We report that the fast droplet transport without additional energy expenditure can be achieved on the spine of cactus (Gymnocalycium baldianum) with the assistance of its special surface structure: the cactus spine exhibits a cone-like structure covered with tilted scales. A single scale and the spine surface under it cooperatively construct a splayed capillary tube. The arrays of capillary tube formed by the overlapping scales build up the out layer of the spine. The serial drops would be driven by the asymmetric structure resulted from tilt-up scales-by-scales on the cone-shaped spine and move directionally toward the bottom from top of spine, by means of the Laplace pressure in differences. In addition, after the past of the first droplet, thin liquid film of drop is trapped in the splayed capillary micro-tube on the surface of spine, which greatly reduces the friction of subsequential droplet transport in efficiency. This finding provides a new biological model which could be used to transport droplet spontaneously and directionally. Also this work offers a way to reduce the surface adhesion by constructing liquid film on the surface, which has great significance in prompting droplet transport efficiency.
Biological kingdom offers the strategies of liquid dynamics that adapt to the natural environment1,2,3,4,5,6,7,8, e.g., fog water collection controlled on biological surfaces such as spider silk1, beetle back2, plant leaf3, etc. in mist. They help researchers to understand the liquid behaviors1,4,8,9,10,11,12,13,14,15,16,17,18 and offers theories to design materials used for droplet transport including surfaces with asymmetric structure1,3,4,7, gradient wettability5 and additive energy to the systems9,10, etc. Up to now, varieties of materials and theories have been investigated to solve the problems in water acquiring task9,19,20,21,22,23,24,25. Cactuses are famous for their abilities to live in the desert where drought is normal and water evaporates so quickly. As has been reported, cactus spine covered with oriented spine and gradient grooves could drive droplet directionally3. Recently, we find that the scale-covered spines of cactus gymnocalycium baldianum (lives in the desert area of Argentina), the structure of which is totally different from the reported one, could also propel fog drops directionally with the assistance of the tilted scales and the splayed capillary tubes. In addition, the subsequent droplets could move more quickly than the first one because the surface adhesion has been greatly reduced by the thin liquid film trapped in the splayed capillary tubes after the past of the first droplet. Our finding could provide researchers with useful guidelines for designing new materials used for drop transport and it also provides researchers with a new way to prompt the droplet transport efficiency.
Here, we show the evolved spines of cactus gymnocalycium baldianum (Fig. 1a), which is observed that the drops are self-transported directionally in mist (Fig. 1b) to achieve water collection in efficiency. The environmental scanning electron microscopy (ESEM) is used to observe the microstructure on spine of cactus gymnocalycium baldianum (Fig. 1c). It is found that there are tilted scales overlapping along the length of the cone spine (~5 cm). The cone-apex angle δ of the spine is ~15° and the tilted angle of the scale (α) is ~20° to baseline of the axis of the spine (Fig. 1c). The scales are ~100–130 μm in length and ~30–50 μm in width (Fig. 1d). Under the tilted-up scales to base of spine, there are some cavities that can fan out with the maximum radius (Rc) of ~20 μm (Fig. 1e) at the opens of scales and the minimum radius (rc) of ~8 μm at the ends of scales (Fig. 1f). The overlapping scales and the surface of the spine construct the gradient splayed capillary micro-tubes array along the cone-shaped spine of cactus (Fig. 1g).
As has been reported, cactus spines can transport fog droplets directionally3. In our experiment, although the structure of the scale-covered cactus spine is totally different from the reported one, it could also transport fog droplets directionally, which reveals the scale-covered spine may have different droplet transport mechanism arising from its special structure. The directional transport of fog drop is observed apparently as shown in Fig. 2a (also see Supplementary Video 1). In water condensation, drop 1′ formed on the tip of the spine and moved to the bottom of the spine (from ~1 s to ~20 s). Then drop 2′ formed on the spine and coalesced with drop 1′ (from ~40 s to ~80 s). With the passing of time, drop 3′ and drop 4′ formed successively and all moved to the bottom of the spine (from ~100 s to ~120 s). In whole process, all of the fog drops moved directionally, which exhibit effective self-gathering capacity along the spine. It is estimated that the average moving velocities of drops 3′ (formed at the time of ~100 s) and 4′ (formed at the time of ~120 s) were ~0.25 mm/s and ~0.27 mm/s, respectively. Both velocities were larger than the average moving velocity of drop 1′ (i.e., ~0.05 mm/s) (Fig. 2b). In addition, on tilted spine, fog drops can also be transported directionally (see Fig. S1).
