9452 results about "Hydrogen peroxide" patented technology

The invention relates to the field of concrete, and provides high-strength concrete and a preparation method thereof, and the high-strength concrete comprises modified basalt chopped fiber, a self-repairing agent, cement, fly ash, slag powder, coarse aggregate, natural sand, a water reducing agent and an air entraining agent. The modified basalt chopped fiber is oxidized by hydrogen peroxide, etched by hydrochloric acid and modified by a nano silicon dioxide coating, so that the interface bonding force is enhanced. The self-repairing agent is prepared by adopting expanded perlite to load bacillus through thallus culture, purification, dipping adsorption and low-temperature vacuum drying, CaCO3 deposition can be induced at concrete cracks, and self-repairing is achieved. The invention further provides a preparation method of the concrete. The preparation method comprises the steps of aggregate screening, hydrated liquid preparation, wet mixing, fiber and self-repairing agent adding, vibration forming and curing. The crack resistance of the concrete is improved by enhancing the fiber-matrix interface bonding force, meanwhile, the service life of the concrete is prolonged by utilizing a biological self-repairing technology, and the concrete is suitable for high-durability concrete engineering.

The invention relates to a bioelectrochemical sensor used for detecting hydrogen peroxide and a manufacturing method of the bioelectrochemical sensor. The novel bioelectrochemical sensor is a sensor with a three-electrode system, wherein the counter electrode is a platinum electrode, the reference electrode is saturated calomel electrode and the working electrode is gold electrode. The sensor is based on orientation combination of a polypeptide horse radish peroxidase with characteristic sequence, the promotion effect of the polypeptide horse radish peroxidase on the activity of the enzyme and the characteristic of high sensitivity of electrochemical detection methods. The sensitivity of hydrogen peroxide sensors is effectively improved and satisfactory results are obtained.

The invention relates to the technical field, and particularly discloses a nano-modified epoxy building thermal insulation material and a preparation method thereof. The nano modified epoxy building thermal insulation material is prepared from the following raw materials in parts by mass: 80 to 120 parts of Portland cement, 20 to 40 parts of slag powder, 5 to 10 parts of hollow mesoporous silicon dioxide, 0.1 to 1 part of pyrrole, 0.1 to 0.2 part of ammonium persulfate, 5 to 10 parts of nano silicon dioxide, 10 to 15 parts of bisphenol S epoxy resin, 1 to 5 parts of acrylic acid, 1 to 2 parts of polylysine, 0.01 to 0.1 part of catalyst and 1 to 2 parts of curing agent. The concrete is prepared from the following raw materials in parts by weight: 20-30 parts of epoxy resin, 4-8 parts of loaded aerogel, 0.1-1 part of polycarboxylate superplasticizer, 1-4 parts of composite fiber and 0.2-1.25 parts of hydrogen peroxide. The fireproof building material has excellent toughness, can better resist cracking and absorb energy, effectively avoids cracking and damage under the action of thermal stress, and ensures that the building material has a fireproof effect.

The invention provides a method for preparing low-chromium low-potassium vanadium oxide by using a sodium vanadium solution, which comprises the following steps: S1) adjusting the pH value of the sodium vanadium solution to 10.5-11.0, and reacting with a chromium removal agent to obtain initial chromium removal slurry; s2) adjusting the pH value of the initial chromium removal slurry to 9.0-9.5, reacting with a silicon removal agent, and carrying out solid-liquid separation to obtain a filtrate; s3) reacting the filtrate with hydrogen peroxide, adding ammonium salt, precipitating vanadium, and performing solid-liquid separation to obtain ammonium metavanadate and primary vanadium precipitation wastewater; s4) adjusting the pH value of the primary vanadium precipitation wastewater to 6-7, reacting with ferrous sulfate, adding a complexing agent, mixing with the sodium vanadium solution, precipitating, and performing solid-liquid separation to obtain ammonium polyvanadate; and oxidizing and calcining the ammonium metavanadate to obtain the low-chromium low-potassium vanadium oxide. According to the method provided by the invention, the low-chromium and low-potassium vanadium oxide is prepared from the sodium vanadium solution, meanwhile, ammonium salt and vanadium in the primary vanadium precipitation wastewater are recycled, and the comprehensive production cost of the vanadium oxide is reduced.

