• Je něco špatně v tomto záznamu ?

Application of a fully integrated photodegradation-detection flow-batch analysis system with an on-line preconcentration step for the determination of metsulfuron methyl in water samples

CC. Acebal, M. Grünhut, I. Srámková, P. Chocholouš, AG. Lista, H. Sklenářová, P. Solich, BS. Band,

. 2014 ; 129 (-) : 233-40.

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc15023127

This work presents the development of a fully automated flow-batch analysis (FBA) system as a new approach for on-line preconcentration, photodegradation and fluorescence detection in a lab-constructed mixing chamber that was designed to perform these processes without sample dispersion. The system positions the mixing chamber into the detection system and varies the instrumental parameters according to the required photodegradation conditions. The developed FBA system is simple and easily coupled with any sample pretreatment without altering the configuration. This FBA system was implemented to photodegrade and determine the fluorescence of the degradation products of metsulfuron methyl (MSM), a naturally non-fluorescent herbicide of the sulfonylurea׳s family. An on-line solid phase extraction (SPE) and clean up procedure using a C18 minicolumn was coupled to the photodegradation-detection mixing chamber (PDMC) that was located in the spectrofluorometer. An enrichment factor of 27 was achieved. Photodegradation conditions have been optimized by considering the influence of the elution solvent on both the formation of the photoproduct and on the fluorescence signal. Under optimal conditions, the calibration for the MSM determination was linear over the range of 1.00-7.20 µg L(-1). The limit of detection (LOD) was 0.28 µg L(-1); the relative standard deviation was 2.0% and the sample throughput for the entire process was 3h(-1). The proposed method was applied to real water samples from the Bahía Blanca׳s agricultural region (Bahía Blanca, Buenos Aires, Argentina). This method obtained satisfactory recoveries with a range of 94.7-109.8%.

000      
00000naa a2200000 a 4500
001      
bmc15023127
003      
CZ-PrNML
005      
20150709122421.0
007      
ta
008      
150709s2014 ne f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.talanta.2014.05.024 $2 doi
035    __
$a (PubMed)25127589
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a ne
100    1_
$a Acebal, Carolina C $u INQUISUR (UNS-CONICET), Department of Chemistry, National University of the South, 1253 Alem Avenue, B8000CPB Bahía Blanca, Argentina. Electronic address: cacebal@uns.edu.ar. $7 gn_A_00000968
245    10
$a Application of a fully integrated photodegradation-detection flow-batch analysis system with an on-line preconcentration step for the determination of metsulfuron methyl in water samples / $c CC. Acebal, M. Grünhut, I. Srámková, P. Chocholouš, AG. Lista, H. Sklenářová, P. Solich, BS. Band,
520    9_
$a This work presents the development of a fully automated flow-batch analysis (FBA) system as a new approach for on-line preconcentration, photodegradation and fluorescence detection in a lab-constructed mixing chamber that was designed to perform these processes without sample dispersion. The system positions the mixing chamber into the detection system and varies the instrumental parameters according to the required photodegradation conditions. The developed FBA system is simple and easily coupled with any sample pretreatment without altering the configuration. This FBA system was implemented to photodegrade and determine the fluorescence of the degradation products of metsulfuron methyl (MSM), a naturally non-fluorescent herbicide of the sulfonylurea׳s family. An on-line solid phase extraction (SPE) and clean up procedure using a C18 minicolumn was coupled to the photodegradation-detection mixing chamber (PDMC) that was located in the spectrofluorometer. An enrichment factor of 27 was achieved. Photodegradation conditions have been optimized by considering the influence of the elution solvent on both the formation of the photoproduct and on the fluorescence signal. Under optimal conditions, the calibration for the MSM determination was linear over the range of 1.00-7.20 µg L(-1). The limit of detection (LOD) was 0.28 µg L(-1); the relative standard deviation was 2.0% and the sample throughput for the entire process was 3h(-1). The proposed method was applied to real water samples from the Bahía Blanca׳s agricultural region (Bahía Blanca, Buenos Aires, Argentina). This method obtained satisfactory recoveries with a range of 94.7-109.8%.
650    _2
$a arylsulfonany $x analýza $7 D001190
650    _2
$a kalibrace $7 D002138
650    _2
$a technologie zelené chemie $7 D055772
650    _2
$a herbicidy $x analýza $7 D006540
650    _2
$a koncentrace vodíkových iontů $7 D006863
650    _2
$a světlo $7 D008027
650    _2
$a limita detekce $7 D057230
650    _2
$a fotochemie $x metody $7 D010777
650    _2
$a fotolýza $7 D010782
650    _2
$a reprodukovatelnost výsledků $7 D015203
650    _2
$a extrakce na pevné fázi $7 D052616
650    _2
$a fluorescenční spektrometrie $7 D013050
650    _2
$a sulfonylmočovinové sloučeniny $x analýza $7 D013453
650    _2
$a voda $x chemie $7 D014867
650    _2
$a látky znečišťující vodu $x analýza $7 D014873
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Grünhut, Marcos $u INQUISUR (UNS-CONICET), Department of Chemistry, National University of the South, 1253 Alem Avenue, B8000CPB Bahía Blanca, Argentina.
700    1_
$a Srámková, Ivana $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Chocholouš, Petr $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Lista, Adriana G $u INQUISUR (UNS-CONICET), Department of Chemistry, National University of the South, 1253 Alem Avenue, B8000CPB Bahía Blanca, Argentina.
700    1_
$a Sklenářová, Hana $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Solich, Petr $u Department of Analytical Chemistry, Faculty of Pharmacy, Charles University, 500 05 Hradec Králové, Czech Republic.
700    1_
$a Band, Beatriz S Fernández $u INQUISUR (UNS-CONICET), Department of Chemistry, National University of the South, 1253 Alem Avenue, B8000CPB Bahía Blanca, Argentina.
773    0_
$w MED00004484 $t Talanta $x 1873-3573 $g Roč. 129, č. - (2014), s. 233-40
856    41
$u https://pubmed.ncbi.nlm.nih.gov/25127589 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20150709 $b ABA008
991    __
$a 20150709122440 $b ABA008
999    __
$a ok $b bmc $g 1083465 $s 906120
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2014 $b 129 $c - $d 233-40 $i 1873-3573 $m Talanta $n Talanta $x MED00004484
LZP    __
$a Pubmed-20150709

Najít záznam

Citační ukazatele

Nahrávání dat...

Možnosti archivace

Nahrávání dat...