927 results about "Tris" patented technology

The invention relates to a hyaluronic acid-polyurethane composite material based on a double dynamic network and a preparation method and application thereof, and the preparation method comprises the following steps: carrying out hydrophobic modification reaction on hyaluronic acid and aminophenylboronic acid to obtain aminophenylboronic acid modified hyaluronic acid; the preparation method comprises the following steps: mixing polytetrahydrofuran ether glycol, polyethylene glycol and isophorone diisocyanate, carrying out a primary reaction, adding trimethylolpropane tri (3-mercaptopropionic acid) ester, carrying out a secondary reaction, adding tannic acid, and carrying out a third reaction to obtain tannic acid-terminated dynamic thionocarbamate polyurethane; and mixing the amino phenylboronic acid modified hyaluronic acid with the tannic acid terminated dynamic thionocarbamate polyurethane for reaction to obtain the hyaluronic acid-polyurethane composite material with the double dynamic networks. Compared with the prior art, by introducing a'thionocarbamate-borate 'double-dynamic network, high toughness, high strength, good self-repairability and repeatable processability in an extreme environment are realized, and the material is particularly suitable for manufacturing and repairing of key components in an LNG ship body and a heat insulation system thereof.

The present invention relates to the field of water treatment technology, and more particularly to a kind of reverse osmosis membrane and preparation method thereof.The preparation method of the reverse osmosis membrane includes:Basement membrane is soaked in aqueous phase solution, after taking out surface drying, oil phase solution is coated on basement membrane and carries out interfacial polymerization reaction, after solidification, coating modifier solution, after drying, obtain reverse osmosis membrane;The modifier includes 2,4,6-tris (4-aminophenyl) ‑1,3,5-triazine ‑1,3,5-tris (4-methylphenyl) benzene.The COFs successfully grafted by the present invention can improve the water permeability of membrane to a certain extent, and can also improve the anti-pollution property, acid resistance and oxidation resistance of membrane, and then improve the service life of membrane.The present invention further compares the different effects that the same type of imino COFs are introduced into reverse osmosis membrane, so as to highlight the excellence of the imino COFs selected by the present invention.

The invention relates to the technical field of metal working fluids, in particular to a degradable environment-friendly vegetable oil-based semi-synthetic cutting fluid and a preparation method thereof. The cutting fluid comprises 20-30 parts of vegetable lubricating oil, 10-20 parts of an alkali storage agent, 2-5 parts of a corrosion inhibitor, 3-5 parts of a coupling agent, 5-8 parts of a surfactant and 6-11 parts of a composite anti-rust agent, the composite anti-rust agent comprises an anti-rust agent A and an anti-rust agent B, the anti-rust agent A comprises N-[3-(dimethylamino) propyl]-N, N-dimethylformamide, and the anti-rust agent B comprises N-[3-(dimethylamino) propyl]-N, N-dimethylformamide. The antirust agent A comprises at least one of N, N ', N'-trimethyl-1, 3-propanediamine, benzotriazole, sebacic acid and 2, 4, 6-tri (aminocaproic acid)-1, 3, 5-triazine, and the antirust agent B comprises at least one of an imidazoline compound and fatty acid sarcosine ester. The cutting fluid provided by the invention has excellent corrosion resistance, rust resistance, defoaming property, biodegradability and storage stability, and has a good application prospect.

The invention discloses a reaction buffer solution for improving endotoxin detection sensitivity of a recombinant tachypleus amebocyte lysate, a kit containing the reaction buffer solution and application of the reaction buffer solution. The reaction buffer solution comprises the following components: a Tris-HCl buffer solution, magnesium ions, sodium chloride, cane sugar, ethylene glycol diethyl ether diamine tetraacetic acid, a nonionic surfactant and cyclodextrin or a derivative thereof. The invention also discloses a preparation method of the reaction buffer solution and a kit containing the reaction buffer solution. When the reaction buffer solution or the kit is used for detecting the endotoxin of the recombinant tachypleus amebocyte lysate, the sensitivity of the recombinant tachypleus amebocyte lysate for detecting the endotoxin can be improved by one order of magnitude, the lowest detection limit can reach 0.0005 EU / ml, the reaction buffer solution or the kit has strong anti-interference capability and short reaction time, and the detection efficiency is greatly improved.

