3287 results about "Sulfonic acid" patented technology

Improved performance ion exchange membranes for use in REM, AEM and DMFC fuel cells, buffered fuel cells, hydrolysis, other applications comprise a molecular matrix of homopolymers, di-monomer, heteropolymers, copolymers, or block-polymers of fluorocarbon and hydrocarbon compounds combined with (i) skeletal support grid to improve durability, handling, reduce membrane swelling, and sequester dopants and nanoparticles from leakage; (ii) microporous membrane formed using a sacrificial filler process enhancing conductivity and limiting fuel crossover; (iii) hetero-ionomeric matrix of two-or-more membrane-bound acids e.g. sulphonic and phosphonic acid expanding usable range; (iv) permanent fillers enhancing conductivity and porosity including nanoparticles, metal-oxides, zeolites, silicates, GOs, CNTs, MOFs, POSS, and others; (v) ionic liquid doping to enhance membrane conductivity; (vi) membrane nanocoating preventing H2O2 diffusion; and / or (vii) catalytic nanocoating with metals, metal-oxides, and MOFs preventing atmospheric toxin catalyst poisoning. Combined with a heterogenous GDI, the IEM is integrated into iBFC power blade and energy bank applications.

The invention discloses a self-crosslinking temperature-resistant salt-resistant emulsion type fracturing fluid thickening agent and a preparation method thereof, and belongs to the technical field of oilfield chemistry. The raw materials adopted by the invention comprise 30 to 50 parts of an oily solvent, 15 to 25 parts of deionized water, 10 to 20 parts of acrylamide, 5 to 10 parts of acrylic acid, 2 to 4 parts of 2-acrylamido-2-methylpropanesulfonic acid, 0.05 to 0.2 part of a crosslinking monomer, 0.5 to 1 part of a quaternary ammonium salt type hydrophobic association monomer, 4 to 8 parts of an emulsifier and 1 to 2 parts of a phase inversion agent. The self-crosslinking emulsion is formed through water phase-oil phase mixing, high-speed emulsification, low-temperature initiation polymerization and phase inversion treatment. Based on physical-chemical double-crosslinking temperature control cooperation, a salt-resistant-hydrophobic double-shielding mechanism and an integrated design without an exogenous crosslinking agent, the contradiction between the temperature-resistant and salt-resistant performance of a traditional thickening agent and the process complexity is broken through, and a technical support is provided for efficient development of high-temperature and high-salt oil and gas reservoirs.

The invention relates to the technical field of environmental science, in particular to a box-type model-based inversion method for methane sulfonic acid particles in marine droplet aerosol, which comprises the following steps of: 1, acquiring satellite remote sensing data, ground observation data and laboratory simulation data, and carrying out data standardization processing; 2, dividing the target sea area into a plurality of sub-areas as independent box bodies; 3, calculating the discharge flux of the marine droplet aerosol based on the dimethyl sulfide concentration and the wind speed, and updating the spatial and temporal distribution of the discharge source; 4, embedding a chemical reaction path for oxidizing dimethyl sulfide on the surface of the aerosol into the box-type model to generate methanesulfonic acid, and introducing the specific surface area of the aerosol to correct the reaction rate; and step 5, outputting spatio-temporal distribution of the concentration of the methane sulfonic acid, and comparing measured data for verification. The accuracy of aerosol source item estimation is improved, the fusion efficiency of multi-source data is improved, and the adaptive capacity of the model in a complex environment is enhanced.

The present invention uses commercially available 3-aminopropylsilane coupling agent, diallylamino polyether acrylate, and an alkylating agent, or γ-propanesultone, or γ-butyrolactone as raw materials, and through an aza-Michael addition reaction and a quaternization reaction, a multifunctional silane coupling agent containing one or more quaternary ammonium cations, or sulfobetaine, or carboxybetaine in its molecular structure is prepared, which is used for the surface modification of bioactive glass, and the bioactivity, antibacterial and antifungal properties, and hydrophilicity enhancement effects after the surface modification of bioactive glass are obtained.

