生物炭
吸附
吸附
化学
水溶液
核化学
朗缪尔吸附模型
铬
打赌理论
解吸
镉
朗缪尔
水溶液中的金属离子
热解
比表面积
金属
有机化学
催化作用
作者
Amali Herath,Cody A. Layne,Felio Pérez,Ei Barbary Hassan,Charles U. Pittman,Todd Mlsna
出处
期刊:Chemosphere
[Elsevier]
日期:2021-04-01
卷期号:269: 128409-128409
被引量:158
标识
DOI:10.1016/j.chemosphere.2020.128409
摘要
Biochar has become a popular research topic in sustainable chemistry for use both in agriculture and pollution abatement. To enhance aqueous Cr(VI), Pb(II) and Cd(II) removal efficiency, high surface area (535 m2/g) byproduct Douglas fir biochar (DFBC) from commercial syn-gas production obtained by fast pyrolysis (900–1000 °C, 1–10 s), was subjected to a KOH activation. KOH-activated biochar (KOHBC) underwent a remarkable surface area increase to 1049 m2/g and a three-fold increase in pore volume (BET analysis). Batch sorption studies on KOHBC verses pH revealed that the highest chromium, lead and cadmium removal capacities occurred at pH 2.0, 5.0 and 6.0, respectively. KOHBC exhibited much higher adsorption capacities than unactivated DFBC. Heavy metal loadings onto KOHBC were characterized by scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. Sorption of Cr(VI), Pb(II) and Cd(II) all followed pseudo-second order kinetics and the Langmuir adsorption model. The highest Langmuir adsorption capacities at the respective pH’s of maximum adsorption were 140.0 mg g−1 Pb(II), 127.2 mg g-1 Cr(VI) and 29.0 mg g−1 Cd(II). Metal ions spiked into natural and laboratory waste water systems exhibited high sorption capacities. Desorption studies carried out using 0.1 M HCl revealed that Pb(II) adsorption onto the KOHBC surface is reversible. Portions of Cd(II) and Cr(VI) adsorbed strongly onto KOHBC were unable to be desorbed by 0.1 M HCl and 0.1 M NaOH.
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