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On the self-similarity of unbounded viscous Marangoni flows

Published online by Cambridge University Press:  16 October 2024

Fernando Temprano-Coleto*
Affiliation:
Andlinger Center for Energy and the Environment, Princeton University, Princeton, NJ 08544, USA Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544, USA
H.A. Stone*
Affiliation:
Department of Mechanical and Aerospace Engineering, Princeton University, Princeton, NJ 08544, USA
*
†Email addresses for correspondence: ftempranocoleto@princeton.edu, hastone@princeton.edu
†Email addresses for correspondence: ftempranocoleto@princeton.edu, hastone@princeton.edu

Abstract

The Marangoni flow induced by an insoluble surfactant on a fluid–fluid interface is a fundamental problem investigated extensively due to its implications in colloid science, biology, the environment and industrial applications. Here, we study the limit of a deep liquid subphase with negligible inertia (low Reynolds number, $Re\ll {1}$), where the two-dimensional problem has been shown to be described by the complex Burgers equation. We analyse the problem through a self-similar formulation, providing further insights into its structure and revealing its universal features. Six different similarity solutions are found. One of the solutions includes surfactant diffusion, whereas the other five, which are identified through a phase-plane formalism, hold only in the limit of negligible diffusion (high surface Péclet number $Pe_s\gg {1}$). Surfactant ‘pulses’, with a locally higher concentration that spreads outward, lead to two similarity solutions of the first kind with a similarity exponent $\beta =1/2$. On the other hand, distributions that are locally depleted and flow inwards lead to similarity of the second kind, with two different exponents that we obtain exactly using stability arguments. We distinguish between ‘dimple’ solutions, where the surfactant has a quadratic minimum and $\beta =2$, from ‘hole’ solutions, where the concentration profile is flatter than quadratic and $\beta =3/2$. Each of these two cases exhibits two similarity solutions, one valid prior to a critical time $t_*$ when the derivative of the concentration is singular, and another one valid after $t_*$. We obtain all six solutions in closed form, and discuss predictions that can be extracted from these results.

Information

Type
JFM Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press.
Figure 0

Figure 1. A non-homogeneous distribution of insoluble surfactant, with concentration $\varGamma (x,t)$, induces a velocity field $\boldsymbol {u}(\boldsymbol {x},t)$ within its fluid subphase through interfacial Marangoni stresses. The surfactant is itself advected by the resulting interfacial velocity $u_s(x,t)=\boldsymbol {u}\boldsymbol {\cdot }\boldsymbol {e}_x|_{y=0}$, leading to a two-way coupled problem. (a) For a localized pulse of surfactant, the Marangoni flow results in outward ‘spreading’. (b) When the surfactant distribution is instead depleted at its centre (a ‘hole’ or a ‘dimple’), the result is an inward ‘filling’ flow. All the dimensional parameters of the model considered here are highlighted in panel (b).

Figure 1

Table 1. Alternative formulations of the problem found in the literature, alongside the transformations required to convert them to (2.16), (2.18) and their variants with $Pe_s^{-1}=0$. Here, we have that $\tilde {\mathcal {H}}\left [\varGamma \right ] = {\rm \pi}^{-1}{\int\hskip -1,05em -\,} _{-\infty }^\infty (x'-x)^{-1}\varGamma (x',t)\,\,\mathrm {d}\kern 0.06em {x'}$ is an alternative definition of the Hilbert transform, such that $\tilde {\mathcal {H}}\left [\varGamma \right ]=-\mathcal {H}\left [\varGamma \right ]$. Subindices indicate partial derivatives.

Figure 2

Figure 2. Phase portraits of (3.1), for six different values of $\beta >0$, $\beta \neq {1}$. Any given two trajectories that are symmetric with respect to the horizontal axis represent one possible similarity solution $f(\eta )=\eta \,{g(\eta )}$, with the origin of the trajectory denoting $\eta =0$ and the endpoint denoting $|\eta |\to \infty$. The three fixed points $O=(0,0)$ (stable node), $P=(1,0)$ (node) and $S=(\beta,0)$ (saddle) have horizontal and vertical eigendirections for all $\beta >0$. Points $M$, $N$, $R$ are the fixed points of the ODE satisfied by the reciprocals of the solution (see Appendix A). Only green, purple, orange and yellow trajectories represent similarity solutions that are physically relevant, as illustrated in table 3. Stability criteria (§ 3.2) select the only five solutions that can be obtained in practice, which are highlighted with a wider streak. The dashed vertical line corresponds to $U/\eta =1-\beta$.

Figure 3

Table 2. Fixed points of the ODE system given by the real and imaginary parts of (3.1), for $\beta >0$ and $\beta \neq {1}$; SN denotes a stable node, UN an unstable node, and S a saddle. Points $M$, $N$ and $R$ are obtained as fixed points of ODE systems involving the reciprocals $\eta /U$ and $\eta /C$, as detailed in Appendix A. The entries for $U(\eta )$ and $C(\eta )$ denote every possible asymptotic expansion about each fixed point, where $K$ and $K'$ are independent, real, non-zero constants of integration, and $\eta _f$ is the (real, non-zero) location of the front occurring at the saddle point $S$. When more than one entry for $U(\eta )$ and $C(\eta )$ is provided, the first row corresponds to the trajectory along the horizontal eigendirection, the second row to the trajectory along the vertical eigendirection and the third (if provided) to generic curves along any other direction.

