2355 results about "Backbone chain" patented technology

The invention belongs to the technical field of anion exchange membranes, and relates to a cross-linked polyaromatic piperidine anion exchange membrane and a preparation method thereof. The exchange membrane structure comprises a copolymer structure of the following repetitive structural units, the selected rigid main chain polyaromatic hydrocarbon can ensure the mechanical strength of the anion exchange membrane, meanwhile, the toughness of the anion exchange membrane is further enhanced by adopting a cross-linked structure, and a formed cross-linked network can reduce swelling of the anion exchange membrane, so that the anion exchange membrane is more stable in performance. The mechanical performance is improved; according to the invention, ether-free skeleton polyaromatic hydrocarbon is selected as a main chain and has the characteristic of strong alkali-resistant stability, six-membered nitrogen heterocyclic ions are adopted as functional groups, and a large steric hindrance structure can hinder nucleophilic substitution and elimination reaction, so that the alkali-resistant stability of the anion exchange membrane is improved, and the service life of the anion exchange membrane is prolonged. And in the # imgabs0 #, X is equal to 0.05 to 0.15.

The invention provides a comb-shaped polymer binder, a pole piece and a battery, the comb-shaped polymer binder comprises an acrylate main chain, a flexible soft segment, a polar hard segment and a functional chain segment, the flexible soft segment, the polar hard segment and the functional chain segment are respectively grafted on the acrylate main chain, the flexible soft segment comprises an ether chain segment and / or an ester chain segment, the polar hard segment comprises a polar group and / or a first heteroaromatic ring group, and the functional chain segment comprises a functional group and a second heteroaromatic ring group. The functional chain segment comprises an aromatic ring group containing a pi-conjugated structure and / or a second heteroaromatic ring group containing a pi-conjugated structure. The comb-shaped binder adopts a structural design of'hard section anchoring + soft section buffering + functional side chain ', is helpful for enabling the binder to have high peel strength, stress buffering and electron conduction capabilities at the same time, is compatible with an existing wet coating-rolling process, is helpful for improving the peel strength and prolonging the cycle life of an electrode plate when being used for preparing the electrode plate, and is beneficial for improving the service life of the electrode plate. And the rate capability of the battery is improved.

The invention provides a novel polynorbornene anion exchange ionomer containing a polar functional group as well as a preparation method and application of the novel polynorbornene anion exchange ionomer. The polynorbornene has excellent thermal stability and chemical stability. Meanwhile, the AEI main chain of the polynorbornene has no aryl group, so that the adsorption influence caused by the aryl group is avoided. The synthesized addition polynorbornene AEI in the form of quaternary ammonium salt can be dissolved in a low-boiling-point solvent, and it is ensured that a membrane electrode can be prepared through a solvent casting method. Besides the solubility of the AEI, the addition polynorbornene-based AEI in the form of quaternary ammonium salt is modified by utilizing a thiol-ene click reaction, an anion exchange ionomer containing a polar functional group can be prepared, the interaction between the AEI and an electrolytic catalyst is improved, the reaction is simple and easy to operate, the universality is high, and the method is suitable for industrial production. And the current density in the AEMWE system containing the AEI can be effectively improved.

The invention discloses a modified organic silicon resin, a high-temperature-resistant coating and a preparation method thereof, the modified organic silicon resin is prepared by hydrolyzing at least two different siloxane monomers and then carrying out condensation reaction on the hydrolyzed siloxane monomers and at least one boric acid monomer, and the main chain of the organic silicon resin is of a heteroatom doped structure formed by a Si-O bond, a B-O bond and a B-O-Si bond; at 200-250 DEG C, the modified organic-inorganic high-temperature-resistant composite material is subjected to a self-crosslinking reaction. The high-temperature-resistant coating overcomes the defect that the high-temperature-resistant coating in the prior art cannot meet the high-temperature test, and avoids the defects that organic and inorganic high-temperature-resistant coatings crack, the impact resistance and hardness are not matched, the water resistance is poor, and the wear resistance is poor.

