Hey guys,
My first extraction was going well, unfortunately ive used mineral turpentine (which is basically a mix of C6-C10 alkanes) which i thought you americans would call naphtha. I looked up the MSDS yesterday and it has a boiling point of 140-200 degrees celsius which explains why the evap is going so damn slow. Is there anyway to speed it up (there is still 2L+ with a huge amount of crystals already precipitated out)? for using baking trays to heighten the surface area as well as hot water baths (My sister yelled at me) and using a fan (and the aussies sun which is around ~25 degrees most days) with a muslin cloth over the top to evaporate.
I have 1L shellite (very pure heptane or octane) and 2L acetone which both aren't anywhere as cheap and i was saving for the purification steps. Is there a way to lower the boiling point/speed up the evaporation process further than i have already
HELP?!?
** help has been give. will freeze precipitate then recrystalise from hexane
My first extraction was going well, unfortunately ive used mineral turpentine (which is basically a mix of C6-C10 alkanes) which i thought you americans would call naphtha. I looked up the MSDS yesterday and it has a boiling point of 140-200 degrees celsius which explains why the evap is going so damn slow. Is there anyway to speed it up (there is still 2L+ with a huge amount of crystals already precipitated out)? for using baking trays to heighten the surface area as well as hot water baths (My sister yelled at me) and using a fan (and the aussies sun which is around ~25 degrees most days) with a muslin cloth over the top to evaporate.
I have 1L shellite (very pure heptane or octane) and 2L acetone which both aren't anywhere as cheap and i was saving for the purification steps. Is there a way to lower the boiling point/speed up the evaporation process further than i have already
HELP?!?
** help has been give. will freeze precipitate then recrystalise from hexane