983 results about "Polyamine" patented technology

Described herein are sorbents functionalized with polyamines having oxygen-containing units selected from carbonyl units, hydroxyl units, and combinations thereof, methods of making same, and methods of using same.

The invention discloses a colorful acid and alkali resistant laser printing ink and a preparation method thereof. The printing ink is composed of the following components in parts by weight: 0 to 30 parts of butanone, 10 to 30 parts of isopropanol, 2 to 6 parts of curing agent, 10 to 15 parts of pigment, and 10 to 30 parts of glycidyl ether epoxy resin. The glycidyl ether epoxy resin is adopted to produce the printing ink, aliphatic polyamine is further chosen as the curing agent, the acid and alkali resistant performance of the printing ink is strengthened through optimizing the formula, thus the shortage that the colorful laser printing ink is lost when being mixed with acid and alkali is overcome, moreover, the color of the laser printing product is more abundant, and the patterns are more clear.

The invention provides an antifouling self-cleaning fluorocarbon finish paint as well as a preparation method and application thereof, and particularly relates to the technical field of special coatings. The antifouling self-cleaning fluorocarbon finish paint is composed of a component A and a component B in a ratio of (80-87): 16, the component A is prepared from the following components in parts by weight: 560 to 580 parts of fluorocarbon resin, 30 to 35 parts of a first solvent, 20 to 40 parts of a second solvent, 180 to 220 parts of titanium dioxide, 90 to 110 parts of filler, 11 to 20 parts of a light stabilizer, 3 to 5 parts of a thickening agent and 13 to 28 parts of an auxiliary agent; the component B comprises the following components in parts by weight: 20-22 parts of fluorocarbon resin, 4-5 parts of a chain extender, 15-20 parts of a diamine curing agent, 15-20 parts of a polyamine curing agent and 25-35 parts of a second solvent. According to the finishing paint, on the basis of enhancing the self-cleaning capability, the weather resistance of a coating is improved, and the aging and damage of the coating are delayed, so that the service life of the coating is prolonged.

The invention discloses a two-phase absorbent and application thereof. The two-phase absorbent comprises the following components in percentage by mass: 10-35% of a main absorbent, 20-50% of a phase-splitting agent, 0-15% of an accelerant and 0-70% of water, wherein the total mass of the two-phase absorbent is 100%; wherein the main absorbent is polyamine, the polyamine contains more than three amino groups, more than three carbon atoms are arranged between the adjacent amino groups, and at least one of the more than three amino groups is a tertiary amino group; the phase splitting agent is an alcohol ether compound. The two-phase absorbent provided by the invention has better absorption performance, can reduce the generation of oxidative degradation, and has higher oxidation stability.

The invention discloses a polyamine type porous polymer as well as a preparation method and application thereof, and belongs to the technical field of synthesis of porous organic polymers. The specific method comprises the following steps: dispersing beta-mercaptoethylamine, a photoinitiator and a porous framework polymer with carbon-carbon double bond connection in a polar organic solvent; under the ultraviolet light initiation condition, the photoinitiator excites beta-mercaptoethylamine to generate sulfydryl free radicals, and the sulfydryl free radicals and the porous framework polymer with carbon-carbon double bond connection are subjected to an addition reaction; and washing and drying the product after the addition reaction to obtain the amino-modified polyamine porous polymer. The preparation method provided by the invention is rapid in reaction, extremely high in reactant utilization rate and simple in post-treatment, and the prepared polyamine type porous polymer has rich adsorption sites, good stability and excellent carbon dioxide adsorption performance, and can be applied to the field of carbon capture and the like.

