4058 results about "Silanes" patented technology

Disclosed herein are bonded structures and methods of forming the bonded structures. In some embodiments, the bonded structures include a first element having an inorganic dielectric surface, a second element having an organic dielectric surface, an interface layer between the first and second elements and bonded to the inorganic and organic dielectric surfaces. The method of forming the bonded structure includes providing the first and second elements, exposing the inorganic dielectric surface to a silane coupling agent to form the interface layer, contacting the organic dielectric surface to the interface layer, and heating the first element, second element, and interface layer to bond the first element to the second element.

A doped or undoped silicon carbide film can be deposited using a remote plasma chemical vapor deposition (CVD) technique. One or more silicon-containing precursors are provided to a reaction chamber. Radical species, such as hydrogen radical species, are provided in a substantially low energy state or ground state and interact with the one or more silicon-containing precursors to deposit the silicon carbide film. A co-reactant may be flowed with the one or more silicon-containing precursors, where the co-reactant is a carbon-containing precursor and each silicon-containing precursor is a silane-based precursor with at least a silicon atom having two or more hydrogen atoms bonded to the silicon atom.

The invention discloses a nano blocking agent for drilling fluid and a preparation method thereof, and belongs to the technical field of blocking agents, the nano blocking agent for drilling fluid is prepared by reaction of a core layer blocking agent and a shell layer blocking agent, the core layer blocking agent is prepared by reacting nano silicon dioxide, gamma-methacryloxypropyltrimethoxysilane and a first part of vinylphosphonic acid, and has secondary blocking capability; and the shell blocking agent is prepared by reacting a second part of vinyl phosphonic acid, styrene and 2-dodecene-1-yl succinic anhydride, and has the characteristic of flexibility. The nano plugging agent has rigid supporting and flexible deformation capabilities, and the high-temperature stability and compressive strength of a plugging layer are remarkably improved. The chemical binding force of the plugging agent and the rock is enhanced; the hydrolysable methoxyl reserved in the core layer provides a secondary plugging function, and the plugging validity period is prolonged. The invention relates to a preparation method of a nano blocking agent for drilling fluid, which is used for preparing the nano blocking agent for drilling fluid.

The invention discloses a high-strength polyethylene film and a preparation method thereof, and relates to the technical field of high polymer materials. The invention discloses a high-strength polyethylene film. The high-density polyethylene composite material is prepared from the following raw materials in parts by weight: 35 to 45 parts of high-density polyethylene, 25 to 35 parts of linear low-density polyethylene, 12 to 18 parts of ethylene-vinyl acetate copolymer, 5 to 10 parts of nano silicon dioxide, 3 to 7 parts of organic montmorillonite, 1.5 to 3.5 parts of hindered amine light stabilizer, 1.5 to 2.5 parts of antioxidant 1010, 0.8 to 1.2 parts of calcium stearate, 0.8 to 1.2 parts of zinc stearate, 0.8 to 1.2 parts of silane coupling agent and 4 to 6 parts of maleic anhydride grafted polyethylene. The composite material is prepared from the following components in parts by weight: 1.5-3.5 parts of a quaternized chitosan-nano silver compound, 6-9 parts of a modified toughening agent, 4-7 parts of a modified heat-resistant agent, 1.5-3.5 parts of a processing aid, 0.15-0.35 part of dibenzoyl peroxide and 0.5-1.5 parts of a nucleating agent DBS. The composite material is excellent in comprehensive performance, high in strength, good in flexibility and puncture resistance, excellent in aging resistance, heat resistance, chemical resistance and antibacterial property, good in processability, capable of meeting the requirements of multiple fields such as packaging and agriculture, scientific in preparation method and high in practical value.

