Nitrogen-Doped Porous Carbons Derived from Carbonization of a Nitrogen-Containing Polymer: Efficient Adsorbents for Selective CO2 Capture
Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO2 capture. Carbonization of N-containing polymers is frequently used for the preparation of NPCs, while such an approach is hindered by the high cost of some p...
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Published in | Industrial & engineering chemistry research Vol. 55; no. 41; pp. 10916 - 10925 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
19.10.2016
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Abstract | Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO2 capture. Carbonization of N-containing polymers is frequently used for the preparation of NPCs, while such an approach is hindered by the high cost of some polymer precursors. In the present study, we report for the first time the fabrication of NPCs through the rational choice of the low-cost, N-rich polymer NUT-2 (NUT indicates Nanjing Tech University) as the precursor, which was obtained from polymerization of easily available monomers under mild conditions in the absence of any catalysts. Through carbonization at different temperatures (500–800 °C), NPCs with various porosity and nitrogen contents are obtained. The pore structure and CO2-philic (N-doped) sites are responsible for the adsorption performance, while the highest surface area does not lead to the highest CO2 adsorption capacity. For the sample carbonized at 600 °C (NPC-2-600), the adsorption capacity on CO2 is as high as 164.7 cm3 g–1 at 0 °C and 1 bar, which is much better than that of the benchmarks, such as activated carbon (62.5 cm3 g–1) and 13X zeolite (91.8 cm3 g–1), as well as most reported carbon-based adsorbents. We also demonstrate that the present NPCs can be regenerated completely under mild conditions. The present adsorbents may provide promising candidates for the capture of CO2 from various mixtures, such as flue gas and natural gas. |
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AbstractList | Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO₂ capture. Carbonization of N-containing polymers is frequently used for the preparation of NPCs, while such an approach is hindered by the high cost of some polymer precursors. In the present study, we report for the first time the fabrication of NPCs through the rational choice of the low-cost, N-rich polymer NUT-2 (NUT indicates Nanjing Tech University) as the precursor, which was obtained from polymerization of easily available monomers under mild conditions in the absence of any catalysts. Through carbonization at different temperatures (500–800 °C), NPCs with various porosity and nitrogen contents are obtained. The pore structure and CO₂-philic (N-doped) sites are responsible for the adsorption performance, while the highest surface area does not lead to the highest CO₂ adsorption capacity. For the sample carbonized at 600 °C (NPC-2-600), the adsorption capacity on CO₂ is as high as 164.7 cm³ g–¹ at 0 °C and 1 bar, which is much better than that of the benchmarks, such as activated carbon (62.5 cm³ g–¹) and 13X zeolite (91.8 cm³ g–¹), as well as most reported carbon-based adsorbents. We also demonstrate that the present NPCs can be regenerated completely under mild conditions. The present adsorbents may provide promising candidates for the capture of CO₂ from various mixtures, such as flue gas and natural gas. Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO2 capture. Carbonization of N-containing polymers is frequently used for the preparation of NPCs, while such an approach is hindered by the high cost of some polymer precursors. In the present study, we report for the first time the fabrication of NPCs through the rational choice of the low-cost, N-rich polymer NUT-2 (NUT indicates Nanjing Tech University) as the precursor, which was obtained from polymerization of easily available monomers under mild conditions in the absence of any catalysts. Through carbonization at different temperatures (500–800 °C), NPCs with various porosity and nitrogen contents are obtained. The pore structure and CO2-philic (N-doped) sites are responsible for the adsorption performance, while the highest surface area does not lead to the highest CO2 adsorption capacity. For the sample carbonized at 600 °C (NPC-2-600), the adsorption capacity on CO2 is as high as 164.7 cm3 g–1 at 0 °C and 1 bar, which is much better than that of the benchmarks, such as activated carbon (62.5 cm3 g–1) and 13X zeolite (91.8 cm3 g–1), as well as most reported carbon-based adsorbents. We also demonstrate that the present NPCs can be regenerated completely under mild conditions. The present adsorbents may provide promising candidates for the capture of CO2 from various mixtures, such as flue gas and natural gas. |
Author | Sun, Lin-Bing Kou, Jiahui |
AuthorAffiliation | College of Materials Science and Engineering Nanjing Tech University College of Chemistry and Chemical Engineering |
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Snippet | Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO2 capture.... Because of their abundant porosity, tunable surface properties, and high stability, N-doped porous carbons (NPCs) are highly promising for CO₂ capture.... |
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SubjectTerms | activated carbon adsorbents adsorption carbon dioxide carbonization catalysts engineering flue gas natural gas nitrogen content polymerization polymers porosity surface area temperature zeolites |
Title | Nitrogen-Doped Porous Carbons Derived from Carbonization of a Nitrogen-Containing Polymer: Efficient Adsorbents for Selective CO2 Capture |
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