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COMPLETELY PHOTODEGRADABLE PLASTICS
Qiang Yue1; Fanling Meng1; Ben Zhong Tang2; Liang Luo1
1Huazhong University of Science and Technology, Wuhan, China; 2The Chinese University of Hong Kong, Shenzhen, China

PAPER: 123/Polymers/Regular (Oral) OL
SCHEDULED: 14:25/Wed. 19 Nov. 2025/Sampaguita

ABSTRACT:

The global plastic waste crisis persists as a pressing environmental challenge, with conventional degradation methods revealing fundamental technical constraints. Current industrial-scale recycling approaches suffer from downcycling effect, restricted applicability, and concomitant microplastic generation, [1,2] which underscores the urgent demand for transformative recycling paradigms that harmonize operational simplicity, economic feasibility, and minimal resource expenditure.

Sunlight-drive decomposition represents a revolutionary paradigm, which operates under ambient conditions with near-zero energy input, positioning a scalable and environmentally benign management solution. [3] However, achieving complete decomposition while maintaining essential material performance constitutes a critical technological hurdle.

we present a transformative materials design strategy as a potential solution to the problem. This design philosophy stems from our previous discovery that a polydiacetylene containing short carboxylic acid side groups undergoes complete degradation into small molecules under sunlight in either air or aqueous environments, primarily through the cleavage of its C=C and C≡C bonds in the backbone. [4] Intriguingly, the topochemical polymerization mechanism inherent to polydiacetylenes is particularly advantageous for crystalline engineering plastics with regularly aligned polymer strands. Using industrial crystalline engineering plastic polyamide 6/10 (nylon 6/10, or PA610) as a model system, our design introduces diacetylene moieties within the strands of PA610 while maintaining the commercial-grade properties of the materials in terms of mechanical properties and transparency. When exposed to sunlight, the inter-chain topochemical polymerization among adjacent diacetylene units occurs, creating a crosslinked network embedding photodegradable elements in both crosslinkers and polymer strands. The derived material then completely degrades in natural environment within 5 months. 

This sunlight-responsive switching mechanism elegantly reconciles the conflicting requirements of structural robustness during service life and controlled degradability at end-of-life, establishing a new paradigm for sustainable materials engineering.

REFERENCES:
[1] J. M. Garcia, M. L. Robertson, Science 358 (2017) 870-872
[2] L. T. J. Korley, T. H. Epps, B. A. Helms, A. J. Ryan, Science, 373 (2021) 66-69
[3] O. G. Mountanea, E. Skolia, C. G. Kokotos, Green Chemistry, 26 (2024) 8528-8549
[4] S. Tian, Q. Yue, C. Liu, M. Li, M. Yin, Y. Gao, et al. J. Am. Chem. Soc. 143 (2021) 10054-10058