2082 results about "Hydrogen bond" patented technology

The invention discloses an amorphous tigorasone solid dispersion which has excellent stability and dissolvability, by adding copovidone, a powerful hydrogen bond is formed between tigorasone and copovidone, and by adjusting the type of an adhesive and the proportion of the adhesive to tigorasone, the problems of easy crystal transformation of amorphous tigorasone, poor solubility and the like are solved. And the technical problem is solved. The tigorazan tablet prepared from the amorphous solid dispersion provided by the invention does not generate crystal transformation after being placed for 30 days under the conditions of 60 DEG C and 75% RH, and the dissolution curve in a standard medium is consistent with that of a reference preparation.

The invention relates to the technical field of high polymer materials, and particularly provides a self-repairing type UV curing alumite color layer coating and a preparation method thereof. The water-based ink is prepared from, by weight, 30-50 parts of polyurethane acrylic resin, 10-25 parts of modified acrylic oligomer containing dynamic covalent bonds, 2-5 parts of photoinitiator, 3-8 parts of hydrophobic modified nano filler and 1-3 parts of cross-linking agent, and the dynamic covalent bonds are selected from at least one of hydrazide bonds, boric acid ester bonds and Diels-Alder bonds. By introducing a gradient energy collaborative network of dynamic covalent bonds and quadruple hydrogen bonds, rapid self-repairing of the coating at normal temperature and thermal triggering recombination of deep damage are achieved, and meanwhile through the micro-phase separation design of the hydrophobic core-shell filler and the graft modified silicon carbide nanowires, the hydrolysis resistance is improved.

The invention relates to a self-repairing high-mechanical-property film and a preparation method and application thereof, and the preparation method comprises the following steps: adding ureido pyrimidone and a chain extender into a solvent to obtain a mixed solution, adding the mixed solution into a polyurethane prepolymer, reacting, and drying to obtain the self-repairing high-mechanical-property film. UPy containing hydrogen bonds is introduced into the polymer to prepare the self-repairing high-mechanical-property film, and the hydrogen bond density can be adjusted by adjusting the UPy content of ureido pyrimidone, so that the composite material has excellent self-healing property; and density hydrogen bonds are introduced to construct a physical cross-linked network, so that the mechanical properties of the composite material can be remarkably improved.

The invention relates to the technical field of biological extraction, in particular to a green synergistic extraction system and an extraction method and application thereof.The green synergistic extraction system comprises a deep eutectic solvent system, an enzymolysis system and an ultrasonic-assisted extraction system, and the deep eutectic solvent system comprises a DES solvent; the DES solvent is composed of a hydrogen bond acceptor and a hydrogen bond donor, and the hydrogen bond acceptor is choline, choline chloride or L-proline; the hydrogen bond donor is lactic acid, urea or ethylene glycol; enzyme preparations in the enzymolysis system are at least two of cellulase, pectinase and beta-glucosidase; the problems that a traditional organic solvent is high in toxicity and poor in biodegradability and synthetic deep eutectic solvent raw materials are non-renewable are solved, a green synergistic extraction system which is environmentally friendly, low in cost and excellent in performance is developed, the mass transfer efficiency and the extraction yield are improved, the used DES and enzyme preparations can be recycled, and the cost is reduced while the environment is protected.

The invention relates to the technical field of petrochemical engineering, and discloses a temperature-resistant anti-swelling agent for fracturing and a preparation process thereof.The preparation method comprises the steps that glycerol triglycidyl ether and diethanol amine are subjected to a ring-opening reaction, a polyhydroxy tertiary amine monomer is obtained, then the polyhydroxy tertiary amine monomer and chloromethylated polystyrene are subjected to a quaternization reaction, and the temperature-resistant anti-swelling agent for fracturing is obtained. Quaternary ammonium salt groups of the anti-swelling agent and negative charges on the surface of clay form electrostatic interaction, and hydroxyl groups and the surface of the clay form hydrogen-bond interaction, so that the anti-swelling agent can be firmly adsorbed on the surface of the clay to form a layer of polymer film, the clay is prevented from being in contact with water, the phenomenon that the clay swells when encountering water is effectively inhibited, and the anti-swelling rate is very high. And the anti-swelling agent contains a heat-resistant polystyrene molecular chain, has excellent high temperature resistance, can maintain good structural stability at high temperature, still maintains high anti-swelling rate, and is suitable for a fracturing fluid system for high-temperature oil reservoir exploitation.

