Abstract: A method of producing fine particles of an oxide of a metal, comprising the steps of: preparing an acidic solution which contains ions of the metal; precipitating fine particles of a hydroxide of the metal by adding an alkaline solution to the acidic solution; collecting the fine particles of the hydroxide of the metal precipitated in a mixed solution of the acidic solution and the alkaline solution; mixing fine particles of a carbon with the collected fine particles of the hydroxide of the metal; and heat-treating a mixture of the fine particles of the hydroxide of the metal and the fine particles of the carbon at a predetermined temperature in a non-reducing atmosphere, whereby the fine particles of the oxide of the metal are produced.

Abstract: Nanostructured chromium(III)-oxide-based materials using sol-gel processing and a synthetic route for producing such materials are disclosed herein. Monolithic aerogels and xerogels having surface areas between 150 m2/g and 520 m2/g have been produced. The synthetic method employs the use of stable and inexpensive hydrated-chromium(III) inorganic salts and common solvents such as water, ethanol, methanol, 1-propanol, t-butanol, 2-ethoxy ethanol, and ethylene glycol, DMSO, and dimethyl formamide. The synthesis involves the dissolution of the metal salt in a solvent followed by an addition of a proton scavenger, such as an epoxide, which induces gel formation in a timely manner. Both critical point (supercritical extraction) and atmospheric (low temperature evaporation) drying may be employed to produce monolithic aerogels and xerogels, respectively.

Abstract: A chromium catalyst is disclosed for use in dehydrogenation and dehydrocyclization processes.

Abstract: A process for producing a strontium chromate corrosion inhibitor includes the steps of providing an aqueous slurry containing dispersed particulate strontium chromate, adding to the slurry a phosphoric acid or a neutral or acidic soluble salt of a phosphoric acid selected from the group consisting of ortho-phosphoric, pyro-phosphoric, tri-phosphoric, polyphosphoric, metaphosphoric, polymetaphosphoric, cyclic tri-metaphosphoric acid, and phosphorous acid, and, filtering and drying the resultant material whereby particulate strontium chromate of reduced solubility is produced.

Abstract: A method of producing fine particles of an oxide of a metal, comprising the steps of: preparing an acidic solution which contains ions of the metal; precipitating fine particles of a hydroxide of the metal by adding an alkaline solution to the acidic solution; collecting the fine particles of the hydroxide of the metal precipitated in a mixed solution of the acidic solution and the alkaline solution; mixing fine particles of a carbon with the collected fine particles of the hydroxide of the metal; and heat-treating a mixture of the fine particles of the hydroxide of the metal and the fine particles of the carbon at a predetermined temperature in a non-reducing atmosphere, whereby the fine particles of the oxide of the metal are produced.

Abstract: It is found that calcining chromium oxide powders having a particle size component smaller than 10 microns reduces the volume proportion of smaller particles and increases the general uniformity of particle sizes in the distribution and the roundness of the particles.

Abstract: A process for the preparation of nanostructured materials in high phase purities using cavitation is disclosed. The method comprises mixing a metal containing solution with a precipitating agent and passing the mixture into a cavitation chamber. The chamber consists of a first element to produce cavitation bubbles, and a second element that creates a pressure zone sufficient to collapse the bubbles. The process is useful for the preparation of mixed metal oxide catalysts and materials for piezoelectrics and superconductors.

Abstract: A new, cost effective process for the production of ultrafine particles which is based on mechanically activated chemical reaction of a metal compound with a suitable reagent. The process involves subjecting a mixture of a metal compound and a suitable reagent to mechanical activation to increase the chemical reactivity of the reactants and/or reaction kinetics such that a chemical reaction can occur which produces a solid nano-phase substance. Concomitantly, a by-product phase is also formed. This by-product phase is removed so that the solid nano-phase substance is left behind in the form of ultrafine particles. During mechanical activation a composite structure is formed which consists of an intimate mixture of nano-sized grains of the nano-phase substance and the reaction by-product phase.

