4779 results about "Hydrogen peroxide" patented technology

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 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 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 provides an electrochemical active oxygen supply device for a washing machine and a preparation method. The device comprises a shell, a single closed reaction chamber is formed in the shell, a bifunctional anode electrode and a bifunctional cathode electrode are integrated in the reaction chamber, and a compact and uniform reaction area is formed between the anode electrode and the cathode electrode. When water flows through the reaction area, hydrogen peroxide (H2O2) and / or hydroxyl radicals (OH) are / is electrochemically generated on the surface in situ by accurately adjusting the electrode potential of the difunctional anode, so that instant generation and instant utilization of active oxygen are realized. The active oxygen directly enters a washing system of the washing machine along with water flow, bacteria, viruses and fungi can be efficiently inactivated under the normal-temperature or low-temperature washing condition without additionally adding chemical disinfectants, organic stains and peculiar smell molecules are synchronously degraded, and green, efficient and intelligent healthy washing is achieved.

The invention belongs to the technical field of pharmaceutical chemical processes, and particularly relates to a preparation method of a penem antibiotic intermediate 4-BMA, which comprises the following steps: adding Zn powder, chlorosilane, aliphatic tertiary amine, zinc salt and 4-AA in a formula (I) into THF (tetrahydrofuran), uniformly stirring, dropwise adding a THF solution of alpha-haloamide with an induction group in a formula (II) for reaction, filtering the reaction solution, removing the zinc powder, and drying to obtain the penem antibiotic intermediate 4-BMA. Extracting the filtrate to obtain a THF phase, washing with an aqueous solution of potassium oxalate, and recovering THF to obtain a formula (III); and carrying out oxidative hydrolysis, sulfur dioxide quenching, sulfur dioxide acid regulation crystallization and recrystallization on the formula (III) to obtain the intermediate 4-BMA. According to the preparation method disclosed by the invention, a zinc salt is used as a catalyst during preparation of the formula (III), potassium oxalate is used for removing residual Zn (II) in a THF phase, SO2 is used for quenching hydrogen peroxide and acid regulation and crystallization of 4-BMA, the oxygenolysis problem of 4-BMA is solved, and the preparation method has the characteristics of greenness, safety and high efficiency, is strong in product competitive advantage and is suitable for industrial production.

The invention relates to the technical field of state monitoring, and discloses a hydrogen peroxide purification process state monitoring method. The method comprises the following steps: performing multi-point real-time monitoring and hydrogen peroxide decomposition risk target factor calculation on the temperature, pressure, conductivity and organic matter content of hydrogen peroxide purification equipment to obtain an evaluation result of the influence of temperature gradient and impurity content on hydrogen peroxide stability; carrying out predictive control parameter calculation on the heating power, the cooling flow and the feeding rate to obtain a safe operation parameter range of the equipment; and performing dynamic safety boundary calculation on the temperature distribution and the concentration boundary in the purification process to obtain a hydrogen peroxide decomposition risk early warning index. Through construction of the dynamic safety boundary and calculation of the risk early warning index, stable operation of the hydrogen peroxide purification equipment is realized, so that the production process of the electronic-grade high-purity hydrogen peroxide is safer, more stable and more efficient.

The invention belongs to the technical field of rare and precious metal recovery, and particularly relates to a method for recovering metallic silver from waste crystalline silicon battery pieces, which comprises the following steps: (1) putting the waste crystalline silicon battery pieces into an inorganic alkali aqueous solution for soaking reaction to obtain an aluminum-containing solution and dealuminized crystalline silicon pieces; (2) adding the dealuminized crystal silicon wafer into a mixed solution of organic acid and hydrogen peroxide for soaking reaction, filtering and washing to respectively obtain silver-containing filtrate and a silver-removed silicon wafer; (3) carrying out chlorination precipitation reaction on the silver-containing filtrate and a chlorine source, filtering and drying to obtain silver chloride powder; (4) adding silver chloride powder into an ammonia water solution, heating and stirring to completely dissolve silver chloride to obtain a silver-ammonia solution; (5) adding PVP (Polyvinyl Pyrrolidone) into the silver-ammonia solution, heating and stirring until the PVP is completely dissolved, adding ascorbic acid, and carrying out reduction reaction at room temperature to obtain metal silver powder precipitate; and filtering, washing and drying the precipitate to obtain the spherical silver powder. According to the method, the silver recovery efficiency is high, the spherical nanoscale silver powder can be prepared, and the purity is high.

