241 results about "Boric acid" patented technology

A process or method for manufacturing a fire-retardant treated wood composite board or panel, such as oriented-strand board, with a low melting point fire retardant (FR) material, such as boric acid, while the press is operating at typical press temperatures above the FR material melting point. An intervening overlay is applied to the top surface of the mat on the forming line, after the use or application of any FR material within or on the mat, prior to entry into the press. The intervening overlay covers the top surface so as to prevent the melting fire retardant material from contacting the press platen(s). After pressing, the intervening overlay may be removed from the top surface by sanding, buffing, or other methods. The intervening overlay also may be sized so as to extend over one or more edges of the underlying panel, for ease of removal post-process.

A boron-containing polyethylene glycol fatty acid ester surfactant belongs to the field of organic chemistry and functional materials. The boron-containing polyethylene glycol fatty acid ester surfactant is prepared as follows: polyethylene glycol (PEG), boric acid and fatty acid are used as raw materials, first esterification reaction of the PEG and the boric acid is performed, then esterification reaction of the PEG and the fatty acid is performed to obtain boron-containing poly ethylene glycol fatty acid ester; by changing the species of fatty acids and catalysts and molecular weight of the PEG, the esterification rate can be enhanced, the boron-containing poly ethylene glycol fatty acid ester product can be used as a surfactant, and the boron-containing poly ethylene glycol fatty acid ester can reduce water surface tension and has good emulsifying properties.

The invention provides a biaxially oriented nylon light conversion film as well as a preparation method and application thereof. A nylon / flaky nano silicon dioxide blend is used as a supporting layer, a nylon / boric acid functionalized terbium metal organic framework material blend is used as a variable light conversion characteristic layer, and the two-way stretching nylon light conversion film is obtained through synchronous two-way stretching. The film has dripping and variable light conversion characteristics, and can convert ultraviolet light into red orange light or blue light.

The invention provides a thermal response self-ceramization fireproof coating and a preparation method thereof. The thermal response self-ceramization fireproof coating is prepared from the following raw materials in parts by mass: 3 to 10 parts of acrylic monomer, 3 to 10 parts of organic sulfonate, 1 to 4 parts of silane coupling agent, 0.5 to 3 parts of silicate ester, 4 to 6 parts of ceramic precursor, 3 to 6 parts of fluxing agent and 0.05 to 0.4 part of initiator. The fluxing agent comprises a component A and a component B, the component A is one of boric oxide, zinc borate or low-melting-point glass powder, and the component B is one of phosphorus pentoxide and ammonium polyphosphate. The silane coupling agent can be copolymerized with an acrylic monomer to construct a C-C main chain, the C-C main chain and silicate ester are subjected to hydrolytic condensation to form a Si-O-Si three-dimensional network, a chemical cross-linked skeleton is formed, and the chemical cross-linked skeleton can generate silicon dioxide at high temperature to participate in a ceramization reaction; the ceramic precursor and silicate ester can form a strong physical cross-linking effect, so that the fireproof coating with a chemical and physical double-cross-linked network can be formed, and the fireproof coating has excellent mechanical property and machinability at normal temperature.

The invention discloses a wood-based composite phase-change material and a preparation method thereof, and belongs to the technical field of phase-change materials.The preparation method of the wood-based composite phase-change material comprises the following steps that wood is cut and then added into delignification liquid to be heated, the wood is taken out and washed with water, and delignified wood is obtained; the delignification wood is added into the modification liquid to be heated, and after being taken out, the delignification wood is washed and dried to obtain pretreated wood; mixing polyethylene glycol, citric acid and boric acid, heating and stirring to obtain a phase change material; dipping the pretreated wood into the phase change material for vacuum dipping, taking out and drying to obtain the phase change material. The modified liquid is prepared from an ethanol water solution, a modified filler, 2-(3, 4-cyclohexene oxide) ethyltrimethoxysilane and triethylamine. The delignification liquid and the modification liquid are adopted for pretreating the wood, so that the wood can be better firmly combined with the phase change material, leakage is prevented, and the finally prepared wood-based composite phase change material has excellent heat management capacity and stability.

