13572 results about "Mixed solution" patented technology

The invention relates to a method for preparing a lithium iron phosphate / carbon composite material of a lithium ion battery, which belongs to the technical field of lithium ion batteries. The method for preparing the lithium iron phosphate / carbon composite material of the lithium ion battery comprises the following steps of: 1) preparing a suspending graphene-dispersed aqueous solution system, namely, crushing graphite to 1 to 5 microns, adding the crushed graphite into distilled water or purified water, adding 0.1 to 5 percent of surfactant, heating with stirring the mixed solution to 180 to 250 DEG C in a sealing way, performing stirring for 2 to 6 hours and reducing the temperature; 2) crushing lithium iron phosphate to the particle size of 1 to 5 microns, adding the crushed lithium iron phosphate into the distilled water or the purified water, adding with stirring 0.01 to 1 percent of coupling agent, performing uniform stirring, adding the graphene-dispersed aqueous solution, and performing stirring and filtration; and 3) vacuum-drying solid powder obtained by the filtration, and calcinating the dried solid powder for 2 to 12 hours to obtain the graphene-coated lithium iron phosphate cathode material. The method has the advantages of simple process, high material performance, high conductivity, high bulk density, high compacted density and the like.

The invention belongs to the technical field of aerogel materials, and particularly relates to antistatic aerogel for 3D printing as well as a preparation method and application of the antistatic aerogel. The preparation method comprises the following steps: (1) dispersing inorganic nanoparticles modified by a silane coupling agent containing epoxy groups and an aniline monomer in an acidic solvent to obtain a monomer mixed solution; (2) stirring and dissolving polyamide in the monomer mixed solution; (3) initiating a reaction to obtain a polyaniline modified polyamide solution; and (4) freeze-drying to obtain the antistatic aerogel for 3D printing. By controlling synthesis conditions, a core-shell structure of acid-doped polyaniline coated inorganic nanoparticles is formed, and a good conductive path is formed in polyamide with a small addition amount of polyaniline. The antistatic aerogel for 3D printing can be applied to technologies such as photocuring molding and fused deposition of polyurethane resin in a 3D printing technology, and the antistatic property and the mechanical property of a 3D printed product are improved.

The invention relates to the technical field of adsorbents, and particularly discloses an aluminum oxide type adsorbent and a preparation method thereof.The preparation method comprises the following steps that lanthanum salt, cerium salt and a polyethylene glycol aqueous solution are mixed to be uniform, then the mixture is mixed with gamma-Al2O3 to be uniform, pH is adjusted, standing is conducted, solid-liquid separation is conducted, drying and roasting are conducted, and a double-doped carrier is obtained; dispersing the double-doped carrier in a mixed solution containing 2-methylimidazole, ferric salt and zinc salt, adjusting the pH value, carrying out heating reaction, solid-liquid separation and drying in an inert atmosphere, grinding to obtain powder, and carrying out molding treatment on the powder to obtain a composite carrier; uniformly mixing the Ag modified molecular sieve with silica sol, coating the surface of the composite carrier with the mixture, and drying to obtain an adsorbent precursor; dipping an adsorbent precursor in the dispersion liquid, and after dipping, solid-liquid separation and drying, reactivating to obtain the aluminum oxide type adsorbent; the prepared adsorbent can synergistically and efficiently remove multiple impurities and is excellent in corrosion resistance.

The invention discloses a composite electrode material for removing uranium through photoelectrocatalysis and a preparation method and application of the composite electrode material, and belongs to the technical field of catalytic materials and wastewater treatment.The preparation method of the composite electrode material comprises the following steps that a ZIF-8 material, copper salt and ferric salt are mixed, and a first metal composite material is prepared; reacting the first metal composite material with a KOH solution to prepare a second metal composite material; carrying out carbonization treatment on the second metal composite material, and then carrying out acid treatment by using acid to obtain a bimetallic atom catalytic material; the preparation method comprises the following steps: dispersing a bimetallic atom catalytic material and a g-C3N4 material in a mixed solution containing phytic acid and a Nafion solution to obtain catalyst ink; and coating the catalyst ink on a substrate, and carrying out illumination drying to obtain the composite electrode material. According to the composite electrode material, under the synergistic effect of the bimetallic single atomic cluster catalyst and g-C3N4, respective advantages are fully exerted, and efficient deposition removal of uranium is achieved.