To reveal the unique behaviors of drops on the spine, a drop in volume of 2 μl is used to mimic the fog drop because of the growing fog drop on fibers similar to the advancing behaviors of the deposited drop26. Firstly, the drop deposits on the tip of the spine (Fig. 3a). At the beginning, the drop spreads slightly (Fig. 3a, from 0 s to ~20 s) and then climbs up the first scale and expands in shape. Subsequently it moves near to the second scale quickly and then climbs up the second scale and expands and then covers the third scale (Supplementary Video 2). After passing through scale by scale, the drop moves finally to the bottom of spine (Fig. 3a, from ~20 s to ~160 s). Further observation is focused on solid-liquid interfaces in details as drop moves in time of ~20.20–20.27 s. It is found the liquid meniscus at the right side of droplet seemed to be dragged to the left and its curvature changed not obviously during the droplet motion (as indicated in the right-side images of Fig. 3b). In contrast, the curvature change of liquid meniscus at the left side of droplet (as indicated in the left-side images of Fig. 3b) was relatively obvious: at the beginning it spread slowly from scale 1 to scale 2 (from ~20.20 s to ~20.25 s). The curvature of the liquid meniscus between scale 1 and scale 2 grew gradually and finally reached the maximum (at the time of ~20.26 s). Then the liquid covered scale 2 and its curvature became relatively small in a short time (from ~20.26 s to ~20.27 s), whereby the entire droplet moved for a distance about the length of a single scale. In addition, the contacting angles measurements (see Fig. S2) during the droplet motion reveals there is no obvious difference between the contacting angles of the left and right sides of the drop. This result excludes the influence of the cone structure of the spine on droplet motion5. It also predicts the tilted scales on the spine surface plays an important role in the directional droplet motion.
Aimed to find out whether the tilted scale plays the key role in the droplet transport process, we performed the following controlling experiments. We deposited droplets with the fixed volume of 2 μl on spines with different surface structures: scale-off spine and normal groove spine of cactus (the structures are shown in Fig. S3–4). The drop placed on scale-covered spine spread asymmetrically (Fig. S5a). The droplets placed scale-cleared-off and groove spine showed no asymmetric spreading (Fig. S5b,c) and didn’t move (Fig. S6a,b). From these experiments we deduce that the scales and the splayed capillary tubes formed by the scales on the spine are most possibly responsible for the directional and spontaneous motion of the first droplet.
We further deposited a second drop on the scale-covered spine to find the reason for the relative fast movement of fog drops 3′ and 4′ (Fig. 4a). After the movement of the first drop from the top to bottom of spine at ~152 s, the second droplet acts fast subsequently. As shown in Fig. 4a, the second deposited drop (drop 2) took about 0.07 s to move the same distance. The different moving velocities of these drops can be estimated by the slope degrees of the lines which represent the relationship between the drop moving distance and the moving time (as showed in Fig. 4b). The drop 1 moves with a velocity ~0.03 mm/s and drop 2 moves with a velocity ~70 mm/s. The high speed video helped us to observe the moving activities of the second drop in detail (see Fig. S7). The second drop firstly moved towards the first drop stably (from 0.000 s to 0.030 s) and then coalesced with it (from 0.036 s to 0.058 s). The fast motion of droplet before coalescence could rule out the coalescence influence on droplet movement. In addition, we found after the passing of drop 1, there would remains ultra thin water film on the spine (Fig. 4a, from the time ~20 s to ~120 s, see the white bright area on the surface of the spine). According to the above observations, we conclude the water ultra thin liquid film may contribute to the fast transport of the subsequential droplet.
Base on the above observations, we give explanations for the directional droplet motion on scale-covered spine. Figure 5 is used to illustrate the behaviors of part of droplet liquid on the spine. The other parts of the droplet liquid exhibit the similar behaviors because the spine is symmetric in cross section. It is understood that when a drop firstly forms on the spine, its shape is distorted by the asymmetric structure of the scales (Fig. 5b). The drop tends to spread along the scale due to the disparity between the local contact angle of the drop on the spine and the nascent contact angle of the related drop end, thus the initial spreading of the drop is triggered26. Influenced by the asymmetric scale-by-scale, the contact angle of the right side of the drop (θr) on the spine is larger than the contact angle of the left side of the drop on the spine (θl) (the inset of Fig. 5b, frame b1). A driving force Fd is described as follow27,28:
where θr is the contact angle of the right side of the drop, θl is the contact angle of the left side of the drop, γ is the liquid-solid surface tension and ds is the integrating variety along the length from the right to the left side of the drop. Because θr > θl, Fd points to the bottom of the spine and it propels the drop move to the left.
