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Matrix fill

Although the reinforcing fibers may be present in the liquid precursor prior to dispensing, better properties are typically obtained when the fibers are initially present in the mold as a preform. The liquid is then dispensed into the mold such that the final matrix fills the mold and surrounds the fibers. Preforms may be arranged as mats or meshes. The fibers within the preform may be randomly oriented or may be oriented in one or more directions. [Pg.22]

Physical and mechanical properties of the filled polymer composite materials (PCM) in dependence on the extent of filling, the rate of deformation were investigated. It was found out that structural properties of the filled composite materials are determined with the nature of polymer matrix, filling degree, nature of the fillers, structural organization of FCM, that is being formed in the process of receiving of the composite materials, and conditions of tests. [Pg.89]

It was logical to suggest that maleated polymers introduced into a polymer matrix filled with cellulose fiber form—at hot melt temperature—covalent ester links between the anhydride groups of the coupling agents and hydroxyl groups on the surface of wood fiber, as they do in model chemical systems. However, studies into the matter have presented no conclusive evidence of such covalent bonds in WPC, except maybe in some isolated cases. [Pg.180]

Figure 2.3 IgG levels after administration of drug delivery systems in rats. Controlled-delivery systems for antibody class IgG. The insert figures show the release of antibody from the delivery system during incubation in buffered saline. The panel (a) inset shows release from poly(lactic acid) microspheres these spherical particles were 10-100/rm in diameter. The panel (b) inset shows release from a poly[ethylene-co-(vinyl acetate)] matrix these disk-shaped matrices were 1 cm in diameter and 1 mm thick. In both cases, molecules of IgG were dispersed throughout the solid polymer phase. Although the amount of IgG released during the initial 1-2 days is greater for the matrix, the delivery systems have released comparable amounts after day 5. (a) Comparison of plasma IgG levels after direct injection of IgG (open circles) or subcutaneous injection of the IgG-releasing polymeric microspheres characterized in the inset (filled circles). The delivery system produces sustained IgG concentrations in the blood [3]. (b) Comparison of plasma IgG levels after direct intracranial injection of IgG (open squares) or implantation of an IgG-releasing matrix (filled squares) [4]. The influence of the delivery is less dramatic in this situation, probably because the rate of IgG movement from the brain into the plasma controls the kinetics of the overall process. Figure 2.3 IgG levels after administration of drug delivery systems in rats. Controlled-delivery systems for antibody class IgG. The insert figures show the release of antibody from the delivery system during incubation in buffered saline. The panel (a) inset shows release from poly(lactic acid) microspheres these spherical particles were 10-100/rm in diameter. The panel (b) inset shows release from a poly[ethylene-co-(vinyl acetate)] matrix these disk-shaped matrices were 1 cm in diameter and 1 mm thick. In both cases, molecules of IgG were dispersed throughout the solid polymer phase. Although the amount of IgG released during the initial 1-2 days is greater for the matrix, the delivery systems have released comparable amounts after day 5. (a) Comparison of plasma IgG levels after direct injection of IgG (open circles) or subcutaneous injection of the IgG-releasing polymeric microspheres characterized in the inset (filled circles). The delivery system produces sustained IgG concentrations in the blood [3]. (b) Comparison of plasma IgG levels after direct intracranial injection of IgG (open squares) or implantation of an IgG-releasing matrix (filled squares) [4]. The influence of the delivery is less dramatic in this situation, probably because the rate of IgG movement from the brain into the plasma controls the kinetics of the overall process.
As Cl concentration in the film exceeds 10w%, it acquires the structure of an open-pore polymer matrix filled with the PI. The sorption mechanism of the liquid Cl by such film is, evidently, similar to that of mass exchange. The inhibitor partly forces PI out of the pores of the polymer matrix and, if its density is lower than that of the PI, this sorption will be accompanied by a mass drop of the film (Table 2.6). [Pg.103]

At the time Tiof setting the pendulum into motion the electrode potential of the tray AU shifts to the positive side (Fig. 4.26). This is because of the mechanochemical activation of metals and damage to the film of the products of electrochemical reactions on the tray surface. At time T2 the pendulum stops. Time At, during which the potential returns to its initial value (before actuation), is seen to reduce with increasing liquid phase in the composite. This regularity is attributed to structural features of the studied composites, which is characterized by a porous polymer matrix filled by the liquid phase liberating from the material in the process of syneresis. [Pg.313]

