Abstract: Embodiments of the present disclosure, in one aspect, relate to solid acid catalysts, methods of making solid acid catalysts, methods of using solid acid catalysts, and the like. An embodiment of the present disclosure can include a reusable and recoverable solid, carbon supported, porous acid catalyst for biodiesel generation using activated carbon or biochar generated from agricultural or forestry residues.

Abstract: Provided herein is a new material, periodic mesoporous phosphorus-nitrogen compound, which may be used in a variety of emerging technologies. Its surface properties render it promising as a component in a variety of applications, including gas separation and purification systems in which waste gases such as SO2, SO3, or CO2 are separated from other gases. It may also be used as an interlayer dielectric in microelectronic chips. Its structure and composition are useful due to an advantageous and favorable combination of thermal stability, elastic modulus, and dielectric properties. The surface properties and the regularity of the pores furthermore provides utility as shape selective base catalysts. Protonated forms of the material are expected to be useful as a solid acid, and in applications such as acid catalysis. Additionally, because of the thermal behavior of the material, it is useful as “hard” template for other porous materials, without the need of an external reagent.

Abstract: The present invention aims to realize (1) manufacture of a mesoporous composite powder or thin film composed of nanocrystalline metal oxide—glass having a three-dimensional structure with a large specific surface area, (2) construction of a porous structure framework with nanocrystalline metal oxide crystal and a slight amount of glass phase (SiO2 or P2O5, B2O3), (3) control of crystal growth of metal oxide with a slight amount of glass phase (SiO2 or P2O5, B2O3), (4) simplification of the manufacturing process, and (5) use thereof in manufacture of a lithium intercalation electric device, photocatalytic device, solar battery and energy storage device. Provided are a nanocrystal oxide—glass mesoporous composite powder or thin film having a three-dimensional structure with regularly arranged mesopores, and a secondary battery comprising the same.

Abstract: Disclosed is a compound represented by the following formula 1. A lithium secondary battery using the same compound as electrode active material, preferably as cathode active material, is also disclosed. LiMP1-xAxO4??[Formula 1] wherein M is a transition metal, A is an element having an oxidation number of +4 or less and 0<x<1. The electrode active material comprising a compound represented by the formula of LiMP1-xAxO4 shows excellent conductivity and charge/discharge capacity compared to LiMPO4.

Abstract: Disclosed herein are a particle production method whereby spherical fine particles of a crystalline calcium phosphate-based compound can be efficiently produced at low cost, fine particles (especially, spherical particles) with good flowability produced by the particle production method, and a high-quality sintered body obtained by sintering a molded body of the particles.

Abstract: By using phosphorus compounds, diesters of dicarbonic acid may be stabilized against thermal and chemical decomposition over a relatively long period. Mixtures of diesters of dicarbonic acid and phosphorus compounds are outstandingly suitable for preserving foods.

Abstract: A method is provided for making inexpensive synthetic inorganic resins that are stable, mix easily with water and may be conveniently diluted to form an easy-to-use paste for commercial applications. The method uses environmentally friendly techniques to provide improved efficiencies in the commercial production of these resins. The resins are produced by the partial reaction of phosphoric acid with sparsely-soluble oxides, or sparsely-soluble oxide minerals, that are added to the phosphoric acid under controlled conditions. In certain specific embodiments, methods are provided for modifying synthetic inorganic resins so as to produce rapid-setting phosphate cements and ceramics having high flexural strength. Unique synthetic inorganic resin formulations are also disclosed.

Abstract: The present invention provides a method for advantageously producing an iron oxyhydroxide exhibiting excellent capability of adsorbing harmful substances, such as a phosphrous components and endocrine disrupting chemicals, which are contained in industrial wastewater, exhaust gases, etc., and an adsorbent material comprising the iron oxyhydroxide produced by the method as a main component. Specifically, the present invention provides an adsorbent material produced by a method comprising the steps of: (a) adding a base to an aqueous iron ion-containing solution, adjusting the pH of the resultant mixture to 9 or less, to form a precipitate that contains an iron oxyhydroxide; (b) drying the precipitate at a temperature of 100° C. or lower to obtain an iron oxyhydroxide; (c) contacting the resultant iron oxyhydroxide with water; and (d) subjecting the resultant iron oxyhydroxide to a heat treatment under a gas atmosphere having an inert gas concentration of 80% or greater at a temperature of 100 to 280° C.

