Key determinants of hydrolytic stability of PLA/PBS blend fibers: The role of aromatic sulfonate derivative and carbodiimide

The hydrolytic stability of poly (lactic acid) (PLA)/poly (butylene succinate) (PBS) blend fibers was systematically investigated by incorporating an aromatic sulfonate derivative (nucleating agent, N) and carbodiimide (anti-hydrolysis agent, Anti-H). Neat PLA/PBS blend fibers (3 wt% PBS) retained only ∼53.9% of their initial tensile strength after hydrolysis, whereas fibers containing both the nucleating agent (N) and anti-hydrolysis agent (Anti-H) preserved up to 97.2% of their initial strength. DSC and 2D-WAXD analyses showed that N selectively promoted the development and retention of the PLA (203) crystalline reflection, accompanied by enhanced crystallinity and molecular orientation along the PLA (200)/(110) planes. 1D-WAXD demonstrated that the intensity ratio of PLA (203) to PLA (200)/(110) reflections correlates with hydrolytic retention following a Boltzmann-type sigmoidal relationship, with a critical threshold x 0 ≈ 0.227. Time-dependent FTIR and XPS analyses demonstrated that Anti-H effectively capped the terminal –COOH groups, suppressing autocatalytic chain scission and providing complementary chemical stabilization. Hydrolysis decreased –COOH and –C O functional groups, while the H-bonded –OH increased. Correlation analysis indicated that changes in –C O most strongly influenced tensile retention. SEM observations revealed smooth fiber surfaces with no discernible defects or phase separation, as well as minimal morphological and compositional changes in the optimized fibers after hydrolysis. Collectively, these results demonstrate that the exceptional hydrolytic durability of PLA/PBS blend fibers arises from the synergistic interplay of selective (203) crystalline coherence, preserved molecular orientation, and chemical end-group stabilization. • Key factors governing the hydrolytic stability of PLA/PBS fiber were investigated. • Reinforcement of the (203) crystalline plane is the primary factor. • Sustained molecular orientation along (200)/(110) planes is a secondary factor. • Stabilization of –COOH groups in PLA is the third factor. • Optimized fibers retain up to 97% of their tensile strength after hydrolysis.

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Journal
Polymer
Published
2026-02-04
DOI
https://doi.org/10.1016/j.polymer.2026.129669
Primary Topic
biodegradable polymer synthesis and properties
Type
article
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article

Key determinants of hydrolytic stability of PLA/PBS blend fibers: The role of aromatic sulfonate derivative and carbodiimide

Ik Sung Choi, Hyun Woo Song, Sang Kyoo Lim, Seong Hui Hong et al.
Polymer
biodegradable polymer synthesis and properties
article

Key determinants of hydrolytic stability of PLA/PBS blend fibers: The role of aromatic sulfonate derivative and carbodiimide

Ik Sung Choi, Hyun Woo Song, Sang Kyoo Lim, Seong Hui Hong, Chang-Hun Lee, Young Kwang Kim, Hye-Jin Seo
article en

Abstract

The hydrolytic stability of poly (lactic acid) (PLA)/poly (butylene succinate) (PBS) blend fibers was systematically investigated by incorporating an aromatic sulfonate derivative (nucleating agent, N) and carbodiimide (anti-hydrolysis agent, Anti-H). Neat PLA/PBS blend fibers (3 wt% PBS) retained only ∼53.9% of their initial tensile strength after hydrolysis, whereas fibers containing both the nucleating agent (N) and anti-hydrolysis agent (Anti-H) preserved up to 97.2% of their initial strength. DSC and 2D-WAXD analyses showed that N selectively promoted the development and retention of the PLA (203) crystalline reflection, accompanied by enhanced crystallinity and molecular orientation along the PLA (200)/(110) planes. 1D-WAXD demonstrated that the intensity ratio of PLA (203) to PLA (200)/(110) reflections correlates with hydrolytic retention following a Boltzmann-type sigmoidal relationship, with a critical threshold x 0 ≈ 0.227. Time-dependent FTIR and XPS analyses demonstrated that Anti-H effectively capped the terminal –COOH groups, suppressing autocatalytic chain scission and providing complementary chemical stabilization. Hydrolysis decreased –COOH and –C O functional groups, while the H-bonded –OH increased. Correlation analysis indicated that changes in –C O most strongly influenced tensile retention. SEM observations revealed smooth fiber surfaces with no discernible defects or phase separation, as well as minimal morphological and compositional changes in the optimized fibers after hydrolysis. Collectively, these results demonstrate that the exceptional hydrolytic durability of PLA/PBS blend fibers arises from the synergistic interplay of selective (203) crystalline coherence, preserved molecular orientation, and chemical end-group stabilization. • Key factors governing the hydrolytic stability of PLA/PBS fiber were investigated. • Reinforcement of the (203) crystalline plane is the primary factor. • Sustained molecular orientation along (200)/(110) planes is a secondary factor. • Stabilization of –COOH groups in PLA is the third factor. • Optimized fibers retain up to 97% of their tensile strength after hydrolysis.

PolymerVol. 347
Daegu Gyeongbuk Institute of Science and Technology (KR), Daewoo Electronics (South Korea) (KR), Textile Research Institute (US), Yeonsung University (KR)
Openalex Percentile: Top 69%
biodegradable polymer synthesis and properties
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