The invention belongs to the technical field of molecular diagnosis, and particularly discloses a high-risk HPV16 rapid detection system based on RPA-CRISPR / Cas12a, which is prepared by the following steps: (1) mixing a nucleic acid lysis solution containing Tris (pH = 8.0), NaHCO3, polyvinylpyrrolidone and Tween-20 with Proteinase K to treat a sample, and performing pyrolysis at room temperature for 5 minutes to obtain a nucleic acid template; (2) an RPA reaction system contains an RNA inhibitor, a reverse transcriptase and an RPA reaction essential enzyme, and after the template and the starting agent in the step (1) are added, RPA amplification is carried out at 37 DEG C; (3) dropping the reaction liquid on a colloidal gold test strip subjected to position exchange and transformation of a sample pad and a water absorption pad, and carrying out result interpretation; and (4) adding the RPA product into a CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) reaction system containing the LbCas12a protein, the specific gRNA and the probe. According to the scheme, a rapid, high-sensitivity and cross-reaction-free detection system of the HPV16 is realized by optimizing a nucleic acid lysis solution formula, designing a specific primer and gRNA and modifying a test strip for detection.

The invention discloses an anti-yellowing PVB (Polyvinyl Butyral) adhesive for laminated glass and a preparation method thereof, and relates to the technical field of adhesives. The yellowing-resistant PVB glue for the laminated glass has the advantages that the yellowing resistance is high; the modified PVB / nano silicon dioxide composite material is prepared from the following raw materials in parts by weight: 55 to 65 parts of modified PVB resin, 4 to 6 parts of modified nano silicon dioxide, 15 to 20 parts of dioctyl adipate, 0.5 to 1 part of a compound antioxidant, 0.3 to 0.8 part of an ultraviolet absorbent UV-327, 0.2 to 0.5 part of a silane coupling agent KH-560, 0.3 to 0.6 part of ethylene bis stearamide, 0.1 to 0.3 part of 2-benzimidazole methyl carbamate, 3 to 5 parts of tris (1-chloro-2-propyl) phosphate and 0.1 to 0.3 part of nano titanium dioxide. 5 to 8 parts of isopropanol; 0.8 to 1.2 parts of polycarbodiimide. The special modified PVB resin and the nano silicon dioxide are matched with the auxiliary agents such as the compound antioxidant, the anti-yellowing performance of the PVB glue for the laminated glass is remarkably improved through precise process preparation, the components have a synergistic effect, the process is controllable, the product performance is stable, and the cohesiveness is good.

The invention belongs to the technical field of organic porous materials, and relates to an acenaphthequinone diimine palladium functionalized super-crosslinked microporous polymer as well as a preparation method and application thereof. The preparation method specifically comprises the following steps: carrying out Friedel-Crafts alkylation reaction on (1E, 2E)-N1, N2-bis [2, 4, 6-tri-(benzhydryl phenyl)] acenaphthylene-1, 2-diimine and dimethyl formal, 1, 3, 5-triphenylbenzene or tetraphenylmethane, so as to obtain an organic porous polymer; and carrying out coordination on the organic porous polymer and PdCl2 to obtain the acenaphthequinone diimine palladium functionalized super-crosslinked microporous polymer with catalytic activity. The super-crosslinked microporous polymer has the advantages of high stability, large specific surface area and high palladium loading capacity, and can catalyze the direct C-H bond arylation reaction of brominated aromatic hydrocarbon and heteroaromatic hydrocarbon to synthesize a linked heteroaryl compound; the preparation method of the organic porous polymer catalytic material is simple and suitable for industrial production.

The invention discloses a preserving fluid for stably preserving sample DNA at normal temperature and a preparation method thereof, and belongs to the technical field of biological sample preservation. The preserving fluid comprises a lysis system, a nucleic acid protection system and a buffering and stabilizing system, the cracking system comprises a composite surfactant and an enzymolysis auxiliary agent; the composite surface active agent is prepared from polyether polyol fatty acid ester and cocamidopropyl hydroxy sulfobetaine; the enzymolysis auxiliary agent comprises lysozyme Lyso-V and protease K; the nucleic acid protection system comprises a nitrogen heterocyclic polyamine-carboxylic acid derivative and dextran sulfate; the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N' ', N ''tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N''-triacetic acid, disodium ethylene diamine tetraacetate-nitrogen heterocyclic derivative, and diethylenetriamine pentaacetic acid-piperazine derivative, and the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N '', N'' tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N ''-triacetic acid. The buffering and stabilizing system comprises an amphoteric buffering agent and a polymer stabilizer; the amphoteric buffering agent comprises 2-(N-morpholino) ethanesulfonic acid and N-tri (hydroxymethyl) methylglycine.

