Ostwald ripening is a phenomenon observed in solid solutions and liquid sols that involves the change of an inhomogeneous structure over time, in that small crystals or sol particles first dissolve and then redeposit onto larger crystals or sol particles.
Dissolution of small crystals or sol particles and the redeposition of the dissolved species on the surfaces of larger crystals or sol particles was first described by Wilhelm Ostwald in 1896.[1] [2] For colloidal systems, Ostwald ripening is also found in water-in-oil emulsions, while flocculation is found in oil-in-water emulsions.[3]
This thermodynamically-driven spontaneous process occurs because larger particles are more energetically favored than smaller particles.[4] This stems from the fact that molecules on the surface of a particle are energetically less stable than the ones in the interior.
Consider a cubic crystal of atoms: all the atoms inside are bonded to 6 neighbours and are quite stable, but atoms on the surface are only bonded to 5 neighbors or fewer, which makes these surface atoms less stable. Large particles are more energetically favorable since, continuing with this example, more atoms are bonded to 6 neighbors and fewer atoms are at the unfavorable surface. As the system tries to lower its overall energy, molecules on the surface of a small particle (energetically unfavorable, with only 3 or 4 or 5 bonded neighbors) will tend to detach from the particle and diffuse into the solution.
Kelvin's equation describes the relationship between the radius of curvature and the chemical potential between the surface and the inner volume:
\Delta\mu=
| 2\sigma\nuat | |
| r |
\mu
\sigma
\nuat
r
\mu=kBTlog(Ceq)
kB
T
Ceq
Combining both expressions the following equation is obtained:
kBTlog\left(
| Ceq | |
| Cinfty |
\right)=
| 2\sigma\nuat | |
| r |
→ Ceq(r)=Ceq(infty)
| ||||
| e |
Ceq
Ceq(r)>Ceq(R)
r
R
r<R
t → infty
The history of research progress in quantitatively modeling Ostwald ripening is long, with many derivations.[5] In 1958, Lifshitz and Slyozov[6] performed a mathematical investigation of Ostwald ripening in the case where diffusion of material is the slowest process. They began by stating how a single particle grows in a solution. This equation describes where the boundary is between small, shrinking particles and large, growing particles. They finally conclude that the average radius of the particles ⟨R⟩, grows as follows:
\langleR\rangle3-\langleR\rangle
| 3 | |
| 0 |
=
| 8\gammacinftyv2D | |
| 9RgT |
t
\langleR\rangle | average radius of all the particles | |
\gamma | particle surface tension or surface energy | |
cinfty | solubility of the particle material | |
v | molar volume of the particle material | |
D | diffusion coefficient of the particle material | |
Rg | ideal gas constant | |
T | absolute temperature and | |
t | time. |
Note that the quantity is different from, and only the former one can be used to calculate average volume, and that the statement that ⟨R⟩ goes as relies on being zero; but because nucleation is a separate process from growth, this places outside the bounds of validity of the equation. In contexts where the actual value of is irrelevant, an approach that respects the meanings of all terms is to take the time derivative of the equation to eliminate and . Another such approach is to change the to with the initial time having a positive value.
Also contained in the Lifshitz and Slyozov derivation is an equation for the size distribution function of particles. For convenience, the radius of particles is divided by the average radius to form a new variable, ρ = .
f(R,t)=
| 4 | |
| 9 |
\rho2\left(
| 3 | |
| 3+\rho |
| |||||
| \right) | \left( |
| 1.5 | |
| 1.5-\rho |
| ||||
| \right) |
\exp\left(-
| 1.5 | |
| 1.5-\rho |
\right),\rho<1.5
Three years after that Lifshitz and Slyozov published their findings (in Russian, 1958), Carl Wagner performed his own mathematical investigation of Ostwald ripening,[7] examining both systems where diffusion was slow and also where attachment and detachment at the particle surface was slow. Although his calculations and approach were different, Wagner came to the same conclusions as Lifshitz and Slyozov for slow-diffusion systems. This duplicate derivation went unnoticed for years because the two scientific papers were published on opposite sides of the Iron Curtain in 1961. It was not until 1975 that Kahlweit addressed the fact that the theories were identical[8] and combined them into the Lifshitz-Slyozov-Wagner or LSW theory of Ostwald ripening. Many experiments and simulations have shown LSW theory to be robust and accurate. Even some systems that undergo spinodal decomposition have been shown to quantitatively obey LSW theory after initial stages of growth.[9]
Wagner derived that when attachment and detachment of molecules is slower than diffusion, then the growth rate becomes
\langleR\rangle2=
| 64\gammacinftyv2ks | |
| 81RgT |
t
Although LSW theory and Ostwald ripening were intended for solids ripening in a fluid, Ostwald ripening is also observed in liquid-liquid systems, for example, in an oil-in-water emulsion polymerization.[3] In this case, Ostwald ripening causes the diffusion of monomers (i.e. individual molecules or atoms) from smaller droplets to larger droplets due to greater solubility of the single monomer molecules in the larger monomer droplets. The rate of this diffusion process is linked to the solubility of the monomer in the continuous (water) phase of the emulsion. This can lead to the destabilization of emulsions (for example, by creaming and sedimentation).[10]
One example of Ostwald ripening is the re-crystallization of water within ice cream which gives old ice cream a gritty, crunchy texture. Larger ice crystals grow at the expense of smaller ones within the ice cream, creating a coarser texture.[11]
Another gastronomical example is the ouzo effect, where the droplets in the cloudy microemulsion grow by Ostwald ripening.
In geology, it is the textural coarsening, aging or growth of phenocrysts and crystals in solid rock which is below the solidus temperature. It is often ascribed as a process in the formation of orthoclase megacrysts,[12] as an alternative to the physical processes governing crystal growth from nucleation and growth rate thermochemical limitations.
In aqueous solution chemistry and precipitates ageing, the term refers to the growth of larger crystals from those of smaller size which have a higher solubility than the larger ones. In the process, many small crystals formed initially (nuclei) slowly disappear, except for a few that grow larger, at the expense of the small crystals (crystal growth). The smaller crystals act as fuel for the growth of bigger crystals. Limiting Ostwald ripening is fundamental in modern technology for the solution synthesis of quantum dots.[13] Ostwald ripening is also the key process in the digestion and aging of precipitates, an important step in gravimetric analysis. The digested precipitate is generally purer, and easier to wash and filter.
Ostwald ripening can also occur in emulsion systems, with molecules diffusing from small droplets to large ones through the continuous phase. When a miniemulsion is desired, an extremely hydrophobic compound is added to stop this process from taking place.[14]
Diffusional growth of larger drops in liquid water clouds in the atmosphere at the expense of smaller drops is also characterized as Ostwald ripening.[15]