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基于壳聚糖-聚苯并恶嗪的生物基碳吸附剂整体材料的合成与优化,用于高效捕获二氧化碳。

Synthesis and optimization of biobased carbon adsorbent monoliths from chitosan-polybenzoxazine for efficient CO capture.

作者信息

Mosquera José E, Delevingne Liana, Delbecq Frédéric, Daouk Elias, Drelich Audrey, Saleh Khashayar, Gautier Rémi, Leturia Mikel

机构信息

Université de Technologie de Compiègne, ESCOM, TIMR Compiègne France

IMT Nord Europe, Institut Mines-Télécom, CERI Energie et Environnement F-59508 Douai France.

出版信息

RSC Adv. 2025 Mar 3;15(9):6783-6793. doi: 10.1039/d5ra00110b. eCollection 2025 Feb 26.

Abstract

The present study introduces a novel method for the preparation of a CO carbon adsorbent derived from biobased precursors. Porous carbon adsorbents were synthesized through the carbonization and thermal activation of biobased chitosan-polybenzoxazine. First, the study explored the influence of varying amounts of the key polymer precursors, lysine (0.05-0.1 g) and chitosan (0.6-0.12 g), on the surface and adsorption characteristics of the obtained carbons. This aimed to identify the most favourable amounts of these precursors that resulted in the highest CO adsorption performance. In the subsequent stage, the study investigated the impact of different activation times (1-7 h) to enhance the surface characteristics and CO adsorption capacity of the activated carbon. Both carbonization and activation processes were conducted in a tubular furnace at 900 °C under N and CO atmospheres, respectively. After carbonization, the resulting carbon monoliths exhibited a char yield of approximately 49 wt%, with a BET surface area of up to 541 m g and a CO uptake of 4.0 mmol g at 0 °C and 1 bar. After activation, the obtained samples displayed a surface area in the range of 650-1000 m g, with CO adsorption capacities at 1 bar ranging from 4.5 to 5.6 mmol g at 0 °C and 3.2 to 4 mmol g at 25 °C. The activated carbons also demonstrated excellent selectivities for CO/N and CO/CH mixtures, along with a stable CO adsorption-desorption performance after 10 cycles.

摘要

本研究介绍了一种制备源自生物基前驱体的CO碳吸附剂的新方法。通过生物基壳聚糖-聚苯并恶嗪的碳化和热活化合成了多孔碳吸附剂。首先,该研究探讨了不同用量的关键聚合物前驱体赖氨酸(0.05 - 0.1 g)和壳聚糖(0.6 - 0.12 g)对所得碳材料的表面和吸附特性的影响。目的是确定能产生最高CO吸附性能的这些前驱体的最适宜用量。在随后阶段,该研究考察了不同活化时间(1 - 7 h)对活性炭表面特性和CO吸附容量的影响。碳化和活化过程分别在管式炉中于900℃下在N和CO气氛中进行。碳化后,所得碳块的焦炭产率约为49 wt%,BET表面积高达541 m²/g,在0℃和1 bar下的CO吸附量为4.0 mmol/g。活化后,所得样品的表面积在650 - 1000 m²/g范围内,在1 bar下,0℃时的CO吸附容量为4.5至5.6 mmol/g,25℃时为3.2至4 mmol/g。这些活性炭对CO/N₂和CO/CH₄混合物也表现出优异的选择性,并且在10次循环后具有稳定的CO吸附-解吸性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e76/11873787/e076a230c0ec/d5ra00110b-f1.jpg

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