The invention discloses a preparation method and application of an aminated MIL-101 (Cr) material for enhancing adsorption of perfluorinated compounds, relates to the technical field of metal organic framework materials, and aims to enhance the adsorption effect of the aminated MIL-101 (Cr) material on the perfluorinated compounds. The preparation method comprises the following steps: taking MIL-101 (Cr) as a skeleton raw material and tris (2-aminoethyl) amine as an amination raw material, and then synthesizing and modifying to prepare the MIL-101 (Cr)-TAEA, the average pore size of which can be more than 7 times of that of the MIL-101 (Cr); the MIL-101 (Cr)-TAEA can be applied to removal of perfluorinated compounds in water, and after four times of cyclic regeneration, the total removal rate of PFASs is reduced by less than 5% compared with that of first adsorption; the preparation steps are simple and easy to operate, the raw materials are easy to obtain, the preparation cost is low, the average pore size of the prepared aminated MIL-101 (Cr) material is greatly increased, the flexibility of the material is enhanced, the adsorption performance on perfluorinated compounds is good, the saturation adsorption capacity is high, and the cyclic regeneration performance of the material is excellent.

The invention relates to preparation of a crystalline allyl covalent organic framework material and application research of the crystalline allyl covalent organic framework material in benzamide cyclization green photocatalytic conversion. The SF-COF material is prepared by adopting a step-by-step synthesis method. The preparation method comprises the following steps: synthesizing a COF precursor by taking 1, 3-benzenetricarboxaldehyde and p-aminophenylacetonitrile as raw materials, and preparing the allylation covalent organic framework material with the electronic push-pull effect from the COF precursor and 5, 5 ', 5'-(benzene-1, 3, 5-triyl) tri (thiophene-2-formaldehyde) through a solvothermal method. The material is applied to the field of photocatalytic organic conversion, and benzamide cyclization and conversion of derivatives of benzamide are achieved under irradiation of a blue light LED. The prepared SF-COF has the advantages of efficient charge separation and electron conduction performance, good structural stability and chemical stability and the like. And a catalyzed organic reaction substrate has the advantages of wide universality range, good cycle stability and the like, and shows excellent photocatalytic conversion capability.

The invention provides a bacteriostatic and scale-inhibiting PE material and a preparation method thereof, and belongs to the technical field of high polymer materials, the preparation method comprises the following preparation steps: dissolving polyethylene in xylene, dissolving, adding perfluorohexylethylene and dicumyl peroxide, reacting, precipitating, washing, and drying to obtain perfluoro modified PE; the preparation method comprises the following steps: dissolving four-arm polyethylene glycol amine in a PBS buffer solution, adding 4-carboxyphenylboronic acid, EDC.HCl and NHS, carrying out a stirring reaction in a dark place, carrying out ultrafiltration and freeze drying to obtain PBA-PEG, dissolving the PBA-PEG in a Tris-HCl buffer solution, adding dopamine hydrochloride, and carrying out mixing, oxidation reaction, dialysis purification and drying to obtain a PBA-DA-PEG compound; the preparation method comprises the following steps: pre-mixing perfluorinated modified PE, mixing with an antioxidant and a compatibilizer, injecting the PBA-DA-PEG compound, continuously mixing, extruding, and carrying out water-cooling pelletizing to obtain the antibacterial and scale-inhibiting PE material. According to the PE material obtained by the invention, the antibacterial performance and the scale inhibition performance of the material can be improved at the same time.

