Hruska Vlastimil, Evenhuis Christopher J, Guijt Rosanne M, Macka Miroslav, Gas Bohuslav, Marriott Philip J, Haddad Paul R
Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague, Prague, Czech Republic.
Electrophoresis. 2009 Mar;30(5):910-20. doi: 10.1002/elps.200800647.
A knowledge of the heat-transfer coefficient, h(s), for the external surface of the capillary or the overall heat coefficient, h(OA), is of great value in predicting the mean increase in temperature of the electrolyte, DeltaT(Mean), during electrokinetic separations. For CE, traditional indirect methods of determining h(s) were time-consuming and tended to overestimate cooling efficiency; a novel method is introduced, which is based on curve-fitting of plots of conductance versus voltage to calculate several important parameters including DeltaT(Mean), h(s), the conductance free of Joule heating effects (G(0)) and the voltage that causes autothermal runaway, V(lim). The new method is superior to previously published methods in that it can be performed more quickly and that it corrects for systematic errors in the measurement of electric current for voltages <5 kV. These errors tended to exaggerate the cooling efficiency of commercial instruments so that the calculated increases in electrolyte temperature were smaller than their actual values. Axially averaged values for h(s) were determined for three different commercial CE instruments ranging from 164 W m(-2) K(-1) for a passively cooled instrument in a drafty environment to 460 W m(-2) K(-1) for a liquid-cooled instrument.
了解毛细管外表面的传热系数h(s)或总传热系数h(OA),对于预测电动分离过程中电解质的平均温度升高ΔT(Mean)具有重要价值。对于毛细管电泳,传统的间接测定h(s)的方法耗时且往往高估冷却效率;本文介绍了一种基于电导与电压关系曲线拟合的新方法,用于计算包括ΔT(Mean)、h(s)、无焦耳热效应的电导(G(0))以及导致自热失控的电压V(lim)等几个重要参数。该新方法优于先前发表的方法,因为它可以更快地执行,并且能够校正电压<5 kV时电流测量中的系统误差。这些误差往往会夸大商业仪器的冷却效率,从而使计算出的电解质温度升高值小于其实际值。针对三种不同的商业毛细管电泳仪器测定了h(s)的轴向平均值,范围从通风环境中被动冷却仪器的164 W m(-2) K(-1)到液冷仪器的460 W m(-2) K(-1)。