931 results about "Thiourea" patented technology

A corrosion inhibitor composition includes a fatty acid ethoxylate, a thiourea, an arylthiourea, a thiazole, and two or more solvents. A metal article in contact with the composition has a corrosion rate of about 25 to about 45 mils penetration per year (mpy), as determined by an ASTM G111 standard test method. A method for inhibiting corrosion of a metal in contact with a corrosive fluid.

The invention discloses an application of a molybdenum disulfide-based piezoelectric catalytic material in a seawater uranium extraction material, and relates to the technical field of seawater uranium extraction, thiourea and sodium molybdate are used as precursors, and a MoS2 nanoflower with a specific 1T / 2H composite crystal structure is constructed through a hydrothermal synthesis technology. The method is placed in a uranyl nitrate solution, ultrasonic treatment is combined, efficient extraction of uranium can be achieved, and the method has potential application to extraction of uranium from seawater. The method is simple in process and environment-friendly, almost does not generate harmful waste in the synthesis process, does not need complex operation, and has good amplification preparation potential.

The invention discloses a La2O3-ZnO-NiO / ZrO2 oxygen carrier as well as a preparation method and application thereof, and belongs to the technical field of ammonia decomposition. According to the technical scheme, the method comprises the following steps: 1) synthesis of a ZrO2 carrier: adding NH3.H2O into a zirconyl nitrate solution to induce precipitation; 2) preparation of La2O3 / ZrO2: adding lanthanum nitrate hexahydrate and urea to obtain a precipitate, drying the precipitate, and finally calcining the precipitate; 3) preparation of La2O3-ZnO / ZrO2: adding zinc nitrate hexahydrate and urea, standing to obtain a precipitate, drying and calcining; and 4) preparation of La2O3-ZnO-NiO / ZrO2: adding NH3.H2O, then adding nickel acetate and thiourea, reacting, drying, and calcining twice to obtain the target product. Lattice oxygen in the oxygen carrier is used for catalytic oxidation of ammonia decomposition, the oxygen carrier can be recycled for multiple times, and the method is suitable for industrial application in the future.

The invention discloses a preparation method of a 3-micron ultrathin lithium battery copper foil. The preparation method comprises the following steps: preparing a copper sulfate electrolyte; a wetting agent, a brightening agent and a high resistance agent are added into the copper sulfate electrolyte, the high resistance agent is at least one of thiazolidinethione, polyethyleneimine, 2-mercaptobenzimidazole and ethylene thiourea, and a mixed additive is formed; polishing and grinding a cathode roller by adopting a flying wing wheel, and carrying out electrolytic treatment on the mixed additive through the polished and ground cathode roller to obtain a first-stage copper foil; and the first-stage copper foil is placed in a nitrogen furnace to be subjected to annealing treatment, and the 3-micron ultrathin lithium battery copper foil is obtained. The invention aims to solve the technical problems that in the prior art, edge tearing, foil breaking, warping, dark appearance oxidation and the like are prone to occurring in the production process of the ultrathin copper foil, the tensile strength and the ductility are difficult to consider at the same time, and stable mass production of the 3-micron copper foil is still difficult.

The invention discloses a monatomic-cluster double-active-site efficient ammonia cracking hydrogen production catalyst and a preparation method thereof, and belongs to the field of new energy catalytic materials. The catalyst comprises a 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier, a molybdenum disulfide nanosheet-loaded iron cluster carrier, monatomic active metal, cluster active metal and an auxiliary agent. Wherein the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier is prepared by the following steps: stirring 2-methylimidazole, zinc acetate and cobalt nitrate hexahydrate in methanol to generate a ZIF-8 precursor, washing, drying, and calcining in an H2 / Ar mixed atmosphere, thereby obtaining the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier; the molybdenum disulfide nanosheet loaded iron cluster carrier is prepared by carrying out hydrothermal reaction on ammonium molybdate and thiourea to generate MoS2 nanosheets and then loading iron clusters. The catalyst prepared by the invention has high activity, long service life and industrial applicability.