The invention discloses efficient sound-absorbing lightweight aggregate foam concrete as well as a preparation method and application thereof, and belongs to the field of inorganic non-metallic materials. The high-efficiency sound-absorbing lightweight aggregate foam concrete is prepared from the following components in parts by weight: 85 to 95 parts of a sulfur-aluminum-iron series low-carbon cementing material, 5 to 15 parts of an auxiliary cementing material, 0.6 to 1.5 parts of a functional additive, 20 to 60 parts of unfired lightweight aggregate, 0.35 to 0.45 part of water and 0.5 to 1.5 L of prefabricated foam, the baking-free lightweight aggregate comprises the following components in parts by weight: 40-50 parts of a sulfur-aluminum-iron series low-carbon cementing material, 50-60 parts of byproduct gypsum, 0.7-1.5 parts of a chemical foaming agent, 15-22 parts of water and 5-8 parts of expanded perlite. According to the invention, a multi-stage-multi-scale pore structure body with expanded perlite pores, hydrogen peroxide foaming pores and physical foaming pores is constructed, so that the balanced broadband sound absorption performance of the material is realized, the sound absorption frequency range is adjustable, the sound absorption and noise reduction coefficient (NRC) of the material is greater than or equal to 0.80, the volume weight is less than or equal to 500 kg / m < 3 >, and the breaking strength is greater than or equal to 1.5 MPa.

The invention relates to the technical field of organic synthesis, in particular to a method for preparing pyroxasulfone with the IPC classification number of C07D413 / 12, and particularly relates to a method for preparing pyroxasulfone with ozone as an oxidizing agent. The preparation method provided by the invention comprises the following steps: at a certain temperature and pressure, taking ozone as an oxidizing agent, and carrying out oxidation reaction between a compound 1 and the oxidizing agent in the presence of a catalyst to obtain pyroxasulfone. According to the preparation method, ozone is used as an oxidizing agent, ozone can be automatically decomposed into oxygen at normal temperature and normal pressure, and the defect that a hydrogen peroxide solution needs to be treated when hydrogen peroxide is used as the oxidizing agent is avoided, so that the preparation method is environment-friendly, and the defect of harmful emission is overcome; the preparation method disclosed by the invention is high in product purity and yield, simple and easy to control in operation process, and beneficial to industrial application.

The invention relates to the technical field of chemical safety and intelligent control, in particular to an explosion-proof intelligent temperature control method and system for a hydrogen peroxide storage tank based on multi-modal monitoring, and the method comprises the steps: collecting multi-dimensional data such as temperature, pressure and H2O2 concentration through a sensor array, carrying out the Kalman filtering and wavelet transform denoising, recognizing local abnormal points through an improved WMDS-DBSCAN algorithm, and obtaining the explosion-proof intelligent temperature control of the hydrogen peroxide storage tank based on the WMDS-DBSCAN algorithm. Predicting a hot spot diffusion trend in combination with an unsteady heat conduction equation and an RF-ADI algorithm; weighted Delaunay triangulation is utilized to construct a self-adaptive monitoring grid, risk area probability distribution is output through an SAM-LSTM-CNN hybrid neural network, and a dynamic amplitude limiting fuzzy PID controller adjusts the opening degree of a nozzle to achieve temperature control. According to the method, multi-modal data and an intelligent algorithm are fused, abnormal accurate detection, risk prediction and self-adaptive temperature control are realized, a closed-loop optimization mechanism is formed, and the operation safety and reliability of the hydrogen peroxide storage tank are effectively improved.

