Next Article in Journal
Wettability of DPPC Monolayers Deposited from the Titanium Dioxide–Chitosan–Hyaluronic Acid Subphases on Glass
Next Article in Special Issue
Anomalously Slow Dewetting of Colloidal Particles at a Liquid/Gas Interface
Previous Article in Journal
Adsorption and Decomposition of Peroxides on the Surfaces of Dispersed Oxides Fe2O3, Cr2O3 and V2O5
Previous Article in Special Issue
Facile Fabrication of Multifunctional ZnO Urchins on Surfaces
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Wetting and Spreading of Commercially Available Aqueous Surfactants on Porous Materials

1
Department of Chemical Engineering, Loughborough University, Loughborough LE11 3TU, UK
2
Proctor and Gamble Ltd., 1853 Grimbergen, Belgium
*
Author to whom correspondence should be addressed.
Colloids Interfaces 2019, 3(1), 14; https://doi.org/10.3390/colloids3010014
Submission received: 5 December 2018 / Revised: 11 January 2019 / Accepted: 17 January 2019 / Published: 21 January 2019
(This article belongs to the Special Issue Wetting on Micro/Nano-Scale: From Fundamentals to Application)

Abstract

:
The wetting properties of aqueous solutions of a commercially available surfactant at various concentrations on porous media are investigated using the KRUSS DSA100 shape analyzer and the ADVANCED software to process the data. Time evolution of both the contact angle and drop base diameter at each surfactant concentration after deposition were monitored. Three different porous substrates (sponges) were examined. The sponges used were a car sponge, dish sponge and audio sponge. The sponges were investigated both dry and at different degrees of saturation, that is, the amount of water absorbed into the sponge. It was found that pure distilled water droplets deposited on the dry porous media showed non-wetting. However, if droplets of surfactant solutions were deposited, then a change to a complete wetting case was found at all surfactant concentrations used. It has been observed that for all sponges, no matter the degree of saturation, they display a minimum contact angle after which the droplet is rapidly absorbed into the porous media.

1. Introduction

The wetting and spreading of aqueous surfactant solutions over porous materials is currently used in a wide range of applications (shampoos, sponges, cleaning, application of drugs on skin and hair) and in near infinite examples in the natural world, from the absorption of water through the xylem of plants, to allowing insects to move on the surface of water.
Scientific interest in wetting and spreading behaviour has increased exponentially in recent years, primarily due to the expanding range of medical and biological science, and environmental engineering applications [1], for example, maintaining biodiversity in soil ecology [2]. Much of the experimental research and theory published related to contact angle characteristics has focussed on smooth and homogenous substrates. In such cases, when a liquid is deposited on the solid’s surface, the three-phase dynamic contact angle will reach an equilibrium value in accordance with Young’s equation [3,4]. Dynamic contact angles and hysteresis have been extensively investigated, and the general consensus is that for impermeable solids, contact angle and spreading behaviour depend on the degree of surface roughness, heterogeneity and hydrophobicity [5]. For example, rough surfaces effectively have multiple barriers to liquid spreading.
More recently, investigations into the wetting properties of porous media specifically have become more prominent. The latter is because numerous real-world substrates exhibit a porosity throughout their structure, or have a thin porous sub-layer [6]. These include sponges, filters and biomedical tissue scaffolds. It has been highlighted that the mechanism for the wetting and spreading of liquids on porous substrates differs from non-porous solids because two competing processes of surface spreading and imbibition into porous substrate are occurring simultaneously. There have been some successful attempts to develop hydrodynamic models for spreading over both dry and saturated porous substrates [6], using Brinkman’s equations [7] to predict inter-porous layer flows. Other theoretical works of the spreading, wetting and dewetting have been conducted by Bonn et al. [8] and Dietrich et al. [9], and the wetting of real surfaces has also been investigated by Bormashenko [10].
The research below is focussed on characterising the wetting and spreading behaviour of droplets of aqueous surfactant solutions using commercially available surfactants deposited on porous substrates under different degrees of saturation. The latter process is of great interest for multiple industries for understanding how surfactant products interact with porous media. For example, in enhanced oil recovery, where surfactant solutions are used to extract oil or gas, the rocks where the oil/gas is located are usually porous. The relationship between contact angle characteristics and foam production is significant when assessing the conditions in which the surfactant products are most effective.
The influence of surfactants on wettability is well understood; however, it has also been established that employing surfactants to enhance spreading on solid porous substrates substantially modifies the wetting process [4,11,12]. The rate of surface spreading increases as the surfactant concentration increases [4] on a smooth homogeneous surface; however, it could be more complicated in the case of spreading over porous materials. It is easy to distinguish between complete and partial wetting in the case of smooth homogeneous substrates: in the case of complete spreading, the final contact angel tends to zero over time, while in the case of partial wetting the droplet stops after reaching a static advancing contact angle, which is different from a zero value [1]. However, a definition of complete and partial wetting in the case of spreading over a porous substrate is not so straightforward and has been given in [1]. In the case of partial wetting (Figure 1), there are three stages of spreading/imbibition of droplet over porous substrate: (i) during the first stage the droplets spread out until the maximum radius of droplet base, Lad, is reached at moment tad; during this stage the contact angle decreases until the static advancing contact angle, θad, is reached at the same moment tad; (ii) during the second stage, which lasts from tad to tr, the droplet base does not change but the contact angle decreases linearly from the static advancing contact angle θad to static receding contact angle θr; (iii) during the third stage the contact angle remains constant and equal to the static receding contact angle, while the droplet base decreases until the complete penetration of the droplet at t* (Figure 1).
In the case of complete wetting, the spreading behaviour is different from the partial wetting case (Figure 2). In this case: (i) stage 2 is absent, (ii) the duration of the stage 1 is much longer, and (iii) the constancy of the contact angle over the duration of stage 3 is only approximately satisfied [1].
Common sponges such as those studied below are often made of polyester and other polymers. They have a soft porous structure, allowing them to be easily compressed to absorb liquids. The wettability of sponges is an important factor that can vary between synthetic sponges. Other important properties include structural properties such as porosity and pore size.

