1005 results about "Hydroxymethyl" patented technology

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

The invention 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 discloses high-performance anti-wear engine lubricating oil as well as a preparation method and application thereof. The high-performance anti-wear engine lubricating oil is prepared from the following raw materials: self-developed lubricating oil base oil, poly-alpha-olefin, zinc dialkyl dithiophosphate, calcium sulfonate, polyisobutylene succinimide, an antioxidant, polymethacrylate, an organic molybdenum complex, a de-foaming agent and a pour point depressant. The preparation method comprises the following steps: 1) synthesizing 9, 10-bis (2-tert-butyl-4-methylphenoxy) trimethylolethane stearate as base oil of the lubricating oil; and 2) mixing the base oil with other assistants to obtain the high-performance anti-wear engine lubricating oil. According to the preparation method, novel-like synthetic ester oil is firstly prepared, a phenol group and a large steric hindrance substituent group are introduced into a polymer, the anti-oxidation function is directly built in base oil molecules, meanwhile, super-strong heat resistance is achieved, and finally the high-performance anti-wear engine lubricating oil is obtained and can be applied to high-end application scenes such as aero-engines or gas turbines.

The invention relates to the technical field of biological detection, and discloses a mycoplasma pneumoniae nucleic acid rapid detection method, which comprises the following steps: mixing a sample to be detected with a multifunctional pretreatment buffer solution containing tris (hydroxymethyl) aminomethane, potassium acetate, polyethylene glycol, saponin, spermine tetrahydrochloride and tris (2-carboxyethyl) phosphine hydrochloride, and carrying out cracking treatment; a cracking mixed solution is obtained; redissolving the enzymatic isothermal amplification basic reagent, the specific primer and the probe to obtain a redissolving amplification system; sucking the supernatant of the cracking mixed solution, adding the supernatant into a redissolving amplification system, and adding a magnesium acetate solution to obtain a reaction mixed solution to be detected; and carrying out isothermal amplification and signal acquisition to obtain a detection conclusion. The multifunctional pretreatment buffer solution is used for cracking the to-be-detected sample, sample liquefaction, cracking and nucleic acid release are completed in a single system, the nucleic acid extraction and purification step of centrifugal column adsorption or magnetic bead elution is avoided, and the operation process is simplified.

The application provides a temperature-resistant and salt-resistant wall stabilizer for a ten-thousand-meter deep well water-based drilling fluid and a preparation method and application thereof, and belongs to the technical field of drilling. The preparation method of the wall stabilizer comprises the following steps: acrylic acid is added into deionized water, the pH of the system is adjusted to 7.0, then N-hydroxymethyl acrylamide, N-[2-(3,4-dihydroxyphenyl)ethyl]-2-acrylamide, an emulsifier, octadecyl vinyl ether and a complexing agent are sequentially added into the system, shearing is performed, a monomer solution is obtained, an initiator is added into the monomer solution, and reaction is performed; after the reaction is completed, washing, drying and crushing are performed, and the wall stabilizer is obtained. The wall stabilizer has a temperature resistance of 200 DEG C and a salt resistance of saturation, has strong adsorption and high cohesion, can effectively adsorb, plug and cement micro-pores and micro-cracks of rocks, thereby consolidating the rocks, effectively enhancing the well wall stability, preventing drilling fluid leakage and providing technical support for safe and efficient drilling of deep wells.

The invention provides an Au nanocluster-Cu monatomic / titanium dioxide photocatalyst as well as a preparation method and application thereof, and belongs to the technical field of photocatalysis. According to the invention, the Cu monatomic atom is used as a catalyst for hydrogen evolution reaction, the Cu monatomic atom and the Au nano-cluster are loaded at the same time, the Cu monatomic atom can be used as an electron transport bridge to regulate the electronic structure of the Au nano-cluster, the synergistic effect of the Cu monatomic atom and the Au nano-cluster is realized, the catalytic activity is regulated and controlled together, and efficient series connection of multi-step reaction is realized; therefore, the product selectivity can be accurately regulated and controlled; the catalytic oxidation reaction can be dynamically adjusted through carrier mediation or direct contact by virtue of the electron interaction between the Cu monatomic and the Au nano-cluster, so that the electron distribution in the catalytic process is favorably optimized, the reaction energy barrier of C-C bond breakage and hydroxymethyl oxidation is regulated and controlled, and the dynamic performance of generating GA and hydrogen through photocatalytic oxidation of EG is improved.

