523 results about "Glycidol" patented technology

The invention belongs to the technical field of recoverable epoxy resin, and relates to a degradable epoxy resin system material and application thereof, a body, a composite material and a recovery method thereof. The degradable epoxy resin system material comprises a first component and a second component, the first component comprises first epoxy resin and second epoxy resin, and the second component comprises a first curing agent, a second curing agent and an accelerant; the first epoxy resin is a mixture of one or more of glycidyl ether epoxy resin and glycidyl amine epoxy resin and accounts for 15-35% of the first component by mass, the second epoxy resin is selected from one or more of epoxy resin with the structure containing # imgabs0 #, and the second epoxy resin accounts for 60-80% of the first component by mass; the first curing agent is one or a mixture of more of alicyclic amines and accounts for 40%-60% of the second component by mass, the second curing agent is one or a mixture of more of polyether amines and accounts for 40%-60% of the second component by mass, and the accelerant accounts for 0.5%-3% of the second component by mass. The requirement for vacuum infusion of the wind power blade can be met.

The invention discloses an organic plugging agent, a preparation method thereof and application of the organic plugging agent to inhibition of SAGD steam cavity edge water invasion. The organic plugging agent is prepared from the following raw materials: epoxy resin, a curing agent, nano aerogel, mineral fibers, plant fibers, a reactive diluent, a heat stabilizer and water, the epoxy resin is at least one of glycidyl amine epoxy resin and alicyclic epoxy resin; the curing agent is at least one of amino resin, dicyandiamide and hydrazide; the heat stabilizer is at least one of thiourea, sodium thiosulfate and cobalt chloride. The organic plugging agent is excellent in high temperature resistance, mineralization resistance and plugging performance, the organic plugging agent, nitrogen and an inorganic plugging agent are injected into a water plugging system of an SAGD steam cavity edge well in a slug mode, the organic plugging agent is applied to SAGD high-temperature and high-leakage well conditions, and the SAGD production effect can be effectively improved.

The invention discloses a waterproof anticorrosive coating and a preparation method and application thereof, and relates to the technical field of coatings, and the waterproof anticorrosive coating is prepared from the following raw materials in parts by weight: 30-40 parts of carboxyl-terminated hyperbranched polyester resin, 20-30 parts of carboxyl-terminated functional polyamide, 10-15 parts of hyperbranched polyurethane containing epoxy groups, 15-20 parts of filler, 1-3 parts of (3, 6-diamino acridine-9-yl) boric acid, 1-3 parts of 1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5-trimethyl-1, 3, 5- the component A is prepared from the following components in parts by weight: 3-5 parts of 2, 3, 5-triglycidyl-S-triazinetrione, 1-2 parts of a coupling agent, 0.8-1.2 parts of a flatting agent and 0.6-1.3 parts of a defoaming agent; the carboxyl-terminated functional polyamide comprises a structural unit introduced by the following monomers: N-(4H-1, 2, 4-triazole-4-yl) diphenylamine-4, 4 '-dicarboxylic acid, and 3, 3'-diamino-4, 4 '-difluorodiphenyl sulfone. The coating is good in waterproof and anti-corrosion performance, high in adhesive force with a base material, sufficient in solvent resistance and aging resistance and long in service life.

The invention relates to the technical field of surfactants, and discloses a preparation method of a modified polycarboxylate surfactant and application of the modified polycarboxylate surfactant in pesticide preparations. 3-hexene-1, 6-diamine and epoxy chloropropane are used as raw materials, 1, 6-tetraglycidylamine-3-hexene is obtained through ring-opening and ring-closing reactions, 1, 6-tetraglycidylamine-3-hexene is utilized twice, and the yield of the 1, 6-tetraglycidylamine-3-hexene is increased. The preparation method comprises the following steps: sequentially reacting 2, 3, 4, 6-tetraglycidylamine-3-hexene with sodium hydrogen sulfite and phosphoric acid to obtain tetrasulfonate hexene and tetraphosphate hexene, and copolymerizing the tetrasulfonate hexene and the tetraphosphate hexene with acrylic acid and methacrylate to obtain the modified polycarboxylate surfactant. The modified polycarboxylate surfactant prepared by the preparation method disclosed by the invention has excellent dispersing performance, heat storage stability and relatively high suspension rate.