2. Materials and Methods

2.1. Preparation of Surfactant Solutions

A commercially available surfactant solution is used during the investigation, wherein a serial dilution was carried out for 0–100% (w/w). The CMC point of the commercial surfactant was found to be 0.2% and the concentration of all solutions used was above CMC. The surface tension was constant and equal to 25 mN/m.

2.2. Experimental Apparatus

The wetting data (contact angle and spreading diameter) were collected using a KRUSS (Hamburg, Germany) DSA100 drop-shape analyser.
It was operated via a purpose-designed ‘ADVANCE (KRUSS software, Hamburg, Germany)’ interfacial software package.

2.3. Sponge Characteristics

Three porous sponge types were tested: a dish sponge (Spondex(France) Washup sponge), a car sponge (Tesco (Hertfordshire, England) car sponge) and an audio sponge (used in sound proofing, Basotect acoustic foam). The sponges used in this investigation are made out of 100% polyester; they are all soft, approximately 3–4 cm in height, and swell slightly when water is absorbed. The contact angle of distilled water was found to be 128.9° ± 2.8° on the dish sponge and 106.9° ± 2.1° on the car sponge; that is, both sponges show non-wetting behavior. The audio sponge completely absorbed the water droplet immediately after deposition.
A scanning electron microscope was used to analyse the pore characteristics of each type of sponges; the porosity was calculated using Matlab (Massachusetts, U.S.A.) by comparing the total area of the image to the combined area of the dark contrast pores. The results of this study are presented in Table 1, which shows that all three sponges have similar porosity but the pore size is smaller in the audio sponge as compared with the dish and car sponges.

2.4. Dry/Wet Sponge

All three sponge samples used (see below) were cut into uniform cylinders using an aluminium cutting tool. A 10–100 µL ‘Finnipipette’ micropipette was used to deposit droplets of surfactant solution (approx. 40 µL) onto a sponge sample placed on the platform in the KRUSS device. Once the droplet had been fully absorbed into the sponge, the recording was stopped, and the recorded data were exported to Microsoft Excel for analysis. When recording liquid droplets on sponges that were fully or partially wetted, there was an additional preparatory phase arranged. First, a beaker of distilled water was filled and weighed. A cylinder of the sponge sample being tested was thoroughly soaked in the distilled water. The beaker of water was then weighed again. The difference between the initial and final measurements equated to the mass of water contained within a fully saturated sponge sample. This information could then be used to create sponge samples of known percentage saturation (in this case 10% and 50%), by weighing out fractions of the saturated mass of water and using a dry sponge to soak the water onto the sponge surface. The amount of water used was 30 g for complete saturation; this was the amount of water observed to completely saturate the sponge without drainage being observed. The data recording technique was the same as for a dry sponge.

