Crawford / Ivanova Superhydrophobic Surfaces

1. Auflage 2015
ISBN: 978-0-12-801331-1
Verlag: Elsevier Science & Techn.
Format: EPUB
Kopierschutz: 6 - ePub Watermark

E-Book, Englisch, 180 Seiten

Superhydrophobic Surfaces analyzes the fundamental concepts of superhydrophobicity and gives insight into the design of superhydrophobic surfaces. The book serves as a reference for the manufacturing of materials with superior water-repellency, self-cleaning, anti-icing and corrosion resistance. It thoroughly discusses many types of hydrophobic surfaces such as natural superhydrophobic surfaces, superhydrophobic polymers, metallic superhydrophobic surfaces, biological interfaces, and advanced/hybrid superhydrophobic surfaces. - Provides an adequate blend of complex engineering concepts with in-depth explanations of biological principles guiding the advancement of these technologies - Describes complex ideas in simple scientific language, avoiding overcomplicated equations and discipline-specific jargon - Includes practical information for manufacturing superhydrophobic surfaces - Written by experts with complementary skills and diverse scientific backgrounds in engineering, microbiology and surface sciences

Professor Russell Crawford is currently the Dean of the Faculty of Life & Social Sciences at Swinburne University of Technology in Melbourne, Australia. He obtained his MSc from Swinburne in 1987, followed by a PhD from The University of Melbourne in 1995. He is the President of the Australian Council of Deans of Science and is a Fellow of the Royal Austraian Chemical Institute. His research is in the area of surface and colloid science, with his early work focusing on the surface chemistry of mineral flotation and the removal of heavy metals from aqueous environments. His more recent research has investigated the ways in which biological organisms interact with solid substrate surfaces, particularly those used in the construction of medical implants.

Autoren/Hrsg.

Crawford, Russell J.

Ivanova, Elena P.

Inhaltsverzeichnis

1;Front Cover;1
2;SUPERHYDROPHOBIC SURFACES;4
3;Copyright;5
4;CONTENTS;6
5;CONTRIBUTORS;8
6;EDITORS BIOGRAPHIES;10
7;PREFACE;12
8;ACKNOWLEDGEMENT;14
9;Chapter One - Superhydrophobicity – An Introductory Review;16
9.1;REFERENCES;21
10;Chapter Two - Natural Superhydrophobic Surfaces;22
10.1;INTRODUCTION;22
10.2;SELF-CLEANING PROPERTIES ARISING FROM HIERARCHICAL STRUCTURES;23
10.3;HIERARCHICAL STRUCTURE OF SURFACES ON AQUATIC SPECIES;36
10.4;SUMMARY;37
10.5;REFERENCES;37
11;Chapter Three - The Design of Superhydrophobic Surfaces;42
11.1;METHODS TO PREPARE SUPERHYDROPHOBIC SURFACES;42
11.2;CONCLUSIONS AND OUTLOOK;58
11.3;REFERENCES;59
12;Chapter Four - Hydrophobicity of Nonwetting Soils;66
12.1;NONWETTING SOIL AND ITS IMPACT ON WATER TRANSPORT;66
12.2;SUPERHYDROPHOBICITY OF SOIL SURFACES;67
12.3;ROLE OF SOIL ORGANIC MATTER ON WATER REPELLENCY;68
12.4;MICROSTRUCTURE OF SOIL ORGANIC MATTER COATINGS;70
12.5;ASSESSMENT OF WATER REPELLENCY OF SOIL SURFACES;72
12.6;INFLUENCE OF SURFACTANTS ON NONWETTING SOILS;75
12.7;REFERENCES;78
13;Chapter Five - Superhydrophobic Polymers;82
13.1;INTRODUCTION;82
13.2;DESIGN OF SUPERHYDROPHOBIC POLYMERS;82
13.3;FABRICATION TECHNIQUES;85
13.4;CONCLUSIONS;97
13.5;REFERENCES;97
14;Chapter Six - Metallic Superhydrophobic Surfaces;102
14.1;INTRODUCTION;103
14.2;STRUCTURING OF METAL SURFACES BY ULTRA-SHORT PULSED LASER IRRADIATION;104
14.3;INFLUENCE OF LASER IRRADIATION ON THE CHEMICAL COMPOSITION OF METAL SURFACES;112
14.4;WETTING CHARACTERIZATION;113
14.5;COMBINATION OF LASER STRUCTURING WITH COATINGS AND LUBRICANTS;119
14.6;SUMMARY;123
14.7;REFERENCES;124
15;Chapter Seven - Applications of Nanotextured Surfaces: Three-dimensional Aspects of Nanofabrication;128
15.1;INTRODUCTION;128
15.2;NANOSCALE STRUCTURES AND THEIR FUNCTIONS;128
15.3;EMERGING 3D NANOSTRUCTURING TECHNOLOGIES;158
15.4;CONCLUSIONS AND OUTLOOK;161
15.5;ACKNOWLEDGMENTS;161
15.6;REFERENCES;161
16;Chapter Eight - Biological Interactions with Superhydrophobic Surfaces;166
16.1;INTRODUCTION;166
16.2;COMPLEXITY AND DYNAMICS;167
16.3;PROTEIN ADSORPTION ON SUPERHYDROPHOBIC SURFACES;167
16.4;BACTERIAL INTERACTIONS WITH SUPERHYDROPHOBIC SURFACES;169
16.5;EUKARYOTIC CELL–TISSUE INTERACTIONS WITH SUPERHYDROPHOBIC SURFACES;171
16.6;SUMMARY;173
16.7;REFERENCES;173
17;INDEX;176

