首页 | 本学科首页   官方微博 | 高级检索  
     检索      

氨基酸螯合吸附树脂对Cu2+的吸附行为
引用本文:孟冠华,欧承慧,陶冬民,刘宝河.氨基酸螯合吸附树脂对Cu2+的吸附行为[J].应用化学,2009,26(12):1450-1455.
作者姓名:孟冠华  欧承慧  陶冬民  刘宝河
作者单位:(安徽工业大学建筑工程学院 马鞍山 243002)
基金项目:安徽省教育厅自然科学研究项目 
摘    要:合成了一种L-酪氨酸修饰的螯合吸附树脂(AJS-02),并与超高交联树脂NDA-150作对比,研究了其 对Cu2+的吸附和脱附行为。静态实验结果表明,在研究的浓度范围内,吸附平衡数据符合Langmuir等温吸附方程。Cu2+在AJS-02上的吸附量大于其在NDA-150上的吸附量。Cu2+在2种树脂上的吸附过程为物理和化学作用的共同结果。吸附动力学符合液膜扩散方程,液膜扩散为吸附速率的主要控制步骤。动态吸附-脱附实验表明,动态穿透吸附量和总吸附量分别为4.05×10-3和6.44×10-3 mol/L,使用5%HCl进行脱附,脱附率达到90%以上。

关 键 词:AJS-02树脂,NDA-150树脂,Cu2+,吸附,脱附  
收稿时间:2008-12-04
修稿时间:2009-04-20

Study on Adsorption of Copper Ions onto Amine Acid Chelated Adsorption Resin
MENG Guan-Hua,OU Cheng-Hui,TAO Dong-Min,LIU Bao-He.Study on Adsorption of Copper Ions onto Amine Acid Chelated Adsorption Resin[J].Chinese Journal of Applied Chemistry,2009,26(12):1450-1455.
Authors:MENG Guan-Hua  OU Cheng-Hui  TAO Dong-Min  LIU Bao-He
Institution:(School of Civil Engineering & Architecture,Anhui University of Technology,Ma′anshan 243002)
Abstract:The synthesis of AJS-02 modified by L-tyrosine acid and a comparison of adsorption-desorption performance toward Cu2+ between NDA-150 and AJS-02 were investigated. The results showed that equilibrium adsorption data fitted to Langmuir isotherms and the adsorption capacity is higher on AJS-02 thanon NDA-150 in our study, which may be attributed to the polar groups on the network of AJS-02. The adsorption of Cu2+ on AJS-02 is a procedure of the coexistence of physisorption and chemisorption. Kinetic analysis shows that the adsorption rate was mainly governed by film diffusion. Dynamic adsorption and desorption studies for Cu2+on AJS-02 show that the breakthrough adsorption capacity and the total adsorption capacity are 4.05×10-3 and 6.44×10-3 mmol per milliliter resin, respectively. Above 90% regeneration efficiency for the adsorbent was achieved by the desorption of 5% hydrochloric acid.  
Keywords:Cu~(2+)  AJS-02  NDA-150 resin  Cu~(2+)  adsorption  desorption
本文献已被 万方数据 等数据库收录!
点击此处可从《应用化学》浏览原始摘要信息
点击此处可从《应用化学》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号