The invention relates to a method for preparing high-purity bismuth by removing impurity lead in refined bismuth through oxidation slagging, and belongs to the technical field of non-ferrous metals. Melting and oxidizing: melting a lead-containing refined bismuth raw material at 300-400 DEG C, adding bismuth oxide into the molten bismuth, and fully stirring to enable the bismuth oxide and lead to generate oxidation reaction to generate lead oxide; slagging reaction: adding boric anhydride (B2O3) into the melt, and enabling the boric anhydride (B2O3) to react with the generated lead oxide to generate lead borate slag; slag salvaging and lead removal: stirring for 30-60 minutes at the temperature of 300-400 DEG C in a heat preservation manner, so that the slagging reaction is fully carried out, generated lead borate slag with lower density floats to the surface of a melt, and a lead-containing slag phase is removed in a mechanical or manual slag salvaging manner; and after the slag salvaging process is finished, cooling the bismuth melt under a protective atmosphere until the bismuth melt is solidified to obtain a lead-removed high-purity bismuth product. According to the method, bismuth oxide and boric anhydride are introduced, metal lead is converted into lead borate slag easy to float, efficient and deep separation of lead and bismuth melt is achieved through the density difference, and the lead content can be reduced to 1 ppm or below.

The invention discloses a method for measuring the content of calcium fluoride in dolomite-containing fluorite mine. The method comprises an acetic acid solution, a hydrochloric acid solution, a triethanolamine solution, a potassium hydroxide solution and boric acid. The method for measuring the content of calcium fluoride in the dolomite-containing fluorite mine comprises the following steps: S1, reagent proportioning; s2, preparing a calcium standard solution; s3, preparing an EDTA standard titration solution; s4, selecting an instrument; s5, preparing a sample; s6, step analysis; s7, content correction and determination; and S8, calculating a result. The invention belongs to the technical field of calcium fluoride content determination, and particularly relates to a method for measuring the content of calcium fluoride in dolomite-containing fluorite mine, compared with the prior art, the method solves the problem of dolomite dissolution when calcium carbonate is leached by acetic acid, and the content of calcium fluoride in the fluorite mine can be measured by accurately calculating the dissolution amount of dolomite. The measured calcium fluoride content is clearer, more reasonable and more reliable and approaches to a true value, and the process operation is simple and rapid, and is suitable for the requirements in the fields of mine production, assay detection and the like.

A particulate nanocomposite material comprising, as determined by X-ray diffraction (XRD): elemental carbon (C); elemental nickel (Ni) in a cubic crystalline phase; a cubic nickel oxide (NiO) crystalline phase; an orthorhombic calcium borate (CaB2O4) crystalline phase; and, a magnesium borate (MgB2O4) crystalline phase. The porous particulate nanocomposite is characterized in that, based on the total number of atoms in the particulate nanocomposite material: the atomic concentration of carbon is from about 1 atomic percent (at. %) to about 10 at. %; the atomic concentration of nickel is from about 1 at. % to about 10 at. %; the atomic concentration of boron (B) is from about 1 at. % to about 10 at. %; the atomic concentration of magnesium (Mg) is from about 5 at. % to about 15 at. %; and, the atomic concentration of calcium (Ca) is from about 1 at. % to about 10 at. %.

The invention relates to the technical field of power cables, and provides a flame-retardant power cable and a preparation method thereof. The flame-retardant power cable comprises a conductor, an insulating layer and a sheath layer which are sequentially arranged from inside to outside, and the sheath layer is prepared from, by weight, 40-60 parts of polyethylene, 60-80 parts of ethylene-vinyl acetate copolymer, 8-10 parts of compatilizer, 3-5 parts of auxiliaries, 15-20 parts of filler and 60-70 parts of flame retardant. The flame retardant is prepared from magnesium hydroxide, antimony trioxide, hydrated zinc borate and an aromatic bromine-containing compound in a mass ratio of 45: 8: 12: (25-30), and the number of bromine atoms of the aromatic bromine-containing compound is 6-8. According to the technical scheme, the problem of insufficient flame retardant property of the power cable in the prior art is solved.

The invention discloses a ceramic fire-resistant sealant for a bridge, a fireproof structure, a preparation device and a preparation method, and relates to the technical field of sealants for the bridge. The ceramic fire-resistant sealant for the bridge comprises the following specific components in parts by weight: 100 parts of an MS polymer; 0 to 100 parts of a plasticizer; 80 to 150 parts of aluminum hydroxide; 80 to 150 parts of modified wollastonite; 50 to 100 parts of calcium carbonate; 10 to 20 parts of zinc borate; 10 to 20 parts of melamine polyphosphate; 5 to 10 parts of dipentaerythritol; 5 to 10 parts of a dewatering agent; 5 to 10 parts of an adhesion promoter; and 0.5-2 parts of a catalyst. According to the ceramic fire-resistant sealant for the bridge, a rubber body formed after vulcanization is converted into a self-supporting ceramic body under the condition of high temperature or open fire, flame is prevented from diffusing into a material, so that the purposes of flame retardance and fire prevention are achieved, meanwhile, the mechanical property is not obviously attenuated before and after thermal aging, and good elasticity is still kept; and the vulcanized paint has excellent adhesive force to the paint, so that the use effect of the paint is guaranteed.

