807 results about "Sodium acetate" patented technology

The invention provides aqueous ophthalmic solutions of phentolamine or pharmaceutically acceptable salts thereof, medical kits, and methods for using such ophthalmic solutions to improve visual performance in a patient. Exemplary aqueous ophthalmic solutions include those containing phentolamine mesylate, mannitol, sodium acetate, and water.

The invention provides aqueous ophthalmic solutions of phentolamine or pharmaceutically acceptable salts thereof, medical kits, and methods for using such ophthalmic solutions to improve visual performance in a patient. Exemplary aqueous ophthalmic solutions include those containing phentolamine mesylate, mannitol, sodium acetate, and water.

The invention provides aqueous ophthalmic solutions of phentolamine or pharmaceutically acceptable salts thereof, medical kits, and methods for using such ophthalmic solutions to improve visual performance in a patient. Exemplary aqueous ophthalmic solutions include those containing phentolamine mesylate, mannitol, sodium acetate, and water.

The invention relates to the technical field of plant polysaccharide extraction, in particular to a process for synergistically extracting rape pollen polysaccharide by a compound enzyme, which comprises the following steps: crushing rape pollen to 200-300 meshes by pulse airflow, performing microwave-ultrasonic degreasing by using a 85% ethanol solution, mixing with an acetic acid-sodium acetate buffer solution with the pH value of 4.8, and performing ultrasonic extraction to obtain a crude extract; the method comprises the following steps: adding a compound enzyme system which is immobilized by Fe3O4 (at) SiO2 nanoparticles by cellulase, pectinase, protease and beta-glucosidase according to a mass ratio of 2: 1: 1: 0.5, carrying out enzymolysis for 4 hours in a 50 DEG C constant-temperature water bath and a 15V / cm pulsed electric field, carrying out enzyme deactivation on enzymatic hydrolysate, carrying out gradient ethanol precipitation, carrying out ultrafiltration deproteinization, and carrying out vacuum pulsation freeze drying to obtain the polysaccharide. According to the method disclosed by the invention, the cell wall breakage rate and the enzymolysis efficiency are improved through pulsed airflow crushing, magnetic nano immobilized enzyme and pulsed electric field assistance, the polysaccharide yield reaches 7.32%, the purity is 91%, the beta-glucosidic bond proportion and the antioxidant activity are remarkably improved, the enzyme can be recycled and reused, the drying time is shortened, and efficient and low-consumption extraction is realized.

The invention discloses a high-entropy P2-O3 composite system sodium ion positive electrode material, a preparation method thereof and a sodium battery, and belongs to a new energy material technology. The method comprises the steps that a first reactant, metal oxide and solid powder of a sodium source are blended, sintered and cooled, the component of the first reactant is NiyFezMn (1-3y-z) (OH) (2-4y), and the particle size of the first reactant is 1-20 micrometers; the metal oxide is any two of TiO2, MgO, Co3O4, SnO2, ZrO2, La2O3 and CeO2, and the particle size D50 of the metal oxide is less than or equal to 5 microns; the sodium source is selected from any one of sodium carbonate, sodium bicarbonate, sodium nitrate and sodium acetate, and the particle size D50 is less than or equal to 10 microns; the particle size of the first reactant is larger than the particle size D50 of the metal oxide, and the particle size D50 of the sodium source is larger than the particle size D50 of the metal oxide.

The present invention provides an anti-fatigue essential oil composition and a preparation method thereof, belonging to the technical field of compound essential oils. The essential oil composition comprises a compound essential oil and a eutectic composition; the compound essential oil comprises 1 to 25 parts of Torreya grandis aril essential oil, 1 to 20 parts of cinnamon leaf essential oil, 1 to 20 parts of lemon essential oil, and 1 to 15 parts of ginger essential oil; the eutectic composition comprises 1 to 3 parts of borneol and 1 to 10.5 parts of menthol. A potassium citrate solution is added to Torreya grandis arils, a sodium acetate solution is added to cinnamon leaves, a potassium citrate solution is added to fresh lemons, and purified water is added to ginger. The juices are squeezed separately and then distilled to obtain Torreya grandis aril essential oil, cinnamon leaf essential oil, lemon essential oil, and ginger essential oil. The present invention combines the four essential oils in a proportioned mixture to produce a compound essential oil, and adds the eutectic composition to produce an essential oil composition. The essential oil composition has significant fatigue-relieving and mentally refreshing effects, and is not easily tolerated.

