1. Introduction
Nowadays, the scientific community working in this field is perfectly aware that the two-phase nucleate boiling regime is one of the most efficient heat dissipation processes. This regime exhibits a considerably improved heat transfer performance, especially when compared with the single-phase heat transfer procedures. Hence, the two-phase pool boiling is used in a wide variety of purposes and technologies, which require the removal of high heat fluxes, including the cooling and thermal stabilization of high-power electronic components and systems [
1], thermal and nuclear power plants [
2], thermal desalination systems [
3], aviation and space equipment [
4], cryogenic engineering [
5], and thermal management procedures based on the vaporization and condensation cycles using heat pipes, heat exchangers, and thermosyphons [
6]. The pool boiling process depends on a considerable number of factors including the temperature, pressure, and intrinsic thermophysical characteristics of the working fluid, and heating surface morphology and properties. In certain cases, an alteration in one of these factors may lead to serious consequences in the heat transfer behavior and in the nucleate boiling crisis and may even lead to the erosion or corrosion of the equipment in practical situations. These factors are also directly linked with the achievable heat transfer coefficient (HTC) and critical heat flux (CHF) of the boiling system, since they affect the saturation point of the operating fluid, nucleation active sites’ density, nucleation frequency, and postponing of the onset pool boiling. Moreover, the most common strategies to enhance the HTC and CHF are based on the modification of the heating surface, either by changing its morphology through structuring at micro- and nanoscale or by tuning its wettability. In this sense, the first studies examining the nucleate pool boiling heat transfer enhancement proposed, for instance, machining procedures to modify the heating surface [
7], the formation of re-entrant cavities [
8], and porous coatings [
9]. The main conclusion of these approaches was related to increases in the HTC and CHF during the pool boiling process on such surfaces, which were caused by the formation of more nucleation sites and additional vapor trapping in the re-entrant cavities. The fast development of nanotechnologies in the past few years has significantly provided more feasible options for surface modification, especially at nanoscale, which have been explored by various researchers to develop novel processes for boiling performance improvement. All these works demonstrated that the usage of modified enhanced surfaces at nanoscale led to a noticeable heat transfer enhancement caused by the augmented vapor entrapment and thin liquid film evaporation in the pores. Both effects can reduce the surface superheating degree for a given working heat flux. Simultaneously, the stability and durability of the coatings are still relevant concerns, given that they can make difficult, or even impede, the implementation of one surface modification technique in practical applications. Because of this, the search for the most adequate coating configuration and fabrication techniques to improve the boiling heat transfer continues today. Nonetheless, in this direction, Shi et al. [
10] developed a multifunctional aviation aluminum alloy with improved superhydrophobicity and corrosion resistance through a two-step process of etching followed by polymer modification. The superhydrophobicity was achieved after the polymer modification with fluorsilane, and the contact angle increased by about 101° after the etching process. Additionally, the corrosion resistance of the metallic alloy increased by up to 83.2% after etching for 7 min. The authors stated that the superhydrophobic character of the surface appreciably enhanced its liquid repellence, leading to an improved counter corrosion capability. Additionally, this type of surface should be applied in future pool boiling studies. Another possible way to control the heat transfer during the pool boiling process is to alter the wettability of the heating surface [
11]. Particularly, the boiling process on hydrophobic surfaces, with a contact angle superior to 90°, can be characterized by an appreciable decrease in the onset of nucleate boiling (ONB) [
12]. On the other hand, the usage of a hydrophilic heating surface, with a contact angle inferior to 90°, results in an increment in the CHF during the boiling process [
13]. This is the rationale behind the interest of the scientific community recently directed to the utilization of surfaces with heterogeneous wettability, usually designated by biphilic surfaces. Hence, many authors [
14,
15,
16,
17,
18] have performed boiling heat transfer studies on the wettability of heterogeneous heating surfaces to take advantage of the wettability gradient effect by a mixture of hydrophilic and hydrophobic properties. The appeal of biphilic surfaces comes fundamentally from the decrease in the ONB and, at the same time, increase in the HTC and CHF during the pool boiling process. Moreover, Lim et al. [
19] studied the diameter and position of the vapor bubbles by changing the size of the hydrophobic regions on the hydrophilic surface. The researchers found that the bubble departure diameter decreased with decreasing size of the hydrophobic regions, and the CHF increased with decreasing bubble departure diameter. Additionally, Jo et al. [
