3767 results about "Phosphoric acid" patented technology

The invention discloses a fluoride salt-free nitrate-free cast iron enamel semitransparent glaze as well as a preparation method and application thereof, and belongs to the technical field of enamel. The semitransparent glaze is prepared from quartz, anhydrous borax, sodium carbonate, potassium carbonate, calcium carbonate, potassium feldspar, zinc oxide, lithium carbonate, zirconium silicate, titanium dioxide, aluminum oxide, trisodium phosphate, antimony oxide, magnesium carbonate and barium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The semitransparent glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, meanwhile, the product has good porcelain surface, luster and low-temperature firing adaptability, and is suitable for cast iron matrixes, the firing temperature is 740-760 DEG C, and the firing time is 2-3 hours. The method can be used for producing green and environment-friendly enamel products.

The invention belongs to the technical field of flame-retardant macromolecules, and particularly relates to intrinsic heat-conducting flame-retardant recycled epoxy resin and a preparation method thereof. The preparation method comprises the following steps: (1) carrying out a reaction on diethanol amine and 9, 10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO) to obtain an intermediate A; and (2) carrying out condensation polymerization on the intermediate A and phenylphosphonic acid to prepare the phosphate-terminated polyester flame retardant (PEF). And (3) carrying out epoxidation on 4, 4 '-biphenol to prepare the liquid crystal epoxy precursor LEP. And (4) mixing PEF, LEP and 3, 3 '-dithiodipropionic acid, and heating and curing to prepare the epoxy resin. The prepared epoxy resin has intrinsic heat conduction, flame retardance and efficient recoverability, and is a high polymer material with great potential.

The invention relates to a modified chrome corundum ramming material and a preparation and construction process thereof, and belongs to the technical field of chrome corundum ramming materials. The ramming material comprises a material A, a material B and a material C, wherein the material A comprises chrome corundum aggregate, titanium dioxide coated aluminum oxide microspheres, calcium sulfide dehydrate and silicon carbide porous microspheres; the material B comprises chromium oxide-zirconium oxide composite nano powder, sodium thiosulfate pentahydrate, tricalcium phosphate and hexagonal boron nitride flaky crystals; and the material C comprises an aluminum dihydrogen phosphate-magnesium hydroxide compound, a calcium fluoride-aluminum oxide co-melt and a silane coupling agent. The preparation process comprises the steps of pretreatment of all the components, preparation of composite powder and layered preparation. The construction process comprises the steps of pretreatment, wet-process mixing, layered ramming, negative-pressure permeation, medium-temperature reaction, spraying curing, integral firing and the like. Generation of hexavalent chromium can be effectively inhibited, the thermal shock resistance, the mechanical strength and the heat-conducting property of the material are remarkably improved, and the material has the advantages of being good in environment friendliness, long in service life, excellent in construction performance and the like.

This invention discloses a method for leaching lithium iron phosphate mixed powder with iron salts and recovering all components, belonging to the field of battery recycling. The invention uses an iron salt solution to leach the mixed powder, obtaining a lithium-containing leachate and leaching residue. Ferrous ions in the leachate are regenerated into ferric iron through acidification and oxidation, and recycled for leaching the next batch of mixed powder. After reaching a preset number of cycles, the leachate is used for re-leaching multiple batches of leaching residue to improve the lithium leaching rate. Ultimately, a enriched solution containing Li, Fe, Cu, and Al and graphite-containing iron phosphate residue are obtained. Copper is recovered from the enriched solution through iron powder replacement, and a high-purity lithium chloride solution is obtained through extraction and separation, while ferric chloride (recycled) and aluminum chloride crystals are also recovered. The leaching residue is treated with hydrochloric acid to obtain regenerated graphite, and the pH is adjusted with alkali to obtain high-purity iron phosphate. This method achieves full component recovery under mild conditions, reducing separation steps and chemical consumption through a "leaching-regeneration-leaching" cycle mechanism, thus achieving both environmental and economic benefits.

