We performed H-cell
and flow cell experiments to study the electrochemical
reduction of CO2 to oxalic acid (OA) on a lead (Pb) cathode
in various nonaqueous solvents. The effects of anolyte, catholyte,
supporting electrolyte, temperature, water content, and cathode potential
on the Faraday efficiency (FE), current density (CD), and product
concentration were investigated. We show that a high FE for OA can
be achieved (up to 90%) at a cathode potential of −2.5 V vs
Ag/AgCl but at relatively low CDs (10–20 mA/cm2).
The FE of OA decreases significantly with increasing water content
of the catholyte, which causes byproduct formation (e.g., formate,
glycolic acid, and glyoxylic acid). A process design and techno-economic
evaluation of the electrochemical conversion of CO2 to
OA is presented. The results show that the electrochemical route for
OA production can compete with the fossil-fuel based route for the
base case scenario (CD of 100 mA/cm2, OA FE of 80%, cell
voltage of 4 V, electrolyzer CAPEX of $20000/m2, electricity
price of $30/MWh, and OA price of $1000/ton). A sensitivity analysis
shows that the market price of OA has a huge influence on the economics.
A market price of at least $700/ton is required to have a positive
net present value and a payback time of less than 10 years. The performance
and economics of the process can be further improved by increasing
the CD and FE of OA by using gas diffusion electrodes and eliminating
water from the cathode, lowering the cell voltage by increasing the
conductivity of the electrolyte solutions, and developing better OA
separation methods.