4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
How to start the dissolution development for unknown tab?
iam using ph instrument lab india make.3ponit and 5point.in calibration time 3point slope will come 98.89and 96.87.that limit is 85 to 105.what basis slope will come.any calucalation between them.5point wiicome slope 99.89?why 3p0int came 2 values
What is viod volume and peak purity in HPLC?
what are the sources in ELSD,PDA, RI and UV Detectors?
why we are use metthanol variously in kfr?why don't use other solutions?
I want analyze my compound at 325 nm so which standard shall i use to calibrate my HPLC system? How i can assure my hplc detector is suitable or not?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
UV and PDA detector, which have less signal to noise ratio?
why we are analyzing purity on HPLC why not in gc
What is the difference between Capillary column and Packed column.