Preparation method of Ruddlesden-Popper-like perovskite type catalytic material

A perovskite-type, catalytic material technology, applied in the direction of chemical instruments and methods, separation methods, physical/chemical process catalysts, etc., can solve the problems of catalyst deactivation, complex preparation process, selectivity reduction, etc., to achieve energy reduction consumption, preparation method and process are simple, and the effect of improving catalytic activity

Active Publication Date: 2018-10-19
HEBEI UNIVERSITY OF SCIENCE AND TECHNOLOGY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Ruddlesden-Popper type perovskite type catalytic materials mostly have AX and ABX 3 The advantages and disadvantages of the two types of catalysts can degrade VOCs more efficiently. At the same time, the homogeneity of the elements leads to the amplification of the disadvantages of the catalysts, such as reduced lifespan, reduced selectivity, etc.
[0004] The preparation methods of Ruddlesden-Popper type perovskite catalytic materials include: impregnation method, mechanical stirring method and other methods. poisoning phenomenon

Method used

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  • Preparation method of Ruddlesden-Popper-like perovskite type catalytic material
  • Preparation method of Ruddlesden-Popper-like perovskite type catalytic material
  • Preparation method of Ruddlesden-Popper-like perovskite type catalytic material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] (1) Weigh the perovskite metal precursor, metal oxide precursor and complexing agent respectively, the perovskite metal precursor is composed of rare earth nitrate and transition metal nitrate, and the metal oxide precursor is composed of The nitrate composition of one of the alkaline earth elements, boron group elements or transition metal elements; the nitrate in the rare earth nitrate, transition metal nitrate and metal oxide precursor is according to the molar ratio 1:x:y (0< The ratio of x≤1; 0<y≤1) is dissolved in deionized water in turn, and the total molar concentration of metal ions in the solution is controlled to be 0.5-2.0 mol / L, then a complexing agent is added, and stirred at room temperature for 0.5h to obtain a precursor compound solution; the number of moles of the complexing agent added is 1 to 2 times the sum of the number of moles of all metal ions added. The rare earth nitrate in the perovskite metal precursor is one of lanthanum nitrate, cerium nit...

Embodiment 2

[0041] (1) In this example, the rare earth nitrate and transition metal nitrate in the perovskite metal precursor are selected from La nitrate and Co nitrate respectively, and the metal elements in the metal oxide precursor are selected from alkaline earth elements. Mg, that is, the metal oxide precursor is the nitrate of Mg. Weigh the rare earth nitrate, transition metal nitrate and metal oxide precursor according to the molar ratio La:Co:Mg=1:1:0.2. La(NO 3 ) 3 •6H 2 O 17.67g, Co(NO 3 ) 2 •6H 2 O 11.76g, Mg(NO 3 ) 2 •6H 2 O 2.07g was dissolved in deionized water successively, and the total molar concentration of metal ions in the control solution was 2mol / L, then 18.59g of complexing agent citric acid was added, stirred at room temperature for 0.5h, and the components were mixed uniformly to obtain the precursor The solution is mixed, and the number of moles of citric acid added is 1 times of the sum of the number of moles of all metal ions added.

[0042] (2) Heat ...

Embodiment 3

[0049] (1) In this example, the rare earth nitrate and transition metal nitrate in the perovskite metal precursor are selected from La nitrate and Co nitrate respectively, and the metal oxide precursor is selected from Mn in transition metal nitrate Nitrate, the nitrate in the rare earth nitrate, transition metal nitrate and metal oxide precursor according to the molar ratio La:Co:Mn=1:1:0.6, weigh La(NO3) 3 •6H 2 O 17.67 g, Mn(NO3) 2 •6H 2 O 8.59 g, Co(NO3) 2 •6H 2 O 11.76g and be dissolved in deionized water successively, the total molar concentration of metal ions in the control solution is 2mol / L, then add complexing agent ethylenediaminetetraacetic acid 30.55g, stir 0.5h at room temperature, make each composition mix homogeneously, A precursor mixed solution is obtained, and the mole number of ethylenediaminetetraacetic acid is one time of the sum of the mole numbers of all metal ions added.

[0050] (2) Heat the precursor mixed solution obtained in step (1) to 90°C ...

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Abstract

The invention relates to a preparation method of a Ruddlesden-Popper-like perovskite type catalytic material, and the method comprises the following steps: 1, respectively weighing a perovskite metalprecursor comprising a rare earth nitrate and a transition metal nitrate, a metal oxide precursor comprising a nitrate of one element of an alkaline earth element, a boron group element or a transition metal element, and a complexing agent; dissolving the rare earth nitrate and the transition metal nitrate and the nitrate in the metal oxide precursor into deionized water, and then adding the complexing agent; 2, stirring to form a wet gel; 3, standing to obtain a dry gel; 4, adding the dry gel to a reaction kettle, meanwhile adding a surfactant and deionized water to the reaction vessel, adjusting the pH, and reacting at 200 DEG C; 5, drying; and 6, roasting. The catalyst prepared by the method not only has the original advantages of high-efficiency catalysis of perovskite, but also achieves multi-metal synergistic catalysis, thereby more efficiently catalyzing the oxidation of VOCs and avoiding the amplification of defects of homogenous metals.

Description

technical field [0001] The invention belongs to the technical field of catalytic materials, in particular, it relates to a preparation method of a Ruddlesden-Popper type perovskite type catalytic material. Background technique [0002] With the development of society and economy, air pollution has intensified, especially petroleum, chemical, pharmaceutical, packaging, printing, furniture, automobile and shipbuilding industries produce a large amount of volatile organic compounds (VOCs) in the production process, VOCs can cause headaches, nausea, etc. Uncomfortable symptoms, long-term exposure can cause chronic poisoning, damage the liver and nervous system, and even have the risk of teratogenicity and cancer. It is also one of the precursors of smog. VOCs have caused great harm to the social environment, economic environment and residents’ health. . In order to improve VOCs pollution control technology, promote enterprises to reduce VOCs emissions, and improve the quality o...

Claims

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Application Information

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IPC IPC(8): B01J23/83B01J23/00B01J23/889B01D53/86B01D53/44
CPCB01D53/8687B01D2257/708B01J23/002B01J23/83B01J23/8892
Inventor 段二红刘洁王赛飞王曼钱恒力刘浩彬牛建瑞
Owner HEBEI UNIVERSITY OF SCIENCE AND TECHNOLOGY
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