Spinel compositions and applications thereof

Abstract

Spinels having a general formula of AB2O4, where A and B are a transition metal but not the same transition metal are disclosed. Spinel and spinel compositions of the application are useful in various applications and methods as further described.

Description

BACKGROUND

The present disclosure relates to spinel compositions and in particular, spinel catalysts. Spinel compositions as disclosed herein can be used for various applications, such as a catalyst to clean emissions, an oxygen storage material, petrochemical catalyst, etc.

SUMMARY

Spinels and spinel compositions are disclosed herein. In particular, a spinel has a general formula of AB₂O₄, where A and B are a transition metal but not the same transition metal. A spinel as disclosed herein can be rare-earth metal free. In an illustrative embodiment, a spinel can include a minor component. In an embodiment, a spinel includes a minor component that is a dopant. A spinel composition can include a spinel as disclosed herein on a substrate.

Spinel and spinel compositions have useful applications in catalysts, oxygen support materials, and batteries. Catalysts comprising a spinel have useful applications in converting exhaust from a combustion engine into useful gases or non-toxic gases. Spinels can also be incorporated into or coated on polymers. Battery anodes and/or cathodes can include a spinel in an active ingredient.

DETAILED DESCRIPTION

Spinel Compositions

Spinel compositions have a variety of applications, including but not limited to catalysts, oxygen support material, anodes and cathodes, gas sensors, etc. Spinels are a mineral oxide having the general formula of AB₂O₄ and may be supported on a plurality of support oxides. Thereby the A component is tetrahedrally coordinated with the oxygens and the B component is octahedrally coordinated with the oxygens. Spinels may include a transition metal (e.g., iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), etc.) and an “other metal” (i.e., aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), or indium (In)).

In an illustrative embodiment, a spinel composition includes copper, nickel, cobalt, iron, manganese, or chromium at any concentration, including quaternary, ternary, and binary combinations thereof. Ternary combinations include Cu—Mn—Fe, Cu—Mn—Co, Cu—Fe—Ni, Cu—Co—Fe, Cu—Mn—Ni, Cu—Mn—Co, and Cu—Co—Ni. Binary combinations include Cu—Mn, Cu—Fe, Cu—Co, Cu—Ni, Cu—Ni, Mn—Fe, Mn—Co, Mn—Ni, Co—Ni, and Co—Fe.

In another embodiment, a spinel composition can be rare-earth metal free. In an embodiment, a spinel composition can also be substantially rare-earth metal free (i.e., trace amounts). In an embodiment, a rare-earth metal free spinel can include copper, nickel, cobalt, iron, manganese, or chromium at any concentration, including quaternary, ternary, and binary combinations thereof. In a further embodiment, a spinel composition as disclosed herein can also include dopants or minor components.

In an illustrative embodiment, the spinel can also include a dopant. A dopant is present in low levels and sits on the A or B site of the spinel. Thus, a doped spinel would have a formula of AB_2-xD_xO₄ or A_1-xD_xB₂O₄, where D is the dopant. In an embodiment, a dopant can be vanadium, silver, palladium, ruthenium, rhodium, platinum, molybdenum, tin, calcium (Ca), strontium (Sr), barium (Ba), lithium (Li), titanium, lanthanum (La), samarium (Sm), gadolinium (Gd), yttrium (Y), neodymium (Nd), cerium (Ce), aluminum, gallium, magnesium, zirconium (Zr), and tungsten (W). In an example, a spinel composition comprising CuFe₂O₄ can be doped by aluminum to form CuFe_2-xAl_xO₄.

A spinel made with any transition metal and either a low valence or a high valence dopant. A low valence dopant is a dopant whose oxidation state is lower than the expected oxidation state of transition metal. A high valence dopant is one which has an oxidation state that is higher than the expected oxidation state of the transition metal. In an embodiment, a spinel composition can be built from the group consisting of copper, nickel, cobalt, iron, manganese, chromium, and combinations thereof with deliberate doping of aliovalant cations (cations with valence different from the host). Aliovalant cations can be lower or higher than the host cation. For example, CuFe₂O₄ includes Cu²⁺ and Fe³⁺. This spinel can be doped with Nb⁵⁺ to form CuFe_2-xNb_xO₄—with the pentavalent Nb⁵⁺ doping the trivalent Fe³⁺ site. Another example is Ca²⁺ doping a Fe³⁺ site (i.e., a lower valence dopant).

Supports

A substrate may be, without ion, a refractive material, a ceramic substrate, a honeycomb structure, a metallic substrate, a ceramic foam, a metallic foam, a reticulated foam, or suitable combinations, where the substrate has a plurality of channels and at least the required porosity. Porosity is substrate dependent as is known in the art. Additionally, the number of channels may vary depending upon the substrate used as is known in the art. Preferably, substrates, either metallic or ceramic, offer a three-dimensional support structure.

