2050 results about "Raffinate" patented technology

The invention discloses a method for comprehensively recycling valuable metals from a spent lithium ion battery. The method comprises the following steps: carrying out electric discharge treatment on a spent battery, crushing, pre-roasting at 300-400 DEG C, adding a reducing agent, and carrying out reduction roasting at 450-700 DEG C; carrying out water extraction and evaporative crystallization on fine aggregates obtained through the reduction roasting, so as to obtain a high-purity lithium product, leaching copper, nickel and cobalt from leached slag and roasted lump materials by virtue of ammonia oxide, carrying out magnetic separation and sieving on ammonia leaching slag so as to obtain iron and aluminum enriched products, and carrying out reduction acid leaching, purification and edulcoration on sieved products, so as to obtain a high-purity manganese sulfate solution; and carrying out extraction and selective reverse extraction on ammonia leaching liquid, so as to obtain a high-purity nickel sulfate solution and a high-purity copper sulfate solution, and carrying out vulcanization cobalt precipitation, oxidation acid leaching and extraction purification on raffinate, so as to obtain a high-purity cobalt sulfate solution. The method is high in extraction rate of valuable metals and applicable to the treatment of multiple waste lithium ion battery raw materials and efficient utilization of multiple elements, and sorting is not required.

The invention relates to a preparation method of an SCR denitration catalyst, which comprises the following steps: (1) Al2O3 sol is prepared, which comprises the steps that hot ammonia, the Al2O3 is added in drops into the ammonia and then HCI is added and the mixture is stirred; (2) Al2O3-SiO2-TiO2 composite sol is prepared, which comprises the steps that tetratethoxy-silane, butyl titanate, deionized water are sequentially put into ethanol to be aging and then the sol prepared by step (1) is adding to be stirred and aging; (3) vector is coated, which comprises the steps that cordierite honeycomb immersed into the sol of step (2) and the raffinate in a channel is cleaned, dried and roasted after being taken out; (4) active component impregnating solution is prepared, which comprises the steps that lanthanum nitrate, ammonium metavanadate and ammonium paratungstate are dissolved into the deionized water after being mixed together and oxalate acid is added to be aging; (5) the active component is loaded, which comprises the steps that the vector of the step (3) is immersed into the impregnating solution of the step (4) and then the raffinate in the channel is cleaned to be dried and roasted. The invention also relates to the denitration catalyst which is prepared by the method.

The invention relates to a catalytic conversion method for preparing lower olefins and aromatics. Raw oil with different cracking performances enters different reaction zones of a first riser reactor to contact with a catalytic cracking catalyst for cracking reaction to separate a spent catalyst from reaction oil gas, wherein the reaction oil gas is separated to obtain a product containing lower olefins, gasoline, distillates with distillation range of 180-250 DEG C and catalytic wax oil, wherein the gasoline is extracted by light aromatics to obtain light aromatics and gasoline raffinate; the raw materials are cracked to be sent into a second riser reactor to contract with a hot regenerated catalyst for catalytic conversion; and the spent catalysts of the two riser reactors are burned and regenerated in the same one regenerator and then returns to the two riser reactors. The method uses heavy raw materials to furthest produce the lower olefins, such as propylene, ethylene, and the like, particularly the propylene, the production rate can exceed 40 wt%, and at the same time the method can coproduce the aromatics, such as toluene, xylene, and the like.

A process for upgrading hydrocarbonaceous oil containing heteroatom-containing compounds where the hydrocarbonaceous oil is contacted with a solvent system that is a mixture of a major portion of a polar solvent having a dipole moment greater than about 1 debye and a minor portion of water to selectively separate the constituents of the carbonaceous oil into a heteroatom-depleted raffinate fraction and heteroatom-enriched extract fraction. The polar solvent and the water-in-solvent system are formulated at a ratio where the water is an antisolvent in an amount to inhibit solubility of heteroatom-containing compounds and the polar solvent in the raffinate, and to inhibit solubility of non-heteroatom-containing compounds in the extract. The ratio of the hydrocarbonaceous oil to the solvent system is such that a coefficient of separation is at least 50%. The coefficient of separation is the mole percent of heteroatom-containing compounds from the carbonaceous oil that are recovered in the extract fraction minus the mole percent of non-heteroatom-containing compounds from the carbonaceous oil that are recovered in the extract fraction. The solvent-free extract and the raffinate concentrates may be used directly or processed to make valuable petroleum, chemical or industrial products.

