Patent Application
20200406240
The present invention provides lanthanide-supported transition metal catalysts synthesized using high-nitrogen energetic precursors, and uses thereof, e.g., in reforming of methane.
Abbreviations: BTA, bis(1H-tetrazole-5-yl)amine; DRM, dry reforming of methane; DSC, differential scanning calorimetry; EDS, energy dispersive spectroscopy (nominal composition analysis and elemental dot mapping); FID, flame ionization detector; FTIR, Fourier-transform infrared; GHSV, gas hourly space velocity (hourly process gas flow per gram of catalyst); RT, room temperature; RWGS, reverse water-gas shift; sccm, standard cubic centimeters per minute; SEM, scanning electron microscopy; TCD, thermal conductivity detector; TEM, transmission electron microscopy; TGA, thermographic analysis; TPO, temperature program oxidation; TPR, temperature program reduction; TPR/O/R, temperature-programmed reduction, oxidation, and subsequent reduction; XPS, X-ray photoelectron spectroscopy (composition, oxidation states); XRD, X-ray diffraction (phase analysis).
Nitrogen-rich energetic materials (EMs) belong to a class of compounds that can release a significant amount of energy and gasses upon their deflagration or detonation. These materials are commonly used as explosives, propellants, pyrotechnics, and as gas generators (Talawar et al., 2009). In recent years, nitrogen-rich EMs have undergone extensive research and development due to the capability of such materials to release N2 as the main combustion product (“green” EMs).
During an investigation of the combustion behavior of various complexes of nitrogen-rich ligands for use in pyrotechnics, Tappan and coworkers found a novel way of synthesizing ultralow-density monolithic metal nanofoams (Tappan et al., 2010). This was achieved by self-propagating combustion of energetic metal complexes containing nitrogen-rich ligands. These researchers showed that the combustion behavior of the energetic metal complex played an important role in determining the metal nanofoam structure in an apparent “Goldilocks” effect. They found that energetic complexes that were too sensitive to mechanical impact and friction (“too hot”) detonated rapidly and failed to create monolithic foams, while complexes which were too inert (“too cold”) could not sustain a self-propagating combustion process. The use of such metal nanofoams in catalytic systems and other applications was recently reported. For example, gold nanofoams showed modest activity as electrocatalysts (Mueller et al., 2009), while self-combustion generated palladium nanofoams were investigated as a material for H2 storage (Tappan et al., 2010). The latter Pd nanofoams showed a low capacity for storage of H2 compared to bulk Pd metal (in a powdered form), possibly due to a presence of combustion-related impurities and residues. In addition to the synthesis of metal nanofoams, the only other reported use of high-nitrogen EMs for metal synthesis was from Qu and coworkers who made copper micro-rods by thermal decomposition of the Cu-[bis(1H-tetrazol-5-yl)amine]2 (Cu(BTA)2) complex under inert atmosphere (Qu et al., 2015).
DRM, the reforming of methane using CO2, is considered to be a promising technology among several other processes for the reforming of methane (steam reforming, partial oxidation, autothermal reforming, etc.). One of the main interests in this process is due to the consumption of two major greenhouse gases (CO2 and CH4) by their conversion to synthesis gas (syngas), which is a mixture of CO and H2 (Eq. 1) (Theofanidis et al., 2015; Baltrusaitis and Luyben, 2015; Shang et al., 2017; Littlewood et al., 2015).
CH4+CO2→2CO+2H2, ΔH°298K=+247 kJmol−1 (eq. 1)
CH4→C+2H2, ΔH°298K=+75 kJmol−1 (eq. 2)
2 CO→CO2+C, ΔH°298K=−172 kJmol−1 (eq. 3)
CO2+H2->CO+H2O, ΔH°298K=+41 kJmol−1 (eq. 4)
The syngas produced from the DRM process could be further utilized as a starting material for Fischer-Tropsch reaction used for the production of various liquid hydrocarbons and fine chemicals. However, till now, the DRM technology is not heavily industrialized, due to the lack of availability of stable, efficient and economical catalysts (Li et al., 2011; Baudouin et al., 2012; Muraleedharan Nair and Kaliaguine, 2016).
Considering their cost, availability and activity, Ni-based catalysts, rather than catalysts containing some noble transition metals (such as ruthenium, rhodium, palladium, osmium, iridium and platinum) are most commonly used to promote the DRM process. On the other hand, Ni-based catalysts deactivate quite rapidly, due to coke formation and sintering, caused by CH4 cracking (Eq. 2), CO dispersion (Boudouard reaction, Eq. 3), and high operational temperature. Different strategies for synthesis of supported Ni-based catalysts were reported (Dai et al., 2015; Kawi et al., 2015; Pakhare and Spivey, 2014; Pan and Bao, 2011; Prieto et al., 2013; Xie et al., 2014). For example, Singh et al. (2016) have synthesized shape-controlled LaNiO3 nanoparticles and converted them into active Ni/La2O3 catalyst by a solid-crystallization method. These authors have shown that their catalyst is capable of a stable methane conversion for 100 hours at 650° C., without any carbon accumulation and sintering effects. Similarly, Li et al. (2017) have stabilized Ni nanoparticles on La2O2CO3 nano-rods by wet impregnation method for DRM and reached a 70% stable methane conversion for 50 hours.
