Catalyst for electronically regulating straight-chain alkane aromatic reaction as well as preparation method and application thereof
A technology for straight-chain alkanes and catalysts, which is applied in the field of catalysts for the dehydrogenation and cyclization of straight-chain alkanes, can solve the problems of difficulty in industrial application of catalysts, high catalyst costs, easy deactivation of catalysts, etc., and achieves improved selectivity and catalytic deactivation. The effect of hydrogen activity, improvement of electron-deficient state, and improvement of carbon deposition resistance
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Embodiment 1
[0027] Mix 10 g of ethylene glycol with 40 g of deionized water, dissolve 0.018 g of tetraammineplatinum dichloride in the mixed system of water and ethylene glycol, then add 2 g of commercial grade KL molecular sieves, and then sonicate for 20 min. Stir at 60 °C until the solvent evaporates completely, and then dry in an oven at 120 °C for 24 h. The catalyst was then ground into powder and calcined in a muffle furnace at 300 °C for 3 h with a heating rate of 2 °C min −1 .
[0028] Then, the performance evaluation of the n-hexane dehydrocyclization aromatization reaction was carried out. The catalyst dosage was 100 mg, the reaction pressure was 0.1 MPa, the raw material gas was a mixture of n-hexane and hydrogen, and the space velocity was 1 h. −1 .
Embodiment 2
[0030] Mix 10 g of ethylene glycol with 40 g of deionized water, 0.018 g of platinum dichlorotetraammine and 0.060 g of Ga(NO 3 ) 3 9H 2 O was dissolved in a mixed system of water and ethylene glycol, then 2 g of commercial grade KL molecular sieves were added, then ultrasonicated for 20 min, stirred at 60 °C until the solvent evaporated completely, and then dried in an oven at 120 °C for 24 h . The catalyst was then ground into powder and calcined in a muffle furnace at 300 °C for 3 h with a heating rate of 2 °C min −1 .
[0031] Then, the performance evaluation of the n-hexane dehydrocyclization aromatization reaction was carried out. The catalyst dosage was 100 mg, the reaction pressure was 0.1 MPa, the raw material gas was a mixture of n-hexane and hydrogen, and the space velocity was 1 h. −1 .
Embodiment 3
[0033] 10 g ethylene glycol was mixed with 40 g deionized water, 0.018 g dichlorotetraammine platinum and 0.072 g Fe(NO 3 ) 3 9H 2 O was dissolved in a mixed system of water and ethylene glycol, then 2 g of commercial grade KL molecular sieves were added, then ultrasonicated for 20 min, stirred at 60 °C until the solvent evaporated completely, and then dried in an oven at 120 °C for 24 h . The catalyst was then ground into powder and calcined in a muffle furnace at 300 °C for 3 h with a heating rate of 2 °C min −1 .
[0034] Then, the performance evaluation of the n-hexane dehydrocyclization aromatization reaction was carried out. The catalyst dosage was 100 mg, the reaction pressure was 0.1 MPa, the raw material gas was a mixture of n-hexane and hydrogen, and the space velocity was 1 h. −1 .
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