814 results about "Rhodium" patented technology

The invention provides a method and system for detecting the content of platinum, palladium and rhodium in an automobile exhaust purification catalyst and application, and relates to the technical field of automobile exhaust purification, the method comprises the following steps: crushing, grinding, sieving, performing microwave acidolysis, neutralizing, washing and drying a catalyst sample to obtain dry filter residues; a trapping agent and a fluxing agent are added into the dry filter residues, constant-temperature heating is conducted in inert gas, then cooling forming is conducted, and an alloy button is obtained; blowing ash on the alloy, then adding mixed acid into the alloy, heating the alloy in a water bath at 95 DEG C for 25-35 minutes to obtain a dissolved solution, then adding a masking agent into the dissolved solution, and oscillating to obtain a solution to be detected; and filtering the liquid to be detected, fixing the volume and detecting. According to the method, precise quantification of trace platinum, palladium and rhodium in the complex matrix catalyst can be realized, and the method has a relatively high recovery rate; meanwhile, pollution elements are prevented from being used, and the method is green and efficient and better conforms to the concept of green chemistry.

The invention provides a multi-component platinum-bismuth-based intermetallic ordered nanosheet as well as a preparation method and application thereof, and relates to the technical field of multi-metal alloy catalysts. The multi-component platinum-bismuth-based intermetallic ordered nanosheet provided by the invention comprises a platinum element, a bismuth element and auxiliary metal elements, the auxiliary elements comprise 1-4 of an iridium element, a ruthenium element, an osmium element, a rhodium element, a tin element and a lead element, and the multi-component platinum-bismuth-based intermetallic ordered nanosheet has an intermetallic ordered structure and a two-dimensional nanosheet morphology. The multi-component platinum-bismuth-based intermetallic ordered nanosheet provided by the invention is stable in structure, is applied to a fuel cell as a catalyst, and has excellent electro-catalytic performance, including formic acid oxidation electro-catalytic performance and alcohol oxidation electro-catalytic performance. The invention provides the preparation method of the multi-component platinum-bismuth-based intermetallic ordered nanosheet, the preparation condition is mild, the operation is simple, and the problems of catalyst agglomeration and the like caused by conversion from high-temperature calcination to an ordered phase are effectively avoided.

A light-emitting device including an organometallic compound having a metal such as is platinum (Pt), palladium (Pd), copper (Cu), silver (Ag), gold (Au), rhodium (Rh), ruthenium (Ru), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), or thulium (Tm) is provided. The light-emitting device may include a first electrode, a second electrode facing the first electrode, an interlayer between the first electrode and the second electrode and comprising an emission layer. The light-emitting device may be included in an electronic apparatus.

Disclosed herein is a catalyst including a multicomponent alloy including a seed and al least four elements. The seed includes at least one platinum group metal, wherein the platinum group metal includes platinum, ruthenium, iridium, palladium, or rhodium. Methods of preparing the catalyst are also provided herein.

The invention relates to a method for manufacturing a bipolar plate (2), comprising the following steps: - Provision of two steel half-sheets (3, 4), wherein at least one of the two half-sheets (3, 4) has an embossed structure (5), - Construction of a three-dimensional metal structure (7) from at least one powder (12) of a metal different from the steel of the half-sheets (3, 4), wherein the metal is selected from the group comprising titanium, titanium alloys, nickel, nickel alloys, chromium, chromium alloys, ferrochrome alloys, copper, copper alloys, silver, silver alloys, or gold, platinum, iridium, rhodium, ruthenium and their alloys, on a first half-sheet (3) of the two half-sheets (3, 4) by means of a laser (10) with green laser light and consequently a wavelength in the range of 495 nm to 550 nm, and - Forming a material-bonded connection of the 3D metal structure (7) with a second half-sheet (4) of the two half-sheets (3, 4) using the same laser (10), wherein the half-sheets (3, 4) are joined to form a bipolar plate (2). The invention further relates to a bipolar plate (2) for an electrochemical cell (20).