Abstract: Fine powders of ceramic materials can be obtained by firing a precursor powder in a rotary kiln while carried on coarse carrier particles.

Abstract: A process for producing acrylic acid from propane and oxygen gas through a vapor-phase catalytic oxidation reaction, said process comprising conducting the reaction using as a catalyst a metal oxide containing metallic elements Mo, V, Sb, and A (provided that A is at least one element selected from the group consisting of Nb, Ta, Sn, W, Ti, Ni, Fe, Cr, and Co). The metal oxide is prepared by a process including specific steps (1) and (2). The metal oxide may be supported on a compound containing specific elements.

Abstract: Formation of hexavalent chromium is reduced during incineration/combustion of materials containing hexavalent chromium by adding to the waste prior to or during combustion a small amount of sulfur. The sulfur can be added as elemental sulfur, as sulfur dioxide, or as high sulfur fuels or high sulfur waste.

Abstract: A continuous hydrothermal synthesis method which comprises pressurizing and heating a material slurry below a saturated vapor temperature or pressurizing a material slurry at normal temperature, pressurizing and heating an aqueous liquid above the saturated vapor temperature, atomizing and mixing the slurry and the aqueous liquid, effecting hydrothermal synthesis in a reaction section above the saturated vapor temperature, cooling the reaction product and taking out the product while retaining the pressurized state in the system by alternately opening and closing shut-off valves provided above and below a product discharging section or through a thin pipe provided in the product discharging section. The method is performed using an apparatus comprising heating-pressurizing sections respectively connected to a material slurry feeding section and an aqueous liquid feeding section, an atomizing-mixing section and a reaction section provided after these feeding sections, and a product discharging section.

Abstract: A method for preparing an oxide (P), which includes the steps of (i) forming a solid phase compound (O) based on an oxide containing molecular entities (1) chosen from optionally substituted ammonium, diammonium, diazan-ium or diazandium, the entities being distributed within the solid matrix, and (ii) eliminating the entities (1) from the solid phase compound (O) by reacting the solid phase compound (O) with a gaseous stream containing a break-down reactant for the entities (1), and isolating the resulting solid material (P).

Abstract: A method for producing a metal oxide powder which comprises heating a metal or metals in an atmosphere gas comprising a halogen gas, a hydrogen halide gas or a mixture of these gases in a concentration of from 0.5% by volume or more to 99.5% by volume or less; and oxygen, water vapor or a mixture of these gases in a concentration of from 0.5% by volume or more to 99.5% by volume or less.

Abstract: Disclosed is a method for producing oxide powders and complex oxide powders having an oxygen amount smaller than the stoichiometric amount. The method comprises: spraying a combustible liquid that contains at least one raw material of metals capable of having a plural number of valences and compounds of such metals; and firing the raw material to give a powder of an oxide of at least one of said metals. The oxygen amount in the atmosphere in which the combustible liquid containing said raw material is sprayed and fired is smaller than the total of the oxygen amount necessary for the complete combustion of said combustible liquid and the oxygen amount necessary for the conversion of said raw material into an oxide that is the most stable in air at room temperature.

Abstract: A method of decorating a firable article which includes the step of mixing a metallic salt with a fuel material which can supply oxygen to the salt in a reaction. This mixture causes complex formation of the salt, characterized by raising the pH of the mixture to at least 5. Additives in the mixture promote stability and provide the required viscosity surface tension and conductivity for use in an ink jet printer. When applying a solution of this mixture onto a firable article by ink jet printing, the mixture is such that upon drying, the mixture reacts to form an oxide of the metal to provide a decorative color pigment on the article.

Abstract: Disclosed herein is a process for producing fine metal oxide particles comprising the step of heat-treating an aqueous solution of a metal salt at a temperature of not lower than 200.degree. C. under a pressure of not less than 160 kg/cm.sup.2 for 1 second to 1 hour so as to bring into the decomposition reaction of said metal salt.

