761results about How to "Small volume change" patented technology

The present invention discloses a preparation method of a complex lithium negative pole of a solid state battery, and belongs to the technical field of electrochemistry and new energy resources. The preparation method mainly comprises the steps: depositing lithium metal on three-dimensional carbon material or foam porous material gaps by using a heat infusing melting method or an electrodeposition method to obtain the complex lithium negative pole, wherein the application of a three-dimensional framework plays two roles, namely, providing adequate space for pre-storing lithium in the preparation process; providing a carrier for receiving metal lithium in a battery circulation process. The complex lithium negative pole can be widely applied in lithium metal batteries such as lithium ion batteries, lithium-air batteries, lithium-sulfur batteries, and solid state batteries. In the assembled symmetric solid state battery, under large electric current density of 5mA cm-2, a stable voltage decay (200mV) can still be kept after circulation for 100 times, in the battery circulation, the growth of lithium dendrites can be inhibited and the pole volume change can be stabilized, and the advantages of being good in circulation stability, and long service life can be realized; in the present invention, a carrier material is rich, and low in price; the process is controlled, the cost is low, and the batch production can be realized.

A silicon composite comprises silicon particles whose surface is at least partially coated with a silicon carbide layer. It is prepared by subjecting a silicon powder to thermal CVD with an organic hydrocarbon gas and / or vapor at 900-1,400° C., and heating the powder for removing an excess free carbon layer from the surface through oxidative decomposition.

A reaction-bonded alpha-alumina filter element is provided. The filter element includes a monolith of porous material having multiple passageways extending from one end face to an opposing end face. The monolith is extruded from a mixture containing at least aluminum metal and alumina powders in a proportion such that on sintering the volume change of the monolith is minimized. The filter body can be used as a filter or as a membrane support for crossflow or dead end flow filter elements. A method for making the filter element is also provided.

The invention discloses a preparation method of a nano Ni3S2 material and belongs to the field of novel energy resources and electrochemistry. The preparation method of the nano Ni3S2 material is characterized by synthesizing the nano Ni3S2 material by taking a Ni net with a three-dimensional porous structure by virtue of a solvothermal method. A nano Ni3S2 active substance formed during the solvothermal process is directly loaded on an upper matrix of the Ni net, so that the active substance Ni3S2 is in relatively firm contact with a Ni net of a current collector; gaps of the porous Ni net can effectively buffer the volume change of the Ni3S2 in the processes of removing and embedding lithium, so that the cycle stability of the composite material can be improved; meanwhile, by virtue of a three-dimensional conductive network of the Ni net, the electronic conductivity of the composite material can be improved, so that the rate performance of the material is improved. The preparation method of the nano Ni3S2 material is simple, green, free from pollution, low in cost and suitable for industrial production. The Ni3S2 material prepared by adopting the method is small in particle size and uniform in particle distribution; according to an electrode prepared from the material, a polymer adhesive and a conductive agent do not need to be added in the electrode; the electrode has the high electrochemical performance and can be widely used in the fields of various portable electronic devices, electric automobiles, aeronautics and astronautics, and the like.

The invention relates to a two-dimensional transition metal carbon (nitrogen) compound and two-dimensional transition metal sulfide nano-composite powder, and a preparation and application thereof. The nano-composite powder is formed by the uniform scattered recombination of a two-dimensional transition metal carbon (nitrogen) compound nanosheet and a two-dimensional transition metal sulfide nanosheet, wherein the percentage of the mass of the two-dimensional transition metal sulfide to the total mass of the nano-composite powder is 10%-99%. The method comprises the steps: enabling the steady suspension liquid of the two-dimensional transition metal carbon (nitrogen) compound nanosheet and the suspension liquid of the two-dimensional transition metal sulfide nanosheet are mixed according to a proportion; carrying out cooling and drying after supersonic mixing, and then obtaining the nano-composite powder. The nano-composite powder is simple in preparation, is safe and high in efficiency, is low in cost, remarkably irons out the defects of conductivity of the two-dimensional transition metal sulfide, and can regulate the conductivity through proportion change. The nano-composite powder serves as a negative electrode of a lithium ion battery and the electrode material of a supercapacitor, is good in application prospect in the field of energy storage devices, and is better in electrochemical performance than the two-dimensional transition metal sulfide.

