16243 results about "Nanoparticle" 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 belongs to the technical field of industrial automation control, and particularly relates to a dynamic optimization control method and system for multi-component batching of a paste making machine, and the method comprises the steps: generating a characteristic waveform spectrum corresponding to a residue molecular structure; dynamically generating electric lubricating medium parameters containing the electroosmotic liquid concentration and the release rate; triggering a low-frequency vibration module of the material layer to generate vibration waves, and enabling the solution and the vibration waves to form a molecular-level synergistic stripping effect; calculating a nanoparticle dispersity index, and generating an inverse gradient mixing instruction when the index exceeds a threshold value; activating a hot vortex ring in a spiral flow guide convex pattern area and establishing a directional heat energy migration channel; and verifying the dynamic equilibrium state of the temperature of the paste core area and the viscoelasticity of the target formula, and triggering a phase lock control signal to terminate the parameter adjustment chain when the energy consumption rate reaches a stable interval. According to the invention, the problems that the transition period during formula switching is prolonged and the phase differences among the execution mechanisms are difficult to match in real time due to a traditional staged regulation and control mode are solved.

The invention relates to a dialkyl imidazole bionic lipid compound and a preparation method and application thereof.The structure of the dialkyl imidazole bionic lipid compound imitates natural phospholipid design, alkyl with no less than 10 carbon atoms is modified on the fourth site and the fifth site of imidazole, and primary amines with different alkyl chain lengths are modified on the second site; the dialkyl imidazole bionic lipid compound is mixed with a therapeutic drug and other auxiliary materials to prepare lipid nanoparticles loaded with the therapeutic drug, and the lipid nanoparticles can be used as a drug delivery system for preparation of brain-targeted drugs. The dialkyl imidazole bionic lipid has the function of dynamically regulating and controlling the blood-brain barrier, and can realize reversible opening of the blood-brain barrier; the formed drug-loaded lipid composition can pass through a blood brain barrier and well realize brain-targeted delivery of loaded therapeutic drugs; the drug-loaded lipid composition composed of the dialkyl imidazole bionic lipid belongs to a new generation of bionic nano-drug carriers, and provides a new strategy for realizing brain-targeted delivery of different types of drugs.

The invention relates to a preparation method of a graphene oxide loaded nanoparticle functional anticorrosive coating. The preparation method comprises the following steps: (1) preparing a graphene oxide loaded nanoparticle composite material; and (2) preparing the anticorrosive coating, namely weighing dimethylbenzene, n-butyl alcohol and filler according to a ratio, performing ultrasonic treatment, weighing epoxy resin, continuously performing ultrasonic treatment and stirring, dropwise adding a defoaming agent, a flatting agent, a wetting dispersant and a curing agent, stirring, standing, and spraying on the surface of a matrix to serve as the anticorrosive coating. According to the anticorrosive filler prepared by the preparation method, the problem that graphene oxide agglomerates in a coating is solved, nano-particles are introduced to optimize a coating structure, micropores and microcracks in the coating are filled, the compactness of the coating is enhanced, defects in the coating are reduced, and the protective performance of the coating is improved.

The invention provides a high-temperature-resistant and high-salt-resistant nano imbibition agent as well as a preparation method and application thereof. The high-temperature-resistant and high-salt-resistant nano imbibition agent is prepared from amination modified mesoporous silica nanoparticles, nano cellulose, rhamnolipid, an anionic surfactant, citrate modified sodium zirconium phosphate, polyethylene glycol-b-polycaprolactone and a sulfydryl-carboxyl imidazoline derivative, therefore, the composite carrier formed by the aminated mesoporous silica nanoparticles and the nanocellulose has high mechanical strength and uniform dispersity, the oil-water interfacial tension is reduced through the synergistic effect of the rhamnolipid and the anionic surfactant, and the crude oil stripping efficiency is remarkably improved; the citrate modified sodium zirconium phosphate enables the salt resistance of the system to be greatly improved, and in a high-temperature and high-salt oil reservoir environment, the nano imbibition agent can remarkably improve the crude oil recovery rate and reduce the injection pressure and dosage; meanwhile, good adsorption resistance is achieved, and reservoir blockage is prevented; in addition, low-toxicity corrosion inhibition components protect equipment, and the service life of an oil well is prolonged.

