METHOD FOR REFORMING HYDROGENIC CARBONS IN THE PRESENCE OF A HEXAALUMINATE-CONTAINING CATALYST

Description

[0001] The invention relates to a process for reforming hydrocarbons, preferably CH 4 , in the presence of CO 2 using a hexaaluminate-containing catalyst. To produce the catalyst, an aluminum source, preferably an aluminum hydroxide, preferably consisting of small-sized primary particles, preferably with a primary particle size of less than or equal to 500 nm, is contacted with a cobalt-containing metal salt solution, dried, and calcined. In addition to the cobalt species, the metal salt solution contains at least one element from the group consisting of La, Ba, and Sr.

[0002] The reforming of methane and carbon dioxide is of great economic interest because it can be used to produce synthesis gas. Synthesis gas is a raw material for the production of basic chemicals. Furthermore, the utilization of carbon dioxide as a starting material in chemical syntheses is of significant importance for chemically binding carbon dioxide, which is a waste product in numerous processes, and thus preventing its emission into the atmosphere.

[0003] Due to its great economic importance, the reforming of hydrocarbons in the presence of carbon dioxide has been the subject of numerous publications. The following provides a brief overview of the main topics of these publications.

[0004] The catalytic properties of nickel-modified hexaaluminates for reforming methane and carbon dioxide to synthesis gas can be found, for example, in a publication by Zhalin Xu et al. (Zhalin Xu, Ming Zhen, Yingli Bi Kaiji Zhen, Applied Catalysis A: General 198 (2000), pp. 267-273). The nickel-modified hexaaluminates used here exhibit greater activity and better stability than conventional nickel-containing catalysts, in which the nickel is deposited on the support materials.

[0005] In a publication by Yokata et al. the use of hexaaluminate-containing catalysts for the production of synthesis gas from the reforming of methane in the presence of CO 2 and steam is reported (O. Yokata, T. Tanaka, Z. Hou, T. Yashima; Stud. Surf. Sci. and Cat. 153 (2004) p. 141 - 144). The investigation concerns nickel- and manganese-containing hexaaluminates, whereby the manganese-containing hexaaluminates can contain elements from the group Ba, La and Sr as well as a mixture of Sr 0.8 La 0.2. The catalytic characterization of the catalysts takes place in the presence of CH 4 / H 2 O / CO 2 (in the volume ratio of 150 / 100 / 50) under atmospheric pressure at a temperature of 700 °C. The flow rate is 18000 hr -1< .

[0006] J. Wang et al. report on the reforming of methane to synthesis gas using catalysts made of nickel-containing magnetoplumbites that are doped with cobalt or in which the nickel has been completely replaced by cobalt (J. Wang, Y. Liu, TX. Cheng, WX. Li, YL. Bi, KJ. ​​Zhen, Appl. Catalysis A: General 250 (2003) pp. 13-23). ​​The catalysts disclosed by Wang et al. are described by the molecular formula LaNi x Co 1-x Al 11 O 19 . A cobalt-lanthanum-containing hexaaluminate with x=0, which is free of nickel, is also disclosed. The preparation of the catalysts disclosed by Wang et al. is based on the use of aluminum nitrate salt, which is decomposed together with the other metal nitrate salts (i.e., La, Ni, and Co, or La and Co) in the presence of PEG-isopropyl alcohol. The catalytic reforming investigations are carried out at temperatures up to 800 °C and a GHSV of 9600 hr -1<.The nickel-free hexaaluminate catalyst with the composition LaCoAl 11 O 19 shows only very low activity with regard to the investigated conversion of methane and CO 2 . In general, the results of Wang et al. indicate that the catalytic efficiency of the catalysts is adversely affected by the addition of cobalt.

[0007] In US Pat. No. 7,442,669 B2, D. Wickham et al. disclose an oxidation catalyst comprising metal-exchanged hexaaluminates. The catalyst exhibits good catalytic activity and stability at high temperatures, with activity being maintained even over extended periods. In general, the catalysts are suitable as oxidation catalysts, particularly in methane combustion, with particular importance for use in natural gas-fired turbines. The synthesis of the hexaaluminate-containing catalysts is based on the use of boehmite particles.

[0008] The hexaaluminates disclosed in US 7,442,669 B2 contain up to three different metal species from groups M 1 , M 2 and M 3 . Group M 1 comprises elements from the rare earth group, group M 2 comprises elements from the alkaline earth group and group M 3 comprises elements from the transition metal group, namely Mn, Fe, Co, Ni, Cu, Ag, Au, Rh, Ru, Pd, Ir and Pt. To characterise the catalysts, they were tested with regard to their methane decomposition activity by exposing the catalysts to a gas stream containing 3 vol% methane. The tests were carried out at a pressure of 5 bar and a GHSV of 17,000 hr -1<. The temperature T 1 / 2, which is required to convert fifty percent of the methane, was determined as a measure of the efficiency of the catalysts. The tested catalysts were subjected to different aging protocols before the catalytic investigation.

[0009] EP 2 119 671 discloses the synthesis of hexaaluminate-containing catalysts in the presence of template materials. The template materials are advantageous for the formation of specific pore structures in the hexaaluminates produced by the inventive process according to EP 2 119 671.

[0010] A large number of publications relate to the use of hexaaluminate-containing catalysts for the oxidation or partial oxidation of hydrocarbons in the presence of oxygen. When carrying out partial oxidations, very short contact times are desirable to prevent complete oxidation of the hydrocarbons. This requires conducting the reactions at high flow rates, low hydrocarbon concentrations, and in the presence of oxygen. Examples of such disclosures include: Kikuchi et al. (R. Kikuchi, Y. Iwasa, T. Takeguchi, K. Eguchi; Applied Catalysis A: General 281 (2005) pp. 61-67), G. Groppi (Applied Catalysis A: General 104 (1993) pp. 101-108).

[0011] In general, various processes for the preparation of hexaaluminate-containing catalysts have been published in the prior art, but all of them are characterized by the fact that the corresponding starting components are subjected to a thermal treatment at temperatures of 1200 °C and above.

[0012] For example, S. Nugroho et al. describe the preparation of phase-pure barium hexaaluminate obtained by annealing barium oxide and aluminum oxide (i.e., BaO and Al 2 O 3 ) by a solid-state reaction at temperatures of 1450 °C (see S. Nugroho et al., Journal of Alloys and Compounds, 2010, 502, pp. 466-471).

[0013] M. Machida et al. (M. Machida et al., Journal of Catalysis, 1987, 103, pp. 385-393) disclose the preparation of phase-pure barium hexaaluminates obtained by hydrolysis of the corresponding alkoxides, which are treated at temperatures up to 1300 °C. The resulting hexaaluminate phases have surface areas of 11 m² / g.

[0014] Chu et al. describe the preparation of barium hexaaluminates by carbonate precipitation (see W. Chu et al., Catalysis Letters, 2001, 74, pp. 139-144). Thermal treatment required temperatures of 1200 °C to obtain materials with high phase purity with respect to the barium hexaaluminate phase. The materials are reported to have surface areas of 17 m² / g.

[0015] Apart from that, the prior art also includes a single disclosure by F. Yin et al. for the production of hexaaluminates by means of urea combustion (i.e., the so-called urea combustion process), which differs from other disclosures in that the thermal treatment of the starting materials takes place at a much lower temperature than in other known processes. F. Yin et al. state that the phase-pure hexaaluminate material was obtained at temperatures as low as 500 °C. The resulting material had a surface area of ​​20 m 2 / g.

[0016] US2007 / 0111884 A1 (Laiyuan Chen et al. and Delphi as applicants) discloses and claims catalyst support materials comprising hexaaluminates and aluminas, which contain rhodium as the active component. To produce the catalyst material, the starting materials are combined with a stoichiometric excess of an aluminum-containing component, so that, in addition to the hexaaluminate-containing phase, the alumina secondary phase is also formed during synthesis. US2007 / 0111884 A1 discloses hexaaluminates that may contain various cations, including lanthanum-containing hexaaluminates that may contain various divalent cations such as Mg, Ca, Ni, Co, Zn, and Fe. Different processes are disclosed for producing the catalyst support materials and catalysts, each of which differs from the other with regard to the mixing steps and the thermal treatment steps used.The catalysts according to the invention, all of which are doped with rhodium as the active metal according to the disclosure, are used in a process for the partial oxidation of gasoline in the presence of oxygen, which serves to produce a hydrogen-rich gas mixture. In the partial oxidation reactions used for fuel reforming, temperatures in the range of 1000°C and higher can occur, and due to the high temperatures, it is necessary to develop particularly sinter-resistant catalysts for this purpose.

