3138 results about "Thermal reaction" patented technology

The invention relates to a carbon quantum dot for strengthening and promoting growth of microalgae and application thereof. In the process of preparing the carbon quantum dots by a conventional hydrothermal method, a precursor mixture is subjected to acidification modification in advance, the pH value is adjusted to 2 by using nitric acid, and then a hydrothermal reaction is performed, so that the prepared carbon quantum dots have the capability of promoting the growth of microalgae. However, if other acids are adopted or pH adjustment is not in place, the effect cannot be achieved, and even the inhibition effect can be achieved. The obtained product is good in effect and stable in performance, no special reaction device needs to be additionally arranged in the acidification modification process, and the method has the advantages that operation is easy and convenient, raw materials are easy to obtain, and the process can be quantified; the method is simple and convenient in process operation, has universality and is easy for industrial production.

The invention discloses preparation of a bionic copper-based MOF nano-enzyme and application of the bionic copper-based MOF nano-enzyme in hydroquinone detection, and the bionic copper-based MOF nano-enzyme is prepared by the following method: dissolving terephthalic acid H2BDC and L-histidine His in N, N-dimethylformamide DMF to obtain a solution A; adding copper chloride CuCl2. 2H2O into the solution A obtained by C1, and stirring to form a uniform mixed solution; carrying out hydrothermal reaction on the mixed solution obtained from C2 for a certain time, centrifuging to obtain a solid precipitate, cleaning the solid precipitate, and drying to obtain the bionic Cu / His-MOF nano-enzyme; the invention also discloses an application of the sensor in hydroquinone detection. The bionic copper-based MOF nano-enzyme has the advantages of being simple and convenient to synthesize, high in substrate affinity, high in catalytic capacity and the like, and meanwhile, a rapid, sensitive and reliable HQ detection method is provided.

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 relates to the technical field of environmental chemistry, in particular to a double-vacancy Fe0. 96S (at) MoS2 nano composite material as well as a wet-type mechanochemical synthesis method and application thereof. The preparation method comprises the following steps: firstly carrying out co-ball milling by utilizing a wet mechanical chemical synthesis method to obtain a low-crystallinity Fe0. 96S (at) MoS2 precursor, and then carrying out further calcination treatment to accelerate the thermal reaction of the precursor, improve the crystallinity and remove redundant sulfur powder impurities, thereby obtaining the high-crystallinity Fe0. 96S (at) MoS2 nano composite material. Iron powder is introduced in the process of preparing MoS2 nanosheets from molybdenum powder and sulfur powder, the reaction activity of the molybdenum powder and the sulfur powder is improved and the formation energy of MoS2 is reduced by utilizing the characteristic of ball-milling heat release of the iron powder and the sulfur powder, the reaction barrier that MoS2 is difficult to prepare between Mo and S through a mechanical ball-milling process originally is broken, and the generation of the MoS2 nanosheets is promoted.

The invention discloses a method for preparing a carbon monoxide oxidation catalyst by using titanium gypsum and a waste hydrogenation catalyst, which comprises the following steps: crushing and pickling the waste hydrogenation catalyst, washing with clear water until the waste hydrogenation catalyst is neutral, and drying to obtain pretreated waste catalytic powder; uniformly mixing and stirring titanium gypsum and the pretreated waste catalytic powder to obtain gypsum doped pretreated waste catalytic powder; mixing a plant extract, crop powder and gypsum, doping the pretreated waste catalytic powder, uniformly stirring, feeding into mixed bacteria consisting of bacillus and aspergillus, and fermenting under a stirring condition to obtain a biological activated mixture; adding water into the biological activation mixture for hydrothermal reaction, filtering, separating and washing the material after the hydrothermal reaction is finished, roasting the washed filter cake, naturally cooling the roasted material, and crushing to obtain the carbon monoxide oxidation catalyst. According to the invention, the titanium gypsum and the waste hydrogenation catalyst are combined, and the biomass material is used for activating treatment, so that the use of chemical precursors is reduced, and the oxidation catalyst with excellent catalytic performance is obtained.

