EFFECT OF TEMPERATURE AND ORGANIC MODIFIER ON THE ISOCRATIC RETENTION CHARACTERISTICS OF NITRATED POLYCYCLIC AROMATIC-HYDROCARBONS ON A REVERSED-PHASE OCTADECYLSILANE COLUMN

被引:32
作者
ROBBAT, A
LIU, TY
机构
[1] Chemistry Department, Trace Analytical Measurement Laboratory, Tufts University, Medford
来源
JOURNAL OF CHROMATOGRAPHY | 1990年 / 513卷
关键词
D O I
10.1016/S0021-9673(01)89430-9
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Nitrated polycyclic aromatic hydrocarbon (nitro-PAH) retention behavior was evaluated on a reversed-phase polymeric octadecylsilane column under isocratic conditions as a function of organic modifier and temperature. Several conclusions can be drawn from the retention and organic modifier study (viz., methanol and acetonitrile-water). First, the logarithm of the capacity factor (log k′) was linearly dependent on organic-water volume fraction (φ{symbol}). Second, nitro-PAH k′ values increased with decrease in organic modifier concentration. Third, the slopes of log k′ vs. φ{symbol} plots were solvent-dependent. Larger slope values were found for nitro-PAHs in methanol-water than in acetonitrile-water mixtures for a particular compound. Fourth, slope values were dependent on the molecular structure of individual nitro-PAHs. Nitro-PAH retention times decreased with increase in column temperature. A linear dependence of log k′ on the reciprocal of the absolute column temperature, the Van `t Hoff plott, was observed for both organic modifiers over the temperature range studied. The standard enthalpic range (ΔH0) for nitro-PAH transfer from the mobile to the stationary pahse was determined. ΔH0 was dependent on organic modifier tupe and composition as well as solute structure. The enthalpy-entropy compensation effect was evaluated by plotting log k′ vs. - ΔH0 and used to interpret nitro-PAH retention mechanisms. A compensation effect was found for some mononitrated PAHs for both organic modifiers. The compensation temperatures were within the accepted range described for reversed-phase high-performance liquid chromatography systems. © 1990.
引用
收藏
页码:117 / 135
页数:19
相关论文
共 20 条
[11]   ENTHALPY-ENTROPY COMPENSATION IN REVERSED-PHASE CHROMATOGRAPHY [J].
MELANDER, W ;
CAMPBELL, DE ;
HORVATH, C .
JOURNAL OF CHROMATOGRAPHY, 1978, 158 (OCT) :215-225
[12]  
OPPERHUIZEN A, 1987, J CHROMATOGR, V338, P51
[13]   BAND-SPACING IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AS A FUNCTION OF SOLVENT STRENGTH - A SIMPLE AND FAST ALTERNATIVE TO SOLVENT OPTIMIZATION FOR METHOD DEVELOPMENT [J].
QUARRY, MA ;
GROB, RL ;
SNYDER, LR ;
DOLAN, JW ;
RIGNEY, MP .
JOURNAL OF CHROMATOGRAPHY, 1987, 384 :163-180
[14]   FUNCTIONAL-GROUP BEHAVIOR IN ION-PAIR REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING SURFACE-ACTIVE PAIRING IONS [J].
RILEY, CM ;
TOMLINSON, E ;
JEFFERIES, TM .
JOURNAL OF CHROMATOGRAPHY, 1979, 185 (DEC) :197-224
[15]   APPLICATIONS OF HIGH SPEED REVERSED-PHASE LIQUID CHROMATOGRAPHY [J].
SCHMIT, JA ;
HENRY, RA ;
WILLIAMS, RC ;
DIECKMAN, JF .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 1971, 9 (11) :645-&
[16]   GRADIENT SELECTION IN REVERSED-PHASE LIQUID-CHROMATOGRAPHY [J].
SCHOENMAKERS, PJ ;
BILLIET, HAH ;
TIJSSEN, R ;
DEGALAN, L .
JOURNAL OF CHROMATOGRAPHY, 1978, 149 (FEB) :519-537
[17]  
SCHOENMAKERS PJ, 1979, J CHROMATOGR, V185, P179
[18]  
Snyder L.R., 2012, PRACTICAL HPLC METHO
[19]   SOLVENT-STRENGTH SELECTIVITY IN REVERSED-PHASE HPLC [J].
SNYDER, LR ;
QUARRY, MA ;
GLAJCH, JL .
CHROMATOGRAPHIA, 1987, 24 :33-44
[20]   INFLUENCE OF TEMPERATURE ON THE RETENTION BEHAVIOR OF MEMBERS OF HOMOLOGOUS SERIES IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
VIGH, G ;
VARGAPUCHONY, Z .
JOURNAL OF CHROMATOGRAPHY, 1980, 196 (01) :1-9