952 results about "Strong acids" patented technology

The invention relates to the technical field of municipal sludge treatment, in particular to a method for recycling nitrogen and phosphorus elements from municipal sludge. According to the method, the municipal sludge is subjected to hydrothermal carbonization treatment, the treated solid-phase product is dried and ground to a specific particle size, the solid-phase product is subjected to acid leaching under a specific condition to extract the phosphorus element, and then heavy metal and metal elements such as Al and Fe in the acid leaching liquid are removed by adopting strong-acid ion exchange resin and a chemical precipitant, so that the phosphorus element is obtained. And finally, mixing the struvite with a hydrolyzate which is subjected to hydrothermal carbonization treatment and is rich in ammonia nitrogen, and precipitating by adjusting the element proportion and the pH value to obtain a solid-phase product struvite crystal. According to the method, external nitrogen-containing substances do not need to be added, the content of heavy metal in the solid-phase product struvite can be effectively reduced, the recovery rate of phosphorus can reach 93% or above, the recovery rate of ammonia nitrogen can reach 63% or above, the recovery rate of nitrogen and phosphorus is high, energy consumption is low, and the treatment cost is low.

The invention relates to the field of organic chemical synthesis, in particular to a synthetic method and application of pyrimidone compounds. The invention provides a synthesis method, reactants are o-amino heterocyclic formamide and triethyl orthoformate respectively, a solvent system is a hexafluoroisopropanol solvent, and a product is a heterocyclic pyrimidone compound. The reaction does not need strong acid or strong alkali conditions, does not need additional reducing agents or oxidizing agents, does not need transition metal catalysis, is economical and practical, the reaction conditions are relatively mild, and the synthesized pyrimidone compound has a good antibacterial effect.

The invention relates to the technical field of new material application, and discloses a magnetic bead material for enriching a sulfydryl peptide fragment and a preparation method thereof.The magnetic bead material prepared from micron carboxyl magnetic beads, dodecane dicarboxylic acid dihydrazide and SPSP has a long chemical reaction connecting arm, so that a reaction group has the better freedom degree, the reaction with sulfydryl is better facilitated, and the magnetic bead material can be used for enriching the sulfydryl peptide fragment. The enrichment efficiency is relatively high. When the magnetic bead material is prepared, micron carboxyl magnetic beads and dodecane dicarboxylic acid dihydrazide are based on hydrazine group and carboxyl condensation, the condensation reaction is more selective and more stable, the reaction is carried out under a milder condition, the reaction product is stable, and the reaction efficiency is higher at a lower reaction temperature. Dodecane dicarboxylic acid dihydrazide and SPSP are based on a reaction of N-succinimide and hydrazine, N-succinimide has high specificity to amino-containing molecules, side reactions are reduced, the reaction is generally carried out at room temperature, strong acid and alkali conditions are not needed, and protection of other sensitive groups is facilitated.

The invention provides a high-quality potassium hydroxide refining and impurity removal process, belongs to the field of potassium hydroxide impurity removal, and aims to overcome the defect that the purity of a potassium hydroxide product is reduced due to defects in removal precision and process stability during potassium hydroxide impurity removal in the prior art. The method comprises the following steps: carrying out oxidation decomposition on organic matters and precipitating calcium and magnesium ions, carrying out coarse filtration to remove large-particle impurities, carrying out graded filtration by adopting a three-stage series inorganic membrane module, carrying out efficient interception on impurities with different particle sizes by accurately controlling the pressure, temperature and flow rate of each membrane layer, and carrying out hydrochloric acid neutralization and potassium sulfite dechlorination to optimize the indexes of the brine. And finally, trace calcium and magnesium ions are deeply removed by utilizing the selective adsorption characteristics of the chelate resin and the strong acid cation resin, and after the resin is saturated, the resin is eluted, regenerated and recycled through acid and alkali with specific concentration, so that the impurity removal effect of potassium hydroxide is improved.

The invention relates to an acylhydrazone bond-connected covalent organic framework material, in particular to an acylhydrazone bond-connected covalent organic framework material as well as a preparation method and application thereof, and aims to overcome the defects of various materials for adsorbing Pd (II) in one aspect or the defects of poor stability and durability in high-acidity and high-radioactivity environments. Or the adsorption selectivity on Pd (II) is not strong. As an emerging crystalline organic porous polymer, the covalent organic framework is mainly formed by connecting pure organic structural units through dynamic covalent bonds, has the advantages of permanent high porosity, low density, high chemical stability, high thermal stability and the like, and is expected to realize Pd (II) adsorption in strong acid and ray irradiation environments.