The present specification discloses the unprecedented synthesis of a supported nanocatalyst prepared by the co-deflagration of a mixture of two high-nitrogen energetic metal complexes containing nickel and lanthanum. The term “co-deflagration” as used herein denotes the combustion of at least two metal-containing energetic complexes resulting in the sub-sonic release of gasses as well as a solid-phase product. As surprisingly found, the kinetic energy available to nickel and lanthanum atoms during the crystallization process gives rise to strong catalyst-support bonding and therefore stable catalytic activity. Ni/La2O2CO3 and Ni/LaOCl were selected as our targets since they have a great potential to enable the large-scale industrialization of DRM, which is highly important due to its consumption of two green-house gasses. Additionally, the co-deflagration technique can be used to make catalysts for other industrial processes such as the water-gas shift reaction and the reverse water-gas shift reaction, potentially catalyzed by Fe/La2O2CO3 or Fe2O3/La2O2CO3.
In one aspect, the present invention relates to a lanthanum-N,N-bis(1H-tetrazole-5-yl)-amine (La-BTA) complex, e.g., the La-BTA pentahydrate complex exemplified herein.
La-BTA Pentahydrate Complex
In another aspect, the present invention provides a catalyst, more specifically a supported catalyst, prepared by a combustion of a mixture of a lanthanum-BTA complex as defined above, and a transition metal (excluding lanthanides and actinides)-BTA complex, wherein the said supported catalyst comprises discrete particles each comprising a lanthanum-containing support material (i.e., core) and nanoparticles of said transition metal or oxide thereof, wherein said support material comprises lanthanum oxycarbonate in the form of both La2O2CO3 and La2O(CO3)2, and optionally lanthanum oxide (La2O3) and/or lanthanum oxychloride (LaOCl), and said nanoparticles are impregnated within or attached to said support material. A particular such supported catalyst exemplified herein comprises lanthanum oxycarbonate-based support material, and nanoparticles comprising nickel and nickel oxide, impregnated within or attached to said support material, wherein the amounts of said lanthanum oxycarbonate, nickel, and nickel oxide are about 50-52%, about 40-42%, and about 9-10%, by weight, of said supported catalyst, respectively. Such a catalyst exhibits an increase of about 0.8 eV in the binding energy of the Ni3p XPS spectrum, as compared to that of unbound (pure) Ni, indicating a formation of strong interactions between the nickel nanoparticles and the lanthanum oxycarbonate support, as a result of the kinetic energy imparted on the metal atoms during the combustion-based preparation of this catalyst. As further shown, while a pure Ni catalyst produced from the combustion of pure Ni-BTA suffered from severe sintering, the Ni/La oxycarbonate catalyst was found to be coke- and sintering-resistant after 100 h of catalytic activity, at various GHSVs. Said Ni/La oxycarbonate catalyst exhibited a high methane and carbon dioxide conversion rate of above 80% and with up to 150 L/g-h GHSV due to the strong interaction between the nickel and the lanthanum oxycarbonate support, and the relatively uniform distribution of the nickel nanoparticles on said support.
In yet another aspect, the present invention thus relates to methods for reforming of a hydrocarbon, e.g., an alkane such as methane, carried out in the presence of a catalyst as defined above. In one particular such aspect, the invention provides a method for dry reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide. In another particular such aspect, the invention provides a method for steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon dioxide. In a further particular such aspect, the invention provides a method for mixed carbon dioxide and steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide and steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide. In certain embodiments, the hydrocarbon reformed according to any one of the methods is a (C1-C8)alkane, preferably methane. In particular embodiments of each one of the methods, the transition metal is nickel, and the nanoparticles impregnated within or attached to said core comprise both nickel and nickel oxide.
In a further aspect, the present invention relates to a process for coating an inert ceramic monolith with a catalyst as defined above, said process comprising:
In another aspect, the present invention provides a process for the preparation of a catalyst, more specifically a supported catalyst, comprising discrete particles comprising a lanthanide-based support material (i.e., a lanthanide-based core) and nanoparticles of a transition metal excluding lanthanides and actinides or an oxide thereof impregnated within or attached to said support material, said process comprising:
In one embodiment, the process disclosed herein is used for the preparation of a catalyst as defined above, i.e., a supported catalyst comprising discrete particles comprising a lanthanum-based support material, and nickel nanoparticles impregnated within or attached to said support material, wherein said process comprises: (i) mixing a La-BTA complex such as the La-BTA pentahydrate complex with a Ni-BTA complex and optionally an organic or inorganic oxidant, each in the form of a solid or semi-solid material, to obtain a homogeneous solid or semi-solid material; (ii) optionally grinding and mixing said homogeneous solid or semi-solid material; (iii) optionally pressing said homogeneous solid or semi-solid material into a form (pellet); (iv) heating said optionally pressed homogeneous solid or semi-solid material to about 350° C. to thereby combust said BTA ligand and said oxidant, if present, and consequently obtain a catalyst material; (v) subjecting said catalyst material to a temperature of about 400° C., in the flow of a gas mixture comprising O2 and an inert gas selected from Ar, He or N2, to thereby oxidize said lanthanum; and (vi) subjecting the product obtained in step (v) to a temperature of about 800° C., in the flow of a gas mixture comprising O2 and an inert gas selected from Ar, He or N2, to thereby reduce the nickel oxide obtained in step (iv) (when said homogeneous solid/semi-solid material is heated and ignites), and consequently obtain said catalyst.
In still another aspect, the present invention provides a catalyst, more specifically a supported catalyst, comprising discrete particles comprising a lanthanide-based support material (i.e., a lanthanide-based core), and nanoparticles of a transition metal excluding lanthanides and actinides or an oxide thereof impregnated within or attached to said support material, obtained by the process defined above.
