High performance liquid chromatography cationic surfactants

Harrison, C.R., Lucy, C.A. (2002). Determination of zwitterionic and cationic surfactants by high-performance liquid chromatography with chemiluminescent nitrogen detection. J. Chromatogr. A 956(1-2), 237-244. [Pg.443]

Several techniques have been developed for the trace analysis of cationic surfactants. Most of the methodologies are based on high-performance liquid chromatography (HPLC) techniques, because most of the commercial cationic surfactants are produced as homologous... [Pg.382]

Fig. 4.3. High performance liquid chromatography (HPLC) of the monosaccharides obtained from a partially purified preparation of microbubble glycopeptide surfactant from forest soil. Following hydrolysis (in 2 N HC1 for 6 hr at 100°C) and filtration, the carbohydrate mixture was charged on a Bio-Rad HPX-87 cation exchange column. For comparison, part A shows the chromatogram (using the same HPLC column) of a standard solution, which contained 4 pg of each of three different monosaccharides (i.e., the last three peaks shown are glucose, xylose and fiicose, in the order of increasing retention times). Part B shows the chromatogram obtained from hydrolysis of the partially purified (see text) microbubble surfactant (approximately 30 pg). All other experimental conditions were identical in the two cases, i.e., water eluent, 0.5 ml/min flow rate, 85°C, refractive index detector attenuation -2x. (Taken from ref. 322.)...

$Fig. 4.3. High performance liquid chromatography (HPLC) of the monosaccharides obtained from a partially purified preparation of microbubble glycopeptide surfactant from forest soil. Following hydrolysis (in 2 N HC1 for 6 hr at 100°C) and filtration, the carbohydrate mixture was charged on a Bio-Rad HPX-87 cation exchange column. For comparison, part A shows the chromatogram (using the same HPLC column) of a standard solution, which contained 4 pg of each of three different monosaccharides (i.e., the last three peaks shown are glucose, xylose and fiicose, in the order of increasing retention times). Part B shows the chromatogram obtained from hydrolysis of the partially purified (see text) microbubble surfactant (approximately 30 pg). All other experimental conditions were identical in the two cases, i.e., water eluent, 0.5 ml/min flow rate, 85°C, refractive index detector attenuation -2x. (Taken from ref. 322.)...$

The same relates to the analytical methods, where for anionic, nonionic and cationic surfactants, various colorimetric procedures (MBAS, bismuth active substance(s) (BiAS), and disulfine blue active substance(s) (DSBAS)) were introduced. Since these methods analyse only the loss of surface-activity or primary degradation, other analytical approaches have been employed in the last 10 years in order to characterize the total or ultimate degradation. These include methods such as high performance liquid chromatography (HPLC), gas chromatography (GC) GC/mass spectrometry (MS), and the measurement of total organic carbon (TOC) and chemical oxygen demand (COD). [Pg.513]

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