750 results about "Molybdic acid" patented technology

The invention discloses an aerogel fire extinguishing agent for fire fighting, a fire extinguishing device and a releasing method.The aerogel fire extinguishing agent for fire fighting is prepared from, by mass, 8-12 parts of silicon dioxide aerogel powder, 40-45 parts of perfluorohexanone, 1.5-2 parts of zinc molybdate, 0.8-1.2 parts of nano cerium oxide, 2-3 parts of hyperbranched polysiloxane and 0.2-0.3 part of 18-crown-6 ether. Solid-phase silicon dioxide aerogel powder is matched with liquid-phase perfluorohexanone, zinc molybdate, nano cerium oxide, hyperbranched polysiloxane, 18-crown-6 ether and the like are compounded to serve as auxiliaries, efficient fire extinguishing can be conducted on precise electrical elements, residues are few, loss of instruments and equipment is small, and the fire extinguishing agent is suitable for being applied to the electrical field.

The invention relates to the field of anticorrosive paint, in particular to anticorrosive paint containing lanthanum cerium oxide and a preparation method of the anticorrosive paint. The invention relates to an anticorrosive coating containing lanthanum cerium oxide. The anticorrosive coating is prepared from the following raw materials: 28 to 45 parts of ultraviolet stable composite film forming matter, 5 to 10 parts of composite rare earth filler, 6 to 12 parts of supported synergistic antirust agent, 18 to 30 parts of mixed solvent, 0.8 to 2.5 parts of dispersing agent, 2.7 to 5.3 parts of functional additive and 0.5 to 1.2 parts of nano montmorillonite, the composite rare earth filler is lanthanum cerium oxide-hydroxyapatite composite powder with a core-shell structure, wherein lanthanum cerium oxide is used as a core, hydroxyapatite is used as a shell, and the thickness of the shell layer is 10-20 nm; the ultraviolet stable composite film forming substance comprises epoxy resin and ultraviolet grafting modified polyurethane in a weight ratio of 1: (0.6-2.2); the supported synergistic antirust agent is a mixture of mesoporous silica supported benzotriazole and zinc molybdate. And the obtained coating is high in adhesive force and long in service life.

The invention relates to the technical field of total phosphorus detection, in particular to a method for determining total phosphorus in water, which comprises the following steps: 1) digestion treatment: adding an oxidant into a water sample to be detected, and then performing microwave digestion treatment to obtain digested water; a molybdate reagent is added into the digested water, then an improved ascorbic acid solution is added, a chromogenic reaction is completed at the set temperature, and the improved ascorbic acid solution is obtained by mixing an ascorbic acid solution and sodium ethylene diamine tetracetate; measuring the concentration: measuring the absorbance value of the obtained color development product by using a spectrophotometer and a long-optical-path cuvette; and drawing a standard curve: using a phosphorus standard solution as a quality control sample, adding a plurality of calibration points in a low-concentration interval of 0.0-0.1 mg / L, carrying out colorimetric determination, and establishing quadratic equation fitting according to absorbance and concentration so as to determine the total phosphorus content of the water sample to be detected, and the method has the advantages of high sensitivity and good accuracy in total phosphorus testing.

The invention relates to a composite reverse osmosis membrane acidic cleaning agent, a preparation method and a cleaning process thereof, and belongs to the technical field of environment-friendly water treatment. The cleaning agent comprises the following components in percentage by mass: 4-8% of inorganic acid, 20-40% of organic acid, 1-3% of a surfactant, 0.5-1% of a chelating agent, 0.5-1% of a compound corrosion inhibitor and the balance of deionized water. The composite corrosion inhibitor is formed by compounding 2-mercaptobenzothiazole and the like according to a specific mass ratio, the molecular weight of polyaspartic acid is 5000, and the molar ratio of Zn to Mo in the zinc-molybdate compound is 2: 1. The preparation method comprises the following four steps: firstly preparing a compound corrosion inhibitor premix, then preparing an acidic base solution, and then sequentially adding the components to finally obtain the cleaning solution. According to the cleaning process, a cleaning agent and deionized water are mixed, the membrane flux recovery rate is larger than or equal to 85% through cleaning of a specific process, the reverse osmosis membrane can be effectively cleaned, and the performance of the reverse osmosis membrane can be recovered.

