144 results about "Phenylacetylene" patented technology

The invention belongs to the field of advanced materials, and particularly relates to polyimide resin with low curing temperature and high heat resistance and a preparation method thereof. According to the invention, pararosaniline is introduced into the molecular chain structure of the phenylacetylene-terminated polyimide resin, and the curing temperature of the phenylacetylene-terminated polyimide resin is reduced by changing the spatial distortion degree of the polyimide molecular chain and introducing free radicals to catalyze the curing process. The polyimide resin can be cured and molded at a relatively low temperature, and keeps excellent heat resistance and mechanical properties. The forming temperature of the high-performance polyimide and the composite material thereof is effectively reduced, so that the manufacturing difficulty and cost are reduced, and the preparation method has important application prospects.

The invention relates to the technical field of battery binders, in particular to a water-based binder, a preparation method of the water-based binder and a carbon-coated aluminum foil. The water-based binder comprises a water-soluble monomer, an oil-soluble monomer, an amphiphilic monomer, a functional monomer, an initiator and a neutralizer, the amphiphilic monomer is prepared from at least one of sodium vinyl sulfonate, sodium p-styrenesulfonate, 2-acrylamide-2-methylpropanesulfonic acid and N-vinyl pyrrolidone; the functional monomer comprises at least one of divinylbenzene, pyrrole, phenylacetylene and 3, 4-ethylenedioxythiophene. According to the water-based binder, the water-soluble monomer, the oil-soluble monomer, the amphiphilic monomer and the functional monomer are compounded in proportion, the conductivity of the binder, the wettability to a conductive carbon material and an aluminum foil, the adhesion to the aluminum foil and the like are improved, the prepared battery has excellent cycle stability, and the service life of the battery is prolonged.

The invention discloses a glass fiber reinforced polyurethane material and a preparation method thereof, and relates to the technical field of high polymer materials. When the glass fiber reinforced polyurethane material is prepared, bis (4, 4 '-dihydroxy) phenylacetylene reacts with bis (pinacolato) diboron and 4-bromopyridine in sequence to prepare an ultraviolet absorption monomer; the preparation method comprises the following steps: polymerizing polyether glycol, an ultraviolet absorption monomer, a sulfonium salt diol monomer and 1, 6-hexamethylene diisocyanate to prepare functional polyurethane; the preparation method comprises the following steps: polymerizing and coating a boron-containing flame-retardant monomer and bis (2-aminoethyl) phosphine on glass fibers to prepare pre-modified glass fibers; the pre-modified glass fiber and hydroxymethylated triazoline diketone are subjected to a reaction, and modified glass fiber is prepared; and uniformly mixing the functionalized polyurethane and the modified glass fiber, and carrying out injection molding to obtain the glass fiber reinforced polyurethane material. The glass fiber reinforced polyurethane material prepared by the invention has excellent anti-aging, antibacterial, flame-retardant, self-repairing and mechanical properties.

The invention relates to the technical field of organic photoelectric materials, in particular to a co-assembly method for improving energy transfer efficiency of chromophores, a co-assembly body and application. The specific method comprises the following steps: co-assembling a donor substance and perfluorinated aromatic hydrocarbon in a solvent system to prepare a donor-perfluorinated aromatic hydrocarbon compound; the method comprises the following steps: co-assembling an acceptor substance and perfluorinated aromatic hydrocarbon in a solvent system to prepare an acceptor-perfluorinated aromatic hydrocarbon compound; the preparation method comprises the following steps: co-assembling a donor-perfluorinated aromatic hydrocarbon compound and an acceptor-perfluorinated aromatic hydrocarbon compound in a solvent system to prepare a crystal-induced energy transfer precise co-assembly body; the donor substance is 9, 10-bis (phenylethynyl) anthracene, and the perfluorinated aromatic hydrocarbon is octafluoronaphthalene; the acceptor substance is 5, 12-bis (phenylethynyl) tetracene. The problems of high energy dissipation and low FRET efficiency of the donor-acceptor pair with weak aggregation emission in the fluorescence resonance energy transfer process are solved.