The present invention relates to the field of catalyst technology, discloses a supported noble metal catalyst and its preparation method and application, the catalyst includes a first carrier and a coating loaded on the first carrier, the raw material composition for preparing the coating includes a second carrier, an active component precursor, an auxiliary agent precursor, a binder and a dispersant; the first carrier is cordierite, mullite or cordierite-mullite; the second carrier is titanium dioxide and / or aluminum oxide; the active component precursor is selected from at least one of a platinum precursor, a palladium precursor and a rhodium precursor; the auxiliary agent precursor is a combination of a cerium precursor, a zirconium precursor and a neodymium precursor; the binder is a mixture of an organic binder, an inorganic binder and a coupling agent. The supported noble metal catalyst has low production cost, high catalytic activity, strong anti-poisoning ability and long service life, can be used for the removal of volatile organic compounds, and is particularly suitable for the removal of flue gases such as ethylene and propane with large air volume and low concentration of organic small molecule hydrocarbons.

A sensor comprising one or more metal oxides as sensor material is used to detect pathogen-derived VOCs, such as those released from an infected wound. The metal oxides can comprise one or more metal elements selected from aluminum, antimony, bismuth, boron, cerium, chromium, cobalt, copper, gold, indium, iridium, iron, lanthanum, lead, manganese, molybdenum, nickel, niobium, osmium, palladium, platinum, rhodium, ruthenium, selenium, silicon, silver, tantalum, tellurium, terbium, tin, titanium, tungsten, vanadium, ytterbium, yttrium, zinc, and zirconium. The sensor device can have one or more sensors that detect and record various VOCs indicative of the presence of pathogens, which are associated with mortality and / or infection.

To provide a method for effectively separating and recovering rhodium from an acidic aqueous solution containing platinum, palladium, and rhodium.SOLUTION: A method for recovering rhodium includes the steps for: adding dimethyl sulfoxide to an acidic aqueous solution containing platinum, palladium, and rhodium, followed by adding a reducing agent to the acidic aqueous solution for the precipitation of platinum and palladium, and then separating the solid and liquid phases to recover platinum and palladium; and recovering rhodium from the platinum and palladium post-recovery solution obtained in the platinum and palladium recovery step.SELECTED DRAWING: Figure 1

To provide an EUV mask blank which prevents damage to a multilayer reflective film due to dry etching using a halogen gas as an etching gas, and dry etching using an oxygen-based gas as an etching gas.SOLUTION: In a reflective mask blank for EUV lithography, a multilayer reflective film reflecting EUV light, a protective film for the multilayer reflective film, and an absorption layer absorbing EUV light are formed in this order. The protective film is made of rhodium (Rh) or a rhodium material including Rh and at least one element selected from the group consisting of nitrogen (N), oxygen (O), carbon (C), boron (B), ruthenium (Ru), niobium (Nb), molybdenum (Mo), tantalum (Ta), iridium (Ir), palladium (Pd), zirconium (Zr), and titanium (Ti).SELECTED DRAWING: None

The invention relates to a method for purifying rhodium from a complex-component rhodium leaching solution, and belongs to the technical field of precious metal refining and purification. The method comprises the following steps: adding a reducing agent into rhodium leaching liquid for reduction to obtain RhCl3 primary purification liquid and insoluble slag; simultaneously adding sulfite and ammonium salt into the RhCl3 primary purification liquid to precipitate rhodium in the form of (NH4) 3Rh (SO3) 3; hydrochloric acid is added into the (NH4) 3Rh (SO3) 3 precipitation residues, heating and boiling are conducted, the (NH4) 3Rh (SO3) 3 precipitation residues are dissolved in the form of RhCl3 and enter a solution, SO3 < 2-> in the solution is removed in the form of SO2, and a secondary purification solution of RhCl3 is obtained; adding a strong oxidant into the secondary purified solution of RhCl3, and carrying out oxidation reaction to obtain RhCl4; adding alkali into the RhCl4 solution to adjust the pH value, and boiling to obtain RhO2. 2H2O precipitation slag; and the RhO2. 2H2O precipitation slag is sequentially subjected to pure water slurrying, hydrazine hydrate reduction, calcination and hydrogen reduction to obtain the high-purity metal rhodium. According to the method disclosed by the invention, the high-purity metal rhodium of which the purity is greater than 99.95% can be prepared, and the direct recovery rate of rhodium is greater than 97%.

The invention discloses a method for electrocatalytic hydrogenation dehalogenation of haloacetic acid or halomethane in a water body, which is characterized in that a conductive material of which the surface is modified with ruthenium or platinum is used as a catalytic cathode, water is used as a hydrogen source, and the haloacetic acid or halomethane in the water body is subjected to electrochemical hydrogenation dehalogenation to form acetic acid or methane. The price of precious metal in the catalytic cathode is lower, and the unit price of ruthenium is far lower than that of palladium and rhodium; and compared with a palladium-modified catalytic cathode, the dechlorination selectivity is higher, and the selectivity of hydrodechlorination of trichloroacetic acid into acetic acid in a water body is improved by 11.7%.

