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INFLUENCE OF THE NATURE OF ACTIVE SURFACE SITES OF HIGHLY DISPERSE OXIDES ON ADSORPTION OF HEAVY METAL IONS

机译:高分子氧化物活性表面位点对重金属离子吸附的影响

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Different surface sites of silica, alumina, titania, and related mixed oxides, and pre-adsorbed poly(vinyl alcohol) (PVA) and poly(ethylene glycol) (PEG), affect the interaction with Ni(II), Cd(II), and Pb(II) studied using adsorption and potentiometric titration methods. Bridging hydroxyls (Bronsted acid sites) capable of taking part in ion-exchange reactions, and pre-adsorbed polymers, enhance the adsorption of metal ions at pH < 7. At pH > 7 PVA adsorbed on silica slightly enhances the adsorption of metal ions but pre-adsorbed PEG gives the opposite result. PEG has only electron-donor functionalities (C-O-C) which reduce the number of possible adsorption sites. PVA has COH groups with both electron-donor and proton-donor properties, which can effectively interact with metal ions and their hydroxy species.
机译:二氧化硅,氧化铝,二氧化钛和相关混合氧化物的不同表面位点,以及预吸附的聚(乙烯醇)(PVA)和聚(乙二醇)(PEG),影响与Ni(II),CD(II)的相互作用和使用吸附和电位滴定方法研究的PB(II)。能够参与离子交换反应的桥接羟基(刚性酸位点)和预吸附的聚合物,增强金属离子在pH <7时的吸附。在硅胶上吸附的pH> 7 PVA略微增强金属离子的吸附但是预先吸附的PEG给出相反的结果。 PEG仅具有电子给体功能(C-O-C),减少可能的吸附位点的数量。 PVA具有具有电子供体和质子供体性的COH基团,其可以有效地与金属离子及其羟基物质相互作用。

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