材料科学
极限抗拉强度
热重分析
锥形量热计
环氧树脂
燃烧性
维卡软化点
阻燃剂
复合材料
傅里叶变换红外光谱
化学工程
化学
燃烧
软化点
热解
有机化学
烧焦
工程类
作者
Yuze Zhang,Lijuan Li,Dong Shi,Fugen Song
标识
DOI:10.1016/j.jcis.2021.03.088
摘要
Abstract Epoxy resin (EP) is a polymer that is widely used in different aspects of life, but its flammability property limits its fields of applications. Most flame retardants at present cannot be applied practically in scale due to their toxicity, incompatibility in polymers, degraded mechanical property or high cost of raw materials and comprehensive preparation process. Layered double hydroxides intercalated by gluconic acid anion (GLDHs) may serve as a new approach. GLDHs with Mg/Al ratio of 3/1 and 2/1 were first coprecipitated with low-cost green reactants, MgCl2·6H2O, AlCl3·6H2O, NaOH and sodium gluconate. Their structures were confirmed by X-ray diffractions (XRD), transmission electron microscope (TEM), Fourier transform infrared spectroscopy (FTIR) and elemental analysis; their thermal properties were analyzed by thermo gravimetric analysis (TGA). Composites containing 40 wt.% GLDHs were easily manufactured with normal magnetic stirring without any filler precipitation. The combustion properties of the composites filled with 40 wt.% GLDHs2 are as follows: the limit oxygen index (LOI) could rise to 29.8% from 25.2% of pristine EP; UL-94 can reach V-1 level with total burning time of only 12.1 s without dropping; compared to pristine EP, the heat release rate peak (PHRR) could drop to 30% with heavy decrease in the smoke production rate and CO production rate. Dynamic mechanical thermal analysis (DMA) tests showed that the addition of 40 wt.% GLDHs had little impact on the glass transition temperature of the composites and could slightly improve their rigidity and toughness. Tensile strength of the composites filled with 40 wt.% GLDHs2 was almost close to 88% of the tensile strength of pristine EP. Above all, GLDHs with good compatibility in polymers can serve as a promising environmental friendly and low-cost flame retardant for EP and other heterochain polymers.
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