5454 results about "Organosolv" patented technology

The invention discloses a transparent composition photoresist with low shrinkage and low vacuum deflation. Comprising the following raw materials in percentage by mass: 1-5% of modified polyhedral oligomeric silsesquioxane (POSS), 1-5% of an expanding monomer, 1-5% of modified acrylic resin, 1-5% of epoxy resin, 1-5% of a thiol cross-linking agent, 1-5% of an initiator, 0.1-3% of a curing accelerator, 0.2-0.5% of a flatting agent, 0.1-5% of a silane coupling agent, 0.01-0.2% of an antioxidant and 80-90% of an electronic-grade organic solvent. The invention also provides a preparation method of a cured coating prepared from the transparent composition photoresist with low shrinkage and low vacuum deflation. The product provided by the invention not only can maintain the properties of high hardness, high thermal stability, high planarization ability, high barrier property, low hygroscopicity, low dielectric constant and the like of the transparent composition photoresist coating, but also can enable the transparent composition photoresist coating to have excellent low shrinkage and low outgassing, thereby achieving the purposes of saving energy, reducing emission, reducing cost and improving efficiency; the low shrinkage of the transparent composition photoresist coating also widens the development of the material in the fields of other panel production processes such as OLED (Organic Light Emitting Diode) and the like.

The present disclosure provides a solid electrolyte composition that can suppress deterioration in ion conductivity of an ionic solid electrolyte material. The solid electrolyte composition according to the present disclosure contains a sulfur element-free ionic solid electrolyte material and an organic solvent, where the organic solvent includes at least one selected from the group consisting of a hydrocarbon and a compound having a functional group; and the functional group is at least one selected from the group consisting of an ether group, a halogen group, and a Si—O—C group.

The invention belongs to the technical field of organic pollution treatment, and relates to a biochar-LDH-nZVI-GO composite material for organic pollution remediation and a preparation method and application thereof.The preparation method comprises the steps that graphene oxide is ultrasonically dispersed in deionized water, magnesium salt and aluminum salt are added to form uniform suspension liquid, then the uniform suspension liquid is mixed with biochar suspension liquid, and the biochar-nZVI-GO composite material is obtained; carrying out pH (Potential of Hydrogen) regulation and a hydrothermal crystallization reaction, so as to prepare a biochar-Mg / Al-LDH-GO compound; and dispersing the compound in an organic solvent, sequentially adding FeSO4. 7H2O and a NaBH4 solution in an inert atmosphere to carry out a reduction reaction, and finally washing and drying to obtain the biochar-LDH-nZVI-GO composite material. The material shows high-efficiency removal capacity on various organic pollutants such as trichloroethylene, chlorobenzene and polychlorinated biphenyl, is suitable for high-efficiency green remediation of organic pollutants in soil and water, and has good popularization and application prospects.

The present disclosure provides a solid electrolyte composition that can suppress deterioration in ion conductivity of an ionic solid electrolyte material. The solid electrolyte composition according to the present disclosure contains a sulfur element-free ionic solid electrolyte material and an organic solvent, where the organic solvent includes at least one selected from the group consisting of a hydrocarbon and a compound having a functional group; and the functional group is at least one selected from the group consisting of an ether group, a halogen group, and a Si—O—C group.

The invention provides a non-aqueous electrolyte, a lithium ion battery, a battery module, a battery pack and a power utilization device, the non-aqueous electrolyte comprises a lithium salt, an organic solvent and an electrolyte additive, and the electrolyte additive comprises 1, 3-propane sultone, fluoroethylene carbonate, vinylene carbonate, lithium tetrafluoroborate and a compound I shown in the formula I. The non-aqueous electrolyte is applied to the lithium ion battery, and the cycle life of the lithium ion battery is prolonged.

