115results about "Chromium compounds" patented technology

The invention provides a method for preparing an iron-chromium electrolyte and electronic-grade ferrous chloride by using a stainless steel waste liquid. The method comprises the following steps: firstly, adding elemental iron and / or elemental chromium into the stainless steel waste liquid to obtain a chromium-containing ferrous chloride solution; then, sulfide is added, and nickel is removed; adding iron powder to increase the pH value to obtain chromium hydroxide precipitate and a ferrous chloride solution; dissolving chromic hydroxide in hydrochloric acid to obtain a chromic chloride solution; purifying the ferrous chloride solution to obtain an electronic-grade ferrous chloride crystal; and finally, adding a chromium chloride solution, the electronic-grade ferrous chloride crystal and hydrochloric acid according to a certain proportion, and stirring and mixing to obtain the iron-chromium electrolyte. The ferrous chloride prepared by the steps is relatively high in purity and less in waste; meanwhile, the prepared electrolyte is good in electrical property, low in attenuation rate and low in cost, the purpose of comprehensive recycling of resources is achieved, and the general trend of technical improvement is met.

The invention belongs to the technical field of lithium ion batteries, and particularly discloses a metal organic framework packaged polyoxometallate coated ternary positive electrode material and a preparation method thereof. The preparation method of the ternary positive electrode material comprises the following steps: a) preparing metal A salt into a metal A salt solution; the preparation method comprises the following steps: preparing an ammonium molybdate compound into an ammonium molybdate compound solution, heating the ammonium molybdate compound solution to boiling, dropwise adding a metal A salt solution, and after dropwise adding, carrying out a constant-temperature reaction, filtering and recrystallizing to obtain Anderson type polyoxometallate; b) dissolving Anderson type polyoxometallate, a metal B salt and an organic ligand in water, and reacting at a certain temperature to obtain polyoxometallate packaged by a metal organic framework; and c) mixing a positive electrode material and the polyoxometallate packaged by the metal organic framework prepared in the step b) according to a ratio, and carrying out ball milling to obtain the ternary positive electrode material coated by the polyoxometallate packaged by the metal organic framework.

The invention relates to active electrode materials and to methods for the manufacture of active electrode materials. Such materials are of interest as active electrode materials in lithium-ion or sodium-ion batteries. The invention provides an active electrode material expressed by the general formula [M1]x[M2](1−x)[Nb]y[O]z, wherein: M1 and M2 are different; M1 represents one or more of Ti, Mg, V, Cr, W, Zr, Mo, Cu, Fe, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Te, Se, Si, Sb, Y, La, Hf, Ta, Re, Zn, In, or Cd; M2 represents one or more of Mg, V, Cr, W, Zr, Mo, Cu, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Sb, Y, La, Hf, Ta, Zn, In, or Cd; and wherein x satisfies 0<x<0.5; y satisfies 0.5≤y≤49 z satisfies 4≤z≤124.

The invention belongs to the technical field of micro-nano composite materials, and particularly relates to a chromium-based bimetallic sulfide-porous carbon composite material and a preparation method and application thereof. The preparation method of the chromium-based bimetallic sulfide-porous carbon composite material provided by the invention comprises the following steps: mixing chromium salt and zinc salt, or chromium salt and manganese salt with a sulfur source, sodium gluconate and a pore-forming agent, and preparing the composite material through heat treatment and vulcanization technologies. The chromium-zinc or chromium-manganese bimetallic sulfide-porous carbon composite material prepared by the preparation method has good structural stability and conductivity, and the cycling stability of a battery can be remarkably improved when the chromium-zinc or chromium-manganese bimetallic sulfide-porous carbon composite material is used as a battery material. The prepared chromium-based bimetallic sulfide-porous carbon composite material has important application value in the field of lithium ion battery electrode materials.