[0017] In his 2007 doctoral thesis, Todd H. Gardner addressed in a very fundamental way the use of hexaaluminates as catalysts for the partial oxidation of fuels obtained in the middle fraction during distillation. In particular, lanthanum-containing, barium-containing, and strontium-containing hexaaluminates, which may contain different transition metal cations, are described. The focus of the work is the investigation of hexaaluminates containing nickel, cobalt, or iron, with the transition metals present in varying proportions and combined with cations from the Sr, La, or Ba group, which are also present in varying proportions. The work is specifically directed at the investigation of pure-phase hexaaluminates. Gardner reports that, although phase impurities cannot be ruled out, they were present only in very low concentrations.To characterize the catalytic properties, the catalysts were used for the partial oxidation of n-tetradecane. The partial oxidations were carried out at a pressure of approximately 2 bar, a GHSV of 50,000 h-1, and an oxygen-to-carbon ratio (i.e., O to C) of 1.2.

[0018] A publication by J. Kirchnerova (in Catalysis Letters 67 (2000) pp. 175-181) describes the criteria for the design of new high-temperature catalysts for catalyzing combustion reactions. The publication also refers to the preparation and testing of materials with a perovskite structure and materials with a hexaaluminate structure. Hexaaluminates containing Sr, La, and Mn (i.e., the structural formula Sr 08 La 0.2 MnAl 11 O 19 ) are described. It is also worth mentioning that the use of boehmite as a starting material in the synthesis of the materials is disclosed. One conclusion drawn by Kircherova et al. is that perovskites containing certain transition metals may exhibit activity in catalytic combustion.The catalytic experiments for characterizing the catalysts refer to the oxidation of methane to carbon dioxide in the presence of air, with the methane content being given as 2%.

[0019] CN 101306361 A discloses hexaaluminates used as catalysts for hydrocarbon oxidation reactions. The hexaaluminates contain the cationic species La, Ba, or Ca as stabilizing elements, and the hexaaluminates can contain Cr, Mn, Fe, Co, Ni, or Cu as transition metal cations.

[0020] Z.-L. Xu et al. disclose hexaaluminates for catalyzing CO2 reforming of methane to synthesis gas (in Kao Ten Hsueh Hsiao Hua Heush Hsueh Pao / Chemical Journal of Chinese Universities. Vol. 21, No. 2, (2000-02), pp. 298 - 300, XP9510765, ISSN: 0251-0790). The publication describes the production of phase-pure hexaaluminates which can contain different transition metals from the group Ni, Co, Fe, Mn and Cu. During the catalytic test investigations, different catalyst samples were investigated in a quartz reactor, with the nickel-containing catalyst samples showing better activity than those catalyst samples which contained transition metals other than nickel. The object underlying the invention is to provide an improved catalytic process for reforming hydrocarbons and CO2 to synthesis gas.

[0021] The objects mentioned here and others are achieved by providing a process for reforming hydrocarbons, preferably methane, and CO2, in which a hexaaluminate-containing catalyst is used. Catalysts and processes for producing catalysts used in the process according to the invention are first described below. The process according to the invention for reforming hydrocarbons in the presence of carbon dioxide is then described in more detail.

[0022] In the process according to the invention for reforming hydrocarbons, preferably methane, in the presence of CO 2 , a hexaaluminate-containing catalyst is used, which is characterized in that the catalyst contains cobalt and at least one further element from the group Ba, Sr, La, wherein the hexaaluminate-containing catalyst, which has a BET surface area greater than 2 m 2 / g, has a Co content in the range of 2 - 15 mol%, preferably 3 - 10 mol% and more preferably in the range of 4 - 8 mol%, the content of the at least one further element from the group Ba, Sr, La is in a range of 2 - 25 mol%, preferably 3 - 15 mol%, more preferably 4 - 10 mol%, the content of Al is in a range of 70 - 90 mol% and wherein the catalyst has an oxidic secondary phase in the range of 3 - 40 wt.% and further preferably in the range of 5 - 30 wt.-%, which is selected from the group alpha-aluminum oxide, theta-aluminum oxide, LaAlO 3 , BaAl 2 O 4 , SrAl 2 O 4 , CoAl 2 O 4 , La-stabilized alumina and / or La-stabilized alumina hydroxide.

[0023] Based on the ranges of molar proportions given here, the following molar ratios for the metal ion species can be determined: The molar ratio of Co to Al (i.e., the n Co / n Al ratio) is in the range of 0.03 - 0.17, preferably 0.043 - 0.11, and more preferably 0.057 - 0.08. The molar ratio of M BaSrLa< to Al (i.e., the n MBaSrLa / n Al ratio) is in the range of 0.029 - 0.28, preferably 0.043 - 0.17, and more preferably 0.057 - 0.11. The molar ratio of Co to M BaSrLa< (i.e. the n Co / n MBaSrLa ratio) is in the range of 1.0 - 0.6, preferably 1.0 - 0.67 and more preferably 1.0 - 0.8.

[0024] Furthermore, it is particularly preferred that the molar ratios of the elements present in the catalyst are in the ranges stated below: The ratio of cobalt to aluminum (ie the n Co / n Al ratio) is in the range from 0.05 to 0.09 and particularly preferably in the range from 0.06 to 0.08. In a preferred embodiment of the catalyst used, the molar ratio of M BaSrLa< to aluminum (ie the n MBaSrLa / n Al ratio) is in a range from 0.09 to 0.25, particularly preferably in the range from 0.092 to 0.20. Furthermore, the molar ratio of Co to M BaSrLa< (ie the n Co / n MBaSrLa ratio) is in the range from 1.0 to 0.3 and particularly preferably in the range from 0.85 to 0.40.

[0025] A material consisting entirely of cobalt hexaaluminate and containing at least one element from the group Ba, Sr, La can be described by the molecular formula CoM BaSrLa< Al 11 O 19 . In this case, the metallic species have the following stoichiometric ratios: the molar ratio of Co to Al (i.e., the n Co / n Al ratio) is 1, the molar ratio of M BaSrLa< to Al (i.e., the n MBaSrLa / n Al ratio) is 0.091, and the molar ratio of Co to M BaSrLa< (i.e., the n Co / n MBaSrLa ratio) is 1.

[0026] A comparison of the composition of the catalyst used in the process according to the invention for reforming hydrocarbons in the presence of CO2 with a material consisting entirely of cobalt hexaaluminate phase shows that, compared to the pure-phase cobalt hexaaluminate, the catalyst (preferably) has a lower proportion of cobalt (relative to aluminum) and a higher proportion of cationic species from the group Ba, Sr, La (relative to cobalt). With respect to the pure-phase cobalt hexaaluminate, this means that the catalyst has a substoichiometric amount of cobalt and a superstoichiometric amount of cationic species from the group Ba, Sr, La.

[0027] One explanation for the formation of the catalyst is that the cobalt-containing species added to the synthesis system are almost completely or entirely incorporated into the structure of the cobalt hexaaluminate phase, leaving no cobalt available for the formation of the secondary phase. The secondary phase is formed from the aluminum-containing species and the cationic species used from the group Ba, Sr, La, which leads to the secondary phase predominantly consisting of aluminates or perovskites (e.g. SrAl 2 O 4, LaAlO 3, etc.) or other phases of the elements La, Sr, Ba, Al known to those skilled in the art. This means that the proportion of free aluminum oxide and the associated number of Lewis acid centers can be minimized. However, the above explanation is not intended to limit the invention in any way.

[0028] In a preferred embodiment, the catalyst contains at least one noble metal-containing promoter from the group Pt, Rh, Pd, Ir, wherein the proportion of noble metal-containing promoters is in the range of 0.1 - 3 mol%.

[0029] In a further embodiment, the catalyst also comprises a proportion of further cations, which are preferably selected from the group Mg, Ca, Ga, Be, Ni, Fe, Cr, Mn, with Mg being particularly preferred.

[0030] It is also conceivable that, as an alternative to at least one element from the group consisting of Ba, Sr, and La, one or more elements from the lanthanide group could also be present in the catalyst used. It cannot be ruled out that the performance properties of the catalyst could be further enhanced by incorporating special secondary phases or combining them within the catalyst.

[0031] Process for the preparation of a hexaaluminate-containing catalyst which is used in the process according to the invention for reforming hydrocarbons in the presence of carbon dioxide, wherein the hexaaluminate-containing catalyst is characterized in that it can be prepared by the following steps: (i) Providing an aluminum source, preferably a finely divided aluminum oxide and / or hydroxide modification, (ii) Contacting the finely divided aluminum source with a meltable or soluble cobalt-containing compound and at least one further meltable or soluble metal salt, (iii) Intense mixing of the aluminum source and the dissolved or melted metal salt, (iv) Drying the mixture, (v) Low-temperature calcination of the mixture, (vi) Molding or shaping, (vii) High-temperature calcination of the mixture.

