From sugars to FDCA: a techno-economic assessment using a design concept based on solvent selection and carbon dioxide emissions
Open Access
- 18 January 2021
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Green Chemistry
- Vol. 23 (4) , 1716-1733
Abstract
The synthesis of the molecule 2,5-furandicarboxylic acid (FDCA) from sugars is key to unlocking the potential for the replacement of the oil derivative PET (polyethylene terephthalate) by polyethylene furanoate (PEF). Although much research and investment has been dedicated to the synthesis of FDCA, there remains limited commercial activity in this area due to the challenges related to the stability and isolation of the FDCA precursor, 5-hydroxymethylfurfural (HMF). High yields of HMF can be obtained from fructose at high loadings in water–organic solvent mixtures (methyl isobutyl ketone, MIBK; γ-valerolactone, GVL), dimethyl sulfoxide (DMSO) or ionic liquids. Each of these approaches suffers from various drawbacks in terms of catalyst development, product separation and environmental impact. It is therefore necessary to understand which of these processes has the potential for scale-up, while ensuring low environmental impact and a competitive selling price. In this study, a process simulation (rather than a life cycle assessment) was performed to evaluate the associated emissions and selling price of FDCA based on its production using different solvents. It was determined that the cost and CO2 emissions associated with the isolation of HMF undermine the economic and environmental viability of the transformation of sugars to FDCA. In contrast, a two-step, one-pot reaction represents an ideal solution to reduce both cost and environmental impact, making FDCA competitive with terephthalic acid (the corresponding precursor for PET). The choice of solvent and the process were then evaluated and ranked based on safety, CO2 emissions, selling price and state of development though a scoring methodology. A system based on a water/GVL mixture is closer to commercial applicability but the process is limited by extensive formation of humins, which reduces the overall yield of the process, increasing the minimum selling price of FDCA. Using DMSO or ionic liquids minimises emissions and leads to the lowest cost of FDCA but further study is needed to improve the oxidation step. This investigation analyses the possible routes to FDCA from sugars based on the current literature, placing the emphasis on process economics but also considering the CO2 emissions from processing the sugars.Keywords
Funding Information
- Engineering and Physical Sciences Research Council (Doctoral Prize Fellowship)
- Imperial College London (President’s PhD Scholarship)
This publication has 87 references indexed in Scilit:
- Aerobic Oxidation of 5-(Hydroxymethyl)furfural in Ionic Liquids with Solid Ruthenium Hydroxide CatalystsCatalysis Letters, 2012
- Dehydration of Highly Concentrated Solutions of Fructose to 5‐Hydroxymethylfurfural in a Cheap and Sustainable Choline Chloride/Carbon Dioxide SystemChemSusChem, 2012
- The effect of solvent addition on fructose dehydration to 5-hydroxymethylfurfural in biphasic system over zeolitesJournal of Catalysis, 2012
- Catalytic conversion of cellulose into 5-hydroxymethylfurfural in high yields via a two-step processCellulose, 2011
- A One-Pot Two-Step Approach for the Catalytic Conversion of Glucose into 2,5-DiformylfuranCatalysis Letters, 2011
- Ionic Liquid-Mediated Formation of 5-Hydroxymethylfurfural—A Promising Biomass-Derived Building BlockChemical Reviews, 2010
- Efficient Route to Hydroxymethylfurans from Sugars via Transfer HydrogenationChemSusChem, 2010
- Efficient Catalytic Conversion of Fructose into 5‐Hydroxymethylfurfural in Ionic Liquids at Room TemperatureChemSusChem, 2009
- Assessment of the environmental profile of PLA, PET and PS clamshell containers using LCA methodologyJournal of Cleaner Production, 2009
- Toxicity and carcinogenicity of methyl isobutyl ketone in F344N rats and B6C3F1 mice following 2-year inhalation exposureToxicology, 2008