The invention provides a zeolite imidazate framework fluorescent material and a preparation method and application thereof, and belongs to the technical field of detection material preparation and environment. Quantum dots, a molecular imprinting technology and an MOFs material are combined, firstly, Mg and N co-doped graphene quantum dots and ZIF-8 are compounded, then imprinting is carried out on the surface of ZIF-8, and the zeolite imidazate framework fluorescent material based on MOFs is obtained. In the zeolite imidazate framework fluorescent material, Mg and N co-doped graphene quantum dots not only have good fluorescence performance, but also can generate electron transfer with SDZ to form hydrogen-bond-like acting force, imprinted holes similar to a target object in size and shape are reserved in the surface of the imprinted material, and the target object needing to be detected can be selectively recognized; the zeolite imidazate framework fluorescent material can be used for detecting sulfadiazine in the environment and has good practicability.

The present invention relates to a preparation method of an intelligent self-repairing, flame-retardant and light-resistant water-based polyurethane coating. The method comprises the following steps: preparing a self-made hyperbranched flame retardant and using it in the synthesis of a polyurethane prepolymer; cooling the mixture to 58° C., adding 2,2-dimethylolpropionic acid, reacting the mixture for 1 to 2 hours, adding 1 to 2 parts of a disulfide compound, reacting the mixture for 1 to 2 hours at 60 to 80° C., adding 1 to 2 parts of a hydrogen bonding agent, reacting the mixture for 1 hour at 60 to 80° C., adding 0.5 to 1.5 parts of a coumarin derivative, and reacting the mixture for 60 to 90° C. The mixture was stirred for 1-2 hours, and then spiropyran, diethanol monoisopropanolamine, and 0.01 parts of p-toluenesulfonamide were added, and the mixture was reacted at 50°C for 30 minutes. The temperature was lowered to 40-45°C, and 1-2 parts of triethylamine were added, and the mixture was reacted for 1-2 hours. The mixture was cooled to room temperature, and 60-65 parts of water were added. The mixture was stirred at a speed of 1800-2000 r / min for 0.5-1 hour to obtain an intelligent self-healing, flame-retardant, and light-resistant water-based polyurethane coating. The flame retardancy and self-healing properties of the obtained water-based polyurethane were significantly improved.

The invention discloses a high-toughness seawater low-temperature environment self-repairing epoxy coating as well as a preparation method and application thereof. The preparation method comprises the following steps: providing a modified epoxy adaptive network material; the modified epoxy adaptive network material is prepared from epoxy resin, polyol, diisocyanate and a monomer containing dynamic chemical bonds through a reaction. Providing a modified Ti < 3 > C < 2 > T < x > two-dimensional nanosheet; the modified Ti < 3 > C < 2 > T < x > two-dimensional nanosheet is obtained by modifying Ti < 3 > C < 2 > T < x >-MXene by using dopamine and a modifier containing a quadruple hydrogen bond motif; and mixing the modified epoxy adaptive network material with the modified Ti < 3 > C < 2 > T < x > two-dimensional nanosheets, and carrying out an interface ordered cross-linking reaction, so as to prepare the high-toughness seawater low-temperature environment self-repairing epoxy coating. The high-toughness seawater low-temperature environment self-repairing epoxy coating provided by the invention has multiple types of dynamic chemical bonds, has excellent properties of thermosetting resin and thermoplastic resin, and shows high toughness and self-repairing characteristics.

