Multiscale Analysis of Elastoplastic-to-Cracking Mechanisms in PLLA

Poly(L-lactic acid) (PLLA) is a semicrystalline polymer of central importance in biomedical engineering, yet accurately predicting its complex failure evolution from plastic yielding to crazing remains a significant challenge. This study establishes a novel multiscale physical-mechanical framework to investigate the elastoplastic-to-cracking transition mechanisms in PLLA specimens across different molecular weights ((1.4–5.0) × 10⁵ g/mol). Surface characterization via atomic force microscopy (AFM) and macroscopic uniaxial tensile testing revealed a distinct three-stage failure process—comprising elastic deformation, plastic hardening, and craze-mediated cracking—that is heavily influenced by molecular weight-dependent lateral intermolecular linkages. To computationally model this sequence, an Extended Finite Element Method (XFEM) platform was developed, employing 3D Voronoi tessellations to map the semicrystalline aggregates and a cohesive element insertion method to simulate the fibrillated plastic process zone. The plastic hardening response was captured using the Johnson-Cook model, wherein the hardening modulus increased from 9.8 to 141 MPa with rising molecular weight. Concurrently, craze damage evolution was governed by a traction-separation law, demonstrating a critical energy release rate increase from 1.43 to 4.63 N/m. The numerical framework demonstrated strong quantitative agreement with experimental stress-strain trajectories and fracture morphologies, accurately capturing localized stress concentrations (e.g., ~55.2 MPa at crack initiation) and the transition toward a crystalline-like fracture mode in higher molecular weight variants. This multiscale approach provides a fundamental theoretical framework for understanding the micro-mechanical failure of PLLA, serving as a preliminary baseline for the future design of load-bearing implants under complex physiological conditions. Increasing PLLA MW enhances intermolecular entanglement and structural homogeneity. The J-C model is suitable for the elastoplastic-to-cracking mechanical feature of PLLA. Multiscale analysis method can reveal the cracking process of crazing in PLLA.

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Publication Details

Journal
Materials Today Communications
Published
2026-03-01
DOI
https://doi.org/10.1016/j.mtcomm.2026.115092
Primary Topic
biodegradable polymer synthesis and properties
Type
article
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article

Multiscale Analysis of Elastoplastic-to-Cracking Mechanisms in PLLA

Dayi Guo, ZiYi Guo, Chao Guo, Zhengran Lu
Materials Today Communications
biodegradable polymer synthesis and properties
article

Multiscale Analysis of Elastoplastic-to-Cracking Mechanisms in PLLA

Dayi Guo, ZiYi Guo, Chao Guo, Zhengran Lu
article en

Abstract

Poly(L-lactic acid) (PLLA) is a semicrystalline polymer of central importance in biomedical engineering, yet accurately predicting its complex failure evolution from plastic yielding to crazing remains a significant challenge. This study establishes a novel multiscale physical-mechanical framework to investigate the elastoplastic-to-cracking transition mechanisms in PLLA specimens across different molecular weights ((1.4–5.0) × 10⁵ g/mol). Surface characterization via atomic force microscopy (AFM) and macroscopic uniaxial tensile testing revealed a distinct three-stage failure process—comprising elastic deformation, plastic hardening, and craze-mediated cracking—that is heavily influenced by molecular weight-dependent lateral intermolecular linkages. To computationally model this sequence, an Extended Finite Element Method (XFEM) platform was developed, employing 3D Voronoi tessellations to map the semicrystalline aggregates and a cohesive element insertion method to simulate the fibrillated plastic process zone. The plastic hardening response was captured using the Johnson-Cook model, wherein the hardening modulus increased from 9.8 to 141 MPa with rising molecular weight. Concurrently, craze damage evolution was governed by a traction-separation law, demonstrating a critical energy release rate increase from 1.43 to 4.63 N/m. The numerical framework demonstrated strong quantitative agreement with experimental stress-strain trajectories and fracture morphologies, accurately capturing localized stress concentrations (e.g., ~55.2 MPa at crack initiation) and the transition toward a crystalline-like fracture mode in higher molecular weight variants. This multiscale approach provides a fundamental theoretical framework for understanding the micro-mechanical failure of PLLA, serving as a preliminary baseline for the future design of load-bearing implants under complex physiological conditions. Increasing PLLA MW enhances intermolecular entanglement and structural homogeneity. The J-C model is suitable for the elastoplastic-to-cracking mechanical feature of PLLA. Multiscale analysis method can reveal the cracking process of crazing in PLLA.

Materials Today Communications
Guangdong University of Petrochemical Technology (CN), Affiliated Hospital of Jining Medical University (CN), Jinzhou Medical University (CN), China Medical University (CN)
Affordable and clean energy
Openalex Percentile: Top 4%
biodegradable polymer synthesis and properties
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