The invention discloses a method for preparing a carbon monoxide oxidation catalyst by using red mud and tungsten-molybdenum smelting slag, which comprises the following steps of: uniformly stirring and mixing the red mud and the tungsten-molybdenum smelting slag at a high speed, mixing with inorganic strong acid, and performing ultrasonic-assisted stirring to obtain acid leaching slag; the acid leaching residues are subjected to low-temperature plasma activating treatment and then microwave activating treatment, and microwave activated plasma residues are obtained; weighing tricalcium phosphate and microwave activated plasma slag, and uniformly stirring to obtain phosphorus-calcium doped activated slag; weighing an ammonium sulfide solution and the phosphorus-calcium doped activated slag, uniformly stirring, transferring the obtained sulfur-phosphorus-calcium doped activated slag into a hydrothermal reaction kettle, carrying out hydrothermal reaction, carrying out compression molding on the obtained hydrothermal composite material, and carrying out pyrolysis carbonization treatment in an inert gas atmosphere to obtain the phosphorus-calcium doped activated slag. The obtained pyrolysis composite material is soaked with a silane coupling agent solution and then roasted again, and the carbon monoxide oxidation catalyst is obtained. The catalyst prepared by the invention can realize efficient oxidation photocatalysis of carbon monoxide under the conditions of normal temperature and normal pressure.

The invention provides a biochar composite porous material for heavy metal contaminated soil remediation and a preparation method and application of the biochar composite porous material. The preparation method comprises the steps that biomass raw materials are subjected to high-temperature pyrolysis carbonization and then smashed, ground and sieved, and biochar powder is obtained; dispersing in a phosphoric acid solution to obtain a biochar solution, and filtering, washing and drying after a hydrothermal activation reaction to obtain activated biochar; dispersing in a chitosan solution, carrying out ultrasonic oscillation, filtering, washing and drying to obtain modified charcoal; mixing sodium bentonite, attapulgite and deionized water, uniformly mixing the modified charcoal, the functional slurry and a sodium carboxymethyl cellulose solution to obtain composite slurry, performing compression molding to obtain a green body, and then drying and calcining the green body. The biochar composite porous material prepared by the invention can simultaneously play multiple roles of physical adsorption, chemical chelation, ion exchange and the like in a heavy metal contaminated soil treatment process, so that efficient fixation of various heavy metal ions is realized.

The invention relates to the technical field of biochemical engineering, in particular to a method for preparing chiral alpha-trifluoromethyl alcohol by using imine reductase AtRedAm, trifluoromethyl ketone is reduced into corresponding chiral trifluoromethyl alcohol at an excellent conversion rate by using the imine reductase AtRedAm, and enantioselectivity is high. The reaction depends on an NADPH (Nicotinamide Adenine Dinucleotide Phosphate) coenzyme circulation system, 10% dimethyl sulfoxide is used as a reaction cosolvent, the reaction is carried out in a 100mM (pH = 7.5) phosphate buffer solution for 16 hours, the highest molar conversion rate reaches 99%, and the highest optical purity reaches 95%.

The invention provides a self-assembled monomolecular layer hole transport material based on a polycarbazole derivative and a preparation method and application thereof, and the self-assembled monomolecular layer hole transport material has a structure as shown in a formula I. The self-assembled monomolecular layer hole transport material is simple in structure, high in hole transport property, strong in interface passivation ability, high in thermal stability, and suitable for large-scale application; a polycarbazole derivative is taken as a mother nucleus, an alkyl / aryl chain is taken as a linking group, phosphoric acid is taken as an anchoring group, and rigid conjugated large-plane polycarbazole with a specific structure is taken as the mother nucleus, so that molecular accumulation can be improved, and the hole transport performance of the material can be improved. By taking a phosphate group as a tail end, single-molecule self-assembly can be realized, a perovskite interface can be passivated, the energy loss at the interface is reduced, and the battery performance is improved.

