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Fig. 2.13 Flow system for the simultaneous determination of chloride and
sulphate. Sampling rate 200 samples h −1 . Tube length and i.d. are
given in cm and mm respectively
Source: Reproduced with permission from Elsevier Science [179]
a measure of the chloride concentration in the initial sample. Not surprisingly, many
anions interfere with this method when present in concentrations comparable to that of
the chloride.
2.17.3 Flow injection analysis
Van Staden [178] has described an automated prevalve dilution inflow injection analysis
method for the determination of chloride in ground water. This method can analyse
samples containing up to 800mg L −1 chloride. By adjusting the ratio of sample flow rate
to dilution water flow rate, the concentration could be reduced to a level at which
linearity of the calibration was preserved (about 160mg L −1 maximum). The method was
based on reaction with mercury thiocyanate in the presence of ferric ions, giving the
deeply coloured ferric thiocyanate. Absorption was measured at 480nm.
Table 2.8 Precision of the proposed FIA method for chloride in surface, ground and
domestic waters
Sample Number of
tests
Automated segmented
method [Cl ] (mg L −1 )
FIA method
[Cl ] (mg l −1 )
Coefficient of
variation (%)
1
15
8
11
1.21
2
15
66
74
0.87
3
15
7
10
1.05
4
15
239
251
0.21
5
15
26
26
0.99
6
15
107
110
0.74
7
15
149
150
0.66
8
15
6
4
1.30
9
15
239
245
0.15
10
15
7
5
1.14
11
15
26
30
0.91
12
15
302
291
0.17
Student's t -test at 5% probability level: calculated t -value=1.298; critical t -value=2.060
Source: Reproduced with permission from Elsevier Science [179]
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