248 results about "Lanthanoid Series Elements" patented technology

The invention provides a high performance lithium ion battery anode material lithium manganate and a preparation method of the material. The lithium manganate is a doped lithium manganate LiMn2-yXy04 which is doped with one kind or a plurality of other metal elements X, wherein X element is at least one kind selected form the group of aluminium, lithium, fluorine, silver, copper, chromium, zinc, titanium, bismuth, germanium, gallium, zirconium, stannum, silicon, cobalt, nickel, vanadium, magnesium, calcium, strontium, barium and rare earth elements lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium and lutetium, and y is larger than 0 but less than or equal to 0.11. The lithium ion battery anode material lithium manganate provided in the invention has extraordinary charge and discharge cycle performance both in the environments of normal temperature and high temperature. According to the invention, the preparation method of the material is a solid phase method, the operation is simple and controllable and the cost is low so that it is easy to realize large-scale productions.

This invention provides a petroleum hydrocarbon catalytic decomposition accelerant and its application. This accelerant includes following components: (1) lanthanide, its weight amount is 0.1-25%; (2) phosphorus or boron, its weight amount is 0.1-10%; (3) base metal, alkali metal and transition metal, their weight amount is 0.1-15%; (4) The others are ZSM-5,ZRP used as carrier. This accelerant used for production of low carbon alkenes by cracking heavy magnesium alkanes, with space velocity of gas 1-25hr-1, such as naphtha, diesel oil, educed pressure diesel and so on. The yield of ethylene, propylene, butylenes and butadiene will improve by 5%.

The invention relates to a lanthanon Y which is utilized to strengthen magnesium alloy effectively and a preparation technology thereof, in particular to a quasicrystal phase which is utilized to strengthen Mg-Zn-Y-Zr magnesium alloy and a preparation method thereof, and the problems such as magnesium alloy strengthening, etc. are solved. On the premise of definite Y contents, the volume percentage of the quasicrystal phase which is led into a magnesium alloy matrix to reach the maximum through reasonably choosing the rate between Zn and Y in the alloy (the rate between Zn and Y ranges from 6 to 15), so as to prepare the Mg-Zn-Y-Zr magnesium alloy with low density, high strength and better plasticity. The magnesium alloy material has the components and the contents thereof as follows: the content of zinc (Zn) ranges from 5 to 30 percent; the content of yttrium (Y) ranges from 0.5 to 5 percent; the content of zirconium (Zr) ranges from 0.3 to 0.8 percent, and the others are magnesium (Mg); all the percentage are weight percentage. The magnesium alloy material are processed through alloy melting and subsequent hot extrusion processing and deformed into products, and the operation of the processing technology is simple and convenient. The tensile strength of the material satisfies that Sigma (b) ranges from 290 to 360MPa, the yield stress delta0.2 ranges from 175 to 260MPa, the unit extension Delta ranges from 10 to 18 percent, and the density is 1.84 to 2.73g/cm<3>.

The invention relates to a catalyst for changing and transforming carbon monoxide in hydrogen-rich fuel gas of coke-oven gas according to a water gas shift reaction and a preparation method thereof, which belong to the technical field of water gas shift processes and catalysts. The catalyst takes copper or iron as an active component, takes zinc, rare earth element cerium or lanthanum and one of boron, aluminum or indium as auxiliary agents, and is prepared by adopting a solution precipitation method. A mixed salt solution of metal nitrates or sulfates is subjected to processes such as homogenization treatment by ultrasonic wave, co-precipitation, constant-temperature aging, drying, baking and the like to finally obtain the mixed metal solid catalyst. The catalyst prepared by the method has the advantages of higher activity, good dispersivity, and large specific surface area, and has high water gas shift activity in the hydrogen-rich fuel gas (VH2 is more than 75 percent), and the transformation ratio of carbon monoxide of the catalyst can approach 100 percent.

A semiconductor processing component includes a substrate and a layer overlying the substrate. The layer has a composition ReA_yO_1.5+2y, wherein Re is Y, La, a Lanthanoid series element, or a combination thereof, A is (Si_1−aGe_a), 0.25≦y≦1.2, and 0≦a≦1.