The invention discloses a compensation method based on ultraviolet-visible spectrum interaction interference, which relates to the technical field of spectral analysis, and comprises the following steps: acquiring ultraviolet-visible spectrum data of turbidity, COD, nitrate single gradient solution and mixed solution of the turbidity, COD and nitrate single gradient solution, and preprocessing the data; constructing a mapping relation model of the turbidity and the spectral data; for spectral data within the wavelength range of 260-320nm, calculating interactive interference data, establishing a relationship between the turbidity and the interactive interference data, and performing interactive interference compensation and spectral analysis; for the spectral data in the wavelength range of 220-260nm, constructing a COD and spectral data relation model, and calculating interactive interference data; and based on the interactive interference data characteristics, establishing a regression model, analyzing the relationship between the interference spectrum characteristics and other substances, and performing interactive interference compensation and spectral analysis. According to the method, the resolution of the spectral signal is remarkably improved, the reliability of data analysis is improved, and the method has a wide application prospect.

The invention discloses a preparation method of a degradable transparent conductive polymer film, and belongs to the technical field of film preparation. Preparing dispersion liquid I through graphene oxide quantum dots; preparing a dispersion liquid II from polyaniline nanofibers; dissolving pyrrole and toluenesulfonic acid in N, N-dimethylformamide to prepare a reaction solution, adding the dispersion liquid I and the dispersion liquid II, stirring, and adding ferric chloride hexahydrate to obtain a reaction solution; adjusting the pH value of the reaction solution to 1.5, and heating to obtain a polypyrrole solution; preparing cellulose acetate, polyvinyl alcohol and N, N-dimethylformamide to obtain a cellulose acetate solution; mixing the polypyrrole solution and the cellulose acetate solution, adding glutaraldehyde to obtain a mixed solution, and pouring the mixed solution into a mold to prepare a composite wet film; and putting the composite wet film into a hot-pressing forming machine for hot-pressing to generate the polymer film. The conductive polymer film prepared by the invention can be applied to the fields of supercapacitor electrode materials, electromagnetic shielding materials, flexible sensors and the like, and provides a new high-performance material choice for the development of related fields.

The utility model provides a detergent putting device and clothes processing equipment. The detergent feeding device comprises a detergent supply assembly, a liquid outlet water path, a first water path and a second water path. The detergent supply assembly is provided with a first water outlet for discharging a detergent mixed solution; the first water path and the second water path are used for conveying fluid, the first water path communicates with a water source, the first water outlet and the water inlet end of the liquid outlet water path, and fluid in the first water path is detergent mixed solution; the second waterway is communicated with the water source and the water inlet end of the liquid outlet waterway, and at least part of the second waterway is arranged in the detergent supply assembly. The detergent putting device provided by the utility model can promote dissolution of the detergent, is compact in structure and small in occupied space, and can be conveniently arranged in the clothes treatment equipment.

The invention belongs to the technical field of rare earth functional materials, and particularly relates to a rare earth aluminate low-temperature magnetic refrigeration material and a preparation method and application thereof.The preparation method comprises the following steps that 1, rare earth metal nitrate and aluminum nitrate are added into water to be mixed, and a mixed solution is prepared; adding ammonia water into the mixed solution to prepare a precipitate; (2) carrying out annealing treatment on the precipitate to prepare a metal oxide; and (3) calcining the metal oxide to obtain the rare earth aluminate low-temperature magnetic refrigeration material. The rare earth aluminate which has the characteristics of stable structure, low preparation cost, strong mechanical property, high magnetic density and the like and is prepared by adopting a coprecipitation method and combining a high-temperature sintering technology has more excellent magnetocaloric properties in a low-temperature region.

