787 results about "Propylsulfonic acid" patented technology

The invention relates to a battery monomer, a battery device and a power utilization device, the battery monomer comprises an electrode assembly and an electrolyte, and the electrode assembly comprises a positive pole piece and a negative pole piece; the positive pole piece comprises a positive pole current collecting part and a positive pole film layer; the positive pole film layer comprises lithium-containing phosphate with an olivine structure; the negative pole piece comprises a negative pole current collecting part and a negative pole film layer, and the negative pole film layer comprises a carbon-based material; the electrolyte comprises a carboxylic ester solvent, a first additive and fluorine-containing lithium sulfimide, and the mass content of the carboxylic ester solvent is 8%-60%; the total mass content of the first additive is 2.5%-10%, the first additive comprises 1, 3-propane sultone with the mass content larger than or equal to 0, an ethylene carbonate derivative with the mass content larger than or equal to 0 and vinylene carbonate with the mass content larger than 0, and the ethylene carbonate derivative comprises a compound shown in the formula A; the mass content of the fluorine-containing lithium sulfimide is 4%-8%. According to the invention, the rapid charging performance and the cycle performance of the battery monomer can be improved. # imgabs0 # formula A

The invention relates to a battery monomer, a battery device and a power utilization device, the battery monomer comprises an electrode assembly and an electrolyte, and the electrode assembly comprises a positive pole piece and a negative pole piece; the positive pole piece comprises lithium-containing phosphate with an olivine structure; the negative pole piece comprises graphite particles; the electrolyte comprises a carboxylic ester solvent and a first additive, the thickness of the single-side negative electrode film layer is 50 microns to 75 microns, and the volume average particle size of the graphite particles is 8.5 microns to 13.5 microns; based on the mass of the electrolyte, the mass content of the carboxylic ester solvent is 8%-60%, the total mass content of the first additive is 3%-10%, the first additive comprises 1, 3-propane sultone with the mass content larger than or equal to 0, an ethylene carbonate derivative with the mass content larger than or equal to 0 and vinylene carbonate with the mass content larger than or equal to 3%, and the ethylene carbonate derivative comprises a compound shown in the formula A. According to the invention, the rapid charging performance and the cycle performance of the battery monomer under high energy density can be improved. # imgabs0 # formula A

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 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 application of poly-2-acrylamide-2-methylpropanesulfonic acid in removal of residual lithium on the surface of a high-nickel NCM ternary material, and relates to the technical field of surface treatment of the high-nickel NCM ternary material. The method aims at solving the problem that an existing method for removing lithium carbonate on the surface of an NCM material through high-temperature calcination or high-concentration ethyl alcohol soaking and cleaning has adverse effects on the structure and performance of the high-nickel NCM ternary material. According to the invention, the cleaning agent using poly-2-acrylamide-2-methylpropanesulfonic acid as a main component is provided for cleaning the residual lithium of the high-nickel NCM ternary material, and verification proves that the high-nickel NCM ternary material can be effectively prevented from being damaged by existing high-temperature calcination and high-concentration ethanol soaking and cleaning treatment, and meanwhile, the electrochemical performance of the high-nickel NCM ternary material is remarkably improved.

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 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 relates to the technical field of petroleum drilling fluids, in particular to a preparation method of an anti-calcium tackifier, a brine-based drilling fluid and a preparation method. The preparation method of the anti-calcium tackifier comprises the following steps: A, uniformly mixing the white oil and the emulsifier to form an oil phase for later use; b, dissolving 2-acrylamido-2-methyl-1-propanesulfonic acid, acrylonitrile, a cationic monomer and a vinyl monomer with carboxyl in pure water, adjusting the pH value to 7.0, and uniformly stirring to form a water phase; c, dropwise adding the water phase in the step B into the oil phase in the step A, and uniformly mixing to obtain a stable inverse emulsion; and D, in a nitrogen atmosphere, adding an initiator into the stable inverse emulsion in the step C, and reacting to obtain the anti-calcium tackifier. The brine-based drilling fluid disclosed by the invention can keep good rheological property and stability in a high-temperature environment of 180 DEG C.

