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Aerobic Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Furandicarboxylic Acid over Holey 2 D Mn 2 O 3 Nanoflakes from a Mn‐based MOF
Author(s) -
Bao Liwei,
Sun FangZhou,
Zhang GuoYing,
Hu TongLiang
Publication year - 2020
Publication title -
chemsuschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.412
H-Index - 157
eISSN - 1864-564X
pISSN - 1864-5631
DOI - 10.1002/cssc.201903018
Subject(s) - catalysis , calcination , redox , yield (engineering) , chemistry , monomer , manganese , fourier transform infrared spectroscopy , chemical engineering , metal organic framework , polymer , materials science , inorganic chemistry , organic chemistry , adsorption , metallurgy , engineering
Abstract The aerobic oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐furandicarboxylic acid (FDCA), a promising renewable monomer to produce bio‐based polymers such as polyethylene furanoate (PEF), has recently emerged as the subject of increasing interest. Here, holey 2 D Mn 2 O 3 nanoflakes were obtained by a facile thermal treatment of a Mn‐based metal–organic framework (MOF) precursor. The structural and morphological properties of the nanoflakes were characterized by powder XRD, FTIR, SEM and TEM to explore the formation process. It was inferred that the linker loss in the MOF precursor and the oxidation of the Mn cation induced by the heat‐treatment in air were responsible for the formation of holey 2 D Mn 2 O 3 nanoflakes. The specific morphology and redox cycle of the Mn cation on the surface endowed the synthesized nanoflakes with promising performance on the selective oxidation. The obtained nanoflakes calcined at 400 °C (M400) afforded over 99.5 % yield of FDCA at complete conversion of HMF, which is superior to the catalytic activity of commercial Mn 2 O 3 and activated MnO 2 . To our knowledge, Mn 2 O 3 exhibiting such a high performance on the aerobic oxidation of HMF to FDCA has not yet been reported. Based on the investigation of the experimental parameters, a plausible reaction mechanism was proposed.