The invention provides a method for recovering tungsten and rhenium from tungsten-rhenium alloy waste, which comprises the following steps: S1, collecting the tungsten-rhenium alloy waste, and crushing to obtain tungsten-rhenium alloy waste powder; s2, the cleaned tungsten-rhenium alloy waste powder is put into a reactor, and then a strong alkaline solution containing hydrogen peroxide is added into the reactor for a reaction; in the strong alkaline solution, the concentration of OH <-> dissociated by the strong alkaline substance is 2.0-4.0 mol / L, and the mass fraction of hydrogen peroxide in the strong alkaline solution is 5-15%; in the reaction process, synchronously and continuously introducing oxidizing gas into the reactor and applying ultrasonic treatment; and S3, after the reaction is finished, carrying out solid-liquid separation, collecting a leaching solution, then separating tungsten-containing ions and rhenium-containing ions in the leaching solution to respectively obtain a tungsten-containing ion solution and a rhenium-containing ion solution, and carrying out subsequent treatment to obtain tungsten salt or metal tungsten and rhenium salt or metal rhenium. According to the method, the passivation problem can be effectively solved, and the leaching rate and recovery rate of W and Re can be increased.

The preparation method comprises the following steps: S1, preparing a phosphoric acid solution, a hydrogen peroxide solution, a Ti salt, a phosphor salt solution and a ferrite solution; s2, Ti salt and the ferrite solution are mixed, and a titanium iron salt solution is obtained; mixing the phosphoric acid solution and the phosphorus salt solution to obtain a phosphorus source solution; s3, adding the titanium iron salt solution into a reaction kettle, and adding the hydrogen peroxide solution; s4, adding the phosphorus salt solution into the reaction kettle to obtain yellow slurry; s5, after the color of the slurry is heated to be white, white slurry is obtained; s6, carrying out solid-liquid separation on the white slurry to obtain an iron phosphate dihydrate filter cake; and S7, drying and calcining the iron phosphate dihydrate filter cake to obtain the Ti-doped battery-grade anhydrous iron phosphate. The titanium-doped iron phosphate is firstly prepared by a one-step method, the pH value of the reaction system is controlled by controlling the molar ratio of the iron element to all phosphorus elements in total phosphorus, ammonium phosphate and phosphoric acid in the reaction system, and the retention of the Ti element in the finished product and the regulation and control of the iron-phosphorus ratio in a specified range are ensured.

The invention provides a method for recycling a waste lithium iron phosphate battery positive electrode material based on organic solvent soaking. The method comprises the following steps: mixing waste lithium iron phosphate positive electrode material powder and a crown ether chelating type co-dissolving agent to obtain a leaching solution; hydrogen peroxide is added into the leachate, the pH is adjusted, a diammonium hydrogen phosphate solution is added, and iron phosphate and filtrate containing lithium ions are obtained; adding sodium carbonate into the filtrate containing lithium ions, and adjusting the pH value to obtain lithium carbonate; mixing the iron phosphate with a phosphoric acid solution to obtain purified iron phosphate; and mixing the purified iron phosphate, lithium carbonate and acetylene black to obtain the regenerated lithium iron phosphate positive electrode material. According to the method for recycling the positive electrode material of the waste lithium iron phosphate battery based on soaking of the organic solvent, the leaching rate of the lithium element is effectively increased, the selectivity to other metal ions is low, and the regenerated positive electrode material of the lithium iron phosphate battery has relatively high discharge capacity and good cycling stability.

