13 results about "Electron exchange" patented technology

The utility model provides a carbon black iodine absorption value measuring device which comprises a rotating wheel disc, a magnetic stirrer, a transmission filtering device and a reaction tank, a plurality of sample cups can be placed on the rotating wheel disc, after a mixed liquid sample is stirred by the magnetic stirrer, an iodine solution and a sodium thiosulfate solution are extracted by a plunger pump, and the iodine absorption value of the carbon black is measured. In the extraction process, carbon black in the iodine solution is filtered through the filter pipe, filtrate is added into the reaction tank and chemically reacts with the sodium thiosulfate, and the iodine ion electrode in the reaction tank can judge the end point of the reaction by detecting the electron exchange capacity of the iodine solution and the sodium thiosulfate in the reaction tank when the iodine solution and the sodium thiosulfate are subjected to oxidation-reduction reaction. And meanwhile, the measured current data is transmitted to a microcomputer for automatic processing, so that accurate carbon black iodine absorption value data is obtained. The problems that manual operation is low in efficiency and the precision is greatly influenced by human factors are solved, and the advantages of high efficiency and high precision are achieved.

This item is an electrochemical cell. An electrochemical cell is an item that generates electrical energy through a chemical reaction, or conversely, uses electrical energy to cause a chemical reaction. Specifically, it consists of at least two electrodes and an electrolyte, and utilizes an oxidation-reduction reaction that involves the exchange of electrons between the electrodes. Examples of electrochemical cells include batteries and electrolytic cells.

This invention discloses a method for monitoring liquid-gas conversion using artificial intelligence in nanofabrication. The liquid-gas converter comprises a cathode electron exchanger and an anode electron exchanger placed vertically, separated from left to right into a cathode gas chamber, a liquid flow controller within the liquid conversion chamber, and an anode gas chamber. The electron exchanger faces the central liquid conversion chamber and directly contacts the liquid flow controller. The other side of the electron exchanger faces the open gas chamber. By applying voltage to the anode and cathode electron exchangers, the liquid-to-gas conversion is transformed into gas. The liquid flow controller has numerous puncture channels on its surface, the dimensions of which are designed using critical surface area and surface adsorption force calculations. These puncture channels are patterned and manufactured using precision processes. The converter is equipped with an intelligent microprocessor and multiple sensors. A liquid-to-gas flow guide valve is placed on top of the liquid flow controller. Under the control of the intelligent microprocessor, the liquid-to-gas flow is guided from the reservoir to the liquid flow controller. The microprocessor handles the liquid flow guide valve and artificial intelligence machine learning calculations, which are also transmitted to a cloud computing server for further calculations.

This invention discloses a conductive filter material and its preparation method. The conductive filter material includes a carrier, the surface of which has a conductive layer formed by conductive particles. In this invention, the conductive filter material can directly utilize its inherent properties to provide an environment conducive to electron donor and acceptor exchange by bacteria, allowing reducing and oxidizing substances to exchange electrons. This enables substances requiring electron exchange energy to undergo continuous biochemical reactions under the action of bacteria, thereby avoiding secondary chemical pollution from oxides or reducing agents required for biochemical treatment and reducing pollutant treatment costs. The conductive filter material of this invention can be applied to biochemical treatment in various scenarios, with a wide range of applications. In this invention, cable bacteria can be used as the main bacteria in the biochemical reaction. Due to the conductivity of the conductive filter material surface, cable bacteria can be cultured, multiplied, and attached to the conductive filter material surface in large quantities, increasing the number of cable bacteria and thus improving biochemical efficiency.

The invention relates to the technical field of catalyst preparation, and discloses a polyphthalocyanine / metal oxide composite catalyst as well as a preparation method and application thereof. The composite catalyst comprises a carbon carrier and metal polyphthalocyanine loaded on the carbon carrier; wherein the carbon carrier is a carbon material modified by metal oxide nanoparticles. The polyphthalocyanine / metal oxide composite catalyst provided by the invention can form a double-electron exchange channel, can effectively stabilize a metal active site in the center of polyphthalocyanine through electron transfer, remarkably inhibits dissolution and inactivation of the polyphthalocyanine in a severe environment, and has high catalytic activity and high stability.