The invention belongs to the technical field of new energy, and discloses a preparation method and application of a LiaMXb-based composite solid electrolyte membrane, and the preparation method comprises the following steps: S1, carrying out spray drying on a mixed solution in which a Li source, an M source and an ammonium salt are dissolved, placing the mixed solution in a crucible of which the bottom is paved with the ammonium salt, and annealing for 2-10 hours at 350-800 DEG C in an inert atmosphere to obtain a LiaMXb solid electrolyte; s2, mixing the LiaMXb solid electrolyte with a fluorine-containing monomer A and a dispersing agent, and performing spray drying to obtain electrolyte powder wrapped by the fluorine-containing monomer A; s3, ball-milling and uniformly mixing the electrolyte powder wrapped by the fluorine-containing monomer A, a lithium salt, a thermal curing agent and a monomer B in an inert atmosphere to obtain composite electrolyte powder; and S4, carrying out cold isostatic pressing and hot pressing curing on the composite electrolyte powder to prepare the LiaMXb-based composite solid electrolyte membrane. The prepared LiaMXb-based composite solid electrolyte membrane not only has excellent air stability, flexibility and machinability, but also has a continuous three-dimensional ion conduction path, and the assembled all-solid-state lithium battery has good electrochemical performance.

The invention discloses a preparation method of capillary crystalline self-repairing concrete, which comprises the following steps: adding zeolite powder into a urease solution for dipping treatment to obtain pretreated zeolite powder; adding the pretreated zeolite powder into a mixed solution A containing urea and sodium alginate, adding a calcium chloride solution A, and separating a solid phase to obtain coated zeolite powder; fumed silica is added into a magnesium chloride solution to be mixed, polyethylene glycol is added, ultrasonic dispersion is conducted, and dispersion liquid is obtained; mixing the coated zeolite powder with the dispersion liquid, adding a sodium alginate solution, mixing, adding a calcium chloride solution B, and separating a solid phase to obtain modified zeolite powder; mixing preparation raw materials including the modified zeolite powder, the cement, the fly ash, the polycarboxylic acid water reducing agent and the aggregate to obtain the concrete. The concrete prepared through the method is good in crack self-repairing effect and good in mechanical strength, and the durability and the service life of the concrete can be improved easily.

The utility model provides a spray head unit and a clothes treating apparatus. The spray head unit comprises a mixing space and a water outlet, and the water outlet is formed in the wall face of the mixing space. A first water path and a second water path for conveying fluid are arranged in the nozzle unit. The fluid in the first water path and the fluid in the second water path converge in the mixing space, the mixed fluid in the mixing space is sprayed to a clothes processing cavity of the clothes processing equipment through the water outlet, and the fluid in the first water path is a detergent mixed solution. The water outlet end of the first water path and the water outlet end of the second water path are located in the spray head unit, the water outlet end of one of the first water path and the second water path is provided with a flow guide channel, and the flow guide channel is used for guiding fluid to the water outlet end of the other one. According to the spray head unit and the clothes treatment equipment, dissolution of the detergent can be promoted, and the cleaning effect is improved.

The invention relates to a preparation method and application of an artificially synthesized exosome with an anti-aging effect, and belongs to the technical field of cosmetics and biology. The artificially synthesized exosome is prepared from hydrogenated lecithin, phytosphingosine, cholesterol, ceramide, squalane, sodium stearoyl glutamate, a surface modification structure, polyol, an active component and water. The preparation method comprises the steps of preparation of an alcohol phase, preparation of a water phase, preparation of a mixed solution and high-pressure homogenization treatment. The artificially synthesized exosome prepared by the preparation method provided by the invention is good in stability and high in anti-aging activity.

The invention provides a method for recovering a BHET monomer from a waste polyester textile alcoholysis solution, and is characterized in that the recovery method comprises the following steps: (1) filtering: mixing the waste polyester textile alcoholysis solution with water under a stirring condition, and filtering at 55-70 DEG C; and (2) cooling crystallization: under a stirring condition, carrying out primary cooling on the filtrate obtained by filtering in the step (1) from 55-70 DEG C to 45-55 DEG C, then adding a BHET seed crystal, then carrying out secondary cooling to 5-15 DEG C, and maintaining the temperature for 20-60 min to obtain the BHET monomer. The mixed solution cooling crystallization method is developed on the basis of complexity of components of the waste polyester textile fabric, the problems that in the conventional production process, a BHET crystal product is low in quality, prone to scaling, difficult to filter and dry and the like are solved, and the obtained BHET product is large in particle size, narrow in particle size distribution, high in purity, good in fluidity and high in stability.

