Choose a buffer that is well within 1+/- pH unit of its pKa to ensure the best use. Details of buffer preparations can be found within the internet.
Ensure the pH of your mobile phase is at a point at which it will hinder ionisation of the compound under analysis, i.e. very low pH for an acidic compound (low pKa) and high pH for a basic compound (high pKa/low pKb) to prevent ionisation. In this form more reproduce able analysis can be governed.
The pH for the individual component to be analysed, will depend on the chemical affinity of the component towards the stationary phase. The same will be different at different pH. Hence e.g. at pH 4.0 the system suitability is passing or the desired results are obtained then the pH for that analysis decided is to be 4.0
With increase in pH i.e. making solvents basic - you will get increase RT for most compounds and reduced peak tailing.
With decrease in pH i.e. making solvents acidid - you will get decrease RT for most compounds.
However this WONT be true for all columns. You cannot use random column at pH 1.5 - this will damage your column and same applies to working at high pHs - i.e. working at pH 13 - will damage most columns.
Always check the pH capacity in HPLC before choosing mobile phase pHs
Source: I am analytical scientist.
i have plant park immersed in methanol How i can select mobile phase
based on which criteria s mobile phase is selected
mobile phase is the phase that consist of the analyte and stationary phase is the phase that is standstill
because in normal phase HPLC mobile phase is non polar and stationary phase is polar. Most of the compound of interest are polar, if you increase the polarity of mobile phase compound of analyte will stay in mobile phase and will elute faster and retention time will be shorter.
The mobile phase as indicated is the moving phase. Either the mobile or stationary phase is polar and the other is Non-polar. A common polar phase is Methanol, and non-polar is hexane
stationary phase stays at the bottom of the paper chromatography while mobile phase is moving on the stationary phase and move on stationary phase till it gets its right place on the top of the paper or somwhere else.
stationary phase is the solid called the filter paper and mobile phase is the liquid or organic solvent present in the developing tank or beaker by ayesha zulfiqar
mobile phase is the phase that consist of the analyte and stationary phase is the phase that is standstill
The mobile phase as indicated is the moving phase. Either the mobile or stationary phase is polar and the other is Non-polar. A common polar phase is Methanol, and non-polar is hexane
because in normal phase HPLC mobile phase is non polar and stationary phase is polar. Most of the compound of interest are polar, if you increase the polarity of mobile phase compound of analyte will stay in mobile phase and will elute faster and retention time will be shorter.
Mobile protection
a moving or mobile phase is a mixture you want to separate , dissolved in a solvent.
stationary phase is the solid called the filter paper and mobile phase is the liquid or organic solvent present in the developing tank or beaker by ayesha zulfiqar
The mobile phase as indicated is the moving phase. Either the mobile or stationary phase is polar and the other is Non-polar. A common polar phase is Methanol, and non-polar is hexane
Normal Phase: It has a polar stationary phase and a non-polar mobile phase.Reverse Phase: It has a non-polar stationary phase and a moderately polar mobile phase
stationary phase stays at the bottom of the paper chromatography while mobile phase is moving on the stationary phase and move on stationary phase till it gets its right place on the top of the paper or somwhere else.
stationary phase is the solid called the filter paper and mobile phase is the liquid or organic solvent present in the developing tank or beaker by ayesha zulfiqar
Paper Chromatography is based on two phases i.e stationary phase & mobile phase. The mixture we use to separate or purify is a stationary phase that we put onto paper (which is usually Watmann's chromatographic paper #1 ) while the other solvent in tank is mobile phase (e.g. gasoline, water, ethanol etc.)Thus it depends upon chemical compositions of stationary phase & mobile phase.
Mobile phase.