Catalysts obtained by the process defined above can be used, e.g., for reforming of a hydrocarbon, e.g., an alkane such as methane. In yet another aspect, the present invention thus relates to methods for reforming of a hydrocarbon carried out in the presence of a catalyst as defined hereinabove, i.e., a catalyst comprising discrete particles comprising a lanthanide-based support material, and a transition metal nanoparticles impregnated within or attached to said support material. In one particular such aspect, the invention provides a method for dry reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide. In another particular such aspect, the invention provides a method for steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon dioxide. In a further particular such aspect, the invention provides a method for mixed carbon dioxide and steam reforming of said hydrocarbon, comprising reacting methane with carbon dioxide and steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide.
In one aspect, the present invention relates to a lanthanum-N,N-bis(1H-tetrazole-5-yl)-amine (La-BTA) complex. In a particular embodiment, said La-BTA complex is in pentahydrate form as exemplified herein.
In another aspect, the present invention provides a catalyst comprising discretem i.e., separate or distinct, particles each comprising a lanthanum-containing support material and nanoparticles of a transition metal excluding lanthanides and actinides or an oxide thereof, wherein said support material comprises lanthanum oxycarbonate (both La2O2CO3 and La2O(CO3)2) and optionally lanthanum oxide and/or lanthanum oxychloride, and said nanoparticles are decorating said support material, more specifically impregnated within or attached to said support material. The term “lanthanum oxycarbonate” as used herein refers to both La2O2CO3 and La2O(CO3)2. Accordingly, catalysts of the present invention referred to herein (for the sake of simplicity) as metal/La2O2CO3 or metal/La2O(CO3)2, e.g., Ni/La2O2CO3 or Ni/La2O(CO3)2, comprise in all cases discrete particles comprising said metal/lanthanum oxycarbonate- and optionally said metal/La2O3— and/or said metal/LaOCl-based support material. Similarly, the term “lanthanum oxycarbonate-based support material” or “lanthanum oxycarbonate-based core” as used herein interchangeably refers to a support material (core) comprising, or made of, lanthanum oxycarbonate and optionally one or both of lanthanum oxide and lanthanum oxychloride.
According to the present invention, the support material composing the catalyst, i.e., the particle core, is decorated, rather than completely coated or covered, by the transition metal nanoparticles, as shown, e.g., in
In certain embodiments, the catalyst of the present invention does not comprise molecular carbon. The term “molecular carbon” as used herein denotes a compound consisting solely of carbon atoms, including macromolecules such as fullerenes; carbon nanomaterials such as single-walled carbon nanotubes, multi-walled carbon nanotubes, or graphene; carbon microstructures such as vitreous carbon; carbon polymorphic forms such as graphite; and amorphous carbon.
In certain embodiments, the nanoparticles impregnated within or attached to the lanthanum oxycarbonate-based support material comprise both said transition metal and said oxide thereof. In other embodiments, said nanoparticles comprise either said transition metal or said oxide thereof.
The term “transition metal” as used herein refers to any element in the d-block (columns 3 through 12) of the Periodic Table, excluding the lanthanides (the elements with atomic numbers from 57 to 71) and the actinides (the elements with atomic numbers from 89 to 103). Examples of transition metals include, without being limited to, titanium (Ti), vanadium (V), manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu), zinc (Zn), molybdenum (Mo), ruthenium (Ru), rhodium (Rh), palladium (Pd), tungsten (W), rhenium (Re), osmium (Os), iridium (Ir), or platinum (Pt). In certain embodiments, the transition metal is nickel or iron.
The term “impregnated” as used herein with respect to the transition metal nanoparticles means that said nanoparticles are not only attached to the support material but, could be partially or completely imbedded within said lanthanum oxycarbonate-based support material, as a result of the combustion process used for the preparation of the catalyst.
In certain embodiments, the transition metal nanoparticles impregnated within or attached to the lanthanum oxycarbonate-based support material are relatively uniformly distributed on said support material.
In certain embodiments, the present invention provides a catalyst as defined in any one of the embodiments above, wherein said transition metal is nickel; and (a) the overall amount of said lanthanum oxycarbonate, lanthanum oxide and lanthanum oxychloride is about 45-60%, preferably about 50-55%, more preferably about 50-52%, by weight, of said catalyst; (b) the amount of said nickel is about 35-50%, preferably about 40-45%, more preferably about 40-42%, by weight, of said catalyst; or (c) the amount of said nickel oxide, when present, is about 5-15%, preferably about 8-12%, more preferably about 9-10%, by weight, of said catalyst. In particular such embodiments, the amounts of said lanthanum oxycarbonate (including lanthanum oxide and/or lanthanum oxychloride, when present), nickel, and nickel oxide are about 50-52%, about 40-42%, and about 9-10%, by weight, of said catalyst, respectively, e.g., about 50.0%, 50.1%, 50.2%, 50.3%, 50.4%, 50.5%, 50.6%, 50.7%, 50.8%, 50.9%, 51.0%, 51.1%, 51.2%, 51.3%, 51.4%, 51.5%, 51.6%, 51.7%, 51.8%, 51.9% or 52.0% lanthanum oxycarbonate (including lanthanum oxide and/or lanthanum oxychloride, when present); about 40.0%, 40.1%, 40.2%, 40.3%, 40.4%, 40.5%, 40.6%, 40.7%, 40.8%, 40.9%, 41.0%, 41.0%, 41.1%, 41.2%, 41.3%, 41.4%, 41.5%, 41.6%, 41.7%, 41.8%, 41.9%, or 42.0% nickel; and about 9.0%, 9.1%, 9.2%, 9.3%, 9.4%, 9.5%, 9.6%, 9.7%, 9.8%, 9.9% or 10.0% nickel oxide, by weight, of said catalyst, wherein each combination of these amounts represents a separate embodiment. Particular such catalysts exhibit an increase of about 0.8 eV or more, e.g., about 0.8 eV, about 0.85 eV, about 0.9 eV, about 0.95 eV, about 1.0 eV, about 1.05 eV, about 1.1 eV, or more, in the binding energy of the Ni3p XPS spectrum compared to that of unbound Ni.
