Chemistry Reference
In-Depth Information
2.108
Valerate
2.108.1
Ion chromatography
The application of this technique is discussed under multianion analysis in section 12.2.4.
2.109
Vanadate
2.109.1
Spectrophotometric methods
Murthy
et al.
[872] determined vanadium(IV) and vanadium(V) in water by solvent
extraction of the complexes with 2-hydroxy-acetophenone oxime followed by
spectrophotometry.
Mori [873] described a spectrophotometric method for the determination of vanadate
ion in non saline water which utilised
o
-hydroxyhydroquinonephthalein as the
complexing agent. Hexadecyltri-methylammonium chloride and L-ascorbic acid serve as
a reducing agent. The method was applied to the determination of total vanadium in the
range of 0-8µg.
2.109.2
Spectrofluorometric method
Bishop [236] has discussed the fluorometric methods for the determination of vanadate.
2.109.3
Chemilumnescence method
Zhang [874] applied chemiluminescence analysis to the determination of vanadium in
non saline waters. Oxidation of thiosulphate by hydrogen peroxide is catalysed by
vanadate (VO
3
−
) and is coupled to the chemiluminescent redox reaction of luminol and
hydrogen peroxide. The detection limit is reported as 4.3×10
−7
µg of vanadium L
−1
with a
relative standard deviation of 3.2% at 2µg L
−1
vanadium.
2.109.4
Preconcentration
The preconcentration of vanadate is discussed in section 15.1.13.
References
1 Hasson, S.S.M., Ahmed, M.A. and Mageed, A.
Analytical Chemistry
,
66
,
492 (1944).
2 Yu, M. and Dovichi, N.
Analytical Chemistry
,
61
,
37 (1989).
3 Gardner, W.S. and Lea, G.E.
Journal of Environmental Science and Technology
,
7
,
719 (1973).
4 Matsuhara, C., Yamamoto, Y. and Takamura, K.
Analyst (London)
,
112
,
1257 (1987).
5 Fogg, A.G. and Bselsn, S.K.
Analyst (London)
,
106
,
1288 (1981).
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