Novel N-doped hierarchically porous carbons derived from sustainable shrimp shell for high-performance removal of sulfamethazine and chloramphenicol

吸附 朗缪尔吸附模型 单层 化学 碳化 比表面积 化学工程 材料科学 核化学 纳米技术 有机化学 催化作用 工程类
作者
Ling Qin,Zhiping Zhou,Jiangdong Dai,Ping Ma,Haibin Zhao,Jinsong He,Atian Xie,Chunxiang Li,Yongshen Yan
出处
期刊:Journal of The Taiwan Institute of Chemical Engineers [Elsevier BV]
卷期号:62: 228-238 被引量:66
标识
DOI:10.1016/j.jtice.2016.02.009
摘要

In this research, shrimp shell, as an abundant, environmental-friendly and renewable biomass source, was successfully converted into novel N-doped hierarchically porous carbons (N-HPCs) via a simple self-template carbonization and KOH activation. The physical–chemical properties of N-HPCs were characterized by FT-IR, SEM, TEM, Raman, BET and elemental analysis. The optimum N-HPCs (named N-HPC-850-2) exhibited the highest specific surface area (3171 m2/g) and total pore volume (1.934 cm3/g), and was used to effectively eliminate sulfamethazine (SMZ) and chloramphenicol (CAP) from water. Batch adsorption results showed increasing temperature was in favor of adsorption and the N-HPC-850-2 had a high adsorption affinity toward two antibiotics over a broad pH range. Adsorption isotherm data were fitted with Langmuir model very well, with the maximum monolayer adsorption capacity of 699.3 and 742.4 mg/g for SMZ and CAP at 318 K, respectively. The pseudo-second-order rate model described adsorption kinetics data well and adsorption processes were governed predominately by intra-particle diffusion and film diffusion. The thermodynamic parameters indicated the spontaneous and endothermic adsorption. Importantly, the N-HPC-850-2 adsorbent also exhibited a good regeneration capacity. Here, we provided a promising approach to prepare low-cost and high-performance biomass-based N-HPCs for fast and highly efficient removal of antibiotics from aquatic system.

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