Metal Oxide Compounds with Enhanced Reactivity

Abstract

Metal oxide ceramic compounds are described that have a high capacity for oxidation of chemical or biological entities through the generation of reactive oxygen species spontaneously without the need for light, heat, electricity, or additional chemical constituents. These materials have at least one metal ion which displays multiple valence states. Applications include the decomposition of toxic chemicals, the inactivation of pathogens, and the prevention of biofouling.

Claims

1. A material or blend of materials with an average stoichiometry Ca.sub.xMn.sub.yO.sub.z wherein x0.1, y0.1, and z1, which generates spontaneously reactive oxygen species.

2. The material or blend of materials of claim 1, blended with a material capable of a Fenton reaction.

3. The material or blend of materials of claim 1, having added thereto one or more alkali metal, alkaline earth, transition metal, lanthanide, and/or main group element(s).

4. The material or blend of materials of claim 1, wherein at least some of the oxygen is replaced by one or more halogen and/or chalcogenide atoms.

5. The material or blend of materials of claim 1, comprising a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more A-site cation(s) selected from the group consisting of strontium, barium, sodium, potassium, lanthanum, cerium, and bismuth.

6. The material or blend of materials of claim 1, comprising a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more B-site cation(s) selected from the group consisting of titanium, vanadium, iron, nickel, copper, zinc, cerium, aluminum, and antimony.

7. The material or blend of materials of claim 1, comprising a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more anion(s) selected from the group consisting of sulfur, fluorine, and chlorine.

8. The material or blend of materials of claim 1, coated on the surface of an object.

9. The material or blend of materials of claim 1, coated on the surface of a particle.

10. The material or blend of materials of claim 1, mixed with a binder and coated on a surface.

11. A method of decomposing a chemical, inactivating a pathogen, or preventing biofouling at a biofouling-susceptible locus, comprising contacting the chemical, pathogen, or biofouling-susceptible locus with the material or blend of materials of claim 1.

12. A material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z wherein Ae is one or more alkaline earth elements, Tm is one or more transition metals or lanthanides with at least one having multiple valences, and x0.1, y0.1, and z1, which generates spontaneously reactive oxygen species.

13. The material or blend of materials of claim 12, blended with a material capable of a Fenton reaction.

14. The material or blend of materials of claim 12, wherein at least some of the oxygen is replaced by one or more halogen and/or chalcogenide atoms.

15. The material or blend of materials of claim 12, coated on the surface of an object.

16. The material or blend of materials of claim 12, coated on the surface of a particle.

17. The material or blend of materials of claim 12, mixed with a binder and coated on a surface.

18. A method of decomposing a chemical, inactivating a pathogen, or preventing biofouling at a biofouling-susceptible locus, comprising contacting the chemical, pathogen, or biofouling-susceptible locus with the material or blend of materials of claim 12.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1 in (a) shows a representative powder X-ray diffraction pattern confirming the perovskite structure of a sub-stoichiometric CaMnO.sub.3- prepared by a solution-based synthesis procedure and in (b) shows a scanning electron micrograph of such sub-stoichiometric CaMnO.sub.3- in which the particle shape and size of such sub-stoichiometric CaMnO.sub.3- is observable.

[0015] FIG. 2 shows in (a) the spontaneous generation of H.sub.2O.sub.2 on CaMnO.sub.3- as detected by UV-Vis spectroscopy using leuco crystal violet as a selective trapping agent, at room temperature (25 C.), and in (b) shows the spontaneous generation of .sup.1O.sub.2 from the same material detected by fluorescence spectroscopy using singlet oxygen sensor green (SOSG) as a selective trapping agent (excitation max 480 nm, emission max 528 nm) at room temperature (25 C.).

[0016] FIG. 3 in (a) shows a graph of absorbance as a function of wavelength, in nanometers, for decomposition of acetaminophen in the presence of CaMnO.sub.3- at room temperature, as detected by UV-Vis spectroscopy, and in (b) shows a graph of absorbance as a function of wavelength, in nanometers, for decomposition of tryptophan in the presence of CaMnO.sub.3- at room temperature, as detected by UV-Vis spectroscopy.

[0017] FIG. 4 in (a) shows a powder x-ray diffraction pattern of CaMnO.sub.3- synthesized by a sol-gel procedure, in (b) shows a powder X-ray diffraction pattern of CaMnO.sub.3- synthesized by a solid-state procedure, in (c) shows a scanning electron micrograph of CaMnO.sub.3- synthesized by the sol-gel procedure, and in (d) shows a scanning electron micrograph of CaMnO.sub.3- synthesized by the solid-state procedure.