Figure 4

Table 3. List of all possible phase-plane trajectories of the reduced similarity ODE (3.1), for different values of the exponent $\beta$. The last column indicates whether a given trajectory represents a physically relevant solution. If the solution is classified as not relevant, the reasons are provided, based on three criteria: (i) having a non-zero concentration $C(\eta )\neq {0}$ representative of Marangoni flow, (ii) compatibility with the far-field condition (2.26) and (iii) continuity at $\eta =0$. If the trajectory is physically relevant, its colour in figure 2 is indicated.

Figure 5

Figure 3. Spreading solutions with $Pe_s^{-1}=0$, for initial profiles of surfactant given by (a) a Cauchy pulse, (b) a rectangular pulse and (c) a double quartic pulse, with their functional forms given in Appendix E. For each example, panels (a i,iii,b i,iii,c i,iii) show the concentration $\varGamma (x,t)$ and interfacial velocity $u_s(x,t)$ obtained through the exact solution of (2.19), while panels (a ii,iv,b ii,iv,c ii,iv) show the same data rescaled in similarity variables (colour curves), superimposed on the similarity solution (4.7) (black curves) valid at long times $t\gg {1}$. For the double quartic pulse (c), the reference position in (2.20) is $x_*=1/2$; in all other examples $x_*=t_*=0$.

Figure 6

Figure 4. Spreading solutions for an initially rectangular pulse of surfactant, with a functional form given in Appendix E, for (a) $Pe_s=1/50$, (b) $Pe_s=1$ and (c) $Pe_s=50$. For each example, panels (a i,iii,b i,iii,c i,iii) show the concentration $\varGamma (x,t)$ and interfacial velocity $u_s(x,t)$ obtained through the exact solution of (2.18), while panels (a ii,iv,b ii,iv,c ii,iv) show the same data rescaled in similarity variables (colour curves), superimposed on the similarity solution (4.24) (black curves) valid at long times $t\gg {1}$. In all examples, $x_*=t_*=0$.

Figure 7

Figure 5. Filling solutions with $Pe_s^{-1}=0$, for initial ‘dimple’ distributions of surfactant given by (a) a Cauchy dimple, (b) a squared Cauchy dimple and (c) an arctangent dimple, with their functional forms given in Appendix E. For each example, panels (a i,iv,b i,iv,c i,iv) show the concentration $\varGamma (x,t)$ and interfacial velocity $u_s(x,t)$ obtained through the exact solution of (2.19). Panels (a ii,v,b ii,v,c ii,v) and (a iii,vi,b iii,vi,c iii,vi) show exact solutions rescaled in similarity variables (colour curves), superimposed on the closure (5.7) and levelling (5.5) similarity solutions (black curves) valid prior and subsequent to the singularity, respectively. In all examples, $x_*=0$.

Figure 8

Figure 6. Filling solutions with $Pe_s^{-1}=0$, for initial ‘hole’ distributions of surfactant given by (a) a rectangular hole, (b) a quartic hole and (c) an asymmetric hole, with their functional forms given in Appendix E. For each example, panels (a i,iv,b i,iv,c i,iv) show the concentration $\varGamma (x,t)$ and interfacial velocity $u_s(x,t)$ obtained through the exact solution of (2.19). Panels (a ii,v,b ii,v,c ii,v) and (a iii,vi,b iii,vi,c iii,vi) show exact solutions rescaled in similarity variables (colour curves), superimposed on the closure (5.13) and levelling (5.10) similarity solutions (black curves) valid prior and subsequent to the singularity, respectively. The asymmetric hole (c) has $x_*\approx {0.562}$, otherwise $x_*=0$.

Figure 9

Table 4. Summary of the six similarity solutions found in this study, indicating the equation number of each solution $f(\eta )$ obtained in closed form. Here, $M_0$ is the dimensionless surfactant mass as defined in (C2), and $Pe_s$ is the Péclet number given by (2.17). In the case of pulses, the reference position $x_*$ is the centre of mass of the surfactant distribution given by (4.10), and in the case of dimples and holes $x_*$ is the ‘closure position’ at which the solution has a weak singularity, which can be calculated a priori from the initial conditions as described in Appendix D. The parameters $t_*$ and $u_*$ are the closure time and instantaneous velocity of the singular point, respectively, and can also be calculated using Appendix D. For solutions of the second kind, the constant $A$ depends on local properties of the initial condition $\varGamma _0(x)$.

Figure 10

Figure 7. Physical interpretation of each quadrant of the phase plane in figure 2, for (a) spreading solutions with an outward flow (as in figure 1a), and (b) filling solutions with an inward flow (as in figure 1b). In order for the concentration $\varGamma (x,t)$ to be strictly non-negative, each quadrant must correspond to a specific definition of the similarity variable, either forward time as in (2.22a) or backward time as in (2.22b). In addition, each quadrant represents one half of the real line, either $x>x_*$ or $x< x_*$.

Figure 11

Table 5. Initial conditions $\varGamma _0(x)$ and $u_{s0}(x)$ used in the article. The fourth column lists the lower-analytic complex function $\psi _0(z)$, with $z=x+\mathrm {i} y$, that results in ${\psi _0(x)=u_{s0}(x)+\mathrm {i}\varGamma _0(x)}$ on the real axis $y=0$. The fifth column denotes the mass of surfactant, as defined in (4.1), for the case of pulses. The last column specifies the singularity time $t_*$ for holes or dimples, as defined in (D6) and (D7). Here, $H(x)$ denotes the Heaviside step function.