The invention relates to a modified lithium ion positive electrode material, a manufacturing method thereof and a lithium ion battery. The invention provides a modified lithium ion positive electrode material which comprises a positive electrode material body and a surface coating layer, the chemical composition of the surface coating layer is high-entropy solid electrolyte Li < 7 > La < 3 > (M < x > M < 1 > a M < 2 > b M < 3 > c... Mij) 2O12, M is Zr or Ti, and x is greater than 0; m1, M2, M3... Mi are elements other than Li, La, Zr and Ti, i is a positive integer, 5 < = i < = 10, a, b, c... j are stoichiometric coefficients of the elements, a, b, c... j > = 0, and x + a + b + c +... + j = 1. The high entropy of the solid electrolyte is realized, so that the ionic conductivity at the interface is further improved, and the problem of energy density reduction caused by surface coating is further solved through lithium enrichment.

The invention discloses a chromium-site high-entropy chromium lithium titanate material as well as a preparation method and application thereof, and belongs to the technical field of electrochemical energy storage materials. The crystal structure of the chromium-site high-entropy chromium lithium titanate material is a single spinel solid solution phase, and the chemical general formula of the chromium-site high-entropy chromium lithium titanate material is Li (Cr < 1-x-y-z-w > V < x > Fe < y > Mn < z > Al < w >) TiO4. According to the preparation method, chromium trioxide serves as an oxidizing agent, carbohydrate serves as a reducing agent, and rapid synthesis is achieved through a one-step combustion method. The process is simple and efficient, and the prepared chromium-site high-entropy chromium lithium titanate material has relatively high specific capacity and excellent cycling stability and can be applied as a lithium ion battery negative electrode material. According to the invention, the problems of limited theoretical capacity and poor rate capability of the existing chromium lithium titanate material are effectively solved, and a new way is provided for developing a high-performance lithium ion battery negative electrode material.

An object is to provide a copper-chromium oxide spinel having excellent dispersibility in a resin composition and excellent adhesion to plating, and a resin composition and a resin molded article containing the copper-chromium oxide spinel. Specifically, provided is a copper-chromium oxide spinel with a particle size distribution spread SPAN = (D90 - D10) / D50 of 2 or less where, in volume-converted particle size distribution obtained by a laser diffraction and scattering method, particle sizes with a cumulative frequency from a smaller particle size side of 10%, 50%, and 90% are D10, D50, and D90, respectively.

The present invention relates to an oxygen ion conductor material with high oxygen ion conductivity in the medium and low temperature range and a preparation method thereof. The chemical composition of the material is represented by: Bi4(V 1‑y M y ) x O 11+z , wherein M is a metal cation, 1.7≤x≤2.2 and x≠2, 0<y≤0.3, and z depends on the neutral balance of the metal cation composition. The modified bismuth vanadate Bi4 (V 1‑y M y ) x O 11+z Materials have simple preparation process, low cost, stable structure and high conductivity, among which Bi4(V 0.9 Cu 0.1 ) 1.9 O 10.465 At 300℃, the grain conductivity is 10 ‑2 S / cm level, the total ionic conductivity of ceramics reaches 1.2×10 ‑3 S / cm, which is about 1 order of magnitude higher than the current highest value reported in the literature, and can meet the application requirements of medium and low temperature oxide fuel cells and oxygen sensors.

A method for the resource utilization of chromium-containing sludge involves conditioning, decomposition, and roasting of the sludge. During roasting, a non-oxidizing atmosphere is introduced for protection, ensuring that chromium (Cr) is enriched in the residue in a non-toxic, non-volatile, low-valence state, thus producing high-value-added calcium-chromium sand. Simultaneously, sulfur-containing flue gas is collected during roasting to produce sulfuric acid or sodium sulfite, preventing sulfur diffusion and air pollution. This significantly reduces hazardous solid waste emissions from related production processes and lowers hazardous waste disposal costs. This method achieves both the harmless treatment of chromium-containing sludge and the comprehensive resource utilization of chromium, calcium, and sulfur within the sludge.

The present invention discloses a method for preparing a spinel-type lithium chromium titanate negative electrode material, which belongs to the field of lithium-ion battery electrode materials. The present invention grinds a low-valent compound of solid chromium or metallic chromium powder with a solid titanium compound, a solid lithium-containing compound, and a solid carbohydrate evenly, adds a trace amount of liquid medium to continue grinding and mixing, and then performs a thermal decomposition treatment; the material is taken out and cooled, then ground for a second time, and then placed in a muffle furnace for a second calcination. After cooling, it is ground and carbonized to obtain a spinel-type lithium chromium titanate negative electrode material. The method of the present invention has low preparation cost, is easy to operate and control, has a low reaction temperature, a high yield of the target product, good uniformity, and stable electrochemical performance, and can effectively solve the problem that the existing LCT preparation method is relatively complex and costly.

