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Journal ArticleDOI

Chelating ion-exchangers containing 8-hydroxyquinoline as the functional group

F. Vernon, +1 more
- 01 Feb 1973 - 
- Vol. 63, Iss: 2, pp 403-414
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TLDR
In this article, the oxine-containing chelating ion-exchangers described in the literature have been synthesized and their properties determined, together with equilibration rates and swelling properties.
About
This article is published in Analytica Chimica Acta.The article was published on 1973-02-01. It has received 86 citations till now. The article focuses on the topics: Uranyl & Chelation.

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Citations
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Coordination chemistry of chelating resins and ion exchangers

TL;DR: In this paper, the synthese des resines echangeuses d'ions chelatantes et complexantes is discussed, together with leurs complexes metalliques and their properties.
Journal ArticleDOI

Amberlite XAD-2 functionalized with o-aminophenol: synthesis and applications as extractant for copper(II), cobalt(II), cadmium(II), nickel(II), zinc(II) and lead(II).

TL;DR: A stable chelating resin matrix was synthesized by covalently linking o-aminophenol with the benzene ring of the polystyrene-divinylbenzene resin, Amberlite XAD-2, through a -NN- group to preconcentrate Cu, Cd, Co, Ni, Zn and Pb, prior to their determination by flame atomic absorption spectrometry.
Journal ArticleDOI

Amberlite XAD-4 functionalized with succinic acid for the solid phase extractive preconcentration and separation of uranium(VI).

TL;DR: The accuracy of the developed solid phase extractive preconcentration method in conjunction with Arsenazo III procedure was tested by analyzing marine sediment and soil reference material and has been successfully employed for the analysis of soil and sediment samples.
Journal ArticleDOI

Vinyl polymer agglomerate based transition-metal cation chelating ion-exchange resin containing the 8-hydroxyquinoline functional-group

TL;DR: In this paper, a simple synthetic route has been developed for the immobilization of 8-hydroxyquinoline onto Fractogel TSK, a highly porous, mechanically and chemically stable, hydrophilic organic resin gel.
References
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Preparation and chelating properties of 8‐hydroxy‐quinoline—formaldehyde polymers

TL;DR: In this paper, 8-hydroxyquinoline with formaldehyde in acid solution yielded a polymer of molecular weight ∽3300, which can be used as selective chelating ion exchange rains which permit separation of various cations.
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