As shown herein, the Ni/La2O2CO3 catalyst of the present invention is highly efficient in dry reforming of methane at 800° C., exhibiting excellent catalytic activity at GHSVs, as high as 150 L/g-h, without any coking and sintering even after 100 hours of activity. As discussed in the Experimental section herein, this unexpected stability probably results from the kinetic energy imparted onto the metal atoms during the combustion synthesis used for the preparation of the catalyst; and it seems to be due to strong interaction between the nickel and the lanthanum-based support, as evident from the increase in the binding energy of the Ni3p XPS spectrum compared to that of unbound nickel, which leads to relatively uniform distribution of the nickel nanoparticles formed on the lanthanum oxide/oxychloride support material, and to impregnation of at least part of said nickel nanoparticles into the support material. The strength of the interaction is also supported by the lack of multi-walled carbon nanotube growth after 100 h of methane dry reforming, a catalyst deactivation mechanism typical of weakly bound Ni nanoparticles.
In yet another aspect, the present invention thus relates to methods for reforming of a hydrocarbon, e.g., an alkane such as methane, carried out in the presence of the catalyst of the invention as defined in any one of the embodiments above. The term “alkane” as used herein means a linear or branched hydrocarbon having, e.g., 1-8 carbon atoms and includes methane, ethane, n-propane, isopropane, n-butane, sec-butane, isobutane, tert-butane, n-pentane, isopentane, 2,2-dimethylpropane, n-hexane, n-heptane, n-octane, and the like. In one particular such aspect, disclosed herein is a method for dry reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide as the oxidizing agent, in the presence of said catalyst, so as to crack said hydrocarbon into a H2+CO mixture, which may then be used in a gas-to-liquid conversion for the production of hydrocarbon fuels and other materials. In another particular such aspect, disclosed herein is a method for steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon dioxide. In a further particular such aspect, disclosed herein is a method for mixed dry and steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with both carbon dioxide and steam as the oxidizing agents, in the presence of said catalyst, so as to crack said hydrocarbon into a H2+CO mixture, which may then be used in a gas-to-liquid conversion for the production of hydrocarbon fuels and other materials. In certain embodiments, the hydrocarbon reformed according to any one of the methods is a (C1-C8)alkane, preferably methane. In particular embodiments of each one of the methods, said transition metal is nickel, and the nanoparticles impregnated within or attached to said core comprise both nickel and nickel oxide.
In a further aspect, the present invention relates to a process for coating an inert ceramic monolith with a catalyst as defined above, said process comprising: (i) activating the surface of said inert ceramic monolith; (ii) mixing said catalyst with a metal oxide; a polysaccharide; a polyalkylene glycol, more specifically polyethylene glycol; a polyvinyl compound; and water to form a slurry; (iii) coating the activated ceramic monolith with said slurry; and (iv) drying and then calcinating the coated ceramic monolith.
In certain embodiments, the inert ceramic monolith coated by the process disclosed herein is alumina such as γ-Al2O3, cordierite, mullite, or silicon carbide.
The activation of the inert ceramic monolith in step (i) of the process is necessary to make sure that the monolith's surface is available and contaminant-free, prior to coating with the catalyst. In certain embodiments, the inert ceramic monolith is activated by cleaning with an acid such as nitric acid, sulfuric acid, hydrochloric acid, or acetic acid, but preferably with nitric acid, and then optionally calcinating at a temperature in a range of 500-1600° C.
In certain embodiments, the metal oxide mixed with said catalyst in step (ii) of the process is alumina such as γ-Al2O3, colloidal alumina, pseudoboehmite, silica, colloidal silica, or sodium silicate. In preferred embodiments, said metal oxide is alumina such as γ-Al2O3.
In certain embodiments, the polysaccharide mixed with said catalyst in step (ii) of the process is hydroxyalkyl cellulose such as hydroxypropyl cellulose and hydroxyethyl cellulose. In preferred embodiments, said polysaccharide is hydroxypropyl cellulose.
In certain embodiments, the polyethylene glycol mixed with said catalyst in step (ii) of the process has a molecular weight in a range of about 600 dalton (Da) to about 6000 Da. In preferred embodiments, said polyethylene glycol has a molecular weight of about 6000 Da.
In certain embodiments, the polyvinyl compound mixed with said catalyst in step (ii) of the process is polyvinyl alcohol, polyvinyl pyrrolidone, polyvinyl butyral, or polyvinyl chloride. In preferred embodiments, said polyvinyl compound is polyvinyl alcohol.
In certain embodiments, the activated ceramic monolith is coated with said slurry in step (iii) by dipping in said slurry.
In particular embodiments, the inert ceramic monolith is activated in step (i) by cleaning with nitric acid; the metal oxide mixed with said catalyst in step (ii) is alumina, e.g., γ-Al2O3; the polysaccharide mixed with said catalyst in step (ii) is hydroxypropyl cellulose; the polyethylene glycol mixed with said catalyst in step (ii) has a molecular weight of about 6000 Da; said polyvinyl compound mixed with said catalyst in step (ii) is polyvinyl alcohol; and the activated ceramic monolith is coated with said slurry in step (iii), e.g., by dipping in said slurry. In more particular such embodiments, the inert ceramic monolith is activated in step (i) by cleaning with nitric acid and then calcinated at about 550° C.; the concentration of the alumina mixed in step (ii) is 0.1-10%, preferably 1-3%, by weight; the concentration of the hydroxypropyl cellulose mixed in step (ii) is 0.01-5%, preferably 0.3-1%, by weight; the concentration of the polyethylene glycol mixed in step (ii) is 0.01-5%, preferably 0.1-0.5%, by weight; and the concentration of the polyvinyl alcohol mixed in step (ii) is 0.01-5%, preferably 0.1-0.5%, by weight.
