1920 results about "Sulfidation" patented technology

The invention discloses high-purity lithium sulfide as well as a preparation method and application thereof. The preparation method comprises the step that lithium hydride, lithium hydroxide and a sulfur source are subjected to a heating reaction in a dry inert atmosphere, and the high-purity lithium sulfide is obtained. The molar ratio of lithium hydride to lithium hydroxide is X: (10-X), and X is 1-6. The invention also discloses the prepared high-purity lithium sulfide and application of the high-purity lithium sulfide in preparation of sulfide solid electrolyte. Lithium hydroxide and lithium hydride are mixed to serve as a lithium source in lithium sulfide preparation, the lithium hydroxide quickly and uniformly reaches the reaction temperature by means of the characteristic that the lithium hydride reacts with a sulfur source to release heat and produce gas, the lithium hydride reacts to produce gas, meanwhile, discharging of product water vapor is facilitated, and oxygen in the environment is isolated; and hardening and generation of a side reaction product lithium sulfate are prevented, the conversion rate of lithium hydroxide to lithium sulfide is improved, and the raw material and process cost for preparing lithium sulfide is remarkably reduced.

The invention provides a composite reagent system and a chalcopyrite and sphalerite collecting method, and belongs to the technical field of mineral processing. The composite reagent system comprises a histidine derived functional group collecting agent and a black agent, and the histidine derived functional group collecting agent (containing a total sulfur ester group, a sulfydryl functional group and a side chain imidazole ring) serves as a core and is compounded with the black agent according to a specific proportion to form a target combination-synergistic interaction flotation mechanism. The histidine derivative collecting agent derives high-activity functional groups under the alkaline condition, and after sulfydryl is dissociated, stable chemical bonds are formed by the dissociated sulfydryl and metal ions on the surfaces of the chalcopyrite and the zinc sulfide. The black powder serves as an auxiliary collecting agent, and the collecting capacity of fine-grain or low-activity sulfide minerals is enhanced through chemical adsorption of dithiophosphate radicals and metal ions on the surfaces of the chalcopyrite and the sphalerite. After the two components are compounded, the selective enrichment efficiency of copper-zinc minerals in the flotation process is remarkably improved.

The invention discloses a method for preparing a carbon monoxide oxidation catalyst by using red mud and tungsten-molybdenum smelting slag, which comprises the following steps of: uniformly stirring and mixing the red mud and the tungsten-molybdenum smelting slag at a high speed, mixing with inorganic strong acid, and performing ultrasonic-assisted stirring to obtain acid leaching slag; the acid leaching residues are subjected to low-temperature plasma activating treatment and then microwave activating treatment, and microwave activated plasma residues are obtained; weighing tricalcium phosphate and microwave activated plasma slag, and uniformly stirring to obtain phosphorus-calcium doped activated slag; weighing an ammonium sulfide solution and the phosphorus-calcium doped activated slag, uniformly stirring, transferring the obtained sulfur-phosphorus-calcium doped activated slag into a hydrothermal reaction kettle, carrying out hydrothermal reaction, carrying out compression molding on the obtained hydrothermal composite material, and carrying out pyrolysis carbonization treatment in an inert gas atmosphere to obtain the phosphorus-calcium doped activated slag. The obtained pyrolysis composite material is soaked with a silane coupling agent solution and then roasted again, and the carbon monoxide oxidation catalyst is obtained. The catalyst prepared by the invention can realize efficient oxidation photocatalysis of carbon monoxide under the conditions of normal temperature and normal pressure.

The invention relates to the technical field of preparation of lithium sulfide, in particular to a method for preparing lithium sulfide through hydrogen reduction of lithium sulfate. According to the specific technical scheme, the method for preparing the lithium sulfide by reducing the lithium sulfate through the hydrogen comprises the steps that the lithium sulfate is smashed to be micron-sized and then fed into a fluidized bed reactor, then high-purity hydrogen preheated to 850 DEG C is introduced into the fluidized bed reactor from the bottom of the fluidized bed reactor, the reaction temperature is controlled to be 850 + / -20 DEG C, and the reaction time is controlled to be 5-10 min. The hydrogen reduction method is relatively low in reaction temperature (700-900 DEG C), hydrogen is used as a clean reducing agent, a reaction byproduct is only water, and the problems of insufficient purity, high energy consumption, serious environmental pollution and the like in a traditional lithium sulfide preparation method can be avoided. The introduction of the fluidized bed technology can greatly enhance the gas-solid phase heat and mass transfer efficiency, realizes the continuity and automation of the process, and is an important path for realizing the industrialization of the reaction.