The invention discloses a preparation method of CoWO (cobalt tungsten oxide) modified NbOp-n heterojunction NbO5 / CoWO photocatalyst powder. The preparation method comprises the following steps: dissolving cobalt salt and tungsten salt in deionized water, stirring and mixing, carrying out hydrothermal reaction in an autoclave, washing and drying to obtain CoWO powder; the preparation method comprises the following steps: dissolving niobium oxalate and ammonium carbonate in deionized water, adding CoWO powder, carrying out a hydrothermal reaction in an autoclave, and carrying out washing and drying treatment to prepare NbO / CoWO photocatalyst powder. According to the method, the hydrothermal reaction temperature is regulated and controlled, and the mass ratio of raw materials is optimized, so that the catalyst forms a p-n heterojunction structure of NbOmicron flower loaded CoWOnano particles. The prepared catalyst has high norfloxacin wastewater degradation efficiency under visible light irradiation, has the advantages of simple preparation process, low reagent cost, high catalytic activity and good structural stability, and can be effectively applied to purification treatment of antibiotic polluted water.

The invention discloses a method for preparing a carbon monoxide normal-temperature oxidation catalyst based on electrolytic manganese residues and landfill leachate. The method comprises the following steps: soaking and purifying the electrolytic manganese residues with deionized water to obtain preliminarily purified electrolytic manganese residues; mixing aryl alcohol dehydrogenase, the preliminarily purified electrolytic manganese residues and the landfill leachate, and standing to obtain enzymolysis electrolytic manganese residue slurry; mixing fly ash, red mud and the enzymolysis electrolytic manganese slag slurry, uniformly stirring, drying and grinding to obtain a multi-component composite raw material; placing the multi-component composite raw material in low-temperature plasma equipment for irradiation to obtain a plasma activated composite material; and carrying out hydrothermal reaction on the plasma activated composite material to obtain a hydrothermal structure composite material, dipping the hydrothermal structure composite material in a solution containing cerium nitrate, drying, and roasting to obtain the carbon monoxide normal-temperature oxidation catalyst. The carbon monoxide normal-temperature oxidation catalyst with high activity and high moisture resistance is prepared by utilizing industrial wastes and landfill leachate enzymolysis derivative liquid.

The invention provides high-performance silver powder suitable for TOPCon battery fine grid silver paste, a preparation method of the high-performance silver powder and the silver paste, and belongs to the technical field of photovoltaic materials. The preparation method comprises the steps that a silver salt solution and a composite reducing agent are mixed, a first-stage hydrothermal reaction is carried out at the first temperature, a second-stage hydrothermal reaction is carried out at the second temperature, and silver powder is obtained after centrifugation, washing and drying; wherein the composite reducing agent is selected from a mixture of two of potassium tartrate, sodium sulfite and ferrous sulfate. According to the method, gradual growth and crystallinity improvement of silver crystal nucleuses are achieved through two-stage heating, particle aggregation or uneven morphology caused by rapid reduction is avoided, in addition, the adopted composite reducing agent combination is remarkably superior to a single reducing agent (such as ascorbic acid), and the morphology and particle size distribution of the silver powder can be more accurately regulated and controlled.

The invention discloses a monatomic-cluster double-active-site efficient ammonia cracking hydrogen production catalyst and a preparation method thereof, and belongs to the field of new energy catalytic materials. The catalyst comprises a 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier, a molybdenum disulfide nanosheet-loaded iron cluster carrier, monatomic active metal, cluster active metal and an auxiliary agent. Wherein the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier is prepared by the following steps: stirring 2-methylimidazole, zinc acetate and cobalt nitrate hexahydrate in methanol to generate a ZIF-8 precursor, washing, drying, and calcining in an H2 / Ar mixed atmosphere, thereby obtaining the 2-methylimidazole zinc derived nitrogen-doped carbon-loaded cobalt monatomic carrier; the molybdenum disulfide nanosheet loaded iron cluster carrier is prepared by carrying out hydrothermal reaction on ammonium molybdate and thiourea to generate MoS2 nanosheets and then loading iron clusters. The catalyst prepared by the invention has high activity, long service life and industrial applicability.