A pharmaceutical composition and a method of administering the pharmaceutical composition to a patient suffering from edema, heart failure, kidney or liver disease or having symptoms thereof is disclosed. The pharmaceutical composition includes furosemide, or a pharmaceutically acceptable salt, hydrate or ester thereof and tris(hydroxymethyl)aminomethane. The furosemide is present in the pharmaceutical composition at a concentration from about 10 mg / mL to about 30 mg / mL and the tris(hydroxymethyl)aminomethane is present at a concentration of less than or equal to 40 mM. The pH value of the pharmaceutical composition is maintained between about 8.0 and about 8.5 for parenteral administration.

The invention provides a synthesis method of tris (dimethylamino) cyclopentadienyl hafnium, which comprises the following steps: reacting hafnium tetrachloride with sodium dimethylamino at a first temperature under the protection of inert gas to form an intermediate; heating and settling, cooling to a second temperature, dropwise adding cyclopentadiene, and filtering, distilling and purifying to obtain a target product. According to the method, high yield and high purity are achieved by optimizing the raw material ratio and controlling the dropwise adding temperature and the use amount of cyclopentadiene. The byproduct sodium chloride is large in particle and easy to filter, the post-treatment process is remarkably simplified, and the process safety, controllability and industrial adaptability are improved.

An aqueous pharmaceutical composition including compound having the formula of tetragadolinium [4,10-bis(carboxylatomethyl)-7-{-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({2-[4,7,10-tris(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate wherein the stereochemistry at the chiral carbon of the four alanine substituents is selected from the group consisting of RRRR, SSSS, RSSS, RRSS, and RRRS stereoisomers, and racemic and diastereomeric mixtures of any thereof, or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same is described. The compounds may be used as an MRI contrast imaging agent.

The invention belongs to the technical field of water treatment, and particularly relates to a preparation method and application of a PDA / CS composite adsorbent loaded with a bimetallic system, and the preparation method comprises the following steps: 1) dissolving dopamine in a Tris buffer solution to prepare a dopamine prepolymer solution; then adding FeCl3, and carrying out constant-temperature water bath; centrifuging the obtained black suspension, performing suction filtration, washing, collecting a filter cake, and performing freeze drying to obtain PDA microspheres; 2) dispersing PDA microspheres in deionized water, and carrying out ultrasonic treatment until the PDA microspheres are uniformly dispersed; 3) dissolving chitosan in an acetic acid solution, and adding CuCl2 to prepare a mixed solution; the suspension obtained in the step 2 is dropwise added into a mixed solution for constant-temperature water bath, the pH of the mixed solution is adjusted through a NaOH solution, glutaraldehyde is added for constant-temperature water bath after constant-temperature water bath, and 4, the obtained suspension is subjected to centrifugation, suction filtration, washing, filter cake collection and freeze drying.

The invention provides a preparation method and application of a high-activity salmon salmon sperm PDRN (DNA sodium) raw material. The preparation method comprises the following steps: crushing and freezing a salmon testis at an ultralow temperature, adding a mixed solution of a Tris-HCl buffer solution and sodium chloride, and dispersing at a low temperature; adding a compound enzyme preparation with the total enzyme activity of more than or equal to 350KU / L, and carrying out low-temperature appropriate pH enzymolysis; and adjusting the pH value to a suitable range, and carrying out frequency conversion ultrasonic and high-pressure homogenization alternate synergistic treatment in an ice-water bath to obtain the DNA fragmentation liquid, so that the defects of low PDRN activity retention rate, insufficient purity and high protein residue in the prior art are overcome.

The invention relates to the technical field of biomedical materials, in particular to photo-thermal antibacterial healing-promoting hydrogel as well as a preparation method and application thereof. The preparation method of the hydrogel comprises the following steps: dispersing mesoporous polydopamine (MPDA) into a Tris-HCl solution, and then adding L-arginine to prepare L-MPDA; the preparation method comprises the following steps: fully dissolving 3-(aminomethyl) phenylboronic acid hydrochloride and 4-(4, 6-dimethoxytriazine-2-yl)-4-methylmorpholine hydrochloride into hyaluronic acid (HA), regulating the pH value to 6.5 by using alkali liquor to obtain phenylboronic acid modified hyaluronic acid mixed liquor, and dialyzing and freeze-drying to obtain HA-PBA. The preparation method comprises the following steps: dissolving metformin and purified L-MPDA in deionized water, sequentially adding purified HA-PBA and a polyvinyl alcohol (PVA) solution, and uniformly mixing to obtain the hydrogel. The hydrogel prepared by the invention has excellent hemostasis, antibacterial and adhesion properties. When the hydrogel is used as a hydrogel dressing for treating a diabetic wound surface, the healing speed of the diabetic wound surface can be effectively improved.

