4.7 Article

Effect of active zinc oxide dispersion on reduced graphite oxide for hydrogen sulfide adsorption at mid-temperature

Journal

APPLIED SURFACE SCIENCE
Volume 280, Issue -, Pages 360-365

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2013.04.161

Keywords

ZnO/rGO composite; H2S adsorption; Reduced graphite oxide; Zinc oxide

Funding

  1. National Sciences and Engineering Research Council of Canada (NSERC)
  2. Energy Efficiency & Resources Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP)
  3. Korea government Ministry of Knowledge Economy [2011201020004B]
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [2011201020004B] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Composites of Zinc oxide (ZnO) with reduced graphite oxide (rGO) were synthesized and used as adsorbents for hydrogen sulfide (H2S) at 300 degrees C. Various characterization methods (TGA, XRD, FT-IR, TEM and XPS) were performed in order to link their H2S adsorption performance to the properties of the adsorbent's surface. Microwave-assisted reduction process of graphite oxide (GO) provided mild reduction environment, allowing oxygen-containing functional groups to remain on the rGO surface. It was confirmed that for the ZnO/rGO synthesize using the microwave-assisted reduction method, the ZnO particle size and the degree of ZnO dispersion remained stable over time at 300 degrees C, which was not the case for only the ZnO particles themselves. This stable highly dispersed feature allows for sustained high surface area over time. This was confirmed through breakthrough experiments for H2S adsorption where it was found that the ZnO/rGO composite showed almost four times higher ZnO utilization efficiency than ZnO itself. The effect of the H-2 and CO2 on H2S adsorption was also investigated. The presence of hydrogen in the H2S stream had a positive effect on the removal of H2S since it allows a reducing environment for Zn-O and Zn-S bonds, leading to more active sites (Zn2+) to sulfur molecules. On the other hand, the presence of carbon dioxide (CO2) showed the opposite trend, likely due to the oxidation environment and also due to possible competitive adsorption between H2S and CO2. (C) 2013 Elsevier B.V. All rights reserved.

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