The invention discloses a preparation method of an acid-resistant chlorine-resistant selective palladium adsorbent, and relates to a preparation method of a selective palladium adsorbent. The invention aims to solve the technical problems of poor structural stability, low adsorption capacity, poor selectivity and difficulty in cyclic regeneration of the existing palladium adsorbent in strong acid and high chlorine systems. According to the preparation method, fumarinonitrile is taken as a cyanogen-containing monomer, zinc chloride is taken as a catalyst, a triazine skeleton network is constructed through an ionothermal trimerization reaction, no organic solvent or expensive catalyst is needed in the process, the reaction condition is mild, the process is simple and convenient, and good environmental compatibility is achieved; the PdCl4 < 2->-doped porous carbon material provides abundant coordination sites, has a relatively large specific surface area and a developed porous structure, can effectively promote mass transfer and adsorption of metal ions, can form stable complexation with PdCl4 < 2->, shows extremely high palladium adsorption capacity and selectivity, and can still keep structural integrity and adsorption activity under strong acid and high chlorine conditions.

The invention relates to the technical field of cables, and provides a corrosion-resistant insulated power cable. The corrosion-resistant insulated power cable is sequentially provided with a conductor layer, an insulating layer and a sheath layer from inside to outside, and the insulating layer is prepared from the following raw materials in parts by weight: low-density polyethylene, magnesium hydroxide and calcium carbonate composite powder, an antioxidant, dicumyl peroxide, zinc stearate and polyethylene wax; the sheath layer comprises the following raw materials in parts by weight: PVC resin, magnesium hydroxide and calcium carbonate composite powder, diisononyl phthalate, a calcium-zinc composite stabilizer, an antioxidant, polyethylene wax and calcium stearate. According to the corrosion-resistant insulated power cable prepared in the invention, the corrosion resistance of the power cable in extreme corrosion environments such as strong acid, strong alkali, high-concentration salt mist and the like is improved, and the condition that a common cable sheath is easy to expand and crack in the extreme corrosion environments is improved.

The invention relates to a method for constructing a composite super-hydrophobic coating through double bonding. The preparation method comprises the following steps: taking a clean copper sheet which is not pretreated as a substrate, dipping the copper sheet in a suspension consisting of nanoparticles and sulfydryl-containing siloxane ethanol, taking out, washing, drying, dipping in a perfluoromercaptan ethanol solution, taking out, washing, and drying to obtain the copper-based super-hydrophobic surface coating. The coating prepared by the method has excellent super-hydrophobicity, icing resistance and stability. Different from an existing conventional preparation method, the method has the advantages that pretreatment operation such as abrasive paper polishing, strong acid etching or anodic oxidation does not need to be carried out on a copper sheet, and micro-nano roughening and low-surface-energy self-assembly can be completed on the copper surface only through two-step normal-temperature dipping. The method is simple in preparation process, mild in condition, free of expensive equipment, thin in coating thickness and small in influence on electric conduction and heat conduction of the copper substrate, intrinsic performance of copper can be reserved, the electric conduction / heat conduction characteristic of the copper substrate is considered, and the method has wide application value and prospects.

The invention discloses a method for recovering platinum and palladium from high-cobalt nickel-containing carbonylation slag, and relates to the technical field of non-ferrous metal carbonylation metallurgy, the method comprises the following steps: S1, hydrogen reduction and activation; s2, feeding into a high-pressure carbonylation reactor; and S3, efficient carbonylation. According to the method, the carbonylation slag is subjected to hydrogen reduction activation treatment, nickel protoxide and cobalt oxide are changed into simple substance nickel, the simple substance nickel is fed into a carbonylation reactor for carbonylation under the protection of reducing gas or inert gas after activation treatment, 95% of Ni, 85% of Fe and 80% of Co are carbonylated to enter a gas phase after carbonylation, bonding of cobalt and a platinum solid solution is broken through carbonylation, and the nickel-cobalt-cobalt-cobalt-cobalt alloy is obtained. Nickel protoxide is difficult to dissolve in various strong acids and oxidizing acids, and a foundation is laid for further separation of base metals and non-metallic element sulfur from precious metals to produce high-grade platinum concentrate.

