Method for preparing metal oxide hollow microcapsule

A technology of oxide and hollow micro, which is applied in the preparation of microspheres, microcapsule preparations, etc., can solve the problems of cumbersome steps, safety and economy, and complicated operation process. The method is simple and easy to control, and the shell component Adjustable, high-efficiency preparation effects

Inactive Publication Date: 2005-10-19
FUDAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The first method is to prepare the precursor species (such as easily hydrolyzed metal alkoxide, etc.) that constitute the hollow microcapsule shell components into an aqueous solution, and form atomized droplets through a nozzle. Since the operation is generally carried out in a dry atmosphere, the formation of The solvent in the droplet evaporates rapidly, which promotes the rapid hydrolysis of the hard-to-volatile precursor species on the surface of the droplet to form the shell structure of the hollow microcapsule. This method can quickly and conveniently synthesize the hollow microcapsule, but it involves high pressure and high energy. The use of expensive spray equipment and the provision of a strictly dry atmosphere create safety and economical issues during the preparation process; the second method is to hydrolyze the components that form the microcapsule shell at the oil / water interface to form hollow microcapsules. Capsule shell structure, this method is suitable for the synthesis of most shell component microcapsules, but the operation process is complicated and the repeatability is poor, and the size of the obtained microcapsules is strictly limited by the size of the droplet, and it is difficult to obtain the particle size distribution uniform microcapsules
The third method uses removable microspheres (such as polymers and silica microspheres) as templates, and then deposits the desired species layer by layer on the surface of the template spheres to form nuclei through surface chemical reactions or electrostatic physical adsorption- shell structure, and finally the template is removed by roasting or chemical corrosion to obtain hollow microcapsules. A shell with a certain strength often requires multi-layer deposition operations, and the steps are relatively cumbersome, which is not suitable for large-scale synthesis

Method used

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  • Method for preparing metal oxide hollow microcapsule
  • Method for preparing metal oxide hollow microcapsule
  • Method for preparing metal oxide hollow microcapsule

Examples

Experimental program
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Effect test

example 1

[0033] Mix 1g of hexadecylamine, 100ml of isopropanol, 90ml of distilled water and 1.4ml of ammonia water, stir well at room temperature, then inject 5.8ml of tetraethoxy silicon into the above solution, stop stirring after 30 seconds, and let it stand at room temperature for 1 day , filter the product, wash it with distilled water, dry it and bake it in an air atmosphere at 600°C for 6 hours to remove hexadecylamine, and obtain mesoporous silica microsphere A 1 .

example 2

[0035] 1.96g CTAB, 2.32gNa 2 SiO 3 9H 2 O mixed with 17g of distilled water, stirred evenly at room temperature, then injected 1.75ml of ethyl acetate into the above solution, stopped stirring after 30 seconds, and heated the mixed solution after standing at room temperature for 5 hours in an oil bath at 90°C for 50 hours, The product was filtered and washed with distilled water, dried and calcined at 600°C in an air atmosphere for 6 hours to remove CTAB to obtain mesoporous silica microspheres B 1 .

example 3

[0037] 0.5g A 1 Immerse in 30ml of 2w.t.% amino silicon ester ethanol solution and stir for 6 hours, wash with ethanol for 1 to 6 times, filter to obtain silica microspheres modified with amino groups in the pores, denoted as A 2 . 0.5g A 1 Immerse in 30ml of 2w.t.% mercaptosilyl ester toluene solution and stir for 6 hours, wash with toluene for 1-6 times, filter to obtain silica microspheres modified with mercapto groups in the pores, denoted as C 1 . Immerse 0.5g of A1 in 30ml of 2w.t.% cyclohexane solution of trimethylchlorosilane and stir for 6 hours, wash with cyclohexane for 1 to 6 times, filter to obtain methyl-modified silicon oxide microspheres in the pores, denoted as D 1 .

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Abstract

The present invention relates to the preparation process of a kind of hollow metal oxide microcapsule. After mesoporous silica microball as template is alkyl group modified, nano metal oxide is filled into the microball hole canal and one layer of polyelectrolyte is adsorbed to the surface, and silica is finally leached out through treatment in alkali solution condition to prepare the hollow metal oxide microcapsule. Said process is simple, has adjustable shell material component and is suitable for the preparation of functional microcapsule. The microcapsule product has fine appearance and excellent performance, and may find its wide application in different fields, such as medicine preparation, catalyzing, electrochemistry, etc.

Description

technical field [0001] The invention relates to a method for preparing metal oxide hollow microcapsules by using mesoporous silicon oxide microspheres as a template. Background technique [0002] Hollow microcapsules with different shell components such as metal oxides, sulfides and noble metals have great potential in catalytic, optical, electrochemical and other functions due to their unique large cavity volume, functional shell components and high specific surface area. There are broad application prospects in the field of materials, and it has become one of the main research hotspots in recent years. [0003] At present, the synthesis of hollow microcapsules mainly relies on spray drying (P.J.Bminsma, A.Y.Kim, J.Liu, S.Baskaran, Chem.Mater., 1997,9,2507), emulsion / phase separation (H.Lin, Y. Cheng, C.Mou, Chem.Mater., 1998, 10, 3772) and sacrificial nuclear technology (L.Dlhne, S.Leporatti,; E.Donath, H.Mhwald, J.Am.Chem.Soc., 2001, 123, 5431; S.M.Marinakos, J.P.Nova...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J13/02C01G1/02
Inventor 任楠唐颐王波陈平杨佑浩
Owner FUDAN UNIV
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