720 results about "End-group" patented technology

The invention belongs to the technical field of optical materials, and discloses a holographic polymer dispersed liquid crystal composition, a holographic grating and a preparation method. The composition comprises the following components in parts by mass: 0.5-1.5 parts of a photoinitiator, 2-5 parts of a co-initiator, 15-20 parts of a first monomer, 15-20 parts of a second monomer, 10-15 parts of a third monomer, 10-15 parts of a solvent and 10-20 parts of mixed liquid crystal. Wherein the first monomer is a monofunctional acrylic monomer, the second monomer is a bifunctional acrylic monomer, the third monomer is a polyfunctional acrylic monomer, the mixed liquid crystal comprises 10-25 wt% of a monomer liquid crystal and 75-90 wt% of a nematic liquid crystal, and the monomer liquid crystal contains fluorine as a benzene ring substituent and contains cyano or isothiocyano as an end group. Through cooperation of the monomer liquid crystal and the nematic liquid crystal in the mixed liquid crystal and cooperation of fluorine atoms and cyano / isothiocyano groups in the monomer liquid crystal, the holographic grating prepared from the composition has the characteristics of low haze and high diffraction efficiency, and the grating can be thinner, so that the requirements of light weight and clearness of AR glasses can be met.

The invention relates to the technical field of BOPP (biaxially-oriented polypropylene) films, in particular to a scratch-resistant adhesive-free matt film and a preparation method thereof, and the scratch-resistant adhesive-free matt film comprises a matt layer, a core layer and a thermal composite layer which are sequentially arranged, the matt layer comprises co-polypropylene, high-density polyethylene, 2.0-2.5 wt% of linear alkyl silicone (the weight-average molecular weight is 12-150 thousands, and the surface tension is 42-45 mN / m) taking maleic anhydride modified aziridine as a terminal group, and 2000-4000 ppm of spherical polymethyl methacrylate (the particle size D50 is 4.0-5.0 microns); the core layer comprises homo-polypropylene; and the thermal composite layer comprises an ethylene-vinyl acetate copolymer and 2000 to 4000 ppm of a spherical anti-blocking agent. According to the scratch-resistant adhesive-free matt film, through collaborative design of the components of the matt layer and the thermal composite layer, balance of scratch resistance, high surface tension (printing applicability) and winding and unwinding smoothness of the surface of the matt layer is achieved, and a solution for the scratch-resistant generality problem of the matt surface of the high-end BOPP matt film is provided.

The present application relates to the technical field of polyimides and relates to a preparation method for a high-performance polyimide and an application thereof, aiming to solve the problems in the prior art such as numerous side reactions and severe impact on transparency caused by an excessively high imidization reaction temperature during the use of a high-temperature thermal imidization method for the preparation of polyimides. The preparation method comprises: (1) preparing a polyamic acid solution; (2) adding a chemical catalyst and a polyamic acid solution to partially complete an imidization reaction; (3) adding an end group auxiliary agent, performing coating with the solution, heating, and maintaining the heat to complete the imidization reaction; and (4) carrying out high-temperature treatment to obtain a high-performance polyimide. The present application can significantly reduce numerous side reactions present in a traditional imidization reaction, eliminate an adverse effect of high-temperature imidization on the optical performance, greatly improve the mechanical properties, heat resistance, optical performance, etc. of a material, and also achieve both high heat resistance and high transparency.

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 discloses an ether polymerization inhibitor special for a butadiene extraction system and a preparation method of the ether polymerization inhibitor. The ether polymerization inhibitor comprises the following raw materials: a polymerization inhibitor intermediate, a solvent and a dispersing agent, the production process comprises the following steps: preparing a polymerization inhibitor intermediate, preparing a solvent, compounding, feeding and mixing, filtering, removing impurities and detecting. According to the method, firstly, a polymerization inhibitor 701 and diethylene glycol normal pressure etherification process is adopted, and beta-hydroxyethyl methyl ether is introduced to seal a terminal group, so that the power consumption is reduced, the generation of byproducts is inhibited, the solubility of an intermediate acetonitrile is improved to be greater than or equal to 30g / L, and the anti-interference performance is greatly enhanced; the solvent doped with a small amount of silane modified nano diatomite is prepared, impurities can be adsorbed, metal ions can be chelated, the dispersing agent can be assisted to be evenly distributed, the problems that a pure water solvent is single in function and the dispersing agent is prone to agglomeration are solved, and the polymerization inhibition efficiency and the stability of an extraction system are guaranteed.