The invention discloses an internal-acid and external-alkali type organic-inorganic hybrid molecular sieve catalyst as well as a preparation method and application thereof, and belongs to the technical field of heterogeneous catalytic materials and chemical processes. According to the catalyst, a hydrogen type Beta molecular sieve is used as an acidic inner core, polyvinylpyrrolidone (PVP) is used as an organic shell, and a unique inner-acid outer-alkali structure is formed. The preparation method comprises the following steps: hydrothermally synthesizing a hydrogen type Beta molecular sieve with a specific silica-alumina ratio, and then coating PVP through surface adsorption. The catalyst is used for catalyzing the condensation of methylal and trioxymethylene under mild conditions (40-70 DEG C and normal pressure) to prepare polyoxymethylene dimethyl ethers (DMMn). The PVP shell covers acidic sites on the outer surface of the molecular sieve to form an external neutral / weak base and internal strong acid microenvironment, so that the secondary side reaction of the product is effectively inhibited, the trioxymethylene conversion rate of more than 98% and the DMMn selectivity of more than 96% can be obtained in the reaction at 50 DEG C and normal pressure, the product distribution can be regulated and controlled, and the traditional Anderson-Schulz-Flory distribution limitation is broken through. The catalyst disclosed by the invention has the advantages of high activity, high selectivity, mild conditions and easiness in separation, and has a good industrial application prospect.

The invention provides a high-temperature-resistant degradable temporary plugging agent and fracturing fluid synergistic system and an application method thereof, and the synergistic system maintains a weak acid environment in a construction stage, protects the core strength of the temporary plugging agent to be slowly attenuated, and ensures stable pressure bearing of a plugging layer; in the flow-back stage, a coating layer of the temporary plugging agent is rapidly damaged by injecting a strong acid activating solution, the specific surface area of the temporary plugging agent is rapidly increased, and rapid hydrolysis of an inner core polymer chain is commonly catalyzed by cooperating with high temperature, so that rapid and thorough degradation of the temporary plugging agent is realized. By means of the design, the temporary plugging agent perfectly balances the contradiction between tough plugging in the construction period and rapid plugging removal after construction is completed, the application window of the temporary plugging fracturing technology in a complex high-temperature reservoir is greatly widened, the reservoir damage risk caused by temporary plugging agent residues is effectively reduced, and the fracturing transformation efficiency and the oil and gas well flowback rate are improved.

A treatment composition that includes a treatment adjunct and a population of core / shell delivery particles, where the shell is made from an acid-treated chitosan and a cross-linking agent, where the acid-treated chitosan results from treating chitosan with a weak acid, or even a mixture of a strong acid and a weak acid. Related methods of making and using such compositions.

The present application discloses a kind of dispersing fast, low turbidity, high temperature and high pressure resistant, strong acid and strong alkali defoaming agent, which is prepared from the following components: 5-50% of white carbon black silica paste, 1-25% of capped polyether modified polysiloxane, 0.1-10% of spherical poly siesquioxane, 1-25% of compound polyether, 0.1-10% of thickening agent, 0.05-0.5% of sterilizing agent, and the balance of water, wherein the sum of the weight percentages of the components is 100%. The present application also provides a production process of the defoaming agent, which comprises the following steps: stirring the white carbon black silica paste, spherical poly siesquioxane and capped polyether modified polysiloxane with a homogenizer to mix them thoroughly, then adding the compound polyether, thickening agent and sterilizing agent, stirring them uniformly, and continuing to stir them rapidly with the homogenizer for 25-35 minutes to obtain the mixed uniform polyether modified polysiloxane defoaming agent. The purpose of the present application is to provide a defoaming agent with fast dispersion speed, low turbidity, high temperature and high pressure resistance, and strong acid and strong alkali resistance.