The invention relates to the technical field of precious metal recovery, in particular to a process for separating precious metal from copper-nickel smelting waste, which comprises the following steps: crushing and grading the waste, adding a sulfuric acid solution containing etidronic acid, leaching, and washing, drying and crushing filter residues to obtain a pretreated material; mixing the pretreated material with a sodium peroxide-sodium carbonate composite flux, roasting, leaching with water, and filtering to obtain a filter residue B; adding a leaching agent containing hydrochloric acid, sodium chlorate and 1, 2-cyclohexanediamine tetraacetic acid into the filter residue B according to the ratio of 1: 3-1: 5, and filtering to obtain filtrate C and filter residue C; adjusting the pH value of the filtrate C to 1.5-2.5, adding an ethanol solution of sodium N, N-diethyldithiocarbamate, precipitating, washing and calcining to obtain sponge palladium; adding ammonium chloride into the filtrate D, precipitating and calcining to obtain sponge platinum; and leaching the filter residue C by using a hydrochloric acid-chloroauric acid mixed solution containing diphenylthiourea, and replacing and calcining zinc powder to obtain crude gold. According to the process, the leaching rates of platinum, palladium and gold and the product purity are greatly improved; flux and reagent systems are optimized, consumption and energy consumption are reduced, waste liquid treatment is matched for up-to-standard discharge, and efficient resource recovery and environment-friendly cooperation are achieved.

The invention discloses a method for preparing a sulfur-doped nickel hydroxide-based self-supporting electrolyzed water anode, and belongs to the technical field of preparation of electrolyzed water catalytic electrodes, and the method comprises the following steps: S1, preparing strong oxidizing salt, thiourea and transition metal salt into an active solution; s2, pretreating the nickel-containing metal substrate to obtain a precursor; and S3, immersing the precursor in an active solution for ultrasonic impregnation, and performing in-situ oxidation to prepare the sulfur-doped nickel hydroxide-based self-supporting electrolytic water anode. According to the method for preparing the sulfur-doped nickel hydroxide-based self-supporting electrolytic water anode, an oxidizing agent-thiourea-transition metal salt synergistic reaction system is adopted, an ultrasonic-assisted technology is combined, and a high-performance catalytic layer is directly grown on the surface of the metal substrate in situ at room temperature; the invention aims to synchronously realize high catalytic activity, excellent stability and macro preparation of the electrode and fundamentally solve the core pain points of long process, high energy consumption, difficulty in amplification and the like in the prior art.

This application relates to the field of printed circuit board processing technology, and more specifically, to a low-electrical-loss copper bonding compound, its preparation method, and its application. The compound has the following structural formula: a polythiourea molecule with a nitrazole structure, wherein the degree of polymerization n is 3-10. This application benefits from the compound's special structure (C=S and -NH2), effectively achieving bonding under copper-free etching conditions, and the smooth copper surface meets the requirements for high-frequency signal transmission.

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 relates to the technical field of membrane separation, and discloses a polythiourea composite nanofiltration membrane as well as a preparation method and application thereof. The composite nanofiltration membrane comprises a bottom layer, a porous support layer and a polythiourea separation layer which are arranged in sequence, wherein the polythiourea separation layer comprises a structural unit A from polyamine and a structural unit B from a polyisothiocyano compound; wherein the structural unit A and the structural unit B are connected through a structure shown in a formula I, Ar1 is a residue obtained after a reaction of a compound containing polyisothiocyano groups, and Ar2 is a residue obtained after a reaction of polyamine. The separation layer structure of the polythiourea composite nanofiltration membrane contains C = S bonds, a large number of hydrogen bonds can be formed, the polythiourea composite nanofiltration membrane has excellent chemical stability, the structural stability of the composite nanofiltration membrane in a strong acid environment is remarkably improved on the premise that the separation performance of the composite nanofiltration membrane is guaranteed, and the acid resistance of the composite nanofiltration membrane is improved.

