6722 results about "Polymerization" patented technology

The invention belongs to the technical field of solid-state lithium batteries, and relates to a fluorinated double-salt cross-linked solid-state electrolyte adaptive to a lithium-free negative electrode, a solid-state lithium battery and a preparation method thereof.The preparation method comprises the steps that double-lithium salt is dissolved in a fluorinated solvent to obtain an electrolyte, then a monomer, a cross-linking agent and an initiator are added, the mixture is stirred to be uniform to obtain a precursor solution, and the precursor solution is prepared; and assembling the precursor solution, a positive electrode, a negative electrode and a solid-state electrolyte composite diaphragm into a battery, and performing gradient polymerization to form the solid-state lithium battery. According to the invention, the ionic conductivity of the solid electrolyte is more than 5 * 10 <-4 > S / cm and the oxidation potential of the solid electrolyte is more than 5.8 V by adopting a fluorinated solvent consisting of fluorinated carbonate and fluorinated carboxylate and a double-lithium-salt synergistic system and combining an in-situ interface fusion technology, so that the solid electrolyte can be matched with a 4.8 V high-voltage lithium-rich manganese-based positive electrode and a lithium-free negative electrode; and the energy density and the safety of the solid-state lithium battery are improved. The electrolyte scheme is low in cost, high in safety and good in positive and negative electrode matching performance, can be compatible with an existing battery production line, and is convenient for large-scale production.

The invention provides a preparation method of an h-BN / PI high-temperature-resistant anticorrosive coating, and relates to the technical field of polymer composites.The preparation method of the h-BN / PI high-temperature-resistant anticorrosive coating comprises the steps that under the protection of inert atmosphere, aromatic diamine containing impurity element five-membered rings and aromatic dianhydride containing ether bonds are taken and subjected to a polymerization reaction in a polar aprotic solvent, and the h-BN / PI high-temperature-resistant anticorrosive coating is obtained. A polyamide acid solution is obtained; performing ultrasonic-assisted liquid phase stripping on the micron-sized hexagonal boron nitride to obtain single-layer hexagonal boron nitride; adding the single-layer hexagonal boron nitride into the polyamide acid solution for multiple times, and uniformly stirring to obtain a hexagonal boron nitride / polyimide composite solution; and coating the hexagonal boron nitride / polyimide composite liquid on a to-be-coated surface, and carrying out gradient heating curing to obtain the h-BN / PI high-temperature-resistant anticorrosive coating. The h-BN / PI high-temperature-resistant anticorrosive coating based on interaction of multiple hydrogen bonds has relatively good high temperature resistance, relatively good resistance mechanical property and excellent corrosion resistance.

The invention belongs to the field of bioinformatics, and relates to an anti-cancer drug response prediction method based on an attention mechanism. The method comprises the following steps: firstly, capturing uniform-dimension drug and cancer cell line characteristics through a multi-layer perceptron; secondly, fusing drug characteristics by adopting a Transform encoder, and constructing a cell encoder for cancer cell line characteristic polymerization; then, designing a cross-modal cross fusion module to promote information interaction between the two; and finally, predicting a semi-suppressed concentration value subjected to logarithmic transformation between the two through a multi-layer perceptron. Experimental results show that compared with an existing optimal method, the method has the advantage that the RMSE is reduced by 2.9%. According to the method, accurate prediction of the anti-cancer drug response is achieved by integrating drug and cancer cell line data, screening of potential anti-cancer drugs can be accelerated, personalized treatment schemes can be optimized, the cure rate of cancer patients is further increased, and the method has great significance in cancer treatment.

The invention discloses a method for evaluating enhancement and release seedling resources based on environmental DNA polymerization analysis. The method comprises the following steps: carrying out gridding partition on a target water area, collecting a water sample through a designed sampling scheme, and carrying out DNA extraction and high-throughput sequencing to obtain species sequence information of each sampling point. Sequencing data is subjected to species identification by using a bioinformatics method, released species are identified, a spatial abundance model is established, and a preliminary distribution map is generated. And establishing a DNA degradation kinetic model in combination with water area environmental parameters, and carrying out reverse correction on abundance distribution. And through a resource inversion model coupled with hydrodynamics, analyzing biomass distribution characteristics and migration laws of the release group, and obtaining a resource evaluation result. And finally, a species environment preference model is constructed based on migration path analysis, an optimal release area is matched in a target water area, a scientific scheme including release point locations, opportunities and quantity is generated, and a whole-process technical support and a decision basis are provided for enhancement and release.