The invention relates to a catalytic material for purifying tail gas of an automobile, in particular to a cerium oxide and zirconium oxide based sosoloid catalyst, a preparation method and application thereof. The cerium oxide and zirconium oxide based sosoloid catalyst comprises 50-79.5wt% of zirconium oxide, 20-49.5wt% of cerium oxide and 0.5-25wt% of oxides of other elements, wherein the zirconium oxide, the cerium oxide and the oxides of other elements is present in a sosoloid form, and the oxides of other elements are one or more oxides of lanthanons except cerium. The preparation method is as follows: continuous coprecipitation is carried out on zirconium oxychloride, saline solution of cerium and saline solution of lanthanons except cerium to obtain the cerium oxide and zirconium oxide based sosoloid catalyst. In the invention, by adding the zirconium oxide and the oxides of the lanthanons except cerium, the prepared cerium oxide and zirconium oxide based sosoloid catalyst has favorable catalytic performance and greatly improved thermal stability. The preparation method can prepare the cerium oxide and zirconium oxide based sosoloid catalyst under relatively lower temperature and normal pressure.

The invention provides a novel sintered neodymium-iron-boron permanent-magnet material containing holmium and a manufacture method thereof. The novel sintered neodymium-iron-boron permanent-magnet material has the structural formula as follows: LnAlphaHoBetaBGammaMxNyFe100-Alpha-Beta-Gamma-x-y, wherein Ln is lanthanon comprising Nd and one or more selected from Pr, Dy and Tb; M is an additive element comprising Co and Cu; N is an additive element comprising one or more selected from Al, Ga, Nb, Zr and Ti; Alpha, Beta, Gamma, x and y are weight percentages of each element; Fe is an Fe element or unavoidable impurities; and Alpha is mare than or equal to 29 and less than or equal to 33, Beta is more than or equal to 0.5 and less than or equal to 4, Gamma is more than or equal to 0.95 and less than or equal to 1.20, x is more than or equal to 0 and less than or equal to 3.5, and y is more than or equal to 0 and less than or equal to 1.50. In the invention, the addition of Ho has a remarkable function in improving the Hcj of a magnet.

This invention discloses a fin heat-exchanger made of aluminum alloy foil and its preparation method. The ingredient and ratio of the alloy are as follows: iron is 0.15-0.40%, silicon is 0.05-0.30%, copper is 0-0.10%, manganese is 0.05-0.30%, the element of rare-earth is 0.05-0.4%, titanium is 0.010-0.060%, the other is aluminum. The ingredient and ratio of rare-earth is as follows: lanthanum is 20-40%, cerium is 45-65%, praseodymium is 5-15%, neodymium is 1-9%, samarium is 0-0.05%, yttrium is 0-0.05%,the other is impurities. The preparation method includes four processes: the preparation of rare-earth aluminum alloy, the casting of blank, cold-rolling of slat and heat treating. Contrasting to the existing aluminum alloy material, the product has the better extension and toughness, the smaller aeolotropism at the same thickness and hardness, and it can be suitable to punch at high flanged fill heat-exchanger and could not crack.

The present invention relates to a new type of green luminophore composed of mixed rare-earth phosphates, and a method of preparation of these new luminophores from precursors comprising particles having a mean diameter of between 1.5 and 15 microns, these particles comprising an inorganic core and a shell composed of a mixed lanthanum and/or cerium phosphate, optionally doped with terbium, evenly covering the inorganic core with a thickness greater than or equal to 300 nm.

The invention provides a manganese-copper based composite oxide doped rare earth element catalyst for catalyzing volatile organic compounds (VOCs) as well as a preparation method and application of the catalyst. The catalyst disclosed by the invention adopts a high-pore-volume cordierite honeycomb ceramic material as a carrier, and the carrier is sequentially coated with a first metal oxide coating layer, a second metal oxide coating layer and a third metal oxide coating layer from the inside to the outside, wherein the first metal oxide coating layer is active aluminum oxide, the second metaloxide coating layer is a hafnium-lanthanum-cerium oxide, and the third metal oxide coating layer is a manganese-copper based oxide. The catalyst provided by the invention adopts a non-precious metalinstead of a precious metal; and the catalyst provided by the invention has uniformly-dispersed coating layers, binding force between an active component and a matrix is strong, the coating layers arenot easy to fall or crack, and the catalyst can maintain higher activity under high-speed airflow and thermal shock, has stable activity when being used repeatedly, strong catalytic activity to the VOCs, a simple preparation process and low costs, and is suitable for large-scale production.

A method is provided for forming a rare earth (RE) element-doped silicon (Si) oxide film with nanocrystalline (nc) Si particles. The method comprises: providing a first target of Si, embedded with a first rare earth element; providing a second target of Si; co-sputtering the first and second targets; forming a Si-rich Si oxide (SRSO) film on a substrate, doped with the first rare earth element; and, annealing the rare earth element-doped SRSO film. The first target is doped with a rare earth element such as erbium (Er), ytterbium (Yb), cerium (Ce), praseodymium (Pr), or terbium (Tb). The sputtering power is in the range of about 75 to 300 watts (W). Different sputtering powers are applied to the two targets. Also, deposition can be controlled by varying the effective areas of the two targets. For example, one of the targets can be partially covered.