The invention provides a molecular identity authentication system and method based on DNA origami framework layered assembly. The molecular identity authentication system comprises a disclosed skeleton chain and a plurality of shared staple chains, the shared staple chain comprises staple chains shared by three groups of single bodies and staple chains shared in pairs, and the staple chains are used as secret keys to be distributed to three participants so as to prepare the three groups of single bodies respectively, and then the three groups of single bodies are combined and spliced into a tripolymer with a dot matrix pattern, so that multi-user collaborative layered chain type assembly is realized. According to the molecular identity authentication system based on DNA origami framework layered assembly, the system combination complexity is improved to the information theory security level, so that the biological information security protection capability is improved, and brute force cracking is prevented.

The invention discloses a hyperbranched water reducing agent for high-tensile wet joint UHPC (Ultra High Performance Concrete) as well as a preparation method and application of the hyperbranched water reducing agent, and belongs to the technical field of concrete admixtures. The preparation method comprises the following steps: mixing pentaerythritol and maleic anhydride, adding a catalyst p-toluenesulfonic acid, and carrying out an esterification reaction to prepare an esterification product; carrying out amidation reaction on the esterification product, diethanol amine and a catalyst sodium ethoxide to obtain a prepolymer; acrylic acid, maleic anhydride and the prepolymer are dissolved in deionized water, an initiator ammonium persulfate is added for a free radical copolymerization reaction, and a main chain polymer is obtained; carrying out phosphorylation reaction on the main chain polymer and phosphorus pentoxide to obtain a phosphorylated main chain polymer; the phosphorylated main chain polymer, methoxypolyethylene glycol and a catalyst p-toluenesulfonic acid are subjected to an etherification reaction, a hyperbranched comb-shaped polymer water reducing agent solution is obtained and then subjected to aftertreatment, and the water reducing agent is prepared. According to the hyperbranched comb-shaped polymer water reducing agent prepared by the preparation method disclosed by the invention, the problems of poor flowability and high viscosity of ultra-high performance concrete (UHPC) are solved by combining a linear side chain of a comb-shaped structure and a three-dimensional branch of hyperbranched topology.

The invention discloses a comb-type polyphosphate polymeric dispersant and a preparation method thereof, the dispersant is prepared by preparing a phosphate monomer from acrylate and phosphorus pentoxide, then copolymerizing the phosphate monomer with phenyl alkene or alkyl alkene, and finally adding alkali liquor for neutralization. A phosphate-polyether bifunctional side chain is introduced to a main chain, a phosphate group provides electrostatic repulsion, and a polyether group enhances steric hindrance, so that the dispersing agent can meet the requirements of strong adsorption and long-range stability at the same time, and a more durable and effective stabilizing effect is provided for a dispersion system.

The invention discloses a bidirectional reversible conversion method and system between a peptide molecule SMILES and a sequence expression. The core innovation lies in that a new sequence description syntax is defined to retain information of a polypeptide special bond and specific modification of amino acid; a main chain atom index and adjacency traversal topology identification algorithm is adopted, and end group and topology integrated detection and coding are carried out; a residue recognition algorithm for main chain cutting and template library matching is compatible with any standard or non-standard amino acid residues, an extensible end group library / monomer template library and an automatic increment mechanism, and automatic recognition and sequence annotation of S-S disulfide bonds; the invention relates to a high-fidelity assembly algorithm of HELM anchor points and topology aware cyclic peptide processing. The method solves the problems of incapability of supporting a complex polypeptide topological structure, poor reversibility, insufficient expansibility of a monomer library and the like in the prior art, can be widely applied to scenes of quantitative structure-activity relationship model construction, large-scale polypeptide data cleaning and the like, and has remarkable practicability and innovativeness.

