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Updated: Feb 17, 2026

Separation of Aldehydes and Reactive Ketones from Mixtures Using a Bisulfite Extraction Protocol
Published on: April 2, 2018
A surfactant-mediated Ni/MgAl bifunctional catalyst for highly selective tandem conversion of acetone to methyl
Zhongxu Zhang1, Shuangshuang Huang2, Jingya Sun3
1State Key Laboratory of Coordination Chemistry, Key Laboratory of Mesoscopic Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Abstract:
Highly efficient conversion of acetone to methyl isobutyl ketone (MIBK) remains a challenging task due to the complicated reaction pathways. Herein, a surfactant-assisted impregnation strategy was developed to modify Ni/MgAl catalysts for acetone conversion. Interestingly, the introduction of surfactants can effectively modulate the catalyst acidity and basicity, thereby blocking the reaction pathway, leading to the isophorone by-product. Moreover, a sodium dodecyl sulfate (SDS) modified catalyst (Ni/MgAl-SDS) exhibited a Ni2+-doped solid solution structure, as well as the conventional impregnated Ni/MgAl catalyst, while a sodium dodecylbenzene sulfonate (SDBS) modified catalyst (Ni/MgAl-SDBS) generated highly dispersed metallic nanoparticles with coexisting Ni0/Ni2+ species. This unique structure efficiently drove the hydrogenation of a mesityl oxide intermediate, achieving a high MIBK selectivity of 94.5% in the acetone conversion process. This strategy provides a novel approach for the synergistic regulation of the metal state, acidity and basicity in tandem reactions.
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