Non‐isothermal crystallization kinetic of recycled PET and its blends with PBT modified with epoxy‐based multifunctional chain extender
Andreas Himmelsbach,
Christian Brütting,
Yavuz Akdevelioglu
et al.
Abstract:A fundamental understanding of crystallization behavior is essential for the processing of both virgin and recycled polymers. This research delves into the crystallization characteristics and non‐isothermal crystallization kinetics of recycled polyethylene terephthalate (rPET) and its blends with poly butylene terephthalate (PBT), which have been modified using epoxy‐based multifunctional chain extenders (CE). The preparation of rPET/PBT blends involved a twin‐screw extruder, with varying weight ratios and dif… Show more
“…In a previous study, it was demonstrated that when the processed PET/PBT blends are fast-cooled, crystalline phases are immiscible, whereas slow cooling could cause the cocrystallization of PET and PBT, leading to the full miscibility of PET and PBT polymers . The crystallization kinetics of the 25/75 blend sample, which confirms our discussion, is comprehensively studied elsewhere …”
Section: Results
and Discussionsupporting
confidence: 83%
“…54 The crystallization kinetics of the 25/75 blend sample, which confirms our discussion, is comprehensively studied elsewhere. 94 3.3. Bead Foaming Behavior.…”
This study investigates the melt rheological properties and foamability of recycled polyethylene terephthalate (rPET) and its blends with polybutylene terephthalate (PBT) modified through an epoxy-based Joncryl ADR 4468 chain extender. A twinscrew extruder was used to prepare rPET/PBT blends at various weight ratios (i.e., 100/0, 75/25, 50/50, 25/75, and 0/100) and with varying Joncryl chain extender contents (i.e., 0.25, 0.5, 0.75, and 1.0 wt %). The small-amplitude oscillatory shear rheological experiments were conducted to analyze the melt viscoelastic behavior of the samples. The melt strength and strain-hardening behavior of the compounds were examined by measuring the extensional rheology and Rheotens tests. Crystallization analysis was conducted on the processed samples by using differential scanning calorimetry. The bead foaming behavior of the samples was investigated using a batch-based foaming reactor with supercritical CO 2 . Both compounding with PBT and Joncryl chain modification increased the complex viscosity, melt strength, and strain-hardening behavior of the blends, while their synergistic effect revealed a more noticeable enhancement. Although direct modification of rPET with Joncryl and its direct compounding with PBT could not generate a meaningful foam structure, a homogeneous microcellular foam structure could successfully be induced when 25 wt % rPET was incorporated in blends with PBT modified with 1.0 wt % Joncryl.
“…In a previous study, it was demonstrated that when the processed PET/PBT blends are fast-cooled, crystalline phases are immiscible, whereas slow cooling could cause the cocrystallization of PET and PBT, leading to the full miscibility of PET and PBT polymers . The crystallization kinetics of the 25/75 blend sample, which confirms our discussion, is comprehensively studied elsewhere …”
Section: Results
and Discussionsupporting
confidence: 83%
“…54 The crystallization kinetics of the 25/75 blend sample, which confirms our discussion, is comprehensively studied elsewhere. 94 3.3. Bead Foaming Behavior.…”
This study investigates the melt rheological properties and foamability of recycled polyethylene terephthalate (rPET) and its blends with polybutylene terephthalate (PBT) modified through an epoxy-based Joncryl ADR 4468 chain extender. A twinscrew extruder was used to prepare rPET/PBT blends at various weight ratios (i.e., 100/0, 75/25, 50/50, 25/75, and 0/100) and with varying Joncryl chain extender contents (i.e., 0.25, 0.5, 0.75, and 1.0 wt %). The small-amplitude oscillatory shear rheological experiments were conducted to analyze the melt viscoelastic behavior of the samples. The melt strength and strain-hardening behavior of the compounds were examined by measuring the extensional rheology and Rheotens tests. Crystallization analysis was conducted on the processed samples by using differential scanning calorimetry. The bead foaming behavior of the samples was investigated using a batch-based foaming reactor with supercritical CO 2 . Both compounding with PBT and Joncryl chain modification increased the complex viscosity, melt strength, and strain-hardening behavior of the blends, while their synergistic effect revealed a more noticeable enhancement. Although direct modification of rPET with Joncryl and its direct compounding with PBT could not generate a meaningful foam structure, a homogeneous microcellular foam structure could successfully be induced when 25 wt % rPET was incorporated in blends with PBT modified with 1.0 wt % Joncryl.
Poly(ethylene terephthalate) (PET) is a thermoplastic polyester with excellent thermal and mechanical properties, widely used in a variety of industrial fields. It is a semicrystalline polymer, and most of the industrial success of PET derives from its easily tunable crystallization kinetics, which allow users to produce the polymer with a high crystal fraction for applications that demand high thermomechanical resistance and barrier properties, or a fully amorphous polymer when high transparency of the product is needed. The main properties of the polymer are presented and discussed in this contribution, together with the literature data on the crystal structure and morphology of PET. This is followed by an in-depth analysis of its crystallization kinetics, including both primary crystal nucleation and crystal growth, as well as secondary crystallization. The effect of molar mass, catalyst residues, chain composition, and thermo-mechanical treatments on the crystallization kinetics, structure, and morphology of PET are also reviewed in this contribution.
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