A method of fabricating plasmonic gold prism arrays for digital surface enhanced Raman spectroscopy, a plasmonic gold prism array arranged on a substrate for digital surface enhanced Raman spectroscopy, and a method of using a plasmonic gold prism array that is arranged on a substrate for digital surface enhanced Raman spectroscopy are disclosed. The method of fabricating plasmonic gold prism arrays for digital surface enhanced Raman spectroscopy includes depositing more than one layers of chromium and gold onto a plasmonic substrate comprising a monolayer of polystyrene beads and removing the monolayer of polystyrene beads under sonication in ethanol.

An object is to provide a copper-chromium oxide spinel having excellent dispersibility in a resin composition and excellent adhesion to plating, and a resin composition and a resin molded article containing the copper-chromium oxide spinel. Specifically, provided is a copper-chromium oxide spinel with a particle size distribution spread SPAN = (D90 - D10) / D50 of 2 or less where, in volume-converted particle size distribution obtained by a laser diffraction and scattering method, particle sizes with a cumulative frequency from a smaller particle size side of 10%, 50%, and 90% are D10, D50, and D90, respectively.

Methods of forming spinel ferrite nanoparticles containing a chromium-substituted copper ferrite as well as properties (e.g. particle size, crystallite size, pore size, surface area) of these spinel ferrite nanoparticles are described. Methods of preventing or reducing microbe growth on a surface by applying these spinel ferrite nanoparticles onto the surface in the form of a suspension or an antimicrobial product are also described.

The present invention provides a method for preparing a rare earth-site-modified hydrotalcite-based oxygen evolution catalyst. The preparation method comprises the following steps: constructing a hydrotalcite precursor with selective metal vacancies by hydrothermal-alkali etching, and then introducing rare earth elements into the hydrotalcite precursor at specific points to obtain a rare earth-precisely modified hydrotalcite-based oxygen evolution catalyst. The hydrotalcite-based oxygen evolution catalyst of the present invention has a stable structure, abundant active sites, excellent oxygen evolution catalytic performance and stability, and has a prospect for large-scale promotion and application.

The invention relates to active electrode materials and to methods for the manufacture of active electrode materials. Such materials are of interest as active electrode materials in lithium-ion or sodium-ion batteries. The invention provides an active electrode material expressed by the general formula [M][Nb]y[O]z; wherein the active electrode material is oxygen deficient; wherein M consists of one of Mg, Cr, W, Mo, Cu, Ga, Ge, Ca, K, Ni, Co, Al, Sn, Mn, Ce, Sb, Y, La, Hf, Ta, Zn, In, or Cd; y satisfies 0.5≤y≤49; and z satisfies 4≤z≤124.

The present invention provides a method for resource recovery of chromium-containing electroplating sludge, including the process steps of pigment preparation and metal recovery. Among them, the ceramic pigment is prepared by a solid-phase method using chromium-containing electroplating sludge and calcium-silicon substances as raw materials. The waste liquid generated during the preparation process realizes the cascade recovery of metals through the methods of adding iron powder to reduce and precipitate copper, hydrogen peroxide to oxidize and precipitate iron, and reduction and flocculation to precipitate chromium. The recovered chromium hydroxide can be returned to the raw material electroplating sludge for secondary utilization. The present invention prepares a ceramic pigment with good color rendering effect and excellent acid and alkali resistance through a simple solid-phase reaction method. Moreover, the purity of the grossularite phase Ca3Cr2(SiO4)3 is relatively high, with stable properties, acid and alkali resistance, and at the same time realizes the cascade recovery of metals. The present invention realizes the resource utilization of chromium-containing sludge, a solid hazardous waste, in the field of ceramic pigments. The process is simple, easy to control, environmentally friendly, and the raw materials are cheap and easily available, greatly reducing the production cost and having good economic and environmental benefits.