The invention discloses a high-initial-efficiency fast-charge graphite composite material and a preparation method thereof, the composite material is of a core-shell structure, the core is graphite, and the shell is lithium sulfonate / lithium molybdate and an amorphous carbon coating layer thereof; the mass ratio of the shell is 5-15 wt% according to the mass ratio of the composite material being 100%. The preparation method comprises the following steps: adding a molybdenum compound into a solvent to prepare a solution, adding graphite oxide, an inorganic lithium salt and a carbon nanotube conductive solution, reacting for 2-12 hours at the temperature of 50-120 DEG C, filtering, carbonizing filter residues to obtain a lithium molybdate conductive agent coated graphite material, and depositing a lithium sulfonate derivative on the surface of the lithium molybdate conductive agent coated graphite material by an atomization method to obtain the lithium molybdate conductive agent coated graphite material. The electron and ion conductivity of the material can be improved, and the rate and the first efficiency of the material can be improved.

The invention provides a visual detection method for interface water droplet induced electron generation in a high-temperature and high-pressure hydrocarbon-water system, and belongs to the technical field of in-situ analysis of electrons in mixed fluid. The detection method comprises the following steps: preparing a fused quartz capillary reaction cavity; loading a sample in a fused quartz capillary reaction cavity: sequentially inserting a thin capillary syringe filled with a silicomolybdic acid aqueous solution and a thin capillary syringe filled with a hydrocarbon liquid into the fused quartz capillary reaction cavity, and injecting the silicomolybdic acid aqueous solution and the hydrocarbon liquid; and carrying out visual detection on the water droplets. Through the visual fused quartz capillary thermal simulation experiment device, the color change of the water droplets at the interface of the silicomolybdic acid aqueous solution and the hydrocarbon fluid under the conditions of high temperature and high pressure is visually displayed, and the color characteristics of the water droplets are observed in real time by using a microscope, so that whether the water droplets induce electron generation or not is judged; the problem that electrons generated by water droplets cannot be directly observed and detected under high-temperature and high-pressure conditions is solved.

The invention relates to the technical field of electro-catalysis oxygen evolution, and particularly discloses a nickel-molybdenum foam composite oxygen evolution electro-catalysis material with high-valence nickel induced by molybdate radicals and a preparation method of the nickel-molybdenum foam composite oxygen evolution electro-catalysis material aiming at the problem that an existing oxygen evolution electro-catalysis material is insufficient in comprehensive performance or poor in performance stability. Soaking in a NaCl aqueous solution, and taking out; s2, mixing the nickel-molybdenum alloy foam with a K3 [Fe (CN) 6] aqueous solution, heating, and carrying out a hydrothermal reaction; and S3, finally, the nickel-molybdenum alloy foam is placed in the air or oxygen atmosphere and heated to 350-450 DEG C, heat preservation treatment is conducted for 2 h, and the nickel-molybdenum foam composite oxygen evolution electro-catalysis material is obtained. Molybdate anions are adopted as a sustainable induction source to be coupled with a NixOy / Fe3O4 heterogeneous interface, integrated construction is achieved on a nickel-molybdenum foam framework, and the nickel-molybdenum foam composite material has the advantages of being low in overpotential, high in stability, high in activity, high in binding force and long-term in durability and meanwhile being simple in process, easy to amplify on a large scale and the like.

