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A. D. Drozdov

Publications and source records attributed to A. D. Drozdov.

21 records · Page 2Linked to original sources

The nonlinear time-dependent response of isotactic polypropylene

Tensile creep tests, tensile relaxation tests and a tensile test with a constant rate of strain are performed on injection-molded isotactic polypropylene at room temperature in the vicinity of the yield point. A constitutive model is derived for the time-dependent behavior of semi-crystalline polymers. A polymer is treated as an equivalent network of chains bridged by permanent junctions. The network is modelled as an ensemble of passive meso-regions (with affine nodes) and active meso-domains (where junctions slip with respect to their positions in the bulk medium with various rates). The distribution of activation energies for sliding in active meso-regions is described by a random energy model. Adjustable parameters in the stress--strain relations are found by fitting experimental data. It is demonstrated that the concentration of active meso-domains monotonically grows with strain, whereas the average potential energy for sliding of junctions and the standard deviation of activation energies suffer substantial drops at the yield point. With reference to the concept of dual population of crystalline lamellae, these changes in material parameters are attributed to transition from breakage of subsidiary (thin) lamellae in the sub-yield region to fragmentation of primary (thick) lamellae in the post-yield region of deformation.

cond-mat.mtrl-sci↗

The effect of annealing on the nonlinear viscoelastic response of isotactic polypropylene

Three series of tensile relaxation tests are performed on isotactic polypropylene at room temperature in the vicinity of the yield point. In the first series of experiments, injection-molded samples are used without thermal pre-treatment. In the second and third series, prior to testing the specimens are annealed at 130 C for 4 and 24 hours, respectively. Constitutive equations are derived for the time-dependent response of semicrystalline polymers at isothermal loading. A polymer is treated as an equivalent temporary network of macromolecules bridged by junctions (physical cross-links, entanglements and crystalline lamellae). Under loading, junctions slip with respect to their positions in the bulk material (which reflects the viscoplastic behavior), whereas chains separate from their junctions and merge with new ones at random times (which reflects the viscoelastic response). The network is thought of as an ensemble of meso-regions (MR) with various activation energies for detachment of chains from temporary nodes. Adjustable parameters in the stress-strain relations are found by fitting observations. Experimental data demonstrate that the shape of the relaxation spectrum (characterized by the distribution of MRs with various potential energies) is independent of mechanical factors, but is altered at annealing. For specimens not subjected to thermal treatment, the growth of longitudinal strain does not affect the volume fraction of active MRs and the attempt rate for detachment of chains from their junctons. For annealed samples, the concentration of active MRs increases and the attempt rate decreases with strain. These changes in the time-dependent response are attributed to broadening of the distribution of strengths of crystalline lamellae at annealing.

cond-mat.mtrl-sci↗

The nonlinear viscoelastic behavior of polypropylene

A series of tensile relaxation tests is performed on isotactic polypropylene in the sub-yield and post-yield regions at room temperature. Constitutive equations are derived for the time-dependent response of a semicrystalline polymer at isothermal loading with small strains. Adjustable parameters in the stress-strain relations are found by fitting experimental data. It is demonstrated that the growth of the longitudinal strain results in an increase in the relaxation rate in a small interval of strains in the sub-yield domain. When the strain exceeds some critical value which is substantially less than the apparent yield strain, the relaxation process becomes strain-independent.

cond-mat.mtrl-sci↗