Abstrakt
Toluene steam reforming was performed over three wood-derived chars and compared with a previously-reported pyrolytic conversion study. The heterogeneous mechanism of toluene decomposition was not directly affected by the introduction of steam, but it caused gasification of char and toluene-derived coke, which prolonged the initial high conversion efficiency. Conversely, when oxygen was used as a substitute for steam, a direct ring-opening reaction of toluene was observed, rather than solid carbon combustion. A comparison of benzene, toluene, and p-xylene conversion revealed that the presence of a methyl group on the aromatic ring enhanced its decomposition, regardless of the catalyst's activity. However, a second methyl group did not further improve the conversion and only served to increase the intensity of secondary recombination reactions.
| Język oryginału | angielski |
|---|---|
| Numer artykułu | 118521 |
| Czasopismo | Fuel |
| Tom | 280 |
| Identyfikatory DOI | |
| Status publikacji | Opublikowano - 15 lis 2020 |
Obszary tematyczne ASJC Scopus
- Ogólna inżynieria chemiczna
- Technologia paliwowa
- Inżynieria energetyczna i technologia energetyczna
- Chemia organiczna
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