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1062. Katoh, K., “Contact angle and surface tension measurement,” in Surface and Interfacial Tension: Measurement, Theory, and Applications, Hartland, S., ed., 375-424, Marcel Dekker, 2004.

The wetting phenomenon is an important issue in various technological processes. In some fields, liquids are desired to spread over solid surfaces, e.g., lubrication oils on metallic surfaces or paint on paper. On the other hand, it is necessary for hydrophobic coatings to repel water such as Teflon film on frying pans. The behavior of bubbles on solid surfaces immersed in liquid often has important effects on the performance of industrial apparatus dealing boiling or condensation. In these problems regarding wetting, it is known that the behavior of a drop or bubble on a solid surface is dependent on the three interfacial tensions between solid, gas, and liquid phases, as shown in Fig. 1. The tangential force balance between these interfacial tensions on the three-phase contact line leads to the following well-known Young’s equation [1]: σSV−σSL=σLV cos αY. (1) σSV, σSL, and σLV indicate solid-vapor, solid-liquid, and liquid-vapor interfacial tensions, respectively. The environmental atmosphere is assumed to be filled with saturated vapor of liquid. When a drop is exposed to air, however, σLV usually does not change because a thin layer of saturated vapor may be formed around the drop [2]. In the right-hand side of Eq. (1), αY is the angle between the solid surface and the liquid-vapor interface measured from the inside of the liquid phase and is called the contact angle. When the difference between the two interfacial tensions on the left-hand side of Eq. (1) is large enough to make αY on the right-hand side small, the solid is favorably wetted by the liquid. As the drop size becomes sufficiently small and the curvature of the solid-gas-liquid contact line becomes quite large, we should add a term representing the effect of line tension to the above equation [3].

1063. Song, B., A. Bismarck, and J. Springer, “Contact angle measurements on fibers and fiber assemblies, bundles, fabrics, and textiles,” in Surface and Interfacial Tension: Measurement, Theory, and Applications, Hartland, S., ed., 425-482, Marcel Dekker, 2004.

1064. Eriksson, J.C., and S. Ljunggren, “Thermodynamics of curved interfaces in relation to the Helfrich curvature free energy approach,” in Surface and Interfacial Tension: Measurement, Theory, and Applications, Hartland, S., ed., 547-614, Marcel Dekker, 2004.

In 1878, Gibbs [1] published his celebrated “Theory of Capillarity,” the standard reference of surface thermodynamics ever since. In a rather compact-yet exhaustive and profound-manner, Gibbs treated fluid-fluid, as well as solid-fluid, interfaces and their equilibrium properties while representing the interfacial region in an Euclidean manner by a single dividing interface, preferably the so-called surface of tension. For this particular dividing surface, the standard Laplace (or Young-Laplace) equation [2]: ∆P=2Hγ (1) holds exactly for a majority of cases. Here H=(c1+c2)/2 denotes the mean curvature, γ is the interfacial tension, and ∆P is the pressure jump at the interface, and c1 and c2 are the principal curvatures of the surface of tension. Moreover, for any given interface, the interfacial tension γ attains a minimum value when the surface of tension is chosen to be the dividing surface, as may readily be verified.

1106. Yasuda, H., Luminous Chemical Vapor Deposition and Interface, Marcel Dekker, 2005.

1153. Harrington, W.F. Jr., “Surface treatment of plastics,” in Coatings Technology Handbook, D. Satas, ed., Marcel Dekker, 1991 (also in Coatings Technology Handbook, 2nd Ed., D. Satas and A.A. Tracton, eds., p. 335-342, Marcel Dekker, Jan 2001, and Coatings Technology: Fundamentals, Testing, and Processing Techniques, A.A. Tracton, ed., p. 38/1-38/7, CRC Press, Oct 2006).

No single step in the coating process has more impact on film adhesion than surface preparation. Film adhesion to a plastic is primarily a surface phenomenon and requires intimate contact between the substrate surface and the coating. However, intimate contact of that plastic surface is not possible without appropriate conditioning and cleansing. Plastic surfaces present a number of unique problems for the coater. Many plastics, such as polyethylene or the fluorinated polymers, have a low surface energy. Low surface energy often means that few materials will readily adhere to the surface. Plastic materials often are blends of one or more polymer types or have various quantities of inorganic fillers added to achieve specific properties. The coefficient of thermal expansion is usually quite high for plastic compounds, but it can vary widely depending on polymer blend, filler content, and filler type. Finally, the flexibility of plastic materials puts more stress on the coating, and significant problems can develop if film adhesion is low due to poor surface preparation.

1477. Della Volpe, C., and S. Siboni, “Acid-base behaviour of (polymer) surfaces: Theory,” in Encyclopedia of Surface and Colloid Science, Hubbard, A., ed., Marcel Dekker, 2002.

1724. no author cited, “Surface free energy of polymers - Optimisation of the determination of polymer surface free energy,” Materials Australia, 33, (Dec 2001).

