1801 results about "Phosphoric Acid Esters" patented technology

The invention provides a low-smoke halogen-free flame-retardant cable material and a preparation method thereof, and belongs to the field of cable materials. The low-smoke halogen-free flame-retardant cable material is prepared from the following chemical components: 32 to 40 parts of nitrile rubber, 22 to 27 parts of natural rubber, 8 to 12 parts of benzoxazole-siloxane copolymer containing phosphate dynamic bonds, 13 to 15 parts of core-shell-sheath three-stage structure flame retardant, 4 to 6 parts of hexaphenoxy cyclotriphosphazene modified carbon nanotubes, 2 to 3 parts of europium-doped mesoporous cerium dioxide and 3 to 4 parts of nano zinc oxide. The composite material is prepared from the following components in parts by weight: 3 to 4 parts of carbon nanotube grafted montmorillonite hybrid, 2 to 3 parts of lubricant, 0.8 to 1.2 parts of cross-linking agent, 0.3 to 0.4 part of accelerant, 0.4 to 0.6 part of dicumyl peroxide and 0.1 to 0.2 part of antioxidant. Unification of high flame retardance, low smoke, excellent mechanical property and processability of the cable material is realized.

The present disclosure provides methods of manufacturing psilocybin and crystalline psilocybin via a reaction of psilocin and tetrabenzylpyrophosphate in the presence of lithium chloride complex Grignard reagent, which is followed by hydrogenation. Methods of producing psilocin from 4-hydroxyindole or 4-acetoxyindole are also provided.

The invention discloses a battery monomer, a battery device and electric equipment, the battery monomer comprises an electrode assembly and an electrolyte, the electrode assembly comprises a positive pole piece, the positive pole piece comprises a positive current collector and a positive active material layer arranged on at least one side of the positive current collector, and the positive active material layer comprises lithium-containing phosphate; the electrolyte comprises a carboxylic ester solvent and a linear carbonic ester solvent, based on the total mass of the electrolyte, the mass ratio of the carboxylic ester solvent is 5%-25%, and the mass ratio of the linear carbonic ester solvent is 20%-49%; the electrolyte further comprises a non-lithium salt additive, the non-lithium salt additive comprises a phosphate ester additive, and the non-lithium salt additive further comprises at least one of a carbonate ester additive, a sulfate ester additive, a borate ester additive, a silane additive and a sultone additive. The total mass of the non-lithium salt additive accounts for 0.1%-5%.

The invention relates to the technical field of protective glue, in particular to extreme high and low temperature impact resistant UV (ultraviolet) photocuring electronic protective glue which is prepared from the following raw materials in parts by weight: 30-50 parts of synergistically modified epoxy-urethane acrylate oligomer, 20-35 parts of composite active monomer, 1.5-5 parts of composite photoinitiator and 10-20 parts of core-shell structure inorganic composite filler, 0.6 to 2.2 parts of a silane coupling agent, 0.12 to 1.1 parts of an antioxidant and 0.11 to 1 part of a leveling agent; the preparation method of the synergistically modified epoxy-urethane acrylate oligomer comprises the following steps: reacting resin acid modified epoxy resin with phosphoric acid di (hydroxyethyl acrylate) ester at 80-90 DEG C, and introducing a phosphate group to obtain a phosphate modified epoxy acrylate intermediate; the protection glue unifies rigidity, flexibility and flame retardance on the molecular level through the cooperation of the hybrid oligomer and the core-shell filler, realizes high heat conductivity, strong adhesion and extremely low internal stress, and has extreme temperature impact resistance, long-term damp-heat aging resistance and high-reliability protection performance.