The invention relates to a method for preparing luminescent nano-particles of rare earth doped with lanthanum phosphate, comprising the following steps: preparing stock solutions including lanthanum nitrate polyol solution doped with rare earth element of Ln and polyol solution of NaH2PO4-2H2O; mixing the stock solutions in a micro mixer and heating the mixture in oil under constant temperature after the mixture enters the micro-channels, after which the mixture will react to produce polyol solution of luminescent nano-particles of rare earth doped with lanthanum phosphate; obtaining luminescence nano-particles of rare earth doped with lanthanum phosphate by extracting, washing and centrifugal separation. With simple technology and easy for batch production, the obtained nano-particles are provided with small particles, good dispersibility and fluorescence.

The invention relates to a nuclear power pipe fittings material forging and a manufacture process, the manufacture process comprises the following steps: selecting materials, blanking, heating, forging, performing thermal treatment after forging, machining, performing physical and chemical inspection and ultrasonic flaw detection, performing thermal treatment, performing finish machining and ultrasonic flaw detection or magnetic powder inspection, cleaning the package and packaging. According to the limitation of components and technological parameters, a proper amount of lanthanide series rare earth element is added, the thermal treatment process with twice normalizing and twice tempering can avoid the intergranular precipitation of a carbide, carburization and nitridation during the thermal treatment process can be avoided, and the corrosion resistance of the material can be avoided.

The invention discloses a high-melt-strength polypropylene material, and a preparation method and application thereof. The polypropylene material is prepared from 65-99.79 parts of polypropylene, 0.01-10 parts of initiator, 0.1-10 parts of polyfunctional group monomer, 0.1-5 parts of free radical stabilizer and 0-10 parts of inert processing assistant, wherein the free radical stabilizer is a lanthanide rare-earth oxide, carboxylate of lanthanide rare-earth element, naphthenate complex of lanthanide rare-earth element or dithiocarbamic acid rare-earth compound. The lanthanide rare-earth element does not include promethium. The proportion of the polypropylene, initiator and polyfunctional group monomer is controlled, the grafting reaction time is prolonged, and the rare-earth substances are utilized to inhibit the degradation of the polypropylene and prolong the service life of the free radical, thereby obtaining long-branched-chain high-melt-strength polypropylene with stable performance and enhancing the service performance of the conventional polypropylene. The method disclosed by the invention is easy to operate and convenient to control, and can easily implement industrial production.

The invention is relates to components of electric contact material and fabricating technique. Weight percentage of each component is a following: 70-95% Ag, 2.5-20% stannic oxide, 0.025-1% magnesia and 0.025-9% lanthanum or cerium. Compound powder of Ag, SnO2, MgO, La or Ce in Nano amorphous or crystalloid is prepared through high-octane ball milling. Structure, decentrality and dimensional stability of Nano granules are improved by adding lanthanide series into material. Thus, formability and electrical property of electric contact alloy are improved as well as ablation rate of contact is reduced and service life is increased.

The invention relates to the technical field of rare earth resource recovery, in particular to a diphenylamino oxocarboxylic acid extraction agent and a preparation method and application thereof. The diphenylamino oxocarboxylic acid extraction agent has a structure shown in a formula (I); and in the formula (I), R1 and R2 are independently selected from H or C1-C9 alkyl groups, and n is a natural number from 1 to 6. The diphenylamino oxocarboxylic acid extraction agent provided by the invention can be used for effectively separating yttrium from lanthanide, and compared with an industrially applied naphthenic acid extraction agent, the extraction agent provided by the invention has the advantages of simplex component, stable chemical structure, no reduction of the concentration of an extracted organic phase and stable extraction performance; and moreover, the coefficient of the diphenylamino oxocarboxylic acid extraction agent for separating yttrium from light rare earth elements is obviously higher than that of the naphthenic acid extraction agent, the coefficient of the diphenylamino oxocarboxylic acid extraction agent for separating yttrium from heavy rare earth elements is also higher than that of the naphthenic acid extraction agent, and the diphenylamino oxocarboxylic acid extraction agent can completely replace the naphthenic acid extraction agent in the aspect of separation efficiency and has quite good application prospects.