The invention relates to the technical field of battery raw materials, in particular to a preparation method of lithium sulfide powder, the lithium sulfide powder and application, and the preparation method comprises the following steps: uniformly mixing lithium sulfate and a carbon source according to a preset proportion to obtain a first mixture; performing first heat treatment on the first mixture in inert gas to obtain a second mixture; and performing second heat treatment on the second mixture in reducing gas to obtain the lithium sulfide powder. The product obtained by the preparation method disclosed by the invention is the lithium sulfide powder, and the obtained lithium sulfide powder has the advantages of less oxygen and carbon impurities, higher purity and high reaction activity, and meets the synthesis requirements of the electrolyte; according to the preparation method, in the process of preparing lithium sulfide, toxic gas and organic solvent are not used, the reaction temperature is low, the energy consumption is low, the requirement on production equipment is low, the process is simple, the cost is low, harmful gas emission is avoided, safety and environment friendliness are achieved, and industrialization is easy to achieve.

A method for synergistically preparing lithium sulfide by vacuum molten salt based on hydrogen sulfide-lithium salt reaction belongs to the technical field of battery materials, and comprises the following steps: placing a lithium salt solid in a reactor, introducing a molten salt medium on the surface of the lithium salt or in a reaction system, introducing purified hydrogen sulfide gas under a vacuum auxiliary condition, controlling the reaction temperature to be 200-500 DEG C, and reacting for 1-2 hours; and adjusting the flow rate of hydrogen sulfide to be 50-1000mL / min and the retention time to be 5-180min, continuously exhausting gas to discharge water vapor in the reaction process, stopping introducing hydrogen sulfide gas after the reaction is finished, cooling the system to room temperature under the protection of inert gas, taking out the product, washing to remove residual fused salt, and carrying out vacuum drying to obtain the high-purity lithium sulfide. The prepared lithium sulfide has high purity (greater than or equal to 99.90%), low defect density and an excellent crystal structure, and can be widely applied to lithium-sulfur batteries, all-solid-state batteries and novel energy storage technologies, so that the energy density is improved, the cycle life is prolonged, and the energy consumption is reduced.

The invention discloses a concrete crack self-repairing material based on microorganism immobilization and a preparation method of the concrete crack self-repairing material, and belongs to the crossing field of microorganism materials and civil engineering. The material is prepared from peptone, sodium lactate, volcanic rock, bacillus pasteurii and other raw materials through the steps of culture medium preparation, carrier modification, microorganism immobilization, microcapsule and gel protection layer formation and the like, the prepared volcanic rock-chitosan carrier provides an inhabiting environment for microorganisms, and the survival rate of the microorganisms in a high-alkali environment is increased to 70%. When the concrete cracks and the alkaline environment triggers the protective layer to disintegrate, the bacillus pasteurii and the desulfurization vibrio are subjected to a reduction reaction with sulfate through urealysis, and calcium carbonate and calcium sulfide are generated to fill cracks. The 28-day repair rate of the material is larger than or equal to 99%, the maximum crack repair width reaches 1.2 mm, the compressive strength recovery rate is larger than or equal to 85%, excellent durability and environment friendliness are achieved, and the concrete crack repair problem is effectively solved.

The invention provides a cyanide-containing wastewater resource recovery and cyclic utilization method, and belongs to the technical field of environmental protection and water treatment. According to the method, firstly, copper is collected through sulfuration under the weak acid condition with the pH being 5-6, so that a copper-cyanogen complex ([Cu (CN) 43-]) in wastewater is converted into a mixed material of copper sulfide (CuS) and cuprous cyanide (CuCN), and primary recovery of copper is achieved; and then, adding a pH regulator 2 to control the pH of the reaction system to be 9-11, adding a separation agent to control the ORP of the reaction system to be-400mV to-200mV, and carrying out a separation reaction. In the process, cuprous cyanide reacts with free cyanide (CN <->) to generate a soluble copper-cyanogen complex, and copper sulfide is retained, so that cuprous cyanide is accurately separated from the copper-containing material, the content of cyanide in the material is reduced, and the obtained copper-containing material meets the requirements of industrial product quality standards and pollution control standards; the problems that in the prior art, the cyanide content in the copper-containing material obtained by recycling copper from the cyanide-containing wastewater exceeds the standard, and the environmental risk is high in storage, transportation and comprehensive utilization are solved.

