20 results about "Miniemulsion" patented technology

The application provides a miniemulsion polymer, which is prepared by a miniemulsion polymerization method through controlling pre-emulsion droplet particle size by a high-pressure homogenizer, using specific auxiliary stabilizers and specific primary emulsifiers. After the miniemulsion polymer is incorporated into a base material, an engineering material with high air tightness, high water tightness, high bonding strength and excellent durability can be obtained, which is used for the durability protection or sealing of engineering structures or the bonding between different materials, and has the advantages of simple process, low cost and outstanding comprehensive performance.

The preparation method of the agar nanogel interface modification spray is prepared from the following raw materials by weight: agarose 35-70 parts, Tween 80 40-50 parts, dimethyl silicone oil 60-150 parts, and tetrahydrofuran 50-120 parts. The preparation method comprises the following steps: S1: placing agarose into heated deionized water to obtain an agarose aqueous solution, adding Tween 80 and dimethyl silicone oil to obtain a coarse emulsion; S2: ultrasonic dissolving the coarse emulsion to obtain a fine emulsion, cooling and centrifuging, taking the lower liquid, adding tetrahydrofuran to obtain an agar nanogel mixture; S3: rotary evaporation and drying the mixture to obtain agar nanogel; and S4: adding the gel into ethanol or water to obtain the agar nanogel interface modification spray. The agar nanogel spray formed based on the molecular self-assembly strategy has a hexagonal phase columnar structure, the spray can form a modified layer with excellent light-heat conversion efficiency and water transport performance on the water surface, and can significantly enhance the evaporation efficiency.

The present application belongs to the technical field of compressed air energy storage power station engineering materials and underground engineering sealing, and specifically provides a composition containing a miniemulsion polymer emulsion for compressed air energy storage, the composition forms a closed gas storage space through sealing and / or filling, and more specifically, the polymer forms a flexible, air impermeable, dense and continuous sealing material or sealing layer between the same substrate or across substrates. The composition has excellent interfacial bonding capacity for different substrates, and can maintain continuous bonding and sealing when relative displacement occurs due to the difference in thermal expansion of different substrates. In addition, a continuous and dense barrier is formed after curing, which can simultaneously achieve "deep plugging + surface air tightness", thereby adapting to the sealing of underground scenes and key weak positions. Therefore, the composition of the present application has a wide application prospect in the field of sealing and filling of the gas storage space of compressed air energy storage.

The invention belongs to the technical field of high polymer materials, and particularly relates to a rubber label containing an epoxy group agglomerated siloxane microsphere emulsion and a preparation method thereof.The preparation method comprises the steps that S1, sodium dodecyl sulfate, sodium bicarbonate and sodium dihydrogen phosphate serve as raw materials to prepare a water phase, modified silane, n-hexadecane and azodiisobutyronitrile serve as raw materials to prepare an oil phase, and the oil phase is prepared into an oil phase; carrying out emulsification treatment on the water phase and the oil phase to obtain a miniemulsion, and carrying out polymerization reaction on the miniemulsion to obtain an epoxy group-containing agglomerated siloxane microsphere emulsion; s2, polyol, isocyanate, a chain extender, 1, 4-butanediol and stannous octoate are used as raw materials to prepare a prepolymer; and S3, adding the epoxy group-containing agglomerated siloxane microsphere emulsion into the prepolymer for stirring reaction, and then pouring into a mold for molding to obtain the rubber label containing the epoxy group-containing agglomerated siloxane microsphere emulsion. The hardness and heat resistance of the material are effectively improved, and good flame retardant property is obtained.

The invention herein disclosed refers to a method for preparation of glycerol nanocapsules (GNCs), adapted as an additive in a hydrophobic lubricant for improving lubricity in a tribological system, further to a glycerol nanocapsule (GNC) and finally to the respective use. The method comprises the steps of providing a continuous phase comprising at least a polyalphaolefin (PAO) and a dispersed phase comprising at least glycerol (GLY), of - mixing the continuous phase and the dispersed phase and performing high-pressure homogenization with a microfluidizer resulting in a minielmulsion comprising glycerol nanodroplets (GNPs). Further, adding a diisocyanate crosslinking agent (TDI) to the miniemulsion is comprised, leading to a polymerization reaction of the diisocyanate cross-linking agent (TDI) and glycerol (GLY) at the interfaces of the glycerol nanodroplets (GNPs) dispersed in the polyalphaolefin (PAO), resulting in formation of crosslinked glycerol-based polyurethan shells encapsulating a core of unreacted glycerol (GLY). Thereby glycerol nanocapsules (GNCs) are obtained, comprising a core of unreacted glycerol (GLY) encapsulated in a crosslinked glycerol-based polyurethan shell.