The invention relates to the technical field of catalysts, in particular to a molybdenum-based oxide / carbide / GO heterojunction catalyst, a preparation method thereof and application of the molybdenum-based oxide / carbide / GO heterojunction catalyst in the field of fuel oxidation desulfurization. The preparation method comprises the following steps: S1, adding dimethylimidazole and metal salt into a graphene oxide aqueous solution, and stirring for reaction; s2, adding an aniline monomer and an initiator, dropwise adding phosphomolybdic acid as a molybdenum source, and centrifuging, washing and freeze-drying a product after the reaction is finished to obtain a polyaniline modified ZIFs / GO composite precursor adsorbed with the molybdenum source; and S3, performing high-temperature pyrolysis on the composite precursor in a protective atmosphere to obtain the catalyst. The invention provides a mode of constructing a molybdenum-based oxide / carbide heterostructure by enhancing the electron-donating capability and conductivity of a carrier through double-doped electron-donating elements, and develops a catalyst with high catalytic activity and low cost. The catalytic efficiency in the oxidative desulfurization process can be effectively improved.

The invention discloses cobalt molybdenum nitride / cobalt modified nitrogen-doped hollow carbon microspheres as well as preparation and application thereof, and relates to the technical field of electrochemical energy storage devices. Carboxylated polystyrene microspheres, soluble zinc salt and cobalt salt, phosphomolybdic acid and 2-methylimidazole are dispersed in methanol, a PMA (at) ZnCo-ZIFs / PS precursor of a spherical structure is obtained, then the PMA (at) ZnCo-ZIFs / PS precursor is placed in an inert atmosphere for carbonization treatment, and the cobalt molybdenum nitride / cobalt modified nitrogen-doped hollow carbon microsphere material is obtained. According to the structure and the preparation method, the nitride / metal cobalt component and the nitrogen-doped sodium affinity sites are introduced at the same time, uniform transportation and nucleation of sodium ions are effectively induced, sodium metal is guided to deposit in a specific three-dimensional structure, growth of sodium dendrites is effectively inhibited, volume expansion of metal sodium in the reaction process is relieved, the preparation method is simple and convenient, and the preparation method is suitable for industrial production. The cost is low, the electrochemical performance of the sodium metal battery assembled by using the composite material can be remarkably improved, and the composite material has a good large-scale application prospect.

The invention provides a double-defect-modified porous carbon nitride photocatalyst prepared by one step from ferromolybdic acid as well as a preparation method and application of the double-defect-modified porous carbon nitride photocatalyst. The catalyst is of a thin-layer porous structure, so that the specific surface area of the catalyst is increased, and more surface active sites are provided for adsorption and reaction; compared with pure g-C3N4, the visible light absorption intensity of the catalyst is obviously enhanced, due to the existence of surface N vacancies and defects formed by doping of metal oxides, effective charge separation is enhanced, the photon-generated carrier separation and transfer capacity is higher under visible light irradiation, and the catalytic activity is remarkably improved. When the photocatalyst is applied to degradation of tetracycline antibiotic pollutants, photocatalytic degradation of tetracycline can be realized only under the condition of low-power 5W LED visible light, the preparation process is simple, and the cost is lower.

The invention relates to the technical field of molybdenum slag resource recycling, in particular to a molybdenum slag resource recycling method which comprises the following steps: performing crushing, washing and drying pretreatment on molybdenum slag; naCl, KCl and NaF serve as fused salt, the fused salt, the cathode and the anode form a fused salt electrochemical system, the pretreated molybdenum slag is added into the fused salt for an electrochemical reduction reaction, and molybdenum in the molybdenum slag is reduced and separated out at the cathode; washing the precipitated metal molybdenum, and drying to obtain Mo powder. Resourceful treatment of the molybdenum-containing solid waste residues is achieved by adopting a molten salt electrochemical reduction recovery mode, and molybdenum elements are efficiently recovered into a metal state from complex molybdenum residues through electrochemical selective reduction in a molten salt system.