The invention relates to the field of preparation of polyurethane damping materials, in particular to a preparation method of a repairable polyurethane damping material based on multiple hydrogen bonds and metal coordination. Compared with a traditional damping material, the damping material has a higher damping temperature range and has a good damping effect at the temperature of-20 DEG C to 60 DEG C. Multiple reversible hydrogen bonds are introduced through diamine containing amido bonds, the material is endowed with self-repairing and high mechanical strength, and damping and self-repairing performance is further enhanced through pyridine nitrogen atom metal coordination. Starting from molecular structure design, multiple hydrogen bonds and metal-ligand coordination bonds constructed on a polyurethane molecular main chain play a role in synergistic enhancement, energy can be effectively dissipated through dissociation and recombination of the multiple hydrogen bonds and fracture and association of the metal coordination bonds, and the energy consumption is reduced. The polyurethane material is endowed with excellent damping performance and self-healing capability by the dual dynamic action.

The invention discloses a dynamic borate bond-based self-healing polyacrylic acid binder and a preparation method thereof. The dynamic borate bond-based self-healing polyacrylic acid binder comprises a polymer main chain and a dynamic cross-linking agent, the dynamic cross-linking agent is a polyol compound containing at least two pairs of ortho-hydroxyl groups; the polymer main chain is formed by copolymerizing the following monomers: an acrylic structural monomer, the molar fraction of which accounts for 85-94% of the total monomer; a functional monomer containing a boric acid group, wherein the molar fraction of the functional monomer accounts for 3-8% of the total monomer; the mole fraction of the flexible monomer containing the acrylate group accounts for 3-8% of the total monomer. Various stresses generated by different negative electrode materials in circulation can be effectively adapted and buffered through a network formed by dynamic boric acid ester bonds and reversible fracture and combination of the boric acid ester bonds, so that the service life of the battery is generally prolonged, the working temperature range of the battery can be remarkably widened, the low-temperature discharge capacity can be remarkably increased, and the high-temperature cycle life can be prolonged.

The invention discloses a crown ether grafted polyarylether sulfone ion separation membrane as well as a preparation method and application thereof, and belongs to the technical field of ion separation membranes, collaborative optimization is realized through crown ether accurate grafting and ultrathin ordered membrane formation: a main chain of polyarylether sulfone is grafted with 4 '-aminobenzo-12-crown-4 to form an inherent channel adapted to Li, and the specific surface area of the main chain is increased; the ultrathin film is prepared by a water surface spreading method, and the ion transmission path is shortened. Finally, in a LiCl / MgCl system, Liion flux has high selectivity, high permeation-high selectivity cooperation is preliminarily realized, the chemical synthesis step can be amplified to a kilogram level, and after a DPAES-g-CE / dichloromethane solution is dropwise added to the water surface, the DPAES-g-CE / dichloromethane solution is rapidly spread to form a film without precise equipment; the raw materials are industrial-grade monomers and have no toxic residues, the membrane can be recycled and reused through dichloromethane, the equipment cost is reduced by about 90%, and industrialization is easy; the main chain of the polyaryl ether sulfone is high in rigidity and resistant to high temperature and chemical corrosion; crown ether grafting avoids molecular chain agglomeration, and the swelling rate is far lower than that of a traditional sulfonated membrane.

The invention relates to a composite binder, an electrolyte membrane, a preparation method and a battery. The composite binder comprises a binder main material and cross-linked molecules, the binder main material has a first functional group; the cross-linked molecule comprises a main chain and second functional groups, the main chain comprises a dynamic cross-linked structure sensitive to heat, the dynamic cross-linked structure comprises at least one of reversible chemical bonds and heat-sensitive functional groups, and the two ends of the main chain are provided with the second functional groups which are combined with the first functional groups in a reaction mode. The problem of poor mechanical property of the binder in the related art can be solved.

