592 results about "Catechol" patented technology

The invention provides a low-temperature-impact-resistant food packaging material and a preparation method and application thereof.The low-temperature-impact-resistant food packaging material is prepared from, by mass, 100 parts of polylactic acid, 1-10 parts of modified layered double hydroxide and 5-40 parts of hyperbranched polyester; wherein the modified layered double hydroxide is obtained by treating layered double hydroxide with a composite anionic surfactant and then treating the treated layered double hydroxide with an organic cationic compound with a long alkyl chain; the composite anionic surfactant comprises a first anionic surfactant and a second anionic surfactant; wherein the first anionic surfactant comprises sodium dodecyl sulfate; the second anionic surfactant comprises a sulfonate anionic surfactant containing an amido bond and a catechol structure. Through the formula design, the impact toughness of the material at low temperature can be improved while the mechanical property of polylactic acid is maintained, and the material can be suitable for the field of food packaging.

The invention discloses an alkali-free accelerator and a preparation method and application thereof in the technical field of concrete additives, and the alkali-free accelerator provided by the invention comprises the following components in percentage by mass: 40%-50% of aluminum sulfate, 10%-15% of magnesium sulfate, 0.2%-0.6% of diethanol amine, 0.5%-1% of catechol-4-ammonium sulfonate, 5%-10% of a stabilizer and the balance of water. The stabilizer comprises silicate dispersion liquid and silica sol. The alkali-free accelerator provided by the invention can be used for spraying concrete, the mixing amount of the alkali-free accelerator is generally 4-6% of the mass of cement, the alkali-free accelerator is good in rapid setting effect and has excellent early and later compressive strength, and meanwhile, the alkali-free accelerator has relatively excellent stability.

The invention discloses a triggering probiotic-drug conjugate and a preparation method and application thereof, and belongs to the technical field of oral drug delivery systems, the triggering probiotic-drug conjugate comprises probiotics, an adhesive inner layer formed by coordination of tannic acid and Fe < 3 + >, and an outer layer formed by pterostilbene-phospholipid bridged by ROS-responsive thioether bonds and cholesterol; the inner layer coats the surfaces of the probiotics through coordination, and the outer layer coats the outer part of the inner layer through self-assembly. An outer lipid layer is decomposed under high-concentration ROS in an inflammation colon area, and probiotics coated with pterostilbene and a tannic acid layer are released. Pterostilbene relieves inflammation and rebuilds a pathological microenvironment, and catechol groups in a tannic acid layer and the surface of the intestinal tract generate multiple interactions to promote planting of probiotics. In UC mouse models, the conjugates exhibit enhanced therapeutic effects by inhibiting inflammation, restoring intestinal barrier function, and improving intestinal microbiota homeostasis. The invention has important transformation potential in clinical application of gastrointestinal diseases.

The invention discloses a method for rapidly adsorbing heavy metal ions by a sulfydryl-functionalized non-woven fabric, relates to preparation of the sulfydryl-functionalized non-woven fabric and heavy metal adsorption application, and belongs to the technical field of functional materials and environmental protection. A catechol derivative, an oxidizing agent, a sulfur-containing coupling agent and the like are prepared into a reaction solution according to a certain proportion, then the non-woven fabric is immersed into the reaction solution for surface modification, the sulfydryl-functionalized non-woven fabric is prepared through reduction, and finally the sulfydryl-functionalized non-woven fabric is applied to adsorption and removal of heavy metal ions in water. The method has the advantages of being mild in condition, high in reaction speed and short in preparation period, the operation process is simple, universality is achieved, and the prepared functional material has the advantages of being good in heavy metal ion adsorption effect, good in functional modification layer stability and the like.

The invention provides a Ni-molybdenum oxide / Nb2O5 nano composite catalyst as well as a preparation method and application thereof, and belongs to the technical field of catalysts. The catalyst precursor is prepared by adopting an excessive impregnation method, then the Ni-molybdenum oxide / Nb2O5 nano-composite catalyst is prepared by adopting a hydrogen reduction treatment method, active components in the catalyst are uniformly loaded, and the catalyst has excellent self-hydrogen hydrothermal catalytic performance. The Ni-molybdenum oxide / Nb2O5 nano composite catalyst prepared by the invention can minimize the dissociation energy of a C-O bond, promote the breakage of the C-O bond, enable the reaction to be carried out in a forward direction, and realize high-value conversion of guaiacol to catechol under mild reaction conditions without exogenous hydrogen.