The invention belongs to the technical field of water-based resin synthesis, and particularly relates to a polyurethane / acrylate hybrid miniemulsion for water-based industrial paint and a preparation method of the polyurethane / acrylate hybrid miniemulsion. The preparation method comprises the following steps: S1, preparing low-viscosity water dispersible sulfonated phthalic anhydride polyester polyol; s2, preparation of a dipropenyl-terminated polyurethane miniemulsion: preparing the sulfonated phthalic anhydride polyester polyol prepared in the step S1 into a semitransparent miniemulsion of which the capsule core is an acrylate monomer droplet and the outer layer is a dipropenyl-terminated amphiphilic polyurethane block polymer dispersant; s3, preparation of polyurethane / acrylate hybrid miniemulsion: transferring the bispropenyl polyurethane miniemulsion prepared in the step S2 into a polymerization reaction device, and slowly heating to initiate free radical polymerization reaction to prepare the polyurethane / acrylate hybrid miniemulsion. The hybrid miniemulsion disclosed by the invention can meet the special grinding and dispersing requirements of water-based industrial paint manufacturing, and the production risk of unstable gel is avoided.

The invention discloses a photochromic fabric sensor and also discloses a preparation method of the sensor, and the preparation method comprises the following steps: preparing a spiropyran compound by using salicylaldehyde and indole; wrapping a spiropyrane compound by using a miniemulsion polymerization method to obtain a photochromic microcapsule dispersion liquid; after the photochromic microcapsule dispersion liquid is diluted, the fabric is soaked in the photochromic microcapsule dispersion liquid, and the photochromic fabric is obtained; the preparation method comprises the following steps: dehydrating polyether polyol, reacting the dehydrated polyether polyol with a hydrophilic monomer, an organic silicon modifier, an organic tin catalyst and diisocyanate to obtain a polyurethane prepolymer, and adding a chain extender and a neutralizer for continuous reaction to obtain an organic silicon modified polyurethane dispersion liquid; and mixing the organic silicon modified polyurethane dispersion liquid with a conductive material, and spraying the mixture on the surface of the photochromic fabric to obtain the photochromic fabric sensor. The preparation method is simple in process and low in cost, and the prepared sensor has the photochromic characteristic and excellent sensing performance.

The invention belongs to the technical field of food, medicine and cosmetic processing, and relates to a preparation method of electrostatic self-assembly high-load powdered oil, which comprises the following steps: mixing cellulose nanocrystal, soy protein isolate, water and algal oil to prepare a miniemulsion, and then heating in a water bath to obtain a precursor emulsion; adding type A gelatin into the precursor emulsion, and then adding an anion stabilizer to obtain an electrostatic self-assembly emulsion; and carrying out spray drying on the electrostatic self-assembled emulsion to obtain the high-oil-loading-capacity powdered oil. The packaging of electrostatic self-assembly is realized by using the type A gelatin and the anionic polymer, the utilization rate of the algal oil is improved, and the high-oil-loading powdered oil which is uniform in granularity, high in solubility and excellent in storage stability, thermal stability and oxidation stability is prepared by using a simple process with mild conditions.

The present application relates to the field of polymer synthesis, and discloses a copolymer emulsion, a preparation method and application thereof. The copolymer emulsion comprises a copolymer hydrogel, an organic solvent, an oil-soluble emulsifier and a water-soluble emulsifier, the average particle size of the copolymer hydrogel is 100-600 nm, the copolymer hydrogel comprises structural unit A, structural unit B and structural unit C, the copolymer emulsion has the characteristics of miniemulsion, is obtained by inverse emulsion polymerization of monomers, and the purity of monomer A is less than 99%; the copolymer emulsion can improve the flowability of crude oil when used for oil exploitation, thereby improving the recovery rate of crude oil.

