Affiliation:
1. Laboratoire des Procédés, Matériaux et Environnement (LPME) Faculté des Sciences et Techniques de Fès Université Sidi Mohamed Ben Abdellah Fès BP. 2202 Morocco
2. Laboratoire des Procédés, Matériaux et Environnement (LPME) Faculté Polydisciplinaire (FP-Taza) Université Sidi Mohamed Ben Abdellah Taza BP. 1223 Morocco
Abstract
AbstractDirect catalytic oxidation of alcohols to acetals in one step process is very attractive, because the two steps process leads firstly to aldehydes, which are unstable species serving as reactive intermediates to generate several by‐products reducing process efficiency and selectivity. In this work, a new selective catalytic acetalization of 1‐butanol into 1‐1‐dibutoxybutane acetal using H2O2 in one step process is investigated using Keggin‐type polyoxometalates catalysts. The materials developed consisted of new lacunary phophotungstate salts Cs5MPW11(H2O)O39 (M=Fe, Co and Cu) which were prepared by inorganic solution condensation method and characterized using XRD, IR, SEM and EDX analysis to verify their structure, surface morphology and chemical composition. Cs5CuPW11(H2O)O39 catalyst allowed the highest performance for the oxidation of 1‐butanol at 60 °C using H2O2 excess with a yield approaching 92 % and a turnover number of 784. Such activity is related to a bifunctional behavior of the catalyst as superacid and redox operating system and the synergistic effect created between the [PW11O39]7− Keggin framework, Cs+ and Cu2+.