20] reported that the HTC enhancement on biphilic surfaces was due to the rapid ONB on the hydrophobic regions and the absence of waiting time caused by the remaining vapor bubbles on the hydrophobic regions after the detachment stage. Additionally, Betz et al. [
21] showed that the mixed hydrophilic and hydrophobic surfaces enhanced both HTC and CHF by performing experiments on hydrophilic networks (hydrophilic surface with circular hydrophobic regions) and hydrophobic networks (hydrophobic surface with circular hydrophilic regions). The authors reported that the hydrophilic networks had the best performance in preventing the formation of an insulating vapor blanket. Additionally, Motezakker et al. [
22] conducted pool boiling experiments on hydrophilic surfaces with different hydrophilic to hydrophobic region ratios and found that the optimal ratio was around 38.5%. Furthermore, Sun et al. [
23] studied the boiling dynamics and heat transfer during the pool boiling of biphilic surfaces composed of a silica oxide hydrophilic surface and polytetrafluorethylene (PTFE) rectangular hydrophobic spots. The researchers concluded that the nucleation site density of the biphilic surface was much higher than that of the constitutive homogeneous surfaces. Hence, more than 70% of the hydrophobic spots could be activated with a heat flux of 206 w/cm
2. Additionally, it was confirmed that the bubbles nucleated on the interface of the hydrophobic and hydrophilic regions and, after that, moved into the middle of the hydrophobic regions. Hence, the circular hydrophobic spots played the role of improved active nucleation sites for the bubbles to grow until their departure from the surface. The bubble departure periods scattered between 80 ms and around 1500 ms. Similarly, Xia et al. [
24] investigated the influence of the surface wettability on the bubble formation and motion of superhydrophilic and superhydrophobic homogeneous surfaces, as well as biphilic surfaces with symmetrically arranged superhydrophobic regions in the superhydrophilic base region. The different surfaces were obtained by the surface laser texturing ablation technique and by sililation grafting to obtain superhydrophobic characteristics. The authors reported that the surface wettability had an appreciable role in the bubble formation, growth, and departure. Once again, on the developed biphilic surface, the bubbles spread toward the superhydrophobic region under the driving force provided by the Laplace pressure difference. The vapor bubbles generated on the superhydrophilic region close to the biphilic boundary could be displaced and spread into the superhydrophobic region when the bubbles contacted the superhydrophobic boundary, which in turn induced the horizontal motion of the vapor and surrounding fluid. Moreover, Serdyukov et al. [
25] developed a biphilic surface to improve the pool boiling in a vacuum. They used a sapphire hydrophilic surface and NeverWet
® solution spray-coated hydrophobic spots. The results showed that the biphilic surface provided a significant increase in the number of detached bubbles over time when compared to that of a bare sapphire surface under the same pressure range. It was also reported that, under a pressure of 10 kPa, the bubble departure diameters during the pool boiling of the biphilic surface were six times lower than the ones of the bare hydrophilic surface. Additionally, it was found that for subatmospheric pressures inferior to 39 kPa, the departure frequency of the bubbles increased considerably compared to that using the bare sapphire surface. The results revealed that, in contrast with the bare surface, the boiling curves for the biphilic surface coincide with each other during the pressure variation between 10 kPa and 39 kPa. Moreover, an appreciable near-four-fold HTC enhancement was reported for the biphilic surface compared to the one verified with the bare surface. Recently, Liu et al. [
26] studied the boiling heat transfer in hydrophilic and hydrophobic copper surfaces. The research team found that at low heat fluxes, the HTC of the hydrophobic surface was higher than that of the hydrophilic surface, whereas at high heat fluxes, the opposite took place. The heat transfer capability modification caused by the wettability is due to the bubble growth behavior difference in these surfaces. At low heat fluxes, the bubbles on the hydrophobic surface presented an extended growth period and enlarged diameter at departure, which are features that augment the heat transfer capability since the phase change can continuously proceed. As the heat fluxes increased, the large contact area between vapor and heating surface turned into an obstacle to the heat transfer on the hydrophobic surface; hence, its HTC became lower than that of the hydrophilic surface. Additionally, the large vapor areas on the surface may break the vapor channel, leading to a precocious deterioration of the heat transfer performance. All the mentioned published studies aim to obtain the ideal parametric configuration for CHF enhancement and heat-transfer-improved capability of the biphilic surfaces under pool boiling regimes. Nevertheless, some fundamental issues need further investigation and more complete understanding. This is the reason for the search for an optimal configuration for a biphilic surface that enables a maximum HTC and CHF during the pool boiling process. According to the aforementioned published studies, the influencing factors of the optimal arrangement are mainly the number and location of the superhydrophobic spots, the size of the spots, the pitch between the spots, and the ratio of hydrophobic to hydrophilic areas, which are all factors closely linked with the bubble and vaporization dynamics of the biphilic surfaces. In addition, there are already some publications proposing optimal configurations for biphilic surfaces at atmospheric pressure [