The invention provides a lithium ion battery cathode material and a preparation method of the lithium ion battery cathode material as well as a lithium ion battery. The lithium ion battery cathode material comprises an inner core, a middle layer outside the inner core and an outer shell wrapping the middle layer, the inner core is Si-C particles, the middle layer is a foam layer, the outer shell is an amorphous carbon layer and the Si-C particles are formed by Si particles and C materials. Compared with the prior art, a middle carbon foam layer existing between the Si-C particle inner core and the amorphous carbon outer shell can form an conductive network structure, thus improving conductivity of a material and buffering enormous volume change of Si particles in the charge-discharge processes; and the amorphous carbon outer shell layer can maintain the core-shell structure of the cathode material, and the cladding layer of the core-shell structure can buffer the volume change, improve cycling stability of electrodes, reduce contact between active substances and an electrolyte, improve first coulombic efficiency of an electrode, prevent nanoparticle aggregation and enhance electrode conductivity.

A negative electrode for a rechargeable lithium battery and a rechargeable lithium battery including the same are provided. The negative electrode for a rechargeable lithium battery includes a current collector, and a negative active material layer on the current collector. The negative active material layer includes an interpenetrating network, and a negative active material in the interpenetrating network. The interpenetrating network is formed by cross-linking a first polymer having a hydroxyl or amine group and a second polymer having a carboxylic acid group. The negative electrode for a rechargeable lithium battery minimizes volume expansion and imparts good cycle-life characteristics and initial formation efficiency.

The invention discloses a spherical silicon-oxygen-carbon negative electrode composite material, which is of a three-layer structure comprising an inner layer, an intermediate layer and an outer layer, wherein the inner layer is an SiOx / graphite substrate; the intermediate layer is an amorphous carbon coating layer; the outer layer is a carbon nanotube coating layer; the mass of the inner layer SiOx / graphite substrate accounts for 80%-90% of total mass of the spherical silicon-oxygen-carbon negative electrode composite material; the mass of the intermediate layer amorphous carbon accounts for 5%-10% of total mass of the spherical silicon-oxygen-carbon negative electrode composite material; and the outer layer carbon nanotube accounts for 5%-10% of total mass of the spherical silicon-oxygen-carbon negative electrode composite material. The grain diameter of the adopted SiOx substrate is smaller than 5 microns; the grain diameter is relatively small; intercalation and deintercalation of active substances are facilitated; higher specific capacity can be obtained; meanwhile, a dispersing agent is added when an SiOx sample is ground; and condition that the SiOx with a relatively small grain diameter is agglomerated in quantity to affect the performance is prevented.

The invention puts forwards a preparation method of a lithium ion battery porous silicon carbon composite negative material. The prepared porous silicon carbon composite material simultaneously has the characteristics of high capacity and excellent circulating stability. Micron silicon and nanometer aluminum powder are promoted to be compounded by utilizing a high-energy ball milling method, a porous silicon material can be formed through acid etching, and through a porous structure, the volume change of silicon in the discharging process is relieved to a great extent. Meanwhile, the stress generated by the volume change of the silicon can be effectively buffered through taking graphite as a dispersion matrix and in combination with a secondary surface amorphous carbon coating technology of the composite material, so that the circulating stability of the material is improved. The preparation method of the material has the advantages of simplicity, low cost and easiness in industrial production.

The invention provides a lithium ion battery cathode material, comprising graphene, nanometer silicon particles distributed in a graphene lamellar structure, and net-shaped carbon materials distributed between the graphene lamellar structure and the nanometer silicon particles. According to the invention, the graphene has a good lamellar structure, nanometer silicon particles are distributed in the graphene lamellar structure, and net-shaped carbon materials are distributed between the graphene lamellar layer and the nanometer silicon particles. According to the lithium ion battery cathode material provided by the invention, carbon materials between the graphene lamellar layer and the network structure are in tight contact with the nanometer silicon particles, thereby improving conductivity of the cathode material, and at the same time, effectively buffering enormous volume change of silicon particles, thus the lithium ion battery cathode material has good cycle performance.