Abstract: A phosphorous pentoxide producing method includes forming a kiln bed using feed agglomerates with a calcium-to-silica mole ratio of from 0.5 to 1.0 and maintaining a bed temperature at or above 1260° C. along a portion of the bed length without exceeding 1380° C. along the entire bed length. Less than 10% of the agglomerates' phosphate input to the kiln remains in the kiln residue as phosphate. Another method includes maintaining a bed temperature at or above 1180° C. along a portion of the bed length and establishing a bed surface-to-volume ratio multiplied by a time for bed heat up to 1180° C. of less than 50 minutes-ft2/ft3.

Abstract: Disclosed herein are methods directed toward the synthesis of ordered structures of hydroxyapatite and hydroxyapatite derivatives. More specifically, disclosed herein is a method of preparing ordered hydroxyapatite nanorod structures including the steps of suspending calcium and phosphate in a solvent, adjusting the pH to above 5, and heating to a temperature sufficient to support formation of the ordered hydroxyapatite nanorod structures. In some cases, the methods may include ethylenediamine tetraacetic acid or ethylenediamine tetraacetic acid derivatives. Also disclosed are methods that additionally involve a step of coating hydroxyapatite nanorods with a protein or an amphiphile such as a surfactant or polymer.

Abstract: A phosphorous pentoxide producing method includes forming a kiln bed using feed agglomerates with a calcium-to-silica mole ratio of less than 1.0 and maintaining a bed temperature at or above 1180° C. along at least 50% of the bed length without exceeding 1380° C. along the entire bed length. Less than 10% of the agglomerates' phosphate input to the kiln remains in the kiln residue as phosphate. Another method includes maintaining a bed temperature at or above 1180° C. along a portion of the bed length and establishing a bed surface-to-volume ratio multiplied by a time for bed heat up to 1180° C. of less than 50 minutes-ft2/ft3.

Abstract: A phosphorous pentoxide producing method includes forming a kiln bed using feed agglomerates with a calcium-to-silica mole ratio of less than 1.0 and maintaining a bed temperature at or above 1180° C. along at least 50% of the bed length without exceeding 1380° C. along the entire bed length. Less than 10% of the agglomerates' phosphate input to the kiln remains in the kiln residue as phosphate. Another method includes maintaining a bed temperature at or above 1180° C. along a portion of the bed length and establishing a bed surface-to-volume ratio multiplied by a time for bed heat up to 1180° C. of less than 50 minutes-ft2/ft3.

Abstract: A method for manufacturing a highly-crystallized double oxide powder composed of a single crystal phase which can be used as a phosphor material, a dielectric material, a magnetic material, etc. The method involves forming fine droplets of a raw material solution containing a raw material compound that includes at least one metal element and/or at least one semi-metal element that constitutes a double oxide, and heating these droplets at a high temperature, wherein the raw material solution is a solution which exhibits only one main peak attributable to the decomposition reaction of the raw material compound or a reaction intermediate thereof in a DTA profile when the solution is dried and solidified and subjected to TG-DTA measurement.

Abstract: The invention is directed to a method of synthesizing silicoaluminophosphate molecular sieves using synthesis templates that contain at least one dimethylamino moiety, selected from one or more of N,N-dimethylethanolamine, N,N-dimethylpropanolamine, N,N-dimethylbutanolamine, N,N-dimethylheptanolamine, N,N-dimethylhexanolamine, N,N-dimethylethylenediamine, N,N-dimethylbutylenediamine, N,N-dimethylheptylenediamine, N,N-dimethylhexylenediamine 1-dimethylamino-2-propanol, N,N-dimethylethylamine, N,N-dimethylpropylamine, N,N-dimethylpentylamine, N,N-dimethylhexylamine and N,N-dimethylheptylamine. The use of dimethylamino moiety containing templates results in good quality SAPO molecular sieves of CHA framework type.

