21412 results about "Nitric acid" patented technology

The invention provides a method for preparing lithium cobaltate by directly using an invalid lithium ion battery. The method comprises the following steps: crushing the invalid lithium ion battery or scraps generated when a lithium cobaltate battery is produced by a mechanical crusher at normal temperature; adding water and one or more of acetic acid, sulfuric acid, hydrochloric acid or nitric acid to produce mixed aqueous solution of the battery scraps and acid; filling the mixed aqueous solution into a hermetic pressure reactor, and controlling the temperature in the reactor to be between 50 and 150 DEG C; introducing or adding one leaching additive of sulfur dioxide or hydrogen, or adding hydrazine hydrate; stirring and leaching, cooling, and filtering; adding one precipitator of sodium carbonate, potassium carbonate and ammonium carbonate, or adding composite precipitator consisting of one of the sodium carbonate, the potassium carbonate and the ammonium carbonate and one of sodium hydroxide and potassium hydroxide to obtain mixture of lithium carbonate, cobalt carbonate and cobalt hydroxide; drying and calcining at high temperature to produce a lithium cobaltate product. The method is particularly suitable for the treatment scale of medium-sized and small enterprises, and is an effective method for directly materializing cobalt secondary resources.

The invention discloses a method for producing humic acid and salt thereof through the oxidative degradation of young lignite. The method comprises the following steps: carrying out the oxidation reaction of the lignite containing the humic acid and aqueous hydrogen peroxide solution; after the reaction, obtaining water soluble fulvic acid through centrifugal separation, supernatant filtration, concentration and drying; adding alkali into the fulvic acid to prepare a fulvic acid salt product; carrying out the alkaline extraction and centrifugal separation of the residue deposit of the production of the fulvic acid, adding acid into the supernatant till the pH value is 1 to 2, carrying out a reaction at an increased temperature or room temperature, carrying out centrifugal separation after the reaction is finished, and obtaining purified ulmic acid after precipitation and drying; and directly concentrating and drying the supernatant in the previous step to obtain the humate. The method can improve the yield of the fulvic acid and total humic acid in the young lignite, and simultaneously increase the active group in the humic acid. The method can be used for producing fulvic acid, fulvic acid salt, ulmic acid and ulmic acid salt products. In particular, the method puts an end to the environmental pollution caused by the nitric acid which is taken as an oxidation degradation agent. In addition, the method has a short technological line, low cost, simple requirements on equipment, and moderate conditions. The method which can be applied to the industrialized production has good application prospect.

The invention relates to a manufacturing mode of environment-friendly and energy-saving M15_M85 methanol diesel oil. The methanol diesel oil is composed of diesel oil, methanol, and additives. The methanol diesel oil is prepared with operations under normal temperatures and normal pressures. The invention discloses a plurality of common additives used for preparing methanol diesel oil in modern times. If explosives and aviation fuels are appropriately utilized, methanol defalcated heat value can be well compensated. The theory is tentatively considered as a gaseous detonation theory. The additives can be selected from nitric acid esters, nitrates, nitro compounds, non-aromatic compounds, peroxides, and the like.

A method of producing nano-scaled graphene platelets with an average thickness smaller than 30 nm from a layered graphite material. The method comprises (a) forming a carboxylic acid-intercalated graphite compound by an electrochemical reaction which uses a carboxylic acid as both an electrolyte and an intercalate source, the layered graphite material as an anode material, and a metal or graphite as a cathode material, and wherein a current is imposed upon the cathode and the anode at a current density for a duration of time sufficient for effecting the electrochemical reaction; (b) exposing the intercalated graphite compound to a thermal shock to produce exfoliated graphite; and (c) subjecting the exfoliated graphite to a mechanical shearing treatment to produce the nano-scaled graphene platelets. Preferred carboxylic acids are formic acid and acetic acid. The exfoliation step in the instant invention does not involve the evolution of undesirable species, such as NO_x and SO_x, which are common by-products of exfoliating conventional sulfuric or nitric acid-intercalated graphite compounds. The nano-scaled platelets are candidate reinforcement fillers for polymer nanocomposites. Nano-scaled graphene platelets are much lower-cost alternatives to carbon nano-tubes or carbon nano-fibers.

