82 results about "Birnessite" patented technology

The invention relates to an air purification material and a preparation method and application thereof, belonging to the technical field of chemical catalytic decomposition, in particular belonging to the technical field of decomposition of formaldehyde pollutants in environment air. The air purification material comprises a base material and manganese oxide, wherein the manganese oxide is supported on the base material, the base material is honeycomb ceramics or a fiber material with a particle filtering function, and the manganese oxide is birnessite manganese oxide prepared from permanganate and oxalate. The air purification material can effectively decompose formaldehyde pollutants in indoor air and can rapidly and constantly remove the formaldehyde pollutants in indoor air at room temperature. The air purification material can be regenerated through heating, so that the service life of the material is prolonged and the practical application is facilitated.

The invention relates to an air cleaning material, and a preparation method and an application thereof, and belongs to the technical field of chemical catalytic decomposition. The air cleaning material comprise a base material and a manganese oxide loaded on the base material; the manganese oxide is a birnessite type manganese oxide prepared by performing in-situ reduction on a permanganate and a reducing agent; and the base material is filter cotton, non-woven fabrics, cotton cloth, gauze, or fiber with particle filtering function. The preparation method comprises the following steps: step 1, dissolving a quaternary ammonium salt and the permanganate in water, adding the base material; step 2, adding the reducing agent into the solution obtained in the step 1, mixing uniformly; step 3, heating the solution obtained in the step 2 at a constant temperature; and step 4, taking out the base material and drying to obtain the finished product. According to the technical scheme, the manganese oxide is simple loaded on the fiber material base material such as filter cotton and the like, so that the obtained low-wind-resistance cleaning material is capable of continuously rapid degrading formaldehyde and ozone in the air at room temperature; and the preparation method of the air cleaning material is simple and low in cost, and no other pollutions are introduced.

Disclosed is a preparation method of a hollow manganese oxide nanosphere of large specific surface area, comprising steps of preparing a silicon dioxide nanosphere, preparing a silicon dioxide composite nanosphere covered by manganese dioxide and preparing hollow manganese oxide nanosphere. Because the preparation method adopts the process steps, which are simple, the production cost is low; the prepared hollow manganese oxide nanosphere is tested by an X-ray diffraction instrument, a scanning electron microscope, a transmission electron microscope, a Fourier transform infrared spectrometer and a physisorption instrument; the hollow manganese oxide nanosphere belongs to natrium-manganese crystal phase and is characterized by spherical morphology, having particle sizes ranging from 300 to 450nm and large specific surface area, and can be used as electrode materials to produce electrochemical capacitors.

The invention provides a preparation method of a catalyst for ozone decomposition. The preparation method comprises the following steps: S1, adding a reducing agent into permanganate water solution, heating, and continuously stirring to obtain birnessite manganese dioxide; and S2, adding the birnessite manganese dioxide into an ammonium salt water solution, heating and continuously stirring to obtain the catalyst.

A secondary alkaline battery using manganese dioxide is described. The battery includes a mixed cathode material with birnessite-phase manganese dioxide or electrolytic manganese dioxide (EMD), a bismuth compound and a copper compound selected from the group consisting of elemental copper and a copper salt. In some embodiments, a conductive carbon and/or a binder may also be included.

The invention discloses a birnessite manganese oxide powder with ultrahigh specific capacitance characteristic as well as a preparation method and application thereof. The manganese oxide powder has an ideal chemical formula of M[2x]MnO[2+x], and in the formula, M is any combination of Li, Na and K positive ions and x is 0.1-0.5. The preparation method comprises the following steps: controlling the mole ratio of permanganate and organic fuel, and dropwise adding an organic fuel solution into a permanganate aqueous solution; heating in a muffle furnace to obtain the required birnessite manganese oxide powder. According to the birnessite manganese oxide powder disclosed by the invention, production raw materials are low in price, equipment is simple, the production efficiency is high, and the specific capacitance characteristic is excellent (the specific capacitance can reach 1,055F.g<-1> under the current density of 1A.g<-1>); the birnessite manganese oxide powder can be applied to the fields of supercapacitors, lithium/sodium/magnesium ion batteries, ion exchange, water photolysis and the like, and is wide in application range.

The invention discloses a method for preparing a potassium type birnessite manganese ore layered crystal potassium ion battery electrode material from a potassium salt and tetravalence manganite witha high-temperature solid-phase method together with an ion exchange method process. Due to adoption of the ion exchange process, the content of potassium ions in potassium type birnessite manganese ore can be increased, and properties of a potassium ion battery electrode are improved. The high-potassium type birnessite electrode material of water solution exchange is high in electric property, thecurrent density of the material is 16mA*g<-1>, the mass specific capacity of the material is up to 125mAh*g<-1>, and when the current density of the material is increased to 400mA*g<-1>, the mass specific capacity of the material is still maintained at 68mAh*g<-1>. After 50 times of circulation at a current density of 80mA*g<-1>, the mass specific capacity of the material is still maintained at 68mAh*g<-1>, and the capacity retention rate of the material is 79%. When being used as a potassium ion battery electrode material, a sample prepared with the method is excellent in rate capability andcirculation stability.

