Liquid chromatography capillary columns dry-packed with polar and nonpolar stationary phases

1991 ◽  
Vol 3 (6) ◽  
pp. 539-545 ◽  
Author(s):  
Giancarlo Crescentini ◽  
Anna Rita Mastrogiacomo
1977 ◽  
Vol 49 (1) ◽  
pp. 142-154 ◽  
Author(s):  
Csaba. Horvath ◽  
Wayne. Melander ◽  
Imre. Molnar

1977 ◽  
Vol 49 (14) ◽  
pp. 2295-2305 ◽  
Author(s):  
Csaba. Horvath ◽  
Wayne. Melander ◽  
Imre. Molnar ◽  
Petra. Molnar

1989 ◽  
Vol 54 (6) ◽  
pp. 1530-1537 ◽  
Author(s):  
Joanna Masłowska ◽  
Grzegorz Bazylak

Stationary phases composed of squalane and some nickel(II)-β-keto amine complexes were prepared and used for the separation of complex mixtures of pyridines. The resolution achieved on short classical columns was comparable with that obtained on capillary columns.


Foods ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 553
Author(s):  
Lorena Manzano-Sánchez ◽  
José Antonio Martínez-Martínez ◽  
Irene Domínguez ◽  
José Luis Martínez Vidal ◽  
Antonia Garrido Frenich ◽  
...  

Nowadays, highly polar pesticides are not included in multiresidue methods due to their physico-chemical characteristics and therefore, specific analytical methodologies are required for their analysis. Laboratories are still looking for a pluri-residue method that encompasses the largest number of polar pesticides. The aim of this work was the simultaneous determination of ethephon, 2-hydroxyethylphosphonic acid (HEPA), fosetyl aluminum, glyphosate, aminomethylphosphonic acid (AMPA), N-acetyl-glyphosate and N-acetyl-AMPA in tomatoes, oranges, aubergines and grapes. For that purpose, an ultra high performance liquid chromatography (UHPLC) coupled to a high resolution single mass spectrometer Orbitrap-MS were used. Different stationary phases were evaluated for chromatographic separation, and among them, the stationary phase Torus DEA provided the best separation of the selected compounds. The QuPPe method was used for the extraction of the analytes, but slight modifications were needed depending on the matrix. The developed method was validated, observing matrix effect in all matrices. Intra- and inter-day precision were estimated, and relative standard deviation were lower than 19%. Recoveries were satisfactory, and mean values ranged from 70% to 110%. Limits of quantification were between 25 and 100 µg kg−1. Finally, the analytical method was applied to different fruits and vegetables (oranges, tomatoes, aubergines and grapes).


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