TY - JOUR
T1 - Inspired by the catalytic properties of biological enzymes
T2 - Design of bifunctional catalytic flame retardants for enhanced polyurethane flame retardancy
AU - Li, Xingyao
AU - Xu, Kangcheng
AU - Wang, Lin
AU - Zhang, Yulu
AU - Geng, Zhishuai
AU - Li, Xangmei
AU - He, Jiyu
AU - Yang, Rongjie
N1 - Publisher Copyright:
© 2025
PY - 2026/3
Y1 - 2026/3
N2 - The flammability of polymers limits their use, and traditional flame-retardant approaches no longer meet modern performance needs. To address issues with metal-based flame retardants—such as poor char-forming efficiency and mismatched decomposition—we designed a metal–ligand coordination system that mimics enzymatic catalysis to regulate polyurethane degradation. Under heat, the metal centers selectively cleave weak bonds, suppressing flammable small-molecule formation and promoting the generation of high-molecular-weight, carbon-rich intermediates. These intermediates rapidly crosslink and carbonize, forming a dense char layer that shifts degradation from gasification to carbonization. As a result, (Co-ATMP)₁-co-PU reduces HRR by 69.9%, SPR by 33%, and CO₂ release by 73.4%, while increasing char yield. This catalytic strategy significantly enhances flame retardancy and improves char stability at high temperature, offering a promising route to intrinsically flame-retardant polymers.
AB - The flammability of polymers limits their use, and traditional flame-retardant approaches no longer meet modern performance needs. To address issues with metal-based flame retardants—such as poor char-forming efficiency and mismatched decomposition—we designed a metal–ligand coordination system that mimics enzymatic catalysis to regulate polyurethane degradation. Under heat, the metal centers selectively cleave weak bonds, suppressing flammable small-molecule formation and promoting the generation of high-molecular-weight, carbon-rich intermediates. These intermediates rapidly crosslink and carbonize, forming a dense char layer that shifts degradation from gasification to carbonization. As a result, (Co-ATMP)₁-co-PU reduces HRR by 69.9%, SPR by 33%, and CO₂ release by 73.4%, while increasing char yield. This catalytic strategy significantly enhances flame retardancy and improves char stability at high temperature, offering a promising route to intrinsically flame-retardant polymers.
KW - Bifunctional catalytic
KW - Intrinsic flame retardant
KW - Thermal degradation pathway
UR - https://www.scopus.com/pages/publications/105025020404
U2 - 10.1016/j.polymdegradstab.2025.111860
DO - 10.1016/j.polymdegradstab.2025.111860
M3 - Article
AN - SCOPUS:105025020404
SN - 0141-3910
VL - 245
JO - Polymer Degradation and Stability
JF - Polymer Degradation and Stability
M1 - 111860
ER -