

FOLLOWUS
a.College of Chemistry and Materials Science, Shanghai Normal University, Shanghai 200234, China
b.Shanghai Engineering Research Center of Green Energy Chemical Engineering, Shanghai 200234, China
weichao107@shnu.edu.cn (C.W.)
zhangchunlei@shnu.edu.cn (C.L.Z.)
Received:19 October 2025,
Accepted:16 December 2025,
Online First:06 February 2026,
Published:15 March 2026
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Wang, Y. H.; Wang, J.; Gong, S. H.; Li, D. H.; Luo, B. J.; Wei, C.; Zhang, C. L. Achieving simultaneous high thermal stability and rapid seawater degradation in poly(butylene succinate-co-glycolide) copolyesters. Chinese J. Polym. Sci. 2026, 44, 653–663
Yu-Hao Wang, Jie Wang, Shi-Hong Gong, et al. Achieving Simultaneous High Thermal Stability and Rapid Seawater Degradation in Poly(butylene succinate-
Wang, Y. H.; Wang, J.; Gong, S. H.; Li, D. H.; Luo, B. J.; Wei, C.; Zhang, C. L. Achieving simultaneous high thermal stability and rapid seawater degradation in poly(butylene succinate-co-glycolide) copolyesters. Chinese J. Polym. Sci. 2026, 44, 653–663 DOI: 10.1007/s10118-025-3535-z.
Yu-Hao Wang, Jie Wang, Shi-Hong Gong, et al. Achieving Simultaneous High Thermal Stability and Rapid Seawater Degradation in Poly(butylene succinate-
Here
a mild ring-opening copolymerization strategy for the efficient synthesis of high molecular weight poly(butylene succinate-
co
-glycolate) (PBSGL) copolymers with narrow dispersion and controllable sequence structure was reported
and PBSGL possesses high thermal stability and rapid degradation in seawater.
Ocean-degradable polyesters incorporating hydrophilic and rapidly degradable glycolide (GL) units into the polymer chain are the most promising for addressing marine plastic pollution
however
it is challenging to obtain high-molecular-weight copolymers with narrow molecular weight distributions. Herein
we prepared a novel biodegradable material
poly(butylene succinate-
co
-glycolide) (PBSGL)
through ring-opening copolymerization using glycolide
succinic anhydride
and 1
4-butanediol as raw materials
providing a new solution strategy for marine pollution. GL could be polymerized according to the pre-designed composition by
1
H-nuclear magnetic resonance (
1
H-NMR) and gel permeation chromatography (GPC) results
indicating controlled polymerization with the synthesized PBSGLs having a weight-average molecular weight of up to 12.30×10
4
g/mol and a narrow molecular weight distribution (1.33–1.65). Differential scanning calorimeter (DSC) and thermogravimetric analysis (TGA) results showed that
T
g
of PBSGLs increased from –32.5 °C to –26.5 °C with the increase of GL content from 0% to 40%
while
T
m
(
>
76 °C) was much lower than
T
d
5%
(
>
314 °C)
which indicated that PBSGLs had good thermal stability and expanded the processing window and application range of the original poly(butylene succinate) (PBS) materials. Under simulated difficult conditions
PBSGL copolyesters could degrade faster with increasing GL content
where PBSGL40 degraded by 22.6% in 12 days
showing good biodegradability. Currently
most biodegradable polyesters with good performance slowly degrade in seawater. In a 30-d
ay artificial seawater degradation test
the amorphous PBSGL40 copolyester showed a about 15-fold (2.33% weight loss) improvement in degradation ability compared to pure PBS
demonstrating rapid seawater degradation capability.
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