Abstract
Zeolites with high framework Si/Al ratios are of interest for industrial applications due to their hydrothermal stability. They are usually synthesized in the presence of pre‐prepared organic structure directing agents (OSDAs). The high silica ERS‐7 zeolite (topology type ESV) can be crystallized using N, N‐dimethylpyrrolidinium (dmpyrr) that is formed in situ via cyclization of N, N, N’, N’‐tetramethyl‐1,4‐diaminobutane (tmdab) when a cationic polymer is also present. The in situ generation of dmpyrr is demonstrated by solid‐state 13C NMR spectroscopy and supported by both chemical analyses and comparative syntheses using pre‐prepared dmpyrr. The cationic polymer inhibits the crystallization of mordenite, which is otherwise observed to be the favored product. The ERS‐7 prepared via in situ dmpyrr synthesis (Si/Al = 14) is characterized by PXRD and solid‐state NMR spectroscopy. The CO2 adsorption seen for the H‐ and Na‐forms indicates interactions with accessible Na+ cations. The synthetic studies indicate the potential for in situ generation of OSDAs to reduce the need for extended OSDA syntheses.
| Original language | English |
|---|---|
| Article number | e202500327 |
| Journal | Chemistry - A European Journal |
| Volume | 31 |
| Issue number | 30 |
| Early online date | 7 May 2025 |
| DOIs | |
| Publication status | Published - 27 May 2025 |
Keywords
- ESV topology type
- in situ OSDA formation
- zeolite synthesis
- cationic polymer