(643e) Capture and Conversion of CO2 into Methane Using Catalytic Sorbent of NaNO3/MgO + Ru/Al2O3 | AIChE

(643e) Capture and Conversion of CO2 into Methane Using Catalytic Sorbent of NaNO3/MgO + Ru/Al2O3

Authors 

Park, S. J. - Presenter, Georgia Institute of Technology
Jones, C. - Presenter, Georgia Institute of Technology
Bukhovko, M. P., Aramco Services Company: Aramco Research Center - Boston
A concerted process combining CO2 capture and utilization can compliment traditional CO2 capture processes, offering unique advantages, as storage and transportation of CO2 can be removed, and the produced renewable fuel source can be directly used again in nearby plants. Specifically in case of CO2 capture & methanation, the energy intensive temperature swing sorption process may also be removed by performing both steps under isothermal conditions. While first generation of catalytic sorbents, such as Ru/CaO/Al2O3, has previously been shown to be effective in this task, like all first generation materials, it has some drawbacks, including modest CO2 sorption and methane production capacities.[1] In this work, a catalytic sorbent composed of a physical mixture of NaNO3/MgO and Ru/Al2O3, was examined for combined capture & conversion. A material comprised of 17% NaNO3/MgO was found to be effective at capturing CO2 under 10% CO2/15%H2O/N2 flows akin to those in flue gas, showing 7.5 mmol CO2/g sorption capacity. It was also capable of capturing and desorbing CO2 over 8 cycles at isothermal conditions at 300 °C by switching the feed gas from CO2 flow to inert flow.[2]

To evaluate performance of the new catalytic sorbent synthesized, both CO2 sorption capacity and methane production capacity, equivalent to number of moles of methane produced per mass of catalytic sorbent in one cycle of capture and methanation, were measured. A catalytic sorbent of 2:1 mass ratio of 17%NaNO3/MgO and 0.5%Ru/Al2O3 showed a sorption capacity of 3.5 mmol CO2/g, and methane production capacity of 1.3 mmol CH4/g at 300 °C. Both the sorption capacity and methane production capacity are comparable to the highest values reported to date using flue gas relevant CO2 concentrations (~10% CO2), making such catalytic sorbents promising materials for further development of combined capture & conversion applications. Ongoing work targets assessment of reaction kinetics and elucidation of reaction pathways using these materials.

Reference:

(1) Duyar, M. S.; Treviño, M. A. A.; Farrauto, R. J. Dual Function Materials for CO2 Capture and Conversion Using Renewable H2. Appl. Catal. B Environ. 2015, 168–169, 370–376.

(2) Park, S.J.; Y. Kim.; Jones, C.W. NaNO3 Promoted Mesoporous MgO for High Capacity CO2 Capture from Simulated Flue Gas with Isothermal Regeneration. ChemSusChem 2020.