To provide a calcined body that is processed easier than a conventional calcined body and where differences in hardness between production lots are suppressed.SOLUTION: A calcined body comprises: at least one first transition metal element selected from the group consisting of manganese (Mn), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu), molybdenum (Mo), technetium (Tc), ruthenium (Ru), rhodium (Rh), palladium (Pd), and silver (Ag); a coloring element of at least one of a lanthanoid rare earth element and a second transition metal element different in kind from the first transition metal element; and zirconia containing a stabilizing element. A content of the first transition metal element is 100 mass.ppm or more, a content of the second transition metal element is less than 100 mass.ppm, and an absolute value of a difference in hardness relative to a hardness of a calcined body obtained from a commercially available powder is 10 HV or less.SELECTED DRAWING: None

A method may include operating a dehydrogenation process whereby a hydrocarbon-containing feed is converted to light olefins, wherein the dehydrogenation process utilizes a fluidized process catalyst that circulates between a reactor and a combustor. The method may comprise withdrawing the process catalyst from the dehydrogenation process, modifying the process catalyst to form a modified catalyst, and adding the modified catalyst back to the dehydrogenation process. The process catalyst may include from 0.1 wt. % to 10 wt. % of one or more metals chosen from gallium, indium, thallium, or combinations thereof, from 1 ppmw to 1000 ppmw of one or more metals chosen from platinum, palladium, rhodium, iridium, ruthenium, osmium, or combinations thereof, and at least 85 wt. % support. Modifying the process catalyst may include adding one or more of manganese, iron, chromium, or vanadium.

The invention provides a method for recovering platinum group metal from a waste automobile exhaust purification catalyst, and belongs to the field of precious metal recovery. The method comprises the following steps: carrying out crushing and impurity removal pretreatment on the waste catalyst to obtain solid residues; mixing the obtained solid slag with alkali liquor, and performing hot-pressing activation to obtain active slag; leaching the active slag by using an acid leaching system of hydrochloric acid-hydrogen peroxide-sodium chloride to obtain a leaching solution enriched with platinum group metals; adjusting the acidity of the leachate, adding a first adsorption material, selectively adsorbing platinum and palladium, and separating supernate and a platinum / palladium enrichment material; adjusting the acidity of the supernate, adding a second adsorption material, selectively adsorbing rhodium, carrying out solid-liquid separation, and collecting a rhodium enrichment material; respectively eluting and refining the platinum / palladium enrichment material and the rhodium enrichment material, and recovering platinum, palladium and rhodium; through the optimally designed recovery method of alkaline hot-pressing activation-mild acidic directional leaching-two-stage magnetic adsorption separation, efficient recovery of platinum, palladium and rhodium in the waste automobile exhaust catalyst is realized.

The invention discloses a catalyst for dealkylation in a chlorine-containing environment as well as a preparation method and application of the catalyst, and belongs to the technical field of catalyst reaction. The catalyst comprises a carrier and an active component, wherein the carrier comprises ZrO2 and MgFeO4; the active component comprises an auxiliary agent and a noble metal component, the auxiliary agent comprises a V2O5-WO3 composite oxide and a CeO2-MnO2 composite oxide, and the noble metal component comprises at least three of rhodium, ruthenium, platinum, palladium and gold. The noble metal components grow in mesopores of the carrier in a confined manner, and the auxiliaries with dechlorination and catalytic oxidation functions are uniformly distributed on the surface of the carrier, so that a two-step catalytic strategy of dechlorination and oxidation of chlorine-containing waste gas is realized, the poisoning phenomenon of the catalyst is effectively avoided, and an excellent catalytic effect is formed. Moreover, the catalyst is stable in property, still keeps an excellent catalytic function after being used for a long time, and is higher in practicability and better in economical efficiency.

