2002
DOI: 10.1016/s0003-2670(02)00724-9
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Simultaneous UV and electrochemical determination of the herbicide asulam in tap water samples by micellar electrokinetic capillary chromatography

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Cited by 32 publications
(29 citation statements)
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“…Enhancement of the base reaction by means of asulam is a novel method for a procedure for the determination of asulam by an automated method using standard instrumentation. [28] Tap water 10 μg/mL 86 6.50 MECK-UV detection [29] Tap water 10 μg/mL 88 5.80 MECK-electrochemical detection [24] Tap water 0.04 ng 90-118 1.13 HPLC with derivatization [25] Natural water 10.9 μg/mL 98 <5.3 CE-UV detection [27] Natural water 0.9 μg/mL 99 <6.5 CE-electrochemical detection [27] Water Samples 40 μg/mL -4.1 Photochemiluminometric [22] Water Samples 5 μg/mL -1 FIA-fluorescence [21] Soil 1 mg/mL --TLC [26] Peaches 0.043 μg/mL 85-106 1.6 Synchronous fluorescence with derivatization [23] …”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Enhancement of the base reaction by means of asulam is a novel method for a procedure for the determination of asulam by an automated method using standard instrumentation. [28] Tap water 10 μg/mL 86 6.50 MECK-UV detection [29] Tap water 10 μg/mL 88 5.80 MECK-electrochemical detection [24] Tap water 0.04 ng 90-118 1.13 HPLC with derivatization [25] Natural water 10.9 μg/mL 98 <5.3 CE-UV detection [27] Natural water 0.9 μg/mL 99 <6.5 CE-electrochemical detection [27] Water Samples 40 μg/mL -4.1 Photochemiluminometric [22] Water Samples 5 μg/mL -1 FIA-fluorescence [21] Soil 1 mg/mL --TLC [26] Peaches 0.043 μg/mL 85-106 1.6 Synchronous fluorescence with derivatization [23] …”
Section: Discussionmentioning
confidence: 99%
“…The current guideline value for asulam in drinking waters is 0.1 μg/L, [19] justifying the development of suitable analytical methods. Asulam has been determined in several matrices by fluorescence [20] and photo-CL [21] determination using flow injections systems, derivatization methods, [22] UV and electrochemical detection, [23] HPLCfluorescence, [24] thin-layer chromatography [25] and electrophoretic detection. [26] In a previous paper [27] a stopped flow chemiluminescence determination of asulam, based on its inhibition action over the system luminol-H 2 O 2 -HRP in the first instants of the reaction, has been proposed.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with the presented asulam determination method, the methods in Table 5 show some disadvantages in the limit of detection, 1,4,5,7,8,12,37 linear dynamic range [3][4][5]10 , and the range of the sample analyzed. [1][2][3][4][5][6][7][8][9][10]12,37 Moreover, the analytical characteristics of the presented sulfide determination method were compared with the others as shown in Table 6. Compared with the presented sulfide enrichment/determination method, the others show some limitations in the limit of detection, 19,20,38−44 linear dynamic range, 20,42 and the range of the sample analyzed.…”
Section: Comparison With the Other Methodsmentioning
confidence: 99%
“…17,18 Other authors have investigated isotachophoresis along with conductimetric or UV-vis detection 19 or micellar electrokinetic capillary chromatography. 20 For complex matrices, combinations of these methods have been employed: one of them for the sample pretreatment; preparative capillary isotachophoresis for humic matrices 21 and HPLC; or, sample pretreatment for soil samples followed by capillary electrophoresis. 22 Other non-separation procedures have been published for Asulam determination.…”
Section: Introductionmentioning
confidence: 99%