2974. Deshmukh, R.R., and N.V. Bhat, “The mechanism of adhesion and printability of plasma processed PET films,” Materials Research Innovations, 22, 283-290, (Sep 2003).

Of the several techniques available for the surface modification, plasma processing has proved to be very appropriate. The low temperature plasma is a soft radiation source and it affects the material only over a few hundred Å deep, the bulk properties remaining unaffected. Plasma surface treatment also offers the advantage of greater chemical flexibility. PET films are widely used for packaging and electrical insulation. The studies of adhesion and printability properties are important. In the present study PET films are treated in air plasma for different time of treatment. The improvement in adhesion is studied by measuring T-peel and Lap shear strength. In addition, printability of plasma treated PET films is studied by cross test method. It has been found that printability increases considerably for plasma treatment of short duration. Therefore it is interesting to study the surface composition and morphology by contact angle measurement, ESCA and AFM. Surface energy and surface roughness can be directly correlated to the improvement in above-mentioned surface related properties. It has been found that the surface oxidation occurs containing polar functional groups such as CSingle BondO, COO. A correlation of all such observations from different techniques gives a comprehensive picture of the structure and surface composition of plasma treated PET films.

541. Occhiello, E., M. Morra, G. Morini, and F. Garbassi, “Effect of oxygen plasma treatments on polypropylene - epoxy interfacial strength,” in Interfaces Between Polymers, Metals, and Ceramics, Ishida, H., 199-204, Materials Research Society, 1989.

The effect of oxygen plasma treatment on adhesion and surface properties of polypropylene (PP) was assessed. An oxygen rich modified PP layer, immiscible with bulk PP, was formed by the treatment. Contact angle measurements showed that macromolecular motions led with time to rearrangements of the surface layer drastically decreasing its wettability, while its composition, measured by XPS, remained unaffected.The shear strength of PP-epoxy joints increased after plasma treatment. The locus of failure was found to occur at the PP/epoxy interface for untreated PP, within PP in the case of oxygen-plasma-treated samples, close to the modified PP/bulk PP interface. This result suggests that the plasma treament improves the interaction at the PP/epoxy interface, but weakens the mechanical strength of the surface layer thereby creating a weak point at the modified PP/bulk PP interface.

2625. Rudawska, A., and J. Kuczmaszewski, “Surface free energy of zinc coating after finishing treatment,” Materials Science - Poland, 24, (2006).

Protective properties of zinc coating increase with an additional coating such as: chromate, phosphate, paint and polymer coating. Besides, additional treatment of zinc coating serves decorative purposes as well. The paper presents the influence of additional coating of zinc coating on their adhesive properties which are especially helpful in processes where adhesion plays an essential role. These processes include among others: gluing, painting or varnishing. Adhesive properties are characterized by the value of surface free energy.

2975. Nowak, S., and O.M. Kuttel, “Plasma treatment of polymers for improved adhesion properties,” Materials Science Forum, 142, 705-726, (1993).

387. Winters, H.F., R.P.H. Chang, C.J. Mogab, J. Evans, J.A. Thornton, and H. Yasuda, “Coatings and surface modification using low pressure non-equilibrium plasmas,” Materials Science and Engineering, 70, 53-77, (1985).

2081. Lawrence, J., and L. Li, “Modification of the wettability characteristics of polymethyl methacrylate (PMMA) by means of CO2, Nd:YAG, excimer and high power diode laser radiation,” Materials Science and Engineering A, 303, 142-149, (May 2001).

The surface of the bio-material polymethyl methacrylate (PMMA) was treated with CO2, Nd:YAG, excimer and high power diode laser (HPDL) radiation. The laser radiation was found to effect varying degrees of change to the wettability characteristics of the material depending upon the laser used. It was observed that interaction with CO2, Nd:YAG and HPDL effected very little change to wettability characteristics of the PMMA. In contrast, interaction of the PMMA with excimer laser radiation resulted an increase in a marked improvement in the wettability characteristics. After excimer laser treatment the surface O2 content was found to have increased and the material was seen to be more polar in nature. The work has shown that the wettability characteristics of the PMMA could be controlled and/or modified with laser surface treatment. However, a wavelength dependence of the change of the wetting properties could not be deduced from the findings of this work.

2979. Pichal, J., J. Cerman, H. Sourkova, and P. Spatenka, “Plasma pre-treatment of polypropylene surface for industrial purposes,” Materials and Manufacturing Processes, 37, 1483-1489, (2022).

The paper describes an experimental investigation of the possibility of industrial modification of surface wettability and adhesion of polymers by the action of a plasma of a gliding discharge generated in air at atmospheric pressure in a simulated production process. The test material was polypropylene plates (PP). The modification was performed by a device with a multi-electrode (four pairs) system, which is not common. The quality of pre-processing and usability was evaluated primarily in terms of the industrial requirements, which means a change in wettability and adhesion expressed by the contact angle/surface free energy value in dependence to sample exposure time expressed by the conveyor belt speed. The surface free energy assessment of a treated polymeric surface by contact angle measurement was carried out by analyzing static sessile drops and evaluated by Owens–Wendt–Rabel–Kaelble (OWRK) model. The results determined a set of operating parameters at which the modification process meets the industrial requirements. By evaluating the change in surface free energy in relation to the storage time, the degree of hydrophobic recovery of the treated samples, i.e. the time stability of the plasma-treated surface, was also determined. It has been found that plasma-treated PP surface fully meets industrial demands and can be stored for at least 50 days.