The invention relates to a lithium ion battery composite cathode material and a preparation method thereof, which belongs to the technical field of lithium ion battery. The invention aims at improving the cycle performance of silicon cathode material at the same time when keeping the high ratio volume of lithium ion battery silicon cathode material. The proposal of the invention is that silica-based material coated by disordered carbon is treated with surface modification processing by utilizing lithium salt, namely, the lithium salt is coated on the surface of Si / G / DC (silicon / graphite / disordered carbon) to be prepared into the composite cathode material, therefore, the lithium-embedding and removing depth of the silicon can be effectively controlled, and the material is the lithium ion battery composite cathode material which has high specific capacity and good cyclical stability; furthermore, the material is safe and pollution-free, and presents higher thermal stability in various lithium salt electrolytes and solvents.

The invention provides a lithium ion battery cathode material and a preparation method of the lithium ion battery cathode material. The lithium ion battery cathode material comprises an inner core and an outer shell wrapping the inner core, a hollow layer exists between the outer shell and the inner core, the inner core is made of a Si-C composite material, the outer shell is made of a C composite material, and the C composite material is formed by a C material and a first amorphous carbon precursor. Compared with the existing Si-C composite material, the hollow layer between the inner core Si-C composite material and the outer shell C composite material can buffer enormous volume change of Si particles in the discharge process, thus endowing the cathode material with good cycle performance; and at the same time, the outer shell can be buffer volume change, reduce stress, improve cycling stability of electrodes, reduce contact between active substances and an electrolyte, improve first coulombic efficiency of an electrode, prevent nanoparticle aggregation and enhance electrode conductivity.

The invention relates to the field of lithium ion battery electrode materials, in particular to a graphene-coated silicon nanoparticle with a novel structure, and a preparation method thereof. The graphene-coated silicon nanoparticle is characterized by being formed by a reduced graphene oxide / carbon shell coating an outer layer, a silicon nanoparticle core located in the reduced graphene oxide / carbon shell, and a cavity layer between the reduced graphene oxide / carbon shell and the silicon nanoparticle core. Compared with the prior art, according to the graphene-coated silicon nanoparticle provided by the invention, the thickness of a surface oxidation layer of a silicon particle is easy to control; surface oxidation silicon powder is dispersed in a solvent easily, and hydroxy on the surface of the particle enables the particle to be combined with a modifier easily; graphene coating the particle surface helps increase electric contact between particles as well as between the particle and a current collector, and is beneficial for electron transfer in a composite material to reduce impedance; carbon produced through high-temperature pyrolyzing of a modifier carbon chain and graphene jointly form a shell with a certain strength, and a stable SEI can be formed favorably.

The invention discloses a polymer composite solid electrolyte and a preparation method and application thereof. The polymer composite solid electrolyte is prepared from polyphenylene sulfide, a lithium salt and an organic quinones electron acceptor and is taken as a polymer composite solid electrolyte of a lithium-sulfur battery, the polymer composite solid electrolyte, carbon black and elemental sulfur are fabricated to a composite sulfur electrode material, and thus, a novel lithium-sulfur battery system is formed. The high-molecular polymer composite solid electrolyte provides a relatively good lithium ion migration passage, the lithium ion conductivity of a composite positive electrode material is improved, the high-molecular polymer composite solid electrolyte has certain rigidity and toughness, the volume change of a positive electrode after charge and discharge of the lithium-sulfur battery is buffered, the discharge specific capacity of the lithium-sulfur battery is improved, and the cycle lifetime of the lithium-sulfur battery is prolonged.

The invention discloses an asphalt pavement repair material, and belongs to the field of engineering materials. The asphalt pavement repair material is prepared from 20-60 parts of monomers of thermosetting polymers and / or prepolymers of the thermosetting polymers, 2-8 parts of an antioxidant, 1-8 parts of an accelerant, 10-30 parts of an admixture, 5-60 parts of the thermosetting polymers, 10-40parts of an initiator, 10-20 parts of a reinforcing agent, 1-60 parts of a diluent and 10-40 parts of aggregates. The asphalt pavement repair material has the advantages of being high in condensationrate, strength, waterproofness and abrasion performance and capable of repairing pavement and getting the traffic to move again in 30 minutes and making construction easy. According to a pavement repaired with the asphalt pavement repair material, the compressive strength can reach 100 MPa, the wet wheel abrasion value is smaller than 800 g*m<-2>, and the load wheel adhesion sand amount water immersion 1d is smaller than 450 g*m<-2>.