The invention discloses a filtering aid method for improving the filtering efficiency of monazite superior soluble slag, which comprises the following steps: step 1, carrying out solid-liquid separation on mixed slurry after alkali cake superior soluble callback to obtain filter residue 1 and filtrate 1; step 2, adding water into the filter residue 1, mixing and stirring according to a liquid-solid ratio of (1-2.5): 1 to react for 0.5-4 hours, and carrying out solid-liquid separation on ore pulp after the reaction to obtain a filter residue 2 and a filtrate 2; 3, if the ore pulp filtering speed in the step 2 is lower than 20 L / (m < 2 > * h) or the water content of obtained filter residues 2 is larger than 60%, the step 2 is repeated for the filter residues 2, the composite reducing agent with the preset mass is added, and stirring reaction is conducted for 2 hours till the water content of the filter residues is smaller than or equal to 60% or the ore pulp filtering speed in the plate and frame filtering process is larger than or equal to 20 L / (m < 2 > * h); in the step 3, the mass ratio of the added composite reducing agent to the original dry slag is (5-50) kg: 1t, and the composite reducing agent comprises sodium sulfite and thiourea in the mass ratio of (1-2): 1. The invention aims at shortening and improving the slag filtering performance so as to shorten the filtering time.

The invention relates to a preparation method of a niobium pentoxide loaded molybdenum disulfide catalyst and application of the niobium pentoxide loaded molybdenum disulfide catalyst in lignin conversion. The preparation method comprises the following steps: dissolving ammonium molybdate heptahydrate and thiourea in distilled water, adding Nb2O5, and adjusting the pH value of the mixture to 0.8-1.1 by using hydrochloric acid; transferring the solution into a stainless steel autoclave for hydrothermal reaction; centrifugally separating to obtain a black precipitate, washing with water and absolute ethyl alcohol, and drying in vacuum overnight; and placing the obtained substance in a high-temperature and high-pressure reaction kettle, screwing the reaction kettle to seal the reaction kettle, discharging gas after introducing H2, discharging air in the device, pressurizing to 3-5 MPa, and reacting to obtain the catalyst Nb2O5-MoS2. The catalyst shows excellent activity of aromatic phenol and ether compound hydrodeoxygenation for aromatic hydrocarbon preparation. The invention provides the catalyst which is low in cost, simple and convenient to prepare and excellent in performance, after ten cycle experiments, the activity of the catalyst is still stable, and the indexes of the conversion rate and the yield are reduced by less than 5%.

The invention discloses a method for separating and recovering selenium and mercury from acid mud containing selenium and mercury. The method comprises the following steps: mixing the acid mud containing selenium and mercury with water, performing wet ball milling, filtering and drying to obtain a ball milling material; adding a hydrogen peroxide solution into the ball-milled material, adding hydrochloric acid to adjust the acidity, carrying out oxidation acid leaching, and carrying out solid-liquid separation to obtain selenium-containing mercury liquid and selenium-removed mercury slag; adding thiourea into the selenium-containing mercury liquid for selective reduction, and performing solid-liquid separation to obtain crude selenium and reduction liquid; zinc powder is added into the reduction liquid for mercury replacement and precipitation, and crude mercury and precipitation liquid are obtained after solid-liquid separation; wherein the selenium-removed mercury slag and the precipitation solution are subjected to centralized treatment. The method is simple in process, convenient to operate and easy to process, selenium and mercury in the acid mud containing selenium and mercury can be removed at a time, efficient separation and recovery of selenium and mercury in the acid mud containing selenium and mercury are achieved, harmless treatment of hazardous waste and effective utilization of resources are achieved, and the method conforms to the concept of green sustainable development.

The invention discloses a preparation method of modified salicornia biochar, and belongs to the technical field of environmental protection. The preparation method comprises the following steps: washing, drying and crushing salicornia europaea serving as a raw material, mixing the salicornia europaea with a nitrogen source modifier according to a certain mass ratio, adding water, uniformly stirring, dipping and drying; the nitrogen source modifier is one or more of urea, melamine or thiourea; then carrying out pyrolysis and carbonization, grinding, washing and drying the obtained carbon material, and finally preparing the modified salicornia biochar. The prepared modified salicornia biochar is used for adsorbing organic matters in sewage or wastewater, can effectively remove dissolved organic carbon (DOC, 86.34%), UV254 (89.33%) and chromaticity (CN, 94.74%) in an adsorption experiment of livestock and poultry biogas slurry, and shows excellent adsorption performance. The method follows the principle of treating waste with waste, the salicornia europaea waste is effectively treated, the obtained biochar has good application potential in the aspect of sewage and wastewater treatment, and high-value utilization of the waste is achieved.

