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影响过渡金属在氧化碳纳米管上吸附的因素研究。

Investigation of factors affecting adsorption of transition metals on oxidized carbon nanotubes.

作者信息

Gao Zhanming, Bandosz Teresa J, Zhao Zongbin, Han Mei, Qiu Jieshan

机构信息

Carbon Research Laboratory, Center for Nano Materials and Science, State Key Lab of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, 158 Zhongshan Road, Dalian, China.

出版信息

J Hazard Mater. 2009 Aug 15;167(1-3):357-65. doi: 10.1016/j.jhazmat.2009.01.050. Epub 2009 Jan 22.

Abstract

Adsorption of nickel, copper, zinc and cadmium from aqueous solutions on carbon nanotubes oxidized with concentrated nitric acid was carried out in single, binary, ternary and quaternary systems. TEM and adsorption of nitrogen were used to determine texture and structural parameters, respectively. The surface chemistry was evaluated using the pH at the point of zero charge, FTIR spectroscopy and XPS analysis. The experimental results showed that all isotherms for Cu(2+)(aq) fit to Langmuir model in each system. On the other hand, the isotherms for Ni(2+)(aq), Cd(2+)(aq) and Zn(2+)(aq) in multi-component systems reveal the effect of competition for adsorption sites seen as a decrease in the amount adsorbed. The uptakes at the equilibrium concentration of 0-0.04 mmol L(-1) in single system and 0-0.15 mmol L(-1) in binary system are in the order Cu(2+)(aq)>Ni(2+)(aq)>Cd(2+)(aq)>Zn(2+)(aq) while for the ternary and quaternary, the order is Cu(2+)(aq)>Cd(2+)(aq)>Zn(2+)(aq)>Ni(2+)(aq). The results indicate that the mechanism of adsorption is governed by the surface features, ion exchange process and electrochemical potential. The latter plays a significant role in multi-component adsorption where redox reactions, not only on the adsorbent surface but also between the adsorbates, are likely to occur.

摘要

在单组分、双组分、三组分和四组分体系中,研究了用浓硝酸氧化的碳纳米管对水溶液中镍、铜、锌和镉的吸附。分别采用透射电子显微镜(TEM)和氮气吸附法测定织构和结构参数。通过零电荷点的pH值、傅里叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)分析对表面化学性质进行了评估。实验结果表明,在每个体系中,Cu(2+)(aq)的所有等温线均符合朗缪尔模型。另一方面,多组分体系中Ni(2+)(aq)、Cd(2+)(aq)和Zn(2+)(aq)的等温线显示出吸附位点竞争的影响,表现为吸附量的减少。在单组分体系中平衡浓度为0 - 0.04 mmol L(-1)以及双组分体系中平衡浓度为0 - 0.15 mmol L(-1)时,吸附量顺序为Cu(2+)(aq)>Ni(2+)(aq)>Cd(2+)(aq)>Zn(2+)(aq),而在三组分和四组分体系中,顺序为Cu(2+)(aq)>Cd(2+)(aq)>Zn(2+)(aq)>Ni(2+)(aq)。结果表明,吸附机理受表面特征、离子交换过程和电化学势的控制。后者在多组分吸附中起重要作用,其中不仅在吸附剂表面,而且在吸附质之间都可能发生氧化还原反应。

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