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Wetting interaction

Metal-ceramic interface interactions wetting and interfacial energies... [Pg.156]

Metal Chemical interaction Wetting angle Remarks ... [Pg.124]

S/L interactions, which are both metallic. No wetting is observed in the CU/AI2O3 system (0 = 128°, Table 6.1) which features strong L/L but weak S/L interactions. However, many organic liquids, whose cohesion is due to weak, physical, interactions, wet silica well despite the fact that their S/L interactions are rather weak (Johnson and Dettre 1993). [Pg.45]

Irrespective of the method of preparation there are two fundamental and critical issues associated with translating or transferring the unique properties of carbon nanotubes to a polymer matrix. Firstly, the nanotubes must be uniformly distributed and dispersed throughout the polymer matrix, and secondly, there must be enhanced interfacial interaction/wetting between the polymer and the nanotubes. For example, any load applied to the polymer matrix should be transferred to the nanotube. This load relies on the effective interfacial stress transfer at the polymer-nanotube interface, which tends to be polymer dependent (7). Three general approaches have been adopted in attempts to modify the surface of CNTs to promote such interfacial interactions chemical, electrochemical and plasma treatment. For example, Castafio et al. (8) placed different organofunctional groups... [Pg.2257]

Notice in Table XVIII-1 a value for the self-diffusion of Ni on Ni(lll) measured using radioactive Ni. More gross processes can occur. Supported Ni crystallites (on alumina) may show spreading and wetting phenomena due to complex interactions with the substrate [146]. [Pg.711]

Figure B3.6.3. Sketch of the coarse-grained description of a binary blend in contact with a wall, (a) Composition profile at the wall, (b) Effective interaction g(l) between the interface and the wall. The different potentials correspond to complete wettmg, a first-order wetting transition and the non-wet state (from above to below). In case of a second-order transition there is no double-well structure close to the transition, but g(l) exhibits a single minimum which moves to larger distances as the wetting transition temperature is approached from below, (c) Temperature dependence of the thickness / of the enriclnnent layer at the wall. The jump of the layer thickness indicates a first-order wetting transition. In the case of a conthuious transition the layer thickness would diverge continuously upon approaching from below. Figure B3.6.3. Sketch of the coarse-grained description of a binary blend in contact with a wall, (a) Composition profile at the wall, (b) Effective interaction g(l) between the interface and the wall. The different potentials correspond to complete wettmg, a first-order wetting transition and the non-wet state (from above to below). In case of a second-order transition there is no double-well structure close to the transition, but g(l) exhibits a single minimum which moves to larger distances as the wetting transition temperature is approached from below, (c) Temperature dependence of the thickness / of the enriclnnent layer at the wall. The jump of the layer thickness indicates a first-order wetting transition. In the case of a conthuious transition the layer thickness would diverge continuously upon approaching from below.
Many of the unusual properties of the perfluorinated inert fluids are the result of the extremely low intermolecular interactions. This is manifested in, for example, the very low surface tensions of the perfluorinated materials (on the order of 9-19 mN jm. = dyn/cm) at 25°C which enables these Hquids to wet any surface including polytetrafluoroethene. Their refractive indexes are lower than those of any other organic Hquids, as are theh acoustic velocities. They have isothermal compressibilities almost twice as high as water. Densities range from 1.7 to 1.9 g/cm (l )-... [Pg.297]

It is also important to study the interactions of papermaking additives (4) in the paper machine water system some additives act synergisticaHy, so that the performance of each is enhanced by the presence of the other. However, some additives have a negative impact on the performance of other additives, or on other desirable paper properties. Thus, optimization of the addition points and usage rates of the entire additive system is necessary in order to maximize performance of the chemical additives and the paper sheet properties, and to minimize cost and negative interactions both on the paper machine and in the white-water system. This is especially tme as unanticipated additives enter the wet end of the paper machine from recycled furnishes, including coated broke (5). [Pg.15]

Pigments Aftertreatments. The surfaces of pigment particles can have different properties and composition than the particle centers. This disparity can be caused by the absorption of ions during wet milling, eg, the —OH groups, on the surface. In some cases, surfaces are modified intentionaHy to improve the pigments appHcation properties, interaction with the organic matrix, and weather resistance. [Pg.5]

The surface film or sprea ding pressure, FI, is used to account for the change in gas—soHd interaction caused by adsorption of vapor evaporated from the Hquid. A Hquid is called wetting if the contact angle from soHd to Hquid through gas, 65 0 nonwetting if > 90°. Because it is easier to... [Pg.541]

The abiHty to tailor both head and tail groups of the constituent molecules makes SAMs exceUent systems for a more fundamental understanding of phenomena affected by competing intermolecular, molecular—substrate and molecule—solvent interactions, such as ordering and growth, wetting, adhesion, lubrication, and corrosion. Because SAMs are weU-defined and accessible, they are good model systems for studies of physical chemistry and statistical physics in two dimensions, and the crossover to three dimensions. [Pg.536]

In addition to the restrictions on their mobiHty caused by steric and polar interactions between chemical groups, the protein molecules in wool fibers are covalentiy cross-linked by disulfide bonds. Permanent setting only occurs if these disulfide bonds are also rearranged to be in equiHbrium with the new shape of the fiber. Disulfide bond rearrangement occurs only at high temperature (>70° C) in wet wool and at even higher temperatures (above 100°C) in... [Pg.350]

Cross-linked finishes are not permanent in the tme sense of the word however, under optimum conditions the finish can last for the usehil life of the material. Wet abrasion during laundering is probably the principal cause of gradual removal of the finish. In order to retain antistatic protection for extended use, an excess of finish is often appHed The extent of chemical interaction between the durable antistatic agents and the fiber substrates to which they are appHed is not perfectiy understood. Certain oxidizing agents such as hypochlorite bleaches tend to depolymerize and remove some durable antistatic finishes. Some of the durable finishes have also produced undesirable side effects on textile materials, ie, harsh hand, discoloration, and loss of tensile properties. [Pg.294]


See other pages where Wetting interaction is mentioned: [Pg.126]    [Pg.206]    [Pg.283]    [Pg.420]    [Pg.737]    [Pg.125]    [Pg.125]    [Pg.397]    [Pg.129]    [Pg.126]    [Pg.700]    [Pg.41]    [Pg.2331]    [Pg.126]    [Pg.206]    [Pg.283]    [Pg.420]    [Pg.737]    [Pg.125]    [Pg.125]    [Pg.397]    [Pg.129]    [Pg.126]    [Pg.700]    [Pg.41]    [Pg.2331]    [Pg.411]    [Pg.466]    [Pg.467]    [Pg.519]    [Pg.314]    [Pg.1642]    [Pg.1714]    [Pg.2374]    [Pg.2374]    [Pg.117]    [Pg.79]    [Pg.347]    [Pg.428]    [Pg.432]    [Pg.149]    [Pg.154]    [Pg.15]    [Pg.320]    [Pg.541]    [Pg.363]    [Pg.381]    [Pg.50]    [Pg.347]   
See also in sourсe #XX -- [ Pg.482 ]




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Wetting interaction PDMS surfaces

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