The invention relates to the field of fire-resistant oil, in particular to phosphate-based fire-resistant oil with synergistically optimized flame resistance and stability and a preparation method of the phosphate-based fire-resistant oil. The fire-resistant oil comprises base oil and an additive, the base oil is a mixture obtained by esterification of mixed alkylphenol and phosphorus oxychloride; the molar percentage of the mixed alkylphenol is as follows: 4-6% of phenol; 11 to 14 percent of p-methylphenol; 22 to 26 percent of 2, 5-position dimethyl phenol; 0.8 to 1.5 percent of 2, 4-position dimethyl phenol; 2.5 to 4 percent of 2, 3-position dimethyl phenol; 0.4 to 0.6 percent of 4-ethyl phenol; 40 to 48 percent of 3, 5-position dimethyl phenol; 8 to 11% of 3-ethyl phenol; 3 to 5 percent of 3, 4-position dimethyl phenol; the additives comprise an antioxidant, a corrosion inhibitor, an anti-foaming agent and an anti-hydrolysis agent; the addition amount of the antioxidant is 0.05-5% of the total mass of the base oil; the addition amount of the corrosion inhibitor is 0.001%-0.08% of the total mass of the base oil; the addition amount of the anti-foaming agent is 0.001%-0.009% of the total mass of the base oil; the addition amount of the anti-hydrolysis agent is 0.001%-0.005% of the total mass of the base oil. The fire-resistant oil provided by the invention can be safely used under the working conditions of high temperature and extreme pressure.

The invention relates to the technical field of high polymer materials, and particularly discloses a fluoride-free halogen-free flame-retardant polycarbonate material and a preparation method and application thereof.The fluoride-free halogen-free flame-retardant polycarbonate material is prepared from, by weight, 70-90 parts of polycarbonate resin, 8-15 parts of phosphorus-nitrogen flame retardant and 3-8 parts of silicon flame-retardant synergist, the composite material is prepared from the following raw materials in parts by weight: 20-30 parts of polypropylene, 2-5 parts of nano reinforcing filler, 0.1-0.5 part of hindered phenol antioxidant, 0.1-0.5 part of phosphite ester antioxidant and 0.1-0.5 part of pentaerythritol stearate. Through the synergistic effect of the composite flame-retardant system and the nanofiller, high flame retardance (UL94 V-0 level, 1.5 mm thickness), high heat resistance (the heat distortion temperature is greater than or equal to 130 DEG C) and excellent mechanical property are realized, the control is easy, the processing is stable, good balance of flame retardance and mechanical property is achieved on the premise of environmental protection, and the composite flame-retardant material is suitable for the fields of high-end household appliances and consumer electronics.

The invention discloses a method for separating iron and lithium in a lithium iron phosphate iron salt leaching solution and recycling iron phosphate, and belongs to the technical field of waste lithium battery recycling. The method comprises the following steps: constructing a bis (2-ethylhexyl) phosphate and trioctyl decyl tertiary amine mixed extraction system for selective extraction of Fe < 3 + >, adopting phosphoric acid for reverse extraction, recycling phosphoric acid reverse extraction liquid, preparing iron phosphate and the like. According to the method, efficient enrichment of Fe < 3 + > and efficient elution of Fe < 3 + > from a loaded organic phase are realized. The purity of the raffinate Li solution is relatively high, so that the subsequent preparation of battery-grade lithium carbonate is facilitated. The strip liquor can be recycled for multiple times, an iron intermediate is precipitated through pH adjustment, and the FePO4 product can be finally prepared through washing, aging and high-temperature calcination. The method is high in extraction selectivity, recyclable in process and mild in operation condition, has good separation effect and resource utilization efficiency, and is suitable for popularization and application of a Fe / Li separation process in lithium battery recovery.

The invention provides a hole transport layer precursor solution, a hole transport layer, a preparation method and application of the hole transport layer, and a perovskite cell, and belongs to the technical field of hole transport layers. The hole transport layer precursor solution comprises a self-assembled single molecule and an organic solvent; the organic solvent comprises a solvent A, a solvent B and a solvent C; the solvent A comprises more than one of a phosphate ester solvent and an alcohol ether solvent; the solvent A contains four hydrogen bond receptors; the boiling point of the solvent A is 215-290 DEG C; the solvent B comprises more than one of ethanol, isopropanol, normal propyl alcohol, butanol, ethylene glycol and N, N-dimethylformamide; the solvent C comprises more than one of ethyl acetate and normal hexane. A ternary hydrogen bond network is formed through the solvent A, the solvent B and the solvent C, the agglomeration degree of SAM molecules is remarkably reduced, and the device performance is improved.