Fig. 6.10 Shows a microsize Mg(OH)2 flakes b date palm fiber-reinfoiced PO matrix filled with... Fig. 6.10 Shows a microsize Mg(OH)2 flakes b date palm fiber-reinfoiced PO matrix filled with...
Nanocomposites refer to the combination of nanosized fillers (10 m diameter) with polymers, rather than the combination of polymer matrix (filled with nanoparticles) and fiber reinforcement The most popular fillers used as fire retardants are layered silicates. Loading of 10% or less (by weight) of such fillers significantly reduces peak heat release rates and facilitates greater char production [7]. The char layer provides a shielding effect for the composites below and the creation of char also reduces the toxicity of the combustion products, as less carbon is available to form the CO and CO2. [Pg.213]

The Mori-Tanaka model is derived based on the principles of Eshelby s inclusion model for predicting an elastic stress field in and around elUpsoidal filler in an infinite matrix. The complete analytical solufions for longitudinal SI and transverse elastic moduh of an isotropic matrix filled with aligned spherical inclusion are [45,... [Pg.165]

Identifying its possible special structures if structured, it is not necessary to reorder rows and columns to reduce the matrix filling. [Pg.153]

When E is large and sparse, LQ factorization can be computationally onerous and lead to the dangerous matrix filling as well in this case a stable Gauss factorization is required to calculate the null space of the matrix (see Chapter 8). [Pg.404]

The updating of the Hessian of the Lagrange function is often computationally ( ) infeasible because of matrix filling due to the BFGS formula. Conversely, the updating of each Hessian with Schubert s formula minimizes the overall matrix filling. [Pg.455]

The favorable conditions for the superparaelectricity observation in small ferroelectric nanoparticles at room temperatures are small Curie-Weiss constants, high nonlinear coefficients an and narrow distribution function of particles radii. The ensemble of noninteracting ferroelectric nanoparticles could be realized in nanoporous nonferroelectric matrix with the pores filled at least partly by some ferroelectric material. Another type of composite material can be considered also. Namely, it is the material with cylindrical geometry of nanopores in the nonferroelectric matrix filled with ferroelectric nanorods. However some difference in polar behavior for this geometry in comparison with spherical case can be expected. [Pg.278]

The composites can be classified on the basis of the form of their structural components fibrous (composed of fibers in a matrix), laminar (composed of layers of materials), and particulate (composed of particles in a matrix). The particulate class can be further subdivided into flake (flat flakes in a matrix) or skeletal (composed of a continuous skeletal matrix filled by a second material). In general, the reinforcing agent can be either fibrous, powdered, spherical, crystalline, or whiskered and either an organic, inorganic, metallic, or ceramic material. [Pg.214]

Composite kam- pa-z3t, kom-, esp British kam-po-zit [L compositus, pp of compo-nere] (1563) adj. (1) An article or substance made up of two or more distinct phases of different substances. In the plastics industry the term applies broadly to structures of reinforcing members dispersed phase) incorporated in compatible resinous binders continuous phase). Such composites are subdivided into classes on the basis of the reinforcing constituents laminate, particulate (the dispersed phase consists of unlayered fibers) flake (flat flakes forming the dispersed phase) and skeletal (composed of a continuous skeletal matrix filled by a resin). (2) Hard or soft constructions in which the fibers themselves are consolidated to form structures rather than being formed into yarns. Rigidity of these constructions is controlled by the density, the modulus of the load-bearing fibers, and the fraction of fusible... [Pg.216]

The topic of polymer nanocomposites pertains to the synthesis, characterization, and applications of polymer materials with at least one or more dimensions less than 100 nm. According to the Rayleigh criterion, the maximum resolution or the minimum detectable size achievable was believed to be half the wave length of light, that is, 200 nm. The first clay nanocomposite was commercialized by Toyota with a belt cover made of a nylon-6 matrix filled with 5% clay. General Motors commercialized the first exterior trim application of nanocomposite in their 2002 mid-sized vans. [Pg.162]

The suggested grading scheme is 2 for an identity (match), -1 for mismatch, and -2 for the gap penalty show the initialization, matrix fill, and traceback steps. Recover all the possible alignments. [Pg.275]


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See also in sourсe #XX -- [ Pg.86 , Pg.809 ]




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