Sciencemadness Discussion Board - Relation between solubility and temperature

Relation between solubility and temperature

r0749547 - 10-1-2019 at 09:22

Is there a real mathematical relation between solubility and temperature?
Exmp. molality ~ epx(temperature),
molarity ~ exp(temperature),
...
I've seen a few documents where they say the relation is exponentially.

But some solubility curves look like they have no relation at all (CaCl2).

Sulaiman - 10-1-2019 at 10:18

Most things approximately double for every 10^oC change,
https://en.wikipedia.org/wiki/Arrhenius_equation
but solubility has to be looked up.
Attachment: AlphabeticalSolubilityOfSalts.ods (55kB)
This file has been downloaded 410 times

[Edited on 11-1-2019 by Sulaiman]

Metacelsus - 10-1-2019 at 10:25

The relationship between temperature and solubility will vary depending on the solute and solvent in question. Generally, it can be described by the van't Hoff equation. See: https://en.wikipedia.org/wiki/Van_%27t_Hoff_equation

This equation uses the changes in enthalpy and entropy to describe changes in equilibrium with temperature. Therefore, in order to use it, the changes in enthalpy and entropy must be known beforehand. Practically speaking, it's often easier to just use a solubility table for the particular substance.

[Edited on 2019-1-10 by Metacelsus]

DraconicAcid - 10-1-2019 at 10:29

Quote: Originally posted by Metacelsus

This equation uses the changes in enthalpy and entropy to describe changes in equilibrium with temperature. Therefore, in order to use it, the changes in enthalpy and entropy must be known beforehand.

You don't need to know the entropy change; just the enthalpy of solution. If you've got that and a solubility at one temp, you can calculate the solubilities at other ones.

r0749547 - 10-1-2019 at 12:36

Quote: Originally posted by DraconicAcid

Quote: Originally posted by Metacelsus

You don't need to know the entropy change; just the enthalpy of solution. If you've got that and a solubility at one temp, you can calculate the solubilities at other ones.

Don't you need the Gibbs free energy? to get the ln(K) = -G0/RT
(I can't write the delta of the Gibbs free energy)

[Edited on 10-1-2019 by r0749547]

DraconicAcid - 10-1-2019 at 13:10

ln(K1/K2)= (-(delta)H/R)*(1/T1-1/T2) The delta H, and the solubility at one temp, is all you need.

This doesn't apply to something like calcium chloride, because you have calcium chloride hexahydrate dissolving at lower temperatures, and then calcium chloride tetrahydrate dissolving at higher temperatures (and the two hydrates have different enthalpies of solution).

[Edited on 10-1-2019 by DraconicAcid]

lordcookies24 - 10-1-2019 at 13:10

i don't think there is a general formula since every solute and solvent would have different solubility.

edit: changed equation to formula

[Edited on 10-1-2019 by lordcookies24]

r0749547 - 11-1-2019 at 02:04

Quote: Originally posted by DraconicAcid

The delta H, and the solubility at one temp, is all you need.

Can't you use the solubility at two different temps to calculate the change in enthalpy?

[Edited on 11-1-2019 by r0749547]

DraconicAcid - 11-1-2019 at 11:13

Quote: Originally posted by r0749547

Quote: Originally posted by DraconicAcid

The delta H, and the solubility at one temp, is all you need.

Can't you use the solubility at two different temps to calculate the change in enthalpy?

[Edited on 11-1-2019 by r0749547]

Yes, that works, too.

r0749547 - 11-1-2019 at 11:32

Last question.
since solubility tables are always in molality,
to go from the molality to molarity I would need the density of the solution.
But that's hard to find. Do you just assume that the volume stays constant at 100ml?
at first I tought to calculate the mole fraction equilibrium constant and to convert that to the concentration equilibrium constant,
using Kc = Kx(P/RT)^delta(v) (but that only applies to gasses right?)

[Edited on 11-1-2019 by r0749547]

DraconicAcid - 11-1-2019 at 12:00

Mole fraction equilibrium constant? I've never heard of that- equilibrium constants are always in molarity for solutes (with gases, you can use Kc or Kp, but that's not relevant here).

If you ignore the difference between molarity and molality, it really won't make much difference for the van't Hoff eq'n.

For example, let's look at what chemister.ru says about the solubility of benzoic acid in ethanol:

ethanol: 47.1 (15°C) [Ref.]
ethanol: 52.4 (19.2°C) [Ref.]
ethanol: 55.9 (23°C) [Ref.]

Because benzoic acid doesn't dissociate in ethanol, we can just use the solubility as the equilbrium constant (unlike an ionic compound in water, where we'd have to convert solubility to Ksp). The van't Hoff eq'n gives us 15.2 kJ/mol for the enthalpy of solution (based on the 15 and 23 oC values).

