Minimizing non-volatile matter in the mobile phase
NOTICE
Long-term exposure of the detector to non-volatile mobile phases will damage the detector. Do not use non-volatile buffers.
Observe the following guidelines to minimize the concentration of non-volatile matter in the mobile phase:
Prepare all mobile phases with volatile solvents. As a general rule, use solvents that are at least as volatile as water, that is lower boiling point and higher vapor pressure.
Use ultra-pure water with high resistivity and low total organic carbon obtained fresh from a thoroughly flushed and well-maintained point-of-use purification system.
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Bottled water and stagnant water from a purification system typically contain a higher level of non-volatile impurities than freshly obtained ultra-pure water.
Choose solvents that are specified to have low residue after evaporation.
For example, LC/MS-grade solvents typically have a lower residue after evaporation specification than HPLC-grade solvents and are often the better choice to achieve consistently low baseline noise.
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Many organic solvents have low viscosity, low surface tension and high volatility, which lead to a high mass transport efficiency within the detector. For such solvents, it is especially recommended to select a grade with lowest residue after evaporation.
If a particular solvent causes high background current or noise, try a different grade or vendor.
Most HPLC-grade or better solvents are pre-filtered and additional filtration may increase the concentration of impurities within the mobile phase. It is therefore recommended to only filter the aqueous buffer salt portion of a mobile phase.
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With solvent gradients, non-volatile impurities in the more polar solvent (for example, water in reversed-phase) can be concentrated on the column and elute later to produce large peaks or baseline artifacts.
With highly combustible mobile phases, such as tetrahydrofuran (THF) and other ethers or ketones, use only nitrogen as supply gas.
When changing the operating mobile phase: Make sure that the solvents are miscible and will not cause precipitation of buffer salts. If required, use an appropriate intermediate solvent.
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Keep this in mind particularly when switching between chromatographic methods.
Water or highly aqueous (< 5% organic modifier) mobile phases are highly susceptible to microbial growth. Prepare such mobile phases freshly on a daily basis.
Select an optimal evaporation temperature to selectively evaporate background components of the mobile phase. Observe the guidelines in Evaporation Temperature.
If the detector is inadvertently exposed to a non-volatile mobile phase, use water or appropriate solvent with no additives to remove the salts from the detector.
Typical compatible solvents for use with the detector
Water
Methanol
Isopropanol
Acetonitrile
Acetone
Methylene chloride
Hexane
Chloroform
Tetrahydrofuran
NOTE: Use THF with nitrogen gas only.