The invention relates to the technical field of refractory materials, in particular to a waste magnesia-calcium brick-containing refractory material and a preparation method thereof, and the waste magnesia-calcium brick-containing refractory material comprises the following components: composite aggregate, calcium aluminate cement, urea resin-aluminum dihydrogen phosphate, active alpha-Al2O3 micro powder, silica micro powder and sodium tripolyphosphate. In the room-temperature spraying maintenance and low-temperature working stage, hydration of free CaO in the waste magnesia-calcium bricks and erosion of OH <-> are prevented through the hydrophobic effect of fluorinated polyphosphazene and modified zirconium oxide sol, and the compatibility and wettability of the composite aggregate and cement paste are improved through carboxylic acid groups of carboxyethyl silanetriol and polyethylene glycol monomethyl ether. According to the present invention, with the temperature rising, the aluminum dihydrogen phosphate forms the viscous liquid phase to wrap the aggregate so as to provide the temporary protection, the temperature continues to rise, the zirconium oxide and the nanometer Al2O3 react with the CaO and the MgO to generate the CaZrO3 and the MgAl2O3, the aluminum dihydrogen phosphate reacts with the nanometer Al2O3 in the system to generate the AlPO4, and the CaZrO3, the MgAl2O3 and the AlPO4 form the multi-phase fire-resistant structure so as to further improve the fire resistance of the fire-resistant material;

The invention discloses an endoglucanase truncated mutant and an application of the endoglucanase truncated mutant. According to the invention, based on endoglucanase BsEGL from bacillus subtilis DLG, a truncated mutant is constructed by deleting a carbohydrate binding domain (CBM) of the endoglucanase BsEGL, and the truncated mutant is named as BsEGL [delta] CBM. Compared with BsEGL, the truncated mutant BsEGL delta CBM has the advantages that the thermal stability, the pH stability, the organic solvent tolerance and the like are remarkably improved, and the activity of degrading phosphoric acid expanded cellulose and corncob xylan is obtained. In addition, the enzymatic activity of the truncated mutant BsEGL delta CBM is remarkably improved by 6.41%, and the catalytic efficiency is remarkably improved. Due to the characteristics, the mutant can be suitable for industrial processes such as feed processing, papermaking, biological energy sources, spinning and food brewing, and is particularly suitable for enzyme catalytic reaction under extreme environments such as high temperature and low pH. The invention provides an enzyme preparation tool with excellent performance for efficient degradation of cellulose biomass, and has important application value.

The invention relates to the technical field of metal material hot working, and discloses a hot-rolled coiled plate production process which comprises the following steps: preparing a reaction type protective agent, the high-temperature-resistant coating is prepared from the following raw materials in parts by weight: 20 to 40 parts of tetraethoxysilane, 5 to 15 parts of triethyl phosphate, 1 to 5 parts of triethyl borate, 0.5 to 2.0 parts of cerous nitrate (III) hexahydrate, 0.1 to 1.0 part of lithium acetate and 0.01 to 0.05 part of vanadyl acetylacetonate (IV). Coating the surface of a hot-rolled plate blank with the protective agent; the coated plate blank is heated in a heating furnace, so that the protective agent forms a molten-state protective layer in situ; carrying out hot rolling on the plate blank with the molten protective layer; and cooling and coiling the hot-rolled steel strip. In the whole heating and hot rolling process, the molten protective layer isolates the contact between the steel and the oxidizing atmosphere, so that the generation of oxide scales is fundamentally inhibited, the production process is simplified, and the metal yield is increased.