Disclosed in the present invention are a PET release film base film having low surface roughness and a preparation method therefor. The release film base film comprises three layers which are stacked: a core layer and two surface layers located on both sides of the core layer. The release film base film is obtained via three-layer co-extrusion by means of taking an auxiliary extrusion resin as a raw material of the two surface layers and a primary extrusion resin as a raw material of the core layer; the auxiliary extrusion resin is obtained by mixing an anti-blocking agent PET masterbatch and a PET base material in a mass ratio of 1:5-1:15; and the primary extrusion resin is a pure PET base material. The release film base film of the present invention has low surface roughness, low haze and excellent overall performance. Since large-particle benzoic acid-modified nano aluminum oxide has the refractive index very close to that of PET base films, the present invention can effectively avoid adverse visual impacts caused by a difference in the refractive index at interfaces between nanoparticles having large particle diameters and resin matrixes, thus effectively reducing the haze.

The present disclosure provides compounds according to Formulae I, II, III, IV, V, VI, VII, VIII, IX, X, XI, XII, XIII, XIII, and XIV for use as a component in a lipid nanoparticle composition for the delivery of biological and / or therapeutic agents. The present disclosure also provides novel, stable lipid nanoparticle compositions comprising one or more biological and / or therapeutic agents, as well as methods of making and delivering lipid nanoparticle compositions.

Ionizable cationic lipids, methods for synthesizing the same, intermediates useful in synthesis of the ionizable cationic lipids, and methods of synthesizing the intermediates are disclosed. The ionizable cationic lipids are useful as a component of lipid nanoparticles (LNP), which in turn can be used for delivering nucleic acids into cells in vivo or ex vivo. LNP compositions are also disclosed, including LNP comprising a functionalized lipid to enable conjugation of a binding moiety, and targeted LNP (tLNP), that is a LNP in which a binding moiety has been conjugated to the functionalized lipid and can serve as a targeting moiety to direct the tLNP to a desired tissue or cell type.

The disclosure relates to ribonucleic acid (RNA) vaccines and combination vaccines, as well as methods of using the vaccines and compositions comprising the vaccines. Specific embodiments relate to RNA betacoronavirus vaccines formulated in a lipid nanoparticle.

The disclosure relates to ribonucleic acid (RNA) vaccines and combination vaccines, as well as methods of using the vaccines and compositions comprising the vaccines. Specific embodiments relate to RNA betacoronavirus vaccines formulated in a lipid nanoparticle.

The present disclosure describes improved LNP-based RNA vaccines, nucleobase editing systems, and therapeutics for use in treating and / or immunization against disease. In particular, the disclosure describes improved LNPs, including novel and improved ionizable lipids for making LNPs, that enhance the targeted delivery of LNP-based RNA vaccines and therapeutics based on linear and / or circular mRNAs. The improved LNPs protect linear and / or circular mRNA payloads from degradation and clearance while achieving targeted systemic or local delivery for use as enhanced vaccines and / or therapeutic agents.

The invention provides a gradient crosslinking process of photosensitive resin for photocuring 3D printing, and relates to the technical field of photocuring 3D printing materials. The gradient crosslinking process of the photosensitive resin for photocuring 3D printing comprises the following steps: S1, based on double-initiator system design, adopting molecular dynamics simulation screening, respectively adding a 405nm sensitive type TPO-L initiator and a 365nm sensitive type I TX initiator into an epoxy acrylate prepolymer, and verifying initiation energy barrier matching through quantum chemistry calculation, and generating a pre-initiation gradient resin formula. Through molecular dynamics simulation, initiator combinations are screened, energy barrier matching is verified, the ratio of dual-wavelength sensitive initiators is optimized, and accurate triggering of surface layer and deep layer cross-linking reaction is ensured. And a three-roller grinding and dispersing process is combined with ultrasonic oscillation to eliminate nanoparticle aggregation, so that the mechanical uniformity and light scattering effect of a resin system are improved.

The present disclosure provides humanized antibodies and antigen binding domains thereof that bind CD8α and other antibody formats comprising these antigen binding domains, their use as a targeting moiety on lipid nanoparticles (tLNP) to deliver a therapeutic payload (such as a nucleic acid molecule) or other types of payloads. The present disclosure further relates to pharmaceutical compositions comprising the humanized anti-CD8α antibodies and CD8-targeted tLNP encapsulating a payload.

