115 results about "Intermolecular force" patented technology

The invention belongs to the technical field of medicines, and particularly provides a solid dispersion as well as a preparation method and application thereof. The solid dispersion comprises a carrier material, and further comprises quercetagetin and phospholipid, the mass ratio of the quercetagetin to the phospholipid is 1: (0.3-1.5), and the carrier material comprises one or more of a hydrophilic polymer and a pH-dependent polymer. Wherein the quercetagetin and the phospholipid are combined through an intermolecular force, so that the quercetagetin obtains a lipid material similar to a cell membrane structure, a cell membrane bionic phospholipid compound is formed, the cell membrane bionic phospholipid compound can be naturally compatible with an upper wall cell membrane of a small intestine, and the permeation transmembrane capability of the quercetagetin is better promoted; the quercetagetin is added into the solid dispersion, so that more quercetagetin can enter systemic circulation and lymphatic circulation, and therefore, the solid dispersion can strengthen transmembrane absorption while strengthening dissolution, so that the solid dispersion has high bioavailability.

The invention discloses an artemisinin derivative nano assembly with anti-tumor activity and a preparation method and application thereof. The nano assembly is formed by self-assembling artemisinin derivatives through intermolecular force and modifying the artemisinin derivatives with a PEG modifier; the artemisinin derivative is artesunate or dihydroartemisinin of which the side chain is binary acid or saturated fatty alcohol or unsaturated fatty alcohol; the mass ratio of the artemisinin derivative to the PEG modifier is (10: 90)-(90: 10), so that the technical effects of high drug loading capacity, good stability, low toxic and side effects and the like are realized, the urgent demand on high-efficiency and low-toxicity preparations in clinic is met, a new strategy is provided for the assembly of homotype synergistic drug nanoparticles, and the application prospect is broad. An effective nano platform is provided for developing a carrier-free nano assembly and a high-efficiency and low-toxicity nano preparation.

The invention provides ionic liquid grafting modified high-temperature-resistant bio-based nylon as well as a preparation method and application thereof, and belongs to the technical field of bio-based high polymer materials. After nylon 5T salt is subjected to prepolymerization reaction, imidazolium ionic liquid is added for final polymerization, and the ionic liquid grafting modified high-temperature-resistant bio-based nylon is obtained. In the polymerization process, the imidazole ionic liquid enters a polyamide macromolecular chain, so that the intermolecular acting force can be reduced, and the molecular chain spacing can be increased, thereby reducing the melting point of the bio-based nylon, increasing the flowability of the bio-based nylon and improving the thermal property, crystallization and other behaviors of the bio-based nylon; the processing stability and the spinning performance of the bio-based nylon in the later period are effectively improved, meanwhile, the energy consumption is reduced, and the bio-based nylon with high strength, high orientation and high crystallization is obtained.

The invention discloses a polymer resin and a preparation method and application thereof, the polymer resin has the following structural general formula as shown in the formula I: # imgabs0 #, and n is a positive integer between 1 and 10000; r1 is a group capable of providing hydrogen atoms, and R2 is an aromatic group or a substituted aromatic group. The polymer resin provided by the invention has more groups and atoms with high refractive index; multiple hydrogen-bond interactions with different strengths are generated among a plurality of hydrogen-bond acceptors and hydrogen-bond donors contained in molecules, so that the intermolecular acting force in the polymer resin is enhanced, and the refractive index of the whole polymer resin is further improved and is higher than 1.8. The aromatic group has certain rigidity, and the thioether bond has certain flexibility, so that the structural toughness and machinability of the whole molecule can be improved.

The invention belongs to the technical field of protective materials, and particularly relates to a preparation method of a boron-based polymer based on a'strong-weak 'dynamic bond, which comprises the following steps: destroying intermolecular force of a boron-based siloxane material and another supramolecular material through a polar solvent, and then fully blending to recombine into a dual-network structure, thereby obtaining the boron-based polymer based on the'strong-weak' dynamic bond. And fully evaporating the solvent to obtain the boron-based polymer based on the strong-weak dynamic bond. According to the invention, the strong-bond silicon-based supramolecular material and the weak-bond silicon-based supramolecular material are subjected to structural interpenetration under the driving of an intermolecular acting force, so that the compatible integration of the two components is promoted, and the novel shear thickening material is formed; by constructing a composite system of a boron-based siloxane material (component A) and siloxane containing a strong dynamic bond (component B), dual-function optimization is realized: a dynamic bond network of the component B not only effectively inhibits the intrinsic cold fluidity defect of the component A, but also inhibits the intrinsic cold fluidity defect of the component B through a dynamic bond synergistic effect on the premise of maintaining the shear thickening characteristic of the system; the mechanical property and the environmental stability of the composite material are obviously improved.