The invention relates to lithium sulfide and a preparation method thereof.The preparation method includes the following steps that sublimed sulfur powder and a lithium source are mixed and subjected to a heating reaction, and the lithium source comprises at least one of anhydrous lithium hydroxide, lithium hydroxide monohydrate, lithium oxide, lithium hydride and lithium carbonate; a reducing gas is introduced while the heating reaction is performed, or the reducing gas is introduced after the heating reaction is finished, and a reduction reaction is performed; and after the reaction is finished, introducing protective gas for calcining to prepare the lithium sulfide. The preparation method provided by the invention can realize low-cost and high-purity production of lithium sulfide, and ensures the safety and environmental protection of the production process.

The invention discloses a water quality monitoring device and a monitoring method thereof, belongs to the technical field of water quality monitoring, and solves the problems that trace hydrogen sulfide generated by sulfate reducing bacteria in a deposited layer at the bottom of a water tank which is not cleaned for a long time in a low-oxygen environment reacts with a platinum membrane electrode of a residual chlorine sensor to generate a platinum sulfide covering layer; and the electrode reading is continuously virtually high and drifts slowly. Comprising an optical transmitting module, an optical receiving module, a spectrum separation module, a signal conditioning module, a lock-in amplification module, a spectrum feature extraction module and a hydrogen sulfide recognition engine. Residual chlorine is monitored in a non-contact mode, deep ultraviolet pulse light is emitted to penetrate through a water body, a reflection spectrum is received, second derivative spectral characteristics are extracted through multichannel signal processing, and multivariable regression compensation is executed to calculate a real residual chlorine value after hydrogen sulfide interference characteristics are recognized. Meanwhile, the drift trend is quantified based on the double-time-constant integral, graded early warning is triggered, industrial standard signals are finally output, and the problem of electrode contact pollution is avoided in the whole process.

The invention relates to a method for preparing lithium sulfide at low temperature by microwave molten salt assisted carbon disulfide-lithium salt reaction, and belongs to the technical field of key materials of lithium-sulfur batteries and solid-state batteries. The technical problems of high energy consumption, difficulty in inhibiting by-products, insufficient purity and crystal phase stability, difficulty in continuous amplification and the like in the existing lithium sulfide preparation process are solved. Comprising the following steps: step 1, performing crushing, screening and grading treatment on lithium source powder; step 2, placing the treated lithium source powder and molten salt in a closed reactor, and introducing CS2 in a gas or liquid form; 3, applying microwave radiation, and reacting at a gas-solid-liquid multiphase interface to generate lithium sulfide; and 4, cooling the material after the reaction to room temperature, separating and recovering the fused salt to obtain the lithium sulfide powder. The method is low in reaction temperature, low in energy consumption, high in reaction rate, high in product purity and suitable for continuous and industrial production.

The invention provides a process for preparing high-purity lithium sulfide based on industrial waste salt recycling, which comprises the following steps: S1, mixing sulfur-containing waste salt and a waste carbon material, granulating, reducing, calcining, separating and purifying to obtain solid sodium sulfide; s2, mixing and ball-milling the obtained solid sodium sulfide and lithium chloride, adding a mixture of a catalyst and ethanol, and performing catalytic reaction to obtain a lithium sulfide crude product; and S3, purifying and drying the obtained lithium sulfide crude product to obtain the lithium sulfide. The method not only can break through the bottleneck of the existing production route, but also can realize the strategic direction of high-value utilization of bulk solid wastes, and has far-reaching significance for promoting sustainable development and green transformation of the battery industry.

A beneficiation method for improving a grade of a magnesium-containing copper sulfide ore concentrate includes: crushing and grinding an ore to a fineness degree allowing 55% to 65% of particles to pass through a 0.074 mm sieve, adding an adjusting agent lime, collecting agents butylxanthate and kerosene, and a foaming agent methyl isobutyl carbinol (MIBC) to obtain a copper-molybdenum-sulfur mixed concentrate; re-grinding the copper-molybdenum-sulfur mixed concentrate to a fineness degree allowing 75% to 82% of particles to pass through a 0.048 mm sieve, adding lime, a magnesium-containing silicate inhibitor, a collecting agent 1, and MIBC to obtain a copper-molybdenum mixed concentrate; and adding sodium sulfide, kerosene, and MIBC to the copper-molybdenum mixed concentrate to obtain a high-grade copper concentrate. The beneficiation method adopts mixed flotation of copper-molybdenum, regrinding for separating copper and molybdenum from sulfur, and magnesium removal from a copper concentrate to allow quality improvement for the copper concentrate.