The invention provides a thermal protection coating as well as a preparation method and application thereof. The thermal protection coating comprises a NiCoCrAlY first bonding layer, a NiCoCrAlY second bonding layer, a CeYSZ first ceramic layer and a GdYbYSZ second ceramic layer which are sequentially arranged on the surface of a base material, and the second NiCoCrAlY bonding layer is made of CeO2 (CeO2) and Al2O3 (Al2O3). According to the invention, a thermal protection coating structure with double bonding layers and double ceramic layers is constructed on the surface of the base material, and CeO2 and Al2O3 nano-particle reinforced phases are introduced, so that the use temperature of the thermal protection coating is increased, and the thermal strain tolerance, the crack resistance and the oxidation resistance are greatly improved.

Ionizable cationic lipids, methods for synthesizing the same, intermediates useful in synthesis of the ionizable cationic lipids and methods of synthesizing the intermediates are disclosed. The ionizable cationic lipids are useful as a component of lipid nanoparticles (LNP), which in turn can be used for the delivery of nucleic acids into cells in vivo or ex vivo. LNP compositions are also disclosed, including LNP comprising a functionalized lipid to enable conjugation of a binding moiety, and targeted LNP (tLNP), that is an LNP in which a binding moiety has been conjugated to the functionalized lipid and can serve as a targeting moiety to direct the tLNP to a desired tissue or cell type.

Disclosed are compositions of lipid nanoparticles (LNP) comprising an ionizable cationic lipid, a phospholipid, a sterol, and a PEG-lipid (non-functionalized and optionally functionalized). The functionalized PEG-lipid can be conjugated with a binding moiety to create a targeted LNP (tLNP). The disclosed tLNP preferentially deliver a nucleic acid molecule or other negatively charged payload to cells expressing a cell surface antigen recognized by the binding moiety of the tLNP, and are better tolerated, as compared to LNPs and tLNPs comprising ionizable cationic lipids found in marketed pharmaceuticals comprising LNPs.

The invention discloses an intelligent sealing test method and system for a wafer in a semiconductor chip, and relates to the technical field of semiconductor manufacturing, and the method comprises the steps: initializing a magneto-electric field cooperation parameter, optimizing the magneto-electric field cooperation parameter through a multi-target genetic algorithm, and driving core-shell nanoparticles to carry out the metallization filling of a high-precision through hole wafer, generating a wafer with a metalized through hole structure; based on the metalized through hole structure wafer, bonding parameters are generated through a laser Doppler frequency vibration spectrum analysis method, flip interconnection is achieved through a thermal ultrasonic virtual process, and a low-defect bonding wafer is generated; a finite element inversion algorithm is adopted, a stress distribution map of a bonding interface is established, an anti-thermal-stress packaging layer is constructed through an intelligent stress matching algorithm, and the low-defect bonding wafer is packaged; and through a multi-target genetic algorithm, magnetoelectric field cooperation parameters are optimized, core-shell nano-particles are driven to directionally deposit, and accurate control over the metallization filling process is achieved.

The invention relates to the technical field of alloy coatings, and discloses a laser cladding high-entropy alloy coating and a preparation method thereof.The laser cladding high-entropy alloy coating is prepared from, by mass, 25%-45% of Fe, 15%-25% of Cr, 10%-20% of Ni, 5%-15% of Mn, 3%-10% of Al, 0%-5% of Ti, 1%-5% of a nanometer reinforcing phase and 0.1%-0.5% of a flow promoter. Lorentz force generated by an alternating electromagnetic field drives melt convection, so that the diffusion coefficient of segregation-prone elements such as Cr and Ni is increased, the ultrasonic cavitation effect is matched to crush dendritic crystals and promote dispersion of nanoparticles, the segregation index of the elements is reduced, a uniform nanocrystalline-amorphous composite structure is formed through the synergistic effect, and uniform distribution of elements in a molten pool is achieved.

The invention discloses a photopolymer type holographic recording medium and a preparation method and application thereof.The photopolymer type holographic recording medium comprises a writing monomer, film-forming resin, a photosensitive initiation combination agent and a catalyst, the writing monomer comprises nanoparticles and a polymerizable monomer, and the film-forming resin is prepared from the nanoparticles and the polymerizable monomer; the refractive index of the polymerizable monomer is smaller than that of the nanoparticles, and the difference between the refractive index of the nanoparticles and the refractive index of the polymerizable monomer is larger than 0.5. The film-forming resin includes a polyol compound and an isocyanate-based compound. The catalyst is used for catalyzing a polyol compound and an isocyanate compound to react to form a film. The photosensitive initiation combination agent is used for sensing light and inducing polymerization of the polymerizable monomer. According to the photopolymer type holographic recording medium disclosed by the invention, after exposure, the polymerizable monomers located in the bright area and the nanoparticles extruded to the dark area have relatively large refractive index difference, so that the refractive index modulation degree of the recording grating can be improved; the film-forming resin provides effective support for the nanoparticles, and the nanoparticles are not agglomerated.