The invention provides a carbon nanotube / polyvinyl alcohol hydrogel and a preparation method and application thereof, and belongs to the technical field of composite materials and flexible electron cross materials. Cellulose nanofibers and multi-walled carbon nanotubes are dispersed in deionized water to obtain dispersion liquid; uniformly mixing a polyvinyl alcohol solution and the dispersion liquid to obtain a mixed solution; carrying out oriented freezing forming on the mixed solution, and then freeze-drying the mixed solution to obtain an aerogel sample; performing hot pressing on the aerogel sample to obtain a thin film material; and swelling and balancing the film material in deionized water to obtain the carbon nanotube / polyvinyl alcohol hydrogel. According to the invention, collaborative optimization of conductive network continuity, interface bonding strength and energy dissipation capability is realized, so that high conductivity, high stress and obdurability are considered, and the material is endowed with multi-dimensional strain sensing capability and signal stability; and a new idea is provided for realizing effective balance between high conductivity and excellent mechanical properties of the hydrogel material.

The invention relates to the technical field of new energy battery materials, in particular to a surface-coated sulfide solid electrolyte as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing and stirring a sulfide solid electrolyte and a first solvent to obtain a first mixed solution; mixing and stirring nanoparticles with oxygen-containing functional groups and a second solvent to obtain a second mixed solution; adding the second mixed solution into the first mixed solution, and stirring to obtain a third mixed solution; and carrying out vacuum drying on the third mixed solution to obtain the surface-coated sulfide solid electrolyte. The sulfide solid electrolyte is subjected to surface particle coating through simple mixing and vacuum drying, oxygen-containing functional groups are attached to the surfaces of the particles, so that the material is more oxygen-loving, the air stability of the sulfide solid electrolyte is improved, and the material still keeps high ionic conductivity and has good electrochemical performance. And moreover, the machining process is reduced, the machining cost is reduced, and the practical application value is higher.

The invention discloses an A-site high-entropy solid oxide fuel cell cathode material as well as a preparation method and application thereof, and provides an A-site high-entropy solid oxide fuel cell cathode material Pr < 0.2 > M < 0.2 > La < 0.2 > Ba < 0.2 > Sr < 0.2 > Co < 0.8 > Fe < 0.2 > O < 3-delta > with a perovskite phase. The preparation method comprises the following steps: S1, weighing multi-element metal nitrates, and mixing to obtain a first mixed solution; s2, dissolving ethylenediamine tetraacetic acid in ammonia water to obtain a second mixed solution; mixing the first mixed solution, the second mixed solution and citric acid to form a mixed precursor solution; s3, carrying out second heating treatment on the mixed precursor solution, and adjusting the pH value to form a gel precursor; and S4, carrying out pre-sintering treatment, third heat treatment and calcination treatment on the gel precursor to obtain a high-grade powder precursor, and carrying out ball milling and sieving treatment to obtain the A-site high-entropy solid oxide fuel cell cathode material. The cathode material is high in stability and good in chemical compatibility with a barrier layer GDC, provides high-quality mass transfer channels and active sites for O2 / O- / O2-, and has good electrochemical performance at medium and low temperatures.

The invention provides a sample pretreatment automation method for flow cytometry, and belongs to the technical field of sample pretreatment for flow cytometry. A biological sample to be detected is collected and placed in a collection tube containing an EDTA-K2 anticoagulant for pretreatment; an automatic pipetting system is used for carrying out incubation reaction on an anticoagulant whole blood sample and an intelligent matching fluorescence labeling antibody mixed solution, and a double-layer game optimization verification system is used for verifying the rationality of an antibody adding proportion and reaction condition parameters; carrying out fluorescence characteristic readability index prediction on the incubated cell suspension by adopting an intelligent dilution parameter regulator model, dynamically adjusting hemolysis parameters and suspension conditions, and adding 1 * hemolysin working solution by using an automatic liquid adding device to carry out hemolysis treatment so as to finish pretreatment; the technical problems that in the pretreatment process of flow cytometry detection samples, parameters are often based on artificial experience, and the reproducibility and standardization degree of detection results are insufficient are solved.