In a particular such aspect, the present invention relates to a process for coating an inert ceramic monolith with a catalyst as defined in any one of the embodiments above, wherein said transition metal is nickel, i.e., a process for coating an inert ceramic monolith with a catalyst comprising discrete particles comprising lanthanum oxycarbonate- and optionally lanthanum oxide- and/or lanthanum oxychloride-core, and nanoparticles of nickel or an oxide thereof impregnated within or attached to said core.
In another aspect, the present invention provides a process for the preparation of a catalyst, more specifically a supported catalyst, comprising discrete particles comprising a lanthanide-based core, and nanoparticles of a transition metal excluding lanthanides and actinides or an oxide thereof impregnated within or attached to said core, said process comprising: (i) mixing a complex of said lanthanide and an energetic nitrogen-rich ligand with a complex of said transition metal and the same or a different energetic nitrogen-rich ligand(s); and optionally an organic or inorganic oxidant, each in the form of a solid or semi-solid material, to obtain a homogeneous solid or semi-solid material; (ii) optionally grinding and mixing said homogeneous solid or semi-solid material; (iii) optionally pressing said homogeneous solid or semi-solid material into a form (pellet); (iv) heating said optionally pressed homogeneous solid or semi-solid material at a temperature sufficient to combust said energetic nitrogen-rich ligand(s), but lower than the melting temperature of each one of said lanthanide and transition metal to thereby obtain a catalyst material; (v) subjecting said catalyst material to a temperature sufficient to oxidize residual organic matter, but lower than the melting temperature of each one of said lanthanide and transition metal, in the flow of a gas mixture comprising (more specifically consisting of) O2 and an inert gas selected from Ar, He or N2; and (vi) subjecting the product obtained in step (v) to a temperature sufficient to reduce the oxide of said transition metal obtained, but lower than the melting temperature of each one of said lanthanide and transition metal, in the flow of a gas mixture comprising (more specifically consisting of) O2 and an inert gas selected from Ar, He or N2, to thereby obtain said catalyst.
According to the process of the present invention, an organic or inorganic oxidant is optionally mixed in step (i) with the lanthanide complex of energetic nitrogen-rich ligand(s) and the transition metal complex of the same or different energetic nitrogen-rich ligand(s), depending on the particular lanthanide and transition metal complexes used. The amount of such an organic or inorganic oxidant mixed with the lanthanide and transition metal complexes may be up to about 70%, by weight, of the overall solid powder mixture, e.g., up to about 10%, up to about 15%, up to about 20%, up to about 25%, up to about 30%, up to about 35%, up to about 40%, up to about 45%, up to about 50%, up to about 55%, up to about 60%, up to about 65%, or up to about 70%, by weight, of the overall solid powder mixture. Non-limiting examples of inorganic oxidants include ammonium nitrate, ammonium dinitramide, and ammonium perchlorate; and examples of organic oxidants include, without being limited to, peroxides, trinitromethane salts, 2,2,2-trinitroethanol and derivatives thereof, 2,2-dinitromethane and salts and derivatives thereof, and 2,2-dinitroethanol and salts and derivatives thereof.
The term “lanthanide” as used herein refers to any one of the series of fifteen metallic elements from lanthanum to lutetium in the Periodic Table, also known as “rare earth elements”, i.e., lanthanum (La), cerium (Ce), praseodymium (Pr), neodymium (Nd), promethium (Pm), samarium (Sm), europium (Eu), gadolinium (Gd), terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium (Yb), and lutetium (Lu). In particular embodiments, the lanthanide used for the preparation of the supported catalyst according to the process of the present invention is La, Ce, Pr, Nd, Pm, Sm, or Gd. In a more particular such embodiment, said lanthanide is La.
In certain embodiments, the energetic nitrogen-rich ligand(s) being complexed with either or both the lanthanide or transition metal, according to the process disclosed herein, is selected from triazole, tetrazole, N,N-bis(1H-tetrazole-5-yl)-amine (BTA), 5,5-diazotetrazolate triazole, tetrazine, nitramines, guanidines, guanylureas, nitroguanidines, nitroureas, or aminoguanidines.
According to the process of the present invention, the lanthanide and transition-metal complexes, optionally together with an organic or inorganic oxidant, are heated at a temperature sufficient to combust the energetic nitrogen-rich ligand(s); and then subjected to a temperature sufficient to oxidize residual organic matter. The supported catalyst obtained by this process thus comprises very low amounts of carbon or carbon-containing materials, and in certain embodiments, does not comprise carbon or carbon-containing materials at all.
In certain embodiments, the lanthanide complex used according to the process of the present invention is a La-BTA complex, e.g., the La-BTA pentahydrate complex, and the transition metal complex used is a Ni-BTA complex.