The invention discloses a preparation method and application of a biomass-based hard carbon negative electrode material based on a microwave solvothermal method, and the preparation method comprises the following steps: fully mixing a pretreated biomass carbon source with a sulfuric acid solution, transferring into a microwave hydrothermal reaction kettle, and carrying out microwave hydrothermal treatment to obtain a hydrothermal reaction product; carrying out solid-liquid separation on a hydrothermal reaction product, collecting filter residues, cleaning until filtrate is neutral, and drying to obtain a hard carbon precursor; performing high-temperature carbonization on the hard carbon precursor under the protection of an inert atmosphere to obtain the biomass-based hard carbon negative electrode material; according to the method, a mixed system of the biomass carbon source and sulfuric acid is pre-carbonized in a microwave solvothermal mode, uniform deliming of the biomass carbon source is achieved under the controllable acidity condition, and the uniformity of the biomass carbon source is improved; the pre-carbonized biomass material is subjected to high-temperature carbonization in an inert atmosphere, so that a hard carbon material with a moderate extension interlayer spacing can be obtained, and the synergistic improvement of high-rate charge-discharge performance and long cycle stability is realized.

The invention relates to the technical field of catalyst preparation, and discloses a preparation method and application of a ruthenium / cerium oxide composite nanofiber catalyst, and the preparation method comprises the following steps: (1) adding cerium salt and P123 into a mixed solution of DMF (Dimethyl Formamide) and an alcohol solvent according to a molar ratio of 1: (0.1-0.4), stirring and mixing, and carrying out hydrothermal reaction at 160-180 DEG C for 4-12 hours to obtain a spinning solution; (2) performing electrostatic spinning on the spinning solution to obtain a cerium fiber precursor; (3) pre-oxidizing the cerium fiber precursor, and then carrying out aerobic roasting to obtain a cerium oxide nanofiber carrier; and (4) dipping the cerium oxide nanofiber carrier in a ruthenium salt solution, drying, and performing hydrogen reduction to obtain the catalyst. According to the invention, the ruthenium / cerium oxide composite nanofiber catalyst with a unique cavity-containing nanofiber form is prepared by adopting an electrostatic spinning technology, and the ruthenium / cerium oxide composite nanofiber catalyst has good catalytic selectivity and stability in an ammonia decomposition reaction.

The invention discloses a self-lubricating aluminum coating and a preparation method thereof.The preparation method comprises the steps that molybdenum disulfide is pretreated through a silane coupling agent, tetraethoxysilane mixed liquor is added, the pH is adjusted to be 9-10, a water bath reaction is conducted, and molybdenum disulfide-silicon dioxide microcapsules are obtained after high-temperature strengthening treatment; respectively adding a zinc nitrate solution and a hexamethylenetetramine solution, adjusting the pH value to 10-11, carrying out a high-temperature and high-pressure hydrothermal reaction to obtain zinc oxide nanorods, and carrying out ball milling treatment on the zinc oxide nanorods, microcapsules, stearic acid and zirconium oxide balls under the protection of argon to obtain doped microcapsules; after raw materials are pretreated, the raw materials and a dispersing agent solution are added into a mixer respectively, spraying powder, a pretreated base body and the spraying powder are obtained after mixing treatment, spraying treatment is conducted on the surface of the base body through a plasma spraying method, and the self-lubricating aluminum coating is obtained after vacuum annealing treatment. Therefore, the obtained self-lubricating aluminum coating is low in friction coefficient, high in performance and excellent in self-lubricating property.

The invention provides a preparation method for preparing porous carbon based on an aerogel method, the porous carbon and application of the porous carbon, and belongs to the technical field of porous carbon material preparation. The preparation method comprises the following steps: mixing polyhydroxy phenol, aromatic aldehyde, acrylamide, graphene oxide and lithium salt according to a mass ratio of 100: (50-200): (5-30): (1-5): (1-5), carrying out hydrothermal reaction at 100-200 DEG C for 1-6 hours, and freeze-drying at-40 DEG C to obtain a hydrogel precursor; and carbonizing the precursor in organic heteroatom gas at 500-800 DEG C, mixing the intermediate with alkali according to the ratio of 100: (100-500), activating at 900-1100 DEG C, pickling and drying to obtain the porous carbon. The conductivity of the product is improved by means of graphene, lithium salt and heteroatoms, and the aerogel method obtains large aperture, has the characteristics of low impedance, high first efficiency and small charge-discharge expansion, and can be efficiently applied to silicon-carbon materials.