27,
28]. However, the number of published scientific articles concerning the influence of the experimental parameters on the dynamics of the vapor bubbles during the pool boiling of biphilic surfaces is still relatively low. Particularly, factors such as the nucleation frequency of the bubbles and their departure diameters remain somewhat poorly understood. Once again, it should be emphasized further comprehensive research in this field using modern measuring techniques is required. Furthermore, more studies are required on the pool boiling processes of biphilic surfaces that use nanofluids, such as the one by Kamatchi and Venkatachalapathy [
29]. Additionally, some practical applications in the electronics cooling field using heat exchangers, such as the one described by Kannan and Kamatchi [
30], should be further addressed. Accordingly, the current experimental work’s goal is to study the effect of different configurations of a biphilic surface composed of a hydrophilic stainless-steel foil and Neverwet™ spray formulation producing superhydrophobic spots on the heat transfer performance during water pool boiling at atmospheric pressure. The aim is to obtain the optimum diameter of the superhydrophobic arrangements in the biphilic surfaces, which enables the general amelioration of the pool boiling characteristics and the CHF enhancement. This work intends to contribute a parametric study for nucleate boiling heat transfer enhancement. Additionally, it suggests further research studies with the use of nanofluids and nanoscale superhydrophobic regions.
Figure 1 shows some of the parameters and forces involved in the nucleation and growing of a symmetrically shaped bubble in a superhydrophobic region.
3. Results and Discussion
One of the main objectives of the present work was the production of biphilic surfaces with only one superhydrophobic region with a variable diameter. This procedure resulted in a more accurate evaluation of the bubble dynamics. We also intended to develop superhydrophobic spot matrixes with a diameter of less than 1 mm. First, we evaluated the dynamic behavior of the bubbles.
Figure 5 presents the different stages of the development of the bubbles generated in the largest tested circular superhydrophobic region with a diameter of 5.2 mm. The figure shows the high-speed images of the fundamental evolution stages of a bubble from its nucleation to its departure from the heat transfer surface: the nucleation stage, hemisphere formation, vertical elongation, departure beginning, necking, and departure or detachment from the heating surface. On the first image on the left, the bubble is at the early nucleation stage after the departure of the preceding bubble, and the corresponding nucleation waiting time is 5 ms. As seen in the second and third images, the bubble formed a hemisphere, which is vertically elongated in the two following Images. This effect is due to the prevalence of the impulsion forces over the adhesion forces present. It should be noted that the growing of the bubble is restricted to the superhydrophobic region and, consequently, the relative weight of the surface tension forces can be attributed to the geometry and size of that region. Additionally, the boundary region between the hydrophilic and superhydrophobic regions of the biphilic surface also has a considerable influence on the set of the forces present. In the period between 1200 ms and 1225 ms, the departure of the bubble started, and the surface tension forces promoted the necking of the base of the bubble, which gradually developed until the departure of the bubble. On the two following images corresponding to 1260 ms and 1270 ms, the departure of the bubble is eminent, with only a small connection between the base of the bubble and its upper part, resulting from a sharp necking. This necking of the base of the bubble promotes, by the vapor mass conservation law inside the bubble, an acceleration of the vapor to the zone of the bubble, which results in a complete detachment of the bubble from the heating surface. At the moment of departure, 1280 ms, a vapor layer was left behind on the superhydrophobic region. This time evolution of the bubble is consistent with findings reported by Teodori et al. [
33]. It is also proper to state that the last stages of the evolution of the bubble were carried out in a very short period, 80 ms, as compared to the total time required for the nucleation and development of the bubble. The vapor mass left deposited on the heating surface may be due to the fact that in the superhydrophobic region, there is no solid–vapor–liquid surface tension component that favors the detachment of that vapor mass from the surface. Hence, and considering that the nucleation of a bubble in a superhydrophobic region can occur at a temperature between 1 °C and 3 °C higher than the saturation temperature, the fast nucleation and coalescence of microscale bubbles produces a continuous vapor film over the superhydrophobic region. These mechanisms were also detailed by Malavasi et al. [
34] and Teodori et al. [
35].