The invention relates to a degradable epoxy resin composite material with an adjustable curing speed, and a preparation method and a mild total recycling method thereof. Existing degradable epoxy resin has the problems of high cost, harsh degradation conditions and the like, and is difficult to meet the requirements of different application scenes on curing speed and temperature at the same time. The invention provides an epoxy resin composite material which comprises curing agent components (an epoxy resin amine curing agent and an ester-containing polythiol curing agent) and epoxy resin components (glycidyl ether epoxy resin, glycidyl amine epoxy resin and glycidyl ester epoxy resin). The cured composite material can be fully recycled through catalytic degradation under mild conditions by using a lewis acid and an amino group breaking ester bond mechanism, and the degradation product can be directly used as a curing agent, a toughening agent and a chain extender. The epoxy resin composite material disclosed by the invention not only has adjustable curing speed and high use performance, but also realizes environmental friendliness and resource recycling, and provides a new solution for sustainable development of epoxy resin.

The invention provides a modified amine curing agent, a preparation method, epoxy resin anticorrosive paint and application, and belongs to the technical field of paint. The modified amine curing agent provided by the invention is prepared from preparation raw materials including alicyclic diamine, m-xylylenediamine, a first glycidyl ether reagent, a second glycidyl ether reagent and a glycidyl ester reagent through amination reaction, the alicyclic diamine contains at least one primary amine group; the first glycidyl ether reagent is ethylene glycol diglycidyl ether and / or bisphenol A type diglycidyl ether; and the second glycidyl ether reagent is 1, 4-butanediol diglycidyl ether and / or C12-14 glycidyl ether. The modified amine curing agent is combined with the curing characteristics of amide and phenolic aldehyde amine, the epoxy resin anticorrosive paint prepared from the modified amine curing agent has a proper curing speed, the adhesive force of a cured coating is high, the anticorrosive effect is good, and the epoxy resin anticorrosive paint is particularly suitable for a high-humidity environment and an underwater environment.

The present invention relates to the technical field of surfactants, and discloses a preparation method of a modified polycarboxylate surfactant and its application in pesticide preparations. The present invention uses 3-hexene-1,6-diamine and epichlorohydrin as raw materials, and obtains 1,6-tetraglycidylamine-3-hexene through ring opening and ring closing reactions. 1,6-tetraglycidylamine-3-hexene is used twice to react with sodium bisulfite and phosphoric acid in sequence to obtain tetrasulfonate-based hexene and tetraphosphate-based hexene, and then the two are copolymerized with acrylic acid and methacrylate to obtain a modified polycarboxylate surfactant. The modified polycarboxylate surfactant prepared by the present invention has excellent dispersibility, heat storage stability and high suspension rate.

The invention discloses a harmonica-shaped tube and a preparation method thereof, a liquid cooling plate, a battery and electric equipment. The harmonica-shaped tube is made of a polyphenylene sulfide composition, and the polyphenylene sulfide composition comprises polyphenylene sulfide resin and a toughening agent; the flexibilizer includes a copolymer of an olefin and a glycidyl ester. According to the application, the polyphenylene sulfide composition is used as the material of the harmonica-shaped tube, so that the occurrence of the conditions that the extruded material is easily broken, the extrusion process is not smooth and the like in the extrusion molding process of the harmonica-shaped tube is reduced; the harmonica-shaped tube has good mechanical strength, deformation resistance, corrosion resistance, heat resistance, heat dissipation performance, creep resistance and the like, the risk that cracking occurs when the harmonica-shaped tube is extruded in the working condition using process is reduced, and the production capacity and the product quality are improved.

The invention provides impact-resistant high-toughness plastic as well as a preparation method and application thereof, and relates to the technical field of high polymer materials. Comprising the following raw materials in parts by weight: 35-45 parts of hydroxyl-terminated hyperbranched polycarbonate, 15-25 parts of LDPE (Low-Density Polyethylene) resin, 8-12 parts of inorganic filler, 4-6 parts of isocyano ethyl methacrylate, 1-3 parts of bis (1-vinyl imidazole-2-) ketone, 1-3 parts of bis (trimethylsilylated) vinyl phosphate, 1-3 parts of 1, 3, 5-triglycidyl-S-triazinetrione, 1-3 parts of 3, 3 '-diamino-4, 4'-diphenyl-1, 3, 4-triazole-2-ketone, 1-3 parts of 1, 3, 5-triazole-2-ketone, 1-3 parts of 1, 3 '-trimethylsilylated vinyl phosphate, 1-3 parts of 2, 3'-diphenyl-1, 3, 4, 5- The material is prepared from the following components in parts by weight: 1-3 parts of 4, 4 '-difluorodiphenyl sulfone, 2-4 parts of a coupling agent, 0.5-1.5 parts of an antioxidant, 0.8-1.2 parts of a compatilizer, 0.7-1 part of a catalyst and 0.8-1 part of an initiator. The plastic has the advantages of favorable mechanical properties, favorable heat aging resistance, favorable impact toughness, favorable flame retardancy and favorable environmental friendliness.

