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 Tao-Eldrup model. The combination of both methods can be useful for the advanced characterization of microporous, mesoporous and hierarchical materials.
| Original language | English |
|---|---|
| Pages (from-to) | 15269-15277 |
| Number of pages | 9 |
| Journal | Physical Chemistry Chemical Physics |
| Volume | 18 |
| Issue number | 22 |
| Early online date | 16 May 2016 |
| DOIs | |
| Publication status | Published - 14 Jun 2016 |
Keywords
- IPC zeolites
- Positron annihilation spectroscopy
- Pore size distribution
- High-resolution absorption
- ADOR
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