14733 results about "Meth-" patented technology

The invention relates to a crystal form of a benzothiophene substituted fused ring compound and a preparation method thereof. Specifically, the invention provides a crystal form A and a crystal form D of 2-amino-7-fluoro-4-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxyl)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptano-2-yl) benzo [b] thiophene-3-formonitrile, and the crystal form A and the crystal form D have the advantages that the crystal form A and the crystal form D are good in stability; and the medicine can be better used for clinical treatment. # imgabs0 #

The invention relates to a crystal form of a benzothiophene substituted fused ring compound and a preparation method thereof. Specifically, the invention provides a crystal form E, a crystal form G and a crystal form H of 2-amino-7-fluoro-4-((5S, 5aS, 6S, 9R)-1-fluoro-12-((1-((4-(fluoromethylsubunit) piperidine-1-yl) methyl) cyclopropyl) methoxyl)-5-methyl-5a, 6, 7, 8, 9, 10-hexahydro-5H-4-oxa-3, 10a, 11, 13, 14-pentaaza-6, 9-methylbridged naphtho [1, 8-ab] heptano-2-yl) benzo [b] thiophene-3-formonitrile, and the crystal form E, the crystal form G and the crystal form H have the advantages that the stability is good; and the medicine can be better used for clinical treatment. # imgabs0 #

The invention belongs to the technical field of battery electrolytes, and particularly relates to a gel polymer electrolyte as well as a preparation method and application thereof. The gel polymer electrolyte is prepared through in-situ polymerization, and the electrolyte is composed of a monomer, a cross-linking agent, an initiator, an organic solvent and a lithium salt. The monomer is selected from fluorine-containing monomers such as trifluoroethyl acrylate, 2, 2, 3, 3-tetrafluoropropyl methacrylate and the like, and the cross-linking agent is selected from NH-containing cross-linking agents such as N, N '-methylene bisacrylamide, hexamethylene bisacrylamide and the like, so that a polymer side chain fluorine-containing functional group is formed in situ and interacts with lithium ions, and lithium ion transmission is promoted; and the NH functional group on the main chain limits the migration of anions, so that the ion migration number is increased. Therefore, the copolymerized fluorine-containing monomer and nitrogen-containing cross-linking agent gel polymer electrolyte enables the battery to show good specific discharge capacity and cycling stability under high current density.

The invention relates to the field of electric heating materials, and provides a graphene-based heating coating and a preparation method thereof. The coating is prepared from functionalized graphene, a surface modified bismuth telluride nanobelt, polyaniline, bisphenol A epoxy acrylate, polyurethane acrylate, a dispersing agent, a flatting agent, a silane coupling agent, a defoaming agent and a propylene glycol methyl ether acetate / N-methyl pyrrolidone mixed solvent. The functionalized graphene is obtained by modifying a hyperbranched polyolefin-acryloyl-POSS copolymer, and carrying out ultrasonic stripping, centrifugal separation, gradient washing and vacuum drying; the surface-modified bismuth telluride nanobelt is modified by an amino silane coupling agent, so that the interfacial compatibility is improved. The preparation method comprises the steps of solvent premixing, nanofiller dispersion, ultrasonic homogenization, coupling agent modification, ultraviolet curing and thermocuring. The heating coating provided by the invention has high conductivity, excellent thermal stability and adhesive force, and can be widely applied to heating electric appliances and intelligent temperature control equipment.

The invention discloses an OCA optical adhesive and a preparation method thereof, and relates to the technical field of adhesives, and the OCA optical adhesive is prepared from the following raw materials in parts by weight: 35-45 parts of acrylate-terminated hyperbranched organosilicon modified polyurethane, 2-4 parts of allyl succinimido carbonate, 1-3 parts of hexafluorobisphenol A diacrylate, 1-3 parts of 1, 2, 4-trimethyl-1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol monoisobutyrate, 1-3 parts of 1, 3-pentanediol The invention relates to a photocurable adhesive, which is prepared from the following components in parts by weight: 20 to 30 parts of a diluent, 0.6 to 1.2 parts of a photoinitiator, 0.5 to 1 part of an antioxidant and 0.5 to 1 part of a de-foaming agent. The photocurable adhesive is prepared from the following components in parts by weight: 1 to 5 parts of 1, 3-bis (oxiranyl methyl)-5-(2-propenyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone, 3 to 5 parts of 2, 2 '-bis (trifluoromethyl) diaminodiphenyl, 6 to 8 parts of other polymerizable monomers, 20 to 30 parts of the diluent, 0.6 to 1.2 parts of the photoinitiator, 0.5 to 1 part of the antioxidant and 0.5 to 1 part of the de-foaming agent. The OCA optical adhesive is good in bonding performance, sufficient in weather resistance and environmental protection performance and good in oil resistance.

