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
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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