The invention discloses a chiral alpha alkyl beta hydroxyl phosphate compound as well as a preparation method and application thereof, and belongs to the technical field of chemical synthesis. In the presence of a catalyst, carbonyl of a substrate is reduced into hydroxyl to obtain a chiral alcohol compound, alpha-alkyl beta-ketophosphonate is reduced by an asymmetric catalytic hydrogen transfer method, and a reduced product can be used as a core skeleton of various drug molecules, so that the chiral alcohol compound is prepared. The compound has an obvious promotion effect on migration and repair of keratinocytes, and has great application potential in the aspects of wound healing, skin tissue soothing, repair, aging resistance and the like.

To provide synthetic fibers and a synthetic fiber treatment agent capable of improving heat resistance.SOLUTION: The synthetic fiber treatment agent contains (A) the following smoothing agent, and (B) organic phosphite ester. The smoothing agent contains at least one selected from (A1) a tri-fatty acid ester of glycerin and (A2) a tri-fatty acid ester of trimethylolpropane.SELECTED DRAWING: None

The invention relates to the technical field of chemical synthesis, and particularly discloses an alpha methyl beta phosphonate compound and a synthesis method thereof.The alpha methyl beta phosphonate compound is obtained by directly oxidizing the alpha position of aryl ketone into carbon positive and combining the carbon positive with diethyl phosphite anions under the alkaline condition by using hydrogen peroxide and iodine as oxidizing agents. The alpha methyl substituted beta phosphate ester compound can be generated by a one-step method. The method is suitable for synthesizing compounds of phosphoric acid (methyl, ethyl, propyl and the like) with different alkyl substitutes (methyl, ethyl, propyl and the like) at carbonyl alpha positions. According to the method, the alpha-methyl substituted beta phosphate compound can be synthesized only by using commercial cheap and easily available aryl ketone as a raw material, using hydrogen peroxide and iodine as oxidants and using diethyl hypophosphite as a phosphine source, and reacting in the DMSO solvent at 100 DEG C for 12 hours, so that the target product can be obtained, and the yield is excellent. Compared with previously reported methods, the method does not need low-temperature operation, is simple to operate, adopts a one-pot method, does not need a metal catalyst, and all raw materials are common bulk chemicals.

The invention discloses a flame-retardant reinforced polycarbonate composite material and a preparation method thereof, and belongs to the technical field of polycarbonate composites.The flame-retardant reinforced polycarbonate composite material comprises 70%-90% of polycarbonate resin, the polycarbonate resin is aromatic polycarbonate with the viscosity average molecular weight ranging from 20000 to 35000; the glass fiber is alkali-free chopped E glass fiber, and the surface of the glass fiber is treated by an amino silane coupling agent; the flame retardant comprises 5-15% of a phosphorus-nitrogen-silicon composite flame retardant, the composite flame retardant is a synergistic system formed by physically premixing a phosphate ester compound, a nitrogen charring agent and a silicone polymer, and the phosphate ester compound plays a role in gas-phase flame retardance and partial condensed-phase flame retardance during combustion. By adopting a phosphorus-nitrogen-silicon composite flame-retardant synergistic system, high flame-retardant efficiency is realized under the condition of low additive amount, the halogen-free and environment-friendly effects are realized, and the environmental and health hidden dangers of the traditional brominated flame retardant are overcome.

The invention discloses an antistatic agent for polyolefin film material production and a preparation method thereof. According to the invention, through reasonable molecular structure design, raw material selection and synthesis process optimization, the antistatic agent has multiple functions of high-efficiency antistatic property, oxidation resistance, antibacterial property, mechanical property enhancement and the like. The polyolefin material added with the multifunctional antistatic agent has good antistatic performance under different environmental conditions, and the oxidation resistance, the antibacterial property and the mechanical property are also remarkably improved. The antistatic agent has good adaptability with processing of a polyolefin film material and has wide application prospects and market competitive advantages, and the comprehensive performance of the polyolefin film material is remarkably improved through multi-component collaborative design. The composite system of the polyolefin quaternary ammonium salt and the graphene quantum dots strengthens the long-term effect of the antistatic effect, and meanwhile, the synergistic effect of the hindered phenol and the phosphite strengthens the antioxidant stability of the material in the processing and using processes.

