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For teaching purpose only
8/28/22
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2
Introduction
High-performance liquid chromatography (HPLC) is a standard technique in
analytical chemistry to separate, identify and/or quantify compounds that are
dissolved in a solution.
HPLC instruments consists of a pump, an injector, a separation column and
a detector. An aliquot of the sample is injected onto the column. Each
compound in the sample interacts slightly differently with the column
material, and therefore, causing different flow rates for the different
components and leading to the separation of the components.
For teaching purpose only
8/28/22
© Agilent Technologies, Inc. 2016
3
Table of Content (ToC)
Introduction Van Deemter Equation
• What happens inside the column? • Eddy Diffusion
Key Parameters • Axial Diffusion
• Retention Time & Peak Width • Resistance to Mass Transfer
• Resolution – Baseline Separation • More on Van Deemter
• Resolution – The Fundamental Equation Peak Capacity
• Efficiency or Number of Theoretical Plates • Gradient Analysis
• Retention Factor • Definition
• Selectivity or Separation Factor • Calculation of Peak Capacity
How to Influence Selectivity? • Peak Width
• Selectivity – Example 1 • Example
• Selectivity – Example 2
• Selectivity – Example 3
• Plate Number
For teaching purpose only
8/28/22
© Agilent Technologies, Inc. 2016
4
Introduction
What happens inside the column?
Time t
Separation t -t
r2 r1
Peak width Wb1,2
ToC
For teaching purpose only
8/28/22
© Agilent Technologies, Inc. 2016
5
Introduction
What happens inside the column?
t -t t -t
r2 r1 r2 r1
Superior separation vs Inferior separation
W W W W
b1 b2 b1 b2
Superior separation vs Inferior separation
ToC
For teaching purpose only
8/28/22
© Agilent Technologies, Inc. 2016
6
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