Abstract: A process for recovery of chromium in an aqueous solution comprising converting the chromium to chromyl chloride, separating the chromyl chloride from the aqueous solution, either as a heavy underlayer, or by extraction into a solvent, purifying the chromyl chloride, hydrolyzing the purified chromyl chloride to form a solution, and drying or precipitating the solution to form chromium, either as chromic acid or a chromate salt.

Abstract: Disclosed is a process for making orthorhombic Na.sub.2 SO.sub.4 containing less than 0.1 ppm chromium from a solution of Na.sub.2 SO.sub.4 containing 0.1 to 100 ppm Cr(III). The Cr(III) is oxidized to Cr(VI) at a pH greater than 7, water is evaporated from the solution to precipitate the orthorhombic Na.sub.2 SO.sub.4, and the precipitated orthorhombic Na.sub.2 SO.sub.4 is separated from the solution.

Abstract: A magnetic recording medium comprising a nonmagnetic substrate and at least one magnetic layer applied thereon and containing an acicular chromium dioxide uniformly distributed in a polymeric binder and additives and having a coercive force of at least 60 kA/m, a mean particle length of the chromium dioxide of less than 300 nm, whose factor HD according to the formula ##EQU1## where KT is the coercive force of the magnetic layer in [kA/m], measured in an external field of 380 kA/m, L is the mean particle length and .DELTA.L is the range of the particle size distribution, determined from the numerical distribution of the particle length, both measured in [nm], is greater than 1.85, and a process for the preparation of this chromium dioxide.

Abstract: A method has been devised for removing chromium ions from a chromium ion containing liquid and recovering chromium oxide in a usable form by (a) adjusting the temperature of the liquid to an optimal temperature to maximize reduction and simultaneous precipitation of the chromium oxide; (b) adding a reducing agent to the liquid to form a mixture, where the reducing agent is at least one inorganic sulfur compound selected from the group of sulfur compounds where sulfur is in the 4.sup.+ oxidation state; and (c) adjusting the pH of the mixture to a pH between 5 and 7; (d) optionally further adjusting the pH of the mixture to a pH between above 7 to 12; and (e) separating the chromium from the mixture.

Abstract: The present invention provides a composition and process for the treatment of waste water containing chromium compound, for example water from a plating operation which includes significant concentration of a toxic chromium compound such as chromic acid. The chromium bearing solution is mixed with sufficient amount of hydrazine which can include selected minor concentrations of a cobalt salt to react with the chromium compound and render it insoluble. The chromium bearing water is introduced to a vessel which can have a baffle so that water introduced on one side of the baffle flows along a side of, then under the baffle and overflows on the other side. The hydrazine, which can include cobalt salt, is introduced to the incoming water at a rate to control the pH of the effluent from the vessel at a selected value of pH sufficient to remove all chromium from the effluent.

Abstract: A method has been devised for removing chromium ion from a chromium ion containing liquid and recovering chromium oxide in an usable form by (a) adjusting the temperature of the liquid to an optimal temperature to maximize reduction and simultaneous precipitation of the chromium oxide; (b) adding a reducing agent to the liquid to form a mixture, where the reducing agent is at least one inorganic sulfur compound selected from the group of sulfur compounds where sulfur is in the 4.sup.+ oxidation state and (c) adjusting the pH of the mixture to a pH between 5 and 7.

Abstract: A process for precipitating and removing chromium compounds in which chromium is in the hexavalent state from aqueous liquids, particularly, alkaline earth metal or alkali metal chlorate-rich solutions containing chloride, chlorate, and bichromate ions produced by the electrolysis of brine. In the process, hydroxylamine, hydroxylamine sulfate, hydroxylamine formate or hydroxylamine hydrochloride is used as a reducing agent to react and co-precipitate at a neutral or acid pH with hexavalent chromium ions present in the aqueous liquid, the reaction and precipitation taking place, generally, at a pH of about 4.0 to about 6.5 and, a temperature of about 50.degree. C. to about 100.degree. C. Precipitated oxides and hydroxides of divalent and trivalent chromium can be removed, for instance, by filtration.