The invention belongs to the technical field of preparation and application of nano materials, and relates to a preparation method and application of amino-functionalized cerium oxide nano enzyme, and the preparation method comprises the following steps: adding 3-aminophenylboronic acid into a cerous nitrate hexahydrate aqueous solution to obtain a mixed solution; dropwise adding a sodium hydroxide aqueous solution into the mixed solution, carrying out hydrothermal reaction, cooling after the reaction is finished, centrifuging, washing and drying to obtain milk white powder, namely the amino-functionalized cerium oxide nano-enzyme. The boron element is introduced in the preparation of the cerium oxide nano-enzyme, and the amino-functionalized cerium oxide nano-enzyme is prepared by adopting a simple one-step hydrothermal synthesis method, so that the nano-enzyme has good phosphatase-like activity, has high selectivity and sensitivity to LPS, and is short in detection time, high in sensitivity, low in detection limit, simple in preparation process and high in preparation efficiency; the product is good in quality, high in stability, environment-friendly and extremely wide in market prospect.

The invention relates to a preparation method and a preparation device of isocyanate, and the preparation method comprises the following steps: carrying out cold reaction on a phosgene solution and an amine solution in a cold reactor to obtain an intermediate mixed solution; separating the intermediate mixed solution by adopting a cyclone, obtaining a carbamoyl chloride mixed solution from an underflow port of the cyclone, and obtaining an amine hydrochloride mixed solution from an overflow port of the cyclone; the carbamyl chloride mixed solution enters a first thermal reactor for thermal reaction to obtain a first reaction product, and the amine hydrochloride mixed solution enters a second thermal reactor for thermal reaction to obtain a second reaction product; mixing the first reaction product and the second reaction product in a staying reactor to obtain an isocyanate reaction solution; and carrying out post-treatment on the isocyanate reaction liquid to obtain the isocyanate. The method can reduce the generation amount of urea by-products, further inhibits the generation of other subsequent by-products, reduces the chromaticity of the product, and improves the quality of isocyanate.

The invention discloses a preparation method of a metal doped type hydroxyapatite nanoflower. The method specifically comprises the following steps: dispersing a calcium source and soluble metal salt into water, adding acid phosphate, urea and L-histidine, uniformly mixing, carrying out a hydrothermal reaction, mechanically stirring, filtering, washing, and drying a hydrothermal system precipitate to obtain the corresponding metal-doped hydroxyapatite nanoflower. Compared with the prior art, the metal-doped hydroxyapatite nanoflower prepared by the preparation method disclosed by the invention is directly assembled by nanosheets, and a single metal type can be doped in a customized manner. According to the method, water is used as a unique solvent, the use of an organic solvent is avoided, the pH does not need to be adjusted in advance, the technological process is simple, operation is convenient, equipment investment is small, and the method is suitable for industrial production.

The application provides a preparation method of a self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon composite material, a product and application, high-content nitrogen-doped porous carbon material is synthesized by inducing dicyandiamide molecules to undergo a supramolecular self-assembly process, and on this basis, a hydrothermal reaction is carried out to coat molybdenum sulfide sheet layer material on the surface, and finally, a self-heating coiling treatment is carried out to form a carbon-based electrocatalyst of the self-coiled structure molybdenum disulfide / nitrogen-doped porous carbon. Compared with a high specific surface area carbon-based catalyst, high doping concentration of nitrogen atoms can provide more electron-rich properties to facilitate the adsorption of substances, and the self-coiled carbon-based material can exhibit very excellent electrochemical performance, especially in the aspect of electrochemical hydrogen production. The preparation method is simple in operation, low in preparation cost and suitable for large-scale production.

The present application belongs to the technical field of nanometer material, and discloses a kind of sheet porous nanometer zinc oxide and its preparation method and application.The present application first prepares basic zinc carbonate precursor, then nitrogen is passed into, the pressure of system is >0.4MPa and <0.6MPa, hydrothermal reaction is carried out, and the reaction product is calcined, and sheet porous nanometer zinc oxide is prepared.The sheet porous nanometer zinc oxide prepared by the method of the present application has uniform and regular sheet porous structure, the holes on the sheet are uniform and regular, dense, small in particle size, large in specific surface area, and can be widely applied in the degradation of organic pollutants in photocatalytic system and the field of heavy metal adsorption.The preparation method of the present application can obtain raw materials easily and can be mass-produced.