In sum, the bubble diameter is constrained by the diameter of the circular superhydrophobic spot, growing up to the limit of the boundaries between the superhydrophobic spot and the remaining hydrophilic surface. Additionally, given that there are no surface tension forces acting on the superhydrophobic spots contributing to the detachment of the bubble, these forces mainly act at the boundary of the superhydrophobic spots. Therefore, for smaller superhydrophobic spots, the necking occurs earlier, and the departure frequency of the bubbles increases. As the bubble detaches from the heating surface, the superhydrophobic spots are instantly covered by a new vapor layer, and there is no quenching promoted by the rewetting of the liquid on the superhydrophobic spots. Nevertheless, the liquid in the larger hydrophilic region may flow, promoted by the bubble departure and coalescence processes. Moreover, the bubble departure frequency and the bubble diameter are affected by the balance between the adhesive forces related to the surface tension at the boundary of the superhydrophobic spots and the buoyancy forces, which are also linked to the size of the superhydrophobic spots. The balance of the forces in play may affect the interaction or coalescence of the vapor bubbles and, consequently, contribute to the latent heat of evaporation and induced heat transfer by convection. Additionally, we observed a larger bubble departure diameter in the larger superhydrophobic areas, which can be explained by the fact that in these larger areas, the surface tension forces act only in the boundary of the superhydrophobic/hydrophilic regions. Hence, the bubble grows freely in the superhydrophobic spot, and the surface tension forces can also act at later growth stages, delaying the detachment of the bubbles. Furthermore, it should be noted that it has already been demonstrated that the superhydrophobic regions attract the vapor, thus contributing to the onset of nucleate boiling just 1-3K above saturation, as reported by Malavasi et al. [
34] and Teodori et al. [
35]. Hence, the superhydrophobic regions act as nucleation sites, where boiling starts just 1-3K above saturation. The maximum superheating values obtained for the range of imposed heat flux and for the configuration used here are of the order of 4K–8K (e.g., [
14,
32]). Furthermore, the bubbles stay constrained inside the hydrophobic regions, as observed in the present work. Nonetheless, it can be stated that the superheating at the boiling surface can affect the shape and dynamics behavior of the vapor bubbles. A high superheat may lead to the formation of large and unstable bubbles, which are more difficult to control than smaller bubbles. The general effects of an increased superheat on the shape and behavior of the bubbles in film boiling are influenced by several factors such as the geometry of the heat transfer surface, thermophysical properties of the operating fluid, and the specific superheating conditions. At high superheats, the bubbles present irregular shapes, which can affect the heat transfer capability of the system and the behavior of the vapor film. Moreover, at high superheats, a second bubble of small size is formed immediately after the detachment of the first bubble. After that, a third bubble of small size is formed, and after a very small fraction of time, the first and second bubble coalesce and merge into a larger bubble. This one detaches from the surface, and a new bubble with the same dimension is formed as the third one detaches from the surface. This bubble dynamics pattern continues with the detachment of more bubbles, disturbing the vapor film and leading to an enhanced heat transfer capability. At high superheats, a large amount of vapor is generated, and the bubbles burst with different sizes, forming a vapor blanket over the heating surface, inducing film boiling or Leidenfrost boiling. Additionally, the high values of the superheat lead to the rapid formation of vapor, which causes the attachment of the bubbles to the vapor blanket. In addition, the increase in the superheat implies an increase in the bubble detachment frequencies. Superheating plays a very important role in augmenting the frequency of the detachment of the bubbles, thereby increasing the heat flux. The imposed heat flux vs. superheat curves for the hydrophilic region and superhydrophobic region, with a diameter of 5.2 mm, of the biphilic surface are presented in
Figure 6.
