Determination of the accessible volume and the interaction parameter in the adsorption mode of liquid chromatography

被引:28
作者
Trathnigg, Bernd [1 ]
Skvortsov, Alexander
机构
[1] Karl Franzens Univ Graz, Inst Chem, A-8010 Graz, Austria
[2] Chem Pharmaceut Acad, St Petersburg 197376, Russia
关键词
void volume; accessible volume; adsorption chromatography; retention factor; reversed phase;
D O I
10.1016/j.chroma.2006.05.099
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The main physical parameters in liquid chromatography of oligomers - the accessible volume and the adsorption interaction parameter-are discussed. It is shown, that in liquid adsorption chromatography (LAC) there is a linear relation between elution volume and the distance of two subsequent peaks of a homologous series. From the intercept of the regression lines in such a plot the accessible volume can be easily determined at any mobile phase in LAC (corresponding to conditions of weak or strong adsorption) without any information about the molar mass of the peaks. From the slope of this dependence the adsorption interaction parameter of a given repeat unit can be obtained. The accurate determination of the accessible volume and the adsorption interaction parameter in the LAC regime is presented for PEG, PPG and fatty alcohols on various reversed phase columns with different pore size in methanol-water or acetone-water mobile phases. The difference between the void volume, the dead volume or hold-up volume (from the solvent peak position) and the acessible volume (obtained by this procedure) is discussed. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 125
页数:9
相关论文
共 36 条
[1]   EVALUATION OF DEAD SPACE IN CHROMATOGRAPHIC SYSTEMS [J].
ALTHAMIR, WK ;
PURNELL, JH ;
WELLINGTON, CA ;
LAUB, RJ .
JOURNAL OF CHROMATOGRAPHY, 1979, 173 (02) :388-391
[2]  
[Anonymous], POLYM HDB
[3]   ON THE DETERMINATION OF THE HOLD-UP TIME IN REVERSED PHASE LIQUID-CHROMATOGRAPHY [J].
BERENDSEN, GE ;
SCHOENMAKERS, PJ ;
GALAN, LD ;
VIGH, G ;
VARGAPUCHONY, Z .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1980, 3 (11) :1669-1686
[4]   ROLE OF THE CHAIN-LENGTH OF CHEMICALLY BONDED PHASES AND THE RETENTION MECHANISM IN REVERSED-PHASE LIQUID-CHROMATOGRAPHY [J].
BERENDSEN, GE ;
DEGALAN, L .
JOURNAL OF CHROMATOGRAPHY, 1980, 196 (01) :21-37
[5]   AN EQUILIBRIUM THEORY FOR EXCLUSION CHROMATOGRAPHY OF BRANCHED AND LINEAR POLYMER CHAINS [J].
CASASSA, EF ;
TAGAMI, Y .
MACROMOLECULES, 1969, 2 (01) :14-+
[6]   EQUILIBRIUM DISTRIBUTION OF FLEXIBLE POLYMER CHAINS BETWEEN A MACROSCOPIC SOLUTION PHASE AND SMALL VOIDS [J].
CASASSA, EF .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER LETTERS, 1967, 5 (9PB) :773-&
[7]   THEORETICAL MODELS FOR PEAK MIGRATION IN GEL PERMEATION CHROMATOGRAPHY [J].
CASASSA, EF .
JOURNAL OF PHYSICAL CHEMISTRY, 1971, 75 (26) :3929-+
[8]   INVESTIGATION OF SELECTIVITY IN REVERSED-PHASE LIQUID-CHROMATOGRAPHY - EFFECTS OF STATIONARY AND MOBILE PHASES ON RETENTION OF HOMOLOGOUS SERIES [J].
COLIN, H ;
KRSTULOVIC, AM ;
GONNORD, MF ;
GUIOCHON, G ;
YUN, Z ;
JANDERA, P .
CHROMATOGRAPHIA, 1983, 17 (01) :9-15
[9]   Permeation of small molecules in aqueous size-exclusion chromatography vis-a-vis models for separation [J].
Dai, H ;
Dubin, PL ;
Andersson, T .
ANALYTICAL CHEMISTRY, 1998, 70 (08) :1576-1580
[10]   SOME CONFORMATION PROBLEMS FOR LONG MACROMOLECULES [J].
DEGENNES, PG .
REPORTS ON PROGRESS IN PHYSICS, 1969, 32 (02) :187-&