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A kind of preparation method of yttrium stannate spherical grade structure material

A hierarchical structure and spherical technology, which is applied in chemical instruments and methods, tin compounds, physical/chemical process catalysts, etc., can solve the problems of small specific surface area, waste of resources, and prone to impurities in products, and achieve simple process routes and easy operation The effect of control and high productivity

Inactive Publication Date: 2019-03-15
BOHAI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The traditional high-temperature solid-phase synthesis method not only wastes resources, but also has disadvantages such as impurity and large size of the product.
Co-precipitation method is easy to produce heterogeneous phases, and the specific surface area is small, which affects its performance as a catalyst or catalyst carrier
In the co-precipitation preparation process, a large amount of precipitant is used, which increases the preparation cost, and the prepared yttrium stannate is not high in purity, resulting in defects such as low density and poor strength.

Method used

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  • A kind of preparation method of yttrium stannate spherical grade structure material
  • A kind of preparation method of yttrium stannate spherical grade structure material
  • A kind of preparation method of yttrium stannate spherical grade structure material

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Effect test

Embodiment 1

[0035] The molar ratio of yttrium acetylacetonate and tin tetrachloride is 1:1, accurately weighed and put into methanol (12C, 99.95%) to stir and dissolve. The molar concentration of yttrium acetylacetonate is 0.01 mol / L. The resulting mixed solution was subjected to solvothermal reaction, the solvothermal reaction temperature was 200 ° C, and the solvothermal reaction time was 24 hours. After the solvothermal reaction was completed, it was naturally cooled to room temperature, and the product obtained by the reaction was filtered and washed and placed in an oven at a programmed temperature increase rate of 5°C / min, and dried at 120°C for 5 hours. Then place it in a muffle furnace for calcination, the calcination time is 8 hours, the calcination temperature is 500 °C, and the heating rate is 10 °C / min. After natural cooling, the spherical grade structure material of yttrium stannate can be obtained. The size of the large spheres is 5 mm, the size of the nanoparticles is 10 n...

Embodiment 2

[0037] The molar ratio of yttrium acetylacetonate and tin tetrachloride is 1:1, accurately weighed and put into methanol (12C, 99.95%) to stir and dissolve. The molar concentration of yttrium acetylacetonate is 0.2 mol / L. The mixed solution obtained is carried out solvothermal reaction, and the solvothermal reaction temperature is 110 ℃, and the solvothermal reaction time is 48 hours. After the solvothermal reaction was completed, it was naturally cooled to room temperature, and the product obtained by the reaction was filtered and washed and placed in an oven at a programmed temperature increase rate of 5°C / min, and dried at 120°C for 1 hour. Then place it in a muffle furnace for calcination, the calcination time is 2 hours, the calcination temperature is 800 °C, and the heating rate is 20 °C / min. After natural cooling, the spherical grade structure material of yttrium stannate can be obtained. The size of the large spheres is 8 mm, the size of the nanoparticles is 20 nm, th...

Embodiment 3

[0039]The molar ratio of yttrium acetylacetonate and tin tetrachloride is 1:1, accurately weighed and put into methanol (12C, 99.95%) to stir and dissolve. The molar concentration of yttrium acetylacetonate is 0.1 mol / L. The resulting mixed solution was subjected to solvothermal reaction, the solvothermal reaction temperature was 200 ° C, and the solvothermal reaction time was 12 hours. After the solvothermal reaction was completed, it was naturally cooled to room temperature, and the product obtained by the reaction was filtered and washed and placed in an oven at a programmed temperature increase rate of 5°C / min, and dried at 120°C for 3 hours. Then place it in a muffle furnace for calcination, the calcination time is 2 hours, the calcination temperature is 600 °C, and the heating rate is 10 °C / min. After natural cooling, the spherical grade structure material of yttrium stannate can be obtained. The size of the large spheres is 6 mm, the size of the nanoparticles is 15 nm,...

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Abstract

The invention belongs to the field of inorganic nonmetal material preparation, and particularly relates to a preparation method of an yttrium stannate spherical hierarchical structure material. The method comprises the steps that after yttrium(III) 2,4-pentanedionate hydrate and tin tetrachloride are sufficiently dissolved in a methanol solution, a solvothermal reaction is conducted, after filtration and washing are conducted, drying and calcination cooling are conducted, and the yttrium stannate spherical hierarchical structure material is obtained. The molar ratio of yttrium(III) 2,4-pentanedionate hydrate to tin tetrachloride is 1:1; the molar concentration of yttrium(III) 2,4-pentanedionate hydrate ranges from 0.01 mol / L to 0.2 mol / L. The technology is simple and convenient and easy to implement, the product is high in purity, the preparation cost is low, the size of the whole large ball of the obtained product ranges from 5 mm to 8 mm, and the sizes of the nano particles range from 10 nm to 20 nm. The homogeneity and dispersibility of the product are very good, the production technology is simple, the calcination temperature is low, and the method is likely to be applied to actual large-scale production.

Description

technical field [0001] The invention belongs to the technical field of preparation of inorganic non-metallic materials, and in particular relates to a preparation method of a spherical grade structure material of yttrium stannate. Background technique [0002] The chemical structure of pyrochlore oxide is A 2 B 2 o 7 , where A and B are metals. The pyrochlore structure contains two different metal cation coordination polyhedra. The metal ion with a larger ionic radius occupies the A site to form an octahedral coordination, and the metal ion with a smaller ionic radius occupies the B site to form a tetrahedral coordination. The coordination polyhedron interpenetrates to form A 2 B 2 o 7 crystal structure. Because the ratio of A-site atoms and B-site atoms' radii can vary within a certain range, pyrochlore-structured compounds have excellent optical, electromagnetic and other physical properties, and have become the most active research objects in the field of nanomater...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G19/00B01J23/14
CPCB01J23/14B01J35/004C01G19/00C01P2002/72C01P2002/84C01P2004/03C01P2004/32C01P2004/64C01P2006/80
Inventor 张杰许家胜王莉丽崔岩孙啸虎杨喜宝于禄
Owner BOHAI UNIV