The invention relates to the technical field of nano-catalysts, and discloses a preparation method and application of a ZnxCd1-xS nano-catalyst rich in sulfur vacancies, the preparation method of the ZnxCd1-xS nano-catalyst rich in sulfur vacancies is characterized by comprising the following steps: S1, mixing cadmium salt, zinc salt and thiourea in deionized water to obtain a mixed solution; and S2, putting the mixed solution into a reaction kettle for heating reaction, cooling, collecting a reaction product, washing the reaction product with deionized water, and drying the washed reaction product to prepare the ZnxCd1-xS nano-catalyst. The ZnxCd1-xS nano-catalyst synthesized by the method is uniform in dispersion, uniform in size and regular in morphology, the morphology of the obtained ZnxCd1-xS nano-catalyst is evolved into a litchi-shaped transition state with a rough surface from a spherical shape along with the rise of the reaction temperature, and then a pine tree-shaped morphology with the regular morphology is generated. In addition, the prepared catalyst is rich in certain sulfur vacancies, and the performance is remarkably improved when the catalyst is applied to the field of photocatalytic hydrogen evolution.

The invention discloses a graphene quantum dot material as well as a preparation method and application thereof, and belongs to the technical field of biomedical materials. The preparation method comprises the following steps: S1, carrying out hydrothermal reaction on a mixed solution of mesoporous SiO2 and a carbon source to obtain a product I; s2, the product I and a fluoride solution are mixed to remove SiO2, and a product II is obtained; and S3, refining the product II to obtain the graphene quantum dot material. The carbon source is selected from at least one of triammonium citrate, diammonium hydrogen citrate, citric acid, folic acid, urea, thiourea and dicyanodiamine; the fluoride is selected from ammonium bifluoride and / or hydrogen fluoride. The particle size of the graphene quantum dot material provided by the invention is 15-30nm, the distribution is controllable, and the raw materials are easy to obtain; the prepared platinum nanoparticle / graphene quantum dot composite nanomaterial is high in solubility, stable in physical and chemical properties and remarkable in chemotherapy effect.

The invention discloses a preparation method of protecting group cefdil side chain acid. The preparation method comprises the following reaction steps: step 1, performing oximation reaction on a compound IV to obtain a compound V; 2, cyclizing the compound V and thiourea to obtain a compound VI; 3, condensing the compound VI and tert-butyl alpha-bromoisobutyrate to obtain a compound VII; 4, the compound VII passes through a protective group to obtain a compound VIII; and 5, hydrolyzing the compound VIII to obtain the product protecting group cefdil side chain acid. The raw materials used in the method are simple and easy to obtain, expensive reagents and customized raw and auxiliary materials are not used, the process operation is simple, a major dangerous process is not involved, and the method has industrial advantages.

The invention relates to the technical field of photocatalysts, in particular to a bismuth-defect bismuth oxybromide-sulfur-defect bismuth sulfide bromide heterojunction and a preparation method and application thereof in photocatalytic CO2 reduction, Bi (NO3) 3.5 H2O, thiourea, cetyltrimethylammonium bromide (CTAB) and the like are used as raw materials, and the VBi-Bi4O5Br2 / VS-Bi19Br3S27 heterojunction is prepared through a two-step hydrothermal method. According to the VBi-Bi4O5Br2 / VS-Bi19Br3S27 heterojunction, bismuth vacancies and sulfur vacancies are introduced, the visible light absorption range of the material is expanded through a proper amount of double vacancies, more electron capture centers are provided, and the separation efficiency of photo-induced electrons and the vacancies is improved, so that the VBi-Bi4O5Br2 / VS-Bi19Br3S27 heterojunction has excellent performance of photocatalytic reduction of CO2, and the preparation method of the VBi-Bi4O5Br2 / VS-Bi19Br3S27 heterojunction is suitable for large-scale production and application of the VBi-Bi4O5Br2 / VS-Bi19Br3S27 heterojunction. CO2 can be reduced into a single product CO, and the photoreduction efficiency of the carbon dioxide can be improved.