The invention relates to the technical field of metal surface protection, and discloses a corrosion-resistant self-repairing metal fastener and a preparation method thereof.The corrosion-resistant self-repairing metal fastener comprises a zinc alloy matrix, a nanometer passivation layer, a slow-release corrosion-resistant layer and a self-repairing functional layer, and the nanometer passivation layer, the slow-release corrosion-resistant layer and the self-repairing functional layer sequentially wrap the zinc alloy matrix; the zinc alloy matrix consists of Al, Cu, Mg, Ce and Zn; the nano passivation layer adopts zinc phosphate / silane composite sol to construct a Si-O-P covalent bond network, and plasma is combined to graft epoxy groups to enhance the interface bonding strength; the slow-release anti-corrosion layer is used for loading a pH response type benzotriazole derivative through gradient aperture mesoporous silica, so that the dynamic controlled release of a corrosion inhibitor is realized; the self-repairing functional layer adopts a synergistic effect of a mechanical triggering type sulfydryl siloxane microcapsule and a pH triggering type EDTA chelating agent microcapsule to form a physical plugging-chemical passivation dual-mode repairing mechanism. Through four-stage cooperation of matrix modification, interface strengthening, slow-release regulation and control and intelligent repair, the corrosion resistance of the corrosion-resistant self-repairing metal fastener in a complex environment is remarkably enhanced.

The invention relates to the field of oil well opening and killing fluid production, in particular to a solid-free well killing fluid for shale oil reservoir and a preparation method of the solid-free well killing fluid. The solid-free well killing fluid for the shale oil reservoir comprises the following raw materials in parts by mass: 50-70 parts of water, 10-30 parts of a density regulator, 3-6 parts of a copolymer tackifier, 1-3 parts of a dispersant, 3-7 parts of a filtrate reducer and 2-4 parts of a corrosion inhibitor. The copolymer tackifier is obtained by initiating copolymerization by taking acrylamide, a quaternary ammonium salt-containing monomer, an unsaturated silane coupling agent and polyethylene glycol diacrylamide as monomer free radicals, and the dispersing agent comprises gas-phase nano silicon dioxide and a fluorine-containing surfactant. Through reasonable compatibility of all the components in the formula, especially the copolymer tackifier, the effect that one agent has multiple functions is achieved, and meanwhile the high temperature resistance, the corrosion inhibition performance and the clay stability of the well killing fluid are improved.

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 field of metal surface treatment, and discloses an efficient electroplating process for a cotton picker spindle and an electroplating liquid formula, the efficient electroplating process comprises the following steps: step 1, substrate pretreatment: sequentially carrying out alkali washing, acid washing and plasma activation on the spindle; step 2, preparing an electroplating solution: dissolving nickel sulfate, sodium hypophosphite, a composite nano additive and a complexing agent in water, and adjusting the pH value to 4.8-5.3; step 3, gradient pulse electroplating: carrying out pulse electroplating in three stages, including bottom layer deposition, transition layer deposition and composite layer deposition; 4, post-treatment is conducted, specifically, silane sealing and curing are conducted on the plating layer; the base body pretreatment in the first step comprises the following sub-steps of alkali washing and oil removal, wherein the picking ingot is soaked in a NaOH solution with the concentration being 45-55 g / L. According to the method, high-density hydroxyl active sites are constructed on the surface of the metal base material through a plasma activation process, strong chemical bonding is formed between a plating layer and the base material, and the interface bonding strength is remarkably improved.

The invention discloses a crosslinked polyethylene reinforced high-strength insulating aerial cable, and belongs to the technical field of crosslinked polyethylene cable materials.The crosslinked polyethylene reinforced high-strength insulating aerial cable is prepared by the steps that hydroxyl is introduced to nano boron nitride powder, then amino is grafted through KH-550, nano alpha-Al2O3 powder is modified through gamma-glycidyl ether oxypropyl trimethoxy silane, and the cross-linked polyethylene reinforced high-strength insulating aerial cable is obtained; the preparation method comprises the following steps: preparing low-density polyethylene, compounding the low-density polyethylene with aminated nano boron nitride powder to form nano composite powder, improving the interface bonding force between the low-density polyethylene and the nano composite powder, carrying out melt blending on the low-density polyethylene and the nano composite powder to improve the dispersity of the nano composite powder in the low-density polyethylene, and carrying out nucleophilic acyl substitution reaction to obtain a fluorine-containing modified monomer. The nano boron nitride powder and the nano alpha-Al2O3 powder are subjected to a cross-linking reaction under the initiation action of an initiator and then coat the exterior of the thermal insulation layer, and the nano boron nitride powder and the nano alpha-Al2O3 powder are bridged through siloxane bonds to form a three-dimensional heat-conducting network, so that the heat resistance of the outer insulating layer is improved.