The invention relates to a low-smoke halogen-free flame-retardant plastic and a preparation method thereof, and belongs to the technical field of flame-retardant high polymer materials. The flame-retardant plastic is prepared from the following components: 12 to 17 weight percent of magnesium hydroxide superfine powder, 4.5 to 6.2 weight percent of modified flame retardant, 5 to 7 weight percent of flexibilizer, 0.9 to 1.2 weight percent of lubricant, 0.3 to 0.4 weight percent of antioxidant and the balance of PBT (Polybutylene Terephthalate) resin, the modified flame retardant is prepared by the following steps: reacting pentaerythritol with phosphorus oxychloride to prepare hydroxyl-containing polyhedral oligomeric phosphate, esterifying acryloyl chloride and the hydroxyl of the polyhedral oligomeric phosphate to prepare a monoester intermediate, and finally performing click addition on sulfydryl of pentaerythritol tetramercaptoacetate and double bonds of the monoester intermediate. The modified flame retardant interacts with magnesium hydroxide, a stable hollow carbon net is formed in the flame retardant process, and the hollow carbon net has a multi-layer adsorption and filtration effect on smoke particles, so that the release of smoke is reduced, and the smoke density is greatly reduced.

The invention discloses an environment-friendly tundish magnesium-calcium dry material for thin-strip cast-rolling short-process steelmaking, and belongs to the technical field of refractory materials. The invention discloses an environment-friendly tundish magnesium-calcium dry material for thin-strip cast-rolling short-process steelmaking. The tundish magnesium-calcium dry material is prepared from the following raw materials in percentage by mass: 44-62.5% of magnesia aggregate, 22.5-24% of dolomite aggregate, 11-28% of magnesia fine powder and 3-5% of a binding agent, the binding agent is silica sol modified by a phosphate esterification aluminic acid ester coupling agent. The preparation method comprises the following specific steps: putting magnesia fine powder, a binding agent, magnesia aggregate and dolomite aggregate into a V-shaped mixing mill, uniformly stirring for 5 minutes, putting the stirred mixture into a mold, ramming, vibrating and molding to obtain a molded green body, curing at room temperature for 24 hours, demolding, drying at 200 DEG C for 24 hours, and carrying out heat treatment in an air atmosphere to obtain a dry material sample. According to the invention, the binding agent with good compatibility with a matrix is prepared by improving the binding agent, so that the binding agent can play a reinforcing role.

The invention discloses a phosphate ester type composite binder for a sulfide battery, the phosphate ester type composite binder comprises a solute and a solvent, the solute comprises the following components in percentage by mass: 49.75%-88.5% of a binder, 9.5%-49.75% of phosphate ester and 0.45%-1.96% of silanol; the solvent is a non-polar solvent, and the mass ratio of the solute to the solvent is 1%: (10%-90%); the preparation method comprises the following steps: S1, placing the binder in a non-polar solvent, and heating and stirring until the binder is completely dissolved to obtain a solution A; s2, mixing a silane coupling agent with absolute ethyl alcohol, adjusting the pH value with acetic acid, and stirring to generate silanol; s3, silanol is added into the solution A, so that one end of silanol reacts with active hydrogen of the binder for bonding; and S4, adding phosphate into the solution A, so that the other end of the silanol is combined with a group of the phosphate to obtain a reaction solution with a binder-silanol-phosphate structure. According to the invention, stable combination of the binder and phosphate is realized through a silanol-mediated grafting structure, and the interface stability, the ionic conductivity and the mechanical strength are improved.