The invention relates to the technical field of plugging agents, and discloses a viscoelastic polymer type self-assembly plugging agent and a preparation method thereof. The preparation method comprises the following steps: adding acrylamide, butyl acrylate, 2-acrylamide-2-methylpropanesulfonic acid, quaternized cyclodextrin, gamma-glycidyl ether oxypropyl trimethoxy silane modified bentonite, Schiff base styrene, a sodium dodecyl benzene sulfonate emulsifier and octadecyl dimethyl allyl ammonium chloride into a reaction kettle; and adding an azodiisobutyronitrile initiator into the deionized water, uniformly mixing, and reacting for 4-5 hours at 50-65 DEG C to obtain the viscoelastic polymer type self-assembled plugging agent after the reaction is finished. The plugging agent disclosed by the invention has a relatively good plugging effect, and effectively solves the problem that the gel strength is weakened or the gelling is not thorough due to the formation shearing effect in a continuous gel migration process.

The invention provides a non-aqueous electrolyte, a lithium ion battery, a battery module, a battery pack and a power utilization device, the non-aqueous electrolyte comprises a lithium salt, an organic solvent and an electrolyte additive, and the electrolyte additive comprises 1, 3-propane sultone, fluoroethylene carbonate, vinylene carbonate, lithium tetrafluoroborate and a compound I shown in the formula I. The non-aqueous electrolyte is applied to the lithium ion battery, and the cycle life of the lithium ion battery is prolonged.

The invention discloses a microporous diaphragm for a low-electrical-impedance lithium battery and a preparation method of the microporous diaphragm. The diaphragm comprises: a base film layer, wherein the base film layer is of a microporous structure formed by biaxially stretching polypropylene and / or polyethylene; the surface of the base film layer is coated with the functional coating, and the functional coating contains mixed slurry of inorganic nanoparticles and a binder; the surface modification layer is formed by introducing a hydrophilic electrolyte group on the surface of the functional coating through plasma treatment or chemical grafting. The base membrane layer forms a uniform micropore structure through a two-way stretching process, the functional coating is formed by compounding nano silicon dioxide or aluminum oxide and polyvinylidene fluoride according to a specific proportion, a porous layer with gradient pore diameter is formed, the pore size of the porous layer is smaller than that of the base membrane layer, and efficient permeation of electrolyte is ensured. Electrolyte-philic groups such as sulfonic groups are introduced into the surface modification layer, so that the wettability of the diaphragm to an electrolyte is remarkably improved. During preparation, the base membrane is formed through melt blending, two-way stretching and pore-forming agent extraction, and then the functional layer is constructed through slurry coating and a low-temperature plasma treatment or sulfonation process. The diaphragm combines gradient aperture design, inorganic filler enhancement and surface chemical modification, and realizes low impedance, high thermal stability and excellent mechanical strength.

The invention belongs to the technical field of drilling fluid, and particularly relates to a free radical polymerization water-based drilling fluid composition and a preparation method thereof. The invention relates to a core-shell composite particle-containing water reducer which comprises deionized water, salts (NaCl / KCl), alkalis (Na2CO3 and NaOH), barium sulfate and core-shell composite particles X. The particle is composed of a silicon dioxide core and a polymer shell layer, and the shell layer is formed by free radical copolymerization of acrylamide, 2-acrylamido-2-methylpropanesulfonic acid and acrylic acid and is covalently connected with the core through silanization treatment. Under the conditions of high salinity, strong alkali and high solid phase weighting, the drilling fluid simultaneously realizes the following effects: (1) high-density bearing and low-viscosity pumpability are realized; (2) compact plugging and water loss reduction and low formation damage flowback can be realized; and (3) stable rheology rock carrying, lubrication and friction resistance reduction. The problem that three aspects of performance are difficult to consider in the prior art is solved, and the drilling fluid is suitable for drilling of deep wells, ultra-deep wells and complex stratums and has remarkable industrial application value.

The invention relates to the technical field of purification of organic chemicals, in particular to an aroma purification method of leaf alcohol. Comprising the following steps: preparing a methanesulfonic acid magnetic catalyst; esterification of leaf alcohol; and alcoholysis and fractionation of the esterification solution. According to the method, acetic acid is used for esterification of leaf alcohol, then clear water and a sodium carbonate solution are used for washing, the clear water can effectively remove some water-soluble impurities and acidic byproducts, and the sodium carbonate solution not only can neutralize residual acidic substances, but also can promote siloxane impurities in initial leaf alcohol to be hydrolyzed and then taken away by a water phase, so that the content of the siloxane impurities in the leaf alcohol is reduced; in the subsequent process of producing leaf alcohol through alcoholysis of the organic phase I, pure water and ethanol, silyl ether impurities are hydrolyzed in a high-temperature and strong-alkali environment, products are dissolved in waste liquid to be removed, olefine aldehyde impurities with the boiling point lower than that of leaf alcohol are removed through azeotropic fractionation with ethanol, in conclusion, the impurities in the finished product leaf alcohol can be effectively reduced, and the yield of the finished product leaf alcohol is increased. And the prepared finished product leaf alcohol is high in purity and pure in fragrance.