The invention discloses a Pd-coated S-COF catalyst for a reaction of preparing styrene through phenylacetylene hydrogenation as well as preparation and application of the Pd-coated S-COF catalyst. The Pd (at) S-COF catalyst comprises a covalent organic framework carrier S-COF and Pd nanoparticles, the covalent organic framework carrier S-COF is an imine bonded covalent organic framework prepared by using 2, 4, 6-tri (4-aminophenyl)-1, 3, 5-triazine and 2, 5-dimethyl thioether-1, 4-phthalaldehyde as raw materials, and the Pd nanoparticles are used for modifying Pd nanoparticles. The Pd nano-particles are encapsulated in pore channels of the S-COF and are loaded on the surface of the S-COF. The invention provides an application of the Pd-coated S-COF catalyst in a reaction for preparing styrene through phenylacetylene hydrogenation, and high phenylacetylene conversion rate and high styrene selectivity can be realized within a short reaction time.

The invention relates to a green catalysis method for improving phenylacetylene hydrogenation selectivity and a catalyst preparation method. The method mainly solves the problems of high catalyst cost, difficult realization of large-scale commercialization and the like caused by large usage amount of noble metals in alkene preparation through alkyne selective hydrogenation at present. According to the green catalysis method for improving phenylacetylene hydrogenation selectivity and the catalyst preparation method, preparation is simple, the usage amount of precious metal is low, H2Ti3O7 intrinsic ion exchange performance is utilized, a Pd active phase is inserted into crystal lattices of the catalyst, continuous active sites are separated, styrene excessive hydrogenation reaction is inhibited, and the selectivity of the catalyst is improved.

The application relates to a catalyst for selectively hydrogenating nitrophenylacetylene to prepare aminophenylacetylene. The Fe2O3-CeO2 / TiO2 catalyst is used, the solvent is anhydrous ethanol, the hydrogen source is hydrazine hydrate, and the nitrophenylacetylene is catalytically hydrogenated to prepare aminophenylacetylene at 80-150 DEG C. The catalyst can realize efficient hydrogenation of the nitro group in the nitrophenylacetylene, the selectivity of the aminophenylacetylene can reach 94.8% when the nitrophenylacetylene is completely converted, the selectivity of the aminophenylacetylene is basically unchanged when the reaction time is continuously prolonged, and there is no accumulation of harmful intermediates such as phenylhydroxylamine in the reaction process.

The invention relates to a method for preparing a molecular sieve confinement active metal catalyst and application of the catalyst. According to the preparation method of the molecular sieve confinement active metal catalyst, a traditional organic structure directing agent is replaced with a seed crystal method, and a metal-molecular sieve catalyst is prepared in an in-situ confinement mode by directly adding molecular sieve seed crystals into a metal silicon-aluminum sol precursor. The metal-coated molecular sieve prepared by the method has metal species with smaller size, the synthesis method is simple and convenient, the use of an organic structure-directing agent is saved, and the cost of the catalyst is reduced. The metal scale of the metal-at-molecular sieve is monatomic, sub-nano, and nano-scale. The sub-nano palladium-coated molecular sieve catalyst is applied to catalysis of semi-hydrogenation reaction of phenylacetylene, has excellent catalytic performance, and shows accurate catalytic selectivity on alkyne molecules less than # imgabs0 #.

The invention provides a silicon composite negative electrode material with a multi-level coating structure, a preparation method of the silicon composite negative electrode material and a secondary battery. An inner core of the silicon composite negative electrode material with the multi-level coating structure comprises a silicon negative electrode material, a middle layer comprises an artificial SEI film layer, and an outermost layer comprises an oxide coating layer; wherein the material of the artificial SEI film layer comprises a phenylacetylene copolymer, and the structure of the phenylacetylene copolymer comprises a combination of a halogen group, an ether group and a group capable of forming a hydrogen bond. According to the invention, the silicon negative electrode material is modified by adopting a differentiated multi-stage surface coating structure, so that the heat resistance, the mechanical property and the interface dynamic property of the silicon negative electrode material are comprehensively improved, and the electrochemical property of a secondary battery under high magnification and high-temperature environment is improved.

The invention discloses a method for preparing a fluorine-containing compound and its application, and relates to the technical field of perovskite material additives. The preparation method is as follows: naphthaleneboric acid, potassium carbonate and bis(triphenylphosphine)palladium chloride are added to a drying container, the container is evacuated to a vacuum state and then filled with nitrogen, phenylacetylene and nine fluoro-4-iodobutane are added to the container, dichloromethane and distilled water are then added to the container, and heated for reaction; the obtained reaction mixture is subjected to extraction and drying, separation and purification, and a fluorine-containing compound is obtained. The fluorine-containing compound prepared by the present invention has good compatibility with the perovskite material, and there will be no heterogeneous phase generation; it is applied as an additive in the perovskite material to suppress the migration and loss of ions, reduce the defect state density at the perovskite grain boundary, extend the carrier lifetime, and improve the charge transfer efficiency; it can also promote the nucleation and growth of perovskite, and improve the quality and morphology of the perovskite film.

