-
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,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- chemické látky znečišťující vodu analýza MeSH
- chromatografie metody MeSH
- formiáty chemie MeSH
- měď analýza MeSH
- minerální vody analýza MeSH
- pitná voda analýza MeSH
- pyridiny chemie MeSH
- resorcinoly chemie MeSH
- sírany chemie MeSH
- sladká voda analýza MeSH
- železo analýza MeSH
- zinek analýza MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
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