The invention relates to a preparation method of a ZIF-67 derived cobalt-manganese catalyst and application of the ZIF-67 derived cobalt-manganese catalyst in catalytic oxidation of benzene, and belongs to the technical field of catalyst preparation. The preparation method comprises the following steps: preparing a ZIF-67 precursor; dispersing ZIF-67 in water to form a turbid liquid, and adding a potassium permanganate aqueous solution to carry out an etching reaction to obtain a mixed system; transferring the mixed system into a reaction kettle for hydrothermal reaction to obtain a black precipitate; and washing the black precipitate, drying, roasting, and grinding to obtain the ZIF-67 derived cobalt-manganese catalyst. According to the preparation method, the problem that residues are usually easy to remain in the conventional preparation method of the ZIF-67 catalyst is solved, and the Co-Mn8-T140 catalyst prepared by the preparation method disclosed by the invention can realize 90% of benzene conversion rate at the reaction temperature of about 210 DEG C under the reaction conditions that the air speed is up to 60000mL / (g.h), the benzene concentration is 1000ppm and the oxygen content is 20%.

The invention discloses a preparation method and application of a bimetallic sulfide / three-dimensional porous carbon catalyst, and relates to the technical field of electrolyzed water catalysts.The preparation method comprises the following steps that melamine sponge is cleaned, and the clean melamine sponge is obtained; the preparation method comprises the following steps: dissolving metal salt 1 and metal salt 2 in an ethanol aqueous solution, and adding alkali and an aniline monomer to obtain a precursor solution; completely soaking the clean melamine sponge in a precursor solution, carrying out constant-temperature hydrothermal reaction, and sequentially washing and drying to obtain the melamine sponge anchored with bimetal ions; introducing inert gas for protection, and performing high-temperature vulcanization treatment to obtain the three-dimensional porous carbon catalyst embedded with the bimetallic sulfide heterostructure. The catalyst comprises uniformly dispersed bimetallic sulfide nanoparticles and a spongy three-dimensional porous carbon carrier, shows excellent bifunctional catalytic activity and stability when being applied to an electro-catalytic water decomposition reaction, and has a wide application prospect.

The invention relates to a platinum-zinc alloy supported nitrogen-doped porous multi-layer carbon material and preparation and application thereof, the carbon material takes a rod-like graded porous carbon nanomaterial as a carrier, and platinum-zinc alloy particles and zinc monatomic are jointly supported on the surface of the carrier; the preparation method comprises the following steps: S1, adding zinc acetate and hexadecyl trimethyl ammonium bromide into DMF (Dimethyl Formamide), carrying out ultrasonic treatment, adding into a polyacrylonitrile solution, and stirring; s2, performing electrostatic spinning on the obtained spinning precursor solution; s3, adding the obtained nanofiber into a zinc acetate dihydrate solution, then adding a dimethylimidazole solution, carrying out hydrothermal reaction, soaking the obtained product in a chloroplatinic acid methanol solution, and then carrying out freeze drying; and S4, heating carbonization is carried out under the protection of an inert atmosphere, then annealing and cooling are carried out, and the PtZn-Zn-N4-HPCNFs material is obtained. Compared with the prior art, the catalytic performance and the like in the reaction processes of oxygen reduction reaction (ORR), chlorine evolution reaction (CER) and the like can be effectively improved.

The application discloses a preparation method of a manganese residue-based catalyst and application thereof, and belongs to the technical field of solid waste treatment. The application comprises the following steps: manganese residue is added into water and uniformly mixed to obtain a manganese residue turbid liquid; a soluble manganese salt solution and a potassium permanganate solution are mixed, and then added into the manganese residue turbid liquid to perform a hydrothermal reaction; and after washing and drying, a manganese residue-based catalyst is obtained. The catalyst prepared by using the manganese residue as a main raw material can efficiently degrade common organic wastewater, and the purpose of "waste treatment by waste" is achieved. In addition, the raw material manganese residue and the modifier are cheap and easy to obtain, the preparation method is simple, the production cost is low, and the application is beneficial to industrial popularization and use.