The invention discloses a preparation method of a chemical composite plating solution based on nano niobium carbide. The preparation method comprises the following steps: step 1, pretreating niobium carbide (NbC) powder; step 2, preparing a chemical plating solution, wherein every 1L of the chemical plating solution contains 30g of nickel chloride, 20g of sodium hypophosphite, 10g of sodium citrate, 5g of glycine, 10g of sodium acetate, 0.3 g of sodium dodecyl benzene sulfonate and 80mg of zinc molybdate; fixing the volume to 1L by using distilled water; 3, measuring the niobium carbide suspension liquid, mixing the niobium carbide suspension liquid with the chemical plating solution, and fixing the volume, so that the content of niobium carbide in the chemical composite plating solution is 0.01-0.3 g / L; adjusting the pH value of the solution to 5.8; according to the method, niobium carbide nanoparticles are added into the chemical composite plating solution, so that the surface of a plated part and metal gold are combined with the particles, and the hardness and wear resistance of a base material are effectively improved; the effect on a 60-80-micron nickel-phosphorus coating in the industry is achieved through the ultrathin chemical composite coating (8-10 microns), so that the corrosion resistance and the wear resistance of the product are enhanced.

The invention discloses a preparation method of chromium-free fingerprint-resistant liquid for an aluminized zinc plate, and relates to the technical field of metal surface treatment materials.The preparation method comprises the steps that a benzotriazole-cerium molybdate composite corrosion inhibition system is constructed, and multiple layers of adsorption films are formed through intermolecular pi-pi accumulation and rare earth ion coordination; meanwhile, a graphene oxide / nano silicon dioxide synergistic enhancement system is introduced, graphene sheet layers are directionally arranged to form a physical barrier, and micropores are filled with nano particles to improve compactness; and meanwhile, a lanthanide rare earth compound is adopted for modifying the flash-rust inhibitor, the stability of a passivation film on the metal surface is enhanced through the empty orbital characteristic of rare earth elements, the nanometer material gradient dispersion technology is combined with the ultrasonic-mechanical coupling dispersion technology, filler uniform distribution and interface bonding strengthening are achieved, and the fingerprint resistance, corrosion resistance and the like of the film layer are effectively guaranteed.

The invention provides a preparation method of a high-temperature-resistant graphite pipe for spectral analysis, and belongs to the technical field of spectral analysis, and the preparation method comprises the following steps: S1, preparing a high-purity graphite pipe matrix and carrying out surface activation treatment; s2, preparing composite sol, wherein the composite sol is formed by mixing silica sol, molybdate and phytic acid; s3, infiltrating the composite sol into the graphite matrix by adopting a vacuum-pressurization alternate impregnation process; s4, carrying out stepped heating heat treatment in an inert environment to form a SiC-MoSi composite reinforced phase; and S5, depositing a pyrolytic carbon layer on the inner wall of the graphite pipe. The silica sol, the molybdate and the phytic acid have a synergistic effect to form a SiC-MoSi composite phase, the phytic acid can prevent the molybdate from gathering and can promote the growth of SiC whiskers in heat treatment, so that the anti-oxidation temperature of the graphite pipe is increased, the temperature resistance and the heat stability of the graphite pipe are improved, and the anti-oxidation performance of the graphite pipe is improved. And finally, the use frequency of the graphite pipe is greatly increased.

The present invention relates to a Glycol based antifreeze liquid composition for combustion engines, electric vehicles, industrial and submersible motors. More particularly, the present invention relates to a Glycol based corrosion-inhibited antifreeze liquid composition, the said liquid composition comprises glycols, deionized water, alkali molybdate, alkali metal octoate or neodecanoate, rare-metal octoate or neodecanoate, dyes. The liquid composition of the present invention is environment-friendly, ready to use composition that will improve efficiency of combustion engines, industrial and submersible motors to the great extent and also provides excellent corrosion protection to the internal parts of the cooling system of combustion engines, electric vehicles and industrial and submersible motors.

