Insight into the Structure and Redox Chemistry of [Carbonatotetraamminecobalt(III)] Permanganate and Its Monohydrate as Co-Mn-Oxide Catalyst Precursors of the Fischer-Tropsch Synthesis

Author:

Béres Kende Attila12ORCID,Dürvanger Zsolt34ORCID,Homonnay Zoltán5,Bereczki Laura16ORCID,Barta Holló Berta7ORCID,Farkas Attila8ORCID,Petruševski Vladimir M.9,Kótai László110ORCID

Affiliation:

1. Institute of Materials and Environmental Chemistry, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary

2. György Hevesy PhD School of Chemistry, ELTE Eötvös Loránd University, H-1053 Budapest, Hungary

3. Structural Chemistry and Biology Laboratory, Institute of Chemistry, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary

4. ELKH-ELTE Protein Modelling Research Group, H-1117 Budapest, Hungary

5. Institute of Chemistry, ELTE Eötvös Loránd University, H-1053 Budapest, Hungary

6. Centre for Structural Science, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary

7. Department of Chemistry, Biochemistry and Environmental Protection, Faculty of Sciences, University of Novi Sad, SRB-21000 Novi Sad, Serbia

8. Department of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, H-1117 Budapest, Hungary

9. Institute of Chemistry, Faculty of Natural Sciences and Mathematics, Ss. Cyril and Methodius University, MK-1000 Skopje, North Macedonia

10. Deuton-X Ltd., H-2030 Érd, Hungary

Abstract

[Carbonatotetraamminecobalt(III)] permanganate monohydrate was synthesized first in the metathesis reaction of [Co(NH3)4CO3]NO3 and NaMnO4 in aqueous solution. Its thermal dehydration at 100 °C resulted in phase-pure [Co(NH3)4CO3]MnO4 (compound 1). Compounds 1 and 2 (i.e., the hydrated form) were studied with IR, far-IR, and low-temperature Raman spectroscopies, and their vibrational modes were assigned. The lattice parameters were determined by powder X-ray diffraction (PXRD) and single crystal X-ray diffraction (SXRD) methods for the triclinic and orthorhombic compounds 1 and 2, respectively. The detailed structure of compound 2 was determined, and the role of hydrogen bonds in the structural motifs was clarified. UV studies on compounds 1 and 2 showed the distortion of the octahedral geometry of the complex cation during dehydration because of the partial loss of the hydrogen bonds between the crystal water and the ligands of the complex cation. The thermal decomposition consists of a solid phase quasi-intramolecular redox reaction between the ammonia ligands and permanganate anions with the formation of ammonia oxidation products (H2O, NO, N2O, and CO2). The solid phase reaction product is amorphous cobalt manganese oxide containing ammonium, carbonate (and nitrate) anions. The temperature-controlled thermal decomposition of compound 2 in toluene at 110 °C showed that one of the decomposition intermediates is ammonium nitrate. The decomposition intermediates are transformed into Co1.5Mn1.5O4 spinel with MnCo2O4 structure upon further heating. Solid compound 2 gave the spinel at 500 °C both in an inert and air atmosphere, whereas the sample pre-treated in toluene at 110 °C without and with the removal of ammonium nitrate by aqueous washing, gave the spinel already at 300 and 400 °C, respectively. The molten NH4NO3 is a medium to start spinel crystallization, but its decomposition stops further crystal growth of the spinel phase. By this procedure, the particle size of the spinel product as low as ~4.0 nm could be achieved for the treatments at 300 and 400 °C, and it increased only to 5.7 nm at 500 °C. The nano-sized mixed cobalt manganese oxides are potential candidates as Fischer-Tropsch catalysts.

Funder

New National Excellence Program of the Ministry for Culture and Innovation from the Source of The National Research, Development and Innovation found

European Union and the State of Hungary

Publisher

MDPI AG

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