A spinel as described herein can be deposited on a substrate with a separate platinum group metal (PGM) component. For example, a PGM can be one or more of platinum, palladium, rhodium, etc. and can be mixed with a spinel to produce a coated substrate. In an embodiment, a single layer catalyst with two phases is inter-mixed. In an embodiment, the spinel is combined with a PGM component, on its own or supported on a conventional carrier like alumina, titania, zirconia, ceria, cerium-based OSM, tin oxide, zeolite etc. In a double layer catalyst, a spinel layer can be distinct from a PGM containing layer. In another double layer embodiment, a first PGM is combined with a spinel in a first layer, and a second PGM is combined with a spinel in a second layer. In another embodiment, a PGM component can be impregnated or coated onto a surface of a spinel composition. In yet another embodiment, a substrate may be zone-coated with a spinel in one region and with a PGM component in a different region. In another embodiment, a substrate may be zone-coated with a PGM on a spinel composition in one region of the substrate and with a spinel without PGM in a different region.

A substrate can be of any suitable material, e.g., cordierite.

In an illustrative embodiment, a spinel composition as described herein can be deposited on a substrate with a separate zero platinum group metal (ZPGM) component. A carrier material oxide may include TiO₂, doped TiO₂, Ti_1-xNb_xO₂, SiO₂, Alumina and doped alumina, ZrO₂ and doped ZrO₂, Nb₂O₅—ZrO₂, Nb₂O₅—ZrO₂—CeO₂ and combinations thereof.

A spinel can be supported or mixed with any individual or combination of refractory oxides (e.g., transition alumina, alpha alumina, titania, zeolite, silica, silicate, magnesium-silicate, silica-alumina, ceria, ceria-zirconia, lanthanide-doped ceria-zirconia, lanthanum doped alumina, etc.). A support oxide can be a mixed metal oxide such as a Ceria-Zirconia type material; a Sn—Ti—Zr oxide; an A₂B₂O₇ pyrochlore; an ABO₃ perovskite; an AB₂O₅ pseudo-brookite; a non-transition metal spinel such as MgAl₂O₄; etc.

A support oxide can be a composite or multi-phase material. A class of such materials (a mixture but not physical mixed, e.g., two components where the phases are immediately adjacent to one another) would be alumina-zirconia, alumina-ceria-zirconia, or alumina-ceria materials. In an embodiment, a support oxide can be a 2-phase oxide comprising an alumina and a fluorite phase. Alternatively, a composite can be a three-phase material such as Al—Zr—Nb—O, where the three phases are alumina, zirconia and niobia, or Al—Zr—La—O, where the three phases are alumina, zirconia and lanthanum. Using different support oxides provides flexibility for a range of environments and “promotional effects” on the spinel catalyst phase activity. For example, cerium dioxide or doped cerium dioxide can be a physical support for a spinel but that can also promote or enhance catalytic activity through the donation or acceptance of active oxygen species to the spinel surface. In embodiments disclosed herein, spinel reactivity with support components is minimized, thereby reducing or preventing formation of deleterious second phases and damaging phase transformations in the support oxide that can lead to a significant loss of surface area.

In an embodiment, a spinel can be formed into a composite powder. The powder can be formed with at least one oxide support known in the field by traditional methods of mixing, milling, co-precipitation, incipient wetness, impregnation, etc.

In an illustrative embodiment, a co-precipitation method includes adding an appropriate amount of at least one of NaOH solution, Na₂CO₃ solution, and ammonium hydroxide (NH₄OH) solution. The pH of a carrier oxide support slurry may be adjusted to about 7 to about 9, and the slurry may be aged for a period of time of about 12 to 24 hours, while stirring. A precipitate may be formed over a slurry including at least one suitable carrier material oxide, where the slurry may include any number of additional suitable carrier material oxides, and may include one or more suitable oxygen storage materials. After precipitation, a metal oxide slurry may then undergo filtering and washing, where the resulting material may be dried and may later be calcined at any suitable temperature of about 300° C. to about 600° C., preferably about 500° C. for about 5 hours. Metal salt solutions are also suitable for use in co-precipitation reactions. Suitable metal salt solutions include, but are not limited to, copper nitrate, copper acetate, manganese nitrate, and manganese acetate.

In one embodiment, a substrate may be in the form of beads or pellets. Beads or pellets may be formed from, without limitation, alumina, silica alumina, silica, titania, mixtures thereof, or any suitable material. In another embodiment, a substrate may be, without limitation, a honeycomb substrate. A honeycomb substrate may be a ceramic honeycomb substrate or a metal honeycomb substrate. A ceramic honeycomb substrate may be formed from, for example without limitation, sillimanite, zirconia, petalite, spodumene (lithium aluminum silicate), magnesium silicates, mullite, alumina, cordierite (e.g. Mg₂A₁₄Si₅O₁₈), other alumino-silicate materials, silicon carbide, aluminum nitride, or combinations thereof. Other ceramic substrates would be apparent to one of ordinary skill in the art.

