不同阳离子磷酸钼酸盐对聚酰胺56阻燃性能的影响

IF 7.4 2区 化学 Q1 POLYMER SCIENCE Polymer Degradation and Stability Pub Date : 2025-04-01 Epub Date: 2025-01-24 DOI:10.1016/j.polymdegradstab.2025.111214
Shiya Wang , Miaojun Xu , Wei Huang , Yingke Zhu , Juan Li , Peng Chen
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引用次数: 0

摘要

聚酰胺56 (PA56)是一种基于生物基化学材料的聚酰胺,受到了广泛的关注。本文将Keggin结构的磷酸钼酸盐(POMs)掺入PA56中,对其阻燃性能进行了改性。不同的聚甲醛对PA56的阻燃效果有不同的影响。少量3 wt%的磷钼酸钠(PMoNa)或磷钼酸镍(PMoNi)使PA56达到UL-94 V-0等级,而含有其他磷钼酸钠的样品在测试中不分类。聚甲醛促进了PA56在低温下的降解和高温下的炭化,提高了PA56在空气中的热稳定性。特别是PMoNa和PMoNi通过在燃烧过程中形成更多的炭,改变热解途径,抑制了热量、可燃挥发物和有毒气体的释放,从而有效地改变了PA56的阻燃性。其力学性能或多或少出现了恶化,需要进一步改进。
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Roles of degradation and charring in the flame retardancy of polyamide 56 induced by phosphomolybdates with different cations
Polyamide 56 (PA56) is a polyamide based on bio-based chemical and has attracted widespread attentions. In this paper, a series of phosphomolybdates (POMs) with Keggin structure were incorporated into PA56 to modify its flame-retardant properties. Different POMs show different effects on the flame-retardant efficiency in PA56. A small amount of 3 wt% sodium phosphomolybdate (PMoNa) or nickel phosphomolybdate (PMoNi) enable PA56 to achieve the UL-94 V-0 rating, while the samples containing other POMs are not classified in the test. The POMs promote the degradation of PA56 at low temperature and char formation at high temperature, and improves the thermal stability in air. Especially, the PMoNa and PMoNi restrain the release of heat, flammable volatiles and toxic gas by forming more char and changing the pyrolysis pathway during combustion, thus modify the flame retardancy of PA56 effectively. The mechanical properties are deteriorated more or less which need to be modified further.
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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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