you know, this whole ordeal is quite rightly pissing me off now( the whole crystalization)
before the x-tal would come out like the first post swim posted. swim was letting it cool only to room temp in about 2 hours with just the beaker in a glass of water.
then I tried your method nmk8743.
I used a thermos that was supose to retain heat up to 6 hours (with out the cooler step)
I left it for a day and put it in the fridge over night the next morning I put in in the frezzer and what came out is pictured above, so it worked!
Now to answer your question nmk8743, the big one is like layered and kinda brittle
the other pieces are like little rocks, but still no where near the quality of yours.
heres where EVERYTHING goes to shit.
before swim had only used naphtha, swim decided to try using heptane. this time swim did add the cooler step to allow a much slower cool down time. what swim has is a foam thermal chest not to big not to small. swim did everything the same except thoes 2 changes.
end result are tiny tiny slivers of x-tals in clusters and when you go to pick it up its like slush cause the x-tals are so fine.
now Ive tried everthing I can think of
added cooling time
reduced cooling time
not using the thermal chest
using the thermal chest
different amounts of solvent where tried to no luck
starting the cooling process from different temps
and heres where chemistry decides its fun to mess with me
swim decided to go back to start and use naphtha again.
to his suprize !.....tiny tiny x-tals
I literally cant get anything to grow larger then the thickness of a human hair
all of a sudden.
so I did some reading about crystalization in general
supposedly, there are zillions of factors such as the content of the air in the environment
and thats not something swim can change all to easily
I can't for the life of me figure out what variable changed
perhapse my beaker is shot?
some info on general crystal growing
http://xray.tamu.edu/pdf...guidetocrystalgrowth.pdf