Title page for ETD etd-12062002-051420


Type of Document Dissertation
Author Smith, Jennifer Houston
URN etd-12062002-051420
Title Chromatographic Properties of Silica-Based Monolithic HPLC Columns
Degree PhD
Department Chemistry
Advisory Committee
Advisor Name Title
McNair, Harold M. Committee Chair
Anderson, Mark R. Committee Member
Glanville, James O. Committee Member
Taylor, Larry T. Committee Member
Viers, Jimmy W. Committee Member
Keywords
  • chromatography
  • monolith
  • HPLC
Date of Defense 2002-09-23
Availability unrestricted
Abstract
Silica-based monolithic HPLC columns contain a novel chromatographic support in which the traditional particulate packing has been replaced with a single, continuous network (monolith) of porous silica. The main advantage of such a network is decreased backpressure due to macropores (2 μm) throughout the network. This allows high flow rates, and hence fast analyses that are unattainable with traditional particulate columns.

The Chromolith SpeedROD™ (EM Science, Gibbstown NJ) is a commercially available silica-based monolithic column. This work investigated the chromatographic properties of the 50x4.60 mm (ODS) SpeedROD™. Data fit to the van Deemter equation (mean square error=0.834) indicated that the van Deemter model was valid for monolithic columns. An effective particle size of 4 μm for the SpeedROD™ column was assigned by comparing the minimum of van Deemter curves with a series of particulate columns having various particle diameters. Separation Impedance (E), an empirically derived measure of column performance, was calculated as an alternate method of evaluating column efficiency. Data collected using this model confirmed monolithic columns behaves as a (more efficient) 3 μm column.

A series of experiments were designed to compare the effects of mobile phase strength and mobile phase viscosity between the SpeedROD™ column and a particulate column. The results indicated both solvent strength and viscosity have effects on the monolithic column at the optimum linear velocity.

A fast (90 s) HPLC method was developed using the SpeedROD™ column and a seven-component test mixture with a large range of hydrophobicities. The precision for both retention time and peak area was measured at high linear velocities (8 mL/min) and the percent relative standard deviation (RSD) calculated. Column to column reproducibility (n=6) was measured. The overall percent RSD ranged from 0.25% to 4.56% for retention time and from 1.08% to 6.77% for peak area. Run to run reproducibility (n=15) was measured for all six columns. Averages ranged for retention time from 0.89% to 5.09% RSD and for peak area from 4.65% to 6.18% RSD.

Applications for the SpeedROD™ column with various sample types were developed and discussed. These methods demonstrated the effectiveness of the SpeedROD™ at fast flow rates.

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