Leseproben

Chapter One Superhydrophobicity – An Introductory Review
Abstract
Superhydrophobicity as a phenomenon has become an increasing focus of research and technological activity, where its fundamental aspects span surface chemistry, chemical physics, and cellular biology. Additionally, its significance to the behavior of natural systems, interfacial fluid dynamics, and biotechnology represents an area rapidly gaining potential importance. Detailed reviews have progressively explored superhydrophobicity from a number of viewpoints (e.g., Ma and Hill, 2006; Quéré, 2002; Shirtcliffe et al., 2010). Here, aspects underlying this wetting behavior are illustrated. It has long been recognized that surface roughness has a profound effect on wetting behavior, in particular through apparent contact angles and subsequent contact angle hysteresis (Bico et al., 2001; Quéré, 2008). Quéré (2008) points out that both chemical and structural surface heterogeneity can cause pinning of the three-phase contact line (TPL) of an advancing wetting front, whereby the difference in the advancing and receding contact angles produces a Laplace pressure and hence a force resisting further liquid advancement. Movement of the wetting front (advancing and receding) can be viewed as a kinetic process in response to changing forces at the TPL that characteristically produce jumps in the movement of this line. Rough and microstructured surfaces inherently increase hydrophobicity of hydrophobic surfaces through two very different mechanisms: a purely geometrical increase in the actual surface area with respect to its projected area generally termed the Wenzel state (Wenzel, 1936) and a composite interfacial effect arising from an air–water interface when air is trapped between microstructural features of the surface ahead of the advancing wetting front forming a Cassie–Baxter state (Cassie and Baxter, 1944), as illustrated in Figure 1. As such, these conditions represent homogeneous and heterogeneous surface wetting systems, respectively, and in both cases are derived from the result of variations in the interfacial energy of the substrate phase(s) solid or solid-vapor. Keywords
Biotechnology; Natural systems; Superhydrophobicity; Three-phase contact line; Wettability Glossary TPL    three-phase contact line S-L-V    solid-liquid-vapour phases CMC    critical micelle concentration Superhydrophobicity as a phenomenon has become an increasing focus of research and technological activity, where its fundamental aspects span surface chemistry, chemical physics, and cellular biology. Additionally, its significance to the behavior of natural systems, interfacial fluid dynamics, and biotechnology represents an area rapidly gaining potential importance. Detailed reviews have progressively explored superhydrophobicity from a number of viewpoints (e.g., Ma and Hill, 2006; Quéré, 2002; Shirtcliffe et al., 2010). Here, aspects underlying this wetting behavior are illustrated. It has long been recognized that surface roughness has a profound effect on wetting behavior, in particular through apparent contact angles and subsequent contact angle hysteresis (Bico et al., 2001; Quéré, 2008). Quéré (2008) points out that both chemical and structural surface heterogeneity can cause pinning of the three-phase contact line (TPL) of an advancing wetting front, whereby the difference in the advancing and receding contact angles produces a Laplace pressure and hence a force resisting further liquid advancement. Movement of the wetting front (advancing and receding) can be viewed as a kinetic process in response to changing forces at the TPL that characteristically produce jumps in the movement of this line. Rough and microstructured surfaces inherently increase hydrophobicity of hydrophobic surfaces through two very different mechanisms: a purely geometrical increase in the actual surface area with respect to its projected area generally termed the Wenzel state (Wenzel, 1936) and a composite interfacial effect arising from an air–water interface when air is trapped between microstructural features of the surface ahead of the advancing wetting front forming a Cassie–Baxter state (Cassie and Baxter, 1944), as illustrated in Figure 1. As such, these conditions represent homogeneous and heterogeneous surface wetting systems, respectively, and in both cases are derived from the result of variations in the interfacial energy of the substrate phase(s) solid or solid-vapor.