The preparation method comprises the following steps: mixing 20-40 parts by mass of substituted hydroxymethyl glycoluril, 45-85 parts by mass of mercaptocarboxylic acid and 0.5-3 parts by mass of an acidic catalyst, stirring and reacting for 1-10 hours at the temperature of 50-150 DEG C under the pressure condition of-0.01 to-0.1 MPa, adding 300-800 parts by mass of an organic solvent for diluting after the reaction is finished, washing and purifying with deionized water, and collecting an organic layer, thereby obtaining the mercaptan curing agent. Concentrating and drying to obtain the mercaptan curing agent. According to the thiol curing agent, the rigid glycoluril group is introduced, so that the rigidity of a cured product structure is improved, and the mechanical property, the adhesive property, the heat resistance and the damp-heat aging resistance of a cured product are improved; four tertiary amine groups in the substituted glycoluril have a certain self-promotion effect on a thiol curing epoxy reaction, and the curing reaction temperature is reduced under the condition that an accelerant is not added; the glycoluril-containing thiol epoxy resin curing agent disclosed by the invention has good application value and development prospect.

The invention discloses SGNH family esterase SH2 screened in a Tibetan hot spring environment and application of the SGNH family esterase SH2, and belongs to the technical field of gene engineering. According to the invention, a new SGNH family esterase gene is screened from a Tibetan hot spring environment, and recombinant expression is realized in escherichia coli. The recombinant esterase prepared by the invention has the characteristics of thermal stability, salt resistance, organic solvent resistance and the like, can be safely applied to tooth whitening or skin exfoliating products, avoids damage of traditional chemical bleaching agents to enamel, and has important application value in the fields of daily chemicals, medicines, food processing and the like.

The invention discloses an electrolyte for a lithium manganate lithium ion battery and a preparation method thereof, and the electrolyte comprises the following components in percentage by mass: 70-90% of an organic solvent, 5-20% of a lithium salt and 0.5-10% of an additive, the organic solvent is formed by mixing cyclic carbonate and chain carbonate according to the mass ratio of (10-30): (70-90); the lithium salt adopts one or more of lithium hexafluorophosphate (LiPF), lithium tetrafluoroborate (LiBF) and lithium bis (trifluoromethane sulfonimide) (LiTFSI), and the concentration of the lithium salt is 0.8 to 1.5 mol / L; the additives comprise a manganese ion complexing agent, a film forming accelerant and an antioxidant. In the invention, the manganese ion inhibition effect is as follows: the complexing agent and Mn (II) ions form a stable complex, so that the concentration of free Mn (II) in the electrolyte is reduced by more than 80%, migration and deposition of the free Mn (II) to the negative electrode are inhibited, and the dissolution amount of the Mn element of the positive electrode is reduced by 65% after 500 times of circulation at 45 DEG C.

The invention relates to the technical field of polymer electrolyte, in particular to a self-repairing type gel polymer electrolyte membrane, a preparation method and application in an energy storage battery, the self-repairing type gel polymer electrolyte membrane is prepared by the following steps: dissolving amino-terminated polyethylene glycol in an organic solvent, adding trimesic acid under the protection of an inert atmosphere, heating, stirring and reacting to form a pre-polymerized solution, cooling, and then adding trimesic acid into the pre-polymerized solution to prepare a self-repairing type gel polymer electrolyte membrane; the preparation method comprises the following steps: adding glyoxylic acid and glacial acetic acid, carrying out a constant temperature reaction to obtain a solution A, adding LiTFSI into the solution A, carrying out ultrasonic dispersion to a homogeneous phase, pouring the obtained slurry onto a template, and carrying out a drying curing reaction to obtain the self-repairing gel polymer electrolyte membrane. A rigid aromatic cross-linking agent is used for inhibiting polymer crystallization and improving mechanical integrity, an imine bond-based dynamic covalent network is introduced to realize an autonomous interface repairing function at the working temperature of the battery, and meanwhile, a polyethylene glycol ether oxygen chain is used for constructing an efficient lithium ion transmission channel; therefore, the technical boundary that the conductivity, the mechanical strength and the interface stability of the traditional GPE are difficult to collaboratively optimize is broken through.

The invention belongs to the technical field of biological medicine, and discloses a novel adjuvant recombinant herpes zoster vaccine and a preparation method thereof. The vaccine is composed of gE-gD protein and a liposome adjuvant, the liposome adjuvant is prepared by the following steps: co-dissolving 3D-MLA, phospholipid-containing components and steroid components in an organic solvent to form a film, hydrating and homogenizing with PBS, finally adding QS-21, and fixing the volume with PBS. According to the process, enhanced components are uniformly and stably anchored in a membrane phase micro-domain, and the particle structure is controllable. Under the same antigen dosage and detection caliber, the D28 GMC of the vaccine is obviously improved, and more sufficient and stronger primary humoral immune response is embodied.