Abstract: A method for controlling the formation of a hydroxyapatite bone filler from dry calcium phosphate precursors in an aqueous solution uses coated sodium phosphate powder. The sodium phosphate powder is coated with a water soluble cellulose. Until the cellulose dissolves in the aqueous solution setting of the calcium phosphate cements proceeds slowly but when the exposed sodium phosphate particles start to solubilize in the aqueous solution the setting rate increases.

Abstract: The invention provides novel lithium-mixed metal materials which, upon electrochemical interaction, release lithium ions, and are capable of reversibly cycling lithium ions. The invention provides a rechargeable lithium battery which comprises an electrode formed from the novel lithium-mixed metal materials. Methods for making the novel lithium-mixed metal materials and methods for using such lithium-mixed metal materials in electrochemical cells are also provided. The lithium-mixed metal materials comprise lithium and at least one other metal besides lithium. Preferred materials are lithium-mixed metal phosphates which contain lithium and two other metals besides lithium.

Abstract: Disclosed is a process for producing phosphorous trichloride, phosphorous pentachloride, or phosphorous tribromide by reacting phosphine gas with chlorine gas or bromine gas, in a mixture with hydrogen gas. The phosphine is dried and the reaction is performed at a temperature up to about 250° C. The phosphorous trichloride or phosphorous tribromide product can be reacted with oxygen to form phosphorous oxychloride or phosphorous oxybromide, respectively.

Abstract: The invention is directed to a method of synthesising silicoaluminophosphate molecular sieves using synthesis templates that contain at least one dimethylamino moiety. The use of dimethylamino moiety containing templates results in good quality SAPO molecular sieves of CHA framework type.

Abstract: Bismuth- and phosphorus-containing catalyst supports, naphtha reforming catalysts made from such supports, methods of making both support and catalyst, and a naphtha reforming process using such catalysts.

Abstract: Novel compounds are provided in the form of nucleoside pyrophosphate and triphosphate analogs. In these analogs, the pyrophosphate or triphosphate group is replaced with a moiety that is isosterically and electronically identical thereto, but is hydrolytically and enzymatically more stable. The compounds are useful as therapeutic agents, e.g., as antiviral agents, anticancer agents, metabolic moderators and the like. The invention also provides pharmaceutical compositions containing a compound of the invention as an active agent, and in addition provides methods of treating disease, including viral infections, cancer, bacterial infections, inflammatory and/or autoimmune diseases, and the like, by administering a compound of the invention to a patient in need of such treatment.

Abstract: The invention concerns a method for preparing phosphorus pentoxide powder having enhanced fluidity, said method consisting in subjecting said phosphorus pentoxide powder to mechanical stirring at room temperature.

Abstract: A method for controlling the formation of a hydroxyapatite bone filler from dry calcium phosphate precursors in an aqueous solution uses coated sodium phosphate powder. The sodium phosphate powder is coated with a water soluble cellulose. Until the cellulose dissolves in the aqueous solution setting of the calcium phosphate cements proceeds slowly but when the exposed sodium phosphate particles start to solubilize in the aqueous solution the setting rate increases.

Abstract: The present invention relates to a pharmaceutical composition comprising lisinopril and dibasic calcium phosphate dihydrate (DCPD), produced by a process comprising mixing lisinopril and DCPD with a specific surface area of less than 1.5 m2g−1. The use of large particle sized DCPD in a lisinopril formulation/composition has the effect of reducing the amount of the lisinopril degradation product DKP that is formed, thereby increasing the shelf-life of tablets formulated with the larger sized DCPD, particularly those with low doses of lisinopril.

Abstract: A process for the manufacture of phosphorus (I) species, phosphorus (III) species, and lower hydrides of phosphorus from phosphorus (V) species is provided. Particularly, the present invention is directed to a process for the preparation of P(I) species, P(III) species, and lower hydrides of phosphorus, wherein the process comprises contacting a P(V) species with a reducing agent in the presence of a catalyst effective to promote reduction of the P(V) species by reaction with a reducing agent. Preferably the reducing agent comprises hydrogen.