The application provides a preparation method of a self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon composite material, a product and application, high-content nitrogen-doped porous carbon material is synthesized by inducing dicyandiamide molecules to undergo a supramolecular self-assembly process, and on this basis, a hydrothermal reaction is carried out to coat molybdenum sulfide sheet layer material on the surface, and finally, a self-heating coiling treatment is carried out to form a carbon-based electrocatalyst of the self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon. Compared with a high specific surface area carbon-based catalyst, high doping concentration of nitrogen atoms can provide more electron-rich properties to facilitate the adsorption of substances, and the self-coiled carbon-based material can exhibit very excellent electrochemical performance, especially in the aspect of electrochemical hydrogen production. The preparation method is simple in operation, low in preparation cost and suitable for large-scale production.

The invention provides an impurity removal method of a gallium-rich solution for a gallium-based fluorescent powder precursor, and belongs to the field of preparation of gallium-based fluorescent powder precursors. The method comprises the following steps: adding an oxidizing agent into an initial gallium-rich solution to carry out a first reaction so as to remove organic impurities in the initial gallium-rich solution and obtain a first gallium-rich solution; adding a composite impurity removal reagent into the first gallium-rich solution to carry out a second reaction to remove impurity elements such as calcium, silicon and vanadium in the first gallium-rich solution so as to obtain a second gallium-rich solution; and adding a sulfide type reagent into the second gallium-rich solution to carry out a third reaction so as to remove copper and iron impurity elements in the second gallium-rich solution, thereby obtaining the gallium-rich solution for the gallium-based fluorescent powder precursor. According to the method, various key impurity elements such as organic matters, alkaline earth metals, metalloids and heavy metals are directionally and efficiently removed through the impurity removal logic of oxidation impurity breaking, synergistic precipitation and deep vulcanization, so that the total content of the key impurity elements in the gallium-rich solution is remarkably reduced.

A method for treating hazardous waste using a coal-based short-process system belongs to the field of hazardous waste treatment technology. The method of the present invention first performs deep reduction on the material, then uses a coal-based lance to generate heat in a molten bath to heat the material to a molten state, and then uses electrodes to heat the melt to separate the slag and matte, resulting in qualified matte. The molten bath produces high-temperature flue gas rich in carbon monoxide, which is fully combusted in a rotary kiln. When producing alloys, ore and coal are heated and deep reduction is performed. No reducing agent is required to produce matte, and sufficient sulfide allows the ore to be sulfided in the rotary kiln. The rotary kiln and molten bath furnace adopt an integrated configuration to reduce heat loss. Coal powder is directly delivered to the working surface, effectively avoiding the ineffective consumption of carbonaceous reducing agents and further enhancing the reduction effect. The method of the present invention has the characteristics of a short process, simple operation, easy control, strong raw material adaptability, high production efficiency, low production cost, low equipment investment, low energy consumption, high copper recovery rate, and environmental friendliness.

The present application relates to electrolytic manganese technology field, specifically to a kind of method for removing heavy metal ions in manganese sulfate solution.The method for removing heavy metal ions in manganese sulfate solution provided by the present application includes the following steps: adding oxidizing agent to pretreated manganese sulfate solution, mixing and stirring, then adjusting the pH value of solution to 5.5-6.0, filtering, to obtain the first purified manganese sulfate solution;Add sulfidation agent to the first purified manganese sulfate solution, filter, to obtain the second purified manganese sulfate solution;Add porous resin polymer to the second purified manganese sulfate solution, add the mixed solution into a sealed container, introduce nitrogen, make the pressure in the sealed container reach 1.1-1.5MPa and maintain for 2-10min, then open the air valve and release pressure instantaneously, stand, filter, fine filter, to obtain the purified manganese sulfate solution.The method provided by the present application can not only effectively remove heavy metal ions in solution, but also effectively reduce the COD value of the purified solution, reduce the loss of manganese content in solution.