The invention relates to the technical field of adsorption materials, and discloses a preparation method and application of a hydrogel adsorption material prepared by copolymerizing cellulose with acrylic acid and acrylamide. The method comprises the following steps: extracting cellulose from corn straws; placing cellulose in a sodium hydroxide / urea / water system, stirring and dissolving; the preparation method comprises the following steps: uniformly mixing acrylamide and acrylic acid in water to prepare a modified solution; sequentially adding the modified solution, N, N '-methylene bisacrylamide and potassium persulfate into the cellulose solution, and stirring and mixing; putting the mixed solution into a drying oven for gelation to obtain the cellulose co-polyacrylamide and acrylic acid hydrogel adsorption material. A large number of groups such as hydroxyl and carboxyl are introduced to the surface of the hydrogel adsorption material prepared by the method, the adsorption capacities of heavy metals such as lead, cadmium and copper reach 434.8 mg / g, 277.7 mg / g and 261.8 mg / g respectively, and heavy metal ions in a water body can be effectively and quickly removed.

The present invention discloses a method for detecting and applying C1-C2-alkyl-substituted phenol isomers, which relates to the technical field of environmental detection and includes: selecting a corresponding sample pretreatment process to prepare a test sample according to the petroleum content range in the sample; under a mobile phase of methanol-5.0-6.5 mmol / L ammonia water, using LC-MS to detect the test sample to obtain the concentration of the first component and the standardized concentrations of co-eluted 3,5-dimethylphenol and 2,6-dimethylphenol; under a mobile phase of acetonitrile-4.0-10.0 mmol / L ammonia water, using LC-MS to detect the test sample to obtain the concentration of 3,5-dimethylphenol, or the standardized concentrations of co-eluted 3,5-methylphenol and 3-ethylphenol, or the standardized concentrations of co-eluted 2,6-dimethylphenol and 2,4-dimethylphenol; under a mobile phase of methanol-5.0-6.5 mmol / L ammonia water or acetonitrile-4.0-10.0 mmol / L ammonia water, using LC-MS to separately detect the calibration samples of the co-eluted components, and calculate the conversion factor of the co-eluted components and the concentration of the other component. The present invention realizes the accurate quantification of phenol and 12 C1-C2-alkyl-substituted phenol isomers.

The invention relates to the technical field of textiles, and discloses a cool and washable bio-based nylon 56 fabric and a preparation method thereof. The preparation method of the cool and washable bio-based nylon 56 fabric comprises the following steps: loading modified nano aluminum oxide on modified aluminum nitride microchips to obtain a composite cool material; nylon 56, an ethylene-methyl acrylate-glycidyl methacrylate terpolymer, polypentamethylene guanidine hydrochloride and a composite cool feeling material are subjected to blending extrusion and melt spinning, and then the bio-based nylon 56 fabric is woven. Mixing the composite modified boron nitride and ethanol to obtain finishing liquid; spraying the finishing liquid on one side of the bio-based nylon 56 fabric, and drying to obtain the cool washable bio-based nylon 56 fabric. The cool and washable bio-based nylon 56 fabric disclosed by the invention has excellent cool feeling, antibacterial property, washable property, moisture absorption property and unidirectional perspiration property.