The invention belongs to the technical field of organic photoelectric materials, and particularly relates to a boron-nitrogen heterocyclic compound and an organic electroluminescent device thereof. The boron-nitrogen heterocyclic compound provided by the invention has relatively large steric hindrance, on one hand, molecular vibration is reduced, and the boron-nitrogen heterocyclic compound has relatively narrow half-peak width and can effectively improve the color purity of light emitted by a device; on the other hand, the distance between molecules is increased, the acting force between the molecules is weakened, quenching caused by aggregation is overcome, the luminous efficiency of the device can be improved, and the service life of the device can be prolonged.

The invention provides a wide-temperature-range high-damping polyurethane IPN material, and in the preparation of the polyurethane IPN material, the R value of polyurethane is accurately controlled to be 1, so that an isocyanate group (-NCO) and a hydroxyl group (-OH) in polyhydric alcohol are completely reacted in a stoichiometric ratio, and a stable carbamate group (-NH-COO-) is generated. A polybutyl methacrylate molecular chain introduced into the system contains strong polar ester groups (-COO <->), and the polar groups and-NH <-> in carbamate groups form strong intermolecular hydrogen bonds. The multiple hydrogen bonds interact to jointly form a complex network structure of the IPN material, and the hydrogen bonds between the hard segment and the soft segment of the polyurethane and the interface hydrogen bonds between the polyurethane and the polybutyl methacrylate have a synergistic effect, so that the internal friction between molecular chains is remarkably increased. The multi-layer and multi-type intermolecular acting force synergistic effect enables the polyurethane IPN material to show more excellent damping performance.

The application discloses a sensitized ferroptosis lipid nano regulator and a preparation method and application thereof, and belongs to the technical field of new adjuvants and new dosage forms of drug preparation combined treatment. The lipid nano regulator is co-assembled by a GPX4 inhibitor and a FASN inhibitor through intermolecular forces, and is modified with an oxidation-reduction sensitive PEG modifier, a molar ratio of the GPX4 inhibitor and the FASN inhibitor is 10:1-1:10, a mass ratio of the sum of the GPX4 inhibitor and the FASN inhibitor to the PEG modifier is 10:90-90:10, and the intermolecular forces include pi-pi stacking force, hydrophobic force and hydrogen bond. The co-assembled nano preparation provides a new strategy and more choices for the development of drug delivery, and meets the urgent needs of high-efficiency and diverse ferroptosis treatment strategies in preparations in the clinic.

The application relates to a carrier-free self-driven nanomotor and a preparation method and application thereof, and belongs to the technical field of biological medicines. The nanomotor is a nanometer assembly formed by co-assembly of a photothermal / light motion dual-enhanced photosensitizer and a near-infrared light response type nitric oxide donor BNN6 through intermolecular force, or is a nanometer assembly formed by co-assembly of a photothermal / light motion dual-enhanced photosensitizer and a near-infrared light response type nitric oxide donor BNN6 through intermolecular force and modified by a polyethylene glycol modifier. The application realizes a synergistic treatment mode of deep tumor penetration and high-efficiency killing by constructing a functional coupling system of "photothermal driving-NO release-motion enhancement-RNS cascade generation".

According to the preparation method for improving the metal / polymer bonding strength, a polar polymer film layer is pre-plated on the metal surface, the prepared polar polymer film layer and the metal surface containing hydroxyl generate intermolecular acting force, polymer entanglement occurs between the prepared polar polymer film layer and a polymer plate in subsequent thermal connection, and finally the metal / polymer interface acting force is enhanced; and the interface heat transfer efficiency is improved, the interface temperature is increased to 378 DEG C from 331 DEG C, and the metal / polymer interface connection area is increased to 224 mm < 2 > from 179 mm < 2 >. The metal / polymer interface bonding strength is improved by enhancing the metal / polymer interface acting force and improving the interface heat conduction efficiency, the film thickness control freedom degree is high, the film with any thickness can be obtained by controlling spin-coating parameters, and the method has the advantages of being easy to prepare, high in processing efficiency, low in economic cost and wide in application range.