The invention relates to a preparation method of an oxygen vacancy-rich bismuth molybdate / bismuth vanadate composite photo-anode and a product and application thereof, and belongs to the technical field of photoelectrocatalysis. The invention discloses a preparation method of an oxygen vacancy-rich bismuth molybdate / bismuth vanadate (Bi2Mo2O9 / BiVO4) composite photo-anode, which mainly comprises the following steps: immersing a fluorine ion-doped tin dioxide (FTO) conductive glass substrate into a Bi < 3 + > ion solution and an I <-> ion solution to form a bismuth oxyiodide (BiOI) film, dropwise adding a dimethyl sulfoxide solution of vanadyl acetylacetonate (VO (acac) 2), and putting into a muffle furnace to prepare the BiVO4 photo-anode. And then vertically immersing into a Bi < 3 + > ion solution and a Mo < 6 + > ion solution, and carrying out annealing treatment in an argon atmosphere to prepare the Bi2Mo2O9 / BiVO4 composite photoanode rich in oxygen vacancies. The Bi2Mo2O9 / BiVO4 material rich in oxygen vacancies is a metal oxide composite photo-anode, the photoelectrocatalysis efficiency can be improved, and hydrogen peroxide (H2O2) can be continuously generated in natural seawater through photoelectrocatalytic oxidation of water for a long time.

The invention provides an anodic oxidation passivation method of a neodymium-iron-boron permanent magnet zinc coating, which comprises the following steps of: performing electrochemical anodic oxidation by taking a neodymium-iron-boron permanent magnet with a zinc coating on the surface as an anode, a Pt sheet as a cathode and a passivation solution as an electrolyte, forming a passivation layer on the surface of the neodymium-iron-boron permanent magnet with the zinc coating on the surface, and cleaning and drying to obtain the neodymium-iron-boron permanent magnet with the zinc coating on the surface. A chromium-free passivation film is formed on the neodymium-iron-boron permanent magnet zinc coating, and passivation of the neodymium-iron-boron permanent magnet zinc coating is completed; the passivation solution is prepared from 10 g / L to 20 g / L of molybdate, 10 g / L to 15 g / L of ammonium fluozirconate, 1 g / L to 10 g / L of etidronic acid, 1 g / L to 10 g / L of sodium dihydrogen phosphate, 1 g / L to 10 g / L of nitric acid, 1 g / L to 10 g / L of phosphoric acid and the balance distilled water. According to the method disclosed by the invention, a complete, uniform and compact passivation film is formed on the surface of the zinc coating after passivation, the corrosion potential is improved while the corrosion current is effectively reduced, and the time for generating a rust spot in a salt spray test exceeds 72 hours.

The invention relates to the field of waste catalyst recovery, and discloses a method for recovering molybdenum from a waste hydrofining catalyst. The method comprises the following steps: (1) roasting the molybdenum-containing waste hydrofining catalyst in an inert atmosphere; (2) carrying out contact reaction on the roasted product obtained in the step (1) and an alkali solution, and then carrying out microwave treatment under the power of 300-900W to obtain a liquid product; and (3) evaporating and concentrating the liquid product under the condition that the pH value is 10-12 to obtain molybdate crystals. The method can obviously improve the recovery rate of molybdenum.

According to the low-temperature plasma activated water preparation system, the preparation method and the application, a direct-current voltage-driven air jet plasma generation device which is small and convenient and does not need a complex gas circuit is utilized in the preparation system, and air is adopted as working gas to treat an aqueous solution; an aqueous solution rich in active oxygen, active nitrogen and other active ingredients is efficiently generated, and the active ingredients have high oxidation-reduction potential and can effectively degrade PhSMe. The concentration of active particles in PAW is improved by optimizing the discharge voltage, the discharge time and the concentration of the sodium molybdate solution, so that the degradation effect of PhSMe is improved. An auxiliary agent sodium molybdate is introduced in the degradation process, and the degradation effect is two times higher than the pure PAW treatment effect.