The invention discloses a preparation method and application of a bimetallic sulfide / three-dimensional porous carbon catalyst, and relates to the technical field of electrolyzed water catalysts.The preparation method comprises the following steps that melamine sponge is cleaned, and the clean melamine sponge is obtained; the preparation method comprises the following steps: dissolving metal salt 1 and metal salt 2 in an ethanol aqueous solution, and adding alkali and an aniline monomer to obtain a precursor solution; completely soaking the clean melamine sponge in a precursor solution, carrying out constant-temperature hydrothermal reaction, and sequentially washing and drying to obtain the melamine sponge anchored with bimetal ions; introducing inert gas for protection, and performing high-temperature vulcanization treatment to obtain the three-dimensional porous carbon catalyst embedded with the bimetallic sulfide heterostructure. The catalyst comprises uniformly dispersed bimetallic sulfide nanoparticles and a spongy three-dimensional porous carbon carrier, shows excellent bifunctional catalytic activity and stability when being applied to an electro-catalytic water decomposition reaction, and has a wide application prospect.

The invention discloses asphalt-based hard carbon, a preparation method thereof and a sodium-ion battery negative electrode material, and relates to the technical field of sodium-ion batteries. The preparation method of the asphalt-based hard carbon comprises the following steps: S1, mixing an asphalt precursor, a sulfur source and a cross-linking agent, and performing cross-linking vulcanization treatment at a first temperature to obtain a primary product; s2, performing carbonization treatment on the primary product at a second temperature to obtain asphalt-based hard carbon; the sulfur source is any one of elemental sulfur, thiourea, dimethyl sulfide and sulfide, or any two of elemental sulfur, concentrated sulfuric acid, thiourea, dimethyl sulfide and sulfide. By adopting the method, the type of the sulfur source is controlled, and the sulfur source and the cross-linking agent are added, so that the reversible capacity and the rate capability of the asphalt-based negative electrode material can be effectively improved, and the application field of the asphalt-based negative electrode material is widened.

The invention discloses a method for separating valuable metal in a waste photovoltaic welding strip through reduction smelting-vacuum gasification-vulcanization, and belongs to the technical field of resource recycling. The method comprises the steps that the waste photovoltaic welding strip is placed in a reducing atmosphere and heated for reduction smelting, so that carbon impurities on the surface of the waste photovoltaic welding strip are removed, tin, lead, silver and copper oxides on the surface are reduced, and a copper-tin-lead-silver alloy is obtained; then, heating the decarbonized and deoxidized photovoltaic welding strip under a vacuum condition, and carrying out vacuum gasification separation to obtain condensed metal lead and a copper-tin-silver alloy; and finally, sulfur is added into the copper-tin-silver alloy for vacuum vulcanization-separation, and volatile matter stannous sulfide and residual copper-silver alloy are obtained. According to the method, valuable metals in the waste photovoltaic solder strip can be efficiently separated, and the method has the advantages of being green and economical.

The present invention relates to a method for preparing lithium sulfide, according to the present invention, when preparing lithium sulfide by a reaction between a lithium raw material and hydrogen sulfide, the reaction is carried out under relatively mild conditions compared to the prior art, so that frequent maintenance or replacement due to corrosion and failure of a reactor and various pipes is not required, thereby improving the economical efficiency of the process. Further, by reusing the unreacted hydrogen sulfide from which moisture has been removed and the solvent, process costs can be reduced, and economical efficiency can be ensured during mass production. Furthermore, moisture and water vapor generated in the lithium sulfide generation reaction are effectively removed, thereby preventing a reverse reaction for generating lithium hydroxide, promoting a positive reaction, and producing high-quality lithium sulfide with high purity and high yield. In addition, the particle size can be adjusted in units, and a separate pulverizing space or pulverizing table is not required, so that convenience and mass productivity are excellent.

The utility model provides a device suitable for preparing lithium sulfide by a continuous double decomposition method. The device mainly comprises a material stirring reaction kettle, a solvent storage tank, continuous solid-liquid separation equipment, continuous solvent evaporation equipment, a first condensing tower and continuous dynamic vacuum calcination equipment, the device disclosed by the utility model can smoothly realize continuous production and preparation of lithium sulfide, and is simple in operation process and free from harmful gas pollution; in the preparation process, a single solvent is used and the solvent is recycled, so that the preparation method has the advantages of energy conservation and low cost, and cross contamination of multiple solvents is avoided; in addition, during continuous production of lithium sulfide, only one-time high-temperature calcination operation is carried out, and a lithium sulfide product with high purity and small particle size is successfully prepared; the composite cathode material can be directly used for preparing a sulfide solid electrolyte and a lithium-sulfur battery. The method has high industrial application value.

