane reaction, the method comprising contacting a reactant feed that includes methane and an oxygen containing gas with any one of the metal oxide catalysts of claim 1 under conditions sufficient to produce a first product gas stream comprising C.sub.2+ hydrocarbons.

12. The method of claim 11, wherein the oxidative coupling of methane reaction occurs at an average temperature of 400 C. to 550 C. and a gas hourly space velocity of 10,000 hr-1 or more.

13. The method of claim 11, wherein C.sub.2+ hydrocarbon selectivity is at least 60%.

14. The method of claim 13, wherein the O.sub.2 conversion is at least 90%.

15. The method of claim 13, further comprising contacting the first product stream with a second catalyst that is capable of catalyzing an oxidative coupling of methane reaction to produce a second product stream that includes C.sub.2+ hydrocarbons, wherein the amount of C.sub.2+ hydrocarbons in the second product stream is greater than the amount of C.sub.2+ hydrocarbons in the first product stream, wherein the second catalyst is positioned downstream from the first catalyst.

16. The method of claim 15, wherein heat produced during the oxidative coupling of methane reaction between the reactant feed and the metal oxide catalyst is at least partially used to heat the first product stream.

17. The method of claim 16, wherein the average temperature of the first product stream is at least 700 C. just prior to or during contact with the second catalyst.

18. The method of claim 15, wherein the second catalyst comprises manganese or a compound thereof, tungsten or a compound thereof, lanthanum or a compound thereof, sodium or a compound thereof, cerium or a compound thereof, silicon or a compound thereof, and any combination thereof.

19. The method of claim 18, wherein the second catalyst is a supported catalyst comprising MnNa.sub.2WO.sub.4/SiO.sub.2.

20. A method of making a metal oxide catalyst of claim 1, the method comprising: obtaining an aqueous solution comprising lanthanum nitrate and cerium salts, wherein the molar ratio of La to Ce is 5<La:Ce<30; heating the aqueous mixture to remove the water to obtain a dried material; and calcining the dried material at a temperature of 400 to 675 C. for a sufficient period of time to obtain the metal oxide catalyst.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic of an embodiment of a system to produce ethylene using the catalytic material of the present invention.

(2) FIGS. 2A and 2B are schematics of embodiments of a system to produce ethylene using the catalytic material of the present invention and an additional catalyst.

(3) FIG. 3 is an image of an X-Ray Diffraction pattern of catalyst of the present invention having a molar ratio of La:Ce of 15.

(4) FIG. 4 is an image of X-Ray Diffraction pattern of catalyst having a molar ratio of La:Ce of 1.

(5) FIG. 5 are graphs of temperature in Celsius versus O.sub.2 conversion in percent, CH.sub.4 conversion in percent and C.sub.2+ selectivity in percent for Sample 1 (La:Ce ratio of 10:1) in an oxidative coupling of methane reaction at a methane to oxygen ratio of 7.4.

(6) FIG. 6 are graphs of temperature in Celsius versus O.sub.2 conversion in percent, CH.sub.4 conversion in percent for Sample 3 (La:Ce ratio of 15:1) in an oxidative coupling of methane reaction at a methane to oxygen ratio of 4.

(7) While the invention is susceptible to various modifications and alternative forms, specific embodiments thereof are shown by way of example in the drawings and may herein be described in detail. The drawings may not be to scale.

DETAILED DESCRIPTION OF THE INVENTION

(8) The currently available catalysts used in oxidative coupling of methane reactions to produce hydrocarbons having two or more carbon atoms (C.sub.2+ hydrocarbons) are prone to sintering and coking, both of which can lead to inefficient catalyst performance and ultimately failure of the catalyst after relatively short periods of use. This can lead to inefficient C.sub.2+ hydrocarbon production as well as increased costs associated with their production. Further, current technology require the feed to be heated to elevated temperatures (e.g., greater than 750 C.) prior to contacting the catalyst to initiate (e.g., ignite) and maintain the oxidative coupling reaction.

