Abstract: A method of additive manufacturing. The method comprises: i) positioning porous particles on a substrate, the porous particles having an average porosity and comprising at least one material chosen from metals and metalloids; ii) heating at least a portion of the porous particles to a reaction temperature; and iii) exposing the porous particles to a reactant gas to form a layer comprising a non-oxide ceramic. A method of making porous particles is also disclosed.

Abstract: The present invention is directed to methods for formation of refractory carbide, nitride, and boride coatings without use of a binding agent. The present invention is directed to methods of creating refractory coatings with controlled porosity. Refractory coatings can be formed from refractory metal, metal oxide, or metal/metal oxide composite refractory coating precursor of the 9 refractory metals encompassed by groups 4-6 and periods 4-6 of the periodic table; non-metallic elements (e.g. Si & B) and their oxides (i.e. SiO2 & B2O3) are also pertinent. The conversion of the refractory coating precursor to refractory carbide, nitride or boride is achieved via carburization, nitridization, or boridization in the presence of carbon-containing (e.g. CH4), nitrogen containing (e.g. NH3), and boron-containing (e.g. B2H6) gaseous species. Any known technique of applying the refractory coating precursor can be used.

Abstract: Processes for preparing a niobate material are provided, in which the processes include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: Processes for preparing a niobate material are provided, in which the processes include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: Processes for preparing a niobate material are provided, in which the processes include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: Processes for preparing a niobate material are provided, in which the processes include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: Processes for preparing a niobate material include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: The present invention is directed to methods for formation of refractory carbide, nitride, and boride coatings without use of a binding agent. The present invention is directed to methods of creating refractory coatings with controlled porosity. Refractory coatings can be formed from refractory metal, metal oxide, or metal/metal oxide composite refractory coating precursor of the 9 refractory metals encompassed by groups 4-6 and periods 4-6 of the periodic table; non-metallic elements (e.g. Si & B) and their oxides (i.e. SiO2 & B2O3) are also pertinent. The conversion of the refractory coating precursor to refractory carbide, nitride or boride is achieved via carburization, nitridization, or boridization in the presence of carbon-containing (e.g. CH4), nitrogen containing (e.g. NH3), and boron-containing (e.g. B2H6) gaseous species. Any known technique of applying the refractory coating precursor can be used.

Abstract: A contaminant-sequestering coating includes a network of hydrolyzed silane compounds. The hydrolyzed silane compounds include a hydrophilic polar head region, a hydrophobic linker, and an anchor region including a silicon atom. The network of hydrolyzed silane compounds is devoid or substantially devoid of fluorine atoms. Methods of destroying one or more perfluoroalkyl and/or polyfluoroalkyl (PFAS) compounds present in a contaminant-containing liquid are also provided.

Abstract: A composite precursor powder, including one or more metals or metalloids, and one or more oxides, wherein a molar ratio of the one or more metals or metalloids to the one or more oxides is from about 1:0.01 to about 1:4, and wherein the molar ratio of the one or more metals or metalloids to the one or more oxides is configured according to a desired volumetric change of the composite precursor powder when converted to a non-oxide ceramic.

Abstract: Processes for preparing a niobate material include the following steps: (i) providing a niobium-containing source; (ii) providing a transitional metal source (TMS), a post-transitional metal source (PTMS), or both; (iii) dissolving (a) the niobium-containing source, and (b) the TMS, the PTMS, or both in an aqueous medium to form an intermediate solution; (iv) forming an intermediate paste by admixing an inert support material with the intermediate solution; (v) optionally coating the intermediate paste on a support substrate; and (vi) removing the inert support material by subjecting the intermediate paste to a calcination process and providing a transition-metal-niobate (TMN) and/or a post-transition-metal-niobate (PTMN). Anodes including a TMN and/or PTMN are also provided.

Abstract: Disclosed is a hydrogen generation furnace using decomposition of biomass steam, which employs an infrared source and a furnace body with a water-accommodating structure. A steam separation-drying device is cylindrical and provided at an upper part of an interior of the furnace body and a cavity of the steam separation-drying device forms a secondary gasifier. A lattice plate is provided at a bottom of the interior of the furnace body. A lattice combustion grate is provided above a middle of the lattice plate. A steam distributor is provided outside a lower part of the furnace body. The furnace of the invention performs gasified gas separation as well as secondary oxidation and gasification and mixes steam with gas generated from biomass to perform a decomposition reaction for generating hydrogen.

Abstract: The invention provides a hydrogen boiler based on coal gasification and water decomposition, including a steam boiler which includes an upper furnace and a lower furnace; water and steam in the upper furnace are respectively communicated with water and steam in the lower furnace; and the steam boiler is provided with a casing which has a narrow gap for containing water and a wide wall for heating to generate gas. The steam boiler contains multistage reactors. A coal modification and gasification device is provided at an outer side of the steam boiler and is provided with two chambers. The steam and gasified gas of coal are mixed and enter the reactors for direct burning to promote respective reactions. After several stages of modification and decomposition, the steam and the gasified gas of coal are completely converted to hydrogen.