The invention discloses nano UV light-cured printing ink and a preparation method thereof, and relates to the technical field of printing ink preparation. The nano UV light-cured printing ink is prepared from nano UV light, the invention discloses a UV (ultraviolet) photoinitiator, which is prepared from the following raw materials in parts by weight: 20 to 40 parts of polyurethane acrylate oligomer, 15 to 30 parts of modified bisphenol A type epoxy acrylate, 10 to 15 parts of tripropylene glycol diacrylate, 5 to 10 parts of ethoxylated trimethylolpropane triacrylate, 5 to 15 parts of modified nano titanium dioxide, 3 to 8 parts of nano silver wire, 2 to 5 parts of photoinitiator 1173 and 1 to 3 parts of benzoin dimethyl ether. The invention relates to a silver-loaded zirconium phosphate composite material which is prepared from the following components in parts by weight: 0.5-2 parts of polyether modified polydimethylsiloxane, 0.3-1 part of a defoaming agent, 1-3 parts of a dispersing agent, 1-5 parts of silver-loaded zirconium phosphate, 0.5-2 parts of an antioxidant 1010, 0.5-2 parts of a coupling agent KH-550 and 10-25 parts of propylene glycol methyl ether acetate. The raw materials are scientifically proportioned and contain various modified components, and parameters of each step are clear. The preparation method is reasonable in process, the performance of the ink is improved through multi-step modification, and the obtained ink is good in dispersity and compatibility, high in curing efficiency and excellent in comprehensive performance and has good practicability and innovativeness.

The invention discloses a polydopamine modified metatitanic acid type lithium ion sieve and a preparation method thereof, and belongs to the technical field of lithium ion sieves, the preparation method comprises the following steps: grinding and uniformly mixing lithium acetate dihydrate and titanium dioxide in an organic solvent, and calcining the mixture at 650-800 DEG C for 3-5 hours to prepare a Li2TiO3 precursor; the preparation method comprises the following steps: putting dopamine hydrochloride, aminated crown ether and a Li2TiO3 precursor into a tris (hydroxymethyl) aminomethane solution with the pH value of 8-9, carrying out a constant-temperature oscillation reaction, carrying out suction filtration, and drying at low temperature, so as to obtain the polydopamine modified metatitanic acid type lithium ion sieve. According to the lithium ion sieve, the adsorption effect on lithium ions can be improved, the lithium extraction efficiency is improved, and the problem of low adsorption capacity of a lithium ion sieve in the prior art is solved.

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 hyperbranched flame retardant as well as a preparation method and application thereof. The flame retardant is prepared by the following steps: dehydrating and pre-polymerizing a boron-containing component (such as tetrahydroxy diborane) and dihydric alcohol (such as 1, 3-propylene glycol), and condensing with trihydroxymethyl phosphine oxide. 4 parts of the flame retardant is added into epoxy resin, phosphorus-containing free radicals can be released in a gas phase for quenching and smoke suppression, a compact boron-containing expanded carbon layer is formed in a condensed phase, and synergistic flame retardance is achieved. The hyperbranched structure can be embedded into an epoxy network, synchronous reinforcement and toughening are achieved, the impact strength is improved by 123.5%, and the tensile strength is improved by 47.7%. The flame retardant has efficient flame retardance (the limit oxygen index is 33.9%, UL-94V-0 level), high transparency and excellent mechanical properties, and is suitable for epoxy resin composite materials in the fields of electronic packaging, aerospace and the like.

The present application relates to a kind of phosphine oxy group covalent modification composite adsorption material and its preparation method and purposes, the preparation method includes the following steps: (1) mixing dopamine hydrochloride, phosphine-containing substrate, tris-hydroxymethyl aminomethane hydrochloride and sodium hydroxide in solvent, to obtain mixed solution;(2) the mixed solution obtained in step (1) and solid phase material are mixed, then oscillation reaction is carried out, to obtain solid-liquid mixture;(3) the solid-liquid mixture obtained in step (2) is carried out solid-liquid separation, and the solid phase part obtained is sequentially washed and dried, to obtain phosphine oxy group covalent modification composite adsorption material.The phosphine oxy group covalent modification composite adsorption material provided by the present application has excellent adsorption selectivity and material stability, and can be used for the high-selectivity separation and recovery of rare metals indium and gallium.

