Effect of solution viscosity on dynamic surface tension detection

被引:8
作者
Staggemeier, BA
Collier, TO
Prazen, BJ
Synovec, RE
机构
[1] Univ Washington, Dept Chem, Ctr Proc Analyt Chem, Seattle, WA 98195 USA
[2] 3M Ctr, 3M Engn Syst Technol Ctr, St Paul, MN 55144 USA
基金
美国国家科学基金会;
关键词
surface activity surface tension; surface pressure; surfactant; polymer; viscosity; diffusion coefficient;
D O I
10.1016/j.aca.2004.11.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A dynamic surface tension detector (DSTD) was used to examine the molecular diffusion and surface adsorption characteristics of surface-active analytes as a function of solution viscosity. Dynamic surface tension is determined by measuring the differential pressure across the air/liquid interface of repeatedly growing and detaching drops. Continuous surface tension measurement throughout the entire drop growth is achieved for each eluting drop (at a rate of 30 drops/min for 2 mu l drops), providing insight into the kinetic behavior of molecular diffusion and orientation processes at the air/liquid interface. Three-dimensional data are obtained through a calibration procedure previously developed, but extended herein for viscous solutions, with surface tension first converted to surface pressure, which is plotted as a function of elution time axis versus drop time axis. Thus, an analyte that lowers the surface tension results in an increase in surface pressure. The calibration procedure derived for the pressure-based DSTD was successfully extended and implemented in this report to experimentally determine standard surface pressures in solutions of varied viscosity. Analysis of analytes in viscous solution was performed at low analyte concentration, where the observed analyte surface activity indicates that the surface concentration is at or near equilibrium when in a water mobile phase (viscosity of 1.0 Cp). Two surface-active analytes, sodium dodecyl sulfate (SDS) and polyethylene glycol (MW 1470 g/mol, PEG 1470), were analyzed in solutions ranging from 0 to 60% (v/v) glycerol in water, corresponding to a viscosity range of 1.0-15.0 Cp. Finally, the diffusion-limited surface activity of SDS and PEG 1470 were observed in viscous solution, whereby an increase in viscosity resulted in a decreased surface pressure early in drop growth. The dynamic surface pressure results reported for SDS and PEG 1470 are found to correlate with solution viscosity and analyte diffusion coefficient via the Stokes-Einstein equation. (c) 2004 Published by Elsevier B.V.
引用
收藏
页码:79 / 87
页数:9
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