1350 results about "Tris" patented technology

The invention discloses a polyrotaxane covalent organic framework material capable of regulating interlayer spacing through cyclodextrin and application of the polyrotaxane covalent organic framework material, and belongs to the technical field of biological medicine. The polyrotaalkylated covalent organic framework material is obtained by taking a cyclodextrin aromatic multi-amino inclusion compound and a (multi-aldehyde bipyridine) ruthenium (II) complex as structural units and carrying out copolymerization; the cyclodextrin aromatic polyamine inclusion compound is a beta-cyclodextrin p-phenylenediamine inclusion compound with a hydroxyl group or without a hydroxyl group; the (multi-aldehyde dipyridyl) ruthenium (II) complex is tris (4, 4 '-diformaldehyde-2, 2'-dipyridyl) ruthenium (II). The interlayer spacing of the polyrotaxane covalent organic framework material is greatly increased by utilizing a cavity of gamma-cyclodextrin, and meanwhile, the material has excellent photo-thermal and photodynamic activity, is positively charged, and can better adsorb negatively charged bacteria; and the hydrogel is good in biocompatibility and free of toxic and side effects, and has an excellent treatment effect on wounds infected with staphylococcus aureus.

The invention discloses tris (dimethylamino) cyclopentadienyl hafnium and a preparation process thereof.The preparation process of the tris (dimethylamino) cyclopentadienyl hafnium comprises the following steps that S1, an n-hexane solution of n-butyllithium and dimethylamine are subjected to a reaction, and a lithium dimethylamino emulsion is obtained; s2, adding hafnium tetrachloride into the lithium dimethylamino emulsion for reaction, and separating to obtain a liquid-phase product; s3, the liquid-phase product is heated, a tetra (dimethylamino) hafnium concentrated solution is obtained, and the volume of the tetra (dimethylamino) hafnium concentrated solution is 20%-30% of the volume of the liquid-phase product; and S4, obtaining cyclopentadiene, adding the cyclopentadiene into the tetra (dimethylamino) hafnium concentrated solution to react, and filtering to obtain tris (dimethylamino) cyclopentadienyl hafnium. According to the preparation process of the tris (dimethylamino) cyclopentadienyl hafnium, complex solvent components are not needed, the preparation efficiency is improved, and the use amount of the solvent and the preparation cost are reduced.

The invention relates to the field of heat shrinkage films, in particular to an antistatic PETG heat shrinkage film. The PETG heat shrink film comprises the following components in parts by weight: 100 parts of PETG resin, 2-6 parts of an anti-adhesion agent, 2-5 parts of a lubricant, 1-5 parts of an antistatic modifier, 1-2 parts of an antioxidant and 0.5-1 part of a light stabilizer. In the preparation process of the PETG heat shrink film, a novel borate antistatic agent is introduced, and the antistatic agent is synthesized by taking tris (2-carboxyethyl) isocyanurate and 4-aminophenylboronic acid pinacol ester as raw materials, so that compared with a traditional antistatic agent, the antistatic property is better, the heat stability is obviously improved, and the service life of the heat shrink film is prolonged. And the phenomenon of local deformation or poor arc-shaped shrinkage of the PETG heat shrinkage film when the PETG heat shrinkage film shrinks at a non-uniform interface is reduced.

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 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 invention relates to the technical field of polyurethane adhesives, and provides a heat-conducting polyurethane structural adhesive and a preparation and use method thereof.The heat-conducting polyurethane structural adhesive comprises a first component and a second component, and the first component comprises modified bio-based polyol, polythiol, heat-conducting filler, a first water removal agent, a thixotropic agent, a first catalyst and a second catalyst; the second component comprises epoxy resin, diisocyanate, polyisocyanate, a heat-conducting filler, a coupling agent, a second dewatering agent, a dispersing agent and a retarder; the modified bio-based polyol is selected from at least one of modified castor oil polyol, modified grease polyol and modified cashew nut shell oil polyol; the polythiol is selected from at least one of trimethylolpropane tri (3-mercaptopropionic acid ester), pentaerythritol tetra (3-mercaptopropionic acid ester), butanediol mercaptopropionic acid ester and polythiol. Through the arrangement, the heat-conducting polyurethane structural adhesive has relatively long openable time, and is rapidly cured at room temperature within a short time to generate relatively high initial curing strength.