The invention relates to the technical field of fabric preparation, in particular to environment-friendly breathable polyester silk fabric and a preparation process thereof. The preparation method comprises the following steps: preparing an epoxy polyurethane emulsion by taking glycidyl as an end-capping reagent; eugenol and phenyl dichlorophosphate are used as raw materials to react, and m-chloroperoxybenzoic acid is used as an oxidizing agent to prepare an epoxy flame retardant; the preparation method comprises the following steps: carrying out reaction on N, N-diethylaminopropyl methyl dimethoxy silane and epoxy chloropropane to obtain epoxy organosilicon quaternary ammonium salt; mixing the epoxy-based polyurethane emulsion, the epoxy-based flame retardant, the epoxy-based organosilicon quaternary ammonium salt and the curing agent, and modifying the polyester silk; preparing bio-based spinning fibers from a mixed solution of a carboxymethyl cellulose solution and a chitosan solution through an electrostatic spinning technology, and then blending the bio-based spinning fibers with the modified polyester to obtain the polyester fabric. The polyester silk fabric prepared by the method has good flame retardant property, antibacterial property and air permeability, and part of materials are renewable materials, so that the polyester silk fabric is economical and environment-friendly and meets the requirement of green development.

The invention relates to the technical field of epoxy splicing adhesives, in particular to a high-performance prefabricated part epoxy splicing adhesive and a preparation method thereof.The epoxy splicing adhesive comprises a component A and a component B. The component A is prepared from 3%-8% of polyether polyol, 2%-4% of hydrophobic fumed silica, 0.1%-1% of a silane coupling agent, 0.01%-0.5% of a defoaming agent, 50%-75% of modified quartz sand, 1%-5% of color paste and the balance epoxy resin; the modified quartz sand is prepared by grafting an amino silane coupling agent on the surface of quartz sand, then reacting with polychlorophosphazene, and then reacting with glycidol; the component B comprises the following components in percentage by weight: 0.2-4% of color paste, 1-5% of hydrophobic fumed silica, 0.1-1% of an amino silane coupling agent, 10-25% of 0.5 mm quartz sand, 40-60% of 0.1 mm quartz sand and the balance of a modified amine curing agent; the preparation method has the advantage that the mechanical strength and the bonding strength of the epoxy splicing adhesive are improved.

The invention discloses a high-molecular-weight phosphamide aggregate flame retardant and a preparation method thereof.The method comprises the steps that phosphoryl dichloride compounds and piperazine anhydrous serve as raw materials, an amino-terminated phosphamide polymer is synthesized through a condensation reaction, and the phosphamide polymer flame retardant is obtained. The high-molecular-weight phosphamide aggregate flame retardant is obtained through a ring-opening reaction of amino-terminated groups and epoxy groups between the high-molecular-weight phosphamide aggregate flame retardant and triglycidyl isocyanurate. Compared with an existing small-molecule flame retardant, the flame retardant is higher in thermal stability, better in compatibility with a high polymer material matrix, not prone to migration and capable of achieving synergistic flame retardance due to the fact that the flame retardant contains phosphorus and nitrogen structural units at the same time, and when the prepared flame retardant is added into TPU, PC, EP, PET and other transparent matrixes, the flame retardance is improved. The flame retardant property of the transparent base material can be improved, and meanwhile, good mechanical property and high light transmittance can be kept. In addition, the preparation method disclosed by the invention is simple and easy to control, high in yield, wide in source of required raw materials, easy for industrial production and wide in industrial application prospect.