The invention discloses a high-interface-stability composite solid electrolyte membrane as well as a preparation method and application thereof. The composite solid electrolyte membrane comprises a gradient aperture three-dimensional porous skeleton formed by sintering inorganic solid electrolyte particles, a polymer electrolyte filled in a pore channel, and a plastic interface stable layer positioned between the electrolyte membrane and an electrode. The preparation method comprises the following steps: preparing a gradient aperture porous framework through a pore-forming agent template method and a tape casting technology, dipping and filling a polymer electrolyte precursor solution in a solution, accelerating in-situ polymerization by adopting electric induction, and performing hot-pressing treatment. The composite solid-state electrolyte membrane has high ionic conductivity, excellent interface compatibility and high mechanical strength, can effectively inhibit the growth of lithium dendrites, can be applied to solid-state batteries such as lithium metal batteries, lithium sulfur batteries and lithium air batteries, and can remarkably prolong the cycle life and improve the safety performance of the batteries, and the preparation process is suitable for large-scale production.

The invention discloses a layered pore structure geopolymer based on combination of multi-stage low-temperature in-situ polymerization and an ice template method and a preparation method of the layered pore structure geopolymer. The preparation method comprises the following steps: preparing geopolymer slurry; performing one-way freezing on the slurry to form a frozen green body containing a directionally arranged ice crystal template; before the frozen green body is subjected to freeze drying to remove an ice crystal template, specific multi-stage low-temperature in-situ polymerization treatment is carried out, and the treatment comprises at least two different low-temperature heat preservation stages which are sequentially carried out within the temperature range of-10 DEG C to + 5 DEG C, and the temperature of the low-temperature heat preservation stages is gradually increased; and then the treated green body is subjected to freeze drying and maintenance. According to the method, the multi-stage low-temperature in-situ polymerization step aiming at the reaction characteristics of the geopolymer is introduced before the ice crystal template is removed, so that the problems of low mechanical property and unstable pore structure of the geopolymer prepared by a traditional ice template method are solved, and the mechanical strength and structural integrity of the product are remarkably improved; meanwhile, a good layered pore structure and pore channel connectivity are kept.

The invention discloses a bionic lignin-based saline-alkali soil improvement material and a preparation method thereof, and belongs to the technical field of high polymer materials and soil improvement. According to the saline-alkali soil improving material, lignin or a derivative thereof serves as a framework, glutenin charge distribution and a dynamic disulfide bond sodium ion response function are simulated, and the sequence and the proportion of chain segments of sulfonic acid groups and quaternary ammonium salt groups are accurately regulated and controlled through step-by-step activation and alternate copolymerization in an aqueous solution polymerization reaction system; positive and negative charges form more uniform sequence distribution, so that the amphipathy of the lignin compound is realized; then, sulfydryl is introduced through click chemistry, linear regulation and control of material viscosity and water solubility are achieved through the chain transfer characteristic of multi-sulfydryl functional groups, and the requirements of different saline-alkali soil application scenes are met. The limitation that a traditional lignin product is single in function is broken through, efficient utilization of lignin is achieved, and the intelligent saline-alkali soil improvement material integrating high stability and pH and Na < + > multi-environment response is developed.

The invention relates to environment-friendly hydrophobic ink and a preparation method thereof, and belongs to the technical field of water-based ink. A copolymerization modifier capable of being combined in a water-based polyacrylate emulsion in an initiation polymerization mode in the stage of preparing the modified water-based polyacrylate emulsion is prepared, and an o-hydroxy aromatic ketone structure in the copolymerization modifier can endow water-based ink with lasting ultraviolet absorption performance; the trifluoromethyl structure can reduce the surface energy of the water-based ink, and the benzimidazole ring structure can form stable coordinate bonds with metal ions, so that the bonding performance of the water-based ink and a metal substrate is enhanced; when the copolymerization modifier is used for modifying the water-based polyacrylate emulsion, the long-term performance, the hydrophobic and oil-resistant performance and the adhesion performance on the surface of a metal base material of the finished water-based ink can be effectively improved.