The invention discloses a quality-divided treatment and recycling method for lead-zinc beneficiation wastewater, and belongs to the technical field of beneficiation wastewater treatment.The method comprises the steps that beneficiation tail water is introduced into a Fenton reaction tank, a catalyst is added firstly, then hydrogen peroxide is added, a Fenton oxidation reaction is conducted, after the Fenton oxidation reaction is finished, the beneficiation tail water is introduced into a coagulation reaction tank, caustic soda liquid is added, and the mixture is stirred and mixed uniformly; adding a precipitating agent, a flocculating agent and a stabilizing agent, and flocculating and settling the precipitate; introducing the beneficiation tail water added with the treatment agent into a honeycomb inclined tube sedimentation tank, further flocculating and settling, then returning flocculated precipitates in a bottom tank to a coagulation reaction tank, and discharging redundant bottom mud into a tailing pond; and settled clear water enters a clear water tank and is used as production water for ore grinding classification and flotation operation. According to the invention, through quality-divided treatment-quality-divided recycling of the beneficiation wastewater, it is ensured that the beneficiation tail water meets the requirements of ore grinding and flotation production indexes, the treatment cost of concentrate overflow water and filtered water is reduced, and the purpose of 100% recycling of the beneficiation wastewater after quality-divided treatment is achieved.

The invention belongs to the technical field of chemical catalysis, and particularly relates to a preparation method of an alkali metal cation modified cobalt-nitrogen-carbon monatomic catalyst and application of the catalyst in electrosynthesis of hydrogen peroxide. The Co-N-C / X catalyst is obtained by taking a cobalt-containing compound as a metal source, mixing the metal source with a nitrogen-containing organic matter and a carbon material, performing rotary evaporation, grinding and high-temperature pyrolysis in an inert atmosphere, performing acid washing with strong acid to construct surface defects, and finally performing stirring adsorption with an alkali metal salt solution, suction filtration and drying. Alkali metal cations are physically adsorbed and anchored on the surface and interface of the Co-N-C catalyst instead of being dissolved in a solution, so that the electronic structure of Co active sites and the adsorption energy of the * OOH intermediate are optimized, and the problem of separation of alkali metal and a product is solved. When the catalyst is used for electro-catalytic oxygen reduction reaction, the H2O2 selectivity reaches up to 98%, the preparation process is simple, the cost is low, large-scale production can be realized, and the problems that the traditional method is high in energy consumption and large in pollution and the existing catalyst is insufficient in selectivity are solved.

The invention belongs to the technical field of antibiosis and wound healing promotion, and relates to double-response (near-infrared light and hydrogen peroxide double-response photo-thermal / carbon monoxide therapy) antibacterial hydrogel as well as preparation and application thereof. The invention relates to a double-response antibacterial hydrogel. The antibacterial hydrogel is prepared from the following components: drug-loaded nano particles and a hydrogel matrix. The drug-loaded nano particles are prepared by loading dimanganese decacarbonyl (MnCO) into cavities of hollow mesoporous copper sulphide nano particles (HMCuS NPs) and coating the surfaces of the particles with a polydopamine layer (PDA). According to the invention, CO / PTT synergistic treatment of bacterial infected wounds is realized, and the antibacterial effect is significantly improved. An in-vitro antibacterial experiment result shows that the antibacterial hydrogel shows extremely strong inhibition capability on escherichia coli and staphylococcus aureus, and the problem of drug resistance caused by a bacterial biofilm is effectively solved.

The invention discloses a method for producing docosahexaenoic acid by strengthening schizochytrium limacinum, which comprises the following steps: carrying out fermentation culture on a schizochytrium limacinum strain until the growth period is ended (a nitrogen source is used up); when the growth period of the schizochytrium limacinum is ended, exogenously adding hydrogen peroxide, culturing, exogenously adding para aminobenzoic acid, and culturing; and repeating for several times, and ending the fermentation to obtain the DHA-containing fermentation liquor. Compared with execution of a blank group without addition of exogenous additives, an independent hydrogen peroxide intermittent feeding control strategy and an independent aminobenzoic acid intermittent feeding control strategy, the DHA yield is increased by 25.21% or above when the hydrogen peroxide-p-aminobenzoic acid periodic control method is adopted, and the highest level of 1.49 g / L is achieved.