The invention belongs to the technical field of metal surface rust prevention, and discloses a treating fluid for metal surface rust prevention and a preparation method of the treating fluid. The coating is prepared from components in parts by mass as follows: 5-15 parts of a silane coupling agent, 3-10 parts of nano titanium dioxide, 1-4 parts of benzotriazole, 1-4 parts of molybdate, 1-5 parts of a dispersing agent, 2-6 parts of a coalescing agent, 1-4 parts of a surfactant, 0.5-3 parts of an accelerant, 0.5-3 parts of citric acid, 1-5 parts of acetic acid and 50-80 parts of deionized water. The preparation method comprises the following steps: sequentially adding the components into a stirring processing container according to a certain sequence, and stirring at a certain speed to obtain a treating fluid; according to the technical scheme, through synergistic interaction of all the components, rust can be removed, a layer of compact and continuous protective film can be formed on the metal surface, a very good anti-rust effect is achieved, benzotriazole and molybdate can also form an adsorption film, metal is protected through a large number of films of various types, the anti-corrosion effect of the protective film is improved, and the service life of the protective film is prolonged. The anti-rust effect is greatly improved.

The invention relates to a halogen-free flame-retardant rubber conveying belt and a preparation method thereof, and belongs to the field of rubber composite materials. The conveying belt comprises the following raw materials in percentage by mass: 55-65% of a rubber matrix (20-50nm EPDM / SBR blend), 5-10% of microencapsulated red phosphorus (the particle size is less than or equal to 10 microns), 12-15% of modified magnesium hydroxide, 4-6% of a pentaerythritol / melamine cyanurate compounded charring agent, 5-10% of a zinc molybdate / zinc borate compound (the mass ratio is 3: 1) and 3-8% of a maleic anhydride compatibilizer. The halogen-free, environment-friendly and high-flame-retardant performance is achieved, meanwhile, the tensile strength is kept to be larger than or equal to 16 MPa, and the problems that a traditional flame-retardant belt is large in toxicity and poor in mechanical property are solved.

A process method for preparing acrylonitrile through propylene ammoxidation belongs to the field of chemical engineering, and is characterized in that in a corresponding device and a reaction system of the method, propylene, ammonia gas and air (in terms of O2) enter a fluidized bed reactor at 400-450 DEG C and 0.01-0.15 MPa for reaction according to a ratio of 1: (1-1.5): (2-10) at a weight hourly space velocity of 0.04-0.1 h <-1 >; the micro-sphere catalyst with the particle size of 40-60 microns in the dense-phase section and the dilute-phase section has alpha-phase bismuth molybdate, gamma-phase bismuth molybdate and lattice oxygen active centers and meets the chemical formula MoaBibNicWdTleVfPgSixOy, the atomic ratio a in the formula is 21-22, the atomic ratio b in the formula is 1.5-2, the atomic ratio c in the formula is 4-5, the atomic ratio d in the formula is 0.8-1, the atomic ratio e in the formula is 0.09-0.1, the atomic ratio f in the formula is 0.15-0.2, the atomic ratio g in the formula is 0.8-1, the atomic ratio x in the formula is 70-71, and y is the number of oxygen atoms needed by the atomic valence of all elements; a product enters a quench tower and a water absorption tower to be neutralized and cooled, and then passes through a recovery tower, an acetonitrile tower, a decyanation tower, a layering device and a finished product tower to realize separation of a water phase and an organic phase, so that crude acetonitrile, hydrocyanic acid and refined acrylonitrile are further obtained. The process is good in conversion degree and product selectivity, stable and reliable in operation, energy-saving and environment-friendly.

The invention belongs to the technical field of preparation of membrane materials and adsorption separation materials, and particularly relates to an MOFs / PVA cross-linked composite film as well as a preparation method and application thereof. The preparation method comprises the following steps: modifying MOFs with amino on the surface to enable the surface of the MOFs to have silicon hydroxyl, then mixing with polyvinyl alcohol (PVA), and heating and drying in a mold to obtain the MOFs / PVA cross-linked composite film. The cross-linked composite film provided by the invention is uniform and continuous, and the problem of poor dispersibility of the MOFs material in the mixed matrix film is solved. The film has good adsorption capacity on metal ions such as molybdate radicals, is high in hydrophilicity and still has a stable film structure in an acid environment, and an effective solution is provided for treatment of heavy metal pollution in industrial wastewater.