The invention belongs to the technical field of material and energy and particularly relates to three-dimensional porous carbon-coated zinc selenide material for lithium ion battery anodes and a preparation method of the material. The preparation method comprises the specific steps of sintering zinc-based zeolite imidazate metal organic framework material (ZIF-8) as a precursor or template with selenium powder under the protection of an inert atmosphere at high temperature for a certain time, and carrying out synchronous selenization and carbonization to finally prepare the carbon-coated zinc selenide composite material. The composite material prepared herein and the preparation method thereof provide effective composition of zinc selenide and graphite carbon, the component ingredients generate great interfacial coupling effect, volume expansion effect of the zinc selenide material during charging and discharging can be effectively relieved and inhibited, the conductivity of the material is improved, and accordingly the composite material has very high specific capacity and excellent cycle stability and rate performance when applied as lithium ion battery anode material. The preparation process is simple, the preparation conditions are mild, and the cost is low.

The invention discloses a polypropylene material used for automobile bumpers and a preparation method thereof. The polypropylene material comprises polypropylene, thermoplastic elastomer, inorganic fillers, lubricants, antioxidants, coupling agents, volume stabilizer and light stabilizers. The invention has the preparation method that the inorganic fillers, the lubricants, the chemical inhibitors, the coupling agents, the volume stabilizers and the light stabilizers are added into a mixer for mixing and stirring, then the polypropylene and the thermoplastic elastomer are added into the mixture for mixing and stirring and are added into an extruder to be extruded for molding, so the polypropylene material is obtained. The invention has the advantages of high impact strength, excellent mechanical property, simple and practical preparation process and low cost, is suitable for industrial production and can be used for preparing the automobile bumpers.

The invention discloses a three-dimensional self-supported lithium-loving carrier-packaged metal lithium composite negative electrode and a preparation method thereof. The three-dimensional self-supported lithium-loving carrier-packaged metal lithium composite negative electrode comprises the following steps of 1) carbonizing melamine foam in an inertia atmosphere to obtain a nitrogen-rich lithium-loving three-dimensional self-supported carrier; and 2) packaging metal lithium in holes of the three-dimensional self-supported carrier to obtain the metal lithium composite negative electrode. Carbon sponge obtained by carbonization of melamine foam is used as a metal lithium carrier, and the metal lithium composite negative electrode has effects of guiding metal lithium to be uniformly deposited and preventing dendrite from being generated. Lithium-loving functional groups are uniformly arranged on the carrier, a lithium-loving coating layer is deposited on a hole surface of the carrier, the lithium-loving performance of the carrier is improved, the volume change of the metal lithium electrode during the circulation process is effectively buffered, moreover, the lithium-loving functional groups uniformly arranged on the three-dimensional carrier are used as active sites for metal lithium deposition, the nucleation over-potential is reduced, uniform nucleation of metal lithium can be effectively controlled, so that the dendrite generation is prevented.

The invention provides a conductive coating material for a lithium ion battery. The conductive coating material comprises components in parts by weight as follows: 100 parts of a conductive agent, 20-150 parts of a binding agent, 0-30 parts of polyvinylpyrrolidone and 500-10,000 parts of water, wherein in terms of 100 parts by weight of the conductive agent, the conductive coating material further comprises components of 70-100 parts by weight of conductive carbon black and 0-30 parts by weight of carbon nano-tubes. The invention further provides a preparation method of the conductive coating material and the lithium ion battery adopting the conductive coating material. The conductive coating material is safe and environment-friendly, has good stability after dispersed and can improve the electrochemical performance of the lithium ion battery remarkably.

The invention discloses a graphene-based protection layer on the surface of a metal lithium anode and a corresponding lithium-sulfur battery. A composite protection layer containing a graphene material is built on the surface of a metal lithium anode of a lithium-sulfur battery through in-situ electrochemical reaction. Materials required for preparing the protection layer are divided into inorganic compounds and organic polymer materials; a layered stack structure of the graphene in the protection layer is capable of inhibiting the lithium anode from generating lithium dendrites in repeated deposition and dissolution processes; and inorganic components between graphene sheets are subjected to in-situ electrochemical reaction with the lithium anode after being infiltrated through an electrolyte to form a lithium ion channel between graphene layers, thereby isolating the contact of the lithium anode and the electrolyte and playing a role in protecting a cathode. Relatively high capacitydeveloping performance and stable cycle performance can be obtained through applying the lithium anode with the graphene-based protection layer to a lithium-sulfur battery system.