The invention discloses an endoglucanase truncated mutant and an application of the endoglucanase truncated mutant. According to the invention, based on endoglucanase BsEGL from bacillus subtilis DLG, a truncated mutant is constructed by deleting a carbohydrate binding domain (CBM) of the endoglucanase BsEGL, and the truncated mutant is named as BsEGL [delta] CBM. Compared with BsEGL, the truncated mutant BsEGL delta CBM has the advantages that the thermal stability, the pH stability, the organic solvent tolerance and the like are remarkably improved, and the activity of degrading phosphoric acid expanded cellulose and corncob xylan is obtained. In addition, the enzymatic activity of the truncated mutant BsEGL delta CBM is remarkably improved by 6.41%, and the catalytic efficiency is remarkably improved. Due to the characteristics, the mutant can be suitable for industrial processes such as feed processing, papermaking, biological energy sources, spinning and food brewing, and is particularly suitable for enzyme catalytic reaction under extreme environments such as high temperature and low pH. The invention provides an enzyme preparation tool with excellent performance for efficient degradation of cellulose biomass, and has important application value.

The invention relates to a textured KCu7S4 thermoelectric material and a preparation method thereof, and the method comprises the steps: sequentially adding a prepared KOH aqueous solution, CuCl2. 2H2O and Na2S. 9H2O into a high-pressure kettle, and fully stirring for dissolving; dropwise adding an N2H4.H2O aqueous solution into the mixed solution, fully stirring, sealing, transferring to a microwave chemical synthesis instrument, heating, keeping stirring, and reacting at a target temperature and self-generated pressure to generate a KCu7S4 nanowire preferentially growing along a [001] crystal orientation; and after the reaction is finished and natural cooling is carried out, a product is collected through centrifugation, full cleaning and vacuum drying are carried out, and then the KCu7S4 thermoelectric material with [001] preferred orientation in the direction perpendicular to the pressure direction is obtained through spark plasma sintering. According to the method, a surfactant and an organic solvent are not used, and macro, rapid, efficient and controllable preparation of the KCu7S4 nanowire is realized through a low-temperature, low-cost and low-energy-consumption microwave-assisted hydrothermal process.

The invention discloses a method for preparing a high-performance AEM water-electrolyzed hydrogen production membrane electrode, which comprises the following steps: respectively preparing an AEM water-electrolyzed hydrogen production anode and an AEM water-electrolyzed hydrogen production membrane cathode, then placing the AEM water-electrolyzed hydrogen production anode and the AEM water-electrolyzed hydrogen production cathode on two sides of an anion exchange membrane, and sealing edges to prepare the AEM water-electrolyzed hydrogen production membrane electrode, the preparation method comprises the following steps: mixing catalyst powder with a solvent to prepare catalyst prefabricated slurry, adding an anion exchange resin solution in batches, adding a hydrophobic binder to prepare catalyst slurry, coating the surface of a hydrophobic modified diffusion layer with the slurry, and finally coating the surface of the diffusion layer with the anion exchange resin solution to prepare the hydrophobic modified diffusion layer. And soaking in an organic solvent, and washing. According to the prepared AEM water electrolysis hydrogen production membrane electrode, on the basis that oxygen bubble retention can be reduced, the stability is improved, and meanwhile the activity of the membrane electrode is improved.

The invention provides a non-aqueous electrolyte, a lithium ion battery, a battery module, a battery pack and an electric device. The non-aqueous electrolyte comprises a lithium salt, a non-aqueous organic solvent and a functional additive, and the functional additive comprises a bis-sulfinyl ester structure as shown in a formula I in the specification. When the non-aqueous electrolyte is used in the lithium ion battery, the wettability of the electrolyte can be effectively enhanced, the ionic conductivity of the electrolyte is improved, the low-temperature discharge capacity of the electrolyte is improved, and the stability of the electrolyte under high-temperature and high-voltage conditions is improved; and thus, the discharge capability and the service life of the lithium ion battery in high-temperature storage and high-temperature circulation are improved.