The invention relates to the technical field of oil and gas field exploitation, and discloses a drag reducer for a multifunctional fracturing fluid and a preparation method thereof.The preparation method of the drag reducer for the multifunctional fracturing fluid comprises the steps that acrylic acid, acrylamide, 2-acrylamido-2-methylpropanesulfonic acid and modified itaconic acid are added into deionized water, stirring and mixing are conducted, and the drag reducer for the multifunctional fracturing fluid is obtained. Nitrogen is introduced for 30-40 min to remove oxygen, then azobis (isobutylamidine) hydrochloride is added, the mixture is stirred to react for 48-72 h at the temperature of 45-50 DEG C, and a polymer solution is obtained; and directly and uniformly mixing the polymer solution, the compatilizer and the modified nano silicon dioxide, and reacting in a magnetic stirrer at 60-70 DEG C for 1.5-2 hours to obtain the drag reducer for the multifunctional fracturing fluid. The drag reducer has a good drag reduction effect, and the hydrophobicity, the temperature resistance, the salt resistance and the shear resistance are improved.

The invention discloses an all-solid-state composite dry conductive agent and a preparation method thereof, and belongs to the technical field of batteries. The all-solid-state composite dry conductive agent is prepared by the following steps: uniformly mixing carbon nanotubes, high-dispersion carbon black and graphene to obtain a primary mixture; then preparing a uniformly dispersed glue solution from the composite dispersant and water; and then adding the primary mixture into the glue solution, uniformly mixing, sanding, homogenizing, drying and crushing to obtain the product, the high-dispersion carbon black is obtained by oxidizing carbon black to form active groups such as carboxyl and hydroxyl on the surface of the carbon black, halogenating acyl and then reacting with lithium 2, 5-diaminobenzene sulfonate. The preparation method comprises the following steps: grafting histidine ester into carboxymethyl cellulose by using propylene glycol diglycidyl ester as a cross-linking agent, then introducing allyl-1, 3-sultone, then copolymerizing with lithium 2-acrylamido-2-methylpropanesulfonate and 3-aminobenzoic acid allyl ester protected by fluorenylmethoxycarbonyl, and then deprotecting to obtain the composite dispersant.

The invention provides a diaphragm and a preparation method thereof and a lithium ion battery, the diaphragm comprises a base membrane layer and a composite functional layer, the composite functional layer comprises hydrophobic SiO2 aerogel modified by a hydrophobic agent, a conductive ion polymer and a solid electrolyte, and the composite functional layer respectively accounts for 3-12wt%, 0.5-1.0 wt% and 0.5-1.5 wt% of the total mass of the diaphragm; the hydrophobic agent comprises trimethylchlorosilane, hexamethyldisilazane, perfluorooctyltriethoxysilane, polyvinylidene fluoride, polydimethylsiloxane and the like, the conductive ionic polymer comprises polyvinylpyrrolidone, lithium polymethacrylate, lithium polystyrene sulfonate, polyacrylamide and the like, and the solid electrolyte comprises lithium lanthanum titanium oxide, lithium lanthanum zirconium oxide, lithium lanthanum zirconium tantalum oxide and the like. The wettability is improved by the high porosity of the hydrophobic SiO2 aerogel, the stability and strong conductivity of a physical conductive network of the solid electrolyte and the ion affinity and amphoteric binding capacity of the conductive ion polymer are optimized, the electrochemical performance and thermal stability of the interface are optimized, and comprehensive optimization of the thermal-electric-interface performance of the diaphragm is realized through combination.

The invention discloses a high-initial-efficiency fast-charge graphite composite material and a preparation method thereof, the composite material is of a core-shell structure, the core is graphite, and the shell is lithium sulfonate / lithium molybdate and an amorphous carbon coating layer thereof; the mass ratio of the shell is 5-15 wt% according to the mass ratio of the composite material being 100%. The preparation method comprises the following steps: adding a molybdenum compound into a solvent to prepare a solution, adding graphite oxide, an inorganic lithium salt and a carbon nanotube conductive solution, reacting for 2-12 hours at the temperature of 50-120 DEG C, filtering, carbonizing filter residues to obtain a lithium molybdate conductive agent coated graphite material, and depositing a lithium sulfonate derivative on the surface of the lithium molybdate conductive agent coated graphite material by an atomization method to obtain the lithium molybdate conductive agent coated graphite material. The electron and ion conductivity of the material can be improved, and the rate and the first efficiency of the material can be improved.