The invention discloses a flexible PI heat-conducting insulating film pad and a preparation method thereof, and relates to the field of film pads. The preparation method comprises the following steps: preparing Fe3O4 magnetic heat-conducting core and SiO2 insulating shell composite nanoparticles by a sol-gel method, treating and grafting epoxy groups by a silane coupling agent, performing ring-opening addition with one end amino group of amino-terminated polydimethylsiloxane, and reacting the other end amino group with polyethylene glycol diglycidyl ether, so that two flexible long chains are grafted on SiO2. Due to the modified composite nanoparticles and the flexible long-chain structure, the flexibility of the film pad is remarkably improved; thermal vibration of silicon-oxygen bonds and ether bonds promotes heat transfer, a hydrogen bond network is formed with a PI substrate to improve dispersion stability, particles are orderly arranged under the action of a high-frequency magnetic field to construct a three-dimensional heat conduction network, and heat conduction efficiency is enhanced; the SiO2 isolates the inner core from conducting and improves the insulating property of the film pad by virtue of good insulativity and no free charge in the flexible long-chain polymer. The flexible PI heat-conducting insulating film pad prepared by the invention has the effects of flexibility, heat conduction and insulation.

The invention discloses a nano material modified alcohol amine grinding aid as well as a preparation method and application thereof, and the preparation method comprises the following steps: firstly, carrying out esterification reaction on alcohol amine and an acid small monomer containing double bonds to generate an esterification product; then, carrying out bulk polymerization on the esterification product and a silane coupling agent KH-570; and finally, combining the bulk polymerization product with the nano-material through a dehydration reaction of a silane coupling agent and hydroxyl on the surface of the nano-material to form the nano-material modified alcohol amine grinding aid. According to the invention, the nano material is directly grafted into the alcohol amine, so that the dispersity of the nano material in the cement grinding process can be effectively optimized, the friction force and energy consumption among cement particles can be reduced, the efficiency and stability of the cement production process can be improved, and the strength and durability of the cement product are improved.

The invention discloses a silane coupling agent grafted MXene composite material and a preparation method thereof, relates to the technical field of composite materials, and aims to provide a surface modification method to enable the MXene composite material to be in good contact with a PDMS (polydimethylsiloxane) material. The surface modification method comprises the following steps: S1, performing wet chemical etching on an MAX phase material in combination with mechanical stripping to obtain a few-layer MXene dispersion liquid; s2, strong base is added into the few-layer MXene dispersion liquid in the step S1, the PH value of the few-layer MXene dispersion liquid is adjusted, a reaction is conducted in the argon environment, and hydroxyl modified MXene dispersion liquid, namely h-MXene dispersion liquid is obtained; and S3, adding a silane coupling agent and a catalyst into the h-MXene dispersion liquid in the step S2, and reacting in an argon environment to obtain the silane coupling agent grafted MXene composite material.

The invention discloses a water-borne epoxy resin coating which comprises a component A and a component B, the component A is prepared from 60 to 80 parts of 50 percent modified water-borne epoxy resin emulsion, 5 to 15 parts of deionized water, 0.5 to 1 part of wetting dispersant, 0.2 to 0.8 part of defoaming agent, 5 to 10 parts of modified zinc phosphate, 3 to 5 parts of ion exchange antirust pigment, 4 to 6 parts of sericite powder, 3 to 5 parts of glass flake, 5 to 10 parts of precipitated barium sulphate, 1 to 5 parts of nano silicon dioxide and 0.5 to 1 part of rheological additive; 1 to 2 parts of modified organic bentonite slurry; 0.1 to 0.3 part of a pH conditioning agent; and 0.2 to 0.8 part of a flash rust inhibitor. The component B is prepared from 40 to 50 parts of waterborne epoxy-amine adduct, 20 to 30 parts of 50 percent modified polyamide curing agent, 5 to 15 parts of 60 percent Mannich base phenolic aldehyde amine curing agent, 0.5 to 1.5 parts of epoxy silane coupling agent, 1 to 2 parts of nonionic surfactant and 15 to 20 parts of deionized water. The emulsion stability of the waterborne epoxy resin coating is improved through a bisphenol A / F mixed epoxy emulsion and a grafted polyethylene glycol hydrophilic chain segment.