The invention relates to the technical field of process control, in particular to a polyphenylene sulfide polymerizer temperature self-adaptive control method, which comprises the following steps: acquiring melt viscosity, heat release power and residence time deviation of a polymerizer in real time, and constructing a normalized multi-dimensional time sequence input vector by using a sliding window technology; and then, through fusing a weight control model of a long short-term memory network and an attention mechanism, combining static working condition characteristics, and analyzing and outputting adaptive weight coefficients for different deviation dimensions in real time. Meanwhile, based on the shear heat effect and the reaction accumulation effect, specific temperature compensation components for the inlet of the heating medium jacket are calculated, and independent amplitude limiting processing is carried out on all the components. And finally, a target set temperature is synthesized through weighting, and an execution mechanism is driven to act accurately by utilizing cascade PID control and a valve flow characteristic inverse mapping model. According to the invention, through deep fusion and mechanism compensation, accurate steady-state control of the polymerization reaction is realized.

The invention relates to the technical field of PC transparent flame-retardant toughening modification, in particular to phenolic hydroxyl-terminated modified polysiloxane with a side chain containing phenyl and sulfonate groups and a preparation method of copolymerized PC. The modified polysiloxane is prepared by the following steps: performing ring opening polymerization on phenol-containing double end sockets and cyclotetrasiloxane to obtain modified polysiloxane containing double bonds and phenyl functional groups, and grafting sulfonate through a thiol-ene click chemical reaction. Diphenyl carbonate, bisphenol A and the modified polysiloxane are used as raw materials, a polysiloxane-PC block copolymer is formed through copolymerization, efficient flame retardance and high transparency are achieved, and meanwhile extremely high low-temperature impact strength is achieved.

The invention discloses a conductive yarn and a preparation method thereof, relates to the technical field of functional textile materials and composite conductive fiber preparation, and can solve the problems that an existing conductive yarn is poor in flexibility, insufficient in durability, prone to oxidation failure and difficult to integrate multiple functional performances. The preparation method comprises the following steps that S1, PBO yarn is soaked in a dopamine solution, a PDA modification layer is formed on the surface of the PBO yarn through a polydopamine self-polymerization reaction, and the PDA modification layer provides a chelation site and a bonding interface for metal deposition; s2, the PDA modified PBO yarn obtained in the step S1 is subjected to chemical silver plating, silver is deposited on a PDA modified layer to form a continuous conductive layer, and conductive PBO core yarn is prepared; s3, carrying out melt blending and granulation on the low-dielectric-constant flame-retardant filler and thermoplastic polymer resin to prepare flame-retardant composite particles; and S4, spinning by taking the conductive PBO core yarn prepared in the step S2 as a core layer and a melt formed by melting the flame-retardant composite particles prepared in the step S3 as a skin layer to prepare the conductive yarn.

The invention provides a self-assembled hypha flexible carbon electrode material and a preparation method and application thereof, and belongs to the technical field of battery packs. The preparation method of the self-assembled hypha flexible carbon electrode material comprises the following steps: treating basswood with white rot fungus mycelia, crushing and roasting to obtain porous basswood / hypha composite carbon powder; and putting the porous basswood / hypha composite carbon powder and a carbon nanotube into a sterilized conical flask containing a potato glucose culture solution, inoculating gloeophyllum trabeum, performing activation culture, adding a dopamine hydrochloride aqueous solution, performing polymerization after ultraviolet irradiation, taking out and tabletting to obtain the self-assembled hypha flexible carbon electrode material. In the preparation process of the self-assembled hypha flexible carbon electrode material, the flexible carbon electrode material is synthesized by taking porous basswood / hypha composite carbon powder as a matrix, taking gloeophyllum trabeum hypha as an adhesive, taking polydopamine as a reinforcing agent and adding carbon nanotubes as a conductive reinforcing material, so that the technical problem of poor cycle performance of a lithium ion battery is solved.

The invention belongs to the technical field of new energy materials, and particularly relates to siloxane crosslinking modified polyether solid electrolyte and a preparation method thereof. According to the solid electrolyte, the electrophilic ring-opening polymerization reaction of a polymer monomer with an epoxy group is utilized, siloxane is used as a cross-linking agent, polyether chain structures are connected together to form a cross-linked network structure, the ionic conductivity can be increased, and the mechanical strength and the high-temperature dimensional stability can be improved; the lithium ion transference number is increased, the polarization is reduced, and the battery rate capability is improved; the oxidation stability of the electrolyte is improved; the decomposition reaction of polyether at high temperature is inhibited; the thermal stability and the flame retardant property of the polymer electrolyte are remarkably improved, so that the safety of a solid-state battery is improved.

