过硫酸盐
电子顺磁共振
吸附
电子转移
化学
X射线光电子能谱
双酚A
碳纤维
降级(电信)
催化作用
朗缪尔吸附模型
硫黄
比表面积
分析化学(期刊)
核化学
化学工程
材料科学
光化学
物理化学
有机化学
复合材料
核磁共振
复合数
计算机科学
工程类
环氧树脂
物理
电信
作者
Shijin Zhang,Xiaowei Huo,Suzhou Xu,Yanting Zhang,Benyin Zhang,Mingming Wang,Qingguo Wang,Jing Zhang
标识
DOI:10.1016/j.psep.2022.10.073
摘要
In this work, sulfur-doped (S-doped) carbon materials (SCs) were successfully synthesized by using coffee grounds which are relatively cheap and easily available. Results show that SCs exhibit excellent catalytic activity for persulfate (PS) activation and a more than 99% bisphenol A (BPA) degradation rate was achieved. Meanwhile, 82.3% of total organic carbon (TOC) can be removed in 40 min at 25 °C when applying a dosage of 0.15 g/L SCs and 1 mM PS under an initial pH of about 4.0. SEM and BET characterization methods were used to reveal the surface characteristics of the material. It is found that SCs had a porous structure and a specific surface area of 159.319 m2/g, which conferred to SCs superior adsorption (17.3 mg/g). Additionally, kinetic and adsorption isotherm models for adsorption by SCs were obtained via linear fitting, which proved that the process was better described by the pseudo-second-order model (R2 = 0.9989) and Langmuir model (R2 = 0.9890). The free radical quenching experiments, electron paramagnetic resonance (EPR), and open circuit potential (OCP) tests together demonstrated that the system achieved BPA degradation via non-radical pathways (singlet oxygen and electron transfer). It is speculated that S-doping is able to effectively promote electron transfer given the XPS results. Finally, batch control experiments were run to investigate the influence of PS concentration (0.2 – 2.0 mM), BPA concentration (0.005 – 0.03 mM), SCs dose (0.05 – 0.25 g/L), pH (4.0 – 10.0), and Cl− and HCO3− (1 or 5 mM) on the degradation of BPA. Evidently, the catalysts could be used for a wide range of BPA removal scenarios. In a word, S-doped carbon materials prepared from coffee grounds can improve the degradation of BPA and activation of PS under a wide range of operating conditions. Simultaneously it was strongly associated with electron transfer in non-radical pathways. This research lays the foundation for the rational design of a persulfate-based system for use as an actual water purification catalyst.
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