RESUMO
This paper reports on the thermally-driven and non-thermal plasma-driven reaction of IsoPropyl Alcohol (IPA) on ceria (CeO2) with the aim to investigate the differences between plasma catalytic interactions and the analogous thermal reactions. Both were studied by in situ infrared spectroscopy: using diffuse reflectance for the thermal reaction and reflectance infrared for the plasma. For the thermal reaction, the activity towards the formation of acetone and acetaldehyde and, at higher temperatures, CO2 was dependent upon the coverage of surface carbonates and bicarbonates, suggesting at least some of these species blocked the relevant active sites. However, for the first time, methane and cold CO was observed and this was interpreted in terms of a roaming mechanism taking place at the surface via a loose transition state. By contrast, the plasma-driven process was not inhibited by adsorbed carbonaceous species producing acetone followed by isophorone and a polymethylacetylene-like polymer. Comparisons are made between the equivalent thermal and plasma reactions of isopropyl alcohol on Macor and tin oxide surfaces. On Macor the plasma produced similar products whereas on tin oxide there was no reaction. This suggests that the selection of catalysts for plasma processing cannot necessarily be determined from the equivalent thermal process.
RESUMO
This paper reports in situ Fourier transform infrared (FTIR) spectroscopic studies on the nonthermal plasma reaction of isopropyl alcohol in dinitrogen at Macor (a ceramic containing oxides of Al, Mg, and Si) and the analogous thermally driven process. While isopropyl alcohol did not react at the Macor at temperatures up to 600 °C, the study of the nonthermal plasma-driven process at the ceramic led to unexpected chemistry hitherto not observed, primarily the reaction of IPA in dinitrogen at short time scales to produce methane, HCN, acetone and "cold" CO at ca. 115 K. The CO, methane, and HCN rapidly established steady state concentrations, pointing to the need for faster FTIR studies: at longer times, isophorone and a "polymethylacetylene-like" polymer were formed as a brown oil. The observation of the steady-state gases and brown oil suggested parallel pathways in the plasma, the latter taking place at the plasma/catalyst interface, and the former in the plasma remote from the catalyst. Replacing dinitrogen with argon completely inhibited or negated the production of the oil, had no effect upon the processes taking place in the plasma remote from the Macor, and instead resulted in the production of acetylene.
RESUMO
This paper reports the application of in situ reflectance Fourier Transform InfraRed spectroscopy to the study of the thermal and plasma driven reaction of IsoPropyl Alcohol (IPA) at SnO2-coated Macor, the latter a ceramic material comprised of the oxides of Al, Mg and Si. The data so obtained were compared to those obtained using uncoated Macor. When uncoated Macor was employed, no reaction of the IPA was observed up to 600 °C in the thermal experiments, whereas a number of products were observed in the plasma-driven experiments. The results obtained using coated Macor were somewhat different, with no reaction taking place in the plasma-driven experiments, whilst significant reaction took place in the thermally-driven process. In the latter experiments, the chemistry was observed to show four distinct temperature regions, with electron injection into the conduction band of the SnO2 playing a significant role, culminating in the production of CO2. The data were interpreted in terms of a model in which physisorbed IPA was converted to two forms of isopropoxide: this was converted to acetone and acetaldehyde via adsorbed enolate. The data clearly support the catalytic activity of Macor in the plasma-driven conversion of IPA.