The invention relates to the technical field of proton exchange membranes, and provides a covalent grafted heteropoly acid modified perfluorosulfonic acid membrane as well as a preparation method and application thereof. According to the invention, polypropylene glycol monoalkyl ether and Keggin type vacancy heteropoly acid are subjected to covalent grafting, and then the obtained covalent grafted heteropoly acid is used as an additive to modify the perfluorosulfonic acid membrane, so that the leakage problem of heteropoly acid in the proton exchange membrane can be effectively relieved, and meanwhile, the excellent proton conduction performance of heteropoly acid is also retained; moreover, the polypropylene glycol monoalkyl ether has relatively large molecular weight, so that the heteropoly acid can be anchored more firmly in the perfluorosulfonic acid membrane, and the proton conduction capability of the heteropoly acid is fully exerted. The result of the embodiment shows that the covalent grafted heteropoly acid modified perfluorosulfonic acid membrane provided by the invention shows excellent proton conduction performance and chemical stability, and has a wide application prospect.

The invention relates to a fluorine-containing binder for a sulfide all-solid-state battery and a preparation method and application thereof.The binder is formed by copolymerizing isoprene and lithium perfluorovinyl ether sulfonate, specifically, the lithium perfluorovinyl ether sulfonate, a chelating agent, an emulsifying agent, ferrous sulfate, a reducing agent and an acid-base buffering agent are dissolved in water, cooling is conducted in the inert atmosphere, and the fluorine-containing binder for the sulfide all-solid-state battery is obtained. And adding isoprene, an initiator and a molecular weight regulator, and carrying out polymerization reaction to obtain the fluorine-containing binder. The isoprene can enhance the solubility of the lithium perfluorovinyl ether sulfonate fragment in the non-polar solvent, so that the whole polymer is dissolved in the non-polar solvent; the perfluorovinyl ether lithium sulfonate has a large space proportion of fluorocarbon groups, and has a shielding effect on hydrocarbon groups on isoprene, so that the stability of the whole polymer can be improved. The fluorine-containing binder prepared by the preparation method disclosed by the invention is a binder with high elasticity, high ionic conductivity and high stability.

Provided is a porous separator selected from (a) to (c). (a) Porous membranes containing hydrophilic inorganic particles, an aromatic porous support, and an organic polymer including a hydrophilic organic polymer that has a sulfo group and / or a carboxy group and has an acid value of 0.3 mmol / g or higher; (b) porous membranes containing no porous support and containing hydrophilic inorganic particles and an organic polymer including a hydrophilic organic polymer that has a sulfo group and / or a carboxy group and has an acid value of 0.3 mmol / g or higher, the hydrophilic inorganic particle content of said porous membranes being 10 mass% or greater; (c) porous membranes containing no hydrophilic inorganic particles and containing an aromatic porous support and an organic polymer including a hydrophilic organic polymer that has a sulfo group and / or a carboxy group and has an acid value of 0.3 mmol / g or higher.

The invention relates to the technical field of hydraulic fracturing exploitation of deep / ultra-deep oil and gas reservoirs, and discloses a gel-coated temporary plugging agent and a preparation method and application thereof.The gel-coated temporary plugging agent comprises a proppant inner core and a degradable gel shell coating the outer surface of the proppant inner core; the degradable gel shell is formed by a gel shell gelling solution, the gel shell gelling solution comprises small-molecule comonomers and a degradable cross-linking agent, and the small-molecule comonomers comprise acrylamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide, N, N-dimethylformamide the initiator is one or more of N, N-dimethylacrylamide, acrylic acid, hydroxyethyl acrylate, benzyl acrylate, 2-propyl acrylic acid, 2-acrylamide-2-methylpropanesulfonic acid and N-vinyl pyrrolidone; and the initiator is one or more of N, N-dimethylacrylamide, acrylic acid, hydroxyethyl acrylate, benzyl acrylate, 2-propyl acrylic acid, 2-acrylamide-2-methylpropanesulfonic acid and N-vinyl pyrrolidone. The gel-coated temporary plugging agent can be used for effectively plugging in a fracturing time period at high temperature / ultrahigh temperature, and the flow conductivity of fractured cracks can be enhanced by exposing an internal propping agent after the gel-coated temporary plugging agent is degraded.

