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金属离子改性活性炭对二氯甲烷/三氯甲烷吸附性能的影响

Effects of metal ions loaded onto activated carbons on adsorption capability of dichloromethane/trichloromethane

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【作者】 夏启斌黄思思肖利民张伟李忠

【Author】 XIA Qi-bin,HUANG Si-si,XIAO Li-ming,ZHANG Wei,LI Zhong(The Key Lab. of Enhanced Heat Transfer and Energy Conversation Ministry of Education College of Chemical and Chemical Engineering,South China University of Technology,Guangzhou 510640,China)

【机构】 华南理工大学化学与化工学院,传热强化与过程节能教育部重点实验室

【摘要】 主要研究了不同金属改性活性炭对三氯甲烷和二氯甲烷吸附性能的影响。采用浸渍法将4种不同金属离子负载改性活性炭,测定了三氯甲烷和二氯甲烷在改性活性炭上的吸附透过曲线,应用软硬酸碱理论分析和讨论了活性炭表面负载不同金属离子对二氯甲烷吸附性能的影响。结果表明,不同金属负载活性炭对三氯甲烷和二氯甲烷的吸附能力依次为:Fe(Ⅲ)-AC>Mg(Ⅱ)-AC>Cu(Ⅱ)-AC>AC>Ag(I)-AC,根据软硬酸碱理论分类,三氯甲烷和二氯甲烷属于硬碱,当活性炭表面负载硬酸类金属离子Fe3+、Mg2+,增大了活性炭表面的硬酸性,对三氯甲烷和二氯甲烷的吸附能力加强,Ag+属于软酸,它的负载局部增强了活性炭表面的软酸性,降低了其对三氯甲烷和二氯甲烷的吸附能力。

【Abstract】 The effects of metal ions loaded onto activated carbons on adsorption capability of dichloromethane/ trichloromethane were investgated. Four kinds of metal ions loaded activated carbons were prepared by the impregnated method. Breakthrough curves for dichloromethane/ trichloromethane adsorption on modified activated carbons in a fixed bed were measured. The effects of metal ions loaded onto activated carbons on adsorption capability of dichloromethane/ trichloromethane was discussed with the help of the hard soft acid base principle.The results showed that the adsorption capability of the modified activated carbons for dichloromethane/ trichloromethane decreased in the order of Fe(Ⅲ)-AC>Mg(Ⅱ)-AC>Cu(Ⅱ)-AC>AC>Ag(Ⅰ)-AC. Based on the hard soft acid base principle,dichloromethane and trichloromethane are hard base. The loading of Fe3+,Mg2+ enhanced the interaction between dichloromethane/ trichloromethane and the surfaces of modification activated carbons because Fe3+,Mg2+ are hard acid ,and the loading of Ag+ weakened the interaction between dichloromethane/trichloromethane and the Ag (Ⅰ)/AC surfaces because Ag+ is a soft acid.

【基金】 国家自然科学基金重点资助项目(20336020);广东省科技攻关资助项目(2005A30401004)
  • 【文献出处】 功能材料 ,Journal of Functional Materials , 编辑部邮箱 ,2009年11期
  • 【分类号】O647.32
  • 【被引频次】48
  • 【下载频次】1101
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