The present invention relates to the technical field of daily chemical technology, and specifically provides a whitening and freckle-removing cream. The freckle-removing cream comprises the following components in parts by weight: water, glycerin, mineral oil, antioxidant microcapsules, polydimethylsiloxane, sodium ascorbyl phosphate, niacinamide, a plant compound extract, essence, and cetearyl alcohol. The present invention adds natural plant extract ingredients, which is safe and effective. A circulation device is used to promote the effective combination of active ingredients, so that the active ingredients can quickly penetrate into the inner layer of the skin, thereby improving the transdermal absorption ability of the active ingredients. A unique encapsulation technology is used to firmly adhere the active ingredients to the skin surface, thereby effectively lightening facial spots, removing dullness from the skin, and restoring luster.

The invention provides an environment-friendly heat-resistant photovoltaic cable and a preparation method thereof. The environment-friendly heat-resistant photovoltaic cable comprises a conductor, an insulating layer and a sheath layer, the insulating layer is prepared from the following component raw materials: 20 to 30 percent of polylactic acid, 10 to 20 percent of polyhydroxyalkanoate, 25 to 35 percent of halogen-free flame-retardant crosslinked polyethylene, 5 to 15 percent of phosphate esterified lignin microspheres, 3 to 8 percent of quaternary ammonium salt chitosan nanofiber, 1 to 3 percent of modified graphene, 2 to 6 percent of epoxidized soybean oil, 1 to 5 percent of modified montmorillonite and 0.5 to 1.5 percent of nano silicon dioxide aerogel. The invention discloses an anti-aging agent which is prepared from the following components in percentage by weight: 2-4% of sodium alginate microcapsules, 0.5-1.5% of polydimethylsiloxane, 0.1-0.8% of a silane coupling agent and 0.1-0.8% of a plant polyphenol antioxidant. The sheath layer comprises the following raw material components: 45-55% of halogen-free flame-retardant crosslinked polyethylene, 10-20% of lignin-based carbon nanotubes, 5-15% of sulfonated chitosan / sodium alginate microspheres, 1-6% of graphene, 5-15% of epoxidized soybean oil, 2-8% of nano silicon dioxide, 1-3% of polydimethylsiloxane, 1-3% of peppermint oil microcapsules, 1-3% of a silane coupling agent and 0.1-0.8% of an antioxidant. And 0.1-0.8% of an ultraviolet light absorber. The photovoltaic cable disclosed by the invention has the advantages of flame retardance and difficulty in generating drippings after combustion.

The invention provides a high-performance concrete anticorrosive paint and a preparation method of a coating, and relates to the technical field of building materials and corrosion prevention. The coating is composed of a component A and a component B, the component A comprises epoxy resin, a composite solvent, an organic solvent, a dispersant, fumed silica and a leveling agent, and the component B comprises an epoxy hardener, a conductive polymer dispersion liquid and an organic solvent. The composite solvent is formed by compounding one or more of orthotitanate, phosphate and orthosilicate with an ester, ketone, alcohol, aromatic hydrocarbon, aliphatic hydrocarbon or ether organic solvent. The preparation method of the anticorrosive coating comprises the following steps: preparing the component A and the component B, mixing to form a coating, applying the coating to the surface of concrete, and curing. The coating is compact in structure and strong in adhesive force, can obviously improve the durability and corrosion resistance of concrete in extreme environments such as high salinity and high acid, and is particularly suitable for infrastructure protection in coastal and heavy corrosion industrial areas.

An extreme-cold resistant low-fume halogen-free flame-retardant polyolefin sheath, a preparation method therefor, and a cable. The sheath comprises the following raw materials in parts by mass: 4-16 parts of an ethylene-vinyl acetate copolymer, 7-13 parts of a phosphate group functionalized linear low-density polyethylene, 9-15 parts of an ethylene-octene copolymer, 5-10 parts of a maleic anhydride-grafted ethylene-methyl methacrylate copolymer, 10-15 parts of magnesium hydroxide, 40-50 parts of aluminum hydroxide, etc. The preparation method for the phosphate group functionalized linear low-density polyethylene comprises: adding a catalyst to a pre-cooled ethylene monomer, adding a vinyl phosphate ester and an initiator after the reaction, and reacting for 1-2 hours at a temperature of 65-75°C and a pressure of 15-35 Mpa and then terminating the reaction, thereby obtaining the phosphate group functionalized linear low-density polyethylene. Compared with unfunctionalized polyethylene, the phosphate group functionalized polyethylene used has greatly improved low-temperature and flame-retardant performance, and can improve the overall flame-retardant and low-temperature performance of the formula.

