4.7 Article

Core-shell structured Y zeolite/hydrophobic organic polymer with improved toluene adsorption capacity under dry and wet conditions

期刊

CHEMICAL ENGINEERING JOURNAL
卷 409, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.128194

关键词

Zeolite; Hydrophobic organic polymer; Hydrophobicity; VOCs; Adsorption

资金

  1. National Key R&D Program of China [2019YFC1904100, 2019YFC1904102, 2019YFC1903902, 2016YFC0205300]
  2. National Engineering Laboratory for Mobile Source Emission Control Technology of China [NELMS2017A03]
  3. Natural National Science Foundation of China [21503144, 21690083]
  4. Tianjin Research Program of Ecological Environmental Treatment [18ZXSZSF00210, 18ZXSZSF00060]
  5. Tianjin Research Program of Application Foundation and Advanced Technique [16JCQNJC05400]
  6. Major Science and Technology Project for Ecological Environment Management in Tianjin [18ZXSZSF00210]

向作者/读者索取更多资源

This study reports a strategy to synthesize Y zeolite and hydrophobic organic polymer core-shell composites, significantly improving the hydrophobicity and toluene adsorption capacity of Y zeolite. The composite exhibits excellent adsorption performance under both dry and wet conditions, suitable for practical applications. Such composite strategy can be applied to other zeolites for hydrophobic modification, increasing the adsorption capacity under wet conditions.
Zeolites with high specific surface area and good stability are considered ideal adsorbent for volatile organic compounds (VOCs) adsorption. However, the hydrophilicity of zeolites surface limits their practical application because of the competitive adsorption between water and VOCs. In this work, we reported a strategy to synthesise Y zeolite and hydrophobic organic polymer core-shell composites (Y@St-DVB), which significantly improved the hydrophobicity and toluene adsorption capacity of Y zeolite. The TEM results showed that hydrophobic organic polymer was uniformly coated on the external surface of Y zeolite through the bridging effect of phenylsilane. The adsorption capacity of Y@St-DVB-12h was 69.9% higher than that of Y zeolite at dry condition, and increased about 96% under 90% relative humidity (RH). It also exhibited excellent adsorption and desorption performance under 60% RH, which was suitable for the practical application. In addition, such composite strategy was suitable for other zeolites (EMT, ZSM-5, and Beta zeolite) to realise hydrophobic modification, which increased the adsorption capacity under wet conditions. This work not only proposes a new hydrophobic zeolite-based VOCs adsorbent, but also provides a new idea for the preparation of a series of hydrophobic adsorbents.

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