Abstract: Disclosed is a polyphosphate for use in promoting wound healing and scar abatement, represented by the following chemical formula 1. The polyphosphate can effectively promote the healing of wounds resulting from surgical operation or cutting without leaving scars, thereby encouraging patients to overcome loss of self-esteem. In addition, the medicinal aid can heal wounds effectively and economically while lessening scars.

Abstract: A process for the preparation of an oxyacid of phosphorus comprising contacting elemental phosphorus with water in the presence of a catalyst effective to promote oxidation of phosphorus by reaction with water. The use of a noble metal catalyst such as Pd under moderate agitation and low severity conditions is effective for the preparation of P(III) oxyacid in high selectivity. Other suitable catalysts may comprise, for example, other Group VIII metals (particularly other platinum metals); oxides, salts, phosphides, and/or coordination compounds of Group VIII metals; Group IB metals; and/or oxides, salts, phosphides, and/or coordination compounds of Group IB metals. Various apparatus and process as schemes for the preparation of phosphoric and phosphorous acid are also disclosed.

Abstract: The invention relates to a process for producing a unique phosphation reagent and to a simple, single-stage process utilizing is reagent to produce alkyl phosphate esters having high monoalkyl phosphate content in combination with low dialkyl phosphate, trialkyl phosphate, phosphoric acid and residual alcohol.

Abstract: The present invention is directed to an apparatus and method for recovering the group III elemental component of a group III-V material waste material. The method includes heating, under a reduced pressure, solid waste materials which contain group III-V material to cause the group III-V material to separate into a group III element and a group V element vapor; drawing off the group V element vapor; condensing the group V element vapor to produce a condensed group V element solid; and zone refining the group III element to produce a purified group III element. The apparatus is designed to carry out this method in the plant which manufactures the group III-V waste material.

Abstract: The invention relates to a method of manufacturing compounds of the Monazite type, doped or not doped with actinides, to a method of packaging radioactive waste, high in actinides and in lanthanides by incorporating this waste in a confining matrix based on Monazite, and to a block for the packaging of radioactive waste that includes a Monazite matrix containing the radioactive elements. This method includes mixing, in the solid phase, reactants comprising an inactive compound of the lanthanide metaphosphate type Ln (PO.sub.3).sub.3 and one or more lanthanide oxides and/or one or more compounds capable of reacting with this oxide or these oxides during a thermal sintering process; the shaping of the mixture thus obtained, and the reaction sintering of said formed mixture, as a result of which a Monazite or a compound of the Monazite type is obtained.

Abstract: This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents.

Abstract: The invention relates to a process for the conditioning of radioactive waste using silicated apatites as the confinement matrix.This process consists of incorporating the waste (1) into a phosphosilicated apatite-based confinement matrix (3) e.g. complying with the formula:M.sub.t Ca.sub.x Ln.sub.y A.sub.z (PO.sub.4).sub.u (SiO.sub.4).sub.6-u X (I)in which M is an alkali metal, Ln a rare earth, A an actinide, X is S.sup.2-, 2F.sup.-, 2Cl.sup.-, 2Br.sup.-, 2I.sup.- or 2OH.sup.- and u is between 0 and 6.

Abstract: The invention relates to methods and processes for the photoassisted oxidation of dissolved species such as arsenic, iron, phosphorous and sulphur. Each aspect of the invention involves supplying to a solution including the species to be oxidized, an oxidant and a photoabsorber, and then irradiating the resultant solution with UV/electromagnetic radiation. The resulting oxidised species can then be subsequently treated, used and/or removed (e.g. through precipation/co-precipitation).

Abstract: The invention relates to a process for preparing organosilanes which contain at least one Si-bonded hydrogen in the presence of a phosphonium catalyst, the phosphonium catalyst itself and also a process for its preparation.

Abstract: Electroluminescent phosphors having substantially increased luminance and maintenance over that of prior art electroluminescent phosphors may be made by (1) doping an inorganic intercalation compound having an atomic structure interspersed with vacant spaces, with selected activator ions capable of luminescent emission, and (2) introducing organic monomers or other conductive material into the vacant spaces of the atomic structure of the doped inorganic intercalation compound. The organic monomers may be polymerized in situ to form conductive polymers therein.

