Acetone adsorption on hierarchically porous carbon foams: Effect of nitrogen doping and oxygen functional groups

Porous carbons are promising materials for volatile organic compound (VOC) capture, but the interplay between pore structure and surface chemistry remains poorly understood. Here, we report the synthesis of graphene-like carbon foams (CFs) with ultra-high surface area (2563 m 2 g −1 ) and tunable surface functionalities for efficient acetone vapour adsorption. Using sodium ethoxide as a precursor, we prepared pristine CFs and systematically modified them via oxygen and nitrogen doping. Moderate oxygen doping (∼11 at.%) preserved microporosity, resulting in exceptional acetone uptake (1206 mg g −1 ), superior N 2 /acetone selectivity (∼11,500) and excellent regeneration stability compared to undoped CF samples. In contrast, aggressive oxidation (∼26 at.% O) and high nitrogen doping (7–13 at.%) significantly reduced porosity and adsorption capacity, with the most heavily doped samples showing the poorest performance. Near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) was employed to gain further insight into the adsorption mechanisms, which were dominated by pore filling and weak electrostatic interactions from surface groups enhancing low-pressure uptake. Our findings establish a clear structure – function relationship, highlighting the critical balance between porosity and surface chemistry for VOC capture. These results also position CFs as scalable, regenerable adsorbents for industrial air purification and environmental remediation. Furthermore, the work provides a robust platform for engineering next-generation adsorbents with tailored performance, contributing to cleaner air technologies and sustainable chemical engineering solutions. • Carbon foams doped with oxygen (11–26 at.%) and nitrogen (7–13 at.%) were prepared. • Oxidation and nitrogen doping modify surface chemistry while reducing porosity. • Surface functional groups enhance acetone uptake through dipole-dipole interactions. • Micropore and mesopore filling determined acetone uptake capacity. • Optimized carbon foam exhibited superior acetone uptake and regenerative ability.

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Publication Details

Journal
Chemical Engineering Journal
Published
2025-08-08
DOI
https://doi.org/10.1016/j.cej.2025.166784
Citations
4
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
2.07

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article

Acetone adsorption on hierarchically porous carbon foams: Effect of nitrogen doping and oxygen functional groups

Stephen Matthew Lyth, Muhammad Irfan Maulana Kusdhany, Maryna Vorokhta, Kazunari Sasaki et al.
4 citations
Chemical Engineering Journal
Catalytic Processes in Materials Science
2.07
article

Acetone adsorption on hierarchically porous carbon foams: Effect of nitrogen doping and oxygen functional groups

Stephen Matthew Lyth, Muhammad Irfan Maulana Kusdhany, Maryna Vorokhta, Kazunari Sasaki, Masamichi Nishihara, Martina Švábová, Michael Vorochta
article en
4 citations

Abstract

Porous carbons are promising materials for volatile organic compound (VOC) capture, but the interplay between pore structure and surface chemistry remains poorly understood. Here, we report the synthesis of graphene-like carbon foams (CFs) with ultra-high surface area (2563 m 2 g −1 ) and tunable surface functionalities for efficient acetone vapour adsorption. Using sodium ethoxide as a precursor, we prepared pristine CFs and systematically modified them via oxygen and nitrogen doping. Moderate oxygen doping (∼11 at.%) preserved microporosity, resulting in exceptional acetone uptake (1206 mg g −1 ), superior N 2 /acetone selectivity (∼11,500) and excellent regeneration stability compared to undoped CF samples. In contrast, aggressive oxidation (∼26 at.% O) and high nitrogen doping (7–13 at.%) significantly reduced porosity and adsorption capacity, with the most heavily doped samples showing the poorest performance. Near-ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) was employed to gain further insight into the adsorption mechanisms, which were dominated by pore filling and weak electrostatic interactions from surface groups enhancing low-pressure uptake. Our findings establish a clear structure – function relationship, highlighting the critical balance between porosity and surface chemistry for VOC capture. These results also position CFs as scalable, regenerable adsorbents for industrial air purification and environmental remediation. Furthermore, the work provides a robust platform for engineering next-generation adsorbents with tailored performance, contributing to cleaner air technologies and sustainable chemical engineering solutions. • Carbon foams doped with oxygen (11–26 at.%) and nitrogen (7–13 at.%) were prepared. • Oxidation and nitrogen doping modify surface chemistry while reducing porosity. • Surface functional groups enhance acetone uptake through dipole-dipole interactions. • Micropore and mesopore filling determined acetone uptake capacity. • Optimized carbon foam exhibited superior acetone uptake and regenerative ability.

Chemical Engineering JournalVol. 521
Kyushu University (JP), Charles University (CZ), Czech Academy of Sciences, Institute of Rock Structure and Mechanics (CZ)
Japan Society for the Promotion of Science London, Akademie Věd České Republiky, Japan Society for the Promotion of Science, Institute of Rock and Soil Mechanics, Chinese Academy of Sciences
Clean water and sanitation
Openalex Percentile: Top 12%
Catalytic Processes in Materials Science
2.07
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