The invention discloses a durable low-surface-energy polymer modifier capable of freezing on the surface of a matrix and a preparation method thereof, the main chain of the durable low-surface-energy polymer modifier comprises a polydentate hydrogen bond monomer structure, and the end group of the polymer chain is a fluorinated structure. The durable low-surface-energy polymer modifier disclosed by the invention is co-mixed with matrix resin through a conventional processing and mixing means in a standard production process, and is migrated to the surface of a material in processing, heat treatment and use processes, so that the durable low-surface-energy polymer modifier can achieve multiple effects of water resistance, pollution resistance, dust prevention, anticoagulation, antithrombosis, antibiosis, self-cleaning and the like; the multidentate hydrogen bond monomer structure in the modifier structure realizes freezing of the modifier on the surface of matrix resin, so that the risk of elution and loss of the modifier is effectively reduced, the possibility of migration, washing or dissolution in blood is reduced, and the low surface energy durability effect of the matrix surface is enhanced.

The invention discloses a preparation method of a grafted and substituted thiophene polymer material, which comprises the following steps: mixing poly (3-hexylthiophene), a grafting monomer, a catalyst and an auxiliary agent, and heating for reaction to obtain the grafted and substituted thiophene polymer material, the structural formula of the grafting monomer is as shown in formula (I); wherein B is fluorine, chlorine, bromine or iodine, A is a carbon atom or a nitrogen atom, and R is cyano, formyl, methoxycarbonyl or; according to the method, pre-synthesis of complex functional monomers is avoided, the main chain of the poly (3-hexylthiophene) can be directly modified without using an expensive catalyst or ligand, the polymerization reaction of the poly (3-hexylthiophene) is not interfered, and meanwhile, the method has the advantages of simplified steps and low cost.

The invention relates to the technical field of polymer degradable materials, in particular to a biodegradable material as well as a preparation method and application thereof. The material takes modified polylactic acid as a main body, and an antioxidant, a plasticizer, a flame retardant and an inorganic filler are used as auxiliary materials in parts by weight. The method is characterized in that lactic acid and an epicatechin imidazole ammonium chloride polymer are polymerized under the catalysis of stannous octoate, and an epicatechin bioactive group is introduced into a polylactic acid main chain in a chemical bonding manner, so that the biodegradation rate, the mechanical property and the thermal stability of the material are remarkably improved. Bioactive substances and ionic groups in the material promote microbial degradation, and the material can be completely decomposed in a compost environment in a short time; meanwhile, the strength, the toughness and the high-temperature processability of the polylactic acid are effectively improved through molecular-level enhancement and an ionic cross-linking effect. The material can be widely applied to the fields of disposable tableware, food packaging films, degradable agricultural mulching films and the like.

The invention relates to a high-temperature-resistant polymer binder and a preparation method thereof. The binder is composed of a mixture of resin containing a siloxane unit polyimide main chain and an epoxy group side chain and tannic acid. Wherein the main chain containing siloxane and imide units endows the adhesive with excellent heat-resistant stability, excellent processability and excellent adhesion with glass and ceramic materials, and the adhesive can be cured at room temperature through the epoxy side group; the mixed tannic acid can form strong interface bonding with a polymer film and a metal material through a multiple hydrogen bond network, so that the tannic acid has important application prospects in the fields of semiconductor packaging, thermal interface materials and the like.

The invention relates to a PVB (Polyvinyl Butyral) film for PDLC (Polymer Dispersed Liquid Crystal) dimming glass, a preparation method and the PDLC dimming glass, and belongs to the technical field of dimming glass. The PVB film for the PDLC dimming glass comprises PVB resin and a plasticizer, at least one end group of the plasticizer is a benzoate group, and the plasticizer belongs to benzoate. Through molecular structure design, the main chain of the plasticizer can be a polyether type [-CH2-CHY-O-] n chain segment or a polyol skeleton, and meanwhile, benzoate groups or specific end group structures (such as branched chain alkyl, aromatic hydrocarbon and the like) are introduced, so that the interaction (such as hydrogen bond damage, dipole interaction, pi-pi accumulation and the like) between the plasticizer and PVB resin is enhanced, and the plasticizer can be used for preparing PVB resin. By introducing structures such as branched chains and aromatic rings, the steric hindrance and rigidity of molecules are greatly improved, and migration and precipitation phenomena of the plasticizer in the PVB film are effectively inhibited.