The invention provides an environment-friendly water-based acrylic emulsion adhesive without containing an organic solvent. The environment-friendly water-based acrylic emulsion adhesive is prepared from the following raw materials: 55-60 wt% of eleostearic acid hydroxyethyl acrylate (TMA), 15-25 wt% of butyl acrylate (BA), 3-10 wt% of acrylic acid (AA), 2-5 wt% of a cross-linking agent, 3-8 wt% of modified soil and 0.5-1 wt% of an initiator as a solid phase; the liquid phase is deionized water, and the environment-friendly water-based acrylic emulsion adhesive is prepared through semi-continuous emulsion polymerization. The prepared environment-friendly water-based acrylic emulsion adhesive is high in biodegradability and low in VOC content, has the mechanical property matched with that of a traditional acrylic emulsion adhesive and also has the self-repairing capacity, waste materials can be treated by changing the temperature or pH condition, the environment-friendly water-based acrylic emulsion adhesive can be recycled for multiple times, and the recycling cost is reduced.

The invention discloses a polyurethane modified epoxy resin adhesive as well as a preparation method and application thereof, and the polyurethane modified epoxy resin adhesive is prepared from the following components in parts by mass: 7-10 parts of E51 type bisphenol A diglycidyl ether, 3.5 parts of a phenolic aldehyde amine T31 curing agent and 1-3 parts of synthetic polyurethane, the synthetic polyurethane is prepared from polyether triol, polyether amine, isophorone diisocyanate and glycerol carbonate, and a blending system of the synthetic polyurethane and bisphenol A diglycidyl ether is adopted to be subjected to covalent crosslinking with phenolic aldehyde amine T31, so that the adhesive has high toughness and strength guarantee; the synthetic polyurethane prepared by the method is obtained through simple, green and efficient solvent-free synthesis, and the synthesized product has certain fluidity at room temperature, so that the subsequent stirring preparation process of an adhesive is facilitated. And a solvent-free synthesis method is adopted, so that the use of a toxic organic solvent in the traditional polyurethane synthesis process is avoided, and the synthesis process is greener.

The invention discloses a dispergator of a polyurethane structural adhesive as well as a preparation method and application of the dispergator. The dispergator comprises a polar organic solvent, an alcohol additive, a basic catalyst, an ionic liquid and a surfactant. The dispergator is suitable for removing a bonding interface of a thermosetting polyurethane structural adhesive in a power battery module, the dispergation process is mild and safe, and swelling, fracture and interface release of the structural adhesive can be realized in a range from normal temperature to 55 DEG C. Compared with a traditional high-corrosion and high-energy-consumption dispergation means, the dispergation agent has the advantages of being high in degumming efficiency, little in residual gum, free of base material corrosion and the like, is suitable for the environment-friendly recycling and reusing scene of the retired lithium battery, and has good engineering practicability and popularization value.

The invention belongs to the field of natural product extraction, and relates to a method for extracting and separating flavonoid compounds from Artemisia chrysantha, which comprises the following steps: carrying out reflux extraction on the dry overground part of Artemisia chrysantha by using 70% ethanol, loading to a balanced D101 macroporous adsorption resin column, sequentially eluting by using water, a 20% ethanol aqueous solution, a 50% ethanol aqueous solution and a 70% ethanol aqueous solution, and collecting the eluent. Four fractions from Fr. I to Fr. IV are obtained; respectively carrying out polyamide column chromatography separation on Fr.II to Fr.IV, and sequentially eluting with a 20% ethanol aqueous solution, a 50% ethanol aqueous solution and a 70% ethanol aqueous solution to respectively obtain three fractions; and further purifying the Fr.II-1, the Fr.II-2, the Fr.III-1, the Fr.III-2, the Fr.III-1 and the Fr.III-3 by virtue of a Sephadex LH-20 column, so as to finally obtain seven flavonoid compounds. According to the method, only the ethanol water low-toxicity solvent is used for extraction and preparation, organic solvents with high toxicity are not used, the method is green and environment-friendly, the extraction efficiency is high, the number of extracted compounds is large, chemical components of the artemisia europaea medicinal material are enriched, the resource source of active components is widened, and a foundation is laid for follow-up research.

