2017
DOI: 10.1016/j.chroma.2017.02.039
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Micellar liquid chromatography of terephthalic acid impurities

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Cited by 10 publications
(2 citation statements)
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“…These results indicate that this mobile phase improves the penetration of the solutes and has a minor interaction with the silanol chains, which may be due to a greater association between the ionic monomer surfactant and the alkyl bonded to the silica stationary phase . The surfactant monolayer was thus partially coated in the stationary phase, resulting in short retention times . In these conditions, the submicellar mobile phase of SDS (0.007 M SDS/ACN 50:50 v/v) was selected to analyze low concentrations of NAP in tissues such as the brain.…”
Section: Resultsmentioning
confidence: 99%
“…These results indicate that this mobile phase improves the penetration of the solutes and has a minor interaction with the silanol chains, which may be due to a greater association between the ionic monomer surfactant and the alkyl bonded to the silica stationary phase . The surfactant monolayer was thus partially coated in the stationary phase, resulting in short retention times . In these conditions, the submicellar mobile phase of SDS (0.007 M SDS/ACN 50:50 v/v) was selected to analyze low concentrations of NAP in tissues such as the brain.…”
Section: Resultsmentioning
confidence: 99%
“…[11]. Various mono-, di-, and tri-carboxylated aromatics, and eight impurities that were formed in the synthesis of terephthalic acid, were separated isocratically on a C18 column in about 17 min using 1% SDS adjusted to pH 3 [12]. A recent study involving the separation of the same terephthalic acid impurities, but using simply a C18 column coated with the nonionic surfactant polyoxyethylene (20), sorbitan monolaurate (Tween 20) and present at 0.001% or less in the isocratic mobile phase, was possible in under 20 min [13].…”
Section: Introductionmentioning
confidence: 99%