3. Results and Discussion

Initially the droplet dynamics of pure water on each of the sponge types was investigated to identify the relative degrees of hydrophobicity. In Figure 3 the obtained time dependencies of contact angle and droplet base, determined in the case of the dry dish sponge, are presented. For the dish sponge (Figure 3), it is evident that the initial contact is high, at approximately 116°. The contact angle reduces quite rapidly during the first 30 s. Mirroring this, the droplet base diameter increases quickly as the water begins to spread. This stage is followed by the second stage, when the contact angle decreases linearly, while the droplet base remains constant. Comparison of the data presented in Figure 3 shows that the case under consideration corresponds to the partial wetting. However, we did not reach the third and final stage, when the contact angle reaches the static receding value. The droplet is still very stable on the surface after 5 min has passed, with a contact angle of 104° when recording ceased, and only a 0.1 mm increase in diameter. Hence, it is evident that the dish sponge exhibits a high degree of hydrophobicity.
The car sponges exhibited very similar partial wetting behaviour to that in Figure 3 when distilled water droplets were applied. The average initial contact angle for the car sponge was 111°, reducing to 102° after 5 min. Therefore, the car sponge is highly hydrophobic since the initial contact angle is over 90° [5]. The dish sponge is the most hydrophobic, closely followed by the car sponge. When distilled water droplets were introduced to the audio sponge, they did not finish in spherical shapes with a non-zero contact angle at the surface of the sponge but were very quickly absorbed. The differences in hydrophobicity (initial contact angle) of the four sponges mentioned are determined by the difference in the polymers that the sponges were manufactured from.
The data presented in Figure 4 show complete wetting behaviour according to Figure 2. The experimental data from all experimental runs across the range of dry sponges using various surfactant concentrations have been compiled into dimensionless plots such as those shown in Figure 5 using the following procedure: the contact angle values are divided by the maximum contact angle θM and the base diameter is divided by the maximum base diameter LM, changing them into dimensionless values θ* and L*, respectively. Both θ* and L* are plotted against dimensionless time, t*, which is calculated by dividing the time values by the total time period of the process tp, where the time period is determined by the point where the droplet absorbs into the substrate. In all cases the initial contact angle is around 107° and the rate at which the contact angle decreases also decreases over time. The measurement of contact angles below 25° is impossible due to surface heterogeneity; the curves in Figure 4 do not go below this point because, once a certain contact angle is reached, the droplets rapidly absorb into the substrate.
The droplet base diameter time dependency in Figure 4 gives an indication of the relative rates of surface spreading and absorption or capillary imbibition into the porous structure of the sponge. The total time over which spreading and absorption occurs reduces as the surfactant concentration increases. Comparison of the data presented in Figure 5 proves that at all concentrations of surfactants considered compete wetting is observed The same dimensionless form was used to present the experimental data on spreading of surfactant solutions over the dish sponge in Figure 6. The data were converted to a dimensionless form, giving universal profiles for contact angle and spreading diameter such as those shown in Figure 6, which confirms that the spreading/imbibition of surfactant solutions shows the complete wetting behaviour of the dish-washing sponge.
Despite the dish and audio sponges having significantly different pore sizes and hydrophilicities, the overall wetting characteristics are very similar. The dish sponge raw data (not shown) follows the same trend as in Figure 4, whereby contact angle reduction and spreading occur faster for lower concentrations of surfactant. The initial contact angle for surfactant droplets is around 95°. Figure 6 demonstrates that dish sponge data for contact angle and spreading diameter align to universal dimensionless profiles and show complete wetting. Again, it is evident that the rate at which the contact angle is decreasing reduces over time. The dimensionless diameter profile in Figure 6 shows that the dish sponge encourages significant surface spreading of surfactant solutions before absorption, and that the final stages of droplet imbibition transpired relatively quickly.
The raw data for the car sponge also match the same trend of the contact angle reducing faster for lower concentrations of surfactant solution and show universal complete wetting behaviour if the same dimensionless variables are used. The data on spreading of surfactant solutions over a car sponge (not shown) demonstrate similarly complete wetting behaviour, as shown in Figure 5 and Figure 6.