The invention discloses a low-cost nano porous silicon-carbon composite material based on a solid waste silicon source as well as a preparation method and application thereof. The preparation method comprises the following steps: taking a solid raw material containing silicon dioxide as a silicon source; carrying out wet ball milling on the pretreated raw materials; mixing the ball-milled material with magnesium powder, aluminum chloride and lithium chloride; carrying out heating reduction reaction on the mixed material; sequentially performing hydrochloric acid pickling and hydrofluoric acid pickling on the reduction product, and then washing to be neutral; mixing the washed silicon particles with a carbon precursor containing nitrogen and sulfur, coating by adopting a spray coating method, and then carrying out carbonization treatment; the carbon precursor containing nitrogen and sulfur is composed of asphalt and thiourea; the carbonization temperature is 750-850 DEG C, the carbonization time is 1-2 hours, and the heating procedure comprises a desolventizing section, an asphalt decomposition section and a carbonization section. The preparation method is low in raw material cost, low in energy consumption, environment-friendly and excellent in product comprehensive performance, and has wide application prospects in the fields of power batteries, energy storage, catalysis and the like.

The invention relates to the technical field of solid-state batteries, and provides a MoS2 / MoN / C conductive agent, a preparation method thereof and an application of the MoS2 / MoN / C conductive agent in a sulfide all-solid-state battery. The preparation method comprises the following steps: firstly preparing formaldehyde-melamine polymer microspheres, then enabling the formaldehyde-melamine polymer microspheres to adsorb molybdenum salt and ammonia water through impregnation to obtain a polymer precursor, and then obtaining the MoS2 / MoN / C conductive agent through pyrolytic reaction of the polymer precursor and thiourea. Compared with the traditional conductive agent, the MoS2 / MoN / C conductive agent prepared by the invention does not induce the sulfide solid electrolyte positive electrode material to generate chemical / electrochemical side reaction, has excellent electronic conductivity and ion mobility, has excellent stability, and can promote the development of sulfide electrolyte all-solid-state batteries.

The invention relates to the technical field of immunochromatography analysis, and discloses a signal enhancer of a colloidal gold immunochromatography rapid detection card and a preparation method thereof, the signal enhancer comprises a silver ion solution, a thiourea-ascorbic acid synergistic reducing agent, a pH buffer system and a surfactant stabilizing system, the signal amplification is realized by catalyzing and depositing silver nanoparticles on the surface of colloidal gold, the operation is simple and convenient, one-time addition is realized, and the reaction is completed within 5-10 minutes; the sensitivity is improved by 5-10 times, and the specificity is higher than 98%; the stability is excellent, and the storage time is 12 months at 4 DEG C; various colloidal gold rapid detection cards are universally compatible; compared with the prior art, the colloidal gold immunochromatography rapid detection card has the advantages that the cost is controllable, the single detection is increased by 0.3-0.5 yuan, and the colloidal gold immunochromatography rapid detection card is particularly suitable for ultra-sensitive detection of small molecular substances in the field of food safety, for example, the detection limit of malachite green reaches 0.1 microgram per liter, the detection limit of fipronil reaches 0.5 microgram per liter, and the application range of the colloidal gold immunochromatography rapid detection card is obviously expanded.

The invention relates to the technical field of etching solutions, and discloses a molybdenum-aluminum-niobium etching solution for a TFT-LCD (Thin Film Transistor Liquid Crystal Display), which comprises the following components in percentage by mass: 50 to 60 percent of phosphoric acid, 3 to 8 percent of nitric acid, 5 to 10 percent of glacial acetic acid, 1 to 5 percent of aluminum nitrate, 0.1 to 0.5 percent of diphenyl thiourea, 1 to 5 percent of etidronic acid, 3.0 to 5.0 percent of sodium hexametaphosphate, 0.1 to 0.2 percent of fatty alcohol-polyoxyethylene ether, 0.5 to 0.8 percent of amino trimethylene phosphonic acid and the balance of ultrapure water. The invention further discloses a preparation method of the molybdenum-aluminum-niobium etching solution. According to the invention, a phosphorus nitrate vinegar system, a composite additive, a novel corrosion inhibitor, a metal ion chelating agent and a surfactant matched with the etching liquid are adopted, so that the molybdenum-aluminum-niobium multi-layer composite metal film can be simultaneously etched at one time; the etching solution has the advantages of being uniform in etching, capable of inhibiting Mo / Nb etching, high in selectivity, controllable in etching rate, free of residues, long in service life, high in stability and the like.

