4.8 Article

Silicon redistribution, acid site loss and the formation of a core-shell texture upon steaming SAPO-34 and their impact on catalytic performance in the Methanol-to-Olefins (MTO) reaction

Journal

JOURNAL OF CATALYSIS
Volume 395, Issue -, Pages 425-444

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2021.01.012

Keywords

Steamed SAPO-34; Methanol-to-olefins; IR spectroscopy and microscopy; FIB SEM

Funding

  1. Engineering and Physical Sciences Research Council (EPSRC, Centre for Doctoral Training in Critical Resource Catalysis) [EP/I017008/1]
  2. Scotland's Chemistry departments (ScotCHEM)
  3. ScotCHEM
  4. SCI
  5. Santander
  6. EPSRC [EP/L017008/1, EP/R023751/1]
  7. EPSRC [EP/L017008/1, EP/R023751/1, EP/T019298/1] Funding Source: UKRI

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SAPO-34 is a commercially-implemented catalyst for selective production of ethene and propene from methanol, but high temperature regeneration leads to deactivation. Prolonged hydrothermal treatment affects the structure and properties of SAPO-34, explaining changes in its catalytic performance. Steaming improves the lifetime of SAPO-34 in MTO catalysis, but irreversible changes occur, especially in crystals with higher Si contents.
SAPO-34 is a commercially-implemented silicoaluminophosphate catalyst for selective high yield production of ethene and propene from methanol, but high temperature regeneration in the presence of steam leads to its deactivation. A comprehensive investigation of the effect of prolonged hydrothermal treatment on the structure and properties of SAPO-34 explains the changes in its catalytic methanol-to-olefins (MTO) performance. Microcrystalline powdered SAPO-34 (ca. 3 mu m crystals, Al17.1P15.6Si3.3O72) and two batches of larger single crystals of SAPO-34 of different Si concentration (20-100 mu m; Al17.3P14.7Si4.0O72 and Al17.7P12.3Si5.9O72) were steamed (p(H2O) = 0.95 atm) at 873-1023 K for up to 240 h. The acidity (NH3-TPD), crystallinity (PXRD), framework cation environment (solid-state Al-27, Si-29 and P-31 MAS NMR) and porosity were followed for all materials; larger crystals were amenable to single crystal X-ray diffraction, FIB-SEM and synchrotron IR microspectroscopy, including operando study during methanol and dimethyl ether conversions. Some level of steaming improved the lifetime of all SAPO-34 materials in MTO catalysis without affecting their olefin selectivity, although more severe conditions led to the formation of core-shell structures, microporosity loss and eventually at 1023 K, recrystallization to a dense phase. All these irreversible changes occurred faster in crystals with higher Si contents. The initial increase in catalytic lifetime results from an activated reduction in acid site density (E-act = 146(18) kJ mol(-1)), a result of redistribution of Si within the SAPO framework without porosity loss. Operando IR with online product analysis during methanol conversion suggests similar reaction pathways in calcined and steamed crystals, but with greatly reduced methoxy group densities in the latter. The gradual development of optically dark crystal cores upon progressive steaming was shown by FIB-SEM to be due to the formation of regions with meso- and macropores, and these were shown by IR mapping to possess low hydroxyl densities. (C) 2021 Elsevier Inc. All rights reserved.

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