The invention discloses a wear-resistant and high-temperature-resistant synchronous belt and a preparation method thereof. The wear-resistant and high-temperature-resistant synchronous belt comprises a synchronous belt framework and a synchronous belt rubber sheet, the synchronous belt rubber sheet is prepared from the following raw materials: a fluorosilicone thermoplastic polyurethane elastomer containing a benzene ring structure, an amino-containing hyperbranched liquid crystal polymer, methyl vinyl phenyl silicone rubber, epoxidized natural rubber, molybdenum sulfide nanosheets, reinforced fibers, bis (1-vinyl imidazole-2-) ketone, 2-acrylamido-2-methylpropanesulfonic acid, 4, 4 '-difluoro-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1, 3, 4-trimethyl-1 The high-temperature-resistant rubber is prepared from 2, 6-hydroxy-2-cyanobenzothiazole, bis (3-aminophenyl) 3, 5-bis (trifluoromethyl) phenylphosphine oxide, a catalyst, a coupling agent, a vulcanizing agent, an anti-aging agent, a scorch retarder and a lubricating agent. The synchronous belt is good in mechanical property, sufficient in high-temperature resistance and cold resistance, good in wear resistance and excellent in aging resistance and flame retardance.

The invention discloses a self-crosslinking temperature-resistant salt-resistant emulsion type fracturing fluid thickening agent and a preparation method thereof, and belongs to the technical field of oilfield chemistry. The raw materials adopted by the invention comprise 30 to 50 parts of an oily solvent, 15 to 25 parts of deionized water, 10 to 20 parts of acrylamide, 5 to 10 parts of acrylic acid, 2 to 4 parts of 2-acrylamido-2-methylpropanesulfonic acid, 0.05 to 0.2 part of a crosslinking monomer, 0.5 to 1 part of a quaternary ammonium salt type hydrophobic association monomer, 4 to 8 parts of an emulsifier and 1 to 2 parts of a phase inversion agent. The self-crosslinking emulsion is formed through water phase-oil phase mixing, high-speed emulsification, low-temperature initiation polymerization and phase inversion treatment. Based on physical-chemical double-crosslinking temperature control cooperation, a salt-resistant-hydrophobic double-shielding mechanism and an integrated design without an exogenous crosslinking agent, the contradiction between the temperature-resistant and salt-resistant performance of a traditional thickening agent and the process complexity is broken through, and a technical support is provided for efficient development of high-temperature and high-salt oil and gas reservoirs.

The invention relates to a flame-retardant inorganic quick-setting material and a preparation method thereof, and the flame-retardant inorganic quick-setting material is prepared from the following raw materials: sulphoaluminate cement, aluminum-magnesium hydrotalcite, phosphorus slag powder, waste PBO fiber, an accelerator, a water reducer, a functional auxiliary agent, and 3, 3 '-diamino-4, 4'-difluorodiphenyl sulfone. The functional auxiliary agent comprises structural units introduced by the following monomers: 3-[N, N-dimethyl-[2-(2-methylpropyl-2-enoyloxy) ethyl] ammonium] propane-1-sulfonic acid inner salt, diphenyl (4-vinyl phenyl) phosphine oxide, 1, 3-bis (oxirane methyl)-5-(2-allyl)-1, 3, 5-triazine-2, 4, 6 (1H, 3H, 5H)-triketone, 10-(4-vinyl phenyl)-10H-phenoxazine and itaconic acid. The material is high in strength, remarkable in rapid hardening and flame-retardant effect, and safe and environment-friendly to use.

The invention relates to the technical field of oilfield chemistry, and discloses a graft modified cellulose filtrate reducer and a preparation method thereof.The preparation method comprises the following steps that modified hydroxyethyl cellulose, 2-acrylamide-2-methyl propane sulfonic acid, dimethyl diallyl ammonium chloride, alkenylated cardanol and N, N '-methylene bisacrylamide are added into deionized water, stirring is conducted, and a mixture is obtained; the preparation method comprises the following steps: adding cellulose into a reaction kettle, stirring for 10-15 minutes at the temperature of 40-60 DEG C at the speed of 300-400 rpm, dropwise adding ammonium persulfate and sodium hydrogen sulfite into a system, and continuously reacting for 4-6 hours to obtain the grafted modified cellulose filtrate reducer. The filtrate reducer disclosed by the invention has good high temperature resistance and salt resistance.

The invention belongs to the technical field of photocatalysts, and particularly relates to a coal gasification fine slag doped g-C3N4 photocatalyst and a preparation method and application thereof.The coal gasification fine slag and g-C3N4 are evenly mixed and calcined, the coal gasification fine slag is doped to the surface of g-C3N4, and the coal gasification fine slag doped g-C3N4 photocatalyst is constructed and used for degrading methylene blue under visible light; the separation of photon-generated carriers is promoted, the hole electron recombination efficiency is reduced, and the photocatalytic activity is improved. According to the method, the utilization way of the coal gasification slag is widened, and meanwhile, the dye wastewater is effectively degraded.