[0032] The at least one further soluble or meltable metal salt comprises a metal salt selected from the group consisting of barium, strontium and lanthanum.

[0033] In a preferred embodiment, the further soluble metal salt comprises at least two metal salts in which at least barium-containing species are present in combination with strontium-containing species or at least barium-containing species are present in combination with lanthanum-containing species or strontium-containing species are present in combination with lanthanum-containing species.

[0034] In the event that the metal salts are not present in the form of a melt but in the form of dissolved metal salts during the mixing in step (iii), a solvent is also added to the metal salts, unless they were used in the dissolved state.

[0035] In a particularly preferred embodiment, the aluminum source is selected from the group of highly reactive aluminum oxides and hydroxides. The aluminum source preferably contains dispersible primary particles, with a primary particle size of less than or equal to 500 nm being preferred.

[0036] Process for the preparation of the hexaaluminate-containing catalyst used for the process according to the invention for reforming hydrocarbons in the presence of carbon dioxide.

[0037] Hexaaluminate-containing catalyst / hexaaluminate phase

[0038] In the context of the present disclosure, the term "hexaaluminate-containing catalyst" encompasses materials characterized by a high proportion of hexaaluminate phase. This means that the hexaaluminate-containing catalyst used in the process according to the invention contains secondary phases. The term "hexaaluminate phase" encompasses phases that have layered structures similar to or identical to the magnetoplumbite structure and / or the beta-aluminate structure—such as the beta' or beta" aluminate structure. The proportion of secondary phase is in a range of 3-40 wt.% and more preferably in a range of 5-30 wt.%.

[0039] The proportion of hexaaluminate-containing phase can be determined using diffractometric methods such as Rietfeld refinement. In the case of particularly fine-particle or nanocrystalline materials, the proportion of hexaaluminate phase is determined using optical analysis according to Kubelka-Munk. A highly sintered reference sample with the same stoichiometry as the sample to be measured (in terms of the proportion of crystalline phase) is prepared and then designated as the standard sample. The samples to be measured are compared against the standard sample as a reference, with the reference previously assigned a value of 100 percent. The optical analysis method is preferred for nanocrystalline materials when they have very small crystallites with a short coherence length.Low coherence lengths (in diffractometric studies with an X-ray wavelength of 0.154 nm) are particularly present when the crystallite sizes are less than 0.5 nm, preferably less than 0.4 nm, and more preferably less than 0.3 nm. Such nanocrystalline materials can be such that they appear amorphous in powder diffraction and crystalline in UV analysis. Aluminum source

[0040] In principle, any aluminum-containing starting material can be used as an aluminum source, with a preferred aluminum source being selected from the group consisting of pseudoboehmite, boehmite, gibbsite, bayerite, gamma aluminum oxide, theta aluminum oxide, hydrotalcites such as magnesium hydrotalcite, colloidal basic aluminum oxides, and other colloidal aluminum sources known to those skilled in the art, as well as mixtures thereof. This includes, among others, the following Sasol products: Disperal and all Disperal types, Dispal, Pural, Puralox, Catalox, Catapal, and all Pural MG types.

[0041] Without wishing to limit the process for producing a catalyst material that is a component of the process according to the invention by any theory, it is assumed that the surface structure of the highly reactive aluminum oxide or hydroxide source, such as theta aluminum oxide, gamma aluminum oxide, pseudoboehmite, boehmite, gibbsite, bayerite, and mixtures of the aforementioned and other highly reactive aluminum oxide or hydroxide sources, could have a significant influence on the formation of an active catalyst. The boehmite used preferably consists of dispersible particles, and the primary particle size is preferably in the range of less than or equal to 500 nm. The term "dispersible particles" means that the particles dispersed or suspended in water form a stable dispersion and only settle to the bottom after a long time.

[0042] The aluminum source is preferably a nanoparticulate aluminum-containing starting material or colloidal primary particles. Peptidized aluminum hydroxides, oxide hydrates, or oxides can be used as nanoparticulate aluminum-containing starting materials. Peptidization can be carried out using organic acids, such as acetic acid, propionic acid, or inorganic acids, such as nitric acid or hydrochloric acid. The colloidal particles can be mixed with stabilizers such as surfactants, soluble polymers, or salts, or such stabilizers can be used in the production process. The colloidal primary particles can also consist of partially hydrolyzed alcoholates.

[0043] In a specific embodiment, shaped bodies of the aforementioned aluminum oxide sources can also be used, which are then brought into contact with the metal compounds. Examples of such shaped bodies can include tablets, extrudates, granules, or other shaped bodies known to those skilled in the art.

[0044] The use of a highly reactive aluminum oxide or hydroxide source proves to be particularly advantageous because it facilitates the formation of desired phases.

[0045] The preferred metal compounds are those that are soluble in solvents or meltable at temperatures up to 250 °C, and that are inexpensive and readily available on an industrial scale. Preferred solvents include the following: water, acidic or alkaline aqueous solutions, alcohols such as methanol, ethanol, propanol, isopropanol, and butanol, ketones such as acetone or methyl ethyl ketone, aromatic solvents such as toluene or xylenes, aliphatic solvents such as cyclohexane or n-hexane, ethers and polyethers such as tetrahydrofuran, diethyl ether, or diglyme, and esters such as methyl acetate or ethyl acetate.

[0046] Particularly preferred metal compounds are soluble salts, complex compounds, or organometallic compounds. Examples of salts include nitrates, nitrites, carbonates, halides, acetates, and octanoates. Examples of complex compounds include EDTA complexes, complexes with amino acids or amines, complexes with polyols or polyacids, and complexes with phosphines. Examples of organometallic compounds include acetylacetonates, alcoholates, alkyl compounds, and compounds with aromatics such as cyclopentadienyl adducts.

[0047] As meltable metal compounds, metal salts are preferably used that do not decompose during melting, or for which decomposition is strongly inhibited kinetically. Examples of such metal salts include nitrates, nitrites, halides, chlorates, bromates, iodates, sulfates, and sulfites. Nitrates, nitrites, or salt melts containing nitrates and nitrites are particularly preferred.

[0048] Suitable methods for contacting the metal compounds with the aluminum source include impregnation processes, in which the metal compounds are dissolved in suitable solvents, which are then removed by drying. Such a drying step can be carried out, for example, by freeze-drying or spray-drying when the aluminum source is in powder form. Alternatively, spray granulation or purely static drying of the resulting composites can also be used. Within the scope of the invention, impregnation is a particularly preferred method.

[0049] Other suitable contacting processes include kneading or grinding the aluminum source in the presence of the metal compounds, with or without the addition of liquids. Kneading, in particular, is a preferred process within the scope of the invention, as it allows for coupling with subsequent extrusion and can thus be advantageous for shaping.

[0050] In the context of the invention, particular preference is given to those metal salts which facilitate the formation of the hexaaluminate phase in the presence of cobalt.

[0051] These include lanthanum, barium, and strontium. Lanthanum, barium, and strontium are incorporated as so-called interlevel cations. The invention includes the use of one or more of these cations. This can result in materials that incorporate different cations into the interlevel (solid solution formation, i.e., individual crystallites that incorporate, for example, both strontium and barium into the interlevels), as well as materials in which only crystallites with one type of cation species form in the interlevel and then exist as a mixture of crystallites with different types of cation species (i.e., for example, a crystal mixture of crystallites that only have barium as interlevel cations with crystallites that only have strontium as interlevel cations). According to the invention, both types of mixture (i.e.Mixed crystals and crystal mixtures).

[0052] Other cations preferred within the scope of the invention are those that, like cobalt, are also incorporated into the spinel blocks. Preferred cations include magnesium, calcium, gallium, beryllium, nickel, iron, chromium, and manganese. Magnesium is particularly preferred.

[0053] Completely surprisingly, it was found that carrying out the high-temperature calcination at relatively low temperatures in the temperature range from 800 °C to 1300 °C, preferably in the temperature range from 850 °C to 1200 °C, particularly preferably in a temperature range from 900 °C to 1100 °C, leads to catalysts which have very good catalytic performance properties with regard to the process according to the invention for producing synthesis gas.

[0054] For the high-temperature calcination and the production of the catalyst, an advantageous temperature window was thus found, which forms a synergistic effect between the performance properties of the materials according to the invention with regard to synthesis gas production and the particularly high energy efficiency in the catalyst production process.

[0055] It is particularly preferred to carry out the catalyst or catalyst precursor material production process in the presence of seed crystals. Particular preference is given to using seed crystals that have a hexaaluminate structure or a composition similar to that of the target phase. The seed crystals most preferably have high crystallinity. It is particularly preferred to carry out the catalyst or catalyst precursor material production process in the presence of seed crystals.