The invention provides a gold ore phase analysis method, and belongs to the field of mineral analys.The gold ore phase analysis method comprises the steps that a gold ore sample is prepared into ore pulp, the pH value is adjusted to 10-11, ultrasonic cavitation treatment is conducted after polyethylene glycol is added, and limonite turbid liquid and sedimentation bottom mud are obtained through separation; the turbid liquid is subjected to flocculation precipitation, drying, roasting, acid dissolution and impurity removal, and the limonite gold-loaded grade is obtained through the mass difference before and after dissolution and gold concentration determination; separating metal sulfide ore heavy minerals and gangue minerals from the settled bottom mud through artificial heavy elutriation, performing acid dissolution and impurity removal on the metal sulfide heavy minerals, and calculating the gold loading grade of the metal sulfide heavy minerals through mass difference and gold concentration determination; after gangue minerals are subjected to oxidizing roasting, the gold content is measured after concentrated acid dissolution; and calculating the distribution rate of gold based on the result. The gold loading grade and distribution of the limonite phase, the metal sulfide ore phase and the gangue mineral phase are measured in a split-phase mode, the method is highly matched with the gold ore development process, operation is easy and convenient, the result is reliable, and beneficiation and metallurgy technological process formulation and technical index pre-judgment can be effectively served.

The invention provides a sulphide ore alkaline desulfurization and cyanidation gold leaching agent system and a method for extracting gold through the sulphide ore alkaline desulfurization and cyanidation gold leaching agent system, and belongs to the technical field of hydrometallurgy. According to the method, a ternary agent system consisting of potassium ferricyanide, low-concentration sodium cyanide and thioguanosine is constructed. An efficient'oxidation-inhibition 'synergistic system is formed between the auxiliary desulfurization agent potassium ferricyanide and the thioguanosine. The rapid and selective oxidation of potassium ferricyanide is smoothly carried out under the synergistic effect of thioguanosine, minerals are thoroughly decomposed, and the surface keeps high activity; meanwhile, due to the existence of the thioguanosine, the local microcell passivation risk and catalytic electron transfer can be eliminated more directionally. The sodium cyanide and the sodium cyanide complement each other, it is jointly guaranteed that the exposed gold can be smoothly and efficiently leached through follow-up low-concentration sodium cyanide, finally, the total consumption of reagents is reduced, environmental pollution is reduced, and meanwhile high-recovery-rate extraction of the gold in the sulfide ore difficult to treat is achieved.

The invention belongs to the technical field of new energy materials and bioelectrochemistry, and particularly relates to an iron-based multi-metal sulfide composite carbon anode material and a preparation method of the iron-based multi-metal sulfide composite carbon anode material. The preparation method is simple in process flow, convenient to operate, easy for large-scale production, wide in raw material source, low in cost and environment-friendly, and can be used for preparing the three-dimensional porous carbon matrix which is formed by foaming and carbonizing polyvinylpyrrolidone and is provided with interconnected carbon nanosheets. Through reasonable composition design and structural regulation, and optimization of metal ratio and vulcanization conditions, accurate regulation of material performance can be realized, electrochemical performance and biocompatibility are significantly improved, electricity generation performance and operation stability of a microbial fuel cell are improved, and good industrial application prospects are achieved.

The invention relates to a method for recovering platinum in nickel-platinum waste. The method comprises the steps of hot nitric acid dissolution, filtration, pH adjustment, selective precipitation and drying. The characteristic that hot nitric acid can completely dissolve Ni and partially dissolve Pt is utilized to achieve preliminary separation of NiPt, sodium sulfide is used as a precipitator, selective precipitation of platinum is achieved through the Ksp difference of platinum sulfide and base metal sulfide within the pH range of 1-2, the recovery rate of platinum is greatly increased, and energy consumption of the platinum recovery process is reduced. Emission of a large amount of volatile acid is avoided while economic benefits are improved, and the method is more suitable for actual production.