The invention discloses a nano blocking agent for drilling fluid and a preparation method thereof, and belongs to the technical field of blocking agents, the nano blocking agent for drilling fluid is prepared by reaction of a core layer blocking agent and a shell layer blocking agent, the core layer blocking agent is prepared by reacting nano silicon dioxide, gamma-methacryloxypropyltrimethoxysilane and a first part of vinylphosphonic acid, and has secondary blocking capability; and the shell blocking agent is prepared by reacting a second part of vinyl phosphonic acid, styrene and 2-dodecene-1-yl succinic anhydride, and has the characteristic of flexibility. The nano plugging agent has rigid supporting and flexible deformation capabilities, and the high-temperature stability and compressive strength of a plugging layer are remarkably improved. The chemical binding force of the plugging agent and the rock is enhanced; the hydrolysable methoxyl reserved in the core layer provides a secondary plugging function, and the plugging validity period is prolonged. The invention relates to a preparation method of a nano blocking agent for drilling fluid, which is used for preparing the nano blocking agent for drilling fluid.

The invention discloses a multifunctional water-retaining agent adapted to acid soil and a preparation method thereof, and the multifunctional water-retaining agent is prepared from the following raw materials in parts by weight: 9-11 parts of a chitosan solution with the concentration of 0.019-0.021 g / mL, 9-11 parts of a sodium polyphosphate solution with the mass concentration of 0.5-1%, 24-25 parts of an acrylic acid solution with the neutralization degree of 80-85%, 9-11 parts of a guar gum solution with the concentration of 0.019-0.021 g / mL and the balance of water. The mass of the methylene bisacrylamide accounts for 0.01-0.03% of the total dry matter mass of the chitosan, the guar gum and the acrylic acid, the mass of the ammonium persulfate accounts for 0.25-0.35% of the total dry matter mass of the chitosan, the guar gum and the acrylic acid, and the clay mineral accounts for 10-12 parts; the preparation method comprises the following steps: S1, pre-preparation; S2, mixing; and S3, post-treatment. The prepared water-retaining agent not only can greatly improve the water absorption and water retention performance of the chitosan water-retaining agent, but also can reduce the acidity of acid soil and improve the CEC and fertilizer retention capacity of the soil, and is a multifunctional acid red and yellow soil conditioner.

To provide an active energy ray-curable composition capable of forming a cured coating that offers low viscosity and high hardness, and excels in adhesion and curling resistance; a cured coating; and a laminated film.SOLUTION: An active energy ray-curable composition comprises the following components (A) and (B). The component (A) is 40 mass%-89 mass% and the component (B) is 10 mass%-60 mass%. The organic solvent content is 5 mass% or less. The component (A): a polyfunctional (meth)acrylate with a viscosity at 25°C of 100 mPa s or less (excluding the component (B)). The component (B): a bifunctional monomer with a viscosity at 25°C of 10 mPa s or less, incorporating a reactive site represented by the formula below.SELECTED DRAWING: None

The invention relates to a preparation method and application of an inner-rigid outer-soft core-shell structure silicon dioxide blocking agent for marine drilling fluid, and belongs to the field of deepwater oil and gas drilling. N-vinyl-2-pyrrolidone, dimethyl diallyl ammonium chloride, acrylamide and 2-acrylamide-2-methylpropanesulfonic acid are polymerized and grafted on the surface of nano silicon dioxide to form the silicon dioxide blocking agent with a core-shell structure and a rigid inside and a soft outside; by means of rigid plugging of a nano material and deformation filling flexible plugging of a high-molecular polymer, shale micro-nano pores are efficiently plugged with rigid inside and flexible outside, so that the stability of a well wall is maintained, meanwhile, secondary generation of hydrates is effectively inhibited, and the safety and efficiency of deepwater drilling are improved; the plugging agent provided by the invention reduces the demand on a large number of thermodynamic inhibitors, not only saves the cost, but also has the characteristic of environmental protection.