The invention discloses a distribution network multi-source roof photovoltaic cluster collaborative aggregation regulation and control method, and belongs to the technical field of distribution network large-scale roof photovoltaic aggregation upgrading consumption, and the method comprises the following steps: collecting a power distribution network topological structure and line impedance parameters in real time, calculating the electrical distance modularity between nodes, and calculating the electrical distance modularity between the nodes; taking the reactive voltage sensitivity as a clustering core index, dividing the power distribution network into a plurality of photovoltaic clusters, selecting a node with the highest comprehensive sensitivity as a dominant node for each cluster, and establishing an inter-cluster reactive voltage sensitivity relation matrix; multi-stage collaborative optimization regulation and control are carried out, day-ahead, intra-day and real-time three-stage optimization models are constructed, and a cluster-stage optimization model is established by taking the minimum voltage deviation as a target; and carrying out multi-agent cooperative voltage regulation and strategy verification and updating. According to the method, the power grid topology is collected, node impedance is calculated, clustering is carried out through reactive sensitivity, a target function is solved through day-ahead optimization, intra-day voltage out-of-limit correction is carried out, margins are distributed in real time, and the technical problem of slow voltage regulation response is solved.

The invention relates to the technical field of soil remediation, in particular to a biochar-humic acid-calcium alginic acid composite saline-alkali soil modifier and a preparation and application method thereof. The modifier adopts a multi-layer structure design: biochar is pre-adsorbed by calcium chloride, compounded with sodium humate, and then crosslinked with sodium alginate to form a gel to form a composite inner core; secondly, sulfobetaine methacrylate and vinyl phosphonic acid are introduced into a sodium alginate molecular chain through graft polymerization, and modified sodium alginate is obtained to serve as an outer layer coating material; and finally, dipping the composite inner core into the outer layer solution, and carrying out graded recalcification by calcium chloride and short-time treatment by sodium sulfate to obtain a final product. Through the synergistic effect of calcium ion slow release of the inner core and zwitterionic characteristics of the outer layer, efficient replacement and long-term stable regulation and control of soil sodium ions are achieved, the pH value, the conductivity and the alkalization degree of soil are remarkably reduced, the water holding capacity is effectively improved, and the soil conditioner is suitable for sustainable improvement of moderate and severe saline-alkali soil.

The invention discloses a polyetherketoneketone high-temperature-resistant wear-resistant non-stick coating and a preparation method thereof. The coating is prepared from the following components in parts by mass: 13 to 30 parts of a resin matrix group (containing 12 to 25 parts of titanium modified polyether ketone ketone resin, 1 to 5 parts of fluorine-free viscous resin and 0.65 to 6 parts of aluminum oxide), 0.5 to 3 parts of a nano reinforced group (containing 0.5 to 3 parts of KH-550 modified nano titanium dioxide, 0.025 to 0.6 part of cerium dioxide and 0.5 to 3 parts of boron nitride) and 62 to 71 parts of an auxiliary agent group. The preparation method comprises the following steps: 1) taking diphenyl ether, paraphthaloyl chloride and isophthaloyl chloride as monomers, and synthesizing titanium modified polyether ketone ketone resins with different viscosities through segmented polymerization (1.5-2.0 hours or 3.0-4.0 hours); 2) respectively preparing a smooth bottom layer water dispersion slurry and a wrinkled surface layer water dispersion slurry; and (3) forming a compact bottom layer and a micro-wrinkle surface layer on the base material by adopting a layered spraying and stepped sintering process (280-320 DEG C, 10-20 minutes). The whole system of the coating is fluorine-free and has temperature resistance gt; the coating has the characteristics of high temperature resistance (350DEG C), wear resistance (Taber wear rate of 3-5mg / 1000r), non-sticking (contact angle gt, 100 DEG C) and heavy corrosion resistance, and is suitable for cooking utensils and chemical equipment.

The present application provides a preparation method for a filtrate reducer and the use thereof. The preparation method comprises: dropwise adding a silane coupling agent containing double bonds into a graphite dispersion under an acidic condition for grafting reaction to obtain silane-coupling-agent-modified graphite, then adding a cross-linking agent into the silane-coupling-agent-modified graphite, adjusting the pH to neutrality to obtain a first intermediate solution, mixing acrylamide, a sulfonic monomer, a cationic monomer and a monomer containing a cyclic group, then adjusting the pH to neutrality to form a second intermediate solution, finally adding an initiator into the first intermediate solution, then dropwise adding the second intermediate solution for polymerization reaction to obtain the filtrate reducer. The filtrate reducer prepared by such a method has a better high-temperature-resistant filtrate loss reduction property, and better pressure bearing capacity and plugging capacity.