The invention discloses a functional intermediate for polycarboxylic acid synthesis modification and a preparation process thereof, the intermediate is a copolymer containing a phosphate group, an acrylate group and a hyperbranched polyether polyol chain segment, the molar ratio of all structural units is 1: (1-3): (0.5-2), and the preparation method comprises the following steps: esterification reaction; carrying out phosphorylation reaction; and carrying out gradient vacuum to remove small molecules. The intermediate is high in content of effective components, the viscosity is 500-2000mPa. S, the dispersing performance and the slump loss resistance of the polycarboxylate superplasticizer are remarkably improved through the synergistic effect of phosphate tackifying, acrylate dispersing and hyperbranched compatibilizing, the intermediate is particularly suitable for concrete construction under complex gravel geological conditions, the doping amount is reduced compared with that of traditional hydroxyethyl acrylate, and the service life of the polycarboxylate superplasticizer is prolonged. And the slump of the mother liquor can be kept lossless for a long time.

The invention discloses hydrolysis-resistant liquid phosphite ester and a preparation method and application thereof.The hydrolysis-resistant liquid phosphite ester is prepared by the steps that 2, 2, 4-trimethyl-1, 3-pentanediol and phosphorus trichloride or phosphite triester serve as raw materials, a cyclization reaction is conducted firstly, and then the hydrolysis-resistant liquid phosphite ester is obtained; and then carrying out nucleophilic substitution on Cl or aryl and alkyl on the cyclized intermediate by using higher saturated monohydric alcohol with more than C8, wherein the molecular structure is as shown in formula I in the specification. The liquid phosphite ester is novel liquid phosphite ester, the main body of the liquid phosphite ester is of a six-membered ring structure, the basic structure of the phosphite ester is reserved to the maximum extent, and the anti-oxidation effect of the phosphite ester is guaranteed; hydrophobic aliphatic chain structures on phosphorus atoms and branched chains of the phosphorus atoms prevent water molecules from approaching P-O bonds, so that the phosphorus atoms and the branched chains are prevented from being attacked by the water molecules, and the hydrolysis resistance is improved under the conditions that any additional amine hydrolysis-resistant agent is not used and any steric hindrance group is not introduced; good practical value, economic value and market prospect are realized.

This invention discloses a gypsum-based lightweight flame-retardant board and its preparation method, relating to the field of building materials technology. The gypsum-based lightweight flame-retardant board prepared by this invention is made by foaming a gypsum substrate with a foaming agent and a composite stabilizer, then introducing a self-made flame retardant and other raw materials, casting it between two layers of facing paper, and drying it. The composite stabilizer includes a modified acrylamide copolymer and acrylamide hydrogel. The modified acrylamide copolymer is obtained by copolymerizing N-isopropylacrylamide with silane acrylic acid and then reacting it with hyperbranched polyphosphate. The acrylamide hydrogel is obtained by polymerizing acrylic acid and acrylamide through an aqueous solution. The self-made flame retardant is obtained by reacting ammonium polyphosphate with a hydroxy heterocyclic amino alcohol. The hydroxy heterocyclic amino alcohol is obtained by reacting a heterocyclic amino alcohol with a double-terminated hydroxyl polyphenylene ether. This process gives the gypsum-based lightweight flame-retardant board excellent flame retardancy, mechanical properties, and flame-retardant stability.

This disclosure provides compounds of Formula (X), and pharmaceutically acceptable salts thereof, that reduce levels of phosphatidylinositol 4,5-bisphosphate 3-kinase (PI3K) isoform alpha (PI3Kα), as well as methods of making and using same, and compositions comprising Formula (X), and pharmaceutically acceptable salts thereof.