The invention relates to a thiourea-polyamine condensation polymer, an epoxy adhesive and a preparation method of the thiourea-polyamine condensation polymer, and the thiourea-polyamine condensation polymer is obtained by reacting thiourea with 3, 3 '-dimethyl-4, 4'-diaminodicyclohexylmethane. According to the preparation method, thiourea is used for modifying 3, 3 '-dimethyl-4, 4'-diaminodicyclohexylmethane under a proper condition, so that the modified thiourea-polyamine condensation polymer is obtained. The modified thiourea-polyamine polycondensate is simple in preparation process and high in yield. Moreover, the modified thiourea-polyamine polycondensate can be used as a chain extender for preparing an epoxy adhesive, the impact toughness and tensile property of the epoxy adhesive can be remarkably improved, the epoxy adhesive has better heat resistance, and the application field and scene of the epoxy adhesive are expanded.

The invention discloses a thiochromanone derivative containing a thiosemicarbazone structure and application of the thiochromanone derivative, relates to the technical field of medicines, and particularly relates to the technical field that the compound has better oxidation resistance and alpha-glucosidase resistance activity, the IC50 value of the compound 1-(7-chloro-4, 4-dioxothiochromanone-3-N-propyl) thiosemicarbazone to ABTS clearance activity is 2.86 [mu] g / mL, the IC50 value of the compound 1-(7-chloro-4, 4-dioxothiochromanone-3-N-propyl) thiosemicarbazone to alpha-glucosidase inhibition activity is 9.51 [mu] g / mL, and the effect is the best and is superior to that of a control agent vitamin E and acarbose. The thiochromanone derivative containing the thiosemicarbazone structure has a general formula shown in the specification,

The application discloses a method for synthesizing a single-atom catalyst, which comprises the following steps of mixing raw materials: taking dimethyl imidazole, zinc nitrate and graphene oxide as solutes, and taking anhydrous methanol as a solvent to form ZIF-8@GO through stirring; taking ZIF-8@GO and thiourea as solutes, and taking anhydrous methanol as a solvent to form S / ZIF-8@GO through stirring and adsorption; first-stage pyrolysis: pyrolyzing S / ZIF-8@GO in a protective gas atmosphere to form porous carbon (S, N-C); precursor preparation: after the porous carbon is cooled, phenanthroline (Phen) and a transition metal source (M) are added into the porous carbon to form a precursor M / S, N-C@Phen; and second-stage pyrolysis: pyrolyzing the M / S, N-C@Phen precursor in a protective gas atmosphere to obtain a M / S, N-C single-atom catalyst. The synthesis method is simple and effective, can be used for large-scale synthesis of a single-atom catalyst, is suitable for synthesis of various metal single-atom catalysts, and solves the problems of complexity in the prior art and difficulty in large-scale preparation.

The invention discloses a stepped recovery method for key components of a core layer laminated structure of a waste photovoltaic module, which comprises the following steps: crushing and pyrolyzing the core layer laminated structure of the waste photovoltaic module to obtain granular powder, and sequentially carrying out selective aluminum leaching and aluminum recovery treatment by using a composite organic acid solution, the step-by-step recovery of key components such as aluminum, silver, lead and silicon elements is realized through selective silver-lead leaching and silver recovery treatment of a thiourea composite complexing oxidation solution, precipitation and solidification treatment of lead and purification and recovery treatment of silicon. According to the recycling method, selective separation and efficient recycling of corresponding metal and silicon resources are carried out on the composite waste containing a silicon substrate (containing an antireflection layer SiNx and SiO2), silver, aluminum, EVA and PbO according to the gradient separation sequence of aluminum, silver, lead and silicon.

