4.5 Article

Synthesis effects on activity and stability of Pt-CeO2 catalysts for partial oxidation of methane

Journal

MOLECULAR CATALYSIS
Volume 432, Issue -, Pages 131-143

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mcat.2017.01.006

Keywords

Pt-nanoparticles; CeO2; Metal-support interaction; Partial oxidation; Methane

Funding

  1. UGC, New Delhi, India
  2. CSIR [CSC-0125, CSC-0117]
  3. DST Government of India [DST/INT/Aus/GCP-4/13(C)]
  4. Nanomission Scheme [SR/NM/NS-1105/2015]
  5. Italian CNR
  6. Indian CSIR
  7. Proton Factory Advisory Committee [2013G210, 2014G070]

Ask authors/readers for more resources

The objective of this study is to explore the effect of catalyst synthesis procedure on the activity of catalysts for partial oxidation of methane. In this aspect, Pt-nanoparticles supported CeO2 catalysts were prepared by Hydrothermal, co-precipitation, impregnation and by controlled deposition of platinum nanoparticles on hydrothermally prepared cerium oxide. Prepared catalysts were characterized by BET-surface area, X-ray diffraction, H-2-Chemisorption, Transmission electron microscopy, Temperature programmed reduction, Inductively coupled plasma atomic emission spectroscopy and X-ray photoelectron spectroscopy. The study revealed that the catalyst preparation procedure plays a very crucial role on morphology, catalyst particle size, metal support interaction and activity of the catalysts. Catalytic activities were tested for partial oxidation of methane in the temperature range 350-800 degrees C. The study revealed that the catalyst prepared by controlled deposition of Pt-nanoparticles on hydrothermally prepared cerium oxide showed better activity for partial oxidation of methane compared to the catalysts prepared by other conventional methods. Controlled deposition of Pt-nanoparticles generated better metal-support interaction compared to the catalysts prepared by conventional hydrothermal, co-precipitation and impregnation methods. All the catalysts showed excellent coke resisting ability but the deactivation of most of the catalyst was found to be caused by catalyst particles sintering and re-oxidation of the Pt particles during catalysis. (C) 2017 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available