The invention discloses a zinc-bromine flow battery electrolyte, a negative electrode cosolvent and a preparation method thereof, and belongs to the technical field of electrochemical energy storage, the negative electrode cosolvent of the zinc-bromine flow battery electrolyte is a carboxyl-containing butenoic acid substance, the butenoic acid substance is used as the cosolvent, and zinc is induced to preferentially deposit on a (002) plane by modifying a solid-liquid interface, so that the zinc-bromine flow battery electrolyte is obtained. And the deposition process of zinc is converted from an irregular form which tends to form a dendritic crystal shape and a moss shape into a deposition layer which tends to form a flat and compact deposition layer which is parallel to the substrate. The highly uniform zinc deposition fundamentally and effectively inhibits the formation and growth of zinc dendrites, and greatly improves the stability of the negative electrode and the cycle life of the battery. Chlorides improve ionic conductivity to reduce internal resistance, and sodium acetate buffer inhibits hydrogen evolution on stable pH; and synergistic optimization of positive and negative components ensures efficient reaction. And moreover, the raw materials are easy to obtain, the preparation is simple and convenient, the industrialization threshold is reduced, and the large-scale energy storage requirement is met.

The invention discloses a ratio-type fluorescence analysis method for determining sodium dehydroacetate, which comprises the following steps: under an alkaline condition, synthesizing tetrafluoroterephthalic acid oxide, namely a fluorescent substance TFAox, by oxidizing tetrafluoroterephthalic acid with hydrogen peroxide, and forming a ratio-type fluorescence probe by the fluorescent substance and rhodamine B, a ratio-type fluorescence analysis method of sodium dehydroacetate is constructed based on the ratio-type fluorescence probe, and the method can be successfully applied to determination of sodium dehydroacetate in a water sample and a bread sample. The ratio-dependent fluorescence detection method for determining sodium dehydroacetate provided by the invention has the characteristics of wide linear range, high detection sensitivity, no interference of coexisting substances on determination, good selectivity and the like.

The invention discloses a zinc-bromine flow battery multifunctional electrolyte and a preparation method thereof, and belongs to the technical field of electrochemical energy storage, and the method comprises the following steps: dissolving an electrolyte in a solvent, and sequentially adding a supporting electrolyte, a positive electrode complexing agent and a positive electrode additive to obtain a positive electrode electrolyte; the positive electrode additive is zinc iodide; i <-> in zinc iodide and Br2 in a Br2 / Br <-> reaction system form mixed halide ions, so that the bromine resistance function is achieved, and the overall conductivity and comprehensive electrochemical performance of the electrolyte are improved; dissolving an electrolyte in a solvent, and sequentially adding a supporting electrolyte and a first negative electrode additive to obtain a negative electrode electrolyte; the first negative electrode additive comprises sodium acetate and sodium citrate; sodium acetate and sodium citrate are combined to form a wide-range buffer system, the pH value of the electrolyte can be dynamically adjusted and stabilized, the long-term stability of the battery is improved, the cycle life is prolonged, and the positive electrode electrolyte and the negative electrode electrolyte form the multifunctional electrolyte for the zinc-bromine flow battery; and the zinc deposition behavior is cooperatively regulated and controlled through sodium salt buffering and ion coordination.

The invention discloses a preparation method of a chemical composite plating solution based on nano niobium carbide. The preparation method comprises the following steps: step 1, pretreating niobium carbide (NbC) powder; step 2, preparing a chemical plating solution, wherein every 1L of the chemical plating solution contains 30g of nickel chloride, 20g of sodium hypophosphite, 10g of sodium citrate, 5g of glycine, 10g of sodium acetate, 0.3 g of sodium dodecyl benzene sulfonate and 80mg of zinc molybdate; fixing the volume to 1L by using distilled water; 3, measuring the niobium carbide suspension liquid, mixing the niobium carbide suspension liquid with the chemical plating solution, and fixing the volume, so that the content of niobium carbide in the chemical composite plating solution is 0.01-0.3 g / L; adjusting the pH value of the solution to 5.8; according to the method, niobium carbide nanoparticles are added into the chemical composite plating solution, so that the surface of a plated part and metal gold are combined with the particles, and the hardness and wear resistance of a base material are effectively improved; the effect on a 60-80-micron nickel-phosphorus coating in the industry is achieved through the ultrathin chemical composite coating (8-10 microns), so that the corrosion resistance and the wear resistance of the product are enhanced.