[0018] FIG. 5 in (a) shows powder x-ray diffraction patterns as a function of Ca:Mn ratio in CaMnO.sub.3-, ranging from pure perovskite to a mix of pure perovskite and Ruddlesden-Popper layered perovskite, and in (b) depicts a bar graph of H.sub.2O.sub.2 concentration, in ppm, for the calcium manganese oxide CaMnO.sub.3- compounds identified in such graph, showing the variation in spontaneous generation of hydrogen peroxide as a function of the Ca:Mn ratio, as detected using UV-Vis spectroscopy with leuco crystal violet as a selective trapping agent, and demonstrating that hydrogen peroxide production was maximized with a mixture of pure perovskite and Ruddlesden-Popper layered perovskite.

[0019] FIG. 6 in (a) thereof shows the powder X-ray diffraction patterns of CaTi.sub.0.1Mn0.9O.sub.3 (top) and Ca.sub.2Ti0.1Mn.sub.0.9O.sub.4 (bottom) synthesized by the solid-state procedure, and scanning electron micrographs are shown in (b) of FIG. 6 for such CaTi.sub.0.1Mn0.9O.sub.3 and Ca.sub.2Ti0.1Mn.sub.0.9O.sub.4 compounds.

[0020] FIG. 7 shows a representative powder X-ray diffraction pattern of CuMnO.sub.3 synthesized by a solid-state process confirming the perovskite structure.

[0021] FIG. 8 in (a) thereof shows a scanning electron micrograph of CaMnO.sub.3- blended with a polyurethane/polyurea binder and coated at 10% by weight on an aluminum foil disc, and in (b) shows an energy dispersive X-ray analysis of both calcium (red) and manganese (purple) evidencing a uniform distribution of ceramic particles across the coating.

[0022] FIG. 9 top panel shows a powder X-ray diffraction pattern of 10 micron diameter rutile TiO.sub.2 particles coated with CaMnOs by a sol-gel process. The middle and lower panels are the diffraction patterns of pure rutile TiO.sub.2 and CaMnO.sub.3, respectively.

DETAILED DESCRIPTION

[0023] The present disclosure provides metal oxide ceramic compounds that are effective to generate reactive oxygen species and provide oxidizing properties in the absence of light, heat, electricity, and/or chemical oxidants, although light, heat, electricity, and/or chemical oxidants may additionally be employed with such metal oxide ceramic compounds to augment or enhance their ROS-generating and oxidizing properties.

[0024] The present disclosure is based on the discovery that with the proper stoichiometry and structure, spontaneous generation of reactive oxygen species may be observed when Ca.sub.xMn.sub.yO.sub.z, doped Ca.sub.xMn.sub.yO.sub.z, and related compounds such as Ca.sub.xFe.sub.yO.sub.z, Cu.sub.xMn.sub.yO.sub.z, or Ce.sub.xMn.sub.yO.sub.z wherein at least one metal ion can exist in multiple oxidation states, are exposed to oxygen (air), water (humidity), and an organic moiety including toxic chemicals and biological species (bacteria, virus, fungi, algae) at room temperature (e.g., 25 C.), or other ambient temperature range such as 10 C. to 40 C.no light, heat, electricity, or chemical additives are required, although their use and/or addition is not precluded.

[0025] The present disclosure further reflects the finding that while Ca.sub.xMn.sub.yO.sub.z has only one metal ion (manganese) that can be present in a mixed valence state, adding a second metal ion with multiple valence states and/or replacing calcium with one or metals such as vanadium, chromium, iron, cerium, cobalt, nickel, and/or copper can introduce strong oxidizing properties while maintaining the capacity to spontaneously generate ROS.

[0026] Applications of the metal oxide compounds of the present disclosure include the decomposition of toxic chemicals, the inactivation of pathogens, and the prevention of biofouling.

[0027] As used herein in reference to a material or blend of materials, generates spontaneously reactive oxygen species means that the material or blend of materials spontaneously produces reactive oxygen species in the presence of (i) oxygen or oxygen-containing gas, e.g., air, (ii) water, e.g., humidity, and (iii) an organic moiety selected from among organic chemicals, e.g., acetaminophen or tryptophan, and biological species (bacteria, virus, fungi, algae), at temperature in a range of 10 C. to 40 C., and in the absence of added or inputted light, heat, electricity, or chemical additives.

[0028] As used herein, material capable of a Fenton reaction means a material that reacts with hydrogen peroxide to form hydroxyl radicals that are effective to decompose organic or other materials, e.g., chemicals, and pathogenic species.