The invention belongs to the technical field of chemical synthesis, and particularly relates to a method for preparing 5-methylfurfural by using 2-methylfuran. The special solid acid catalyst is used for replacing traditional phosphorus oxychloride, hydrogen chloride and phosphorus-containing wastewater are eliminated from the source, and the sulfolane is used for replacing DMF (Dimethyl Formamide), so that solvent residues in the product are reduced. The solid catalyst SO4 < 2-> is modified to form a strong Bronsted acid site (-SO3H) which cooperates with Ce < 3 + > / Ce < 4 + > redox to inhibit carbon deposition, selectively activate 2-methylfuran alpha-C and inhibit side reactions, so that the selectivity and yield of a target product are improved. Na2CO3 neutralization is replaced by electrochemical neutralization, salt slag solid waste is eliminated, and environmental pollution is reduced. After the organic phase is dried and dewatered through a molecular sieve, most of the solvent is removed through rotary evaporation, and the residual crude product is subjected to centrifugal molecular distillation, so that unreacted raw materials and trace impurities are effectively removed, and the product purity is remarkably improved.

The synthesis method comprises the following steps: S1, adding furandicarboxylic acid into a reaction container, adding a certain amount of methanol, adding a double-acid-site strong acid solid catalyst, starting stirring, controlling the reaction temperature to carry out esterification reaction, and after the reaction is finished, filtering, washing and drying to obtain furandihydrazide; separating out the double-acid-site strong acid solid catalyst to obtain clear liquid, namely dimethyl furandicarboxylate; s2, transferring dimethyl furandicarboxylate serving as a raw material into another reaction container, adding a certain amount of sodium formate serving as a catalyst, then adding a proper amount of hydrazine hydrate, controlling the reaction temperature, keeping a reflux state, reacting for a period of time, cooling to room temperature after the reaction is finished, and performing centrifugal separation to obtain white solid furandihydrazide. The synthesis method has the advantages of simple reaction steps, no need of toxic and harmful catalysts, mild reaction conditions, high conversion rate and high yield, and can realize efficient, green and low-cost production of furandihydrazide.

The invention discloses a compound environment-friendly corrosion inhibitor as well as a preparation method and application thereof. The choline ionic liquid comprises choline ionic liquid and amino acid, the choline ionic liquid is choline cations; the amino acid is one or more of cysteine and tryptophan. The compound environment-friendly corrosion inhibitor has high corrosion inhibition efficiency, and the compound structure of the compound environment-friendly corrosion inhibitor further improves the protection performance of the compound environment-friendly corrosion inhibitor through a dual adsorption mechanism of the synergistic effect of physical adsorption and chemical adsorption on the metal surface. According to the compound environment-friendly corrosion inhibitor, a full-green ionic liquid corrosion inhibition system is constructed, the environment-friendly requirement is met, and a metal protection solution can be provided for industrial acid pickling and other strong acid working conditions. Not only is the progress of a corrosion inhibition technology promoted, but also more economic and environment-friendly anti-corrosion application can be provided for actual industrial scenes.

The invention provides an antistatic derusting neutralizing acid agent and a preparation method thereof, and belongs to the technical field of commercial cleaning. The antistatic derusting neutralizing acid agent provided by the invention comprises the following components in percentage by mass: 2.0-6.0% of an antistatic agent which is Gemini-type quaternary ammonium salt, 2.0-6.0% of an anti-rust agent, 2.0-6.0% of a neutralizing agent and the balance of water. 15.5-41.0% of a composite acid agent, wherein the composite acid agent is methanesulfonic acid, glycollic acid and ammonium bifluoride; 1.0 to 5.0 percent of chelating agent, wherein the chelating agent is a strong acid resistant chelating agent; 0.5 to 2.0 percent of corrosion inhibitor; and the balance of water. The antistatic derusting neutralizing acid agent provided by the invention has excellent antistatic performance, and can efficiently improve the antistatic performance of linen at low cost when being used in a neutralizing treatment stage of the linen.

The invention relates to a method for preparing a hydrated magnesium silicate cementing material by using sepiolite, which comprises the following steps: dissolving sepiolite by using strong acid, and separating to obtain a solution and residues; naOH is added into the solution, and Mg (OH) 2 sediment is obtained; and separating the Mg (OH) 2 precipitate, calcining to obtain MgO, mixing a water reducing agent, the residues and the MgO, and adding water for curing to obtain the hydrated magnesium silicate cementing material. Rich sepiolite in the earth crust is used as a main raw material, so that low-cost and large-scale preparation of the hydrated magnesium silicate cementing material is realized.