The invention discloses polyphenylene sulfide resin and a preparation method thereof. The weight-average molecular weight of the polyphenylene sulfide resin is 20000-50000, the molar ratio of a sulfydryl terminal group to a chlorine terminal group is 1-9, and the content of the chlorine terminal group is 15-60 [mu] mol / g. In the preparation method of the polyphenylene sulfide resin, a sulfur source, an alkali metal hydroxide and a dihalogen aromatic compound are taken as raw materials and subjected to a polymerization reaction in N-methyl pyrrolidone, and self-blocking is performed by accurately controlling the adding time of the dihalogen aromatic compound, so that controllable adjustment of an active end group is realized. The polyphenylene sulfide resin provided by the invention has excellent processability, and has excellent reactivity with silane coupling agents such as gamma-aminopropyltriethoxysilane and the like.

In some aspects, the present disclosure provides systems for forming hydrogels that comprise (i) a reactive multi-arm polymer that comprises three or more polymer arms linked to a core region, each arm comprising a polyether segment and a reactive moiety comprising a cyclic imide carboxy-C1-C5-alkyl ester end group or each arm comprising a polyether segment and a reactive moiety comprising a C2-C6-isocyanoalkyl end group and (ii) a polyamino compound comprising at least two amino (-NH2) groups, wherein the reactive multi-arm polymer and the polyamino compound react to form a crosslinked hydrogel that does not contain ester groups and has long-term stability in vivo. In some aspects, the present disclosure provides methods of treatment using such systems and hydrolysis-resistant crosslinked hydrogels formed from such systems.

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 embodiment of the invention provides a connecting unit for chemical modification of a nucleic acid end group, a preparation method of the connecting unit and a nucleic acid probe. The connecting unit for chemical modification of the nucleic acid end group has a triethylene glycol structure, and the connecting unit has the following structure. Therefore, the connecting unit with the triethylene glycol structure is relatively simple in synthesis process, relatively high in yield, efficient in synthesis, good in nucleic acid end group chemical modification effect, applicable to connection of various types of probe molecules and nucleic acid molecules, capable of simply and efficiently preparing nucleic acid probes and wide in application range.

The invention relates to a tin-free one-component moisture-curable composition, comprising at least one organic polymer containing reactive silane end groups, at least one latent curing catalyst comprising at least one latent amine and at least one latent carboxylic acid, preferably adhesion promoters, plasticizers, fillers and optionally additives. The one-component moisture curable composition can be formulated to show excellent properties for storage stability and curing speed and is free of tin-based catalysts.

The invention relates to the technical field of organic photoelectric materials, and particularly discloses a non-condensed ring small molecule acceptor material based on a quinonoid structure as well as a preparation method and application of the non-condensed ring small molecule acceptor material. According to the invention, easily available 1, 4-diacetyl piperazine-2, 5-diketone is used as a center, an alkyl chain and Ar are used for modification, EG is used as an end group, the non-condensed ring A-D-A '-D-A type structure acceptor material based on a quinone structure is constructed, and the general formula is shown in the specification. Wherein the PCE of the acceptor material which is modified by bithiophene and takes 2-(3-ethyl-4-oxothiazolidine-2-subunit) malononitrile as a terminal group reaches 15%. The non-condensed ring small molecule acceptor material based on the quinonoid structure is simple in synthesis process, and an effective strategy is provided for solving the problem of the overall performance of an organic solar cell.

