Analysis of the Phase Structure Development during the Melt Mixing of Polymer Blends

1996 ◽  
Vol 28 (2) ◽  
pp. 106-139 ◽  
Author(s):  
Ivan Fortelný ◽  
Josef Kovář ◽  
Michael Stephan
Polymers ◽  
2020 ◽  
Vol 12 (6) ◽  
pp. 1226 ◽  
Author(s):  
Ivo Kuřitka ◽  
Vladimír Sedlařík ◽  
Diana Harea ◽  
Evghenii Harea ◽  
Pavel Urbánek ◽  
...  

In this paper, we present the use of a disubstituted polyacetylene with high thermal stability and quantum yield as a fluorescence label for the identification, tracing, recycling, and eventually anti-counterfeiting applications of thermoplastics. A new method was developed for the dispersion of poly[1-phenyl-2-[p-(trimethylsilyl)phenyl]acetylene] (PTMSDPA) into polymer blends. For such purposes, four representative commodity plastics were selected, i.e., polypropylene, low-density polyethylene, poly(methyl methacrylate), and polylactide. Polymer recycling was mimicked by two reprocessing cycles of the material, which imparted intensive luminescence to the labelled polymer blends when excited by proper illumination. The concentration of the labelling polymer in the matrices was approximately a few tens ppm by weight. Luminescence was visible to the naked eye and survived the simulated recycling successfully. In addition, luminescence emission maxima were correlated with polymer polarity and glass transition temperature, showing a marked blueshift in luminescence emission maxima with the increase in processing temperature and time. This blueshift results from the dispersion of the labelling polymer into the labelled polymer matrix. During processing, the polyacetylene chains disentangled, thereby suppressing their intermolecular interactions. Moreover, shear forces imposed during viscous polymer melt mixing enforced conformational changes, which shortened the average conjugation length of PTMSDPA chain segments. Combined, these two mechanisms shift the luminescence of the probe from a solid- to a more solution-like state. Thus, PTMSDPA can be used as a luminescent probe for dispersion quality, polymer blend homogeneity, and processing history, in addition to the identification, tracing, and recycling of thermoplastics.


Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 761 ◽  
Author(s):  
Fortelný ◽  
Jůza

Control of the phase structure evolution in flowing immiscible polymer blends during their mixing and processing is fundamental for tailoring of their performance. This review summarizes present state of understanding and predictability of the phase structure evolution in flowing immiscible polymer blends with dispersed structure. Results of the studies of the droplet breakup in flow, important for determination of the droplet breakup frequency and of the size distribution of the daughter droplets, are reviewed. Theories of the flow-induced coalescence providing equations for collision efficiency are discussed. Approximate analytic expressions reliably describing dependence of the collision efficiency on system parameters are presented. Available theories describing the competition between the droplet breakup and coalescence in flow are summarized and approximations used in their derivation are discussed. Problems with applicability of available theories on prediction of the droplet size evolution during mixing and processing of immiscible polymer blends, which have not been broadly discussed so far, are addressed.


2013 ◽  
Vol 291-294 ◽  
pp. 2654-2656
Author(s):  
Nor Azwin Ahad ◽  
Sahrim Hj Ahmad ◽  
Norazwani Muhammad Zain

The blends of thermoplastic polyurethane (TPU) with natural rubber (NR) were prepared via melt mixing technique, at four different blending temperature at range 180°C - 210°C and mixing times of 8, 10, 12, 14 min. The effects of both mixing parameters on tensile strength of the blends were investigated. The blend of 85TPU15NR shows the maximum tensile strength at 180°C and 10 min mixing. The viscosity of the polymer blends will decrease as the temperature increased. The movements of molecules are more worthy because of the poor molecules interaction. The increasing of mixing time will increase the compatibility of the blends and also increase in mechanical properties. Mixing time and mixing temperature are important parameters in acquiring blends having optimum mechanical properties.


2015 ◽  
Vol 26 (1) ◽  
pp. 015014 ◽  
Author(s):  
Xiong Liang ◽  
Xiaoyu Wu ◽  
Bin Xu ◽  
Jiang Ma ◽  
Zhiyuan Liu ◽  
...  

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