The invention belongs to the technical field of high polymer chemical materials, and particularly relates to a self-repairing composite waterproof board and a preparation method thereof. The invention relates to a high-temperature-resistant graphene coating which is prepared from the following raw materials: bisphenol A diglycidyl ether, fluorosilane modified nano SiO2, graphene slurry, polydimethylsiloxane, epoxy-terminated polydimethylsiloxane, a urea-formaldehyde prepolymer, a silane coupling agent, sodium dodecyl benzene sulfonate, an FSO-100 fluorocarbon surfactant, a CTBN adhesive, a curing agent, an epoxy accelerator DMP-30 and a diluent. Through the collaborative design of the gradient structure of the hard framework and the soft coating, low-surface-energy filler chemical anchoring, microcapsule local material supplementing and thermal triggering dynamic bond rearrangement, the board obtains balance among the bearing strength, long-term hydrophobicity, weather-proof barrier and repeatable thermal self-repairing; and meanwhile, the common defects that room-temperature self-repairing is difficult to realize, hydrophobic particles are easy to agglomerate, a coating is easy to layer and the like are avoided.

The invention provides a high-insulation black organic silicon coloring agent and a preparation method thereof. The high-insulation black organic silicon coloring agent comprises the following raw materials in parts by mass: 100 parts of a silicone oil carrier; 3-5 parts of passivated carbon black; 1-3 parts of fumed silica; wherein the passivated carbon black comprises carbon black and an organic silicon layer coated on the surface of the carbon black; the organic silicon layer is obtained by graft polymerization of polymethyltriethoxysilane and a functionalized silane coupling agent on the surface of the carbon black; the functionalized silane coupling agent comprises at least one of an aryl silane coupling agent and a fluorine-containing silane coupling agent. According to the black coloring agent, the advantage of high blackness of carbon black is maintained, meanwhile, the electric insulation performance and dispersion stability of the black coloring agent in a silicone oil system are remarkably improved, the problems that the carbon black is high in conductivity, poor in interface compatibility and prone to agglomeration are solved, and the black coloring agent is especially suitable for being applied to organic silicon materials with the high requirement for the insulation performance.

The invention belongs to the technical field of environmental protection, and provides a preparation method of an imine-modified functionalized mesoporous magnetic silicon dioxide nano material. The method comprises the following steps: synthesizing Fe3O4 magnetic nanoparticles in a Fe < 2 + > / Fe < 3 + > alkaline hydrolysis system through a coprecipitation method; then coating the magnetic nanoparticles with an amorphous silicon dioxide layer by taking TEOS (tetraethoxysilane) as a silicon source by adopting a sol-gel method, so as to prepare magnetic silicon coated nanoparticles; the prepared nano-particles are subjected to secondary silicon coating guided by a cetyl trimethyl ammonium bromide (CTAB) mesoporous template agent, and mesoporous magnetic silicon nano-particles are formed after calcination; and finally, carrying out surface amination modification on the mesoporous magnetic silicon nano-particles by utilizing an amino silane coupling agent, and then carrying out condensation reaction on the mesoporous magnetic silicon nano-particles and various aldehyde derivatives to construct imine bonds, so as to obtain the imine-modified functionalized mesoporous magnetic silicon dioxide nano-material. The imine-modified functionalized mesoporous magnetic silicon dioxide nano-material formed by the invention has the characteristics of efficient adsorption, rapid magnetic recovery and excellent environmental stability, and can effectively remove polystyrene micro-plastics and organic pollutants in a water body.

The invention discloses a preparation method and application of a hydrophobic core-shell structure catalyst, and the method comprises the following steps: adding a metal oxide and a surfactant into a first solvent to obtain a first dispersion liquid; adding an alkaline solution and a silicon source into the first dispersion liquid to obtain a first turbid liquid; calcining the first turbid liquid to obtain a porous core-shell material of silicon dioxide coated metal oxide; adding the porous core-shell material into a third solvent to obtain a second suspension; and adding an alkaline solution and a silane agent into the second turbid liquid to obtain the hydrophobic core-shell structure catalyst of the hydrophobic silicon dioxide coated metal oxide. The oxidation reaction of the inner core of the silicon dioxide layer does not destroy hydrophobic groups on the outer layer, so that the hydrophobic performance is maintained for a long time, organosilane is grafted on the surface of the silicon dioxide shell layer, inhibition of water vapor on the activity of the catalyst is reduced, and competitive adsorption of water vapor and reaction gas is prevented; the activity and the service life of the catalyst under high-temperature and high-humidity conditions are effectively improved.

