Youngeun Park, Suhyeon Jo, Xuancheng Tie, Woo Geun Kim, Geon Hui Lee, Ka Yeon Ryu, Sang‐Hyun Pyo, Hoyoul Kong
High Resolution Image Download MS PowerPoint Slide To address the flammability issues limiting polymer applications, phosphorus-containing flame retardants have received increasing attention as halogen-free alternatives. In this study, two phosphorus-containing methacrylate monomers, diphenylphosphinyl methacrylate ( DPMA, +1 oxidation state, P–Ph bond) and diphenylphosphoryloxy methacrylate ( DPOMA, +5 oxidation state, P–O–C bond), were synthesized and selectively incorporated into the shell of core–shell polymers via seeded emulsion polymerization. The resulting particles were uniform, spherical, and low polydispersity (PDI < 0.07). The flame-retardant behavior was strongly affected by the oxidation state of phosphorus. When 70 wt % of each monomer was placed in the shell, PA-DPMA70 reduced the peak heat release rate (pk-HRR) by 44% and showed a significant decrease in the fire growth index (FGI) and average effective heat of combustion (av-EHC), indicating a dominant gas-phase inhibition. In contrast, PA-DPOMA70 reduced the pk-HRR by 19% but greatly increased the residual char yield, producing a dense and highly graphitized structure with an I D / I G ratio of 1.56, which is characteristic of condensed-phase protection. These findings clearly demonstrate that the oxidation state of phosphorus determines whether gas-phase radical quenching or condensed-phase char formation governs the flame-retardant mechanism. In addition to earlier reports on incorporating phosphorus methacrylates into bulk matrices or silicone–acrylic adhesives, this work establishes a shell-specific localization strategy that clarifies the oxidation state mechanism relationship and offers guidance for the rational design of next-generation halogen-free flame-retardant polymers.