The invention belongs to the field of soil remediation materials, and particularly relates to a humic acid composite remediation material for a coal chemical industry polluted site and a preparation method of the humic acid composite remediation material. The method comprises the following steps: 1) uniformly mixing raw materials, alkali liquor and phosphide, standing, taking supernate, adding acid liquor to adjust the pH value of a system, and performing suction filtration to obtain a humic acid solution; 2) drying the solid obtained by the standing operation in the step 1), adding an acid solution, uniformly mixing, filtering, cleaning, adding a strong acid for corrosion, filtering again, cleaning, and drying to obtain a base material; and (3) heating the organic raw material, the emulsifier and the solvent, adding the mixed solution of the acyclic carboxylic acid and the humic acid solution while keeping stirring, adding the initiator, performing thermal reaction, adding the base material while being hot, uniformly mixing, drying and grinding to obtain the humic acid composite repair material. The humic acid composite remediation material can effectively improve the structure and quality of soil and effectively improve the soil remediation efficiency.

The invention discloses a strong acid and alkali resistant plastic material for fume hood surface decoration and a preparation method of the strong acid and alkali resistant plastic material, belongs to the technical field of plastic material processing, and aims at solving the technical problem that in the prior art, the acid and alkali resistance and the bending modulus of a plastic material for fume hood surface decoration need to be further improved. The preparation method specifically comprises the following steps: stirring amino-modified fluorosilicone resin, paraformaldehyde and 1, 4-dioxane in a reaction kettle, dropwise adding an anacardol solution, heating the reaction kettle to 85-95 DEG C, carrying out heat preservation reaction for 6-8 hours, and carrying out post-treatment to obtain the anacardol-based benzoxazine resin. Perfluoro-modified polysiloxane benzoxazine is prepared, naphthalene-containing epoxy resin and imidazole-modified silicon carbide microspheres are compounded, in-situ catalysis synergistic curing is carried out by using filler interface imidazole, a compact organic-inorganic hybrid interpenetrating network is constructed, and the strong acid and alkali corrosion resistance and bending modulus of the material are remarkably improved.

The invention relates to a high-temperature acidolysis reaction defluorination method, and belongs to the technical field of phosphorus chemical resource recycling. The technical problem to be solved by the invention is to provide a high-temperature acidolysis reaction defluorination method which is simple to operate and high in defluorination rate. According to the method, phosphorite powder / white fertilizer is subjected to high-temperature acidolysis, fluoride in the phosphorite powder / white fertilizer reacts with strong acid, fluorine is separated from a reaction system in a gas form, and hydrofluoric acid is obtained through condensation. The method is simple, is simple and convenient to operate, and is easy to realize technologized large-scale production. Meanwhile, due to the destructive effect of the strong acid on the lattice structure of the phosphorus-calcium compound, citrate-soluble phosphorus can be converted into soluble phosphate, subsequent phosphorus recovery is facilitated, comprehensive utilization of phosphorite and elimination of white fertilizer output are achieved, meanwhile, the problems of material accumulation and resource waste of enterprises are solved, and the method conforms to the circular economy concept of green development.

The invention provides a method for synthesizing diethyl adipate through dynamic covalent chemical regulation. Comprising the following steps: S1, sequentially adding 80-120g of adipic acid, 160-240mL of absolute ethyl alcohol, 5-8g of a difunctional dynamic regulation and control carrier, 2-4g of a ternary composite catalyst, 1-2g of a synergistic additive and 100-150mL of a mixed solvent consisting of cyclohexane and methylbenzene into a 500mL four-neck flask provided with a thermometer, a water segregator and a pH sensor, and adjusting the initial pH value to 8.0-8.5; stirring and reacting for 6 to 8 hours at the rotating speed of 450 to 500r / min under the condition of 70 to 75 DEG C; and S2, after the reaction is finished, cooling to 25 DEG C, separating and recovering the bifunctional dynamic regulation and control carrier and the ternary composite catalyst, introducing CO2 into the filtrate to regulate the pH value to 5.0-5.5, releasing the captured moisture, and carrying out reduced pressure distillation under the conditions of 80-90 DEG C and-0.08 MPa to obtain diethyl adipate. By means of the rare earth ion-carbon quantum dot-ionic liquid ternary composite catalyst, efficient catalysis under the strong acid-free condition is achieved, and the catalyst recovery rate and the product purity are greatly improved.