The invention relates to an selective dry film for a circuit board and a preparation method of the selective dry film. The selective dry film for the circuit board comprises the following components: acrylic resin, an active monomer, modified boron nitride, hyperbranched polyether, an auxiliary agent and a solvent, wherein the modified boron nitride is obtained by reacting a silane coupling agent, trifluoromethacrylic acid and glycidyl methacrylate with boron nitride. The hyperbranched polyether is a polymer of glycerol and glycidyl. Materials such as acrylic resin are adopted as main components and compounded with modified boron nitride, so that compatibility and stability among the components are improved, more active groups are introduced, a firmer cross-linked structure is obtained, the strength of the dry film is further improved, and improvement of properties such as adhesive force and precision is facilitated; and the method has important significance on development and popularization of selective dry film products.

A composition for the surface treatment of a polymer material includes a hyperbranched polyglycerol comprising a glycidol-derived repeating unit and an unsubstituted or substituted acrylate group at least at one end thereof. The composition has the effect of suppressing fibrosis, thrombus formation, or inflammatory cell adsorption by preventing proteins from being adsorbed to the surface of a polymer material that is surface-treated with the composition or an in-vivo implantation material including a polymer material.

The present invention belongs to the technical field of waterborne polyurethane, and specifically relates to a method for synthesizing an internally cross-linked cationic waterborne polyurethane emulsion. The method comprises the following steps: 1) reacting glycidol and diethanolamine until the infrared spectrum analysis shows that the glycidol and diethanolamine are at 908 cm ‑1 and 845cm ‑1 The epoxy groups disappear, the reaction is stopped, and the product EDEOA, a tertiary amino crosslinking agent, is obtained as a light yellow viscous liquid; 2) polyol and diisocyanate are added to a reactor and heated and kept warm under stirring for reaction; 3) solvent, tertiary amino crosslinking agent, tertiary amino small molecule alcohol amine chain extender, solvent and catalyst are then added to react to obtain a polyurethane intermediate; 4) a neutralizing agent is then added to the reaction system for neutralization reaction, and the temperature is lowered after the reaction is completed; 5) water is added to quickly disperse the mixture uniformly, and the solvent is removed in vacuo to obtain a waterborne polyurethane emulsion. The present invention mainly solves the technical problems existing in the synthesis of cationic waterborne polyurethanes, such as poor emulsion stability, low film mechanical properties, and poor water and solvent resistance.

The invention relates to the technical field of high polymer materials, in particular to polyolefin thermoplastic elastomer / silicone rubber thermoplastic vulcanized rubber as well as a preparation method and application thereof. According to the invention, the polyolefin thermoplastic elastomer grafted silane or / and the polyolefin thermoplastic elastomer grafted maleic anhydride / glycidyl ester terpolymer, the platinum catalyst and the inhibitor are added during blending and dynamic vulcanization of the silicone rubber and the polyolefin thermoplastic elastomer to regulate and control the dynamic vulcanization process; therefore, the thermoplastic vulcanized rubber with ideal mechanical properties is obtained. The polyolefin thermoplastic elastomer / silicone rubber thermoplastic vulcanizate provided by the invention is high in strength, good in elasticity, good in toughness, smooth in surface, fine in phase state, good in somatosensory compatibility and good in skin touch, and also has good stain resistance, sweat resistance, yellowing resistance and ultraviolet resistance.

The inorganic quick-setting filling material comprises a material A and a material B. The material A is prepared from the following components in parts by weight: 25-35 parts of sulphoaluminate cement, 30-40 parts of blast furnace slag, 10-20 parts of waste gypsum, 1-3 parts of recycled alumina fiber, 5-10 parts of volcanic ash and 0.8-1.2 parts of (3, 6-diamino acridine-9-yl) boric acid. The material B is prepared from the following raw materials in parts by weight: 4 to 6 parts of functional water-soluble resin, 1 to 2 parts of sodium 3-(N-morpholinyl)-2-hydroxypropanesulfonate, 0.5 to 0.8 part of sucralose, 0.1 to 1 part of sodium lignin sulfonate, 0.8 to 1.2 parts of 1, 3, 5-triglycidyl-S-triazinetrione and 0.1 to 0.5 part of sodium N-(trimethoxysilylpropyl) ethylenediamine triacetate. The material is good in rapid hardening effect, high in compressive strength, good in flame-retardant and antistatic performance and long in service life.