The application belongs to the technical field of polymer materials and engineering, and discloses a preparation method of a phosphate cross-linked organic porous uranium extractant. A phenylacetylene is cross-linked with 1,4-dithioerythritol through a click chemistry reaction by using a photo-induced cross-linking method. Compared with common mercaptans, 1,4-dithioerythritol contains an adsorption group. The cross-linking reaction is carried out under the condition that the ratio is 1:3 and the light irradiation time is 1h. An organic polymer PCM with a porous structure is synthesized. After the synthesized polymer is subjected to Soxhlet extraction for 48h, the polymer is modified by phosphating with phosphorus oxychloride to prepare a porous polymer containing a phosphate group. After the synthesized polymer is subjected to Soxhlet extraction for 48h and is dried, a purple black powder P-PCM is obtained. The target polymer can be synthesized only through three steps of reactions. The polymer preparation is relatively simple under the photo-induced cross-linking, which is of great significance to improving the uranium adsorption capacity. The preparation is simple, the reaction is stable, the safety is high, and the cost is low through the click chemistry reaction.

The invention relates to a method and a catalyst for preparing amino aromatic hydrocarbon through hydrogenation of nitroaromatic hydrocarbon containing easily reduced groups such as nitrophenylacetylene. According to the method, Fe-N / C prepared by an impregnation-pyrolysis method is used as a catalyst, absolute ethyl alcohol is used as a solvent, hydrazine hydrate is used as a hydrogen source, and nitro-aromatic hydrocarbon is catalyzed to be hydrogenated at 30-100 DEG C to prepare amino-aromatic hydrocarbon. The catalyst has high activity and high selectivity on nitro hydrogenation in nitro aromatic hydrocarbon, and when the conversion rate of nitrophenylacetylene is 100%, the selectivity of aminophenylacetylene is gt; the reaction time is continuously prolonged, and the selectivity of the aminophenylacetylene is basically unchanged. For hydrogenation of other nitro aromatic hydrocarbons, the selectivity gt of amino aromatic hydrocarbons can be realized under the conversion rate of 100%; 96%.

The application discloses a kind of all-substituted pyrrole compounds, the raw material alkyne compound of the application has structural diversity with isonitrile compound, can be used to synthesize different types and structures of all-substituted pyrrole compounds;Reaction raw material diphenylacetylene and its same type substrate compared with the raw material of the reaction reported by predecessors, have the advantages of simple and easy to obtain, stable nature;All-substituted pyrrole compounds have good diversity and functional group tolerance, so it has wide application;Further modification is carried out to different substitution sites on the heterocyclic skeleton of all-substituted pyrrole compounds, and intermediates of chemical products and drug structures can be obtained;The target product of the application takes pyrrole as the key mother nucleus, while amide and other unsaturated groups are introduced on the ring, and the structure has potential pharmacological activity;Cheap transition metal nickel is used as catalyst;The yield of the application is good.

The application discloses a preparation method of high-adhesion carbon paper for fuel cells and relates to the technical field of fuel cells.The method comprises the following steps: performing cleaning treatment on carbon fibers to obtain carbon fiber precursors; performing modification treatment on the carbon fiber precursors to obtain modified carbon fibers; performing wet forming treatment on the modified carbon fibers to obtain carbon fiber base paper; placing the carbon fiber base paper in phenylacetylene to obtain carbon fiber paper precursors; performing heat preservation on the carbon fiber paper precursors to obtain carbon fiber paper; performing impregnation on the carbon fiber paper, and then performing solidification treatment and carbonization treatment to obtain the high-adhesion carbon paper for fuel cells.The preparation method simultaneously adopts polyurethane and carbon nanotubes to modify the carbon fibers, polyacetylene to modify the carbon fiber base paper and vinyltrichlorosilane to modify phenolic resin, and the high-adhesion carbon paper for fuel cells prepared by the method has high density and excellent heat conduction performance and electric conduction performance.

The present application describes methods for disinfecting physical or biological surfaces by contact with antimicrobial formulations comprising substituted tolan compounds, such as one or more alkoxy (e.g., methoxy) and hydroxy substituents on one or two phenyl rings of the tolan. The compounds and methods are microbial and / or microbicidal, depending on the dose and suspected microorganism. Suspected pathogenic microorganisms include gram-negative bacteria, such as Pseudomonas aeruginosa (P.aeruginosa) and Escherichia coli (E.coli); gram-positive bacteria, such as Staphylococcus aureus (S.aureus), including MRSA; and fungal pathogens, such as Candida and Candida albicans (C.albicans). The present application also describes methods for inhibiting or disrupting biofilm formation of one or more microorganisms.