If a substrate is a metal honeycomb substrate, the metal may be, without limitation, a heat-resistant base metal alloy, particularly an alloy in which iron is a substantial or major component. A surface of the metal substrate may he oxidized at elevated temperatures above about 1000° C. to improve (he corrosion resistance of an alloy by forming an oxide layer on the surface of the alloy. This oxide layer on the surface of the alloy may also enhance the adherence of a washcoat to the surface of the monolith substrate.

In one embodiment, a substrate may be a monolithic carrier having a plurality of fine, parallel flow passages extending through the monolith. Passages can be of any suitable cross-sectional shape and/or size. Passages may be, for example without limitation, trapezoidal, rectangular, square, sinusoidal, hexagonal, oval, or circular, although other shapes are also suitable. A monolith may contain from about 9 to about 1200 or more gas inlet openings or passages per square inch of cross section, although fewer passages may be used.

A substrate can also be any suitable filter for particulates. Some suitable forms of substrates may include, without limitation, woven filters, particularly woven ceramic fiber filters, wire meshes, disk filters, ceramic honeycomb monoliths, ceramic or metallic foams, wall flow filters, and other suitable filters. Wall flow filters are similar to honeycomb substrates for automobile exhaust gas catalysts. Wall flow filters may differ from the honeycomb substrate that may be used to form normal automobile exhaust gas catalysts in that the channels of the wall flow filter may be alternately plugged at an inlet and an outlet so that the exhaust gas is forced to flow through the porous walls of the wall flow filter while traveling from the inlet to the outlet of the wall flow filler.

Washcoats

According to an embodiment, at least a portion of a catalyst may be placed on a substrate in the form of a washcoat. Oxide solids in a washcoat may be one or more carrier material oxide, one or more catalyst, or a mixture of carrier triate oxide(s) and catalyst(s). Carrier triaterial oxides are normally stable at high temperatures (>1000° C.) and under a range of reducing and oxidizing conditions. Examples of oxygen storage material include, but are not limited to a mixture of ceria and zirconia; more preferably a mix re of (1) ceria, zirconia, and lanthanum or (2) ceria, zirconia, neodymium, and praseodymium.

According to an embodiment, if a catalyst comprises at least one oxygen storage material, the catalyst may comprise about 10 to about 90 weight percent oxygen storage material, preferably about 20 to about 80 weight percent, more preferably about 40 to about 75 weight percent. The weight percent of the oxygen storage material is on the basis of the oxides. Various amounts washcoats may be coupled with a substrate, preferably an amount that covers most of, or all of, the surface area of a substrate. In an embodiment, about 80 g/L to about 250 g/L of a washcoat may be coupled with a substrate.

In an embodiment, a washcoat may be formed on a substrate by suspending oxide solids in water to form an aqueous slurry and depositing the aqueous slurry on the substrate as a washcoat. Other components may optionally be added to an aqueous slurry. Other components such as acid or base solutions or various salts or organic compounds may be added to an aqueous slurry adjust the rheology of the slurry and/or enhance binding of the washcoat to the substrate. Some examples of compounds that can be used to adjust the rheology include, but are not limited to, ammonium hydroxide, aluminum hydroxide, acetic acid, citric acid, tetraethylammonium hydroxide, other tetraalkylamnionium salts, ammonium acetate, ammonium citrate, glycerol, commercial polymers such as polyethylene glycol, polyvinyl alcohol anti other suitable polymers.

The slurry may be placed on a substrate in any suitable manner. For example, without limitation, a substrate may be dipped into the slurry, or the slurry may be sprayed on the substrate. Other methods of depositing a slurry onto a substrate known to those skilled in the art may be used in alternative embodiments. If a substrate is a monolithic carrier with parallel flow passages, a washcoat may be formed on the walls of the passages. Gas flowing through the flow passages can contact a washcoat on the walls of the passages as well as materials that are supported on the washcoat.

Spinel with a Second Phase Oxide

A spinel can be mixed with a second phase oxide. Second phase oxides include, but are not limited to, fluorites, pyrochlores, perovskites, pseudo-brookites, rock-salts, lanthanum oxide, titanium oxide, tin oxide, and silver oxide. In an embodiment, a composite multi-phase mixture as described herein can be deposited on any of conventional oxide carrier materials known in the art (e.g., alumina, silica, zeolite, Ceria-Zirconia, titania, etc.).