The invention relates to the technical field of preparation of copper-clad plates, and discloses a preparation method of a phosphorus-containing flame-retardant halogen-free copper-clad plate, which comprises the following steps: uniformly stirring and mixing bisphenol A type epoxy resin, linear phenolic resin, phosphorus-containing tetraglycidyl ester and the like, smearing the mixture on E-glass fabric, baking to obtain prepregs, overlapping eight prepregs, coating copper foils on the two surfaces, and drying to obtain the phosphorus-containing flame-retardant halogen-free copper-clad plate. According to the preparation method, bisphenol A type epoxy resin is taken as matrix resin, linear phenolic resin is taken as a curing agent, phosphorus-containing tetraglycidyl ester is added, flame-retardant elements and a heat-resistant structure contained in the phosphorus-containing tetraglycidyl ester are utilized, the flame-retardant halogen-free copper-clad plate is obtained, and the flame-retardant halogen-free copper-clad plate is obtained. The flame retardant property, the heat resistance and the mechanical property of the copper-clad plate material are improved.

The invention discloses waterborne epoxy resin, a coating and a preparation method and application thereof, and relates to the technical field of high polymer materials. The water-borne epoxy resin has a specific structure, the structure contains units of glycidol, bisphenol A and fluorophthalic anhydride, the water-borne epoxy resin does not contain chloride ions and can be used for preparing low-chlorine, low-sulfur and low-lead water-borne epoxy coatings, the corrosion resistance of coatings formed by the water-borne epoxy coatings is improved, the service life of the coatings formed by the water-borne epoxy coatings is prolonged, and the service life of the coatings is prolonged. The obtained coating is improved in acid and alkali resistance, water resistance and salt spray resistance, has good adhesive force, is suitable for preparing the coating for stainless steel, and can effectively prevent free chloride ions from damaging a stainless steel passive film protective layer.

The invention relates to the technical field of chemical detection, in particular to a sample pretreatment method and a GC-MS (Gas Chromatography-Mass Spectrometer) method for simultaneously detecting glycidol and monochloropropanol in heated cigarette aerosol. The sample pretreatment method for simultaneously detecting the glycidol and the monochloropropanol in the heated cigarette aerosol comprises the following steps: capturing particulate matters in the heated cigarette aerosol; mixing the trapping material with ethyl acetate and an internal standard substance, extracting to obtain an extracting solution, and diluting with n-hexane; adding heptafluorobutyrylimidazole to perform derivatization reaction, washing with water after the derivatization reaction is completed, and drying to obtain a solution to be detected. According to the present invention, ethyl acetate is adopted for extraction, and detection analysis can be performed through dilution, HFBI derivatization, water washing and drying, such that the sample pretreatment step is substantially simplified, and the analysis sensitivity and the accuracy of the simultaneous detection of the three compounds such as the glycidyl, the 3-chloro-1, 2-propylene glycol and the 2-chloro-1, 2-propylene glycol can be easily improved.

The invention relates to the field of biomedical polymer materials, and discloses a preparation method of high-viscosity photo-crosslinking sodium hyaluronate hydrogel, which comprises the following steps: dissolving sodium hyaluronate in deionized water / N, N-dimethylformamide to obtain a sodium hyaluronate solution; mixing the sodium hyaluronate solution and the conjugated diene glycidyl ester / N, N-dimethylformamide solution to obtain a pre-formed sodium hyaluronate glue solution; composite antibacterial microspheres and a photoinitiator are added into the preformed sodium hyaluronate glue solution, a photo-crosslinking reaction is performed, conjugated diene glycidyl ester is prepared from raw materials including n-butyllithium, ethyl acetate, 2, 3-dibromo-1-propylene, vinyl magnesium chloride, sodium hydroxide and glycidol, and the conjugated diene glycidyl ester is prepared from raw materials including sodium hyaluronate, sodium hyaluronate and sodium hyaluronate. According to the preparation method disclosed by the invention, the modification reaction and photo-crosslinking time is shortened through the grafting of conjugated diene glycidyl ester, the viscosity of the hydrogel is greatly improved, and the antibacterial property of the hydrogel is improved through the addition of the composite antibacterial microspheres.