The invention discloses a high-temperature-resistant temporary plugging agent for an oil field and a preparation method thereof.The temporary plugging agent is prepared by taking acrylamide, acrylic acid, 2-acrylamide-2-methylpropanesulfonic acid and castor oil as reaction raw materials, cross-linking the reaction raw materials with a modified cross-linking agent and carrying out blending polymerization with a modified filler, the molecular structure of the temporary plugging agent is latticed polyacrylamide, a polyacrylamide molecular chain contains an amide group, a sulfonic acid group and carboxyl, the amide group is an uncharged group and is not easily influenced by high-salinity bottom water, the sulfonic acid group can improve the salt resistance of the temporary plugging agent, and the carboxyl can be complexed with hydrogen ions in water, so that the salt resistance of the temporary plugging agent is improved. A side chain contains a polysiloxane chain segment and a long-chain alkyl group, so that the temporary plugging agent can still be normally used in a high-temperature environment, and the long-chain alkyl group forms a hydrophobic micro-area and can be adsorbed with a hydrophobic surface of stratum rock, so that the temporary plugging agent is kept in a stable state in a construction process.

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 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 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 provides application of sodium 2, 3-dimercaptopropanesulfonate as an inhibitor in low-alkalinity copper-sulfur flotation separation, and relates to the technical field of mineral separation. When the compound serves as an inhibitor, the compound, a collecting agent and a foaming agent are prepared into a composite flotation reagent and used for low-alkalinity flotation separation of chalcopyrite and pyrite, flotation separation is conducted through the steps of one-time roughing, at least one-time scavenging and at least one-time concentration after ore grinding and grading, and copper concentrate is collected; the method can effectively solve the problems that the copper-iron separation effect is poor in the process of flotation separation of the chalcopyrite and the pyrite, the copper recovery rate is low due to addition of a large amount of lime and the like, the chalcopyrite and the pyrite can be efficiently separated under the low-alkalinity condition through the specific flotation process, and the flotation effect on the chalcopyrite is improved.

The invention relates to a novel salt-resistant drilling fluid filtrate reducer and a preparation method thereof, and belongs to the technical field of drilling fluid filtrate reducers, the novel salt-resistant drilling fluid filtrate reducer comprises the following raw materials by weight: 15-20 parts of N, N-dimethylacrylamide, 10-14 parts of 2-acrylamido-2-methylpropanesulfonic acid, 6-8 parts of N-vinyl pyrrolidone, 0.9-1.2 parts of a silane coupling agent KH570, and 1-3 parts of nano clay. The adhesive is prepared from the following components in parts by weight: 5-6 parts of polyethylene glycol, 0.5-0.8 part of hexadecyl methyl ammonium bromide, 20-30 parts of hydroxyethyl cellulose, 0.5-1 part of an initiator, 0.3-0.5 part of a cross-linking agent and 60-70 parts of deionized water. The filtrate reducer disclosed by the invention has excellent salt resistance, filtrate reduction performance and good thermal stability.

The invention provides a dry powder drag reducer for fracturing fluid and a preparation method of the dry powder drag reducer, and belongs to the technical field of fracturing materials for well drilling, and the preparation method comprises the following steps: dissolving 4-bromobutyryl chloride and N-dodecyl methylamine in acetonitrile, heating and stirring for reaction, adding polyethylene glycol monomethyl ether acrylate and dichloromethane, stirring and purifying in a nitrogen atmosphere to obtain a dry powder drag reducer; a double-tailed hydrophobic monomer is obtained; uniformly mixing the core-shell SiO2 / Fe3O4 composite nanoparticles, an ethanol water solution, KH570 and an ammonia solution, stirring, and purifying to obtain modified SiO2 / Fe3O4; the preparation method comprises the following steps: adding acrylamide, acrylic acid, sodium 2-acrylamido-2-methylpropanesulfonate, a double-tailed hydrophobic monomer and modified SiO2 / Fe3O4 into water, uniformly mixing, adjusting the pH value, introducing nitrogen, mixing and stirring, adding an azo initiator, stirring, cooling, purifying, carrying out vacuum drying, and crushing into powder, thereby obtaining the dry powder drag reducer for the fracturing fluid. The drag reducer has certain heat resistance while achieving good drag reduction performance, and can be better applied to fracturing operation in the well drilling process.