The invention discloses a real-time feedback method and system for a hydrogen peroxide production process, and relates to the technical field of intelligent feedback. The real-time feedback method and system for the hydrogen peroxide production process comprises the following steps: S1, preprocessing production process data and historical process data; s2, self-adaptive time sequence prediction feedback regulation and control analysis is carried out, the rotating speed of a servo motor is adjusted, and a sampling flow error value is corrected; s3, performing regulation and control characteristic attribution analysis, and performing mixed solution transfer; s4, performing process equipment self-diagnosis for efficient emulsion separation and multi-parameter mahalanobis distance discrimination; and S5, carrying out process parameter optimization and risk early warning. The problems that an existing system is difficult to achieve automatic continuous sampling and flow self-adaptive regulation and control in the hydrogen peroxide production process, and high-precision real-time monitoring and intelligent early warning are difficult to achieve are solved.

The invention relates to a method for treating a waste iron phosphate positive electrode material by a phosphoric acid-hydrogen peroxide method matched with a specific complexing agent. The method comprises the following steps: crushing the positive electrode material of the waste lithium iron phosphate battery, adding the crushed positive electrode material into deionized water, and stirring to prepare slurry; heating the slurry, dropwise adding a phosphoric acid-hydrogen peroxide mixed solution and a complexing agent, adding a NaOH solution to adjust the pH value to 3.5, and filtering to obtain a filtrate and a filter cake; adding a NaOH solution into the filtrate, and adjusting the pH value to 10 to obtain lithium phosphate; performing evaporative crystallization on the filter cake to obtain trisodium phosphate; the complexing agent is prepared by adding pentasodium salt of amino trimethylene phosphonic acid, triallyl citrate, epoxysuccinic acid and DMF (Dimethyl Formamide) into a reaction kettle, mixing, adding ammonia water to adjust the pH value to be 10, and distilling to remove the DMF after the reaction is finished. The precipitation rate of Fe reaches up to 99.99%, the leaching rate of Li reaches up to 99.91%, and efficient separation and recycling of lithium and iron are achieved.

The invention discloses preparation of a phenanthroline-based covalent organic framework photocatalyst and application of the phenanthroline-based covalent organic framework photocatalyst in photocatalytic production of hydrogen peroxide. According to the method, a hydrogen peroxide production experiment is carried out in a water-oxygen system or a benzyl alcohol-water-oxygen system by taking phenanthroline-based COF as a photocatalyst. According to the invention, through regulation and control of molecular flatness engineering, an electron-rich phenanthroline unit (Phen) anchored by a pyridine expansion plane and electron-deficient triazine (TTA) are integrated into a COF skeleton, and a novel electron donor-acceptor (D-A) type COF is synthesized. The COF has the advantages of proper energy band structure, excellent photo-induced electron and hole separation efficiency, strong D-A interaction, good hydrophilicity and the like, and the efficiency of photocatalytic hydrogen peroxide production reaction within a short time is greatly improved. The invention provides a use method of the COF photocatalyst which is cheap, convenient, rapid, efficient and environment-friendly, and has a potential application prospect.

Provided is a stabilized aqueous hydrogen peroxide composition comprising a sugar alcohol that does not contain silver, organophosphonate, peroxyacetic acid or other peracid, or stannate. The composition optionally includes a carboxylic acid. The composition is suitable as a disinfectant and oxidizer, and for the treatment, inhibition, or eradication of fungi or nematodes. Also provided is a method for reversing a bacterial or fungal infection in an infected plant, and a method for enhancing plant growth and / or productivity. Also provided is a method for inhibiting or preventing fungal spore germination in soil in a fungal infested area. Also provide is a method of controlling or preventing nematode infestation of a plant, and a method of reversing damage of a plant caused by nematode infestation. Also provided is a method for treating or reversing Panama disease in an infected banana plant.

