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 O ). 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.
This paper presents a techno-economic analysis of a low-cost and high-efficiency technology for the production of 2,5-furandicarboxylic acid (FDCA) from starch, glucose, or high-fructose corn syrup (HFCS). With the design presented here, it is viable to convert starch to glucose through enzymatic hydrolysis followed by catalytic dehydration of glucose with niobium phosphate, an innovative low-cost catalyst, to produce 5-hydroxymethyl furfural (HMF). The HMF produced is then converted into FDCA via air oxidation over a cobalt-manganese mixed oxide catalyst. Three variations of this design are assessed: Scenario 1 starts with starch, and Scenarios 2 and 3 start directly with glucose or HFCS, without the initial starch hydrolysis step. The minimum selling price (MSP) and discounted payback period (PBP) were calculated to investigate the feasibility of the scenarios. A sensitivity analysis was also performed for the key cost drivers, selling price of FDCA, and spent catalysts. All scenarios were feasible; however, the HFCS to FDCA process was the most profitable (MSP 1802 US$/t and a PBP below 5 years). Above all, the feasibility of this technology is mostly affected by variations in recovered catalysts and FDCA selling prices.
Catalytic conversion of biomass or biomass-derived carbohydrates into 5-hydroxymethylfurfural (HMF) is an important reaction for the synthesis of bio-based polymers, fuels, and other industrially useful products.
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