In an embodiment, a second phase oxide can be a fluorite such as CeO₂, ZrO₂, or solid solutions of both. In an embodiment, a second phase oxide can be Zircona, ceria-zirconia, or Ln-doped ceria-zirconia solid solutions. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be a pyrochlore. A spinel composition as disclosed herein can be mixed with a second phase pyrochlore with a formula of A₂B₂O₇, where A is La, Y, or any element known in the art to occupy the Pyrochlore A-site; and B can be a smaller cation such as Mn, Ti, Sn or any element known in the art to occupy the B site. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be a perovskite. A spinel composition as disclosed herein can be mixed with a second phase perovskite with a formula of ABO₃, where A can be any lanthanide, alkali metal, alkaline earth, and any element known in the art to occupy the Perovskite A-site; and B can be any transitional metal (e.g., Mn, Co, Cu, Fe, Pd, Pt, Rh. Cr, Ni, etc.) or any element known in the art to occupy the B site. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be a pseudo-brookite. A spinel composition as disclosed herein can be mixed with a second phase pseudo-brookite with a formula of AB₂O₅, where A can be Y, La, or any element known in the art to occupy the A-site of this composition; and B can be Mn, Ti; or any element known in the art to occupy the B site. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be a rock-salt. A spinel composition as disclosed herein can be mixed with a second phase rock-salt composition such as VO₂, NiO, MnO, and any oxide composition known in the art to form this composition. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be a rare earth sesquioxide, such as lanthanide oxide (Ln₂O₃). A spinel can be mixed a second phase of a lanthanide oxide, where Ln can be La, Y, Nd, Sm, Gd, Tb or any other lanthanide or rare-earth metal. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In another embodiment, the second phase oxide can be tin, silver, or titanium oxide. The mixed phase material of a spinel with a tin, silver, or titanium oxide can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm.

In an embodiment, a transition metal based spinel (e.g., vanadium, titanium, yttrium, iron, manganese, niobium, zirconium, molybdenum, cobalt, rhodium, etc.) is mixed (e.g., in a phase mixture) with a second or third spinel of different composition. For example, a spinel composition as disclosed herein is mixed with a second spinel phase of CuMn₂O₄+FeAL₂O₄. A mixed phase material such as these can provide improved sintering resistance of the spinel phase. Both phases can be made with crystallite sizes of about 2 nm to about 50 nm

In an embodiment, a phase mixture comprising a spinel composition and a second phase and/or second spinel on a support oxide can be made from a common solution by any technique known in the art (e.g., co-precipitation, nitrate decomposition, sol-gel, Pechini method, etc.). In an embodiment, a phase mixture of a spinel and cerium dioxide in the final material can be formed from a common solution of spinel components and cerium made from nitrates or any other method known in the art. In an embodiment, the phase mixture can be dried and calcinated. In another embodiment, a phase mixture of a spinel and zirconia can be formed from a common solution of spinel components and zirconium made from nitrates or any other method known in the art. In an embodiment, the phase mixture can be dried and calcinated to form a phase mixture of a spinel and zirconium dioxide. In yet another embodiment, a phase mixture of a spinel and alumina can be formed from a common solution of spinel components and aluminum made from nitrates or any other method known in the art. In an embodiment, the phase mixture can be dried and calcinated to form a phase mixture of a spinel and alumina.

Catalyst Systems

The spinel compositions described herein can be utilized as part of a catalyst system. A catalyst system can be used to clean emissions from a combustion engine or vehicle powered completely or in part by a combustion engine. The catalyst can be an oxidation catalyst for carbon monoxide, hydrocarbons, and nitrate oxidation. In an embodiment, the catalyst can be a three way catalyst for carbon monoxide, hydrocarbons, and nitric oxide conversion. In another embodiment, a catalyst can be on a filter for particulate matter (PM) control. In another embodiment, a catalyst can be on a filter for carbon monoxide, hydrocarbon, and nitric oxide removal from a gasoline direct injection engine.

A spinel catalyst or spinel-based catalyst coating can be placed in the close-couple position near an engine in a vehicle's emission control system. In another embodiment, a spinel catalyst or spinel-based catalyst coating can be placed as a second coated substrate downstream from a conventional PGM based catalyst (i.e., “second position”, also known as an underfloor catalyst). In an embodiment, a spinel catalyst or spinel-based catalyst can be upstream from a conventional PGM based underfloor converter

In yet another embodiment, a spinel composition can also be used as an oxygen storage material. For example, an after treatment system in a vehicle powered completely or in part by a combustion

In an embodiment, a catalyst system includes a spinel composition, a substrate, and a washcoat. In an embodiment, the catalyst system is substantially free of platinum group metals. A washcoat can include at least one oxide solid, wherein the oxide solid can be a carrier material oxide, a catalyst, or a mixture thereof. A carrier material oxide can be one or more of an oxygen storage material, aluminum oxide, doped aluminum oxide, spinel, delafossite, lyonsite, garnet, perovskite, pyrochlore, doped ceria, fluorite, zirconium oxide, doped zirconia, titanium, tin oxide, silicon dioxide, and mixtures thereof. In an embodiment, a catalyst comprises one or more selected from the group consisting of a PGM transition metal catalyst, ZPGM transition metal catalyst, a mixed metal oxide catalyst, a zeolite catalyst, and mixtures thereof. In an embodiment, an oxygen storage material comprises one or more of cerium, zirconium, lanthanum, yttirum, lanthanides, actinides, and mixtures thereof. A catalyst system may optionally comprise an overcoat comprising at least one oxide solid, wherein the overcoat oxide solid comprises one or more of a carrier material oxide, a catalyst, and mixtures thereof. In an embodiment a spinel composition can be a coating on a ceramic or metallic flow-through.