(9) A discovery has been made that avoids the coking and sintering described above and lowers the average ignition temperature of the exothermic oxidative coupling reaction. The discovery is premised on the use of a bulk metal catalyst that includes a La(OH).sub.3 crystal phase in a LaCe oxide catalyst. This catalyst can catalyze the oxidative coupling of methane at milder conditions than conditions being used with currently available catalysts. The LaCe oxide catalyst with La(OH).sub.3 has structural characteristics that are believed to provide for an environment that has both high oxygen capacity and mobility characteristics thereby promoting ignition at lower temperatures (e.g., less than 700 C.) and to produce C.sub.2 and/or higher hydrocarbons at higher selectivities.

(10) These and other non-limiting aspects of the present invention are discussed in further detail in the following sections.

(11) A. Catalytic Material

(12) 1. First/Upstream Catalytic Material

(13) The metals that can be used in the context of the present invention to create bulk metal oxides or supported catalysts include at least two metals (M.sup.1 and M.sup.2) from the lanthanide series (Group IIIB, Column 3) of the Periodic Table. The metals or metal compounds can be purchased from any chemical supplier such as Sigma-Aldrich, Alfa-Aeaser, Strem, etc. Lanthanides metals and metal compounds include lanthanum, cerium, praseodymium (Pr), neodymium (Nd), promethium (Pm), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), lutetium (Lu) or any combination thereof, with lantheum and cerium oxides being preferred. In a particular embodiment, the catalyst does not contain a dopant. In a preferred embodiment, the catalyst consists essentially of lanthanum-cerium oxide and lanthanum hydroxide. In a non-limiting example, lanthanum nitrate and cerium nitrate are used in combination to create the catalysts of the present invention.

(14) The catalysts are crystalline in structure and can include one or more crystalline phases. The phases can have a common crystal framework and structure. At least one phase contains a trinary structure of two metals and oxygen (M.sup.1M.sup.2O) where at least one of M.sup.1 and M.sup.2 is in a trivalent state. For example, the metal oxide catalyst can be LaCe oxides, where La is in the trivalent state (III).

(15) A second phase is a M.sup.1(OH).sub.3 crystal phase, where M.sup.1 is the trivalent ion of the M.sup.1M.sup.2O compound, (e.g., lanthanum). In the most preferred embodiment, M.sup.1 is lanthanum and the second phase is La(OH).sub.3. The M.sup.1(OH).sub.3 crystal phase is believed to have a hexagonal crystal structure and that the M.sup.1(OH).sub.3 (e.g., La(OH).sub.3) is incorporated in the M.sup.1M.sup.2O (e.g., LaCe oxide) crystal lattice.

(16) The bulk metal oxide catalysts of the present invention can be made by processes that provide a crystalline structure as exemplified in the Examples section. A non-limiting example includes dissolving salts of lantheum and cerium (for example, La(NO.sub.3).sub.3 and Ce(NO.sub.3).sub.3) in de-ionized water with agitation. The metal salts can be in a 2:1 to 30:1 molar ratio, preferably a 5:1 to 30:1, or most preferably a 5:1 to 15:1 molar ratio, of M.sup.1:M.sup.2 (for example, La(NO.sub.3).sub.3 and Ce(NO.sub.3).sub.3). The molar ratio of M.sup.1 to M.sup.2 (e.g., La:Ce) can be greater than 1, or 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30 or any value there between. In a particular instance, the M.sup.1 to M.sup.2 (e.g., La:Ce) molar ratio is from 5 to 30, 5 to 15, or 7 to 12. The aqueous mixture of the salts can be dried at a temperature from 110 C. to 130 C., for example, 125 C. The dried material can be calcined by heating the pellets to an average temperature between 400 C. and 850 C., 500 C. to 700 C., with 600 C. and 650 C. being preferred, at a rate of about 1 C. per minute and holding at between 600 C. and 650 C. for 3 to 12 hours, or 4 to 8 hours, and then cooled at a rate of about 1 C. per minute to ambient temperature (about 72 to 80 C.). In a preferred aspect of the invention, the calcining temperature is 650 C. at 4 to 8 hours. The resulting catalyst has discrete M.sup.1(OH).sub.3 (e.g., La(OH).sub.3) phase in the crystal lattice). In a preferred embodiment, the LaCe oxide has La(OH).sub.3 incorporated in its crystal lattice.