The invention discloses a copper surface micro-etching coarsening solution for a fine circuit as well as a preparation method and application of the copper surface micro-etching coarsening solution, and relates to the technical field of printed circuit board manufacturing. The copper surface micro-etching coarsening solution for the fine circuit is prepared from, by mass concentration, 60 g / L to 100 g / L of sulfuric acid, 40 g / L to 60 g / L of hydrogen peroxide, 0.5 g / L to 2 g / L of zinc sulfate, 10 g / L to 30 g / L of copper ions, 0.5 g / L to 1 g / L of pyridine heterocycle-containing Schiff base, 10 g / L to 100 g / L of ethyl alcohol, 1 g / L to 3 g / L of 2-mercaptobenzothiazole, 1 g / L to 5 g / L of methionine and 1 g / L to 5 g / L of polyacrylamide. According to the copper surface micro-etching coarsening solution, the 2-mercaptobenzothiazole and the methionine in the copper surface micro-etching coarsening solution can enable the copper surface to form a honeycomb structure under the low micro-etching amount, the zinc sulfate and the pyridine heterocyclic ring-containing Schiff base can form a composite film layer with copper ions on the surface of the honeycomb structure, and the interlayer binding force is improved.

The invention provides a preparation method of grain size grading iron phosphate and high compaction type lithium iron phosphate. Removing impurities from the titanium dioxide byproduct ferrous sulfate, and filtering to obtain a purified ferrous sulfate base solution; the method comprises the following steps: reacting phosphoric acid with ammonia water to prepare ammonium phosphate solutions with different reaction pH values and phosphorus molar concentrations, respectively mixing the ammonium phosphate solutions with a certain amount of hydrogen peroxide, and sequentially adding an iron source, a first phosphorus salt solution, a second phosphorus salt solution and a third phosphorus salt solution into a tubular reactor for reaction to obtain iron phosphate slurry; and sequentially converting, filtering, washing, drying and calcining the completely reacted slurry to finally prepare the anhydrous iron phosphate. According to the invention, a mode of controlling solution nucleation and growth is adopted, nucleation and growth rates are controlled by preparing phosphorus salt solutions with different concentrations, size grading of precursor particles is directly realized in a synthesis reaction section, and slurry grading uniformity is further realized through aging crystal transformation. Lithium iron phosphate prepared from the iron phosphate precursor has high compaction density.

The present invention generally relates to a process for synthesizing a graphene oxide quantum dots-iron phthalocyanine (FePc-GOQDs) nanocomposite with enhanced electrochemical properties, particularly for oxygen reduction reactions (ORR). The process begins by dispersing 500 mg of graphene oxide (GO) in a hydrogen peroxide and deionized water solution in a 1:10 volume ratio, followed by hydrothermal treatment at 180° C. for 8 hours to produce GO quantum dots (GOQDs). The resulting material is freeze-dried to obtain GOQDs powder. Subsequently, 60 mg of GOQDs are combined with 10 mg of iron phthalocyanine (FePc) and 20 mL of dimethyl sulfoxide (DMSO), and the mixture is subjected to microwave irradiation at 500 W and 150° C. for 30 minutes. The resulting composite is rinsed repeatedly with deionized water and ethanol, then dried at 120° C. to yield the FePc-GOQDs nanocomposite. This composite demonstrates superior ORR performance due to strong Fe—O bonding and optimized electronic interactions.

