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Performance of platinum doping on spent alkaline battery-based catalyst for complete oxidation of o-xylene. | LitMetric

AI Article Synopsis

  • The study explores the oxidation of o-xylene, a type of volatile organic compound (VOC), using a platinum-doped alkaline battery-based catalyst to assess its properties and effectiveness.
  • Various characterization techniques, such as FE/TEM, BET, and XRD, were employed to analyze the catalysts, which included elements like manganese, zinc, and iron, indicating their complex structure.
  • Increasing the platinum doping from 0.1 to 1 wt% improved the catalyst's performance, allowing complete oxidation of o-xylene at lower temperatures, particularly with the 1.0 wt% Pt/SAB (400) catalyst achieving success at 280 °C.

Article Abstract

Oxidation of o-xylene was performed using alkaline battery-based catalyst doped with platinum to investigate the properties and activities. O-xylene was selected as the model of volatile organic compound (VOC) in this work. Physicochemical properties of the selected catalysts were characterized by FE/TEM (field emission transmission electron microscopy), BET (Brunauer-Emmett-Teller) analysis, XRD (X-ray powder diffraction), SEM/EDX (scanning electron microscopy/energy dispersive X-ray spectroscopy), and H-TPR (hydrogen temperature programmed reduction). Major elements of the spent alkaline battery-based catalyst treated with sulfuric acid solution [SAB (400) catalyst] were manganese, zinc, iron, oxygen, carbon, chlorine, aluminum, sodium, silicon, and potassium. Increasing the doping amount of platinum on SAB (400) catalyst from 0.1 to 1 wt% increased particle size of platinum and lowered the temperature of TPR (TTP) for SAB (400) catalyst. Better redox properties were achieved with an increase in the o-xylene conversion according to the doping amount of platinum. When GHSV (gas hourly space velocity) was 40,000 h, o-xylene was oxidized completely over SAB (400) catalyst and 1.0 wt% Pt/SAB(400) catalyst at temperatures of 400 °C and 280 °C, respectively.

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Source
http://dx.doi.org/10.1007/s11356-020-09575-6DOI Listing

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