[0056] One possible effect that can be achieved by adding seed crystals is a reduction in the formation temperature of the hexaaluminate phase during the process according to the invention, or an increase in the yield of the hexaaluminate-containing phase. It is also possible that both the formation temperature and the yield can be reduced. Another advantageous effect associated with the addition of seed crystals is a possible reduction in the crystallization time.

[0057] With regard to the seed crystals, it should be noted that in a preferred embodiment of the process, these consist of a material with a hexaaluminate phase—the target product—more preferably of phase-pure hexaaluminate. Furthermore, it is also preferred if the seed crystals have a small grain size with a high specific surface area, or consist of agglomerates with a small crystallite size and a high specific surface area.

[0058] Seed crystals can be produced from a corresponding hexaaluminate material by subjecting it to a suitable mechanical and / or chemical treatment, such as grinding in the dry state, grinding in the presence of water or grinding in the presence of acids or bases.

[0059] In a particularly preferred embodiment, the seed crystals are brought into contact with the aluminum source by intensive mixing. This mixing can be carried out by grinding, kneading, mulling, or other methods known to those skilled in the art. The mixing of the aluminum source with the seed crystals can take place before, during, or after contacting with the cobalt-containing compound and the at least one metal compound.

[0060] The aluminum oxide source can be provided in the form of a solid such as powder or granules, or in liquid form. If the aluminum oxide source is in liquid form, it is preferred that the aluminum-containing species be dispersed in the solvent—or present therein as colloidal particles. The stability of the colloidal aluminas, or rather the formation of the colloidal aluminas, can be improved by selecting a pH value that is either in the range of 2 to 4.5 or in the range of 8 to 12.5. Suitable agents for producing or stabilizing the colloidal aluminas are acids such as HNO3, acetic acid, or formic acid, or bases such as aqueous NaOH, KOH, or ammonia solution.

[0061] In a preferred embodiment of the process, a colloidal alumina solution is used which comprises peptidized alumina particles and whose pH is in the range of 2 to 4.5.

[0062] The aluminum source is brought into contact with at least one metal compound. During addition to the aluminum source, which is present as a liquid, particular care is taken to ensure that no precipitation of the metal compounds or colloids is observed. The seed crystals can be added before, during, or after the addition of the metal compounds. Alternatively, the seed crystals can also be added after the drying step.

[0063] In a further preferred embodiment of the process, a dispersible nanoparticulate aluminum oxide source is used as a finely divided powder. The finely divided powder consists of primary particles smaller than or equal to 500 nm, which are present as agglomerates with a D 50 value of 1 to 100 µm.

[0064] In this preferred embodiment, the aluminum source is brought into contact with at least one metal compound. The metal compound can be added either as a solution or as a solid. In the case of a solid, a liquid is subsequently added. When adding the solution or the liquid, particular care is taken to ensure that a homogeneous, dough-like mass is formed which is kneadable and which is characterized by very intimate mixing of the aluminum oxide source and the metal compound. The seed crystals can be added before or after the addition of the metal compounds. An essential feature of this preferred embodiment is that the drying (i.e. step (iv)) is preceded by extrusion as a shaping step (i.e. step (vi)).

[0065] In another preferred embodiment of the process according to the invention, the finely divided powder of the aluminum source is brought into contact with at least one fusible metal compound. The intimate mixing of the aluminum oxide source and the fusible metal compound is carried out at a temperature in the range of 25°C to 250°C. When selecting the temperature, particular care is taken to ensure that it lies above the melting point of the metal compound. By melting the metal compound, a particularly homogeneous distribution of the components in the mixture is achieved. The addition of the seed crystals can take place before, during, or after the addition of the metal compounds. Alternatively, the seed crystals can also be added after the mixture has cooled.

[0066] The low-temperature calcination of the dried mixture or the molded and dried material obtained after the above-mentioned process steps essentially serves to remove the anions from the metal compounds used and convert them into the corresponding metal oxides. The calcination temperature depends on the metal compounds used; preferably, the temperature is less than or equal to 550 °C, and more preferably, in the temperature range of 150 °C to 550 °C.

[0067] The high-temperature calcination of the molded and dried mixture or the low-temperature calcined mixture obtained according to the above-mentioned process steps is an essential process step in the production of the catalyst. The temperature during the high-temperature calcination must be higher than 800 °C, preferably the temperature is equal to or higher than 850 °C, and more preferably the temperature is equal to or higher than 900 °C.

[0068] Furthermore, it is important to carry out the calcination over a period of time greater than 0.5 hours, more preferably greater than 1 hour, and particularly preferably a period of time greater than 12 hours.

[0069] In a further preferred embodiment of the process according to the invention, the low-temperature calcination (v) and high-temperature calcination steps (vii) can be carried out in a single, continuous process step. This is particularly advantageous if the drying step is preceded by a shaping step.

[0070] If the target temperature of 800 °C is not reached during calcination, catalyst production will be negatively affected, as the formation of hexaaluminate fails or the amount of hexaaluminate formed is too low. If a calcination temperature is selected that lies above the appropriate temperature range, phases with a certain degree of catalytic activity will be formed, but the materials will have too small a surface area. The upper limit for the calcination temperature is 1500 °C, preferably 1450 °C, and more preferably 1400 °C.

[0071] It is conceivable that the invention could be further specified by specifying specific calcination conditions. However, in large-scale operation, a very long calcination time is uneconomical and undesirable.

[0072] For the specific application of the material as a catalyst for producing synthesis gas, a high specific surface area is advantageous. Materials with surface areas greater than 2 m² / g are used within the scope of the invention; particularly preferred are materials with surface areas greater than 4 m² / g, even more preferred are materials with surface areas greater than 8 m² / g, and even more preferred are materials with surface areas greater than 15 m² / g.

[0073] A shaping process is important for catalyst production so that the catalyst can be used in a tubular reactor in a suitable manner. This is also due to the fact that the boehmite, which is particularly preferred as an alumina source, is preferably very finely divided, with the primary particle size preferably in the range of 10 to 500 nm. The direct introduction of a very finely divided catalyst, produced from a finely divided powder, into a tubular reactor would lead to a high pressure drop or complete blockage of the reactor, which would impair the catalytic reforming process.

[0074] The material produced by this process can be used in reforming to produce syngas in the form of bulk material, pellets, or extrudates. The choice of the appropriate catalyst form depends on the specific process conditions relevant to the production of syngas.

[0075] Shaping is usually carried out after process steps (iii) or (v), but can also be carried out after process step (vii).

[0076] The production of a tablet body takes place through the steps (x.1) compaction, (x.2) sieving, and (x.3) tabletting. Binders and lubricants can be added to the catalyst material or precursor material used for compaction and tabletting. Graphite or stearic acid, for example, can be used as lubricants. Graphite is preferred. The amount of lubricant is typically no more than 10 wt.% based on the catalyst material.

[0077] It is also possible to produce the target fraction using a compaction machine that performs several steps in succession. The bulk material produced with the compaction machine may have lower mechanical stability than the material produced with the press machine.

[0078] Furthermore, it is also possible for a molded body to be produced by means of an extrusion step. Such extrusion can take place after step (ii) or step (iii) of the production process.

[0079] Apart from that, it is also possible for the suspension to be dried using a spray dryer and then subjected to a calcination process.

[0080] One or more oxides can be added to the catalyst as a binder material for compaction and tabletting, or specific oxides can be formed through specific process features or process steps during the synthesis of the material. Such process features or process steps can include, among others: preferred choice of the stoichiometry of the starting compounds, preferred choice of the type of starting compounds and, in particular, the aluminum source, and preferred choice of thermal treatment steps. A particularly suitable binder material has a positive effect on the formation of a high surface area of ​​the catalyst.

[0081] Examples of such oxides which form from the binder material during calcination and which represent particularly preferred secondary phases include: theta-alumina, alpha-alumina, lanthanum aluminate (LaAlO 3 ), barium aluminate (BaAl 2 O 4 ), strontium aluminate (SrAl 2 O 4 ), La-stabilized alumina, La-stabilized alumina hydroxide.

[0082] In another embodiment, it is possible, for example, to apply the catalyst or catalyst precursor material to a ceramic support material through a coating process. A ceramic honeycomb body or other shaped bodies could be used as the support material.

[0083] To produce a particularly effective catalyst, it is necessary that the stoichiometry of the elements forming the catalyst material lies within a certain preferred range.

[0084] In this paper, the preferred range of composition is based on the metallic elements and is expressed as a mole percentage. The figures are to be completed to the nearest hundred parts, disregarding the presence of oxygen.