The invention provides a method for reclaiming a rare earth element from abandoned fluorescent lamp. The invention is characterized in that the method comprises the following steps of: melting fluorescent powder by NaOH or KOH and adding water into an alkali melted substance to produce water insoluble substances and alkaline filtrate; dissolving the water insoluble substances into hydrochloric acid to produce neutral filtrate; extracting the neutral filtrate by P204 or P507 to produce extraction liquid and raffinate; back extracting the extraction liquid by HCl to produce back-extraction liquid, and precipitating the back-extraction liquid by H2C2O4 or NH4HCO3 to produce rare earth precipitate containing mixed Y, Ce, Tb and Eu; precipitating the raffinate by the NH4HCO3 to produce precipitate containing Mg, Ba and Sb; adjusting the pH value of the alkaline filtrate to between 3 and 5 to produce Al(OH)3 precipitate and manganiferous filtrate; washing, filtering and calcining the Al(OH) precipitate to produce alumina; and adding oxalic acid into the manganiferous filtrate to produce manganous carbonate. The method realizes that the rare earth element, Eu, Tb, Ce and Y are separated from Mg, Ba, Ca and other alkaline-earth metals, ensures that resources are comprehensively reclaimed and used, and has the advantages of reasonable process flow, economy and practicality.

The invention discloses an extracting polyphenol, theanine, tea polysaccharide and tea pigment method from tea, which is characterized by the following: using deionized water for lixiviating tea at constant temperature with continuous flow upstream at multi-speed; adopting microstrainer to dislodge the foreign matter of raffinate; using hyperfiltration for putting-off pectin and protein; concentrating by hyperfiltration and dehydration; extracting tea polyphenol by acetic acid ethyl ester and recovering dissolvant; stripping caffeine of extracting extract phase, pesticide residue and dissolvant by CO2 supercritical fluid; getting tea polyphenol by low-temperature nitrogen spray-drying; using alcohol separation and low temperation vacuum drying by hyperfiltration trapped fluid to prepare tea polysaccharide; separating alcohol recrystallization by basic copper carbonate and hydrogen sulfide to get theanine; using enzymatic oxidation and alkaline air to oxygenate remain polyphenols substance of liquid phantom; getting tea pigment by hyperfiltration dehydration compression and vacuum drying; merging caffeine form carbon dioxide above-critical fluid and caffeine from carrene; recovering dissolvent; using deionized water for washing; obtaining caffeine by recrystallization vacuum drying.

The invention discloses a comprehensive recovery method of complex polymetal sulphide ore containing copper, lead and zinc and adopts dressing-metallurgy combination method and hydrometallurgy-pyrometallurgy combination method to recover metals. The recovery method comprises the following steps: first performing bulk flotation to the complex polymetal sulphide ore, fine grinding the obtained concentrate, leaching by using two-step counter flow oxygen pressure leaching process, extracting and separating copper and zinc from the obtained leachate, electrodepositing the strip liquor of copper-loaded organic phase to obtain cathode copper, cleaning the obtained raffinate and electrodepositing to obtain cathode zinc; pressurizing leaching residue to perform flotation separation and obtain sulfur concentrate and lead silver residue, distilling sulfur concentrate to obtain sulfur; performing lead smelting process to lead silver residue to obtain electrolytic lead product and lead anodic slime; and comprehensively recovering noble metals such as gold, silver and the like from lead anodic slime. The method can greatly improve the metal recovery rate, resource utilization and the economic efficiency of mines and generate a lot of sulfur so as to obviously reduce the sulfur dioxide pollution to the atmosphere.

A process for recovering nickel and cobalt values from nickel- and cobalt-containing laterite ores as an enriched mixed nickel and cobalt sulphide intermediate and for producing nickel and cobalt metal from the nickel and cobalt sulphide intermediate. The laterite ore is leached as a slurry in a pressure acid leach containing an excess of aqueous sulphuric acid at high pressure and temperature, excess free acid in the leach slurry is partially neutralized to a range of 5 to 10 g/L residual free H₂SO₄ and washed to yield a nickel- and cobalt-containing product liquor, the product liquor is subjected to a reductant to reduce any Cr(VI) in solution to Cr(III), the reduced product liquor is neutralized to precipitate ferric iron and silicon at a pH of about 3.5 to 4.0, and the neutralized and reduced product liquor is contacted with hydrogen sulphide gas to precipitate nickel and cobalt sulphides. The precipitated nickel and cobalt sulphides can be leached in a water slurry in a pressure oxidation leach, the leach solution subjected to iron hydrolysis and precipitation, the iron-free solution contacted with zinc sulphide to precipitate copper, the iron- and copper-free solution subjected to zinc and cobalt extraction by solvent extraction to produce a nickel raffinate, the nickel raffinate contacted with hydrogen gas to produce nickel powder and the cobalt strip solution from the solvent extraction step contacted with hydrogen gas to produce cobalt powder.