The heat flux was controlled and kept at low values, always in early stages of nucleate boiling so that bubbles only appeared on the superhydrophobic region and nowhere else. That is the purpose of using the superhydrophobic region in a biphilic surface. It can be observed from the plot in
Figure 6 that for heat fluxes values lower than 1300 w/m
2, the superheat of the hydrophilic region and that of the superhydrophobic region were practically the same. In the case where the imposed heat flux was higher than 1300 w/m
2, the superhydrophobic region exhibited a higher superheat than that of the hydrophilic region. This occurs due to the continuous presence of vapor in the superhydrophobic region right after the onset of boiling. This effect, which has been widely reported in the literature, including our previous works, assures that the superhydrophobic region is the nucleation site and that there is no nucleation in other unwanted and stochastic places. Playing with their location is then possible by pumping fresh fluid into the hydrophilic region as the bubbles leave the surface, keeping the overall superheat values low (which is beneficial for cooling purposes). Hence, for heat fluxes superior to 1300 w/m
2, the presence of the superhydrophobic region enhances the heat transfer capability, which is the main reason for the enhanced heat transfer when using superhydrophobic heating surfaces or biphilic surfaces. Due to the early-onset nucleate boiling and this superheat, bubbles were restricted to hydrophobic regions, and if we put then in a pattern, as the bubbles left these hydrophobic regions, they did not coalesce or coalesced far away from the surface, enough to promote the pumping of fresh fluid into the hydrophilic region, so the biphilic surface had a higher heat flux for a low superheat (we see that only the superhydrophobic region increased the superheat, but overall in low values). Nevertheless, if the heat flux is excessive, one observes an increased bubble coalescence, and a vapor film forms in both superhydrophobic and hydrophilic regions, limiting the flow of fresh fluid and, consequently, leading to a reduction in the heat transfer coefficient compared to that of a bare homogeneous hydrophilic surface. This effect is in agreement with that previously reported and clearly shown in [
36]. The following figures show the plots of the evolution of the bubble dynamics’ influencing parameters of biphilic surfaces with a single superhydrophobic spot. For the acquisition of the plots, we applied a crescent electric current between 3A and 9A, thus obtaining the different heat fluxes between 0.03 W/cm
2 and 0.22 W/cm
2. In the X axis of the first set of plots, we used the nondimensional time
t* given by Equation (2):
where
t is the time and
tmax is the maximum time required for the bubbles to reach their maximum base diameter for each value of imposed heat flux. This nondimensional time
t* is used to minimize the discrepancies in the obtained frequencies for each case. It is also worth mentioning that the curves of the plots are the result of the average of at least four repeated experiments for applied current intensities of 3A, 5A, 7A, and 9A, which correspond to heat fluxes of 0.03 W/cm
2, 0.07 W/cm
2, 0.13 W/cm
2, and 0.22 W/cm
2. Thereafter, we present the results according to the influencing factors of the bubble dynamics of biphilic surfaces with a single superhydrophobic spot. The superhydrophobic spots had the following diameters: 0.8 mm, 1.3 mm, 2.4 mm, 3.6 mm, 4.4 mm, and 5.2 mm. The analyzed parameters were the contact angle, base of the bubble diameter, maximum bubble diameter, centroid height, and volume of the bubble.
Figure 7 illustrates the evolution of the contact angle as a function of the non-dimensional time. From
Figure 7, it is possible to confirm that the contact angle of the generated bubbles decreased with the decreasing superhydrophobic spot diameter. For instance, the superhydrophobic region with a diameter of 1.3 mm generated bubbles with contact angles inferior to 70°, whereas the 5.2 mm-diameter region formed bubbles with contact angles equal or superior to 110°. It can also be verified that in the early growing stages of the bubbles, the decreasing of the contact angle was less pronounced in the superhydrophobic spots with larger diameters. This was likely due to the slower enlargement of the diameter of the bubble occurring in the larger superhydrophobic spots. The contact angle evolution was determined by the balance between the impulsion forces and the surface tension forces. In the absence of the surface tension component, which contributes more to the necking stage of development, the bubbles generated in the larger superhydrophobic regions tended to keep growing without any restriction, along with their base diameter. In the earliest stage of the formation of the bubbles, the contact angle inside the bubbles was near 140°. This angle decreased sharply as the bubbles grew until a gradual stabilization occurred, which began at
t* = 0.25 during the hemisphere-like growing. The contact angle remained almost constant until
t* = 0.85, which marked the beginning of the departure stage of the bubbles. After this time value, the contact angle increased gradually. When the contact angle surpassed 90°, the necking of the base of the bubble commenced and the angle increased significantly in a very short time. At the moment of the complete detachment of the bubble from the heating surface, the contact angle again reached 140°. The evolution of the contact angle of the bubbles was not affected by the heat flux and exhibited some similarity with the evolutions reported for a hydrophilic surface by Phan et al. [