The invention relates to a rapid detection kit for large yellow croaker pyramidal worm, and belongs to the field of pathogen biological diagnosis in aquaculture. The kit comprises a nucleic acid releasing agent and further comprises a primer and a probe which are used for detecting the large yellow croaker pyramidal worm. The kit comprises a nucleic acid releaser; the formula of the nucleic acid releasing agent comprises tris (hydroxymethyl) aminomethane hydrochloride with the final concentration of 100 mM, sodium chloride with the final concentration of 100 mM, sodium dodecyl sulfate with the final concentration of 1 wt%, sodium alpha-olefin sulfonate with the final concentration of 3 wt%, sodium lauroyl glutamate with the final concentration of 1.2 wt%, betaine with the final concentration of 1 wt% and water as a solvent. The sequences of the primer and the probe for detecting the Pseudosciaena crocea pyramidal are 5 '-TATGGGCAATTCTGAATCCT-3', 5 '-TCTTTTCTGATCCCTGAAT-3' and 5 '-FAM-GTCGGTGGAGTGATTTGTTTG-3'. The kit disclosed by the invention is simple to operate, provides a tool for diagnosis, prevalence monitoring, prevention and control of the Pseudosciaena crocea pyramidal, and has a very high application value.

The invention belongs to the field of novel environment-friendly materials, and particularly relates to a modified covalent organic framework material for simultaneously adsorbing multiple heavy metal ions as well as a preparation method and application of the modified covalent organic framework material. The preparation method of the material comprises the following steps: dissolving 1, 3, 5-tri (4-aminophenyl) benzene and 2, 5-dihydroxy terephthalaldehyde in a mixed solvent, and standing and reacting at room temperature to obtain a mixed solution; adding scandium trifluoromethanesulfonate into the obtained mixed solution, carrying out standing reaction at room temperature, after the reaction is finished, separating insoluble substances from the reaction solution, and washing and drying the insoluble substances to obtain a covalent organic framework base material; a covalent organic framework base material prepared by adopting a neutral solution is subjected to ultrasonic modification treatment, and then the modified base material is washed and dried to obtain the modified covalent organic framework material. The material modified by the neutral solution shows a good adsorption effect on multiple heavy metal mixed ions in water, and has a good application prospect in the aspect of adsorbing and removing heavy metal ions in a water environment.

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 discloses a 3-ketosteroid-delta1-dehydrogenase mutant and application thereof in synthesis of prednisone acetate, the mutant with high catalytic activity on cortisone acetate is obtained through screening, and a methanol-water phase (Tris-HCl buffer solution) system is adopted to increase the solubility of a substrate so as to improve the biological catalytic efficiency. In a single water phase system (Tris-HCl buffer solution) without methanol, the conversion efficiency is only 64.8% for 60g / L of cortisone acetate, and under the condition that other conditions are the same, the conversion rate in the Tris-HCl buffer solution system with methanol is increased to 92.1%, and the conversion rate is increased by 1.42 times.

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 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 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 discloses an antistatic protective glove and a preparation method thereof, and relates to the technical field of protective gloves. The antistatic protective glove is prepared from the following raw materials in parts by weight: 50 to 60 parts of natural latex, 40 to 50 parts of neoprene latex, 0.4 to 2 parts of potassium hydroxide, 1.2 to 1.8 parts of peregal O, 1.5 to 3 parts of sulfur, 1 to 2 parts of accelerant BZ, 3.5 to 5 parts of antistatic agent, 0.5 to 1 part of sodium carboxymethyl cellulose and 1.2 to 1.8 parts of anti-aging agent. The preparation method of the antistatic agent comprises the following steps: firstly, reacting 1, 3, 5-tri (2, 3-epoxypropoxy) benzene with N1, N7 dimethyl heptane-1, 7-diamine to obtain a hyperbranched polymer, and then carrying out quaternization on the hyperbranched polymer and chlorinated octadecane to obtain the antistatic agent. The antistatic protective glove provided by the invention has excellent antistatic performance and anti-aging performance.

The invention relates to a method for constructing a C-N bond or a C-C bond through an insertion reaction of oxygen-sulfur ylide and aromatic amine. According to the method, tris (pentafluorophenyl) borane is taken as a catalyst, oxygen-sulfur ylide and aromatic amine are taken as raw materials, and N-H or C-H insertion reaction is carried out under different temperatures and solvents. According to the method, the defect that a metal catalyst or an oxidizing agent is used traditionally is overcome, and on the basis of the method, various alpha-amino-acid ester derivatives or diaryl acetate derivatives can be obtained by using different aromatic amines and oxygen-sulfur ylide as substrates. According to the method, the raw materials are easy to obtain, the operation is simple, the use of a catalyst and an oxidizing agent is avoided, and the method is a mild, effective, feasible and environment-friendly method for preparing the alpha-amino-acid ester and the diaryl acetate and has important application value.