Wet Sponge Results

Following the dry sponge analysis, the sponges were tested whilst being subjected to three different degrees of saturation: 10%, 50%, and 100%, where 100% saturation is 30 g of water absorbed into the porous media. The addition of water to the sponges prior to the deposition of surfactant droplets increases the speed of the wetting and spreading processes significantly. Despite this, the overall trends in contact angle and spreading diameter showed the same behaviour as for the dry sponges described above. For this reason, the figures and graphs from this part of the investigation are not included, but the key findings are summarised by Table 2. When any quantity of water is used to pre-wet the sponge, it is no longer possible to observe the contact angle or spreading diameter for droplets of pure distilled water such as in Figure 3. These are very quickly absorbed into the sponge structure. When any amount of surfactant is present in the droplets, it demonstrates complete wetting (Figure 2).
Table 2 shows that for any degree of saturation the process time (time drop remains on the surface) is significantly reduced; the process time between different degrees of saturation is similar, indicating that increasing the saturation of an already wet sponge does not increase the spreading rate. The maximum droplet base diameter increases from a dry sponge to a wet sponge. The base diameter increases as saturation increases until after 50%; once the sponge is saturated, the base diameter decreases to a value similar to that of a dry sponge.
Initial contact of the droplet decreases as the degree of saturation increases and, in the case of the car sponge, increases as the sponge becomes saturated, whereas for the dish sponge the initial contact angle decreases only slightly and still lies within the error range of a droplet on a dry sponge. All the sponges, wet or dry, display a minimum contact angle after which the droplet rapidly absorbs into the porous media. For the car sponge the contact angle at which this phenomenon occurs decreases as the saturation increases. This is unlike the dish sponge, where this point of rapid absorption occurs at a larger contact angle, indicating that the initial contact angle and complete absorption contact angle are more heavily affected by the material and structural behaviour of the media than by the degree of saturation of the media.

4. Conclusions

When distilled water droplets are deposited on porous sponges, we have a case of partial wetting; when any concentration of commercial surfactant solution is used, on both wet and dry sponges, there is a change to a complete wetting scenario.
The methods used are proven to be effective at characterising the overall wetting and spreading characteristics of the sponges via the generation of universal dimensionless dependences in each case.
Pre-wetting the sponges to any degree increases the speed of spreading and the rate of contact angle reduction. Partially wetting the sponge increases the base diameter, whereas with saturated sponges the base diameter is the same as that of a dry sponge.
All the sponges, no matter the saturation, display a minimum contact angle after which the droplet absorbs rapidly into the porous media.
Initial contact angle and complete absorption contact angle are more dependent on the material and structural behaviour of the media than the degree of saturation of the media.

Author Contributions

Conceptualization, V.S. and A.T.; Methodology, P.J.; Validation, T.R., P.J. and A.T.; Formal Analysis, P.J. and T.R.; Investigation, T.R. and P.J.; Resources, A.T. and M.V.; Data Curation, T.R. and P.J., Writing—Original Draft, T.R. and P.J.; Writing—Review and Editing, A.T., V.S., M.V. and P.J.; Visualization, P.J., T.R. and V.S.; Supervision, A.T. and V.S.; Project Administration, A.T.

Acknowledgments

This research was supported by Procter and Gamble Ltd., Loughborough Materials Characterisation Centre, MAP EVAPORATION and PASTA projects, European Space Agency.

Conflicts of Interest

The authors declare no conflict of interest.

