吸附
化学
生物炭
镉
朗缪尔吸附模型
离子交换
降水
热解
水溶液
吸附
朗缪尔
无机化学
环境化学
离子
有机化学
物理
气象学
作者
Xiaoqiang Cui,Siyu Fang,Yiqiang Yao,Tingqiang Li,Qijun Ni,Xiaoe Yang,Zhenli He
标识
DOI:10.1016/j.scitotenv.2016.03.248
摘要
The objective of this study was to investigate the mechanisms of cadmium (Cd) sorption on biochars produced at different temperature (300–600 °C) and their quantitative contribution. The sorption isotherms and kinetics of Cd2 + sorption on biochars were determined and fitted to different models. The Cd2 + sorption data could be well described by a simple Langmuir model, and the pseudo second order kinetic model best fitted the kinetic data. The maximum sorption capacity (Qm) obtained from the Langmuir model for CIB500 was 188.8 mg g− 1, which was greater than that of biochars produced at other temperature. Precipitation with minerals, ion exchange, complexation with surface oxygen-containing functional groups, and coordination with π electrons were the possible mechanisms of Cd2 + sorption on the biochars. The contribution of each mechanism varied with the pyrolysis temperature. With increasing pyrolysis temperature, the contribution of surface complexation and metal ion exchange decreased from 24.5% and 43.3% to 0.7% and 4.7%, while the contribution of precipitation and Cd2 +-π interaction significantly increased from 29.7% and 2.5% to 89.5% and 5.1%, respectively. Overall, the precipitation with minerals and metal ion exchange dominated Cd2 + sorption on the biochars (accounted for 73.0–94.1%), and precipitation with minerals was the primary mechanism of Cd2 + sorption on the high-temperature biochars (≥ 500 °C) (accounted for 86.1–89.5%).
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