37], and those recently reported for a superhydrophobic surface by Teodori et al. [
33]. On the one hand, the verified stabilization plateau during a long period had already been reported by Teodori et al. [
35]. At this stage, the growing of the bubble was promoted only by the vapor layer produced in the superhydrophobic region and not by the solid–vapor–liquid surface tension in the perimeter of the superhydrophobic region and at the boundary with the hydrophilic region. On the other hand, at the initial and final stages of the growing evolution of the bubbles, these are subjected to the surface tension at the interface between the hydrophilic and superhydrophobic region and, consequently, the involved mechanisms are comparable with the ones observed at the same stages for bubbles generated in hydrophilic surfaces by Phan et al. [
37]. Nevertheless, the bubbles which were generated in the smaller superhydrophobic region with a diameter of 0.8 mm displayed the smoothest contact angle evolution, with a difference of only about 10° between the angle of the early growing stage and the departure, indicating the slowest bubble growing rate of all the tested superhydrophobic regions. The noise in the spectral lines is associated with the processing mode of the developed MATLAB algorithm, as well as with some instability and oscillation of the bubbles during their growing. As already reported by Teodori et al. [
35], the instability may be the result of three distinct effects. The first one is related to the upward impulsion forces along with the successively lower surface tension forces, which make the bubbles more prone to suffer instabilities from the vapor layer formed at the surface. The second effect is the alteration in the size of the bubbles, which is promoted by the vapor transport between the produced vapor layer and the bubbles. The last one derives from the slowness of the growing process of the bubbles, making them more sensitive to local pressure variations. The second possible effect is less likely to occur in the present situation, since this effect is primarily observed when the vapor layer is much larger than the bubble. In addition,
Figure 8 shows the mean base diameter evolution of a generated bubble over time.
The plot in
Figure 8 shows that the base diameter of the bubbles reached its maximum when the bubbles totally occupied the corresponding superhydrophobic regions. These results are consistent with the findings of published studies, suggesting that the base diameter of the bubbles is closely related to the area of the superhydrophobic region [
38]. It can be stated that the base of the bubbles is confined to its corresponding superhydrophobic region, which is consistent with the reported results, for instance, by Teodori et al. [
35]. However, after the vertical elongation stage in the smaller superhydrophobic regions, the bubble grows radially and reaches a dimension that is higher than that of the base. This fact is not noticeable in the larger superhydrophobic regions. Nevertheless, it is possible to verify that the base diameter has its lowest values at the beginning and at the end of the bubble nucleation process, and this effect is more noticeable in the case of bigger bubbles. In addition, in our experiment, the base diameters of the bubbles in all superhydrophobic regions underwent an initial increase until they momentarily stabilized in a near-plateau region. After that, the base diameters decreased in the final stages of the development of the bubbles until the detachment of the bubbles from the heat transfer surface. The period that the base diameter stayed approximately constant increased as the size of the superhydrophobic region decreased. It is also possible to verify from this plot, as well as from the plot in
Figure 9, that the larger the size of the bubble, the bigger the plot line noise. This is likely due to the interference of the preceding bubble in the case of the bigger bubbles. This effect is somewhat attenuated along the development of the new bubble.
Figure 9 depicts the mean evolution of the maximum diameter of the bubble over time. This figure shows, in detail, the marked difference in the maximum diameter evolution for the superhydrophobic regions with distinct diameters. It is possible to verify that for the larger superhydrophobic regions, the almost-linear increasing trend in the maximum diameter of the bubbles is gradually replaced by a trend like that of the base diameter evolution over time, which is depicted in
Figure 7. The maximum diameter of the bubbles progressively increased and reached, or even surpassed, the value of the corresponding base diameter in the hemispheric growing stage around
t* = 0.4 for all the superhydrophobic regions. The slope of the curves seems to be approximately constant until the stages before the departure of the bubbles. The departure can be identified by the steeper decrease in the maximum diameter at around
t* = 1. Additionally, the bubbles had their biggest enlargement in the smallest superhydrophobic circular region with a diameter of 0.8 mm, where the mean maximum diameter reached 2.5 mm, which is more than three times greater than the diameter of the corresponding superhydrophobic region.