(17) The bulk metal oxide catalysts of the present invention can be put on a support. Supported metal oxide catalysts of the present invention can be made by generally known catalyst preparation techniques. The support can be Al.sub.2O.sub.3, SiO.sub.2 or other materials. In some embodiments, the support may be combined with the catalytic metal to form a catalyst (for example, an incipient impregnation technique). In a particular embodiment, the catalyst is not a nanowire or present in a nanowire substrate. As illustrated in the Examples section, the produced bulk metal oxide catalysts of the invention are coke resistant materials at elevated temperatures, such as those typically used in oxidative coupling of methane reactions (e.g., 400 C. up to 1000 C. or range from 400 C., 450 C., 500 C., 525 C., 550 C., 600 C., 700 C., 750 C., to 950 C.). Further, the produced catalysts can be used effectively in oxidative coupling reactions of methane at an average temperature range from 275 C. up to 1000 C. or from 400 C. to 525 C., at a gas hourly space velocity (GHSV) range from 500 to 100,000 h.sup.1 or more at atmospheric or elevated pressures, preferably a temperature of 400 C. to 525 C. and a GHSV of 50,000 h.sup.1 or more. The metal oxide catalyst can have a C.sub.2+ hydrocarbon selectivity of at least 60%, 60% to 80%, or 60% to 70%, or at least 60%, 65%, 70%, 75%, 80% or any range there between. The metal oxide catalyst can have O.sub.2 conversion of at least 90% or 100%.

(18) 2. Additional Catalytic Material

(19) Additional catalysts can be used in combination with the catalyst of the present invention. The additional catalysts (e.g., a second catalyst, third catalyst, fourth catalyst, etc.) can be positioned downstream of the catalyst (first catalyst). The second catalyst can be the same catalysts, different catalysts, or a mixture of catalysts. The catalysts can be supported, bulk metal catalysts, or unsupported catalysts. The support can be active or inactive. The catalyst support can include MgO, Al.sub.2O.sub.3, SiO.sub.2, or the like. All of the support materials can be purchased or be made by processes known to those of ordinary skill in the art (e.g., precipitation/co-precipitation, sol-gel, templates/surface derivatized metal oxides synthesis, solid-state synthesis, of mixed metal oxides, microemulsion technique, solvothermal, sonochemical, combustion synthesis, etc.). One or more of the catalysts can include one or more metals or metal compounds thereof. Catalytic metals include Li, Na, Ca, Cs, Mg, La, Ce, W, Mn, Ru, Rh, Ni, and Pt. Non-limiting examples of catalysts of the invention include La on a MgO support, Na, Mn, and La.sub.2O.sub.3 on an aluminum support, Na and Mn oxides on a silicon dioxide support, Na.sub.2WO.sub.4 and Mn on a silicon dioxide support, or any combination thereof. Non-limiting examples of catalysts that promote oxidative coupling of methane to produce ethylene are Li.sub.2O, Na.sub.2O, Cs.sub.2O, MgO, WO.sub.3, Mn.sub.3O.sub.4, or any combination thereof. A non-limiting example of a mixture of catalysts is a catalyst mixture that includes a supported catalyst containing Ni, Ce and La, and another supported catalyst containing Mn, W, and Na (e.g., MnNa.sub.2WO.sub.4 on SiO.sub.2). In some instances, the second catalyst has a C.sub.2+ selectivity that is greater than the first catalyst.

(20) B. Reactants

(21) The reactant mixture in the context of the present invention is a gaseous mixture that includes, but is not limited to, a hydrocarbon or mixtures of hydrocarbons and oxygen. The hydrocarbon or mixtures of hydrocarbons can include natural gas, liquefied petroleum gas containing of C.sub.2-C.sub.5 hydrocarbons, C.sub.6+ heavy hydrocarbons (e.g., C.sub.6 to C.sub.24 hydrocarbons such as diesel fuel, jet fuel, gasoline, tars, kerosene, etc.), oxygenated hydrocarbons, and/or biodiesel, alcohols, or dimethyl ether. In a preferred aspect, the hydrocarbon is a mixture of hydrocarbons that is predominately methane (e.g., natural gas). The oxygen containing gas used in the present invention can be air, oxygen enriched air, oxygen gas, and can be obtained from various sources. The reactant mixture may further contain other gases, provided that these do not negatively affect the reaction. Examples of such other gases include carbon dioxide, nitrogen and hydrogen. The hydrogen may be from various sources, including streams coming from other chemical processes, like ethane cracking, methanol synthesis, or conversion of methane to aromatics. Carbon dioxide may be from natural gas, or a waste or recycle gas stream (e.g. from a plant on the same site, like for example from ammonia synthesis) or after recovering the carbon dioxide from a gas stream.