The application belongs to the field of functional materials and surface engineering, and particularly relates to an ant nest-like photo-thermal super-hydrophobic sponge as well as a preparation method and application thereof. The preparation method comprises the following steps: repeatedly soaking melamine sponge in anhydrous ethanol solution and drying; adding dopamine hydrochloride into a tris buffer solution to obtain a mixed solution by stirring, and then immersing the surface of the dried melamine sponge into the mixed solution and drying to obtain PDA@MS; adding PDMS and a curing agent into a cyclohexane solution to stir, then adding MWCNTs, MnO2 and CuO to stir to form a mixed solution, and then spraying the mixed solution on the surface of the PDA@MS and drying to obtain PMOS; and immersing the surface of the PMOS into a mixed solution of ethanol and deionized water containing PFOTES, and then taking out and drying. Through fine cross-scale multi-layer gap structure design, high mechanical durability, excellent light absorption capacity, efficient anti-icing, de-icing, interface evaporation and fresh water production in extreme environments are realized.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2,2′,2″-(1,3,5,2,4,6-trioxatriborinane-2,4,6-triyl)tris (3-fluorophenol), useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

The invention discloses a preparation method and application of a fluorinated amino covalent organic framework adsorption material, and relates to the technical field of covalent organic framework materials. According to the preparation method, 2, 4, 6,-tri (4-aminophenyl)-1, 3, 5-triazine is adopted as a point monomer, 2, 3, 5, 6-tetrafluorop-dibenzaldehyde and 2, 5-divinyl-1, 4-phthalaldehyde are adopted as side monomers, and the fluorinated covalent organic framework adsorption material is obtained through reaction; and carrying out post-modification reaction on the fluorinated amino covalent organic framework by adopting cysteamine hydrochloride to obtain the fluorinated amino covalent organic framework adsorption material. The prepared fluorinated amino covalent organic framework adsorption material has high selective adsorption and high adsorption capacity on PFAS, and due to the characteristics, the material has excellent adsorption performance on PFAS in water.

The invention belongs to the technical field of flame-retardant master batches, and particularly relates to a flame-retardant master batch for polypropylene and a preparation method thereof.The preparation method comprises the steps that tris (2-hydroxyethyl) isocyanurate is heated and molten, tetrabutyl titanate and DOPO-DPP are added into the molten tris (2-hydroxyethyl) isocyanurate, the mixture reacts for 3-4 h, melamine and cyanuric acid are added into the molten tris (2-hydroxyethyl) isocyanurate, the mixture reacts for 30 min, cooling and smashing are conducted, and a macromolecular flame retardant TDMC is obtained; the preparation method comprises the following steps: carrying out ester exchange reaction on 2, 4-diphenyl-6-[2-hydroxy-4-(ethoxycarbonyl methoxy) phenyl]-1, 3, 5-triazine and 2, 2, 6, 6-tetramethyl piperidinol to prepare a free radical capturing agent; the polypropylene, the TDMC, the free radical scavenger and the zeolite are put into a high-speed mixer to be stirred and mixed, and then extrusion granulation is performed. The macromolecular flame retardant TDMC is adopted, the molecular weight of the macromolecular flame retardant TDMC is large, the water resistance is good, and the compatibility and damp-heat stability of the flame-retardant master batch in polypropylene are improved.

The invention belongs to the technical field of sensor materials and malathion detection, and relates to a nano-silver modified covalent organic framework composite material, a preparation method and application thereof, and an electrochemical aptamer sensor. The preparation method comprises the following steps: S1, dissolving 1, 3, 5-tri (4-aminophenyl) benzene and 2, 5-divinyl-1, 4-phthalaldehyde in acetonitrile, adding a catalyst to carry out condensation reaction, standing, separating, washing and drying to obtain a covalent organic framework material; s2, dispersing the covalent organic framework material and silver nitrate in water, adding sodium citrate after ultrasonic dispersion, and washing and drying to obtain the nano-silver modified covalent organic framework composite material. The nano-silver modified covalent organic framework composite material prepared by the invention shows excellent crystallinity, extremely high porosity and good conductivity, and realizes high-sensitivity, rapid and accurate quantitative analysis of malathion in traditional Chinese medicinal materials.