The invention provides a preparation method and application of low-bath-ratio and high-viscosity hydroxypropyl carboxymethyl composite starch ether, and relates to the technical field of starch deep processing. The method comprises the following steps: S1, premixing corn starch with a compound base catalyst and magnesium stearate, and spraying an ethanol water solution for alkalization; s2, adding epoxypropane to carry out first-stage etherification, and then adding sodium chloroacetate to carry out second-stage etherification; and S3, after the reaction is finished, performing vacuum drying, crushing and sieving to obtain the high-viscosity hydroxypropyl carboxymethyl composite starch ether. Wherein the composite alkali catalyst comprises sodium hydroxide, sodium carbonate and calcium oxide. The starch ether obtained by the method has the advantages of high substitution degree, high viscosity, low solvent consumption and low energy consumption, and overcomes the defects of the traditional semi-dry method.

The invention discloses a salt-spray-corrosion-resistant stainless steel rod and a preparation method thereof, and belongs to the technical field of salt-spray-corrosion-resistant stainless steel. The salt-spray-corrosion-resistant stainless steel rod comprises a stainless steel rod body and a corrosion-resistant layer attached to the outer surface of the stainless steel rod body. The method comprises the following steps: sequentially polishing, deoiling, activating and cleaning a stainless steel rod, then putting the stainless steel rod into a chemical composite plating solution for chemical composite plating, then putting the stainless steel rod into a nitric acid solution for chemical etching, introducing hydrogen and hydrocarbon gas in a high-temperature atmosphere, and then continuously heating and introducing composite hydrogen to obtain the salt-spray-corrosion-resistant stainless steel rod, wherein the chemical composite plating solution comprises the following components: 30-40 g / L of nickel sulfate, 15-35 g / L of sodium hypophosphite, 4-6 g / L of citric acid, 32-36 g / L of boric acid, 16-20 g / L of sodium acetate, 0.03-0.05 g / L of carbon black and 20-35 g / L of tungsten carbide particles; the salt-spray-corrosion-resistant stainless steel rod prepared by the invention is relatively good in corrosion resistance, wear resistance and toughness.

The invention discloses an electrolytic medium, an acidic oxygen evolution non-noble metal manganese-based catalyst, a process and application, and belongs to the field of water electrolysis hydrogen production. The preparation process comprises the following steps: (1) dissolving a metal salt of M, a metal salt of Mn, sodium sulfate, sulfuric acid and sodium acetate in deionized water to serve as an electrolyte; (2) carrying out electrodeposition reaction by using an electrochemical workstation and a three-electrode system at room temperature, and loading a manganese-based component on a conductive carrier; (3) cleaning the conductive carrier loaded with the manganese-based component in deionized water, and drying; calcining the loaded manganese-based component in the air at the temperature of 300-500 DEG C; the molar ratio of M to Mn is smaller than 1: 5, the metal manganese-based catalyst is metal element doped manganese oxide M-MnOx, and when the molar ratio is larger than or equal to 1: 5, the metal manganese-based catalyst is metal oxide coupled manganese oxide MOx / MnOx. According to the scheme, the problem that the activity and the stability of the existing MnO2 which is directly used as an excellent acidic oxygen evolution catalyst are insufficient is solved.

The invention discloses a pH-responsive low-temperature gel temporary plugging agent and a preparation method thereof, and belongs to the technical field of oil-gas field development. The pH response type low-temperature gel temporary plugging agent is prepared from the following substances in parts by weight: 2.8 to 5.7 parts of acrylamide, 1.4 to 2.6 parts of 2-acrylamido-2-methylpropanesulfonic acid, 0.05 to 1.04 parts of a cross-linking agent, 0.01 to 0.1 part of an initiator, 2 to 3.33 parts of amylopectin, 1 to 1.67 parts of sodium alginate, 0.27 to 0.35 part of acetic acid, 2.14 to 2.61 parts of sodium acetate, 0.9 to 1.5 parts of glycerol and the balance of water, and the sum of the parts by weight of the components is 100. The cross-linking agent is obtained by synthesizing dihydrazide and diacetone acrylamide. The gel temporary plugging agent is easy and convenient to prepare, raw materials are cheap and easy to obtain, and the production process is controllable. The fracturing fluid is applied to a temporary plugging diversion fracturing process of a low-temperature tight oil reservoir, and has important significance on efficient development of oil and gas fields.