Solid electrolyte compositions and solid-state batteries are disclosed, which comprise a solid electrolyte layer including a sulfide-containing solid-state electrolyte material and a compound of Chemical Formula 1. The sulfide-containing solid-state electrolyte material includes but is not limited to Li6PS5Cl (“LPSC”), an LPS-based glass or glass ceramic of formula xLi2S·yP2S5, wherein x+y=1, or an argyrodite-based sulfide-based solid electrolyte or formula Li6PS5X, wherein X═Cl, Br, or I) or Li6-yPS5-yCl1+y, where y is <1. In some aspects, the compound of Chemical Formula 1 is sodium 3-mercapto-1-propanesulfonate (3M1P).

The invention belongs to the technical field of oilfield auxiliaries, and particularly relates to an oil-soluble demulsifier for a heavy oil field and a preparation method of the oil-soluble demulsifier. The oil-soluble demulsifier for the heavy oil field, provided by the invention, is prepared from a block polymer emulsion, nonylphenol polyoxyethylene ether, modified nanoparticles and a cross-linking agent. According to the invention, methoxystyrene, dodecyl vinyl ether, N, N-dimethylaminopropyl acrylamide and 2-acrylamide-2-methylpropanesulfonic acid are adopted to prepare a quaternary block comb-shaped polymer, the quaternary block comb-shaped polymer and nonylphenol polyoxyethylene ether are subjected to molecular-level cross-linking through a cross-linking agent, nano modified particles are added, and the quaternary block comb-shaped polymer is prepared. The prepared demulsifier can be rapidly adsorbed on an oil-water interface and respectively adsorb an oil phase and a water phase, so that the tension of the oil-water interface is reduced, rapid separation of the oil phase and the water phase is realized, and the demulsification performance is improved.

The invention belongs to the technical field of lithium ion battery solid electrolytes, and discloses a multi-component in-situ polymerized gel solid electrolyte and a preparation method and application thereof, the gel solid electrolyte is prepared by adding an amide cross-linking agent and a polymeric monomer into a basic electrolyte to obtain a precursor solution, then adding an initiator, and carrying out in-situ polymerization at 45-70 DEG C for 6-12 hours, the amide cross-linking agent is one or more of N, N '-methylene bisacrylamide, polyacrylamide, poly (2-acrylamide-2-methyl-1-propanesulfonic acid), polymethacrylamide, polyethylene glycol diacrylamide, polyether amide or adipamide. The first coulombic efficiency of an LCOLi button cell assembled by the multi-component in-situ polymerization solid-state gel electrolyte reaches 94.81%, the capacity retention rate after 500 cycles at 3-4.6 V still reaches 80% or above, and the LCOLi button cell can safely pass a needle test and can be applied to the field of solid-state electrolytes.

The invention relates to the technical field of thickening agents for fracturing fluids, and particularly discloses a composite fracturing fluid thickening agent for an oil and gas well and a preparation process of the composite fracturing fluid thickening agent. The invention relates to a composite fracturing fluid densifier for oil and gas wells. The composite fracturing fluid densifier comprises 30-50 parts of acrylamide; 20 to 35 parts of 2-acrylamide-2-methyl propane sulfonic acid; 10 to 25 parts of acryloyl morpholine; 3-8 parts of a polyether amine modified organic zirconium cross-linking agent; 2-6 parts of sulfonated konjac gum; 1-5 parts of a salt-tolerant synergistic aid; 0.5-2 parts of a composite initiator; 0.1 to 0.8 part of an inhibitor; and 150 to 180 parts of deionized water. The fracturing fluid thickening agent provided by the invention has the advantages of high viscosity, high temperature resistance and high salt resistance.

The invention relates to the technical field of electrolytic copper foil processing, and particularly provides a method for reducing the rough surface roughness of an HVLP copper foil by using a composite additive, which comprises the following steps: step (1): enabling the composite additive to flow into a high-level tank through an additive flow pump, uniformly mixing the composite additive with a copper sulfate electrolyte, and enabling the mixture to flow into a crude foil machine; step (2), then adjusting process parameters of a crude foil machine, including current and line speed of a cathode roller; (3) foil generation and foil drawing are carried out; the composite additive comprises one or two of gelatin and collagen. One or more composite additives composed of gelatin, collagen, sodium dithiodipropane sulfonate, N, N-dimethyl-dithioformamide sodium propanesulfonate, 3-sulfydryl-1-sodium propane sulfonate, hydroxyethyl cellulose and polyethylene glycol are added into the raw foil electrolyte, so that the copper electrodeposition reaction potential can be effectively changed; and uniform and compact copper crystallization peaks are obtained, the rough surface roughness of the raw foil is reduced, and the uniformity of a plating layer is improved.