The invention relates to the technical field of fabrics, and discloses a preparation method of an anti-wrinkle comfortable fabric, which comprises the following steps: by taking alkyl diamine, acrylonitrile, gamma-chloropropyl methyl dimethoxy silane and the like as raw materials, carrying out addition reaction, hydrolysis reaction and quaternization reaction to obtain polycarboxyl disilane gemini quaternary ammonium salt; octamethylcyclotetrasiloxane, polycarboxyl disilane gemini quaternary ammonium salt and the like are used as raw materials, quaternary ammonium salt modified polysiloxane is obtained through base catalysis copolymerization, then the quaternary ammonium salt modified polysiloxane is emulsified and prepared into finishing liquid, pure cotton fabric is soaked in the finishing liquid, and the anti-wrinkle comfortable fabric is obtained through two-dipping and two-rolling finishing. The crease resistance of the fabric is improved by utilizing a large number of amino groups and carboxyl groups contained in the finishing liquid, and the antibacterial property of the fabric is improved by utilizing a quaternary ammonium salt structure contained in the finishing liquid. Experiments prove that the prepared fabric has good crease-resistant comfort performance and antibacterial performance.

A biodegradable polymer composite, a method of making the same and use for same are provided. The biodegradable polymer composite has about 30 to 99.5% by weight of a polymer selected from a group consisting of polybutylene adipate terephthalate (PBAT), polybutylene succinate (PBS), polyhydroxyalkanoates (PHA), and polycaprolactone (PCL) grafted with a compatibilizer selected from a group consisting of maleic anhydride, glycidyl methacrylate, pyromellitic anhydride, acrylic acid, polyacrylic acid, methylene diphenyl diisocyanate, poly(glycidyl methacrylate, copolymer(s) of glycidyl methacrylate; and about 0.5 to 50 % by weight a nano-filler or a micro-filler. The biodegradable polymer composite does not contain polylactic acid. Surfaces of the nano-filler or the micro-filler may be modified using a grafting agent so that the biodegradable polymer composite has enhanced mechanical properties, increased heat resistance, compostablity and / or improved processability. The biodegradable polymer composite may be used to make flexible articles, such as a freezer wrap and a farming sheet.

The invention discloses a preparation method of a non-additive nitrogen-phosphorus-cerium synergistic flame-retardant polyurethane elastomer, and the polyurethane elastomer is prepared by taking isocyanate as a hard segment and poly (1, 4-butanediol adipate) as a soft segment, and compounding the hard segment and the soft segment with 2-amino-4-hydroxy-6-methylpyrimidine, a phosphorus reactive flame retardant and cerium oxide. The preparation method is simple, the process is easy to control, and the prepared polyurethane elastomer has good tensile strength; besides, the limit oxygen index of the polyurethane elastomer reaches 27.4, the polyurethane elastomer meets commercial standards of flame-retardant materials and UL-94 V-0 flame-retardant grade requirements, the ultraviolet band light transmittance is 0%, ultraviolet rays can be completely isolated, and the polyurethane elastomer has a good anti-oxidation function and can be applied to the industries of wires, cables, pipe profiles, films, general molding and the like.

The invention provides a salt-responsive temperature-resistant salt-resistant water-based drilling fluid tackifying filtrate reducer as well as a preparation method and application thereof, and belongs to the technical field of drilling. The tackifying filtrate reducer is prepared from the following raw materials in parts by mass: 30 to 50 parts of 1-(2-carboxyethyl)-2-vinylpyridine, 20 to 40 parts of (3-(methacrylamido) propyl) dimethyl (3-thiopropyl) ammonium hydroxide inner salt, 35 to 55 parts of N, N-dimethylacrylamide, 10 to 25 parts of 4-vinylpyridine, 300 to 500 parts of water and 1 to 5 parts of an initiator. According to the filtrate reducer, cations and anions are concentrated on one monomer molecule, so that the synthesized product contains the cations and the anions with the same charge number, has good adsorption capacity and salt response characteristics, is compatible with salt essentially, can effectively resist high temperature and high salt, and can be recycled. And the viscosity-increasing and filtrate-reducing agent has good viscosity-increasing and filtrate-reducing effects on the drilling fluid.