The invention discloses a polyphenol modified carbon fiber reinforced sulfonated polyetheretherketone composite material and a preparation method thereof, and belongs to the field of polymer composites.The preparation method comprises the steps that a resin matrix and filler are filled into a mold to be sintered, the resin matrix is sulfonated polyetheretherketone, the filler comprises modified carbon fibers and nano-silicon dioxide, and the modified carbon fibers and the nano-silicon dioxide are sintered to obtain the polyphenol modified carbon fiber reinforced sulfonated polyetheretherketone composite material; the modified carbon fiber is prepared by taking carbon fiber, catechol and polyethyleneimine as raw materials in a Tris buffer solution. The hydration lubrication performance of a resin matrix is improved through sulfonated polyetheretherketone, the hydrophilic property is enhanced, a polyphenol coating is formed through self-polymerization reaction on the surfaces of the carbon fibers, the adhesion performance of the surfaces of the fibers is improved through the pi-pi stacking effect, and the interface bonding force between the carbon fibers and the modified resin matrix is enhanced; the nano silicon dioxide is introduced to modify the matrix of the composite material, so that not only is the overall wettability of the material optimized, but also the mechanical property and the wear resistance are effectively improved, and the final composite material has the characteristics of high strength and low friction.

The invention relates to the technical field of solid-state batteries, and provides a positive plate, a preparation method thereof and a solid-state battery. The positive plate comprises a positive current collector and a positive active material layer arranged on at least one side surface of the positive current collector; the positive electrode active material layer comprises a nickel-containing positive electrode active material, a solid electrolyte, a conductive agent and a binder; the binder comprises a first binder and a second binder; the first binder comprises polymer nanofibers, and the length-diameter ratio of the polymer nanofibers is 30-90; the mass ratio of the first binder in the positive active material layer is 0.8%-5%; the second binder includes a catechol group-containing polymer. According to the invention, the first binder and the second binder are combined for use to form a tough composite adhesion system, so that the adhesion of the positive plate is remarkably improved, and the high and low temperature performance and flexibility of the solid-state battery are improved.

The application discloses a mussel-inspired multifunctional double-network crosslinked hydrogel wound dressing. A hydrogel network formed by dynamic covalent crosslinking between carboxymethyl chitosan and oxidized sodium alginate is utilized; further, a natural antioxidant, gallic acid, with a catechol structure is introduced to enhance the tightness of the hydrogel network combination and endow the hydrogel with certain adhesion and antioxidant properties; finally, a mussel adhesive fluid containing catechol and iron is imitated to have strong tissue adhesion behavior under alkaline conditions, which is suitable for dynamic wound treatment, so as to prepare a mussel-inspired multifunctional double-network crosslinked hydrogel wound dressing. In addition, catechol-Fe 3+ Metal coordination also shows strong antibacterial effect, and under the irradiation of near-infrared light, light energy can be converted into heat energy for preventing and treating wound infection, shortening wound closure time and preventing scar formation.

The invention relates to an oxidase response type molecular probe as well as a preparation method and application thereof, and belongs to the technical field of medical imaging. Aiming at the problem that the inflammation activity is difficult to accurately evaluate in the prior art, the invention provides a molecular imaging probe capable of responding to the activity of in-vivo myeloperoxidase (MPO), and the molecular imaging probe can be used for real-time and non-invasive imaging monitoring of the activity of the in-vivo MPO, so that the activity of the inflammatory reaction of a focus is accurately evaluated. The invention provides a chelating agent with structural characteristics of a chelating unit and an enzyme response unit, and is characterized in that the enzyme response molecular probe is constructed by taking rigid framework cyclohexanediamine (CDTA) as a transition metal chelating unit and taking electron-rich functional groups (such as phenol, catechol or 5-hydroxytryptamine) as the enzyme response unit. The probe is chelated with paramagnetic metal (such as Mn < 2 + >) for magnetic resonance imaging (MRI) or radioactive metal (such as 68Ga) for positron emission tomography (PET), so that specific response to MPO activity is realized. The dynamic stability of the probe is remarkably improved; after the MPO is responded, the relaxation efficiency is improved by 2-3 times, and the sensitivity is optimized; the cytotoxicity is low; in an acute pancreatitis model, the MRI contrast noise ratio (delta CNR) reaches 77.39 + / -7.04 and is 4.2 times that of a control group, the PET uptake rate is remarkably improved, bimodal imaging is supported, and accurate positioning and quantitative evaluation of the inflammation activity are achieved.

