EasyManua.ls Logo

Waters 2475 - Mobile phase solvent degassing

Waters 2475
228 pages
Print Icon
To Next Page IconTo Next Page
To Next Page IconTo Next Page
To Previous Page IconTo Previous Page
To Previous Page IconTo Previous Page
Loading...
Mobile phase solvent degassing C-7
If the extent to which the pressure changes will affect the analysis is not
known, monitor the pressure during the run using the Chart Out terminal.
Mobile phase solvent degassing
Mobile phase difficulties account for 70% or more of all liquid
chromatographic problems. Using degassed solvents is important, especially
at excitation wavelengths below 220 nm. Degassing provides these benefits:
Stable baselines and enhanced sensitivity
Reproducible retention times for eluting peaks
Reproducible injection volumes for quantitation
Stable pump operation
This section explains the solubility of gases, solvent degassing methods, and
solvent degassing considerations.
Gas solubility
Only a finite amount of gas can be dissolved in a given volume of liquid. This
amount depends on:
The chemical affinity of the gas for the liquid
The temperature of the liquid
The pressure applied to the liquid
Changes in the composition, temperature, or pressure of the mobile phase can
all lead to outgassing.
Effects of intermolecular forces
Nonpolar gases (N
2
, O
2
, CO
2
, He) are more soluble in nonpolar solvents than
in polar solvents. Generally, a gas is most soluble in a solvent with
intermolecular attractive forces similar to those in the gas (like dissolves like).
Effects of temperature
Temperature affects the solubility of gases. If the heat of solution is
exothermic, the solubility of the gas decreases when you heat the solvent. If
the heat of solution is endothermic, the solubility increases when you heat the
solvent. For example, the solubility of He in H
2
O decreases with an increase in

Table of Contents

Related product manuals