The invention belongs to the technical field of all-vanadium redox flow battery diaphragms, and particularly discloses a sulfonated polyetheretherketone / polyaniline composite membrane as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing polyetheretherketone and concentrated sulfuric acid, and carrying out water bath heating reaction to prepare a sulfonated polyetheretherketone solid; molybdenum disulfide and methylbenzene are mixed and subjected to ultrasonic treatment, 1, 3-propane sultone is added, oil bath heating is conducted, and sulfonated molybdenum disulfide powder is prepared; the preparation method comprises the following steps: mixing and stirring sulfonated molybdenum disulfide powder, polyaniline and a DMF (Dimethyl Formamide) solution, performing ultrasonic treatment, adding a sulfonated polyether-ether-ketone solid, stirring to obtain membrane casting slurry, coating a glass plate with the membrane casting slurry, drying to form a membrane, and soaking the membrane in a sulfuric acid solution and deionized water in sequence to obtain the sulfonated polyether-ether-ketone / polyaniline composite membrane. The invention discloses a sulfonated polyetheretherketone / polyaniline composite membrane as well as a preparation method and application thereof. The sulfonated polyetheretherketone / polyaniline composite membrane has high proton conductivity, can maintain relatively low vanadium ion permeability and can improve the electrochemical performance of an all-vanadium redox flow battery.

The invention discloses a concave-convex high-skid-resistance archaized brick and a preparation process thereof, and relates to the field of building materials. When the concave-convex high-skid-resistance archaized brick is prepared, ferrochrome waste residues, coal ash, argil, quartz sand, clay powder and red soil powder are subjected to mold pressing and roasting, and a green brick is prepared; mixing albite, quartz, calcite, zinc oxide, barium carbonate, deionized water, water glass and American water, glazing the surface of a green brick, and roasting to obtain an archaized brick matrix; the archaized brick base body is sequentially subjected to a reaction with 3-aminopropyltrimethoxysilane, 5, 7-dihydroxyflavone, 1H, 1H-perfluorooctylamine and 1, 3-propane sultone, and the concave-convex high-skid-resistance archaized brick is prepared. The concave-convex high-skid-resistance archaized brick prepared by the invention has good antibacterial, antifouling and coating durability effects.

The invention relates to the technical field of films, in particular to a high-surface tension aluminized base film and a preparation method thereof. The method comprises the following steps: grafting modified fumed silica with a silane coupling agent KH-570, and grafting a ternary polymerization shell layer composed of 2-acrylamide-2-methylpropanesulfonic acid, lauryl methacrylate and glycidyl methacrylate on the surface of the modified fumed silica to obtain organic anti-sticking silica; secondly, synthesizing an aromatic sulfonated polyester prepolymer, loading nano titanium dioxide, and carrying out melt blending extrusion with polypropylene to form polar cluster polypropylene master batches; and finally, blending polypropylene resin, the master batch and maleic anhydride grafted polypropylene, and carrying out melt extrusion, air cooling and slow cooling and two-way stretching molding. The obtained base film is high in surface tension, high in aluminized layer adhesive force, excellent in oxygen and water vapor barrier property, good in thermal stability and suitable for the field of high-end packaging.

The invention belongs to the technical field of hydrogel materials, and particularly relates to hydrogel as well as a preparation method and application thereof. The preparation method of the hydrogel provided by the invention comprises the following steps: mixing polyvinyl alcohol, 2-acrylamide-2-methylpropanesulfonic acid, strong alkali, a photoinitiator, a cross-linking agent and water, and carrying out photo-crosslinking to obtain pre-gel; the pre-gel is circularly frozen and thawed and then salted out, and the hydrogel material is obtained. The hydrogel prepared according to the preparation method disclosed by the invention has relatively high strength, elongation at break and toughness and has good anti-freezing and anti-swelling properties, and a flexible sensor prepared from the hydrogel can be used in various environments and can better realize long-time monitoring on a human body.

According to the scheme, the expanded polytetrafluoroethylene artificial blood vessel with the anticoagulant coating and preparation and application are provided, firstly, groups such as carboxyl and amino are formed on the inner surface of the expanded polytetrafluoroethylene artificial blood vessel through co-auto-polymerization reaction of L-dopamine and polyethyleneimine in a Tris aqueous alkali, then epoxy chloropropane serves as a cross-linking agent, and the expanded polytetrafluoroethylene artificial blood vessel with the anticoagulant coating is prepared. Trihydroxymethyl methylamino propanesulfonic acid is cross-linked to the inner surface of the membrane, carboxyl and sulfonic acid groups on the surface of the membrane endow the expanded polytetrafluoroethylene artificial blood vessel with anticoagulation performance, meanwhile, the hydrophobic performance of the outer surface is reserved, anticoagulation finishing is conducted on the inner wall of the expanded polytetrafluoroethylene artificial blood vessel, and the hydrophobic performance of the outer wall of the blood vessel is reserved; the expanded polytetrafluoroethylene artificial blood vessel has an anticoagulation function and does not influence the growth of fiber cells and fiber connective tissues on the surface of the blood vessel.

The invention belongs to the technical field of insulating materials, and particularly relates to a high-voltage-resistant wear-resistant insulating photocureable coating, a preparation method thereof and a power battery shell coating. The high-pressure-resistant wear-resistant insulating photocureable coating is formed by mixing sulfonated bisphenol A epoxy acrylate, modified polyurethane acrylate and a photoinitiator; the sulfonated bisphenol A epoxy acrylate is prepared by carrying out epoxy ring-opening reaction on bisphenol A epoxy resin and 2-acrylamide-2-methylpropanesulfonic acid under the catalytic action; and the modified polyurethane acrylate is bifunctional organic silicon grafted polyurethane acrylate. A coating for a power battery shell, which is formed by the high-voltage-resistant wear-resistant insulating photocureable coating disclosed by the invention, is excellent in insulating property, can meet the insulating requirement of the power battery shell under a 800V framework at the present stage, and in addition, the formed coating has excellent wear resistance and shows good application and popularization prospects.

The invention relates to a super-absorbent paper diaper and a preparation method and application thereof.The super-absorbent paper diaper comprises a bottom film, a core layer, a surface layer and elastic side seals and is characterized in that the core layer is prepared from, by weight, 50-60 parts of acrylic water-absorbent resin, 20-30 parts of polyacrylamide microspheres, 20-30 parts of quaternized chitosan, 10-15 parts of modifier and 1-5 parts of catalyst; wherein the modifier is a composition of tartaric acid, 2-acrylamide-2-methylpropanesulfonic acid and N, N '-bis (acryloyl) cystamine in a mass ratio of 1: (2-3): (1-1.5). Wherein the acrylic water-absorbent resin provides basic water-absorbent capacity, the polyacrylamide microspheres enhance adsorption and prevent gel blockage, the quaternized chitosan improves antibacterial property and electrolyte adsorption capacity, the catalyst ensures that the reaction is fully carried out, and all the components of the modifier cooperate with one another to enhance hydrophilicity; the water absorption performance, the structural stability and the salt tolerance of the core layer are jointly improved.

The invention relates to the technical field of oilfield chemistry and high-temperature and high-salt oil reservoir profile control and water shutoff, in particular to a preparation method, a product and application of polymer gel particles with enhanced mechanical properties through a double-crosslinking domain structure. The preparation method comprises the following steps: dissolving a monomer, a cross-linking agent and an initiator in water, and carrying out free radical polymerization reaction to obtain polymer hydrogel; and drying the polymer hydrogel to obtain the polymer gel particles, the monomers comprise acrylamide, acrylic acid, N-(hydroxymethyl) acrylamide and 2-acrylamide-2-methylpropanesulfonic acid; the cross-linking agent comprises methacrylic acid esterified lignosulfonate and / or N, N '-methylene bisacrylamide. The preparation method disclosed by the invention is simple, and the polymer gel particles prepared by utilizing the method have a unique double-crosslinking domain structure, have excellent mechanical properties and excellent temperature resistance and salt tolerance, and are suitable for profile control and water shutoff of high-temperature and high-salt oil reservoirs.