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Yield stress fluids solidifying in capillary imbibition

Published online by Cambridge University Press:  03 October 2024

Hanul Kim
Affiliation:
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea
Siyoung Q. Choi*
Affiliation:
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea KAIST Institute for the Nanocentury, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yusseong-gu, Daejeon 34141, Republic of Korea
*
†Email address for correspondence: sqchoi@kaist.ac.kr

Abstract

When subjected to external stress exceeding their yield stress ($\sigma _{Y}$), yield stress fluids (YSFs) undergo transition from solid to liquid. While the flow dynamics of capillary flows – including wetting, coating, spreading, and wicking – can be predicted accurately for fluids without yield stress, only a few asymptotic solutions have been validated against experiments for YSFs. In this study, we explore experimentally and theoretically the entire dynamics and solidifying process during capillary imbibition of YSFs, representing the fundamental aspect of capillarity-driven flow. We observe that during the gradual deceleration of capillary rise, YSFs exhibit apparent flow below $\sigma _{Y}$. This unexpected behaviour is linked to wall slip, manifested as plug flow in particle image velocimetry analyses. We introduce a model with numerical solutions, grounded in the rheological properties of YSFs and slip mechanisms, to accurately describe this liquid–solid transitional behaviour.

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) Schematic for the capillary rise experiment. Capillary rise $h(t)$ of (b) 85 $\%$ glycerol (Newtonian fluid, $\sigma _{Y}=0$) and (c) 0.12 wt. $\%$ Carbopol (YSF, $\sigma _{Y}=10$ Pa). Dashed lines in (b,c) are (1.1) combined with (1.2) for Newtonian and simple power law fluids ($\sigma _{Y}=0$), respectively. The solid line is (1.1) with (2.1). The shading is an error bar. Experimental parameters follow table 1.

Figure 1

Table 1. Rheological properties and slip layer thicknesses: $\sigma _{HB}$ is fitted from a rheology measure, while $\sigma _{Y}$ is fitted from capillary rise $h(t)$. Theoretical prediction follows $\sigma _{Y}$.

Figure 2

Figure 2. (a–c) Slip demonstration of horizontal imbibition using 0.12 wt. $\%$ Carbopol. (a) Microscope image of 0.12 wt. $\%$ Carbopol inside a glass capillary. The solution is seeded with 10 $\mathrm {\mu }$m hollow glass spheres. The scale bar is 100 $\mathrm {\mu }$m. The scheme on the right describes the depletion layer at the YSF–glass interface. (b) Horizontal capillary imbibition curve. (c) The PIV analysis result. The solid line is the plug flow velocity profile from the bulk imbibition speed. (d,e) Stress-velocity plots during the vertical capillary imbibition for (d) 0.12 wt. $\%$ and (e) various YSFs. The solid line is the Newtonian slip model (2.4). The shading in (d) shows the error bar. Insets in (c,d) show the vertical capillary rise curve $h(t)$, and coloured markers denote corresponding regimes. Velocity in (e) is normalized with $\mu$ and $l_{s}$. The concentrations in the legend in (e) are given in wt. $\%$.

Figure 3

Figure 3. (a,b) Proposed model prediction (solid lines) against experiments. From top to bottom, concentrations are 0.08 and 0.12 wt. $\%$ in (a), and 0.3, 0.7, 1.0 and 1.3 wt. $\%$ in (b). Marker colours match the colour map for $\sigma _{Y}$. (c,d) Normalized numerical solutions of (1.1) and (2.4) varying yield stress and slip conditions. From the bottom, (c) $\sigma _{Y} = 40$, 10 and 2 Pa, while (d) $(l_{s},\phi ) = (0.01\ {\rm nm},0.006)$, (0.2 nm, 0.1) and (16 nm, 9) nm. Dashed lines in (c,d) are shear thinning curves without slip. (e) Contour plot of $\varDelta$. The solid line shows $l_{s} = 10$ nm, and the dashed line is $l_{s}=0.1$ nm. The lower inset is the graphical definition of $\varDelta$, while the upper inset shows the same contour over $l_{s}$ versus $\sigma _{Y}$. For (c–e), rheological properties other than $\sigma _{Y}$, surface tension and DCA parameters follow the Carbopol 0.12 wt. $\%$ values shown in table 1 and table 2.

Figure 4

Table 2. DCA model parameters, slip dominance and plateau intensity.

Figure 5

Figure 4. (a) Ramp-up and ramp-down cycles of shear-rate–stress measurement for Carbopol 0.12 wt. $\%$. The inset is the corresponding stress–stress curve. Solid lines are for power 1. (b,c) The measured up-ramp cycles of shear rate versus stress flow curves for (b) Carbopol and (c) xanthan solutions. Concentrations in (b,c) are given in wt. $\%$.

Figure 6

Figure 5. (a,b) The contact angle change during the capillary rise of (a) xanthan and (b) Carbopol. (c1,d1) The raw meniscus images of (b) before and after solidification. (c2,d2) The corresponding contact angle measurement results. The measurement method is validated in Kim et al. (2020).

Figure 7

Figure 6. (a) Salt effects on the capillary imbibition of xanthan solutions. (b) Capillary rise on surfaces without (circle) and with (triangle) the APTES modification. The insets in (a,b) are the same curves in linear scale.