The invention relates to a method for preparing high-molecular-weight polyethylene furandicarboxylate by a one-step method, and belongs to the technical field of bio-based polyester materials. The method comprises the following steps: weighing raw materials including 2, 5-furandicarboxylic acid, ethylene glycol, an end group regulator, a protective agent, a decarboxylation inhibitor and a catalyst, mixing and adding into a reaction container, introducing nitrogen, maintaining the pressure of the nitrogen in the reaction container to be 50-150 kPa, carrying out esterification reaction, heating and vacuumizing until the pressure is less than or equal to 50 Pa after the esterification reaction is completed, and carrying out polycondensation reaction to obtain the 2, 5-furandicarboxylic acid. And carrying out extrusion and drying so as to obtain the high-molecular-weight polyethylene furandicarboxylate, wherein the high-molecular-weight polyethylene furandicarboxylate is obtained. According to the method, the FDCA conversion rate is larger than or equal to 98%, the number-average molecular weight of the obtained product is larger than or equal to 32 kg / mol, no heavy metal residues exist, and the method is suitable for large-scale production of high-end bio-based packaging materials.

The invention discloses vinyl fluorine-containing polysiloxane and a preparation method thereof, and relates to the technical field of organic silicon materials. According to the invention, high-activity fluorine-containing potassium hydroxide silanolate is used as a catalyst to realize high-efficiency catalysis; d3F serves as a main monomer, D3Vi serves as a comonomer, deionized water is introduced for the first time to serve as a retarder, and implosion is effectively inhibited; vinyl dimethyl ethyoxyl silane is used as an end-capping reagent for the first time, end group vinylation is synchronously realized, and end group and side chain divinyl polysiloxane is prepared; through cooperation of ring-opening polymerization and condensation polymerization, the reaction process is mild and controllable, the product viscosity is controllable, the crosslinking activity is high, and the application range is remarkably widened.

The invention belongs to the technical field of high-molecular polymer synthesis, and particularly relates to a high-performance special polyether material with a directionally-modified terminal group and a preparation method of the high-performance special polyether material. The preparation method comprises the following steps: sequentially grafting 4-bromobenzoate to methylene of crown ether and aminating bromine atoms to prepare an intermediate, and reacting amino of the intermediate with isocyanate-terminated polyether to form a urea bond, so that a terminal group of a polyether structure is chemically modified, and a special polyether material is endowed with separation performance; when the composite membrane is applied to a nanofiltration separation membrane, the water permeability can be remarkably improved, and magnesium ions and lithium ions can be efficiently and selectively separated. According to the invention, a terminal group of a polyether structure is chemically modified through a specific reaction, and the application potential of a special polyether material in emerging fields such as high-performance separation membranes is expanded.

The invention discloses a preparation method of modified thermostable polycaprolactone, and belongs to the technical field of high polymer materials. The method comprises the following steps: selecting branched monomers such as 3-methyl-epsilon-caprolactone, inhibiting molecular chain slippage through a side group steric effect, and improving chain rigidity; a super-crosslinking metalloporphyrin porous material catalyst is adopted; (3) introducing a light / heat reversible group to an end group; and (4) optimizing process conditions and narrowing molecular weight distribution. Experiments show that the modified PCL obtained by the method is high in thermal decomposition temperature, small in melt flow rate change rate, low in yellowing index and high in tensile strength, and the comprehensive performance of the modified PCL is far better than that of the modified PCL obtained by a traditional method. The material is suitable for the fields of medical instruments, intelligent packaging and the like, and has the characteristics of high thermal stability, rapid shape recovery and controllable degradation.

The invention discloses cyano-terminated modified polysulfone and a preparation method thereof. The terminal cyano group is selected from at least one of the following groups: n, m, p, q and r are independently 0 or 1; r1, R2, R3 and R4 are respectively and independently selected from any one of H, methyl, trifluoromethyl and cyano. Through molecular structure design, a polar group (cyano) with large dipole moment is introduced into the end group of polysulfone to prepare the cyano-terminated modified polysulfone and the film thereof. According to the polysulfone provided by the invention, the cyano group at the chain end has a relatively large degree of freedom, and when the cyano group is subjected to sub-Tg polarization, the steric hindrance is relatively small. Therefore, the cyano-terminated modified polysulfone can maintain relatively low dielectric loss and high Tg while increasing the dielectric constant.