[0029] In one aspect, the disclosure relates to a material or blend of materials with an average stoichiometry Ca.sub.xMn.sub.yO.sub.z wherein x0.1, y0.1, and z1, which generates spontaneously reactive oxygen species.

[0030] In various embodiments, such material or blend of materials may be additionally blended with a material capable of a Fenton reaction.

[0031] In other embodiments, such material or blend of materials may have added thereto one or more alkali metal, alkaline earth, transition metal, lanthanide, and/or main group element(s). Alkali metal elements useful for such purpose include lithium, sodium, potassium, rubidium, and cesium. Alkaline earth elements useful for such purpose include magnesium, strontium, and barium. Transition elements that may be employed include scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, yttrium, zirconium, niobium, molybdenum, ruthenium, rhodium, palladium, silver, cadmium, hafnium, tantalum, tungsten, rhenium, osmium, iridium, platinum, and gold. Lanthanide elements for such purpose include cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium. Main group elements that may be useful for such purpose include elements of Groups 1, 2, and 13 to 18 of the Periodic Table.

[0032] In various embodiments, the above-described material or blend of materials may be constituted, wherein at least some of the oxygen is replaced by one or more halogen and/or chalcogenide atoms. Halogen atoms suitable for such replacement include chlorine, fluorine, bromine, and iodine. Chalcogenide atoms that may be used for such replacement include sulfur, selenium, and tellurium.

[0033] In other embodiments, the material or blend of materials of the disclosure may comprise a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more A-site cation(s) selected from the group consisting of strontium, barium, sodium, potassium, lanthanum, cerium, and bismuth.

[0034] In various embodiments, the material or blend of materials of the disclosure may comprise a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more B-site cation(s) selected from the group consisting of titanium, vanadium, iron, nickel, copper, zinc, cerium, aluminum, and antimony.

[0035] In various embodiments, the material or blend of materials of the disclosure may comprise a Ca.sub.xMn.sub.yO.sub.z perovskite lattice substituted with one or more anion(s) selected from the group consisting of sulfur, fluorine, and chlorine.

[0036] In various embodiments, the material or blend of materials may variously include any one or more of the A-site substitutions and/or B-site substitutions and/or anion substitutions described in the preceding three paragraphs, with respect to substitution(s) selected from the group consisting of the specified A-site cation(s), B-site cation(s), and anion(s).

[0037] The material or blend of materials of the disclosure may be coated on the surface of an object, or coated on the surface of a particle, or mixed with a binder and coated on a surface.

[0038] In a further aspect, the disclosure relates to a method of decomposing a chemical, inactivating a pathogen, or preventing biofouling at a biofouling-susceptible locus, comprising contacting the chemical, pathogen, or biofouling-susceptible locus with the material or blend of materials of the present disclosure, as variously described above.

[0039] Another aspect of the disclosure relates to a material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z wherein Ae is one or more alkaline earth elements, Tm is one or more transition metals or lanthanides with at least one having multiple valences, and x0.1, y0.1, and z1, which generates spontaneously reactive oxygen species. The respective alkaline earth elements, transition metals, and lanthanides may include any the specific types of alkaline earth elements, transition metals, and lanthanides mentioned in the preceding description.

[0040] The material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z may be blended with a material capable of a Fenton reaction.

[0041] Such material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z may be coated on the surface of an object, or on the surface of a particle, or may be mixed with a binder and coated on a surface, in various respective embodiments.

[0042] In particular embodiments, the material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z may have added thereto one or more alkali metal, alkaline earth, transition metal, lanthanide, and/or main group element(s). Specific alkali metal, alkaline earth, transition metal, lanthanide, and/or main group element(s) include those previously described herein.

[0043] In various embodiments, the material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z may be constituted, wherein at least some of the oxygen is replaced by one or more halogen and/or chalcogenide atoms. Suitable halogen and/or chalcogenide species for such purpose include the halogens and chalcogenides previously discussed herein.

[0044] The material or blend of materials with an average stoichiometry Ae.sub.xTm.sub.yO.sub.z may be employed in a method of decomposing a chemical, inactivating a pathogen, or preventing biofouling at a biofouling-susceptible locus, in which the chemical, pathogen, or biofouling-susceptible locus is contacted with such material or blend of materials.

[0045] The features and advantages of the present disclosure are more fully shown by the following non-limiting Examples, as illustrative of specific implementations of the disclosure in corresponding embodiments thereof.

