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Preparation method and application of perovskite type composite oxide catalyst

A composite oxide and perovskite-type technology, applied in metal/metal oxide/metal hydroxide catalysts, physical/chemical process catalysts, chemical instruments and methods, etc., can solve unfavorable scale production, many influencing factors, Problems such as high equipment cost, to achieve the effect of saving cumbersome procedures, simple process operation and low equipment cost

Inactive Publication Date: 2011-08-31
BEIJING CHANGLI UNION ENERGY TECH CO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] At present, there are many methods for preparing perovskite-type oxides, including solid-phase sintering, salt decomposition, sol-gel, co-precipitation, and solution spray-freeze-drying, etc. Among them, although the solid-phase sintering method operates Simple, but it is not commonly used because it is difficult to mix the solid substances evenly, which affects the conversion rate and activity of the product; although the product prepared by the sol-gel method has the advantages of high purity, good uniformity, and simple process equipment, the method There are many influencing factors, and the treatment period is long, which is not conducive to large-scale production; the co-precipitation method needs to sinter the precipitate at high temperature and for a long time, which is easy to cause the agglomeration of particles and the reduction of specific surface area; and the solution spray-freeze-drying method is also Because of its harsh preparation conditions and high equipment cost, it is not conducive to production and wide application

Method used

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  • Preparation method and application of perovskite type composite oxide catalyst
  • Preparation method and application of perovskite type composite oxide catalyst
  • Preparation method and application of perovskite type composite oxide catalyst

Examples

Experimental program
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Effect test

Embodiment 1

[0021] Select the constituent elements and chemical composition of the perovskite oxide, and according to the stoichiometric ratio, the selected three water-soluble salts: lanthanum nitrate (La(NO3)3 6H2O), calcium nitrate (Ca(NO3)2 4H2O) and manganese nitrate (50%Mn(NO3)2 solution) to form a solution with a total solute concentration of 5%, then weigh the coconut shell carbon mass of 3 / 4 of the total mass of the water-soluble salt added, and add it to the solution The activation solution was obtained, put it into an oven for drying at 80°C after standing for 10 hours, and then grind the obtained mixed powder, then send it to a muffle furnace for sintering at 700°C for 10 hours, and cool to room temperature with the furnace to obtain a perovskite type Composite oxide catalyst, the X-ray diffraction spectrum of gained oxide is as figure 1 As shown, the results show that the method can be used to prepare perovskite-type composite oxides.

Embodiment 2

[0023] According to the stoichiometric ratio, three selected water-soluble salts: lanthanum nitrate (La(NO 3 ) 3 ·6H 2 O), calcium nitrate (Ca(NO 3 ) 2 4H 2 O) and cobalt nitrate (Co(NO 3 ) 2 ·6H 2 O) Make a solution with a total solute concentration of 15%, then weigh XC-72 activated carbon that is 1 / 2 of the added water-soluble salt, add it to the solution to obtain an activation solution, put it into an oven at 85°C to dry after standing for 12 hours After drying, the obtained mixed powder was ground, then sent to a muffle furnace for sintering at 750° C. for 9 hours, and cooled to room temperature with the furnace to obtain a perovskite composite oxide catalyst.

Embodiment 3

[0025] According to the stoichiometric ratio, three selected water-soluble salts: lanthanum nitrate (La(NO 3 ) 3 ·6H 2 O), strontium nitrate (Sr(NO 3 ) 2 ) and manganese nitrate (50%Mn(NO 3 ) 2 solution) to make a solution with a concentration of 20% of the total solute, then weigh the fruit stone charcoal of the same quality as the added water-soluble salt, add it into the solution and stir to obtain an activation solution, and put it into an oven at 90°C to dry after standing for 8 hours. Then put the ground mixed powder into a muffle furnace for sintering at 800° C. for 8 hours, and cool down to room temperature with the furnace to obtain a perovskite composite oxide catalyst.

[0026] The use of the perovskite oxide catalyst prepared by the method of the present invention is preferably to prepare an air electrode.

[0027] The air electrode prepared by the catalyst of the present invention is synthesized by rolling a catalytic membrane, a hydrophobic membrane and a c...

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Abstract

The invention discloses a preparation method and application of a perovskite type composite oxide catalyst. The perovskite type composite oxide catalyst is an A-position substituted perovskite type composite oxide. The structural formula of the catalyst is A1-xA'xBO3, wherein x is larger than 0 and smaller than 1; A is La or Nd element; the A'-position substitution ion is one of Ca, Sr, Ba, Ce and the like; and the B-position ion is one of Mn, Co, Ni, Fe and the like. The preparation method comprises the following steps of: according to a chemical metering ratio, weighing a water-soluble salt which contains the A-position, A'-position and B-position elements; mixing the salt and deionized water to obtain 5 to 20 percent salt solution; adding the solution into a beaker; adding activated carbon of which the mass is 0.1 to 1.5 times of the salt into the solution; completely soaking the activated carbon and standing; heating and stirring the mixture, continuously heating until the water content is completely evaporated, wherein the co-crystallized solid mixture is uniformly carried on the activated carbon, and after drying the mixture, grinding the mixture into powder; and sintering the powder in a muffle furnace, cooling the sintered powder with the furnace to room temperature, and grinding the cooled powder to obtain the powder of the perovskite type composite oxide mixed catalyst. The preparation method is suitable for production; and the electrode activity of the perovskite type catalyst can be greatly improved in a zinc air cell structure.

Description

technical field [0001] The invention belongs to the field of inorganic non-metallic materials, and in particular relates to a preparation method and application of a perovskite-type oxide catalyst. Background technique [0002] Perovskite-type composite oxides generally refer to inorganic non-metallic oxides composed of rare earth or alkaline earth elements and transition elements, which have the same crystal structure as perovskite. Because of their good catalytic performance, the performance in alkaline solution is relatively Stable, resistant to oxidation, high conductivity at room temperature, and low price, it is a promising bifunctional oxygen electrode material, and thus has become a research hotspot in the field of positive electrode materials for zinc-air batteries. [0003] At present, there are many methods for preparing perovskite oxides, including solid-phase sintering, salt decomposition, sol-gel, co-precipitation, and solution spray-freeze-drying, etc. It is ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/34B01J23/83B01J23/889H01M4/90
CPCY02E60/50
Inventor 赵亮
Owner BEIJING CHANGLI UNION ENERGY TECH CO
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