The invention relates to the technical field of rare earth element separation methods, in particular to a method for separating ytterbium and lutetium by using a phosphate adsorbent, which comprises the following steps: loading a phosphate solution on a porous solid-phase carrier by using a vacuum impregnation method, and carrying out reduced pressure evaporation and drying to obtain a phosphate solid adsorbent; filling an exchange column with the solid adsorbent to obtain the exchange column filled with the solid adsorbent; enabling a nitric acid solution containing ytterbium and lutetium to flow through an exchange column filled with a solid adsorbent to complete a column adsorption process; and performing elution, performing desorption by using a desorption solution to obtain the regenerated exchange column filled with the solid adsorbent, respectively collecting the ytterbium solution and the lutetium solution, completing the separation process, and repeating the steps. By adopting the steps, the separation of ytterbium and lutetium is directly realized from the nitric acid solution containing ytterbium Yb and lutetium Lu through column adsorption separation, leaching and desorption processes, and high-purity ytterbium and lutetium products are prepared.

The invention relates to synergistic herbicidal mixtures and compositions comprising triclopyr (3,5,6-Trichloro-2-pyridinyloxyacetic acid), a salt thereof and / or an ester thereof, and at least one phosphate ester adjuvant, and methods of use thereof.

The invention relates to high-tinting-strength intaglio printing ink and a preparation method thereof, preparation raw materials of the high-tinting-strength intaglio printing ink comprise the following components in parts by weight: 30-40 parts of resin, 10-14 parts of a modified pigment, 40-60 parts of a solvent, 0.8-1.2 parts of a rheology modifier and 1-3 parts of a functional aid, and the surface of the modified pigment is modified by an epoxy silane coupling agent, a phosphate coupling agent and ionic quaternary ammonium salt. After the pigment in the ink prepared by the invention is modified, the surface contains an epoxy group, a phosphate group and a quaternary ammonium salt group, so that the compatibility of the pigment and resin is remarkably improved, the dispersion stability of the pigment in an ink layer and the anchoring effect of the pigment on a base material are improved, and the ink has high adhesive force and high tinting strength.

The invention relates to a corrosion-resistant polypropylene modified plastic and a preparation method thereof, and belongs to the technical field of polypropylene plastic modification. The modified plastic is prepared from isotactic polypropylene, exfoliated montmorillonite, polyvinylidene fluoride powder, anhydride grafted polypropylene, a beta-crystal nucleating agent, diethyl aluminum chloride, peroxide, hindered phenol, phosphite ester and N, N-distearoyl hydroxylamine. The preparation method comprises the steps of low-shear melting and blending, high-shear supercritical COviscosity reduction, vacuum exhaust, bidirectional orientation, infrared local crosslinking, co-extrusion cooling and the like. The obtained material is excellent in tensile strength, elongation at break, low-temperature impact strength, strong acid corrosion resistance and the like.

The invention discloses a high-performance coiled material powder coating and a preparation method thereof, and belongs to the technical field of powder paints.The high-performance coiled material powder coating has the advantages that organosilicon modified epoxy resin and carboxyl-terminated polyester resin are compounded, a-Si-O-Si-chain segment is introduced into a system after organosilicon modification, the flexibility is high, and the high-performance coiled material powder coating has a synergistic effect with nano calcium carbonate; the adhesive force and the flexibility of the coating are balanced, and the mechanical strength of the coating can be obviously improved by adding the grafted modified graphene oxide and the active chromic oxide; then, phosphite ester groups are grafted to the graphene oxide, the graphene oxide is applied to a powder coating system, a three-dimensional network structure and chemical bonding can be formed in the system, the crosslinking stability of the graphene oxide in the system can be improved, and a certain barrier property can be achieved due to the flaky structure of the graphene oxide; and the coating is endowed with long-acting weather resistance, and the weather resistance and the corrosion resistance of the coating are further improved through the synergistic effect with the active chromic oxide.

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.