The invention discloses a carbon material rich in intrinsic defects as well as a preparation method and application thereof, and belongs to the technical field of catalysts, fullerene or fullerene derivative carbon cages adopted by the invention have a pi conjugated structure, so that relatively strong pi-pi interaction force exists among molecules. Fullerene or a fullerene derivative is used as a raw material, a macroscopic crystalline material, namely a fullerene condensed state precursor, is obtained through self-assembly based on intermolecular acting force, the fullerene condensed state precursor is subjected to pre-etching treatment through oxygen plasma, surface modification is conducted on the fullerene condensed state precursor, and the fullerene or fullerene derivative is obtained. The preparation method comprises the following steps: preparing a fullerene condensed state precursor, performing two-stage temperature programming heat treatment of low-temperature pre-etching treatment and high-temperature roasting in ZnCl2 molten salt, endowing the fullerene condensed state precursor with five-membered ring topological defects and carbon intrinsic defects of boundaries and curvatures, so as to obtain the carbon material rich in intrinsic defects, and endowing the carbon material with good electro-catalytic performance by the intrinsic defect sites.

This invention relates to the field of optical thin film fabrication technology, specifically to a method for fabricating a high extinction ratio, adhesive-free polarizing beam splitter film resistant to high and low temperature environments. The method includes the following steps: S1, substrate pretreatment; S2, polarizing beam splitter film deposition; S3, adhesive-free bonding treatment; S4, annealing strengthening; and S5, post-treatment. This invention uses an adhesive-free optical contact bonding process to replace the traditional organic bonding process, completely eliminating the temperature adaptability bottleneck caused by organic adhesive layers. The bonding interface relies on intermolecular forces for adhesion, eliminating problems such as aging and debonding of organic adhesives. This allows the device to operate stably in a wide temperature range of -60℃ to 120℃, greatly improving the device's environmental adaptability and meeting the needs of extreme environments such as deep space exploration and polar observation.

The invention discloses a preparation method of egg white protein nanogel. The preparation method comprises the following steps: firstly, adding an ethanol solution with the volume fraction of 0.1-11.5% into egg white liquid, and diluting until the protein concentration is 1-2%; the egg white protein ethanol solution is subjected to microwave and ultrasonic combined treatment, the treatment time is set to be 3-7 min, ultrasonic is in an intermittent mode, the ultrasonic power is 200-800 W, and the microwave heating temperature is 65-75 DEG C. And finally, removing ethanol in the solution subjected to microwave ultrasonic treatment to obtain the egg white protein nanogel particles. The method is different from an existing'bottom-to-top 'preparation method and comprises the following steps: firstly, carrying out mild denaturation on protein by adopting low-concentration ethanol, changing a protein structure and an intermolecular acting force to expose a hydrophobic structure and expand the structure, and then moderately gathering and crushing the protein into microgel by utilizing an ultrasonic cavitation effect and a microwave heat effect; the nanogel has smaller particle size, higher system stability and interface stability, and the preparation method is simple and low in cost.

The application discloses a heating transmission device suitable for in-situ detection of ultrahigh-temperature pyrolysis reaction, comprising a heating pipe and an adjusting assembly; a sample outlet end of the heating pipe is connectable to a detection device; the heating pipe is divided into a low-temperature zone, a high-temperature zone and an annealing zone; a first water-cooled electrode is arranged outside the low-temperature zone; and a second water-cooled electrode is arranged outside the annealing zone; the adjusting assembly comprises a guide rail and a sliding block; and the sliding block is connected with the first water-cooled electrode or not. The application forms a variable-diameter and variable-temperature zone through combination design of the heating pipe and the water-cooled electrode, guarantees contact between the heating pipe and the protective electrode, builds a relatively slow and uniform temperature gradient in the annealing zone, guarantees generation and dispersion of product molecules and improves transmission efficiency of macromolecular compounds. The application is convenient to connect with a mass spectrometer, can realize in-situ analysis of ultrahigh-temperature pyrolysis reaction and solves the problem that macromolecular products such as polycyclic aromatic hydrocarbons, fullerenes and the like cannot be detected in-situ due to aggregation caused by intermolecular forces in the pyrolysis reaction.