The comprehensive process of extracting tea polysaccharide, tea polyphenol, theanine and coffine from tea includes the following steps: water or organic solvent extraction of tea powder under the action of microwave, concentration, precipitation and water dissolving the extract liquid, salt separating to eliminate protein and separation in gel column and drying to obtain tea polysaccharide; chloroform extraction of the raffinate, ethyl acetate extraction of the chloroform raffinate and drying to obtain tea polyphenol; No. 732 cationic exchange resin extraction of the ethyl acetate raffinate, concentration, crystallization and drying to obtain theanine; and crystallizing and drying the chloroform extract liquid to obtain coffine. The present invention has the advantages of short extraction time, high extraction rate, less loss of active matter, etc.

The invention relates to a method for preparing high-purity vanadium from heteropolyacid impurities in an amine extraction mode. Generally an ordinary vanadium solution is doped with impurities such as chromium, silicon, phosphorus, tungsten, molybdenum and arsenic, if acid is added into the solution, heteropolyacids such as phosphorus tungsten, phosphorus vanadium tungsten, silicon tungsten, phosphorus molybdenum tungsten, silicon molybdenum tungsten, molybdenum vanadium arsenic and tungsten arsenic can be formed, the impurities in the solution are removed by carrying out compounding synergic extraction on the heteropolyacids in the ordinary vanadium solution by using amines and a synergist so as to obtain a purified vanadium-containing raffinate, subsequently the vanadium-containing raffinate is evaporated and concentrated to be the concentration that each liter of the solution contains 40g vanadium, ammonium salt is further added into the concentrated liquid to obtain ammonium metavanadate solid, vanadium pentoxide with the purity greater than 99.9% is obtained through washing in pure water, drying and calcining in an oxygen atmosphere, the organic phase after the heteropolyacid is extracted is subjected to reverse extraction by using an alkali solution so as to form a heteropolyacid water phase, and the organic phase is recycled and circulated. The method has low requirement on equipment, and is simple to operate, key extraction agents are good in thermal stability and not sensitive in acid and alkali, and a recycling and circulating method is simple and easy to be industrialized.

Disclosed is a process for extracting tea polyphenol, caffeine as a byproduct thereof and tea polysaccharide from tea, which comprises, (1) extracting active ingredients including tea polyphenol, caffeine and tea polysaccharide from the tea through composite enzymolysis abstraction and water abstraction, (2) filtering the raffinate with hyperfiltration membrane, (3) subjecting the membrane compression liquid to ethanol deposition so as to obtain crude polysaccharides, removing protein and carrying out ethanol deposition, drying to obtain the tea polysaccharides, (4) separating and purifying through second level resin adsorption chromatography, thus obtaining tea polyphenol as well as caffeine as by-product.

The invention provides a recovery method of a copper indium gallium selenide thin-film solar panel. The method comprises the steps that: the copper indium gallium selenide thin-film solar panel is crushed into pieces; the pieces are soaked by using a H2SO4+H2O2 system, such that a soaking liquid is obtained; the soaking liquid is filtered, such that a first leachate is obtained; with a first phase ratio of 1, the first leachate is extracted by using an extraction agent; separation is carried out, such that a first extraction liquid and a first raffinate are obtained; the extraction agent is composed of 30% of P2O4 and 70% of kerosene by volume percentage, the extraction and balance time is 5-20min; an HCl solution is adopted as a stripping agent, and the first extraction liquid is striped by using a second phase ratio, such that In and stripping residual liquid are obtained; a reducing agent is added into the first raffinate; when a reduction reaction is finished, crude Se and a second leachate are obtained by filtering; alkali is added into the second leachate, and a pH value is regulated such that the pH value is constantly higher than 14; when a reaction is finished, filtering is carried out, such that a filtering slag comprising a hydroxide of Cu and a water solution comprising Ga are obtained; the alkali is NaOH, the pH value adjustment process is to add the NaOH in the reaction process after pH=14 so that the pH is always kept more than 14 during the reaction process, and the reaction time is kept for 0.5-2h; and the water solution is electrolyzed.