The application relates to a dry powder drag reducer for fracturing fluid and a preparation method thereof, and belongs to the technical field of drag reducers; the dry powder drag reducer is copolymerized and modified by preparing a polymerizable modifier, aromatic rings and sulfonic acid ion structures are introduced into the dry powder drag reducer, the high-temperature resistance and salt resistance of the dry powder drag reducer are effectively improved, in addition, the modified dry powder drag reducer structure also has a catechol structure, can form a stable five-membered ring borate with a boron crosslinking agent, and the dry powder drag reducer can be mixed with a guar gum drag reducer when the boron drag reducer is used, so that the problem of poor sand carrying capacity of the dry powder drag reducer is effectively solved.

The invention discloses a catechol side group-containing polylysine derivative as well as a preparation method and application thereof. The preparation method comprises the following steps: (1) dissolving catechol acid in an organic phase, firstly adding NHS, stirring and dissolving until the materials are uniformly mixed, then adding EDC.HCl, and stirring and reacting to obtain a catechol-NHS intermediate solution; (2) dissolving polylysine or a salt thereof in a water phase, and adjusting the pH value to 6.0-7.0 by using an alkaline solution to obtain a solution of polylysine or a salt thereof; and (3) adding the intermediate solution obtained in the step (1) into the polylysine or the salt solution thereof obtained in the step (2), and maintaining the pH value of the reaction system at 5.0-6.0 by using an alkaline solution to obtain the catechol side group-containing polylysine derivative. The preparation method is short in reaction time and mild in reaction condition, and the obtained product is high in grafting rate and high in raw material conversion rate and has a good application prospect in the aspects of tissue adhesives and the like.

The invention relates to a dry powder drag reducer for fracturing fluid and a preparation method thereof, and belongs to the technical field of drag reducers. The dry powder drag reducer is subjected to copolymerization modification by preparing the polymerizable modifier, an aromatic ring and sulfonic acid ion structure is introduced into the dry powder drag reducer, the high temperature resistance and salt resistance of the dry powder drag reducer are effectively improved, in addition, the modified dry powder drag reducer structure further has a catechol structure, and the modified dry powder drag reducer has a good application prospect. The dry powder drag reducer can form stable five-membered ring boric acid ester with a boron cross-linking agent, when the boron drag reducer is used, the dry powder drag reducer can be mixed with a guar gum drag reducer for use, and the problem that the dry powder drag reducer is poor in sand carrying capacity is effectively solved.

The invention discloses a bio-based polymer emulsion as well as a preparation method and application thereof, and belongs to the technical field of aqueous polymer emulsions. The emulsion comprises an aqueous continuous phase, bio-based polymer particles, a stabilizing system, and a bionic catechol adhesion component. Specific modified starch is innovatively utilized for assistance, and a bionic adhesion shell layer is constructed on the surface of a bio-based polymer core in situ. Compared with similar products in the market that adhesion to inert substrates can be improved only by adding a large amount of tackifying components, the scheme has the advantages that excellent dry and wet adhesion can be realized on the surfaces of difficult-to-adhere substrates such as polypropylene and polyethylene only by constructing an extremely thin interface functional layer, and the functionalization efficiency and economical efficiency of the bio-based material are greatly improved. Meanwhile, the system effectively overcomes the industrial problem that the high-solid-content emulsion is easy to settle, has excellent storage stability and construction adaptability, and conforms to the development trend of sustainable barrier packaging and high-performance water-based coatings in the future.