This invention provides a high-performance, high-precision gradient pore ultrafiltration membrane and its preparation method, belonging to the field of membrane preparation technology. Lithium chloride can alter the thermodynamic properties of the casting solution, affecting the aggregation state of polymer molecules and the phase separation process. CTAB has multiple functions in the phase inversion membrane preparation process; as a non-solvent additive, it regulates the phase separation behavior of the polymer PVDF, promoting the formation of more uniform nanoscale channels. DOP has a unique molecular structure and physicochemical properties, playing a multifaceted role in improving membrane performance; by inserting itself between PVDF molecular chains, it weakens the intermolecular forces, making the molecular chains more loosely arranged, thereby forming more interconnected channels and increasing flux. Simultaneously, it helps to form a narrow pore size distribution, reducing macropore defects and improving retention accuracy. This invention, through the mixing of the above substances, effectively achieves a high-porosity, nanoscale pore structure, realizing a high-performance, high-precision gradient pore ultrafiltration membrane preparation method.

The application discloses a kind of nano-assemblies of enhanced photodynamic-immunotherapy and its preparation method and application, belong to the technical field of pharmaceutical preparation.The nano-assemblies are co-assembled by photodynamic photosensitizer and cystine / glutamate antiporter inhibitor through intermolecular force of π-π stacking and hydrophobic interaction, and are surface-modified with amphiphilic PEG modifier, the molar ratio of the photodynamic photosensitizer and cystine / glutamate antiporter inhibitor is 10:1~1:10, and the mass ratio of the total mass of the photodynamic photosensitizer and cystine / glutamate antiporter inhibitor and the mass of PEG modifier is 60:40~95:5.The preparation method of the nano-assemblies of the application is simple and convenient, the drug loading efficiency is high, the efficient co-loading of drug can be realized, and the effect of enhancing photodynamic-immunotherapy is achieved, so the nano-assemblies have good clinical application prospect.

The invention relates to a graphitized carbon nanotube as well as a preparation method and application thereof, and belongs to the technical field of nano materials and fibers. An electrolyte with strong ionization property, moderate ion size and a certain hydration effect is added into a precursor solution, and in a low-temperature freezing process, an environment provided by the electrolyte and the precursor solution enables natural high-molecular or polymer molecules to generate a self-assembly behavior based on an intermolecular acting force, so as to obtain the nanotube with ordered molecular arrangement. And carrying out carbonization and graphitization on the obtained nanotube to obtain the graphitized carbon nanotube. The graphitized carbon nanotubes have graphite lattice stripes, the internal height of the graphitized carbon nanotubes is ordered, the number of defects is extremely small, and the crystallinity is extremely high, so that the material has ultrahigh strength, ultrahigh modulus, excellent electric conductivity and thermal conductivity and excellent stability.

The invention provides a physical experiment simulation system, and relates to the technical field of material mechanics tests, the physical experiment simulation system is based on an actual stress-strain curve, a simulation test piece three-dimensional model with a gap is established, cells are divided, a typical plane is selected, a groove cell, a slope bottom cell, a stretching cell and a gap cell are divided, and the physical experiment simulation system is obtained. The method comprises the following steps of: performing accurate simulation analysis on each position conveniently, directly simulating a real stretching effect in a stretching cell, acquiring radial stress at a groove cell according to a rotation trend generated by an intermolecular acting force, judging whether a notch cell and a slope bottom cell which serve as stress concentration points are in an elastic deformation stage or not through a vonMises yield criterion, and judging whether the notch cell and the slope bottom cell are in an elastic deformation stage or not. And the deformation condition of each cell caused by the influence of the stress is visualized, and the process and the result of the abnormal test result caused by the gap are intuitively displayed.

The invention discloses a photovoltaic cell, a photovoltaic module and a processing method of the photovoltaic cell, the surface of the photovoltaic cell is provided with an antireflection layer, and the antireflection layer has a saturated bond; when the anti-reflection layer on the surface of the photovoltaic cell is characterized by adopting a Raman scattering spectrum analysis test, a Raman spectrum chart obtained by the anti-reflection layer has a characteristic peak A, and the ratio range of the peak intensity of the characteristic peak A to the half-peak width is 1-25. According to the photovoltaic cell, a Raman spectrum chart in the antireflection layer has a characteristic peak A at the position, the ratio range of peak intensity to half-peak width is 1-25, the characteristic peak A is relatively sharp, intermolecular acting force in a molecular structure of the characteristic peak A is high, chemical bonds are not prone to breakage, and therefore the characteristic peak A at the position is the characteristic peak corresponding to a saturated bond; therefore, a large number of saturated bonds exist in the antireflection layer, and only a small number of unsaturated bonds or dangling bonds exist in the antireflection layer, so that the stability and passivation effect of the antireflection layer are ensured, and the photovoltaic cell is further ensured to have relatively good power generation efficiency.