The invention relates to a water treatment system for removing PFOA (perfluorooctanoic acid) in soil washing wastewater through electrooxidation coupled hydrogen peroxide reduction and application, CF / FeCo-N-C with high H2O2RR activity is prepared as a cathode to replace the traditional HER cathode reaction, the cathode potential is improved, the cathode polarization is reduced, and the input voltage and energy consumption of the system are reduced. Besides, the water treatment system is used for electrooxidative degradation of actual PFOA-containing soil washing wastewater, and compared with the prior art, the water treatment system has the advantages that the theoretical value of cathode potential can be increased from 0V vs.RHE of HER to 1.78 V vs.RHE, the ultra-low thermodynamic equilibrium potential of 1.02 V is achieved, deep treatment of the PFOA-containing soil washing wastewater is achieved, energy consumption is remarkably reduced, and the method is suitable for industrial production. New theoretical insight and practical significance are provided for sustainable treatment of PFOA-containing soil washing wastewater, and a new technical mode is provided for a post-treatment stage in soil remediation.

The invention discloses a colorimetric and fluorescent dual-mode nano-enzyme sensor. The colorimetric and fluorescent dual-mode nano-enzyme sensor comprises nano-enzyme, hydrogen peroxide and a colorimetric probe, wherein the nano-enzyme is prepared from ZrCl4, 2-aminobiphenyl dicarboxylic acid and Cu (NO3) 2 by a one-pot method; the colorimetric probe is TMB, can oxidize colorless TMB into blue oxTMB, generates an ultraviolet absorption peak at 652 nm, and has a strong fluorescence emission peak at 405 + / -5 nm. The zirconium-based metal organic framework UiO-67-NH2 with high stability is used as a carrier, Zr < 4 + > sites are replaced by part of Cu < 2 + >, the fluorescent nano-enzyme with peroxidase activity is formed, and the problems that free enzyme is difficult to recover, the stability is low and the like are solved.

The invention provides a low-cost preparation method of high-performance titanium-doped iron phosphate, and relates to the technical field of batteries. The low-cost preparation method comprises the following steps: S1, respectively preparing a phosphoric acid solution, a hydrogen peroxide solution, a phosphorus salt solution and a ferrite solution; s2, adding titanium sulfate into the ferrite solution to obtain an iron-titanium mixed solution; s3, directly adding ammonia water and a hydrogen peroxide solution into the phosphorus salt solution to obtain a phosphorus-oxygen mixed solution; s4, the iron-titanium mixed solution is heated, the phosphorus-oxygen mixed solution is put into the iron-titanium mixed solution, and slurry A is obtained; s5, obtaining a filter cake A; s6, adding pure water and a phosphoric acid solution, and heating to obtain slurry B; s7, obtaining anhydrous iron phosphate; the synthesized iron phosphate is compact and compact in morphology, internal pore channels of primary particles are still rich, the compaction density of the lithium iron phosphate material obtained through grinding and sintering reaches 2.613 g / cc, the 0.1 C discharge capacity can still reach 156.35 mAh / g, and the 1C discharge capacity reaches 131.47 mAh / g.

The invention provides a single-crystal-like dense iron phosphate material and a preparation method thereof.The iron phosphate material is prepared through the following steps that S1, a certain amount of pure water is added into a reaction kettle for bottoming, a ferrite solution and a phosphorus salt solution are added at the temperature of 30-60 DEG C, and ferrous phosphate slurry A is obtained; s2, carrying out solid-liquid separation and washing treatment on the ferrous phosphate slurry A to obtain a ferrous phosphate filter cake; s3, pulping the ferrous phosphate filter cake with pure water, uniformly stirring, transferring into a reaction kettle, continuously stirring, heating, mixing a phosphoric acid solution and a hydrogen peroxide solution, and adding to obtain white slurry B; and S4, carrying out solid-liquid separation, washing treatment and flash evaporation drying on the white slurry B to obtain iron phosphate dihydrate, and calcining the iron phosphate dihydrate to obtain the monocrystal-like dense iron phosphate material with the high iron-phosphorus ratio. When the iron phosphate provided by the invention is matched with conventional iron phosphate to prepare lithium iron phosphate, the quantity ratio of small-particle lithium iron phosphate can be effectively controlled.