Only considered into the fiber with normal scale-by-scale along its axis, drop motion would cease when the drop reaches the equilibrium configuration, e.g., the ends of drops can be “hinged” by the edges of scales29. Interestingly, the scales on spine of cactus gymnocalycium baldianum open separately. The stable conformation of the drop will be disturbed by the liquid flow in the space among the tilted-up scales30,31,32. When the drop reaches the hinge of scale 2 (on the left side of the droplet) and scale 0 (on the right side of the droplet), the liquid on the right and left sides of the drop could continue to spread along the direction parallel to the axis of spine. Because of the asymmetric radius from the bottom and the top cavities of the scales (inset of Fig. 5b, frame b2, rc ~8 μm < Rc ~20 μm), the spaces of cavities can be regarded as typical splayed capillary micro-tubes in array. In the spreading process, the liquid of the right side of the drop firstly enters into the bottom of the scale 0 and exhibit a concave curvature owing to the hydrophilicity of the scale surface. The Laplace pressure resulted from this curvature is defined as P0, which points to the tip of the scale (inset of Fig. 5b, frame b3). P0 will drag the droplet liquid move to the left of the spine. Influenced by the hinge scales 0 and 2, the main liquid of the drop exhibits a nearly symmetrical shape, so the Laplace pressure (P1) resulted from the convex drop curvature points vertically to the axis of spine, which have no influence on droplet motion in horizontal direction. The liquid of the left side of the drop exhibits concave curvatures when it contacts with scale 3. The Laplace pressures introduced by the meniscuses at top and bottom of scale 3 are defined as P2 and P3, respectively. P2 points to the top of the scale and P3 points to the bottom of the scale. Both of P2 and P3 will drag more droplet liquid into scale 3, in a way, they will help the more droplet liquid move to the left (inset of Fig. 5b, frame b4). Therefore, according to the different dragging effect applied on the whole droplet, the Laplace pressure difference for the entire drop can be described as . can be further written as , where r0, r2 and r3 are the curvature radii of the related liquid menisci, respectively. As for a liquid menisci in a capillary tube with a radii of R, its curvature radii r can be written as , θ is the contacting angle of the liquid on the capillary tube surface. Based on this equation it can be deduced r decreases with R. The curvature radii difference between the meniscuses at bottom and top of liquid leads to the difference between P2 and P3,which generates a force pointing to location of the micro-tube with minimum radius33,34. So the liquid of drop reaches the micro-tube end firstly and then extends along the scale. From this aspect the bottom liquid menisci in scale 3 will keep the smallest curvature radius r3 because the liquid has reached the bottom of the scale. r0 will grow large as more liquid has entered into the space under scale 0. So with the liquid spreading, r3 > r0and > 0. points to the left side of the drop and will drive the drop liquid to move left. When the droplet liquid totally fills the space between scale 2 and scale 3, this part of droplet liquid will merge with the main droplet. Thus the hinge effect of scale 2 will be overcome and the whole droplet will move to the left (Fig. 5c). This hypothesis is supported by the observed phenomenon that the drop showed a obvious movement when the space between scale 1 and scale 2 was filled (Fig. 3b, from 20.26 s to 20.27 s). The drop also could overcome the hinge effect of the scale 3 by the same way (Fig. 5d). The droplet thereby moves continuously along the scale-by-scale array surface of the spine.
The subsequent drops with fast moving velocity are mostly attributed to the ultra thin liquid film on the scale-covered spine left by the first drop. In fog atmosphere, the direction of the fog flow is vertical to the spine, water will form on the surface of the tiled scale and not easily form under the scale, so in high humidity the channels are not totally wetted and the first droplet encounters high surface adhesion. After the past of the first droplet, the splayed capillary micro-tube makes part of the drop liquid trapped in it by capillary force, thus all the liquid trapped in the capillary micro-tube arrays forms a liquid film on spine surface benefiting from the discontinuous scales (Fig. 5d). The liquid film leads to a more hydrophilic spine surface, which greatly decreases the surface contact angle hysteresis35,36,37. When the subsequent drop is formed on the surface, the unbalanced surface tension force produced from the contacting angle difference between the opposite sides of the drops and the Laplace pressure difference resulting from the liquid curvature disparity cooperatively initiate the directional drop transport. Benefiting from the low friction force, the sequent drop could move more quickly. To confirm the lubricant effect of the liquid film, we imbued the bottom part of the spine in water and found the drop moves much fast on liquid-film area (see Fig. S8), which is a strong support for our theory. Directional droplet transport could renew the surface effectviely19 and this is beneficial for the continuous formation of droplets, hence materials with fast directional droplet transport ability would have a high efficiency in fog collection.
