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Reactive mixing shear

So, for given strain rate s and v (a function of the applied shear stress in the shock front), the rate of mixing that occurs is enhanced by the factor djhy due to strain localization and thermal trapping. This effect is in addition to the greater local temperatures achieved in the shear band (Fig. 7.14). Thus we see in a qualitative way how micromechanical defects can enhance solid-state reactivity. [Pg.245]

Approach ii is applicable to all thermoplastic polymers and offers considerable practical advantage since reactively modified polymers can be readily produced by normal commercial high-shear mixing procedures at no additional cost. [Pg.412]

Tubular flow reactors (TFR) deviate from the idealized PFR, since the applied pressure drop creates with viscous fluids a laminar shear flow field. As discussed in Section 7.1, shear flow leads to mixing. This is shown schematically in Fig. 11.9(a) and 11.9(b). In the former, we show laminar distributive mixing whereby a thin disk of a miscible reactive component is deformed and distributed (somewhat) over the volume whereas, in the latter we show laminar dispersive mixing whereby a thin disk of immiscible fluid, subsequent to being deformed and stretched, breaks up into droplets. In either case, diffusion mixing is superimposed on convective distributive mixing. Figure 11.9(c) shows schematically the... [Pg.616]

Fig. 11.9 Types of linear continuous-flow reactors (LCFRs). (a) Continuous plug flow reactor (CPFR) resembling a batch reactor (BR) with the axial distance z being equivalent to time spent in a BR. (b) A tabular flow reactor (TFR) with (tq) miscible thin disk of reactive component deformed and distributed (somewhat) by the shear field over the volume, and (b2) immiscible thin disk is deformed and stretched and broken up into droplets in a region of sufficiently high shear stresses, (c) SSE reactor with (cj) showing laminar distributive mixing of a miscible reactive component initially placed at z = 0 as a thin slab, stretched into a flat coiled strip at z L, and (c2) showing dispersive mixing of an immiscible reactive component initially placed at z — 0 as a thin slab, stretched and broken up into droplets at z — L. Fig. 11.9 Types of linear continuous-flow reactors (LCFRs). (a) Continuous plug flow reactor (CPFR) resembling a batch reactor (BR) with the axial distance z being equivalent to time spent in a BR. (b) A tabular flow reactor (TFR) with (tq) miscible thin disk of reactive component deformed and distributed (somewhat) by the shear field over the volume, and (b2) immiscible thin disk is deformed and stretched and broken up into droplets in a region of sufficiently high shear stresses, (c) SSE reactor with (cj) showing laminar distributive mixing of a miscible reactive component initially placed at z = 0 as a thin slab, stretched into a flat coiled strip at z L, and (c2) showing dispersive mixing of an immiscible reactive component initially placed at z — 0 as a thin slab, stretched and broken up into droplets at z — L.
First and foremost, the laminar mixing flow created in the reactive processing equipment, must reduce the striation thickness to a level where the diffusion characteristic time, tD = r2/ )AB, is small compared to the reaction characteristic time. Since the molecular diffusivities of low molecular weight components in polymeric melts (see Section 8.3) are very small and of the order of 10 6 cm2/s, the striation thickness must be reduced to the micron level in order to get a characteristic time t of the order of 1 s. Shear flow can accomplish this in reasonable mixing times because the striation thickness is inversely proportional to the total shear (see Section 7.3)... [Pg.623]

As with any crystallization process, reactive crystallization will, in general, produce fine particles unless the entire operation is run within the metastable region. This condition can be realized by provision of heavy seeding and by slow addition to control supersaturation at a low level. Adequate mixing is necessai-y, but shear damage must be avoided by selection of the correct impeller speed and type. [Pg.224]

Some polymers contain reactive functionahty but are also themselves subject to mechano-chemical radical generation. When such polymers are blended under high-shear mixing with a second functionalized polymer, the architectures... [Pg.404]

One way to achieve compatibilization involves physical processes such as shear mixing and thermal history, which modify domain size and shape. The second way is the use of physical additives to increase attraction between molecules and phases. The third method is reactive processing, which is used to change the chemical structure of one or more of the components in the blend and thus increase their attraction to each other. Table 1.5 contains a list of compatibilizers used in the formulation of polyolefin blends. As can be seen from Table 1.5, most of the compatibilizers used in the formulation of polyolefin blends contain compounds such as maleic anhydride, acrylic and methacrylic acid, glycidyl methacrylate, and diblock and triblock copolymers involving styrene, ethylene, and butadiene. [Pg.14]

In a separate vessel, combine the mineral spitits and the reactive amine polymer. Add to the above mixture with high shear mixing. [Pg.207]


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Shear mixing

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