skip to main content


Title: Electrosynthesis of amino acids from biomass-derived α-hydroxyl acids
Electrochemical conversion of biomass-derived intermediate compounds to high-value products has emerged as a promising approach in the field of biorefinery. Biomass upgrading allows for the production of chemicals from non-fossil-based carbon sources and capitalization on electricity as a green energy input. Amino acids, as products of biomass upgrading, have received relatively little attention. Pharmaceutical and food industries will benefit from an alternative strategy for the production of amino acids that does not rely on inefficient fermentation processes. The use of renewable biomass resources as starting materials makes this proposed strategy more desirable. Herein, we report an electrochemical approach for the selective oxidation of biomass-derived α-hydroxyl acids to α-keto acids, followed by electrochemical reductive amination to yield amino acids as the final products. Such a strategy takes advantage of both reactions at the anode and cathode and produces amino acids under ambient conditions with high energy efficiency. A flow electrolyzer was also successfully employed for the conversion of α-hydroxyl acids to amino acids, highlighting its great potential for large-scale application.  more » « less
Award ID(s):
2102220
NSF-PAR ID:
10348787
Author(s) / Creator(s):
; ; ;
Date Published:
Journal Name:
Green Chemistry
Volume:
24
Issue:
13
ISSN:
1463-9262
Page Range / eLocation ID:
5320 to 5325
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    The increasing demand for green chemical products calls for the exploration of sustainable and renewable carbon resources beyond fossil-based materials, whose utilization inevitably results in environmental concerns. As such, biomass valorisation has attracted increasing attention because biomass is the most widely available and sustainable carbon source. Among the available biomass-derived platform chemicals, 5-hydroxymethylfurfural (HMF) has long been regarded as an attractive candidate for the production of numerous value-added products. Nevertheless, the poor stability, and difficult separation and purification of HMF from fructose dehydration significantly inhibit its large-scale application. Herein, we report a two-step process for the direct production of two biopolymer precursors, 2,5-furandicarboxylic acid (FDCA) and 2,5-bis(hydroxymethyl)furan (BHMF), from fructose, bypassing the isolation of HMF. FDCA and BHMF are much easier to separate and purify from the reaction mixture than HMF, and they both can replace petroleum-based counterparts in the syntheses of many industrially important polymers, ranging from polyesters to polyamides. Optimized fructose dehydration under microwave irradiation achieved a high HMF yield (83%) using a biphasic strategy. The subsequent electrocatalytic conversion of the resulting microwave reaction mixture allowed us to carry out either oxidation or reduction via readily tuning the electrochemical parameters to yield FDCA or BHMF, respectively. The integration of microwave irradiation and electrocatalysis in a flow electrolyzer enabled the direct conversion of readily available fructose to highly valuable FDCA and BHMF without the expensive and challenging step of HMF isolation, suggesting an economically attractive approach for upgrading carbohydrates. 
    more » « less
  2. null (Ed.)
    Despite the increasing interest in upgrading biomass-derived molecules to value-added products, the electrochemical conversion of biomass platform chemicals to highly valuable biofuels, such as jet fuel, has not yet received wide attention. Herein, we report a catalyst-free electrochemical route for the production of a jet fuel precursor, hydrofuroin, from the electrohydrodimerization of furfural, which can be readily derived from lignocellulose and already has an industrial production of 300 000 tons per year. Detailed electrochemical studies using carbon and copper electrodes at various pH values enabled us to probe the reduction mechanism of furfural and obtain the kinetic details, such as the diffusion constant and electron transfer rate. Preparative electrolysis in a batch electrolyzer achieved a high yield of hydrofuroin (94%) with an excellent faradaic efficiency of 93%. Finally, a flow electrolyzer was employed to demonstrate the great promise of large-scale production of hydrofuroin from the electrohydrodimerization of furfural. 
    more » « less
  3. Electrocatalytic upgrading of biomass-derived feedstocks driven by renewable electricity offers a greener way to reduce the global carbon footprint associated with the production of value-added chemicals. Paired electrolysis is an emerging platform for cogenerating high-valued chemicals from both the cathode and anode, potentially powered by renewable electricity from wind or solar sources. By pairing with an anodic biomass oxidation upgrading reaction, the elimination of the sluggish and less valuable water oxidation increases flow cell productivity and efficiency. In this presentation, we report our research progress on paired electrolsysis of HMF to production of higher valued chemicals in electrochemical flow cells. We first prepared an oxide-derived Ag (OD-Ag) electrode with high activity and up to 98.2% selectivity for the ECH of 5-(hydroxymethyl)furfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF), and such efficient conversion was achieved in a three-electrode flow cell. The excellent BHMF selectivity was maintained over a broad potential range with long-term operational stability. In HMF-to-BHMF paired with 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO)-mediated HMF-to-FDCA conversion, a markedly reduced cell voltage from ~7.5 V to ~2.0 V was observed by transferring the electrolysis from the H-type cell to the flow cell, corresponding to more than four-fold increase in energy efficiency in operation at 10 mA. A combined faradaic efficiency of 163% was obtained to BHMF and FDCA. Alternatively, the anodic hydrogen oxidation reaction on platinum further reduced the cell voltage to only ~0.85 V at 10 mA. Next, we have demonstrated membrane electrode assembly (MEA)-based flow cells for the paired electrolysis of 5-(hydroxymethyl)furfural (HMF) paired electrolysis to bis(hydroxymethyl)furan (BHMF) and 2,5-furandicarboxylic acid (FDCA). In this work, the oxygen evolution reaction (OER) was substituted by TEMPO-mediated HMF oxidation, dropping the cell voltage was from 1.4 V to 0.7 V at a current density of 1.0 mA cm−2. A minimized cell voltage of ~1.5 V for a continuous 24 h co-electrolysis of HMF was then achieved at the current density of 2 mA cm−2(constant current of 10 mA), leading to the highest combined faradaic efficiency (FE) of 139% for HMF-to-BHMF and HMF-to-FDCA. A NiFe oxide catalyst on carbon cloth further replaced the anodic TEMPO mediator for HMF paired electrolysis in a pH-asymmetric flow cell. We envision renewable electrical energy can potentially drive the whole process, thus providing a sustainable avenue towards distributed, scalable, and energy-efficient electrosynthesis. 
    more » « less
  4. Abstract