The invention discloses a silane cross-linked polyolefin halogen-free flame-retardant cable material and a low-energy-consumption preparation method thereof.The preparation method comprises the steps that EVA / EEA serves as a matrix, silane groups are covalently connected to a polyolefin molecular chain through a free radical grafting reaction, and a grafting material containing an active silane side group is prepared; meanwhile, vinyl isocyanate is adopted to chemically modify hydroxyl on the surface of magnesium hydroxide, vinyl is grafted to the surfaces of particles, the polarity of the particles is reduced, and the dispersity of the particles is enhanced; then carrying out melt blending on the grafted material and modified magnesium hydroxide, constructing an interface bridge by using an anhydride group, and shortening the two-phase distance; finally, through room-temperature natural cross-linking and warm water auxiliary cross-linking, silane groups are promoted to be hydrolyzed into silanol, the silanol is condensed to form a-Si-O-Si-three-dimensional network, meanwhile, vinyl on the surface of magnesium hydroxide and a polyolefin matrix are subjected to free radical copolymerization, and a covalent bond interface layer is formed between inorganic particles and an organic matrix. According to the method, the synergistic improvement of high crosslinking degree, strong stretchability and excellent flame retardance of the cable material is realized through molecular-level interface regulation and cross-linking network optimization.

The invention discloses a solid electrolyte with high ionic conductivity, which comprises the following components: a matrix material: a halide super ion conductor with a LiMXCl4 structure, M being selected from at least one of Ta, Nb and Hf, X being O or F, a chemical general formula being LiM1-aX1-6Cl4, a being equal to 0.1-0.3, and an electrochemical window being regulated to 2.5-4.0 V through fluorine-chlorine mixed anion substitution; the second phase material is a core-shell structure compound, the core is Li3TiCl6, and the shell is a Li3PS4 interface layer; and the sintering aid is a compound of Li3BO3 and LiF. Through fluorine-chlorine mixed anion regulation and control and MO2Cl4 octahedron synergistic tilting mechanism, the ionic conductivity of the solid electrolyte is remarkably improved, the lithium ion conductivity at room temperature is greater than or equal to 10mS / cm, the activation energy is less than or equal to 0.2 eV and is superior to that of the traditional halide electrolyte, and meanwhile, the free volume between chains is optimized through Zr < 4 + > / Sn < 2 + > gradient doping, so that the performance of the solid electrolyte is improved. The core-shell structure compound and the silane coupling agent are combined for modification, so that the electrochemical window is effectively widened to 2.5-4.0 V, the interface side reaction is inhibited, and the composite material is adaptive to a high-voltage positive electrode material.

The invention provides a preparation method and application of a wear-resistant polyimide material, and the preparation method comprises the following steps: S1, adding a polyimide material into an alkali solution for reaction, cleaning reactants with acid and ethanol, and drying to obtain an activated polyimide material; s2, adding the activated polyimide material into a silane coupling agent solution for reaction, cleaning reactants with ethanol and water, and drying to obtain a modified polyimide material with silicon-oxygen bond active sites on the surface; s3, adding the modified polyimide material with silicon-oxygen bond active sites on the surface into a modified epoxy resin solution, adjusting the pH value to be acidic, and reacting to obtain the wear-resistant modified polyimide material, wherein the modified epoxy resin solution is obtained by reacting a silane coupling agent with acrylate. According to the method, the wear resistance of the polyimide can be improved on the premise that other properties of the polyimide material are not influenced.