In certain embodiments, the process of the invention as defined in any one of the embodiments above is used for the preparation of a catalyst as disclosed herein, i.e., a supported catalyst comprising discrete particles comprising a lanthanum-based support material and nickel nanoparticles impregnated within or attached to said support material, wherein said process comprises: (i) mixing a La-BTA complex such as the La-BTA pentahydrate complex with a Ni-BTA complex and optionally an organic or inorganic oxidant, each in the form of a solid or semi-solid material, to obtain a homogeneous solid or semi-solid material; (ii) optionally grinding and mixing said homogeneous solid or semi-solid material; (iii) optionally pressing said homogeneous solid or semi-solid material into a form (pellet); (iv) heating said optionally pressed homogeneous solid or semi-solid material to about 350° C. to thereby combust said BTA ligand and said oxidant, if present, and consequently obtain a catalyst material; (v) subjecting said catalyst material to a temperature of about 400° C., in the flow of a gas mixture comprising O2 and an inert gas selected from Ar, He or N2, to thereby oxidize said lanthanum; and (vi) subjecting the product obtained in step (v) to a temperature of about 800° C., in the flow of a gas mixture comprising O2 and an inert gas selected from Ar, He or N2, to thereby reduce the nickel oxide obtained and consequently obtain said catalyst.
In particular embodiments, the La-BTA complex used for the preparation of said catalyst is the La-BTA pentahydrate complex; and up to 70%, by weight of the overall solid or semi-solid material mixture, organic or inorganic oxidant, as defined above is optionally added to the complexes mixture.
In still another aspect, the present invention provides a catalyst, more specifically a supported catalyst, comprising discrete particles comprising a lanthanide-based core, and nanoparticles of a transition metal excluding lanthanides and actinides or an oxide thereof impregnated within or attached to said core, wherein said catalyst is obtained by the process of the present invention as defined in any one of the embodiments above. Such a catalyst can be used, e.g., for reforming of a hydrocarbon, e.g., an alkane such as methane.
In yet another aspect, the present invention relates to methods for reforming of a hydrocarbon, e.g., an alkane such as methane, carried out in the presence of a catalyst as defined hereinabove, i.e., a catalyst comprising discrete particles comprising a lanthanide-based support material, and transition metal nanoparticles impregnated within or attached to said support material. In one particular such aspect, the invention provides a method for dry reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide. In another particular such aspect, the invention provides a method for steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon dioxide. In a further particular such aspect, the invention provides a method for mixed carbon dioxide and steam reforming of said hydrocarbon, comprising reacting said hydrocarbon with carbon dioxide and steam, in the presence of said catalyst, to thereby obtain hydrogen and carbon monoxide. In certain embodiments, the hydrocarbon reformed according to any one of the methods is a (C1-C8)alkane, preferably methane. In particular embodiments of each one of the methods, said transition metal is nickel, and the nanoparticles impregnated within or attached to said core comprise both nickel and nickel oxide.
Unless otherwise indicated, all numbers referring, e.g., to amounts of lanthanum oxycarbonate, lanthanum oxide, or lanthanum oxychloride, nickel, and nickel oxide in the supported catalyst disclosed herein, or to temperatures used in the process of the invention, used in the present specification are to be understood as being modified in all instances by the term “about”. Accordingly, unless indicated to the contrary, the numerical parameters set forth in this description and claims are approximations that may vary by up to plus or minus 10% depending upon the desired properties sought to be obtained by the invention.
The invention will now be illustrated by the following non-limiting Examples.
Bis(1H-tetrazole-5-yl)amine [BTA]
(U.S. Pat. No. 5,468,866). A solution of boric acid (10.14 g, 164.0 mmol), sodium dicyanamide (7.4 g, 83.1 mmol) and NaN3 (10.8 g, 166.1 mmol) in water (80 mL) was refluxed for 18 h, while the pH was kept at about 8. The reaction mixture was then cooled to RT and acidified by dropwise addition of concentrated hydrochloric acid to pH 1. Formed white precipitate was collected by filtration, washed with water (until pH 3) and vacuum dried to yield pure BTA as a white powder (5.8 g, 46% yield). FTIR (ATR): 495, 1043, 1554, 1645, 2361, 2853, 2941, 3027, 3453 cm−1. DSC (10° C./min)—endotherms: 120.2 and 138.7° C.; exotherm: 244.2° C.
(U.S. Pat. No. 8,350,050). To a dispersion of BTA (6.0 g, 39.2 mmol) in water (100 mL) ammonia solution (28% in water) was added dropwise at RT until a transparent solution was obtained. The resulted solution was evaporated on a rotovap (at 60° C.) and further vacuum dried to yield pure ammonium-BTA as a white powder (6.7 g, 93% yield). FTIR (ATR): 473, 520, 977, 1631, 2164, 2284, 3157, 3392 cm−1. DSC (10° C./min)—endotherms: 115.5, 132.7° C.; exotherms: 253.1, 278.3, 332.1, 536.2° C.
Ni-BTA Complex
(U.S. Pat. No. 7,141,675). A solution of ammonium-BTA (3.03 g, 16.2 mmol) and Ni(ClO4)2.6H2O (2.96 g, 8.1 mmol) in water (50 mL) was refluxed for 12 h under vigorous stirring. After that time, the reaction mixture was allowed to cool down to RT, a solvent was evaporated on a rotovap (at 60° C.) and further vacuum dried to yield Ni-BTA complex as a violet powder (5.5 g). FTIR (ATR): 744, 824, 1041, 1303, 1597, 3195 cm−1. DSC (10° C./min)—endotherm: 243.9° C.; exotherms: 366.6, 566.6° C.
La-BTA Complex.
A solution of ammonium-BTA (3.03 g, 16.2 mmol) and La(NO3)3.6H2O (3.51 g, 8.1 mmol) in water (50 mL) was refluxed for 12 h under vigorous stirring. After that time, the reaction mixture was allowed to cool down to RT, a solvent was evaporated on a rotovap (at 60° C.) and further vacuum dried to yield La-BTA complex as a white powder (2.3 g). FTIR (ATR): 626, 716, 1424, 1511, 1622, 2320, 3099 cm−1. DSC (10° C./min)—endotherms: 91.1, 149.9° C.; exotherms: 285.7, 328.5° C.