[0085] In the context of the invention, a hexaaluminate-containing material is preferred, the cobalt content of which is preferably in a range of 2 - 15 mol%, particularly preferably in a range of 3 - 10 mol%, especially preferably in a range of 4 - 8 mol%.

[0086] In the context of the invention, preference is given to a hexaaluminate-containing material which has at least one metal species which is present in addition to cobalt and which is selected from the group consisting of barium, strontium and lanthanum, wherein the metal content of this at least one metal species is preferably in a range of 2 - 25 mol%, more preferably in a range of 3 - 15 mol% and particularly preferably in a range of 4 - 10 mol%.

[0087] Further promoters such as magnesium, gallium, nickel are preferably added to the material in the context of the invention at less than 10 mol%.

[0088] Some examples of materials having a preferred composition are listed below: A particularly preferred material has a composition in which the La content is in the range of 3 - 20 mol%, the Co content is in the range of 2 - 10 mol%, the content of noble metal-containing promoter or additional promoter is in the range of 0.25 - 3 mol% and the Al content is in the range of 70 - 90 mol%.

[0089] Another example of a material preferred according to the invention has a composition in which the content of La and / or Ba is in the range of 3 - 20 mol%, the content of Co is in the range of 2 - 10 mol%, the content of noble metal-containing promoter is in the range of 0.1 - 3 mol% and the content of aluminum is in the range of 70 - 90 mol%.

[0090] Very particularly preferred is a material with a composition in which the content of La and / or Sr is in the range of 3 - 20 mol%, the Co content is in the range of 2 - 10 mol%, the content of noble metal-containing promoter or additional promoter is in the range of 0.25 - 3 mol% and the Al content is in the range of 70 - 90 mol%.

[0091] Very particularly preferred is a material with a composition in which the Ba content is in the range of 3 - 20 mol%, the Co content is in the range of 2 - 10 mol%, the content of noble metal-containing promoter or additional promoter is in the range of 0.25 - 3 mol% and the Al content is in the range of 70 - 90 mol%.

[0092] Very particularly preferred is a material with a composition in which the Sr content is in the range of 3 - 20 mol-%, the Co content is in the range of 2 - 10 mol-%, the content of noble metal-containing promoter or additional promoter is in the range of 0.25 - 3 mol-% and the Al content is in the range of 70 - 90 mol-%.

[0093] Particularly preferred cobalt hexaaluminate-containing catalysts are those whose molar ratio of cobalt to aluminum (ie the n Co / n Al ratio) is in the range from 0.05 to 0.09 and particularly preferably in the range from 0.06 to 0.08. In a preferred embodiment of the catalyst which is the subject of the reforming process according to the invention, the molar ratio of M BaSrLa< to aluminum (ie the n MBaSrLa / n Al ratio) is in a range from 0.09 to 0.25, particularly preferably in the range from 0.092 to 0.20. Preferably, the molar ratio of Co to M BaSrLa< (ie the n Co / n MBaSrLa ratio) is in the range from 1.0 to 0.3 and particularly preferably in the range from 0.85 to 0.40. The abbreviation M BaSrLa< indicates that at least one element from the group Ba, Sr, La is included.

[0094] In the case that the catalyst is produced by impregnation in conjunction with a metal salt solution: Suitable metal salts are all salts that can be dissolved in a solvent in order to achieve the most homogeneous distribution of the metal species on the surface of the aluminum source, preferably the boehmite.

[0095] For example, the metal salts added are nitrates or hydrated nitrates. Water is used as the preferred solvent.

[0096] Preferably, the aluminum source contains only a small amount of nitrate or is nitrate-free. Considering the nitrate content and the total content of all metallic components in the synthesis system (i.e., Al together with Co and the other metals), the nitrate content is preferably less than 40 mol%, more preferably less than 25 mol%, and even more preferably less than 18 mol%.

[0097] It is conceivable that precious metal-containing salts could be added to the impregnation solution as minor components, acting as promoters and increasing catalyst activity. However, it should also be considered that the use of promoters containing precious metals could increase the cost of the catalyst. Preferred precious metals for promotion include platinum, rhodium, and palladium.

[0098] With regard to the introduction of the noble metal-containing promoters, it should be noted that these can be added during the catalyst synthesis or that they can be deposited on the finished catalyst.

[0099] The invention relates to a process for reforming hydrocarbons, preferably methane, in the presence of carbon dioxide, the process comprising the following steps: (a.1) contacting a reforming gas containing more than 70 vol.% hydrocarbons, preferably methane, and carbon dioxide with a hexaaluminate-containing catalyst, (a.2) heating the reactor or the catalyst therein during contact with the reforming gas at a temperature greater than 700 °C, preferably greater than 800 °C and more preferably greater than 900 °C, (a.3) operating the reactor during the reaction at a process pressure greater than 5 bar, preferably greater than 10 bar and more preferably greater than 15 bar, (a.4) applying to the catalyst a reforming gas stream whose GHSV is in a range from 500 to 20,000 hr -1<, preferably in a range from 1,500 to 10,000 hr -1< and more preferably in a range from 2,000 to 5,000 hr -1< , and where the hexaaluminate-containing catalyst contains cobalt and at least one other element from the group Ba, Sr, La, which has a BET surface area greater than 2 m 2 / g, a Co content in the range of 2 - 15 mol-%, a content of further metal from the group Ba, Sr, La in a range of 2 - 25 mol-%, and an Al content in a range of 70 - 90 mol-% and the catalyst has an oxidic secondary phase in the range of 3 - 40 wt.%, which is selected from the group theta-aluminum oxide, alpha-aluminum oxide, LaAlO 3 , BaAl 2 O 4 , SrAl 2 O 4 , CoAl 2 O 4 , La-stabilized alumina, La-stabilized alumina hydroxide.

[0100] In a preferred embodiment of the process according to the invention, an activation process precedes the reforming process. This activation process makes it possible to adjust the catalyst to the desired process parameters under controlled conditions.

[0101] The activation process comprises thermal treatment of the catalyst in a reducing gas atmosphere at a temperature in the range of 300 °C to 900 °C. Preferably, the catalyst is heated to the process temperature using a controlled heating process. The heating rate is preferably in a range of 1 °C / min to 30 °C / min, with a range of 5 °C / min to 15 °C / min being preferred.

[0102] Preferably, the activation process is coupled with catalyst conditioning, or the conditioning is carried out downstream of the activation. Conditioning is a process in which the catalyst is gradually brought closer to the process parameters of the target reaction. These conditioning steps effectively prevent uncontrolled coking of the catalyst during the so-called start-up phase.

[0103] Catalyst conditioning involves, for example, heating the catalyst to the process temperature in the presence of methane, steam, and / or hydrogen. It is also possible to condition the catalyst in the presence of steam.

[0104] The reforming gas, which forms the main component of the reactant fluid, has a composition in which the proportion of hydrocarbon, preferably methane, and carbon dioxide in total is greater than 70 vol%.

[0105] Preferably, the methane and carbon dioxide are present in the reactant fluid in equimolar or nearly equimolar amounts. A preferred ratio of methane to carbon dioxide is in the range from 4:1 to 1:2, more preferably in the range from 3:1 to 3:4, and most preferably in the range from 2:1 to 3:4. The most preferred ratio of methane to carbon dioxide is—as mentioned above—1:1. If the hydrocarbon-containing starting gas is ethane, carbon dioxide and ethane are present in a ratio of 2:1.

[0106] Steam is added to the reactant fluid during the process. The proportion of steam in the reactant fluid is preferably equal to or less than 30 vol.%, more preferably equal to or less than 20 vol.%, and even more preferably equal to or less than 15 vol.%. A preferred reforming gas composition contains the components CH 4 / CO 2 / H 2 O in a percentage ratio range of the gas volumes from 35 / 35 / 30 to 48 / 48 / 4, and more preferably a range from 43 / 43 / 14 to 45 / 45 / 10.

[0107] For process-related reasons, standard gases or auxiliary gases can be added to the reforming gas. The standard gas, for example, is a noble gas added in a proportion of 1 to 5 vol%. The addition of an internal standard in laboratory tests serves to determine the recovery rate.

[0108] In a preferred process procedure, a synthesis gas is produced by means of the process according to the invention which has an H 2 / CO ratio which is in the range from 0.85 to 1.4, more preferably the H 2 / CO ratio is in a range from 0.9 to 1.2 and even more preferably in a range from 0.95 to 1.1.

[0109] The process according to the invention makes it possible to carry out the reforming process under extreme process conditions without a significant amount of coke being deposited on the hexaaluminate-containing catalyst. Due to the catalyst's very high thermal stability and pressure resistance, it can be used over long process periods.