The invention discloses a perfluorinated compound adsorption material and a preparation method thereof. Comprising the following steps: 1) placing moso bamboo in a high-temperature carbonization furnace for carbonization treatment, after carbonization is completed, taking out bamboo charcoal, carrying out acid treatment to remove surface impurities and part of ash, then repeatedly washing the bamboo charcoal with deionized water until the bamboo charcoal is neutral, and finally drying the bamboo charcoal to obtain pretreated bamboo charcoal; and 2) putting the pretreated bamboo charcoal into a chitosan acetic acid solution to load chitosan on the surface of the bamboo charcoal, repeatedly washing the bamboo charcoal with deionized water to remove unloaded chitosan, and then drying to obtain the perfluorinated compound adsorption material. The prepared adsorption material has high adsorption capacity and selectivity on perfluorinated compounds, the adsorption performance of the adsorption material on the perfluorinated compounds is improved by modifying the bamboo charcoal, and the adsorption capacities of the adsorption material on perfluorooctanoic acid and perfluorooctane sulfonic acid can reach 400 mg / g and 450 mg / g respectively.

The invention discloses a method for preparing a polyvinyl polyamide composite reverse osmosis membrane by coupling reversed-phase interfacial polymerization with lignosulfonate, which adopts a reversed-phase interfacial polymerization method and comprises the following steps: firstly adding an oil phase containing polyacyl chloride, and then adding a water phase containing amine monomers and lignosulfonate. Molecules of the lignosulfonate contain more sulfonate radicals, so that the lignosulfonate is endowed with hydrophilicity, meanwhile, a large number of active functional groups such as phenolic hydroxyl groups, alcoholic hydroxyl groups and carboxymethyl exist, and oxygen atoms, sulfur atoms and the like in the functional groups contain unbonded electron pairs and can participate in interfacial polymerization reaction to form a cross-linked structure; the trade-off effect of the flux and the rejection rate of the reverse osmosis membrane is broken, and the polyvinyl polyamide reverse osmosis membrane with high flux and high rejection rate is obtained. The raw material of the polyethylene base material is low in price, and the product can be applied to the fields of water treatment, seawater desalination, brackish water desalination and the like on a large scale.

The invention relates to a temperature-resistant and salt-resistant gel for deep plugging and a preparation method thereof. The gel comprises a main agent, a cross-linking agent, a cross-linking promoting agent, a reinforcing agent, a stabilizing agent and water. The main agent is an acrylamide / 2-acrylamide-2-methylpropanesulfonic acid / N-vinyl pyrrolidone (AM / AMPS / NVP) terpolymer, the temperature-resistant and salt-resistant gel for deep plugging control is suitable for oil reservoirs with the temperature of 110-130 DEG C and the formation water mineralization degree of 5 * 10 < 5 >-10 * 10 < 5 > mg / L, the gelling time is controllable within 73-98 hours, the gel strength after gelling is high, the thermal stability is good, and the temperature-resistant and salt-resistant gel for deep plugging control is suitable for the oil reservoirs with the temperature of 110-130 DEG C and the formation water mineralization degree of 5 * 10 < 5 >-10 * 10 < 5 > mg / L. And long-time deep effective plugging of high-temperature and high-salt oil reservoirs can be realized.

The invention discloses a composite solid electrolyte and a preparation method and application thereof, and belongs to the technical field of solid lithium batteries. The composite solid electrolyte comprises a polymer matrix, a lithium salt and a lithium ion modified ionic metal organic framework (MOF) material. The metal center of the ion-conducting MOF material can be selected from Zr, Ti, Hf and the like, and the organic ligand can be selected from organic acids containing sulfydryl, sulfo groups and the like. The MOF material can effectively inhibit crystallization of a polymer matrix and increase the proportion of an amorphous region, Lewis acid sites on the surface of the MOF material can promote dissociation of lithium salt, and a lithium ion coordination channel formed in the MOF material can provide an extra rapid transmission path for lithium ions. When the electrolyte is applied to the solid-state lithium battery, the growth of lithium dendrites can be effectively inhibited, and the rate capability, the cycling stability and the safety of the battery can be remarkably improved.