EXAMPLE 1

[0046] Sub-stoichiometric CaMnO.sub.3- was synthesized by a co-precipitation process. Ca(NO.sub.3).sub.2.Math.4H.sub.2O and Mn(NO.sub.3).sub.2.Math.4H.sub.2O were dissolved in distilled water in a 1:1 ratio and stirred for 20 minutes. A 0.5M solution of (NH.sub.4).sub.2CO.sub.3 was added in 3:1 excess and the resulting precipitate was filtered and double washed with warm distilled water, then dried for 18 hours at 80 C., ground in a mortar and pestle, and calcined from 2 10 12 hours at temperatures between 400 and 900 C.

[0047] Mixed manganese valence states are critical for ROS generation. Stoichiometric CaMnO.sub.3 has an average Mn oxidation state of +4 (which does not imply that all manganese ions are in that state). Under the above-described synthesis conditions, the resulting calcium manganese oxide is deficient in oxygen resulting in an average Mn oxidation state of +3.8.

[0048] FIG. 1 in (a) shows a representative powder X-ray diffraction pattern confirming the perovskite structure and in (b) shows a scanning electron micrograph of the sub-stoichiometric CaMnO.sub.3- from the foregoing solution-based synthesis procedure, in which the particle shape and size of such sub-stoichiometric CaMnO.sub.3- is observable.

[0049] The sub-stoichiometric CaMnO.sub.3- was tested to determine its capability for spontaneous generation of H.sub.2O.sub.2 using UV-Vis spectroscopy with leuco crystal violet as a selective trapping agent, at room temperature (25 C.), with the result shown in graph (a) in FIG. 2, of absorbance as a function of wavelength, in nanometers, at time intervals of 30 minutes, 60 minutes, 90 minutes, and 120 minutes.

[0050] The sub-stoichiometric CaMnO.sub.3- was also tested to determine its capability for spontaneous generation of .sup.1O.sub.2 at room temperature (25 C.), by fluorescence spectroscopy using singlet oxygen sensor green (SOSG) as a selective trapping agent (excitation max 480 nm, emission max 528 nm). The results are shown in graph (b) of FIG. 2, in which fluorescence intensity (counts per second, CPS) is plotted as a function of wavelength, in nanometers, at time zero (0 hours) and at 7 hours.

[0051] The data shown in FIG. 2 in (a) thereof thus demonstrate the spontaneous generation of H.sub.2O.sub.2 on the sub-stoichiometric CaMnO.sub.3-. It is noted that a Fenton catalyst (a catalyst that converts H.sub.2O.sub.2 to 2 OH.Math., such as for example Fe.sub.2O.sub.3) may be blended with the sub-stoichiometric CaMnO.sub.3-, to convert some or all of the generated hydrogen peroxide to the more reactive OH.Math..

[0052] The data shown in FIG. 2 in (b) thereof demonstrate the spontaneous generation of .sup.1O.sub.2 from the sub-stoichiometric CaMnO.sub.3-. .sup.1O.sub.2 may be a primary product of the reaction of the sub-stoichiometric CaMnO.sub.3- with oxygen, water, and organic species or may be a decomposition product of the hydrogen peroxide that is generated. It is noted that CaMnO.sub.3- readily reacts with H.sub.2O.sub.2 at room temperature to generate oxygen bubbles.

[0053] Testing was also conducted using the sub-stoichiometric CaMnO.sub.3- to determine its capability to effect decomposition of acetaminophen, a representative pharmaceutical residue found in wastewater, at room temperature (25 C.). 2.5 g of CaMnO.sub.3- was added to 50 ml of a 10 mg/L solution of acetaminophen. UV-Vis spectroscopy spectra were recorded at time zero (0 hours) and after stirring for 4 hours, evidencing decomposition of acetaminophen, as shown in the spectral data graph (a) in FIG. 3, of absorbance as a function of wavelength in nanometers, for the acetaminophen solution (10 mg/liter) without the sub-stoichiometric CaMnO.sub.3-, and for the acetaminophen solution containing the sub-stoichiometric CaMnO.sub.3-.

[0054] The sub-stoichiometric CaMnO.sub.3- was also tested to determine its capability for decomposing tryptophan, a prototypical amino acid, at room temperature (25 C.). 2.5 grams of CaMnO.sub.3- was added to 50 ml of a 10 mg/L solution of tryptophan. UV-Vis spectroscopy spectra were recorded at time zero (0 hours) and after stirring for 4 hours, evidencing decomposition of tryptophan, as shown in the spectral data graph (b) in FIG. 3, of absorbance as a function of wavelength in nanometers, for the tryptophan solution (10 mg/liter) without the sub-stoichiometric CaMnO.sub.3-, and for the tryptophan solution containing the sub-stoichiometric CaMnO.sub.3-.

