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Micron-scale monodisperse porous silica microspheres and preparation method thereof

A technology of porous silicon dioxide and silicon dioxide, which is applied in the direction of silicon dioxide, silicon oxide, nanotechnology, etc., can solve problems such as limitations in application fields, and achieve low raw material costs, adjustable particle size and pore structure, and particle size Narrow distribution effect

Active Publication Date: 2022-01-11
TIANJIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the pore size of the material prepared by the molecular template method is generally less than 4nm, which cannot be directly used as a chromatographic stationary phase filler, and its application field is limited.

Method used

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  • Micron-scale monodisperse porous silica microspheres and preparation method thereof
  • Micron-scale monodisperse porous silica microspheres and preparation method thereof
  • Micron-scale monodisperse porous silica microspheres and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0024] Preparation of Silica Microspheres Using Polymethylsilsesquioxane Microspheres as a Template

[0025] (1) Add 20 g of methyltrimethoxysilane to 100 mL of deionized water, add 0 μL of hydrochloric acid solution at pH 1, and stir and react at room temperature for 1 h to obtain a polysilsesquioxane hydrolyzate;

[0026] (2) Add 10 μL of concentrated ammonia water to the polysilsesquioxane hydrolyzate, stir evenly, let it stand for 4 hours, filter to remove the mother liquor, collect the microspheres, wash with 95% ethanol, and obtain the polysilsesquioxane gel microspheres. ball;

[0027] (3) Disperse 1 g of polysilsesquioxane gel microspheres in 10 mL of 80% ethanol according to the mass volume ratio of 0.1, and mix well;

[0028] (4) Add sodium hydroxide to the mixed solution obtained in step (3) to make the concentration 0.05M, mix well, shake and react in a water bath at 70°C for 10 hours, filter to remove the solvent, and wash the microspheres alternately with 95% et...

Embodiment 2

[0032] Preparation of silica microspheres with different pore sizes using polymethylsilsesquioxane microspheres as template

[0033] (1) Add 20 g of methyltrimethoxysilane to 100 mL of deionized water, add 0 μL of hydrochloric acid solution at pH 1, and stir and react at room temperature for 1 h to obtain a polysilsesquioxane hydrolyzate;

[0034] (2) Add 10 μL of concentrated ammonia water to the polysilsesquioxane hydrolyzate, stir evenly, let it stand for 4 hours, filter to remove the mother liquor, collect the microspheres, wash with 95% ethanol, and obtain the polysilsesquioxane gel microspheres. ball;

[0035] (3) Disperse 1 g of polysilsesquioxane gel microspheres in 10 mL of 80% ethanol according to the mass volume ratio of 0.1, and mix well;

[0036] (4) Add sodium hydroxide to the mixed solution obtained in step (3) so that the concentrations are 0.01 and 0.025M respectively, mix well, shake and react in a water bath at 70°C for 10 hours, filter to remove the solven...

Embodiment 3

[0042] Preparation of silica microspheres with different particle sizes using polymethylsilsesquioxane microspheres as template

[0043] (1) Add 20 g of methyltrimethoxysilane to 100 mL of deionized water, add 0 μL of hydrochloric acid solution at pH 1, and stir and react at room temperature for 1 h to obtain a polysilsesquioxane hydrolyzate;

[0044] (2) Add 5, 20, and 50 μL of concentrated ammonia water to the polysilsesquioxane hydrolyzate, stir evenly, let stand for 4, 3, and 2 hours respectively, filter and remove the mother liquor, collect the microspheres, wash with 95% ethanol, Obtain polysilsesquioxane gel microspheres of different particle sizes;

[0045] (3) Disperse 1 g of polysilsesquioxane gel microspheres in 10 mL of 80% ethanol according to the mass volume ratio of 0.1, and mix well;

[0046] (4) Add sodium hydroxide to the mixed solution obtained in step (3) so that the concentrations are 0.05, 0.1, and 0.6M respectively, mix well, shake and react in a water ...

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Abstract

The invention discloses a method for preparing micron-scale monodisperse porous silica microspheres, which uses a new type of porous polysilsesquioxane microspheres as a template, directly calcines to remove organic components, and then obtains particle size and Monodisperse porous silica microsphere material with controllable pore size. Also disclosed are micron-scale monodisperse porous silica microspheres prepared by the method, the particle diameter of the silica microspheres is 3-10 μm, and the pore volume is 0.3-0.9 cm 3 / g, the specific surface area is 100‑400m 2 / g, the pore size is 3-100nm. Compared with the traditional process, the preparation method is simple, economical, and does not require classification and sieving. The prepared porous silica microspheres are spherical, uniform in particle size distribution, and have a mesoporous structure, which can be directly applied to high-performance liquid chromatography. The stationary phase can also be used in catalytic carriers, coatings, cosmetic additives and other fields.

Description

technical field [0001] The invention belongs to the technical field of preparation of high-efficiency liquid phase monodisperse mesoporous silica microspheres, and in particular relates to a micron-scale monodisperse porous silica microsphere and a preparation method thereof, especially relates to high-performance liquid chromatography immobilization A method for preparing monodisperse porous silica microspheres with a particle size distribution of 3-10 μm. Background technique [0002] Monodisperse porous silica microspheres are widely used in the fields of biomedicine, cosmetics, coatings, chemistry and chromatography due to their high mechanical strength, large specific surface area, mesoporous structure and abundant functionalized silanol on the surface. application prospects. Monodisperse porous silica microspheres with a particle size in the range of 3-10 μm play an important role in the high-efficiency liquid phase stationary phase, which can effectively reduce the f...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01B33/18B82Y30/00B82Y40/00
CPCB82Y30/00B82Y40/00C01B33/18C01P2004/32C01P2006/17C01P2006/14C01P2006/12C01P2004/61C01P2004/52
Inventor 陈磊霍志霞万谦宏
Owner TIANJIN UNIV