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. 2023 Sep 2;13(1):14476.
doi: 10.1038/s41598-023-41683-4.

Exploring the capture and desorption of CO2 on graphene oxide foams supported by computational calculations

Affiliations

Exploring the capture and desorption of CO2 on graphene oxide foams supported by computational calculations

Bryan E Arango Hoyos et al. Sci Rep. .

Erratum in

Abstract

In the last decade, the highest levels of greenhouse gases (GHG) in the atmosphere have been recorded, with carbon dioxide (CO2) being one of the GHGs that most concerns mankind due to the rate at which it is generated on the planet. Given its long time of permanence in the atmosphere (between 100 to 150 years); this has deployed research in the scientific field focused on the absorption and desorption of CO2 in the atmosphere. This work presents the study of CO2 adsorption employing materials based on graphene oxide (GO), such as GO foams with different oxidation percentages (3.00%, 5.25%, and 9.00%) in their structure, obtained via an environmentally friendly method. The characterization of CO2 adsorption was carried out in a closed system, within which were placed the GO foams and other CO2 adsorbent materials (zeolite and silica gel). Through a controlled chemical reaction, production of CO2 was conducted to obtain CO2 concentration curves inside the system and calculate from these the efficiency, obtained between 86.28 and 92.20%, yield between 60.10 and 99.50%, and effectiveness of CO2 adsorption of the materials under study. The results obtained suggest that GO foams are a promising material for carbon capture and the future development of a new clean technology, given their highest CO2 adsorption efficiency and yield.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1
Figure 1
CCS technologies for industrial waste, listing sorbents which can be applied to capture CO2 from air.
Figure 2
Figure 2
Flowchart for the DTD method to obtain the GO foams used in this research.
Figure 3
Figure 3
CO2 adsorption characterization system (GO–Foam–CO2) for GO foams developed herein.
Figure 4
Figure 4
GO foams obtained employing the DTD and characterization methods, (a) 873.15 K (GO 9.00%), (b) 973.15 K (GO 5.25%), (c) 1053.15 K (GO 3.00%), (d) GO–TEM, (e) GO–XRD patterns and (f) GO–Raman at 873 and 973 K.
Figure 5
Figure 5
(a) CO2 generation characterization, CO2 adsorption in (b) Zeolite, (c) Silica gel, and (d) CO2 adsorption using GO-9.00% at 294.15 K.
Figure 6
Figure 6
(a) GO-9.00% with a temperature of 423.15 K, (b) GO-9.00% with a temperature of 523.15 K, and (c) GO-9.00% with a temperature of 573.15 K.
Figure 7
Figure 7
(a) GO-3.00% with re-adsorption temperature of 673.15 K, (b) GO-5.25% with re-adsorption temperature of 673.15 K, and (c) GO-9.00% with re-adsorption temperature of 673.15 K.
Figure 8
Figure 8
(a) GO 9.00% at 260.15 K and (b) GO 9.00% at 253.15 K.
Figure 9
Figure 9
Structures studied. (a) Graphene, (b) GO with hydroxyl bridges, (c) CO2 molecule adsorbed in pristine graphene passivated by hydrogen atoms in its edges, (d) converged CO2/GO structures for the GO-1 position, (e) GO-2 position, (f) GO-3 position, (g) MEP for pristine graphene/CO2, (h) MEP for GO-1 position, (i) NCI for pristine graphene/CO2 and (j) NCI for GO-1 position.
Figure 10
Figure 10
Possible application of GO–Foam–CO2 for carbon removal in a traffic light. (Permissions allowed by Erica Valencia (left figure) and Humberto Franco (right figure). copyright holders).

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