The application discloses a kind of off-site electrocatalytic reaction method and reaction system.The off-site electrocatalytic reaction method includes: electrolyte ion pair in battery system carries out electron exchange reaction with electrode, obtains oxidation potential or reduction potential;Obtain the electrolyte of oxidation potential or reduction potential enters the independent reaction system outside battery system, and carries out oxidation-reduction reaction with reactant in reaction system to obtain mixture containing reaction product;After separation, after oxidation-reduction reaction, electrolyte returns to the battery system again to obtain oxidation potential or reduction potential.The novel off-site electrocatalytic tandem reaction technology provided by the application can move the complex reaction involving gas, liquid, solid and other phases out of the electrode surface, and place the reaction process outside the battery, avoiding the contamination of reactants and / or products on the electrode, catalyst, separator, etc.;The reaction system built by the off-site electrocatalytic synthesis technology runs stably, can be used for basic theory research, and has practical application significance.

The invention discloses a preparation method of a Nia / Cobat Ti3C2Tx bimetal fused salt etched composite electrode material and application of the Nia / Cobat Ti3C2Tx bimetal fused salt etched composite electrode material to removal of fluorine ions in a water body, and belongs to the technical field of water treatment. In the preparation process of the MXene, a relatively safer, green and environment-friendly Lewis acid molten salt etching method is selected, and negative groups brought to the MXene by traditional fluorine-containing reagent etching are reduced. Meanwhile, due to the interaction of metal and the carrier, a large number of uniformly loaded Ni / Co metal nanoparticles or metal alloys are obtained on the surface of the prepared material, the interlamellar spacing of the MXene material is remarkably increased, more active sites are exposed, the ion and electron exchange capacity of the material is greatly improved, and the material shows excellent electrochemical performance; and the material is applied to a capacitive deionization technology, so that the capacitive deionization capability is effectively improved.

This invention discloses a functionalized MXene-supported metal oxide catalytic material, its preparation method, and its applications. The preparation method includes: fully contacting a pretreated metal substrate with a liquid-phase system containing MXene and metal ions and reacting at high temperature, followed by annealing in air to obtain the MXene-supported metal oxide material; and then subjecting it to electrochemical or chemical treatment to obtain the functionalized MXene-supported metal oxide catalytic material. In the functionalized MXene-supported metal oxide catalytic material of this invention, electron transfer occurs between the functionalized MXene and the metal oxide, promoting the formation of more active sites in the metal oxide that are conducive to catalyst-reactant electron exchange, thereby improving the activity of the oxygen evolution reaction (OER). Simultaneously, the functionalized MXene has abundant surface groups, which can generate strong chemical interactions with the metal oxide, improving the stability of the metal oxide in acidic media.

The invention provides a method for preparing gallium trichloride based on a hydrogen chloride gas method, and belongs to the field of gallium trichloride preparation. The method comprises the following steps: mixing metal inorganic salt with metal gallium to obtain a mixture; under the atmosphere of protective gas, hydrogen chloride gas is introduced into the mixture, heating is carried out, an oxidation-reduction reaction is carried out, and gallium trichloride gas is obtained; and cooling the gallium trichloride gas to obtain a gallium trichloride solid. The metal inorganic salt can be used as a reaction catalyst and directly participates in electron exchange on the surface of the metal gallium, the addition of the metal inorganic salt is equivalent to the construction of a micro electrode, the oxidation-reduction reaction can be enhanced, the electron transfer speed is obviously accelerated, and the reaction rate is further greatly improved. In practical application, after the metal inorganic salt is added, the preparation rate of the gallium trichloride is increased by 2-8 times compared with that of the gallium trichloride without the catalyst, and the purity of the finally obtained gallium trichloride can reach 3N-6N, so that the method for efficiently preparing the high-purity gallium trichloride is formed.