According to the microwave reactor and method for recycling the three-way catalytic precious metal, through the synergistic effect of microwave radiation and the telescopic glass stirring rod, the problem that the mass transfer efficiency is low due to high viscosity of a traditional ionic liquid leaching system is solved, the precious metal leaching time is shortened, and the efficiency is improved. Meanwhile, a diamond ATR crystal infrared probe is adopted to monitor components of a reaction solution in real time, multi-parameter linkage control of microwave power, temperature and stirring rate is combined, reaction conditions are dynamically optimized, and the recovery rate of platinum, palladium and rhodium is increased. The method systematically solves the technical bottlenecks of high energy consumption, heavy pollution and low ionic liquid leaching efficiency of the traditional pyrogenic process / wet process, and provides an innovative scheme with high efficiency, low environmental load and industrial feasibility for precious metal recovery.

The invention relates to the field of preparation of nano materials, in particular to a preparation method of a metal-oxide cluster electro-catalytic material based on an ammonia-mediated electrostatic adsorption principle, and aims to solve the problem that a metal-oxide cluster heterogeneous interface is difficult to accurately construct by an existing method. The preparation method comprises the following steps: dispersing a carbon carrier, a soluble inorganic compound containing platinum, ruthenium and rhodium, a soluble metal complex anion salt and dopamine hydrochloride in a water-alcohol mixed solution, adding ammonia water, and preparing a metal-oxide heterogeneous cluster precursor through an ammonia-mediated electrostatic adsorption effect; and pyrolyzing the precursor in a reducing atmosphere to prepare the metal-oxide cluster electro-catalytic material. The prepared electro-catalytic material has a definite heterogeneous cluster interface and has excellent performance in alkaline hydroxide reaction. The method is simple and convenient to operate, low in cost and low in energy consumption, can be popularized to various metal-oxide cluster electro-catalytic materials, and has application potential.

The invention relates to a catalyst for preparing 1, 4-cyclohexanedimethanol (CHDM) by catalyzing dimethyl terephthalate (DMT) hydrogenation and a preparation method thereof, non-noble metals nickel (Ni) and copper (Cu) are used as active components, silicon dioxide is used as a carrier, ammonia water in a solution is evaporated out after ammonia water precipitation, and a catalyst sample is obtained. The active components mainly adopt metal Ni and Cu elements with relatively low price, compared with noble metals such as ruthenium, rhodium, platinum and the like, the use cost of the catalyst is greatly reduced, the bimetallic catalyst Ni-Cu-SiO2 is prepared by an ammonia distillation method, 1, 4-cyclohexanedimethanol can be prepared by catalyzing dimethyl terephthalate hydrogenation by a one-pot method, and the catalyst has a wide application prospect. The preparation cost of the catalyst is relatively low, the dispersity and stability of the catalyst are improved by adopting an ammonia distillation method, the CHDM is prepared by adopting a one-pot method, the energy consumption is further reduced, the reaction procedure is simplified, and the preparation method is simple and is easy to amplify to industrial production.

High entropy alloy catalysts may be used for production of hydrogen. An example method of hydrogen production may include: introducing a hydrocarbon to a reactor, wherein the reactor contains therein a catalyst, wherein the reactor is substantially absent of oxygen and water, wherein the catalyst comprises a high entropy alloy and a catalyst support, wherein the catalyst is present in a form of a first plurality of particles, wherein the first plurality of particles is submicron-sized, wherein the high entropy alloy has an entropy, S, such that S≥12.47 J K−1 mol−1, and wherein the high entropy alloy comprises at least five of: iron, cobalt, manganese, nickel, molybdenum, copper, zinc, titanium, chromium, vanadium, aluminum, gallium, ruthenium, rhodium, palladium, silver, indium, tungsten, rhenium, iridium, platinum, gold, and bismuth; and reacting the hydrocarbon over the catalyst to produce solid carbon and hydrogen gas.

The invention provides electronic-grade quartz glass fiber cloth and a preparation method thereof. The method comprises the following steps: selecting high-purity quartz sand, melting at high temperature, precisely filtering, and homogenizing; preparing a special impregnating compound; drawing fibers through a platinum-rhodium alloy bushing and coating the fibers with an impregnating compound; weaving into a cloth blank; performing high-temperature sintering treatment; the electrical property is improved through electron beam irradiation treatment; and cleaning with ultrapure water and drying to ensure the electronic grade cleanliness. According to the invention, high purity, uniformity and excellent electrical properties of the electronic-grade quartz glass fiber cloth can be ensured, and the requirements of the electronic industry on high-performance materials are met.