Abstract: A composite oxide synthesized by a citrating process and utilized in functional ceramics materials is prepared by the following process. Co-precipitants or mixtures of at least one component selected from the group consisting of carbonates, basic copper and/or hydroxides of elements which compose a composite oxide are reacted with citric acid in an aqueous solution or in an organic solvent. The elements are selected from at least one element of the group consisting of Y, rare earth elements, transition elements, and alkali metal or alkaline earth metal elements. The citrate compound formed is baked to complete the composite oxide.The composite oxide synthesized by this invention has superconduction at the most temperature of 93.degree. K. with excellent Meissner effect.

Abstract: Stabilized acicular ferromagnetic chromium dioxide is prepared by a method in which the chromium dioxide surface formed as a result of a reductive treatment is treated with adsorbed monobasic or polybasic hydroxycarboxylic acids.

Abstract: A low temperature process is described for forming a coating or powder comprising one or more metals or metal compounds by first reacting one or more metal reactants with a halide-containing reactant to form one or more reactive intermediates capable of reacting, disproportionating, or decomposing to form a coating or powder comprising the one or more metal reactants. When one or more metal compounds are formed, either as powders or as coatings, a third reactant may be injected into a second reaction zone in the reactor to contact the one or more reactive intermediates formed in the first reaction zone to thereby form one or more metal compounds such as metal nitrides, carbides, oxides, borides, or mixtures of same.

Abstract: Disclosed is a method of making chromic acid by electrolyzing an aqueous solution of sodium bichromate until the sodium bichromate is converted to chromic acid at a bichromate percent conversion of about 1 to about 48.4. Sulfuric Acid is then added to the aqueous solution in an amount between stoichiometric and about 30 wt % in excess of stoichiometric to convert the remaining sodium bichromate to chromic acid. This results in the precipitation of chromic acid, which is separated from the aqueous solution.

Abstract: This invention is directed to the formation of homogeneous, aqueous precursor mixtures of at least one substantially soluble metal salt and a substantially soluble, combustible co-reactant compound, typically an amino acid. This produces, upon evaporation, a substantially homogeneous intermediate material having a total solids level which would support combustion. The homogeneous intermediate material essentially comprises highly dispersed or solvated metal constituents and the co-reactant compound. The intermediate material is quite flammable. A metal oxide powder results on ignition of the intermediate product which combusts same to produce the product powder.

Abstract: A process for preparing finely-divided oxides of metals of metalloids of the elements of main groups III and IV and sub-groups III, IV, V and VI of the Periodic System of Elements, comprising reacting compounds of these elements with a polymerizable hydrocarbon compound or mixture to form a polymer product, which is then thermally treated to yield the oxide product.

Abstract: Stabilized acicular ferromagnetic chromium dioxide is prepared by reductive treatment of the chromium dioxide with Na.sub.2 [Fe(CO).sub.4 ], and this material is present in magnetic recording media.

Abstract: Disclosed is a method of reducing the turbidity of an aqueous solution of chromic acid which is formed by dissolving melted chromic anhydride in water. The chromic anhydride is contacted with water in an amount in excess of 0.02 wt %, but insufficient to form a solution, at a temperature above ambient but below about 196.degree. C. The water may be in the form of a liquid, water vapor, or steam. When the chromic anhydride is subsequently dissolved in water, the solution is much less turbid than it otherwise would be.

Abstract: Chromium oxide green in the form of donut-shaped, ring-shaped or tire-shaped particles having an internal diameter of from 0.01 to 0.5 mm and an external diameter of from 0.05 to 1.0 mm is prepared by spraying an aqueous chromium oxide green suspension through a liquid pressure nozzle into a spray dryer such that the suspension entering the drying space of the spray dryer is rotating.