The invention discloses a low-temperature curing high-throwing-power cathode electrophoretic coating and a preparation method and application thereof, and belongs to the field of automobile coating materials, the coating is composed of epoxy resin, a fluorosilicone copolymerization type epoxy modifier, a polyamino siloxane-acrylic acid hybrid and other components, and performance improvement is achieved through the synergistic effect of the two brand-new modifiers. Wherein the fluorine-silicon copolymerization type epoxy modifier is prepared by taking bisphenol A epoxy resin as a framework, introducing fluorine-containing alkyl and siloxane groups and carrying out ultraviolet reaction, so that the surface energy is reduced, and low-temperature crosslinking is promoted; the polyamido siloxane-acrylic acid hybrid takes siloxane as a core, and acrylic acid and polyamido are bridged through isocyanate, so that the crosslinking density and the water solubility are enhanced. When the coating is prepared, the two modifiers are mixed with epoxy resin, a solvent and the like, and the coating is prepared through dispersion and dilution. The coating can be cured at low temperature, so that a uniform thick film is obtained in an inner cavity of a complex workpiece, and meanwhile, the coating has excellent corrosion resistance and adhesive force and is suitable for efficient and environment-friendly coating of an automobile body and parts.

A separation membrane, a preparation method therefor and a use thereof in magnesium and lithium separation are provided. The separation membrane includes, in sequence, a base material layer, a porous support layer, a polyamide layer and a modification layer. Cross-linked polymers forming the modification layer has structural units provided by polyphenols and polyamines, at least some of the structural units provided by the polyphenols are connected to the polyamide layer via ortho positions of phenolic hydroxyl groups. The preparation method includes sequentially preparing the porous support layer, the polyamide layer and the modification layer on the base material layer. The method of preparing the modification layer includes under a first pressure, bringing one side of the polyamide layer into first contact with the polyphenol solution; then under a second pressure, bringing one side of the polyamide layer into second contact with the polyamine solution, to complete a self-assembly reaction.

The invention relates to the technical field of coatings, in particular to a corrosion-resistant coating material and a preparation method thereof. The corrosion-resistant coating material comprises the following components in parts by mass: 80-100 parts of epoxy resin, 5-20 parts of a modified phenolic aldehyde amine curing agent, 2-5 parts of a waterproof agent, 5-10 parts of a corrosion inhibitor and 40-55 parts of a lubricant. The modified phenolic aldehyde amine curing agent is obtained by carrying out Mannich reaction on phenol, thymol, aliphatic polyamine and formaldehyde. The phenol provides a rigid benzene ring structure, and endows a cured product with good heat resistance and chemical resistance. Thymol improves the flexibility and adhesive force of the cured product and enhances the hydrophobicity of the cured product at the same time. The epoxy resin and the modified phenolic aldehyde amine curing agent are polymerized, the waterproof agent, the corrosion inhibitor and the lubricant are wrapped, and the obtained coating material has good adhesive force and corrosion resistance.

The invention relates to a brand-new microbial natural metabolite, namely Fcl-8, which is derived from a fermentation solution of Xenorhabdius budapestensis XBD8, and is characterized in that the Fcl-8 is a new microbial natural metabolite, namely Fcl-8, which is derived from the fermentation solution of the Xenorhabdius budapestensis XBD8. The purified Fcl-8 is a snow white flocculent crystal and is very easy to dissolve in water, and the solid state of the purified Fcl-8 is as shown in Figure 1. The chemical structural formula of the Fcl-8 is as shown in a figure 2, the chemical formula is C57H102N14O12, the molecular weight is 1175.78744, and the typical secondary mass spectrum information of the Fcl-8 is as shown in a figure 3. The Fcl-8 is derived from a microbial natural metabolite, is novel in structure and high in biological activity, and has very high potential to be developed into a novel biopesticide.