The invention provides a multi-walled carbon nanotube paste electrode based on gold nanoparticles and C60 modification as well as a preparation method and application thereof, and belongs to the technical field of electrochemical sensors. The preparation method comprises the following steps: firstly, modifying fullerene C60 on the surface of a carbon nanotube paste electrode (MWCNTPE) to form C60 / MWCNTPE, then loading gold nanoparticles on the surface of the C60 / MWCNTPE, and finally constructing the AuNPs / C60 / MWCNTPE composite electrode. The prepared composite electrode is used for environmental estrogen detection, especially for simultaneous detection of hydroquinone, catechol and bisphenol A. The method has the advantages of high sensitivity and low detection limit, can solve the problem that hydroquinone and catechol isomeride are difficult to separate through the detection capability, has the advantages of simplicity and convenience in operation and low cost, and has good practical applicability, stability and reproducibility.

The invention relates to the technical field of fabrics, in particular to a cool-feeling long cilia strip and a preparation method thereof.The cool-feeling long cilia strip is composed of cool-feeling fibers and a long cilia strip base material and is characterized in that the cool-feeling fibers comprise a core layer, a functional skin layer and an outer thin skin layer; the functional skin layer is prepared from the following components: a sulfonated copolyester matrix, catechol grafted master batch, surface modified zeolite nano powder, an anti-hydrolysis agent and an antioxidant, and the functional skin layer also contains introduced Zn < 2 + > and Mg < 2 + >. Zn < 2 + > and Mg < 2 + > which are stably combined on anchoring points of sulfonated copolyester are subjected to hydration endothermic reaction when being in contact with water, so that a cool feeling is generated; the surface modified zeolite nano powder synergistically enhances moisture absorption and water temporary storage by virtue of the specific surface area, and continuously provides water for an ionized hydration reaction to prolong and amplify a cool feeling effect; the catechol grafting structure endows the fiber with antibacterial performance, and long-term stability of the structure is ensured through an interface enhancement effect. And the outer layer hydrophilic polyester is matched, so that the product has comfort, durability and functionality.

The invention discloses a high-color-fastness washable polyethylene fabric and a preparation process thereof in the field of functional polymer materials. The high-color-fastness washable polyethylene fabric is prepared from the following raw materials: polyethylene resin, maleic anhydride-acrylic acid copolymer grafted polyethylene, dopamine-silane composite modified polyethylene, magnesium stearate and an antioxidant. Wherein the maleic anhydride-acrylic acid copolymer grafted polyethylene is prepared by copolymerizing maleic anhydride and acrylic acid and then blending and granulating with polyethylene, and carboxyl and acrylate groups are introduced to enhance the binding force with dye; the dopamine-silane composite modified polyethylene is prepared through polyethylene surface hydroxylation, dopamine self-polymerization modification and silane grafting reaction, and the acting force and hydrophobicity between fibers are doubly improved through a catechol group and an epoxy group. According to the prepared fabric, the color fastness and the washing resistance are remarkably improved, meanwhile, the original characteristics of light weight and chemical corrosion resistance of polyethylene are kept, and the application scene is expanded.

The invention relates to the technical field of high polymer materials, in particular to a corrosion-resistant cable sheath material and a preparation method thereof. The sheath material is prepared by taking an ethylene-octylene copolymer as a matrix and compounding functional fillers such as an aminated magnesium ion exchange A type molecular sieve, dopamine shell silicon dioxide nanoparticles and phenylboronic acid / octadecyl double-grafted silicon dioxide nanoparticles. Wherein the aminated Mg-A molecular sieve is used for efficiently capturing and fixing chloride ions through an ion-dipole effect and a hydrogen bond network; the dopamine shell layer silicon dioxide enhances the interface bonding strength through dual active groups of catechol and amido; phenylboronic acid / octadecyl double-grafted silicon dioxide constructs a dynamic boric acid ester cross-linked network and a hydrophobic barrier, and synergistic protection of crack self-healing and moisture barrier is achieved. The sheath material remarkably improves the long-term corrosion resistance and mechanical stability of the cable in a severe environment.

