Guided Crystallization of Zeolite Beads Composed of ZSM-12 Nanosponges

Kassem Moukahhal, Ludovic Josien, Habiba Nouali, Joumana Toufaily, Tayssir Hamieh, T. Jean Daou*, Benedicte Lebeau*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The direct route using a bifunctional amphiphilic structuring agent for the synthesis of hierarchical nanozeolites coupled with pseudomorphic transformation was used for the crystallization of hierarchized zeolite beads/hollow spheres composed of ZSM-12 (MTW structural-type) with nanosponge morphology. These beads/hollow spheres have the same average diameter of 20 µm as their counterpart amorphous mesoporous silica beads used as precursor in the starting synthesis mixture. The effects of synthesis parameters, such as stirring and treatment time at 140 C, on the morphology, structure, and texture of the materials have been investigated using X-ray diffraction (XRD), N 2 sorption, scanning electronic microscopy (SEM), and transmission electronic microscopy (TEM) techniques. Static conditions were found necessary to maintain the morphology of the starting amorphous silica beads. An Ostwald ripening phenomenon was observed with the increase in hydrothermal treatment time leading to the dissolution of the interior of some beads to form core shell beads or hollow spheres with larger crystals on the outer surface. These ZSM-12 beads/hollow spheres possess higher porous volume than conventional ZSM-12 zeolite powder and can be used directly for industrial applications.

Original languageEnglish
Article number828
Pages (from-to)1-15
Number of pages15
JournalCrystals
Volume10
Issue number9
DOIs
Publication statusPublished - Sept 2020
Externally publishedYes

Keywords

  • zeolite beads
  • hierarchical zeolite
  • pseudomorphic transformation
  • ZSM-12
  • shaping
  • nanosponges
  • CRYSTAL MORPHOLOGY
  • NEW-GENERATION
  • NANOSHEETS
  • MFI
  • SILICALITE-1
  • PERFORMANCE
  • CONVERSION
  • MONOLITHS
  • PROGRESS
  • CAPTURE

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