The invention relates to a bionic strong acid-resistant nanofiltration membrane and a preparation method thereof, and the bionic strong acid-resistant nanofiltration membrane comprises a porous support layer and an active separation layer formed on the surface of the porous support layer, the active separation layer is a polymer network layer formed by carrying out interfacial polymerization reaction on a water-phase solution containing polyamine and an oil-phase solution containing polyacyl chloride on the surface of the porous support layer. The water-phase solution and / or the oil-phase solution also contains a bionic amphiphilic phosphate compound, the bionic amphiphilic phosphate compound participates in interfacial polymerization reaction through an active functional group in a molecular structure of the bionic amphiphilic phosphate compound, and the phosphate structure of the bionic amphiphilic phosphate compound is covalently connected into a skeleton of the polymer network layer. The preparation method has the beneficial effects that the bionic amphiphilic phosphate compound with a hydrophilic phosphate head, a hydrophobic alkyl tail and a reaction site is synthesized, so that the bionic amphiphilic phosphate compound is spontaneously and orderly arranged on a water / oil interface and participates in interfacial polymerization, the film forming uniformity is improved, the pore size distribution is narrowed, and the intelligent response characteristic is given to the film.

This anticorrosive coating composition comprises a main agent (I) and a curing agent (II), wherein: the main agent (I) contains an epoxy resin (a); the epoxy resin (a) contains at least one of a bisphenol A epoxy resin (a-11) and a novolac epoxy resin (a-12) each having a weight average molecular weight of 6,000-12,000; the curing agent (II) contains a polyamine (b) and an alkylphenol (c); the polyamine (b) contains an alicyclic polyamine (b-1) having a cyclic aliphatic hydrocarbon group to which an amino group is bonded and contains a non-alicyclic polyamine (b-2) having no cyclic aliphatic hydrocarbon group to which an amino group is bonded; at least one of the main agent (I) and the curing agent (II) includes a vinyl-based defoaming agent (d) that has a constituent unit derived from at least one monomer selected from the group consisting of alkyl (meth)acrylates, alkyl vinyl ethers, and olefins and that has a number average molecular weight of 30,000-100,000 or 300,000-2,000,000; the content of the alicyclic polyamine (b-1) is 30%-80% by mass of the solid content of the curing agent (II); the content of the non-alicyclic polyamine (b-2) is 2%-45% by mass of the solid content of the curing agent (II); the content of the alkylphenol (c) is 5%-60% by mass of the solid content of the curing agent (II); and the content of the vinyl-based defoaming agent (d) is 0.005-3 parts by mass with respect to 100 parts by mass of the anticorrosive coating composition.

The invention relates to the technical field of antistatic agents, and particularly discloses an oil product antistatic agent and a preparation method thereof. The modified polysulfone is obtained by mixing and treating the following raw materials in parts by mass: 35-40 parts of xylene, 20-25 parts of composite polyamine, 15-20 parts of polysulfone, 5-8 parts of oligomeric dopamine and 1-2 parts of an activating agent, the preparation method comprises the following steps: taking composite polyamine, mixing with oligomeric dopamine, dispersing with xylene, then adding an activator, stirring, then adding polysulfone, and continuously treating, thereby obtaining the product. The preparation method of the composite polyamine comprises the following steps: taking epichlorohydrin, dispersing, adding a mixed amine source, heating, adding sodium carbonate, continuously stirring, cooling, adding a deprotection agent, filtering after treatment, taking a liquid part, drying by distillation, washing, drying again, and grinding to obtain the composite polyamine. The oil product antistatic agent prepared by the invention has relatively strong antistatic capability and relatively long duration time, and can form a firmer double-electric-layer structure.

The invention relates to the technical field of carbon dioxide capture, and discloses a carbon dioxide absorbent and a preparation method thereof, and the carbon dioxide absorbent comprises the following components by weight: 10-15 parts of diethylenetriamine and 2-3 parts of modified mesoporous silica. According to the invention, through a synergistic adsorption mechanism of diethylenetriamine and modified mesoporous silica, a relatively good CO2 capture capability is realized; the cage-shaped structure of the modified mesoporous silica has a high specific surface area and ordered pore channels, and provides sufficient loading sites and diffusion channels for diethylenetriamine; meanwhile, an amino auxiliary (containing a plurality of primary amine and secondary amine groups) introduced in the modification process and a polyamine structure of diethylenetriamine form an amino cluster, and a better adsorption effect is achieved.