The invention relates to the technical field of cables, and provides a corrosion-resistant control cable and a preparation method thereof. The corrosion-resistant control cable sequentially comprises a conductor, an insulating layer, a shielding layer and a sheath layer from inside to outside, wherein the sheath layer comprises the following components in parts by weight: 50-70 parts of polyvinyl chloride, 15-25 parts of ethylene propylene diene monomer, 10-20 parts of modified graphene oxide, 0.5-1.5 parts of an antioxidant, 3-5 parts of a plasticizer, 15-20 parts of a flame retardant, 2-4 parts of a compatilizer, 4-5 parts of an active agent, 1-3 parts of an assistant crosslinking agent and 1-3 parts of a crosslinking agent; wherein the modified graphene oxide is obtained by modifying graphene oxide with dimethyl 5-hydroxyisophthalate and N-hydroxymethyl acrylamide. According to the technical scheme, the problem of insufficient corrosion resistance of the control cable in the prior art is solved.

The present invention provides for methods of epigenetic analysis. In some cases, the methods may include obtaining a sample comprising a nucleic acid sequence. In some cases, the nucleic acid sequence may comprise one or more epigenetic marks. The methods may include performing a sequencing. The methods may include distinguishing a hydroxymethylated base from a methylated base.

In the first aspect, the present disclosure provides a Lactoferrin polypeptide fragment, where the Lactoferrin polypeptide fragment has an amino acid sequence shown in SEQ ID NO: 1. In the second aspect, the present disclosure provides a preparation method of the Lactoferrin polypeptide fragment, including: protecting amino acids using a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group, coupling the amino acids with a P-hydroxymethylphenoxymethyl polyethylene resin (HMP resin) in an order of cysteine, alanine, leucine, cysteine, glutamate, threonine, asparagine, aspartate, asparagine, phenylalanine, leucine, leucine, asparagine, and lysine, and separating the HMP resin to obtain a target Lactoferrin polypeptide fragment. In the third aspect, the present disclosure further provides an anti-Lactoferrin antibody prepared using the Lactoferrin polypeptide fragment, and use of the Lactoferrin polypeptide fragment in preparation of an anti-Lactoferrin flow cytometric antibody and in preparation of a Lactoferrin detection product.

The invention relates to a formaldehyde-free environment-friendly polyurethane adhesive and a preparation method thereof, relates to the technical field of high polymer materials, and aims to solve the problems of formaldehyde residue, poor water resistance, high process energy consumption, high cost and the like of the existing formaldehyde-free adhesive. According to the invention, dimethylolpropionic acid and wood metal ions form coordinate bonds to strengthen interface bonding, trimethylolpropane constructs a three-dimensional hydrophobic network, and toluene diisocynate isomers are subjected to fractional reaction to optimize crosslinking uniformity. The content of free formaldehyde in the adhesive is not detected, the adhesive strength retention rate is greatly improved after the adhesive is boiled in boiling water for 72 hours, the hot pressing time is shortened to 8 minutes, and the raw material cost is reduced by 40% or above compared with similar products.

The invention discloses a low-foam acidic zinc plating additive and a preparation process thereof, and belongs to the technical field of electroplating additives, the additive comprises a low-foam softening agent and a water-based brightener, and the low-foam softening agent comprises the following raw materials in percentage by mass: 0.8-1.2% of polyethyleneimine, 0.03-0.06% of monododecyl phosphate potassium, 0.2-0.6% of water-soluble polyether amine and the balance of water. The water-based brightener is prepared from the following raw materials: 0.6 to 1.2 percent of 5-hydroxymethylfurfural, 0.2 to 0.4 percent of L-cysteine salt, 0.1 to 0.15 percent of 4-amino-2 (1H) pyrimidone, 0.05 to 0.1 percent of sodium salicylate, 1 to 1.5 percent of citric acid, 0.3 to 0.5 percent of alpha-ketoglutaric acid, 0.2 to 0.4 percent of erythorbic acid and the balance of water. The water-based formula is prepared by optimizing the components in the additive, the components are uniformly dispersed, the foam amount is low, and the plating quality is good.

The present invention provides for novel methods for regulating and detecting the cytosine methylation status of DNA. The invention is based upon identification of a novel and surprising catalytic activity for the family of TET proteins, namely TET1, TET2, TET3, and CXXC4. The novel activity is related to the enzymes being capable of converting the cytosine nucleotide 5-methylcytosine into 5-hydroxymethylcytosine by hydroxylation.