The invention discloses a triiodothyronine dissociation agent, a detection kit, a preparation method of the triiodothyronine dissociation agent and application of the triiodothyronine dissociation agent and the detection kit, and the triiodothyronine dissociation agent comprises 10-100 mM of acetic acid-sodium acetate buffer solution, 0.05-1 g / L of ethylene diamine tetraacetic acid disodium salt, 1-10 g / L of perfluoroalkyl ethyl methacrylate, 0.2-1 mL / L of Tween-20 and 0.2-2 mL / L of ProClin 300, the pH (Potential of Hydrogen) of the triiodothyronine dissociation agent is 5.5 + / -1; the kit comprises a triiodothyronine dissociation agent and a reagent strip. According to the present invention, the two sites can be specifically recognized, the sensitivity and the specificity are high, the high-specificity detection on the specific antigen can be achieved, and the low-end sensitivity is high; meanwhile, the interference problem of rare earth europium during detection of triiodothyronine can be solved, and the accuracy of a detection result is further improved.

The utility model provides a byproduct sodium acetate dissolving device, which belongs to the technical field of sodium acetate production, and comprises a dissolving tank and a stirring assembly, the stirring assembly comprises a connecting shaft, a stirring paddle, a crushing paddle, a driving motor and a lifting piece, the connecting shaft is vertically suspended in the dissolving tank, the stirring paddle is arranged on the connecting shaft and is positioned in the dissolving tank, and the crushing paddle is arranged in the dissolving tank. The crushing paddle is installed on the connecting shaft and located below the stirring paddle, the driving motor is arranged at one end of the connecting shaft, and the lifting piece is connected with the driving motor and drives the driving motor to move up and down in the vertical direction. The crushing paddle and the lifting part are additionally arranged, so that the crushing paddle firstly crushes large crystal byproduct sodium acetate, the large crystal byproduct sodium acetate is crushed into small crystal byproduct sodium acetate, dissolution of the crystal byproduct sodium acetate is accelerated, the dissolution rate is increased, and meanwhile, the dissolution rate is increased. The mutual collision between the stirring paddle and the bulk crystal byproduct sodium acetate is avoided, and the stirring paddle is prevented from being damaged.

The invention relates to a liquid detergent composition comprising a first surfactant selected from fatty alcohol ether sulfates, a second surfactant selected from betaines, optionally at least one solvent selected from ethanol, propanol, isopropanol, ethylene glycol, butyl glycol, propylene glycol, polypropylene glycol, alcoholamine, monoethanolamine, glycerol and mixtures thereof, wherein the salt concentration in the composition is about 0.2 to about 10 wt.-% and wherein the salt is selected from the group consisting of sodium salts such as sodium chloride, sodium sulfate, sodium formate, sodium acetate or sodium propionate, potassium salts such as potassium chloride, potassium sulfate, potassium formate, potassium acetate or potassium propionate, magnesium salts such as magnesium chloride, magnesium sulfate, magnesium formate, magnesium acetate or magnesium propionate, and calcium salts such as calcium chloride, calcium sulfate, calcium formate, calcium acetate or calcium propionate, and mixtures thereof, and wherein the composition is a concentrate that can be diluted with water while maintaining or increasing the viscosity.The present invention further relates to the use of such a cleaning composition for cleaning hard surfaces, in particular dishes, and to a process for preparing a cleaning composition, the process comprising diluting the concentrated liquid cleaning composition with water.

The invention provides an electroactive biofilm for degrading enriched sulfonamide antibiotics and a method for identifying microorganisms, and relates to the technical field of environmental microorganisms and wastewater treatment. The method for degrading the electroactive biological membrane by enriching the sulfonamide antibiotics and identifying the microorganisms comprises two steps of directional enrichment of the electroactive biological membrane and identification and analysis of functional microbial communities, the directional enrichment of the electroactive biological membrane is carried out in a double-chamber bioelectrocatalysis system and comprises a single carbon source stage, a common carbon source stage, a single carbon source stage and a common carbon source stage, and the directional enrichment of the electroactive biological membrane is carried out in a double-chamber bioelectrocatalysis system. An isotope labeling stage; the sodium acetate in the single carbon source stage is the only carbon source; sodium acetate and sulfonamide antibiotics are used as a common carbon source in the carbon source sharing stage; in the isotope labeling stage, 13C-labeled antibiotics are used for replacing common antibiotics. According to the method, the effects of efficiently and directionally enriching, accurately identifying active degrading microorganisms and analyzing degrading genes and metabolic pathways are achieved, and technical support is provided for developing efficient degrading bacteria and bioremediation methods.