The invention relates to the technical field of target material preparation, and provides a nickel ferrite target material and a preparation method thereof.The preparation method comprises the steps that NiO powder and Fe2O3 powder are provided and sequentially subjected to mixed ball milling, drying and calcination treatment with a dispersing agent and a solvent, and NiFe2O4 calcined powder is obtained; the A-doped Fe3O4 powder, NiFe2O4 calcined powder, a dispersing agent and a solvent are mixed, ball-milled and dried, and mixed powder is obtained; a is selected from at least one of MnO2, CuO, CoO, Cr2O3 and MgO; and carrying out pre-pressing treatment and hot-pressing treatment on the mixed powder, and then machining to obtain the nickel ferrite target material. The A-doped Fe3O4 powder is introduced, and Fe < 2 + > and Fe < 3 + > exist on octahedral sites in a crystal structure of the A-doped Fe3O4 powder at the same time, so that electron exchange can be realized through an oxygen ion bridge, a conductive path is constructed in the material, the conductivity of the target material is improved, and the requirement of a direct-current sputtering process is met.

Electron exchangers are placed in the conversion cell and divide it into cathode gas chamber, liquid conversion solution chamber filled with a multiple track injection liquid controller, and anode gas chamber. Voltage is applied to the electron exchangers to convert the liquid conversion solution to gases, and gases are released directly to the gas chambers. On the surfaces of the single sheets of the multiple track injection liquid controller, there are many tracks and puncture channels that are designed by critical surface calculations, and manufactured with a precision technology. A computing engine connected to the cloud is responsible for artificial intelligence calculations, and it controls valves, sensors, servo motors, and enhance gas flow devices. In producing the same amount of final gases, our method is energy efficient.

The application relates to the technical field of target material preparation, and provides a nickel ferrite target material and a preparation method thereof, which comprises the following steps: providing NiO powder and Fe2O3 powder, and sequentially mixing, ball milling, drying and calcining the NiO powder and the Fe2O3 powder with a dispersant and a solvent to obtain NiFe2O4 calcined powder; mixing, ball milling and drying Fe3O4 powder doped with A, the NiFe2O4 calcined powder, the dispersant and the solvent to obtain mixed powder; A is at least one selected from MnO2, CuO, CoO, Cr2O3 and MgO; and the mixed powder is subjected to pre-pressing treatment and hot-pressing treatment, and then is machined to obtain the nickel ferrite target material. The Fe3O4 powder doped with A is introduced, Fe 2+ and Fe 3+ exist on octahedral sites in the crystal structure of the Fe3O4 powder doped with A, so that electron exchange can be realized through oxygen ion bridges, a conductive path is constructed in the material, the conductivity of the target material is improved, and the direct-current sputtering process requirement is met.

The application relates to the technical field of lithium ion batteries, in particular to surface-modified lithium iron phosphate and a preparation method thereof, a positive electrode material, a battery and application; the application is used for solving the problems of poor conductivity and low lithium ion diffusion coefficient of existing lithium iron phosphate; tin and vanadium are doped into the lithium iron phosphate, and the ion migration resistance is cooperatively reduced through tin-vanadium co-doping, so that the rate performance, electronic conductivity and discharge specific capacity of the material are improved; the lithium iron phosphate is coated with carbon and polypyrrole, and graphene is introduced into the material, so that the electronic conductivity is improved; the graphene is bridged with each other to form an electronic conduction network, and the rate performance of the material is significantly improved; the coating of the polypyrrole reduces the resistance between particles, accelerates the transmission speed of electrons between the particles, improves the electron exchange rate, forms a continuous conductive grid, improves the surface electronic conductivity, and improves the charge-discharge performance and cycle performance of the positive electrode material under high rate.