Layered composite material as well as preparation method and application thereof
A layered composite material and a composite material technology are applied in the field of layered composite materials and their preparation to achieve the effects of low cost of raw materials, improved selectivity of low-carbon olefins, and increased olefin ratio
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Embodiment 1
[0041] A method for preparing a layered magadiite-supported iron-based catalyst of the present embodiment, the method comprises the following steps:
[0042] (1) Preparation of Precursor 1.
[0043] Weigh 3.6 g gas phase SiO 2 , 0.7 gNaOH, 0.94 gNa 2 CO 3 Transfer to a beaker, add 120 mL of deionized water, stir magnetically for 5 min, transfer the solution to a polytetrafluoroethylene-lined autoclave, and crystallize at 220 °C for 27 h. After the reaction kettle was cooled to room temperature, it was taken out, washed, centrifuged, washed with deionized water until the pH value was 7-8, and dried overnight in a vacuum oven at 80°C to obtain precursor 1.
[0044] (2) Preparation of precursor II.
[0045] Weigh 10 g FeCl 3 ·6H 2 0 and 1 g of Triton X-100 were transferred to a beaker, then 145 mL of ethylene glycol was added to the beaker, fully dissolved to obtain a homogeneous solution. Weigh 15 g of anhydrous sodium acetate and dissolve it in 125 ml of 1-2-ethylene gly...
Embodiment 2
[0048] A method for preparing a layered magadiite-supported iron-based catalyst of the present embodiment, the method comprises the following steps:
[0049] (1) Weigh 3.6 g of gas phase SiO 2 , 0.7 gNaOH, 0.94 gNa 2 CO 3 Transfer to a beaker, add 120 mL of deionized water, stir magnetically for 5 min, transfer the solution to a polytetrafluoroethylene-lined autoclave, and crystallize at 220 °C for 27 h. After the reaction kettle was cooled to room temperature, it was taken out, washed, centrifuged, washed with deionized water until the pH value was 7-8, and dried overnight in a vacuum oven at 80°C to obtain precursor 1.
[0050] (2) Disperse 2.52 g of precursor 1 in 50 mL of deionized water, sonicate for 20 min, and mechanically stir for 12 h to obtain solution 1. 0.02 molFeCl 2 4H 2 O and 0.01 mol FeCl 3 ·6H 2 O in N 2 Add it into a three-necked flask containing 50 mL of deionized water under atmosphere, stir it mechanically for 30 min to obtain solution 2, then add ...
Embodiment 3
[0052] (1) Weigh 3.6 g of gas phase SiO 2 , 0.7 gNaOH, 0.94 gNa 2 CO 3 Transfer to a beaker, add 120 mL of deionized water, stir magnetically for 5 min, transfer the solution to a polytetrafluoroethylene-lined autoclave, and crystallize at 220 °C for 27 h. After the reaction kettle was cooled to room temperature, it was taken out, washed, centrifuged, washed with deionized water until the pH value was 7-8, and dried overnight in a vacuum oven at 80°C to obtain precursor 1.
[0053] (2) Weigh 10 g FeCl 3 ·6H 2 0 and 1 g of Triton X-100 were transferred to a beaker, then 145 mL of ethylene glycol was added to the beaker, fully dissolved to obtain a homogeneous solution. Weigh 15 g of anhydrous sodium acetate and dissolve it in 125 ml of 1-2-ethylene glycol. After fully stirring, pour it into the homogeneous solution prepared in the previous step, keep stirring for 30 min, and transfer it to polytetrafluoroethylene. In a lined high-pressure reactor, dry it in an oven at 180°...
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