Preparation method of all-silicon type amorphous porous material and application of all-silicon type amorphous porous material in cigarette filters
A porous material, cigarette filter technology, applied in the application, e-liquid filter, chemical instruments and methods, etc., can solve the problem of inability to achieve adsorption effect, and achieve easy mass production, convenient operation, and reduce the content of irritating substances. Effect
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Embodiment 1
[0034] 1. Preparation of all-silicon amorphous porous material by hydrothermal synthesis method: 0.25g of cetyltrimethylammonium bromide (CTAB) was completely dissolved in 35g of deionized water, which was recorded as solution A; 10g of diethyl ether and 1.2g Mix tetraethyl silicate (TEOS) evenly, gradually add 20mL of 0.2mol / L hydrochloric acid solution dropwise, and 14-16% TEOS is pre-hydrolyzed, which is recorded as solution B. Under vigorous stirring, solution B was added dropwise into solution A, and then the solution was adjusted to pH 9.0 with 0.5M sodium carbonate. The formed sol was transferred to an airtight container, stirred at room temperature for 12 h, and then aged at 100° C. for 24 h. The reaction product was filtered, washed thoroughly with deionized water, and dried in air for 15 h to powder. Calcined under nitrogen at 550°C for 5 hours to obtain a porous material, which is designated as CTN1. The specific surface area and pore structure data of CTN1 are sh...
Embodiment 2
[0047] 1. Preparation of all-silicon amorphous porous material by hydrothermal synthesis method: completely dissolve 0.25g cetyltrimethylammonium bromide (CTAB) in 35g deionized water, which is recorded as solution A; mix 10g methyl ethyl ether and 1.75 g of silica sol, and gradually add 5mL of 0.2mol / L phosphoric acid solution dropwise to achieve pre-hydrolysis of 14-16% TEOS, which is recorded as solution B. Under vigorous stirring, solution B was added dropwise into solution A, and then the solution was adjusted to pH 12.0 with 0.1 M NaOH solution. The formed sol was transferred to an airtight container, stirred at room temperature for 10 h, and then aged at 120 °C for 20 h. The reaction product was filtered, washed thoroughly with deionized water, and dried in air for 20 h to powder. Calcined with oxygen at 600°C for 8 hours to obtain a porous material, denoted as CTN2. The specific surface area and pore structure data of CTN2 are shown in Table 2, and the scanning elect...
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