The invention provides a coupling method of catalytic cracking gasoline desulfurization. The coupling method comprises the following steps: cutting gasoline raw materials into light fractions, medium fractions and heavy fractions; carrying out extractive distillation on the medium fractions by an organic solvent to obtain olefin-contained raffinate and extracts which contain sulfide and arene; separating the organic solvent in the extracts to obtain extraction oil; carrying out selective hydrodesulfurization on the extraction oil and the heavy fractions to obtain the desulfurization heavy fractions; mixing the light fractions, the raffinate and the desulfurization heavy fractions to obtain desulfurization gasoline, wherein the cutting temperature of the light fractions and the medium fractions is 35 to 60DEG C, and the cutting temperature of the medium fractions and the heavy fractions is 140 to 160DEG C. According to the coupling method of the gasoline desulfurization, the octane value loss of a gasoline product can be obviously reduced, and desulfurization load is drastically lowered while deep desulfurization is realized. The yield of the product is greater than 95%.

An extracting and separating method of high-temperature coal tar belongs to a coal tar separation method. The extracting and separating method includes the step of adding No.1 or No.2 solvent into the coal tar at the ordinary pressure for secondary extraction and separation. Extraction processes are carried out under the pretreatment condition of sufficiently mixing and heating, heating temperature is lower than 150 DEG C, raw materials of the coal tar are respectively mixed with the No.1 or No.2 solvent according to the volume proportion of 1:2 to 4, extraction time ranges from 1 to four hours, extracts and raffinate are obtained after the No.1 solvent and the coal tar are filtered and separated when the system is balanced, and the No.1 solvent is recovered by distillation and recycled. The extracting and separating method has the advantages that energy saving effect of equipment is evident, process is simple and convenient, operation conditions are moderate, manufacturing cost and investment of the equipment are low and benefits are evident. Adding quantity of the solvent and extraction operation parameters are changed, separation depth and process capacity of the coal tar can be flexibly mastered and selectively controlled.

Product purity from or capacity of a simulated-moving-bed adsorptive separation process is increased by flushing the contents of the transfer line previously used to remove the raffinate stream away from the adsorbent chamber, preferably into the raffinate column used to separate desorbent from raffinate product. Preferably a stream from the adsorbent chamber at an intermediate point between the feed entry point and raffinate withdrawal is used as the flushing liquid. This flush step eliminates the passage of a quantity of the raffinate material into the adsorbent chamber in the transfer-line flush period or when the process conduit is subsequently used to charge the feed stream to the adsorbent chamber.

The invention provides a method for extraction and separation of tungsten and molybdenum. Hydrogen peroxide is filled in the tungsten and molybdenum mixed solution, the pH value is regulated to be acidic, and the acid tungsten mixed solution is taken as a water phase feed liquid to carry out extraction and separation with an organic phase. The organic phase comprises trialkylphosphine oxide, tributyl phosphate and a diluting agent; the organic phase conducts the multi-stage extraction with the water phase feed liquid, molybdenum is extracted into the organic phase, and tungsten is left in a raffinate, so that the separation of tungsten and molybdenum is achieved. The load-bearing organic phase adopts an alkaline back-extraction agent to carry out back-extraction to obtain a molybdenum-contained solution, and the organic phase subjected to the back-extraction returns to the extraction process. Tungsten and molybdenum are extracted and separated in the tungsten and molybdenum mixed solution containing H2O2 by adopting a novel binary mixture extracting agent, the method has the advantages that extraction and the back-extraction are high in split-phase speed, the separation effect of tungsten and molybdenum is good, the tungsten co-extraction loss is low, the loss of the organic phase as well as the environmental pollution is low, the industrialization is easy to realize, and the method is especially suitable for separating tungsten and molybdenum in the tungstate solution with high molybdenum content.

