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Direct evidence of nucleation during the induction period of nucleation from the melt is obtained for the first time by means of small angle X-ray scattering (SAXS). This confirmed that the induction period of crystallization from the melt corresponds to the process of nucleation, not to that of spinodal decomposition. This success is due to a significant increase in the scattering intensity (I ...
Model of nucleation on active centers is applied to formation of folded chain crystals of polyethylene at low supercooling. Nucleation rate and the total number of nuclei are determined by numerical solution of kinetic equations. Thermodynamic and kinetic parameters were chosen to get the coincidence with experimental data for the total number of nuclei and the size distribution of nuclei as a function...
Degree of supercooling (ΔT) dependence of nano-nucleation was studied by means of small angle X-ray scattering (SAXS) and a new nucleation theory was proposed. We obtained the ΔT dependence of size distribution f(N,t) directly, where N is number of particle and t is time, which concluded that the “induction period” of crystallization is not controlled by so called “spinodal decomposition” but by nucleation...
The role of “epitaxy” of nucleating agent (NA) in nucleation mechanism of polymers was studied to formulate the nucleation rate (I) as a function of concentration of NA (C NA ) in mixture of polymer and NA and lateral size of a NA crystal (a NA ), I∝C NA /a NA . It is proved that the epitaxy of NA controls nucleation mechanism by confirming above formula experimentally...
Nucleation mechanism of polymers was studied by means of small angle X-ray scattering (SAXS) by improving our two previous studies. The first one showed first direct SAXS observation of nucleation of polyethylene (PE). The second one reported how “size distribution f(N,t)” of nuclei of nano-meter size (nano-nuclei) evolves with time (t), where N is number of “repeating unit” in a nucleus. Unfortunately...
Molecular weight (M) dependence of the lateral growth rate (V) of α form crystal of isotactic polypropylene (iPP) was studied. Reliable equilibrium melting temperature determined in our previous study was used for the analysis of supercooling dependence of V. A power law of M of V, V∝Mn−H, was obtained, where H is a small constant (H=0.7). The small H, which is similar to that of the hexagonal phase...
“How do chain molecules spontaneously entangle from completely disentangled polymer melt?” remains the most interesting unsolved problem. In order to solve this problem, we used the concept that the melt of “nascent” polymer crystallized during polymerization just after melting does not include any entanglements. We succeeded in detecting the increase of entanglement density ν e with the increase...
In part 1 of this series of paper, we have solved the formation mechanism of shish from the oriented melt based on the kinetic observation. In this work, we have shown for the first time the molecular mechanism of the growth of shish by kinetic study. We found that there are two different type of the growth of shish against the flow direction. The growth rate along the flow direction (U) is proportional...
We have solved the molecular mechanism of the formation of shish of isotactic-polypropylene (iPP) and polyethylene (PE) from the sheared melt based on kinetic study by means of polarizing optical microscope. We found that the rate determining process for the formation of shish is a nucleation process in the most range of degree of supercooling (ΔT) except for large ΔT of PE. We have shown a direct...
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