{"title":"Balancing flame retardancy and high toughness in solvent-free reactive polyurethane films via P/Si synergistic strategy","authors":"Jinbiao Zhao , Huimin Duan , Xinxin Xu , Shangchao Ji , Hao Yang , Zhichao Huang , Qi Zhong , Dongming Qi","doi":"10.1016/j.eurpolymj.2025.113810","DOIUrl":null,"url":null,"abstract":"<div><div>Reactive polyurethane (RPU) films in a solvent-free medium exhibit exceptional stability and mechanical properties due to their highly cross-linked structure. Achieving inherent fire resistance, waterproofing, and high mechanical performance in RPUs is challenging. Here, we prepared an intrinsic flame retardant, waterproof, and flexible RPU using a P/Si synergistic system with hydroxylated ammonium polyphosphate aAPP/Si-RPU via <em>in-situ</em> polyaddition of NCO-double capped prepolymer and polyol components, including polydimethylsiloxane (PDMS) and aAPP. The aAPP was synthesized through cation exchange between diethylene glycol amine (DGA) and ammonium polyphosphate (APP). Compared to pure RPU, aAPP/Si<sub>15%</sub>-RPU showed a 60.3 % reduction in peak heat release rate (pk-HRR) and a 14.1 % reduction in total heat release (THR), with the limiting oxygen index (LOI) increasing from 18.2 % to 27.8 %. Mechanical properties and hydrophobicity improved, with tensile strength at 31.9 ± 1.9 MPa, elongation at break at 522.7 ± 20.3 %, and a water contact angle of 127.1°. The balance of properties was due to ordered microphase separation from the organic–inorganic hybrid structure of aAPP and PDMS, where aAPP particles enhanced microstructure and crosslinked interactions, and the Si-O bond in PDMS provided flexibility and water resistance. This study presents a strategy to resolve the conflict between rigidity and toughness, offering design ideas for intrinsic flame retardant polyurethane.</div></div>","PeriodicalId":315,"journal":{"name":"European Polymer Journal","volume":"228 ","pages":"Article 113810"},"PeriodicalIF":5.8000,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Polymer Journal","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014305725000989","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Reactive polyurethane (RPU) films in a solvent-free medium exhibit exceptional stability and mechanical properties due to their highly cross-linked structure. Achieving inherent fire resistance, waterproofing, and high mechanical performance in RPUs is challenging. Here, we prepared an intrinsic flame retardant, waterproof, and flexible RPU using a P/Si synergistic system with hydroxylated ammonium polyphosphate aAPP/Si-RPU via in-situ polyaddition of NCO-double capped prepolymer and polyol components, including polydimethylsiloxane (PDMS) and aAPP. The aAPP was synthesized through cation exchange between diethylene glycol amine (DGA) and ammonium polyphosphate (APP). Compared to pure RPU, aAPP/Si15%-RPU showed a 60.3 % reduction in peak heat release rate (pk-HRR) and a 14.1 % reduction in total heat release (THR), with the limiting oxygen index (LOI) increasing from 18.2 % to 27.8 %. Mechanical properties and hydrophobicity improved, with tensile strength at 31.9 ± 1.9 MPa, elongation at break at 522.7 ± 20.3 %, and a water contact angle of 127.1°. The balance of properties was due to ordered microphase separation from the organic–inorganic hybrid structure of aAPP and PDMS, where aAPP particles enhanced microstructure and crosslinked interactions, and the Si-O bond in PDMS provided flexibility and water resistance. This study presents a strategy to resolve the conflict between rigidity and toughness, offering design ideas for intrinsic flame retardant polyurethane.
期刊介绍:
European Polymer Journal is dedicated to publishing work on fundamental and applied polymer chemistry and macromolecular materials. The journal covers all aspects of polymer synthesis, including polymerization mechanisms and chemical functional transformations, with a focus on novel polymers and the relationships between molecular structure and polymer properties. In addition, we welcome submissions on bio-based or renewable polymers, stimuli-responsive systems and polymer bio-hybrids. European Polymer Journal also publishes research on the biomedical application of polymers, including drug delivery and regenerative medicine. The main scope is covered but not limited to the following core research areas:
Polymer synthesis and functionalization
• Novel synthetic routes for polymerization, functional modification, controlled/living polymerization and precision polymers.
Stimuli-responsive polymers
• Including shape memory and self-healing polymers.
Supramolecular polymers and self-assembly
• Molecular recognition and higher order polymer structures.
Renewable and sustainable polymers
• Bio-based, biodegradable and anti-microbial polymers and polymeric bio-nanocomposites.
Polymers at interfaces and surfaces
• Chemistry and engineering of surfaces with biological relevance, including patterning, antifouling polymers and polymers for membrane applications.
Biomedical applications and nanomedicine
• Polymers for regenerative medicine, drug delivery molecular release and gene therapy
The scope of European Polymer Journal no longer includes Polymer Physics.