The invention provides a metal polyphenol nanoparticle, a preparation method thereof and an application of the metal polyphenol nanoparticle in preparation of a medicine for treating acute lung injury, the metal polyphenol nanoparticle is formed by self-assembly of metal ions and polyphenol, the metal ions are selected from Mg < 2 + >, Zn < 2 + >, Mn < 2 + > or Cu < 2 + >, and the polyphenol is selected from Mg < 2 + >, Zn < 2 + >, Mn < 2 + > or Cu < 2 + >. The polyphenol is selected from epigallocatechin gallate (EGCG), caffeic acid (CA), chlorogenic acid (CGA), gallic acid (GA) and luteolin (LUT). The metal polyphenol nanoparticles are used for preparing a medicine for treating acute lung injury induced by sepsis, pneumonia, serious trauma or inhalation injury, and the medicine further comprises a pharmaceutically acceptable carrier. The metal polyphenol nanoparticles provided by the invention are simple in preparation process and high in biological safety, polyphenol and metal ions synergistically enhance the anti-inflammatory and antioxidant activity, and the metal polyphenol nanoparticles are superior to the single use of polyphenol or metal ions.

The invention relates to the technical field of environmental materials and water treatment, in particular to a graphene amino silica gel composite adsorbent for heavy metal wastewater treatment and a preparation method thereof.The graphene amino silica gel composite adsorbent is prepared from # imgabs0 nanoparticles, an amino-functionalized silicon dioxide coating layer, carboxylated reduced graphene oxide, a polydopamine modification layer and tetraethyl orthosilicate; the coating is prepared from the following raw materials: 3-aminopropyltriethoxysilane, 3-mercaptopropyltrimethoxysilane, N-((4-vinyl benzyl) amino) diacetic acid, chitosan, beta-cyclodextrin, hexadecyl trimethyl ammonium bromide, polyethylene glycol, L-ascorbic acid, 1-ethyl-3-(3-dimethyl aminopropyl) carbodiimide hydrochloride and N-hydroxysuccinimide. The composite adsorbent shows excellent adsorption performance on various heavy metal ions, and the adsorption performance is far higher than that of traditional adsorption materials and existing composite adsorbents.

The present invention relates to the technical field of composite materials. Provided are a glass fiber-reinforced epoxy resin composite material and a preparation method therefor. In the present invention, an epoxy silane coupling agent solution is used for performing surface modification on glass fibers. An epoxy silane coupling agent contains a hydrolyzable group and an epoxy group. Silicon hydroxyl generated when the hydrolyzable group is hydrolyzed can be connected to the glass fibers, so as to effectively modify the surfaces of the glass fibers. The epoxy group can react with an epoxy resin matrix, thereby improving the infiltration effect of the epoxy resin on the glass fibers and improving the bonding performance of the interface of the glass fiber-reinforced epoxy resin composite material, and thus improving the mechanical properties of the glass fiber-reinforced epoxy resin composite material. The epoxy resin is cured and modified by using a functional curing agent or nanoparticles, so as to improve the ductility or strength of the epoxy resin, thereby improving the mechanical properties of the prepared glass fiber-reinforced epoxy resin composite material.

The present application provides guide RNAs and genome-editing complexes or nanoparticles that are useful for specifically targeting a mutated KRAS. Exemplary genome-editing complexes or nanoparticles comprise cell-penetrating peptides, and optionally a DNA nuclease (such as Cas9) or a polynucleotide encoding the DNA nuclease.