The utility model relates to the technical field of clothes treatment, and provides a detergent putting device and clothes treatment equipment, the detergent putting device comprises a first water path and a liquid flow channel, the side wall of the first water path is opened to form a liquid outlet, and the first water path comprises a mixing space; the liquid flow channel is provided with a second water outlet end, and at least one of the first water path and the liquid flow channel conveys a detergent mixed solution; and the second water outlet end is communicated with the liquid outlet through the mixing space. The second water outlet end is communicated with the liquid outlet through the mixing space, fluid discharged from the second water outlet end enters the mixing space to be converged and mixed with fluid of the first water path, the mixing effect is improved, and detergent such as washing powder can be dissolved more sufficiently.

The invention relates to an anion exchange membrane based on isopropyl piperidone and biphenyl and a preparation method of a membrane electrode, the preparation method comprises the following steps: respectively dissolving an aromatic monomer and IPD in a first solvent, and mixing to obtain a mixed solution, the aromatic monomer being BP or TP; dropwise adding an acidic initiator into the mixed solution for reaction at the reaction temperature of-5 DEG C to 0 DEG C to obtain a nitrogen heterocyclic ring polymer intermediate; adding a quaternization reagent into the nitrogen-containing heterocyclic ring polymer intermediate to realize quaternization modification of nitrogen atoms to obtain a quaternization ionomer; and forming a film to obtain the AEM film. The preparation method of the membrane electrode comprises the following steps: respectively forming a cathode catalyst layer and an anode catalyst layer on two opposite sides of an AEM membrane through ultrasonic spraying to obtain the MEA. The AEM membrane and the MEA obtained according to the invention have the characteristics of excellent stability and high water electrolysis performance, can significantly improve the efficiency and durability of AEMWE, and are suitable for the fields of hydrogen production by water electrolysis and the like.

The invention provides a collagen freeze-dried product and a preparation method thereof, and belongs to the technical field of biology. In the formula design, through the synergistic effect of the arginine (salt) and the surfactant, denaturation and aggregation of the collagen freeze-dried product in the production process and the storage period are inhibited, the stability of the product is improved, and the prepared collagen freeze-dried product is high in activity, purity and safety. In the freeze-drying process, pre-freezing parameters are optimized, and the nucleation effect of ice crystals in the freezing process of the collagen mixed solution is controlled by regulating and controlling parameters such as temperature and vacuum degree in the freeze-drying process, so that the shapes and the sizes of the crystals in the collagen freeze-dried product are more uniform, the drying time is shortened, and the production efficiency is improved. And the collagen freeze-dried product with uniform pore diameter and excellent appearance is obtained, and the uniformity and stability of batch and inter-batch products are improved.

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 relates to a PEO-based organic-inorganic composite solid electrolyte membrane and a preparation method thereof. The electrolyte membrane is prepared by heating and curing a blend solution of a PLA organic solution and a PEO / LITFSI / LATP mixed solution. The PEO-based organic-inorganic composite solid electrolyte membrane and the preparation method thereof provided by the invention have the effects that due to the existence of the PLA / PEO blending system, the degradability of the solid electrolyte can be realized, and the mechanical property of the solid electrolyte can be enhanced. In addition, the inorganic lithium salt and the organic lithium salt are mixed, so that the solid electrolyte is endowed with excellent ionic conductivity, and the mechanical property of the solid electrolyte is further improved. Therefore, the PEO-based organic-inorganic solid electrolyte and the preparation method thereof provided by the invention can bring important contributions to high energy density, long cycle life and excellent safety performance of an all-solid-state battery.