The invention discloses a beneficiation method for tin-silver symbiotic polymetallic ore and application of the beneficiation method, and relates to the technical field of mineral separation. Comprising the steps that after tin-silver symbiotic polymetallic ore is ground, undersize minerals are obtained through a high-frequency screen, silver-copper flotation is conducted on the undersize minerals, and silver-copper concentrate and silver-copper tailings are obtained; the silver-copper tailings are subjected to lead-zinc-sulfur flotation, and lead concentrate and zinc-sulfur tailings are obtained; and the zinc-sulfur tailings are subjected to zinc-sulfur flotation, and zinc-sulfur concentrate and tin-sulfur tailings are obtained. The concentration of ore pulp in the ore grinding process is controlled, it is guaranteed that cassiterite and sulfide minerals are fully dissociated, then a first inhibitor is added in the lead-zinc-sulfur flotation process, the valuable metal recovery efficiency can be enhanced by optimizing the flotation process and collaboratively innovating a reagent formula according to the complex characteristics of tin-silver symbiotic polymetallic ore, and the recovery rate of the tin-silver symbiotic polymetallic ore is increased. The contents of silver, copper and tin in the tailings are obviously reduced, and efficient utilization of resources and reduction of solid wastes are realized.

The invention provides a synthesis method and application of a sulfuration modified palladium-iron bimetallic material. The method comprises the steps that potassium borohydride and sodium sulfide nonahydrate are dissolved in a solvent, sodium hydroxide is added into a sulfuration solution, the pH of the sulfuration solution is adjusted to be alkaline, and an alkaline solution is obtained. The method comprises the following steps: dropwise adding an alkaline solution into a mixed aqueous solution of FeSO4. 7H2O and sodium tetrachloropalladate at a speed of 10mL / min in a nitrogen atmosphere; and separating the precipitate from the mixed aqueous solution in a magnetic separation manner, and washing the precipitate for three times by using oxygen-free water and absolute ethyl alcohol to obtain the palladium iron sulfide bimetallic particles. Through a one-step reduction method of vulcanization and palladium doping, vulcanization modification and bimetal modification are combined to act on zero-valent iron, the stability of the zero-valent iron is enhanced through vulcanization, meanwhile, the reactivity of the zero-valent iron is improved through addition of bimetal, especially the selectivity to pollutants such as chlorinated paraffin and the reactivity after surface passivation are improved, and the stability of the zero-valent iron is improved. And the reliability and efficiency of the zero-valent iron in organic pollution remediation are greatly improved.

The invention relates to the technical field of battery materials, in particular to a preparation method of a lithium sulfide material. The preparation method of the lithium sulfide material comprises the following steps: S1, mixing lithium carbonate and sodium sulfide, heating to a first heating temperature to melt lithium carbonate and react with sodium sulfide, separating out a solid phase, and collecting a first solid; s2, the first solid is heated to a second heating temperature, the second heating temperature is higher than the melting point of sodium carbonate and lower than the melting points of lithium sulfide and sodium sulfide, a solid phase is separated out, and a second solid is collected; s3, the second solid is heated to a third heating temperature, the third heating temperature is higher than the melting point of lithium sulfide and lower than the melting point of sodium sulfide, a liquid phase is separated out, and a liquid lithium sulfide material is prepared; and S4, carrying out curing treatment on the liquid lithium sulfide material to prepare a solid lithium sulfide material. The preparation method improves the reaction conversion rate, simplifies the process flow, reduces the cost and improves the product purity.

The invention belongs to the technical field of biological materials, and discloses a PEEK bone implant material of a piezoelectric catalysis biological heterojunction and a preparation method of the PEEK bone implant material, the material comprises a PEEK bone implant loaded with the biological heterojunction, the biological heterojunction is composed of BiVOO and a chalcogenide calcium compound in a molar ratio of 1-3, and the chalcogenide calcium compound is calcium sulfide, calcium selenide or calcium telluride; during preparation, the BiVO / CaX biological heterojunction is firstly prepared by a hydrothermal method or an in-situ composite method, then PEEK is sequentially subjected to acetone, ethanol and deionized water cleaning, sulfuric acid ultrasonic treatment for 5-10 minutes and dopamine modification, the biological heterojunction is in contact with the modified PEEK at 4 DEG C for 12 hours to complete loading, and improvement means can be introduced into part of schemes. The material has the acoustic catalytic antibacterial function and the bone repair promoting function, the antibacterial effect can be regulated and controlled through ultrasound, the process is simple, and the reaction condition is mild; the multi-drug-resistant bacterial infection can be dealt with, and the heterojunction loading stability and the material cell compatibility are improved.