In summary, a kind of scale-covered cactus spine could transport droplet spontaneously and quickly. The asymmetric splayed capillary channel arrays formed by the scales on the spine surface provide the initial propulsion for the drop motion. The trapped liquid left by the first droplet in the splayed tubes contributes to the low friction force of the surface and then the following droplets can move more quickly. Our works find a novel way to transport droplets spontaneously and quickly with liquid trapped in the surface structure acting as the lubricant. This finding is helpful to design artificial cactus spines to develop a fast water transport system without additional energy. It also provides us with an applicable way to prompt the liquid-transferring efficiency on interfaces of materials38.
How to cite this article: Liu, C. et al. Effective directional self-gathering of drops on spine of cactus with splayed capillary arrays. Sci. Rep. 5, 17757; doi: 10.1038/srep17757 (2015).
Zheng, Y. M. et al. Directional water collection on wetted spider silk. Nature 463, 640–643 (2010).
Parker, A. R. & Lawrence, C. R. Water capture by a desert beetle. Nature 414, 33–34 (2001).
Ju, J. et al. A multi-structural and multi-functional integrated fog collection system in cactus. Nat. Commun. 3, 1247–1247 (2012).
Bai, H., Ju, J., Zheng, Y. M. & Jiang, L. Functional Fibers with Unique Wettability Inspired by Spider Silks. Adv. Mater. 24, 2786–2791 (2012).
Bai, H. et al. Direction Controlled Driving of Tiny Water Drops on Bioinspired Artificial Spider Silks. Adv. Mater. 22, 5521–5525 (2010).
Ju, J., Xiao, K., Yao, X., Bai, H. & Jiang, L. Bioinspired Conical Copper Wire with Gradient Wettability for Continuous and Efficient Fog Collection. Adv. Mater. 25, 5937–5942 (2013).
Hou, Y. P., Chen, Y., Xue, Y., Zheng, Y. M. & Jiang, L. Water Collection Behavior and Hanging Ability of Bioinspired Fiber. Langmuir 28, 4737–4743 (2012).
Bai, H. et al. Large-Scale Fabrication of Bioinspired Fibers for Directional Water Collection. Small 7, 3429–3433 (2011).
Prakash, M., Quéré, D. & Bush, J. W. M. Surface tension transport of prey by feeding shorebirds: The capillary ratchet. Science 320, 931–934 (2008).
Rico-Guevara, A. & Rubega, M. A. The hummingbird tongue is a fluid trap, not a capillary tube. P. Natl. Acad. Sci. USA 108, 9356–9360 (2011).
Zheng, Y. M., Gao, X. F. & Jiang, L. Directional adhesion of superhydrophobic butterfly wings. Soft Matter 3, 178–182 (2007).
Liu, C. C., Ju, J., Zheng, Y. M. & Jiang, L. Asymmetric Ratchet Effect for Directional Transport of Fog Drops on Static and Dynamic Butterfly Wings. ACS Nano 8, 1321–1329 (2014).
Reis, P. M., Jung, S. H., Aristoff, J. M. & Stocker, R. How Cats Lap: Water Uptake by Felis catus. Science 330, 1231–1234 (2010).
Guo, P., Zheng, Y. M., Liu, C. C., Ju, J. & Jiang, L. Directional shedding-off of water on natural/bio-mimetic taper-ratchet array surfaces. Soft Matter 8, 1770–1775 (2012).
Mele, E., Girardo, S. & Pisignano, D. Strelitzia reginae Leaf as a Natural Template for Anisotropic Wetting and Superhydrophobicity. Langmuir 28, 5312–5317 (2012).
Chu, K. H., Xiao, R. & Wang, E. N. Uni-directional liquid spreading on asymmetric nanostructured surfaces. Nat. Mater. 9, 413–417 (2010).
Hancock, M. J., Sekeroglu, K. & Demirel, M. C. Bioinspired Directional Surfaces for Adhesion, Wetting and Transport. Adv. Funct. Mater. 22, 2223–2234 (2012).
Lee, S. G., Lim, H. S., Lee, D. Y., Kwak, D. & Cho, K. Tunable Anisotropic Wettability of Rice Leaf-Like Wavy Surfaces. Adv. Funct. Mater. 23, 547–553 (2013).
