The complexation of Tl(III) and Cr(III) with
groundwater
humic acids (HA) was investigated at pH 4.5 and pH 5.5
using
different fluorescence methods. These comprised both
quenching measurements of the continuous and synchronous
fluorescence of the HA ligand and an ion competition
method based on the time-resolved laser-induced
fluorescence
of HA-bound Eu(III). Modeling of the experimental
data
using an electrostatic discrete site approach (Model V),
yielded
comparable values of intrinsic binding constants for each
of the studied metal, independently of sample conditions
(pH, metal:ligand ratio) and fluorescence method used.
The results confirmed the validity of fluorescence
techniques
in the analysis of low concentration metal ion−HA
interac
tions and indicated that, beside the aquo ion and the first
hydroxo complex, other species may also bind to humic
acids.
The simultaneous determination of potassium nitrate and sodium monofluorophosphate in dentifrices by single column ion chromatography is described. Nitrate and monofluorophosphate are extracted from the dentifrice with deionized water and separated by a low capacity anion separator column with 0.2% sodium benzoate (adjusted to pH 5.8 +/- 0.1 with formic acid) as the mobile phase. A conductivity meter is used for concentration measurements. The method has been applied to commercial dentifrices containing both potassium nitrate and sodium monofluorophosphate. The mean recoveries for potassium nitrate and monofluorophosphate from spiked samples were 99.0% and 99.2%, respectively, with corresponding standard deviations of 1.73% and 2.55%. The minimum detectable concentration is 5 micrograms/ml for both nitrate and monofluorophosphate.
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