The invention discloses a polyamide acid-resistant nanofiltration membrane and arsenic removal application thereof in hair dye preparation. According to the amide acid-resistant nanofiltration membrane, a polyamine monomer and trimesoyl chloride are subjected to an interface reaction on an ultrafiltration supporting bottom membrane, and the polyamide acid-resistant nanofiltration membrane containing the Telogen structure is obtained. According to the method for removing the arsenic in the hydroxyethyl diphosphoric acid, a polyamide acid-resistant nanofiltration membrane containing a Troger structure is adopted for at least one time of filtration treatment, the concentration of arsenate in the hydroxyethyl diphosphoric acid after secondary filtration treatment is reduced to 4.60 mg / kg from 480.02 mg / kg, and the arsenic content of the hair dye prepared from the hydroxyethyl diphosphoric acid is smaller than 0.07 mg / kg. According to the polyamide acid-resistant nanofiltration membrane containing the Troger structure, which is obtained by adopting a limited preparation method, the acid resistance is greatly improved, the separation selectivity is higher, arsenic in hydroxyethyl diphosphate can be effectively removed, and the arsenic content in a hair dye is greatly reduced.

The invention relates to the technical field of membrane separation, and discloses a polythiourea composite nanofiltration membrane as well as a preparation method and application thereof. The composite nanofiltration membrane comprises a bottom layer, a porous support layer and a polythiourea separation layer which are arranged in sequence, wherein the polythiourea separation layer comprises a structural unit A from polyamine and a structural unit B from a polyisothiocyano compound; wherein the structural unit A and the structural unit B are connected through a structure shown in a formula I, Ar1 is a residue obtained after a reaction of a compound containing polyisothiocyano groups, and Ar2 is a residue obtained after a reaction of polyamine. The separation layer structure of the polythiourea composite nanofiltration membrane contains C = S bonds, a large number of hydrogen bonds can be formed, the polythiourea composite nanofiltration membrane has excellent chemical stability, the structural stability of the composite nanofiltration membrane in a strong acid environment is remarkably improved on the premise that the separation performance of the composite nanofiltration membrane is guaranteed, and the acid resistance of the composite nanofiltration membrane is improved.

The invention relates to absorbable adhesive styptic powder and a preparation method thereof, and the absorbable adhesive styptic powder is characterized in that the absorbable adhesive styptic powder is formed by cross-linking aldehyde polysaccharide and a polyamino compound through Schiff base reaction, the raw materials are selected from at least one of glucan, sodium carboxymethyl cellulose, sodium hyaluronate, chitosan and carboxymethyl starch; the polyamino compound is selected from at least one of polylysine, polypeptide, bovine serum albumin and polyamine; the styptic powder is porous particles with the particle size of 10-1000 meshes, is cured into gel within 10 seconds after being in contact with body fluid, and is completely degraded within 15-60 days. According to the scheme, the styptic powder has the advantages of rapid wet adhesion, controllable degradation and excellent processability, and is an urgent clinical demand.

The invention provides a functional nanofiber material as well as a preparation method and application thereof, and the preparation method comprises the following steps: (1) adding raw materials into water to form an electrostatic spinning solution; performing electrostatic spinning to obtain a nanofiber membrane; (2) cross-linking the nanofiber membrane in an organic solvent under the catalysis of acid to obtain a cross-linked nanofiber membrane; and (3) carrying out grafting reaction on the cross-linked nanofiber membrane in a polyamine cross-linking agent, and then reacting with a sulfur-containing reagent to obtain the functional nanofiber material, the functionalized nanofiber material prepared by the preparation method disclosed by the invention combines good biocompatibility of polyvinyl alcohol, high specific surface area and high porosity of nanofiber and a synergistic adsorption effect of the polyamine cross-linking agent and cysteine, and has the advantages of large adsorption capacity, high adsorption rate, strong selectivity, good biocompatibility, stable structure and the like; the heavy metal ions in the plasma can be efficiently and safely removed, and a plurality of defects of the existing adsorption material are overcome.

