Separating substances under lower atmos press

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A cyclohexane-toluene mixture can be effectively separated at an external pressure of 350 mm Hg, as this reduced pressure lowers the boiling points of both compounds, facilitating their separation. Cyclohexane boils at approximately 58.5°C and toluene at about 85.5°C under these conditions, which creates a significant difference in boiling points, making distillation feasible. The discussion touches on vacuum distillation, which is typically employed for compounds with high boiling points to prevent thermal decomposition. While vacuum distillation can be useful, it is not strictly necessary for this mixture, as simpler distillation methods may suffice. Additionally, safety considerations are noted due to the flammability of both cyclohexane and toluene, emphasizing the importance of proper equipment and techniques during the separation process.
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Can a cyclohexane-toluene mixture be separated if the external pressure is 350mm HG instead of 760 mmHG ?

My guess is yes, lowering the atmospheric pressure will only lower the boiling point, it won't affect whether separation will occur. By the way, is this what we call vacuum distillation? I need a little greater explanation. DOes anyone have any ideas?
 
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chiefy said:
Can a cyclohexane-toluene mixture be separated if the external pressure is 350mm HG instead of 760 mmHG ?
My guess is yes, lowering the atmospheric pressure will only lower the boiling point, it won't affect whether separation will occur. By the way, is this what we call vacuum distillation? I need a little greater explanation. DOes anyone have any ideas?

yeah, but I think that for the most part vacuum distillation is used for compounds with high boiling points, which decompose under such temperatures.

http://www.Newton.dep.anl.gov/askasci/chem00/chem00635.htm
 
The boiling point of cyclohexane at atmospheric pressure is 81.4 and that of toluene 110.8 which means that they can be separated easily. At reduced pressure,the difference in boiling points will probably be large enough to allow for separation.
 
if you're meaning through simple distillation probably not, I think what they usually do with vacuum distillation is to trap the gaseous organics in a "cryogenic chamber", that is if the organics are gases at that temperature. Fractional distillation may work even at normal pressures.
 
I am not quite sure understand your post. The only reason for vacuum distillation as opposed to atmospheric pressure is that because the boiling points are lowered, it is possible to operate with less thermal decomposition.
 
Mr.Chiefy:
According to my Handbook of Chemistry and Physics,the change in boiling point with pressure is given by:
\deltat=(273.1+t)(2.8808-logp)/phi+.15(2.8808-logp)
where t is temperature,p is pressure and phi can be obtained from a graph. I picked 4.7 for cyclohexane and 4.6 for toluene.

Assuming my arithmetic is fairly correct,this is what transpires:
Cyclohexane at 350mm boils at 58.5 centigrade
Toluene at 350mm boils at 85.5 centigrade.
Consequently distillation at 350mm ought to separate the compounds very well.
 
vacuum distillation is something I just through in there, I simply wanted to know if they separate under a lower pressure, and I think the consensus is that they will. Thanks for the replies.
 
renerob said:
I am not quite sure understand your post. The only reason for vacuum distillation as opposed to atmospheric pressure is that because the boiling points are lowered, it is possible to operate with less thermal decomposition.

thermal decomposition of organics? cyclohexane and toulene?
 
Personally I have had a couple of compounds that I have tried to purify by distillation and I got better results by distilling at atmospheric pressure than at low temperature. Then again, the bp difference was a bit smaller in my case.

Also, you don't necessarily need cryogenic cooling when you do vacuum distillation. A simple, water-cooled distillation apparatus is often good enough when you are dealing with high boiling materials. There definitely are cases where you need to condense the distillate at very cold temps, but not always.
 
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GCT:
Good point. In this particular case one other good reason is that both compounds are very flamable.
 
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