The invention provides a method for extracting lithium salt from lithium brine. The method comprises the following steps: extraction step: adding a co-extracting agent FeCl3 and an extraction agent tributyl phosphate (TBP) to lithium brine to extract lithium so as to obtain an organic phase LiFeCl4.2TBP and a water phase raffinate; reverse extraction step: adding a hydrochloric acid liquor to the organic phase LiFeCl4.2TBP for reverse extraction to obtain organic phase LiFeCl4.2TBP and water phase LiCl; and phase inversion step: inversing phase for the organic phase LiFeCl4.2TBP containing hydrogen ions by a liquor of alkali chloride, alkaline earth chloride or a mixture MCln (n is greater than or equal to 1) as a phase inversion agent to obtain an organic phase M(FeCl4)n.2TBP. According to the method for extracting lithium salt from lithium brine provided by the invention, the production cost of extracting lithium salt can be lowered.

The invention relates to a treatment method and a system of leachate of a garbage incineration plant. The method comprises that: a coagulant is added into the leachate to carry out coagulative precipitation pretreatment and to remove suspended matter; after the pretreatment, evaporation and concentration treatment are carried out on the leachate to obtain condensate water, and residue and raffinate of contaminants are removed; ammonia stripping treatment is carried out on the condensate water to remove ammonia and nitrogen; after ammonia stripping treatment, after-treatment is carried out on the condensate water to meet the environmental discharge standard. The system comprises a pretreatment system, an evaporation and concentration system, an ammonia stripping system and an after-treatment system which are connected in sequence. The invention is applicable to treating various garbage leachates with high concentration, including leachate with low content of biochemical contaminant, and can reach national primary discharge standard; heat energy of garbage incineration is used for treating leachate, thus realizing the purpose of treating waste with waste without secondary pollution; the invention has the advantages of low cost of investment and operation, energy saving, and long-term operational feasibility and load and impact resistance which are superior to prior art; the performance and operation of the invention are not restricted by foreign technology.

The invention relates to a catalytic conversion method for preparing lower olefins and aromatics. Raw oil with different cracking performances enters different reaction zones of a first riser reactor to contact with a catalytic cracking catalyst for cracking reaction to separate a spent catalyst from reaction oil gas, wherein the spent catalyst after stripping enters a first regenerator and returns to a first riser after scorching regeneration, the reaction oil gas is separated to obtain a product containing lower olefins, gasoline, distillates with distillation range of 180-250 DEG C and catalytic wax oil, wherein the gasoline is extracted by light aromatics to obtain light aromatics and gasoline raffinate; the raw materials are cracked to be sent into a second riser reactor to contract with a hot regenerated catalyst for catalytic conversion; and the spent catalyst is burned and regenerated in a second regenerator and then returns to a second riser reactor. The method uses heavy rawmaterials to furthest produce the lower olefins, such as propylene, ethylene, and the like, particularly the propylene, the production rate can exceed 40 wt%, and at the same time the method can coproduce the aromatics, such as toluene, xylene, and the like.

The invention discloses a method for recovering valuable metal from a waste power battery cathode waste material. The method comprises the following steps that (1) the waste power battery cathode waste material is subjected to acid dipping treatment, and a nickel cobalt manganese and lithium containing mixed solution is obtained; (2) the nickel cobalt manganese and lithium containing mixed solution is subjected to impurity removal, nickel cobalt manganese and lithium containing purified liquid and impurity removed liquid or impurity removed residue are obtained; (3) nickel cobalt and manganeseare separated from the nickel cobalt manganese and lithium containing purified liquid through a selective co-extraction method, and nickel cobalt and manganese containing strip liquid and lithium-rich extraction raffinate are obtained; (4) lithium-rich extraction raffinate is subjected to deep impurity removal treatment, and lithium-rich purified liquid and impurity removal liquid or impurity removal residue are obtained; (5) the lithium-rich purified liquid is treated by adopting a bipolar membrane electrodialysis method after being subjected to deep degreasing treatment, and a lithium hydroxide solution and a sulfuric acid solution are generated; and (6) the lithium hydroxide solution is evaporated and concentrated, and a battery-level lithium hydroxide monohydrate and concentrated mother liquid are obtained. The recovery rate of nickel cobalt manganese and lithium is higher than 98%, and appreciation of metal products is achieved while the valuable metal is efficiently recovered.

A process for the recovery of nickel and cobalt from an acidic resin eluate containing at least nickel and cobalt, said process including the steps of: (a) treating the eluate with an immiscible organic reagent (18) to selectively absorb the majority of the cobalt, and a portion of any copper, zinc and manganese present in the eluate, leaving a raffinate containing the nickel and minor impurities; (b) neutralising the raffinate to precipitate the nickel as nickel hydroxide (19); (c) stripping the cobalt from the organic reagent (22); and (d) recovering the cobalt (23).