The invention discloses an inorganic-organic hybrid cross-linked network high-toughness material and a preparation method thereof, and belongs to the technical field of engineering material preparation. The high-toughness material is composed of an inorganic phase component and an organic phase component, the inorganic phase component is prepared from 5 to 10 parts of amino modified silicon dioxide nanoring; the organic phase component is prepared from the following components in parts by weight: 90 to 105 parts of polycaprolactone glycol, 14.5 to 16.5 parts of isophorone diisocyanate, 0.8 to 1.5 parts of dibutyltin dilaurate, 4 to 6 parts of bis-catechol borane and 6 to 10 parts of polydopamine nano particles. The fracture performance of the material can reach 20 kJ / m or above and is far higher than-1 kJ / m of a common elastomer and-10 kJ / m of high-toughness hydrogel, and meanwhile the tensile strength of 30 MPa or above is kept. According to the material disclosed by the invention, the dynamic borate bond is utilized, after the material is in contact with a damaged section, efficient self-repairing can be realized after the material is placed at room temperature for 24 hours, and the repairing efficiency is gt; by heating and applying pressure, the whole material can be reshaped through fracture and recombination of the dynamic bonds, and green and sustainable effects are achieved.

The invention belongs to the technical field of biological fouling protection, and particularly relates to an environment-friendly adhesive hydrogel antifouling coating which is prepared by the following steps: grafting a catechol group to an acryloyl compound with double bonds through acylation reaction to obtain a dopamine-acrylamide compound; the preparation method comprises the following steps: carrying out copolymerization reaction on an acrylamide derivative and a dopamine-acrylamide compound in a water environment to obtain an acrylamide derivative copolymer; and mixing the chitosan and the acrylamide derivative copolymer to obtain the environment-friendly adhesive hydrogel antifouling coating. According to the invention, polyacrylamide and catechol are introduced into a chitosan system at the same time to form a chitosan-polyacrylamide-catechol ternary synergistic network, and the chitosan-polyacrylamide-catechol ternary synergistic network has the effects of self-repairing, high toughness, strong adhesion and intelligent response.

The invention relates to the technical field of copper foil surface treatment, in particular to a copper foil and a preparation method and application thereof. The copper foil comprises an electrolytic copper raw foil, and a roughening treatment layer, a catechol-based polymer layer and a silane coupling agent layer which are sequentially laminated on the rough surface of the electrolytic copper raw foil. According to the copper foil, the catechol-based polymer layer is introduced between the roughening treatment layer and the silane coupling agent layer, the catechol-based polymer layer contains rich functional groups such as hydroxyl and amino, the number of attachment sites of a silane coupling agent on the surface of the copper foil is increased, and then the binding force of the silane coupling agent and the copper foil is increased; meanwhile, rich functional groups can also improve the binding force between the copper foil and various base materials, so that the copper foil has higher peel strength under the condition of keeping lower roughness during application.

The invention discloses a method for in-situ rapid growth of a dual-network hydrogel coating on the surface of a base material by a one-step method, which comprises the following steps: putting the base material with an adhesion initiation layer on the surface into a hydrogel precursor solution, and carrying out in-situ polymerization for 0.1-10 minutes under light irradiation, wherein the adhesion initiation layer comprises an adhesive compound based on a catechol group and a first photoinitiator, and the hydrogel precursor solution comprises a natural polymer containing tyrosine, an acrylic monomer, a cross-linking agent and a second photoinitiator, and wherein the first photoinitiator and the second photoinitiator are different from each other and are independently selected from a divalent ruthenium compound and a persulfate. Compared with the prior art, the natural / synthetic polymer double-network gel coating with biological activity and mechanical property can grow on the surfaces of different substrates more quickly and efficiently through a one-step method; and the base material, the surface of which is modified by the in-situ grown double-network hydrogel coating, obtained by the method can be applied to in-vivo medical apparatuses and instruments.

