Resembling Graphene/Polymer Aerogel Morphology for Advancing the CO2/N2 Selectivity of the Postcombustion CO2 Capture Process

被引:1
|
作者
Barbarin, Iranzu [1 ,2 ]
Fidanchevska, Monika [1 ,2 ]
Politakos, Nikolaos [1 ,2 ]
Serrano-Cantador, Luis [3 ]
Cecilia, Juan Antonio [4 ]
Martin, Dolores [5 ]
Sanz, Oihane [6 ]
Tomovska, Radmila [1 ,2 ,7 ]
机构
[1] Univ Basque Country UPV EHU, POLYMAT, Donostia San Sebastian 20018, Spain
[2] Univ Basque Country UPV EHU, Dept Appl Chem, Donostia San Sebastian 20018, Spain
[3] Univ Cordoba, Nanochem Univ Inst IUNAN, Inorgan Chem & Chem Engn Dept, Biopren Grp, Cordoba 14014, Spain
[4] Univ Malaga, Inorgan Chem Crystallog & Mineral, Malaga 29071, Spain
[5] Univ Basque Country UPV EHU, Fac Engn Gipuzkoa, Macrobehav Mesostruct Nanotechnol SGIker Serv, Donostia San Sebastian 20018, Spain
[6] Univ Basque Country, Dept Appl Chem, Donostia San Sebastian 20018, Spain
[7] Ikerbasque, Basque Fdn Sci, Bilbao 48013, Spain
关键词
CARBON-DIOXIDE CAPTURE; POROUS CARBONS; ORGANIC POLYMERS; HIGH-PERFORMANCE; ADSORPTION; NITROGEN; SURFACE; ADSORBENTS; EFFICIENT; ACTIVATION;
D O I
10.1021/acs.iecr.3c02989
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The separation of CO2 from N-2 remains a highly challenging task in postcombustion CO2 capture processes, primarily due to the relatively low CO2 content (3-15%) compared to that of N-2 (70%). This challenge is particularly prominent for carbon-based adsorbents that exhibit relatively low selectivity. In this study, we present a successfully implemented strategy to enhance the selectivity of composite aerogels made of reduced graphene oxide (rGO) and functionalized polymer particles. Considering that the CO2/N-2 selectivity of the aerogels is affected on the one hand by the surface chemistry (offering more sites for CO2 capture) and fine-tuned microporosity (offering molecular sieve effect), both of these parameters were affected in situ during the synthesis process. The resulting aerogels exhibit improved CO2 adsorption capacity and a significant reduction in N-2 adsorption at a temperature of 25 degrees C and 1 atm, leading to a more than 10-fold increase in selectivity compared to the reference material. This achievement represents the highest selectivity reported thus far for carbon-based adsorbents. Detailed characterization of the aerogel surfaces has revealed an increase in the quantity of surface oxygen functional groups, as well as an augmentation in the fractions of micropores (<2 nm) and small mesopores (<5 nm) as a result of the modified synthesis methodology. Additionally, it was found that the surface morphology of the aerogels has undergone important changes. The reference materials feature a surface rich in curved wrinkles with an approximate diameter of 100 nm, resulting in a selectivity range of 50-100. In contrast, the novel aerogels exhibit a higher degree of oxidation, rendering them stiffer and less elastic, resembling crumpled paper morphology. This transformation, along with the improved functionalization and augmented microporosity in the altered aerogels, has rendered the aerogels almost completely N-2-phobic, with selectivity values ranging from 470 to 621. This finding provides experimental evidence for the theoretically predicted relationship between the elasticity of graphene-based adsorbents and their CO2/N-2 selectivity performance. It introduces a new perspective on the issue of N-2-phobicity. The outstanding performance achieved, including a CO2 adsorption capacity of nearly 2 mmol/g and the highest selectivity of 620, positions these composites as highly promising materials in the field of carbon capture and sequestration (CCS) postcombustion technology.
引用
收藏
页码:7073 / 7087
页数:15
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