The invention discloses a preparation method and application of a metal sulfide adsorbent for adsorbing iodine and methyl iodide. The preparation method comprises the following steps: uniformly mixing an antimony source, a sulfur source, a deep eutectic solvent, polyamine and water to obtain a mixed solution; and transferring the mixed solution into a high-pressure reaction kettle, sealing, carrying out hydrothermal reaction at 110-220 DEG C for 2-9 days, cooling to room temperature to separate out crystals, and filtering, washing and drying to obtain the metal sulfide adsorbent. The invention also discloses application of the metal sulfide adsorbent in adsorption of iodine and methyl iodide. The metal sulfide adsorbent disclosed by the invention has a good adsorption effect on iodine and methyl iodide, and compared with an ethylenediamine-oriented metal sulfide adsorbent, the diethylenetriamine-oriented metal sulfide adsorbent has higher adsorption capacity on iodine and methyl iodide.

The invention belongs to the technical field of nano fluorescent powder, and particularly relates to Ca10 (PO4) 6 (OH) 2: RE < 3 + > nano fluorescent powder as well as a preparation method and application thereof. The preparation method comprises the following steps: mixing Ca (NO3) 2 and RE (NO3) 3 solutions in proportion to prepare a cation solution, dropwise adding a certain amount of H3PO4 to prepare a mixed solution, adjusting the pH value by using a charge compensation agent, uniformly stirring, performing ultrasonic dispersion, performing hydrothermal reaction on the obtained solution, and purifying to obtain the final product Ca10 (PO4) 6 (OH) 2: RE < 3 + > nano fluorescent powder. The charge compensation agent is at least one of KOH and LiOH. By utilizing the methods, the invention provides the Ca10 (PO4) 6 (OH) 2: RE3 + nano fluorescent powder taking K < + > / Li < + > as the charge compensation agent, and the Ca10 (PO4) 6 (OH) 2: RE3 + nano fluorescent powder has the advantages of thermal stability, color stability and high luminescence, and is suitable for temperature sensing, cheilogramma and anti-counterfeiting detection.

The invention belongs to the technical field of iron ion detection, and particularly relates to a rapid detection method for ferric ions in water, which comprises the following steps: a fluorescent probe preparation step: taking trihydrate of copper nitrate and tryptamine, adding into a centrifuge tube in sequence, adding ultrapure water, performing ultrasonic dissolution, transferring into a high-pressure reaction kettle, and performing hydrothermal reaction to obtain a fluorescent probe; cooling to room temperature, centrifuging the obtained yellow green solution in a centrifugal machine, and filtering the supernate through a microfiltration membrane to obtain a copper-doped carbon quantum dot CuCDs stock solution, namely the fluorescent probe; analyzing and determining Fe < 3 + >: taking the diluent of the prepared CuCDs solution, adding the diluent into a centrifugal tube containing a Fe < 3 + > standard solution, uniformly mixing, carrying out fluorescent quantitative analysis and detection, and exploring the change rule of the fluorescence intensity ratio of CuCDs; according to the rapid detection method for Fe < 3 + > provided by the invention, the synthesized CuCDs have high sensitivity, can realize on-site rapid detection of Fe < 3 + > in a water medium, and shows a wide application prospect in the field of environmental monitoring.

According to the red mud-based composite material and the preparation method and application thereof, bentonite, red mud and biomass are mixed in a proper amount of water according to the mass ratio of 1: 1: (1-10), and first suspension liquid is formed; drying the first suspension to obtain a precursor of the red mud-based composite material; the precursor is subjected to a carbon thermal reaction at 300-700 DEG C, ferric oxide in the red mud is converted into zero-valent iron, and the red mud-based composite material is obtained. The red mud is alkaline and promotes manganese ions to form insoluble precipitates, the unique structure and ion exchange capacity of the bentonite can effectively solidify the manganese ions, the biomass has a high specific surface area and a developed pore structure, and the manganese ions are physically adsorbed through Van der Waals' force and pore interception; ferric oxide in the red mud is converted into zero-valent iron in the carbothermal reaction process, and the zero-valent iron can catalytically oxidize ammonia nitrogen, so that the red mud-based composite material synchronously solves the problem of combined pollution of manganese and ammonia nitrogen in the soil.