The invention belongs to the technical field of traditional Chinese medicine detection, and discloses a detection method for a characteristic spectrum of Uighur medicine Kspecific heat extracting tablets and application of the detection method. The detection method provided by the invention comprises the following steps: preparing a test sample solution by taking a 75% methanol solution as a solvent, and determining the test sample solutions prepared from different batches of test samples by adopting ultra-high performance liquid chromatography to obtain a characteristic spectrum; the chromatographic conditions of the ultra-high performance liquid chromatography are as follows: a chromatographic column is a C18 chromatographic column, a mobile phase A is acetonitrile, a mobile phase B is a 0.1 vol% phosphoric acid solution, and the flow velocity is 0.25-0.35 mL / min; the detection wavelength is 0 to 18 minutes, and the wavelength is 327 nm; the time is 18 to 28.5 min, and the wavelength is 254 nm; when the time is 28.5 to 37.6 minutes, the wavelength is 242 nm; after 37.6 to 70 minutes, the wavelength is 210 nm; the sample size is 1 microliter, the column temperature is 20-40 DEG C, and gradient elution is carried out. The invention provides a more scientific identification and quality control method for the Kespecific heat tablets.

The invention discloses fluoride-salt-free and nitrate-free high-temperature acid-resistant translucent glaze for steel plate enamel as well as a preparation method and application of the translucent glaze, and belongs to the technical field of enamel. The semitransparent glaze is prepared from quartz, anhydrous borax, titanium dioxide, trisodium phosphate, potassium carbonate, lithium carbonate, aluminum oxide, zinc oxide and sodium carbonate according to a specific mass ratio. The preparation method comprises the steps of raw material mixing, high-temperature melting under a pure oxygen condition, wiredrawing detection, quenching and the like. The semitransparent glaze is completely free of fluoride salt and nitrate, the problems of fluoride emission and environmental protection equipment blockage are avoided from the source, the fluorine content of the product is not detected through detection, the product meets the requirements of European Union REACH regulations, meanwhile, the product has good porcelain surface, luster and firing adaptability, is suitable for a steel plate matrix, has the firing temperature of 840-880 DEG C and the firing time of 820-830 minutes, and is suitable for a steel plate. The method can be used for producing green and environment-friendly enamel products.

The invention relates to the technical field of polyurethane impermeable materials, and particularly discloses a high-molecular impermeable material with oil resistance and impermeability as well as a preparation method and application thereof, and the high-molecular impermeable material comprises the following components in parts by weight: 120 parts of a polyurethane prepolymer, 20-45 parts of a diluent, 10-30 parts of an auxiliary agent, 15-20 parts of a micro-powder filler, 10-15 parts of carboxymethyl cellulose and 3-8 parts of dibasic hydrogen phosphate; wherein the polyurethane prepolymer is prepared from a diisocyanate compound and polyether polyol through a reaction; wherein the micro powder filler is a mixture of sodium acrylate hydrogel micro powder and sodium alginate hydrogel micro powder; wherein the dibasic hydrogen phosphate is monovalent ion salt. The high-molecular anti-seepage material has excellent anti-seepage performance in an oil storage environment, has relatively high adhesive force, and can be suitable for grouting in a humid environment; and water resistance and oil resistance of an underground water-sealed stone cavern oil depot environment can be better realized.

The invention discloses a preparation method of a lithium iron phosphate positive electrode material, three iron sources with different forms and different particle sizes participate in preparation of the lithium iron phosphate positive electrode material, and gradation is formed to improve the compaction density and rate capability of the material. The EDTMPA reduces the viscosity of the slurry, is anchored on the surface of FePO4 particles through strong adsorption, inhibits particle aggregation through steric hindrance and electrostatic repulsion effect, and introduces hydrophilic groups to enhance wettability, reduce the viscosity of the system, optimize dispersion stability, accelerate particle crushing and refining, reduce the particle size and shorten the grinding time; in the sintering process, a reducing agent is generated through pyrolysis to inhibit too fast oxalic acid decomposition to cooperate with the generated reducing gas, Fe < 3 + > is completely reduced, the reduction temperature is reduced to inhibit grain growth, and the grading effect between large and small particles is improved; in addition, an N-doped carbon coating layer is formed through high-temperature cracking, pores are filled with residual carbon generated through decomposition of ferrous oxalate, the coating density is improved, the carbon-coated graphitization degree is improved, and then the electronic conductivity and the rate capability of the material are improved.