The invention belongs to the field of olefin polymers, and relates to a reversible cross-linked polyolefin elastomer and a preparation method thereof. The reversible cross-linked polyolefin elastomer is a reversible cross-linked polyolefin elastomer in which a cross-linked network is formed through three non-covalent bonds, namely hydrogen bonds, ionic bonds and coordinate bonds, and the hydrogen bonds and the cross-linked bonds account for 0.1-85% by taking the sum of the three non-covalent bonds, namely the hydrogen bonds, the ionic bonds and the coordinate bonds as 100%; the ionic crosslinking bond accounts for 0.5-90%; and the coordination crosslinking bond accounts for 9-99%. Compared with a reversible cross-linked polyolefin elastomer in the prior art, the reversible cross-linked polyolefin elastomer prepared by the invention contains hydrogen bonds, ionic bonds and coordinate bonds at the same time, and a synergistic effect is generated through combination of reversible cross-linked interaction of the coordinate bonds, the hydrogen bonds and the ionic bonds; therefore, the material has excellent physical and mechanical properties and also has recoverability and self-repairability.

The invention relates to the technical field of liquid-liquid homogeneous microextraction, in particular to a method for microextraction analysis of perfluorooctanoic acid by using a switchable eutectic solvent. Comprising the following steps: step 1, mixing a hydrogen bond acceptor and a hydrogen bond donor according to a set proportion value, and stirring and mixing at a set temperature value to obtain a eutectic solvent; step 2, filtering the water sample through a water-based filter membrane, then adding a set amount of deep eutectic solvent, dropwise adding an alkaline solution, carrying out full vortex mixing through a mixer, and then adding an acidic solution to form an emulsion; according to the method, the high selectivity of the green solvent with a specific structure on perfluorooctanoic acid and the characteristic that the solvent is switched between hydrophilic and hydrophobic forms are utilized, so that the microextraction time is shortened, and the impurity removal and enrichment effects are enhanced. The method is simple and convenient to operate, green, environment-friendly, low in cost and good in effect, has the advantage of efficiently and rapidly pretreating the batch small-size complex matrix sample, and has a relatively good application prospect.

The invention relates to the technical field of batteries, and particularly discloses a current collector, a method for preparing the current collector, a pole piece, a lithium ion battery and a power utilization device.The current collector comprises a base material and a conductive coating arranged on at least one side of the base material, and physical crosslinking points are evenly distributed in the conductive coating; the physical cross-linking points are non-covalent bond connecting points and comprise coordinate bonds between the binder and metal ions and / or hydrogen bonds between the binder and the polyhydroxy compound. The physical cross-linking points can effectively improve the adaptability of the conductive coating to the expansion and shrinkage stress of the active material layer in the long-term circulation process, the physical cross-linking points can be self-generated again after being damaged, the cross-linking structure improves the adhesion strength of the conductive coating to the current collector, meanwhile, the conductive coating has excellent fatigue resistance, and the service life of the conductive coating is prolonged. After long-term circulation, the high cohesiveness is still kept, and the phenomena of interface separation and active substance powder falling are not prone to occurring.

The invention belongs to the technical field of membrane material preparation and water treatment, and discloses a La-MOF-COOH / AO-PAN composite membrane material and a preparation method and application thereof, and the preparation method of the membrane comprises the following steps: preparing a PAN membrane; preparing an AO-PAN membrane; the preparation method comprises the following steps: preparing La-MOF-COOH; and the preparation of the La-MOF-COOH / AO-PAN film is carried out. The composite membrane material is composed of modified polyacrylonitrile fibers, metal lanthanum and an organic ligand. Amino groups and hydroxyl groups in amidoximated PAN participate in hydrogen bonds and covalent interaction, so that the interfacial compatibility and stability of La-MOF-COOH and AO-PAN are improved, agglomeration of La-MOF-COOH filler is avoided, the structural uniformity, stability and functionality of the La-MOF-COOH / AO-PAN composite membrane are improved, and the composite membrane has a good application prospect.

