Unveiling the role of CO2 methanation toward single-walled carbon nanotubes synthesis through systematic optimization within a tandem process

Abstract

This study develops a tandem process for the direct conversion of CO2 into SWCNTs via sequential CO2 methanation and CH4 pyrolysis. The process integrates Step 1 (CO2 -> CH4 over 30 wt % Ni/SiO2) and Step 2 (CH4 -> CNTs over 1 wt % Fe-0.1 wt % Mo/MgO), by systematically varying the reaction temperature (T = 300-400 degrees C) and H-2/CO2 ratio (4-8) in Step 1 to investigate their influence on CNT growth in Step 2. At low Step 1 temperatures (<= 300 degrees C), CH4 formation was limited by low CO2 conversion, resulting no CNTs. At elevated Step 1 temperatures, the CO2 methanation pathway shifted from the formate to the CO route, leading to increased formation of CH4 and CO. This enhanced the CNT yield up to 79.1 wt % but reduced crystallinity and wall selectivity due to excessive carbon feedstock. Increasing H-2/CO2 ratio led to residual H-2, which disrupted CH(4 )pyrolysis equilibrium in Step 2, further degrading CNT crystallinity and yield. In particular, three types of CNT growth zones were identified: No CNTs zone (T < 300 degrees C), DWCNTs zone (T > 360 degrees C and H-2/CO2 > 6), and SWCNTs zone (T <= 360 degrees C and H-2/CO2 <= 6), revealing a reaction-property relationship governed by Step 1 reaction conditions. Building on these findings, a life cycle assessment was conducted to evaluate the environmental performance of the tandem process. The process exhibited a global warming potential of 10.58 kg CO2-eq lower than conventional CNT synthesis methods, with further reductions anticipated under renewable electricity input. These results demonstrate a sustainable and scalable route for producing high-value carbon materials directly from CO2.