The present application relates to the field of high-temperature-resistant film, co-doped nanocrystals and surface matrix material, and particularly relates to a polyimide matrix co-doped nanocrystal film and a preparation method thereof. A co-doped nanocrystal precursor modified reverse-phase fine emulsion is prepared first, and then a dispersion containing the co-doped nanocrystal precursor and polyamic acid is prepared; then, the dispersion containing the co-doped nanocrystal precursor and polyamic acid is spin-coated on a clean quartz glass sheet, and is placed in a replaceable air oven for drying to obtain a polymer matrix co-doped film; finally, after sintering and cooling, a polyimide matrix co-doped film is obtained. The thickness of the polyimide matrix co-doped film can be controlled within 80-500 nanometers, and the base film is flat; the co-doped nanocrystals are uniformly distributed in the form of nanodots on the matrix film; the film can be used at high temperature, the base film does not deform, and the co-doped nanodots have good adhesion.

The objective is to provide an emulsifier composition and an emulsifying composition that can easily prepare nanoemulsions with fine emulsion particles without going through heating and cooling processes, and without using high-energy equipment such as high-pressure homogenizers. [Solution] To solve the above problem, an emulsifier composition was prepared by combining (A) a polyglycerin fatty acid ester surfactant with an HLB value of 12 or more and 18 or less with (B) oleyl glyceryl ether or isostearyl glyceryl ether. Furthermore, an emulsifier composition with a particle size of less than 300 nm was obtained by mixing the oil phase containing the emulsifier composition with (G) an aqueous phase containing water.

The application relates to a method for preparing chitosan-hydroxyapatite composite microparticles through high-speed shearing and synergic double-reverse-phase fine emulsion, which continuously acts on the emulsification and homogenization process of the emulsification mixing of a chitosan-containing calcium salt and phosphate precursor aqueous solution and an oil phase system and a triethanolamine precursor aqueous solution and an oil phase system (constituting double-reverse-phase fine emulsion droplets) and the subsequent collision-mixing-neutralization-reaction process of chitosan, calcium salt and phosphate in the dispersed phase emulsion droplets (water droplets) and triethanolamine in another dispersed phase emulsion droplet (water droplet), realizes the continuous operation of the high-speed shearing effect reinforced physical emulsification mixing process and in-situ precipitation chemical reaction process, and achieves the purpose of preparing CS-HAP composite microparticles which are good in dispersity, not prone to agglomeration, closely combined with each other, high in porosity, uniformly dispersed and nano-level dispersed. The method is simple in preparation process, low in equipment requirement and cost, mild in reaction condition, easy to control in preparation process and easy to enlarge.

This invention proposes a fluorine-free waterproof textile finishing agent and its preparation method, belonging to the field of textile auxiliaries technology. The method involves fine emulsion polymerization, using acrylate monomers as the core, and utilizing tetraethyl orthosilicate under alkaline conditions to form nano-SiO2 embedded on the surface of microspheres, constructing a micro-nano rough structure. Further modification with a compound of epoxy-containing silanes and hydrophobic silanes imparts a fully hydrophobic surface to the microspheres and enhances their reactivity with fabric fibers. The resulting finishing agent imparts excellent waterproof performance and superior wash fastness to textiles, and the process is simple, environmentally friendly, and fluorine-free, meeting the market demand for high-end functional textiles.

The invention relates to the technical field of ink-jet printing ink, in particular to a preparation process of polymer coated self-crosslinking dispersant modified pigment ink, which comprises the following steps: 1, weighing an anchoring monomer, a hydrophilic monomer and a crosslinking monomer according to a mass ratio of 3: 5: 2, and mixing; 2, adding deionized water and the self-crosslinking dispersing agent prepared in the step 1 into a dispersing tank; step 3, coating the polymer by adopting a core-shell miniemulsion polymerization method; 4, adding a water-soluble solvent, a defoaming agent and a sterilizing agent into the polymer coated pigment emulsion prepared in the step 3; the self-crosslinking dispersing agent designed by the invention has anchoring groups, hydrophilic chains and crosslinkable active sites, the anchoring groups can be tightly adsorbed on the surface of a pigment, the hydrophilic chains provide steric hindrance to realize preliminary stabilization, and the active sites participate in a crosslinking reaction in a subsequent polymerization process, so that the dispersing agent and a coated polymer form covalent binding; the interface bonding force between the dispersing agent and the pigment and the coating layer is obviously improved, and the desorption of the dispersing agent and the agglomeration of the pigment are effectively avoided.

