Segment length, characteristic

Comparing Eqs. (83), (84) and Eqs. (21), (22) it follows immediately that Rouse and Zimm relaxation result in completely different incoherent quasielastic scattering. These differences are revealed in the line shape of the dynamic structure factor or in the (3-parameter if Eq. (23) is applied, as well as in the structure and Q-dependence of the characteristic frequency. In the case of dominant hydrodynamic interaction, Q(Q) depends on the viscosity of the pure solvent, but on no molecular parameters and varies with the third power of Q, whereas with failing hydrodynamic interaction it is determined by the inverse of the friction per mean square segment length and varies with the fourth power of Q. 

For the segment length we take where the characteristic ratio... 

The unconventional applications of SEC usually produce estimated values of various characteristics, which are valuable for further analyses. These embrace assessment of theta conditions for given polymer (mixed solvent-eluent composition and temperature Section 16.2.2), second virial coefficients A2 [109], coefficients of preferential solvation of macromolecules in mixed solvents (eluents) [40], as well as estimation of pore size distribution within porous bodies (inverse SEC) [136-140] and rates of diffusion of macromolecules within porous bodies. Some semiquantitative information on polymer samples can be obtained from the SEC results indirectly, for example, the assessment of the polymer stereoregularity from the stability of macromolecular aggregates (PVC [140]), of the segment lengths in polymer crystallites after their controlled partial degradation [141], and of the enthalpic interactions between unlike polymers in solution (in eluent) [142], as well as between polymer and column packing [123,143]. 

Mean Electronic Density of PE Segments and Determination of Characteristic Segment Length... 

A high segment length value A of rigid chain polymers leads to many characteristic hydrodynamic properties of their solutions differing from those of flexible polymers. 

Some important properties of polymer chains in dilute solutions [steric hindrance parameter, characteristic ratio, persistence length, radius of gyration, statistical chain segment length (introduced earlier, in Chapter 11), intrinsic viscosity, and viscosity at small but finite concentrations] will be discussed, and new correlations will be presented for the steric hindrance parameter and the molar stiffness function, in Chapter 12. 

Several parameters, most of which are interrelated and can be estimated in terms of each other, are utilized to describe the conformational properties of polymer chains [1,2]. These quantities include the steric hindrance parameter a, the characteristic ratio Cx, the persistence length Ip, the statistical chain segment (or Kuhn segment) length lk, the root mean square radius of gyration Rg (often briefly referred to as simply the "radius of gyration"), and the molar... 

Physics-based methods are implemented when direct analysis of the system or its resources is feasible. With regard to the human system, such methods are commonly applied in biomechanical analysis where unknown parameters, such as joint torque, are derived from known characteristics, such as segment lengths and reaction forces, based on estabhshed physical laws and relationships. 

Hence, the perfonned within the framewoik of fractal approach analysis of behavior of polystirene, modified by Dendron s, in diluted solutions gave the same conclusions, as the analysis within the fiamewoik of classical approaches. The main distinction of the indicated approaches is the fact, that the structural model, allowing to describe quantitatively macromolecules structural state and conformation, was placed in the fractal approach base. Other characteristics (gyration radius, Kuhn segment length and so on) are the function of the indicated structural state of a macromolecule. The fractal analysis methods, used for the description of linear flexible-chain polymers behavior, can be applied successfiilly also in case of polymers with more complex macromolecular architecture. 

---