The invention belongs to the field of chemical engineering, and relates to a process device and method for continuously synthesizing glycidyl (3-chloro-1, 2-propylene glycol and sodium hydroxide (hereinafter referred to as NaOH) as raw materials). The device comprises a raw material feeding pump, a heat exchanger, a micro-reactor, a delay tube reactor 1, a neutralization micro-reactor and a delay tube reactor 2 which are sequentially in fluid communication through pipelines, the heat exchangers are divided into two groups, one group is used for heat exchange of 3-chloro-1, 2-propylene glycol solution, and the other group is used for heat exchange of alkaline solution. According to the method, a 3-chloro-1, 2-propylene glycol solution and a sodium hydroxide solution (NaOH) are adopted as raw materials, glycidol is continuously prepared through a microchannel reactor, on the basis, an acid-base neutralization reaction can be carried out in situ according to needs to remove redundant alkali, redundant heat generated by the acid-base neutralization reaction is absorbed through a low-temperature material, and energy consumption is reduced; the product is analyzed by gas chromatography, and the generated glycidol does not have hydrolysates or auto-polymerization products, so that the product selectivity is higher.

Challenges are to provide an epoxy resin composition for RTM which achieves both viscosity stability at the time of injection and stiffness at the time of demolding, and a cured resin of which is superior in balance among elastic modulus under wet and heat conditions, heat resistance under wet conditions, and fracture toughness, and to provide a large fiber-reinforced composite material having a high Vf and including the epoxy resin composition. Provided is an epoxy resin composition for RTM including an epoxy resin and a curing agent component, containing the following components [A] and [C] as the epoxy resin, containing the component [B] as the curing agent component, and containing 50 to 85 parts by mass of the component [A] in 100 parts by mass of the epoxy resin, [A] Tetrafunctional glycidyl amine type epoxy resin [B] a curing agent that is liquid at 150°C [C] Aniline type epoxy resin represented by Formula (I): (In Formula (I), R1 and R2 each represent at least one selected from the group consisting of aliphatic hydrocarbon groups having a carbon number of 1 to 4; n is an integer of 0 to 4; and m is an integer of 0 to 5; when n or m is 2 or more, R1 and R2 each may be the same or different at each occurrence; X represents -O- or -S-).

The invention discloses modified epoxy resin suitable for oven forming and a preparation method and application thereof, and belongs to the technical field of resin-based composite materials. The modified epoxy resin comprises the following raw materials in parts by mass: 45-60 parts of bisphenol A epoxy resin; 10 to 15 parts of glycidyl amine tetrafunctional epoxy resin; 15 to 20 parts of glycidyl ester type trifunctional epoxy resin; 10 to 16 parts of a toughening agent; 40 to 45 parts of 4, 4 '-diaminodiphenyl sulfone; the toughening agent is thermoplastic phenolphthalein polyaryletherketone resin or thermoplastic phenolphthalein polyethersulfone resin, and the obtained modified epoxy resin has similar viscosity-temperature characteristics, highest exothermic temperature and relatively long gelation time as MTM45-1 oven molding resin applied in airbus certification, and is suitable for being used in preparation of oven molding prepregs. And the obtained oven molded prepreg has good stability, and the difference of products in each batch is small.

The invention relates to the field of resin coatings, and particularly discloses a coating containing a resin composition as well as a preparation method and application of the coating. The coating containing the resin composition is prepared from the following raw materials: the resin composition, a curing agent and an auxiliary material mixture, and the weight ratio of the resin composition to the curing agent to the auxiliary material mixture is 100: (30-50): (50-150). Wherein the resin composition is formed by compounding triglycidyl isocyanurate, bisphenol F type episulfide resin and tetraglycidyl amine type epoxy resin. The preparation method comprises the following steps: respectively adding the auxiliary material mixture into the resin composition and the curing agent according to a certain ratio, uniformly mixing, and then mixing to finally obtain the coating containing the resin composition, the test shows that the coating has good bonding strength, high temperature resistance, acid corrosion resistance, rapid cooling resistance and rapid heating performance, the surface drying time meets the construction requirement, and the coating has good application prospects. The coating can be applied to the inner wall coating of the wet desulphurization chimney.

