Patents
Literature
Patsnap Copilot is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Patsnap Copilot

462 results about "Ultrasonic emulsification" patented technology

Phase change energy storage microcapsule material and its preparation method

The invention relates to a phase change energy storage microcapsule, which takes n-dodecanol as a phase change material and adopts methyl methacrylate-acrylic acid copolymer as a capsule wall material. Ultrasonic-assisted emulsification is adopted, and interfacial polymerization is employed to perform microcapsule packaging. The preparation method of the phase change energy storage material includes: firstly mixing n-dodecanol with an emulsifier, performing ultrasonic emulsification, then conducting mechanical stirring, adding methyl methacrylate and an initiator under 80DEG C water bath to react for certain time, then adding acrylic acid to react, and completing polymerization; and carrying out cooling, filtering, and drying so as to obtain a sample. According to the invention, n-dodecanol is adopted as the phase change material, the phase change temperature can be controlled in the vicinity of room temperature. The methyl methacrylate-acrylic acid copolymer is taken as the capsule wall, which has very good chemical stability and strong adaptability to the environment. Ultrasonic assisted emulsification is employed to form a miniemulsion, and the reaction undergoes more easily. The phase change energy storage microcapsule material provided by invention has the advantages of simple process, low cost, and good stability, and can effectively improve the energy storage effect of a phase change material.
Owner:NANJING UNIV OF TECH

Method for preparing degradable dry beancurd preservation packaging film

The invention provides a method for preparing a degradable dry beancurd preservation packaging film. The method comprises the following steps: adding soybean protein isolates to deionized water, adjusting the pH value and stirring the materials to obtain soybean protein solution; adding pectin to deionized water and stirring the materials to obtain pectin solution; blending the soybean protein solution with the pectin solution, adding a plasticizer and essential oil and carrying out ultrasonic emulsification to obtain film liquid; and pouring the film liquid into an organic glass tank to be formed, drying the formed product in the hot air environment and tearing off the film, thus obtaining the preservation packaging film. The method has the following advantages that 1) interaction between polysaccharides and protein molecules is fused, thus enhancing the moisture resistance and mechanical performances of the preservation packaging film; 2) time is saved by ultrasonic emulsification, the energy consumption is lower than that in the high pressure homogenization method and the emulsion is stable; 3) the loaded essential oil can endow the film material with excellent bacteriostasis performance; and 4) the total number of colonies of the dry beancurd is effectively reduced by utilizing the preservation film to package the dry beancurd.
Owner:BOHAI UNIV

Polystyrene/calcium alginate composite gel microsphere in nuclear shell structure and preparation method thereof

The invention provides a polystyrene/calcium alginate composite gel microsphere in a nuclear shell structure and a preparation method thereof, relating to biopolymer materials. The polystyrene/calcium alginate composite gel microsphere in the nuclear shell structure takes a polystyrene microsphere as a core and calcium alginate gel as a shell, wherein the grain size of the core is 1-100 microns, and the thickness of the shell layer is 50-800 nm. The preparation method comprises the following steps of: mixing polystyrene microsphere with aqueous solution containing a surface active agent I, and carrying out ultrasonic emulsification to obtain mixed solution A; adding sodium alga acid solution in the mixed solution A, and stirring to obtain mixed solution B; adding organic solution containing a surface active agent II into the mixed solution B, and stirring to obtain mixed solution C; adding calcium chloride solution which has the same volume with the sodium alga acid solution into the mixed solution C under stirring to react, and carrying out vacuum filtration, washing the solution until no calcium ion residue exists on the surface and drying to obtain a product D; and dispersing the product D into water, centrifuging the mixture, pouring out supernate and taking out precipitate to obtain the product.
Owner:XIAMEN UNIV