The invention relates to a universal adapter sensor detection platform and application thereof. The detection platform comprises an aptamer sensor module, the aptamer sensor module comprises at least one of a first aptamer sensor and a second aptamer sensor, and the first aptamer sensor comprises a first signal output sequence, a first promoter sequence, a first target aptamer sequence and an Assistor sequence from the 5'end to the 3 'end; the second aptamer sensor comprises a second signal output sequence, a second promoter sequence, a second target aptamer sequence and a Locker sequence from the 5'end to the 3 'end; and the reaction regulation and control module comprises a polymerization reaction unit and a transcription reaction unit. The platform has good sensitivity (subnanomole level) and fast response time (lt, 40 min), and has universality, programmability and portability at the same time.

The recycled bis(4-hydroxybutyl) terephthalate according to one embodiment has a low amount of residual ethylene glycol derivatives and can therefore be used as a polymerization raw material for high crystallinity engineering polyester products or biodegradable polyesters, offering superior qualities, for example, color.

The invention discloses unsaturated polyester resin for an optical cable reinforcing core and a preparation method thereof, and belongs to the technical field of unsaturated polyester resin. The composition is composed of the following components: PG, IPA, a catalyst, maleic anhydride, AA, styrene, an antioxidant, a first polymerization inhibitor, a second polymerization inhibitor and a third polymerization inhibitor. The ratio of alcohol to acid is (1.08-1.12): 1; the activity is (3.4-3.8): 1; the molar ratio of AA to IPA is 1: (12-16); the preparation method comprises the following steps: 1) uniformly mixing propylene glycol, a catalyst and isophthalic acid; 2) raising the temperature, preserving the heat and raising the temperature again; cooling, sequentially adding a first polymerization inhibitor, maleic anhydride and adipic acid, heating, keeping the temperature, and heating again; 3) cooling and adding a second polymerization inhibitor, and 4) cooling and adding styrene, a third polymerization inhibitor and an antioxidant, uniformly mixing, and cooling to less than or equal to 60 DEG C to obtain the unsaturated polyester resin for the optical cable reinforcing core. The unsaturated polyester resin for the optical cable reinforcing core has the characteristics of high bending strength and high temperature resistance.

The invention discloses a preparation method and application of a zinc-bromine flow battery positive electrode material, and belongs to the field of zinc-bromine flow batteries. The preparation method comprises the following steps: firstly, cleaning and activating a carbon-based three-dimensional conductive network substrate by adopting plasmas, performing oxygen / argon plasma etching, and performing chemical vapor deposition on carbon to prepare three-dimensional porous carbon; then growing a metal oxide nanocrystalline array on the three-dimensional porous carbon by a hydrothermal method, and carrying out ammonia gas calcination to convert the metal oxide nanocrystalline array into a metal nitride nanocrystalline array; then preparing an electro-deposition solution containing tin bismuth salt and an aniline-bromine source polymerization solution, and constructing Sn-Bi bimetallic nanoparticles and a polyaniline-bromine complex layer on the metal nitride nanocrystalline array / three-dimensional porous carbon precursor through electro-deposition and electro-polymerization in sequence to finally prepare the high-performance zinc-bromine battery positive electrode material. The positive electrode material has high conductivity, excellent Br2 / Br <-> catalytic activity and structural stability, and the coulombic efficiency, the voltage efficiency and the energy efficiency of the battery are remarkably improved.

The invention discloses a method for constructing a dual-mode sensor through smartphone-assisted surface molecular imprinting for detecting diphenyl phosphate and application of the dual-mode sensor, and belongs to the technical fields of biochemical analysis, functional nano materials and life science. In synthesis, solubility and selectivity of a target object and photo-initiation efficiency in a polymerization process are optimized, and diphenyl phosphate molecularly imprinted nano-enzyme MIPs is rapidly prepared through a molecular imprinting technology; in the detection, H2O2 and 3, 3, 5, 5-tetramethyl benzidine TMB are catalyzed by peroxidase-like activity of Fe and N-CDs to generate a chromogenic reaction and an inner filter effect of oxTMB is used for inhibiting a fluorescence signal, dual-signal cross validation is realized in cooperation with a smart phone, and the colorimetric-fluorescence sensor for detecting diphenyl phosphate is constructed. The sensor has specific recognition selectivity and binding affinity of diphenyl phosphate, is simple to operate and low in cost, can realize sensitive detection of diphenyl phosphate in a wide linear range, has the detection limit as low as 16 pg / mL, and is suitable for field analysis of trace DPhP in a complex water environment.

