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Library / Solution chemistry, equilibria and kinetics / SCH-30

Solution chemistry, equilibria and kinetics

Metal precipitation recovery at a fixed free ligand concentration

Percentage of a metal precipitated as MXᵦ when the free precipitating ion concentration X is held constant, from the Ksp and the initial total metal concentration C₀.

Ref
SCH-30
Rev
v1
Field
Solution chemistry, equilibria and kinetics
Result
recovery [%]

If free precipitating ion X is held at a fixed concentration, the dissolved metal at saturation is Ksp/Xᵇ. When the initial metal concentration C₀ exceeds that, the fraction recovered is 1 − Ksp/(Xᵇ C₀), which here is given as a percentage. Below saturation nothing precipitates, so the recovery is zero. It assumes that no other reactions, such as complexation, hold metal in solution.

Percentage of a metal precipitated as MXᵦ when the free precipitating ion concentration X is held constant, from the Ksp and the initial total metal concentration C₀. The result is zero below saturation.

Calculator

Solve for
%
1e-201e-4
mol/L
1e-41
14
mol/L
1e-51
  • Dissolved metal at equilibrium, min(C₀, Ksp/Xᵇ)1×10−7 mol/L
  • Metal precipitated per litre9.999×10−4 mol/L
  • Precipitant needed for 99.9 % recovery0.001 mol/L

What drives the result

Each variable is moved across its typical range while the others stay at the values above. The longest bar is the key driver.

Metal recovered (%) current value 99.99 %
KspSolubility productKey driver
0100
bPrecipitant ions per formula unit
0
C0Initial metal concentration
99100
XFree precipitant concentration
99100
  • With 0.01 mol/L of free precipitant, 99.99 % of the metal is recovered, leaving 1×10−7 mol/L in solution.
  • Reaching 99.9 % would need 0.001 mol/L of precipitant.
Chart data as tables

Ranked variables

VariableTypical rangeLowest resultHighest resultSwing (%)Local stepChange in result
Ksp Solubility product1e-20 to 1e-4 0100100+10%−0.001 %
b Precipitant ions per formula unit1 to 4 099.9999.99+1 −0.99 %
C0 Initial metal concentration1e-5 to 1 mol/L991001+10%+9.09e-4 %
X Free precipitant concentration1e-4 to 1 mol/L991000.9999+10%+9.09e-4 %

Sweep of Free precipitant concentration

Free precipitant concentration (mol/L)Metal recovered (%)
1e-499
3.162e-499.68
0.00199.9
0.00316299.97
0.0199.99
0.03162100
0.1100
0.3162100
1100

Sweep one variable

Metal recovered (%)Hover, touch, or use the arrow keys on the chart
9999.299.499.699.8100 1e−40.0010.010.11 Free precipitant concentration (mol/L), log scale now 99.99

Variables and how each one contributes

recovery

Metal recovered

Result · %

What the equation gives you. Everything else feeds it.

Ksp

Solubility product

· typical 1e-20 to 1e-4

The solubility product of MXᵦ. A larger Ksp leaves more metal dissolved, so the recovery falls. Raising it by 10 % (to 1.1×10−9) moves the result by −0.001 %, from 99.99 to 99.99 %.

X

Free precipitant concentration

mol/L · typical 1e-4 to 1

The free precipitant concentration, held constant, in mol/L. A higher precipitant level pushes the metal out more completely, so the recovery rises. Raising it by 10 % (to 0.011) moves the result by +9.09×10−4 %, from 99.99 to 99.99 %.

b

Precipitant ions per formula unit

· typical 1 to 4

The number of precipitant ions per formula unit. A larger b makes the precipitant’s concentration matter more, so the recovery rises. Raising it by 10 % (to 1.1) moves the result by −0.00585 %, from 99.99 to 99.98 %.

C0

Initial metal concentration

mol/L · typical 1e-5 to 1

The initial metal concentration, in mol/L. More metal at the start raises the recovered fraction, since the dissolved remainder is fixed. Raising it by 10 % (to 0.0011) moves the result by +9.09×10−4 %, from 99.99 to 99.99 %.

Worked example with the values above

  1. Dissolved metal at saturation: Ksp/Xᵇ = 1×10−9 / 0.01 = 1×10−7 mol/L.
  2. Fraction left: 1×10−7 / 0.001 = 1×10−4.
  3. Recovery = 100 × (1 − that) = 99.99 %.

Assumptions and limits

  • Pure-water dissolution, or the stated common ion, with no complexation, hydrolysis or ion pairing unless stated.
  • Concentration-based Ksp, with the solid present at equilibrium.

Common mistakes

  • Using the formula-unit coefficients in the wrong places in the Ksp expression.
  • Applying the approximation when the added solubility is not small compared with the common-ion concentration.
  • Ignoring complexation, which can raise the solubility by orders of magnitude.

Statistics and uncertainty

Solubility products vary widely between sources, often by a factor of two or more, and activity effects at ionic strengths of 0.1 M change solubility by 20 % to 50 %.

Where it is used

  • Predicting precipitation and the separation of ions.
  • Water treatment, hydroxide precipitation and gravimetric analysis.

Maths you need

  • Solubility product: Ksp, the product of ion concentrations at saturation
  • Common-ion effect: adding a shared ion lowers solubility
  • Ion product: Q, compared with Ksp to predict precipitation

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