Ni Catalyst.
Powder of Ni-BTA (250 mg) was grinded in an agate mortar and pressed into a pellet, by using 13 mm die (suitable for preparation of pellets for FTIR) and 100 kN hydraulic press. The pellet obtained was placed into a stainless-steel autoclave and heated in a furnace at 300° C. for 1 h. After combustion, the catalyst powder was collected, placed into a quartz tube (with diameter 2.54 cm) in a tube oven, and oxidized at 400° C. for 4 h at 100 sccm flow of Ar and O2 gas mixture. Subsequently, the oxidized catalyst powder was reduced at 800° C. for 1 h at 25 sccm flow of Ar and H2 gas mixture.
Ni/LaOCl Catalyst.
Powders of Ni-BTA and ammonium perchlorate (171.0 mg), and La-BTA (85.5 mg) were mixed and grinded together in an agate mortar to obtain a homogeneous solid. This solid was grinded in an agate mortar and pressed into a pellet, by using 13 mm die and 100 kN hydraulic press. The obtained pellet was placed into a stainless-steel autoclave and heated in a furnace at 300° C. for 1 h. After combustion, the catalyst powder (45.7 mg, 18% yield) was collected, placed into a quartz tube in a tube oven, and oxidized at 400° C. for 4 h at 100 sccm flow of Ar and O2 gas mixture, to produce oxidized Ni/LaOCl catalyst (29.5 mg, 11.5% yield). Subsequently, the oxidized catalyst powder was reduced at 800° C. for 1 h at 25 sccm flow of Ar and H2 gas mixture.
Ni/LaO2CO3 Catalyst.
Powders of Ni-BTA and ammonium nitrate (171.0 mg), and La-BTA (85.5 mg) were mixed and grinded together in an agate mortar to obtain a homogeneous solid. This solid was grinded in an agate mortar and pressed into a pellet, by using 13 mm die and 100 kN hydraulic press. The obtained pellet was placed into a stainless-steel autoclave and heated in a furnace at 300° C. for 1 h. After combustion, the catalyst powder (45.7 mg, 18% yield) was collected, placed into a quartz tube in a tube oven, and oxidized at 400° C. for 4 h at 100 sccm flow of Ar and O2 gas mixture, to produce oxidized Ni/LaO2CO3 catalyst (29.5 mg, 11.5% yield). Subsequently, the oxidized catalyst powder was reduced at 800° C. for 1 h at 25 sccm flow of Ar and H2 gas mixture.
Characterization Techniques.
The BTA ligand and metal-BTA complexes were characterized by FTIR spectroscopy and DSC, powder XRD and single-crystal X-ray diffraction. The Ni and Ni/LaO2CO3 catalysts were characterized by electron microscopy, powder XRD, XPS, TPR and TPO. The DSC data was recorded by Netzsch Simultaneous Thermal Analyzer (STA) 449 F5 Jupiter. FTIR spectra were taken using Bruker Tensor 27 spectrometer, equipped with an ATR unit and recorded using Opus software. Electron micrographs were taken using field-emission gun Environmental scanning electron microscope (Quanta 200 FEG ESEM) and field-emission gun transmission electron microscope (Tecnai, Philips) operated at 200 kV. XRD pattern was recorded on Scintag-powder diffractometer equipped with liquid nitrogen cooled germanium solid state detector with Cu Kα radiation. XPS analysis of the catalyst was performed on 5600 AES/XPS system (PHI, USA) using Al Kα (hν=1486.6 eV) as the excitation source. A shift of −1.05 and 0.4 eV in Ni3p XPS spectra of Ni and Ni/LaOCl catalysts respectively were considered during analysis. The TPR and TPO were recorded by a PulsarBET gas analyzer (Quantachrome) instrument. Further, the catalysts prepared were placed at the center of a quartz tube (11 mm or 50 mm ID) on either a quartz wool or a cordierite support. Before testing the catalytic activity, the catalysts were reduced at 800° C. for 1 h at 25 sccm of Ar and H2 gas flows. The dry reforming performance of the catalysts was tested under different GHSV viz. 18.5, 30, 50, 100, 150 and 450 L/(g·h). The catalytic reaction was initiated by feeding a mixture of CH4 and CO2 with a molar ratio of unity over the catalyst. The mixed reforming activity was measured using the same procedure as described above, except with the additional feed of H2O with a molar ratio between 0.1 and 0.5 compared to the inlet CO2 flow. The conversion of methane and carbon dioxide into carbon monoxide and hydrogen was monitored using an SRI gas chromatograph fitted with MS-13X and Haysep-C packed columns. Hydrogen was detected using a nitrogen carrier and TCD detector. CO2, CO and CH4 were detected by a FID detector with a methanizer placed directly upstream.
Characterization of Ni and Ni/LaO2CO3 and LaOCl Catalysts
Combustion synthesis was used to prepare the Ni and Ni/LaOCl catalysts.
The morphology of the Ni/LaOCl catalyst was seen in both SEM and TEM.