887. Veselovsky, R.A., and V.N. Kestelman, Adhesion of Polymers, McGraw-Hill, Dec 2001.

1535. Petrie, E.M., “Surfaces and surface preparation,” in Handbook of Adhesives and Sealants, 2nd Ed., 227-275, McGraw-Hill, Jan 2007.

910. Wettermann, R.P., “Electrical surface treatment of medical plastics,” Medical Device & Diagnostic Industry, (Oct 1990).

2947. Palmers, J., “Surface modification using low-pressure plasma technology,” Medical Device & Diagnostic Industry, (Jan 2000).

352. Stobbe, B.D., “Corona discharge treatment for medical surface preparation,” Medical Device and Diagnostic Industry, (Feb 2000).

179. Jones, W.C., “Testing surfaces for cleanliness,” Metal Finishing, 83, 13-15, (Oct 1985).

452. Dobreva, E.D., M.A. Encheva, and A.T. Trandafilov, “The effect of preliminary treatment with surfactants in the metallization of dielectrics,” Metal Finishing, 90, 29-32, (Mar 1992).

2015. Kuhn, A., “Starting off with a clean slate: Using dyne liquids is one of the easiest and most cost-effective means of assessing surface cleanliness,” Metal Finishing, 103, 72-79, (May 2005).

2869. Kuhn, A., “Determining whether a metal surface is really clean: Two testing methods offer an inexpensive yet accurate means for measuring cleanliness,” Metal Finishing, 103, 16-21, (Sep 2005).

893. Hibbard, D., “Sticky science: new polymer technology makes it easier to paint and glue plastic parts,” Modern Paints & Coatings, 91, 31, (Dec 2001).

27. Blitshteyn, M., and R. Wetterman, “Surface treatment of polyolefins,” Modern Plastics, 67, 424, (Oct 1990).

146. Greene, R., “High energy system prepares molded parts,” Modern Plastics, 68, 30-31, (Aug 1991).

224. Lindsay, K.F., “Process surface-treats PP parts in line, opening market opportunities,” Modern Plastics, 69, 47-48, (Apr 1992).

328. Sewell, J.H., “Polymer critical surface tensions,” Modern Plastics, 48, 66-72, (Jun 1971).

2328. no author cited, “Guide to corona treatment,” Modern Plastics, 38, 199-202+, (Sep 1961).

523. Mapleston, P., “Plasma technology progress improves options in surface treatment,” Modern Plastics Intl., 20, 74-79, (Oct 1990).

610. no author cited, “Corona treatment tackles tough jobs,” Modern Plastics Intl., 17, 56-58, (Jan 1987).

616. no author cited, “Plasma treated plastics parts have improved paintability, bondability,” Modern Plastics Intl., 19, 4-6, (Mar 1989).

972. Gabriele, M.C., “Corona systems keep pace with end-use demands,” Modern Plastics Intl., 29, 28-29, (Feb 1999).

1043. Colvin, R., “Novel plasma method treats polymer rather than part,” Modern Plastics Intl., 29, 33-34, (Apr 1999).

1046. Gabriele, M.C., “'Cold-plasma' system takes on polyolefin parts,” Modern Plastics Intl., 28, 46, (Feb 1998).

1520. Rosato, D., “Plasma bonding polymer to polymer,” Molding Views, (Oct 2006).

1548. Manges, M., “Plasma treatment for medical device assembly,” Moll Medical, Seagrove Div., Apr 2006.

2796. Huber, M.L., “Models for viscosity, thermal conductivity, and surface tension of selected pure fluids as implemented in REFPROP v10.0,” NIST,

2604. Duncan, B., R. Mera, D. Leatherdale, M. Taylor, and R. Musgrove, “Techniques for characterising the wetting,. coating and spreading of adhesives on surfaces (NPL Report DEPC MPR 020),” National Physical Laboratory, Mar 2005.

25. Blake, T.D., and K.J. Ruschak, “A maximum speed of wetting,” Nature, 282, 489-490, (1979).

The wetting (or dewetting) of a solid by a liquid is an integral part of many important processes such as coating, petroleum recovery, distillation and the handling of liquid fuels in low gravity conditions. Several experiments1–4 have shown that wetting lines (where liquid, air and solid phases meet) which are straight at slow rates of movement over the solid have a sawtooth shape at sufficiently high speeds. We now offer a quantitative explanation for this phenomenon based on the postulate that, for a given system, there is a maximum rate at which wetting can proceed. The consequences of this interpretation are likely to be important, since, in many practical situations, the aim is to maximise the speed of wetting without entraining the displaced phase.

 

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