The invention provides a redox imidazole covalent organic framework material as well as a preparation method and application thereof, belongs to the technical field of material preparation and photocatalytic preparation of hydrogen peroxide, and aims to solve the technical problem of low activity of a current covalent organic framework in preparation of hydrogen peroxide. The preparation method of the imidazole-connected redox type imidazole covalent organic framework material comprises the following steps: respectively reacting a reactant 2, 7-di-tert-butylpyrene-4, 5, 9, 10-tetraketone monomer with 4, 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ', 4', 4 ' The preparation method comprises the following steps: mixing 4, 4 '-(pyridine-2, 4, 6-triyl) tribenzaldehyde and a tri (4-formylphenyl) amine monomer, adding a solvent and a catalyst, uniformly stirring, and reacting to obtain the redox type imidazole covalent organic framework material after the reaction is finished. The application comprises the following steps: adding the covalent organic framework, oxygen and the sacrificial agent into water, and reacting under the irradiation of visible light. The preparation method is green, environment-friendly, simple and easy to implement, the prepared material has good thermal stability, and efficient visible light photocatalysis preparation of hydrogen peroxide can be achieved; meanwhile, the catalyst can be recycled and has good photocatalytic stability.

The present application relates to the field of wastewater treatment, and provides a treatment system and method for electroless nickel-plating waste liquid. The treatment system comprises a decomplexing pretreatment system; an oxidation-decomplexing system comprising a redox reactor and a decomplexing reactor which are connected in sequence, wherein an oxidizing agent in the redox reactor is oxygen, and an oxidizing agent in the decomplexing reactor is hydrogen peroxide; a chemical precipitation system comprising a neutralization reaction tank and a sedimentation tank which are connected in sequence, wherein the sedimentation tank is equipped with a filter system; and an evaporation crystallization system comprising an evaporation device, a crystallization device, and a separation device which are arranged in sequence. In the treatment system and method for electroless nickel-plating waste liquid, a two-stage oxidation method is employed to achieve oxidation and decomplexing of the waste liquid; in addition, combining chemical precipitation treatment and evaporation crystallization treatment not only reduces the waste liquid treatment cost but also avoids the introduction of other impurities, and allows for the separation of nickel salts and phosphate salts, so that the operation is easy and convenient, the treatment cost is low, the nickel removal rate is high, and resource utilization of nickel is facilitated.

The invention discloses a multistage circulating fluidized bed hydrogen peroxide integrated production method, and relates to the field of hydrogen peroxide preparation.The method comprises the steps that continuous efficient synthesis of hydrogen peroxide is achieved by constructing a multistage serial circulating fluidized bed reaction system; meanwhile, a genetic algorithm based on historical data is introduced to perform off-line optimization on process parameters such as reaction temperature, flow velocity, catalyst particle size, gas-liquid ratio and retention time, so that the hydrogen peroxide yield is improved, the energy consumption per unit yield is reduced, and the generation of byproducts is inhibited; the constructed optimization objective function adopts a weighted mean square error structure, multiple objectives are balanced, and it is ensured that the overall working condition is optimal; an optimization result is used for guiding initial setting and steady-state operation of a reaction system, and efficient reaction can be realized without real-time sensor control. The system has the advantages of high process structure integration level, high control strategy intelligence degree, good operation stability and the like, and is suitable for continuous optimization operation of medium and large hydrogen peroxide production devices.