The invention discloses a method for constructing a dual-mode sensor through smartphone-assisted surface molecular imprinting for detecting diphenyl phosphate and application of the dual-mode sensor, and belongs to the technical fields of biochemical analysis, functional nano materials and life science. In synthesis, solubility and selectivity of a target object and photo-initiation efficiency in a polymerization process are optimized, and diphenyl phosphate molecularly imprinted nano-enzyme MIPs is rapidly prepared through a molecular imprinting technology; in the detection, H2O2 and 3, 3, 5, 5-tetramethyl benzidine TMB are catalyzed by peroxidase-like activity of Fe and N-CDs to generate a chromogenic reaction and an inner filter effect of oxTMB is used for inhibiting a fluorescence signal, dual-signal cross validation is realized in cooperation with a smart phone, and the colorimetric-fluorescence sensor for detecting diphenyl phosphate is constructed. The sensor has specific recognition selectivity and binding affinity of diphenyl phosphate, is simple to operate and low in cost, can realize sensitive detection of diphenyl phosphate in a wide linear range, has the detection limit as low as 16 pg / mL, and is suitable for field analysis of trace DPhP in a complex water environment.

The invention discloses a multi-network anti-freezing hydrogel electrolyte, a preparation method thereof and application of the multi-network anti-freezing hydrogel electrolyte in an electrochemical device. The hydrogel is prepared by using polyvinyl alcohol (PVA) and polyacrylamide (PAM) to form a basic network skeleton, introducing phytic acid, ethylene glycol and lithium / zinc bimetal salt (Li2SO4 / ZnSO4), and carrying out thermal initiation polymerization and freeze thawing. The hydrogel prepared by the invention has a multiple physical cross-linked network formed by polymer molecular chain entanglement, hydrogen-bond interaction among functional groups and metal coordinate bonds constructed between phosphate groups and divalent metal ions, so that the hydrogel electrolyte has excellent mechanical properties. Due to introduction of ethylene glycol, formation of ice crystals is effectively inhibited, and the hydrogel is endowed with excellent anti-freezing performance; the high-concentration Li < + > and Zn < 2 + > ensure the high ionic conductivity. The supercapacitor assembled by using the hydrogel electrolyte shows relatively high specific capacitance and good capacitance retention rate under bending and freezing conditions, and has good electrochemical properties and safety performance.

The invention discloses an antistatic PET dust-free film and a preparation method thereof, and relates to the technical field of high polymer materials. When the antistatic PET dust-free film is prepared, firstly, 6-bromohexanoic acid reacts with 4-imidazole-1-butyric acid, and then is subjected to ion exchange with potassium hexafluorophosphate to prepare diacid imidazole hexafluorophosphate ionic liquid; the preparation method comprises the following steps: enabling montmorillonite to react with tetraethoxysilane, 3-aminopropyltriethoxysilane and dodecyl triethoxysilane, so as to obtain modified montmorillonite; carrying out copolycondensation on terephthalic acid, the diacid imidazole hexafluorophosphate ionic liquid, ethylene glycol and the modified montmorillonite to prepare a modified polyester master batch; and carrying out melt blending on the modified polyester master batch and a chain extender, and carrying out blow molding to obtain the antistatic PET dust-free film. The prepared antistatic PET dust-free film has the advantages of being antistatic, flame-retardant, super-hydrophobic and low in dust adhesion rate.

The invention relates to the technical field of building materials, in particular to light water-resistant phosphogypsum-based cement concrete mortar and a preparation process thereof. The phosphogypsum-based cement concrete mortar comprises the following components: activated phosphogypsum, sulphoaluminate cement, magnesium phosphate cement, modified zeolite powder, lightweight aggregate, modified nano silicon dioxide, a core-shell toughening agent, a polycarboxylate superplasticizer and water, and the preparation method comprises the following steps: respectively preparing the activated phosphogypsum, the modified zeolite powder, the modified nano silicon dioxide and the core-shell toughening agent; the water resistance of the ardealite is improved through activating treatment, the interface bonding force and the structural compactness are enhanced through multi-component synergism by means of selective adsorption of the modified zeolite powder, the mechanical property of the lightweight aggregate is optimized, the toughness is improved through the core-shell toughening agent, and lightweight, high water resistance, stable performance and durability improvement of the mortar are achieved; the requirements of complex building scenes are met, and environment-friendly and practical values are achieved.