A method for preparing exosomes is provided. The method includes preparing a human platelet, treating the human platelet with a buffer to obtain a platelet solution, centrifuging the platelet solution, and collecting supernatant of the centrifuged platelet solution to obtain an exosome solution. The buffer is calcium ion buffer, phosphate buffered saline (PBS), tris(hydroxymethyl)aminomethane hydrochloride (Tris-HCl) buffer, or 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES) buffer.

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.

According to the scheme, the expanded polytetrafluoroethylene artificial blood vessel with the anticoagulant coating and preparation and application are provided, firstly, groups such as carboxyl and amino are formed on the inner surface of the expanded polytetrafluoroethylene artificial blood vessel through co-auto-polymerization reaction of L-dopamine and polyethyleneimine in a Tris aqueous alkali, then epoxy chloropropane serves as a cross-linking agent, and the expanded polytetrafluoroethylene artificial blood vessel with the anticoagulant coating is prepared. Trihydroxymethyl methylamino propanesulfonic acid is cross-linked to the inner surface of the membrane, carboxyl and sulfonic acid groups on the surface of the membrane endow the expanded polytetrafluoroethylene artificial blood vessel with anticoagulation performance, meanwhile, the hydrophobic performance of the outer surface is reserved, anticoagulation finishing is conducted on the inner wall of the expanded polytetrafluoroethylene artificial blood vessel, and the hydrophobic performance of the outer wall of the blood vessel is reserved; the expanded polytetrafluoroethylene artificial blood vessel has an anticoagulation function and does not influence the growth of fiber cells and fiber connective tissues on the surface of the blood vessel.

The invention relates to the technical field of plastic films, in particular to a preparation method of an environment-friendly plastic bag, which comprises the following steps: S1, mixing polyethyleneimine, ammonium polyphosphate and a first solvent, then carrying out primary reaction, cooling to room temperature, filtering, washing and drying to obtain a solid-phase substance; s2, tannic acid and a second solvent are mixed, tris (hydroxymethyl) aminomethane is added, the pH is adjusted to 7-9, then hydrogen peroxide is added, after a secondary reaction, the solid-phase matter is added for a third reaction, filtering, washing and drying are conducted, and a heat-resistant enhancer is obtained; s3, the modified polylactic acid, the heat-resistant enhancer and the auxiliaries are put into a high-speed mixer to be mixed to be uniform, then the mixture is added into a double-screw extruder to be granulated, then film blowing is conducted through an air blower, and the environment-friendly plastic bag is obtained. The environment-friendly plastic bag provided by the invention has excellent mechanical properties, thermal stability and ultraviolet resistance.

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 discloses a preparation method and application of a salmon salmon sperm DNA sodium raw material, and belongs to the technical field of biomedicines.The preparation method comprises the following steps that S1, raw material pretreatment is conducted, specifically, after frozen salmon or salmon testis tissue is crushed at the ultralow temperature of-30 DEG C to-20 DEG C, a mixed solution containing a Tris-HCl buffer solution, NaOH and NaCl is added, and a mixed solution is obtained; adding a chitosan embedded compound enzyme with the total enzyme activity of more than or equal to 350KU / L, carrying out enzymolysis at 37 + / -1 DEG C for 26-30 hours, and maintaining the pH value to be 7.8-8.0, so as to prepare an enzymatic hydrolysate; s2, DNA synergistic crushing: adjusting the pH value of the enzymatic hydrolysate to 7.8, and in an ice-water bath of less than or equal to 10 DEG C, carrying out 25-35 kHz variable-frequency ultrasound and 100-120 MPa high-pressure homogenization alternate circulation for 3-5 times to carry out synergistic treatment for 40 minutes, so as to obtain a DNA crushing solution; the method solves the problems of high protein residue, non-uniform molecular weight distribution, low transdermal absorption rate, high cost, poor environmental protection property and the like in the traditional process extraction, and has the advantages of high product purity, high activity, low cost, greenness and environmental protection.

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.

