TY - JOUR
T1 - Application of bar adsorptive microextraction-large-volume injection-gas chromatography-mass spectrometric method for the determination of trace levels of agrochemicals in real matrices
AU - Bernarda, João R.
AU - Ahmad, Samir M.
AU - Almeida, Carlos
AU - Neng, Nuno R.
AU - Nogueira, José Manuel F.
N1 - Publisher Copyright:
©2015 Sociedade Brasileira de Química.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - Bar adsorptive microextraction followed by liquid desorption in combination with large volume injection gas chromatography coupled to mass spectrometry, under selected ion monitoring mode acquisition (BAμE-LD/LVI-GC-MS(SIM)), was applied for the determination of trace levels of different classes of agrochemicals (using alachlor, diniconazole, fenpropathrin, as well as cis and trans-permethrin as model compounds) in environmental water and wine matrices. Assays performed on 25 mL of ultra-pure water samples spiked at the 2.0 μg L-1 level, yielded recoveries ranging from 55.2 to 105.6%, under optimized experimental conditions. The analytical performance showed convenient detection limits (8.0 to 32.0 ng L-1 ) and good linear dynamic ranges (0.03 to 4.00 μg L-1 ), with remarkable determination coefficients (r2 > 0.9982). Excellent repeatability, based in relative standard deviation (RSD) was also achieved through intraday (RSD < 7.5%) and interday (RSD < 7.0%) assays. Studies performed on surface and ground water, as well as wine samples, using the standard addition method, revealed good sensitivity at the trace level.
AB - Bar adsorptive microextraction followed by liquid desorption in combination with large volume injection gas chromatography coupled to mass spectrometry, under selected ion monitoring mode acquisition (BAμE-LD/LVI-GC-MS(SIM)), was applied for the determination of trace levels of different classes of agrochemicals (using alachlor, diniconazole, fenpropathrin, as well as cis and trans-permethrin as model compounds) in environmental water and wine matrices. Assays performed on 25 mL of ultra-pure water samples spiked at the 2.0 μg L-1 level, yielded recoveries ranging from 55.2 to 105.6%, under optimized experimental conditions. The analytical performance showed convenient detection limits (8.0 to 32.0 ng L-1 ) and good linear dynamic ranges (0.03 to 4.00 μg L-1 ), with remarkable determination coefficients (r2 > 0.9982). Excellent repeatability, based in relative standard deviation (RSD) was also achieved through intraday (RSD < 7.5%) and interday (RSD < 7.0%) assays. Studies performed on surface and ground water, as well as wine samples, using the standard addition method, revealed good sensitivity at the trace level.
KW - Agrochemicals
KW - Baμe
KW - Environmental water and wine matrices
KW - LVI-GC-MS
KW - Trace analysis
UR - http://www.scopus.com/inward/record.url?scp=84943143807&partnerID=8YFLogxK
U2 - 10.5935/0103-5053.20150202
DO - 10.5935/0103-5053.20150202
M3 - Article
AN - SCOPUS:84943143807
SN - 0103-5053
VL - 26
SP - 2150
EP - 2158
JO - Journal of the Brazilian Chemical Society
JF - Journal of the Brazilian Chemical Society
IS - 10
ER -