研究了MOSw@PDA@NiOOH中Ni(III)对柔性聚氯乙烯复合材料抑烟阻燃的关键作用

IF 7.4 2区 化学 Q1 POLYMER SCIENCE
Xiaoyuan Liu , Jia Liu , Xinyi Bao , Wenqing Ge , Zhihui Lv , Li Dang
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引用次数: 0

摘要

为了克服柔性聚氯乙烯(fPVC)高烟毒性和可燃性的关键挑战,本研究通过聚多巴胺(PDA)界面工程和NiOOH在硫酸镁晶须(MOSw)上的原位沉积,开发了一种核壳阻燃剂(MOSw@PDA@NiOOH)。SEM, TEM和EDS证实了Ni(III)基NiOOH纳米颗粒均匀锚定在MOSw表面的分层界面结构。Cone量热测试表明,与fPVC/MOSw复合材料相比,fPVC/MOSw@PDA@NiOOH的峰值产烟率降低了35.38%,总产烟率降低了75.88%,同时具有UL-94 V-0等级和28.8%的极限氧指数。拉曼、TGA和XPS分析表明:i) Ni(III)的强刘易斯酸性有利于氯离子从PVC中消除,导致共轭多烯结构的形成;ii) Ni(III)强大的氧化能力直接氧化不饱和碳,如CC,生成碳阳离子,随后促进芳构化和交联反应;iii) Ni(iii)诱导MOSw完全分解为MgO,最终形成由石墨碳、MgO、NiO和MgCl2组成的致密碳质残渣层。Py-GC/MS和TGA-FTIR分析进一步表明,Ni(III)的强氧化能力也促进了芳香族/脂肪族中间体的深层裂解和氧化,从而显著减少了烟雾前体的积累。此外,Ni(III)及其还原的Ni(II)都具有部分填充的3d轨道,能够清除气相自由基(例如H·和HO·),从而中断燃烧链反应并提高阻燃效果。此外,PDA的氨基/羟基通过氢键强化了mows - pvc界面,提高了拉伸模量(20.9 MPa)和强度(17.8 MPa),同时保持了冲击强度(83.9 kJ/m2)。本研究建立了一种多功能设计策略,通过协同界面和催化效应,在fPVC复合材料中同时实现阻燃、抑烟和机械增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The critical role of Ni(III) species in MOSw@PDA@NiOOH for effective smoke suppression and flame retardancy in flexible polyvinyl chloride composites

The critical role of Ni(III) species in MOSw@PDA@NiOOH for effective smoke suppression and flame retardancy in flexible polyvinyl chloride composites
To overcome the critical challenges of high smoke toxicity and flammability in flexible polyvinyl chloride (fPVC), this study developed a core-shell flame retardant (MOSw@PDA@NiOOH) via polydopamine (PDA) interfacial engineering and in-situ NiOOH deposition on magnesium oxysulfate whiskers (MOSw). SEM, TEM, and EDS confirm the hierarchical interface structure with Ni(III)-based NiOOH nanoparticles uniformly anchored on MOSw surfaces. Cone calorimetry tests show a 35.38 % reduction in peak smoke production rate and a 75.88 % decrease in total smoke production, respectively, for fPVC/MOSw@PDA@NiOOH compared to fPVC/MOSw composite, along with a UL-94 V-0 rating and 28.8 % limiting oxygen index. Raman, TGA, and XPS analyses reveal that: i) the strong Lewis acidity of Ni(III) facilitates chloride elimination from PVC, leading to the formation of conjugated polyene structures; ii) the powerful oxidizing capability of Ni(III) directly oxidizes unsaturated carbons such as CC, generating carbocations that subsequently promote aromatization and cross-linking reactions; iii) Ni(III) induces complete decomposition of MOSw into MgO, ultimately forming a dense carbonaceous residue layer composed of graphitic carbon, MgO, NiO, and MgCl2. Py-GC/MS and TGA-FTIR analyses further demonstrate that the strong oxidative capacity of Ni(III) also promotes deep cleavage and oxidation of aromatic/aliphatic intermediates, which significantly reduces the accumulation of smoke precursors. Moreover, both the Ni(III) and its reduced Ni(II) possess partially filled 3d orbitals capable of scavenging gas-phase radicals (e.g., H· and HO·), thereby interrupting combustion chain reactions and imparting flame-retardant efficacy. Additionally, PDA’s amino/hydroxyl groups strengthen the MOSw-PVC interface via hydrogen bonding, increasing tensile modulus (20.9 MPa) and strength (17.8 MPa) while maintaining impact strength (83.9 kJ/m2). This work establishes a multifunctional design strategy that simultaneously achieves flame retardancy, smoke suppression, and mechanical reinforcement in fPVC composites through synergistic interfacial and catalytic effects.
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来源期刊
Polymer Degradation and Stability
Polymer Degradation and Stability 化学-高分子科学
CiteScore
10.10
自引率
10.20%
发文量
325
审稿时长
23 days
期刊介绍: Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology. Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal. However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.
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