The present invention relates to a negative electrode active material and its preparation method and application. The negative electrode active material includes a silicon-carbon material and a polymer coating layer coated on the surface of the silicon-carbon material, and the material of the polymer coating layer includes a binder and a hydrophilic grafting monomer; wherein the side chain of the binder contains an end group capable of forming a hydrogen bond; any end group in the hydrophilic grafting monomer structure contains a reactive group; the minimum unit repetition number of the segment that does not contain the end group in the side chain structure of the binder is n1, and the minimum unit repetition number of the segment that does not contain the reactive group in the hydrophilic grafting monomer structure is n2, and n1 / n2 is 1.5-9.5. The negative electrode active material described in the present invention can not only be evenly dispersed in water, but also significantly reduces the gas production problem during the slurrying of the negative electrode active material and the coating of the electrode, thereby improving the quality of the electrode and the performance of the battery.

The invention belongs to the technical field of high polymer material preparation, and provides a low-melting-point toughened copolyester chip and a preparation method thereof. The preparation method comprises the following steps: firstly, preparing hyperbranched polyester of which the surface is rich in carboxyl-terminated functional groups through core growth of polybasic acid alcohol and end group functionalization reaction of anhydride; the other chain extender is a linear chain extender which has a long flexible chain segment and two tail ends of which are also functionalized by carboxyl groups, and is obtained by carrying out end group esterification reaction on polyether glycol; then, in the synthesis process of the main polyester, carrying out multi-stage melt polycondensation on an aromatic dibasic acid component and a polyol component under the action of a composite catalyst system, introducing the hyperbranched polyester and a chain extender into a reaction system in the form of slurry, and covalently bonding a functional additive to a copolyester main chain through a polycondensation process, so as to obtain the hyperbranched polyester. An integrated network reinforced structure is formed, so that the copolyester chip has the characteristics of low melting point and excellent toughness.

According to the prepared MXene / C electrode material based on PAN carbonization, a nitrogen-doped carbon layer generated through polyacrylonitrile (PAN) in-situ carbonization serves as a supporting spacer to be inserted between MXene nanosheet layers, the MXene nanosheet layers are tightly bridged, the interlayer spacing of MXene is effectively enlarged, re-stacking of nanosheets is inhibited, and in the carbonization process, the MXene / C electrode material can be used for preparing the MXene / C electrode material based on PAN carbonization. Abundant mesopores and fissure holes are generated in the composite material by introducing and decomposing a sacrificial template (PMMA nanosphere), and a three-dimensional through ion transmission channel is constructed; the nitrogen-doped carbon layer not only serves as a supporting spacer to be inserted between MXene nanosheet layers, but also coats the surfaces of the MXene nanosheets,-F end groups on the surfaces of the MXene nanosheets are weakened, and C-O (H) and C-N functional groups are enriched, so that the interface wettability, the conductivity and the anti-oxidation stability of the material are improved, and the material can be widely applied to the technical field of electrochemical energy storage materials.

The invention provides polyether base oil and a preparation method and application thereof.According to the polyether base oil, a melt polycondensation method is adopted, a diester group-COO-R-COO-is introduced into a molecular structure through hydroxyl groups at the two ends of polyalkylene oxide, a polyether ester molecular chain with ether bonds and diester bonds distributed alternately is formed, and the polyether base oil is prepared. Then, carboxyl at the end group of a molecular chain is further subjected to an end-capping reaction with an amine compound, a unique amine double-end-capped polyether ester structure is obtained, and the polyether base oil has excellent viscosity-temperature performance, oxidation resistance, anti-rust performance and anti-wear and anti-friction performance.

The invention discloses a dynamically migratable low-surface-energy polymer modifier and a preparation method thereof, the polymer main chain of the low-surface-energy polymer modifier comprises a temperature-sensitive dynamic structure, and the polymer chain end group of the low-surface-energy polymer modifier is a fluorinated structure. The 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 migrates to the surface of a material in a processing heat treatment and use process, so that multiple effects of water resistance, pollution resistance, dust prevention, anticoagulation, antithrombus, antibiosis, self-cleaning and the like can be achieved; the modifier not only can achieve an excellent low surface energy modification effect, but also has no influence on the performance of matrix resin. The invention further discloses a low-surface-energy blending composition containing the low-surface-energy polymer modifier and application of the low-surface-energy blending composition.