[0055] The results shown in FIG. 3 confirmed the capability of the sub-stoichiometric CaMnO.sub.3- to decompose acetaminophen and to decompose tryptophan.

EXAMPLE 2

[0056] Particle size, particle size distribution, and particle shape may be controlled by the synthesis procedure. For sol-gel synthesis, stoichiometric amounts of Ca (NO.sub.3).sub.2.Math.4H.sub.2O and Mn (NO.sub.3).sub.2.Math.4H.sub.2O were dissolved in distilled water, and citric acid was added as a ligand, in 2:1 mole ratio to the metal ions. The solution was heated in an oil bath at 90 C. for 4 hours to evaporate the solvent and promote polymerization until a spongy orange solid was formed. The resulting mass was dried at 180 C. for 20 hours, ground in a mortar and pestle, and then calcined at 600 C. for 4 hours, yielding the sub-stoichiometric CaMnO.sub.3- product. For the solid-state synthesis, stoichiometric amounts of CaCO.sub.3 and MnCO.sub.3 were mixed for 1 hour in a mortar and pestle and then calcined at 1200 C. for 12 hours, yielding the sub-stoichiometric CaMnO.sub.3- product.

[0057] FIG. 4 shows powder X-ray diffraction patterns of (a) the sub-stoichiometric CaMnO.sub.3- product synthesized by the sol gel synthesis procedure, and (b) the sub-stoichiometric CaMnO.sub.3- product synthesized by the solid-state synthesis procedure, as well as scanning electron micrographs of (c) the sub-stoichiometric CaMnO.sub.3- product synthesized by the sol gel synthesis procedure, and (d) the sub-stoichiometric CaMnO.sub.3- product synthesized by the solid-state synthesis procedure. The scanning electron micrographs show that the particle size for the sub-stoichiometric CaMnO.sub.3- product synthesized by the solid-state procedure is larger than that of the sub-stoichiometric CaMnO.sub.3- product synthesized by the sol-gel process.

EXAMPLE 3

[0058] Since the oxidation state of calcium and oxygen are fixed at +2 and 2, respectively, if x, y, and z are known in Ca.sub.xMn.sub.yO.sub.z, then the average oxidation state of manganese is equal to (2*z2*x)/y. The ratio of x to y may be varied by adjusting the Ca to Mn ratio in the starting materials, as shown in Table 1 below.

[0059] The oxygen stoichiometry (z) may be controlled by adding or removing oxygen during the calcining process or by post treatment (for example, by controlled heating (Inorg. Chem. 53 (2014) 9106)). This too changes the average oxidation state of manganese, as shown in Table 1 below.

TABLE-US-00001 TABLE 1 Control of theoretical average manganese oxidation state in CaMnO.sub.3 via stoichiometry. Left table: impact of changes in calcium:manganese atomic ratio. Right table: impact of changes in oxygen stoichiometry. Ca.sub.xMnO.sub.3 CaMnO.sub.z Ca Stoichiometry Theoretical Mn O Stoichiometry Theoretical Mn (x) Oxidation State (z) Oxidation State 0.9 4.2 2.4 2.8 1.0 4.0 2.6 3.2 1.1 3.8 2.8 3.6 1.2 3.6 3.0 4.0 1.3 3.4 3.2 4.4

[0060] Ca.sub.xMn.sub.yO.sub.z with ratios of Ca:Mn of 1:1.4, 1:1.2, 1:1, 1:0.8, 1:0.6, and 1:0.5 were synthesized by a hybrid solution-solid state procedure. Stoichiometric amounts of Ca(C.sub.2H.sub.3O.sub.2).sub.2.Math.H.sub.2O and Mn(C.sub.2H.sub.3O.sub.2).sub.2.Math.4H.sub.2O were dissolved in distilled water and stirred for 20 minutes, then the mixed solution was evaporated in a drying oven at 80 C. overnight. The resulting mix of salts was ground in a mortar and pestle and heated at 400 C. for 2 hours to decompose the acetate ligands, followed by calcination at 1000 C. for 2 hours.

[0061] The respective Ca.sub.xMn.sub.yO.sub.z products were assessed by powder X-ray diffraction, with the resulting powder X-ray diffraction patterns (intensity (CPS) as a function of 2 theta (degrees)) shown in (a) of FIG. 5. The powder x-ray diffraction patterns shown in (a) of FIG. 5 varied as a function of the Ca:Mn ratio from pure perovskite to a mix of pure perovskite and Ruddlesden-Popper layered perovskite. The Ruddlesden-Popper phase consists of two-dimensional perovskite-like layers interleaved with calcium cations and shows high structural flexibility in accommodating oxygen vacancies/oxygen non-stoichiometry. X-ray diffraction patterns of the two individual materials, calcium manganese oxide and dicalcium manganate, are shown at the bottom of (a) in FIG. 5 for reference.

