Cargando…

Nitrogen-Doped Porous Carbon Materials Derived from Graphene Oxide/Melamine Resin Composites for CO(2) Adsorption

CO(2) adsorption in porous carbon materials has attracted great interests for alleviating emission of post-combustion CO(2). In this work, a novel nitrogen-doped porous carbon material was fabricated by carbonizing the precursor of melamine-resorcinol-formaldehyde resin/graphene oxide (MR/GO) compos...

Descripción completa

Detalles Bibliográficos
Autores principales: Ouyang, Like, Xiao, Jianfei, Jiang, Housheng, Yuan, Shaojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434559/
https://www.ncbi.nlm.nih.gov/pubmed/34500736
http://dx.doi.org/10.3390/molecules26175293
Descripción
Sumario:CO(2) adsorption in porous carbon materials has attracted great interests for alleviating emission of post-combustion CO(2). In this work, a novel nitrogen-doped porous carbon material was fabricated by carbonizing the precursor of melamine-resorcinol-formaldehyde resin/graphene oxide (MR/GO) composites with KOH as the activation agent. Detailed characterization results revealed that the fabricated MR(0.25)/GO-500 porous carbon (0.25 represented the amount of GO added in wt.% and 500 denoted activation temperature in °C) had well-defined pore size distribution, high specific surface area (1264 m(2)·g(−1)) and high nitrogen content (6.92 wt.%), which was mainly composed of the pyridinic-N and pyrrolic-N species. Batch adsorption experiments demonstrated that the fabricated MR(0.25)/GO-500 porous carbon delivered excellent CO(2) adsorption ability of 5.21 mmol·g(−1) at 298.15 K and 500 kPa, and such porous carbon also exhibited fast adsorption kinetics, high selectivity of CO(2)/N(2) and good recyclability. With the inherent microstructure features of high surface area and abundant N adsorption sites species, the MR/GO-derived porous carbon materials offer a potentially promising adsorbent for practical CO(2) capture.