    Hydrodeoxygenation chemistries play a key role in the upgrading of biomass‐derived feedstocks. Among these, the removal of targeted hydroxyl groups through selective C−O bond cleavage from molecules containing multiple functionalities over heterogeneous catalysts has shown to be a challenge. Herein, we report a highly selective and stable heterogeneous catalyst for hydrodeoxygenation of tartaric acid to succinic acid. The catalyst consists of reduced Mo5+centers promoted by palladium, which facilitate selective C−O bond cleavage, while leaving intact carboxylic acid end groups. Stable catalytic performance over multiple cycles is demonstrated. This catalytic system opens up opportunities for selective processing of biomass‐derived sugar acids with a high degree of chemical functionality.

     
    more » « less
  5. Abstract

    Among many biomass‐derived intermediate compounds, 5‐hydroxymethylfurfural (HMF) has been regarded as a platform chemical because it can be used to produce numerous valuable products. However, the difficulty of HMF isolation from reaction media coupled with its poor stability have significantly inhibited its large‐scale production and application. In this work, we report a single‐step process for the direct production of HMF from glucose using green chemical methods. Optimized glucose isomerization and dehydration under microwave irradiation achieved a respectable HMF yield (70 %) using a biphasic solvent mixture (water/THF), high glucose concentration (30 % w/v), catalytic amounts of AlCl3(5 mol%) and HCl (15 mol%). The reaction can be completed within minutes at 165 °C. Overall, our microwave‐assisted strategy enables the direct conversion of commercially available glucose to the highly valuable platform chemical HMF without the use of expensive solvents or catalysts, suggesting an economically attractive approach for upgrading carbohydrates.

     
    more » « less