The invention relates to the technical field of fluorescence sensing, in particular to a preparation method and application of an Nd (III)-based hydrogen bond organic framework crystalline material. According to the Nd (III)-based hydrogen bond organic framework crystalline state material, Nd (III) serves as a central metal ion and is coordinated with 9 oxygen atoms, and adjacent Nd (III) are connected through H2 (4-CPCA) ligands to form a one-dimensional chain structure. One-dimensional chains are bridged through H2 (4-CPCA) ligands to form a two-dimensional double-layer planar structure, and two-dimensional surfaces are further stacked through the interaction of a large number of intermolecular hydrogen bonds to form a three-dimensional supramolecular structure. The Nd (III)-based hydrogen bond organic framework crystalline material has good fluorescent property and stability, and can be applied to the field of fluorescence sensing.

The invention discloses an inorganic-organic hybrid compound crystal and a preparation method thereof, and belongs to the technical field of organic-inorganic hybrid materials. The preparation method comprises the following steps: mixing raw materials containing hydroiodic acid, organic cage molecules RCC3 and a lead source with a solvent, and carrying out solvothermal reaction to obtain the inorganic-organic hybrid compound crystal. The chemical formula of the prepared inorganic-organic hybrid compound crystal is ({H18 [C72H108N12] 2 [(Pb10I36)]}. 2I), wherein [C72H108N12] is RCC3 acidified by hydroiodic acid, the crystal has a supramolecular three-dimensional structure assembled by a [Pb5I8] 3-anion cluster unit and a protonated RCC3 molecular cage through electrostatic and hydrogen-bond interaction, and belongs to a monoclinic system, and the space group is P21. The crystal structure is a metal halide-based organic-inorganic hybrid crystal constructed by taking an organic molecular cage as nitrogen-containing cations and lead iodide for the first time.

The invention discloses a coated reflecting film based on an organic fluorescent coating and a preparation method of the coated reflecting film, tetra (4-aminophenyl) methane and tetra-(4-formyl-(1, 1-biphenyl)) ethylene are used as reaction monomers to prepare a novel topological structure [4 + 4] COF (3D-TPE-COF) with a tetraphenylethylene (TPE) unit, and the novel topological structure [4 + 4] COF (3D-TPE-COF) is used for preparing the reflective film based on the organic fluorescent coating. The covalent organic framework material 3D-TPE-COF is added into coating liquid as a fluorescent material to prepare a coating reflecting film based on an organic fluorescent coating, and the obtained reflecting film can convert high-energy blue light, so that the brightness of light emitted by a backlight module is higher and closer to white; meanwhile, the 3D-TPE-COF fluorescent material and the polymer particles can form hydrogen bonds in the coating liquid to avoid aggregation of the polymer particles, so that the wear resistance and scratch resistance of the coating reflecting film are improved.

The invention relates to the field of preparation of polyurethane damping materials, in particular to a preparation method of a repairable polyurethane damping material based on multiple hydrogen bonds and metal coordination. Compared with a traditional damping material, the damping material has a higher damping temperature range and has a good damping effect at the temperature of-20 DEG C to 60 DEG C. Multiple reversible hydrogen bonds are introduced through diamine containing amido bonds, the material is endowed with self-repairing and high mechanical strength, and damping and self-repairing performance is further enhanced through pyridine nitrogen atom metal coordination. Starting from molecular structure design, multiple hydrogen bonds and metal-ligand coordination bonds constructed on a polyurethane molecular main chain play a role in synergistic enhancement, energy can be effectively dissipated through dissociation and recombination of the multiple hydrogen bonds and fracture and association of the metal coordination bonds, and the energy consumption is reduced. The polyurethane material is endowed with excellent damping performance and self-healing capability by the dual dynamic action.

The invention belongs to the technical field of polyfluorosiloxane synthesis, and provides a low-by-product polyfluorosiloxane controllable synthesis method which comprises the following steps: carrying out anionic ring opening polymerization on D3F by adopting a binary organic catalytic system, weakening the strong nucleophilicity of an active center based on hydrogen-bond interaction and steric effect, and inhibiting the occurrence of chain back-biting side reaction, so as to obtain the low-by-product polyfluorosiloxane. The polyfluorosiloxane with low content of by-product DnF (n is greater than or equal to 4), controllable structure and narrow molecular weight distribution is prepared. The polyfluorosiloxane with low byproduct content is catalyzed by the binary organic catalyst, the synthesis method is simple, the operation is convenient, the reaction condition is mild, the catalyst has good stability, large-scale production is easy, and further development of the polyfluorosiloxane in the field of high-end and harsh oil-resistant sealing materials can be promoted.