The invention belongs to the technical field of medical materials, and particularly relates to a tooth whitening composition and a preparation method thereof, the tooth whitening composition comprises the following components by weight: 5%-15% of hydrogen peroxide, 0.5%-1.5% of a gel matrix, 0.2%-1.0% of a thickener, 5%-10% of a humectant, 3%-8% of propylene glycol, 0.05%-0.2% of a chelating agent, 1%-3% of a sweetener, 0.1%-0.5% of sodium fluoride, and the balance of water. Aiming at the problems that an existing tooth whitening product is relatively low in pH value (most of 4.0-5.0), easy to irritate gingiva and sensitive in tooth manufacturing, and the existing tooth whitening product needs to be stored in a dark place at a low temperature and is short in whitening validity period, the pH value of the product is adjusted to 5.5-6.5, so that the product is close to oral saliva, the irritation can be reduced, the stability of the product can be ensured, the product is not easy to decompose, and the tooth whitening effect is good. Active ingredients are prevented from losing efficacy in advance, and the whitening validity period is prolonged.

The invention discloses a catalytic material based on a subject-object three-dimensional network structure as well as a preparation method and application of the catalytic material, and provides a supermolecule electrocatalyst based on dynamic crosslinking by inserting subject-object building blocks into a conjugated microporous molecular skeleton model with pure carbon connectors and triangular knots. A heterocyclic molecule containing procaine and cyclodextrin is used as a substrate, the catalyst is synthesized through a Schiff base reaction, the surface of the catalyst is dynamically linked with a three-dimensional network structure formed by beta-cyclodextrin and procaine through host-guest interaction, and the catalyst has excellent hydrogen peroxide selectivity and stability.

The invention provides a colorimetric / fluorescent dual-mode nano-enzyme sensor, a preparation method thereof and application of the colorimetric / fluorescent dual-mode nano-enzyme sensor in formaldehyde detection. The sensor comprises a metal organic framework nano-enzyme AIE-MOF coated PCN-222 loaded with an AIE-MOF material, hydrogen peroxide and a chromogenic substrate o-phenylenediamine OPD; the metal organic framework nano enzyme PCN-222 in the AIE-MOF-coated PCN-222 can oxidize colorless OPD into yellow 2, 3-diaminophenazine DAP, an ultraviolet absorption peak is generated at the position of 450 nm, a strong fluorescence emission peak is generated at the position of 560 nm, the AIE-MOF-coated PCN-222 has a strong fluorescence emission peak at the position of 446 nm, and the AIE-MOF-coated PCN-222 and a fluorescence signal of the DAP can form a ratio fluorescence sensor. According to the invention, the excellent catalytic ability of the nano-enzyme and the luminescence characteristic of AIE-MOF are integrated in one system, so that high-sensitivity formaldehyde detection is realized.

A novel strategy for wound healing involving the coating of oxygen nanobubbles with exosomes and incorporating them into a polyvinyl alcohol (PVA) / gelatin hybrid hydrogel. In this work, we not only mitigate wound hypoxia but importantly have an efficient delivery method of exosomal nanoparticles, which to date has been confounded by very low to lack of uptake by cells in hypoxia. Furthermore, the self-healing properties of the hydrogel, along with its gelatin component, aids in hemostasis, thereby benefiting acute and surgical wound healing. Additionally, the crosslinking bonds within the hydrogel facilitate the decomposition of hydrogen peroxide (H2O2), alleviating wound inflammation. The multifunctional hydrogel provides for enhanced wound healing through increased angiogenesis, enhanced exosome delivery, hypoxia mitigation, and inflammation inhibition.

The invention relates to the technical field of chemical production, in particular to a method for efficiently synthesizing epichlorohydrin. The method provided by the invention comprises the following steps: adding a mixed solution of chloropropene and methanol and part of hydrogen peroxide into a reactor; then injecting residual hydrogen peroxide through a middle-section feeding hole of the reactor; constant-temperature circulating water is adopted to control a front-section temperature control area of the reactor to be at a first temperature, a middle-section temperature control area of the reactor to be at a second temperature and a rear-section temperature control area of the reactor to be at a third temperature, and the third temperature, the first temperature and the second temperature are gradually increased in sequence. The method provided by the invention can effectively solve the problems of side reaction increase, too fast catalyst deactivation and the like caused by local overheating of the fixed bed reactor, and significantly improves product selectivity and production efficiency.

