ELSEVIER Talanta 44 (1997) 1307-1312
Talanta
Solvent extraction, spectrophotometric and inductively coupled
plasma atomic emission spectroscopic (ICP-AES) determination
of lanthanum(III) with crown hydroxamic acid
Yadvendra K. Agrawal *, Pranav Shrivastav
Chemistry Department, School of' Sciences, Gujaral UniversiO', Ahmedabad 380 009, India
Received 17 July 1996; received in revised form 7 January 1997; accepted 8 January 1997
Abstract
A new crown hydroxamic acid, 5,14-N,N'-hydroxyphenyl-4,15-dioxo-1,5,14,18-tetraaza hexacosane (NHDTAHA)
for the extraction and spectrophotometric determination of lanthanum(III) is described. Lanthanum(III) forms a
yellow coloured complex with NHDTAHA, which is extracted with chloroform, having molar absorptivity 7.7 x 103
I tool- l per cm at 372 nm. The system obeys Beer's law in the range 1.2-20 ppm of lanthanum. The extract is directly
aspirated for ICP-AES measurements, the limits for estimation are 5-140 ppb of lanthanum. Lanthanum has been
determined in monazite sand and standard samples. © 1997 Elsevier Science B.V.
Keywords: Crown hydroxamic acid; Inductively coupled plasma atomic emission spectrophotometry (ICP-AES);
Monazite sand; Lanthanum(III); Spectrophotometry
I. Introduction
Liquid-liquid extraction technique is widely
used for preconcentration and separation of vari-
ous metal ions from an interfering matrix. Hy-
droxamic acids are superior reagents for
extraction and spectrophotometric determination
of metal ions [1-5]. In recent years the macro-
cyclic ligands, crown ethers, have been reported
for metal complexation [6-10]. However, the
methods for the extraction and determination of
lanthanum with crown ethers suffer from low
* Corresponding author.
sensitivity and interference of diverse ions [11,12].
The direct atomic absorption and inductively cou-
pled plasma emission determination of lanthanum
is reported, but a prior ion exchange separation is
required [13,14]. The complexities of lanthanum
emission lines with large number of strong ionic
lines cause some difficulties over line selection
thereby causes overlaps and reduces the detection
limits considerably [15,16]. The very low levels at
which the lanthanum is sought and potential in-
terference from major elements, have led to the
use of separation method to remove the bulk of
major elements and at the same time to concen-
trate the lanthanum from the samples into small
volume of solution.
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