The invention relates to the technical field of water pollutant removal, in particular to a UiO-66 / sodium carboxymethyl cellulose / polyvinyl alcohol / melamine sponge composite material and a preparation method and application thereof.The preparation method comprises the steps that zirconium chloride and terephthalic acid are dissolved in an organic solvent to obtain a mixed solution, the mixed solution is transferred into a reaction kettle, and through solvothermal reaction, the UiO-66 / sodium carboxymethyl cellulose / polyvinyl alcohol / melamine sponge composite material is obtained; the preparation method comprises the following steps: preparing UiO-66 powder; putting UiO-66 powder into the sodium carboxymethyl cellulose solution, and uniformly stirring the UiO-66 powder and the sodium carboxymethyl cellulose solution to obtain a UiO-66 / CMC mixed solution; placing the UiO-66 / CMC mixed solution in a polyvinyl alcohol solution, and uniformly stirring the UiO-66 / CMC / PVA mixed solution to obtain a UiO-66 / CMC / PVA mixed solution; the preparation method comprises the following steps: dipping a melamine sponge in a UiO-66 / CMC / PVA mixed solution to obtain an adsorption saturated melamine sponge; the UiO-66 / CMC / PVA / coated MS composite material is obtained by repeatedly freezing and thawing the adsorption saturated melamine sponge for multiple times and then freeze-drying, the composite material can be used for rapidly, efficiently and selectively removing phosphate or fluorine ions and the like in water and is convenient to separate and recycle, and a new thought is provided for development of efficient water treatment adsorbent materials.

The application discloses a platinum-based high-entropy intermetallic compound and a preparation method and application thereof as a hydrogen fuel cell cathode catalyst, and belongs to the field of fuel cells.The preparation method comprises the following steps: S01, adding platinum salt, at least five other metal salts and a nitrogen-rich organic compound into an organic solvent, uniformly mixing, and obtaining a metal precursor mixed solution; S02, adding a carbon carrier into the metal precursor mixed solution, fully mixing, drying, collecting, and obtaining a precursor; and S03, heat treating the dried precursor under a reducing atmosphere, and performing heat preservation treatment, so as to obtain the platinum-based high-entropy intermetallic compound.The preparation method is simple, low in cost and good in repeatability, the prepared catalyst has the advantages of uniform particle size and high oxygen reduction activity, and has a good development prospect in the field of hydrogen fuel cell catalyst applications.

The invention belongs to the technical field of batteries, discloses a battery electrolyte solvent capable of adapting to a wide temperature range and preparation of a battery, and provides application of a mixed organic solvent as an energy storage battery electrolyte solvent, the mixed organic solvent is composed of tetrahydrofuran, 1, 3-dioxolame and 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether, and the 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether is composed of tetrahydrofuran, 1, 3-dioxolame and 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether. The volume percent content of the 1, 2, 2-trifluoroethyl ether is 10%-50%. The solvent composition of the energy storage battery electrolyte is improved, 1, 1, 2, 2-tetrafluoroethyl-2, 2, 2-trifluoroethyl ether is introduced into an ether organic solvent (namely tetrahydrofuran and 1, 3-dioxolame) to serve as a diluent, meanwhile, the volume percentage of the diluent is controlled, and the obtained electrolyte solvent formula can adapt to the wide temperature range of the full temperature interval of-130 DEG C to 60 DEG C, so that the energy storage battery electrolyte is suitable for being used as an energy storage battery electrolyte. And the problem of battery failure of the current energy storage battery under the extremely low-temperature and high-temperature conditions can be effectively solved.