[0062] FIG. 5 in (b) thereof is a bar graph of H.sub.2O.sub.2 concentration, in ppm, for the calcium manganese oxide compounds identified in such graph, showing the variation in spontaneous generation of hydrogen peroxide as a function of the Ca:Mn ratio, for H.sub.2O.sub.2 production detected using UV-Vis spectroscopy with leuco crystal violet as a selective trapping agent. Hydrogen peroxide production was maximized with a mixture of pure perovskite and Ruddlesden-Popper layered perovskite. As noted in Example 1, a Fenton catalyst such as Fe.sub.2O.sub.3 may be blended with Ca.sub.xMn.sub.yO.sub.z to convert some or all the hydrogen peroxide to the more reactive OH.Math..

EXAMPLE 4

[0063] While mixed valence states in manganese are central to the spontaneous generation of ROS, other factors are also important. This includes oxygen vacancies, which both alter the surface chemistry and control the diffusion rate of oxygen in the lattice, and electrical conductivity which allows electrons and holes to rapidly move both within the crystal lattice as well as on the surface. Calcium (or other A site constituents) also play a role as pure manganese oxides with a mixed valence state (e.g., Mn.sub.3O.sub.4 with Mn.sup.+2/Mn.sup.+3) do not generate comparable quantities of ROS.

[0064] Thus, the properties of Ca.sub.xMn.sub.yO.sub.z may be modified by substitution at the calcium, manganese, and/or oxygen sites with (i) ions of the same valence, but different ionic radius (larger or smaller, which distort the perovskite lattice), (ii) ions of similar ionic radius, but different valence (this too can distort the lattice due to changes in the metal-oxygen bond length), or (iii) both (i) and (ii).

[0065] Table 2 below shows the ionic radius of various ions that may be substituted into the Ca.sub.xMn.sub.yO.sub.z lattice. Metal ions such as vanadium, nickel, iron, copper, cerium, etc. may also be substituted into the A site to form compounds such as vanadium manganese oxide, nickel manganese oxide, iron manganese oxide, copper manganese oxide, cerium manganese oxide, etc., of varying stoichiometries.

TABLE-US-00002 TABLE 2 Ionic radius of representative ions that can substitute into the Ca.sub.xMn.sub.yO.sub.z perovskite lattice A Ionic Radius B Ionic Radius Ionic Radius Cation (nm) Cation (nm) Anion (nm) Ca.sup.+2 0.134 Mn.sup.+2 0.067 O.sup.2 0.14 Sr.sup.+2 0.144 Mn.sup.+3 0.058 S.sup.2 0.184 Ba.sup.+2 0.161 Mn.sup.+4 0.053 Na.sup.+ 0.139 Ti.sup.+4 0.0605 F.sup.1 0.133 K.sup.+ 0.164 V.sup.+3 0.064 Cl.sup.1 0.181 La.sup.+3 0.136 V.sup.+4 0.058 Bi.sup.+3 0.117 Fe.sup.+2 0.061 Fe.sup.+3 0.055 Ni.sup.+2 0.069 Ni.sup.+3 0.056 Cu.sup.+1 0.077 Cu.sup.+2 0.073 Zn.sup.+2 0.074 Ce.sup.+3 0.101 Ce.sup.+4 0.087 Al.sup.+3 0.0535 Sb.sup.+3 0.076

[0066] The perovskite crystal structure tolerates large distortions with respect to the ABO.sub.3 cubic symmetry, allowing for changes in the ideal stoichiometry and for a wide variety of targeted metal substitutions/additions at both the A and B sites. The stability of the perovskite lattice can be determined by the Goldschmidt tolerance factor, t, given by

[00001]$t=\frac{r_A+r_O}{\sqrt{2}\left(r_B+r_O\right)}$

where r.sub.A, r.sub.B, and r.sub.O are the ionic radius of the A cation, B cation, and anion, respectively. When dopants are added at either the A or B sites and/or the charge on an ion changes, the average ionic radius is used in the calculation. t1 yields the idealized cubic perovskite lattice. When t is between 0.85 and 1.1, the lattice can deform slightly due to distortion, rotation, and tilting of the BO.sub.6 octahedra. The perovskite lattice is still stable, however. Table 3 below shows representative compounds by substitution into the A, B, and anion sites, their Goldschmidt tolerance factor, and the theoretical average oxidation state of manganese (which may differ from the actual oxidation state due to the oxygen content). These compounds may be synthesized using solid-state or solution processes and may lead to greater or lesser spontaneous reactive oxygen species generation.