Provided is a dispersant for hydraulic compositions that has high dispersibility and can reduce the viscosity of the hydraulic composition. [Solution] A dispersant for hydraulic compositions comprising: a polymer (P) having a structural unit (1) formed from a compound represented by general formula (1), and a structural unit (2) formed from a compound containing at least one selected from acrylic acid, methacrylic acid, fumaric acid, maleic acid, maleic anhydride, itaconic acid, itaconic anhydride, and salts thereof; and an ether compound (A) which is a compound in which 1 to 500 moles of an alkylene oxide having 2 to 4 carbon atoms are added to 1 mole of a mono- to tetrahydric aliphatic alcohol having 2 to 24 carbon atoms, wherein the mass average molecular weight of the polymer (P) is 5,000 to 5,000,000, and the mass ratio (A / P) of the ether compound (A) to the polymer (P) is greater than 0 and less than or equal to 0.25.

The invention relates to the field of quantum dot ink, and discloses diffusion plate printing quantum dot ink and a preparation method thereof.The diffusion plate printing quantum dot ink comprises acrylic resin, hyperbranched polyester resin, a quantum dot material, modified boron nitride, a reactive diluent, a photoinitiator, a wetting agent and a defoaming agent; the hyperbranched polyester resin is prepared by reacting hyperbranched polyester acrylate and a sulfydryl-terminated silicon-containing reaction monomer, wherein the hyperbranched polyester acrylate is prepared by reacting pentaerythritol with 2, 2-dimethylolpropionic acid and then carrying out esterification reaction with acrylic acid; the sulfydryl-terminated silicon-containing reaction monomer is prepared by reacting eugenol with 1, 1, 3, 3-tetramethyldisiloxane and then carrying out esterification reaction with 3-mercaptopropionic acid; the modified boron nitride is prepared by modifying a cationic polymer which is prepared by carrying out a Mannich reaction on triethylene tetramine, formaldehyde and acetone and then carrying out a condensation polymerization reaction with formaldehyde. After the ink prepared by the invention is cured, a coating film is high in hardness, adhesive force and heat conductivity coefficient, and good in flexibility, heat resistance and migration barrier property.

The invention relates to the technical field of PET optical film coatings, in particular to a coating liquid for a PET optical film coating and a preparation method of the coating liquid. The coating liquid for the PET optical film coating is prepared from the following preparation raw materials in parts by mass: 20 to 25 parts of polyurethane acrylic resin, 10 to 15 parts of N-hydroxymethyl acrylamide, 1 to 2 parts of a coupling agent, 4 to 6 parts of a photoinitiator, 8 to 10 parts of modified nano titanium dioxide, 0.2 to 0.3 part of an ultraviolet light absorber and 40 to 47 parts of a reactive diluent. The coating liquid for the PET optical film coating prepared by the invention is excellent in adhesive force, weather resistance, scratch resistance, light transmittance and the like, and has a wide application prospect.

The invention relates to an antibacterial and anti-fouling ceramic product glaze and a preparation method, and belongs to the technical field of ceramic product glaze preparation, the ceramic product glaze comprises the following raw materials: a component A: a base material, a water glass solution, a sodium bicarbonate solution, a gadolinium nitrate solution, a europium nitrate solution, a silver nitrate solution and sodium cocoate; and the component B comprises the following components: dimethoxy methyl (3, 3, 3-trifluoropropyl) silicon, polysiloxane, dodecenyl succinic anhydride, gamma-methacryloxy propyl trimethoxy silane and white gasoline. Silver nitrate serves as a main material, europium nitrate serves as an auxiliary material, gadolinium nitrate excites the activity of silver and europium ions, and the silver nitrate, the europium nitrate and the gadolinium nitrate cooperate, so that the prepared ceramic product glaze has excellent antibacterial performance; sodium cocoate is added to form a steric hindrance effect, so that agglomeration among system particles is inhibited, and the antibacterial property of the glaze is enhanced; according to the anti-fouling glaze disclosed by the invention, the dimethoxymethyl (3, 3, 3-trifluoropropyl) silicon and the polysiloxane are added, so that the prepared glaze has a lasting anti-fouling effect.