In another embodiment, catalysts to control toxic emissions can have a composite composition including transition metal nano-particles or ions dispersed and supported on a surface of a support material. Support materials may be either micro-particles with a very large specific surface area or a highly porous matrix. In an illustrative embodiment, a catalyst exhibits a high level of heat resistance and is capable of ensuring stability and reliability in long-term service. At higher temperatures at which a catalyst functions, catalytic centers become massed together or agglomerated, and thereby decreases the effective surface area to result in the gradual degradation of the catalytic functions. Catalysts as described herein can be prepared by various methods including the co-precipitation method also disclosed herein.

A specific type of catalyst is a three way catalyst (TWC). Common three way catalysts work by converting carbon monoxide, hydrocarbons, and nitrogen oxides into less harmful compounds or pollutants. A common TWC converts pollutants in vehicle emissions. A lack of sufficient oxygen may occur either when oxygen derived from nitrogen oxide reduction is unavailable, or when certain maneuvers such as hard acceleration enrich the mixture beyond the ability of the converter to supply oxygen, as the TWC catalyst deteriorates because of aging, its ability to store oxygen diminishes, and the efficiency of the catalytic converter decreases.

Further, spinel compositions as disclosed herein can be can be used as oxygen storage materials for application in vehicle (powered completely or partially by a combustion engine) after treatment catalysts. In an embodiment, a TWC comprising a spinel composition as an OSM buffers the effects of rich and lean engine-out A/F transients. Such an OSM can also comply with on-board diagnostics.

A spinel composition can also be used as a substrate honeycomb support. For example, a spinel composition is mixed with appropriate amounts of binder and other additives as appropriate (cordierite, alumina, silicon carbide, aluminum titanate, etc.) followed by extruding and calcining. A honeycomb support with a spinel oxide can be coated with catalyst coatings using platinum group metals and support oxides as is customary for DOC and TWC use. In another embodiment, a honeycomb support with a spinel oxide can be coated with zeolite based materials for SCR performance.

In an embodiment, a method includes directing exhaust from a combustion engine through or flow over a catalyst as disclosed herein. In an embodiment, the catalyst decomposes nitrogen oxide in the exhaust. In an embodiment, the catalyst decomposes nitrogen oxide in the exhaust.

Batteries

In an illustrative embodiment, a spinel composition can be an active component of an anode or cathode in batteries. Spinel compositions as disclosed herein have properties useful for batteries. For example, a spinel composition has reduction-oxidation switching properties. In another example, a spinel composition in a cathode can reduce oxygen (O₂) to oxygen anions (“oxygen reduction reaction”). In an embodiment, a method includes reducing oxygen to oxygen anions by a cathodic spinel composition.

In an embodiment of a metal-air battery or a solid oxide fuel cell, an active component for either the anode and/or the cathode can include a spinel composition as disclosed herein. A spinel composition can also be useful in lithium batteries. In an embodiment, a lithium battery can include a spinel composition as an intercalation compound. In another embodiment, a cathode of a lithium battery or a low temperature fuel cell can include an active component comprising a spinel composition.

Thermoelectric Material

Thermoelectric materials (e.g., used in power generation and refrigeration) produce a phenomena where either a temperature difference creates an electric potential or an electric potential creates a temperature difference. In some embodiments thermoelectric systems comprising thermoelectric materials can convert these temperature differentials to electricity. Conventional systems are based on highly efficient metals and alloys that need to be encapsulated to avoid contact with oxygen and are not stable at higher temperatures. Costs are also a key factor in many applications. Spinel compositions as disclosed herein can be low-cost, air-stable, high-temperature stable thermoelectrics for operation at high temperatures. Spinel compositions as disclosed herein also have desirable electronic properties (carrier electron density and mobility) and thermal conductivity that can be reduced from a variety of mechanisms to enable a high thermoelectric co-efficient.

To improve thermoelectric efficiency of thermoelectric material, nano-scale or microscopic defects are introduced to decrease thermal conductivity of a composite. Atomic level defects can be oxygen vacancies or cation defects introduced by aliovalent metal dopants in the spinel structure itself. Such aliovalent dopants in a spinel include but are not limited to niobium, cerium, praseodymium, calcium, strontium, barium, aluminum, tantalum, tungsten, and tin. Nano-scale defects can be nano-scale second phases decorated at the interface or supported by a spinel oxide. A two-phase system (i.e., spinel and a second phase) can be engineered by exceeding the solid solubility limit of a dopant metal in a spine, thereby forcing the dopant metal to form a second phase oxide on a surface of the spinel. For example, a Cu—Mn—Ce system with Ce concentrations that exceed the solid solubility limit for Ce in a Cu_xMn_3-xO₄ spinel would produce nanoscaled CeO₂ existing as about 1 to about 10 nm crystallites on a surface of a spinel crystallite. A macro-scale defect can be from about 10 to about 1000 nm and engineered through a mixed phase or multi-phase approach. However, second and third phases are not a minor constituent on a spinel but rather a major phase component (i.e., allowed to form larger crystallites and structures).

