Spectrophotometric determination of trace amounts of lead(II) by ion-pair extraction with cryptand (2.2.2) and eosin
Authors:
- Walenty Szczepaniak,
- Bernard Juskowiak
Abstract
The solvent extraction of ion-pair complexes of calcium, strontium and lead (2.2.2) cryptates is described. The extraction equilibrium constants (DC, Kex and KD) at room temperature are reported. The formation of the positively-charged lead cryptate ion and its extraction into chlorobenzene as an ion-pair with eosin are the basis of the proposed spectrophotometric determination of traces of lead. The high molar absorptivity of the ion-pair complex (ε{lunate} = 1.1 × 105 l mol-1 cm-1) and the linearity of the calibration graph over the range 0-10-5 M, allow even 0.1 ppm lead to be determined. The selectivity is high; there is no interference from cations often occurring with lead, such as Bi3+, Sn2+, Hg2+, Zn2+, Cd2+, Cu2+, Ca2+, Pd2+, Ag+ and Tl+. © 1982.
- Record ID
- UAM74a6f1ef27e947f1af09f084187d6f9a
- Author
- Journal series
- Analytica Chimica Acta, ISSN 0003-2670
- Issue year
- 1982
- Vol
- 140
- Pages
- 261-269
- ASJC Classification
- ; ; ;
- DOI
- DOI:10.1016/S0003-2670(01)95472-8 Opening in a new tab
- Language
- (en) English
- Score (nominal)
- 0
- Score source
- journalList
- Publication indicators
- = 25; = 24; : 1999 = 1.182; : 2006 (2 years) = 2.894 - 2007 (5 years) =3.348
- Uniform Resource Identifier
- https://researchportal.amu.edu.pl/info/article/UAM74a6f1ef27e947f1af09f084187d6f9a/
- URN
urn:amu-prod:UAM74a6f1ef27e947f1af09f084187d6f9a
* presented citation count is obtained through Internet information analysis and it is close to the number calculated by the Publish or PerishOpening in a new tab system.