The invention relates to the technical field of production of dipotassium phosphate, discloses a process method for continuously producing food-grade anhydrous dipotassium phosphate, aims to obtain a food-grade anhydrous dipotassium phosphate product through a drying reaction in a rotary polymerization furnace by a one-step method, and effectively solves the problems of multiple control procedures, complicated process control and high production cost. The coke content is greatly reduced under the condition of ensuring the dipotassium phosphate content.

The invention relates to the technical field of inorganic compound preparation, and particularly discloses a method for preparing high-purity iron phosphate through low-temperature acidolysis of phosphated residues, which comprises the following steps: washing, drying and crushing the phosphated residues to obtain phosphated residue powder; carrying out low-temperature acidolysis reaction on the phosphated residue powder and inorganic acid in an aqueous medium at 60-90 DEG C to obtain an acidolysis solution; adding an oxidizing agent into the acidolysis solution, adjusting the pH value of the system to 2.5-4.5 at 65-85 DEG C, carrying out oxidation impurity removal, and filtering to obtain an iron-containing phosphate solution; and selectively supplementing an iron source according to the molar ratio of iron to phosphorus in the solution, adjusting the pH value to 1.0-3.0, and carrying out precipitation reaction at 65-75 DEG C to generate iron phosphate. According to the method, low-energy-consumption resource utilization of the phosphated residues is achieved by combining low-temperature acidolysis with oxidation impurity removal and component regulation and control, the product purity meets the battery-grade requirement, and the method is suitable for preparing the lithium battery positive electrode material precursor.

The invention belongs to the technical field of flame-retardant materials, and particularly relates to a prismatic aluminum hypophosphite compound as well as a preparation method and application thereof. The prismatic aluminum hypophosphite compound is prepared from aluminum hypophosphite, layered montmorillonite and nano silicon dioxide, and the weight percentage of the layered montmorillonite is 0.043 to 0.087 weight percent and the weight percentage of the nano silicon dioxide is 0.0036 to 0.0181 weight percent based on 100 weight percent of the aluminum hypophosphite; the particle size D10 of the prismatic aluminum hypophosphite compound is 1-3 microns, the particle size D50 of the prismatic aluminum hypophosphite compound is 5-8 microns, the particle size D90 of the prismatic aluminum hypophosphite compound is 10-15 microns, the particle size D97 of the prismatic aluminum hypophosphite compound is smaller than 20 microns, and the prismatic aluminum hypophosphite compound is of a single prismatic crystal structure or a regular structure in which a plurality of prismatic crystals are mutually embedded. The prismatic aluminum hypophosphite compound provided by the invention has a specific morphology and is especially suitable for a polyurethane flame-retardant system.

The invention discloses preparation of a phosphate radical modified carbon quantum dot nickel-based catalyst and application of the phosphate radical modified carbon quantum dot nickel-based catalyst in alkaline seawater electrolysis, and belongs to the technical field of hydrogen production through electro-catalysis and seawater electrolysis. The preparation method of the phosphate radical modified carbon quantum dot nickel-based catalyst comprises the following steps: mixing citric acid and urea in water to obtain a carbon quantum dot precursor solution; and mixing the carbon quantum dot precursor solution, phytic acid and a nickel substrate, and reacting to obtain the phosphate radical modified carbon quantum dot nickel-based catalyst. The phosphate radical modified carbon quantum dot nickel-based catalyst is designed by introducing a composite modification layer of carbon quantum dots and phosphate radicals on the surface of a nickel substrate, and the phosphate radical modified carbon quantum dot nickel-based catalyst has an obvious promotion effect on the OER activity through the synergistic effect of PO4 groups and CDs in the phosphate radical modified carbon quantum dot nickel-based catalyst; therefore, the catalyst can show excellent oxygen evolution reaction activity and long-term stability in alkaline seawater containing Br <-> and Cl <->.

The invention discloses a halogen-free compound flame retardant and application thereof in an antistatic nylon 66 composite material, and belongs to the technical field of polymer composite materials. The halogen-free compound flame retardant is prepared by compounding 68 parts of an organic aluminum hypophosphite flame retardant, 20 parts of a nitrogen-phosphorus intumescent flame retardant, 10 parts of a two-dimensional layered inorganic substance and 2 parts of a coupling agent through a high-speed mixing and drying process. The halogen-free compound flame retardant is blended with nylon 66, reinforced fibers, an antioxidant and the like, and the composite material is prepared through melt extrusion. According to the compound system, the total dosage of the flame retardant is remarkably reduced, the V-0 flame retardant grade is still achieved under the condition that the thickness is 0.8 mm, and the limit oxygen index exceeds 32%. The composite material has excellent flame retardancy and antistatic property while maintaining good mechanical properties, is suitable for a high glass fiber content system, effectively solves the problems of high flame retardant addition amount, difficult processing, high cost and the like in the prior art, and has the advantages of simple process and excellent comprehensive performance.

The invention provides an application of inositol monophosphate in an enzyme catalysis reaction system for preparing inositol. The invention also provides a preparation method of the inositol, the starch is used as a substrate, glucan phosphorylase, glucose phosphate mutase, inositol-3-phosphate synthase and inositol monophosphate are added as enzyme catalysts to catalyze the substrate to generate the inositol, the inositol monophosphate is derived from Archaeoglobus fulgidus, the amino acid sequence is shown as SEQ ID NO: 12, or the amino acid sequence is shown as SEQ ID NO: 1, or the amino acid sequence is shown as SEQ ID NO: 2, or the amino acid sequence is shown as SEQ ID NO: 3, or the amino acid sequence is shown as SEQ ID NO: 4, or the amino acid sequence is shown as SEQ ID NO: 5, or the amino acid sequence is shown as SEQ ID NO: 6. The inositol monophosphate is derived from Thermococcus kodakarensis, and the amino acid sequence of the inositol monophosphate is as shown in SEQ ID NO: 13; or the inositol monophosphate is derived from Pseudothermotoga lettinae, and the amino acid sequence of the inositol monophosphate is as shown in SEQ ID NO: 14. Inositol-3-phosphate synthetase and inositol monophosphate with good performance are screened, high-concentration starch is efficiently catalyzed to be converted into inositol by a one-pot method in a whole-cell feeding mode, and NAD < + > and other coenzymes do not need to be used. Under a 60L reaction system, 200g / L of corn starch is catalyzed, the unit yield of the prepared inositol reaches 161g / L, and the method has a good industrial application prospect.

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 belongs to the technical field of preparation of phosphorus removal agents, and particularly relates to a composite phosphorus removal agent and a preparation method and application thereof. The composite phosphorus removal agent comprises a honeycomb carrier and microspheres, the microspheres are loaded on the honeycomb carrier; the microspheres are prepared from the following raw materials: polyvinylidene fluoride particles, graphene oxide, ZrOCl2 and phosphorus-accumulating bacteria. The composite phosphorus removal agent comprises a honeycomb carrier, microspheres and microcapsules, wherein the microspheres and the microcapsules are loaded on the honeycomb carrier; capturing phosphate radicals in a water body by the microspheres and carrying out biological phosphorus removal and adsorption phosphorus removal; the honeycomb carrier also has the effect of adsorbing phosphate; and the two synergistically remove phosphate in the water body, so that the phosphorus removal effect of the phosphorus removal agent is improved, and the burden of the water body is not increased.

The preparation method comprises the following steps: shredding a light fibrous plant raw material which is difficult to process to 1-5mm, adding a certain amount of lignin, fully mixing with diammonium hydrogen phosphate or ammonium dihydrogen phosphate, carrying out hot press molding at 130-190 DEG C by using a pelletizer to prepare heavy particles with the particle size of 8-10mm, and carrying out high-temperature sintering to obtain the columnar activated carbon for desulfurization and denitrification of the fibrous plant raw material, thereby obtaining the columnar activated carbon for desulfurization and denitrification of the fibrous plant raw material and the columnar activated carbon for desulfurization and denitrification of the fibrous plant raw material. Heating the heavy particles to 400-700 DEG C in a rotary furnace, carbonizing for 1-3 hours, introducing a mixed gas of water vapor and air, and carrying out segmented activation at 850-950 DEG C-1000 DEG C to prepare high-quality activated carbon with the iodine value of more than or equal to 950 mg / g; crushing activated carbon to 140-325 meshes, mixing the crushed activated carbon with the composite glue solution, adding a proper amount of water for kneading, and forming the mixture into 2-8mm columnar particles by a hydraulic granulator or a screw extrusion granulator; through drying at the temperature of 100-300 DEG C and heat treatment at the temperature of 700-900 DEG C in a nitrogen, water vapor or anaerobic atmosphere, a basic group generated by the binder in the heat treatment has a very strong chemical adsorption effect on acid gas, later-stage modification is not needed, and excellent desulfurization and denitrification performance is achieved.

The invention discloses a preparation method of monensin fermentation liquor, relates to the technical field of microbial fermentation, and aims to solve the problems of low titer and long period of the existing process. According to the method, streptomyces cinnamomi is taken as a strain, a culture medium with a specific formula is adopted, and fermentation is performed in three stages: in the first stage (0-30-50 hours), pH is not controlled; in the second stage, a phosphoric acid and compound oil mixed solution (accounting for 1-3% of the fermentation solution, and the compound oil contains 20-30% of peanut oil, 20-30% of corn oil and the like) is supplemented at a time; in the third stage, the pH is controlled to be 6.2-6.3, and soybean oil and sterile water are supplemented according to needs. The fermentation adopts a secondary process, the temperature is controlled at 30-33 DEG C, the dissolved oxygen is more than or equal to 35% and the like, the total duration is less than or equal to 320 hours, and the titer is more than or equal to 55000 mu g / ml. By optimizing the culture medium and precisely regulating and controlling, the element production capacity is improved, the method is suitable for industrial production of tanks of 50 L to 100 m < 3 >, the efficiency is improved, and the cost is reduced.

The invention relates to the technical field of material surface corrosion prevention, in particular to a spraying method for a heavy anti-corrosion coating of a port steel structure. The method comprises the following steps that (1) sand blasting derusting treatment is conducted on a steel structure base body, so that the cleanliness of the steel structure base body reaches the Sa2.5 level, and the roughness is controlled to range from 40 micrometers to 75 micrometers; 2) coating the treated substrate with epoxy zinc-rich primer, and doping graphene modified zinc powder accounting for 1-3% of the total mass of the primer to form a primer layer with a dry film thickness of 60-80 [mu] m; (3) after the primer layer is cured, the primer layer is coated with epoxy micaceous iron oxide intermediate paint, aluminum tripolyphosphate accounting for 2-5% of the total mass of the intermediate paint is further added into the epoxy micaceous iron oxide intermediate paint, and an intermediate paint layer with the dry film thickness being 150-200 microns is formed; 4, the middle paint layer is coated with weather-resistant finish paint, and a finish paint layer with the dry film thickness being 60-80 microns is obtained.According to the method, the adhesive force, chloride ion permeation resistance, salt fog resistance (larger than or equal to 3000 hours) and weather resistance of the coating are remarkably improved, the method is suitable for the harsh marine environment, and the service life of the steel structure can be prolonged to 20 years or above.