Elution of organic solutes from different polarity sorbents using subcritical water

被引:149
作者
Yang, Y [1 ]
Belghazi, M [1 ]
Lagadec, A [1 ]
Miller, DJ [1 ]
Hawthorne, SB [1 ]
机构
[1] Univ N Dakota, Energy & Environm Res Ctr, Grand Forks, ND 58202 USA
关键词
mobile phase composition; stationary phases; SFC; extraction methods; chlorophenols; amines; polynuclear aromatic hydrocarbons; n-alkanes; water; subcritical;
D O I
10.1016/S0021-9673(98)00222-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The intermolecular interactions between organic solutes and sorbent matrices under subcritical water conditions have been investigated at a pressure of 50 bar and temperatures ranging from 50 to 250 degrees C. Both polar and nonpolar organics (chlorophenols, amines, n-alkanes, and polycyclic aromatic hydrocarbons) and five different sorbent matrices (glass beads, alumina, Florisil, silica-bonded C-18, and polymeric XAD-4 resins) were used. From the same matrix, the polar solutes always eluted at lower temperatures, while the moderately polar and nonpolar solutes only eluted at higher temperatures. Similar to matrix effects previously observed using supercritical carbon dioxide, the sorbent type greatly influenced the elution efficiency under subcritical water conditions. Lower temperatures are sufficient to elute a particular solute from glass beads, alumina, and Florisil, but higher temperatures (less polar water) are needed to elute the same solute from silica-bonded C-18. The highest temperatures were required to elute aromatic organics from XAD-4. These matrix effects demonstrate that, while low temperature water can break inert or dipole interactions between solutes and glass beads, alumina, and Florisil, higher temperature water is required to interrupt the van der Waals attractions between solutes and silica-bonded C-18, and even higher temperatures needed to overcome the pi-electron interactions between aromatic solutes and XAD-4. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 159
页数:11
相关论文
共 19 条
[1]   SUPERCRITICAL-FLUID EXTRACTION IN ENVIRONMENTAL-ANALYSIS [J].
BOWADT, S ;
HAWTHORNE, SB .
JOURNAL OF CHROMATOGRAPHY A, 1995, 703 (1-2) :549-571
[2]  
Haar L., 1984, NBS NATL RES COUNCIL
[3]   Coupled subcritical water extraction with solid-phase microextraction for determining semivolatile organics in environmental solids [J].
Hageman, KJ ;
Mazeas, L ;
Grabanski, CB ;
Miller, DJ ;
Hawthorne, SB .
ANALYTICAL CHEMISTRY, 1996, 68 (22) :3892-3898
[4]   EXTRACTION OF ORGANIC POLLUTANTS FROM ENVIRONMENTAL SOLIDS WITH SUBCRITICAL AND SUPERCRITICAL WATER [J].
HAWTHORNE, SB ;
YANG, Y ;
MILLER, DJ .
ANALYTICAL CHEMISTRY, 1994, 66 (18) :2912-2920
[5]   EFFECT OF SFE FLOW-RATE ON EXTRACTION RATES - CLASSIFYING SAMPLE EXTRACTION BEHAVIOR [J].
HAWTHORNE, SB ;
GALY, AB ;
SCHMITT, VO ;
MILLER, DJ .
ANALYTICAL CHEMISTRY, 1995, 67 (15) :2723-2732
[6]  
Horvath C., 1980, High Performance Liquid Chromatography Advances and Perspectives, V2, P113
[7]   SUPERCRITICAL-FLUID EXTRACTION IN ENVIRONMENTAL-ANALYSIS [J].
JANDA, V ;
BARTLE, KD ;
CLIFFORD, AA .
JOURNAL OF CHROMATOGRAPHY, 1993, 642 (1-2) :283-299
[9]   AQUEOUS SOLUBILITY OF POLYNUCLEAR AROMATIC-HYDROCARBONS [J].
MACKAY, D ;
SHIU, WY .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1977, 22 (04) :399-402
[10]   ENVIRONMENTAL SFE [J].
MCNALLY, MEP .
ANALYTICAL CHEMISTRY, 1995, 67 (09) :A308-A315