The present invention discloses a method for inducing self-assembly of poly(phenylacetylene) into films by photoirradiation cross-linking polymerization reaction. Two phenylacetylene monomers containing dendrimeric alkoxy ether units and acrylate functional groups are used. Based on the two phenylacetylene monomers, a dendritic phenylacetylene copolymer is prepared by metal-catalyzed copolymerization reaction. The copolymer has a radial amphiphilic structure and temperature-sensitive characteristics. When its aqueous solution is heated above the phase transition temperature, dehydration aggregation occurs to form film-like assemblies. A photoinitiator is added to the copolymer aqueous solution, and under the condition of ultraviolet light irradiation above the phase transition temperature of the copolymer, the polymer further undergoes cross-linking and self-assembly to directly obtain a thin film. The thin film has excellent temperature responsiveness, and its thickness can be regulated by the copolymer concentration, copolymerization ratio, and irradiation time. The invention provides a new way to prepare thin film materials, with short reaction time, simple steps, and the prepared intelligent thin films having good prospects in aspects such as material separation and molecular selective permeation.

The application discloses a five-membered ring containing alkynyl or triazole functional group P The chiral phosphine oxide compound is obtained through Domino Heck-Sonogashira cascade reaction by taking a prochiral tertiary phosphine oxide compound containing a double ethylene group and phenylacetylene as raw materials, transition metal palladium catalyst and chiral TADDOL phosphoramidite ligand under the protection of inert gas P The chiral phosphine oxide compound has a product yield of 96% and an enantioselectivity ee value of 99%, and a diastereoselectivity dr value of greater than 20:1. The application adopts an asymmetric desymmetrization strategy, uses a Heck reaction to start and a Sonogashira reaction to end a cascade reaction, simultaneously constructs P The chiral and quaternary carbon chiral center has mild reaction conditions, simple operation and good substrate universality, provides a compound skeleton with diversity, and is successfully applied to a palladium-catalyzed asymmetric allyl substitution reaction as a chiral ligand.

The invention discloses an alkynyl modified diethylstilbestrol benzoxazine monomer as well as a preparation method and application thereof, and belongs to the technical field of resin synthesis. The diethylstilbestrol, 3-aminophenylacetylene and paraformaldehyde are used as raw materials to successfully prepare the benzoxazine monomer through a solvent-free method, and the preparation method comprises the following steps: mixing diethylstilbestrol, 3-aminophenylacetylene and paraformaldehyde; and carrying out heating reflux, cooling, dichloromethane extraction, reduced pressure evaporation and ethanol recrystallization to obtain a white solid benzoxazine monomer. The method has the advantages of cheap and easily available raw materials, simple synthesis steps, short reaction time and high product purity, and can be used for large-scale production. The prepared benzoxazine monomer is polymerized at a high temperature to obtain alkynyl modified diethylstilbestrol benzoxazine resin, and the alkynyl modified diethylstilbestrol benzoxazine resin shows excellent heat resistance and flame retardance.

The invention belongs to the technical field of chemical analysis and detection. The invention provides a platinum complex fluorescent probe as well as a preparation method and application thereof in detection of water. The chemical formula of the platinum complex fluorescent probe is C23H16ClN3Pt; the preparation method comprises the following steps: 1, under the protection of argon, mixing terpyridine, potassium tetrachloroplatinate, deionized water and dimethyl sulfoxide in a round-bottom flask, heating, stirring, carrying out reflux reaction, cooling to room temperature, adding concentrated hydrochloric acid, carrying out suction filtration to obtain a precipitate, and drying to obtain Pt-Cl; 2, Pt-Cl, phenylacetylene, cuprous iodide, N, N-dimethylformamide and triethylamine are mixed into a round-bottom flask, then argon is pumped and replaced for multiple times, after a reaction, suction filtration is conducted, precipitates are obtained, washing and drying are conducted, and the catalyst is obtained. The platinum complex fluorescent probe is applied to detection of water and has the advantages of specific selectivity, high sensitivity, wide detection concentration range and the like, so that the detection can better meet the current requirements.

