dc.contributor.author |
Mustikasari, Kamilia |
|
dc.contributor.author |
Rodiansono |
|
dc.contributor.author |
Astuti, Maria Dewi |
|
dc.contributor.author |
Husain, Sadang |
|
dc.contributor.author |
Sutomo |
|
dc.date.accessioned |
2021-09-02T03:46:09Z |
|
dc.date.available |
2021-09-02T03:46:09Z |
|
dc.date.issued |
2021-05 |
|
dc.identifier.issn |
1978-2993 |
|
dc.identifier.uri |
https://repo-dosen.ulm.ac.id//handle/123456789/21010 |
|
dc.description.abstract |
Highly efficient and selective hydrogenation of ,-unsaturated carbonyl compounds to unsaturated alcohol using
bimetallic palladium-copper supported on carbon (denoted as Pd-Cu(3.0)/C; 3.0 is Pd/Cu molar ratio) catalyst is
demonstrated. Pd-Cu(3.0)/C catalyst was prepared via a simple hydrothermal route under air atmosphere at 150
°C for 24 h followed by reduction with hydrogen at 400 °C for 1.5 h. The chemoselective hydrogenation of typical
,-unsaturated carbonyl ketone (2-cyclohexene-1-one) and aldehyde (trans-2-hexenaldehyde), and chemoselective
hydrogenation of FFald and (E)-non-3-en-2-one mixture demonstrated high productivity, leading to high selectivity
of unsaturated alcohols. The presence of bimetallic Pd-Cu alloy phase with relatively high H2 uptakes was ob served, enabling to preferentially hydrogenate C=O rather than to C=C bonds under mild reaction conditions. Pd Cu(3.0)/C catalyst was found to stable and reusable for at least four reaction runs and the activity and selectivity
of the catalyst can be restored to the original after rejuvenation with H2 at 400 °C for 1.5 h. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
Universitas Diponegoro Semarang |
en_US |
dc.relation.ispartofseries |
Buletin of Chemical Reaction Engineering & Catalysis;Vol. 16 Issue 2 |
|
dc.subject |
bimetallic palladium-copper; chemoselective hydrogenation; unsaturated carbonyl compounds; unsatu rated alcohol |
en_US |
dc.title |
The Promotion Effect of Cu on the Pd/C Catalyst in the Chemoselective Hydrogenation of Unsaturated Carbonyl Compounds |
en_US |
dc.type |
Article |
en_US |