TABLE-US-00003 TABLE 3 Representative compounds by substitution into the A, B, and anion sites, their Goldschmidt tolerance factor (t), and the theoretical average oxidation state of manganese (which may differ from the actual oxidation state due to the oxygen content) Theoretical Mn Compound t Oxidation State CaMnO.sub.3 1.004 +4 A site substitution (Ca) SrMnO.sub.3 1.041 +4 BaMnO.sub.3 1.103 +4 Ca.sub.0.5Na.sub.0.5MnO.sub.3 1.011 +4.5 Ca.sub.0.5K.sub.0.5MnO.sub.3 1.059 +4.5 La.sub.0.65Ca.sub.0.35MnO.sub.3 1.008 +3.35 Bi.sub.0.65Ca.sub.0.35MnO.sub.3 0.964 +3.35 CeMnO.sub.3 0.861 +3 B site substitution (Mn) CaMn.sub.0.8Ti.sub.0.2O.sub.3 0.996 +4 CaMn.sub.0.8V.sub.0.2O.sub.3 0.999 +4 CaMn.sub.0.8Fe.sub.0.2O.sub.3 1.002 +4.25 CaMn.sub.0.8Ni.sub.0.2O.sub.3 1.001 +4.25 CaMn.sub.0.8Cu.sub.0.2O.sub.3 0.983 +4.5 CaMn.sub.0.8Zn.sub.0.2O.sub.3 0.982 +4.5 CaMn.sub.0.8Al.sub.0.2O.sub.3 1.003 +4.25 CaMn.sub.0.8Bi.sub.0.2O.sub.3 0.981 +4.25 Oxygen substitution CaMnO.sub.2.4S.sub.0.6 0.991 +4 CaMnO.sub.2.4F.sub.0.6 1.005 +3.4 CaMnO.sub.2.4Cl.sub.0.6 0.992 +3.4

[0067] CaTi.sub.0.1Mn.sub.0.9O.sub.3 and Ca.sub.2Ti.sub.0.1Mn.sub.0.9O.sub.4 were synthesized by solid state synthesis, where CaCO.sub.3, MnCO.sub.3 and TiO.sub.2 (rutile) were mixed in a mortar and pestle and calcined at 1200 C. for 12 hours. CaMn.sub.0.8Cu0.2O.sub.3 was synthesized via the acetates route discussed in Example 3, where stoichiometric amounts of Ca(C.sub.2H.sub.3O.sub.2).sub.2.Math.H.sub.2O, Mn(C.sub.2H.sub.3O.sub.2).sub.2.Math.4H.sub.2O and Cu(C.sub.2H.sub.3O.sub.2).sub.2.Math.3H.sub.2O were dissolved in distilled water, mixed and stirred for 20 minutes and the solution was allowed to evaporate in a drying oven at 80 C. overnight. The resulting mixed salt was heated to 400 C. for 2 hours and calcined at 1000 C. for 2 hours. FIG. 6 in (a) thereof shows the powder X-ray diffraction patterns of CaTi.sub.0.1Mn.sub.0.9O.sub.3 (top) and Ca.sub.2Ti0.1Mn.sub.0.9O.sub.4 (bottom) synthesized by the solid-state procedure, and scanning electron micrographs are shown in (b) of FIG. 6 for such CaTi.sub.0.1Mn.sub.0.9O.sub.3 and Ca.sub.2Ti.sub.0.1Mn.sub.0.9O.sub.4 compounds.

EXAMPLE 5

[0068] CuMnO.sub.3 was synthesized by a solid-state method. Equimolar amounts of CuO and MnO.sub.2 powders were ball-milled together and then calcined in air for 20 hours between 800 and 1100 C. The single phase, perovskite structure of the resulting material is confirmed by the powder X-ray diffraction pattern in FIG. 7. The sample generated 4.8 ppm of H.sub.2O.sub.2 at room temperature (25 C.) after 90 min. using the same test procedure outlined above.

EXAMPLE 6

[0069] Mixed metal manganese oxide powders can be blended with paints and/or polymeric binders to form antimicrobial surface coatings since reactive oxygen species are known to inactivate pathogens. ROS can cause oxidative damage to proteins, nucleic acids, lipids, membranes, and organelles and can lead to rapid cell death even without the complete destruction of the biological species. As a representative example, FIG. 8 in (a) thereof shows a scanning electron micrograph of CaMnO.sub.3- blended with a polyurethane/polyurea binder and coated at 10% by weight on an aluminum foil disc. FIG. 8 in (b) shows an energy dispersive X-ray analysis of both calcium (red) and manganese (purple) evidencing a uniform distribution of ceramic particles across the coating. Table 4 below is a summary of the inactivation of various pathogens using CaMnO.sub.3-. The thickness of the dried coating was 40 microns, and exposure times varied from 5 to 10 minutes, with all experiments carried out at room temperature.