The invention discloses a polymer electrolyte composite material for a high-temperature-resistant solid-state battery and a preparation method of the polymer electrolyte composite material, and belongs to the technical field of solid-state battery materials. The preparation method comprises the following steps: preparation of key functional components, preparation of a precursor solution, dispersion and compounding of the filler, film casting and heat treatment, and post-treatment. A dynamic thioether bond is introduced into a main chain to construct an oxygen-sulfur synergistic coordination network, and a multi-component interface chemical bonding and gradient curing process is combined, so that the problems that the ionic conductivity and the mechanical strength of the traditional polymer electrolyte cannot be considered at a high temperature, the filler is easy to agglomerate, the membrane has many defects and the like are solved; the obtained material still keeps high ionic conductivity and excellent mechanical stability at 150 DEG C, has a wide electrochemical window, and is suitable for high-safety and high-energy-density solid-state batteries.

The invention relates to the technical field of fibers, and discloses a thermal insulation polyamide fiber and a preparation method thereof. Polyurethane modified silicon dioxide aerogel with a phase change unit and a heat insulation carrier is prepared, the polyurethane modified silicon dioxide aerogel and epoxidized carbon nanotubes with light absorption and heat generation performance are jointly introduced into PA6 slices, epoxy groups react with carboxyl and amino at the tail end of a PA6 main chain under the melting condition, the dispersity and compatibility of all components in the PA6 slices are improved, and the heat insulation performance of the PA6 is improved. The polyamide fiber prepared by melt spinning not only has good heat insulation performance, but also can utilize the phase change material and the light absorption heating material to store energy and regulate temperature, so that the heat storage and heat preservation performance of the fiber is further improved.

The invention belongs to the related technical field of batteries, and discloses a reversible phase change electrolyte, a preparation method thereof and a secondary battery. The reversible phase change electrolyte is an organic solvent system, a copolymer with a specific structure and an ionic liquid are used as main components, the pi-pi interaction between the copolymer and the ionic liquid is utilized, when the temperature is higher than the LCST temperature, the pi-pi interaction between the copolymer and the ionic liquid breaks, and phase change occurs. Meanwhile, the main chain of the polymer C enables the length of the side chain of the polymer A or the polymer B to be increased, and hindering is formed for the pi-pi interaction between the copolymer and the ionic liquid; and a-CX3 side chain group in the polymer C further promotes the reduction of the phase change temperature of the electrolyte. The phase-change electrolyte disclosed by the invention can generate phase change at a low temperature of 40-60 DEG C, and when the temperature of the battery continues to rise to 77 DEG C or above, the internal reaction of the battery is completely stopped, so that thermal runaway of the battery is prevented, and the battery can efficiently work in a wide temperature range.

The invention belongs to the technical field of liquid crystal alignment agents, and particularly relates to a liquid crystal alignment agent, a liquid crystal alignment film and a liquid crystal display element. The liquid crystal alignment agent comprises polyamic acid, a main chain of the liquid crystal alignment agent contains short side chain diamine and carbonate bonds, the short side chain diamine can slow down direct collision between film surfaces, carbonyl on a short side chain enhances absorption of ultraviolet light, and the compressive strength of a liquid crystal alignment film and the cracking alignment performance of the liquid crystal alignment film are improved; the carbonic ester bond can improve the voltage holding rate thermal stability of the liquid crystal alignment film and can improve the anchoring force of the liquid crystal alignment film and liquid crystals, the liquid crystal alignment agent with high compressive strength, voltage holding rate, high thermal stability and low linear polarization ultraviolet exposure is finally obtained, the stability of the high voltage holding rate improves the residual image of a display device, and the display effect is improved. And due to high compressive strength, the undesirable phenomenon of ZARA of the liquid crystal display device can be reduced.

