-xylene isomerization over IWW zeolite with a three-modal pore structure: The effect of crystal morphology

Xylene isomerization is a key zeolite-catalyzed petrochemical process for the production of p -xylene, a highly demanded intermediate in the polymer industry. While MFI-type zeolites are widely used in industry as shapeselective catalysts, xylene isomerization also serves as a benchmark reaction for evaluating the shapeselectivity of new zeolite catalysts in relation to their porosity. In this study, IWW zeolite with a three-modal pore network of isolated 8- and 12-ring pores intersected by 10-ring channels was investigated for m -xylene isomerization, with a focus on how both the multidimensional pore system and crystal morphology affect catalytic performance. IWW zeolites were synthesized as germanosilicates with platelet-like and needle-like crystals, functionalized by post-synthetic Ge-to-Al substitution, and tested in gas-phase m -xylene isomerization in comparison with reference zeolite catalysts containing unimodal 8-, 10-, or 12-ring channels. Compared to MFI with a similar concentration of acid sites, Al-IWW catalysts exhibited higher m -xylene conversion across a wide range of WHSV values (4.4 – 40 h -1 ), regardless of crystal morphology. Needle-like Al-IWW crystals achieved para -selectivity comparable to that of MFI, while platelet-like Al-IWW outperformed MFI in p -xylene yield at short contact times (WHSV = 40 h -1 ). STEM analysis confirmed that the 10-ring channels are aligned along the length of the needle-like crystals, promoting shapeselective p -xylene formation. In contrast, the 12-ring channels running along the extended dimension of the platelet-like crystals facilitate the diffusion of reactant and product molecules to and from the active sites. All in all, the integration of multi-sized pores and tunable crystal morphology in IWW zeolites may offer a promising strategy for balancing selectivity and activity in p -xylene synthesis. • Multimodal-pore Al-IWW zeolites prepared by post-synthetic Ge-to-Al substitution • Al-IWW with needle- and platelet-like morphology vs. MFI in m -xylene isomerization • Comparable para-selectivity of needle-like Al-IWW and MFI • Higher yield of p-xylene over platelet-like Al-IWW vs. MFI

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Journal
Catalysis Today
Published
2025-09-10
DOI
https://doi.org/10.1016/j.cattod.2025.115563
Primary Topic
Zeolite Catalysis and Synthesis
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article
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article

-xylene isomerization over IWW zeolite with a three-modal pore structure: The effect of crystal morphology

Mariya Shamzhy, Emad Shamma, Subhajyoti Samanta, Michal Mazur et al.
Catalysis Today
Zeolite Catalysis and Synthesis
article

-xylene isomerization over IWW zeolite with a three-modal pore structure: The effect of crystal morphology

Mariya Shamzhy, Emad Shamma, Subhajyoti Samanta, Michal Mazur, Maksym Opanasenko, Alica Seidlová
article en

Abstract

Xylene isomerization is a key zeolite-catalyzed petrochemical process for the production of p -xylene, a highly demanded intermediate in the polymer industry. While MFI-type zeolites are widely used in industry as shapeselective catalysts, xylene isomerization also serves as a benchmark reaction for evaluating the shapeselectivity of new zeolite catalysts in relation to their porosity. In this study, IWW zeolite with a three-modal pore network of isolated 8- and 12-ring pores intersected by 10-ring channels was investigated for m -xylene isomerization, with a focus on how both the multidimensional pore system and crystal morphology affect catalytic performance. IWW zeolites were synthesized as germanosilicates with platelet-like and needle-like crystals, functionalized by post-synthetic Ge-to-Al substitution, and tested in gas-phase m -xylene isomerization in comparison with reference zeolite catalysts containing unimodal 8-, 10-, or 12-ring channels. Compared to MFI with a similar concentration of acid sites, Al-IWW catalysts exhibited higher m -xylene conversion across a wide range of WHSV values (4.4 – 40 h -1 ), regardless of crystal morphology. Needle-like Al-IWW crystals achieved para -selectivity comparable to that of MFI, while platelet-like Al-IWW outperformed MFI in p -xylene yield at short contact times (WHSV = 40 h -1 ). STEM analysis confirmed that the 10-ring channels are aligned along the length of the needle-like crystals, promoting shapeselective p -xylene formation. In contrast, the 12-ring channels running along the extended dimension of the platelet-like crystals facilitate the diffusion of reactant and product molecules to and from the active sites. All in all, the integration of multi-sized pores and tunable crystal morphology in IWW zeolites may offer a promising strategy for balancing selectivity and activity in p -xylene synthesis. • Multimodal-pore Al-IWW zeolites prepared by post-synthetic Ge-to-Al substitution • Al-IWW with needle- and platelet-like morphology vs. MFI in m -xylene isomerization • Comparable para-selectivity of needle-like Al-IWW and MFI • Higher yield of p-xylene over platelet-like Al-IWW vs. MFI

Catalysis TodayVol. 462
Charles University (CZ), Czech Academy of Sciences, Institute of Macromolecular Chemistry (CZ)
Openalex Percentile: Top 80%
Zeolite Catalysis and Synthesis
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