The present invention provides a method for removing a nitrosamine with high selectivity and high efficiency.　More specifically, the present invention provides a method for removing a nitrosamine, the method including a step in which a substance to be irradiated, which contains the nitrosamine, is irradiated with light in the presence of an aromatic polyamine and a photocatalyst.

The invention discloses a preparation method and application of a metal sulfide adsorbent for adsorbing iodine and methyl iodide. The preparation method comprises the following steps: uniformly mixing an antimony source, a sulfur source, a deep eutectic solvent, polyamine and water to obtain a mixed solution; and transferring the mixed solution into a high-pressure reaction kettle, sealing, carrying out hydrothermal reaction at 110-220 DEG C for 2-9 days, cooling to room temperature to separate out crystals, and filtering, washing and drying to obtain the metal sulfide adsorbent. The invention also discloses application of the metal sulfide adsorbent in adsorption of iodine and methyl iodide. The metal sulfide adsorbent disclosed by the invention has a good adsorption effect on iodine and methyl iodide, and compared with an ethylenediamine-oriented metal sulfide adsorbent, the diethylenetriamine-oriented metal sulfide adsorbent has higher adsorption capacity on iodine and methyl iodide.

The invention discloses a preserving fluid for stably preserving sample DNA at normal temperature and a preparation method thereof, and belongs to the technical field of biological sample preservation. The preserving fluid comprises a lysis system, a nucleic acid protection system and a buffering and stabilizing system, the cracking system comprises a composite surfactant and an enzymolysis auxiliary agent; the composite surface active agent is prepared from polyether polyol fatty acid ester and cocamidopropyl hydroxy sulfobetaine; the enzymolysis auxiliary agent comprises lysozyme Lyso-V and protease K; the nucleic acid protection system comprises a nitrogen heterocyclic polyamine-carboxylic acid derivative and dextran sulfate; the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N' ', N ''tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N''-triacetic acid, disodium ethylene diamine tetraacetate-nitrogen heterocyclic derivative, and diethylenetriamine pentaacetic acid-piperazine derivative, and the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N '', N'' tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N ''-triacetic acid. The buffering and stabilizing system comprises an amphoteric buffering agent and a polymer stabilizer; the amphoteric buffering agent comprises 2-(N-morpholino) ethanesulfonic acid and N-tri (hydroxymethyl) methylglycine.

The invention belongs to the technical field of membranes, and particularly relates to a composite membrane with polyfunctional group organic mesoporous nanoparticles as a middle layer and a preparation method of the composite membrane. The composite membrane is of a three-layer structure and comprises a porous supporting layer, a middle layer and a selective separation surface layer, the middle layer is polyfunctional group organic mesoporous nanoparticles with good water dispersibility and excellent stability, and the selective separation surface layer is polyamide; the preparation method comprises the following steps: loading organic mesoporous nanoparticles on the surface of the porous support layer to form the middle layer; and polymerizing on the surface interface of the middle layer to form a selective separation surface layer. The middle layer contains polyfunctional groups, can interact with a water-phase polyamine monomer and controls the diffusion of the monomer in an interfacial polymerization process, so that the structure of the selective polymer separation layer is regulated and controlled, and the surface appearance and thickness of the separation layer are optimized; due to the mesopore hydrophilic property of the middle layer, a rapid water transmission channel can be constructed, and the membrane flux is effectively improved. The composite membrane provided by the invention has excellent water flux, salt rejection rate and monovalent and divalent anion selectivity.