The invention relates to a low-temperature smoke denitration SCR (silicon controlled rectifier) catalyst, which comprises a carrier, a manganese oxide, and composite oxide of one or more of Ce, Zr, Ti, Co, Fe and Cu, the mass content of manganese is 0.1-66 percent, and the total mass content of the Ce, Zr, Ti, Co, Fe or/and Cu is 0-50 percent; and glass fiber and/or kieselguhr is used as the carrier, wherein the glass fiber of the carrier is calcined for 2-4 hours at temperature of 400-600 DEG C, then placed in a nitric acid, sulfuric acid or hydrochloric acid solution with mass concentration of 5-40 percent for acidizing for 1-8 hours, washed by distilled water to be neutered, dried at temperature of 80-120 DEG C, and crushed to have the fineness of 20-325 meshes. The catalyst uses the glass fiber and the kieselguhr as the carriers, so that the dispersion effect of nanoparticles and specific surface area of the catalyst are increased, the high adsorptive capacity and strong heat resistance and corrosion resistance capacity are achieved, stronger toxic resistance capacity to sulfur dioxide and stream contained in the smoke is realized, the invention can be used for 10-200 DEG C of low temperature smoke denitration, and has strong water resisting and sulphur toxic resisting capacities.

An organic-based uniprill fertilizer is provided. To produce the fertilizer, organic matter is sequentially pre-treated by first mixing it in a first grinder with a lime admixture, then adding a slurry of reagents and binders, followed by a mixture of acids. The acids can include sulfuric and phosphoric acids, in addition to nitric acid and various organic acids such as citric and fulvic acid, depending on the end requirements of the fertilizer product. Following the mixing of the pre-product with the mixture of acids and reagents, the resultant raw product is preferably processed through a second grinder. This grinding further dries, mixes and granulates the raw product. The particle size of the completed fertilizer is reduced into a flowable, user safe uniprill product that can be further ground to reduce its moisture. Further drying may be necessary for bag or bulk product, or it can be liquified by high speed blending or micro-fluidized for sprinkler or drip applications. The uniprill fertilizer comprises small, preferably microscopic particles that are homogenous in nature, in that any single particle is substantially identical in composition to all other particles of the fertilizer. Additionally, each uniprill particle contains substantially all sixteen nutriments and minerals required for the growth of healthy plants.

A method of producing metal fibers including melting a mixture of at least a fiber metal and a matrix metal, cooling the mixture to form a bulk matrix comprising at least a fiber phase and a matrix phase and removing at least a substantial portion of the matrix phase from the fiber phase. Additionally, the method may include deforming the bulk matrix. In certain embodiments, the fiber metal may be at least one of niobium, a niobium alloy, tantalum and a tantalum alloy and the matrix metal may be at least one of copper and a copper alloy. The substantial portion of the matrix phase may be removed, in certain embodiments, by dissolving of the matrix phase in a suitable mineral acid, such as, but not limited to, nitric acid, sulfuric acid, hydrochloric acid and phosphoric acid.

SO₂ and/or NO_x are removed from gaseous CO₂ at elevated pressure(s) in the presence of molecular oxygen and water and, when SO₂ is to be removed, NO_x, to convert SO₂ to sulfuric acid and/or NO_x to nitric acid. The sulfuric acid and/or nitric acid is/are then removed from the gaseous carbon dioxide to produce SO₂-free, NO_x-lean carbon dioxide gas. The invention has particular application in the removal of SO₂ and/or NO_x from carbon dioxide flue gas produced in an oxyfuel combustion process, for example, in a pulverized coal fired power station.

Rare earth oxide material is dissolved in dense nitric acid, titrated with potassium hydroxide and made to pass through hydrothermal reaction at 100-250 deg.c inside one sealed container, so that monocrystal nanostring of RE hydroxide may be prepared. When the hydroxide is used as precursor, and through annealing at 400-500 deg.c, corresponding Re oxide nanostring may be prepared; and the hydroxide may be calcined at certain temperature to produce corresponding RE oxide nanopowder. When some other RE is doped, composite RE hydroxide, RE oxide nanostring or nanopowder may be prepared. The nanopowder has great specific surface area and the nanostring is anisotropic, so that they may find wide application in various fields.

The invention includes methods in which silicon is removed from titanium-containing container structures with an etching composition having a phosphorus-and-oxygen-containing compound therein. The etching composition can, for example, include one or both of ammonium hydroxide and tetra-methyl ammonium hydroxide. The invention also includes methods in which titanium-containing whiskers are removed from between titanium-containing capacitor electrodes. Such removal can be, for example, accomplished with an etch utilizing one or more of hydrofluoric acid, ammonium fluoride, nitric acid and hydrogen peroxide.

An aqueous solution of metal chlorate, mineral acid and a reducing agent are continuously or intermittently sprayed, in a pattern to achieve intimate mixing, into a spherical chamber creating an aqueous foam reaction mixture generating chlorine dioxide which is removed in a direction 90 degrees to the axis of the spray nozzles. A baffle plate may be used to reduce the open cross sectional area of the exit port to increase reaction efficiency. The reactants are a mineral acid and an alkali metal chlorate or chloric acid and a reducing agent such as hydrogen peroxide. The mineral acid is either diluted or concentrated sulfuric acid, hydrochloric acid, acetic acid, nitric acid or a blend thereof. The ratio of acid is greater than one and less than 3 kg acid per kg of ClO2 formed. The chlorine dioxide may be removed with a stripper column.