The invention relates to the technical field of electroplating, in particular to a nickel stripping agent, a preparation method of the nickel stripping agent and a nickel plating layer stripping method. The nickel stripping agent comprises the following raw materials: an oxidizing agent, a complexing agent, a dissolution promoter, a surfactant and a corrosion inhibitor, wherein the mass ratio of the oxidizing agent to the complexing agent to the dissolution promoter to the surfactant to the corrosion inhibitor is (4-15): (3-25): (1-11): (0.01-1): (0.01-5); wherein the oxidizing agent is nitrobenzoic acid; the complexing agent is one or more of 2-amino-2-methyl-1-propyl alcohol, acetylacetone, nitrilotriacetic acid, nitrilotriacetic acid sodium salt, acrylate, sodium gluconate and ethylenediamine hydrochloride; the dissolution promoter is an alcohol ether solvent. According to the nickel stripping agent, the oxidizing agent with relatively low toxicity and a non-toxic or low-toxicity non-volatile complexing system are adopted, nickel can be completely removed, a base material cannot be eroded, and the threat to the health of operators can be remarkably reduced.

The invention provides a method for preparing high-purity calcium sulfate dihydrate powder from fluorgypsum. The preparation method comprises the following steps: drying fluorgypsum and preparing fluorgypsum powder; mixing the fluorgypsum powder with a sodium acetate solution, and reacting to obtain a mixed solution; performing solid-liquid separation on the mixed solution to obtain a first filtrate; aging the first filtrate, and separating out a filter cake; washing and drying the filter cake to obtain high-purity calcium sulfate dihydrate powder; wherein the phase of the high-purity calcium sulfate dihydrate powder is a gypsum phase, the content of calcium sulfate dihydrate is greater than 98%, the whiteness is greater than 94, and the microscopic morphology comprises a plate shape and / or a particle shape. The anhydrous calcium sulfate in the fluorgypsum is fully utilized, the added sodium acetate auxiliary exists in the solution in the form of ions all the time and can be circularly used for dissolving the anhydrous calcium sulfate in the raw material, the whole preparation process is carried out at low temperature and normal pressure, the auxiliary can be recycled, and the whole process is free of wastewater discharge.

The invention provides a preparation method of biomass-derived porous carbon with ionic adsorption potential, which comprises the following steps: adding disodium ethylene diamine tetraacetate and ferrous chloride into water, and uniformly mixing to obtain EDTA-Fe; the preparation method comprises the following steps: sequentially adding an acetic acid-sodium acetate buffer solution and a biomass material into EDTA-Fe, uniformly mixing, adding aluminum chloride, carrying out a hydrothermal reaction to obtain a primary product, cleaning the primary product, and drying to obtain biomass hydrothermal carbon; the preparation method comprises the following steps: soaking biomass hydrothermal carbon in a saturated solution of potassium carbonate, then carrying out solid-liquid separation, firstly drying a solid obtained by separation, then calcining in a nitrogen atmosphere, and cleaning to obtain the biomass derived porous carbon. The biomass hydrothermal carbon prepared by the method has regular and controllable morphology, abundant surface functional groups and a stable carbon skeleton structure, and shows excellent electrochemical performance.

