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Microstructures equilibrium

Cohen and Ramost describe some phase equilibrium studies of block copolymers of butadiene (B) and isoprene (I). One such polymer is described as having a 2 1 molar ratio of B to I with the following microstructure ... [Pg.67]

Carbon steels as received "off the shelf" have been worked at high temperature (usually by rolling) and have then been cooled slowly to room temperature ("normalised"). The room-temperature microstructure should then be close to equilibrium and can be inferred from the Fe-C phase diagram (Fig. 11.1) which we have already come across in the Phase Diagrams course (p. 342). Table 11.1 lists the phases in the Fe-FejC system and Table 11.2 gives details of the composite eutectoid and eutectic structures that occur during slow cooling. [Pg.113]

The sequence just outlined provides a salutary lesson in the nature of explanation in materials science. At first the process was a pure mystery. Then the relationship to the shape of the solid-solubility curve was uncovered that was a partial explanation. Next it was found that the microstructural process that leads to age-hardening involves a succession of intermediate phases, none of them in equilibrium (a very common situation in materials science as we now know). An understanding of how these intermediate phases interact with dislocations was a further stage in explanation. Then came an nnderstanding of the shape of the GP zones (planar in some alloys, globniar in others). Next, the kinetics of the hardening needed to be... [Pg.90]

If we look at the mechanistic and crystallographic aspects of the operation of polycomponent electrodes, we see that the incorporation of electroactive species such as lithium into a crystalline electrode can occur in two basic ways. In the examples discussed above, and in which complete equilibrium is assumed, the introduction of the guest species can either involve a simple change in the composition of an existing phase by solid solution, or it can result in the formation of new phases with different crystal structures from that of the initial host material. When the identity and/or amounts of phases present in the electrode change, the process is described as a reconstitution reaction. That is, the microstructure is reconstituted. [Pg.365]

Phase transition occurs at a state of thermodynamic equilibrium, inducing a change in the microstructure of atoms. However, corrosion is a typical nonequilibrium phenomenon accompanied by diffusion and reaction processes. We can also observe that this phenomenon is characterized by much larger scales of length than an atomic order (i.e., masses of a lot of atoms), which is obvious if we can see the morphological change in the pitted surface. [Pg.219]

Membrane reactors are known on the macro scale for combining reaction and separation, with additional profits for the whole process as compared with the same separate functions. Microstructured reactors with permeable membranes are used in the same way, e.g. to increase conversion above the equilibrium limit of sole reaction [8, 10, 11, 83]. One way to achieve this is by preparing thin membranes over the pores of a mesh, e.g. by thin-fihn deposition techniques, separating reactant and product streams [11]. [Pg.288]

The copolymers consist of strictly alternating sequences of diene and olefin. C-NMR measurements Showed the microstructure of the butadiene units in BPR to be exclusively of the trans-1,4 configuration (Figure 8). The isoprene units in isoprene-ethylene copolymer (IER) contain 84 % trans-1,4, 15 % cis-1,4, and 1 % 3,4 structures (Figure 9). Spontaneous crystallization in unstretched BPR samples was detected by dilatometry and confirmed by X-ray diffraction and DSC measurements. The extrapolated equilibrium melting point is about -10 °C. [Pg.67]

Figure 3. Modulus contributions from chemical cross-links (Cx, filled triangles) and from chain entangling (Gx, unfilled symbols) plotted against the extension ratio during cross-linking, A0, for 1,2-polybutadiene. Key O, GN, equibiaxial extension , G.v, pure shear A, Gx, simple extension Gx°, pseudo-equilibrium rubber plateau modulus for a polybutadiene with a similar microstructure. See Ref. 10. Figure 3. Modulus contributions from chemical cross-links (Cx, filled triangles) and from chain entangling (Gx, unfilled symbols) plotted against the extension ratio during cross-linking, A0, for 1,2-polybutadiene. Key O, GN, equibiaxial extension , G.v, pure shear A, Gx, simple extension Gx°, pseudo-equilibrium rubber plateau modulus for a polybutadiene with a similar microstructure. See Ref. 10.
The equilibrium, room temperature structure of pure cobalt is hep. The fee structure is stable at high temperatures (422 °C to 1495 °C) and has been retained at room temperature by rapid solidification techniques [101], X-ray diffraction analysis was used to probe the microstructure of bulk Co-Al alloy deposits containing up to 25 a/o Al and prepared from solutions of Co(II) in the 60.0 m/o AlCfi-EtMelmCl melt. Pure Co deposits had the hep structure no fee Co was observed in any of the deposits. The addition of aluminum to the deposit caused a decrease in the deposit grain size and an increase in the hep lattice volume. A further increase in the aluminum content resulted in amorphization of the deposit [44], Because the equilibrium... [Pg.298]

FLUCTUATION PHENOMENA IN AN EQUILIBRIUM MICROSTRUCTURE ON METAL SURFACES... [Pg.135]

The aim of this chapter is to introduce the reader to some of the ways in which the CALPHAD approach has been combined with kinetics to predict the formation of phases and/or microstructures under conditions which are not considered to be in equilibrium. Broadly speaking, the combination of thermodynamics and kinetics can be broken down into at least two separate approaches (1) the calculation of metastable equilibria and (2) the direct coupling of thermodynamic and kinetic modelling. [Pg.428]

In Table II, the product yields of REY-PILC are compared with PILC, a commercial equilibrium catalyst, and with the same commercial catalyst that had been deactivated in the laboratory to near constant conversion. The addition of REY to PILC maintained activity in the presence of steam while coke yield was reduced and the LCO/HCO ratio was slightly higher than for either of the commercial catalysts. This suggests that the microstructure of the PILC after pretreatment D will still convert large molecules into gasoline range products instead of generating coke as seen in PILC alone. [Pg.263]


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See also in sourсe #XX -- [ Pg.135 ]




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Microstructure equilibrium cooling

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