Methods for the production of rare earth magnetic materials including magnetic crystals of Nd2F14B and the magnetic materials produced thereby. The methods lead to the formation of magnetic materials having a high concentration of Nd2F14B crystals. The method comprises steps of: admixing a neodymium borate powder, iron powder and calcium hydride to form a precursor powder; compacting the precursor powder to form a compacted precursor powder body; and heating the compacted precursor powder body to form a consolidated powder body.

The application discloses a kind of determination methods and program products of core reactivity state, the method includes: the key state parameter in the process of core reaction is collected, key state parameter includes at least one of core power distribution parameter, coolant temperature, coolant density, control rod position, boric acid concentration and burnup;Determine the burnup step of fuel, the evolution process of fissile nuclide and fission product in core is modeled based on the burnup step of fuel and burnup model, to obtain the reactivity parameter related to the burnup of fuel, the burnup model is used to describe the nuclide transmutation and consumption logic of fuel during the operation of core;Corresponding digital twin is constructed with the reactivity state of the core, the reactivity state of the core is mapped by the digital twin based on the reactivity parameter and the key state parameter driving, can realize high-precision, real-time, full life cycle dynamic digital mapping and intelligent detection of core reactivity state.

Provided herein are compositions and methods to improve plant resistance to abiotic and biotic stress, thereby improving crop yield. Provided herein are compositions including zinc, copper, and an acid, where the acid is selected from citric acid, sulfuric acid, oxalic acid, humic acid, fulvic acid, boric acid, acetic acid, and a combination thereof. Certain embodiments optionally include ammonium sulfate. Compositions described herein have plant priming activity where the plant's defenses against abiotic and biotic stress are boosted.

The application discloses a kind of north fruit tree spring frost injury freeze protection fluid and its preparation and application method, the freeze protection fluid is by plant growth regulator, saccharide, amino acid component, mineral nutrient component, boric acid and film-forming protective component and water compound, each raw material is mixed uniformly according to defined mass fraction ratio. When using, stock solution dilution 300-700 times, 24-72h before frost, it is suitable for cherry, apple, pear, apricot and other north fruit tree flowering freeze protection. The application has multiple effects of freeze protection, membrane stabilization, repair and nutrient supplementation, can maximize protect cell integrity and reduce irreversible necrosis at low temperature. Even if suffering from low temperature freeze injury, the flower organ is less damaged after spraying the freeze protection fluid, and recovers quickly.

The present application relates to a kind of EB solidification ecological home cabinet door plate, including the structure of substrate layer, primer layer and topcoat, wherein topcoat is formed after using flame-retardant and reinforcing modifier compound coating by EB electron beam curing, and the composition of reinforcing modifier coating is nanometer silicon powder, alumina powder and boric acid or borax powder;Primer layer is made of water-based fluorinated polyurethane or acrylic emulsion;2-3 layers of primer are coated on substrate layer, and then external topcoat is coated, and after coating, it is cured by EB electron beam in nitrogen environment, to obtain EB solidification ecological home cabinet door plate, and the cabinet door plate produced has the excellent performance of low cost, stain resistance, wear resistance, corrosion resistance, high hardness, impact resistance, yellowing resistance and fingerprint resistance.

The present invention relates to the field of battery recycling, and more particularly to a method for regenerating and repairing waste graphite layer structures. The method comprises mixing acid-washed and impurity-removed waste graphite, a manganese salt and / or nickel salt, boric acid, and an alcohol reagent, followed by drying, followed by high-temperature heating and impurity removal. The method provided by the present invention can efficiently recover electrode graphite powder from waste lithium-ion batteries. The recovered graphite has an excellent layer structure, effectively improving the electrochemical performance of the regenerated graphite.

