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Flame retardancy of organic-anion-intercalated layered double hydroxides in ethylene vinyl acetate copolymer

机译:乙烯乙酸乙烯酯共聚物中有机阴离子插层双氢氧化物的阻燃性

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To gain high efficiency flame retardant, the twin organic anions intercalated layered double hydroxides (PD(x)CA(y)-LDH) were designed and prepared via calcination-reconstruction, where the organic anions were pentaerythritol diphosphate (PD) and cyanuric acid (CA). The morphology, chemical composition and structure of the PD(x)CA(y)-LDH materials were characterized, revealed that the PD(x)CA(y)-LDH materials were successfully intercalated by the PD and CA anions in single or combining form. The incorporation of the PD(x)CA(y)-LDH with ethylene vinyl acetate copolymer (EVA) not only could significantly improve the thermal stability of EVA matrix but also promote the formation of char layer during combustion, owing to the combined advantages of CA, PD and LDH. It was found that the flame retardancy of the PD(x)CA(y)-LDH depended on the mass ratio of PD to CA anions, where the PD(7)CA(3)-LDH with a 7:3 mass ratio of PD/CA had the best flame retardancy due to the presence of an excellent char layer. The EVA/PD(7)CA(3)-LDH composite achieved a LOI value of 28.0% and a UL 94 V-0 rating compared with the EVA/LDH composite with 19.5% and a HB rating, and the peak heat release rate (PHRR) and total heat release (THR) decreased to 340.2 kW.m(-2) and 132.7 MJ.m(-2), respectively. These improvements could be attributed to the catalyzing carbonization of the PD and CA to EVA matrix to form more protective char layers.
机译:为了获得高效阻燃剂,通过煅烧-重构设计并制备了双有机阴离子插层双氢氧化物(PD(x)CA(y)-LDH),其中有机阴离子为季戊四醇二磷酸酯(PD)和氰尿酸( CA)。对PD(x)CA(y)-LDH材料的形貌,化学组成和结构进行了表征,表明PD(x)CA(y)-LDH材料已成功被PD和CA阴离子单次或组合嵌入形成。 PD(x)CA(y)-LDH与乙烯乙酸乙烯酯共聚物(EVA)的结合不仅可以显着提高EVA基体的热稳定性,而且由于燃烧的综合优势还可以促进燃烧过程中炭层的形成。 CA,PD和LDH。发现PD(x)CA(y)-LDH的阻燃性取决于PD与CA阴离子的质量比,其中PD(7)CA(3)-LDH的质量比为7:3由于存在出色的炭层,PD / CA具有最佳的阻燃性。 EVA / PD(7)CA(3)-LDH复合材料的LOI值为28.0%,UL 94 V-0等级,而EVA / LDH复合材料为19.5%且HB等级,并且峰值放热率(PHRR)和总热量释放(THR)分别降至340.2 kW.m(-2)和132.7 MJ.m(-2)。这些改进可以归因于将PD和CA催化碳化为EVA基质以形成更多保护性炭层。

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