The invention discloses a low-viscosity ternary eutectic solvent as well as a preparation method and application thereof, and belongs to the technical field of CO2 absorbents. The low-viscosity ternary eutectic solvent is composed of polyamine hydrochloride, steric hindrance amine and organic alcohol, the polyamine hydrochloride has multiple active amino groups and is used for guaranteeing the high CO2 absorption rate and absorption load of the ternary eutectic solvent, the steric hindrance amine can inhibit formation of a hydrogen bond network due to the unique steric hindrance structure, and the high CO2 absorption rate and absorption load of the ternary eutectic solvent are improved. The organic alcohol can be used as a viscosity regulating agent, active hydroxyl of the organic alcohol can promote proton transfer in a CO2 desorption reaction, and the CO2 desorption efficiency is enhanced. The ternary eutectic solvent provided by the invention can still maintain a low-viscosity homogeneous liquid state after absorbing CO2, can effectively reduce the reduction of mass transfer efficiency caused by high viscosity, influence on contact with a target compound, heat transfer efficiency and the like, and solves the ubiquitous problems of overhigh viscosity and insufficient regeneration efficiency of the existing DESs system.

The invention relates to the use of an epoxy resin adhesive for bonding substrates at least partially coated with a cured epoxy resin adhesive, characterized in that the adhesive comprises a resin component comprising at least one epoxy resin and a curing agent component comprising at least one epoxy resin, the curing agent component comprises at least one amine having at least one aliphatic amino group wherein the amine is selected from the group consisting of polyetheramines and linear or branched but non-cyclic aliphatic polyamines wherein the amine comprises at least 50% by weight of all amine curing agents having at least one amine hydrogen contained in the curing agent component, the curing agent component is based on all amine curing agents in the curing agent component. The use according to the invention allows the adhesion of substrates at least partially coated with a cured epoxy adhesive, forming a stable weather-resistant adhesive connection, and is particularly suitable for repairing rotor blades in wind turbines.

[Problem] To provide: a flame retardant which has excellent flame retardancy and contains, as an active ingredient, an organic phosphoric acid compound reduced in environmental burden; a flame-retardant polyurethane resin composition containing the flame retardant; and a synthetic leather obtained using the flame-retardant polyurethane resin composition.　[Solution] A polyurethane resin composition containing a flame retardant that contains, as an active ingredient, an organophosphorus compound which is a salt obtained by reacting phytic acid with an aliphatic polyamine, preferably an aliphatic polyamine represented by R-(NH2)x (wherein R is a C2-C12 linear aliphatic hydrocarbon group and X is an integer of 2-4).　

The invention relates to a nanofiltration membrane and a preparation method thereof. The nanofiltration membrane sequentially comprises a supporting material and a membrane body from bottom to top, the base film is formed by a base film solution containing a polymer with a polyimide structure, a nano material and a silane coupling agent containing at least one functional group of a primary amino group, a secondary amino group and an epoxy group; the functional layer is formed by treating a prepolymer of aliphatic polyamine and aromatic polyisocyanate with more than three isocyanate groups with an aqueous solution containing hyperbranched polyamine and strong alkali and weak acid salt; the molar amount of the aromatic polyisocyanate having more than three isocyanate groups is excessive relative to the molar amount of the aliphatic polyamine, the prepolymer has unreacted isocyanate groups, the prepolymer is prepared at a temperature range of 10-20 DEG C, and the treatment is carried out at a temperature range of 50-80 DEG C. The nanofiltration membrane can tolerate a temperature of 70 DEG C or above and a high-concentration alkali of 20 wt% or above, and has excellent salt rejection rate and flux.

