Catalyst for producing p-xylene by alkylation of benzene and methanol and preparation method thereof
A p-xylene and fluidized bed catalyst technology, applied in the direction of physical/chemical process catalysts, molecular sieve catalysts, chemical instruments and methods, etc., can solve the cumbersome preparation steps of catalysts, low p-xylene selectivity, low benzene conversion rate, etc. problems, achieve high stability, reduce production costs, and increase single-pass yield
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Embodiment 1
[0031] 3 Kg hydrogen ZSM-5 (SiO 2 / Al 2 o 3 =25, particle size 1-4 μm) molecular sieve, 4 Kg kaolin, 2 Kg silica sol were added to appropriate amount of water, stirred evenly, spray-dried and molded, roasted at 600°C for 3 h, recorded as raw powder A.
[0032] Take 0.9 Kg tetraethyl orthosilicate to make ethanol solution, impregnate it in raw powder A, and obtain raw powder A-I after drying; make 0.1Kg MgO (precursor is magnesium nitrate hexahydrate) into aqueous solution, soak it in roasted raw powder Powder A-I was dried to obtain the original powder A-II. The catalyst BTPX-01 was obtained after the raw powder A-II was roasted.
Embodiment 2
[0034] 3.5 Kg hydrogen ZSM-5 (SiO 2 / Al 2 o 3 =150, particle size 20-500 nm) molecular sieve, 1.5 Kg pseudoboehmite, 0.5 Kg alumina sol, 2 Kg kaolin, add appropriate amount of water, stir evenly, spray dry and form, roast at 600 °C for 3 h, record as raw powder b.
[0035] Take 2 Kg of tetraethyl orthosilicate to prepare ethanol solution, impregnate in raw powder B, and dry to obtain raw powder B-I; make 0.5 KgCaO (precursor is calcium nitrate tetrahydrate) into an aqueous solution, impregnate in raw powder B-I, dry Obtain former powder B-II afterward. The catalyst BTPX-02 was obtained after the raw powder B-II was roasted.
Embodiment 3
[0037] 1.5 Kg sodium ZSM-5 (SiO 2 / Al 2 o 3 =25, particle size 1-4 μm) molecular sieve, 3 Kg pseudo-boehmite, 3 Kg silica, 1.5 Kg alumina sol were added to an appropriate amount of water, stirred evenly, spray-dried and shaped, roasted at 600 °C for 3 h, recorded as the original Powder C.
[0038]Make 0.01 Kg MgO (the precursor is magnesium chloride) into an aqueous solution, impregnate it in Kg raw powder C, and dry it to obtain raw powder C-I; take 0.99 Kg tetrabutyl orthosilicate to make an ethanol solution, and dip it in the roasted raw powder C-I , to obtain the original powder C-II after drying. The catalyst BTPX-03 was obtained after the raw powder C-II was roasted.
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