The invention discloses a negative pole made of a silicon / graphite nanosheet composite material of a lithium ion battery, which comprises the following components in percentage by mass: 85 to 95 percent of nanometer silicon powder-graphite nanosheet composite material, and 5 to 15 percent of polyvinylidene fluoride, wherein the content of nanometer silicon powder is between 20 and 75 percent in the nanometer silicon powder-graphite nanosheet composite material. A preparation method thereof comprises the steps of: preparing graphite oxide, preparing a mixed dispersion system of the nanometer silicon powder and graphite oxide nanosheets; adding a reducing agent, namely hydrazine hydrate into the mixed dispersion system of the nanometer silicon powder and the graphite oxide nanosheets, and reducing the graphite oxide nanosheets into graphite nanosheets to obtain a composite material of the nanometer silicon powder and the graphite nanosheets; and fully mixing the composite material of the nanometer silicon powder and the graphite nanosheets with N-methylpyrrolidone sol of the polyvinylidene fluoride, blending the mixture into paste, evenly coating the paste onto a copper coil, and performing drying and roller compaction. The negative pole made of the silicon / graphite nanosheet composite material of the lithium ion battery has high electrochemical capacity and good cycling stability performance.

The invention relates to the preparation and application of a covalent organic skeleton / titanium carbide nano-sheet composite material, and belongs to the technical field of development and research of new energy materials. The Ti3C2 nano-sheets with single layer or few layers are mixed with organic monomer and solid catalyst and sealed in a vacuum quartz tube, and a covalent organic skeleton / Ti3C2 nano-sheet composite material is obtained by the ionothermal method. The covalent organic skeleton / Ti_3C_2 nanocomposite was coated on aluminum as working electrode after carrying sulfur, lithium metal is used as counter electrode and reference electrode, organic microporous membrane is used as separator, organic solution is used as electrolyte, and a button cell is assembled in the glove box filled with high purity argon. Compared with the prior art, the present invention can be used as a two-dimensional electrode material, is widely used in the energy field such as lithium sulfide batteryand the like, and has excellent charging / discharging performance.

The invention discloses a vanadium phosphate sodium composite nano porous cathode material and a method for preparing the material by using a freeze drying method, which belong to the technical fields of a cell material and its preparation method. The method comprises the following steps: adding a certain amount of a vanadium source in a mixed solvent of deionized water and hydrogen peroxide, after stirring the materials and dissolving the materials, adding a sodium source, a phosphorus source and a carbon source with a stoichiometric ratio to form a mixing solution; then refrigerating the prepared mixing solution in liquid nitrogen to a solid, then performing vacuum drying on the material in a vacuum freeze drier; and finally putting a precursor obtained after freeze drying in mixing gas of argon and hydrogen for calcining to obtain the vanadium phosphate sodium composite nano porous cathode material. The prepared vanadium phosphate sodium composite nano porous cathode material has a three-dimensional porous structure and large specific surface area, and thereby is in favor of infiltration and transmission of an electrolyte, active sites of an electrochemical reaction are multiple, and high specific capacity and good multiplying power performance can be displayed.

The invention relates to a preparation method of core-shell TiO2 / ZnO photocatalyst and the application thereof, which relates to the preparation method of a photocatalyst and the application thereof. The invention solves the problem that the valence band electron of the existing photocatalyst can transit onto a conduction band only under the excitation of ultraviolet radiation. The preparation method of the invention is that: 1. Zn(CH3 / COO)2 / 2H2 / O is mixed into a Polyvinyl alcohol solution and heated in step after being dried and then cooled down to room temperature; 2. tetrabutyl titanate, absolute ethyl alcohol and triethanolamine are mixed together and aged, then the product of the step 1 is added into the solution for dissolving following by drying and heat treatment. The core-shell TiO2 / ZnO photocatalyst prepared by the invention is painted on cross linked ethylene, layered perovskite, molten salt crystal water and salt or Al-Si material as thermal energy storage material. The electron of the TiO2 in the invention can transit onto the conduction band under common lighting condition, which leads photo electron to be effectively separated.

The invention discloses a high-performance silicon monoxide / amorphous carbon / graphite composite negative electrode material. The high-performance silicon monoxide / amorphous carbon / graphite composite negative electrode material comprises the following components in parts by weight: 5-7 parts of silicon monoxide, 1-2 parts of carbohydrate and 1-4 parts of natural flake graphite. The preparation method of the composite negative electrode material comprises the following steps of: mixing the materials; carrying out high-energy ball milling and high-temperature pyrolysis; and grinding and sieving to obtain the composite material. The composite negative electrode material is excellent in cycle performance and capacity performance, so that a certain feasibility choice is provided for practicability of the SiO negative electrode material. Moreover, the preparation method is simple to operate, environment-friendly, pollution-free and easy to popularize.