The invention relates to the field of microfluid chemical synthesis, and discloses a method for preparing gold nanoparticles based on two-phase flow microfluid control. The method comprises the following steps: 1) converging a gold precursor water phase, a reducing agent water phase and an organic phase in a micro-fluidic chip at 0-25 DEG C to form water-in-oil liquid drops; (2) conveying the fluid to a mixing area channel of a micro-fluidic chip, and carrying out instantaneous nucleation reaction to form a gold nanoparticle prototype; 3) conveying the fluid into a capillary reactor, and further nucleating, growing and curing the gold nanoparticle prototype; and (4) the fluid is subjected to phase splitting, and a gold nanoparticle solution is obtained. A three-in-one micro-fluidic chip is adopted, process parameters are optimized, and a gold precursor and a reducing agent are wrapped in an organic phase before reaction to form water-in-oil liquid drops, so that on one hand, the situation of adsorption and scaling of the inner wall of a channel can be avoided, and on the other hand, the heat and mass transfer efficiency of a material can be improved through the generated liquid drops; and the uniformity of a reaction nucleation environment is ensured.

The present disclosure describes improved LNP-based RNA vaccines, nucleobase editing systems, and therapeutics for use in treating and / or immunization against disease. In particular, the disclosure describes improved LNPs, including novel and improved ionizable lipids for making LNPs, that enhance the targeted delivery of LNP-based RNA vaccines and therapeutics based on linear and / or circular mRNAs. The improved LNPs protect linear and / or circular mRNA payloads from degradation and clearance while achieving targeted systemic or local delivery for use as enhanced vaccines and / or therapeutic agents.

The invention relates to a preparation method of a radiation refrigeration coating with super-hydrophobic performance. According to the method, hydrophobic modified nano-particles and nano-particles with high reflectivity and high emissivity are blended in an adhesive solution, an adhesive is separated out to form a micron-sized aggregate through a non-solvent induced phase separation technology, and meanwhile, various nano-particles are uniformly coated on the surface of the aggregate, so that a stable suspension system is prepared. The radiation refrigeration coating has excellent radiation refrigeration performance, excellent super-hydrophobicity and good durability, the preparation process is simple, the radiation refrigeration coating is suitable for large-scale industrial application of outdoor scenes such as building outer walls, and a new technical solution is provided for developing efficient and lasting radiation refrigeration materials.

The invention belongs to the technical field of medical materials, and relates to a titanium-based implant surface dual drug release system and a preparation method and application thereof. Comprising a titanium-based implant and a hydrogel layer attached to the surface of the titanium-based implant, the surface of the titanium-based implant is of a nanotube array structure, zinc oxide nanoparticles and up-conversion luminescent material particles are arranged between the titanium-based implant and the hydrogel layer, and MgO2 nanoparticles are loaded in the hydrogel layer; wherein the material of the up-conversion luminescent material particles is NaYF4: Yb < 3 + >, Er < 3 + >, and the hydrogel layer is composed of gelatin-sodium alginate hydrogel. The titanium-based implant surface dual-drug release system provided by the invention can realize loading of different drugs, can be used for treating various diseases, has a better time sequence control effect, is long in action time and low in cost, and has a wide application prospect.

The invention discloses a shale oil exploitation method based on cooperation of multistage pulse gas fracturing and nano-catalysis, and belongs to the technical field of oilfield development, and the shale oil exploitation method comprises the following steps: S1, determining an optimal drilling position of a target shale layer, and carrying out drilling operation; s2, 0.1-10 Hz adjustable pulse pressure waves are formed through control of a high-frequency electromagnetic valve, a fracturing medium mixed with the functionalized nanoparticles is injected into the stratum through a fracturing pump, the pulse frequency of the high-frequency electromagnetic valve is adjusted, staged pulse fracturing operation is conducted, and a fracture network is formed; s3, after fracturing of each stage is completed, mixed fluid of a propping agent and fracturing fluid is injected into stratum fractures; and S4, after fracturing operation is completed, a microwave field is applied to the stratum, and the stratum temperature is kept within a set range. According to the method, the gas fracturing medium and the functionalized nanoparticles are mixed and then fractured, so that the influence on the environment is remarkably reduced, and the recovery ratio of shale oil is greatly increased under the combined action of multi-stage pulse fracturing, the composite proppant and the microwave field.

Iridium-based catalysts and methods of making the catalysts are described. The catalyst comprises a catalyst material comprising particles comprising iridium or a mixture of iridium and iridium oxide. The particles include an interconnected network of nanoparticles. The particles are in the range of 50 nm to 1 [mu] m, and the nanoparticles are in the range of 2 nm to 15 nm. It may have a BET surface area of 30 m2 / g or greater and a pore volume of at least 0.10 cc / g. The catalyst is prepared using an organic structure directing agent.