Figure 1 Contact angles on structured surfaces in the classic Wenzel (W) and Cassie–Baxter (C–B) states, respectively, where r is the physical amplification of surface area due to roughness and fS is the fractional area in contact with air. Adapted from Shirtcliffe et al. (2010). Marmur characterized superhydrophocity according to two criteria (Marmur, 2004), a very high contact angle and very low drop roll-off angle, as well as addressing the transition between these states in terms of their metastability and its impact on superhydrophobicity (Marmur, 2003). Since the free energy increases with increasing contact angle, the state that is most stable is represented by that with lowest contact angle. Gao and Yan (2009) and Quéré (2008) point out that due to local energy minima, a water drop cannot only assume multiple energy states but also coexist on a particular surface, and from the energy barrier for the transition Cassie–Baxter to the Wenzel state, surface geometry influences the interfacial energy requirement to reach equilibrium whether homogeneous or heterogeneous wetting is involved. Pinning of the advancing TPL is also dependent on the topology (feature size, spacing, and shape). Shirtcliffe et al. (2010) and McHale (2007) note that this also determines the observed contact angle and consistency with the Wenzel and Cassie–Baxter models since the incremental advancing area is assumed to characterize the surface overall. And, as a result, features on either side of the TPL do not influence the contact angle over the increment but must be of sufficiently small size to ensure that an average of the overall topology is sampled by the TPL at any one time, as shown by McHale (2007) and Shirtcliffe et al. (2010) for a random surface, illustrated in Figure 2.
Figure 2 Advancing wetting front across homogeneous zones 1 and 2 with respective contact angles ?1,2 and across a microscopically random surface (1,2) with contact angle ?c-B. Interestingly, these studies also illustrate that a systematic variation in topological pattern within the bounds of a TPL yields a driving force for liquid transport not reliant on capillary suction (Figure 3), which may have implications for microfluidic device design. Transition between a Cassie–Baxter suspended state and complete surface immersional Wenzel wetting readily occurs through the imposition of external forces whether mechanical, hydrostatic, or compositional or through the size of the drop and its internal Laplace pressure (Ishino et al., 2004; Lafuma and Quéré, 2003). The enhancement of superhydrophocity, through a hierarchical surface roughness where a nanoscale topology is superimposed on surface microscale roughness, has now been widely studied. In many cases, this has been related to fractal behavior (Bottiglione and Carbone, 2013). Nosonovsky (2007), in investigating the instability of the Cassie–Baxter wetting state and its transformation to Wenzel wetting, established hierarchical roughness as a criterion enhancing the composite wetting state, which was then shown to apply to both natural and synthetic surfaces and suggested as a general requirement when other destabilizing scale-dependent effects are present such as in microprocesses. Noting the transition to a stable Cassie state under imposed vibration on the Lotus leaf surface (Boreyko and Chen, 2009), Boreyko and Collier (2013) then examined the obverse situation where drops in the Wenzel condition can assume the Cassie–Baxter state through a dewetting transition. Here, they show that pinned Wenzel drops cannot be totally stretched during a transition to reduce their contact angle below a critical curvature since pinch-off of the drop surface occurs, resulting in a partial liquid Wenzel droplet remaining on the surface. They thereby provide a condition for a Wenzel dewetting where the receding contact angle needs to be moderately large (~90°).
Figure 3 Influence of a variation in surface topology producing an additional wetting force and fluid flow. Adapted from Shirtcliffe et al. (2010). Contact angle and movement at the TPL (wetting or dewetting) have been noted as a response to forces at the intersection of interfaces between the three principal phases (S-L-V). Within this line of contact, where the feature size of surface topology exerts influence, an additional line tension (Rusanov et al., 2004) exists akin to a “one dimensional surface tension” that may influence the contact angle and hence the Wenzel and Cassie–Baxter models and their respective transitions, if the droplet and feature size are small. Amirfazli and Neumann (2004) point out, in a detailed analysis of the status of line tension, that line tension influences contact...