The present invention discloses a gas-phase preparation method of 1,1,1,4,4,4-hexafluoro-2-butyne. Using a mixture of 2,3-dichloro-1,1,1,4,4,4-hexafluoro-2-butene and hydrogen as raw materials, under the action of a particulate catalyst, 1,1,1,4,4,4-hexafluoro-2-butyne is obtained through a one-step hydrodechlorination reaction. The catalyst includes a carbon carrier and an active phase in the form of hollow spheres supported on the carbon carrier. The active phase includes: a first metal selected from at least one of silver, copper, nickel, and cobalt; and a second metal selected from at least one of palladium, platinum, and rhodium. The present invention has the advantages of high product selectivity, high catalytic activity, obtaining the reaction product through a one-step reaction, and being suitable for industrial application, etc.

A light emitting device, an electronic device, an electronic apparatus, and an organometallic compound including an organometallic compound having a metal such as platinum (Pt), palladium (Pd), copper (Cu), silver (Ag), gold (Au), rhodium (Rh), ruthenium (Ru), osmium (Os), titanium (Ti), zirconium (Zr), hafnium (Hf), europium (Eu), terbium (Tb), or thulium (Tm) are provided. The light emitting device may include a first electrode, a second electrode facing the first electrode, and an intermediate layer between the first electrode and the second electrode and including an emission layer. A light emitting device may be included in an electronic apparatus.

A method may include contacting a hydrocarbon-containing feed with a catalyst in a reactor to form an olefin-containing effluent, then at least partially separating the olefin-containing effluent from the catalyst. Passing the catalyst to a combustor and heating the catalyst by combusting a supplemental fuel. The supplemental fuel includes methane in an amount greater than or equal to 1 mol. %. Passing the catalyst from the combustor to the reactor, such that at least a portion of the catalyst continuously cycles between the reactor and the combustor. The catalyst includes from 0.1 wt. % to 10 wt. % of one or more metals chosen from gallium, indium, thallium or combinations thereof, from 5 ppmw to 1000 ppmw of one or more metals chosen from platinum, palladium, rhodium, iridium, ruthenium, osmium, or combinations thereof, from 100 ppmw to 30000 ppmw of chromium, and at least 85 wt. % support.

The invention discloses a flexible magnetic sheet for false eyelashes and a preparation process thereof.The flexible magnetic sheet comprises, by mass, 1%-5% of a thermoplastic elastomer TPE, 80%-90% of neodymium iron boron magnet powder, 1%-2% of a coupling agent, 1%-2% of a POE branch toughening agent and the balance co-polypropylene, and the flexible magnetic sheet comprises, by mass, 1%-5% of the thermoplastic elastomer TPE, 80%-90% of the neodymium iron boron magnet powder, 1%-2% of the coupling agent and 1%-2% of the POE branch toughening agent. And the balance of co-polypropylene. According to the technical scheme, the toughness of the flexible magnetic sheet can be effectively improved, the flexible magnetic sheet is more resistant to bending, the service life of the flexible magnetic sheet is effectively prolonged, and the flexible magnetic sheet is elastic, easy to elongate and shape and more comfortable to wear.

The invention provides a method for recovering rhodium in organic residual liquid containing triphenylphosphine / phosphine oxide, and relates to the technical field of precious metal recovery, and the method comprises the following steps: S1, carrying out reduced pressure rectification on the organic residual liquid containing triphenylphosphine / phosphine oxide to remove volatile components until the indexes of the residual liquid meet the feeding requirements of a subsequent process, and collecting light components for independent storage; s2, adding an acidic medium into the organic phase after light component removal, stirring and heating, introducing an oxidizing agent to carry out oxidation-complexation reaction, maintaining reaction conditions until the reaction is complete, standing for phase splitting, and collecting a water phase containing rhodium complex ions; according to the method, a core process combining oxidation-chlorination transfer and anion exchange adsorption is adopted, and key parameters of each process are accurately controlled, so that the rhodium recovery rate is stabilized at 95% or above, the rhodium content in the residual liquid can be reduced to 5 ppm or below, the industrial emission standard is completely met, and compared with the prior art, the resource recovery efficiency is greatly improved, and the cost is reduced. And waste of precious metal resources is effectively reduced.