Infrared phase-changing material and preparation method thereof

InactiveCN101845293AReduce thicknessDoes not involve effective associativity issuesHeat-exchange elementsParaffin waxUltrasonic emulsification
The invention relates to an infrared phase-changing material, which relates to an optoelectronic material. The infrared phase-changing material comprises an inner shell, an outer shell, and a core material, the inner shell comprises a copolymer containing styrene and methylacrylic acid, the outer shell comprises conductive polyaniline, and the core material comprises various kinds of paraffins. The preparation method comprises the following steps: uniformly mixing the paraffins, styrene, methylacrylic acid, dodecyl mercaptan and azobisisobutyronitrile according to a certain proportion; dissolving a certain amount of sodium dodecyl sulfate and TritonX-100 in de-ionized water; completely mixing the two solutions together, moving the solutions in a four-hole bottle after ultrasonic emulsification in ice-bath, filling nitrogen, heating and agitating; after six hours, obtaining a powder sample through cooling, emulsion breaking, filtration, washing and drying; uniformly mixing a certain proportion of powder sample, aniline monomer and dilute hydrochloric acid together, and slowly adding a certain amount of ammonium persulfate and hydrochloric acid solution after cooling down; and after six hours, obtaining the final product through filtration, washing and drying. The invention solves the problem that two materials are needed for the temperature control and the reduction of the infrared emissivity, increases the associative property of different materials, and reduces the coating thickness and the actual construction links.
Owner:BEIJING JIAOTONG UNIV

Method for preparing mono-disperse polymer functional microspheres with photochemical method

The invention discloses a method for preparing mono-disperse polymer functional microspheres with a photochemical method. According to the invention, under the regulation of a reversible addition-fragmentation chain transfer (RAFT) reagent, polymer functional microspheres with various sizes such as nano-grade sizes and micron-grade sizes, and with uniform particle sizes are synthesized by using the photochemical method. First, mono-functional group carbon-carbon double-bond monomers, multifunctional group carbon-carbon double-bond cross-linking agents, monomers containing functional groups, a dispersing agent, a stabilizing agent, the RAFT reagent, a photoinitiator, a pore-forming agent, and the like are added into a mixed solvent; the mixture is subjected to ultrasonic emulsification, such that a uniform and stable dispersion liquid is produced; the dispersion liquid is transferred into a reaction bottle, and is stirred; vacuum pumping is carried upon the reaction bottle, and nitrogen is filled into the reaction bottle until constant pressure is achieved; the reaction bottle is irradiated by using an ultraviolet lamp under room temperature for approximately 8 hours, and the reaction is then stopped; an obtained reaction liquid is subjected to centrifugal sedimentation, washing, and drying, such that the mono-disperse polymer functional microspheres with uniform particle sizes are obtained. The preparation method provided by the invention is advantaged in high production efficiency, and is energy-saving and environment-friendly. According to different requirements, thousands of specifications of mono-disperse microspheres with particle sizes of 5 nanometers to 1000 micrometers can be prepared. The method is widely applied in fields related to paints, adhesives, biomedicines, and electronic information.
Owner:苏州异导光电材料科技有限公司

Chitosan oligosaccharide composite powder with adjuvant hpyerglycemic function and preparation method thereof

The invention relates to a chitosan oligosaccharide composite powder with adjuvant hpyerglycemic function. The chitosan oligosaccharide composite powder comprises, by weight, 40 to 60 parts of oat beta-glucan, 5 to 20 parts of chitosan oligosaccharide, 5 to 20 parts of sealwort extract, 3 to 8 parts of mulberry leaf extract, 2 to 6 parts of balsam pear extract, 0.05 to 0.5 part of chromium-rich yeast and 10 to 20 parts of a filler. The invention has the following advantages: the chitosan oligosaccharide composite powder is a chitosan oligosaccharide compound prepared from chitosan oligosaccharide and oat beta-glucan, used as main effective components, and a plurality of traditional Chinese medicinal active components, used as adjuvant materials, through refining in virtue of ultrasonic emulsification and spray drying technologies; the chitosan oligosaccharide composite powder has the advantages of good dissolvability, good dispersibility and high absorption and availability; all the components of the chitosan oligosaccharide composite powder cooperate with each other to exert substantial effect on promotion of blood glucose metabolism and maintenance and adjustment of the functions of the pancreas islet; moreover, a variety of active components included in the chitosan oligosaccharide composite powder has obvious synergism in improving the sensitivity of insulin and stabilizing postprandial blood sugar.
Owner:颐海产业控股有限公司

