Solute separation by centrifuge

In summary: DNA was sequenced to see how it had changed. It was found that the daughter cells had copied the original DNA exactly, but that the original DNA had changed.The original DNA was not destroyed - DNA is radioactively labelled (e.g. by growing bacteria in radioactive thymidine) all the DNA radioactivity is still found in the DNA of the daughter cells. But what way was it distributed? I.e. if we represent an existing strand as | and a newly produced strand as | , so the original DNA is || , when the cell has duplicated are progeny || and || (called 'conservative replication') or
  • #1
neanderthalphysics
53
6
TL;DR Summary
If energy (in)efficiency was not a factor, is it possible to separate any solute from any solvent by centrifuge? At extreme RPMs, is molecular disassociation possible?
My view is that it is possible to separate any solute from any solvent by centrifuge. Likewise it is possible to separate heavy water from H1 water by centrifuge.

Molecular disassociation is probably a borderline possibility, especially if we consider the molecular disassociation of your centrifuge by too high RPMs! But maybe, if you have a long chain molecule with two heavy atoms on the ends, and it is forced to bend under the rotational forces, then it might break the bonds.
 
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  • #2
neanderthalphysics said:
Summary:: If energy (in)efficiency was not a factor, is it possible to separate any solute from any solvent by centrifuge? At extreme RPMs, is molecular disassociation possible?

My view is that it is possible to separate any solute from any solvent by centrifuge. Likewise it is possible to separate heavy water from H1 water by centrifuge.

Molecular disassociation is probably a borderline possibility, especially if we consider the molecular disassociation of your centrifuge by too high RPMs! But maybe, if you have a long chain molecule with two heavy atoms on the ends, and it is forced to bend under the rotational forces, then it might break the bonds.
No. You can find solvents and solute which are not separable by centrifuge. For example, different variants of hydrocarbons with same density.
Also, the centrifuge itself will break long before any gravity-chemical effects would be noticeable.
 
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trurle said:
No. You can find solvents and solute which are not separable by centrifuge. For example, different variants of hydrocarbons with same density.
Also, the centrifuge itself will break long before any gravity-chemical effects would be noticeable.

Thanks for your inputs.

Can you give some examples of solvents and solute which are not separable by centrifuge?

If we go for something basic (excuse the pun) like KOH in water where the former is highly soluble in the latter, will you get an increasing concentration gradient as you spin the centrifuge faster?

What happens if you have a saturated or even supersaturated solute in a solvent, and then you spin it in a centrifuge? Will you start getting crystallization?

Tom.G said:
It can however be used to separate various isotopes of elements. For instance that is how enriched Uranium is obtained for reactor fuel, and for bombs.

https://science.howstuffworks.com/uranium-centrifuge.htm

I guess with a stretch of imagination one could view the U-235 and U-238 isotopes in a uranium centrifuge as a "solvent" and "solute" both of which are infinitely miscible with the other with interchangeable definitions of solvent and solute.
 
  • #5
neanderthalphysics said:
Thanks for your inputs.

Can you give some examples of solvents and solute which are not separable by centrifuge?

If we go for something basic (excuse the pun) like KOH in water where the former is highly soluble in the latter, will you get an increasing concentration gradient as you spin the centrifuge faster?

What happens if you have a saturated or even supersaturated solute in a solvent, and then you spin it in a centrifuge? Will you start getting crystallization?
I guess with a stretch of imagination one could view the U-235 and U-238 isotopes in a uranium centrifuge as a "solvent" and "solute" both of which are infinitely miscible with the other with interchangeable definitions of solvent and solute.
For example, phenol and water. Densities are very similar.
Saturated solution under centrifuge may become super-saturated if difference in density is large enough.
You need rotational speed about ~100 (m/s)/(g/cm3)
 
  • #6
The Uranium isotope separation mentioned earlier is one example. Of course you don't get some drastic all-or-none separation, your get quantitative enrichment, and a cascade of processes is needed (fortunately).

The principle has a classical application in molecular biology which is in all the textbooks. Centrifuge a solution containing a heavy ion fast enough, long enough you will get an equilibrum density gradient which is just the same principle as the gradient of air density of the atmosphere. Will be a shallow gradient but that is okay for the application, which is to separate macromolecules of closely similar density.

The question was when the (double-stranded) DNA molecule replicates in cellular duplication, how does the original DNA distribute between daughter cells? It was known that the original DNA was not destroyed - DNA is radioactively labelled (e.g. by growing bacteria in radioactive thymidine) all the DNA radioactivity is still found in the DNA of the daughter cells. But what way was it distributed? I.e. if we represent an existing strand as | and a newly produced strand as | , so the original DNA is || , when the cell has duplicated are progeny || and || (called 'conservative replication') or are they || and || (called 'semi conservative replication')? (They are not || and || (nonconservative) from what was mentioned above, the parent DNA strands are conserved.)

Cells were grown in a medium where their nitrogen source was the (nonradioactive) nitrogen isotope 15N. This gives a DNA slightly more dense than that with the normal 14N isotope. So || , || and || have three different densities and will eqiilibrate settling at different heights in the centrifuge tube in which a gradient of CsCl is established, and in this way it was possible to verify that replication produced || i.e. is semiconservative.

See any textbook or look up 'semiconservative replication' or 'Meselson & Stahl experiment'.
 
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Tom.G said:
It can however be used to separate various isotopes of elements. For instance that is how enriched Uranium is obtained for reactor fuel, and for bombs.

In gaseous phase, not in solution.
 
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Surely whether it is in the gaseous or liquid phase just affects separation by a matter of degree?
 
  • #9
neanderthalphysics said:
Surely whether it is in the gaseous or liquid phase just affects separation by a matter of degree?
Yes.
gaseous phase U235:U238 separation: known (I believe as their hexafluorides)

Liquid phase U235:238 separation: unknown
 

1. What is a centrifuge?

A centrifuge is a laboratory instrument that uses centrifugal force to separate mixtures of different substances based on their density. It spins samples at high speeds, causing the heavier components to move towards the bottom and the lighter components to move towards the top.

2. How does a centrifuge separate solutes?

A centrifuge separates solutes by spinning them at high speeds, causing the heavier components to move towards the bottom and the lighter components to move towards the top. This process is known as centrifugation and is based on the principle of sedimentation, where denser particles settle faster than lighter particles.

3. What types of solutes can be separated by a centrifuge?

A centrifuge can separate a variety of solutes, including cells, proteins, DNA, and other biomolecules. It can also separate mixtures of liquids with different densities, such as oil and water.

4. What are the benefits of using a centrifuge for solute separation?

Centrifugation is a quick and efficient method for separating solutes, making it a popular technique in many laboratory settings. It can also be used to purify samples, concentrate substances, and remove impurities.

5. Are there any limitations to using a centrifuge for solute separation?

While centrifugation is a powerful technique, it does have some limitations. It may not be suitable for separating very small particles or for samples with similar densities. Additionally, some substances may be damaged or denatured by the high speeds and forces involved in centrifugation.

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