The application relates to the technical field of battery materials, and discloses a lithium secondary battery positive electrode coating material as well as a preparation method and application thereof. 3+z Nb 1‑ x M x O 4‑y R y wherein M is selected from one of Fe, Ti, Mn, Mo, W, V, Ta and Cr; R is selected from one of F, Cl, Br and I; 0<=x<1, 0<=y<=4, and the values of x, y and z satisfy the charge balance of the positive electrode coating material. The application integrates the triple functions of thermodynamic interface protection, fast ion conduction and charge compensation in a single material through cation, anion or anion-cation co-doping design based on Li3NbO4 as a matrix; the positive electrode coating material can significantly reduce the solid-solid interface impedance in a full solid-state battery, improve the first circle coulomb efficiency, and greatly improve the long cycle stability of an electrode; meanwhile, the positive electrode coating material can effectively inhibit the decomposition of high-voltage electrolyte in a traditional liquid battery, and improve the cycle life of a positive electrode material.

A cold storage material, which has a large specific heat and a small magnetization in an extremely low temperature region and has satisfactory manufacturability, is provided, and a method for manufacturing the same is provided. Further, a refrigerator having high efficiency and excellent cooling performance is provided by filling this refrigerator with the above-described cold storage material. Moreover, a device incorporating a superconducting coil capable of reducing influence of magnetic noise derived from a cold storage material is provided. The cold storage material of embodiments is a granular body composed of an intermetallic compound in which the ThCr2Si2-type structure (11) occupies 80% by volume or more, and has a crystallite size of 70 nm or less.

This provides a new material that exhibits negative thermal expansion. [Solution] The negative thermal expansion material is Ti (3) 2-x M x O3(M contains at least one element selected from Mg, Al, Si, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, Zr, Nb, Mo, Ag, In, Sn, Sb, La, Ta, W, Bi, 0

The invention relates to a class of electrochemical energy storage materials and a preparation method and application thereof. A porous metal oxide-based electrochemical energy storage material at least comprises a host metal oxide with a hierarchical pore structure; wherein, the host metal oxide is a single crystal, quasicrystal, or twin crystal structure with ordered atomic lattice arrangement, the crystal is rich in oxygen atom vacancy defects, the structural general formula is MxOy-z, wherein M is selected from one or more combinations of niobium element, molybdenum element, titanium element, vanadium element, manganese element, iron element, cobalt element, nickel element, copper element, zinc element, tungsten element, tantalum element, and zirconium element; and 1≤x≤2, 1≤y≤5, and 0.1≤z≤0.9, preferably Nb2O5-z.

The present application relates to modified lithium ion positive electrode material and its manufacturing method, and lithium ion battery. A modified lithium ion positive electrode material is provided, which comprises a positive electrode material body and a surface coating layer, wherein the chemical composition of the surface coating layer is high-entropy solid-state electrolyte Li7La3(M x M1 a M2 b M3 c …Mi j )2O 12 , wherein M is Zr or Ti, and x>0; M1, M2, M3…Mi are elements other than Li, La, Zr and Ti, i is a positive integer and 5≤i≤10, a, b, c…j are stoichiometric coefficients of each element, a, b, c…j≥0, and x+a+b+c+…+j=1. The present application further improves the ion conductivity at the interface by high-entropy of the solid-state electrolyte, and further reduces the problem of energy density reduction caused by surface coating by lithium enrichment.

The invention provides a wide-band-gap ferromagnetic insulator material. The chemical formula of the wide-band-gap ferromagnetic insulator material is Cd2CrSbO6. The invention also provides a method for preparing the wide-band-gap ferromagnetic insulator material, which comprises the following steps: (1) sufficiently grinding and mixing CdO, Cr2O3 and Sb2O5 in a protective gas atmosphere to obtain a mixture; (2) sealing and wrapping the mixture, and then carrying out heating and pressurizing treatment; and (3) cooling and depressurizing the treated product obtained in the step (2). The ferromagnetic insulator material Cd2CrSbO6 disclosed by the invention has a potential application value in spintronics devices.