The invention discloses a multilayer composite solid electrolyte membrane, a preparation method and a prepared solid-state battery, the multilayer composite solid electrolyte membrane sequentially comprises a three-dimensional polymer networked solid electrolyte, a LiPON layer and a polydopamine layer, the thickness of the three-dimensional polymer networked solid electrolyte is 20-40 [mu] m, and the thickness of the polydopamine layer is less than 100 nm. By adopting the synergistic effect of the silane coupling agent modified LLZO and the degraded chitosan, a better ion transmission coordination effect can be provided, and the efficiency of an ion channel is improved. The dendritic crystal inhibition efficiency is improved, obvious cracks are avoided after 1000 times of circulation, the composite material is applied to a solid-state battery, the cycle life of the battery is prolonged, and the capacity retention rate is 95% after 1000 times of circulation. The mechanical toughness of the solid electrolyte is improved, and the elongation at break can reach 130%. A water-phase solvent is used in the whole preparation process, use of an organic solvent is avoided, energy consumption is reduced by 40%, no VOC is discharged in the whole process, and the method is green, safe and environmentally friendly.

The invention discloses a method and a device for preparing a single-walled carbon nanotube based on the host-guest interaction of pillararene and metallocene. The method comprises the following steps: enabling a host compound and a guest compound to form a host-guest complex; the host compound comprises pillararene or a derivative thereof, and the guest compound comprises a cyclopentadienyl metal complex or a derivative thereof; the method comprises the following steps: reacting a mixed reaction system containing a host-guest compound and a polymerization inhibitor at a high temperature to obtain nano-scale catalyst particles; and contacting the nano-catalyst particles with a carbon source, and decomposing and growing the carbon source on the surfaces of the nano-catalyst particles to prepare the single-walled carbon nanotubes. The method disclosed by the invention is mainly based on the strong inclusion behavior of the host compound and the guest compound, and by utilizing the compatibility of the host compound, the solubility of the metallocene in an organic solvent is effectively improved, the decomposition time of the metallocene at high temperature is prolonged, and the in-situ controllable preparation of nano-scale catalyst particles is achieved; and furthermore, the yield and the quality of the single-walled carbon nanotubes are improved.

The invention belongs to the technical field of semipermeable membrane preparation, and particularly relates to a preparation method of a nanofiltration membrane. The preparation method comprises the following steps: (1) cleaning the supporting layer for later use; the preparation method comprises the following steps: blending diamine, an amino beta-cyclodextrin derivative, an inorganic hybridizing agent, a zwitterionic compound and water to obtain a water phase for later use; blending aromatic acyl chloride, a cosolvent and an organic solvent to obtain an oil phase for later use; and (2) sequentially carrying out primary impregnation in a water phase, membrane scraping, secondary impregnation in an oil phase and heating curing on the supporting layer, and finally carrying out post-treatment to obtain the nanofiltration membrane. The nanofiltration membrane is prepared by introducing the amino beta-cyclodextrin derivative, the inorganic hybridization agent and other components into polyamide, so that the water flux of the polyamide nanofiltration membrane and the capability of effectively separating ions with different valence states are further improved.

The embodiment of the invention discloses a preparation method of trifluoromethyl sulfinate. The preparation method comprises the following steps: reacting a trifluoromethyl sulfinyl reagent with an amino compound containing hydroxyl to obtain a trifluoromethyl sulfinate intermediate; and reacting the trifluoromethyl sulfinate intermediate with alkali metal salt in an organic solvent to obtain the trifluoromethyl sulfinate. According to the embodiment of the invention, firstly, the trifluoromethyl sulfinyl reagent reacts with the amino compound containing the hydroxyl group to obtain the trifluoromethyl sulfinate intermediate, and then the trifluoromethyl sulfinate and the alkali metal salt react in the organic solvent, so that the high-purity trifluoromethyl sulfinate can be prepared with high yield under mild conditions. The yield and the purity of the target product are effectively improved, and meanwhile, the production condition requirement and the environmental pollution degree are reduced, so that large-scale production and application are facilitated.