The invention discloses a stainless steel material for a food-grade straw and a preparation process of the stainless steel material, and relates to the technical field of stainless steel material plating. The silver coating and the antibacterial coating are arranged on the surface of the stainless steel material, and the stainless steel material has good wear resistance and antibacterial performance through the action of the double protective layers. Sulfonated polyphenylene sulfide is added into a silver plating solution, a plating layer is formed after electroplating, the surface of a stainless steel material is not prone to being scratched, the wear resistance of stainless steel is improved, quaternary ammonium salt modified tea polyphenol-nano-silver composite particles are added into the antibacterial coating, and through the synergistic antibacterial effect of quaternary ammonium salt, tea polyphenol and nano-silver, the wear resistance of the stainless steel material is improved. The broad-spectrum antibacterial property is realized, and the efficient antibacterial effect is achieved.

The invention relates to the technical field of battery electrodes, in particular to a zinc pole piece coated with a sulfonic COF membrane, a preparation method of the zinc pole piece and an aqueous zinc battery, and the preparation method comprises the following steps: dissolving 2, 4, 6-triformyl phloroglucinol and p-phenylenediamine-2, 5-disulfonic acid in an organic solvent to obtain a mixed solution; and putting the zinc foil into the mixed solution, carrying out sealed standing at normal temperature, taking out the zinc foil coated with the sulfonic group COF film, and washing and drying the zinc foil to obtain the zinc pole piece coated with the sulfonic group COF film. The prepared zinc pole piece coated with the sulfonic COF film has good corrosion resistance and dendritic crystal inhibition capacity, and when the zinc pole piece is used as a negative electrode of a water-based zinc battery, the cycle performance of the water-based zinc battery can be improved, and the cycle life of the water-based zinc battery can be prolonged; the problems that a zinc negative electrode of an existing water-based zinc battery is prone to generating dendritic crystal and corrosion passivation side reactions in the battery circulation process, so that the use performance of the water-based zinc battery is reduced, and the service life is greatly shortened are solved.

The invention discloses high-performance anti-wear engine lubricating oil as well as a preparation method and application thereof. The high-performance anti-wear engine lubricating oil is prepared from the following raw materials: self-developed lubricating oil base oil, poly-alpha-olefin, zinc dialkyl dithiophosphate, calcium sulfonate, polyisobutylene succinimide, an antioxidant, polymethacrylate, an organic molybdenum complex, a de-foaming agent and a pour point depressant. The preparation method comprises the following steps: 1) synthesizing 9, 10-bis (2-tert-butyl-4-methylphenoxy) trimethylolethane stearate as base oil of the lubricating oil; and 2) mixing the base oil with other assistants to obtain the high-performance anti-wear engine lubricating oil. According to the preparation method, novel-like synthetic ester oil is firstly prepared, a phenol group and a large steric hindrance substituent group are introduced into a polymer, the anti-oxidation function is directly built in base oil molecules, meanwhile, super-strong heat resistance is achieved, and finally the high-performance anti-wear engine lubricating oil is obtained and can be applied to high-end application scenes such as aero-engines or gas turbines.

The invention discloses a preparation method of lithium trifluoromethanesulfinate, and belongs to the field of lithium ion battery materials. The preparation method of the lithium trifluoromethanesulfinate comprises the following steps: 1, mixing trifluoromethanesulfonyl chloride, lithium sulfite, lithium bicarbonate and a first solvent, and heating to react; 2, dissolving the concentrated crude product in a second solvent, and filtering and separating a lithium sulfate solid; and 3, concentrating the filtrate, adding a third solvent, uniformly stirring, filtering and separating the lithium chloride solid, and concentrating to obtain the lithium trifluoromethanesulfinate. According to the method for preparing the lithium trifluoromethanesulfinate, the yield can reach 94%, the operation is simple, byproducts are easy to separate, and the method is suitable for industrial production. In addition, the obtained by-product lithium sulfate can be used for preparing lithium sulfide, the by-product lithium chloride can be used for preparing solid electrolyte, and resource utilization is achieved.