The invention relates to a chargeable and dischargeable aqueous aluminum ion battery and a preparation process thereof, belonging to the technical field of batteries. The aqueous aluminum ion batterymainly comprises a cathode, an anode, an electrolyte and a diaphragm, wherein the cathode material is birnessite manganate, the anode is metal aluminum and alloy thereof, the electrolyte is an aluminum trifluoromethanesulfonate aqueous solution, and the cathode, the anode, the electrolyte and the diaphragm form a primary battery system. The interlayer spacing of the birnessite manganate MxMnOy.nH2O (M is a metal cation) is about 0.72nm, and lattice water exists between the layers. The secondary aluminum ion battery is high in capacity (530mAhg<-1>, relative to the birnessite manganate), is proper in discharge potential platform (1.0-1.4V vs. A13+/Al), is very good in the corresponding cathode capacity density (530-740Wh g<-1>), is wide in material source, easy to prepare, simple to assemble, low in cost and green and environmental.

The invention relates to a preparation method of a birnessite type manganese oxide catalyst material and application thereof in charcoal smoke particle catalytic combustion. According to the birnessite type manganese oxide catalyst preparation method disclosed by the invention, the material is a manganese oxide catalyst material with a birnessite type structure, a manganese oxide material is K2Mn4O8, and the manganese oxide catalyst is a catalyst material with the molar ratio of K to Mn to O as 2 to 4 to 8. According to the manganese oxide catalyst, potassium permanganate and glucose which arelow in cost are utilized as raw materials; by means of a simple preparation method of using the glucose as a reducing agent, the birnessite type K2Mn4O8 manganese oxide catalyst with higher oxidationreduction ability is further obtained. The preparation method disclosed by the invention avoids special equipment and severe conditions, and the prepared birnessite type manganese oxide catalyst hasthe advantages of simple preparation technology, strong practicability and easiness in achieving large-scale production.

The present invention relates to a multi-walled carbon nano-tube supported manganese oxide-based catalyst preparation method, wherein an active component manganese oxide is loaded on multi-walled carbon nano-tubes by using an oxidation reduction method, and the catalyst manganese-based oxide obtained after drying is loaded on the carbon nano-tubes in a scaly manner, such that the specific surface area is increased, the relatively more active sites are easily exposed compared with the loading-free birnessite type manganese oxide, and the NO catalytic oxidation reaction activity under the normal temperature and normal pressure and the long-term stability are improved; and the process is simple, and the method can be used for the efficient purification treatment of the NO pollutants in parking areas, underground shopping malls and other enclosed spaces or urban highway tunnels, and has important social significance and practical application values.

The invention relates to a method for treating nuclear power plant radioactive waste liquid based on the birnessite in-situ reaction. The method comprises following steps: (1) adding potassium permanganate into the nuclear power plant waste liquid containing radioactive elements and uniformly mixing the liquid; (2) adding manganous salt into the liquid on the basis that the molar ratio of manganous ions (Mn2+) in the potassium permanganate to manganous ions (Mn2+) in the manganous salt is 3:2, and uniformly mixing the liquid to obtain the mixed solution; (3) adding an alkaline solution into the mixed solution drop by drop so as to adjust the pH of the mixed solution to be 8-13, enabling the potassium permanganate to react with the manganous salt to generate birnessite MnO2, then adding magnetic Fe3O4 powder into the solution, and stirring the solution at a constant temperature of 20-80 DEG C for 15-300 minutes; and (4) allowing the solution to stand, performing magnetic separation and removing the precipitate, thereby completing the purification treatment of the nuclear power plant radioactive waste liquid. Compared with the prior art, the method is advantageous in that the steps are simple, conditions are easy to control, the method is economical and practical, the radioactive ion removing efficiency is high, the using range of the method is wide, and no secondary pollution is formed.

A method of producing an oxide of manganese including reacting, in a first aqueous solution, a manganese salt and an alkali agent to form manganese hydroxide; separating the manganese hydroxide from the first solution; mixing the manganese hydroxide into an aqueous medium to form a manganese hydroxide suspension; mixing the manganese hydroxide suspension with alkali metal hydroxide to form a second aqueous solution; and oxidizing the manganese hydroxide in the second aqueous solution to form an oxide of manganese. The dried oxide of manganese includes birnessite, a maximum of 20% hausmannite, and a maximum of 10% feitknechtite, may further include a maximum of 400 ppm of anions, may have a specific surface area of at least 25 m2/g, and may have an average oxidation state of greater than 3.5.

Provided are: manganese dioxide which can cure a liquid polysulfide polymer and enables the production of a cured article that is rarely swollen or rarely undergoes the deterioration in strength even when immersed in warm water for a long period; and a curable composition containing the manganese dioxide. The manganese dioxide can be used as a curing agent for a liquid polysulfide polymer, and is characterized by comprising monoclinic cation-substituted birnessite-type manganese dioxide produced by substituting each of sodium ions existing between layers of monoclinic sodium birnessite represented by the formula: Na0.55Mn2O4·1.5H2O by a monovalent to trivalent cation.