Daniel, S., Chaudhury, M. K. & Chen, J. C. Past drop movements resulting from the phase change on a gradient surface. Science 291, 633–636 (2001).
Yao, X. et al. Running droplet of interfacial chemical reaction flow. Soft Matter 8, 5988–5991 (2012).
Khoo, H. S. & Tseng, F. G. Spontaneous high-speed transport of subnanoliter water droplet on gradient nanotextured surfaces. Appl. Phys. Lett. 95, 063108 (2009).
Linke, H. et al. Self-propelled Leidenfrost droplets. Phys. Rev. Lett. 96, 154502 (2006).
Lagubeau, G., Le Merrer, M., Clanet, C. & Quéré, D. Leidenfrost on a ratchet. Nat. Phys. 7, 395–398 (2011).
Marin, A. G. et al. Capillary droplets on Leidenfrost micro-ratchets. Phys. Fluids 24, 122001 (2012).
Dupeux, G. et al. Viscous mechanism for Leidenfrost propulsion on a ratchet. EPL 96, 58001 (2011).
Carroll, B. J. Droplet Formation and Contact Angles of Liquids on Mammalian Hair Fibres. J. Chem. Soc. 85, 3853–3860 (1989).
Chen, J. C. Surface contact – Its significance for multiphase heat transfer: Diverse examples. J. Heat Trans-T Asme 125, 549–566 (2003).
Chaudhury, M. K. & Whitesides, G. M. How to make water run uphill. Science 256, 1539–1541 (1992).
Lorenceau, E. & Quéré, D. Drops on a conical wire. J. Fluid. Mech. 510, 29–45 (2004).
Chen, Y., He, B., Lee, J. H. & Patankar, N. A. Anisotropy in the wetting of rough surfaces. J. Colloid Interf. Sci. 281, 458–464 (2005).
Xia, D. Y. & Brueck, S. R. J. Strongly anisotropic wetting on one-dimensional nanopatterned surfaces. Nano Lett. 8, 2819–2824 (2008).
Xia, D. Y., He, X., Jiang, Y. B., Lopez, G. P. & Brueck, S. R. J. Tailoring Anisotropic Wetting Properties on Submicrometer-Scale Periodic Grooved Surfaces. Langmuir 26, 2700–2706 (2010).
Renvoise, P., Bush, J. W. M., Prakash, M. & Quéré, D. Drop propulsion in tapered tubes. EPL 86, 64003 (2009).
Tsori, Y. Discontinuous liquid rise in capillaries with varying cross-sections. Langmuir 22, 8860–8863 (2006).
Wong, T. S. et al. Bioinspired self-repairing slippery surfaces with pressure-stable omniphobicity. Nature 477, 443–447 (2011).
Anand, S., Paxson, A. T., Dhiman, R., Smith, J. D. & Varanasi, K. K. Enhanced Condensation on Lubricant-Impregnated Nanotextured Surfaces. Acs Nano 6, 10122–10129 (2012).
Zheng, Y., Jiang, L., Wang, J. & Han, D. Extreme “water repellency” on strong water-spreading surface without tilted degree actuation. Appl. Phys. Lett. 93, 094107 (2008).
Liu, J. L., Xia, R., Li, B. W. & Feng, X. Q. Directional motion of droplets in a conical tube or on a conical fibre. Chinese Phys. Lett. 24, 3210–3213 (2007).
This work is supported by the State Basic Research Program of China (2013CB933000), the National Natural Science Foundation of China (21234001, 21473007) and Doctoral Fund of Ministry of Education of China (20121102110035).
The authors declare no competing financial interests.
About this article
Cite this article
Liu, C., Xue, Y., Chen, Y. et al. Effective directional self-gathering of drops on spine of cactus with splayed capillary arrays. Sci Rep 5, 17757 (2015). https://doi.org/10.1038/srep17757
Structure, function and parallel evolution of the bivalve byssus, with insights from proteomes and the zebra mussel genome
Philosophical Transactions of the Royal Society B: Biological Sciences (2021)
New Phytologist (2021)
Journal of Fluid Mechanics (2021)
Enhanced Movement of Two-Component Droplets on a Wedge-Shaped Ag/Cu Surface by a Wettability Gradient
ACS Applied Materials & Interfaces (2021)
Three-Dimensional Multilayer Vertical Filament Meshes for Enhancing Efficiency in Fog Water Harvesting
ACS Omega (2021)