The present application relates to a special coating for water-cooled wall surface of coal-fired boiler, in particular to a coating for water-cooled wall surface of coal-fired boiler, a preparation method and application thereof. The coating comprises nano-tungsten powder, tungsten carbide, rare earth compound, sodium borate, potassium chromate, rock asphalt, binder, modifier, dispersant, defoaming agent, curing agent and solvent. The coating is fused on the water-cooled wall surface of coal-fired boiler, the obtained coating has good interface bonding with the water-cooled wall base material, low porosity, avoids the penetration of corrosive gas and liquid, solves the corrosion problem of water-cooled wall, and also avoids the reduction of coating hardness and wear resistance; the coating is not easy to wear and damage in long-term use, can improve the high-temperature resistance, hardness, corrosion resistance and wear resistance of the water-cooled wall surface of boiler, effectively prolongs the service life of the water-cooled wall surface of boiler, and further ensures the safe and stable operation of coal-fired boiler.

This invention provides an antistatic and privacy-protecting polarizing film and its preparation process, belonging to the field of polarizing film preparation technology. The preparation process includes the following steps: preparation of an antistatic agent; preparation of a modified adhesive; preparation of a composite polarizing film; and preparation of the polarizing film. This invention introduces an antistatic agent and POSS-modified graphene oxide into the modified adhesive, making the adhesive layer a conductive medium connecting multiple layers such as the polarizing film (PVA), TAC layer, and privacy film, forming a cross-layer conductive path. This avoids static electricity accumulation at the interface, improving the antistatic effect. Boric acid is first used to crosslink the PVA film, followed by glyoxal crosslinking, achieving long-term reliability of the polarizing film under high temperature and high humidity environments.

The invention discloses high-temperature underglaze Chinese red glaze as well as a preparation method and application thereof, and belongs to the technical field of ceramic high-temperature underglaze colored glaze materials. The high-temperature underglaze Chinese red glaze comprises a high-temperature red pigment, a glaze matrix and related additives, wherein the high-temperature red pigment comprises a base material and a coloring element and is a core coloring component of the Chinese red glaze; the glaze matrix comprises potassium feldspar, muscovite, quartz sand, boric acid and wollastonite, and can be fused at high temperature to form a transparent or semitransparent vitreous layer to wrap and protect the pigment and provide good glaze gloss and flatness at the same time; related additives comprise a shaping agent, a dispersing agent and a mineralizing agent, and the colored glaze processing property can be improved. In addition, the invention further provides a preparation method and a sintering process of the high-temperature underglaze Chinese red glaze, Chinese red can be sintered at the temperature of 1300-1400 DEG C, the glaze color is bright, the chroma is full, the color is normal, darkening and blackening are avoided, and the high artistic value and process practicability are achieved.

The invention discloses a copper electroplating solution and application thereof. The invention relates to a copper electroplating solution, which comprises the following raw materials: 20-250g / L of copper sulfate; 4-98g / L of sulfuric acid; the concentration of chloride ions is 50 to 300 mg / L; 0.5 g / L to 10 g / L of a displacement agent; 0.2-15 g / L of an accelerator; 2 to 20 mg / L of a leveling agent; 5-50 mg / L of a stress regulator; wherein the stress regulator comprises one or a combination of more of thiourea, boric acid, nickel salt and cobalt salt. The copper electroplating liquid can be used for rapidly electroplating and preparing a copper plating layer under the condition of high current density, and meanwhile, the obtained copper plating layer has remarkably lower internal stress, good adhesive force and better appearance, and is suitable for being applied to electrode preparation of solar cells.

The application provides an Ag etching solution, a preparation method and application thereof. The Ag etching solution comprises the following components in a weight ratio: 40-80 parts of inorganic acid; 10-50 parts of organic acid; 0.05-1.5 parts of corrosion inhibitor; 0.1-2 parts of chelating agent; 1-7.5 parts of buffer; and 30-50 parts of ultrapure water. The application further discloses a preparation method of the Ag etching solution and application thereof in the field of etching ITO-Ag-ITO composite layers. The inorganic acid is selected from one or more of phosphoric acid, sulfuric acid, carbonic acid, boric acid, hydrobromic acid, iodic acid, hypoiodous acid, hydrofluoric acid and nitric acid. The inorganic acid is preferably phosphoric acid and nitric acid. The Ag etching solution has a stable etching rate for ITO-Ag-ITO, and is not damaged to the insulating layer and photoresist, and can be used in the OLED pixel electrode manufacturing process, and the Ag layer is not provided with burrs and is not shrunk after etching.

