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. 2020 Aug 26;22(9):934. doi: 10.3390/e22090934

Comment on “Crystallization of Supercooled Liquids: Self-Consistency Correction of the Steady-State Nucleation Rate” by Abyzov et al., Entropy 2020, 22, 558

Vitaly A Shneidman 1
PMCID: PMC7597193  PMID: 33286703

Abstract

It is shown that in the growth region (above the critical nucleation size) the transient distributions obtained numerically from the Becker-Döring equation (BDE) by Abyzov et al., Entropy 2020, 22, 558, are in accurate correspondence with the matched asymptotic (singular perturbation) solution by Shneidman, Sov. Phys. Tech. Phys. 1988, 33, 1338. The solution is unmodified by “self-consistency” corrections which affect only the steady state rate. Sensitivity of the results to selection of a specific form of the BDE (the “nucleation model”) also is briefly discussed.

Keywords: transient nucleation, Becker-Döring, comment


As part of a recent study by [1] transient behavior (relaxation to steady state) of the Becker-Döring nucleation equation (BDE) with parameters related to those of lithium disilicate has been examined using numerical methods. Indeed, the time-dependent BDE does not allow a closed form exact solution. Nevertheless, an asymptotically exact solution (AES) is available in the limit of a large nucleation barrier [2,3]. Since the parameters used by [1] lead to ΔGnc>50kBT, the AES is expected to be very accurate in the domain of its applicability. Below I briefly describe the solution and present the comparison; where possible, notations which are identical to those by [1] (except for τ) will be used.

The transient flux at size n in the growth region (i.e., for nncδnc) is given by [2,3]

j(n,t)=Jstexpexpti(n)tτ (1)

Note two time scales τ, the “relaxation time” and ti(n) the “incubation time” which is larger than τ and which depends on the size n where the flux is observed. One has

τ=δnc22w+nc, (2)

while ti(n) is expressed in terms of the “deterministic growth rate” n˙w+(n)w(n) [i.e., in terms of an integral dn/n˙]. One has [3]

ti(n)=tdecncδnc2+tgrnc+δnc2,n (3)

Here tdec is the positive decay time of a subcritical cluster with indicated initial size; tgr is the growth time for a supercritical cluster with initial size nc+δnc2 to reach the size n. The experimentally obseved “induction time” (also, “time lag”) which is defined as tind(n)=01j(n,t)/Jstdt is then given by tind(n)=ti(n)+0.5772τ.

Above is the general solution. To specify the model one needs an explicit growth rate n˙. For the selection w+n2/3 by [1] one has

n˙=dndRR˙,R˙=RcτkBTΔμ1expΔμkBT1RcR (4)

(which is the “Hertz-Knudsen” growth rate in vapor condensation context); R and n are related by (4/3)πR3=nd03. The decay and growth contributions to the incubation time ti(n) in Equation (3) now can be directly evaluated:

ti(n)=1ncδnc2dnn˙+nc+δnc2ndnn˙ (5)

The “self consistency” corrections discussed by [1] do not change the rate n˙ and thus do not affect the transient part of the AES.

In the growth region the distribution function f(n,t) is given by j(n,t)/n˙. For comparison with numerics by [1] it is convenient to express the distribution as a function of radius, i.e., f(R,t)=f(n,t)dn/dR which tends to a constant at large R. Results of comparison are shown in Figure 1. As mentioned, the numerical accuracy of the AES is due to large values of the barrier ΔGnc compared to kBT.

Figure 1.

Figure 1

Comparison of the asymptotic solution [2,3] (lines) with numerics by [1] (symbols) at different times: left t = 2284 s, middle t = 5710 s, right t = 11,420 s. Dashed line is the steady state distribution in the growth region, Jst/R˙. No matching parameters were used.

In addition to the specific BDE considered by [1], other versions of the general BDE (other “models”) are discussed in literature in connection with transient nucleation in lithium disilicate. Such models differ by selection of the attachment rate w+(n), or by the mathematical form, continuous vs. discrete, of the nucleation master equation. The double exponential transient shape in Equation (1) remains unchanged, which allows a robust determination of τ from experimental data [3]. Otherwise, selection of another model leads to a different n˙ compared to Equation (4), affecting the incubation time ti(n). For example, the “Turnbull-Fischer” model leads to R˙=2RckBT/(τΔμ)sinhΔμ/(2kBT)1Rc/R [4,5,6]. In the limit of small Δμ/kBT this growth rate, as well as the one given by Equation (4) tend to a simpler R˙=Rc/τ1Rc/R which is consistent with continuous “Zeldovich-Frenkel” (ZF) version of the BDE. In that case the growth and decay integrals can be evaluated in terms of elementary functions, and one has [3]:

tiZF(n)=τln6ΔGnckBT2+RRc+lnRRc1 (6)

with explicit separation of the barrier- and the size-dependences. In the context of “self-consistent” correction by [1], note that the full barrier ΔGnc, rather than its reduced value ΔGncΔG1 enters the above expression (and thus the correction affects only Jst). The logarithmic dependence on the barrier in Equation (6) is expected to be adequate for parameters used by Abyzov et al. For the size dependence however, due to large values of Δμ/kBT one needs the general Equations (3) and (4) in order to achieve the level of accuracy demonstrated in Figure 1.

Acknowledgments

The author would like to thank A. Abyzov and E. Zanotto for useful correspondence and for sharing the digital version of their Figure 3.

Funding

This research received no external funding.

Conflicts of Interest

The author declares no conflict of interest.

References

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