The invention discloses a microcapsule material, a microcapsule using the microcapsule material and a preparation method of the microcapsule, and relates to the technical field of daily chemical products. The microcapsule material comprises an addition polymer formed by a ring-opening reaction of epoxy resin and bio-based polyamine, poly (beta-amino ester) formed by a Michael addition reaction of acrylate and phenyl polyamine, and at least one cationic polymer containing quaternary ammonium groups. The microcapsule material shows certain biodegradability, the biodegradation rate of the microcapsule material exceeds 20% within 28 days, and the applied microcapsule can effectively meet the friction fragrance release performance requirement required by essence wrapping, so that after the obtained essence-encapsulated microcapsule is stored in a lotion at 45 DEG C for 28 days, the fragrance release performance of the microcapsule material is not influenced by the friction fragrance release performance, and the fragrance release performance of the microcapsule material is not influenced by the friction fragrance release performance. The excellent friction aroma releasing capability and the adhesion capability on the fabric can still be maintained, and the excellent thermal stability is shown.

The invention relates to a culture medium for high-density serum-free suspension culture of BHK-21 cells and application of the culture medium. The culture medium contains inorganic salt, amino acid, vitamins, energy substances, a buffer substance, an antioxidant, sterol, polyamine, an additive and an indicator, and the antioxidant comprises dihydrolipoic acid and S-acetyl-L-glutathione. According to the invention, the culture medium for serum-free suspension culture of the BHK-21 cells, which is clear in components and remarkable in culture effect, can be provided. The added dihydrolipoic acid and S-acetyl-L-glutathione are combined as antioxidants of the culture medium, so that the survival rate of BHK-21 cells cultured in the culture medium is improved while the oxidation resistance of the serum-free suspension culture medium is improved.

The application provides a reverse osmosis membrane and a preparation method and application thereof. The preparation method comprises the following steps: (1) polymeric reaction of a polyamine and a polyacyl chloride on a support membrane to form a polyamide layer on the support membrane; and (2) reaction of the polyamide layer prepared in step (1) and a benzene series A to obtain the reverse osmosis membrane; the benzene series A is a benzene series containing an amino group, an antibacterial group, a disulfide bond and a phenoxy group. The reverse osmosis membrane provided by the application has high flux and high desalination rate, and excellent oxidation resistance, antibacterial property and acid and alkali resistance.

The invention belongs to the technical field of carbon dioxide capture and separation, and particularly relates to a two-phase absorbent for capturing carbon dioxide as well as a preparation method and application thereof, and the two-phase absorbent comprises a polyamino compound, a compound containing amino and ether bonds, a phase splitting agent and water; wherein the compound containing the amido and the ether bond comprises a monoamine compound containing the ether bond and a polyamine compound containing the ether bond; the mass ratio of the monoamine ether bond-containing compound to the polyamine ether bond-containing compound is (0.1-5): 1. Compared with a traditional organic amine absorbent, the two-phase absorbent provided by the invention has the characteristic of high CO2 absorption capacity, and meanwhile, due to the fact that the two-phase absorbent can greatly reduce the volume of a regeneration solution, the regeneration energy consumption can be greatly reduced.

The invention provides a flexible chain cable reinforcing material and a preparation method thereof, flexible chain cable reinforcing material liquid injection equipment and a method for reinforcing a soft outburst coal seam, and belongs to the technical field of coal seam curing materials. The flexible chain cable reinforcing material provided by the invention comprises a material A and a material B which are subpackaged, wherein the volume ratio of the material A to the material B is 1: (0.8-1.2); the material A is prepared from components in percentage by mass as follows: 60%-75% of an epoxy modified polyurea semi-prepolymer, 12%-18% of nanoparticles, 10%-20% of a first flame retardant and 2%-3% of a catalyst; and the material B comprises the following components in percentage by mass: 45-65% of a polyamine curing agent, 25-40% of resin and 10-15% of a second flame retardant. The flexible chain cable reinforcing material provided by the invention is a mining intrinsic safety type rapid solidification high polymer material with high toughness and high strength, is used for reinforcing a soft outburst coal seam, can permeate into a deep crack of the soft outburst coal seam, and is simple to operate and good in safety.