The invention discloses a modified organic silicon marine antifouling paint and coating based on dynamic crosslinking of boric acid ester, and the modified organic silicon marine antifouling paint based on dynamic crosslinking of boric acid ester comprises the following components in parts by weight: 20-40 parts of a component A; 4-10 parts of a component B; 1-3 parts of a component C; wherein the component A comprises hydroxyl-terminated polydimethylsiloxane, borate modified polysiloxane, an auxiliary agent, a pigment filler and a first solvent, the component B comprises a curing agent and a second solvent, and the component C comprises a catalyst and a third solvent. Hydrolysis of boric acid ester bonds increases the hydrogen-bond interaction between the coating and a base material, and meanwhile, ether groups are introduced to strengthen the hydrogen-bond interaction effect, so that the coating can be firmly adhered to the intermediate paint in a seawater soaking environment.

The invention discloses a method for purifying a carbon nano tube by using a deep eutectic solvent. The method comprises the following steps: drying carbon nanotube powder prepared on a supported catalyst by adopting a chemical vapor deposition method; the method comprises the following steps: mixing a hydrogen bond donor and a hydrogen bond acceptor according to a fixed molar ratio, and stirring at a set temperature to obtain a homogeneous eutectic solvent; adding the dried carbon nanotube powder into a deep-eutectic solvent, and dissolving the supported catalyst particles by regulating and controlling the temperature and the time; and carrying out vacuum filtration, cleaning and drying treatment on the reacted liquid to obtain the high-quality carbon nanotube. Compared with a traditional strong acid purification process, the method has the advantages of being simple, environmentally friendly, low in cost and the like, the intrinsic structure and surface characteristics of the carbon nanotubes can be effectively kept, and the method has important industrial application prospects.

The invention discloses a multi-hydrogen bond enhanced fluorine-containing core-shell water-based binder as well as a preparation method and application thereof, and relates to the technical field of lithium ion silicon-based negative electrode binders. The preparation method comprises the following steps: dissolving methyl methacrylate, acrylonitrile and an emulsifier in water, carrying out a polymerization reaction to obtain a rigid core emulsion, adding acrylic acid long-chain ester, a fluorine-containing monomer and acrylamide, carrying out a mixing reaction to obtain a core-shell structure emulsion, mixing the core-shell structure emulsion with a sodium alginate solution, adding nano SiO2, and carrying out a polymerization reaction to obtain the high-temperature-resistant water-based acrylic emulsion. And after the reaction is finished, obtaining the multi-hydrogen bond enhanced fluorine-containing core-shell water-based adhesive. Through core-shell structure design and introduction of a multiple hydrogen bond network, the problem of bonding caused by volume expansion of the silicon negative electrode material in the charging and discharging process is successfully solved, the cycle life and stability of the battery are remarkably prolonged, meanwhile, the environment-friendly characteristic and the process simplicity are considered, and the preparation method is simple and convenient. And an efficient and sustainable development solution is provided for the field of lithium ion batteries.

The invention discloses a durable low-surface-energy polymer modifier capable of freezing on the surface of a matrix and a preparation method thereof, the main chain of the durable low-surface-energy polymer modifier comprises a polydentate hydrogen bond monomer structure, and the end group of the polymer chain is a fluorinated structure. The durable low-surface-energy polymer modifier disclosed by the invention is co-mixed with matrix resin through a conventional processing and mixing means in a standard production process, and is migrated to the surface of a material in processing, heat treatment and use processes, so that the durable low-surface-energy polymer modifier can achieve multiple effects of water resistance, pollution resistance, dust prevention, anticoagulation, antithrombosis, antibiosis, self-cleaning and the like; the multidentate hydrogen bond monomer structure in the modifier structure realizes freezing of the modifier on the surface of matrix resin, so that the risk of elution and loss of the modifier is effectively reduced, the possibility of migration, washing or dissolution in blood is reduced, and the low surface energy durability effect of the matrix surface is enhanced.