LID-PEG-PLGA controlled-release nano microsphere and preparation method thereof

The invention discloses an LID-PEG-PLGA controlled-release nano microsphere and a preparation method thereof. The microsphere is the controlled-release microsphere which contains medicinal lidocaine and a degradable carrier. The degradable carrier contains polylactic-glycolic acid and PEG-2000. The mass percentage of the lidocaine in the controlled-release microsphere is 30 to 35 percent. The preparation method comprises the following steps of: preparing the carrier into matrix solution; dispersing the lidocaine into the matrix solution and preparing the lidocaine into an oil phase; mixing the oil phase and the aqueous solution of polyvinyl alcohol, and performing ultrasonic emulsification on the mixture under a water bath condition to obtain W / O-type protogala; mixing the W / O-type protogala and the aqueous solution of polyvinyl alcohol again, and further emulsifying the mixture into W / O / W-type complex emulsion; volatilizing the emulsion by reducing pressure at the normal temperature to obtain cured lidocaine-carried nano microsphere; and scattering, blending, packaging, freezing, sterilizing and the like. The medicament loading rate of the controlled-release nano microsphere can be up to 15 to 22 percent; the entrapment rate can be up to 68 to 78 percent; and the half-life period can be prolonged to 3 to 4 days. Therefore, the microsphere has relatively good effect of burst in the first day after the microsphere is taken and good effect of slow release in later days.
Owner:ARMY MEDICAL UNIV

Preparation method of copper-free click crosslinking polysaccharide microspheres

The invention discloses a preparation method of copper-free click crosslinking polysaccharide microspheres. The preparation method comprises the following steps that chitosan and 1-hydroxyl benzotriazole are dissolved in water at room temperature, and cyclooctyne-3-glycolic acid is dissolved in a tetrahydrofuran/water mixed solvent; after the two solutions are mixed, diisopropylethylamine is added, stirring reaction is performed, and cyclooctyne chitosan is obtained through dialysis and freeze-drying; sodium alginate and carbodiimide are dissolved in water, 11-azido-3,6,9-triethyl ether-1-amine is added, stirring reaction is performed, and azido sodium alginate is obtained through dialysis and freeze-drying; water solutions of the cyclooctyne chitosan and the azido sodium alginate are respectively prepared, after mixing according to the volume ratio, emulsifier Span-80 containing paraffin oil is added, and an emulsification emulsion is obtained through ultrasonic emulsification; the emulsification emulsion volatilizes and stays overnight and is poured into isopropanol for precipitation of microspheres, and the crosslinking polysaccharide microspheres are obtained through freeze-drying after cleaning. The process is simple, makes products safe and non-toxic and is suitable for the medical fields of drug release, gene therapy, tissue engineering and the like.
Owner:NANJING UNIV OF SCI & TECH

Medicament coating stent capable of preventing blood vessel restenosis and preparation method thereof

The invention provides a medicament coating stent capable of preventing blood vessel restenosis and a preparation method thereof. The stent is coated with a PLGA (polylactic acid-glycollic acid) nano particle coating which comprises a medicament carrier and a medicament material; the medicament carrier is PLGA; and the medicament material is one or two of rapamycin or paclitaxel. The preparation method comprises the following steps of: dissolving PLGA with dichloromethane, adding the medicament material, dissolving fully, and performing ultrasonic emulsification by use of an ultrasonic cell disruptor under an ice bath condition so as to prepare a suspension; slowly adding a 2% PVA (Polyvinyl Alcohol) water solution into the suspension while performing magnetic stirring, and emulsifying the suspension again so as to prepare an emulsion; performing rotary evaporation on the emulsion under reduced pressure so as to enable dichloromethane to volatilize completely, so that a nano particular colloidal dispersion system is obtained; adding a 1% coupling agent into the system, and then soaking the stent into the system for 5 minutes, so as to prepare the coating stent; and freeze-drying the coating stent for 10 hours, and preserving the freeze-dried stent at the temperature of 4 DEG C.
Owner:DONGGUAN KEWEI MEDICAL INSTR
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products