TY - JOUR
T1 - Inexpensive but Highly Efficient Co–Mn Mixed-Oxide Catalysts for Selective Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid
AU - Rao, Kasanneni Tirumala Venkateswara
AU - Rogers, Jennifer Lorraine
AU - Souzanchi, Sadra
AU - Dessbesell, Luana
AU - Ray, Madhumita Bhowmick
AU - Xu, Chunbao (Charles)
N1 - Funding Information:
The authors acknowledge the financial support from NSERC Discovery Grants and the funding from BioFuelNet Canada, a Network of Centres of Excellence. C.X. also gratefully acknowledges the funding from the NSERC/FPInnovations Industrial Research Chair program and the ORF‐RE Program in Forest Biorefinery. L.D. also gratefully acknowledges Brazil Science Without Borders/CNPq Graduate Scholarship.
Publisher Copyright:
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/9/21
Y1 - 2018/9/21
N2 - A highly active and inexpensive Co–Mn mixed-oxide catalyst was prepared and used for selective oxidation of 5-hydroxymethylfurfural (HMF) into 2, 5-furandicarboxylic acid (FDCA). Co–Mn mixed-oxide catalysts with different Co/Mn molar ratios were prepared through a simple solid-state grinding method—a low-cost and green catalyst preparation method. The activity of these catalysts was evaluated for selective aerobic oxidation of HMF into FDCA in water. Excellent HMF conversion (99 %) and FDCA yield (95 %) were obtained under the best reaction conditions (i.e., 120 °C, 5 h, Co–Mn mixed-oxide catalyst with a Co/Mn molar ratio of 0.25 calcined at 300 °C (Co-Mn-0.25) and 1 MPa O2). The catalyst could be reused five times without a significant decrease in activity. The results demonstrated that the catalytic activity and selectivity of the Co–Mn mixed-oxide catalysts prepared through solid-state grinding were superior to the same Co–Mn catalyst prepared through a conventional coprecipitation method. The high catalytic activity of the Co-Mn-0.25 catalyst was attributed to its high lattice oxygen mobility and the presence of different valence states of manganese. The high activity and low cost of the Co–Mn mixed-oxide catalysts prepared by solid-state grinding make it promising for industrial application for the manufacturing of polyethylene furanoate, a bioreplacement for polyethylene terephthalate, from sustainable bioresources.
AB - A highly active and inexpensive Co–Mn mixed-oxide catalyst was prepared and used for selective oxidation of 5-hydroxymethylfurfural (HMF) into 2, 5-furandicarboxylic acid (FDCA). Co–Mn mixed-oxide catalysts with different Co/Mn molar ratios were prepared through a simple solid-state grinding method—a low-cost and green catalyst preparation method. The activity of these catalysts was evaluated for selective aerobic oxidation of HMF into FDCA in water. Excellent HMF conversion (99 %) and FDCA yield (95 %) were obtained under the best reaction conditions (i.e., 120 °C, 5 h, Co–Mn mixed-oxide catalyst with a Co/Mn molar ratio of 0.25 calcined at 300 °C (Co-Mn-0.25) and 1 MPa O2). The catalyst could be reused five times without a significant decrease in activity. The results demonstrated that the catalytic activity and selectivity of the Co–Mn mixed-oxide catalysts prepared through solid-state grinding were superior to the same Co–Mn catalyst prepared through a conventional coprecipitation method. The high catalytic activity of the Co-Mn-0.25 catalyst was attributed to its high lattice oxygen mobility and the presence of different valence states of manganese. The high activity and low cost of the Co–Mn mixed-oxide catalysts prepared by solid-state grinding make it promising for industrial application for the manufacturing of polyethylene furanoate, a bioreplacement for polyethylene terephthalate, from sustainable bioresources.
KW - 2,5-furandicarboxylic acid
KW - 5-hydroxymethylfurfural
KW - heterogeneous catalysis
KW - selective oxidation
KW - solid state
UR - http://www.scopus.com/inward/record.url?scp=85053027300&partnerID=8YFLogxK
U2 - 10.1002/cssc.201800989
DO - 10.1002/cssc.201800989
M3 - Article
C2 - 30006949
AN - SCOPUS:85053027300
SN - 1864-5631
VL - 11
SP - 3323
EP - 3334
JO - ChemSusChem
JF - ChemSusChem
IS - 18
ER -