The invention relates to a method for leaching an anode and cathode mixed material of a waste lithium nickel manganese cobalt battery, which comprises the following steps: putting an anode and cathode mixed material separated out of a waste lithium nickel manganese cobalt battery in a container which is resistant to pressure and the corrosion of sulphuric acid and nitric acid; then sealing the container and pumping the sulphuric acid and the nitric acid into the container; and leading industrial pure oxygen into the container to leach out the anode and cathode mixed material of the waste lithium nickel manganese cobalt battery, wherein leaching temperature is 20-100 DEG C; leaching pressure is 0.05-0.5MPa; the initial concentration of the leaching sulphuric acid is 1-5mol/L; the initial concentration of the nitric acid is 5-20g/L; reaction time is 1-5 hours; stirring is carried out in a reaction process, and stirring speed is 30-100r/min; and the addition of the sulphuric acid is 101-200 percent of the theoretical sulphuric acid consumption of all leached metal in the anode and cathode mixed material added into the container.

The invention relates to acid solution used for processing the magnesium alloy surface. The acid solution is water solution which contains acids, inhibitor and wetting agent, wherein, the acids are first acids or mixture of first acids and second acids; the first acids are selected from one type or a plurality of types among citric acids, oxalic acids, tartaric acids, methanoic acids, acetic acids, metacetonic acids, butyric acids, glutaric acids, phenylformic acids, benzene dicarboxylic acids, lactic acids, glycolic acids, glyoxylic acids and amino acids; and the second acids are hydrochloric acids and/or nitric acids. By adoption of the acid solution, the magnesium alloy surface can be fully activated; the membranous layer of a converting film which is formed on the magnesium alloy surface after chemical conversion process is compact, has erosion resistance and good binding force with a paint film. Moreover, the method is a environment-friendly method for processing the magnesium alloy surface.

The invention discloses a technique method for producing high-concentration nitric phosphate, which comprises the following steps of: adding nitric acid into phosphorus ore for acidolysis, depositing and separating acid non-soluble substance, freezing and crystallizing calcium nitrate, filtering the calcium nitrate, neutralizing the mother liquid, vaporization, pelleting and drying. The invention is characterized in that: a step of thoroughly removing the calcium of the mother liquid is arranged between the steps of filtering the calcium nitrate, and neutralizing the mother liquid. The steps comprise the following steps of: I) thoroughly removing the calcium of the mother liquid and adding sulfuric acid or ammonium sulfate; the calcium ions and the sulfate ions in the mother liquid generate dihydrate calcium sulfate crystal; II) the grading processing of reaction slurry: employing a grading device to carry out grading processing to the reaction slurry; returning the reaction slurry provided with small grain calcium sulfate to the mother liquid for thoroughly removing the calcium, and feeding the reaction slurry provided with large grain calcium sulfate to the calcium sulfate for filtering; and III) filtering and washing the filtering reaction slurry of calcium sulfate by a filter, feeding the primary filtrate and the primary lavage fluid into the working procedure of neutralizing, and returning the secondary lavage fluid to the filter. The invention has the advantage of using middle-low quality phosphorite to prepare the high-concentration nitric phosphate.

The invention discloses an analysis and detection method for impurity elements such as aluminum, calcium, ion, molybdenum, niobium, titanium, tungsten and the like in chromium carbide. The method comprises adding a chromium carbide sample into a dissolving cup, adding hydrofluoric acid, sulphuric acid and nitric acid sequentially, stirring, charging into a sealed high-pressure jar; putting the sealed high-pressure jar into a microwave extinguishing instrument for two times of microwave extinguishment; taking the high-pressure jar out of the microwave extinguishing instrument for cooling, transferring the dissolved chromium carbide liquid sample into a volumeric flask, diluting to a predetermined index, stirring; preparing a chromium substrate matched mixed standard solution series of aluminum, calcium, iron, molybdenum, niobium, titanium and tungsten; measuring element emission power of aluminum, calcium, iron, molybdenum, niobium, titanium, tungsten or the like in a blank liquid sample, a chromium carbide liquid sample and the prepared series mixed standard solution by an inductively coupled plasma atomic emission spectrometer in the same time, obtaining the analysis result by checking a standard working curve or by linear equation calculation. The invention adopts two times of microwave extinguishment using the mixed acid, solves the problem of hardness in chromium carbide decomposition, having a measurement range from 0.010% to 1.00%, which is high in accuracy, and good in precision.

