6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Effect of Pr, Sm, and Tb Doping on the Morphology, Crystallite Size, and N2O Decomposition Activity of Co3O4Nanorods

      , , ,
      Journal of Nanomaterials
      Hindawi Limited

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Cobalt(II,III) oxide, Co 3O 4, is a promising catalyst for nitrous oxide direct decomposition. In this paper we report effect of doping with some rare earth (RE) elements (Pr, Sm, and Tb) on the morphology and crystallite size of Co 3O 4nanorods. The various precursors (RE/Co oxalates) were prepared via the microwave assisted method and subsequent calcination. The decomposition pathway of these precursors was followed using thermogravimetric analysis (TGA). Based on thermal analysis results, Pr-, Sm-, and Tb-doped Co 3O 4samples were obtained via the calcination in static air at 500°C for their oxalate precursors. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and hydrogen temperature programmed reduction (H 2-TPR) were used to characterize the RE-doped cobalt oxide catalysts. The activity of the prepared catalysts was investigated for N 2O direct decomposition and compared with that of the undoped Co 3O 4catalyst. It was shown that the promoted Co 3O 4catalysts revealed higher activity compared to the unpromoted one. The dependence of the activity on both the catalysts particle size and the reduction behaviour was discussed.

          Related collections

          Most cited references32

          • Record: found
          • Abstract: not found
          • Article: not found

          Catalytic decomposition of N2O over CeO2 promoted Co3O4 spinel catalyst

            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Formation and control of N2O in nitric acid production

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Highly sensitive and fast responding CO sensor based on Co3O4 nanorods.

              Co(3)O(4) nanorods (diameters approximately 6-8 nm and lengths approximately 20-30 nm) were synthesized for the first time through a simple co-precipitation/digestion method by calcination of cobalt hydroxyl carbonate in air and their CO gas sensing properties were investigated. The Co(3)O(4) nanorods exhibited outstanding gas sensing characteristics such as, higher gas response (approximately 6.55-50 ppm CO gas at 250 degrees C), extremely rapid response (approximately 3-4s), fast recovery (approximately 5-6s), excellent repeatability, good selectivity and lower operating temperature (approximately 250 degrees C). Furthermore, the Co(3)O(4) nanorods are able to detect up to 5 ppm for CO with reasonable sensitivity (approximately 3.32) at an operating temperature 250 degrees C and they can be reliably used to monitor the concentration of CO over the range (5-50 ppm). The experimental results clearly demonstrate the potential of using the Co(3)O(4) nanorods as sensing material in the fabrication of CO sensors. Plausible CO sensing mechanism of the Co(3)O(4) nanorods is also discussed.
                Bookmark

                Author and article information

                Journal
                Journal of Nanomaterials
                Journal of Nanomaterials
                Hindawi Limited
                1687-4110
                1687-4129
                2015
                2015
                : 2015
                :
                : 1-10
                Article
                10.1155/2015/580582
                a0daf890-cf3e-400b-910f-5ecef3ed2280
                © 2015

                http://creativecommons.org/licenses/by/4.0/

                History

                Comments

                Comment on this article