Abstract: An acicular, ferromagnetic material which has a high coercive force and essentially consists of iron-containing chromium dioxide is prepared by thermal decomposition of hydrated chromium(III) chromate under superatmospheric pressure.

Abstract: Acicular ferromagnetic chromium dioxide is stabilized by treatment with an alkali metal hydroxide in an aqueous alkaline suspension at elevated temperatures.

Abstract: A process is disclosed for producing chromium oxide powders, which comprises forming an aqueous slurry wherein the solids content is a mixture which consists essentially of in percent by weight about 5 to 15 chromium acetate and the balance chromium oxide, agglomerating the mixture, sintering the resulting agglomerated mixture in a hydrogen atmosphere at a temperature at about 1400.degree. C. to about 1550.degree. C. in metallic vessels, entraining the sintered chromium oxide powder in a carrier gas, passing the sintered chromium oxide powder and the carrier gas through a plasma flame at a power of about 10 to about 80 KW using an inert gas as the plasma gas, and cooling the resulting plasma heated chromium oxide powder to produce free flowing chromium oxide powder having a free chromium content of less than about 1% by weight.

Abstract: Process for the manufacture of vitreous metal oxides in which a metal alcoholate derived from an alcohol, the pka of which is less than 15.74, is hydrolysed with an aqueous medium, the pH of which is greater than 1.5. The process is applied especially to the manufacture of vitreous zirconium oxide.

Abstract: Chromium(III) oxide and hydroxide aerogels are produced by the reaction of chromium(VI) oxide with a solvent which is reducing to chromium(VI), such as methanol, heating the solution to hypercritical conditions, and venting the solvent hypercritically. The product aerogels exhibit surface areas above 400 m.sup.2 /g, pore volumes of at least 2 cm.sup.3 /g and a substantially uniform pore size distribution. Also disclosed is a unique process which employs high pore volume, high surface area chromium(III) oxide or hydroxide as a fluorination catalyst. More particularly, reaction of C.sub.2 Cl.sub.3 F.sub.3 with HF over these catalysts produced high yields of C.sub.2 Cl.sub.2 F.sub.4 and C.sub.2 ClF.sub.5.

Abstract: A process for removing dichromates from chlorate-rich solutions containing hypochlorite and dichromate ions and produced by the electrolysis of brine. The dichromate is reduced in a two-stage process by the addition of ammonia under controlled conditions of pH and temperature to a mixed di- and trivalent chromium hydroxide which is precipitated from solution and removed. The process provides an economical method of recovering chromium from electrolytically produced chlorate solutions.

Abstract: A magnetic recording medium comprising a non-magnetic substrate and a magnetic layer formed thereon which contains chromium oxide ferromagnetic powder comprising chromium oxide of the formula:CrO.sub.xwherein x is not smaller than 1.74 and not larger than 1.91, which has improved long term storage stability.

Abstract: Acetic acid is substituted for a portion of the chromic oxide employed in the hydrothermal reaction of chromium trioxide and chromic oxide to form ferromagnetic chromium dioxide.

Abstract: Ultrafine particles of ceramic or metallic material are obtained at low temperatures from a nitrate source capable of endothermic decomposition by molecularly combining under a nitrogen atmosphere the nitrate source with an inorganic reducing fuel compound, such as hydrazine, to provide a chemical precursor for the ceramic or metallic material and then exothermically decomposing the precursor in a controlled atmosphere by heating to a temperature up to about 200.degree. C. below the endothermic decomposition temperature of the nitrate source. The nitrate source is a metal nitrate or a mixture of nitrate salts. Ferrite particles are recovered when the nitrate source is a mixture of nitrate salts containing ferric nitrate in a 2:1 molar ratio with at least one additional metal nitrate.

Abstract: Chromic acid and inexpensive, coarse grained Cr.sub.2 O.sub.3 are dissolved in water prior to adding more costly fine grained Cr.sub.2 O.sub.3 to produce chrome pastes which are more economical than pastes prepared by prior art techniques employing only fine grained Cr.sub.2 O.sub.3. The pastes are equivalent to prior art pastes when reacted to form chromium dioxide.