A conductive carbon nanotube film having high tensile strength and initial tensile modulus comprises primarily oxidized small-diameter carbon nanotubes wherein the diameter of the small-diameter carbon nanotubes are at most about 3 nm. A method for making the film comprises refluxing an aqueous mixture comprising carbon nanotubes and an oxidizing agent to form a refluxed nanotube dispersion; forming a carbon nanotube film from the refluxed carbon nanotube dispersion; optionally removing nitric acid or other oxidizing agent from the carbon nanotube film; drying the carbon nanotube film; and heat-treating the carbon nanotube film to form a heat-treated carbon nanotube film. The method can also comprise sonicating the nanotubes prior to or after refluxing. A heat-treated small-diameter carbon nanotube film can have a tensile strength of over 70 MPa and an initial tensile modulus of about 5 GPa.

The invention discloses the preparation for composite material with nanometal or metal oxide distributed on surface of carbon nanotube uniformly which comprises, stirring and stewing the precursor through long time supersound treatment, the precursor being metal organic compound and concentrated nitric acid treated carbon nano tube, thus resulting in coordination reaction between the metal organic compound and carbon nano tube surface carboxyl and/or carbonyl and/or hydroxyl with the presence of the alcohol solvent action, and forming cores on the carbon nano tube walls so as to form the composite material.

The invention provides a process method for separating and purifying rare earth elements by solvent extraction. The method takes a mixed rare earth sulfate solution obtained from a rare earth ore treated by sulphuric acid as a raw material, directly adopts a nonsaponifiable P507 extraction agent or a synergistic extraction agent containing the P507 to completely extract rare earth in a material liquid into an organic phase, and then takes the organic phase as a rare earth material liquid to extract, separate and purify the rare earth or directly backextract to produce mixed chlorinated rare earth or rare earth nitrate. The process method is simple and flexible, does not saponify the organic phase during the extraction and separation process, does not produce ammonia nitrogen waste water, is easy to backextract middle and heavy rare earths, and has less consumption of acid and base and low production cost.

The invention relates to a method for undergoing a chlorobenzene nitration reaction by using a micro-channel reactor, belonging to the technical field of application of organic synthesis. In the method, nitric acid, sulfuric acid, water and chlorobenzene are taken as initial reaction raw materials, and processes such as mixed acid preparation, mixed acid and chlorobenzene preheating, mixed acid and chlorobenzene reacting and the like are completed in a micro-channel reactor system. In the reaction, nitro-sulfuric mixed acid is taken as a nitrating agent, the effective concentration of sulfuric acid in the mixed acid is 50-90 percent, the molar ratio of the nitric acid to the sulfuric acid in the mixed acid is 1:1-1:10, the molar ratio of the chlorobenzene to the nitric acid is 1:1.0-1:2.0, the reaction temperature is 50-100 DEG C, and the reaction time is 30-120 seconds. The chlorobenzene transformation ratio is up to 97 percent, the selectivity of nitrochlorobenzene serving as a product is over 96.5 percent, and the ratio of ortho-para nitrochlorobenzene is over 0.6. A strengthened mixed micro-channel reactor adopted in the invention is particularly suitable for undergoing a continuous nitration reaction, and has the characteristics of stable temperature control and safe process.

The invention discloses a nitrate molten salt heat transferring and reserving medium and a preparation method and application thereof. The nitrate molten salt heat transferring and reserving medium is prepared with 5 to 40 percent of potassium nitrate, 5 to 25 percent of sodium nitrate, and 10 to 70 percent of calcium nitrate. The melting point of the nitrate molten salt heat transferring and reserving medium can be as low as 120 DEG C, and the upper limit of temperature for use can reach 550 DEG C, the nitrate molten salt heat transferring and reserving medium has a wide temperature scope of application, can work normally at the temperature scope of 180 DEG C to 550 DEG C, and has good thermal stability; the shortcoming of high melting point of binary nitrate molten salt system can be overcome, and the problem of instability caused by easy oxidative decomposition at high temperature of NaNO2 in the Chinese patent 200110027954.1 and ternary nitrate salt system can be solved, and the problems of corrosion and cost increase caused by the existing LiNO3 in the Chinese patent 00111406.9 and the American patent US007588694B1 can also be solved.

One of many universal requirements of dental or orthopedic implants, wherever they are used in the vital body, is that the implant system should be biologically functioning. To achieve the biological functionality, the implant should meet several requirements for compatibility. These include biological compatibility and mechanical compatibility. It has now been recognized that morphological compatibility and crystallographic compatibility should be added to these two compatibility requirements. Hence, the present invention provides a method of forming a certain type of crystalline structure of titanium oxide and controlled surface roughness to meet both morphological and crystallographic compatibilities. It has been further determined that a chemical treatment (using sodium hydroxide) alone or followed by in-air oxidation, or acid treatment (a mixed aqueous solution of hydrofluoric acid and nitric acid), followed by sodium hydroxide treatment, furthermore followed by in-air oxidation provide for advantageous surface modifications to create a complex mixture of rutile with anatase and/or brookite types of titanium oxide and provide a most favorable surface for wettability and an acceptable range of surface roughness.