烧焦
单体
分散性
燃烧
化学工程
聚合物
甲基丙烯酸酯
高分子化学
猝灭(荧光)
阻燃剂
材料科学
乳状液
甲基丙烯酸甲酯
化学
极限氧指数
可燃性
限制
解聚
点火系统
氧化态
工作(物理)
乳液聚合
反应机理
有机化学
硼
作者
Youngeun Park,Suhyeon Jo,Xuancheng Tie,Woo Geun Kim,Geon Hui Lee,Ka Yeon Ryu,Sang‐Hyun Pyo,Hoyoul Kong
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-01-02
卷期号:11 (2): 2917-2929
被引量:3
标识
DOI:10.1021/acsomega.5c09027
摘要
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.
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