Cage-based small-pore catalysts for NH3-SCR prepared by combining bulky organic structure directing agents with modified zeolites as reagents
It has been possible to efficiently synthesize high-silica ERI and AFX zeolites with nano-sized primary crystallites (30–200 nm). This was achieved by using a dicationic and rigid organic structure directing agent (OSDA) that fits within the large cavities of these zeolites, and the use of FAU zeoli...
| Autores: | , , , , , |
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| Tipo de documento: | artigo |
| Estado: | Versión aceptada para publicación |
| Data de publicação: | 2017 |
| País: | España |
| Recursos: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositório: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/162141 |
| Acesso em linha: | http://hdl.handle.net/10261/162141 |
| Access Level: | Acceso aberto |
| Palavra-chave: | Small-pore zeolites Organic structure directing agents (OSDAs) Erionite AFX NOx abatement |
| Resumo: | It has been possible to efficiently synthesize high-silica ERI and AFX zeolites with nano-sized primary crystallites (30–200 nm). This was achieved by using a dicationic and rigid organic structure directing agent (OSDA) that fits within the large cavities of these zeolites, and the use of FAU zeolites as initial Si- and Al-sources. Cu- and Fe-based ERI and AFX materials were prepared following both post-synthetic cation exchange and direct synthesis methodologies, showing good activity for the selective catalytic reduction (SCR) of nitrogen oxide using ammonia. Accelerated hydrothermal ageing of the zeolites at high temperature (i.e. 750 °C) shows the necessity of removing the alkali cations remaining in the zeolites to obtain stable materials. Furthermore, the catalytic performance of the prepared Cu- and Fe-containing AFX catalysts, both before and after ageing treatment, approaches the catalytic activity of Cu- and Fe-CHA. |
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