Method of manufacturing mesoporous silica and method of manufacturing the same
A technology of silica and ethylene glycol, applied in the direction of silica, silica, silicon compounds, etc., can solve the problems that the advantages of mesoporous silica cannot be fully utilized
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Embodiment 1
[0096] Specific examples are given below to further describe the present invention in detail, but the present invention is not limited by these examples.
[0097] First, the production method of the water-soluble silicate monomer used in the present invention will be described.
Synthetic example 1
[0099] Add 20.8g (0.1mol) of tetraethoxysilane and 24.9g (0.4mol) of ethylene glycol to 150ml of acetonitrile, and further add 1.8g of strongly acidic ion exchange resin (Dow EX50W-X8: manufactured by Dow Chemical) as a solid catalyst , and then mixed and stirred at room temperature. The reaction solution which started to separate into two layers was uniformly dissolved after about 1 hour. Stirring was then continued for 5 days, the solid catalyst was separated by filtration, and acetonitrile was distilled off under reduced pressure to obtain 39 g of a transparent viscous liquid. As a result of NMR analysis, it was confirmed that it was the target product (tetrakis(2-hydroxyethoxy)silane) (yield: 72.5%).
[0100] Preparation of mesoporous silica
[0101]The present inventors prepared a water-soluble silicate monomer according to the above synthesis example, and tried to prepare mesoporous silica by using a nonionic surfactant and the water-soluble silicate monomer.
[010...
Embodiment 9
[0118] Add 0.8 g of surfactant POE (10 mol) phytosterol ether into 3.2 g of ion-exchanged water, and stir until uniform. It was confirmed by microscopic observation or the like that this surfactant solution was a nematic chiral liquid crystal phase. 1.0 g of tetrakis(hydroxyethoxy)silane was added to this liquid crystal, and it stirred for 10 minutes. The solution was transparent and homogeneous in appearance. When the solution was left to stand at 25° C. for 3 hours, the entire solution became cloudy, and when it was left to stand for 17 hours, the entire solution formed a gel in a cloudy state. The gel was freeze-dried to remove water, and then ethanol was added and left to stand overnight at 37°C to remove the ethanol solution containing the surfactant. The remaining white powder was dried by a rotary evaporator to obtain silica powder.
[0119] The silica powder obtained in Example 9 above was observed by a transmission electron microscope, and it was confirmed that the...
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