The invention discloses a lithium-sulfur battery positive-pole composite material with an imitated cellular structure and a preparation method thereof. In the positive-pole composite material, a conductive polymer film layer and nanometer oxide inlaid inside the conductive polymer film layer form a cell membrane, an elemental sulfur particle serves as a cell nucleus, and the three portions jointly form the imitated cellular structure. The composite material is prepared by conducting ultrasonic dispersion on the elemental sulfur particle and the nanometer oxide in water in the presence of a surface active agent, adding a conductive polymer monomer and an acid solution, performing even stirring and then adding an oxidizing agent to perform stirring reaction. The preparation method is simple in process, low in cost, low in energy consumption, controllable in sulfur content and good in repeatability and enables large-scale production to be easily achieved. The composite material is made into a lithium-sulfur battery positive pole, loss of active substances in the charging-discharging process can be effectively inhibited, improvement of the specific discharge capacity of a battery material and the utilization ratio of the active substances is facilitated, and accordingly the battery cycle performance is greatly improved.

The invention discloses a method for preparing a composite sodium negative electrode for a sodium-ion battery and belongs to the field of new energy materials. According to the method disclosed by the invention, metal sodium is deposited in gaps of a three-dimensional carbon material or a foamed porous material and other carriers through a hot infusion melting method or an electrodeposition method, so that the composite sodium negative electrode is prepared, wherein the three-dimensional carbon material is applied to providing a sufficient space for pre-stored sodium in the preparation process and providing a carrier for receiving the metal sodium in the battery cycle process. The composite sodium negative electrode can be widely applied to the sodium-ion battery, a sodium air battery, a sodium-sulfur cell and other sodium metal batteries, is assembled into a sodium-ion symmetric cell to still keep a stable voltage platform under high current density, is capable of inhibiting sodium dendritic growth and stabilizing volume change of the sodium electrode in the battery cycle process, and has the advantages of good cycling stability, long service life and the like. The method disclosed by the invention is rich and cheap in carrier materials, controllable in preparation process, low in production cost and capable of realizing batch production.

A fuel system for use in a combustion chamber of a compression ignition internal combustion engine comprises a pump arrangement having a pump chamber for fluid and a piston which is movable outwardly from the combustion chamber in response to pressure generated within the combustion chamber as a result of combustion so as to pressurise fluid within the pump chamber. The system also includes a control valve assembly for controlling the supply of fluid that is pressurised within the pump chamber to an accumulator volume. In one particular aspect, the invention provides a fuel system for use in an engine having at least two engine cylinders, comprising a first pump arrangement associated with one of the engine cylinders and a second pump arrangement associated with the other of the engine cylinders, each of the first and second pump arrangements having a pump chamber for fluid and a piston which is movable outwardly from the combustion chamber in response to pressure generated within the combustion chamber as a result of combustion so as to pressurise fuel within the pump chamber. At least one control valve assembly controls the supply of fluid that is pressurised within the pump chamber of at least one of the pump arrangements to an accumulator volume.

The invention discloses a method for preparing a linear polyurethane phase change material. The method comprises the following steps: dissolving polyethylene glycol and diisocyanate into solvent in inert atmosphere, reacting in the presence of optional catalyst, adding tertiary amine type chain extender containing hydroxyl for chain extension, adding an optional neutralizer for salt formation so as to obtain the linear polyurethane phase change material, wherein the molar ratio of the sum of hydroxyl of polyethylene glycol and hydroxyl of chain extender to the isocyanate group of diisocyanate is 1:1, the add amount of the catalyst accounts for 0-1% the total weight of the polyethylene glycol, diisocyanate and chain extender, the molar ratio of neutralizer to tertiary amine type chain extender is 0-1, and the molecular weight of the polyethylene glycol is higher than 2000. The linear polyurethane phase change material prepared by the method has a linear structure and large enthalpy of phase change, has a simple preparation method, is low in cost, has stable property, can be stored for long time, is not solidified and cross-linked, is easy to process and shape, and is beneficial to large-scale popularization and application.