In some aspects, the present disclosure provides a method for generating a geometrical structure of a binding complex formed between a protein and a ligand. In some embodiments, the method comprises sampling an initial geometrical structure of the binding complex from a geometry prior. In some embodiments, the method comprises denoising, using a machine-learned stochastic differential equation (SDE), the initial geometrical structure to generate the geometrical structure of the binding complex.

The invention belongs to the technical field of polymer composite materials, and particularly relates to a polycarbonate modified composite material as well as a preparation method and application thereof, and the polycarbonate modified composite material comprises 60-85 parts of a PC base material, 10-30 parts of a bio-based monomer, 1-8 parts of surface modified nano cellulose and 0.1-2 parts of a transesterification catalyst. According to the polycarbonate modified composite material as well as the preparation method and the application thereof provided by the invention, chemical bonding of a bio-based monomer and a PC main chain is realized through transesterification, phase separation is avoided, and the core pain point of traditional blending modification is solved; the biodegradation rate is increased by 30% or above compared with pure PC, and meanwhile, the excellent mechanical properties (the tensile strength is larger than or equal to 60 MPa, and the notch impact strength is larger than or equal to 5 kJ / m) of PC are reserved; the melt flow rate is increased by more than 25%, the processing energy consumption is reduced, and the application scene is widened; the carboxylic acid modified nano cellulose and the block copolymer form a synergistic network, so that the mechanical property, the thermal stability and the degradation uniformity are synchronously improved.

The application discloses a PAG bonding type photosensitive photoresist resin and a preparation method and application thereof. The photoresist resin is as follows: formula. The PAG bonding type resin is prepared through the following reaction process: 1) performing a RAFT polymerization reaction on p-acetoxystyrene, p-styrene sulfonamide trifluoromethyl potassium salt and a RAFT chain transfer agent under the action of an initiator to obtain an intermediate I, 2) performing a hydrolysis reaction on the intermediate I to obtain an intermediate II, 3) performing a protection group introduction reaction on the intermediate II and di-tert-butyl dicarbonate to obtain an intermediate III; and 4) performing an ion exchange reaction on the intermediate III and triphenylsulfonium bromide. The application realizes the bonding of the PAG into the resin skeleton, and improves the problems of poor compatibility between the PAG and the resin, phase separation, uneven distribution of the PAG and the like. Therefore, the photoresist prepared from the resin has the photo-generated acid bound by the polymer main chain and limited diffusion, the resolution is improved, and the photoetching effect is excellent.

The present invention provides a polymer production method comprising: (1) a step in which a monomer starting material including a prescribed monomer is polymerized by living radical polymerization using a radical initiator and a RAFT agent to obtain a polymer P-1 having a terminal structure that includes, at a terminal of the main chain thereof, a sulfur atom derived from the RAFT agent; (2) a step in which, subsequent to step (1), a radical generator and a thiol compound are added to a solution including the polymer P-1 and the same is heated to remove the terminal structure from the main chain of the polymer P-1; and (3) a step in which, subsequent to step (2), the solution including the polymer P-1 with the terminal structure removed therefrom is mixed with a poor solvent to precipitate the polymer as a solid and purify the same.

The invention relates to the technical field of sewage treatment, in particular to a preparation method of a degradable bactericide for an oil field. According to the invention, a hydroxypropyl guanidine gum-polycaprolactone-ethylenediamine fragment copolymer is taken as a carrier, a methylisothiazolinone quaternary ammonium salt (Q-MIT) bactericide is loaded, and the degradable bactericide for the oil field is obtained by cooperating with a dodecyl ethyl sulfide (TC-SE) bactericide and combining with sodium polyaspartate. A carrier forms a hydrogen bond with a polar group on the surface of a biological membrane through a hydroxypropyl guanidine gum main chain to realize targeted anchoring, a polycaprolactone branched chain encapsulates Q-MIT through a hydrophobic effect, primary amino groups of ethylenediamine are introduced to form a pH sensitive Schiff base bond with Q-MIT, and the primary amino groups and adipic dihydrazide form a thermal response hydrazide bond to construct a dual dynamic covalent bond, so that controlled release of Q-MIT is realized, and the biomembrane is prepared. And moreover, the components of the whole system are connected through degradable chemical bonds, so that the environmental protection property and sustainability of oil field operation are guaranteed.