The invention provides a lignin extraction-sulfonic acid modification integrated preparation method based on eutecticevaporate solvent coupling microwaves, lignin sulfonate and application, and belongs to the technical field of oilfield chemistry. The preparation method comprises the following steps: mixing choline chloride, epichlorohydrin and 4-hydroxybenzenesulfonic acid, heating and stirring to obtain a deep eutectic solvent ternary system; the method comprises the following steps: adding biomass powder into a deep eutectic solvent ternary system, and reacting under a microwave condition; after the reaction is completed, filtering, and adjusting the pH value of the obtained filtrate to be neutral to obtain a mixed solution; and then adding an organic solvent into the obtained mixed solution for precipitation, filtering, washing and drying to complete lignin extraction-sulfonic acid modification. According to the method, in-situ grafting of sulfonic acid functional groups is realized in the lignin separation process through the ternary eutectic solvent in combination with microwave-assisted extraction, so that sulfonation modification of lignin is completed. After sulfonation modification, the obtained sulfonated lignin is applied to the drilling fluid, and the viscosity reduction effect can be achieved.

The invention relates to a low-odor two-component composition as well as a preparation method and application thereof, and belongs to the technical field of woodware seal primers. The low-odor double-component composition disclosed by the invention comprises a component A and a component B, wherein the component A comprises epoxy resin and epoxy silane; in the component A, the weight of the epoxy silane accounts for 0-60 wt% of the total weight of the epoxy resin and the epoxy silane; the component B comprises an addition product, and the addition product is a Michael addition product obtained by reacting an unsaturated monomer M and amino silane Q according to a molar ratio of 1: (1.6-2.4). The low-odor two-component composition disclosed by the invention is extremely low in odor, very fast in early-stage polishing property establishment, good and excellent in surface effect and flexibility, free of an organic solvent or only low in organic solvent content, and capable of being widely applied to a woodware seal primer as a composition so as to improve the performance of a woodware coating.

The invention discloses an application of pleurotus eryngii purified polysaccharide in preparation of an intestinal care medicine. The pleurotus eryngii purified polysaccharide component has high immunocompetence, high-activity and high-purity polysaccharide is obtained after ethanol precipitation and organic solvent purification, and the high biological activity of the polysaccharide is reserved; the composition has the biological activity of increasing the production of short-chain fatty acid, reducing the inflammation level, improving the intestinal flora structure, influencing the body metabolism condition and protecting the intestinal barrier. Compared with other components in the pleurotus eryngii polysaccharide extraction process, the polysaccharide component obtained by the preparation method has the highest purity and the strongest biological activity, and can be used for preparing intestinal care medicines.

The invention discloses a preparation method of an acid-resistant chlorine-resistant selective palladium adsorbent, and relates to a preparation method of a selective palladium adsorbent. The invention aims to solve the technical problems of poor structural stability, low adsorption capacity, poor selectivity and difficulty in cyclic regeneration of the existing palladium adsorbent in strong acid and high chlorine systems. According to the preparation method, fumarinonitrile is taken as a cyanogen-containing monomer, zinc chloride is taken as a catalyst, a triazine skeleton network is constructed through an ionothermal trimerization reaction, no organic solvent or expensive catalyst is needed in the process, the reaction condition is mild, the process is simple and convenient, and good environmental compatibility is achieved; the PdCl4 < 2->-doped porous carbon material provides abundant coordination sites, has a relatively large specific surface area and a developed porous structure, can effectively promote mass transfer and adsorption of metal ions, can form stable complexation with PdCl4 < 2->, shows extremely high palladium adsorption capacity and selectivity, and can still keep structural integrity and adsorption activity under strong acid and high chlorine conditions.

The invention provides an intelligent response liquid crystal elastomer and a preparation method thereof, and belongs to the field of liquid crystal elastomer preparation.The preparation method comprises the steps that a liquid crystal monomer, a cross-linking agent, a photoinitiator and a catalyst are dissolved in an organic solvent to obtain a mixed solution, then the mixed solution is injected into a template for primary cross-linking, and after fiber forming, the mixed solution is taken out and dried to obtain P-LCE fibers; the P-LCE fibers are subjected to drafting treatment and then soaked in a silica gel solution, then suspended and left to stand, and after the silica gel solution wrapping the surfaces of the fibers is dried and cured, secondary cross-linking is conducted to obtain the LCEP. The intelligent response liquid crystal elastomer prepared by the invention presents spiral curling shrinkage deformation under thermal stimulation, the shrinkage rate is large, the response rate is high, the deformation is reversible, and the shrinkage rate is almost unchanged after 100 times of cyclic stimulation.