The invention discloses an elastic shape-stabilized phase change material and a preparation method and application thereof, and belongs to the technical field of heat insulation materials and preparation thereof.The preparation method comprises the steps that firstly, paraffin and polymer phase change microcapsule emulsion is prepared through a miniemulsion method; then, polyvinyl alcohol is dissolved in the phase change microcapsule emulsion, and steeping liquor is obtained; finally, melamine sponge subjected to carbonization treatment is soaked in the steeping liquor, and the melamine sponge is taken out after being soaked and dried to obtain the elastic shape-stabilized phase change material. The shape-stabilized phase change material prepared by the invention has high paraffin content and phase change latent heat, the microencapsulated paraffin is not easy to leak, the carbonized melamine sponge carrier has good thermal conductivity, the shape can be arbitrarily cut, and the carbonized melamine sponge carrier has good elasticity and has good application prospects in the aspect of thermal insulation materials.

The application provides a composite isolation material for thermal runaway prevention of an electrical energy storage device, which comprises two high-temperature-resistant base layers and a heat-insulating adhesive layer formed by curing of an adhesive material containing a mini-emulsion polymer. The composite isolation material is suitable for being arranged between adjacent heat sources in an electrical energy storage device, and can maintain the interface bonding integrity between the layers inside the composite isolation material under the condition that the electrical energy storage device has thermal runaway, one side of the composite isolation material is under a high-temperature working condition of not lower than 800 DEG C and lasts for a predetermined time, and does not have delamination or through failure, and significantly reduces the heat transfer to the other side of the composite isolation material.

The application relates to a method for preparing hydroxyapatite nanoparticles through high-speed shearing and synergic double reverse-phase fine emulsion, which continuously acts on the emulsification, mixing and homogenization process of a weakly alkaline precursor solution containing a calcium salt and an oil phase system and a precursor solution containing a phosphate and an oil phase system (constituting double reverse-phase fine emulsion droplets), and the collision-mixing reaction process of the calcium salt in the subsequent dispersed phase emulsion droplet (water droplet) and the phosphate in another dispersed phase emulsion droplet (water droplet), realizes the continuous operation of the high-speed shearing effect to intensify the physical emulsification mixing process and the chemical reaction mixing process, and achieves the purpose of preparing nHAP with good dispersity, small size and narrow particle size distribution; the method has simple preparation process, low equipment requirement, low cost, mild reaction condition, easy control in the preparation process, and is easy to enlarge, effectively solves the problems of low yield, high cost, use of a large amount of solvent in the process, easy harm to human body and environment, and difficulty in realizing large-scale production in the prior art.

The present application relates to the field of colloids, surface doping, hydrothermal treatment, and in particular to a method for realizing surface doping of nanocrystals on polymer coating by Pickering miniemulsion. Solid nanocrystal precursor emulsifier capable of stabilizing Pickering emulsion is formed by interfacial reaction, then doping phase is added after maturation, and then doping nanocrystals are formed by hydrothermal treatment, and finally polymer coating surface doping nanocrystals are formed by coating into film. By interfacial reaction, solid emulsifier capable of stabilizing Pickering emulsion can be formed, with original particle size of about 1-2 nanometers and aggregate particle size of about 5 nanometers, and after maturation, maturation nanocrystal precursor with particle size of about 20-30 nanometers can be obtained, and Pickering emulsion after hydrothermal treatment can directly obtain polymer coating surface doping nanocrystals.

The invention discloses a novel method for preparing polyvinylidene fluoride resin through emulsion polymerization, the novel emulsion polymerization is a miniemulsion polymerization process, fluorine-containing polyether carboxylate is used as an emulsifier, fluorine-containing oligomer is used as a co-stabilizer to realize a miniemulsion polymerization system, and the polymerization system is high in stability and moderate in polymerization rate. Compared with traditional emulsion polymerization, the novel emulsion polymerization process has remarkable technical advantages and industrialization potential, efficient preparation of PVDF can be achieved, and the product has the advantages of being narrow in particle size distribution, high in solid content and the like and is suitable for the fields of high-end coatings, lithium battery binders and the like.