The application belongs to the technical field of gene detection, and particularly relates to a biological sample nucleic acid rapid extraction method and kit based on a magnetic bead method. The method comprises the following steps in sequence: S1, liquefying a biological sample by using a liquefying solution; the liquefying treatment is to add 1-4 times the volume of the liquefying solution to the biological sample, shake and mix, and then place at room temperature for 15-30 minutes; the liquefying solution comprises guanidine salt, potassium salt and / or sodium salt, Tris-HCl, EDTA and isopropyl alcohol; S2, lysing the biological sample; adding a lysing solution and magnetic beads to the system obtained in S1, and heating at 90-100 DEG C for 3-20 minutes to lyse the biological sample; S3, cleaning the biological sample; and S4, eluting the nucleic acid. The method does not need centrifugal separation in the operation process, and can realize automatic and efficient extraction of the nucleic acid.

The application discloses a hot-melt injectable adhesive and a preparation method and application thereof, and belongs to the technical field of adhesives. The hot-melt injectable adhesive comprises a co-hot-melt product of alpha-liponic acid, N-alkyl liponic amide and tris(2-carboxyethyl) phosphonium hydrochloride or citric acid, and is specifically prepared by mixing and hot-melting alpha-liponic acid, N-alkyl liponic amide and tris(2-carboxyethyl) phosphonium hydrochloride or citric acid and then cooling and shaping. The hot-melt injectable adhesive is a temperature-responsive crystallization curing mode, the curing process does not involve material exchange with a water phase, and the use of a solvent is omitted, so that the hot-melt injectable adhesive has the advantages of green environmental protection, simple preparation, good universality, strong adhesion and convenient use and operation, and is expected to have great application potential in daily life and industrial engineering fields.

The invention discloses an antibacterial nanofiber hemodialysis membrane and a preparation method thereof, and relates to the technical field of dialysis membranes, and the preparation method comprises the following steps: mixing a chitosan derivative, heparin, dopamine, an unsaturated monomer and an initiator in a DMF / phosphate buffer mixed solution to obtain a surface treating agent; taking the polyethersulfone nanofiber membrane as a supporting layer, dipping in a surface treating agent, and performing UV irradiation to form a functional layer, thereby obtaining the dialysis membrane. The preparation method comprises the following steps: compounding phenanthroline cerium triacrylate hybridized CeO2 with N-vinyl pyrrolidone, sodium p-styrenesulfonate and lauryl methacrylate to obtain an unsaturated monomer, compounding the unsaturated monomer with a chitosan derivative, heparin and dopamine to prepare a surface treating agent, impregnating a polyether sulfone nanofiber membrane, and carrying out irradiation curing to form a functional layer. The prepared hemodialysis membrane has efficient anticoagulation and broad-spectrum antibacterial properties, high permeability, low protein adsorbability and long-term stability.

The invention relates to the field of acetylene purification and new materials, and particularly provides a double-interspersed MOF (Metal Organic Framework) and a preparation method and application thereof in acetylene purification, and the specific synthesis method comprises the following steps: reacting a tricarboxylic acid ligand 1, 3, 5-tris (4-carboxylphenyl) benzene (H3btb) with a nitrogen-containing methyl-containing ligand 3-methyl-1H-1, 2, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3, 4-tetramethyl-1, 3-tetramethyl-1 The MOF (Zn-btb-fmtrz) with ultrahigh stability performance is synthesized from 2, 3, 4-triazole (fmtrz) and a zinc-containing compound, and the material can be used as an adsorbent, has strong acetylene adsorption action force, high selectivity and good stability, is suitable for industrial production, and shows a more excellent separation effect on low-concentration acetylene compared with a traditional method. The synthesized material is stable and has good acetylene adsorption capacity, and a new direction is provided for using MOF as an acetylene purification material.

