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Adsorption Behavior of Divalent Metal Ions onto Surface-functionalized Mesoporous Silicate MCM-41 Having Schiff Base Structure

机译:二价金属离子在表面官能化的中孔硅酸盐MCM-41具有Schiff基础结构的吸附行为

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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~(2+), Ni~(2+), Cu~(2+), Zn~(2+), Cd~(2+), and Pb~(2+), were quantitatively adsorbed on the PI-MCM-41 and QI-MCM-41, except for Mn~(2+). 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.
机译:通过Schiff制备了表面官能化的介孔硅酸盐,具有3-(2-吡啶甲基亚氨基)丙基(PI-MCM-41)或3-(2-喹啉-41)丙基(QI-MCM-41)的丙基(QI-MCM-41)的MCM-41s研究了基础反应,以及金属离子在改性MCM-41s上的吸附行为。通过傅里叶变换红外光谱(FT-IR),X射线光电子能谱(XPS)和元素分析来确认修改的MCM-41表面上的功能组。检查金属离子,CO〜(2+),Ni〜(2+),Cu〜(2+),Zn〜(2+),Cd〜(2+)和PB〜(2+)是定量的吸附在PI-MCM-41和QI-MCM-41上,除了Mn〜(2+)。在与这些金属离子的络合中,建议亚胺-N和杂环-N原子用作供体原子。此外,认为衍生自MCM-41上改性有机官能团的疏水性有助于提高吸附能力。

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