The invention relates to the use of an aqueous alkaline composition having a pH of less than 10.0 for cleaning the surface of a substrate, said composition comprising, in addition to the aqueous hydroxide anion a1), at least one complexing agent a2), at least one surfactant a3) and optionally at least one a4) of phosphate and borate anions condensed, wherein the surface is at least partially made of at least one steel which is at least partially coated with at least one zinc-aluminum-magnesium alloy; a method for cleaning the aforementioned surface by using the aqueous alkaline composition; a substrate having at least one cleaned surface obtainable therefrom; a process for the chemical pretreatment of the aforementioned cleaned substrate surface by further using an aqueous coating composition suitable for forming a preferred conversion coating film on the surface; and a substrate having at least one chemically pretreated surface obtainable therefrom.

The invention relates to a preparation method and application of a Ti3C2Tx nano wave-absorbing material with OBO as a surface terminal. The invention belongs to the technical field of wave-absorbing materials. The problem that an existing Ti3C2Tx material is poor in impedance mismatch and electromagnetic wave absorption capacity is solved. The method comprises the following steps: uniformly mixing anhydrous copper chloride, potassium chloride, sodium chloride, anhydrous sodium tetraborate and Ti3AlC2, heating, cooling, grinding, dissolving in an ammonium persulfate solution, stirring, performing ultrasonic treatment, centrifuging and drying. The preparation process is low in cost, simple, green and pollution-free. By changing the surface groups of the Ti3C2Tx material, the dipole polarization is reduced, and the impedance matching is improved. The absorption thickness is 1-2 mm, the effective absorption bandwidth of the wave-absorbing material covers 9-18 GHz, and the broadband absorption target of the material is completed. At the corresponding frequency of 14.24 GHz, when the thickness of the absorbing layer of the wave-absorbing material is 1.36 mm, strong absorption of the wave-absorbing material is realized, and 99.99% of electromagnetic waves can be absorbed.

The invention relates to the technical field of fireproof materials, and discloses a fireproof plugging material and a preparation method thereof, and the fireproof plugging material comprises the following components by mass: 20-40 parts of a metal oxide enriched phosphate gelling system, 10-25 parts of an expansion main body, 5-15 parts of a synergistic fluxing and heat absorbent, 30-50 parts of an in-situ reactive aggregate, and 1-5 parts of reinforced fibers. According to the preparation method, a four-stage chain reaction system of expansion, synergistic fluxing, volatilization inhibition and in-situ welding is constructed, an oxygen-enriched phosphate gelling system provides BO volatilization inhibition capability and a POprecursor, boric acid provides a low-temperature endothermic effect and a BO precursor, the oxygen-enriched phosphate gelling system and the boric acid form a phosphorus borate eutectic melt at the temperature of 600-900 DEG C, and the low-temperature heat absorption effect and the BO precursor form a low-temperature heat absorption effect and a low-temperature heat absorption effect at the temperature of 600-900 DEG C; and the melt further reacts with wollastonite to generate a calcium-magnesium-boron-phosphorus-silicate glass phase, and a loose carbon layer obtained after expandable graphite is expanded is welded, so that the core contradiction that high expansion rate and high-temperature residual strength cannot be considered at the same time in the prior art is effectively solved.

The present invention provides a method for controlling the reactivity of a boric acid-free reactor in a secondary system of a pressurized light-water reactor, wherein: a turbine and a main water feeding system of a pressurized light-water reactor comprise a steam generator (S / G), a high-pressure turbine, a low-pressure turbine, a high-pressure feedwater heater, and a low-pressure feedwater heater; the high pressure turbine is provided with extracted steam ① and ② capable of heating feedwater, the low pressure turbine is provided with extracted steam ③ and ④ capable of heating feedwater, the high-pressure feedwater heater is provided with high pressure heaters ① and ② for receiving extracted steam from the turbines to heat feedwater, and a low-pressure feedwater heater is provided with low pressure heaters ③ and ④ for receiving extracted steam from the turbines to heat feedwater; and when operated with constant reactivity and temperature set as default values, the high-pressure heater ① receives extracted steam ② of the high-pressure turbine to heat feedwater, the high-pressure heater ② receives extracted steam ① of the high-pressure turbine to heat feedwater, the low-pressure heater ③ receives extracted steam ④ of the low-pressure turbine to heat feedwater, and the low-pressure heater ④ receives extracted steam from the low-pressure turbine ③ to heat feedwater.