The invention relates to the technical field of biology, in particular to a method for extracting PDRN from plants and application. In the preparation process, the casein is added, so that the casein and the PDRN are competitively combined with impurities in plants; enzyme is added for enzymolysis treatment, so that subsequent centrifugation and other operations are facilitated; the impurities are further removed by adding Tris-HCl, NaCl, CTAB (cetyltrimethyl ammonium bromide) and EDTA (ethylene diamine tetraacetic acid) and controlling each concentration. By adopting the method provided by the invention, the A260 / A280 of the PDRN extracted from the plant is greater than or equal to 1.69, the A260 / A230 is greater than or equal to 1.55, the PDRN has the advantage of high purity, and the obtained PDRN has the effects of resisting aging, repairing a barrier, resisting inflammation and the like, and has a good application prospect.

The invention discloses a recyclable water-based metal cutting fluid and a preparation method thereof. The cutting fluid comprises the following raw materials in parts by weight: 32-36 parts of base oil, 8-12 parts of amines, 9-12 parts of a surfactant, 0-8 parts of an extreme pressure agent, 6-9 parts of a lubricant, 4-6 parts of an antirust agent, 0-2 parts of a bactericide, 2-4 parts of a coupling agent, 0.1-1 part of a defoaming agent and the balance of deionized water. The preparation method comprises the following steps: dissolving the amine in water in advance, adding the anti-rust raw material into the amine solution, fully stirring until the anti-rust raw material is completely dissolved, finally adding the base oil, the surfactant and other additives, and continuously stirring until the anti-rust raw material is completely clarified and transparent. The preferable antirust agent is tris (2-carboxyethyl) phosphine oxide, the excellent extreme pressure effect and bactericidal performance are achieved through carboxyethyl and phosphine oxide structures contained in the tris (2-carboxyethyl) phosphine oxide, and the finished product has good long-term stability, high oil film lubricity and excellent antirust and anti-corrosion performance.

The invention relates to the field of veterinary drug residue detection, in particular to a fluorescence sensor based on DNA molecular machine mediated split Cas12a and application of the fluorescence sensor to ofloxacin detection, the fluorescence sensor comprises a system A, a system B and a system C. According to the final concentration of each system, the system A comprises an AP / CP double-stranded compound and a 20 mM Tris-HCl buffer solution 1, the system B comprises a double-stranded compound, an sRNA probe and a 10 mM Tris-HCl buffer solution 2, and the system C comprises a DNA molecular machine mediated split Cas12a. The system C comprises a Cas12a / hRNA compound, a pDNA / psG43 signal probe, ThT and a 20 mM Tris-HCl buffer solution; aP in the AP / CP double-chain compound is an aptamer of ofloxacin, and AP and CP in the AP / CP double-chain compound are paired and connected through complementary base pairing; the sequences of AP, CP, PS, SS, sRNA, hRNA, pDNA and psG43 are respectively as shown in SEQ ID NO.1-SEQ ID NO.8. The invention also discloses a kit for detecting the content of the protein. According to the application, the nucleic acid aptamer of ofloxacin is utilized, based on a DNA molecular machine and SCas12a as a signal amplification technology and sulfo-modified G43 as a fluorescent signal probe, even if the content of ofloxacin in a sample is extremely low, detection can be accurately realized.

The invention relates to the technical field of organic functional material synthesis and mycotoxin removal, in particular to a magnetic covalent organic framework for adsorbing zearalenone and a preparation method and application thereof.The magnetic covalent organic framework is Fe3O4 (at) COF-VPBA and is prepared from 1, 3, 5-tris (4-aminophenyl) benzene, 2, 5-dimethoxy terephthalaldehyde, 4-alkenyl phenylboronic acid, boron trifluoride diethyl etherate, 2, 3-dichloro-5, 5-di (4-aminophenyl) benzene, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2, 5-dimethoxy terephthalaldehyde, 2 The catalyst is prepared from 2, 6-dicyano-1, 4-benzoquinone and nano ferroferric oxide through a four-component one-pot in-situ Povarov reaction. According to the method, the process is simplified, the defects of a fractional step method are avoided, due to specific covalent binding of boric acid groups and ZEN catechol hydroxyl groups, the adsorption capacity and the adsorption rate are remarkably superior to those of traditional and unfunctionalized adsorption materials, the adsorption rate still exceeds 90% after acetonitrile is eluted and regenerated and is repeatedly used for more than 5 times, and the comprehensive requirements of high selectivity, high adsorption capacity, easiness in separation and recyclability are met.