The invention discloses an in-situ autocatalytic forming gel epidermal electrode, an electrophysiological signal monitoring system and an electrophysiological signal monitoring device. The gel precursor includes a supramolecular solvent selected from a specific monomer, a metal ion catalyst, an initiator, a cross-linking agent, and a hydrogen bond acceptor and a hydrogen bond donor. The gel precursor provided by the invention can perform autocatalysis to initiate crosslinking to form a sensing medium with an interlocking structure, and meanwhile, can form a stable interface structure with the skin to ensure that the gel precursor is tightly attached to epidermal tissues, and motion artifacts caused by relative displacement in a motion process are reduced to the greatest extent. According to the invention, the electrode is formed by gelling the gel precursor on the skin surface, and the electrode has low interface impedance so as to ensure high signal fidelity, excellent mechanical stability, dynamic adhesion, stable electrochemical performance and biocompatibility, and can be reliably used for a long time. The method can be widely applied to wearable equipment, electronic skin, medical equipment and the like.

The invention provides a hydrogen bond organic framework material, a preparation method and application of the hydrogen bond organic framework material in dopamine detection, the preparation method of the hydrogen bond organic framework material comprises the following steps: S1, dissolving 1, 3, 5-tri (4-carboxyphenyl) benzene in an organic solvent to obtain an organic solution; and S2, dropwise adding an alcohol solvent into the organic solution to react to obtain turbid liquid, and drying to obtain the hydrogen bond organic framework material. The hydrogen bond organic framework material HOF-BTB prepared by the invention is a porous material, has two-dimensional (2D) pi-pi stacked hexagonal lamellas and complex eight interpenetration, generates a one-dimensional channel in the framework, and is simple in preparation process, mild in synthesis condition, low in cost, good in biocompatibility and low in cytotoxicity; and due to rigid organic construction molecules, the compound shows excellent fluorescence performance. The HOF-BTB material has high selectivity due to differential recognition of binding sites, and can be effectively applied to detection of dopamine.

The invention discloses an alkynyl functionalized hydrogen bond organic framework (HOF) material for efficient reverse separation of propylene / propane as well as a preparation method and application of the alkynyl functionalized hydrogen bond organic framework (HOF) material. The preparation method comprises the following steps: dissolving a tetracarboxylic acid type organic ligand H4L in a benign organic solvent to obtain an H4L solution, then placing the H4L solution in a poor solvent steam atmosphere, and obtaining an HOF material through a gas phase diffusion method; after a low-boiling-point reagent is adopted to carry out solvent exchange on the HOF material, solvent molecules in pore channels of the HOF material are removed through an activation method, and then the alkynyl functionalized HOF material for propylene / propane efficient reverse separation is obtained. The material shows the characteristics of high propane adsorption capacity, excellent propylene / propane reverse separation performance, good cycle performance, easy repair and reproducibility, fills the technical blank of the HOF material in the field of efficient reverse separation of propylene / propane mixed gas, and provides a brand new thought and technical support for research and development in the field of light hydrocarbon separation.

The invention relates to a hydrophobically modified aluminum oxide and polytetrafluoroethylene composite film as well as a preparation method and application thereof. According to the present invention, the aluminum oxide is firstly subjected to hydroxylation treatment, and then the surface of the aluminum oxide is subjected to hydrophobic treatment by using cyclosilazane, such that the Al-OH content of the prepared hydrophobic modified aluminum oxide surface is low, such that the water absorption rate of the aluminum oxide-PTFE composite film is low, and the aluminum oxide-PTFE composite film is not easily interfered by moisture, and has good electrical insulation performance. In addition, amino groups (-NH2) or imino groups (-NH-) are further introduced into the surface of the hydrophobic modified aluminum oxide and can form hydrogen-bond interaction with C-F bonds in PTFE, so that the compatibility of the hydrophobic modified aluminum oxide and the PTFE is improved, and the mechanical property of the aluminum oxide-PTFE composite film can still be kept under the condition of high addition amount of aluminum oxide.