The invention belongs to the field of photovoltaic materials, provides a preparation method and application of reinforced polyurethane resin for a photovoltaic frame, and solves the problem that the existing polyurethane resin for the photovoltaic frame cannot have excellent flame retardant property, water resistance, aging resistance and mechanical property at the same time. Comprising the following steps: carrying out a reaction on polytetrahydrofuran ether glycol and polyisocyanate to obtain a polyurethane prepolymer, and chemically grafting a phosphorus-containing compound onto a polyurethane main chain by using prepared 9, 10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, so as to obtain the flame-retardant polyurethane. Hydroxyl-terminated polydimethylsiloxane and polyhydric alcohol are used as part of flexible chain segments to be embedded into a polyurethane main chain, 2-(2-hydroxy-4-acryloyl)-2H-benzotriazole is added to serve as an anti-ultraviolet agent, and final polyurethane resin is obtained through reaction. And injecting the polyurethane resin and the glass fiber into a mold, and preparing the photovoltaic frame profile through a pultrusion process.

A lithium-sulfur battery including an anode structure, a cathode, a separator, and an electrolyte is provided. A protective layer may form within the anode structure responsive to operational discharge-charge cycling of the lithium-sulfur battery. The protective layer may include a polymeric backbone chain formed of interconnected carbon atoms collectively defining a segmental motion of the protective layer. Additional polymeric chains may be cross-linked to one another and at least some carbon atoms of the polymeric backbone chain. Each additional polymeric chain may be formed of interconnected monomer units. A plasticizer may be dispersed throughout the protective layer without covalently bonding to the polymeric backbone chain. The plasticizer may separate adjacent monomer units of at least some additional polymeric chains. Increasing separation of adjacent monomer units increases a cooperative segmental mobility of the additional polymeric chains and ionic conductivity of the protective layer.

A preparation method of the cardanol-based phosphorus-containing side group novolac epoxy resin comprises the following steps: (1) in the presence of a catalyst A, carrying out a stirring reaction on cardanol and an aldehyde compound at 80-110 DEG C for 3-10 h to prepare an intermediate A; (2) stirring the intermediate A and a phosphorus-containing compound at 50-150 DEG C to react for 10-24 hours to prepare an intermediate B; and (3) in the presence of a catalyst B, stirring and reacting the intermediate B and epichlorohydrin at 70-110 DEG C for 2-6 hours, and in the presence of a catalyst C, stirring and reacting at 30-65 DEG C for 1-4 hours to prepare the cardanol-based phosphorus-containing side group novolac epoxy resin. Through a rigid structure on a main chain of the novolac epoxy resin, a phosphorus-containing structure on a side chain of the novolac epoxy resin and an epoxy group, the toughness and flame retardance of an epoxy cured product can be improved on the premise that the thermal stability is not reduced, and the novolac epoxy resin has an extremely good application research prospect.

The invention relates to a composite current collector and a lithium battery. The composite current collector comprises a metal layer, a supporting layer and an adjusting layer arranged between the metal layer and the supporting layer, the adjusting layer comprises matrix resin, and the glass transition temperature Tg of the matrix resin is less than or equal to 70 DEG C, so that the adjusting layer has excellent flexibility and deformability, can effectively absorb and buffer internal stress generated by thermal expansion coefficient difference of metal and polymer, and prevents interface stripping caused by stress concentration, thereby greatly improving the durability of the binding force. By limiting the number of carbon atoms of a molecular main chain in a range of 12-700, the flexibility and cohesion strength of the adjustment layer can be balanced, so that stress can be buffered, the adjustment layer can serve as a firm whole, the binding force of the metal layer and the polymer layer is further improved, interface separation is avoided, the cycle life of the lithium battery is prolonged, and the use safety of the lithium battery is improved.