J12, are you in a sealed setup? as in your solvent amount stays the same like in a jar?
in a tray or pan type tek that isnt sealed or has a ton of headspace, with the slow evap/boil/loss of solvent one would have to increase temps so as to stay in the sweet spot. In a sealed jar with minimal loss over time the spot would stay similar, as the crystals form the saturation level goes down, so in a sealed system over time one would need to trend down on the temp so as to increase saturation by temp lowering, and wouldnt have to go as high to get dissolution of the fines.
I do think that elevated temps will increase growth rate at the same saturation levels though.
Thats what we’re talking about, cycling temps, but restricting it to levels before nucleation and before dissolution of targeted growth crystals.
I make diamonds in sealed jars only, and no you don’t need to go down in temps. The only time you would want to go down in temperature is if your solution is crashing too fast and your trying to slow it down so it doesn’t sugar out. Only thing I use a Pyrex for is badder and fast crash.
I cannot find the exact quote after digging through my books, but there is a clear statement saying that the cooling cycle for ostwald ripening can be achieved by the evaporative cooling effect of evaporating the solution.
So there may not be a physical temp drop of your heating system (oven, heating pad, etc) but there is still a temp drop in your solution.
What are other ways to increase saturation? Adding solvent back in would have a similar effect and in turn give you more flexibility on your next move.
Yeah, that reminds me I need to implement an N2 then vac purge before opening our ovens…having that butane exhaust through my rated pump makes a whole lot more sense than letting it pour out the door towards the operator and possible ignition sources.
If you have a solute that has a greater affinity for the solvent than the compound you’ve currently got dissolved in that solvent then it should be able to displace that compound from the solution as it’s dissolved into the solvent itself.
Its a half baked idea on my part, but I’m still curious if anyone has took this past thought before me.
from what I recall salting out works with the polar interactions between solute and solvent. you block the positive interactions between the solvent and solute with another solute. With nonpolar you only have minimal and transient positive interactions between components, and the repulsive forces tend to outweigh the attractive ones.