Abstract
AbstractSupercritical carbon dioxide was shown to be a suitable reaction medium for the highly efficient hydrogenation of citral using monometallic Pt and bimetallic Pt‐Ru supported on a mesoporous material, MCM‐48, as catalyst. A remarkable change in the product distribution was observed after the addition of Ru to the monometallic Pt catalyst in supercritical carbon dioxide. The monometallic Pt catalyst was found to be highly selective to the unsaturated alcohol (geraniol+nerol) at a temperature of 323 K within 2 h whereas the bimetallic catalyst becomes selective to the partially saturated aldehyde (citronellal) under the same reaction conditions. Phase behavior plays an important role in the product distribution. Highest conversion and high selectivity to citronellal were achieved in the homogeneous phase for the Pt‐Ru catalyst while on the other hand the unsaturated alcohol (geraniol+nerol) was produced in the heterogeneous phase for the monometallic Pt catalyst. An XPS study offers strong evidence of the electronic modification of Pt after the addition of Ru in the bimetallic catalyst. The change in product distribution on the Pt‐Ru bimetallic catalyst may be explained by the appreciable interaction between the medium and the metal particles promoted by the presence of metallic Ru.
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