The invention provides a composite antifouling system coating as well as a use method and application thereof. The coating sequentially comprises a bottom layer, a copper-containing middle layer and a surface layer in the direction from near to far away from a base material, wherein the copper-containing middle layer comprises 20-30 parts of self-polishing acrylic silicon resin, 5-10 parts of lime rosin, 8-12 parts of zinc oxide, 30-50 parts of cuprous oxide, 2-3 parts of a compound antifouling agent, 0.5-1 part of a thixotropic agent and a first diluent. The surface layer is prepared from 30 to 35 parts of caprolactone and lactic acid grafted linear polyester, 5 to 10 parts of highly hydrolyzed N-(hydroxymethyl) acrylamide (NMA) modified acrylic resin, 15 to 20 parts of copper-free organic antifouling agent, 5 to 12 parts of polytetrafluoroethylene micro powder, 2 to 3 parts of dispersing agent and second diluent. The high-hydrolysis copper-free surface layer forms an isolation barrier, so that the copper-containing middle layer is prevented from being in direct contact with air, and the problem that the antifouling efficiency is reduced due to the fact that water is not discharged for a long time after coating is solved; the stable hydrolysis rate of the surface layer resin can ensure the continuous release of the organic antifouling agent, and the copper-containing intermediate layer can provide deep antifouling guarantee and synergistically realize long-acting antifouling.

The invention belongs to the field of flame-retardant thermal insulation materials, and particularly relates to flame-retardant silicone rubber and a production process thereof. The flame-retardant silicone rubber comprises the following formula components: methyl vinyl silicone rubber, fluorinated silicone rubber, a compound flame retardant, a filler, a silane coupling agent, an antioxidant, a lubricant and a vulcanizing agent, the compound flame retardant is prepared from a carbon nano tube, nano silicon dioxide and a nitrogen-phosphorus complexing agent according to the mass ratio of (4 to 7) to (11 to 13) to (16 to 19). The preparation method comprises the following steps: reacting dimethyl phosphate with methacrylamide to obtain an intermediate, then adding trimethylolpropane, reacting to obtain a nitrogen-phosphorus complexing agent of which the molecular structure simultaneously contains a phosphate group and hydroxymethyl, and preparing nano silicon dioxide with a porous network by taking tetraethoxysilane and methyltrimethoxysilane as silicon sources. The carbon nano tube, the nano silicon dioxide and the nitrogen-phosphorus complexing agent jointly form a compound flame retardant, and the compound flame retardant is added into the flame-retardant silicone rubber, so that the heat insulation property and the flame retardance of the flame-retardant silicone rubber are effectively improved.

The invention provides epoxy resin for halogen-free flame-retardant self-leveling powder coating and a preparation method of the epoxy resin, and belongs to the technical field of powder coating. The flame retardant is mainly prepared from anhydrous piperazine, bisphenol A diglycidyl ether, trihydroxymethyl phosphorus oxide, triethyl phosphite, epoxy chloropropane, sodium hydroxide, N-methyl iminodiacetic acid, ethylene glycol diglycidyl ether and other main raw materials through polymerization. The prepared epoxy resin and 2-phenylimidazoline are subjected to low-temperature curing (135 DEG C / 20 min) on the premise that an additional flatting agent does not need to be used, the flexibility of a coating film is good, the impact resistance grade is high, the impact performance reaches the condition that no cracking phenomenon exists in the front and back 60cm, the leveling grade reaches the grade 7 or above, the gloss is high and reaches 95% or above, the oxygen index reaches 34% or above, and the halogen-free flame retardant performance is excellent.

The invention belongs to the technical field of protein calibration, and particularly relates to an enhanced protein-free confining liquid for protein detection, which comprises the following components: trihydroxymethyl aminomethane, sodium chloride, Tween-20, polyvinyl alcohol, trehalose, EDTA (Ethylene Diamine Tetraacetic Acid) and a polyoxyethylene-polyoxypropylene block copolymer, and sodium chloride and trehalose are matched to provide ions and small molecular compounds to form a stable closed environment. Wherein the trehalose assists in filling and covering small pores of PVDF, the sodium chloride provides ion balance, the EDTA-Na is used for precipitating metal ions, and the Tween-20 assists in repairing the PVDF film. According to the invention, the polyvinyl alcohol and the polyoxyethylene-polyoxypropylene block copolymer are mixed for use, so that non-specific sites on the membrane are blocked while impurity proteins are prevented from being introduced, the sealing effect is achieved, and the problem of false positive or non-specific binding easily caused by the traditional sealing liquid is effectively solved.

The invention discloses a polyphenyl ether modified epoxy resin-based copper-clad plate, and particularly relates to the technical field of copper-clad plates, the polyphenyl ether modified epoxy resin-based copper-clad plate comprises a glue solution, an electronic glass fabric and a copper foil, and the glue solution comprises the following raw materials: modified polyphenyl ether, an inorganic filler, a curing agent, a flame retardant and the balance of epoxy resin. The bisphenol A epoxy resin, toluene and benzoyl peroxide are utilized to treat polyphenyl ether, the molecular weight of the polyphenyl ether can be reduced, the crosslinking property of the polyphenyl ether and the epoxy resin is better, then paraformaldehyde is utilized to catalyze and modify the polyphenyl ether, the terminal of the polyphenyl ether is grafted with hydroxymethyl, and the polyphenyl ether is grafted with polyphenyl ether. The compatibility and interface bonding force of the obtained hydroxymethylated polyphenyl ether and epoxy resin are good, the dielectric loss performance and toughness of the copper-clad plate can be effectively improved, and anhydrous aluminum silicate of an amorphous layered gap structure formed through specific activation treatment can be formed during temperature-controlled calcination of kaolin. The dielectric constant and the dielectric loss of the copper-clad plate can be obviously reduced.

The invention discloses a serine hydroxymethyltransferase mutant and an application thereof in production of L-serin.The serine hydroxymethyltransferase mutant with the specific enzyme activity remarkably improved is obtained by conducting saturated mutation on serine hydroxymethyltransferase from escherichia coli and conducting screening, and the serine hydroxymethyltransferase mutant is applied to synthesis of L-serine. The serine hydroxymethyltransferase disclosed by the invention can be used for effectively improving the efficiency of catalyzing glycine and formaldehyde to synthesize L-serine by using the serine hydroxymethyltransferase, reducing the enzyme dosage, remarkably reducing the production cost and reducing the separation difficulty of downstream products.

The invention belongs to the technical field of synthesis and preparation of high-molecular optical materials, and particularly relates to a multi-mercaptothiol composition as well as a preparation method and application thereof. According to the present invention, the three-step synthesis route of the tetrahydroxymethylation reaction, the thiol precursor introduction and the deprotection is adopted, the reaction conditions are mild, the steps are clear, the yield is high, the complexity of the traditional synthesis route is avoided, the production cost is reduced, and the industrial production is easily achieved. In the aspect of refractive index regulation and control, the compound contains a plurality of sulfur atoms, the coating is endowed with the characteristic of high refractive index, accurate regulation of the refractive index can be realized by adjusting the formula of the composition, the requirements of different optical applications are met, and the application range of the material is widened. The prepared optical coating has excellent light transmittance, light loss can be reduced to the maximum extent, and the efficient performance of an optical device is ensured; meanwhile, the haze value of the coating is low, the light scattering phenomenon is effectively avoided, and the imaging definition and the precision of an optical system are guaranteed.

The invention relates to the technical field of polylactic acid fibers, and discloses a preparation process of an anti-static polylactic acid superfine fiber fabric, star-shaped polylactic acid grafted carbon nanotubes are prepared from tetra (hydroxymethyl) phosphorus chloride, 2-amino-4, 6-dimethoxy-1, 3, 5-triazine and the like as raw materials, and the star-shaped polylactic acid grafted carbon nanotubes and polylactic acid slices are subjected to melt spinning to obtain the polylactic acid superfine fiber fabric; the star-shaped polylactic acid grafted carbon nanotubes have a structure similar to that of a polylactic acid matrix, so that the carbon nanotubes are uniformly dispersed in a polymer matrix and form relatively strong interface bonding, migration and precipitation are avoided, and the star-shaped polylactic acid grafted carbon nanotubes have anti-static durability; the structure of the superfine fiber fabric contains nitrogen and phosphorus synergistic flame-retardant elements, so that the exchange between a fiber matrix and oxygen and heat in the air can be blocked, and the flame-retardant property of the superfine fiber fabric is improved; the density of the fiber fabric can be increased by the formed cross-linked network structure, so that the mechanical property of the superfine fiber fabric is remarkably improved.

The invention provides an inorganic silicon hybrid polyurethane primer as well as a preparation method and application thereof, and belongs to the technical field of primer. The primer provided by the invention is prepared from the following raw materials: polyester polyol, polyether polyol, trimethylolpropane, hexamethylene diisocyanate, 3-(phenylamino) propyltrimethoxysilane, ethyl acetate, xylene, an antioxidant, a light stabilizer, stannous octoate and a catalyst. An isocyanate-terminated polyurethane prepolymer is selected as a base material, a silane hybrid structure is introduced, a Si-O-Si network is formed after silane is hydrolyzed, the Si-O-Si network and Ca < 2 + > in concrete form a coordinate bond, and meanwhile, an isocyanate group reacts with water to generate a urea bond to reinforce anchoring. According to the primer disclosed by the invention, through a chemical-physical synergistic effect, the technical problem of bonding failure of a floating dust hardened layer is systematically solved, and an innovative solution is provided for long-acting sealing of a concrete joint.