The invention relates to lactobacillus crispatus LC30 for preventing and treating female genital tract infection and application of the lactobacillus crispatus LC30. The lactobacillus crispatus LC30 is preserved in the China General Microbiological Culture Collection Center with the preservation number of CGMCC NO.31923. The lactobacillus crispatus LC30 has good hydrogen peroxide production capacity and adhesion capacity, has a strong inhibition effect on main vaginitis pathogenic bacteria, and can be used for preventing and treating female genital tract infection. The composition is effective to nutritional pathogenic bacteria, and can also reduce form transformation and biological membrane formation of the pathogenic bacteria and prevent and treat drug resistance; besides, the fermentation product can reduce the content of pathogenic bacteria metabolites, regulate the secretion of cytokines and achieve the effect of relieving inflammation, so that the fermentation product can be used for preparing products for preventing and treating genital tract pathogenic bacteria infection, preventing and treating vaginitis and / or removing pudendum peculiar smell.

The invention relates to lactobacillus gasseri FMTA1125B with the effect of preventing, relieving or treating vaginitis and application of the lactobacillus gasseri FMTA1125B. The lactobacillus gasseri FMTA1125B is classified and named as lactobacillus gasseri, and the preservation number of the lactobacillus gasseri FMTA1125B is CGMCC No.34292. The lactobacillus gasseri FMTA1125B has the effects of preventing, relieving or treating vaginitis and the application of the lactobacillus gasseri FMTA1125B. The bacterium can produce beneficial components such as lactic acid, gamma-aminobutyric acid and hydrogen peroxide through metabolism so as to regulate the genital tract environment and improve the health degree; and the traditional Chinese medicine composition has relatively good bacteriostasis and sterilization effects on common vaginal pathogenic bacteria such as escherichia coli, staphylococcus aureus, gardnerella vaginalis, candida albicans, neisseria gonorrhoeae and the like. Therefore, the lactobacillus gasseri FMTA1125B strain can be used for preparing a preparation with the effect of improving related genital tract diseases such as vaginitis.

The invention relates to the technical field of organic synthesis, and discloses a preparation method of bromo-pyrrole nitrile. The method comprises the following steps: (1) mixing p-chlorophenylglycine, acetonitrile, trifluoroacetic acid and a catalyst, then dropwise adding acyl chloride and carrying out acylation reaction, and after the reaction is completed, purging with an inert gas; (2) under the inert gas, mixing the mixture obtained in the step (1) with inorganic salt, then dropwise adding 2-chloroacrylonitrile, carrying out cyclization reaction, and separating a liquid phase from the obtained mixture; and (3) under the inert gas, mixing the liquid phase obtained in the step (2), hydrobromic acid and hydrogen peroxide, carrying out a bromination reaction, then extracting with acetonitrile to obtain an acetonitrile layer, then removing the acetonitrile, and then carrying out cooling crystallization to obtain the bromo-pyrrolenitrile. According to the technical scheme, the reaction yield is high, different solvents do not need to be frequently replaced, and the solvents can be recycled.

The invention discloses a method for rapidly preparing a hard carbon negative electrode material from a waste wind turbine blade, an obtained product and application, and the method comprises the following steps: putting the waste wind turbine blade into a mixed solution of acetic acid and hydrogen peroxide, heating for reaction, filtering after the reaction, and distilling filtrate to obtain degraded resin; and carrying out heating curing on the degraded resin to obtain cured resin, carrying out pre-carbonization on the cured resin, and then carrying out Joule heat high-temperature carbonization to obtain the hard carbon negative electrode material. According to the method, fibers and resin in the waste wind turbine blades are separated through one-step reaction by adopting a chemical recovery method, and the hard carbon negative electrode material is prepared by utilizing a Joule heating technology, so that the preparation period of the hard carbon negative electrode material is shortened, the energy consumption is reduced, and the application of the hard carbon negative electrode material in the sodium-ion battery has good application prospects. And the initial coulombic efficiency, platform capacity and total capacity of the prepared sodium ion battery can be simultaneously improved.

