A chromatographic estimate of the degree of surface heterogeneity of RPLC packing materials III. Endcapped amido-embedded reversed phase

被引:11
作者
Gritti, F
Guiochon, G [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Chem Sci, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
liquid chromatography; column heterogeneity; adsorption energy distribution; chromatographic test; adsorption isotherm; frontal analysis; C-18-bonded phase; polar embedded RP phase; multi-Langmuir isotherm; phenol; caffeine; sodium naphthalene sulfonate; propranololium chloride;
D O I
10.1016/j.chroma.2005.11.089
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The difference in adsorption behavior between a conventional monomeric endcapped C-18 stationary phase (3.43 mu mol/m(2)) and an endcapped polymeric RP-Amide phase (3.31 mu mol/m(2)) was investigated. The adsorption isotherms of four compounds (phenol, caffeine. sodium 2-naphthalene sulfonate, and propranololium chloride) were measured by frontal analysis (FA) and the degree of heterogeneity of each phase for each solute was characterized by their adsorption energy distributions (AED), derived using the Expectation-Maximization method. The results show that only certain analytes (phenol and 2-naphthalene sulfonate) are sensitive to the presence of the polar embedded amide groups within the RP phase. Their binding constants on the amide-bonded phase are significantly higher than on conventional RPLC phases. Furthermore. an additional type of adsorption sites was observed for these two compounds. However, these sites having a low density, their presence does not affect much the retention factors of the two analytes. On the other hand, the adsorption behavior of the other two analytes (caffeine and propranololium chloride) is almost unaffected by the presence of the amide group in the bonded layer. Strong selective interactions may explain these observations. For example, hydrogen-bond interactions between an analyte (e.g., phenol or naphthalene sulfonate) and the carbonyl group (acceptor) or the nitrogen (donor) of the amido-embedded group may take place. No such interactions may take place with either caffeine or the cation propranololium chloride. This study confirms the hypothesis that analytes have ready access to locations deep inside the bonded layer. where the amide groups are present. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 82
页数:14
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