Chelating agents extractants

Liquid-liquid extractions using ammonium pyrrolidine dithiocarbamate (APDC) as a metal chelating agent are commonly encountered in the analysis of metal ions in aqueous samples. The sample and APDC are mixed together, and the resulting metal-ligand complexes are extracted into methyl isobutyl ketone before analysis. 

Cupferron is a ligand whose strong affinity for metal ions makes it useful as a chelating agent in liquid-liquid extractions. The following distribution ratios are known for the extraction of Hg +, Pb +, and Zn + from aqueous solutions to an organic solvent. 

The lanthanides form many compounds with organic ligands. Some of these compounds ate water-soluble, others oil-soluble. Water-soluble compounds have been used extensively for rare-earth separation by ion exchange (qv), for example, complexes form with citric acid, ethylenediaminetetraacetic acid (EDTA), and hydroxyethylethylenediaminetriacetic acid (HEEDTA) (see Chelating agents). The complex formation is pH-dependent. Oil-soluble compounds ate used extensively in the industrial separation of rate earths by tiquid—tiquid extraction. The preferred extractants ate catboxyhc acids, otganophosphoms acids and esters, and tetraaLkylammonium salts. 

The carbanions derived from acylthiophenes have been condensed with aldehydes,and, through the Claisen condensation with esters, thienylsubstituted -diketones have been obtained. 2-Thenoyl trifluoroacetone, first prepared by Reid and Calvin through the Claisen condensation of 2-acetylthiophene with ethyl trifluoracetate, has become an extremely useful chelating agent for the extraction of numerous elements from strongly acidic solutions, The tautomeric form which dominates in aqueous solution is the ketone hy-drate. Other thiophenes have also proved useful for analytical purposes. ... 

The nature of the donor atoms in the chelating agent. Ligands which contain donor atoms of the soft-base type form their most stable complexes with the relatively small group of Class B metal ions (i.e. soft acids) and are thus more selective reagents. This is illustrated by the reagent diphenylthiocarbazone (dithizone) used for the solvent extraction of metal ions such as Pd2+, Ag+, Hg2+, Cu2+, Bi3+, Pb2+, and Zn2 +. ... 

The choice of a satisfactory chelating agent for a particular separation should, of course, take all the above factors into account. The critical influence of pH on the solvent extraction of metal chelates is discussed in the following section. 

The solvent extraction of a neutral metal chelate complex formed from a chelating agent HR according to the equation... 

The procedure followed entails the removal of gross interferences by solvent extraction, and the selective extraction and concentration of the trace metal by use of a chelating agent. The alloy used should not contain more than 0.1 g of copper in the sample weighed out. 

Extractive titrations involving chelates and chelating agents. A. Galik, Chelates Anal. Chem., 1972, 3,1-55 (86). 

Sequential extraction was performed as described by Redgwell and Selvendran [1], WUS was sequentially extracted with chelating agent (ChSS), dilute alkali (DASS), 1 M alkali (1 MASS) and 4 M alkali (4 MASS) and a cellulose-rich residue (RES) remained. 

Pectins were extracted from isolated cell walls of 5-week-old wheat plants using different methods. Enzymic digestions of the cell walls involved pectinases such as a commercial pectolayse or recombinant endopolygalacturonase [Maness Mort, 1989]. Chemical extractions involved the chelating agent imidazole [Mort et al., 1991] or solvolysis with anhydrous HF at 0 °C in a closed teflon line [Mort et al., 1989] followed by imidazole extraction. 

Adriano DC, Delaney MS, Hoyt GD, et al. 1977. Availability to plants and soil extraction of americium-241 as influenced by chelating agent, lime, and soil type. Environ Exp Bot 17 69-77. 

Chelates Heavy metals or bases Chelating agents such as by extraction of the metal ions Formation of stable metal chelates ... 

The carbonate-bound trace elements are usually extracted by NaOAc-HOAc (Tessier et al., 1979 Hickey and Kittrick, 1984 Banin et. al., 1990 and Han et al., 1992) or by using chelating agents, such as EDTA (Sposito et al., 1982 Emmerich et al., 1982 Miller and Mcfee, 1983 Chang et al., 1984 Knudtsen and O Connor, 1987 McGrath and Cegarra, 1992). Generally, EDTA lacks the required specificity and selectivity for carbonate phase extractions and tends to extract metals from a number of soil components. 

Bioavailable trace elements in soil correlate with plant uptake and concentrations in plants. Extractants for bioavailable trace elements include chelating agents, diluted inorganic acid, neutral salt solutions, and water (Table 7.2). The most popular extractant for bioavailable trace elements in arid and semi-arid soils is DTPA-TEA (triethanolamine), which was developed by Lindsay and Norvell (1969, 1978) to extract available Cu, Zn, Fe and Mn from neutral and calcareous soils. Use of this chelating agent, DTPA, is based on the fact that it has the most favorable combination of stability constants for simultaneous complexation of Cu, Fe, Mn and Zn... 

In order to suppress interferences due to the presence of inorganic species and reliably determine the proteinaceous composition of the sample, a clean-up step has often been introduced in the analytical procedure. This step may include the extraction of the proteinaceous matter by an ammonia solution [8], the use of a cation-exchange resin [8,55], a chelating agent [9,41,44], the use of a Cig resin or the use of barium chloride solution to suppress sulfates [10,81,82]. Table 9.1 reports the methods used to overcome such problems. 

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