The invention discloses a preparation method of recombinant catechol-2, 3-dioxygenase and an application of the recombinant catechol-2, 3-dioxygenase. According to the invention, a novel catechol-2, 3-dioxygenase group C23O927 is identified from a constructed metagenome library, and the catechol-2, 3-dioxygenase group C23O927 is a key enzyme for catalyzing degradation of polycyclic aromatic hydrocarbon pollutants. A C23O927-pET32a (+) recombinant expression vector is constructed and converted into host bacteria, heterologous expression of target protein is achieved, and the prepared recombinase belongs to acid enzymes and has good resistance to high temperature, acid, alkali, high-concentration metal ions, organic solvents and surfactants. The recombinase provided by the invention can be used in an acidic environment, has very good enzymatic activity, can catalytically degrade various catechol compounds, can be better used for treating polycyclic aromatic hydrocarbon polluted environments, and has important significance for developing more products which can tolerate various extreme environments and efficiently catalyze degradation of polycyclic aromatic hydrocarbons.

The present disclosure provides a method for the chemoselective modification of a target molecule. The subject methods comprise contacting a target molecule comprising a thiol moiety with a biomolecule comprising a reactive moiety, wherein the reactive moiety is produced by reacting a biomolecule comprising a phenol moiety or catechol with an enzyme capable of oxidizing the phenol moiety or the catechol moiety. The contacting is performed under conditions sufficient to conjugate the target molecule to the biomolecule, thereby producing a modified target molecule. The present disclosure provides compositions comprising a subject target molecule comprising a thiol moiety and a biomolecule comprising a phenol moiety or a catechol moiety. The present disclosure provides kits for performing the subject methods. The disclosure also provides modified target molecules and methods of using the same.

The invention provides a diesel oil anti-wear agent and a preparation process thereof, and belongs to the technical field of diesel oil additives, and the preparation process comprises the following steps: mixing and stirring diisooctyl maleate and xylene, adding diethylenetriamine and deionized water, carrying out heating reaction, adding toluene, 4-(aminomethyl) pyridine and ethylene oxide, carrying out mixing reaction, filtering, washing, and drying to obtain the diesel oil anti-wear agent. The pyridinium-based polyester hollow capsule is prepared; the preparation method comprises the following steps: mixing xylene, catechol, ethylene phosphonic acid, ammonium persulfate and deionized water, heating, dispersing in cyclohexane, adding polyvinyl alcohol, octadecyl methacrylate and azodiisobutyronitrile, mixing and reacting to obtain catechol phosphonate nano colloidal particles; mixing and stirring the fatty acid ester solution, the oleoyl fluorocarbon copolymer and the pyridinium-based polyester hollow capsule, adding the catechol phosphonate nano colloidal particles, continuously stirring, performing ultrasonic treatment, and degassing to obtain the diesel oil anti-wear agent. The diesel oil antiwear agent can improve the antiwear property and demulsibility of the diesel oil antiwear agent.

The invention discloses a salicylic acid decarboxylase mutant and application of the salicylic acid decarboxylase mutant in degradation of salicylic acid. The mutant is obtained by carrying out site-specific modification on salicylic acid decarboxylase NahG, and specifically, valine at the 46th site, tyrosine at the 380th site and leucine at the 382nd site of an amino acid sequence shown in SEQ ID NO.2 are mutated into cysteine, phenylalanine and phenylalanine at the same time. The mutant shows remarkably improved catalytic efficiency, and salicylic acid can be efficiently and thoroughly decarboxylated and converted into catechol under mild conditions. The invention also provides a coding gene, a recombinant vector and an engineering bacterium of the mutant. The mutant not only can be used for efficient bioremediation of salicylic acid pollution, but also can effectively break through and accelerate a naphthalene catabolism pathway due to the characteristic of directionally generating catechol, and has important application value in the fields of environmental pollution abatement and biological catalysis.

The invention discloses a fluorosilicone waterborne polyurethane emulsion as well as a preparation method and application thereof, and belongs to the technical field of polyurethane emulsion synthesis. The preparation method comprises the following steps: taking fluorinated diol, sulfonic diol and alkynyl diol as raw materials, preparing a polyurethane prepolymer with a side chain containing a sulfonic group and an alkynyl group through a diisocyanate condensation reaction and organic tertiary amine neutralization salification, and connecting a catechol group and an active siloxy group to the side chain through an alkyne-azide click reaction. And finally, carrying out self-emulsification to obtain the fluorosilicone waterborne polyurethane emulsion. After the fluorosilicone waterborne polyurethane emulsion is dried into a coating, the coating has excellent adhesive force on the surfaces of various base materials, and the coating not only has friction resistance, acid and alkali resistance and organic solvent resistance, but also has super-hydrophobicity, water soaking resistance and pollution resistance.