In another embodiment, a mixed-phase material can include a spinel as disclosed herein and an oxide or oxides from the Ca—Co—O system. Spinets containing cobalt and other transition metals can be synthesized to exist in conjunction with well-known thermoelectric oxide materials such as those found in a Ca—Co—O. Oxides from the modified Ca—Co—M—O system, where M is Mn, Fe, V, Cu, or Ni, system can form a spinel and Ca—Co—O phase mixture. The interfaces between the oxide containing Ca and Co and the spinel phase can lower the thermal conductivity of thermoelectric material because of phonon scattering at the phase boundaries. In yet another embodiment, a mixed-phase material comprises a spinel a second phase thermoelectric material of ZnO and/or doped ZnO.

Reforming Reactions

Spinel compositions as disclosed herein can generate H₂ using CO (water-gas shift reaction or “WGSR”) or hydrocarbons (steam reforming) at high space velocity over a range of temperatures.

Water-gas shift is when CO and steam react with a catalyst to produce a high amount of hydrogen and CO₂. The hydrogen can be captured and used for a range of downstream industrial processes (e.g., synthesis of ammonia), including use in fuel cells. Catalysts for a water-gas shift reactions can comprise a spinel or spinel composition as disclosed herein. In an embodiment, a process of producing a water-gas shift reaction includes catalyzing the reaction with a catalyst comprising a spinel as disclosed herein and capturing produced hydrogen.

Steam reforming is a well-known method of producing hydrogen, carbon monoxide, and other gases from hydrocarbon fuels. A method includes reacting steam with a hydrocarbon in a reforming catalyst (i.e., site of the reaction). In an illustrative embodiment, a reforming catalyst comprises a spinel. In an embodiment, a spinel composition as disclosed herein can be used in steam reforming where the hydrocarbon input is methane, natural gas, methanol, ethanol, etc. In an embodiment, steam reforming is performed at temperatures at about 700° C. to about 1100° C. In an embodiment, the reforming catalyst is a metal-based catalyst (e.g., nickel) comprising a spinel as disclosed herein. In an example, methane reacts with steam to produce carbon monoxide and hydrogen.CH₄+H₂OCO+3H₂ Such steam reforming can be performed in a combustion engine or a fuel cell. A steam reforming can also convert non-methane hydrocarbons to hydrogen. For example, a general formula is the following:C_nH_m+nH₂O(n+m/2)H₂+nCO.In an embodiment, a steam reforming process includes converting a hydrocarbon to hydrogen catalyzed by a catalyst comprising a spinel as disclosed herein and capturing produced hydrogen.Polymers

In an embodiment, a spinel or a spinel composition can be mixed or blended with a polymeric formulation to produce a polymeric material. In an embodiment, a polymer can be a polyolefin. In an embodiment, a polymer can be a polypropylene or a polyethylene. In an embodiment, a polyethylene can be low density polyethylene, linear low density polyethylene, high density polyethylene, or mixtures thereof. In an embodiment, a polymer can be ethylene-vinyl acetate copolymers, ethylene-ethylacrylate copolymers, ethylene-acrylic acid copolymers, polymethylmethacrylate mixtures of at least two of the foregoing and the like. In an embodiment, a spinel can be added to a polymeric formulation, whereby the polymeric formulation is then extruded to form a polymeric material. In another embodiment, a spinel or spinel formulation can be deposited on a polymer (e.g., a film layer).

Definitions

The term “calcination” refers to a thermal treatment process applied to solid materials, in presence of air, to bring about a thermal decomposition, phase transition, or removal of a volatile fraction at temperatures below the melting point of the solid materials.

The term “carrier material oxide (CMO)” refers to support materials used for providing a surface for at least one catalyst.

The term “conversion” refers to the chemical alteration of at least one material into one or more other materials.

The term “co-precipitation” may refer to the carrying down by a precipitate of substances normally soluble under the conditions employed.

The term “catalyst” refers to one or more materials that may be of use in the conversion of one or more other materials.

The term “exhaust” refers to the discharge of gases, vapor, and fumes that may include hydrocarbons, nitrogen oxide, and/or carbon monoxide.

The term “impregnation” refers to the process of imbuing or saturating a solid layer with a liquid compound or the diffusion of some element through a medium or substance.

The term “lean condition” refers to exhaust gas condition with an R-value below 1.

The term “milling” refers to the operation of breaking a solid material into a desired grain or particle size.

The term “minor component” refers generally to a spinel structure having a presence of one or more elements selected from the group consisting of copper, nickel, cobalt, iron, manganese, chromium, and combinations thereof. The minor component can be in-phase (doping a crystallographic site) or second-phase (metal not doping the crystallographic sites of the spinel). Thereby a dopant case is a subset case of a minor component. For example, a minor component can be barium in a CuFe₂O₄ spinel and the structure can be determined in how the minor component is introduced to the spinel. For example, CuFe₂O₄ and BaO can be dissolved in a common solution, dried, and calcined to produce the oxide. The Ba will not dope the spinel site but will exist as a second-phase component. Alternatively, when Cu, Fe and Al are formed into a solution precursor, dried, and calcined to form the oxide phase, the Al dopes the Fe site producing a single phase CuFe_2-xAl_xO₄.