Nomenclature

SymbolMeaningUnits
ΘActual contact angleDegrees
ΘMMax. contact angleDegrees
Θ*Dimensionless C.A.-
LActual Diametermm
LMMax. Diametermm
L*Dimensionless diam.-
ttimes
tpTotal process times
t*Dimensionless time-

References

  1. Arjmandi-Tash, O.; Kovalchuk, N.M.; Trybala, A.; Kuchin, I.V.; Starov, V. Kinetics of Wetting and Spreading of Droplets over Various Substrates. Langmuir 2017, 33, 4367–4385. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Ebrahimi, A.N.; Or, D. Microbial dispersal in unsaturated porous media: Characteristics of motile bacterial cell motions in unsaturated angular pore networks. Water Resour. Res. 2014, 50, 7406–7429. [Google Scholar] [CrossRef] [Green Version]
  3. Young, T. An essay on the cohesion of fluids. Philos. Trans. R. Soc. Lond. 1805, 95, 65–87. [Google Scholar] [CrossRef]
  4. Lee, K.S.; Ivanova, N.; Starov, V.M.; Hilal, N.; Dutschk, V. Kinetics of wetting and spreading by aqueous surfactant solutions. Adv. Colloid Interface Sci. 2008, 144, 54–65. [Google Scholar] [CrossRef] [PubMed]
  5. Yuan, Y.; Lee, T.R. Contact Angle and Wetting Properties. In Surface Science Techniques; Springer: Berlin/Heidelberg, Germany, 2013; Volume 51, pp. 3–34. [Google Scholar]
  6. Starov, V.M.; Zhdanov, S.A.; Kosvintsev, S.R.; Sobolev, V.D.; Velarde, M.G. Velarde, Spreading of liquid drops over porous substrates. Adv. Colloid Interface Sci. 2013, 104, 123–158. [Google Scholar] [CrossRef]
  7. Brinkman, H.C. A calculation of the viscous force exerted by a flowing fluid on a dense swarm of particles. Flow Turbul. Combust. 1949, 1, 27. [Google Scholar] [CrossRef]
  8. Bonn, D.; Eggers, J.; Indekeu, J.; Meunier, J.; Rolley, E. Wetting and spreading. Rev. Mod. Phys. 2009, 81, 739–804. [Google Scholar] [CrossRef]
  9. Rauscher, M.; Dietrich, S. Wetting Phenomena in Nanofluidics. Annu. Rev. Mater. Res. 2008, 38, 143–172. [Google Scholar] [CrossRef]
  10. Bormashenko, E.Y. Wetting of Real Surfaces, 2nd ed.; Walter de Gruyter GmbH: Berlin, Germany; Boston, MA, USA, 2018. [Google Scholar]
  11. Lee, R.; Bong, J. Droplet Dynamics on Non-Porous and Porous Media: Impact, Spreading and Absorption. Ph.D. Thesis, ETH Zurich, Zurich, Switzerland, 2015; pp. 8–15. [Google Scholar]
  12. Henrich, F.; Fell, D.; Truszkowska, D.; Weirich, M.; Anyfantakis, M.; Nguyen, T.H.; Wagner, M.; Auernhammer, G.K.; Butt, H.J. Influence of surfactants in forced dynamic dewetting. Soft Matter 2016, 12, 7782–7791. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Starov, V.; Velarde, M.; Radke, C. Dynamics of Wetting and Spreading; Surfactant Sciences Series; Taylor & Frances: Abingdon, UK, 2007; Volume 138. [Google Scholar]
Figure 1. Three stages of spreading/imbibition of droplet over porous substrate in the case of partial wetting: Lad is the maximum radius of droplet base, θad is the static advancing contact angle, tad is the time when θad is reached, θr is the static receding contact angle, tr is the time when θr is reached and t* is the time when imbibition is finished completely [13].
Figure 1. Three stages of spreading/imbibition of droplet over porous substrate in the case of partial wetting: Lad is the maximum radius of droplet base, θad is the static advancing contact angle, tad is the time when θad is reached, θr is the static receding contact angle, tr is the time when θr is reached and t* is the time when imbibition is finished completely [13].
Colloids 03 00014 g001
Figure 2. Two stages of spreading/imbibition of droplet over porous substrates in the case of complete wetting: Lm is the maximum radius of droplet base, tm is the time when Lm is reached, θm is the contact angle at tm, t* is the time when complete imbibition is finished and θf is the final contact angle at t*. Note, in the case of complete wetting stage 2 is absent (see Figure 1) [13].
