Polyoxometalate-Modified Amphiphilic Polystyrene-block-poly(2-(dimethylamino)ethyl methacrylate) Membranes for Heterogeneous Glucose to Formic Acid Methyl Ester Oxidation

Author:

Utievskyi Yurii1,Neumann Christof2ORCID,Sindlinger Julia3ORCID,Schutjajew Konstantin4,Oschatz Martin45,Turchanin Andrey256,Ueberschaar Nico3ORCID,Schacher Felix H.156ORCID

Affiliation:

1. Institute of Organic Chemistry and Macromolecular Chemistry, Friedrich Schiller University Jena, Humboldtstraße 10, 07743 Jena, Germany

2. Institute of Physical Chemistry, Friedrich Schiller University Jena, Lessingstraße 10, 07743 Jena, Germany

3. Mass Spectrometry Platform, Faculty of Chemistry and Earth Sciences, Friedrich Schiller University Jena, Humboldtstraße 8, 07743 Jena, Germany

4. Institute for Technical Chemistry and Environmental Chemistry (ITUC), Friedrich Schiller University Jena, Philosophenweg 7a, 07743 Jena, Germany

5. Center for Energy and Environmental Chemistry (CEEC), Friedrich Schiller University Jena, 07743 Jena, Germany

6. Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, 07743 Jena, Germany

Abstract

Herein, we present a new heterogeneous catalyst active toward glucose to formic acid methyl ester oxidation. The catalyst was fabricated via electrostatic immobilization of the inorganic polyoxometalate HPA-5 catalyst H8[PMo7V5O40] onto the pore surface of amphiphilic block copolymer membranes prepared via non-solvent-induced phase separation (NIPS). The catalyst immobilization was achieved via wet impregnation due to strong coulombic interactions between protonated tertiary amino groups of the polar poly(2-(dimethylamino)ethyl methacrylate) block and the anionic catalyst. Overall, three sets of five consecutive catalytic cycles were performed in an autoclave under 90 °С and 11.5 bar air pressure in methanol, and the corresponding yields of formic acid methyl ester were quantified via head-space gas chromatography. The obtained results demonstrate that the membrane maintains its catalytic activity over multiple cycles, resulting in high to moderate yields in comparison to a homogeneous catalytic system. Nevertheless, presumably due to leaching, the catalytic activity declines over five catalytic cycles. The morphological and chemical changes of the membrane during the prolonged catalysis under harsh conditions were examined in detail using different analytic tools, and it seems that the underlying block copolymer is not affected by the catalytic process.

Funder

Deutsche Forschungsgemeinschaft

Publisher

MDPI AG

Subject

General Materials Science,General Chemical Engineering

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