[0110] In a preferred embodiment, the reforming process according to the invention using the hexaaluminate-containing catalyst is characterized in that the cobalt species are present in the cobalt hexaaluminate phase of the catalyst and remain predominantly in the hexaaluminate phase during the process. Thus, the catalyst obtained by carrying out this preferred process has only a very low content of metallic cobalt species.

[0111] Carrying out the reforming at high process pressures is advantageous because it produces a synthesis gas that is also under very high pressure. This synthesis gas can be used for further processes that require the synthesis gas as a starting material at high pressure. The subsequent processes can be methanol synthesis, Fischer-Tropsch synthesis, or other gas-to-liquid syntheses. The synthesis gas produced by the process is preferably used for those subsequent processes that require an H2 / CO ratio that can also be provided in the process according to the invention using the hexaaluminate-containing catalysts.

[0112] Since the process according to the invention can provide a synthesis gas which is under a high pressure, the process according to the invention is superior to those processes known from the prior art. I. Example of the preparation of a catalyst used in the reforming process according to the invention

[0113] To prepare catalyst E3, cobalt nitrate and lanthanum nitrate, which are located in a beaker, are first mixed with 250 mL of distilled water and completely dissolved. The cobalt nitrate consists of 83.1 g of Co(NO 3 ) 3 x6H 2 O, and the lanthanum nitrate consists of 284.9 g of La(NO 3 ) 3 x6H 2 O. 250 g of boehmite is added to the metal salt solution, resulting in a suspension. Disperal from SASOL is used as the boehmite.

[0114] The suspension is stirred for 15 minutes with a mechanically driven stirrer at a stirring speed of 2000 rpm. The suspension is then dropped into a liquid nitrogen bath using a pipette to freeze nearly spherical particles with a particle diameter of 5 mm. The frozen suspension particles are first dried using a freeze-dryer and then pressed through a sieve for size reduction. The mesh size of the sieve used here is 500 µm.

[0115] Following freeze-drying and comminution, the material is precalcined in an oven at 520 °C. The calcined material is then compressed into tablets using a punch press, which are then crushed and passed through a 1 mm mesh sieve. The tablets have a diameter of 13 mm and a thickness of 3 mm. The target fraction has a particle size of 500 to 1000 µm.

[0116] For high-temperature calcination, the sieved material is heated in a muffle furnace for 30 hours at 1100 °C, with an air flow of 6 liters / minute directed over the material. The furnace is heated to 1100 °C at a heating rate of 5 °C.

[0117] The preparation of catalysts E1 and E2, which illustrate examples of the claimed process, was carried out according to the synthesis procedure described for E3, whereby the amounts of cobalt nitrate and lanthanum nitrate were chosen to obtain the catalyst samples having the molar stoichiometries given in Table 1.

[0118] To prepare catalyst E4, which is an example of a catalyst containing strontium cobalt hexaaluminate to illustrate the process according to the invention, 64.7 g of cobalt acetate, 71.2 g of strontium acetate, and 250 g of boehmite (Disperal) were used. The preparation was carried out analogously to the synthesis procedure described for E3. II. Catalysis studies

[0119] To illustrate the process according to the invention, six different hexaaluminate-containing catalyst samples (B1 to B3 and E1 to E3) were tested in a laboratory catalysis apparatus with six reactors arranged in parallel under the process conditions for converting reforming gas. Catalyst samples B1 to B3 were hexaaluminate-containing samples prepared from nickel and lanthanum nitrate salts. Samples E1 to E3 were prepared from cobalt and lanthanum nitrate salts. Catalyst samples B1 to B3 were obtained using the same preparation process as catalysts E1 to E3 used for the process according to the invention, which is described under point I., except that a nickel nitrate salt was used instead of the cobalt nitrate salt. An overview of the composition of the catalysts tested is given in Table 1.

[0120] To conduct the tests, the individual reactors were filled with sample, using a minimum amount of 20 mL of sample per test. The reforming tests were conducted at a temperature of 850 °C and a temperature of 950 °C. A pressure of 20 bar and a GHSV of 3800 hr -1 were selected as process parameters. The composition of the product fluids obtained from the reactions was determined by GC analysis using an Agilent GC equipped with two TCDs and an FID. Test series 1

[0121] A summary of the process conditions and the catalysis data obtained from the reforming studies is shown in Table 2.

[0122] With regard to the catalytic tests, it should be noted that the test conditions were gradually changed during the test to increase the severity (the degree of the process conditions) and thus to create more drastic process conditions. The changes affected the composition of the reactant fluid and the temperature of the tests. To identify the different test stages, the sample numbers in Table 2 were each given a suffix from the series S1, S2, S3, ... S9, which refers to the conditions of the respective test stage. The tests on the catalyst samples were discontinued when coke formation occurred, which was demonstrated by a drop in methane conversion activity.

[0123] The investigations were carried out in the presence of 5 vol% argon as a standard gas, which was added to the reactant fluid for analytical reasons to control the substance recovery rate.

[0124] The starting point for each study was the steam reforming conditions of stage 1 (i.e., labeled S1 in Table 2), where the samples were exposed to a reaction temperature of 850 °C and a methane-to-H 2 O ratio of 1:1.

[0125] In the second stage (i.e., stage S2), the catalysts were subjected to tri-reforming conditions in which the reactant fluid contained methane, carbon dioxide, and water vapor.

[0126] In stages 3 to 7, the addition of steam was completely omitted, although hydrogen was added to the reactant fluid. From stages 3 to 7, the hydrogen content was gradually reduced from 40 vol% to 10 vol%, while the methane and carbon dioxide content was increased from 27.5 vol% to 42.5 vol% each. An exception was the transition from stage 4 to stage 5, where the catalyst temperature was increased from 850 °C to 950 °C, but the reactant fluid composition was kept constant.

[0127] From stage 8 onwards, steam was again added to the reactant fluid, but half of the hydrogen (i.e., 5 vol.% H 2 ) was replaced by steam compared to stage 7. From stage 9 onwards, the addition of hydrogen to the reactant fluid was completely omitted, and the steam content was increased from 5 vol.% to 10 vol.%.

[0128] The cobalt-containing hexaaluminates showed greater activity at higher process intensities (i.e., at increased severity) than the nickel-containing hexaaluminates. For samples B1, B2, and B3, coke formation began as early as test stages S5, S7, and S6, so the tests had to be discontinued at these test stages. The time until coke formation began ranged from 260 to 360 hours. The onset of coke formation on the catalyst samples is indicated by the letters KA in Table 2.

