College of Bioscience and Chemistry, Kanazawa Institute of Technology, Ishikawa, 921-8501, Japan.
Technology Planning Div., Nomura Micro Science Co., Ltd., Kanagawa, 243-0021, Japan.
Anal Sci. 2021 Apr 10;37(4):613-617. doi: 10.2116/analsci.20P090. Epub 2020 Oct 23.
Surface functionalized mesoporous silicates, MCM-41s, having 3-(2-pyridylmethylideneimino)propyl group (PI-MCM-41) or 3-(2-quinolylmethylideneimino)propyl group (QI-MCM-41) were prepared via Schiff base reaction, and the adsorption behavior of metal ions onto the modified MCM-41s was investigated. The function groups on the modified MCM-41 surface were confirmed by Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and elemental analysis. The metal ions examined, Co, Ni, Cu, Zn, Cd, and Pb, were quantitatively adsorbed on the PI-MCM-41 and QI-MCM-41, except for Mn. In the complexation with these metal ions, it was suggested that imine-N and heterocyclic-N atoms act as donor atoms. In addition, it was considered that the hydrophobicity derived from the organo-functional groups modified on MCM-41 contributed to improving the adsorption ability.
通过席夫碱反应制备了具有 3-(2-吡啶亚甲基亚氨基)丙基基团(PI-MCM-41)或 3-(2-喹啉基亚甲基亚氨基)丙基基团(QI-MCM-41)的表面功能化介孔硅酸钠 MCM-41,并研究了金属离子对改性 MCM-41 的吸附行为。通过傅里叶变换红外光谱(FT-IR)、X 射线光电子能谱(XPS)和元素分析确认了改性 MCM-41 表面的功能基团。除 Mn 外,Co、Ni、Cu、Zn、Cd 和 Pb 等金属离子都被定量吸附在 PI-MCM-41 和 QI-MCM-41 上。在与这些金属离子的络合中,亚胺-N 和杂环-N 原子被认为是供体原子。此外,还认为修饰在 MCM-41 上的有机官能团的疏水性有助于提高吸附能力。