Abstract
Developing sulfonic-acid-supported catalysts with superacidity and hydrophobicity is of great importance for many acid-catalyzed reactions where H2O is generated. Herein, a novel hydrophobic superacidic biochar is first reported via a diazo grafting method using halogen-substituted amino-benzenesulfonic acids and 4-tert-butylaniline as sulfonating and hydrophobic reagents, respectively. The resultant biochar has a high Brunauer-Emmett-Teller (BET) surface area (400-700 m2·g-1), acid concentration (up to 1.5 mmol·g-1), and H2O contact angle (above 134°). The synergistic effect of superacidity and hydrophobicity greatly improves the catalytic alkylation reactions of 4-ethylphenol-phenylmethanol and 2-methylfuran-cyclic ketones for the synthesis of renewable high-density fuels. The hydrophobic superacidic biochar shows higher catalytic conversion and selectivity than those of its counterparts without hydrophobicity or superacidity. Meanwhile, it is also far superior to commercial Amberlyst-15 and the traditional sulfonated biochar. Finally, the catalyst is stable without obvious activity reduction after cycling.
Original language | English (US) |
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Pages (from-to) | 7785-7794 |
Number of pages | 10 |
Journal | ACS Sustainable Chemistry and Engineering |
Volume | 8 |
Issue number | 21 |
DOIs | |
State | Published - Jun 1 2020 |
Keywords
- alkylation
- biochar
- high-density biofuel
- hydrophobicity
- superacidity
ASJC Scopus subject areas
- Chemistry(all)
- Environmental Chemistry
- Chemical Engineering(all)
- Renewable Energy, Sustainability and the Environment