The invention discloses a two-component heat-conducting gel with high heat conductivity, low viscosity and high thixotropy, a modifier and a treating agent are respectively suitable for forming an intermolecular acting force network structure of polar molecules in a system of a heat-conducting component A and a gel component B, and the improvement of the thixotropy of the heat-conducting component A and the gel component B and the improvement of the room-temperature storage stability are facilitated. Linear isopropenyl-terminated silicone oil and cyano-terminated silicone oil are compounded and interact with the modifier and the treating agent respectively, so that the thixotropy and room temperature stability of the component A and the component B are further improved. The double-component heat-conducting gel disclosed by the invention has the properties of high heat conductivity, low viscosity and high thixotropy, can resist sedimentation and phase splitting during storage at room temperature, is resistant to high temperature and can be used at 200 DEG C.

This invention discloses an environmentally friendly curcumin nanocrystal and its preparation method, relating to the field of nanoparticle technology. The nanocrystal has a core-shell structure, with a core of curcumin crystals and a shell of hepatin peptide molecules bonded together by intermolecular forces. The average particle size of the nanocrystal is 50-200 nanometers, and it is completely dispersed and stable in an aqueous phase, containing no organic solvents or synthetic surfactants. This invention utilizes a pectin-chitosan complex to microencapsulate the nanocrystal, enabling it to resist gastric acid degradation and target release to the colon, thus precisely acting on the gut-hepatic axis and significantly improving bioavailability and hepatoprotective efficacy. While completely avoiding organic solvents and synthetic stabilizers, it simultaneously solves four major industry challenges related to curcumin: solubility, stability, targeted delivery, and synergistic efficacy, providing a new technical path for developing high-end, naturally derived hepatoprotective products.

The present invention relates to the technical field of nucleotide raw materials, and specifically relates to a blocking probe for RNA library construction, a library construction kit, and a preparation method. The blocking probe provided by the present invention has a polymer molecule with a specific structure connected to its 5'-end. The blocking probe targets a target region and binds to RNA to form a double-stranded composite structure. The polymer molecule improves the stability of the double-stranded composite structure through intermolecular forces such as hydrogen bonds and molecular entanglement, as well as the chimeric effect of the linear functional groups in the polymer structure and the double-stranded composite structure in the molecular spatial structure. At the same time, it can effectively prevent the reverse transcriptase from displacing the blocking probe under the action of strand displacement activity, improve the blocking effect of the blocking probe, reduce the library content of unnecessary RNA in the RNA library, optimize the library quality, and improve the convenience and accuracy of RNA sequence information analysis.

The invention discloses an olmesartan medoxomil pharmaceutical co-crystal as well as a preparation, a preparation method and application thereof. The co-crystal is formed by olmesartan medoxomil and a specific co-crystal forming agent through intermolecular force. The invention also particularly provides a compound preparation containing the olmesartan medoxomil pharmaceutical co-crystal and hydrochlorothiazide. Through the eutectic technology, the invention fundamentally overcomes the inherent defects of low solubility and slow dissolution of olmesartan medoxomil as a BCS II drug. Experiments show that the preparation disclosed by the invention can realize rapid and complete drug release in vitro (the dissolution rate within 30 minutes is greater than or equal to 98%), the relative bioavailability of olmesartan in vivo can be improved by at least 180% compared with that of a reference preparation, and meanwhile, the eutectic structure ensures that the preparation has excellent chemical stability under an accelerated test condition. The invention provides an innovative solution for the development of an efficient and stable olmesartan medoxomil preparation.