(22) C. Oxidative Coupling of Methane Process

(23) In one particular aspect of the invention, a method of producing ethylene from a reaction mixture that includes methane (CH.sub.4) and an oxygen (O.sub.2) containing gas is described. The reaction mixture can be contacted with the metal oxide catalyst of the present invention under sufficient conditions to produce a product stream (e.g., a first product stream) that includes ethylene. The ethylene is obtained from oxidative coupling of CH.sub.4. In some instances, continuous flow reactors can be used in the context of the present invention to treat methane with oxygen to produce ethylene. Non-limiting examples of continuous flow reactors include a fixed-bed reactor, a fluidized reactor, a stacked bed reactor, an ebullating bed reactor, or a moving bed reactor. The reactors include conventional components for controlling chemical reactions such as, for example, heating elements, thermocouples, manual and/or automated controllers, valves, and the like. The reactors can be jacketed or unjacketed. Jacketed reactors can be capable of circulating a heat exchange fluid for addition or removal of heat as necessary during the chemical reaction. In some aspects of the present invention, the reactant mixture can have a molar ratio of CH.sub.4 to O.sub.2 ranges from 0.3 to 20, 0.5 to 15, 1 to 10, or 5 to 7.5 or any range there between. The molar ratio of CH.sub.4 to O.sub.2 can be 0.3, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, or 20 or any value there between. Process conditions to effect production of ethylene from methane through oxidative coupling can include an average temperature of less than 1000 C., less than 700 C., 275 C. to 700 C., 400 to 550 C. or from 425 to 525 C. and a pressure of about 1 bara, and/or a gas hourly space velocity (GHSV) from 500 to 50,000 h.sup.1 or more. In a preferred embodiment, the reactant mixture is heated to an average temperature of less than 700 C., preferably 275 C. to 700 C., more preferably 300 C. to 550 C. or most preferably from 300 C. to 450 C. In some embodiments, the metal oxide catalyst and the reactant mixture are heated to the same temperature and the temperature downstream of the metal oxide catalyst is maintained at a different temperature. Severity of the process conditions may be manipulated by changing, the hydrocarbon source, oxygen source, carbon dioxide source, pressure, flow rates, the temperature of the process, the catalyst type, and/or catalyst to feed ratio. A process in accordance with the present invention is carried out at pressures more than atmospheric pressure.

(24) In some embodiments, the catalyst is used in combination with the second catalyst described above that is capable of catalyzing an oxidative coupling of methane reaction to produce a second product stream that includes C.sub.2+ hydrocarbons. Such a combination produces a greater amount of C.sub.2+ hydrocarbons in the second product stream than those produced in the first product stream. The second catalyst can be positioned downstream from the first catalyst. When the metal oxide catalyst of the present invention (first catalyst) is used in combination with the second catalyst and positioned upstream from the second catalyst, the reactant feed can be at a lower average temperature relative to average temperatures conventionally used for oxidative coupling of methane. In some instances, the average temperature of the reactant feed just prior to or during contact with the first catalyst is 275 C. to less than 700 C., 300 to 550 C., or preferably 300 C. to 450 C. at a GHSV of 500 to 10,000 h.sup.1. In some embodiments, the feed can be heated to the same temperature as the first reaction zone. Heat generated during the oxidative coupling of methane between the reactant feed and the first catalyst can be used to heat the first product stream. The use of a catalyst that can ignite the oxidative coupling of methane at relatively low temperature in combination with another catalyst allows for higher C.sub.2+ yield while extending catalyst life by inhibiting sintering of catalytic metals and/or agglomeration of particles in the catalyst.