The invention provides a platinum-carbon catalyst taking hollow carbon nanospheres as a carrier and a preparation method of the platinum-carbon catalyst. The method comprises the following steps: adding a polymer monomer into a nano template dispersion liquid with a uniform size; then adding a proper amount of platinum salt into the solution to obtain a mixed solution, and stirring to react for 0.5-30 hours to obtain a reaction product; and annealing the reaction product, and then removing the nano template to obtain the platinum-carbon catalyst. The obtained platinum-carbon catalyst takes the hollow carbon nanospheres as a carrier and has a larger specific surface area, the platinum catalyst is loaded on the surfaces of the carbon nanospheres and can be in better contact with an electrolyte, and the obtained catalyst has good electrochemical activity and shows excellent electro-catalytic hydrogen evolution performance and oxygen reduction performance; and the related preparation method is simple and reliable, is suitable for preparation of an electrocatalytic hydrogen evolution electrode and an oxygen reduction electrode, and has a good application prospect in the fields of proton exchange membrane electrolytic cells, hydrogen fuel cells and the like.

The invention provides a method for synthesizing 1, 2-bis (4-vinyl phenyl) ethane, which comprises the following steps: adding a first solvent, methyl triphenyl phosphine halide and strong alkali into a reaction flask, and uniformly stirring to obtain a first mixed solution; heating the first mixed solution and carrying out reflux reaction for 1 hour; dropwise adding a 1, 2-bis (p-formaldehyde phenyl) ethane solution until the reflux reaction is finished to obtain a second mixed solution; reducing the temperature of the second mixed solution to room temperature, and adjusting the pH value of the second mixed solution to obtain a first solution; layering the first solution, and taking an organic layer; adding a polymerization inhibitor into the organic layer to obtain a second solution; concentrating the second solution to obtain a 1, 2-bis (4-vinyl phenyl) ethane crude product; adding a poor solvent into the crude product, stirring and crystallizing; filtering the crystal to obtain a filter cake, adding a second solvent into the filter cake, and washing and drying the filter cake to obtain 1, 2-bis (4-vinyl phenyl) ethane; the method for synthesizing the BVPE is simple and low in raw material cost, and the synthesized BVPE is high in purity and free of product isomeride.

The invention discloses a method for preparing regenerated flame-retardant high-shrinkage polyester by a methanol alcoholysis method, and belongs to the technical field of polyester. The method comprises the following steps: (a) mixing the waste polyester fabric with methanol, and carrying out catalytic depolymerization to obtain a regenerated DMT mixed solution; (b) carrying out impurity separation and methanol recovery treatment on the regenerated DMT mixed solution, and then carrying out cooling crystallization, centrifugal drying and rectification purification treatment to obtain pure DMT; (c) carrying out transesterification on pure DMT, ethylene glycol, a transesterification catalyst and a DEG inhibitor; (d) after the ester exchange reaction, adding CEPPA-EG and IPA-EG for copolymerization; adding a polymerization catalyst, a stabilizer and an antioxidant for polymerization reaction to obtain a modified polyester melt; and (e) granulating and drying to obtain the slices. The regenerated polyester prepared by the method has multiple functions of flame retardance, high boiling water shrinkage, low-temperature dyeing and the like, and is suitable for the fields of high-end clothing, automotive trim, electronic packaging materials and the like.

The invention discloses a carbon-doped titanium dioxide nanotube-molybdenum disulfide energy-storage antibacterial material and a preparation method thereof. The preparation method comprises the following steps: carrying out primary anodic oxidation on a clean titanium foil in a mixed electrolyte of ethylene glycol, water and ammonium fluoride; after ultrasonic treatment is carried out in a hydrochloric acid solution for set time, secondary anodic oxidation is carried out, and the mixed electrolyte of the secondary anodic oxidation is the same as that of the primary anodic oxidation; annealing the titanium foil subjected to anodic oxidation twice in an argon atmosphere, putting an annealed sample into a mixed solution of sodium molybdate, a sulfur source and glucose, and carrying out hydrothermal treatment; and the titanium foil subjected to hydro-thermal treatment is cleaned and dried, and the carbon-doped titanium dioxide titanium foil with the surface covered with molybdenum disulfide is obtained. The MoS2-coated carbon-doped titanium dioxide nanotube (TNT-C-atMoS2) with high biocompatibility developed by the invention has a synergistic effect of charge antibiosis and chemical sterilization, so that the problem of intractable biological fouling of a titanium-based metal material in ocean engineering equipment is effectively solved.