The invention discloses a synthetic method of a modified mesoporous material. The synthetic method comprises the following steps: S1, reacting p-bromophenol with dicyandiamide to obtain an intermediate; s2, adding phenol and the intermediate into a reaction container, heating for melting, adding a sodium hydroxide solution, dropwise adding a formaldehyde solution, and performing reflux reaction to obtain a phenolic resin precursor; s3, dropwise adding diluted hydrochloric acid into the reaction solution to adjust pH to be neutral, performing rotary evaporation to remove water, dissolving with ethanol, adding a template agent F127 into the reaction solution, heating to dissolve the template agent F127, mixing and stirring at normal temperature, pouring on a glass plate, evaporating at room temperature, transferring into a drying oven, and curing to obtain ordered mesoporous phenolic resin; taking out, adding into methanol, dispersing and reducing, taking out and drying to obtain the modified mesoporous material. The invention provides the synthetic method of the modified mesoporous material, and the prepared modified mesoporous material can be used for catalytic synthesis of cinnamic acid from phenylacetylene and carbon dioxide, and has excellent catalytic performance and high recycling rate.

The invention discloses a Pd / 3-CN polymer catalyst as well as preparation and application thereof. The preparation method of the Pd / 3-CN polymer catalyst comprises the following steps: fully mixing cyanuric chloride, 3, 5-diamino-1, 2, 4-triazole, potassium carbonate and potassium tetrachloropalladate, uniformly grinding, transferring the obtained solid powder into a hydrothermal reactor, reacting at 80-160 DEG C for 12-24 hours, washing the obtained solid, performing Soxhlet extraction, and drying to obtain the Pd / 3-CN polymer catalyst. The Pd / 3-CN polymer catalyst is obtained. The invention provides the application of the Pd / 3-CN catalyst in the reaction of preparing the styrene compound by hydrogenation of the phenylacetylene compound, and the Pd / 3-CN catalyst can realize high phenylacetylene compound conversion rate and high styrene compound selectivity within a short reaction time.

The invention relates to the technical field of batteries, in particular to a silicon-carbon composite material and a lithium ion secondary battery. The silicon-carbon composite material comprises silicon-carbon particles and an aromatic polymer coating layer on the surface, and a monomer of the silicon-carbon composite material is selected from at least one of aniline, pyrrole, thiophene, 3, 4-ethylenedioxythiophene and phenylacetylene. The silicon content of the central area of the silicon-carbon particle is higher than that of the edge area, in the cross section scanning electron microscope energy spectrum of the silicon-carbon composite material, the silicon content of the central area is x0, the silicon content of any point on the edge is x1, a is equal to x1 / x0, and 0.8 < = alt; 1; the distance from the center of the silicon-carbon particle to the edge is R, the silicon content at a position 0.5 R away from the center of the silicon-carbon particle is x2, and x2 is greater than (x1 + x0) / 2; in a small-angle XRD (X-Ray Diffraction) spectrum of the silicon-carbon composite material, a first characteristic peak exists at 4-5 degrees, and the half-peak width is 0.05-0.6 degree; comprising the silicon-carbon composite material disclosed by the invention is high in cycle retention rate and good in low-temperature performance.

The invention relates to the field of oilfield chemical industry. The invention relates to a temporary plugging agent, in particular to a temperature-resistant and compression-resistant temporary plugging agent and a preparation method and application thereof. The temperature-resistant and compression-resistant temporary plugging agent comprises the following raw material components in parts by weight: 60-80 parts of polyimide; 5-10 parts of calcium carbonate nanofibers of which the surfaces are assembled with amphiphilic block copolymers; 0.2 to 4 parts of an auxiliary agent; wherein the polyimide is prepared by taking biphenyl tetracarboxylic dianhydride, p-phenylenediamine and phenylacetylene phthalic anhydride as polymerization reaction raw materials; the amphiphilic block copolymer assembled on the surface of the calcium carbonate nanofiber is polystyrene-b-polyacrylic acid. The temperature-resistant and compression-resistant temporary plugging agent provided by the invention has excellent high temperature resistance, compression resistance and plugging capacity, can be quickly hydrolyzed and crushed after temporary plugging is finished, can realize quick plugging removal, and is suitable for a high-temperature and high-pressure mining environment with the formation temperature (use environment) of 281-295 DEG C and the formation pressure of more than or equal to 130 MPa.

