这调查瞄准了改进泰勒的表演“为在各种各样的溶剂的极小的溶质的散开系数的快、精确的测量的 s 分散分析。调查被监视溶质脉搏的紫外吸收山峰并且由山峰效率计算散开系数在一台毛状的电气泳动仪器上执行。与是的 L 本氨基丙酸主要测试溶质,一些关键因素后来包括特别毛状的尺寸,搬运人流动速度,注射体积和毛状的调节被揭示。当很快的移植和高样品集中引起了 o ve 休息 i 地席离子时,跟踪的山峰,大量样品注射和慢移植被发现低估散开系数。在 0.1 的中等流动速度—1 cm/s 与一 72.44 毛状嗯 I.D.x60 厘米(50 厘米有效) 在 25 deg C 维持了,水的 L 本氨基丙酸的散开系数被决定,给 7.02X10 ~ 的价值(有错误的 -6) cm~2/s <2% 并且相对标准差 < 0.2 %(n=3 ) 。方法被显示对象水的本氨基丙酸,丙酮,酚,甲苯和苯那样的各种各样的样品的测量适用,并且非水的苯(在乙醇或 1-butanol ) 。
This investigation aimed at improving the performance of Taylor's dispersion analysis for the fast and accurate measurement of diffusion coefficient of a minute solute in various solvents. The investigation was carried out on a capillary electrophoresis instrument by monitoring the UV absorption peak of a solute pulse and calculating the diffusion coefficient by peak efficiency. With L-phenylalanine as a main testing solute, some key factors were afterward disclosed including especially the capillary size, carrier flow velocity, injection volume and capillary conditioning. Peak tailing, large volume of sample injection and slow migration were found to underestimate the diffusion coefficient while very fast migration and high sample concentration caused overestimation. At a moderate flow velocity of 0.1--1 cm/s with a capillary of 72.44μm I.D.x60 cm (50 cm effective) maintained at 25℃, the diffusion coefficient of aque- ous L-phenylalanine was determined, giving a value of 7.02×10^6 cm^2/s with error 〈2% and relative standard deviation 〈0.2 % (n=3). The method was shown to be applicable to the measurement of various samples such as aqueous phenylalanine, acetone, phenol, toluene and benzene, and nonaqueous benzene (in ethanol or 1-butanol).