Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600, USA.
J Chromatogr A. 2013 Jul 5;1297:64-76. doi: 10.1016/j.chroma.2013.04.047. Epub 2013 Apr 27.
The mass transfer kinetics in short and wide 4.6mm×30mm columns packed with 3.0μm Hypurity-C18 fully porous particles were measured for three different configurations of the inlet sample distribution and outlet sample collection: (1) both the inlet and outlet column endfittings are standard, (2) the inlet endfitting is standard while the outlet endfitting allows parallel segmentation of the exiting flow between a central and a peripheral region across the column diameter, and (3) both the inlet and outlet endfittings allow a parallel segmentation of the flow entering and exiting the column, respectively. The total reduced heights equivalent to a theoretical plate (HETP) were carefully measured, using the first and second central moments of the elution band profiles, obtained by its accurate numerical integration. The longitudinal diffusion term was measured at the lowest experimental reduced velocity applied. The solid-liquid mass transfer resistance was estimated from measurements of the intra-particle diffusivity using the Torquato's model of effective diffusion in packed beds. The trans-channel and short-range interchannel eddy diffusion HETP terms were taken from data obtained by solving numerically the Navier-Stokes equations and simulating advective-diffusive transport in computer-generated random sphere packings. The results clearly show that the trans-column eddy diffusion HETP term can account for up to 85% of the total intrinsic HETP (corrected for extra-column contributions) of the standard columns. Parallel segmented flow chromatography can reduce this contribution by half at high velocities, by eliminating most of the baseline peak tailing. This holds true irrespective of the retention factor of the analyte. It was found also that segmenting the inlet/outlet flow increases detection sensitivity by 25-50% for peaks with large to small retention factors, respectively. In practice, the advantage of parallel segmented flow chromatography in gradient elution (thin peak widths) is essentially limited by post-column bandspreading and diffusion in the dwell volume of the instrument used. Analyst should minimize post-column bandspreading (caused by connectors and detection cell volume) and synchronize the eluent composition in the peripheral and central inlet ports of the column, by using two separate pumps with appropriate dwell volumes.
在短而宽的 4.6mm×30mm 柱中,使用 3.0μm Hypurity-C18 全多孔颗粒,对三种不同的入口样品分布和出口样品收集配置的传质动力学进行了测量:(1)入口和出口柱端配件均为标准配置,(2)入口端配件为标准配置,而出口端配件允许在柱直径上从中心到外围区域将流出流并行分段,(3)入口和出口端配件分别允许进入和离开柱的流并行分段。使用洗脱带轮廓的第一和第二中心矩,通过其精确的数值积分,仔细测量了总等效理论板高度(HETP)。在应用的最低实验还原速度下测量了纵向扩散项。使用填充床中有效扩散的 Torquato 模型,通过测量颗粒内扩散率来估计固液传质阻力。跨通道和短程相间涡流扩散 HETP 项取自通过数值求解纳维-斯托克斯方程和模拟计算机生成的随机球堆积中对流扩散传输获得的数据。结果清楚地表明,跨柱涡流扩散 HETP 项可以占标准柱总固有 HETP(校正柱外贡献)的高达 85%。在高速时,平行分段流色谱可以将其减少一半,从而消除大部分基线峰尾。这适用于分析物的保留因子。还发现,无论分析物的保留因子如何,将入口/出口流分段都会使大保留因子和小保留因子的峰的检测灵敏度分别提高 25-50%。实际上,在梯度洗脱(峰宽较窄)中平行分段流色谱的优势主要受所用仪器的柱后带展宽和扩散限制。分析人员应通过使用具有适当停留体积的两个单独泵,使柱的外围和中心入口端口中的洗脱剂组成同步,从而最小化柱后带展宽(由连接器和检测池体积引起)。