4.7 Article

Water vapor adsorption on metal-exchanged hierarchical porous zeolite-Y

Journal

MICROPOROUS AND MESOPOROUS MATERIALS
Volume 326, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.micromeso.2021.111380

Keywords

Zeolite-Y; Cationic polymer; Hierarchical structure; Metal sites; Water; Adsorption

Funding

  1. ADNOC refining, ADNOC, Abu Dhabi, UAE
  2. Khalifa University of Science and Technology [RC2-2018-024]

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The study successfully synthesized zeolite-Y samples with a hierarchical porous structure using a bifunctional cationic polymer and ion-exchange with metal salts. Different metal ions were introduced into the zeolite-Y structure to enhance water adsorption capacity. The results showed that the hierarchical porous zeolites exhibited improved water uptake capacity compared to conventional zeolite-Y, with the introduction of distinct metal ions leading to further enhancements in water adsorption performance.
The development of efficient zeolite-based adsorbents with high water uptake capacity is an essential requirement for water adsorption and moisture removal technologies. In the present study, zeolite-Y samples with interconnected hierarchical micro-mesoporous network were synthesized by employing a bifunctional cationic polymer (namely, polydiallydimethyl-ammonium chloride, PDDA), and ion-exchanged with several metal salts (such as Zn, Mg, Li) targeting high capacity water adsorption. We systematically investigated water adsorption behavior of hierarchically porous NaY (HP-NaY) samples and studied the influence of their distinct metal exchange analogues on water affinity and total adsorption capacity. The water affinity and water uptake increased for the HP-NaY samples compared to conventional NaY. HP-NaY samples demonstrating a high water adsorption capacity (17.32-17.98 mmol/g) at 303 K and 0.7 relative pressure (P/Po) when compared to commercial zeoliteY (CBV-400, 14.83 mmol/g). A further improvement in water uptake was attained by introduction of distinct metal ions into the hierarchical porous zeolite-Y. HP-LiY exhibited the highest water adsorption capacity (19.08 mmol/g at 0.7 P/Po) amounting to 28% and 15% improvement when compared to CBV-400 and CBV-Li respectively. The observed improvements in water adsorption capacity are attributed to (i) the existence of interconnected micro-mesoporous channel network and higher total pore volume and (ii) the enhancement in accessibility of adsorption sites by H2O molecules. The adsorption data of the samples were also fitted using various adsorption models. Hierarchically porous zeolites displayed site heterogeneity, the latter being rendered by the existence of varying chemical environments between sites within the micropores and the mesopores and the nature of the host metals.

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