[0129] When carrying out the process according to the invention with cobalt-containing hexaaluminate samples E1, E2, and E3, the process could be carried out under the reaction conditions of process stages S8 and S9. During test stage S9, the catalyst samples were tested at a temperature of 950 °C, with the reactant gas having a composition of 42.5 vol% methane, 42.5 vol% carbon dioxide, and 10 vol% H2O. Table 1 shows the composition of the catalyst samples B1 to B3 and E1 to E3 (the values ​​given refer to mol%), the corresponding BET surface area and the loose bulk density. sample Ni Co La Al SA [m 2 < / g] LBD [g / mL] B1 6 8 86 6,1 0,953 B2 6 10 84 4,0 1,042 B3 6 14 80 3,1 1,196 E1 6 8 86 13,8 0,953 E2 6 10 84 7,1 1,036 E3 6 14 80 8,3 1,008 Table 2 shows a summary of the composition of the catalysts investigated, the reaction conditions, and the conversions. (Examples demonstrating the process according to the invention are given by the following examples: E1_S6, E1_S7, E1_S8, E1_S9, E2_S6, E2_S7, E2_S8, E2_S9, E3_S6, E3_S7, E3_S8, E3_S9). The examples (i.e., comparative examples) given under examples E1_S1 - E1_S5, E2_S1 - E2_S5, and E3_S1 - E3_S5 are not covered by the claims. Furthermore, the examples (i.e., comparative examples) given under B1 to B3 are not covered by the claims. Example Temperature [°C] CH 4 [vol.%] CO 2 [vol.%] H 2 O [vol.%] H 2 [vol.%] CH 4 -Conv. [%] CO2 conversion [%] H 2 / CO ratio B1_S1 850 47,5 - 47.5 0 32 4,4 B1_S2 850 27.5 27.5 40 50 24 1,7 B1_S3 850 27.5 27.5 - 40 4 56 1,35 B1_S4 850 32.5 32.5 - 30 36 73 1,2 B1_S5 950 32.5 32.5 - 30 KA B2_S1 850 47,5 - 47.5 - 40 4,5 B2_S2 850 27.5 27.5 40 - 65 30 1,6 B2_S3 850 27.5 27.5 - 40 6 58 1,6 B2_S4 850 32.5 32.5 - 30 4 40 1,45 B2_S5 950 32.5 32.5 - 30 40 75 1,2 B2_S6 950 37.5 37.5 - 20 55 85 1,05 B2_S7 950 42.5 42.5 - 10 KA 5 B3_S1 850 47,5 - 47.5 - 34 4,8 B3_S2 850 27.5 27.5 40 52 23 1,7 B3_S3 850 27.5 27.5 - 40 4 56 1,71 B3_S4 850 32.5 32.5 - 30 36 75 1,25 B3_S5 950 32.5 32.5 - 30 58 80 1,4 B3_S6 950 37.5 37.5 - 20 KA E1_S1 850 47,5 - 47.5 - 25 6 E1_S2 850 27.5 27.5 40 - 35 16 1,7 E1_S3 850 27.5 27.5 - 40 17 66 1,6 E1_S4 850 32.5 32.5 - 30 18 63 1,08 E1_S5 950 32.5 32.5 - 30 60 86 1,28 E1_S6 950 37.5 37.5 - 20 62 85 1,05 E1_S7 950 42.5 42.5 - 10 57 79 0,86 E1_S8 950 42.5 42.5 5 5 60 74 0,86 E1_S9 950 42.5 42.5 10 - 82 78 1,1 E2_S1 850 47,5 - 47.5 - 5 12 E2_S2 850 27.5 27.5 40 - 8 2 2,25 E2_S3 850 27.5 27.5 - 40 25 70 1,6 E2_S4 850 32.5 32.5 - 30 41 75 1,2 E2_S5 950 32.5 32.5 - 30 65 90 1,3 E2_S6 950 37.5 37.5 - 20 68 90 1,09 E2_S7 950 42.5 42.5 - 10 71 89 0,93 E2_S8 950 42.5 42.5 5 5 75 85 0,93 E2_S9 950 42.5 42.5 10 - 82 79 1,0 E3_S1 850 47,5 - 47.5 - 6 7,2 E3_S2 850 27.5 27.5 40 - 10 5 1,82 E3_S3 850 27.5 27.5 - 40 30 74 1,55 E3_S4 850 32.5 32.5 - 30 38 74 1,2 E3_S5 950 32.5 32.5 - 30 65 90 1,3 E3_S6 950 37.5 37.5 - 20 68 90 1,08 E3_S7 950 42.5 42.5 - 10 70 88 0,92 E3_S8 950 42.5 42.5 5 5 74 85 0,92 E3_S9 950 42.5 42.5 10 - 85 75 1,15 Test series 2

[0130] A portion of the catalyst sample from experimental example E2 was subjected to another catalytic test under modified test conditions. The feed composition and test protocol 2 are shown in Table 3. In this test, sample E2 was exposed to a feed that exhibited very low water vapor partial pressures compared to the tests shown in Table 2. Test protocol 2 differs from the first test protocol in that hydrogen was added to the feed gas only in a few process steps. In those process steps in which hydrogen was added to the feed gas, the hydrogen content was low, at 5 vol% and 10 vol%, respectively. In the first process steps (S01 to S04), thermodynamic equilibrium was not even close to being reached.A conceivable explanation for the failure to reach a state close to thermodynamic equilibrium would be that the catalyst was initially only incompletely reduced at the high water vapor partial pressures.

[0131] An unexpected finding was that catalyst E2 exhibited very high catalytic activity over an extremely long period under high-severity conditions (i.e., extremely harsh and demanding process conditions), and this activity was maintained for a very long period of more than 250 hours. After the end of the study, the catalyst was removed from the reactor without any coke deposits. The results thus demonstrate the high coke resistance of the catalyst when operated under the process conditions given in Table 3. At the same time, a product stream was obtained that exhibited a favorable H2 to CO ratio. Table 3 shows the test conditions and results obtained when testing catalyst sample E2 using Test Protocol 2 at modified process stages (S01 to S05). The catalytic measurements were performed at 850 °C. Examples demonstrating the process according to the invention are given by the following examples: E2_S03, E2_S04, E2_S05. Examples which do not correspond to the process according to the invention are given by the following examples (ie comparative examples): E2_S01 and E2_S02. Example TOS [h] CH 4 [vol.%] CO 2 [vol.%] H 2 O [vol.%] H 2 [vol.%] CH 4 -Conv. [%] CO2 conversion [%] H 2 / CO ratio E2_S01 0-94 27,5 27,5 40,0 0 10-33 3-9 1,7-1,9 E2_S02 94 - 141 32,5 32,5 30,0 0 37-31 21-19 1,4 E2_S03 141-167 37,5 37,5 20,0 10,0 30 33-31 1,3-1,4 E2_S04 167-191 37,5 37,5 25,0 5,0 29-26 28-27 1,2 E2_S05 191-453 37,5 37,5 20,0 0 26-65 23-57 1,1-1,0 Test series 3

[0132] In a further series of tests, exemplary embodiments of catalysts according to the invention, which had been prepared according to Examples E1, E2, and E4, and a comparative sample prepared according to Example B2, were subjected to catalytic reforming using a hydrogen-free reactant gas. The results of these tests, as well as the experimental conditions with regard to temperature and reactant gas composition, are shown in Table 5. Samples E1 and E2 were hexaaluminate-containing catalysts in which the hexaaluminate phase contained cobalt and lanthanum; Sample E4 was a hexaaluminate-containing catalyst in which the hexaaluminate phase contained cobalt and strontium; and Sample B2 was a hexaaluminate-containing catalyst in which the hexaaluminate phase contained nickel and lanthanum.

[0133] Compared to the catalysis experiments carried out in test series 1 and 2, the results of which are presented in Tables 2 and 3, a smaller amount of water vapor was added to the reactant gas in test series 3. Overall, the reactant gas in test series 3 is characterized by a low water vapor partial pressure and the absence of hydrogen (see Table 5). The test protocol used in test series 3 (i.e., test protocol 3) is divided into different process steps. In the first process step (S001), the catalyst was brought into contact with a reactant gas containing an equimolar ratio of methane to water (H2O to CH4 = 1.0). In the second process step, a reactant gas containing an equimolar ratio of 27.5 vol% methane and 27.5 vol% carbon dioxide, as well as an additional 40 vol% H2O, was used.Subsequently, in the next three process steps (S003 - S005), the equimolar ratio of methane to carbon dioxide was maintained, while the water content was gradually reduced from 30 vol% (at process step S003) to 15 vol% (at process step S005). (In process step S005, the H 2 O to CH 4 ratio is 0.38.)

[0134] The results achieved within test series 3 show that the cobalt hexaaluminate-containing catalyst samples E1, E2, and E4 enable high catalytic activity and stable operation over long periods and under very harsh process conditions (high-severity conditions) – particularly high temperatures and very low H2O partial pressures of only 15 vol.%. In contrast, the nickel hexaaluminate-containing sample B2 could only be operated up to process stage S003 (30 vol.% H2O). Further intensification of the process conditions led to rapid coking of sample B2, so the experiment had to be discontinued.

[0135] The tests conducted on samples E1, E2, and E4 were each terminated after a cumulative runtime of more than 1,000 hours, and the samples were removed from the reactor tube. None of the samples recovered after the test exhibited coke deposits. The results thus represent a further finding demonstrating the extremely high coke resistance of the inventive cobalt hexaaluminate-containing catalysts under the drastic process conditions listed in Table 5. At the same time, as can be seen from Table 5, the catalysis experiments produced a product stream with a favorable H2 to CO ratio. Table 4 shows the composition of catalyst sample E4 (the values ​​given refer to mol%), the corresponding BET surface area and the loose bulk density. sample Co Sr Al SA [m 2 < / g] LBD [g / mL] E4 6 8 86 25,0 1,035 Table 5 shows the test conditions and results obtained during the investigation of catalyst samples E1, E2, E4, and B2 in Test Series 3. In Test Series 3, a test protocol (Test Protocol 3) was used in which the samples were each subjected to five process steps (S001 to S005). The catalytic tests were conducted at a temperature of 850 °C and a pressure of 20 bar. Examples illustrating the process according to the invention are given by the following examples: E1_S004, E1_S005, E2_S004, E2_S005, E3_S004, E2_S005. Examples which do not illustrate the process according to the invention are given by the following examples (ie comparative examples): B2_S001 to B2_S005, E1_S001, E1_S002, E1_S003, E2_S001, E2_S002, E2_S003, E4_S001, E4_S002, E4_S003. Example Temperature [°C] CH 4 [vol.%] CO 2 [vol.%] H 2 O [vol.%] CH 4 -Conv. [%] CO2 conversion [%] H 2 / CO ratio B2_S001 850 47,5 - 47,5 32 - 4,9 B2_S002 850 27,5 27,5 40 43 16 1,7 B2_S003 850 32,5 32,5 30 40 21 1,4 B2_S004 850 37,5 37,5 20 - - KA B2_S005 850 40,0 40,0 15 - - KA E1_S001 850 47,5 - 47,5 58 - 3,8 E1_S002 850 27,5 27,5 40 75 24 1,9 E1_S003 850 32,5 32,5 30 62 33 1,6 E1_S004 850 37,5 37,5 20 71 59 1,1 E1_S005 850 40,0 40,0 15 65 65 1,0 E2_S001 850 47,5 - 47,5 52 - 4,0 E2_S002 850 27,5 27,5 40 77 31 1,8 E2_S003 850 32,5 32,5 30 57 31 1,6 E2_S004 850 37,5 37,5 20 70 58 1,1 E2_S005 850 40,0 40,0 15 65 65 1,0 E4_S001 850 47,5 - 47,5 41 - 4,4 E4_S002 850 27,5 27,5 40 60 21 1,8 E4_S003 850 32,5 32,5 30 72 49 1,3 E4_S004 850 37,5 37,5 20 67 60 1,1 E4_S005 850 40,0 40,0 15 64 64 1,0