The invention discloses a xanthophyll-nicotinamide eutectic crystal and a preparation method and application thereof, the eutectic crystal is formed by xanthophyll and nicotinamide according to the molar ratio of 1: 1 through intermolecular interaction of hydrogen bonds, Van der Waals force and the like, and the molecular formula is C46H62N2O3. According to the invention, xanthophyll and nicotinamide are combined through a co-crystal technology, a novel co-crystal with good water solubility and high bioavailability is formed, and the solubility and absorption efficiency of xanthophyll are significantly improved.

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 provides a piperazinyl steric hindrance type liquid-solid phase change carbon trapping agent and a preparation method thereof, and relates to the field of liquid-solid phase change trapping of CO2. Alkylamine and the like are used as raw materials, piperazinyl steric hindrance type organic amine with secondary amino and tertiary amino structures is designed, and the piperazinyl steric hindrance type organic amine is prepared through ring-opening addition, nucleophilic substitution, cyclization, hydrogenation and other reactions. The piperazinyl steric hindrance type organic amine is compounded with a solvent and a functional additive to prepare the piperazinyl steric hindrance type liquid-solid phase change carbon trapping agent. According to the steric hindrance type phase change carbon trapping agent, on the basis of the electron donating effect of alkyl, the absorption rate of trapping CO2 is increased by 2.2 times compared with that of traditional steric hindrance amine (AMP); on the basis of the steric hindrance effect of the tertiary amine site, the hydrogen-bond interaction between carbamate and the solvent is weakened, liquid-solid phase splitting after the aqueous solution carbon capture system absorbs CO2 is promoted, the problem of poor cycling stability of a non-aqueous solvent system is solved, and the capture efficiency and enrichment degree of CO2 are improved.

The invention relates to the technical field of pharmaceutical preparations, in particular to a preparation process of carbon dots for killing helicobacter pylori and application of the carbon dots in oral pharmaceutical preparations. The preparation method comprises the following steps: mixing microcrystalline cellulose and glycerol, freezing and crushing at an ultralow temperature, and selectively hydrolyzing by combining citric acid-malic acid mixed acid liquor to efficiently prepare a high-crystallinity cellulose nanocrystal template; the controllable synthesis of the carbon dots is realized by utilizing the hydrogen-bond interaction of hydroxyl / carboxyl on the surface of the cellulose nanocrystal and the nitrogen doping effect in the polymerization and carbonization process of citric acid and urea. Besides, when a sodium alginate-chitosan double-layer structure is constructed, carbon dots are introduced into the inner layer to endow the inner layer with special performance, a protein-polysaccharide network is formed on the outer layer through transglutaminase enzymatic crosslinking, and the oxidation resistance and mechanical strength are enhanced through secondary curing of tea polyphenol. According to the invention, food-grade raw materials are used for realizing high-efficiency antibiosis, the oral preparation safety specification is met, and the clinical transformation potential is realized.

According to the hydrogen-bond organic framework material and the preparation method and application thereof, the preparation process is simple, mild and low in cost, the prepared hydrogen-bond organic framework material HOF-BTB-NH2 is one of a few of HOF materials with permanent pore channels, and the porous material has great development potential; the BTB-NH2 linker is connected with carboxyl on an adjacent linker through a hydrogen bond on the carboxyl, a firm 3D porous material is further formed through face-to-face pi-pi stacking interaction between benzene rings, and the 3D porous material is provided with one-dimensional porous channels in the a-axis direction; according to the HOF-BTB-NH2 fluorescent probe, the rigid organic construction molecules enable the HOF-BTB-NH2 fluorescent probe to show excellent fluorescence performance, the porosity and large specific surface area of the HOF-BTB-NH2 material are beneficial to full contact with an analyte and promote interaction with guest molecules, so that the detection sensitivity is improved, and the HOF-BTB-NH2 fluorescent probe has high selectivity due to difference recognition of binding sites. By adopting the fluorescence characteristic of the new material HOF-BTB-NH2, the sensitive and specific detection on the metal ion Cu < 2 + > can be realized.