(25) Referring to FIG. 1, a schematic of system 100 for the production of ethylene is depicted. System 100 may include a continuous flow reactor 102 and a catalytic material 104. In a preferred embodiment, catalytic material 104 is the LaCe oxide catalytic material of the present invention. A reactant stream that includes methane can enter the continuous flow reactor 102 via the feed inlet 106. An oxygen containing gas (oxidant) is provided in via oxidant source inlet 108. In some aspects of the invention, methane and the oxygen containing gas are fed to the reactor via one inlet. The reactants can be provided to the continuous flow reactor 102 such that the reactants mix in the reactor to form a reactant mixture prior to contacting the catalytic material 104. The average temperature of reactant mixture prior to contacting the catalytic material is less than 1000 C., or 275 C., 300 C. to 700 C., 450 C. to 550 C., or 400 C. to 525 C. or any range there between. In some embodiments, the catalytic material is heated to an average temperature of less than 1000 C., or 275 C., 300 C. to 700 C., 450 C. to 550 C., or 400 C. to 525 C. or any range there between. The average temperature of the reactant mixture, the catalytic material, or both can be 300 C., 325 C., 350 C., 375 C., 400 C., 425 C., 450 C., 475 C., 500 C., 525 C., 550 C., 600 C., 625 C., 650 C., or 700 C. In some instances, the catalytic material 104 may be layered in the continuous flow reactor 102. Contact of the reactant mixture with the first catalytic material 104 produces a product stream (for example, ethylene and generates heat (i.e., an exotherm or rise in temperature is observed). After ignition, the reaction conditions are maintained downstream of the first catalyst at temperatures sufficient to promote continuation of the process. Wishing not to be bound by theory, it is believed that the product stream from contact of the feed stream with the catalytic material in the presence of oxygen at lower average temperatures does not generate excessive heat, thus only a small amount or substantially no carbon dioxide or carbon monoxide is formed resulting in a relatively high C.sub.2+ selectivity. The product stream can exit continuous flow reactor 102 via product outlet 110.

(26) Referring to FIGS. 2A and 2B, a schematic of system 200 having the catalyst of the present invention and a second catalyst is described for the production of ethylene. System 200 may include a continuous flow reactor 102, a first catalytic material 104, and a second catalytic material 202 positioned downstream of the first catalytic material. The first catalytic material 104 can be the catalytic material of the present invention and second catalytic material 202 can the same or different as catalytic material 104. In a preferred embodiment, second catalytic material 202 is a catalytic material that has a higher C.sub.2+ selectivity than the first catalytic material 104. A reactant stream that contains methane enters the continuous flow reactor 102 via the feed inlet 106. An oxygen containing gas is provided in via oxidant source inlet 108. The reactants can be provided to the continuous flow reactor 102 such that the reactants mix in the zone 204 to form a reactant mixture prior to contacting the first catalytic layer 104. In some embodiments, the reactants can be provided to the continuous flow reactor 102 are provided as one stream via one inlet. As shown in FIG. 2B, a mixture of methane (e.g., hydrocarbon gas) and an oxygen containing gas can enter continuous flow reactor via inlet 103 and an additional oxygen containing gas can be added via oxidant inlet 108. The average temperature of the reactant mixture in zone 206 prior to contacting the catalytic material is less 1000 C., or 275 C., 300 C. to 700 C., 450 C. to 550 C., or 400 C. to 525 C. or any range there between. The GHSV can be adjusted to, or be maintained at, 500 hr.sup.1 or more. In some embodiments, the reaction zone 206 and/or catalytic material 104 is heated to an average temperature of less than 1000 C., or 275 C., 300 C. to 700 C., 450 C. to 550 C., or 400 C. to 525 C. or any range there between. Contact of the reactant mixture with the first catalytic material 104 in reaction zone 206 produces a first product stream 208 (for example, ethylene and generates heat (i.e., an exotherm or rise in temperature is observed). The first product stream 208 can include unreacted methane, oxygen containing gas, and C.sub.2+ hydrocarbons. A portion of the generated heat in reaction zone 206 is transferred to the first product stream 208. In a preferred embodiment, the first product stream 208 is heated only by heated generated from contact of the reactant mixture with the first catalytic material 104. As shown in FIG. 2B, the first catalytic material 104 and second catalytic material 202 are separated with zone 210, however, the two catalytic materials may be positioned such that there is a minimal amount of space between the two catalytic layers. In some embodiments, the amount of oxygen in the oxygen containing gas is monitored, and if more oxygen is necessary, oxygen can be added to zone 210 via oxygen containing gas source inlet 212. In a preferred embodiment, at least 90% or substantially all (e.g., 100%) of the oxygen provided to the reactant mixture is converted, and thus, additional oxygen is provided via oxidant inlet 212 to zone 210. The first product stream 208 can be heated prior to and during contact with the second catalytic material 202. In a preferred embodiment, heat from reaction zone 206 heats the first product stream and/or the oxygen containing gas to a temperature of at least 700 C., or 700 C. to 1000 C., 700 C. to 900 C. The heated product steam with sufficient oxygen either remaining in the stream or from an external source (e.g., from the oxygen containing gas entering via inlet 212 shown in FIG. 2B) can enter reaction zone 214. The reaction zone 214 can be heated to an average temperature of at least 700 C., or 700 C. to 1000 C., 700 C. to 900 C. by the heat generated in zone 206 and/or by the heat generated in zone 214. The GHSV can be adjusted to, or be maintained at, a rate higher than the first reaction zone (e.g., 5,000 hr.sup.1 or more, 10,000 hr.sup.1 or more, 20,000 hr.sup.1 or more, 50,000 hr.sup.1 or more, 60 hr.sup.1 or more, or 80,000 hr.sup.1 or more, preferably higher than 50,000 hr.sup.1). Contact of the heated first product stream 208 with the second catalytic material in the presence of oxygen in reaction zone 214 generates a second product stream 216. In some embodiments, contact of the reactant mixture with the first catalyst is controlled such that the methane conversion is greater than zero, but as low as possible. Said another way, the reaction is started using the first catalyst and then maintained using the second catalytic material. Use of an igniting catalyst and a high selectivity catalyst can provide high selectivities to C.sub.2+ hydrocarbon with prolonged catalyst life (e.g., sintering and coking of the catalyst are minimized). Second product stream 216 can have more C.sub.2+ hydrocarbons than the first product stream 206. The second product stream 216 can exit continuous flow reactor 102 via product outlet 110. While only two layers of catalytic material is described it should be understood that additional catalysts can be positioned downstream of the second catalytic material to achieve the desired C.sub.2+ hydrocarbons. The additional catalysts can be any of the catalysts described throughout the invention.