Using this enthalpy, we can find the solubility at 19.2 oC as 51.6 g/ 100 g solvent, which is pretty close.

[Edited on 11-1-2019 by DraconicAcid]

r0749547 - 11-1-2019 at 13:32

Quote: Originally posted by DraconicAcid

Mole fraction equilibrium constant? I've never heard of that- equilibrium constants are always in molarity for solutes (with gases, you can use Kc or Kp, but that's not relevant here).

If you ignore the difference between molarity and molality, it really won't make much difference for the van't Hoff eq'n.

For example, let's look at what chemister.ru says about the solubility of benzoic acid in ethanol:

ethanol: 47.1 (15°C) [Ref.]
ethanol: 52.4 (19.2°C) [Ref.]
ethanol: 55.9 (23°C) [Ref.]

Because benzoic acid doesn't dissociate in ethanol, we can just use the solubility as the equilbrium constant (unlike an ionic compound in water, where we'd have to convert solubility to Ksp). The van't Hoff eq'n gives us 15.2 kJ/mol for the enthalpy of solution (based on the 15 and 23 oC values).

Using this enthalpy, we can find the solubility at 19.2 oC as 51.6 g/ 100 g solvent, which is pretty close.

[Edited on 11-1-2019 by DraconicAcid]

But what do you do if it does dissociate and you do need the molarity for the Kst?
Do you simply assume the 100g of water to be 100ml and neglect the volume change of mixing? (ex. NaCl in water)

And about the mole fraction equilibrium constant...
It stands in one of my books I need to know for my exams

[Edited on 11-1-2019 by r0749547]

DraconicAcid - 11-1-2019 at 13:50

If you need the molarity for a dilute solution, then just assume that the 100 g of water makes 100 mL of solution. If it's a concentrated solution (such as saturated sodium chloride in water), then it's not going to work anyway because the ionic strength mucks things up, and you have to use activities instead of concentrations. Even without considering ions, if you have a solution that is 10% non-ionizing solute (such as 2-butanone), the solution doesn't act as a pure aqueous solution (it's only 90% water). That will change K for anything dissolving in it- ionic compounds will be less soluble, and organic compounds will be more soluble.

Even then, the van't Hoff eq'n isn't exact, because the enthalpy of solution will vary slightly with temperature.

Morgan - 11-1-2019 at 18:27

Is there a solid substance that is more soluble at a lower temperature than at a higher temperature?

[Edited on 12-1-2019 by Morgan]

j_sum1 - 11-1-2019 at 19:54

Many lantjanide series salts do this. Ce2(SO4)3 is one if I am not mistaken.

For something a bit less exotic, calcium carbonate. Tdep did a nice video on this on his extractions and ire channel.

Sulaiman - 12-1-2019 at 01:41

the van 't Hoff equation seems to be applicable only over a range of temperature that needs to be chosen by refering to a solubility table or chart.
No doubt useful for optimising/fine-tuning an industrial application but not much use to me.

Praseodymium sulfate^* has a third-order behaviour (see file I posted above)
- fit that with a van 't Hoff equation

^* the first one I spotted, many other salts have anomalies

fusso - 12-1-2019 at 07:55

@Sulaiman I can't open the ods file with excel, something unreadable

Sulaiman - 12-1-2019 at 08:05

The file is just a version of the Wikipedia page https://en.wikipedia.org/wiki/Solubility_table

Attachment: AlphabeticalSolubilityOfSalts.xls (401kB)
This file has been downloaded 412 times

fusso - 12-1-2019 at 08:17

Quote: Originally posted by j_sum1

For something a bit less exotic, calcium carbonate. Tdep did a nice video on this on his extractions and ire channel.

Really? Did he? I can't find that.

Metacelsus - 13-1-2019 at 00:30

Quote: Originally posted by DraconicAcid

Quote: Originally posted by Metacelsus

You don't need to know the entropy change; just the enthalpy of solution. If you've got that and a solubility at one temp, you can calculate the solubilities at other ones.

Yes. Knowing the enthalpy and the solubility at one temperature is equivalent to knowing both the enthalpy and entropy.

nezza - 13-1-2019 at 07:06

Some reagents do follow a simple solubility curve if you plot solubility agaist temperature. There is always a caveat. Reagents which react with the solvent do not, even if it is only hydrate formation. The curve is usually linear or exponential and can be used as a guide for recrystallising reagents. I have attached 2 curves BaNO3 which is just about linear and CuSO4 which approximates to exponential.

Quibbler - 14-1-2019 at 06:31

If you assume that the solute is forming an "ideal solution" then the mole fraction of solute (x) at temperature T is related to the fusion enthalpy (effectively going into solution is similar in energy to melting)

ln(x)=(/\H(fusion)/R)*(1/T(fusion)-1/T)