For both the 0.8 mm- and 1.3 mm-diameter superhydrophobic regions, the maximum diameter of the generated bubbles surpassed the diameter of the region even before
t* = 0.25. Additionally, in these regions, the maximum diameter of the bubbles increased linearly until their departure from the heating surface. Moreover,
Figure 10 presents the evolution of the ratio between the maximum diameter of the bubble and its base diameter according to the diameter of the superhydrophobic regions. Though the bubbles that were generated in the larger superhydrophobic regions had larger diameters, it can be confirmed that the ratio between the maximum diameter and the base diameter decreased with the increasing diameter of the superhydrophobic regions. The observed trend suggests that the larger superhydrophobic regions do not necessarily potentiate the transfer of more evaporation mass over time. This fact, together with the departure frequency of the bubbles, determines the amount of latent heat dissipated from the heating surface. Adding the experimental results of two more superhydrophobic regions of 1.5 mm and 2.6 mm diameters, it is possible to observe an exponential trend line.
Furthermore, in the plot in
Figure 11, we can observe the mean evolution over time of the centroid height of the bubbles at the departure stage. We noticed a linear increase in the centroid height of the bubbles until a nondimensional time of 0.85 for all the evaluated superhydrophobic regions. For time values superior to 0.85, all the curves adopted an exponential progress until the departure of the bubbles from the heating surface. In fact, in the necking stage, the height of the geometrical center of the bubbles grew exponentially during the short period of 0.95 <
t* < 1, until the departure of the bubbles took place. Moreover, the height of the centroid at the departure stage had an average value of 3.5 mm. It was also verified that the height of the centroid evolution was independent of the imposed heat flux value.
As expected, the values of the height of the centroid of the bubbles at departure were higher for the bubbles nucleated in the larger superhydrophobic spots. However, there were some inconsistent centroid height values during the formation of the bubbles in the different superhydrophobic regions. These discrepancies may have arisen from the developed MATLAB code. The plot in
Figure 12 presents the evolution over time of the mean volume of the bubbles.
The plot in
Figure 12 clearly shows distinct tendencies in the variation in the mean vapor volume of the bubbles over time, according to the different sizes of the studied superhydrophobic regions. In the larger regions, bigger bubbles with larger base diameters formed, and consequently, they had higher mean volume values in each stage of their generation. It can also be stated that there was a considerable increase in the slope of the curves with the increasing diameter of the superhydrophobic spots. Hence, there was an appreciable difference of around 140 mm
3 between volumes of the bubbles at the departure stage, which were naturally higher for the superhydrophobic spots, with larger diameters and steeper curve slopes. For values of
t* superior to 0.85, we observed a marked instability in the trend lines of the evolution of the volume of the bubbles generated in all the superhydrophobic spots. This instability may be derived from the convective streams inside the boiling chamber, which affected the bubbles with special emphasis at the necking stage when their connection with the surface was more fragile. The necking stage also enhanced the flow effects induced by the convective streams, given that apart from the base necking, the diameter of the bubbles reached its maximum in this final growing stage. Additionally, the next two plots are relative to the comparative evolution of the departure frequency of the bubbles and evaporation mass transfer rate according to the heat flux. The plot in
Figure 13 exhibits an increasing mean departure frequency of the bubbles with increasing heat flux. This trend is almost linear for all the evaluated superhydrophobic regions. The smaller superhydrophobic spots naturally promoted the departure of bubbles with smaller diameters, thus enabling higher departure frequencies of the bubbles. In the superhydrophobic region with the smallest diameter, 0.8 mm, the mean departure frequency of the bubbles reached a value superior to 2.5 Hz, whereas the departure frequency in the superhydrophobic region with the largest diameter, 4.4 mm, was of only around 0.25 Hz. In the latter case, we also noticed an increase in the departure frequency that was higher than that expected. Indeed, for heat fluxes superior to approximately 0.15 W/cm
2, the mean departure frequency of the bubble generated in the corresponding superhydrophobic spot was higher than the one of the smaller spot with a 3.6 mm diameter. This tendency may be derived from the eventual pressure and temperature fluctuations inside the pool boiling chamber. It should be noted that for a heat flux of 0.03 W/cm
2, corresponding to an applied electric charge of 3A, it was not possible to observe any bubble nucleation in the largest superhydrophobic region, which indicated that this value of heat flux was still too low to assure a stable bubble nucleation.