Abstract: A process for the preparation of chromium(III) oxide by decomposing hydrated ammonium dichromate at elevated temperatures, an apparatus for carrying out this process and the use of the chromium(III) oxide thus prepared as a starting material for the synthesis of chromium dioxide.

Abstract: Soluble hexavalent chromium values are removed from aqueous chlorate solutions by employing a critical effective ratio of OH.sup.- :Cr.sub.2 O.sub.7.sup.= ions of at least 3:1 in the aqueous chlorate solution and by employing a dithionite to reduce the hexavalent chromium to trivalent chromium, preferably in the mole ratio of S.sub.2 O.sub.4.sup.= :Cr.sub.2 O.sub.7.sup.= of at least 3:1. The trivalent chromium forms chromic hydroxide (Cr(OH).sub.3) with the hydroxyl ions and precipitates from the aqueous chlorate solution. The process is rapid and effective in quantitative removal of hexavalent chromium from the aqueous chlorate solutions and is especially useful for the removal of sodium dichromate from cell liquor which is intended to be employed in chlorine dioxide production and which is produced by diaphragmless electrolysis of sodium chloride.

Abstract: A new process for synthesis of ferromagnetic chromium dioxide is provided wherein a chromium trioxide solution is mixed with reducing agent that only partially reacts with chromium trioxide during formation of paste below about 100.degree. C. and completes reaction during the heating of paste to temperatures needed to synthesize ferromagnetic chromium dioxide.

Abstract: A process is disclosed for recovering cobalt in a relatively pure form from an impure cobalt bearing material. The process involves digesting the material in hydrochloric acid to form a solution essentially all of the cobalt and some impurities and insoluble material containing the remainder of the impurities, separating the solution from the insolubles, adding an oxalate producing compound in an amount sufficient to subsequently convert essentially all of the cobalt to cobalt oxalate to the solution, adjusting the pH of the oxalate treated solution to from about 1.5 to about 2.0 with a base to precipitate the cobalt, and finally separating the precipitate from the resulting mother liquor.

Abstract: Spherical, submicronic, monodispersed, and non-agglomerated particles of metal oxides by reacting with steam a gaseous stream containing an aerosol of liquid particles of a hydrolyzable metal compound. Into a duct, in which an inert gas stream containing vapors of a hydrolyzable metal compound flows, there is fed through a nozzle a cold inert gas stream, the temperatures and flows of the two gaseous streams being such as to establish in the duct a temperature lower than the condensation temperature of the metal compound; the mixed gaseous streams having a turbulent flow in the duct, with a Reynolds number equal to or higher than 1800. At the duct outlet, the aerosol of metal compound liquid particles, which has formed in the duct, is caused to react with steam, wherefore solid particles of hydrated metal oxide form, which are subsequently calcined to the oxide.

Abstract: A chromium hydroxide precipitate obtained by a continuous process is described, wherein chromium containing waste waters are subjected to continuous hot treatment with acetic acid or with alkaline acetates and alkaline hydroxides at a temperature from 40.degree. C. to boiling point and at atmospheric pressure, at a pH higher than 6.5, preferably between 7 and 10, particularly about 7.5. Thus, a "sandy" type of chromium hydroxide is obtained, having a titer in Cr.sub.2 O.sub.3 of 20 to 40% by weight, which quickly filters, is easily soluble in acids, and thereby affords an easy valorization both as a tanning agent and as a raw material for preparing other chromium compound.

Abstract: A selectively absorbent layer for solar collectors, comprising a mixture of chromium oxides resulting from thermal decomposition of chromium hexacarbonyl or substituted chromium carbonyl. The absorbent layer is deposited from a process gas containing the carbonyl gaseous phase, oxygen, and inert carrier gas. An intermediate reflective layer is provided between the absorbent layer and the substrate.