Abstract: Phossy water is a toxic liquid waste that is generated when elemental phosphorus is manufactured, stored, or processed into phosphorus-containing products. Elemental phosphorus may be prsent as a solution, as colloidal particles, and as settleable particles.The primary objects of the invention are as follows:1. To provide a process for the disposal of phossy water stored at the TVA National Fertilizer and Environmental Research Center.2. To provide a process for the recovery of phossy water that will be generated when hazardous wastes stored at the TVA National Fertilizer and Environmental Research Center are recycled.Phossy water can be disposed of by using it to quench and granulate molten slag at electric furnaces used to manufacture elemental phosphorus. The elemental phosphorus content of the phossy water is limited to about 2 parts per million.Phossy water that will be generated during recycling of hazardous wastes can be recovered by using it in the process to produce fluid fertilizers.

Abstract: Boron silicates, phosphosilicates and aluminum silicates useful as binding surfaces for DNA purification. These compounds allow DNA to be bound and eluted under native conditions (i.e., in the absence of chaotropes or alcohols) using only water, low salt buffers or physiological buffers. Methods for preparation of the compounds and methods for purifying DNA using the compounds are also provided.

Abstract: A process for preparing borosilicate, aluminosilicate, or phosphosilicate comprising preparing a mixture of SiCl.sub.4 with a specific molar ratio of BCl.sub.3, AlCl.sub.3, or PCl.sub.3 ; cooling said mixture to zero degrees; and adding water to the reaction mixture until the evolution of gas is complete. These silicates are useful for purifying DNA wherein the DNA is bound in water or low salt buffers (i.e., in the absence of a chaotropic agent or alcohol).

Abstract: The present invention relates to a silicon-containing material which exhibits sufficient hydrophilicity and sufficient electropositivity to bind DNA from a suspension containing DNA and permit elution of the DNA from the material. Generally, the hydrophilic and electropositive characteristics are expressed at the surface of the silicon-containing material. Preferred silicon-containing materials of the present invention include boron silicate, aluminum silicate, phosphosilicate, silica carbonyl, silica sulfonyl and silica phosphonyl. The silicon-containing materials of the present invention are particularly useful in processes for purification of DNA from other cellular components. In these processes, a suspension of cellular components is placed in contact with the silicon-containing material, the silicon-containing material is washed to remove all cellular components other than DNA which are bound to the material, and the bound DNA is eluted from the material.

Abstract: Aqueous phosphorus wastes from the electric furnace production of phosphors and containing heavy metal bearing particulates are treated with lime whereby the phosphorus is converted into useful phosphorus compounds and the heavy metals rendered sufficiently non-leachable to permit their release into the environment. The treatment is conducted above about 60.degree. C. at a pH of between about 11.0 to 12.5.

Abstract: There is provided a catalyst comprising a heteropoly acid, such as phosphotungstic acid, supported on a mesoporous crystalline material, such as M41S. A particular form of this M41S support is designated as MCM-41. There is also provided a method for preparing this catalyst by impregnating the heteropoly acid on the support. There is also provided a process for using this catalyst to catalyze acid catalyzed reactions, such as the isomerization of paraffins and the alkylation of aromatics.

Abstract: A method for oxidizing a hypophosphite ion, comprised of bringing a solution containing a hypophosphite ion into contact with at least one catalyst selected from the group consisting of boron-nickel compounds, boron-cobalt compounds, and metallic palladium to oxidize the hypophosphite ion to a phosphite ion.

Abstract: The invention provides metal-phosphorus-nitrogen polymer compounds and methods for their preparation at low temperatures using readily available starting materials. One group of compounds, metal-phosphazene polymers, are comprised of repeating units of [PN].sub.3 rings linked to form polymers through P--X--M--X--P bonds. The linking atoms X are either NH.sub.2 or O, and M is a metal cation. Another group of the compounds have the generic formula M.sub.a (P.sub.2 O.sub.5).sub.b (NH.sub.3).sub.c O.sub.d.eH.sub.2 O. If the metal-phosphorus-nitrogen polymers are heated to a sufficiently high temperature to reduce the nitrogen/phosphorus ratio, additional novel solid metal phosphorus compounds of the invention are formed, many of which have a foamed, porous structure. The properties of the compounds of the invention can be varied by choice of metal and reaction conditions to create materials having useful conductive, magnetic, optical, catalytic, or ion-exchange properties.