The term “overcoat” refers to at least one coating that may be deposited on at least one washcoat layer.

The term “oxidation catalyst” refers to a catalyst suitable for use in converting at least hydrocarbons and carbon monoxide.

The term “oxygen storage material (OSM)” refers to a material able to take up oxygen from oxygen rich streams and able to release oxygen to oxygen deficient streams

The term “platinum group metal (PGM)” refers to platinum, palladium, ruthenium, iridium, osmium, and rhodium.

The term “R Value” refers to the number obtained by dividing the reducing potential by the oxidizing potential.

The term “rich condition” refers to exhaust gas condition with an R-value above 1.

The term “second phase” refers to additional and different compositions from any spinel. A second phase can describe a plurality of phases distinct from a spinel composition.

The term “spinel composition” refers to a combination of components that include a spinel that compose a substance. For example, a spinel composition can be spinel and a substrate.

The term “spinel structure” refers to the spinel molecule.

The term “substrate” refers to any material of any shape or configuration that yields a sufficient surface area for depositing a washcoat and/or overcoat.

The term “three-way catalyst (TWC)” refers to a catalyst that may achieve three simultaneous tasks: reduce nitrogen oxides to nitrogen and oxygen, oxidize carbon monoxide to carbon dioxide, and oxidize unburnt hydrocarbons to carbon dioxide and water.

The terms “treating,” “treated,” or “treatment” refer to drying, firing, heating, evaporating, calcining, or mixtures thereof.

The term “washcoat” refers to at least one coating including at least one oxide solid that may be deposited on a substrate.

The term “zero platinum group metal (ZPGM) catalyst” refers to a catalyst completely or substantially free of platinum group metals.

Claims

1. A catalyst comprising a spinel having the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal, and wherein A is selected from the group consisting of manganese (Mn), nickel (Ni), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and B is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi).

2. The catalyst of claim 1, wherein the transition metal is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), etc.) and an “other metal” (i.e., aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and indium (In).

3. The catalyst of claim 1, wherein the spinel is rare-earth metal free.

4. The catalyst of claim 1, wherein the spinel further comprises a dopant.

5. The catalyst of claim 4, wherein the spinel has a general formula of Ai-xDxB2O4, where D is the dopant.

6. The catalyst of claim 4, wherein the dopant is selected from the group consisting of vanadium, silver, palladium, ruthenium, rhodium, platinum, molybdenum, tin, calcium (Ca), strontium (Sr), barium (Ba), lithium (Li), titanium, lanthanum (La), samarium (Sm), gadolinium (Gd), yttrium (Y), neodymium (Nd), cerium (Ce), aluminum, gallium, magnesium, zirconium (Zr), and tungsten (W), and further wherein D is not the same metal as A or B.

7. The catalyst of claim 4, wherein the dopant is a low valence dopant.

8. The catalyst of claim 4, wherein the dopant is a high valence dopant.

9. The catalyst of claim 1, wherein the spinel is deposited on a substrate.

10. The catalyst of claim 9, wherein the substrate is a support oxide.

11. The catalyst of claim 10, wherein the support oxide is transition alumina, alpha alumina, titania, zeolite, silica, silicate, magnesium-silicate, silica-alumina, ceria, ceria-zirconia, lanthanide-doped ceria-zirconia, lanthanum doped alumina, and mixed metal oxide.

12. The catalyst of claim 11, wherein the mixed metal oxide is selected from the group consisting of fluorite, pyrochlore, perovskite, pseudo-brookite, lanthanide oxide, titanium oxide, silver oxide, and tin oxide.

13. The catalyst of claim 4, wherein the dopant is an aliovalent dopant.

14. A battery comprising an anode or cathode, wherein the anode or the cathode comprise an active ingredient comprising a spinel having the general formula of AB2O4, wherein A and B are each independently a transition metal, wherein A and B are not the same transition metal, and wherein A is selected from the group consisting of nickel (Ni), vanadium (V), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi) and indium (In), and B is selected from the group consisting of iron (Fe), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Ti), lead (Pb), bismuth (Bi), and indium (In).

15. A method of cleaning emissions from a combustion engine comprising directing exhaust from a combustion engine through or flow over a catalyst comprising a spinel having the general formula of AB2O4, wherein A and B are each independently a transition metal, wherein A and B are not the same transition metal, and wherein A is selected from the group consisting of manganese (Mn), nickel (Ni), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and B is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi).

16. A polymeric material comprising a polymeric formulation and a spinel having the general formula of AB2O4, wherein A and B are each independently a transition metal, wherein A and B are not the same transition metal.

17. The polymeric material of claim 16 wherein the polymeric formulation comprises a polyolefin.

18. The polymeric material of claim 16 wherein the polymeric formulation comprises at least one of a polyethylene or a polypropylene.

19. The polymeric material of claim 18, wherein the polyethylene is low density polyethylene, linear low density polyethylene, high density polyethylene, or mixtures thereof.