This invention belongs to the field of polymer composite materials technology, specifically relating to a self-lubricating polyimide resin based on a perfluoroether bond network and carbon dot reinforcement, its preparation method, and applications. The invention involves mixing carboxyl-functionalized carbon dots, an ether-containing aromatic diamine, and a polar aprotic solvent to obtain a carbon dot-diamine pre-assembled system, which is then polymerized with a perfluoroaromatic dianhydride to obtain a linear polyamic acid solution. This linear polyamic acid solution is then reacted with a phenylacetylene-containing active end-capping agent to obtain a polyamic acid solution with a three-dimensional network structure. Finally, the polyamic acid solution with the three-dimensional network structure is cured in a protective gas atmosphere to obtain a self-lubricating polyimide resin. The self-lubricating polyimide resin provided by this invention achieves a synergistic improvement in load-bearing capacity, wear resistance, and structural stability under high temperature and high load conditions, and can be widely applied in aerospace high-temperature bearings, high-load sealing rings, wear-resistant coatings for extreme conditions, and high-temperature sliding components.

The invention belongs to the technical field of photocatalytic materials, and particularly relates to a method based on one-step in-situ synthesis of a copper cyanophenylacetylene / copper phenylacetylene (CN-PhCCu / PhCCu) homogeneous heterojunction composite photocatalyst and application. The homogeneous heterojunction composite photocatalyst with a compact interface structure is synthesized in situ in one step under a mild condition by regulating and controlling the ratio of copper cyanophenylacetylene (CN-PhCCu) to copper phenylacetylene (PhCCu). The heterojunction can effectively promote exciton dissociation and photo-induced electron delocalization, remarkably inhibit charge recombination and improve the utilization efficiency of visible light. Experiments show that the composite photocatalyst shows excellent degradation performance on various water pollutants such as diclofenac (DCF) under irradiation of visible light, and has the advantages of high degradation efficiency, wide pH application range, strong coexisting ion interference resistance and the like. The method disclosed by the invention is simple in process and mild in condition, and provides a new material and technical support for efficient visible light driven water body pollution control.

The application discloses a room-temperature phosphorescent material of a phenylacetylene node-substituted pyrene derivative and a preparation method thereof. The pyrene is used as a substrate, and phenylacetylene is selectively substituted at a node (2 position) of the pyrene. Compared with a pyrene derivative obtained by substituting phenylacetylene at an anti-node (1 position) of the pyrene, the pyrene derivative obtained by substituting phenylacetylene at the node destroys the conjugation of the substitution site, maintains the rotation freedom between the substituent and the pyrene core, thereby enhancing the spin-orbital coupling, and enabling the room-temperature phosphorescence of the pyrene derivative. The obtained room-temperature phosphorescent material has the advantages of high luminous efficiency and long lifetime.

The invention provides a modified polyether-ether-ketone resin composite material as well as a preparation method and application thereof, and belongs to the field of high-molecular polymer materials. The modified polyether-ether-ketone resin / glass fiber composite material with a continuous chemical gradient interface is prepared through the interface bonding design of the polyether-ether-ketone oligomer containing the phenylacetylene functional group, the respective plasticizing and co-extrusion composite process and the reverse gradient structure design with the hard outside and the tough inside; the composite material is used for a high-performance robot exoskeleton device, and the problems that the strength and toughness of a traditional composite material are difficult to maximize at the same time, layers of a multi-layer or gradient material are easy to strip and lose efficacy, and a high-performance complex component is tedious in preparation process and low in efficiency are solved. The composite material provided by the invention has excellent mechanical properties and anti-aging and anti-fatigue properties, shows certain heat resistance during high-temperature heating, and shows great application potential in the field of high-end medical devices.

This invention relates to a low-cost method and system for preparing PEEK materials, belonging to the field of plastics production technology. The method includes: collecting the required quantity and types of raw materials; determining the required quantity of raw materials based on the type of raw material and the required quantity; determining the required quantity of end-capping agent based on the required quantity of raw materials; selecting a type of detergent based on the type of raw materials and the required quantity; adding difluoromonomers and bisphenol monomers to an organic solvent based on the required quantity of raw materials, and adding a salt-forming agent for polymerization; adding a phenylacetylene end-capping agent based on the required quantity of end-capping agent to obtain an initial oligomer; and washing and drying the initial oligomer based on the type of detergent to obtain a self-heating crosslinkable PEEK oligomer. This invention effectively reduces the preparation cost of polyether ether ketone (PEEK).

The invention discloses a modified tetraphenylacetylene silane resin prepolymer and a preparation method thereof. Specifically, the invention discloses a modified tetraphenylacetylene silane resin prepolymer which is of a three-dimensional network structure and has a repeated structural unit shown in the specification. # imgabs0 #