Investigation of deactivation mechanisms of a solid acid catalyst during esterification of the bio-oils from mallee biomass
The oligomers, N-containing organics and metal ions in bio-oil poison the solid acid catalyst via different ways. Processing with a concentrated sulfuric acid significantly improved the catalytic activity via removal of the poisons. [Display omitted] •Deactivation of a solid acid catalyst in bio-oil...
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Veröffentlicht in: | Applied energy 2013-11, Vol.111, p.94-103 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The oligomers, N-containing organics and metal ions in bio-oil poison the solid acid catalyst via different ways. Processing with a concentrated sulfuric acid significantly improved the catalytic activity via removal of the poisons. [Display omitted]
•Deactivation of a solid acid catalyst in bio-oil esterification was investigated.•The bio-oils from wood, bark, and leaves contain quite different catalyst poisons.•Metal ions, N-containing organics and polymer in bio-oil poison catalyst.•Ion exchange can substantially but not completely regenerate the catalyst.•Metal ions and N-containing organics are reversible poisons while polymer is not.
This study reports the deactivation mechanisms of the solid acid catalyst Amberlyst 70 during the esterification of bio-oils from mallee biomass and the methods for catalyst regeneration. The metal ions in bio-oil deactivated Amberlyst 70 via ion exchange with the hydrogen ions on/in catalyst, which changed structure of catalysts and reduced availability of acidic sites. N-containing organics reacted with the hydrogen ions on/in catalyst, forming neutral salts and resulting in complete catalyst deactivation. Polymers formed during the esterification of bio-oils deposited on/in catalyst, reducing the accessibility of catalytic sites. Washing with solvents could remove some adsorbed organics and restore some catalytic activity but not much. In comparison, ion exchange in a concentrated sulfuric acid removes most of metal ions and the N-containing organics and significantly improves the catalytic activity. |
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ISSN: | 0306-2619 1872-9118 |
DOI: | 10.1016/j.apenergy.2013.04.078 |