The invention relates to a co-doped carbon nitride / phosphomolybdic acid composite catalyst as well as a preparation method and application thereof. The composite catalyst is composed of co-doped carbon nitride and phosphomolybdic acid loaded on the co-doped carbon nitride; the co-doped carbon nitride is graphite phase carbon nitride co-doped with sodium, phosphorus and oxygen, and the co-doped carbon nitride is prepared by mixing a cyanamide compound and sodium hexametaphosphate and calcining at high temperature. The composite catalyst is used for photocatalytic production of hydrogen peroxide, and a method for photocatalytic production of hydrogen peroxide comprises the following steps: dispersing the co-doped carbon nitride / phosphomolybdic acid composite catalyst in an aqueous solution containing a sacrificial agent, and performing photocatalytic preparation of hydrogen peroxide under irradiation of a xenon lamp. Compared with the prior art, the preparation method provided by the invention is simple and good in repeatability, the charge separation efficiency of the prepared photocatalytic material is remarkably improved, and the photocatalytic hydrogen peroxide preparation efficiency is high.

The invention belongs to the field of material preparation, and particularly relates to a 2H-phase molybdenum disulfide crystal and a preparation method and application thereof. Comprising the following steps: mixing potassium molybdate and powdered sulfur, grinding, sintering in an Ar / H2 mixed atmosphere, and cooling to room temperature to obtain a product A; mixing the product A with sulfur powder, grinding, sintering in an Ar / H2 mixed atmosphere, and cooling to room temperature to obtain a product B; and sintering the product B in an Ar / H2 mixed atmosphere, cooling to room temperature, washing, and drying to obtain the 2H-phase MoS2 crystal. According to the preparation method disclosed by the invention, the purity and the crystal integrity of the 2H-phase MoS2 crystal are remarkably improved, and meanwhile, the interlayer spacing of the 2H-phase MoS2 crystal is optimized; in addition, the 2H-phase MoS2 crystal disclosed by the invention is used as a catalyst of a Li-CO2 battery positive electrode material, so that the electrochemical performance and the energy conversion efficiency of a Li-CO2 battery are remarkably improved.

The invention relates to the technical field of PE pipes, in particular to a PE pipe and a preparation method thereof. The PE pipe is prepared from, by weight, 40-60 parts of polyethylene, 6-8 parts of filler, 4-6 parts of auxiliaries, 4-6 parts of silicon dioxide, 2-4 parts of stabilizer and 2-4 parts of antioxidant. According to the invention, the filler is added in the preparation process of the PE pipe, and the coconut shell forms a porous carbon structure after being carbonized and ground, so that the interface bonding force between the materials can be effectively enhanced, and the coconut shell is uniformly dispersed in a PE matrix to bear part of external force and play a role in structure enhancement; thiomolybdate ions generated by thioacetamide and sodium molybdate can uniformly precipitate and grow on the surface and in pores of the coconut shell powder, and are tightly combined with the coconut shell powder, so that the structural stability of the PE pipe is effectively improved.

The invention discloses a tetrathiomolybdate intercalated ternary iron-magnesium-zinc layered double hydroxide catalyst, a preparation method thereof and an application of the tetrathiomolybdate intercalated ternary iron-magnesium-zinc layered double hydroxide catalyst in degrading azo dyes by activating peroxymonosulfate. According to the method, a carbonate intercalated ternary LDH precursor is synthesized through a hydrothermal reaction, interlayer anions are replaced with nitrate and tetrathiomolybdate through ion exchange, and the target catalyst is obtained. In the catalyst, a unique Fe-Mg-Zn ternary metal laminate and a MoS < 2-> intercalation structure cooperatively construct a multi-active center, and MoS < 2-> is used as an electron donor to promote cyclic regeneration of Fe < 3 + > / Fe < 2 + >. The catalyst keeps ultrahigh activity in a wide range of pH (potential of hydrogen) of 3-9, can completely degrade 10 mg / L of acid orange 7 within 5 minutes, and is stable in structure and low in metal dissolution risk. The problems of low activity, slow Fe < 3 + > reduction, metal ion dissolution and the like under neutral and alkaline conditions in an advanced oxidation technology based on peroxymonosulfate are solved, and the method has important application value in the field of printing and dyeing wastewater treatment.