To provide an electrolytic silver germanium alloy plating solution capable of codepositing a sufficient amount of germanium in a film, having good liquid stability, and hardly causing foaming.SOLUTION: The problem is solved by an electrolytic silver germanium alloy plating solution containing a silver source and a germanium source characterized by containing a nitrogen-containing coordination compound having a molecular weight of 500 or less. Specific examples of the nitrogen-containing coordination compound include N,N-di(2-hydroxyethyl)glycine, diethanolamine, N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid, triethylenetetramine, glycine, tris(hydroxymethyl) aminomethane, N-methylglucamine, bis(2-hydroxyethyl)aminotris(hydroxymethyl)methane, tricin, N,N,N',N'-tetrakis(2-hydroxypropyl)ethylenediamine, and salts of these compounds.SELECTED DRAWING: None

The invention provides an antibacterial polyurethane acrylate film material embedded with N-substituted benzisothiazolinone and alkenyl functionalized quaternary phosphonium salt, and belongs to the field of organic antibacterial coatings. N-substituted alkenyl of benzisothiazolinone is functionalized, tri (4-methoxyphenyl) phosphine alkenyl is functionalized, and the antibacterial polyurethane acrylate film material is prepared. Double bonds are introduced into a benzisothiazolinone structural unit and a tri (4-methoxyphenyl) phosphine structural unit, N-substituted benzisothiazolinone (NIT) and tri (4-methoxyphenyl) (nonyl-8-ene-1-yl) phosphonium bromide (TPC9) are grafted into a polyurethane acrylate main chain at the same time, and by means of the remarkable antibacterial activity of the NIT and the TPC9 on escherichia coli and staphylococcus aureus, the polyurethane acrylate can be used for preparing the antibacterial polyurethane acrylate. A broad-spectrum antibacterial material is prepared, and a corresponding antibacterial coating can be used for modifying the surface of a base material.

The invention relates to the technical field of oil-water separation, in particular to a renewable oil-water separation material as well as a preparation method and application thereof. According to the preparation method, a melamine foam material is soaked in a mixed solution composed of cane sugar, dopamine and a trihydroxymethyl aminomethane-hydrochloric acid buffer solution, and the renewable oil-water separation material is obtained; the renewable oil-water separation material can quickly and efficiently separate different types of oily wastewater such as kitchen oil, industrial oil and organic solvents, the separation efficiency can reach 99% or above, and the separation flux can reach 104-105 liters per square meter per hour. Moreover, the used renewable oil-water separation material can be repeatedly used after being fully soaked in an ethanol solution, and the separation flux and the separation efficiency are not obviously reduced. In addition, the renewable oil-water separation material has a wide oil-water separation effect and is suitable for industrial production.

The transparent deacidification type long-acting mildew-proof silicone sealant is prepared from the following components in parts by mass: 80 to 110 parts of basic polymer, 15 to 25 parts of plasticizer, 6 to 9 parts of cross-linking agent, 10 to 15 parts of filler, 0.05 to 0.2 part of mildew preventive, 1 to 2 parts of tackifier and 0.05 to 0.2 part of catalyst, the cross-linking agent is any one or a combination of more of methyl triacetoxysilane, ethyl triacetoxysilane, propyl triacetoxysilane, methyl tris (2-ethyl acetoxygroup) silane or methyl tris (benzoyloxy) silane; and the cross-linking agent is any one or a combination of more of methyl triacetoxysilane, ethyl triacetoxysilane, propyl triacetoxysilane, methyl tris (benzoyloxy) silane. Through the design of the sealant formula, the sealant with excellent comprehensive performance can be obtained, the curing speed is high, the bonding performance is good, long-acting mildew prevention is achieved, and the use scene of the sealant is widened.

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 discloses an extraction method and application of high-molecular-weight turbellarian worm genome DNA, and belongs to the field of turbellarian worm genome extraction.The turbellarian worm genome DNA extraction is achieved by improving a lysate formula and removing ethylenediaminetetraacetic acid and increasing Mg < 2 + > on the basis of a conventional reagent in a classic Tris-HCl-phenol-chloroform method to inhibit activity of deoxyribonuclease II in a turbellarian worm body to inhibit degradation of genome DNA, and the high-molecular-weight turbellarian worm genome DNA is obtained. Meanwhile, ribonuclease A is added, RNA in cells can be degraded in the tissue cell digestion process, so that the step of two times of purification is omitted, the loss of DNA yield is reduced, experimental steps are simplified, especially the step of DNA purification is reduced, the problem of degradation in the extraction process of the turbellarian turbellarian worm genome DNA is solved, and the genome DNA yield (gt; 10 micrograms per turbellarian worm), and the turbellarian worm genome ultra-long sequencing or PacBio high-fidelity sequencing requirements are met.