The invention provides a preparation method of a cell culture three-dimensional scaffold and cell culture meat, which comprises the following steps: firstly, preparing a gelatin-carrageenan mixed solution and a gel precursor solution of transglutaminase, dividing into two parts, incubating at constant temperature to obtain two parts of composite hydrogel, randomly freeze-drying one part to obtain aerogel, and freeze-drying the aerogel to obtain the cell culture three-dimensional scaffold. Stacking on the other part and incubating at constant temperature again to obtain the prefabricated double-layer gel. The prefabricated double-layer gel is directionally frozen, ice crystals grow upwards from the bottom, freezing is stopped after the temperature is reduced to the set temperature, and the cell culture three-dimensional scaffold is obtained through drying. The stent adopts an ordered-disordered partition design, parallel micro-channels are formed in the lower layer by using a directional ice template method, and muscle fiber arrangement is simulated; a porous spongy structure is constructed on the upper layer by using a random ice template method, and is adapted to adipocyte proliferation. Two layers of interfaces are interpenetrated and communicated, natural mechanical gradients are combined, natural tissue characteristics are re-engraved, the traditional limitation is broken through, the cell co-culture efficiency and the cultured meat quality are improved, and industrialization is promoted.

The invention relates to the technical field of high performance liquid chromatography detection, in particular to a liquid chromatography determination method and equipment for the content of m-tert-butylphenol, and the method comprises the following steps: determining a to-be-determined mixed solution of the prepared m-tert-butylphenol by using high performance liquid chromatography to obtain chromatographic data; the method comprises the following steps: preparing chromatographic data of standard control group solution samples of m-tert-butylphenol under different concentrations under two preset different wavelengths, and obtaining a nonlinear fitting relationship between the concentrations of m-tert-butylphenol and chromatographic peak areas; analyzing the chromatographic data deviation of the to-be-measured mixed solution, and obtaining the chromatographic peak area of the to-be-measured mixed solution after correction of the intermediate tert-butylphenol; and acquiring the concentration of the intermediate tert-butylphenol in the mixed solution to be measured corresponding to the corrected chromatographic peak area by utilizing a nonlinear fitting relationship. The invention aims to improve the measurement accuracy of the prepared m-tert-butylphenol.

The invention relates to a preparation method of antibacterial gamma-polyglutamic acid superabsorbent hydrogel. The preparation method comprises the following steps: (1) preparing a gamma-polyglutamic acid solution; (2) dissolving an antibacterial agent in the gamma-polyglutamic acid solution, and fully stirring and uniformly mixing to obtain a mixed solution 1; adjusting the pH value of the mixed solution 1, heating the mixed solution 1 to 60 DEG C, and continuously reacting for 1-2 hours to obtain a mixed solution 2; cooling the mixed solution 2 to room temperature, adding a cross-linking agent, and uniformly mixing to obtain a mixed solution 3; standing the mixed solution 3 at room temperature for 1-3 hours and then carrying out gradient heating reaction to obtain an antibacterial gelatinous product; and (3) dehydrating the antibacterial gelatinous product, and carrying out vacuum negative pressure drying to obtain a dried hydrogel product, namely the antibacterial gamma-polyglutamic acid super absorbent hydrogel. The antibacterial gamma-polyglutamic acid superabsorbent hydrogel prepared by the invention has good biocompatibility, is safe and non-toxic, also has excellent water absorption performance and antibacterial performance, and has a good application prospect.

The utility model relates to the technical field of clothes treatment, and provides clothes treatment equipment which comprises a clothes treatment cavity and a mixing space, the mixing space is used for containing a detergent mixed solution, the mixing space is provided with a liquid outlet, and the liquid outlet is directly communicated with the clothes treatment cavity. The mixing space is used for containing a detergent mixed solution, provides space for further mixing of the detergent and water and promotes dissolution of the detergent. The liquid outlet is directly communicated with the clothes processing cavity, fluid from the liquid outlet directly enters the clothes processing cavity, a transfer channel does not need to be arranged between the liquid outlet and the clothes processing cavity, the transfer channel is saved, and the production cost is reduced; fluid such as a detergent mixed solution can directly enter the clothes processing cavity from the liquid outlet and directly act on clothes.