The invention relates to the technical field of rice seed germination accelerating systems and methods. Seed selection is conducted, specifically, rice seeds which are full and free of damage are screened, and impurities are removed; the rice seeds are soaked in a plant growth regulator mixed solution to be subjected to oscillation treatment, the mixed solution is composed of gibberellin with the concentration being 20-50 mg / L, pimacol with the concentration being 5-15 mg / L and polyoxyethylene lauryl ether with the concentration being 0.01-0.03%, the liquid temperature is kept at 30 + / -2 DEG C, and the treatment time is 2-4 hours; gradient disinfection: primary disinfection: putting the pretreated seeds into a 0.3-0.5% hydrogen peroxide solution at the temperature of 40-50 DEG C, and stirring for 15-20 minutes; secondary disinfection: transferring to a 0.8-1.2% sodium hypochlorite solution at the temperature of 25-30 DEG C, adding a 0.05-0.1 mol / L phosphate buffer solution to adjust the pH value to 6.8-7.2, and standing for 40-60 minutes; the disinfected seeds are put into magnetized water containing 0.1%-0.3% of chitosan derivatives and 0.05%-0.15% of sodium alginate, the magnetic field intensity ranges from 300 gauss to 500 gauss, and ultrasonic waves of 30 kHz to 50 kHz are adopted for assisting permeation for 1 h to 2 h; the rice seed germination accelerating system and method are high in germination accelerating efficiency.

The invention discloses a Fe-N-C catalyst and application thereof in degradation of perfluorinated and polyfluoroalkyl substances, and belongs to the technical field of water treatment. The preparation method comprises the following steps: taking nitrogen-doped carbon derived from pine cones as a substrate, dissolving aminated pine cones, FeCl36H2O, sodium acetate and polyethylene glycol in ethylene glycol, reacting at 200 DEG C for 10 hours, putting in an inert gas atmosphere, and calcining at 900 DEG C for 2 hours; the Fe-N-C catalyst which simultaneously contains Fe nano particles (Fe NPs) and Fe-N single atoms (Fe SAs) and has different sizes and double sites is prepared. The catalyst and PMS are mixed and then added into water, and perfluoro and polyfluoroalkyl substances in the water can be degraded; the catalyst can activate PMS to promote formation of a non-free radical pathway, depends on a degradation mechanism of Fe (IV) = O and singlet oxygen (O), the degradation rate of PFOA within 2 hours reaches 90.5%, and the catalyst also shows relatively strong tolerance in different natural water bodies; a key thought is provided for designing the efficient catalyst, and a new technical direction is expected to be provided for environmental treatment of persistent organic pollutants such as PFOA.

The invention relates to the field of water treatment agents, and discloses a composition with scale inhibition and corrosion inhibition functions, the composition comprises a first component, a second component, a third component, a fourth component and an optional Schiff base compound; the first component is selected from at least one of a C2-C6 alcohol amine compound, a C4-C8 cyclic amine compound, a nitrogen-containing heterocyclic compound and gluconate; the second component is selected from at least one of a benzotriazole compound, a benzothiazole compound and a thiourea compound; the third component is an inorganic metal salt; the fourth component is selected from at least one of a sodium acetate compound, sodium polyacrylate, sodium polymaleate and polyepoxysuccinic acid. The composition has relatively strong scale inhibition and scale dissolving effects on a high-hardness and high-alkalinity circulating water system, has long-term corrosion inhibition on metals, and reduces the water supplementing and changing times of the circulating water system.

The utility model discloses a separation device for ethyl acetate and cyclohexane, which belongs to the technical field of separation and purification, solves the problems of incapability of large-scale separation, high process difficulty and poor separation effect in the prior art, and comprises an extractive distillation tower, the upper part is provided with a polyol solvent inlet, the top is connected with a first condenser, the outlet of the first condenser is connected with a cyclohexane outlet on the other side of the upper part of the extractive distillation tower, and the cyclohexane outlet is connected with a re-separation device. According to the device disclosed by the utility model, the problem of azeotropy of ethyl acetate and cyclohexane is solved by adding polar polyol, the relative volatility of the ethyl acetate and the cyclohexane is changed, and large-scale efficient separation of a mixture of the ethyl acetate and the cyclohexane is realized; the dissolubility of cyclohexane, sodium acetate and ethanol in water is different, so that the separation effect of cyclohexane is further improved, and the whole device is simple in structure.

The invention provides aqueous ophthalmic solutions of phentolamine or pharmaceutically acceptable salts thereof, medical kits, and methods for using such ophthalmic solutions to improve visual performance in a patient. Exemplary aqueous ophthalmic solutions include those containing phentolamine mesylate, mannitol, sodium acetate, and water.

