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Polymer chain segment

Fig. XI-4. Schematic diagram of the structure of an adsorbed polymer chain. Segments are distributed into trains directly attached to the surface and loops and tails extending into solution. Fig. XI-4. Schematic diagram of the structure of an adsorbed polymer chain. Segments are distributed into trains directly attached to the surface and loops and tails extending into solution.
More fundamental treatments of polymer solubihty go back to the lattice theory developed independentiy and almost simultaneously by Flory (13) and Huggins (14) in 1942. By imagining the solvent molecules and polymer chain segments to be distributed on a lattice, they statistically evaluated the entropy of solution. The enthalpy of solution was characterized by the Flory-Huggins interaction parameter, which is related to solubihty parameters by equation 5. For high molecular weight polymers in monomeric solvents, the Flory-Huggins solubihty criterion is X A 0.5. [Pg.435]

Classical X-ray diffraction and scattering is carried out in the subarea of wide-angle X-ray scattering (WAXS). The corresponding scattering patterns yield information on the arrangement of polymer-chain segments (e.g., orientation of the amorphous phase, crystalline structure, size of crystals, crystal distortions, WAXS crystallinity). [Pg.25]

H, R and two Polymer chain segments of chain length m and n as shown below ... [Pg.261]

In other words, we try to mimic enzymes by attaching centers for homogeneous catalysis to polymer chains we want to learn from nature how to conduct chemical processes in a cleaner, more selective and milder way. In this respect it is of great importance that we can adapt, just like in enzymes, the micro-environment of the catalytic centers by modification of neighbouring polymer chain segments. [Pg.7]

Figure 4. Schematic of electron transfer processes for 2,6-disubstituted phenol. The ligand groups are indicated as Am and the intermediate polymer chain segments as straight lines, (a) Hydroxo-bridged catalyst (b) chloro-bridged catalyst. Figure 4. Schematic of electron transfer processes for 2,6-disubstituted phenol. The ligand groups are indicated as Am and the intermediate polymer chain segments as straight lines, (a) Hydroxo-bridged catalyst (b) chloro-bridged catalyst.
Polymerization leads to a polymer structure (VII) with a repeating alkene double bond in the polymer chain. The double bond in each repeating unit of the polymer chain is a site of steric isomerism since it can have either a cis or a trans configuration. The polymer chain segments on each carbon atom of the double bond are located on the same side of the double... [Pg.628]

Typical data from such an experiment for PDN6S are seen in Figure 3. For multiphoton exposure, the birefringence initially rises until a saturation value is reached, then begins to diminish. This corresponds to the initial scission of the polymer chain segments aligned with the pulsed laser exposure and subsequent scission of polymer chain segments of other orientations. [Pg.643]

C. M. Ylitalo, G. G. Fuller, V. Abetz, and R. Stadler, and D.S. Pearson, Relaxation dynamics of selected polymer chain segments and comparison with theoretical models, Rheol. Acta, 29, 543 (1990). [Pg.253]

Polymers above their Tg are in a state of equilibrium much like simple liquids. However, upon cooling below Tg, polymers are not able to achieve an equilibrium state since the polymer chain segments lack sufficient mobility to reach this state in realizable time scales. Thus, glassy polymers exist in a nonequilibrium state that is a function of the prior history of the sample. It is useful to think of simple volumetric thermal expansion where at equilibrium the specific volume at a given temperature and pressure is Veq(T,p) the specific volume of a rubbery polymer is given by Veq. The... [Pg.64]

It is noted that the UV absorbance of the 10(g)-32(sc) sample decreased after the annealing treatment, as shown in Fig. 28a. Presumably, most polysilane chains lie down before annealing in the quartz substrate plane, as the film was prepared by the spin-coating technique. However, the thermal annealing treatment of semi-flexible 32 tends to orient some of the polymer chain segments perpendicularly and/or tilt them to the substrate plane, leading to the decrease in the apparent UV absorbance at 321 nm, as illustrated in Fig. 27. [Pg.171]


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See also in sourсe #XX -- [ Pg.3 , Pg.3 , Pg.4 , Pg.4 ]




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