[0136] Fig. 1shows three diffractograms recorded on the catalyst samples E1, E2, and E3 used for the process according to the invention before the catalytic test (i.e., on the fresh catalyst samples E1-f to E3-f). The diffractograms of all three samples exhibit reflections at 32.08, 34.01, and 36.10 °2θ, respectively, which can be assigned to the cobalt hexaaluminate, and one reflection at 33.42 °2θ, which can be assigned to the perovskite phase. No other crystalline phases are detectable based on the present XRD analysis.

[0137] Fig. 2shows two diffraction patterns recorded on catalyst samples E2 before and after the catalytic test, labeled E2-f (fresh catalyst sample) and E2-g (aged catalyst sample). The diffraction pattern recorded on the sample before the catalytic tests shows no difference compared to the diffraction pattern recorded on the aged sample. The investigations show that the cobalt remains in the hexaaluminate phase and is not dissolved out of it. Cobalt in the form of the free metal could not be detected in the aged sample either.

[0138] Fig.3shows two diffractograms recorded on catalyst samples B2 before (i.e., sample B2-f) and after (i.e., sample B2-g) the catalytic test. The diffractogram recorded from the aged sample (B2-g) shows a reflection at 44.40 °2θ, which can be attributed to a metallic nickel phase. The metallic nickel phase is not visible in the diffractogram of the fresh catalyst sample, as a corresponding reflection is not present.

[0139] Fig. 4 shows the results of the XPS analyses, which were measured on a fresh catalyst sample E2-f and an aged catalyst sample E2-g. The cobalt species detected in the fresh sample E2 are entirely attributable to the cobalt hexaaluminate phase. The aged catalyst sample E2-g shows various cobalt species. It is noteworthy that the majority of the cobalt species can be attributed to the hexaaluminate phase, and the metallic cobalt content is only low.

[0140] Samples E2-f (fresh catalyst sample before catalytic testing) and E2-g (aged catalyst sample after catalytic testing) were each subjected to XPS analysis (XPS: X-ray photoelectron spectroscopy). The results of these XPS analyses are presented in Table 6. In catalyst sample E2-f (i.e., the fresh catalyst), the cobalt is present exclusively as cobalt-lanthanum hexaaluminate (Co-HA, 781.2 eV).

[0141] Table 6 shows the relative proportions of cobalt in the cobalt-lanthanum hexaaluminate phase (Co-HA), the cobalt(II) oxide phase (Co(II) oxide), and the metallic cobalt phase (Co-metal). In sample E2-g (i.e., the aged catalyst sample), two additional cobalt species were detected in addition to the cobalt species present in the cobalt-lanthanum hexaaluminate (Co-HA, 781.2 eV): a cobalt(II) oxide (CoO, 780.4 eV) and a cobalt metal (Co-metal, 778.4 eV). The quantification of the XPS data (Table 6) confirmed the unexpected finding that a significant amount of non-metallic cobalt is present in the aged sample and that the cobalt remains essentially in the cobalt-lanthanum hexaaluminate phase.It can be assumed that this unexpected finding represents a crucial characteristic of the catalyst that can be used for the process according to the invention and plays an essential role in the exceptional coking resistance and activity of the catalyst. Table 6 shows a summary of the XPS data of a fresh sample of catalyst E2-f and an aged sample of catalyst E2-g after removal from the test reactor (nd = not detected). Relative proportions of cobalt species (%) Co-HA (781.2 eV) Co(II) oxide (780.4 eV) Co metal (778.4 eV) E2-f (fresh sample) 100 and and E2-g (aged sample) 82,6 9,2 8,3

[0142] Physical characterization of all catalyst samples presented in the examples was performed using XRD analyses, nitrogen sorption, and bulk density measurements. The XRD analyses were performed using a Bruker / AXS D8 Advance Series 2 spectroscopy system using a CuK-alpha source (with a wavelength of 0.154 nm at 40 kV and 40 mA). The measurements were performed over the range: 5–80° (2Theta), 0.02° steps with 4.8 seconds per step.

[0143] The XPS analyses were performed using a PHI 5000 VersaProbe spectrometer using Al K-α X-rays (1486.6 eV, monochromator) and a 180° hemisphere analyzer with a 16-channel detector. A spot size of 200 µm (50 watts) was used for the measurements. The C1s peak (284.8 eV) was used to calibrate the energy axis of the XPS spectrum.

Claims

1. A process for the reforming of hydrocarbons, preferably methane, in the presence of CO2, which comprises the following steps: (a.1) contacting of reforming gas in which the total proportion of hydrocarbons, preferably methane, and CO2 is more than 70% by volume with a hexaaluminate-comprising catalyst, (a.2) heating of the catalyst when coming into contact with the reforming gas at a temperature > 973.15 K, (a.3) operation of the reactor while the reaction is being carried out at a process pressure of > 5 bar, (a.4) the reforming gas brought into contact with the catalyst has a GHSV in a range from 500 to 20 000 hr-1, and wherein the hexaaluminate-comprising catalyst comprises cobalt and at least one further metal from the group consisting of Ba, Sr, La, and wherein the hexaaluminate-comprising catalyst having a BET surface area of greater than 2 m2 / g has a Co content in the range of 2 - 15 mol%, a content of further metal from the group consisting of Ba, Sr, La in a range of 2 - 25 mol%, and a content of Al in the range of 70 - 90 mol%, and the catalyst has an oxidic secondary phase in the range of 3 - 40% by weight, selected from the group consisting of theta-aluminum oxide, alpha-aluminum oxide, LaAlO3, BaAl2O4, SrAl2O4, CoAl2O4, La-stabilized aluminum oxides, La-stabilized aluminum oxide hydroxide.

2. The process for the reforming of hydrocarbons, preferably methane, in the presence of CO2 according to claim 1, wherein the hexaaluminate-comprising catalyst has a molar ratio of cobalt to aluminum in the range from 0.05 to 0.09 and a molar ratio of at least one element from the group consisting of Ba, Sr, La (MBaSrLa) to aluminum in a range from 0.09 to 0.25 and a molar ratio of Co to the at least one element from the group consisting of Ba, Sr, La (MBaSrLa) in the range from 1.0 to 0.3.

3. The process for the reforming of hydrocarbons, preferably methane, in the presence of CO2 according to either of claims 1 and 2, wherein the hexaaluminate-comprising catalyst has a BET surface greater than 4 m2 / g.

4. The process for the reforming of hydrocarbons, preferably methane, in the presence of carbon dioxide according to any of claims 1 to 3, wherein the reforming gas mentioned in step (a.1) has an H2O content of up to 30% by volume.

5. The process for the reforming of hydrocarbons, preferably methane, in the presence of carbon dioxide according to any of claims 1 to 4, wherein the reforming process is preceded by an activation process and / or a conditioning process.

6. The process for the reforming of hydrocarbons, preferably methane, in the presence of carbon dioxide according to any of claims 1 to 5, wherein the feed fluid comprises steam and has a composition in which the components CH4 / CO2 / H2O are present in a ratio range of the gas volumes from 35 / 35 / 30 to 48 / 48 / 4.

7. The process for the reforming of hydrocarbons, preferably methane, in the presence of carbon dioxide according to any of claims 1 to 6, wherein the catalyst comprises at least one noble metal-comprising promoter from the group consisting of Pt, Rh, Pd, Ir and the content of noble metal-comprising promoter is in the range of 0.1 - 3 mol% or the catalyst comprises further cations, preferably from the group consisting of Mg, Ca, Ga, Be, Ni, Fe, Cr, Mn.