In most sources i found Loss on drying /LOD (w/w %)of a sample is determined by putting about 1g of a powdered sample into an oven at about 105°C for some hours.

Afterwards it is placed in a desiccator while cooling.

This is not only used in most papers i found - but also mentioned in Pharmacopoeias or Certificates of Analysis.

In a few articles i found vacuum desiccators mentioned. But so far nothing about how those two methods compare. Or if it is even possible to get comparabe/accurate results when using a vacuum desiccator with siliga gel instead of an oven?

Does anyone of you have experience in drying powdered samples (e.g. herbal extracts) and determing LOD via vaccum desiccator?

How do the two methods compare? How long does it need roughly to dry?

More Daryl Goodrich's questions See All
Similar questions and discussions