The invention provides a hot melt adhesive and a preparation method thereof, and relates to the technical field of adhesives. According to the hot melt adhesive, amorphous polyolefin (APAO) is used as a main body, ethylene-vinyl acetate copolymer (EVA) is added as a compatilizer, and Fischer-Tropsch wax is used as a viscosity modifier. The preparation method comprises the following steps: firstly synthesizing a dopamine functional polymer, and then carrying out melt blending on the dopamine functional polymer, APAO, EVA, tackifying resin and other components so as to stably introduce a catechol group into a hot melt adhesive system. When the hot melt adhesive is bonded with a metal surface, the catechol group can form a firm coordinate bond with metal ions, so that the adhesive force is greatly improved. The product provided by the invention has high adhesive force, excellent flexibility, good compatibility and construction performance, and is suitable for bonding and sealing metal materials.

The application provides a preparation method of a Chlorella-arsene composite drug delivery system and application thereof. The application prepares arsene nanosheets (ANs) through a liquid phase stripping method, and obtains catechol-polyethyleneimine nanoparticles (CA-PEI) through oxidation self-polymerization. The ANs and the CA-PEI are charge-absorbed to form CA-PEI loaded with ANs (CA-PEI@ANs), and then charge-absorbed with protein nucleus Chlorella (CP), so that a Chlorella-arsene composite drug delivery system (CP@CA-PEI@ANs) is successfully constructed. The preparation operation of the drug delivery system is simple, and the reproducibility is good, and the drug delivery system has a good application prospect. The protein nucleus Chlorella is used as a drug delivery carrier, so that the problems of high cost and complex synthesis process commonly existing in a targeted delivery carrier are solved, and the application has good tumor targeting effect, and is beneficial to better drug efficacy.

The utility model provides an energy-saving device for separating and purifying materials after hydroxylation reaction of phenol and hydrogen peroxide, and relates to the technical field of chemical synthesis. Materials obtained after phenol hydrogen peroxide hydroxylation reaction are separated and purified through the extraction tower, the extraction agent recovery tower, the first phenol removal tower, the tar removal tower, the second phenol removal tower, the catechol removal tower, the light component removal tower and the hydroquinone tower, the whole technological process is simple, the yield is high, and the high-purity hydroquinone product and the high-purity catechol product can be obtained; according to the utility model, the extraction tower is adopted to replace a dehydration rectifying tower in the traditional process to remove phenol-containing wastewater, so that the phenol recovery rate is improved, and the subsequent wastewater treatment burden is reduced; and the tar removal tower is arranged behind the phenol removal tower I, so that the retention time of tar impurities in the whole process system is shortened, and the process safety is improved. According to the utility model, the high-temperature waste heat at the top of the dephenolization tower I is recovered by combining waste heat recovery with a mechanical steam recompression energy-saving technology, so that the process energy consumption of the operation of the whole device is effectively reduced.

The application discloses a kind of cement-based material surface biomimetic hydrophobic coating, including 0.1-0.6 parts of organic matter containing catechol group, 0.2-3 parts of dodecylamine, 17-75 parts of tris buffer solution, 13-69 parts of anhydrous ethanol, 0.1-0.5 parts of hydrogen peroxide, 0.1-1 parts of deposition aid;Coating surface microstructure is plate block and small spherical shape.The application also discloses the preparation method of the cement-based material surface biomimetic hydrophobic coating, including the following steps: mixing dopamine, dodecylamine, tris buffer solution and anhydrous ethanol, and loading into the middle part of atomization device container for spraying deposition solution;CuSO4 and H2O2 are divided and loaded into the container on both sides of atomization device;Each face of cement test block is sprayed, dried, and cyclically sprayed-dried;Surface is washed, and naturally dried.The application prepares biomimetic hydrophobic coating on cement-based material surface by one-step co-deposition method, and the prepared coating has the characteristics of good hydrophobicity and uniform deposition.