The invention discloses a composite solid electrolyte layer, a preparation method and application, the composite solid electrolyte layer comprises a porous membrane laminated on a negative pole piece, and pores in the porous membrane and gaps between the porous membrane and the negative pole piece are filled with in-situ generated polymers. Inorganic solid electrolyte is also dispersed in the porous membrane, and lithium salt is dispersed in the polymer and the porous membrane. The composite solid electrolyte layer is obtained through in-situ polymerization of a polymer in pores in the porous membrane and gaps between the porous membrane and the negative electrode plate, and a novel interface structure with the electrode-electrolyte integration characteristic is constructed. By adopting a collaborative optimization strategy of a polymer matrix and inorganic filler double-crosslinking network system and an interface stable layer, the volume effect problem of a silicon-based negative electrode, the electrolyte interface impedance problem and the battery safety problem can be solved at the same time, so that the cycling stability and the rate capability of the lithium ion battery are remarkably improved.

The present invention relates to the field of polyurethane materials and particularly to a temperature-induced color-changing vehicle film and a preparation method therefor. The method of the present invention comprises: firstly, using polyurethane to wrap vanadium dioxide powder to obtain color-changing microcapsules; then using 1,1,1,3,5,5,5-heptamethyltrisiloxane and 3-allyloxy-1,2-propanediol as raw materials to synthesize an organosilicon-modified diol, and enabling trimellitic anhydride to react with toluene diisocyanate to synthesize a dicarboximide compound; enabling the organosilicon-modified diol and the dicarboximide compound to undergo an esterification reaction and a polymerization reaction to obtain an organosilicon-modified imide polyester diol; then mixing the organosilicon-modified imide polyester diol with polytetrahydrofuran ether glycol 2000, and then enabling the mixture to react with toluene diisocyanate to obtain a polyurethane elastomer; and mixing the polyurethane elastomer, the color-changing microcapsules, a silane coupling agent, a plasticizer, an antioxidant, and an ultraviolet light absorber, followed by melt extrusion and blow molding into a film, so as to obtain the temperature-induced color-changing vehicle film.

The invention discloses a multi-network anti-freezing hydrogel electrolyte, a preparation method thereof and application of the multi-network anti-freezing hydrogel electrolyte in an electrochemical device. The hydrogel is prepared by using polyvinyl alcohol (PVA) and polyacrylamide (PAM) to form a basic network skeleton, introducing phytic acid, ethylene glycol and lithium / zinc bimetal salt (Li2SO4 / ZnSO4), and carrying out thermal initiation polymerization and freeze thawing. The hydrogel prepared by the invention has a multiple physical cross-linked network formed by polymer molecular chain entanglement, hydrogen-bond interaction among functional groups and metal coordinate bonds constructed between phosphate groups and divalent metal ions, so that the hydrogel electrolyte has excellent mechanical properties. Due to introduction of ethylene glycol, formation of ice crystals is effectively inhibited, and the hydrogel is endowed with excellent anti-freezing performance; the high-concentration Li < + > and Zn < 2 + > ensure the high ionic conductivity. The supercapacitor assembled by using the hydrogel electrolyte shows relatively high specific capacitance and good capacitance retention rate under bending and freezing conditions, and has good electrochemical properties and safety performance.

The invention relates to the technical field of high polymer materials, and discloses a conductive shielding material for a high-voltage cable. Comprising the following components in parts by weight: 40 to 70 parts of main body polyolefin resin, 10 to 30 parts of ethylene-vinyl acetate copolymer, 5 to 15 parts of maleic anhydride grafted polyolefin, 20 to 40 parts of surface modified conductive carbon black, 0.5 to 2 parts of peroxide cross-linking agent, 0.5 to 3 parts of functionalized silane coupling agent, 0.1 to 1 part of processing aid and 0.1 to 1 part of antioxidant, the surface modified conductive carbon black is high-structure conductive carbon black which is subjected to plasma oxidation treatment, solution graft polymerization and surface coupling agent pretreatment. The conductive carbon black is subjected to multi-step surface modification including plasma oxidation, solution graft polymerization and surface coupling agent pretreatment, and the in-situ chemical bonding effect of maleic anhydride grafted polyolefin is matched, so that the agglomeration problem of the conductive carbon black caused by high surface energy is effectively solved.

