层状双氢氧化物
吸附
生物炭
化学工程
介孔材料
复合数
吸热过程
化学
朗缪尔吸附模型
比表面积
离子强度
离子交换
动力学
无机化学
材料科学
离子
催化作用
水溶液
有机化学
复合材料
热解
工程类
物理
量子力学
作者
Shisuo Fan,Shuo Wang,Weiyu Zhang,Xinru Fan,Zijian Huang,Na Zhou,Huacheng Xu
标识
DOI:10.1016/j.jiec.2024.01.010
摘要
In this study, a promising KOH activated biochar/MnAl-layered double hydroxides (K-BC-LDHs) composite was synthesized using the in-situ chemical co-precipitation method. The results showed that the LDH particles were successfully distributed across the activated biochar during the modification process. More functional groups (Mn − O, Mn − O − Mn) and crystalline minerals (Mn4Al2(OH)12CO3·3H2O) were created and appeared on the surface of the composite. The LDHs modification process decreased the surface area, but increased the pore volume of the activated biochars. In addition, a mesoporous structure was formed, predominately due to the introduction of LDHs particles. The adsorption capacity for TC by K-BC-LDHs reached 1477.67 mg·g−1 and this increase was attributed to the combined actions of pore filling, complexation, and ion exchange, followed by hydrogen bonding, electrostatic attraction, and π-π interactions. The pseudo-second-order kinetics, intra-particle diffusion kinetics, and Langmuir isotherm models well described the adsorption behavior of TC by K-BC-LDHs. Furthermore, TC adsorption by K-BC-LDHs was a spontaneous and endothermic process. The K-BC-LDHs composite exhibited strong adsorption toward TC over a wide pH range (3–9) and there was a certain resistance to coexisting ionic interference. Additionally, the K-BC-LDHs composite showed high adsorption performance toward other pollutants and can potentially be recycled.
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