20. The polymeric material of claim 16 wherein the polymeric formulation comprises ethylene-vinyl acetate copolymers, ethylene-ethylacrylate copolymers, ethylene-acrylic acid copolymers, polymethylmethacrylate mixtures of at least two of the foregoing, or mixtures thereof.

21. A method of generating hydrogen comprising reacting carbon monoxide and steam with a catalyst comprising a spinel having the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal, and wherein A is selected from the group consisting of iron (Fe), manganese (Mn), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and indium (In), and B is selected from the group consisting of iron (Fe), manganese (Mn), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and indium (In).

22. The method of claim 21 further comprising capturing the hydrogen generated.

23. A method of generating hydrogen comprising reacting steam with a hydrocarbon in a reforming catalyst, wherein the reforming catalyst comprises a spinel having the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal.

24. The method of claim 23, wherein the hydrocarbon is selected from the group consisting of methane, natural gas, methanol, and ethanol.

25. The method of claim 23, wherein said reacting is performed at temperatures at about 700° C. to about 1100° C.

26. A thermoelectric composition comprising a spinel and aliovalent dopant, wherein the spinel has an oxygen vacancy or cation defect, and wherein the spinel has the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal, and wherein A is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni) cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi) and B is selected from the group consisting of iron (Fe), manganese (Mn), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi).

27. The thermoelectric composition of claim 26, wherein the aliovalent dopant is selected from the group consisting of niobium, cerium, praseodymium, calcium, strontium, barium, aluminum, tantalum, tungsten, and tin.

28. The thermoelectric composition of claim 26, wherein the dopant forms a second phase oxide on a surface of the spinel.

29. The thermoelectric composition of claim 28, wherein the spinel is CuxMn3-xCexO4.

30. A spinel composition comprising a) spinel having the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal; b) a binder; and optionally, c) an additive, and wherein A is selected from the group consisting of manganese (Mn), nickel (Ni), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and B is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi).

31. A honeycomb support comprising the spinel composition of claim 30 and a platinum group metal catalyst coating.

32. A honeycomb support comprising the spinel composition of claim 30 and an alumina based material.

33. The method of claim 15, wherein the catalyst is a second coated substrate downstream from a conventional PGM based catalyst.

34. The method of claim 15, wherein the catalyst is upstream from a conventional PGM based underfloor converter.

35. An oxygen storage material comprising a spinel having the general formula of AB2O4, wherein A and B are a transition metal, wherein A and B are not the same transition metal.

36. The oxygen storage material of claim 35, wherein the oxygen storage material comprises about 10 to about 90 wt % of a catalytic coating.

37. A catalytic converter comprising i) a spinel having the general formula of AB2O4, wherein A and B are a transition metal, and wherein A and B are not the same transition metal;ii) a platinum group metal (PGM), and wherein A is selected from the group consisting of manganese (Mn), nickel (Ni), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), bismuth (Bi), and B is selected from the group consisting of iron (Fe), manganese (Mn), nickel (Ni), cobalt (Co), copper (Cu), vanadium (V), silver (Ag), palladium (Pd), ruthenium (Ru), rhodium (Rh), platinum (Pt), molybdenum (Mo), niobium (Nb), titanium (Ti), aluminum (Al), magnesium (Mg), gallium (Ga), tin (Sn), thallium (Tl), lead (Pb), and bismuth (Bi).

38. The catalytic converter of claim 37, wherein the spinel and the PGM component or layer is deposited or coated on a substrate.

39. The catalytic converter of claim 38, wherein the substrate is cordierite.

40. The catalytic converter of claim 37, wherein the platinum group metal is selected from the group consisting of platinum, palladium, and rhodium.

41. The catalytic converter of claim 37, wherein the catalytic converter is a single layer catalyst, wherein the spinel and the PGM component are inter-mixed.

42. The catalytic converter of claim 37, wherein the PGM component is supported on a carrier.

43. The catalytic converter of claim 42, wherein the carrier is selected from the group consisting of alumina, titania, zirconia, ceria, cerium-based OSM, tin oxide, and zeolite.

44. The catalytic converter of claim 37, wherein the catalytic converter is a double layer catalyst, wherein the spinel and the PGM are in separate, distinct layers.

45. The catalytic converter of claim 37, wherein the catalytic converter is a double layer catalyst, wherein a first layer comprises a first PGM and a first spinel, and a second layer comprises a second PGM and a second spinel.

46. The catalytic converter of claim 37, wherein the PGM is impregnated onto a surface of the spinel.

47. The catalytic converter of claim 37, wherein the PGM is coated on a surface of the spinel.

48. The catalytic converter of claim 38, wherein the substrate is zone-coated with the spinel and the PGM.

49. The catalytic converter of claim 48, wherein the zone-coated substrate is coated with a spinel in a first region and coated with a PGM in a second region, wherein the first region is not coated with a PGM and the second region is not coated with a spinel.

50. The catalytic converter of claim 48, wherein the zone-coated substrate is coated with a PGM on a spinel composition in a first region and coated with a spinel without PGM in a second region.