Issue 22, 2016

Structural analysis of IPC zeolites and related materials using positron annihilation spectroscopy and high-resolution argon adsorption

Abstract

The advanced investigation of pore networks in isoreticular zeolites and mesoporous materials related to the IPC family was performed using high-resolution argon adsorption experiments coupled with the development of a state-of-the-art non-local density functional theory approach. The optimization of a kernel for model sorption isotherms for materials possessing the same layer structure, differing only in the interlayer connectivity (e.g. oxygen bridges, single- or double-four-ring building units, mesoscale pillars etc.) revealed remarkable differences in their porous systems. Using high-resolution adsorption data, the bimodal pore size distribution consistent with crystallographic data for IPC-6, IPC-7 and UTL samples is shown for the first time. A dynamic assessment by positron annihilation lifetime spectroscopy (PALS) provided complementary insights, simply distinguishing the enhanced accessibility of the pore network in samples incorporating mesoscale pillars and revealing the presence of a certain fraction of micropores undetected by gas sorption. Nonetheless, subtle differences in the pore size could not be discriminated based on the widely-applied TaoEldrup model. The combination of both methods can be useful for the advanced characterization of microporous, mesoporous and hierarchical materials.

Graphical abstract: Structural analysis of IPC zeolites and related materials using positron annihilation spectroscopy and high-resolution argon adsorption

Supplementary files

Article information

Article type
Paper
Submitted
23 Mar 2016
Accepted
16 May 2016
First published
16 May 2016

Phys. Chem. Chem. Phys., 2016,18, 15269-15277

Structural analysis of IPC zeolites and related materials using positron annihilation spectroscopy and high-resolution argon adsorption

J. Jagiello, M. Sterling, P. Eliášová, M. Opanasenko, A. Zukal, R. E. Morris, M. Navaro, A. Mayoral, P. Crivelli, R. Warringham, S. Mitchell, J. Pérez-Ramírez and J. Čejka, Phys. Chem. Chem. Phys., 2016, 18, 15269 DOI: 10.1039/C6CP01950A

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