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Cascade catalytic hydrogenation–cyclization of methyl levulinate to form γ-valerolactone over Ru nanoparticles supported on a sulfonic acid-functionalized UiO-66 catalyst
| Content Provider | Semantic Scholar |
|---|---|
| Author | Lin, Zhenzhen Cai, Xiaoxiong Fu, Yanghe Zhu, Weidong Zhang, Fumin |
| Copyright Year | 2017 |
| Abstract | We herein report a high-yielding one-pot upgrade strategy for converting biomass-derived methyl levulinate (ML) into γ-valerolactone (GVL) over a dual-functional catalyst prepared by depositing Ru nanoparticles on a sulfonic acid-functionalized Zr-based metal–organic framework (SO3H-UiO-66). Under the mild conditions of 80 °C and 0.5 MPa H2 for 4 h in aqueous solution, a quantitative (100%) yield of GVL was obtained over the prepared Ru/SO3H-UiO-66 catalyst. In contrast, a very limited yield of GVL was achieved in the control experiment by first hydrogenating the reactant ML over a metal catalyst without any acidity (e.g. Ru/C) to produce the 4-hydroxypentanoic acid methyl ester (4-HPME) intermediate, followed by treatment of this intermediate over the acidic SO3H-UiO-66 support in the absence of metal. We also found that the catalytic activity and selectivity of Ru/SO3H-UiO-66 were significantly suppressed upon neutralization of its acidic sites, thereby confirming the indispensable role of the sulfonic acid groups in promoting the intramolecular dealcoholation of the 4-HPME intermediate. Furthermore, the Ru/SO3H-UiO-66 catalyst was recyclable over five cycles without any significant loss in its catalytic activity, thus rendering this precious metal/acid dual-functional catalyst a potential candidate for efficient GVL production under mild conditions. |
| Starting Page | 44082 |
| Ending Page | 44088 |
| Page Count | 7 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/C7RA06293A |
| Volume Number | 7 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/c7/ra/c7ra06293a/c7ra06293a1.pdf |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |