Lattice Matching and Microstructure of the Aromatic Amide Fatty Acid Salts Nucleating Agent on the Crystallization Behavior of Recycled Polyethylene Terephthalate
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Published:2024-06-28
Issue:13
Volume:29
Page:3100
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ISSN:1420-3049
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Container-title:Molecules
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language:en
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Short-container-title:Molecules
Author:
Zhao Tianjiao1, Lin Fuhua2ORCID, Dong Yapeng1, Wang Meizhen1, Ning Dingyi1, Hao Xinyu1, Hao Jialiang1, Zhang Yanli1, Zhou Dan1, Zhao Yuying1, Luo Jun3, Lu Jingqiong1, Wang Bo1ORCID
Affiliation:
1. School of Chemical Engineering and Technology, Taiyuan University of Science and Technology, Taiyuan 030024, China 2. School of Traffic Engineering, Shanxi Vocational University of Engineering Science and Technology, Jinzhong 030619, China 3. Guangzhou Fibre Product Testing and Research Institute, Guangzhou 510220, China
Abstract
To solve the decrease in the crystallization, mechanical and thermal properties of recycled polyethylene terephthalate (rPET) during mechanical recycling, the aromatic amide fatty acid salt nucleating agents Na-4-ClBeAmBe, Na-4-ClBeAmGl and Na-4-ClAcAmBe were synthesized and the rPET/nucleating agent blend was prepared by melting blending. The molecular structure, the thermal stability, the microstructure and the crystal structure of the nucleating agent were characterized in detail. The differential scanning calorimetry (DSC) result indicated that the addition of the nucleating agent improved the crystallization temperature and accelerated the crystallization rate of the rPET. The nucleation efficiencies (NE) of the Na-4-ClBeAmBe, Na-4-ClBeAmGl and Na-4-ClAcAmBe were increased by 87.2%, 87.3% and 41.7% compared with rPET which indicated that Na-4-ClBeAmBe and Na-4-ClBeAmGl, with their long-strip microstructures, were more conducive to promoting the nucleation of rPET. The equilibrium melting points (Tm0) of rPET/Na-4-ClBeAmBe, rPET/Na-4-ClBeAmGl and rPET/Na-4-ClAcAmBe were increased by 11.7 °C, 18.6 °C and 1.9 °C compared with rPET, which illustrated that the lower mismatch rate between rPET and Na-4-ClBeAmGl (0.8% in b-axis) caused Na-4-ClBeAmGl to be the most capable in inducing the epitaxial crystallization and orient growth along the b-axis direction of the rPET. The small angle X-ray diffraction (SAXS) result proved this conclusion. Meanwhile, the addition of Na-4-ClBeAmGl caused the clearest increase in the rPET of its flexural strength and heat-distortion temperature (HDT) at 20.4% and 46.7%.
Funder
Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi
Reference43 articles.
1. Acceleration a yeast-based biodegradation process of polyethylene terephthalate microplastics by Tween 20: Efficiency, by-product analysis, and metabolic pathway Prediction;Giyahchi;Environ. Pollut.,2024 2. Muszynski, M., Nowicki, J., Zygadlo, M., and Dudek, G. (2023). Comparsion of catalyst effectiveness in different chemical depolymerization methods of poly(ethylene terephthalate). Molecules, 28. 3. Acetolysis of waste polyethylene terephthalate for upcycling and life-cycle assessment study;Peng;Nat. Commun.,2023 4. Myren, T.H.T., Stinson, T.A., Mast, Z.J., Huntzinger, C.G., and Luca, O.R. (2020). Chemical and electrochemical recycling of end-use poly(ethylene terephthalate) (PET) plastics in batch, microwave and electrochemical reactors. Molecules, 25. 5. Chemical recycling of polyethylene terephthalate: A mini-review;Babaei;J. Environ.,2024
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