The invention relates to a preparation method and application of high-temperature-resistant organic modified bentonite. According to the method, three organic modifiers of long-chain quaternary ammonium salt, amide and a silane coupling agent are compounded to modify bentonite, and the problem that a single modifier is easy to decompose at high temperature is solved through the synergistic effect of physical intercalation, chemical crosslinking and interface bonding; and secondly, a three-dimensional stable structure is constructed by adding nano silicon dioxide and a composite modifier, so that the high temperature resistance and dispersion stability of the modified bentonite are further enhanced. According to the invention, the requirements of deep well and ultra-deep well drilling fluids on the temperature resistance and rheological property of the treating agent can be met, and the ultra-deep well drilling fluid which can tolerate the high temperature of 250-300 DEG C, and is low in filter loss and good in dispersion stability can be obtained.

The invention discloses a super-hydrophobic road ice-inhibiting coating based on a photothermal effect and nano modified particles and a preparation method of the super-hydrophobic road ice-inhibiting coating. The preparation method comprises the following steps: introducing silane modified nano silicon dioxide (SiO2) and titanium dioxide (TiO2) particles into a polyaniline solution, and preparing the composite super-hydrophobic powder through a chemical oxidation polymerization method. The preparation method comprises the following steps: firstly, modifying the surfaces of SiO2 and TiO2 nanoparticles by adopting a silane coupling agent, and endowing the SiO2 and TiO2 nanoparticles with low surface energy and hydrophobic property; and then adding the modified nano-particles into an aniline monomer solution, reacting with doped acid and an oxidizing agent, so that polyaniline molecules are subjected to in-situ polymerization on the surfaces of the particles, and the composite super-hydrophobic powder with a micro-nano structure is formed. The obtained composite material has excellent photothermal conversion performance and super-hydrophobic performance at the same time, and the efficient photothermal material heat absorption ice melting effect and the synergistic ice restraining effect of the photothermal material and the super-hydrophobic material can be achieved. Compared with a traditional ice-inhibiting coating, the coating disclosed by the invention shows stronger ice-resisting capability in a low-temperature and high-humidity environment, has good durability, mechanical stability and environmental protection property, and is suitable for the field of ice prevention and ice inhibition in cold regions such as roads, bridges, airport runways and the like.

The invention discloses a low-warpage damp-heat-resistant liquid epoxy molding compound as well as a preparation method and application thereof. The liquid epoxy molding compound is prepared from the following raw material components in parts by mass: 85 to 90 parts of modified silicon dioxide, 5 to 8 parts of naphthalene type epoxy resin monomer, 5 to 8 parts of anhydride curing agent, 0.1 to 0.3 part of coupling agent, 0.1 to 0.3 part of adhesion promoter and 0.2 to 0.5 part of temperature response type amine catalyst. The modified silicon dioxide is obtained by carrying out surface modification on micron-sized silicon dioxide by adopting a silane coupling agent containing an epoxy group, and the mass of the silane coupling agent containing the epoxy group is 0.3-0.8% of the mass of silicon dioxide. The liquid epoxy molding compound provided by the invention has excellent flowability, adhesive force and heat and humidity resistance, can significantly relieve and reduce the warping of a silicon wafer, and is suitable for integrated circuit packaging.

The invention relates to a fly ash-based MOFs adsorption-catalysis material integrated preparation method, and belongs to the field of solid waste treatment and resource utilization. The material takes industrial solid waste fly ash as a matrix, and is prepared by the following steps: firstly, carrying out alkali modification and silane coupling agent surface activation treatment on fly ash to form a high-activity matrix; then loading a metal organic framework (MOFs) on the surface of the activated fly ash through an in-situ synthesis process to form a porous composite carrier; the integrated material with CO2 adsorption and catalytic conversion functions is further prepared through impregnation of a copper-based active component and a high-temperature calcination process. According to the invention, the problems of high energy consumption, high cost and low comprehensive utilization rate of fly ash of the traditional CO2 capture and utilization technology (ICCU) are solved, high-valued resource utilization of industrial solid waste and efficient capture and conversion of CO2 are synchronously realized, and the method has dual values of environmental protection and economy.

