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Surface energy of the material

Mag., 25(1), 131 (1972)] conclude that these measurements are valid when 50 percent corrections are added for the bending energy of the crystal. Kuznetzov ranks other materials by a relative wear test. His results substantiate the efficiencies given earlier. Attempts to measure efficiency of the grinding process by calorimetiy involve errors that exceed the theoretical surface energy of the material being ground. [Pg.1832]

The usual procedure, however, does not follow Laplace s precedent, but rather uses Dupre s scheme. Consider a bar, of unit area cross section and containing 2n atomic layers perpendicular to the axis of the bar n is a large number. Let the internal energy of the bar be E0. If the bar is cut in two, so that each half contains n atomic layers, the energy of the system changes to Ey. One-half of the difference between the two energies is considered to be (specific) surface energy of the material, that is 7 = 0.5 (Ex - E0). The factor 0.5 appears, of course, because two rupture surfaces are formed by one act of separation. [Pg.11]

Despite limitations, the most common sorption medium is activated charcoal — a form of carbon treated in such a way as to open a large number of pores. The surface energy of the material and the pores combine to produce a material that can first attract and then trap small organic molecules. The attraction is via adsorption rather than absorption. Adsorption applies to attachment to the surface absorption is a bulk effect. Extraction is a bulk phenomenon. Simply put, adsorption is a function of surface area while absorption is a mass effect. [Pg.84]

Now we let G be the surface energy of the material and let s also assume that the material will fail in an ideal brittle fashion by cleanly breaking the bonds across our selected plane (Figure 13-27). If we keep in mind that two surfaces are created when we break our sample and assume that all the strain energy is converted to surface energy we can write Equation 13-20 ... [Pg.415]

The point to notice is that a threshold level of stored energy in the bond is necessary before AG -> 0 and thus before the forward reaction can proceed. This stored energy is, of course, equal to AG and thus (when normalised) to the surface energy of the material. Thus we see that the kinetic model of fracture requires a minimum energy supply equal to the surface energy, which is the fracture criterion employed by Griffith. No contradiction therefore exists between the kinetic and Griffith theories. [Pg.9]

Variations in chemical composition and molecular structure can also have important repercussions on the surface energy of the material. Several techniques have been proposed for the experimental determination of surface tension, the sessile and pendant drop methods being the most promising and commonly used... [Pg.2681]

A plate of high-density polyethylene has a surface crack 7.5 pm in one face. The plate fractures in a brittle fashion when a force of 6 X 10 N m is apphed in a direction perpendicular to the crack. The elastic modulus of the polyethylene is 0.95 GPa. Estimate the surface energy of the material. [Pg.335]

Draw a figure showing the change in equilibrium vapour pressure with the radius of curvature of a material (from 0.01 pm to 10 pm) at 1000°C. Assume the molar volume and the surface energy of the material to be 1 X 10 m and 1 J/m, respectively. [Pg.31]

Nanoscale architecture is defined by a feature or grain size less than 100 nm. This architecture affects the roughness, surface area and surface energy of the material... [Pg.149]

The wettability, and hence ability to bond, of oxidized polyethylene decreases quickly upon heating it to 85°C (66). Apparently, oxygen-containing groups in the surface spontaneously turn inward toward the bulk of the sample, so that the surface energy of the material is reduced and the hydrocarbon character of the surface is increased. At room temperature, the loss of bondability is slower since the chains have less mobility for this redistribution. [Pg.324]

Adhesion is the molecular force of attraction between unlike materials. The strength of attraction is determined by the surface energy of the materials. The higher the surface energy, the greater is the molecular attraction while the lower the surface energy, the weaker is the attractive force. The adhesion energy, or the work of adhesion, is defined as the work per unit area that needs to be provided to separate reversibly a solid-liquid interface so as to create solid-vapor and liquid-vapor interfaces [52]. Thus... [Pg.150]

Hot isostatic pressing (HIP) is carried out at 30 MPa on a ceramic material. The same material was prepared by conventional sintering to get the same pore diameter of 8 p. If the surface energy (%) of the material is 650 mN/m, what are the driving forces for both the processes ... [Pg.269]

In this equation, y is the surface energy of the material. The "2" in the equation represents the two surfaces created. Now, the total internal energy of the parallelepiped has become the sum of Equations 15.50 and 15.51. This sum is given by Equation 15.52. [Pg.296]


See other pages where Surface energy of the material is mentioned: [Pg.25]    [Pg.154]    [Pg.2]    [Pg.25]    [Pg.122]    [Pg.427]    [Pg.41]    [Pg.52]    [Pg.1263]    [Pg.362]    [Pg.885]    [Pg.126]    [Pg.243]    [Pg.243]    [Pg.255]    [Pg.154]    [Pg.220]    [Pg.161]    [Pg.1066]    [Pg.45]    [Pg.303]    [Pg.204]    [Pg.673]    [Pg.694]    [Pg.34]    [Pg.65]    [Pg.333]    [Pg.227]    [Pg.28]    [Pg.420]    [Pg.455]    [Pg.708]    [Pg.398]    [Pg.72]    [Pg.60]    [Pg.299]   
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