Method for synthesizing mobil composition of matters-41(MCM-41) mesoporous molecular sieve
A technology of MCM-41 and mesoporous molecular sieve, which is applied in the direction of crystalline aluminosilicate zeolite, etc., can solve the problems of low synthesis yield of MCM-48, high alkalinity of the synthesis system, low utilization rate of silicon source, etc., and achieve economic benefits As well as the realization of ecological benefits, the reduction of synthesis costs, and the effects of reducing consumption
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Embodiment 1
[0018] Preparation of silicon source for the synthesis of MCM-41 mesoporous materials: high-quality MCM-48 mesoporous molecular sieves were synthesized by referring to the method reported in the literature (Micopor. Mesopor. Mater., 2005, 86, 314). Dry to obtain MCM-48 mesoporous molecular sieve. The mother liquor obtained by the first suction filtration is retained, then titrated with 37% concentrated hydrochloric acid to obtain a white precipitate, and the SiO obtained by filtering and washing 2 The filter cake was directly used as the silicon source for the synthesis of MCM-41 mesoporous materials.
[0019] Synthesis of MCM-41 mesoporous material: Add 8.0g NaOH to a beaker containing 720ml deionized water, then add 60.0g SiO obtained by acid titration of MCM-48 mother liquor 2 The filter cake was stirred at a constant temperature of 60°C for 1 hour to obtain solution A; 32.8g of cetyltrimethyl-p-toluenesulfonate (CTATos) was added to a beaker containing 720ml of deionized ...
Embodiment 2
[0022] Potassium hydroxide is used as an alkali source to prepare high-quality MCM-41 mesoporous molecular sieves:
[0023] Except replacing the sodium hydroxide in embodiment 1 with potassium hydroxide, other preparation conditions are all identical with embodiment 1.
Embodiment 3
[0025] Increase the crystallization temperature and prolong the crystallization time to prepare high-quality MCM-41 mesoporous molecular sieves:
[0026] Keeping the molar composition of the mixture SiO 2 / CTATos / NaOH / H 2 O=1:0.05:0.20:80 remains unchanged, the crystallization temperature is 130° C., and the crystallization time is 24 hours. Other preparation conditions and processes are the same as in Example 1.
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