The invention belongs to the technical field of membrane electrodes, and particularly relates to a hydrogen fuel cell catalyst layer slurry based on hydrophilic and hydrophobic regulation and a preparation method of a membrane electrode. The slurry of the catalyst layer comprises the following contents: the slurry of the PEM close to the cathode side comprises a Pt / C catalyst, deionized water, a perfluorosulfonic acid ionic polymer solution and isopropanol; the mass ratio, namely I / C ratio, of the ionic polymer to the carbon carrier is 0.8-1.2; the GDL cathode side slurry comprises a Pt / C catalyst, deionized water, a perfluorosulfonic acid ionic polymer solution, a PTFE aqueous solution (polytetrafluoroethylene aqueous solution) and isopropanol, and the mass ratio of the ionic polymer to the carbon carrier, namely I / C ratio, is 0.3-0.5. High hydrophilic ionomer content is reserved on the side, close to the cathode, of the PEM, proton conduction and catalyst active site wetting are guaranteed, the proportion of hydrophobic ionomers and hydrophobic materials is increased on the GDL side, a drainage channel is formed, liquid water is prevented from blocking gaps, then the performance of the membrane electrode is remarkably improved, and the interface contact resistance is stabilized to be 1.64-1.76 m omega (2.5 A / cm < 2 >).

The invention discloses a low-temperature-resistant polyacrylamide flocculant suitable for a low-temperature water body and a preparation method of the low-temperature-resistant polyacrylamide flocculant. The flocculant is prepared from the following raw materials in parts by weight: 60 to 85 parts of acrylamide (AM), 15 to 40 parts of low-temperature-resistant functional monomer 2-acrylamide-2-methylpropanesulfonic acid (AMPS), 0.5 to 5 parts of hydrophobic modified monomer, 0.1 to 1.0 part of molecular chain regulator, 0.01 to 0.1 part of initiator, 120 to 200 parts of deionized water and 1 to 5 parts of post-added antifreezing agent. The product is prepared by an aqueous solution polymerization method. According to the invention, by introducing the rigid sulfonic monomer and the functional monomer with large steric hindrance and compounding the specific antifreezing agent, the extensibility and diffusion performance of a polymer molecular chain in low-temperature (less than or equal to 10 DEG C) water are remarkably improved, so that large and dense flocs can be quickly formed under the low-temperature condition, and an excellent flocculating settling effect is kept.

The invention relates to a method for efficiently extracting lithium by roasting lepidolite at low temperature by using composite organic acid. The invention relates to a method for efficiently extracting lithium by roasting lepidolite at low temperature by using composite organic acid, which comprises the following steps of: adding an activating agent into lepidolite concentrate, and pre-activating to obtain activated lepidolite concentrate powder; the lepidolite concentrate powder and a composite organic acid roasting agent are mixed, acidified and roasted, and a roasted product is obtained; adding water into the roasted product for leaching, and carrying out suction filtration to obtain a lithium-containing leachate; the composite organic acid roasting agent at least comprises methanesulfonic acid. According to the method, the problem that the lithium ion extraction efficiency is low due to the fact that the TOT layered structure in the lepidolite is difficult to damage is solved, and the problem that the lithium ion extraction efficiency is low due to the fact that Si-O bonds with high bond energy in an existing lepidolite crystal framework are difficult to dissociate is also solved.

The invention discloses a lithium iron manganese phosphate positive electrode material and a preparation method thereof, and belongs to the technical field of lithium ion batteries, the lithium iron manganese phosphate positive electrode material at least comprises lithium iron manganese phosphate particles and a coating layer coating the lithium iron manganese phosphate particles; the raw material of the coating layer comprises an aluminum fluoride embedded poly (ethylenedioxythiophene)-lithium polystyrene sulfonate compound. And the coating layer can be used as a physical barrier to form dynamic interface protection, so that dissolution of manganese and erosion of electrolyte are directly inhibited, and side reaction between the electrolyte and the positive electrode material is reduced. Meanwhile, a more flexible transmission channel is provided for lithium ions and electrons, the conductivity of the positive electrode material is enhanced while the transmission efficiency of the lithium ions is improved, and the lithium manganese iron phosphate positive electrode material with stable structure, high rate capability and cycling stability is obtained.

The present invention discloses a preparation method of camptothecin derivatives. The present invention provides a preparation method of a compound of formula 7, which comprises the following steps: in an organic solvent, the compound of formula 6 is subjected to a deprotection reaction with methanesulfonic acid to obtain the compound of formula 7. The preparation method of the present invention uses a small amount of solvent during post-treatment, is easy to filter, the obtained product is off-white, the product purity and yield are higher, and it is suitable for industrial production. The recrystallization mother liquor obtained from the deprotection reaction is easier to recover, greatly reducing the raw material cost.