AVS 64th International Symposium & Exhibition | |
Plasma Science and Technology Division | Monday Sessions |
Session PS+AS+SE-MoM |
Session: | Atmospheric Pressure Plasmas |
Presenter: | François Reniers, Université Libre de Bruxelles, Belgium |
Authors: | A. Ozkan, Université Libre de Bruxelles, Belgium S. Chorfi, Université Libre de Bruxelles, Belgium L. Brune, Université Libre de Bruxelles, Belgium T. Visart de Bocarmé, Université Libre de Bruxelles, Belgium F. Reniers, Université Libre de Bruxelles, Belgium |
Correspondent: | Click to Email |
The field of plasma-catalysis, i.e. combining a plasma process and a catalyst, either inside the plasma or in its post-discharge is gaining importance for the conversion of CO2 and CH4 mixtures. Indeed, the combination of plasma and catalysis could not only increase the conversion of these gases, but also orient the reaction(s) towards the synthesis of valuable molecules.
This paper will present first the main factors that influence the conversion and the energy efficiency for the reduction of CO2 using an atmospheric pressure dielectric barrier discharge. Second, an alumina supported catalyst will be added between the electrodes and its effects on the conversion of pure CO2, pure CH4 and CO2/CH4 mixtures will be presented. Ni, Co, Cu have been tested, as well as various loadings of Ni.
The conversion is studied by atmospheric mass spectrometry, and the chemical identification of the end products was obtained either by mass spectrometry or gas chromatography.
It is shown that the frequency, the pulse mode, the dielectric nature and thickness strongly influence the conversion and energy efficiency of the reaction, whereas the residence time and the power injected into the discharge modify the conversion[1]. An increase in the Ni loadings leads to an increase in conversion of both CO2 and CH4. If CO and H2, starting molecules for more complex organic chemistry, are always the main products of reaction, C2, C3 and C4 molecules, oxygenated or not are also detected. The effect of the nature of the catalyst on the relative amounts of these molecules is discussed.
[1] : A. Ozkan, A. Bogaerts, F. Reniers, J. Phys. D: Appl. Phys. 50 (2017) 084004, doi:10.1088/1361-6463/aa562c