(27) The resulting C.sub.2+ hydrocarbons and water produced from the systems of the invention (for example, systems 100 and 200) can be collected in a collection device and/or transported via piping to separation unit. In the separation unit, the C.sub.2+ hydrocarbons are separated using known separation techniques, for example, distillation, absorption, membrane technology to produce an ethylene product. In embodiments when carbon dioxide is in the reactant mixture and/or generated in situ, the resulting gases (for example, CO, H.sub.2, and ethylene) produced from the systems of the invention (for example, systems 100 and 200) is separated from the hydrogen, carbon monoxide, and carbon dioxide (if present) using known separation techniques, for example, a hydrogen selective membrane, a carbon monoxide selective membrane, a carbon dioxide selective membrane, or cryogenic distillation to produce one or more products such as ethylene, carbon monoxide, carbon dioxide, hydrogen or mixtures thereof. The separated or mixture of products can be used in additional downstream reaction schemes to create additional products or for energy production. Examples of other products include chemical products such as methanol production, olefin synthesis (e.g., via Fischer-Tropsch reaction), aromatics production, carbonylation of methanol, carbonylation of olefins, the reduction of iron oxide in steel production, etc. The method can further include isolating and/or storing the produced gaseous mixture or the separated products.

EXAMPLES

(28) The present invention will be described in greater detail by way of specific examples. The following examples are offered for illustrative purposes only, and are not intended to limit the invention in any manner. Those of skill in the art will readily recognize a variety of noncritical parameters which can be changed or modified to yield essentially the same results.

Example 1

Synthesis of Catalysts

(29) All materials for the synthesis of the bulk metal oxide catalysts were obtained from Sigma Aldrich Chemical Company (St. Louis, Mo., USA).

(30) Bulk Metal Oxide Catalyst.