The invention provides isosorbide-based copolyester as well as a preparation method and application thereof, and relates to the technical field of high polymer materials. According to the preparation method, a step-by-step esterification method is adopted, firstly, isosorbide, excessive aromatic dicarboxylic acid and an acylating agent are subjected to a first esterification reaction, so that the acylating agent can efficiently and specifically activate secondary hydroxyl of isosorbide, and the initial esterification rate of isosorbide is greatly increased. Meanwhile, the excessive aromatic dicarboxylic acid ensures that the generated isosorbide prepolymer takes carboxyl as a terminal group, so that isosorbide molecules are'locked 'in the middle of a polymer chain segment. Due to the fact that the isosorbide is embedded in the middle of the chain segment in advance, the problem that the isosorbide falls off in the ester exchange reaction due to the fact that the isosorbide is located at the chain end and low in reaction activity in the subsequent polycondensation stage is effectively solved, and therefore the retention rate of the isosorbide in the final polymer is greatly increased, and the glass-transition temperature of the isosorbide is greatly increased.

The invention relates to the technical field of manufacturing of fusible polytetrafluoroethylene resin, in particular to a method for treating an unstable terminal group of fusible polytetrafluoroethylene, which is used for solving the problem that the unstable terminal group cannot be thoroughly treated in the prior art. The method comprises the following steps: heating fusible polytetrafluoroethylene resin to a molten state, after self-reaction, introducing high-purity fluorine-nitrogen mixed gas to carry out fluoridation reaction, and extracting impurities generated by the reaction to obtain unstable soluble polytetrafluoroethylene resin with a treated terminal group; according to the method, soluble polytetrafluoroethylene resin is heated to a molten state, and unstable terminal groups are thoroughly treated through self-reaction and fluorination reaction.

In some aspects, the present disclosure provides systems for forming hydrogels that comprise (i) a reactive multi-arm polymer that comprises three or more polymer arms linked to a core region, each arm comprising a polyether segment and a reactive moiety comprising a cyclic imide carboxy-C1-C6-alkyl ester end group or each arm comprising a polyether segment and a reactive moiety comprising a C2-C6-isocyanoalkyl end group and (ii) a polyamino compound comprising at least two amino (—NH2) groups, wherein the reactive multi-arm polymer and the polyamino compound react to form a crosslinked hydrogel that does not contain ester groups and has long-term stability in vivo. In some aspects, the present disclosure provides methods of treatment using such systems and hydrolysis-resistant crosslinked hydrogels formed from such systems.

The invention belongs to the field of high polymer material synthesis, and provides a method for preparing polyphenylene sulfide from high-purity p-dichlorobenzene, which adopts the whole process design of pre-construction of a composite sulfur source intermediate, regulation and control of an end group controllable oligomerization polyphenylene sulfide intermediate, segmented polymerization of the high-purity p-dichlorobenzene and precise dehydration-washing-drying. The ultra-low impurity level of 0.05-0.25 wt% of burning residues of the polyphenylene sulfide product, the sodium ion content of 10-200 mg / kg and the chloride ion content of 10-500 mg / kg is achieved, and meanwhile the high-performance stability of the melting point of 270-300 DEG C, the gel fraction of 92-99 wt% and the water content of 0.01-0.20 wt% is kept. The problems of deep removal of inorganic ions and ash content, balance of gel fraction and processability and control of residual solvents in the traditional polyphenylene sulfide preparation process are solved, and the method has wide application value in the fields of high-performance engineering plastics, special fibers, electronic packaging materials and the like.

(Meth)acrylate-functionalized oligomers having a) an oligomeric backbone comprised of first segments and second segments and b) (meth)acrylate-functionalized end groups are provided. Such oligomers are useful as components of curable compositions. The first segments, second segments and (meth)acrylate-functionalized end groups are linked together by linking moieties derived from a polyisocyanate. The first segments are residues of a first segment precursor containing a plurality of repeating units and a plurality of isocyanate-reactive functional groups and having a number average molecular weight of at least 250 daltons. The second segments are residues of a second segment precursor, different from the first segment precursor, containing a plurality of repeating units and a plurality of isocyanate-reactive functional groups and having a number average molecular weight of at least 250 daltons. The first segment and the second segment exhibit a Hansen Solubility Parameter Distance Relative Energy Difference of at least about 4 and not more than about 9.

