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Direct Synthesis of Nano-Ferrierite along the 10-Ring-Channel Direction Boosts Their Catalytic Behavior.
Margarit, Vicente J; Díaz-Rey, M Rocío; Navarro, M Teresa; Martínez, Cristina; Corma, Avelino.
Afiliação
  • Margarit VJ; Instituto de Tecnología Química, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas (UPV-CSIC), Valencia, 46022, Spain.
  • Díaz-Rey MR; Instituto de Tecnología Química, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas (UPV-CSIC), Valencia, 46022, Spain.
  • Navarro MT; Instituto de Tecnología Química, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas (UPV-CSIC), Valencia, 46022, Spain.
  • Martínez C; Instituto de Tecnología Química, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas (UPV-CSIC), Valencia, 46022, Spain.
  • Corma A; Instituto de Tecnología Química, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas (UPV-CSIC), Valencia, 46022, Spain.
Angew Chem Int Ed Engl ; 57(13): 3459-3463, 2018 03 19.
Article em En | MEDLINE | ID: mdl-29485242
Ferrierite zeolites with nanosized crystals and external surface areas higher than 250 m2 g-1 have been prepared at relatively low synthesis temperature (120 °C) by means of the collaborative effect of two organic structure directing agents (OSDA). In this way, hierarchical porosity is achieved without the use of post-synthesis treatments that usually involve leaching of T atoms and solid loss. Adjusting the synthesis conditions it is possible to decrease the crystallite size in the directions of the 8- and 10-ring channels, [010] and [001] respectively, reducing their average pore length to 10-30 nm and increasing the number of pores accessible. The small crystal size of the nano-ferrierites results in an improved accessibility of reactants to the catalytic active centers and enhanced product diffusion, leading to higher conversion and selectivity with lower deactivation rates for the oligomerization of 1-pentene into longer-chain olefins.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article