(31a) Modeling and Techno-Economic Assessment of an Air-to-Syngas Process | AIChE

(31a) Modeling and Techno-Economic Assessment of an Air-to-Syngas Process

Authors 

Almajed, H. - Presenter, Renewable and Sustainable Energy Institute, University of Colorado
Guerra, O. J., Colombian Petroleum Institute (ICP), ECOPETROL S.A.
Smith, W. A., University of Colorado Boulder
Hodge, B. M., National Renewable Energy Laboratory
Integrating carbon capture with utilization is one of the most promising pathways to pursue carbon neutrality1–3. Particularly, valorizing CO2 by integrating Direct Air CO2 Capture (DACC) with renewably-driven carbon electrolysis offers a promising pathway to overcome the high capture costs of DACC. More immediately, syngas production via integrated DACC-electrolysis routes can become economically feasible by 2050 as CO2 electrolysis (CO2ER) systems are well-suited to produce CO as a main product and H2 as a byproduct. In this contribution, we study the integration of hydroxide-based DACC with a low-temperature CO2ER and with conventional Reverse Water Gas Shift (RWGS) to identify improvement opportunities for DACC-Utilization (DACCU) in general and DACC-electrolysis in particular. We define the syngas H2:CO molar ratio to be 2 and the production rate of syngas to be 2.2 Mt-syngas/yr, and we assume hydrogen supply from Alkaline Water Electrolysis (AWE) in both routes due to its higher technological maturity level. We present a verified Aspen Plus model of a hydroxide-based DACC plant and a custom-built model for CO2 and water electrolysis to enable the assessment of the studied routes techno-economically. Herein, we refer to the integrated DACC with RWGS and with CO2ER pathways as DACC-AWE-RWGS and DACC-AWE-CO2ER, respectively.

Our findings indicate that DACC requires energy inputs of 8.58 and 8.55 GJ/t-CO2 when integrated with RWGS and CO2ER, respectively, in line with current literature estimates4,5. In addition, we calculate the power consumption of CO2 electrolysis to be 6.56 MWhel/kg-syngas and of H2O electrolysis to be 6.01 and 9.68 MWhel/kg-syngas for DACC-AWE-RWGS and DACC-AWE-CO2ER, respectively. Such values, in addition to a referenced RWGS energy consumption value, are used to estimate the total energy consumption, and thus cost, of the two routes. Our assessment demonstrates that DACC-AWE-RWGS is a more carbon-efficient and a less energy-consuming pathway than the current state of the DACC-AWE-CO2ER route. However, in terms of marginal energy-associated CO2 emissions, we find DACC-AWE-CO2ER to outperform DACC-AWE-RWGS, although at an insufficient emissions difference that would drive the shift from the conventional RWGS to the emerging CO2ER. In addition, our CAPEX and OPEX calculations provide a lower total syngas cost of $1.44/kg-syngas via DACC-AWE-RWGS compared to that of DACC-AWE-CO2ER ($1.53/kg-syngas). Further, our sensitivity analysis suggests that the H2 production cost and the electricity price to be the main drivers in both pathways, and in that order. Moreover, our future scenario analysis compares three potential technology improvement scenarios and defines research targets for DACC-AWE-CO2ER to compete economically with DACC-AWE-RWGS. Finally, we end with a discussion on the integration of renewable electricity with the investigated pathways.

References:

  1. Mertens, J., Breyer, C., Arning, K., Bardow, A., Belmans, R., Dibenedetto, A., Erkman, S., Gripekoven, J., Léonard, G., Nizou, S., et al. (2023). Carbon capture and utilization: More than hiding CO2 for some time. Joule 0. 10.1016/j.joule.2023.01.005.
  2. IPCC (2022). Climate Change 2022: Mitigation of Climate Change: Summary for Policymakers (Cambridge University Press) 10.1017/9781009157926.001.
  3. International Energy Agency (September 19). Putting CO2 to Use (IEA Publications).
  4. Keith, D.W., Holmes, G., St. Angelo, D., and Heidel, K. (2018). A Process for Capturing CO2 from the Atmosphere. Joule 2, 1573–1594. 10.1016/j.joule.2018.05.006.
  5. Zeman, F. (2007). Energy and Material Balance of CO2 Capture from Ambient Air. Environ. Sci. Technol. 41, 7558–7563. 10.1021/es070874m.