The chemical changes of Ni in both the Ni and Ni/LaOCl catalysts were analyzed by XPS (data not shown). Compared to that of the Ni catalyst, the XPS of the Ni/LaOCl catalyst not only exhibits a relatively low intensity O1s and Ni peaks, but also exhibits additional peaks corresponding to La phase, which confirms the interactions of Ni with La phase. The spectra do not exhibit any carbon peak which implies that the oxidation process completely removes the carbon accumulation of the catalyst. According to standard energy positions, the peaks of Ni2p and La3d overlap strongly and it is thus not possible to analyze the Ni2p peak in both of the catalysts (Liang and Xiaofang, 2011). Therefore, we use Ni3p core levels to see the chemical changes of Ni in both of the catalysts (
Temperature Programmed Reduction and Oxidation of Ni/La LaO2CO3 Catalyst
The catalytic activity and stability of the catalysts were carried out at 800° C. as a thought of avoiding carbon formation from Boudouard reaction (Eq. 3) and the RWGS reaction (Eq. 4) which causes a decrease in H2/CO ratio (Fan et al., 2009). The DRM activity was tested at different GHSVs (18.5 L/g-h to 450 L/g-h).
To encounter the problem of sintering with the Ni catalyst, we have synthesized Ni/LaOCl catalyst. At lower GHSV (18.5 L/g-h), the Ni/LaOCl catalyst exhibits a high CH4 and CO2 conversion rates of ˜90% and ˜100%, respectively, and is stable for more than 60 h of time. To check the catalytic performance capability of the Ni/La LaO2CO3 catalyst, we have increased the GHSVs from 18.5 to 450 L/g-h (closed symbols). The Ni/LaOCl catalyst shows >80% conversion rates of both CH4 and CO2 up to 150 L/g-h GHSV. However, the CH4 conversion rate decreased to 40% at very high GHSV of 450 L/g-h. In contrast, the CO2 conversion rate reached beyond 100% at the highest GHSV. Also, the observed H2/CO ratio at GHSVs 18.5 and 450 L/g-h were much lower than that of the remaining GHSVs. A similar effect in the opposite direction can be observed for CO2 conversion rates at different GHSVs. The observed low H2/CO ratio and the high CO2 conversion rates at 18.5 and 450 L/g-h GHSVs are the adverse effects of RWGS reaction in which most of the CO2 and produced H2 were utilized to form CO and water (Múnera et al., 2007; Tsipouriari and Verykios, 2001). Although the catalytic activity is performed at 800° C., the RWGS effects can be still observed. Depending upon the standard free energies, Wang et al. (1996) concluded that the RWGS and Boudouard reactions will not take place at temperatures above 820° C. On the other hand, the stability of the Ni/LaOCl catalyst over 100 h of catalytic activity can be explained on the basis of the La support. The effect of La support on the catalytic activity of Ni-based catalysts has been elevated in various reports (Singh et al., 2016; Li et al., 2017; Oemar et al., 2016; Ma et al., 2016). For example, Sierra Gallego et al. (2008) proposed that during DRM process of Ni/La2O3, the exposed CO2 gas is adsorbed on La2O3 and forms La2O2CO3. Further, the excellent oxidizing characteristics of the formed oxycarbonate benefit to gasify the dissociated carbon (due to CH4 decomposition) at catalyst and produce CO and H2.
Catalytic Performance and Post-Reaction Characterization of the Ni/La2O2CO3 Catalyst
The catalytic performance of Ni/La2O2CO3 powder was also monitored during an injection of water. The purpose of this test is to validate that the catalyst continues to perform even in moist carbon dioxide is used, and additionally to validate that this catalyst is viable for use in mixed carbon dioxide and steam reforming.
Since most industrial reactors are not packed with powder catalyst as shown in
To coat, the Cordierite was activated by cleaning the support in 1M nitric acid for 2 hours and then calcinating at 550° C. for 4 h. The slurry was prepared by adding 3 wt % of catalyst into deionized water and sonicating for 30 min. An additional 3 wt % of alumina nanoparticles was added to the slurry and the entire mixture was re-sonicated. To this slurry, 0.6 wt % of hydroxyl propyl cellulose and 0.3 wt % of polyethylene glycol and 0.3 wt % of polyvinyl alcohol was added. This mixture was stirred for 2 hours. To form a single coat, the activated Cordierite pieces were dipped in this slurry for 5 min and dried at 100° C. for 3 hours, then calcinated at 600° C. for 6 hours.
The morphological changes of Ni/La2O2CO3 catalyst after 100 hours of methane dry reforming were observed through TEM. As shown in
Combustion synthesis of energetic metal complexes was performed to prepare the new Ni/LaO2CO3 catalyst. This synthetic method produced Ni nanoparticles, which were successfully impregnated into the LaO2CO3 support, as shown by TEM along with minor NiO phase. The temperature-programmed experiments with the catalyst reveal existence of different kinds of Ni particles and their interactions with the support. The newly developed catalyst was found to be highly promising for dry reforming of methane at 800° C., while the Ni nanoparticles catalyst without support, suffered from severe sintering. The Ni/La LaO2CO3 catalyst exhibited excellent catalytic activity at GHSVs as high as 150 L/g-h, without any coking and sintering even after 100 h of activity. The better stability of the Ni—La BTA catalyst was explained on the basis of formation of Ni nanoparticles and their strong interaction with the La LaO2CO3 support.
Study 2. Synthesis and Characterization of Fe2O3/La2O2CO3
A solution of ammonium-BTA (3.03 g, 16.2 mmol) and iron nitrate in water (50 mL) was refluxed for 12 h under vigorous stirring. After that time, the reaction mixture was allowed to cool down to room temperature, a solvent was evaporated on a rotovap (at 60° C.) and further vacuum dried to yield Fe-BTA complex as a black powder. Fe-BTA powder was mixed with La-BTA and ammonium nitrate and compressed into a pellet in a similar manner to the pellet used to produce Ni/La2O2CO3. The pellet was ignited under air at 350° C. to result in Fe2O3/La2O2CO3 catalyst.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IL2018/050655 | 6/14/2018 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62519996 | Jun 2017 | US |