The invention provides a doped ferric sodium pyrophosphate material as well as a preparation method and application thereof. The preparation method comprises the following steps: S1, blending ferrite, phosphate, strong acid and an antioxidant to form a solution A; s2, adding doped metal salt, sodium salt and a chelating agent into the solution A to form a solution B; s3, co-dropwise adding the solution B and the coprecipitation solution into grinding equipment, and maintaining the pH value to be 4.5-5.5 in the grinding process; s4, mixing and stirring the reaction product and water to form a suspension, and freeze-drying to obtain a precursor material; and S5, mixing the precursor material with a carbon source, and performing high-temperature heat treatment to obtain the doped ferric sodium pyrophosphate material. The material has excellent electrochemical performance, high compaction density and regular product morphology.

The invention relates to the technical field of nuclear waste treatment, in particular to a cucurbituril-based supramolecular organic framework material as well as a preparation method and application thereof. A construction unit of the supramolecular organic framework material is constructed by taking cucurbit [8] uril (CB8) as a subject and terephthalyl viologen ligand 1, 1 ''-(1, 4-phenylene) bis ([4, 4 '-bipyridyl]-1-onium) salt (PBV. 2X) as an object through the bonding effect of the subject and the object; in the molecular structure of the supramolecular organic framework material, the construction units are staggered and stacked in parallel in the space, and NO3 <-> is located at the gap of the adjacent CB8. The supramolecular organic framework material disclosed by the invention has high structural stability and cationic framework characteristics, and a rigid framework and a pyridine conjugated system of CB8 endow the material with excellent chemical / irradiation stability, so that the material shows ultrahigh removal rate on ReO4 <-> / TcO4 <-> in extreme environments (strong acid, strong alkali and high irradiation).

The invention discloses a synthesis process of chiral cyclic ether indole. The synthesis process comprises the following steps: reacting 4-bromobenzaldehyde with malonic acid under the catalysis of piperidine to generate olefin carboxylic acid CHP-1; carrying out condensation reaction to prepare CHP-2; under the catalysis of a copper reagent, carrying out Michael addition reaction to obtain CHP-3; preparing a chiral alcohol intermediate CHP-4 through a reduction reaction; trifluoromethanesulfonic acid is used, and a chiral ether intermediate CHP-5 is prepared through ring closing; reacting with protected hydrazine by using a copper ion catalyst to obtain an intermediate CHP-6; the method comprises the following steps: by taking alcohol as a solvent, adding strong acid, and removing a protecting group of hydrazine to obtain an intermediate CHP-7; and carrying out ring closing by taking lewis acid as a catalyst to obtain an indole product CHP-8. The use of a noble metal catalyst palladium is avoided, and the cost is greatly reduced. The chiral center is directly constructed through a chemical method, and SFC is not needed for resolution, so that the cost is remarkably reduced, and industrial production is successfully realized.

The invention provides a collaborative treatment and resource utilization process for CO2 in industrial solid waste and tail gas, and belongs to the technical field of environmental protection. According to the method, carbon residues in the gasified slag are used as a catalyst, and aluminum and silicon are extracted through the gasified slag chemical method under the polybasic acid aqua regia effect and the electrochemical effect. According to the method disclosed by the invention, a stack retting neutralization mode is adopted, so that the superacid and aluminum and iron oxides in the ash residues are converted into soluble salts, and ferric hydroxide, aluminum hydroxide and polybasic acid ammonium are sequentially replaced from a salt solution by virtue of an ammonia replacement method, so that the use safety risk of high oxidability of polybasic acid is overcome; rapid crystallization of the aluminum salt solution in the form of aluminum chloride is promoted by using the same ion effect; performing stack retting neutralization reaction on the slag charge and sodium hydroxide to generate sodium silicate, introducing carbon dioxide to obtain silicic acid and sodium carbonate, and reacting the sodium carbonate solution with calcium hydroxide to obtain sodium hydroxide. The sodium hydroxide, the polyatomic acid, the ammonia gas and the activated carbon are recycled for treating the fly ash and the coal gangue, so that the comprehensive utilization of multi-element solid waste is realized.