Figure 2. Two stages of spreading/imbibition of droplet over porous substrates in the case of complete wetting: Lm is the maximum radius of droplet base, tm is the time when Lm is reached, θm is the contact angle at tm, t* is the time when complete imbibition is finished and θf is the final contact angle at t*. Note, in the case of complete wetting stage 2 is absent (see Figure 1) [13].
Colloids 03 00014 g002
Figure 3. Contact angle and droplet base diameter time dependencies for distilled water on dry dish sponge. Both plots show the presence of stages 1 and 2 according to the partial wetting case in Figure 1.
Figure 3. Contact angle and droplet base diameter time dependencies for distilled water on dry dish sponge. Both plots show the presence of stages 1 and 2 according to the partial wetting case in Figure 1.
Colloids 03 00014 g003
Figure 4. Contact angle and droplet base diameter time dependencies for different concentrations of surfactant (%) on dry audio sponge.
Figure 4. Contact angle and droplet base diameter time dependencies for different concentrations of surfactant (%) on dry audio sponge.
Colloids 03 00014 g004
Figure 5. Contact angle and droplet base diameter dimensionless profiles for different concentrations of surfactant (%) on a dry audio sponge.
Figure 5. Contact angle and droplet base diameter dimensionless profiles for different concentrations of surfactant (%) on a dry audio sponge.
Colloids 03 00014 g005
Figure 6. Contact angle and droplet base diameter dimensionless profiles for different concentrations of surfactant on a dry dish sponge.
Figure 6. Contact angle and droplet base diameter dimensionless profiles for different concentrations of surfactant on a dry dish sponge.
Colloids 03 00014 g006
Table 1. Properties of sponge samples.
Table 1. Properties of sponge samples.
Pore Size (mm)Porosity
Dish0.302 ± 0.0720.689
Audio0.093 ± 0.0280.692
Car0.295 ± 0.0700.694
Table 2. The total time each droplet of concentrated surfactant solutions remained on the porous media with different degrees of saturation before being absorbed; the corresponding maximum base diameter and initial and final contact angle of the droplet.
Table 2. The total time each droplet of concentrated surfactant solutions remained on the porous media with different degrees of saturation before being absorbed; the corresponding maximum base diameter and initial and final contact angle of the droplet.
SpongeDegree of Saturation (%)Total Process Time (s)Maximum Droplet Base Diameter (mm)Initial Contact Angle (degrees)Contact Angle (Final) for Complete Absorption (degrees)
CarDry sponge493.1 ± 0.396.9 ± 8.238.8 ± 0.5
10%73.6 ± 0.281.2 ± 0.522.5 ± 0.5
50%43.9 ± 0.483.2 ± 0.525.4 ± 0.5
100%53.1 ± 0.195.2 ± 0.530.7 ± 0.5
DishDry sponge223.1 ± 0.3101.7 ± 6.226.3 ± 0.5
10%43.6 ± 0.298.2 ± 2.832.4 ± 4.9
100%63.1 ± 0.395.2 ± 0.536.2 ± 9.8

Share and Cite

MDPI and ACS Style

Johnson, P.; Routledge, T.; Trybala, A.; Vaccaro, M.; Starov, V. Wetting and Spreading of Commercially Available Aqueous Surfactants on Porous Materials. Colloids Interfaces 2019, 3, 14. https://doi.org/10.3390/colloids3010014

AMA Style

Johnson P, Routledge T, Trybala A, Vaccaro M, Starov V. Wetting and Spreading of Commercially Available Aqueous Surfactants on Porous Materials. Colloids and Interfaces. 2019; 3(1):14. https://doi.org/10.3390/colloids3010014

Chicago/Turabian Style

Johnson, Phillip, Toby Routledge, Anna Trybala, Mauro Vaccaro, and Victor Starov. 2019. "Wetting and Spreading of Commercially Available Aqueous Surfactants on Porous Materials" Colloids and Interfaces 3, no. 1: 14. https://doi.org/10.3390/colloids3010014

Article Metrics

Back to TopTop