Complexing extractants

Other Metals. Because of the large number of chemical extractants available, virtually any metal can be extracted from its aqueous solution. In many cases extraction has been developed to form part of a viable process (275). A review of more recent developments in metal extraction including those for precious metals and rare earths is also available (262). In China a complex extraction process employing a cascade of 600 mixer—settlers has been developed to treat leach Hquor containing a mixture of rare earths (131). 

Quantitative. Classically, silver concentration ia solution has been determined by titration with a standard solution of thiocyanate. Ferric ion is the iadicator. The deep red ferric thiocyanate color appears only when the silver is completely titrated. GravimetricaHy, silver is determined by precipitation with chloride, sulfide, or 1,2,3-benzotriazole. Silver can be precipitated as the metal by electro deposition or chemical reduciag agents. A colored silver diethjldithiocarbamate complex, extractable by organic solvents, is used for the spectrophotometric determination of silver complexes. 

Gold (III) and palladium (II) are sorbed quantitatively on all studied sorbents, except for methyleneamine, from solutions 0,2-2 M HCI. The degree of platinum (IV) complex extraction substantially depends not only on the nature of sorbent functional groups, but also on geometrical parameters of the matrix. This factor influences gold (III) and palladium (II) soi ption to a lesser extent. 

Complexing extraction of pyridine bases from coal coking products with organic solvents 97KGS3. 

Kuterev, Stoyanov, Bagreev and Zolotov [461] reported on the investigation, using IR spectroscopy, of the composition of niobium and tantalum complexes extracted by amines from fluoride solutions. It was shown that in solutions that contain hydrofluoric acid in concentrations ranging from 1M to 12M, both niobium and tantalum were extracted in the form of NbF6 and TaF6 ... 

Ethylenediamine complexes Extraction Halide complexes structures vibrational spectra... 

Ethylenediamine complexes Extraction Halide complexes structures vibrational spectra Halides +3 state +4 state +5 state +6 state... 

The food industry, following scientific and technological developments and market demands, takes into account consumer wishes to have more naturally colored foods and adapts its methodologies to safer ways of producing food. In recent decades, we experienced a shift from exclusive use of certifiable synthetic colorants to exempt colorants and to natural complex extracts. 

Analysis of Corexit 9527. Corexit 9527 in natural waters can be analyzed. The method is based on the formation of a Z>w(ethylenediamine) copper(II) complex, extraction of the complex into methylisobutylketone, and atomic absorption spectroscopy [1564]. The method is suitable for a concentration range of 2 to 100 mg/liter, with a precision as low as 5% relative to standard deviation for samples in the middle- to high range. Only a small sample volume (10 ml) is required. The sensitivity may be substantially increased for trace analysis by increasing the sample volume. 

An advantage of the microbore gas chromatrography/time-of-flight mass spectrometry (GC/TOFMS) method over the other two approaches is that separation efficiency need not be compromised for speed of analysis. The rapid deconvolution of spectra ( scan rate ) with TOFMS makes it the only MS approach to achieve several data points across a narrow peak in full-scan operation. However, the injection of complex extracts deteriorates performance of microbore columns quickly, and an increased LOD and decreased ruggedness result. Microbore columns may be used in water analysis if the LOD is sufficiently low, but they can rarely be used in real-life applications to complicated extracts. 

In dealing with solvent extraction as applied to uranium, it may at first be pointed out that uranium can exist in aqueous solution either as a neutral complex, a complex anion, or a cation. The organic solvents used in solvent extraction can accordingly be divided into three classes, according to the type of uranium complex extracted. 

Plasticiser/oil in rubber is usually determined by solvent extraction (ISO 1407) and FTIR identification [57] TGA can usually provide good quantifications of plasticiser contents. Antidegradants in rubber compounds may be determined by HS-GC-MS for volatile species (e.g. BHT, IPPD), but usually solvent extraction is required, followed by GC-MS, HPLC, UV or DP-MS analysis. Since cross-linked rubbers are insoluble, more complex extraction procedures must be carried out. The determination of antioxidants in rubbers by means of HPLC and TLC has been reviewed [58], The TLC technique for antidegradants in rubbers is described in ASTM D 3156 and ISO 4645.2 (1984). Direct probe EIMS was also used to analyse antioxidants (hindered phenols and aromatic amines) in rubber extracts [59]. ISO 11089 (1997) deals with the determination of /V-phenyl-/9-naphthylamine and poly-2,2,4-trimethyl-1,2-dihydroquinoline (TMDQ) as well as other generic types of antiozonants such as IV-alkyl-AL-phenyl-p-phenylenediamines (e.g. IPPD and 6PPD) and A-aryl-AL-aryl-p-phenylenediamines (e.g. DPPD), by means of HPLC. 

In an acetone extract from a neoprene/SBR hose compound, Lattimer et al. [92] distinguished dioctylph-thalate (m/z 390), di(r-octyl)diphenylamine (m/z 393), 1,3,5-tris(3,5-di-f-butyl-4-hydroxybenzyl)-isocyanurate m/z 783), hydrocarbon oil and a paraffin wax (numerous molecular ions in the m/z range of 200-500) by means of FD-MS. Since cross-linked rubbers are insoluble, more complex extraction procedures must be carried out (Chapter 2). The method of Dinsmore and Smith [257], or a modification thereof, is normally used. Mass spectrometry (and other analytical techniques) is then used to characterise the various rubber fractions. The mass-spectral identification of numerous antioxidants (hindered phenols and aromatic amines, e.g. phenyl-/ -naphthyl-amine, 6-dodecyl-2,2,4-trimethyl-l,2-dihydroquinoline, butylated bisphenol-A, HPPD, poly-TMDQ, di-(t-octyl)diphenylamine) in rubber extracts by means of direct probe EI-MS with programmed heating, has been reported [252]. The main problem reported consisted of the numerous ions arising from hydrocarbon oil in the recipe. In older work, mass spectrometry has been used to qualitatively identify volatile AOs in sheet samples of SBR and rubber-type vulcanisates after extraction of the polymer with acetone [51,246]. 