The invention discloses an iron-cobalt spinel oxide, which is prepared by the following steps: with ferric salt and cobalt salt as raw materials, dissolving the ferric salt, the cobalt salt and sodium acetate in an ethanol aqueous solution to obtain a precursor solution, carrying out hydrothermal treatment on the precursor solution, and washing and drying a reaction product to obtain the iron-cobalt spinel oxide. The iron-cobalt spinel type oxide is stable in crystal structure, the leaching rate of metal ions is remarkably reduced due to existence of metal-oxygen bonds, the recycling rate is increased, and meanwhile the risk of secondary pollution of water is reduced. In the process of degrading nitrogen-containing organic wastewater by an advanced oxidation technology for generating sulfate free radicals based on peroxymonosulfate, the iron-cobalt spinel type oxide has good catalytic performance, and can basically complete degradation of multi-nitrogen organic pollutants in water; and the method has relatively strong capability of resisting interference of inorganic ions and organic matters, and has relatively great application potential in actual wastewater treatment. The invention also discloses a method for degrading the multi-nitrogen explosive wastewater by using the ferrocobalt spinel type oxide.

The invention provides a high-foaming self-thickening amino acid cleaning composition and a preparation method thereof, and relates to the technical field of cosmetics. The high-foaming self-thickening type amino acid cleaning composition is prepared from the following raw materials in percentage by mass: main surfactants: 15%-20% of potassium cocoyl glycinate, 0.5%-2.0% of sodium cocoyl amino propionate and 0.05%-2% of sodium lauroyl glutamate; the auxiliary surfactant comprises the following components in percentage by weight: 1.2%-1.8% of sodium lauroamphoacetate, 1.8%-3.6% of lauryl hydroxyl sulfobetaine, 0.5%-1.5% of sodium methyl cocoyl taurate and 0.5%-1.5% of lauryl glucoside; and 0.5%-1.8% of an acrylic ester copolymer. The cleaning composition is free of fatty acid components, small in irritation, rich and dense in foam, good in foam performance, high in cleaning power, good in flushing performance, free of false slip after flushing and good in stability.

The invention provides a production device and process for recovering electronic-grade phosphoric acid from waste etching liquid. The device comprises a raw material storage tank, a multi-stage filtration system, a phosphoric acid evaporation kettle, a purification system, a mixed acid storage tank and a neutralization reaction and crystallization system. The waste etching liquid enters an evaporation kettle after being subjected to multi-stage filtration to remove suspended solid particles, and phosphoric acid is separated from volatile nitric acid and acetic acid; and condensing the volatile acid into mixed acid for storage, and removing metal ions from the semi-finished phosphoric acid through a purification system to obtain the electronic-grade phosphoric acid. The mixed acid reacts with alkali to generate a mixed solution of sodium acetate and nitric acid, sodium acetate crystals are separated out through evaporation and concentration, a solid product is obtained after separation, nitric acid is obtained by condensing gas, and suspended particles and metal impurities are subjected to incineration treatment. Through the steps of filtering, negative-pressure evaporation, neutralization and crystallization and the like, the process realizes efficient recovery of electronic-grade phosphoric acid and byproducts of sodium acetate and nitric acid, and has the characteristics of high resource recovery rate and low pollution emission.

The invention discloses a self-crystallization type amino acid cleansing cream composition and a preparation method thereof. Comprising the following components in percentage by weight: 20%-40% of glycerol, 15%-25% of cocoyl glycinate, 1%-10% of cocoyl hydrolyzed collagen potassium, 0.1%-5% of sodium lauroamphoacetate, 0.1%-3% of citric acid, 0.1%-3% of sodium methyl cocoyl taurate, 0.1%-3% of sodium chloride, 0.1%-3% of sodium lauroyl glutamate, 0.1%-3% of ethyoxyl diethylene glycol, 0.1%-3% of propylene glycol laurate, 0.1%-3% of PEG-150 stearate, 0.1%-3% of ethylene glycol distearate, 0.0%-2% of 1, 3-propylene glycol distearate, 0.0%-2% of 1, 3-propylene glycol distearate and the balance of water. The cleaning agent is prepared from the following components in percentage by weight: 0.0 to 2 percent of 1, 2-hexanediol, 0.0 to 2 percent of p-hydroxyacetophenone and The self-crystallization type cleansing cream composition disclosed by the invention is high in crystallization point, good in thermal stability, mild and low in irritation, and has the effects of moisturizing and promoting cell proliferation, and the overall performance is improved.