The invention provides a preparation method of a surface structure of a back contact battery, which relates to the technical field of back contact batteries, and comprises the following steps: S1, carrying out double-sided polishing on the surface of a silicon wafer: firstly carrying out rough polishing, removing a damaged layer on the surface of the silicon wafer, then cleaning with acid and ozone, then carrying out fine polishing, then cleaning with a mixed solution of hydrogen peroxide and alkali, and then carrying out acid pickling with ozone, then cleaning with a mixed solution of acid and hydrogen peroxide, and finally washing and drying; sequentially depositing a tunneling oxide layer and amorphous silicon on a single surface at high temperature; and performing high-temperature diffusion on the surface to form a crystallized first semiconductor region and a mask layer BSG. According to the invention, the specific suede structure is formed on the front surface, and the polished surface is formed on the back isolation base region, so that high reflectivity of the back isolation base region is ensured, the specific suede structure on the front surface can be independently designed, and meanwhile, a double-surface ozone oxidation process is added; therefore, the open-circuit voltage and the short-circuit current of the cell are improved, and the photoelectric conversion efficiency of the cell is improved.

The invention discloses a preparation method of a triazinyl covalent organic framework (COF) material and application of the triazinyl covalent organic framework material in photocatalytic production of hydrogen peroxide. The amino starting monomer is regulated and controlled through a side chain regulation and control strategy to obtain the COF with a functional group, and the COF can be connected into a ring by thienopyridine through post-modification to replace an original imine bond, so that the planarity and the conjugation degree of the COF are obviously improved, and the COF has good light absorption capacity and a proper band gap; therefore, the COFs photocatalyst has excellent photocatalytic hydrogen peroxide production capacity in a water-benzyl alcohol system under a light source, and a beneficial thought can be provided for designing a high-performance COFs photocatalyst.

The invention provides a pharmaceutical wastewater treatment process. The pharmaceutical wastewater treatment process comprises the following steps: A1, pretreatment, A2, adsorption treatment, A3, oxidation treatment and A4, filtration treatment. In the step A2, a composite adsorbent comprising the following raw materials: attapulgite, activated carbon, carbon nanotubes, 4-carboxyphenylboronic acid, polyethyleneimine, sodium dithiocarbamate, epoxy resin E-44, deionized water and modified nano zero-valent iron is used, and self-repairing is realized through dynamic chemical bonds such as boric acid ester bonds, imine bonds and thiol-disulfide bonds; the adsorbent can be self-repaired during microscopic damage, so that the service life is prolonged, and relatively high adsorption capacity is kept. In the step A3, a gel microsphere oxidant comprising the following raw materials: hydrogen peroxide, potassium persulfate, copper-iron sulfide, nitrogen-doped carbon quantum dots, sodium alginate powder, sodium polyacrylate and a phosphate buffer solution is used, and efficient degradation is realized through a synergistic mechanism of free radical oxidation, non-free radical oxidation and photocatalysis.

The invention provides a method for decomposing and mineralizing fluorine-containing organic matter wastewater, which is applied to the technical field of treatment of fluorine-containing organic matter wastewater generated in a perfluoroether elastomer emulsion flocculation process, and comprises the following steps: S1, carrying out adsorption and desorption treatment on the fluorine-containing organic matter wastewater to obtain a concentrated solution of the fluorine-containing organic matter wastewater; s2, hydrogen peroxide and ferrous ions are added into a container containing the concentrated solution to obtain a mixed solution, the pH of the mixed solution is adjusted to be 2-4, the concentration mass ratio of the hydrogen peroxide to organic matter contained in the fluorine-containing organic matter wastewater is 1: 1-2, the molar ratio of the hydrogen peroxide to the ferrous ions is 1-6: 1, micro-nano bubbles are introduced into the mixed solution, and ultrasonic treatment is conducted; s3, calcium hydroxide is added into the treated mixed solution, calcium fluoride precipitates are obtained through centrifugal treatment, and the fluorine-containing organic matter in the wastewater can be degraded and mineralized.