The invention discloses a method for preparing battery-grade iron phosphate and lithium carbonate from a waste lithium iron phosphate battery, and belongs to the technical field of lithium batteries, the method comprises the following steps: slurrying a waste lithium iron phosphate positive electrode material, adding concentrated sulfuric acid for leaching, adding sodium sulfite, controlling reaction potential, and carrying out filter pressing after reaction to obtain a leachate; iron is added into the leachate to remove copper, and copper-removed liquid and copper slag are obtained after filter pressing; adding sodium dihydrogen phosphate into the copper-removed liquid to remove aluminum, and carrying out filter pressing to obtain aluminum slag and impurity-removed liquid; adjusting the pH value of the impurity-removed solution, adding hydrogen peroxide, reacting to obtain an iron phosphate dehydrate precipitate and an iron phosphate mother solution, and treating the iron phosphate dehydrate to obtain battery-grade anhydrous iron phosphate; adjusting the pH value of the iron phosphate mother liquor, carrying out filter pressing to obtain impurity-removed slag and a lithium sulfate solution, adding sodium carbonate into the lithium sulfate solution, carrying out heating reaction, filtering slurry to obtain a lithium carbonate wet material, and treating to obtain battery-grade lithium carbonate. According to the method, the problem of recycling the waste lithium iron phosphate battery material iron phosphate is solved, and comprehensive recycling of the iron phosphate and the lithium material is realized.

The invention discloses a humic acid liquid fertilizer and a preparation method and application thereof, and belongs to the technical field of liquid fertilizers, organic waste and ferric oxide are ball-milled and mixed, transferred into a muffle furnace, roasted for 2-2.5 h at 280-310 DEG C under nitrogen protection, transferred into a reaction kettle and stirred and mixed with a 10 wt% hydrogen peroxide aqueous solution and potassium hydroxide powder, and the humic acid liquid fertilizer is obtained. The preparation method comprises the following steps: adding potassium humate into a potassium humate solution, extracting for 40-60 minutes under the assistance of ultrasonic waves, filtering to obtain a potassium humate extract and filter residues, transferring the potassium humate extract into a stirring kettle, adding urea, dipotassium phosphate, a composite carbon dot lubricant and a suspension stabilizer into the stirring kettle, and uniformly mixing to obtain the humic acid liquid fertilizer. The suspension stabilizer can reduce the generation of flocculation and crystallization in the liquid fertilizer, and through the antifriction and lubrication effects of the composite carbon dot lubricant, the friction force between indissolvable solids and water outlet holes of the drip irrigation equipment is reduced, and the risk of blockage of the drip irrigation equipment is reduced.

The invention discloses an antistatic polyisoprene rubber anesthesia air storage bag, and relates to the technical field of anesthesia air storage bags. The antistatic polyisoprene rubber anesthesia air storage bag is prepared from the following raw materials in parts by weight: 100 parts of polyisoprene latex, 0.5 to 2 parts of a stabilizer, 1 to 2 parts of a sodium p-styrenesulfonate aqueous solution, 3 to 6 parts of nano silicon dioxide suspension dispersion liquid, 1 to 2 parts of an anti-aging agent, 0.8 to 2 parts of conductive graphite and 3 to 6 parts of a vulcanization bag, the anti-aging agent is prepared by the following steps: reacting 3-(3, 5-di-tert-butyl-4-hydroxyphenyl) propionic acid with glycerol 1-oleyl ether-d5 to generate an esterification product, epoxidizing the esterification product with hydrogen peroxide and formic acid, and reacting the epoxidized product with N-phenyl-1, 3-phenylenediamine, and has excellent migration resistance. By adding the anti-aging agent into the polyisoprene rubber, the anti-aging capability of the anesthesia air storage bag is improved.

The invention discloses a lactobacillus delbrueckii subsp. Lactis TG001 and application thereof in improving oral health, and belongs to the technical field of probiotic application, the preservation number of the lactobacillus delbrueckii subsp. Lactis TG001 is CCTCC NO: M 20241941, the preservation place is China Center for Type Culture Collection in Wuhan, and the preservation date is September 9, 2024. The lactobacillus delbrueckii subsp. Lactis TG001 has a good inhibition effect on common oral pathogens such as streptococcus mutans and porphyromonas gingivalis, particularly can inhibit the growth of cariogenic bacteria streptococcus mutans by generating hydrogen peroxide and remove biofilm formation, and has good tolerance to antibacterial substances in an oral environment. Therefore, the oral cavity diseases such as dental caries, periodontitis and ozostomia can be prevented, the micro-ecological environment of the oral cavity is effectively improved, meanwhile, the peculiar smell of the oral cavity is relieved, and good application prospects are achieved in preparation of products for preventing and / or treating the oral cavity diseases such as dental caries and periodontitis.