The invention discloses a corrosion-resistant copper alloy, which comprises the following compositions by weight percent: 1.0-1.2% of Mn, 0.5-0.7% of Si, 0.05-0.15% of Fe, 0.8-1.2% of Mg, 2-4% of Zn, 11-13% of Al, 1.2-1.4% of Ti, 0.3-0.5% of Sc, 5.5-6.5% of Ni and 0.2-0.3% of composite mischmetal, wherein the composite mischmetal contains La and Ce mischmetal elements, the percentage of Ce is 30-50%, and the balance is Cu.

The invention provides a high-strength high-toughness Mg-Al-Mn die cast magnesium alloy containing lanthanum-cerium rare earth compound, which is composed of 97% to 90% by mass of AM60 magnesium alloy and 3% to 10% by mass of magnesium-lanthanum cerium interalloy in a proportion of 3% to 10%. The magnesium-lanthanum cerium interalloy is prepared by 80% by mass of magnesium ingot and 20% by weight of lanthanum-cerium rare earth compound; the lanthanum-cerium rare earth compound is the residual lanthanum-cerium rare earth compound after Pr and Nd are separated from cerium-rich rare earth compound, composed of 20% to 80% by mass of Ce, 80% to 20% by mass of La and no more than 1% of other rare earth elements. Comparing the preparing method with that of traditional magnesium alloy, the differences lies in: magnesium-lanthanum cerium interalloy is first prepared, and then magnesium-lanthanum cerium interalloy is added during smelting process. The rare earth has small lose, is easy to control its compositions, the smelting time is shorted, thus to improve the alloy quality.

The invention discloses a halogen-free flame retardant. The halogen-free flame retardant has a structural formula as follows, wherein M is rare earth element series of lanthanum, cerium or praseodymium; and n2 is an integer from 1 to 4. A method for preparing the halogen-free flame retardant comprises the following steps: 1, synthesizing melamine phosphate; 2, carrying out polycondensation on the melamine phosphate (MP) to form melamine pyrophosphate (MPP); and 3, carrying out end sealing reaction to synthesize metal melamine pyrophosphate (MMPP). A rear earth metal chloride end sealing group is added during the polycondensation of the product, as rare earth elements have unique valence shell structures and physicochemical properties, coordination bonding is realized except chemical bonding, the thermal stability of MMPP is increased, and after the MMPP is mixed with polyvinyl plastics, the flame retardant property of the polyvinyl plastics can be greatly improved. The MMPP does not contain halogen, has high thermal stability and does not generate toxic hydrogen halide gas easily.

The invention discloses a catalyst for producing difluoro acetylfluoride by catalyzing and cracking 1, 1, 2, 2-tetrafluoethyl alkyl ether and a preparation method thereof. The preparation method comprises the following steps of taking pseudo-boehmite powder (specific surface area of 400m2/g) and at least one type of water-soluble salt of other elements such as zirconium, yttrium, lanthanum cerium and praseodymium as an original raw material; mixing the original raw material with water; gradually adding ammonia in the solution during the mixing process till the pH value of colloidal substance achieves 7 to 9; subsequently carrying out ageing, filtering, water washing, drying, roasting in air, pressing and forming; and then pumping HF/N2 mixed gas or fluorochloromethane, thus obtaining the catalyst by activation. The catalyst has the advantages such as a high specific surface area, a plurality of uniformly distributed active acid centers and excellent mechanical strength, thereby having high activity and high stable performance.

The invention belongs to the field of metallurgy, and relates to a lead-antimony rare-earth positive grid alloy and a preparation method thereof. The alloy comprises the following metal elements in percentage by mass: 0.5 to 1 percent of antimony, 0.005 to 0.1 percent of lanthanum, 0.005 to 0.1 percent of samarium, and the balance of lead. The preparation method comprises the following steps: preparing lead-lanthanum and lead-samarium alloy as master alloys; adding pure antimony into molten lead, stirring until the pure antimony is completely molten; and adding the lead-lanthanum and lead-samarium master alloys to perform mixed melting to prepare the lead-antimony rare-earth positive grid alloy. Grains of the prepared alloy become fine, uniform and regular, so that the comprehensive mechanical performance of the alloy can be improved, the impedance of an oxide film can be reduced, and the charge and discharge acceptance and deep cycle performance of a storage battery can be improved. Meanwhile, rare-earth element serves as an additive to prepare the lead-antimony grid alloy, arsenic, cadmium and other elements harming the environment and workers on the forefront of production severely are not contained. Therefore, lead alloy pollution can be reduced furthest.