It is of relevance to determine the evaporation mass transfer rate of each biphilic surface, given that this parameter is closely linked with the latent heat fraction that can be removed from the heating surface in pool boiling scenarios. In fact, the mechanistic models proposed by Kurul and Podowski [
3], for instance, mention that the total heat flux dissipated in pool boiling results from the following fundamental factors: (i) natural convection before the nucleation of the bubbles, (ii) latent heat removed from the surface resulting from the liquid mass evaporation, and (iii) the convection induced by the cooler liquid motion provoked by the displacement of the bubbles during the final stages of development and departure. This last factor can be promoted by the interaction between the bubbles and the nucleation active sites. The evaporation mass transfer rate in each superhydrophobic region can be found using Equation (3):
where
is the evaporation mass per unit of time,
ASHF is the area of the superhydrophobic region,
ρv is the vapor density,
f is the departure frequency of the bubbles,
Vb is the estimated volume of the bubble, estimated by a spherical approach using the diameter of the bubble at departure, and
Φ is the diameter of the superhydrophobic region. The trend displayed in the plot in
Figure 13 is more pronounced in the plot in
Figure 14. In the latter, it is possible to observe that the superhydrophobic region with the smallest diameter, 0.8 mm, presented an evaporation mass transfer rate appreciably higher than the rest of the superhydrophobic regions. Therefore, the superhydrophobic region with smaller dimensions was the one that displayed the best performance and the largest contribution to the latent heat fraction that can be removed from the heating surface.
Additionally, the linear progress in the plot for each superhydrophobic region confirms the general trend in the evolution of the evaporation mass transfer rate per unit of area according to the heat flux. Hence, the evaporation mass transfer rate decreased with the increasing area of the superhydrophobic regions. For instance, with an imposed heat flux of 0.22 W/cm
2, the superhydrophobic region with a 0.8 mm diameter presented an evaporation mass transfer rate of around 2.6 × 10 g/s.cm
2, which was ten-fold superior to that of the superhydrophobic region with a 2.4 mm diameter. Therefore, in this case, a nine-fold decrease in the superhydrophobic region represented a ten-fold increase in the evaporation mass transfer rate. It can be concluded that the superhydrophobic region with the smallest diameter, 0.8 mm, had the most effective heat transfer area, given that it optimized the evaporation mass transfer rate per unit of area, producing proportionally more vapor than the larger superhydrophobic regions. Although the respective plot is not included in the current work, we also performed a surface temperature evolution over the superhydrophobic regions in the function of the nondimensional position x* in the central axis of the base of the bubble. The plot was obtained at a
t* of 0.5 and a current intensity of 9A. An analysis of the plot representing the surface temperature evolution showed a decrease in the surface superheating and in the integral temperature oscillations with the decreasing diameter of the superhydrophobic region. This fact reflects the improved uniformization of the temperature of the surface, along with an enhanced stabilization of the nucleate pool boiling in the smaller superhydrophobic regions. In essence, in accord with the results reported by Pontes et al. [
14] and in view of the obtained results, it can be concluded that the bubble dynamics are directly influenced by the dimensions of the superhydrophobic spots, mainly because of the effect of the surface tension forces at the boundaries between the hydrophilic base region and the superhydrophobic spots. Moreover, the temperature differences were also found to be greater at the interfacial boundaries between the hydrophilic and superhydrophobic regions and, hence, the smaller superhydrophobic regions promoted increased evaporated mass fluxes, increasing the heat fluxes closely linked with the latent heat of evaporation. Considering these facts, the ideal biphilic surface arrangement should exhibit extremely small, millimetric or even micrometric, superhydrophobic spots, which have been demonstrated to achieve higher mass evaporation values in comparison with larger superhydrophobic regions. Additionally, concerning the distance between the superhydrophobic spots, it is recommended to conduct further in-depth experimental works involving influencing factors such as the above-mentioned temperature gradients and the bubble departure dynamics, which promote the flow of the cold liquid in the spaces between the superhydrophobic regions. Nonetheless, the superhydrophobic spots should exhibit enough interspacing to avert the coalescence of the bubbles. If the superhydrophobic spots are not separated by a distance greater than the diameter of the bubbles, as reported by Pontes et al. [
32], the bubbles interact and coalesce, forming a bridge between the vapor layers, and, hence, insulating the heat transfer surface between the spots and provoking the deterioration of the pool boiling heat transfer performance.