Nitrogen-doped porous carbons derived from sustainable biomass via a facile post-treatment nitrogen doping strategy: Efficient CO2 capture and DRM

碳化 催化作用 吸附 氮气 氢氧化钾 微型多孔材料 碳纤维 化学工程 无机化学 热解 材料科学 活性炭 化学 有机化学 复合材料 复合数 工程类
作者
Xiaodi Zhang,Ying Xu,Guojie Zhang,Chenlei Wu,Jun Liu,Yongkang Lv
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:47 (58): 24388-24397 被引量:57
标识
DOI:10.1016/j.ijhydene.2022.05.222
摘要

Nitrogen (N)-doped carbon materials have become promising candidates for many applications. In this paper, the biomass activated carbon (BC) was obtained by carbonization and activation of soybean meal. Using soybean meal as the precursor, potassium hydroxide (KOH) as the activator and melamine as the nitrogen source, a series of N-doped porous biomass carbons (H-NC-X) with different N contents were achieved via a facile post-treatment nitrogen doping strategy. Then these samples were used as a catalyst for dry reforming of methane (DRM) reaction and an adsorbent for CO2 capture. Among all the investigated samples, BC has the largest specific surface area and the best pore structure characteristics, showing the best CO2 adsorption capacity. However, when BC was used as a catalyst for DRM reaction, it showed the worst catalytic performance. After nitrogen doping treatment, the CO2 adsorption capacity of the prepared N-doped biomass porous carbon decreased gradually with the increase of the introduced N content. This is mainly due to the destruction of the microporous structure of porous carbon by post-processing nitrogen doping. In contrast, when nitrogen-doped porous carbon was used as the reforming catalyst, the catalytic activity increased with the increase of the introduced N content. The order was: H-NC-30>H-NC-20>H-NC-10. This indicates that when nitrogen-doped porous carbon was used as an adsorbent, the pore structure plays a major role; while when it was used as a reforming catalyst, nitrogen functional groups are the major active sites. This study provides a promising N-doped carbon material for effect CO2 adsorption and DRM reactions.
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