The invention discloses a preparation process of carboxylated shell-based activated carbon for organic matter adsorption, and particularly relates to the technical field of adsorption materials, and the preparation process comprises the following steps: mixing coconut shell powder and walnut shell powder, crushing, and loading potassium hydroxide in stages in a gradient manner; carrying out two-stage microwave activation in an inert atmosphere, namely low-temperature pre-activation in the first stage and high-temperature activation in the second stage, and introducing carbon dioxide; the activated product, phosphoric acid, a laccase-peroxidase complex enzyme preparation and a buffer solution are subjected to ultrasonic synergistic modification, and then a weak acid reaction is maintained through dynamic pH regulation and control; and finally, performing graded washing and gradient drying to obtain a finished product. According to the method, high-density carboxyl grafting and graded pore construction are synchronously realized under mild conditions through a synergistic effect of directional catalysis of biological enzyme and dynamic regulation of microwave, so that the problems of structural damage caused by strong acid corrosion, pore imbalance caused by fixed parameters and stability reduction caused by insufficient post-treatment in a traditional process are solved; the adsorption performance and the regeneration cycle performance of the material are also obviously improved.

The invention relates to the technical field of wastewater treatment, and discloses a recycling washing water treatment process of sodium chloride high-salinity wastewater, which comprises the following steps: step 1, a pretreatment stage: recycling washing water with a pH value range of 6-9 and main solutes of NaCl and Ca < 2 + lt >; 350mg / L, Mg < 2 + lt >; the method comprises the following steps: introducing washing water with the concentration of 350mg / L and the TDS of more than 100g / L into a multi-medium filter, removing impurities in the washing water through a multi-layer filtering structure by utilizing the adsorption and interception effects of a filtering medium, and controlling the filtering speed to be 8-12m / h; and step 2, a hardness removal stage: the water treated by the multi-medium filter enters a hardness removal resin device, and strong-acid cation exchange resin is adopted to carry out ion exchange reaction with Ca < 2 + > and Mg < 2 + > in the water to remove calcium and magnesium ions in the water. And in the hardness removal process, the flow speed is controlled to be 4-6 m / h. Water resources and salt in washing water are fully separated and recycled, no by-product pollutant is discharged into the environment, pollution to soil, water and atmosphere is greatly reduced, and balance of the ecological environment is protected.

The invention discloses application of a carbon steel corrosion inhibitor based on combination of physical adsorption, chemical adsorption and hydrophobic barrier, and relates to the technical field of metal corrosion inhibition. The technical problem that a corrosion inhibitor in the prior art is low in corrosion inhibition efficiency in a high-temperature strong-acid environment is solved. The preparation method of the carbon steel corrosion inhibitor comprises the following steps: firstly, ultrasonically dissolving 4-aminopyridine to obtain a solution I; then, dropwise adding an isopropanol solution of 2, 3-epoxypropyltrimethylammonium chloride into the solution I according to a molar ratio of 1: 1, removing a solvent through a rotary evaporation method, washing with ethanol, centrifuging to obtain quaternized 4-aminopyridine, and drying the quaternized 4-aminopyridine; and finally, the dried quaternized 4-aminopyridine and bromododecane are added into acetonitrile for a reaction, diethyl ether is dropwise added into obtained reaction liquid for precipitation, and the quaternized 4-aminopyridine-bromododecane carbon steel corrosion inhibitor is obtained after drying. The prepared carbon steel corrosion inhibitor is high in corrosion inhibition efficiency in a high-temperature and strong-acid environment.

The application discloses a preparation method of mesoporous copper oxide and application thereof. The preparation method comprises the following steps: S1, preparing a hydroxyl copper nitrate microplate by taking calcium carbonate paper as a substrate and copper nitrate as a solvent; S2, synthesizing an ordered copper hydroxide nanowire assembly through an alkali solution reaction; and S3, performing annealing treatment in a muffle furnace to obtain the mesoporous copper oxide microplate. Under the conditions of no hard template, no soft template and no strong acid treatment, the application provides a method for synthesizing the mesoporous copper oxide microplate material with uniform pore structure on the carbonic paper by adopting copper nitrate hydrolysis, alkali etching and annealing, and the synthesis method of the mesoporous structure has the advantages of simple operation, good controllability and low cost. The application also relates to application of the mesoporous copper oxide as an electrocatalyst material in the field of glucose electrochemical sensing.