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用于选择性分离铅(II)离子的铅(II)离子印迹微孔颗粒

Pb(II) ion-imprinted micro-porous particles for the selective separation of Pb(II) ions.

作者信息

Jiang Yang, Kim Dukjoon

出版信息

J Nanosci Nanotechnol. 2014 Nov;14(11):8578-83. doi: 10.1166/jnn.2014.10003.

Abstract

Pb(II) ion-imprinted micro-porous particles were prepared from the ionic complexes formed between vinyl pyridine functional monomers and template Pb(II) ions. The self-assembled Pb(II)/monomer complex was suspension polymerized in the presence of divinylbenzene cross-linker. The prepared micro-particles were 400-600 μm in size. Their chemical and physical structures, morphologies, and adsorption capacity were analyzed by energy dispersive X-ray spectrometry (EDX) Brunauer-Emmett-Teller (BET) analysis, scanningelectron microscopy (SEM), and atomic adsorption spectroscopy (AAS). The adsorption capacity of the imprinted polymer for the Pb(II) template ions was significantly affected by the initial concentration and the pH of the feed solution. Adsorptionis rapid in the first 1 h, after which it slowly increases to equilibrium. The imprinted particles showed high selectivity for lead ions; the adsorption capacity for the Pb(II) ions, 28 mg g(-1) polymer, was much higher than those for other metal ions such as Ni(II)Zn(II), Fe(II), or Cd(II). The imprinted particles maintain high standards of their adsorption ability after 10 repeated uses.

摘要

通过乙烯基吡啶功能单体与模板铅(II)离子形成的离子络合物制备了铅(II)离子印迹微孔颗粒。在二乙烯基苯交联剂存在下,将自组装的铅(II)/单体络合物进行悬浮聚合。制备的微粒尺寸为400 - 600μm。通过能量色散X射线光谱法(EDX)、布鲁诺尔-埃米特-泰勒(BET)分析、扫描电子显微镜(SEM)和原子吸收光谱法(AAS)对其化学和物理结构、形态及吸附容量进行了分析。印迹聚合物对铅(II)模板离子的吸附容量受进料溶液的初始浓度和pH值影响显著。吸附在最初1小时内迅速进行,之后缓慢增加至平衡。印迹颗粒对铅离子表现出高选择性;对铅(II)离子的吸附容量为28 mg g⁻¹聚合物,远高于对其他金属离子如镍(II)、锌(II)、铁(II)或镉(II)的吸附容量。印迹颗粒在重复使用10次后仍保持高标准的吸附能力。

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