Flexible-structured systems made of ceramic fibers containing Pt-NaY zeolite used as CO oxidation catalysts

Catalytic ceramic papers were developed by incorporating Pt-NaY zeolite to ceramic papers. The necessary mechanical strength was enhanced by the addition of natural borate compounds, which confer elasticity and resistance similar to those obtained using colloidal suspensions, which are the most comm...

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Detalles Bibliográficos
Autores: Cecchini, Juan Pablo, Banus, Ezequiel David, Leonardi, Sabrina Antonela, Zanuttini, Miguel Angel Mario, Ulla, Maria Alicia del H., Milt, Viviana Guadalupe
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2015
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/17542
Acceso en línea:http://hdl.handle.net/11336/17542
Access Level:acceso abierto
Palabra clave:Ceramic Papers
Zeolite
https://purl.org/becyt/ford/2.4
https://purl.org/becyt/ford/2
Descripción
Sumario:Catalytic ceramic papers were developed by incorporating Pt-NaY zeolite to ceramic papers. The necessary mechanical strength was enhanced by the addition of natural borate compounds, which confer elasticity and resistance similar to those obtained using colloidal suspensions, which are the most commonly used binders. Pt-NaY zeolite was incorporated into ceramic papers either during the papermaking process or by spraying a zeolitic suspension on ceramic papers. The partial encapsulation of the faujasite by the sintering of the borate compound during the calcination step made catalytic ceramic papers less active toward the CO oxidation reaction than the corresponding traditional systems (Pt-NaY zeolite coated onto cordierite monoliths or the powder Pt-NaY faujasite). Light-off curves indicated that the activity of Pt-NaY zeolite was preserved when incorporating the zeolitic component by spray, in which case the CO oxidation reaction ran away at ca. 130 °C, and the total CO conversion was achieved at 150 °C, maintaining 100 % CO conversion for more than 90 h.