The invention relates to the technical field of electrolyte, in particular to a thioether cross-linked solid polymer electrolyte membrane as well as a preparation method and application thereof. The preparation method comprises the following steps: taking N, N-dimethylformamide, respectively adding 3, 6-dioxa-1, 8-octane dithiol and triglycidyl isocyanurate, and uniformly stirring to obtain a mixed solution; adding bis (trifluoromethylsulfonyl) imide lithium into the mixed solution, putting magnetons on a magnetic stirrer, and completely dissolving the magnetons to obtain a precursor solution; and pouring a proper amount of the precursor solution into a polytetrafluoroethylene mold, spreading, and carrying out cross-linking polymerization in a blast oven to form the film. The three-dimensional thioether cross-linked network structure has a large number of weakly coordinated thioether groups, dissociation of lithium salt can be promoted, a large number of free Li < + > is generated, the number of Li < + > is increased, meanwhile, the crystallinity of a polymer is remarkably reduced, the ionic conductivity is improved, the mechanical stability of a film can be improved, and the service life of a battery is effectively prolonged.

The invention relates to the technical field of high polymer materials and protective coatings, and discloses a single-layer anti-ultraviolet heavy-duty powder coating as well as a preparation method and application thereof. The preparation method of the single-layer anti-ultraviolet heavy anti-corrosion powder coating comprises the following steps: adding carboxyl polyester resin, triglycidyl isocyanurate, modified nano silicon dioxide, modified chitosan, 2-(2H-benzotriazole-2-yl)-4, 6-di-tert-pentylphenol, bis (2, 2, 6, 6-tetramethyl-4-piperidinyl) sebacate, flaky aluminum powder, zinc phosphate, BYK-3920, 2-hydroxy-1, 2, 4-triazole-2-yl)-1, 3, 4-triazole-2-yl)-1, 3, 5-triazole-2-yl)-1, 3, 5-triazole-2-yl)-1, 3, 5-triazole-2-yl)-1, 3, 5-triazole-2-yl)-1, 3, 5- The preparation method comprises the following steps: stirring and mixing 2, 2-diphenylethanone and gamma-aminopropyltriethoxysilane at room temperature at 300-350rpm for 10-15min to obtain a mixture, extruding the mixture through a double-screw extruder at the extrusion temperature of 110-120 DEG C and the screw rotation speed of 450-500rpm, and grinding to obtain the single-layer anti-ultraviolet heavy-duty anticorrosive powder coating. The single-layer anti-ultraviolet heavy anti-corrosion powder coating can be applied to metal base material protection. The coating prepared by the invention has good ultraviolet resistance and corrosion resistance.

The invention discloses a high-strength self-degradable gel temporary plugging agent and a preparation method thereof, and relates to the technical field of oil-gas field development. The temporary plugging agent is prepared by the following steps: firstly, reacting a diprimary amine compound with unsaturated glycidyl to prepare a multi-arm cross-linking agent, then reacting an acrylamide monomer, an acidic monomer, a rigid monomer and a 2-methacryloyloxyethyl phosphorylcholine monomer under the action of the multi-arm cross-linking agent and an initiator, and after the reaction is finished, crushing, drying and granulating to obtain the temporary plugging agent. The high-strength self-degradation gel temporary plugging agent prepared by the invention not only has relatively high strength, but also can be self-degraded, and the permeability recovery rate of a reservoir after degradation is relatively high, so that the influence on the reservoir is relatively small.

The invention provides a preparation method of a single-ended vinyl hyperbranched polyether macromonomer, which can be applied to the technical field of hyperbranched polyether synthesis. The method comprises the following steps: carrying out ring-opening polymerization reaction on any one of an epoxy group-containing vinyl monomer, a hydroxyl group-containing vinyl monomer or a carboxyl group-containing vinyl monomer and glycidol in the presence of a catalyst and a polymerization inhibitor to form the single-ended vinyl hyperbranched polyether macromonomer with an amino group, ester group or ether group structure. The invention also provides a single-ended vinyl hyperbranched polyether macromonomer product.

The invention provides a high-flame-retardant burnthrough-resistant PC alloy and a preparation method thereof. The PC alloy comprises the following components: branched PC resin with a special blocking rate, 4-10 parts of aryl p-toluenesulfonate and glycidyl ester, wherein the blocking rate of the branched PC resin is 85-95%. The heat resistance, melt strength and burnthrough resistance of the PC alloy are remarkably improved, the heat deformation temperature is increased to 132 DEG C from 122 DEG C, the needle flame S.2 burnthrough time is increased to 150 s or above from 15 s, high flame retardance and burnthrough resistance of a PC product are achieved, and meanwhile the original mechanical performance and thermal performance of PC resin are not affected.