• Je něco špatně v tomto záznamu ?

Sequential injection chromatography with post-column reaction/derivatization for the determination of transition metal cations in natural water samples

B. Horstkotte, P. Jarošová, P. Chocholouš, H. Sklenářová, P. Solich,

. 2015 ; 136 (-) : 75-83. [pub] 20150112

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16000263

In this work, the applicability of Sequential Injection Chromatography for the determination of transition metals in water is evaluated for the separation of copper(II), zinc(II), and iron(II) cations. Separations were performed using a Dionex IonPAC™ guard column (50mm×2mm i.d., 9 µm). Mobile phase composition and post-column reaction were optimized by modified SIMPLEX method with subsequent study of the concentration of each component. The mobile phase consisted of 2,6-pyridinedicarboxylic acid as analyte-selective compound, sodium sulfate, and formic acid/sodium formate buffer. Post-column addition of 4-(2-pyridylazo)resorcinol was carried out for spectrophotometric detection of the analytes׳ complexes at 530nm. Approaches to achieve higher robustness, baseline stability, and detection sensitivity by on-column stacking of the analytes and initial gradient implementation as well as air-cushion pressure damping for post-column reagent addition were studied. The method allowed the rapid separation of copper(II), zinc(II), and iron(II) within 6.5min including pump refilling and aspiration of sample and 1mmol HNO3 for analyte stacking on the separation column. High sensitivity was achieved applying an injection volume of up to 90µL. A signal repeatability of<2% RSD of peak height was found. Analyte recovery evaluated by spiking of different natural water samples was well suited for routine analysis with sub-micromolar limits of detection.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16000263
003      
CZ-PrNML
005      
20160127114059.0
007      
ta
008      
160108s2015 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.talanta.2015.01.001 $2 doi
035    __
$a (PubMed)25702988
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Horstkotte, Burkhard $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic. Electronic address: Horstkob@faf.cuni.cz.
245    10
$a Sequential injection chromatography with post-column reaction/derivatization for the determination of transition metal cations in natural water samples / $c B. Horstkotte, P. Jarošová, P. Chocholouš, H. Sklenářová, P. Solich,
520    9_
$a In this work, the applicability of Sequential Injection Chromatography for the determination of transition metals in water is evaluated for the separation of copper(II), zinc(II), and iron(II) cations. Separations were performed using a Dionex IonPAC™ guard column (50mm×2mm i.d., 9 µm). Mobile phase composition and post-column reaction were optimized by modified SIMPLEX method with subsequent study of the concentration of each component. The mobile phase consisted of 2,6-pyridinedicarboxylic acid as analyte-selective compound, sodium sulfate, and formic acid/sodium formate buffer. Post-column addition of 4-(2-pyridylazo)resorcinol was carried out for spectrophotometric detection of the analytes׳ complexes at 530nm. Approaches to achieve higher robustness, baseline stability, and detection sensitivity by on-column stacking of the analytes and initial gradient implementation as well as air-cushion pressure damping for post-column reagent addition were studied. The method allowed the rapid separation of copper(II), zinc(II), and iron(II) within 6.5min including pump refilling and aspiration of sample and 1mmol HNO3 for analyte stacking on the separation column. High sensitivity was achieved applying an injection volume of up to 90µL. A signal repeatability of<2% RSD of peak height was found. Analyte recovery evaluated by spiking of different natural water samples was well suited for routine analysis with sub-micromolar limits of detection.
650    _2
$a chromatografie $x metody $7 D002845
650    _2
$a měď $x analýza $7 D003300
650    _2
$a pitná voda $x analýza $7 D060766
650    _2
$a formiáty $x chemie $7 D005561
650    _2
$a sladká voda $x analýza $7 D005618
650    _2
$a železo $x analýza $7 D007501
650    _2
$a minerální vody $x analýza $7 D008900
650    _2
$a pyridiny $x chemie $7 D011725
650    _2
$a resorcinoly $x chemie $7 D012118
650    _2
$a sírany $x chemie $7 D013431
650    _2
$a chemické látky znečišťující vodu $x analýza $7 D014874
650    _2
$a zinek $x analýza $7 D015032
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Jarošová, Patrícia $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Chocholouš, Petr $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Sklenářová, Hana $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Solich, Petr $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University in Prague, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
773    0_
$w MED00004484 $t Talanta $x 1873-3573 $g Roč. 136, č. - (2015), s. 75-83
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25702988 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20160108 $b ABA008
991    __
$a 20160127114224 $b ABA008
999    __
$a ok $b bmc $g 1102544 $s 924469
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 136 $c - $d 75-83 $e 20150112 $i 1873-3573 $m Talanta $n Talanta $x MED00004484
LZP    __
$a Pubmed-20160108

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...