Abstract: The invention aims at a process for preparing phosphated or nitrophosphated fertilizers through reaction of phosphate rock in aqueous pulp, with sulfuric and/or phosphoric acids, with addition, or not, of ammonia, so as to produce fertilizers of the types simple, double or triple superphosphates, nitrogen-bearing (or not) phosphated partially acidulated, and superphosphated ammoniated, the product being adequate for use as a fertilizer, either powdered or slurried.The invention allows for a more complete reaction due to the better contact between the liquid and solid reagents besides the complete utilization of the heat produced in the reaction as well as in the acid dilution in the aqueous medium, for the vaporization of the water present in the process.

Abstract: Luminescent grade, small particle size boron phosphate is prepared by reacting diammonium phosphate with an excess amount of boric acid and washing the product with ammonium hydroxide solution.

Abstract: Phosphorous acid is formed by gaseous phase oxidation of phosphorus with water vapour to form predominantly P.sub.2 O.sub.3 and dissolving the P.sub.2 O.sub.3 so-formed in water. The P.sub.2 O.sub.3 also can be recovered as the product by quenching the P.sub.2 O.sub.3 to a stable temperature using an inert cooling medium rather than water. Oxygen also may be used in conjunction with the water vapour. Sufficiently rapid quenching of reaction products may result in the formation of red amorphous phosphorus from unreacted phosphorus.

Abstract: Compacted shapes of phosphatic material, suitable as a charge for a phosphorus furnace, are produced by compacting a mixture of calcined phosphate fines and phosphoric acid. The compacted shapes are conveniently produced on a roll briquetting press.

Abstract: Essentially pure and colorless N-(dichlorophosphoryl)trichlorophosphazene [P.sub.2 NOCl.sub.5 ] is prepared/purified under relatively moderate conditions, by reacting phosphorous pentachloride with ammonium chloride, treating the resulting medium of reaction, containing P.sub.3 NCl.sub.12, with SO.sub.2, and thin film evaporating the medium of reaction, advantageously in two stages, to eliminate SO.sub.2, POCl.sub.3 and SOCl.sub.2 values therefrom.

Abstract: Metallic constituents, especially heavy metal constituents are removed from dust electrostatically separated from a gas mixture consisting substantially of carbon monoxide and phosphorus in vapor form obtained during the electrothermal production of yellow phosphorus. To this end, the dust is initially calcined with continuous agitation under oxidizing conditions at temperatures of 300.degree. to 800.degree. C.; next, the resulting calcined matter is mixed with carbon and the mixture is treated at temperatures of 950.degree. to 1200.degree. C. under reducing conditions with volatilization of the metallic constituents; and the volatized metallic constituents are ultimately condensed and separated.

Abstract: A method of catalytic oxidation of organophosphonate esters includes introducing the organophosphonate esters in gaseous form into contact with a molybdenum catalyst and effecting such introduction in the presence of oxygen to cause the organophosphonate ester to be oxidized on the molybdenum catalyst surface. The process is preferably carried out at a temperature of at least 900.degree. K. in the presence of excess oxygen. A chemisorbed oxide coating or molybdenum oxide coating or both may be established on all or part of the molybdenum catalyst. Among the organophosphonate esters which may be oxidized in this manner are dimethyl methylphosphonate, diisopropyl methylphosphonate, diphenyl methylphosphonate, and other molecules with the structure: ##STR1## The catalytic oxidation results in emission of carbon monoxide and phosphorus oxides(s) without undesired buildup of carbonaceous or phosphorus overlayers on the Mo catalyst surface.

Abstract: Nodule fines, formed by abrasion of an electric furnace feed material of phosphate shale nodules, are utilized by mixing a recycle stream of the nodule fines with fresh phosphate in the presence of phosphoric acid prior to forming the shale into nodules. The phosphoric acid prevents loss in mechanical strength of the nodule caused by admixture with the nodule fines.