Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6691858 | Applied Energy | 2014 | 8 Pages |
Abstract
This work is concerned with the question of why oxidative desulfurization (ODS) catalyst that show good catalytic performance for ODS of model gasoline thiophenic compounds is not effective for real gasoline. For the first time, the effects of gasoline composition on ODS using a phosphotungstic acid/activated carbon (HPW/AC) catalyst with H2O2 were investigated. ODS of thiophene, one of the most difficult thiophenic compounds to be oxidized, was studied in a model fuel system, where a high thiophene conversion rate of 90% could be reached in 2 h at 90 °C. However, when applying the ODS to a real gasoline, the ODS conversion rate decreased to only 32%, suggesting a strong inhibiting effect of gasoline composition on ODS. The ODS studies in different model fuels suggested that the inhibiting effect can be ascribed to the competitive adsorption and oxidation with the presence of the alkenes and alkylated aromatic hydrocarbons in real gasoline. The active pi-electrons in alkenes and alkyl groups in alkylated aromatic hydrocarbons may react with polyoxoperoxo species or peroxo-metallate complexes formed by phosphotungstic acid-H2O2 interaction. Additionally, it was indicated that the ODS selectivity followed the order of benzothiophene > trimethylthiophene > dimethylthiophene â¼Â methylthiophene > thiophene, suggesting the partial charge on the electron-rich sulfur atom may play a decisive role for its oxidation reactivity. To mitigate the inhibiting effect of gasoline composition on ODS, we propose (a) implementation of selective separation-oxidation processes; (b) choice of suitable selective oxidants; (c) optimization of selective ODS reaction temperature, etc. to improve ODS selectivity for real gasoline desulfurization applications.
Related Topics
Physical Sciences and Engineering
Energy
Energy Engineering and Power Technology
Authors
Jing Xiao, Luoming Wu, Ying Wu, Bing Liu, Lu Dai, Zhong Li, Qibin Xia, Hongxia Xi,