SCI和EI收录∣中国化工学会会刊

Chinese Journal of Chemical Engineering ›› 2020, Vol. 28 ›› Issue (12): 3052-3060.DOI: 10.1016/j.cjche.2020.07.039

• Catalysis, Kinetics and Reaction Engineering • Previous Articles     Next Articles

Enhancing hydrothermal stability of framework Al in ZSM-5: From the view on the transformation between P and Al species by solid-state NMR spectroscopy

Lei Han, Ying Ouyang, Enhui Xing, Yibin Luo, Zhijian Da   

  1. State Key Laboratory of Catalytic Materials and Reaction Engineering, Research Institute of Petroleum Processing, Sinopec, Beijing 100083, China
  • Received:2020-03-18 Revised:2020-06-27 Online:2021-01-11 Published:2020-12-28
  • Contact: Zhijian Da

Enhancing hydrothermal stability of framework Al in ZSM-5: From the view on the transformation between P and Al species by solid-state NMR spectroscopy

Lei Han, Ying Ouyang, Enhui Xing, Yibin Luo, Zhijian Da   

  1. State Key Laboratory of Catalytic Materials and Reaction Engineering, Research Institute of Petroleum Processing, Sinopec, Beijing 100083, China
  • 通讯作者: Zhijian Da

Abstract: HZSM-5, with good surface acidity and shape selectivity, was reported as hydrocarbon cracking catalyst for multiple decades, however the hydrothermal stability, especially dealumination of tetrahedrally coordinated framework aluminum (TFAl), has been proved extensively as one of the major challenges during reactionregeneration process. Phosphorus was proposed to stabilize TFAl and indeed it enhanced the hydrothermal stability. Unfortunately, most of the phosphorus species would remain outside of the zeolite pore, mainly as polyphosphate species, and block the micropore severely, with only a limited portion introduced into the channel being able to interact with TFAl. Enlarging the pore size by alkali treatment (desilication) is one of the most convinced methods, but the details about specific P species during alkali treatment and its transformation upon hydrothermal activation is not acquired, thus the mechanism has not been fully understood. Herein, the P-containing species and its transformation during direct P modification and acid/alkali treatment followed by P modification have been studied, and the mechanism on the interaction between P and Al species has been investigated, using several analytical methods, especially Solid-state nuclear magnetic resonance (SSNMR) spectroscopy. It was found that the combination of desilication and subsequent phosphorus modification can enhance the activity of the ZSM-5 for the cracking of ethylcyclohexane, due to the better hydrothermal stabilization of acid sites by the enhanced interaction between phosphorus and TFAl, resulting from the improved accessibility of TFAl because of the successful generation of mesoporosity. Whereas the acid treatment followed by phosphorus modification, with declined retention of crystallinity and P/Al ratio, monoclinic/orthorhombic transition during steam activation, and the failed generation of mesopores, would cause obvious aggregation of the phosphorus species and could not improve the hydrothermal stability of the ZSM-5effectively, and the direct phosphatation turned out much worse. Finally, a specific index that the intensity of the signal at 39 in 27Al MAS NMR spectra before steam activation was proposed as the indicator for determining the efficiency of phosphorus modification. And the proposed mechanism on the interaction between phosphorus and TFAl during the phosphorus modification could also be applicable in other zeolites.

Key words: Phosphorus modification, TFAl, NaOH/alkali treatment, Interaction, ZSM-5

摘要: HZSM-5, with good surface acidity and shape selectivity, was reported as hydrocarbon cracking catalyst for multiple decades, however the hydrothermal stability, especially dealumination of tetrahedrally coordinated framework aluminum (TFAl), has been proved extensively as one of the major challenges during reactionregeneration process. Phosphorus was proposed to stabilize TFAl and indeed it enhanced the hydrothermal stability. Unfortunately, most of the phosphorus species would remain outside of the zeolite pore, mainly as polyphosphate species, and block the micropore severely, with only a limited portion introduced into the channel being able to interact with TFAl. Enlarging the pore size by alkali treatment (desilication) is one of the most convinced methods, but the details about specific P species during alkali treatment and its transformation upon hydrothermal activation is not acquired, thus the mechanism has not been fully understood. Herein, the P-containing species and its transformation during direct P modification and acid/alkali treatment followed by P modification have been studied, and the mechanism on the interaction between P and Al species has been investigated, using several analytical methods, especially Solid-state nuclear magnetic resonance (SSNMR) spectroscopy. It was found that the combination of desilication and subsequent phosphorus modification can enhance the activity of the ZSM-5 for the cracking of ethylcyclohexane, due to the better hydrothermal stabilization of acid sites by the enhanced interaction between phosphorus and TFAl, resulting from the improved accessibility of TFAl because of the successful generation of mesoporosity. Whereas the acid treatment followed by phosphorus modification, with declined retention of crystallinity and P/Al ratio, monoclinic/orthorhombic transition during steam activation, and the failed generation of mesopores, would cause obvious aggregation of the phosphorus species and could not improve the hydrothermal stability of the ZSM-5effectively, and the direct phosphatation turned out much worse. Finally, a specific index that the intensity of the signal at 39 in 27Al MAS NMR spectra before steam activation was proposed as the indicator for determining the efficiency of phosphorus modification. And the proposed mechanism on the interaction between phosphorus and TFAl during the phosphorus modification could also be applicable in other zeolites.

关键词: Phosphorus modification, TFAl, NaOH/alkali treatment, Interaction, ZSM-5