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Crystallization of Polylactic Acid with Organic Nucleating Agents under Quiescent Conditions.
Gao, Peng; Alanazi, Saeed; Masato, Davide.
Afiliação
  • Gao P; Department of Plastics Engineering, University of Massachusetts Lowell, Lowell, MA 01854, USA.
  • Alanazi S; Department of Engineering and Design, Western Washington University, Bellingham, WA 98225, USA.
  • Masato D; Department of Plastics Engineering, University of Massachusetts Lowell, Lowell, MA 01854, USA.
Polymers (Basel) ; 16(3)2024 Jan 24.
Article em En | MEDLINE | ID: mdl-38337210
ABSTRACT
Polylactic acid (PLA) is a versatile and sustainable polymer used in various applications. This research explores the use of orotic acid (OA) and ethylene bis-stearamide (EBS) as nucleating agents to enhance the quiescent crystallization of PLA within the temperature range of 80 °C to 140 °C. Different blends were produced via melt processing before analyzing via DSC, XRD, and SEM. Our results show that both nucleating agents significantly accelerated the crystallization process and reduced the incubation time and the crystallization half-time. The most promising results were obtained with 1% EBS at 110 °C, achieving the fastest crystallization. The XRD analysis showed that at 80 °C, the disordered α'phase predominated, while more stable α phases formed at 110 °C and 140 °C. Combining the 1% nucleating agent and 110 °C promotes densely packed crystalline lamellae. The nucleated PLA exhibited a well-organized spherulitic morphology in agreement with the Avrami modeling of DSC data. Higher nucleating agent concentrations yielded smaller, more evenly distributed crystalline domains. Utilizing OA or EBS in PLA processing could offer enhanced properties, improved processability, and cost-efficiency, making PLA more competitive in various applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article