This invention discloses a system and method for producing methanol by carbon dioxide hydrogenation. The system includes a feedstock turbine compressor, a first feedstock gas heat exchanger, a second feedstock gas heat exchanger, an adiabatic reactor, an isothermal reactor, a gas-liquid membrane separator, and a molecular sieve. By setting up an isothermal reactor and utilizing the heat from the product produced by the adiabatic reactor in separate streams, heat coupling between the two reactors is achieved. The unreacted feedstock gas remaining after the adiabatic first-stage reaction is circulated in the isothermal reactor, reducing the size requirements of the adiabatic reactor and improving the overall conversion rate of carbon dioxide. This application solves the problems of high energy consumption in the distillation of by-product water in the carbon dioxide hydrogenation to methanol process, large investment in traditional equipment, serious heat loss, and excessive circulating gas volume in existing technologies.

The invention belongs to the technical field of catalyst development, and relates to a cerium oxide-loaded non-noble metal catalyst for a carbon dioxide methanation reaction and a preparation method of the cerium oxide-loaded non-noble metal catalyst. The method comprises the following steps: firstly, obtaining a cerium oxide carrier through a hydrothermal reaction, secondly, impregnating non-noble metal nitrate serving as a precursor on the cerium oxide carrier through an impregnation method, and carrying out ultrasonic treatment, drying, calcining and other steps to obtain the cerium oxide supported non-noble metal catalyst. The prepared catalyst is low in cost and has excellent carbon dioxide methanation catalytic activity. By controlling the loading capacity and the loading type of the non-noble metal, a multi-site synergistic effect is realized, more active sites are exposed, and finally, the catalytic performance of the cerium oxide loaded non-noble metal catalyst for catalyzing methanation of carbon dioxide at low temperature is improved.

The invention belongs to the field of catalysts, and discloses a catalytic material based on lignin derivation and a preparation method and application thereof. The catalytic material is prepared from lignin derived carbon and NiFe LDH; the lignin derived carbon is inserted into the interlayer of the NiFe LDH and is coated on the surface of the NiFe LDH. The preparation method comprises the following steps: S1, dissolving a lignin derivative in water to obtain a first solution; s2, dissolving metal salt in water to obtain a second solution, wherein the metal salt comprises ferric salt and nickel salt; s3, mixing the first solution and the second solution, and adjusting the pH value to obtain a mixed solution; and S4, immersing the conductive current collector into the mixed solution for hydrothermal reaction, taking out the conductive current collector after the reaction is finished, and treating the conductive current collector to obtain the catalytic material. The obtained catalytic material is used for an anode oxygen evolution reaction in an electrolytic seawater environment, and has high activity, high stability and good chlorine corrosion resistance.

The invention relates to a nitrogen-tellurium co-doped carbon-loaded cobalt-lanthanum-gallium triatomic oxygen reduction catalyst as well as a preparation method and application thereof. The catalyst comprises a carbon carrier, doped nitrogen atoms, doped tellurium atoms, supported cobalt atoms, supported lanthanum atoms and supported gallium atoms, wherein the doping proportions of nitrogen atoms and tellurium atoms in the carrier are 3.63 wt%-6.96 wt% and 2.11 wt%-3.83 wt% respectively, the loading capacity of cobalt atoms is 0.86 wt%-1.05 wt%, the loading capacity of lanthanum atoms is 0.38 wt%-0.47 wt%, and the loading capacity of gallium atoms is 0.21 wt%-0.47 wt%; in the preparation method, the nitrogen-tellurium co-doped carbon carrier is fully anchored and coordinated to Co and La atoms through a hydrothermal reaction; and through freeze drying, collapse of a carbon skeleton of the catalyst can be effectively avoided. The obtained catalyst shows good oxygen reduction activity in a solid zinc-air battery, and the peak power density of the catalyst reaches up to 1.68 mW cm <-2 >.