The present invention discloses a two-component thermal conductive gel with high thermal conductivity, low viscosity and high thixotropy. The modifier and the treating agent are respectively suitable for forming an intermolecular force network structure of polar molecules in the system of the thermal conductive component A and the gel component B, which is beneficial to the improvement of the thixotropy of the thermal conductive component A and the gel component B and the improvement of the room temperature storage stability. By compounding the linear isopropenyl-terminated silicone oil and the cyano-terminated silicone oil, and through the interaction with the modifier and the treating agent of the present invention respectively, the thixotropy and the room temperature stability of the A and B components are further improved. The two-component thermal conductive gel of the present invention has the properties of high thermal conductivity, low viscosity and high thixotropy, can resist sedimentation and phase separation at room temperature during storage, is high temperature resistant, and can be used at 200 °C.

The invention discloses modified kappa-carrageenan as well as a preparation method and application thereof, and belongs to the field of development and application of high polymer materials. The prepared modified carrageenan has quaternary ammonium groups with positive charges and sulfate radicals with negative charges at the same time, the sol-gel transition temperature of the carrageenan is remarkably reduced by regulating and controlling the acting force between molecular chains, flexible machinability is achieved, and meanwhile the mechanical strength of the carrageenan is enhanced. According to the modification strategy, efficient fixation of salt ions is achieved, and the material is endowed with excellent atmospheric water trapping capacity and stable moisture power generation performance. On the basis, an intelligent self-powered sensor is constructed, and real-time monitoring of the breathing state can be achieved. Based on the unique salt ion cross-linking characteristic of the kappa-carrageenan, the sol-gel transition temperature of the kappa-carrageenan is optimized, the machinability of the kappa-carrageenan is enhanced, the application of the kappa-carrageenan in the fields of moisture-related water drawing, power generation and sensing is expanded, and the kappa-carrageenan has a wide application prospect.

The invention discloses a foldable screen protective film capable of being reworked and a preparation method thereof, the protective film comprises an HC layer, a silica gel layer, an optical adhesive layer and an isolation layer, and the optical adhesive layer is obtained by coating optical adhesive and then curing. The optical adhesive comprises the following raw material components in parts by weight: 60-90 parts of alkyl (meth) acrylate, 5-25 parts of a polar monomer A, 1-10 parts of tackifying resin, 0.02-2 parts of a photoinitiator and 0.01-1 part of a curing agent. The prepared protective film has reliable bending resistance and good reworkability, the peel strength of the protective film is improved through the (methyl) acrylate tackifying resin added into the optical adhesive layer, and the reliable bending resistance of the protective film is guaranteed. The polar monomer A containing ether bonds can increase intermolecular acting force, improve creep recovery performance and reduce sacrifice of chemical crosslinking to peel strength, meanwhile, a plurality of hydrophilic groups enable the protective film to be easily peeled off when ethanol is wiped, and the protective film is endowed with good reworkability.

A method of directed evolution for developing a membrane includes using a 3D protocol to simulate particle trajectories and determine the effect of intermolecular forces on particle capture performance during membrane filtration to determine the effectiveness of different candidate membranes in optimizing performance.

The purpose of the present invention is to provide composite particles having nanoparticles that are excellent in terms of weather resistance. Composite particles according to an embodiment of the present invention each include at least one nanoparticle complex and an aggregate of a plurality of functional particles. The nanoparticle complex is present inside an aggregate structure that is formed of the aggregate of the functional particles, and the nanoparticle complex is held inside the aggregate structure by intermolecular force between the nanoparticle complex and the functional particles.

The application relates to the technical field of biological materials, and discloses a chitosan electrostatic spinning liquid and a preparation method thereof, which comprises the following steps: preparing chitosan through a homogeneous deacetylation method; and preparing the chitosan electrostatic spinning liquid. The preparation method of the chitosan electrostatic spinning liquid is simple and mild, the crystallinity and the intermolecular force are reduced through the mode of reducing the deacetylation degree and the molecular weight of chitosan, the concentration and the spinnability of the pure chitosan spinning stock solution can be improved, and the pure chitosan nanofiber can be successfully prepared.

This invention provides a simulation method for analyzing changes in the flame retardant properties of polymer insulation materials during aging based on intermolecular forces. The method involves three aspects: 1) simulating and analyzing microscopic parameters related to intermolecular forces during the aging process of polymer insulation materials; 2) analyzing the evolution of intermolecular forces during the aging process of polymer insulation materials; and 3) establishing a structure-activity relationship between intermolecular forces and flame retardant properties of polymer insulation materials. This method provides theoretical guidance for understanding the influence of intermolecular forces on the properties of polymer insulation materials during aging.