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Microscopic shear

Shear controlled orientation technology was developed to optimize plastic properties by orientation of filler particles. In this patented technology, the single feed is split into a plurality of feeds which can supply pressure to the mold cavity independent of the feed channel. Figure 7.3 shows feed arrangements. The shear is applied by a controlled movement of pistons which imposes microscopic shear. A perfect alignment of fibers can be obtained. [Pg.352]

In the measmements, an oscillatory microscopic shear strain of sine form is imposed on the liquid (Kanbara, 1982 Doi, 1993 Guizard, 1992). The sinusoidal strain is expressed as ... [Pg.939]

Carpick R W, Agrait N, Ogletree D F and Salmeron M 1996 Measurement of interfacial shear (friction) with an ultrahigh vacuum atomic force microscope J. Vac. Sc/. Technol. B 14 1289... [Pg.1724]

Using the fluctuation-dissipation theorem [361, which relates microscopic fluctuations at equilibrium to macroscopic behaviour in the limit of linear responses, the time-dependent shear modulus can be evaluated [371 ... [Pg.2528]

Many of the mesoscale techniques have grown out of the polymer SCF mean field computation of microphase diagrams. Mesoscale calculations are able to predict microscopic features such as the formation of capsules, rods, droplets, mazes, cells, coils, shells, rod clusters, and droplet clusters. With enough work, an entire phase diagram can be mapped out. In order to predict these features, the simulation must incorporate shape, dynamics, shear, and interactions between beads. [Pg.273]

Foams that ate relatively stable on experimentally accessible time scales can be considered a form of matter but defy classification as either soHd, Hquid, or vapor. They are sol id-1 ike in being able to support shear elastically they are Hquid-like in being able to flow and deform into arbitrary shapes and they are vapor-like in being highly compressible. The theology of foams is thus both complex and unique, and makes possible a variety of important appHcations. Many features of foam theology can be understood in terms of its microscopic stmcture and its response to macroscopically imposed forces. [Pg.426]

Hardness. The Knoop indentation hardness of vitreous sihca is in the range of 473—593 kg/mm and the diamond pyramidal (Vickers) hardness is in the range of 600—750 kg/mm (1 4). The Vickers hardness for fused quartz decreases with increasing temperature but suddenly decreases at approximately 70°C. In addition, a small positive discontinuity occurs at 570°C, which may result from a memory of quartz stmcture (165). A maximum at 570°C is attributed to the presence of small amounts of quartz microcrystals (166). Scanning electron microscopic (sem) examination of the indentation area indicates that deformation is mainly from material compaction. There is htfle evidence of shear flow (167). [Pg.506]

On a microscopic scale, the deformations are shown in Figure 3-15. Note that the matrix deforms more than the fiber in shear because the matrix has a lower shear modulus. The total shearing deformation is... [Pg.133]

Molecular dynamics, in contrast to MC simulations, is a typical model in which hydrodynamic effects are incorporated in the behavior of polymer solutions and may be properly accounted for. In the so-called nonequilibrium molecular dynamics method [54], Newton s equations of a (classical) many-particle problem are iteratively solved whereby quantities of both macroscopic and microscopic interest are expressed in terms of the configurational quantities such as the space coordinates or velocities of all particles. In addition, shear flow may be imposed by the homogeneous shear flow algorithm of Evans [56]. [Pg.519]

M. Kroger, R. Makhloufi. Wormlike micelles under shear flow A microscopic model studied by nonequihbrium molecular dynamics computer simulations. Phys Rev E 55 2531-2536, 1996. [Pg.552]

Crystals are sohds. Sohds, on the other hand can be crystalhne, quasi-crystal-hne, or amorphous. Sohds differ from liquids by a shear modulus different from zero so that solids can support shearing forces. Microscopically this means that there exists some long-range orientational order in the sohd. The orientation between a pair of atoms at some point in the solid and a second (arbitrary) pair of atoms at a distant point must on average remain fixed if a shear modulus should exist. Crystals have this orientational order and in addition a translational order their atoms are arranged in regular lattices. [Pg.854]

As an indication of the changes in deformation modes that can be produced in ionomers by increase of ion content, consider poly(styrene-co-sodium methacrylate). In ionomers of low ion content, the only observed deformation mode in strained thin films cast from tetra hydrofuran (THF), a nonpolar solvent, is localized crazing. But for ion contents near to or above the critical value of about 6 mol%, both crazing and shear deformation bands have been observed. This is demonstrated in the transmission electron microscope (TEM) scan of Fig. 3 for an ionomer of 8.2 mol% ion content. Somewhat similar deformation patterns have also been observed in a Na-SPS ionomer having an ion content of 7.5 mol%. Clearly, in both of these ionomers, the presence of a... [Pg.146]

The solidity of gel electrolytes results from chain entanglements. At high temperatures they flow like liquids, but on cooling they show a small increase in the shear modulus at temperatures well above T. This is the liquid-to-rubber transition. The values of shear modulus and viscosity for rubbery solids are considerably lower than those for glass forming liquids at an equivalent structural relaxation time. The local or microscopic viscosity relaxation time of the rubbery material, which is reflected in the 7], obeys a VTF equation with a pre-exponential factor equivalent to that for small-molecule liquids. Above the liquid-to-rubber transition, the VTF equation is also obeyed but the pre-exponential term for viscosity is much larger than is typical for small-molecule liquids and is dependent on the polymer molecular weight. [Pg.513]


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