The invention provides a medium / high-entropy metal organic framework material and a preparation method thereof, the configuration entropy delta S of the medium-entropy metal organic framework material is greater than 1R and less than 1.5 R, and the configuration entropy delta Sgt of the high-entropy metal organic framework material is greater than 1R and less than 1.5 R; 1.5 R, R is a gas constant and is 8.314; metal ions in the medium / high-entropy metal organic framework material are at least four of magnesium, calcium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, zinc, zirconium, molybdenum, ruthenium, palladium, silver, cadmium, indium, tin, iridium, rhodium and platinum, the molar weight of each metal ion is 10%-70% of the total molar weight of the metal ions, and the ratio of the total molar weight of the metal ions to the molar weight of the organic ligand is 1: (2-8). The preparation method has the characteristics of being programmable and adjustable, the number of metal types is four or more, and the metal proportion change of the metal content before and after preparation is smaller than 5%. The medium / high-entropy MOFs provided by the invention has the characteristics of uniform metal element distribution, accurate modulation and organic ligand replacement, and can accurately regulate and control the types and proportions of metals in the medium / high-entropy MOFs as well as the structure and performance of the obtained sample.

Discloses a hydrometallurgical process and system for the recovery of precious metals; specifically palladium, rhodium, and platinum metals, at high purity and with limited waste and environmental fouling.

The invention discloses a high-dispersion rhodium-loaded defect-state black titanium dioxide photocatalyst, preparation and application thereof in preparation of propylene through photocatalytic methane conversion, and belongs to the technical field of methane photocatalytic conversion. The preparation method comprises the following steps: firstly, carrying out chemical reduction treatment on titanium dioxide, carrying out high-temperature calcination, and then washing, carrying out suction filtration and drying to obtain black titanium dioxide; carrying out hydrogen peroxide treatment on the titanium dioxide, and further modifying the surface structure of the titanium dioxide to obtain defect-state black titanium dioxide; and finally, mixing with a metal Rh precursor solution, and calcining to obtain the high-dispersion metal Rh loaded defect-state black titanium dioxide photocatalyst. The prepared catalyst has excellent light absorption capacity, energy from visible light to a near-infrared region (accounting for about 96% of solar energy) in sunlight can be fully utilized, efficient and selective conversion from methane to propylene is achieved under the conditions of low temperature and visible light irradiation, the propylene selectivity can reach 70% or above, and reaction activity far exceeding thermodynamic limitation is shown.

The invention provides a composite hydrogen transfer catalyst based on an MOFs material as well as a preparation method and application of the composite hydrogen transfer catalyst. The composite hydrogen transfer catalyst comprises the MOFs material loaded with an active metal component and solid alkali, the active metal component is selected from at least one of palladium, platinum, ruthenium, rhodium and nickel; the active metal component accounts for 0.5-5% of the mass of the catalyst; the MOFs material is selected from at least one of ZIF-8, MIL-101, UiO-66, HKUST-1 and MOF-5 (Metal Organic Frameworks); the solid alkali is selected from at least one of magnesium oxide, calcium oxide, hydroxyapatite and barium oxide. The catalyst provided by the invention has the advantages of high catalytic activity, good selectivity, strong stability, reusability and the like, can efficiently catalyze fatty alcohol to perform hydrogen transfer reaction under a lower-temperature reaction condition to prepare Guerbet alcohol, remarkably improves the yield and purity of a product, and reduces the reaction energy consumption and cost.

The invention relates to the technical field of precious metal recovery and purification, in particular to a metal rhodium recovery and purification method which comprises the following steps: S1, adjusting the pH value of rhodium leaching liquid, heating, adding a reducing agent, and filtering after reaction to obtain primary impurity removal liquid; s2, controlling the pH value of the primary impurity removal liquid to be 1.5-2, heating, adding thiodiglycolic acid and ammonium salt, reacting, and performing solid-liquid separation to obtain primary rhodium-containing precipitate; s3, dispersing the primary rhodium-containing precipitate in an acid solution, adding a strong oxidant, carrying out heating reflux, and adjusting the pH value to 6-7 to obtain a secondary rhodium-containing precipitate; s4, dispersing the secondary rhodium-containing precipitate in a solution with a pH value of 13-14 for pulpifying, adding a reducing agent, carrying out a reduction reaction at 90-100 DEG C, and carrying out solid-liquid separation to obtain a tertiary rhodium-containing precipitate; s5, calcining the third rhodium-containing precipitate, and performing hydrogen reduction to obtain metal rhodium; the method has the advantages that the recovery efficiency of rhodium can be improved, and the pressure on the environment is reduced.