4.7 Article

Phosphorus promotion on hydrothermal stability of ZSM-5 by P precursors with different molecular sizes

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DOI: 10.1016/j.micromeso.2023.112706

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ZSM-5; Phosphorus modification; Catalytic cracking; P precursor; Hydrothermal stability

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The promotional effects of phosphorus modification on ZSM-5 zeolites by different molecular sizes of phosphorus oxyacids (H4P2O7, H3PO4, H3PO3, and H3PO2) were studied using catalytic cracking of n-tetradecane as the probe reaction. The diffusion of P precursor molecules into ZSM-5 channels was found to be important for preventing aggregation of P species and improving stabilization on tetra-coordinated framework aluminum. The presence of P-Al interaction was proposed based on the results of 27Al, 31P, and 29Si MAS NMR. H3PO2 as the P precursor showed easy diffusion into ZSM-5 channels, resulting in less formation of polyphosphates, homogeneous distribution of P species, better reserved crystallinity, microporous area, and acidic sites, leading to improved cracking performance of n-tetradecane.
The promotional effects of phosphorous modification on ZSM-5 zeolites by phosphorus oxyacids (H4P2O7, H3PO4, H3PO3, and H3PO2) with different molecular sizes were investigated with catalytic cracking of n-tetradecane as the probe reaction. It was verified that the diffusion of P precursor molecules into ZSM-5 channels was important to prevent aggregation of P species for better stabilization on tetra-coordinated framework aluminum. Meanwhile, the P-Al interaction was proposed based on results of 27Al, 31P, and 29Si MAS NMR. With H3PO2 as the P precursor, easy diffusion into ZSM-5 channels contributed to less formation of polyphosphates, homogeneous distribution of P species, better reserved crystallinity, microporous area and acidic sites for improving cracking performance of n-tetradecane.

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