The invention discloses a grafted cellulose-based separation membrane and a preparation method thereof. The separation membrane comprises a membrane substrate containing cellulose and double grafting chains growing on the surfaces of the two sides of the membrane, the double-grafted chain comprises a Block A chain grafted to the membrane substrate and a Block B chain grafted to the end of the Block A chain; the structure of the separation membrane is as follows: a substrate-[Block A]-[Block B], a Block A chain is a block copolymerization chain containing a thiourea group and an amidoxime group, and a Block B chain is a block hydrophobic chain containing a vinyl imidazolium salt graft product. The adsorption capacity of a BlockA chain to heavy metal ions can be improved through thiourea group and amidoxime group bidentate synergistic coordination; the BlockB chain can repel harmful anions through static electricity of the vinyl imidazole onium salt and remove organic matters through hydrophobic-hydrophobic interaction. The preparation method of the separation membrane comprises the steps of double-sided activation of a membrane substrate, initiator fixation and double-sided growth of a Block A chain and a Block B chain, the Zeta potential of the obtained grafted cellulose membrane is larger than or equal to + 40 mV, the water contact angle is larger than or equal to 105 degrees, the carbon yield at 600 DEG C is larger than or equal to 30%, and the separation membrane is suitable for treatment of electroplating wastewater and other complex polluted wastewater.

The present application relates to the technical field of anode slime treatment, and discloses a method for removing antimony and tellurium from anode slime by multi-stage pressurization and chlorine-free process, which comprises the following steps: S1, anode slime pretreatment, S2, multi-stage pressurization treatment, S3, separation of antimony and tellurium from the anode slime, S4, preparation of sodium antimonate, S5, tail gas treatment, S6, waste liquid treatment, S7, post-treatment. The method is characterized by the following: one-stage pressurized thiourea transformation is used for deep copper removal, and two-stage pressurized sulfuration is used for chlorine-free antimony and tellurium removal. The process flow does not involve chlorine-containing substances, and the pressurized leaching of alkaline medium does not produce substances with strong corrosivity, thereby reducing the damage to the equipment. In the process of removing antimony and tellurium, the harmful substances generated during the reaction can be treated by waste gas and waste liquid treatment, and the by-products, precipitates, incompletely removed heavy metal ions, trace pollutants and the like in the tail liquid can be removed or converted into harmless substances, so that the tail liquid meets the discharge standard and the environmental pollution caused by the tail liquid discharge is reduced.

The invention relates to a preparation method of a novel anti-freezing rewarming antibacterial medical gel dressing, belongs to the field of composite material-based hydrogel, and is applied to prevention and treatment of frostbite of field operating personnel in high-cold regions. The preparation method comprises the following step: reacting anhydrous copper chloride, polyvinylpyrrolidone and thiourea to obtain copper sulfide. The preparation method comprises the following steps: dispersing copper sulfide, polymerizing dopamine hydrochloride in an alkaline oxygen-containing environment to gather on the surface of the copper sulfide so as to form polydopamine copper sulfide (PDA-coated CuS), adding N 'N-methylene bisacrylamide and ammonium persulfate, stirring, pouring into a mold, and polymerizing in an environment of 60 DEG C, thereby obtaining PDA-coated CuS / Pro / PAM gel. CuS and PDA are combined, so that the biocompatibility and antibacterial property of CuS are enhanced, the photo-thermal property of dopamine is improved, and proline is used as an antifreeze agent to destroy hydrogen bonds of water molecules and inhibit formation of ice crystals. The medical gel dressing has the beneficial effects that the medical gel dressing with the anti-freezing, rewarming and antibacterial functions can be used in a low-temperature environment of-24 DEG C, and a good rewarming environment is provided for a frostbite part.

The invention discloses an online monitoring and regulating system for inhibiting nitration reaction by thiourea for sewage treatment, and relates to the technical field of sewage treatment. Comprising an on-line monitoring module which monitors and obtains nitrification parameters and environmental parameters in the nitrification activity process through an on-line analyzer and a sensor network, and adjusts parameter monitoring frequency according to the nitrification parameters; the intelligent control module is used for determining optimal parameters of a PID (Proportion Integration Differentiation) controller through a virtual reference model according to the nitrification parameters and the environmental parameters, and determining the addition amount of a thiourea solution according to the optimal parameters; and the thiourea adding unit is used for adding the thiourea solution at an adding point through adding equipment according to the adding amount of the thiourea solution. According to the method, excessive inhibition possibly caused by a traditional control model based on historical data is avoided, the risk that fragile nitrifying flora is thoroughly killed is effectively prevented, success of the bacterium cultivation process is ensured, and the system starting time is shortened.