The invention belongs to the field of wastewater treatment, and particularly relates to a method for co-treating high-salt degradation-resistant organic wastewater based on electro-polymerization of in-situ activated chlorine free radicals of a penetrating electrode. The method comprises the following steps: by taking a penetrating electrode as an anode, sequentially and alternately arranging the anode and the cathode to form an electrode group, placing the electrode group in a reaction tank, connecting the cathode and the anode of the electrode group with a direct-current power supply, and carrying out electrocatalytic degradation on the high-salt degradation-resistant organic wastewater to be treated in the reaction tank; the transmission type electrode comprises a porous conductive substrate and a metal oxide catalytic layer loaded on the surface of the porous conductive substrate. Under the action of low current, the metal oxide catalytic layer of the anode activates chloride ions in the wastewater in situ to generate chlorine free radicals, and refractory pollutants are degraded through the action of electrocatalytic oxidation; meanwhile, a low-current polymerization reaction is initiated to generate a polymer to adsorb pollutants, so that electrocatalytic oxidation and polymerization synchronous synergistic decontamination is realized.

The present invention relates to the technical field of tackified adhesive films and specifically to a tackified adhesive film. The tackified adhesive film comprises a substrate layer and a UV-tackified adhesive layer applied onto the substrate layer. The UV-tackified adhesive layer is prepared by using a modified polyester resin, which is obtained by the graft polymerization of a hydroxyl-terminated polyester resin, butyl methacrylate, and isocyanatoethyl methacrylate, as a main resin and mixing the main resin with a tackifying resin, a photo-curing agent and the like. The UV-tackified adhesive layer has relatively high cohesive strength and relatively good adhesion to a PET substrate. Before a UV-induced tackification reaction, an initial peel force is not significantly increased with the extension of standing time, so that an adhesive tape can be easily removed without causing damage and contamination such as residual adhesive to an adherend . After the UV-induced tackification reaction, the modified polyester resin can improve the bonding strength between the adhesive tape and the adherend.

The invention belongs to the field of functional composite materials, and particularly relates to low-viscosity and high-dispersity aluminum oxide slurry and a preparation method thereof.The low-viscosity and high-dispersity aluminum oxide slurry is prepared from a newly-designed phosphono-carboxyl block copolymer and biquaternary ammonium salt polyether silane as composite modifiers; and efficient anchoring and stable dispersion of the surfaces of alumina particles are realized through the synergistic effect of molecular structures. The phosphono-carboxyl block copolymer is prepared through controllable polymerization and deprotection reaction, and strong chemical bonding is formed between a phosphono group and the surface of aluminum oxide; the biquaternary ammonium salt polyether silane is subjected to click chemical synthesis, and electrostatic adsorption of quaternary ammonium salt and the steric hindrance effect of a polyether chain are combined. When the slurry is prepared, the two modifiers are sequentially added into water, the aluminum oxide powder is added after the pH value is adjusted, finally, the isobutylene maleic anhydride copolymer and the defoaming agent are introduced, and the slurry is obtained through vacuum defoaming and filtering. The slurry prepared by the method has the characteristics of high solid content, low viscosity and good dispersion stability.

The invention discloses a kit for detecting miRNAs of multiple extracellular vesicles based on a TtAgo-driven rolling circle amplification technology and application of the kit, a platform combines TtAgo protein and RCA reaction, cooperates with endonuclease activity and DNA polymerase activity of TtAgo, accurately controls reaction kinetic balance between temperature and enzyme activity, not only does not damage the cutting activity of TtAgo, but also can detect miRNAs of multiple extracellular vesicles. The method provided by the invention can be used for detecting multiple extracellular vesicles miRNAs, ensures strong polymerization amplification performance, creates a strong one-step single-tube experiment, greatly simplifies the experimental process, shortens the detection time, realizes ultra-sensitive and specific detection of nucleic acid markers, and can be used for detecting multiple extracellular vesicles miRNAs.