This application belongs to the field of water quality testing technology, specifically relating to a method for testing ammonia nitrogen in wastewater from the hydrometallurgical process of laterite nickel ore. The method includes the following steps: adding sodium thiosulfate and zinc sulfate to the wastewater, adjusting the pH with a boric acid-sodium hydroxide buffer solution to pH 9.5, and allowing the solution to stand; filtering, taking an appropriate amount of filtrate into a colorimetric tube, and adjusting the volume, then adding potassium sodium tartrate and Nessler's reagent, mixing well, and allowing it to stand; measuring the absorbance, and calculating the ammonia nitrogen concentration in the wastewater based on the absorbance. This method can effectively eliminate the interference from high sulfate content and metal ions in high-sulfate industrial wastewater. The resulting colorimetric system is highly stable and has the advantages of being simple to operate and providing reliable results. It holds significant importance for the testing and treatment of wastewater from the hydrometallurgical process of laterite nickel ore.

The invention discloses a wax recovery treatment method which comprises the following steps: stirring, dissolving and precipitating wax in a sodium hydroxide solution to obtain supernate; adding the supernatant into boric acid, stirring to obtain jelly, filtering the jelly, washing, and drying to obtain a dried substance; mixing and stirring the dried substance and methanol, and drying to obtain a wax solid substance; and purifying the wax solid with a distillation extract of petroleum ether. According to the method, impurities in the wax are effectively removed, and the recovery purity and quality of the wax are improved, so that the service life of the wax is prolonged, the production cost is reduced, and the aims of saving resources and protecting the environment are fulfilled.

The invention provides a preparation process of a ceramic zinc borate flame retardant, and relates to the technical field of preparation of zinc borate flame retardants. The preparation process of the ceramic zinc borate flame retardant comprises the following steps: step 1, mixing boric acid and water according to a mass ratio of 1: (1.6-1.9), heating a preparation device to 70 DEG C, adding fatty alcohol-polyoxyethylene ether, and stirring until the fatty alcohol-polyoxyethylene ether is completely dissolved; 2, mixing zinc oxide and boric acid according to the mass ratio of 1: (4-5), stirring for 6-7 hours at the constant temperature of 70-85 DEG C, and then filtering and drying to obtain a zinc borate flame retardant; and 3, mixing the zinc borate flame retardant and the sodium sulfonate modified silane according to a mass ratio of 4: (0.6-1.2), and mechanically grinding to obtain the ceramic zinc borate flame retardant. The zinc borate flame retardant is uniformly mixed during preparation, does not settle and is thorough in reaction.

The application relates to the technical field of saline-alkali soil improvement, and particularly discloses a preparation method of a saline-alkali soil improvement slow-release fertilizer, which comprises the following steps: (1) uniformly mixing carbon powder, plant nutrient solution, molasses and seaweed acid powder, granulating the obtained mixture, mixing the obtained granules with carbon powder again to coat the granules, separating the granules, drying the granules, and obtaining a nutrient core; (2) uniformly mixing gypsum powder, carbon powder and water to form a coating slurry; coating the slurry on the surface of the nutrient core, and drying the nutrient core to obtain precursor granules; (3) uniformly mixing boric acid or lactic acid, carbon powder, gypsum powder and water to form a coating slurry; coating the slurry on the surface of the precursor granules, and drying the precursor granules to obtain the saline-alkali soil improvement slow-release fertilizer. The slow-release fertilizer prepared by the process can improve the exchange capacity of sodium ions in the soil, improve the soil nutrition degree and air permeability, and is beneficial to the growth of plants.

The invention relates to an efficient phosphorus removal embedded bioactive filler and a preparation method thereof, and belongs to the fields of sewage and wastewater treatment and low-carbon and water pollution control. Activated sludge of an urban sewage treatment plant is used as a bacterium source for separation, enrichment and directional culture of a phosphorus-accumulating bacterium flora. The preparation method comprises the following steps: preparing a colloidal embedding material from components (phosphorus-accumulating bacteria culture, PVA, diatomite, wooden activated carbon, calcium carbonate, trace elements and the like); extruding into a pipe strip shape by using an extruder; placing the extrudate in a saturated boric acid solution for cross-linking for 4 hours, washing with clear water, curing and cutting; and finally, soaking the obtained filler in a saturated phosphate solution for 4 hours, and cleaning with clear water to obtain the efficient phosphorus removal embedded bioactive filler. The biological phosphorus removal effect is enhanced by the phosphorus removal embedded bioactive filler, and the system has good mud-water separation performance, supports efficient recovery and resource utilization of phosphorus in water, and has both environmental benefits and economic benefits.