4.6 Article

Enhanced Catalytic Performance and Sulfur Dioxide Resistance of Reduced Graphene Oxide-Promoted MnO2 Nanorods-Supported Pt Nanoparticles for Benzene Oxidation

期刊

CATALYSTS
卷 12, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/catal12111426

关键词

volatile organic compound; benzene oxidation; manganese dioxide nanorod; reduced graphene oxide; supported Pt nanocatalyst; sulfur dioxide resistance

资金

  1. National Natural Science Foundation of China
  2. National Key Research and Development Program of China
  3. [21277008]
  4. [2017YFC0209905]

向作者/读者索取更多资源

This study investigates catalysts for the degradation of volatile organic compounds in exhaust gas. The introduction of Pt and rGO on α-MnO2 nanorods significantly enhances the catalyst's activity. Among the catalysts tested, the 0.94Pt-1.0rGO/α-MnO2 catalyst exhibits the best catalytic performance, with a benzene conversion rate of 90%.
The reduced graphene oxide (rGO)-promoted alpha-MnO2 nanorods-supported Pt (xPt-yrGO/alpha-MnO2, x = 0.93 wt%, y = 0.5, 1.0, and 2.0 wt%) nanocatalysts were prepared using a polyvinyl alcohol (PVA)-protected reduction method. After an appropriate loading of Pt on alpha-MnO2, the strong metal-support interaction between Pt and alpha-MnO2 was beneficial for an increase in catalytic activity. The simultaneous addition of rGO to alpha-MnO2 not only provided a more amount of benzene adsorption sites, but also acted as an electron transfer channel to accelerate charge migration, thus further improving catalytic activity of alpha-MnO2. Among all of the catalyst samples, 0.94Pt-1.0rGO/alpha-MnO2 showed the best catalytic performance with 90% benzene conversion at 160 degrees C and a gas hourly space velocity (GHSV) of 60,000 mL/(g h), which was better than that over the other Pt-based catalysts. The results of in situ DRIFTS characterization revealed that phenol, benzoquinone, and carboxylate species were the intermediates and eventually oxidized to CO2 and H2O. When sulfur dioxide was present, catalytic activity of alpha-MnO2 decreased due to the formation of manganese sulfate that blocked the active sites, while the loading of Pt and rGO hindered the chemisorption of SO2 and prevented the active sites of the catalyst from being poisoned by SO2, thus enhancing sulfur resistance of the catalyst. The 0.94Pt-1.0rGO/alpha-MnO2 catalyst presented in this work can be considered as a cost-effective and promising catalyst for the oxidative removal of volatile organic compounds.

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