The invention further discloses polyethylene glycol carboxyl activated ester, degradation-adjustable amide ester bond hydrogel and a preparation method, and belongs to the technical field of biological application materials. According to the hydrogel, polyethylene glycol succinimide succinate and polyethylene glycol succinimide polyacid ester with different molecular weights, terminal group numbers and ortho-position groups are prepared through molecular design, and then the polyethylene glycol succinimide succinate and polyethylene glycol succinimide polyacid ester are mixed with an amino-rich polymer to prepare the amide ester bond hydrogel with adjustable degradation time. By adjusting the mixing ratio of the polyethylene glycol succinimide succinate to the polyethylene glycol succinimide polybasic acid ester, the degradation rate can be adjusted; wherein the degradation rate of succinimide ester bond hydrogel of the polyethylene glycol succinimide succinate is high, and the degradation rate of multi-amide ester bond hydrogel in the polyethylene glycol succinimide polybasic acid ester is low; the method is high in universality and suitable for reaction of polyethylene glycol carboxyl activated ester and any amino-rich polymer.

The invention discloses a preparation method of a PNLC film and application of the PNLC film in an automobile intelligent dimming awning, and belongs to the technical field of liquid crystal materials for intelligent awning glass and preparation of the liquid crystal materials. The problems that an existing automobile intelligent dimming awning cannot meet the rapid dimming requirement and is poor in reliability and durability and the like are solved. A bifunctional liquid crystal monomer RM82 and a nematic liquid crystal E7 are compounded, acrylate end group polymerization of the RM82 is realized under the initiation of ultraviolet light, meanwhile, a biphenyl core structure and E7 can form a strong pi-pi conjugation effect, a phase separation energy barrier of the PNLC film is remarkably reduced, GQDs serve as a scattering enhancer, the PNLC film is endowed with a dynamic luminescence capability by utilizing the fluorescence characteristic of the GQDs, and the PNLC film has a good application prospect. The orientation of liquid crystal molecules is regulated and controlled through an electric field or temperature, the light scattering state is changed, switching of light transmitting, light scattering and light emitting is achieved, and the starry sky effect is simulated.

The invention discloses a phosphorus-nitrogen-silicon flame retardant with double-end-group siloxane, hydrophobic flame-retardant epoxy resin prepared from the phosphorus-nitrogen-silicon flame retardant and a preparation method of the hydrophobic flame-retardant epoxy resin and belongs to the technical field of flame-retardant materials.The flame retardant contains elements such as P, Si and N and is symmetrical in structure, the double end groups are siloxane, rigid groups such as benzene rings are introduced, and the flame-retardant property is good. Wherein the double-end-group siloxane can be subjected to a cross-linking reaction with hydroxyl in the epoxy resin, so that the epoxy resin is endowed with good thermal stability and relatively high tensile strength; the low surface energy characteristic of siloxane can endow the epoxy resin with hydrophobicity, and the service life is prolonged; meanwhile, P / N / Si multi-elements in the structure can play a synergistic flame-retardant role, and the flame-retardant efficiency can be effectively improved in cooperation with introduction of rigid groups such as benzene rings.

The invention relates to the technical field of development of photovoltaic packaging adhesive film materials, in particular to an anti-aging PVB (Polyvinyl Butyral) adhesive film for packaging a photovoltaic module and a preparation process of the anti-aging PVB adhesive film. The anti-aging PVB composite material is prepared from the following components in parts by weight: 60-80 parts of end group modified PVB resin, 5-10 parts of a novel composite anti-aging agent, 10-20 parts of a vegetable oil-based compound plasticizer, 3-8 parts of modified composite inorganic nano filler, 1-3 parts of a diepoxy group-containing cross-linking agent and 1-3 parts of an ultraviolet absorbent with a multi-conjugated structure, and all the components synergistically improve the performance. Through end group modification and special additives, the anti-aging, flexibility and heat resistance are improved, the binding power is enhanced, the preparation process is optimized, the efficiency is improved, the cost is reduced, the service life of a photovoltaic module is prolonged, the performance is guaranteed, and the development of the photovoltaic industry is promoted.