Disclosed in the present invention are a fluorosilicone-modified low-surface-energy antifouling coating and a preparation method therefor. The coating comprises the following components in parts by weight: 11-15 parts of butyl acrylate, 3-4 parts of dodecafluoroheptyl methacrylate, 3-4 parts of vinyl-terminated polydimethylsiloxane, 3-4 parts of 2-hydroxy-4-acryloyloxybenzophenone, 30-38 parts of methyl isobutyl ketone, 0.15-0.25 parts of azobisisobutyronitrile, 0.1-0.2 parts of sodium hydroxide, 2-3 parts of modified titanium dioxide nanoparticles, and 0.5-1.5 parts of 3-aminopropyltriethoxysilane. In the present invention, vinylpentamethyldisiloxane reacts with decamethylcyclopentasiloxane to prepare vinyl-terminated polydimethylsiloxane; a titanium dioxide precursor is mixed with polydopamine nanoparticles for modification to prepare modified titanium dioxide nanoparticles; and then the components above are mixed to prepare the fluorosilicone-modified low-surface-energy antifouling coating. The coating has low surface energy and good adhesion and ultraviolet resistance.

The invention belongs to the field of medical chemistry, and particularly relates to a crystal form of a heterocyclic compound and a pharmaceutical composition thereof. Specifically, the invention relates to a crystal form of 4-((2R, 3S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl)-5-methyl-5-(trifluoromethyl) thiacyclopentane-2-formamido) pyridine-2-formamide and a pharmaceutical composition of the crystal form of 4-((2R, 3S, 5R)-3-(3, 4-difluoro-2-methoxyphenyl)-5-methyl-5-(trifluoromethyl) thiacyclopentane-2-formamido) pyridine-2-formamide. The crystal form is good in crystallinity, excellent in chemical stability and crystal form stability, high in process safety and capable of playing a good drug effect in various animal models.

Embodiments herein generally relate to protein-based surface coatings. In some examples, disclosed embodiments relate to a process for synthesizing a protein-based surface coating, comprising conjugating acrylate or (meth-)acrylate monomer to serum albumin molecules. In at least one example, the conjugation step comprises: reducing native serum albumin molecules to produce free thiol groups; reacting the reduced serum albumin with (meth-)acrylate or acrylate monomers to react carbon-carbon double bonds with the free thiol groups; and inducing (meth-)acrylate or acrylate polymerization.

The present disclosure relates to the technical field of drilling fluid, and discloses a high density environmentally friendly polymer water-based drilling fluid with resistance to 240° C. and saturated salts, a preparation method therefor and use thereof. The water-based drilling fluid comprises a micro-crosslinked heterocyclic polymer filtrate reducer, a hyper-branched strongly adsorbed filtrate reducer, a nanometer intercalated complex shearing potentiator, a flexible outer and rigid inner microsphere plugging agent, and water, wherein the micro-crosslinked heterocyclic polymer filtrate reducer is prepared by reacting sodium p-styrene sulfonate, N,N,N-trimethyl-3-(2-methylallylamino)-1-propyl ammonium chloride, N,N-diethyl acrylamide, N-vinyl caprolactam, tetramethyl ethylenediamine with phenyl triethoxy silane. The high density environmentally friendly polymer water-based drilling fluid with resistance to 240° C. and saturated salts of the present disclosure can exhibit good performance at high temperature and high salinity conditions, and has desirable weighting capability, it can meet the requirements of drilling well in the deep oil and gas formations.

The invention discloses preparation and application of a block cationic copolymer / quaternary ammonium salt chitosan-based composite hydrogel. The preparation method comprises the following steps: reacting a sodium alginate solution with a NaIO4 solution at room temperature in a dark place to obtain an oxidized sodium alginate solution; adding ethylene glycol into the oxidized sodium alginate solution, reacting, concentrating, dialyzing and drying to obtain oxidized sodium alginate; the preparation method comprises the following steps: mixing acrylamide, 1-butyl-3-vinyl imidazole ammonium bromide, 3-acrylamide phenylboronic acid and quaternary ammonium salt chitosan, dissolving in water, adding ammonium persulfate and N, N-methylene bisacrylamide, heating for reaction, and cooling to obtain a cooling liquid; adding the oxidized sodium alginate solution into the cooling liquid, continuously adding polymerized N, N, N ', N'-tetramethylethylenediamine, reacting and curing to obtain composite hydrogel; and soaking the composite hydrogel in a glycerin / water mixed solution to obtain the composite hydrogel. When the composite hydrogel is used as a wound dressing, the composite hydrogel has the characteristics of good antibacterial activity, high sterilization efficiency, good anti-freezing and anti-drying performance and difficulty in generating drug resistance.