This invention discloses a copper-chromium catalyst, its preparation method, and its application. The preparation method of the catalyst includes: (1) mixing polylactic acid with dichloromethane and ethanol to obtain a polymer solution, adding a soluble copper salt to it, stirring, and obtaining a spinning solution; (2) using a coaxial electrospinning nozzle to perform electrospinning with the obtained spinning solution, and collecting the obtained solid; (3) placing the obtained solid in an ethanol solution of trimesic acid to react, washing and drying after the reaction, and collecting the obtained solid; (4) dissolving a soluble chromium salt in ethanol and reacting it with the obtained solid, then washing and drying, and collecting the obtained catalyst precursor; (5) calcining the obtained catalyst precursor to obtain an unformed catalyst, then pressing it into tablets to obtain the copper-chromium catalyst. This catalyst can improve the conversion rate and selectivity of the catalyst in the hydrogenation of dimethyl maleate to prepare 1,4-butanediol and co-production of γ-butyrolactone and tetrahydrofuran.

The invention relates to the technical field of hazardous waste disposal and utilization, in particular to a technological method for co-disposal of chromic anhydride waste and waste zinc phosphide, which comprises the following steps: dissolving chromic anhydride waste in a dissolving tank according to a certain solid-to-liquid ratio, and hydrolyzing chromic anhydride to generate chromic acid; the method comprises the following steps: adding a certain proportion of an inorganic acid solution into a chromic acid solution, and combining chromate ions with hydrogen ions to generate dichromate ions under an acidic condition; transferring the solution into a closed first-stage reactor, and slowly stirring; according to the method, firstly, the method is suitable for chromic anhydride waste and zinc phosphide waste, waste chromate, dichromate waste and aluminum phosphide waste can be used, harmless treatment of the hazardous waste can be completed, secondly, reagents used in the treatment process only need phosphoric acid, hydrogen peroxide and sodium hydroxide, ferrous sulfate is not used as a reducing agent, and the method is environmentally friendly. The production of a large amount of iron mud is avoided, and finally, the produced secondary waste can be recycled, so that the aim of turning waste into wealth is fulfilled.

A solid electrolyte, a method of preparing the same, and a secondary battery including the same, wherein the solid electrolyte comprises a metal oxide including lithium, silicon, and boron, and a metal comprising at least one of iron, chromium, lanthanum, or thallium, and the solid electrolyte has a glass structure containing 60 mol% or greater of lithium based on 100 mol% of the total amount of the metal and lithium, silicon, and boron, and wherein the solid electrolyte has a softness of 152 1 / BHN or greater, wherein 1 / BHN is an inverse of a Brinell hardness number as measured in accordance with ISO 6506.

Doped titanium niobate is provided, which has a chemical structure of Ti(1-x)M1xNb(2-y)M2yO(7-z)Qz or Ti(2-x′)M1x′Nb(10-y′)M2y′O(29-z′)Qz′, wherein M1 is Li, Mg, or a combination thereof; M2 is Fe, Mn, V, Ni, Cr, or a combination thereof; Q is F, Cl, Br, I, S, or a combination thereof; 0≤x≤0.15; 0≤y≤0.15; 0.01≤z≤2; 0≤x′≤0.3; 0≤y′≤0.9; and 0.01≤z′≤8.

The invention provides an oxygen-containing small-molecule intercalated hydrotalcite, a rubber composite material, and a preparation method and application of the oxygen-containing small-molecule intercalated hydrotalcite and rubber composite material. The oxygen-containing small molecule intercalated hydrotalcite is obtained by mixing and reacting components including ethanol salt, methoxide and a solvent; the ethanol salt comprises divalent ethanol salt and trivalent ethanol salt; the rubber composite material is prepared from the following components: rubber, oxygen-containing small molecule intercalated hydrotalcite and a vulcanizing agent. The oxygen-containing micromolecule intercalated hydrotalcite prepared by the method has larger interlayer spacing and better dispersity in a rubber matrix, interlayer water can be removed at the temperature of 100 DEG C or below, the influence in the vulcanization process is avoided, and the oxygen-containing micromolecule intercalated hydrotalcite is suitable for a high-temperature vulcanization environment, is used in a rubber composite material and can improve the gas barrier property of the composite material.