4.7 Article

Multiple templating strategy for the control of aluminum and phosphorus distributions in AFX zeolite

Journal

MICROPOROUS AND MESOPOROUS MATERIALS
Volume 321, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.micromeso.2021.111124

Keywords

AFX zeolite; Structure-directing agent; Control of aluminum distribution; Alkylphosphonium; Control of phosphorus distributions

Funding

  1. JSPS KAKENHI [JP16H04218, 19H02513]
  2. JSPS Core-to-Core Program
  3. Research Association of Automotive Internal Combustion Engines (AICE) project, Japan
  4. International Network on Polyoxometalate Science at Hiroshima University
  5. Grants-in-Aid for Scientific Research [19H02513] Funding Source: KAKEN

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This study utilized a multiple templating strategy to control the distribution of aluminum and phosphorus in AFX zeolite synthesis. The use of bulky template TEBOP2+ and small template Me4N+ resulted in AFX zeolites with different Si/Al ratios. Characterization by elemental analysis and NMR spectroscopy revealed that TEBOP2+ mainly occupied the wide aft cage, while Me4N+ preferentially occupied the narrow gme cage, impacting the Si/Al ratio.
A multiple templating strategy using both bulky and small organic structure-directing agents (SDAs) was adapted for AFX zeolite synthesis in order to control the distribution of aluminum and phosphorus. An AFX zeolite with an Si/Al ratio of 4.8 was obtained in the presence of a bulky and rigid SDA, N,N,N',N'-tetraethylbicyclo[2.2.2] oct-7-ene-2,3:5,6-dipyrrolidinium cation (TEBOP2+), and co-existing Na+ cations. The use of a tetramethylammonium cation (Me4N+) as the SDA instead of Na+ provided AFX zeolite with a middle Si/Al ratio of 7.9. Elemental analysis and 13C and 29Si magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy suggested that TEBOP2+ existed in the wide aft cage in both AFX zeolites, while the higher Si/Al ratio was derived from the lower charge density of Me4N+ occupying the narrow gme cage. We also attempted to control the distribution of phosphorus in phosphorus-modified AFX zeolite. The large tetraethylphosphonium cation (Et4P+) and small tetramethylphosphonium cation (Me4P+) were selectively incorporated into aft and gme cages during the hydrothermal synthesis, respectively. As a result, phosphorus oxide with different polymerization degrees were formed by calcination treatment according to the size of the cage occupied by the phosphorusmodifying agents (P-MAs). This direct phosphorus modification using alkylphosphonium was characterized by elemental analysis and 13C, 27Al, and 31P MAS NMR and two-dimensional (2D) 31P-27Al heteronuclear correlation NMR spectroscopies.

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