The invention provides a high-hydrophobicity anti-pollution flashover coating and a preparation method thereof, and relates to the field of coatings. The silicone rubber composition is prepared from the following raw materials in parts by weight: 80 to 100 parts of hydroxyl-terminated polydimethylsiloxane; 5 to 15 parts of modified nano silicon dioxide; 10 to 30 parts of a composite self-repairing microcapsule; 10 to 25 parts of a flame retardant; 3-8 parts of a cross-linking agent; 0.5-2 parts of a catalyst; 1-5 parts of an accelerant; 40 to 100 parts of a solvent; the modified nano silicon dioxide is fumed silica subjected to surface treatment by a fluorine-containing silane coupling agent and a platinum catalyst; the capsule wall of the composite self-repairing microcapsule is a polylactic acid-glycolic acid copolymer, and the capsule core of the composite self-repairing microcapsule is a mixed solution of a hydroxyl-terminated polydimethylsiloxane oligomer and methyltris (methylethylketoximino) silane. The coating has excellent hydrophobicity, weather resistance and targeted repair function.

The invention discloses a high heat storage density stable thermochemical adsorption composite heat storage material and a preparation method thereof, the high heat storage density stable thermochemical adsorption composite heat storage material comprises 54%-57% by mass of mixed salt and 43%-46% by mass of a porous material, the mixed salt comprises MgSO4 and MgCl2, the mass ratio of MgSO4 to MgCl2 is 9: 1-6: 4, and the porous material is expanded perlite modified by nano alumina or a silane coupling agent. The high-heat-storage-density stable thermochemical-adsorption composite heat storage material provided by the invention is simple in preparation method, and the modified expanded perlite is used as a carrier of the mixed hydrated salt; the obtained composite heat storage material has excellent performance: the salt-containing load rate is 114-121%, the water absorption rate is 1.2-1.28 g / g, the heat storage density is 1123.5-1208.6 kJ / kg, the heat storage temperature is 133.4-141.3 DEG C, the structural strength is 10.346-12.631 kPa, the structural stability is 99.27-99.53%, and the stability is 79.7-83.3% after circulation for 30 times, that is, the composite heat storage material is high in heat storage density, high in water absorption rate, low in heat storage temperature, high in strength and not easy to scatter and fall off, and the composite heat storage material is suitable for large-scale production. And the material also has relatively good cycling stability.

The present invention provides a multifunctional silane coupling agent, which is prepared from commercially available 3-aminopropylsilane coupling agent, acryloxy polyetheramine, and one of an alkylating agent, polyether sulfonate, γ-propane sultone or γ-butyrolactone through Michael addition reaction and quaternization reaction. The multifunctional silane coupling agent is a new variety carrying zwitterions, quaternary ammonium cations and polyether chains, enriching the functions and application scope of silane coupling agents. It can endow some modified materials with surface hydrophilicity, conductivity, antibacterial, antifogging, antifouling, biocompatibility, anticoagulant and wet lubrication properties, etc. at the same time.

The invention relates to the technical field of building decoration materials, in particular to a high-performance antibacterial mildew-proof sealant and a preparation method thereof. The sealant is prepared from the following raw materials in parts by weight: 20 to 30 parts of silane modified polyurethane, 40 to 50 parts of nano calcium carbonate, 20 to 30 parts of a plasticizer, 3 to 7 parts of a hydroxyl silane coupling agent, 0.4 to 0.8 part of a mildew preventive, 0.3 to 0.7 part of an ultraviolet light absorber, 0.3 to 0.7 part of a de-foaming agent and 0.8 to 1.2 parts of a first catalyst. The high-performance antibacterial and mildew-proof sealant has long-acting antibacterial and mildew-proof performance, and excellent mechanical performance and weather resistance of the sealant can be maintained, so that the requirements of industries such as building, medical treatment and food processing on high-performance, healthy and environment-friendly sealing materials are met; and the preparation method is simple and controllable, the production cost is relatively low, and large-scale production can be realized.

The invention discloses a silicon-carbon material as well as a preparation method and application thereof. The silicon-carbon material comprises nitrogen-doped porous carbon and an amorphous carbon layer coating the nitrogen-doped porous carbon, and pores of the nitrogen-doped porous carbon are filled with boron-doped nano silicon. The nitrogen-doped porous carbon improves the affinity of silane gas while improving the electron conductivity, a high-conductivity and high-density silicon-carbon composite structure is realized, the boron-doped nano silicon and the nitrogen-doped porous carbon form a nano heterojunction site, and the migration rate of lithium ions is improved, so that electrochemical reaction kinetics is improved, and the electrochemical performance of the lithium ion battery is improved. The material has the advantages of high rate and long cycle performance.