In one aspect, a preparation method for ferric phosphate includes the following steps: (a) feeding a ferrous sulfate solution and a phosphate solution including hydrogen peroxide simultaneously into a first reactor for mixing and reacting to obtain nucleated ferric phosphate; wherein a molar ratio of iron element to phosphorus element in the feeding process is 1:1, and a stirring speed is 500-600 r / min; (b) discharging the nucleated ferric phosphate to a second reactor for growth to obtain amorphous ferric phosphate slurry, and post-processing the amorphous ferric phosphate slurry to obtain the high tap density ferric phosphate; wherein a stirring speed is 120-150 r / min. The first reactor is a small-volume reactor, and the second reactor is a large-volume reactor.

The invention belongs to the technical field of organic photoelectric materials, and particularly relates to preparation and application of a benzoselenadiazole covalent organic framework material. According to the invention, benzoselenadiazolyl tetraaldehyde is used as a construction unit, o-toluidine, 4, 4 '-biphenyl diamine or 3, 3'-dihydroxybenzidine is used as a connecting body, and three kinds of novel rigid COFs, namely HBU-COF-CH3, HBU-COF-H and HBU-COF-OH, are synthesized in sequence. The COFs has high cycling stability, has outstanding advantages in the aspect of sustainable heterogeneity of molecular catalysts, and can be used as a heterogeneous photocatalyst to realize efficient hydrogen peroxide production under visible light, and the photocatalytic hydrogen peroxide production performance of the COFs is superior to that of most reported COFs materials. Wherein the yields of HBU-COF-CH3, HBU-COF-H and HBU-COF-OH are as high as 12910 [mu] mol g <-1 > h <-1 >, 8838 [mu] mol g <-1 > h <-1 > and 7679 [mu] mol g <-1 > h <-1 > in sequence.

The invention provides a preparation method of a semiconductor structure and the semiconductor structure, and particularly relates to the technical field of semiconductors. The preparation method of the semiconductor structure comprises the following steps: providing an initial semiconductor structure, wherein a metal layer is deposited on the initial semiconductor structure; performing first annealing treatment on the metal layer to generate a metal silicon compound; processing the initial semiconductor structure by using a first cleaning solution, wherein the first cleaning solution is a mixed solution of sulfuric acid, hydrogen peroxide and ferrous ions; processing the initial semiconductor structure by using a second cleaning solution, wherein the second cleaning solution is a mixed solution of hydrochloric acid, hydrogen peroxide and water; and performing second annealing treatment on the metal silicon compound to generate a self-aligned silicide layer. By adopting the preparation method of the semiconductor structure, the removal temperature of the unreacted metal layer can be reduced, the influence and damage of high temperature on the thermal stability of the metal silicon compound are avoided, and the product yield is improved.

The invention discloses a method for extracting valuable metals from black powder of waste lithium ion batteries, and belongs to the technical field of recycling of waste lithium ion batteries. According to the method, valuable metals are extracted from the waste lithium ion battery black powder by adopting low-temperature roasting and water leaching, the waste lithium ion battery black powder is taken as a raw material, sulfamic acid is taken as a roasting agent, the waste lithium ion battery is pretreated, and roasting for carbon removal, metal extraction and water leaching are performed in sequence, so that the valuable metals are obtained. And leaching liquid and leaching residues containing two or more elements of lithium, nickel, cobalt, manganese, iron and aluminum are obtained and are used for further purification and recovery of valuable metals. According to the method provided by the invention, the influence of aluminum dissolution on recovery of other metals is reduced, the use of hydrogen peroxide is avoided, the process flow is shortened, the process cost is greatly reduced, the roasting and water leaching processes cannot corrode equipment, and the whole process cannot generate waste acid to cause secondary pollution.