The application relates to the technical field of packaging cartons, and discloses a high-strength lightweight packaging carton and a preparation method thereof. The preparation steps are as follows: S1: uniformly mixing trihydroxy heptaoctyl poss, 3-bromopropylene, sodium carbonate and tetrahydrofuran, reacting at 50-60 DEG C for 3-5 h to obtain modified poss; S2: taking hexamethoxymethyl melamine, ethanol and the modified poss to prepare a modified etherified amino resin; S3: uniformly mixing the modified etherified amino resin, mercapto-modified silicon dioxide and a photoinitiator to obtain an additive; uniformly stirring acrylic emulsion, epoxy / acrylic core-shell emulsion, hyperbranched polyurethane acrylate and the additive to obtain reinforcing coating; and coating the reinforcing coating on the surface of the lightweight packaging carton, drying and curing to obtain the high-strength lightweight packaging carton.

The invention discloses a liquid chromatography method for measuring 5-hydroxymethylfurfural in a calcium gluconate and sodium chloride injection. The method comprises the following steps: measuring the calcium gluconate and sodium chloride injection as a test solution; weighing 5-hydroxymethylfurfural, and adding water to dilute the 5-hydroxymethylfurfural to form a reference solution; carrying out continuous sample introduction on the liquid chromatograph by using the reference substance solution to obtain a system applicability solution chromatogram; when the chromatogram of the applicable solution of the system meets the standard, measuring the test solution and the reference solution, respectively injecting the test solution and the reference solution into a liquid chromatograph, and recording the chromatograms; the content of 5-hydroxymethylfurfural in the calcium gluconate and sodium chloride injection is obtained through a 5-hydroxymethylfurfural content calculation formula. The method has the advantages of strong specificity, high sensitivity, good precision, strong durability and the like, and can quantitatively detect 5-hydroxymethylfurfural in the calcium gluconate and sodium chloride injection, so that the safety of clinical medication of the calcium gluconate and sodium chloride injection is improved.

The present application relates to a kind of pharmaceutical composition for treating type 2 diabetes and its application.The pharmaceutical composition includes icariin, hydroxymethyl coumarin and cinnamaldehyde, by three-component synergistic effect, simultaneously act on insulin resistance, pancreatic beta cell apoptosis and systemic metabolic inflammation three type 2 diabetes core pathological links, auxiliary reduce serum lipid level, and reduce drug-related liver injury risk, good safety.Animal experiment results show that three-drug combination group can effectively reduce blood sugar (decrease about 50%), significantly improve islet structure atrophy, restore hepatocyte index arrangement, reduce glomerular hypertrophy, significantly reduce serum TG and CHOL level (P<0.05) and inflammatory factor IL-6 and TNF-alpha level (P<0.05), and avoid the hepatotoxicity risk (ALT / AST restores to close to normal level) of hydroxymethyl coumarin.The present application is composed of three kinds of natural monomers with clear structure, and has clear components and controllable quality, which provides a more optimal comprehensive treatment strategy for the treatment of type 2 diabetes and its complications.

This invention discloses a denitrification agent for low-temperature denitrification and its preparation method, belonging to the field of denitrification technology. The denitrification agent is prepared using diatomaceous earth as the matrix framework, compounded with calcium chloride, calcium bicarbonate, chitosan, sodium lignosulfonate, and TRIS (tris(hydroxymethyl)aminomethane). The components synergistically optimize the pore structure. Chitosan and sodium lignosulfonate achieve self-assembly through hydrogen bonding and electrostatic attraction. Nitrogen oxides are removed through a dual action of alkaline absorption and electrostatic adsorption. The TRIS can be regenerated and reused after alkali washing. This invention's denitrification agent solves the problems of high reaction temperature, poor low-temperature activity, low efficiency in removing low-concentration nitrogen oxides, and easy ammonia escape in traditional SCR denitrification technology, and can meet the requirements for NO removal in flue gas from power plants. x ≤15mg / m 3 It has ultra-low emission indicators, and features excellent low-temperature activity, high denitrification efficiency, and recyclability. It is suitable for denitrification treatment of low-temperature flue gas in power plants, etc.