(31) Lanthanum nitrate (La(NO.sub.3).sub.3) and cerium nitrate (Ce(NO.sub.3).sub.3) in the molar ratios shown below in Table 1 were dissolved in de-ionized water under agitation. Then the mixture was dried at 125 C. overnight. The dried material was then calcined at 625 C. for 5 hours at a ramp rate of 1 C. per minute. FIG. 3 is an X-Ray Diffraction (XRD) patterns of bulk metal oxide catalyst of the present invention (sample 3 in Table 1) showing the La(OH).sub.3 phase. The upside down triangle indicates the peaks attributable to the La(OH).sub.3. As shown in FIG. 3, the La(OH).sub.3 phase is the dominant phase in the catalyst. FIG. 4 is an X-Ray Diffraction (XRD) patterns of Sample 5 which did not include the La(OH).sub.3 phase.

(32) TABLE-US-00001 TABLE 1 Sample La/Ce Presence of La(OH).sub.3 No. (Molar Ratio) Crystal Phase 1 10 yes 2 30 yes 3 15 yes 4 7 yes 5 1 no

Example 2

Oxidative Coupling of Methane

(33) A fixed bed catalyst reactor was filled with a catalytic material of Example 1 (10 mg). The reactor was heated to the required temperature, and a mixture of methane (CH.sub.4) and oxygen (O.sub.2) at a fixed CH.sub.4:O.sub.2 ratio of 7.4 was fed to the reactor at a flow rate of 80 sccm. The ignition temperature, methane conversion, oxygen conversion and selectivity to C.sub.2.sup.+ products under 500 C. for each sample are listed in Table 2. Methane conversion was calculated on the basis of difference of inlet and outlet concentrations of methane. Selectivity was calculated on the basis of concentrations of C.sub.2+ products in comparison all the converted amount of methane. From analysis of the data, it was concluded that the catalysts containing La(OH).sub.3 crystal phase showed higher C.sub.2+ selectivity than the catalyst without the La(OH).sub.3 crystal phase.

(34) TABLE-US-00002 TABLE 2 Ignition Sample Temperature, O.sub.2 CH.sub.4 C.sub.2+ No. C. Conversion, % Conversion, % Selectivity, % 1 500 98.8 15.5 67.0 2 450 78.2 14.2 63.1 3 500 92.1 15.6 62.9 4 450 99.5 16.4 68.5 5 450 93.9 10.6 59.5

(35) FIG. 5 are graphs of O.sub.2 conversion in percent, CH.sub.4 conversion in percent and C.sub.2+ selectivity in percent versus temperature in Celsius for Sample 1 (La:Ce ratio of 10:1) in an oxidative coupling of methane reaction. From analysis of the data, it was concluded that the reaction ignited at 500 C. FIG. 6 are graphs of O.sub.2 conversion in percent, CH.sub.4 conversion in percent versus temperature in Celsius for Sample 3 (La:Ce ratio of 15:1) in an oxidative coupling of methane reaction under a methane to oxygen ratio of 4.0. Under these operation conditions, the reaction ignited at about 475 C. It was observed that the reaction extinction temperature under these conditions was 275 C. Thus, a high level of CH.sub.4 conversion can be obtained at operation temperature above 275 C.

Example 3

Oxidative Coupling of Methane with Second Catalyst

(36) A fixed bed catalyst reactor was filled with a supported catalyst (100 mg, MnNa.sub.2WO.sub.4/SiO.sub.2). The reactor was heated to the required temperature and methane and oxygen was fed to the reactor at a flow rate of 33.3 sccm. The CH.sub.4:O.sub.2 ratio, methane conversion, oxygen conversion and with selectivity to C.sub.2+ products for each sample is listed in Table 3. Methane conversion was calculated on the basis of difference of inlet and outlet concentrations of methane. Selectivity was calculated on the basis of concentrations of C.sub.2+ products in comparison all the converted amount of methane.

(37) TABLE-US-00003 TABLE 3 Reaction Sample CH.sub.4:O.sub.2 Temperature, O.sub.2 Con- CH.sub.4 Con- C.sub.2+ No. ratio C. version, % version, % Selectivity, % 6 4.0 750 100 30.4 73.3 7 7.4 800 100 18.8 79.8
From analysis of the data in Table 3, the selectivities with the second catalyst in the presence of oxygen were determined to be higher than those obtained from the catalysts used in Example 2.