The invention is suitable for the technical field of MCA, and provides an MCA / PA6 flame-retardant composite material and a preparation method thereof. Comprising the following components in parts by weight: 50-60 parts of MCA, 15-20 parts of PA6, 15-25 parts of long glass fiber, 3-8 parts of metal hydroxide, 0.5-1.5 parts of titanium dioxide, 0.3-0.6 part of an antioxidant, 1-2 parts of nano silicon dioxide, 1-3 parts of zinc molybdate, 2-5 parts of aluminum hypophosphite, 1-2 parts of silicone resin, 0.5-1 part of carbodiimide and 5-8 parts of a toughening agent. The MCA / PA6 flame-retardant composite material disclosed by the invention combines the flame-retardant property of MCA and the excellent physical property of PA6, so that the flame-retardant property of the material is remarkably improved, and meanwhile, the original characteristics of light weight, good toughness, chemical resistance, good durability and the like of PA6 are maintained. By adding the long glass fiber, the metal hydroxide, the titanium dioxide, the antioxidant, the nano silicon dioxide, the zinc molybdate, the aluminum hypophosphite, the silicone resin, the carbodiimide, the flexibilizer and other components, the strength, the heat resistance and the flame retardant effect of the composite material are further enhanced.

The invention discloses a Mo in-situ doped transition metal layered double hydroxide derivative catalyst. The Mo in-situ doped transition metal layered double hydroxide derivative catalyst is of a nanometer two-dimensional layered structure; nitrate, aluminum nitrate and molybdate are used as raw materials, and a series of nano flaky Mo-X / Al2O3 composite metal oxide catalysts with high activity, high selectivity and high stability are obtained through co-hydrothermal precipitation and one-step roasting reduction. The invention further discloses a preparation method and application of the Mo in-situ doped transition metal layered double hydroxide derivative catalyst. According to the invention, macromolecules in biomass or biomass waste can be effectively depolymerized and liquefied into high-calorific-value bio-oil, so that the effect of turning waste into wealth from oriented conversion of the waste into bio-fuel is realized, and meanwhile, the bidirectional positive effects of avoiding environmental pollution caused by direct emission of the biomass waste and realizing comprehensive utilization of resources are realized; and a path with more economic benefits is provided for conversion from biomass wastes to renewable energy sources.

The invention relates to the technical field of photocatalysts, and particularly discloses modified bismuth molybdate as well as a preparation method and application thereof. The preparation method comprises the following steps: preparing a homogeneous solution A containing a bismuth source; sO4 < 2-> and a molybdenum source are dispersed in a solvent according to the molar mass ratio of 1: 1-1: 10, and a homogeneous solution B is obtained; uniformly mixing the homogeneous solution A and the homogeneous solution B to obtain a solution C; and carrying out a hydrothermal method on the solution C to obtain the modified bismuth molybdate. By doping SO4 < 2-> into bismuth molybdate, the physicochemical properties of bismuth molybdate are optimized from multiple aspects, the photocatalytic activity of bismuth molybdate is improved, and excellent performance is achieved in the aspect of photocatalytic degradation of tetracycline in actual wastewater. The prepared modified bismuth molybdate not only can efficiently utilize visible light, but also is rich in oxygen vacancies on the surface, has high specific surface area, strong adsorbability and efficient photon-generated carrier separation efficiency, shows strong redox activity, and remarkably promotes pollutant degradation.