TABLE-US-00004 TABLE 4 Inactivation of selected pathogens by 10% weight CaMnO.sub.3-d in a polyurethane/polyurea binder (except C. albicans, which was tested on CaMnO.sub.3-d powder); all experiments were carried out at room temperature Pathogen Time Inactivation Bacteria S. aureus 10 min >99.9% E. coli 10 min >99.9% Fungus C. albicans 24 h 100% Virus Vaccinia 5 min >99.9%

EXAMPLE 7

[0070] Ca.sub.xMn.sub.yO.sub.z and doped-Ca.sub.xMn.sub.yO.sub.z may be deposited on the surface of a particle using either physical or chemical means or combinations thereof. Physical deposition methods include, but are not limited to, sputtering, evaporation, plasma spray, thermal spray, laser deposition, etc. (see, for example, Handbook of Sputter Deposition Technology 2.sup.nd Ed. (2012) and references cited therein). Chemical deposition methods include, but are not limited to, sol gel formation, chemical bath (liquid) deposition, chemical vapor deposition, plasma enhanced chemical vapor deposition, atomic layer deposition, electrochemical deposition (plating), mechano-chemical synthesis, etc. (see, for example, Chemical Solution Deposition of Functional Oxide Thin Films (2013) and references cited therein). Calcining after deposition may also be employed. The films may be continuous or discontinuous (porous) and may be uniform in structure or consist of small particles (and combinations thereof).

[0071] The composition, thickness, and morphology/structure of the film may be either homogenous or heterogeneous. A tie or pretreatment layer may be used to enhance the wetting of the particle surface, alter the morphology of the Ca.sub.xMn.sub.yO.sub.z or doped-Ca.sub.xMn.sub.yO.sub.z coating, and/or improve the adhesion of the coating. Average film thickness may vary between 1 nm and >1 micron.

[0072] The particulate core material in various embodiments may include materials such as silica, alumina, macroreticulate polymers, porous silicon, glass, or ceramic. In other embodiments, the particulate core material may be or comprise metal, metal alloys, carbon nanotubes, graphene, graphene oxide, or diatomaceous earth. Particle core materials may be selected for the provision of high surface area, to maximize presentation of the calcium manganese oxide and may lower costs by using cheap core materials. Active core materials such as metals/metal alloys, carbon nanotubes, graphene/graphene oxides may provide adjunctive or synergistic activity by affecting the electronic structure of the antimicrobial metal oxide.

[0073] In one illustrative experiment, the coating on particles was deposited using a sol-gel process. Stoichiometric amounts of Ca(NO.sub.3).sub.2.Math.4H.sub.2O and Mn(NO.sub.3).sub.2.Math.4H.sub.2O were dissolved in distilled water, and citric acid was added as a ligand in 2:1 mole ratio to the metal ions. The solution was heated on an oil bath at 90 C. for 1 hour to evaporate the solvent and promote polymerization until a thick gel was formed. At this point, heating was removed and an amount of rutile TiO.sub.2 powder was added to the gel in a 90% weight ratio and blended until a homogeneous mixture was obtained. The resulting mass was dried at 180 C. for 20 hours, ground in a mortar and pestle, and then calcined at 600 C. for 4 hours. The top panel of FIG. 9 shows a powder X-ray diffraction pattern of rutile TiO.sub.2 particles coated with CaMnO.sub.3. The main peaks are indexed to that of rutile TiO.sub.2 (dots, middle panel) and CaMnO.sub.3 (inverted triangles, lower panel) at a corresponding ration of approximately 9:1.

[0074] There have thus been described and illustrated certain embodiments of a metal oxide compound according to the disclosure. Although the metal oxide compounds and their preparation and applications have been described and illustrated in detail, it should be clearly understood that the disclosure is illustrative only and is not to be taken as limiting, the spirit and scope of the invention being limited only by the terms of the appended claims and their legal equivalents, as construed in the context of the specification herein. Thus, while the focus of the description herein has been on manganese compounds, this phenomenon can be observed in other transition metal oxides and mixed metal oxides as well, including, but not limited to, vanadium: +2, +3, +4, +5; chromium: +2, +3, +6; iron: +2, +3; cerium: +3, +4, cobalt: +2, +3; nickel: +2, +3, +4; and copper: +1, +2.