The invention discloses equipment and method for preparing double-electrolyzed water based on O3 and H2O2 in parallel, and relates to the technical field of disinfectant fluid preparation, the equipment comprises a lower shell and an upper shell, a self-priming pump, an ozone generation device, a hydrogen peroxide generation device and an ultraviolet device are installed in the lower shell, and the ozone generation device and the hydrogen peroxide generation device are arranged in parallel; a water inlet of the self-priming pump is connected with a first quick connector extending out of the side wall of the lower shell, and an outlet end of the ultraviolet device is connected with a second quick connector extending out of the side wall of the lower shell. The ozone generation device and the hydrogen peroxide generation device are connected in parallel, an aqueous solution containing ozone and hydrogen peroxide at the same time is obtained by controlling the proportion of ozone and hydrogen peroxide, photolysis of ozone and hydrogen peroxide is promoted by utilizing the synergistic effect of ozone and hydrogen peroxide and introducing an ultraviolet light source, and therefore more hydroxyl radicals are generated; and compared with an ozone solution, the sterilization effect of the disinfectant fluid is better.

The invention relates to a copper-molybdenum-titanium etching solution as well as a preparation method and application thereof. The copper-molybdenum-titanium etching solution comprises a main agent, the main agent is prepared from organic acid, a fluorine-containing compound, a surfactant, organic alkali, a corrosion inhibitor, hydrogen peroxide and deionized water. The copper-molybdenum-titanium etching solution provided by the invention does not contain phosphorus, the cost and environmental protection risk in a wastewater treatment link are greatly reduced, and meanwhile, the copper-molybdenum-titanium etching solution contains low fluorine, so that the etching solution has good etching activity, corrosion to equipment is effectively reduced, a powerful guarantee is provided for stable operation of production, and the copper-molybdenum-titanium etching solution is suitable for industrial production. And meanwhile, the safety of an operation environment is improved. Especially, under the condition of low hydrogen peroxide content, the copper-molybdenum-titanium etching solution shows excellent etching performance. In addition, the etching solution also has long copper service life, can effectively inhibit the negative influence of copper ions on the etching performance, prolongs the effective service time of the etching solution in a high copper content state, greatly reduces the replacement frequency of the etching solution, reduces the production cost, and improves the production efficiency.

The invention discloses a photovoltaic cell preparation method for improving ALD passivation and a photovoltaic cell, and belongs to the technical field of photovoltaic cells. The preparation method comprises the following steps: performing texturing, front boron diffusion, oxidation, back etching and polishing on a silicon wafer, preparing a back tunneling oxide layer and an amorphous silicon layer, performing acid pickling, removing the tunneling oxide layers on the back and the side surfaces through cleaning, preparing front and back passivation films, printing electrodes and the like, washing with water: washing with a cleaning solution containing potassium hydroxide and hydrogen peroxide, washing with water, pickling, and washing with water; repeating the steps; and cleaning with the oxidizing liquid again, and washing with water. According to the invention, through the improvement of the processing technology of the tunneling oxide layer and the amorphous silicon back winding plating, the yield of the battery production line is improved, the control of the production line is simpler and more convenient, the promotion of the passivation of the oxide layer before ALD is more stable, and the battery conversion efficiency of the production line is further improved.

The invention relates to a wafer cleaning solution and a cleaning method, the cleaning solution is used for an SC-2 cleaning process, and the cleaning solution comprises hydrochloric acid, hydrogen peroxide and deionized water; wherein the pH value of the cleaning solution is greater than 2. According to the invention, particulate matters can be effectively prevented from depositing on the surface of the wafer, so that the deposition quantity of the particulate matters on the surface of the wafer is reduced, and the cleaning effect on the wafer is improved.