TY - JOUR
T1 - Coupling CO2 electrolysis and downstream processing via heat pump-based waste heat recovery
AU - Dal Mas, Riccardo
AU - Carta, Andrea
AU - Somoza-Tornos, Ana
AU - Kiss, Anton A.
PY - 2026
Y1 - 2026
N2 - The electrification of chemical processes and CO2 utilization are key approaches to improving efficiency and reducing CO2 emissions in the process industry. The development of electrolyzers has gathered momentum, enabling the potential introduction of renewable electrons into the manufacture of CO2-based chemicals. While the performance of electrolyzers is subject to improvements driven by the experimental community, the generation of waste heat is unavoidable due to electrical resistances and process inefficiencies within the electrochemical cells. Nonetheless, reusing this waste heat has yet to be investigated for CO2 electrolyzers. This novel work shows the potential for upgrading the electrolyzer waste heat by means of a heat pump, enabling its utilization in the separation processes downstream of the carbon dioxide electrolyzer. The product chosen is formic acid (60 kt/y), and for our system, the waste heat represents approximately 60 % of the power input to the electrochemical cells, and it can be upgraded from 50 °C to 120 °C to drive the azeotropic distillation of formic acid and water. This integration results in the electrification of 76 % of the separation energy duty, yielding a decrease in CO2 emissions of 29–84 % compared to the conventional production, depending on the source of electricity. The results demonstrate that the use of traditional heating media in thermal separation processes can be offset and substituted with (renewable) electrical energy, allowing for an increased overall system efficiency. This approach can be readily extended to different productions based on carbon dioxide electroreduction, for example for methanol and ethanol manufacture. This eco-efficient process design leads to a deeper penetration of renewable energy into chemical manufacturing, as both reaction and separation are driven by electricity.
AB - The electrification of chemical processes and CO2 utilization are key approaches to improving efficiency and reducing CO2 emissions in the process industry. The development of electrolyzers has gathered momentum, enabling the potential introduction of renewable electrons into the manufacture of CO2-based chemicals. While the performance of electrolyzers is subject to improvements driven by the experimental community, the generation of waste heat is unavoidable due to electrical resistances and process inefficiencies within the electrochemical cells. Nonetheless, reusing this waste heat has yet to be investigated for CO2 electrolyzers. This novel work shows the potential for upgrading the electrolyzer waste heat by means of a heat pump, enabling its utilization in the separation processes downstream of the carbon dioxide electrolyzer. The product chosen is formic acid (60 kt/y), and for our system, the waste heat represents approximately 60 % of the power input to the electrochemical cells, and it can be upgraded from 50 °C to 120 °C to drive the azeotropic distillation of formic acid and water. This integration results in the electrification of 76 % of the separation energy duty, yielding a decrease in CO2 emissions of 29–84 % compared to the conventional production, depending on the source of electricity. The results demonstrate that the use of traditional heating media in thermal separation processes can be offset and substituted with (renewable) electrical energy, allowing for an increased overall system efficiency. This approach can be readily extended to different productions based on carbon dioxide electroreduction, for example for methanol and ethanol manufacture. This eco-efficient process design leads to a deeper penetration of renewable energy into chemical manufacturing, as both reaction and separation are driven by electricity.
KW - CO electrolysis
KW - Downstream processing
KW - Heat pumps
KW - Waste heat recovery
UR - http://www.scopus.com/inward/record.url?scp=105014012504&partnerID=8YFLogxK
U2 - 10.1016/j.compchemeng.2025.109330
DO - 10.1016/j.compchemeng.2025.109330
M3 - Article
AN - SCOPUS:105014012504
SN - 0098-1354
VL - 204
JO - Computers and Chemical Engineering
JF - Computers and Chemical Engineering
M1 - 109330
ER -