Abstract: Disclosed is a hydrogen generation furnace using decomposition of biomass steam, which employs an infrared source and a furnace body with a water-accommodating structure. A steam separation-drying device is cylindrical and provided at an upper part of an interior of the furnace body and a cavity of the steam separation-drying device forms a secondary gasifier. A lattice plate is provided at a bottom of the interior of the furnace body. A lattice combustion grate is provided above a middle of the lattice plate. A steam distributor is provided outside a lower part of the furnace body. The furnace of the invention performs gasified gas separation as well as secondary oxidation and gasification and mixes steam with gas generated from biomass to perform a decomposition reaction for generating hydrogen.

Abstract: The invention provides a hydrogen boiler based on coal gasification and water decomposition, including a steam boiler which includes an upper furnace and a lower furnace; water and steam in the upper furnace are respectively communicated with water and steam in the lower furnace; and the steam boiler is provided with a casing which has a narrow gap for containing water and a wide wall for heating to generate gas. The steam boiler contains multistage reactors. A coal modification and gasification device is provided at an outer side of the steam boiler and is provided with two chambers. The steam and gasified gas of coal are mixed and enter the reactors for direct burning to promote respective reactions. After several stages of modification and decomposition, the steam and the gasified gas of coal are completely converted to hydrogen.

Abstract: In a clean boiler with steam conversion and hydrogen/oxygen pre-blending, the clean boiler comprises two identical boiler bodies integrated to form a single entity. The clean boiler comprises two slim cavities, four water-containing chambers and four combustors, which is heated at wide faces and generates steams rapidly. The boiler comprises an integrate body containing two independent boiler bodies (1), and each of the independent boiler bodies (1) contains an independent boiler chamber (19). A steam conversion and transformation system is simultaneously provided for introducing a part of steam into the independent boiler chamber (19). High temperature of the boiler chamber (19) is utilized to promote a decomposition of the steam into H2 and O2. Water formed by H2 and O2 is utilized as a fuel to provide a self-sustaining combustion and heating, thus reducing a dependence on a primary energy source, reducing carbon emissions and protecting the environment.

Abstract: The present invention provides an infrared hydrogen/oxygen combustor. The structure of the combustor includes a sinus ring (1). A surrounding foot (12) of the angle-shaped sinus ring (1) wraps a material-containing basin (14). A first small tube (16) and a second small tube (7) are connected the material-containing basin (14) and the angle-shaped sinus ring (1). Water solution (3) is contained in the material-containing basin (14). A straight-hole ceramic water-absorbing board (5) is provided on the upper part of the water solution (3), a spacing ring (6) is provided above the side of the material-containing basin (14) and in the upward ring of the angle-shaped sinus ring (1), a two-stage material-containing box (9) with a separated brake is provide on one side of the angle-shaped sinus ring (1). The technical scheme of the invention reduces the production cost, the pollution and protects the environment.

Abstract: In a clean boiler with steam conversion and hydrogen/oxygen pre-blending, the clean boiler comprises two identical boiler bodies integrated to form a single entity. The clean boiler comprises two slim cavities, four water-containing chambers and four combustors, which is heated at wide faces and generates steams rapidly. The boiler comprises an integrate body containing two independent boiler bodies (1), and each of the independent boiler bodies (1) contains an independent boiler chamber (19). A steam conversion and transformation system is simultaneously provided for introducing a part of steam into the independent boiler chamber (19). High temperature of the boiler chamber (19) is utilized to promote a decomposition of the steam into H2 and O2. Water formed by H2 and O2 is utilized as a fuel to provide a self-sustaining combustion and heating, thus reducing a dependence on a primary energy source, reducing carbon emissions and protecting the environment.

Abstract: The present invention provides an infrared hydrogen/oxygen combustor. The structure of the combustor includes a sinus ring (1). A surrounding foot (12) of the angle-shaped sinus ring (1) wraps a material-containing basin (14). A first small tube (16) and a second small tube (7) are connected the material-containing basin (14) and the angle-shaped sinus ring (1). Water solution (3) is contained in the material-containing basin (14). A straight-hole ceramic water-absorbing board (5) is provided on the upper part of the water solution (3), a spacing ring (6) is provided above the side of the material-containing basin (14) and in the upward ring of the angle-shaped sinus ring (1), a two-stage material-containing box (9) with a separated brake is provide on one side of the angle-shaped sinus ring (1). The technical scheme of the invention reduces the production cost, the pollution and protects the environment.

Abstract: The present invention is directed to methods for formation of refractory carbide, nitride, and boride coatings without use of a binding agent. The present invention is directed to methods of creating refractory coatings with controlled porosity. Refractory coatings can be formed from refractory metal, metal oxide, or metal/metal oxide composite refractory coating precursor of the 9 refractory metals encompassed by groups 4-6 and periods 4-6 of the periodic table; non-metallic elements (e.g. Si & B) and their oxides (i.e. SiO2 & B2O3) are also pertinent. The conversion of the refractory coating precursor to refractory carbide, nitride or boride is achieved via carburization, nitridization, or boridization in the presence of carbon-containing (e.g. CH4), nitrogen containing (e.g. NH3), and boron-containing (e.g. B2H6) gaseous species. Any known technique of applying the refractory coating precursor can be used.