Cavrini et al. [32] reported the development of a colorimetric method for the determination of miconazole nitrate in pharmaceutical preparation. The method is based on the formation of a yellow complex between the drug and bromocresol green. The absorption peak of this complex, extracted by chloroform over the pH 2—4 range, was at 424 nm, and linear response was obtained from 3—13 pg/mL. The molar absorptivity of the complex in chloroform was 1.845 x 104. This procedure is suitable for the analysis of miconazole nitrate in commercial dosage forms. 

A system exhibiting chiral recognition. The chiral macrotricyclic tet-raamide (250) (Lehn, Simon Moradpour, 1978) has been used for the complexation, extraction and transport of primary ammonium salts. The tetraamide was used rather than the corresponding tetraamine because of the lower basicity of the nitrogens in the former ligand. This avoids the possibility of proton transfer occurring from the primary ammonium substrates R-NH3+ used as guests. In a typical experiment, a solution of a primary ammonium salt, such as naphthylethyl ammonium or phenylalanine methylester hydrochloride in hydrochloric acid was... 

Moffett [179] determined chromium in seawater by Zeeman corrected graphite tube atomisation atomic absorption spectrometry. The chromium is first complexed with a pentan-2,4 dione solution of ammonium 1 pyrrolidine carbodithioc acid, then this complex extracted from the water with a ketonic solvent such as methyl isobutyl ketone, 4-methylpentan-2-one or diisobutyl ketone. 

Nickel Nickel dimethyl glyoxime complex extracted from water AAS 5 (ig/1 [899]... 

The spectophotometric methylene blue method for anionic surfactants has been applied to seawater. In one version, the surfactants are collected in ethyl acetate. The solvent is then evaporated, the surfactants put back in solution in water, and the standard spectrophotometric methylene blue method is applied to this solution. In this manner, the salt error introduced by seawater is eliminated [195]. A similar method, with the methylene blue-surfactant complex extracted into chloroform, and measured directly was proposed by Hagihara [192]. 

LAS Soil Alkaline methanol Complexation/extraction Photometer [29]... 

A different concept of chiral recognition was used by Lehn et al. (1978) for the differentiation between pairs of enantiomeric anions. Following the terminology used for metallo-enzymes, the chiral crown ether [309] acts as an apo-receptor, complexing a metal cation and thus becoming a chiral metal receptor that may discriminate between enantiomeric anions (cascade-type complexation). Extraction experiments with racemic mandelic acid dissolved in... 

H. Tsuchiya, High-performance liquid chromatographic analysis of polyhydroxyflavones using solid-phase borate-complex extraction. J. Chromatogr.B 720 (1998) 225-230. 

Fig. 4.12 Enhancement of Zn(ll) extraction, D Do, from 1 M NaC104 into carbon tetrachloride containing the complexing extractants acetylacetone (O), trifluoroacetone (A), or hexafluoroacetone ( ) as a function of the concentration of the adduct former trioctyl phosphine oxide (B). The curves are fitted with Eq. (4.50) using the constants log Km = 3.01 (AA), 6.70 (TEA), 7.0 (TEA), and Km = 4.66 (AA), nil (TEA), 11.6 (HEA). (Erom Ref. 24.)...

Evaporation Precipitation, flocculation Flotation Adsorption Formation of inclusion complexes Extraction processes Stripping Reduction chemical, electrochemical ... 

The major sources of folate are green vegetables, citrus fruits, legumes, egg yolk, wheat germ, and yeast [417]. This vitamin can be added only in the form of pteroylmonoglutamic acid [402]. The multiplicity of forms, low stability, low concentration, and the complex extraction and detection techniques make the analysis of folate in food a difficult task. 

DVE does not destroy contaminants it must be used in conjunction with another remediation technology. DVE cannot remove heavy chlorinated compounds or hydrocarbons heavier than the middiesel range. DVE cannot recover pesticides or polychlorinated biphenyls (PCBs). Generally, the deeper the contaminant, the more complex extraction becomes. Problems with iron fouling have been reported at DVE sites. 

Figure 3.2 Drugs from natural sources different molecules can be isolated from the leaves, stems, and roots. From each of these sources, extracts conducted with solvents with different polarities will yield different natural products. This complex extraction system ensures the identification of all possible candidate molecules from a plant source.

For this puq)ose, the photoswitchable bis(crown ether)s 88 and 89 as well as the reference compound 90 have been synthesized. Compounds 88 and 89 are highly lipophilic derivatives of azobis(benzo-15-crown-5). The parent azobis crown ether was originally developed by Shinkai and its photoresponsive changes in complexation, extraction, and transport properties thoroughly examined. Compared to 87, more distinct structural difference between the cis and trans isomers can be expected for 88 and 89 because in the latter compounds the 15-crown-5 rings are directly attached to the azobenzene group. The photoequilibrium concentrations of the cis and trans forms and the photoinduced changes in the complexation constants for alkali metal ions are summarized in Table 7. 

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