Abstract
Reactive compatibilization of immiscible polymer blends using a preferred compatibilizer leaves the following question: How much loading of a compatibilizer is good enough and what maximum properties can be achieved? A good understanding of the process can help solve the reutilization of mixed waste plastics. Here, the reactive compatibilization of polypropylene-graft-maleic anhydride (PP-g-MAH) on polypropylene/polyamide 66 (PP/PA66) blends is quantitatively assessed using thermorheological, microoptical, spectroscopic, and x-ray scattering-based characterization tools. The overall compositions of all PP(60%)/PA66(30%)/PP-g-MAH(10%) blends are kept constant while systematically controlling the degree of the chemical reaction by varying the sequential addition of PP-g-MAH to the melt mixture. The first feeding of PP-g-MAH ((Formula presented.)) is conducted at 280°C and the second feeding of ((Formula presented.))% is at 200°C. During the first step, a larger amount of chemical activity is observed up to 4%–6% addition of PP-g-MAH. The constant chemical composition allows a systematic comparison of the compatibilizer-dependent thermal, rheological, morphological, and mechanical properties. With an increased degree of interfacial reaction, the size of dispersed PA66 domains decreases to register improved interfacial adhesion with the PP matrix, yielding enhanced Young's modulus and absolute failure strength of the isotropic matrix.
Original language | English |
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Pages (from-to) | 2419-2434 |
Number of pages | 16 |
Journal | Polymer Engineering and Science |
Volume | 62 |
Issue number | 8 |
DOIs | |
State | Published - Aug 2022 |
Bibliographical note
Publisher Copyright:© 2022 Society of Plastics Engineers.
Funding
This research at Oak Ridge National Laboratory, managed by UT Battelle, LLC, for the U.S. Department of Energy (DOE) under contract DE-AC05-00OR22725, was sponsored by the Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office Program. This research partly utilized facilities of the Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility. The authors thank Sherry Razo for administrative support. This research at Oak Ridge National Laboratory, managed by UT Battelle, LLC, for the U.S. Department of Energy (DOE) under contract DE‐AC05‐00OR22725, was sponsored by the Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office Program. This research partly utilized facilities of the Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility. The authors thank Sherry Razo for administrative support.
Funders | Funder number |
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U.S. Department of Energy | DE‐AC05‐00OR22725 |
Office of Science | |
Office of Energy Efficiency and Renewable Energy | |
Oak Ridge National Laboratory | |
UT-Battelle |
Keywords
- polyamide 66
- polymer composite
- polymer recycling
- polypropylene
- polypropylene-graft-maleic anhydride
- reactive extrusion