Influence of Ionic Liquid-Based Metal-Organic Hybrid on Thermal Degradation, Flame Retardancy, and Smoke Suppression Properties of Epoxy Resin Composites

被引:40
|
作者
Xiao, Fei [1 ,2 ]
Wu, Kun [1 ]
Luo, Fubin [1 ,2 ]
Yao, Sa [1 ,2 ]
Lv, Maoping [1 ,2 ]
Zou, Haimei [1 ]
Lu, Mangeng [1 ]
机构
[1] Chinese Acad Sci, Guangzhou Inst Chem, Key Lab Cellulose & Lignocellulos Chem, Guangzhou 510650, Guangdong, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 10049, Peoples R China
关键词
AMMONIUM POLYPHOSPHATE; MECHANICAL PROPERTY; HIGH-PERFORMANCE; STABILITY; GRAPHENE; PHOSPHORUS; PHOSPHATE; BEHAVIOR; AGENT;
D O I
10.1007/s10853-018-2318-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A new multifunctional ionic liquid-based metal-organic hybrid (PMAIL) was synthesized by anion exchange between as-synthesized phosphonate-based ionic liquid and phosphomolybdic acid and applied to epoxy resin (EP) as an efficient flame retardant. As expected, with only 1 wt% addition of PMAIL, the char yield of EP-PMAIL1 composite at 700 degrees C was significantly improved by 108.3% from 12.0% for neat epoxy resin to 25.0%, demonstrating the outstanding catalytic charring effect of PMAIL. Meanwhile, EP-PMAIL6 composite (6 wt% addition) can reach V-0 rating in the UL-94 vertical burning tests easily, and its peak heat release rate and total smoke production of EP-PMAIL6 were dropped by 31.0 and 15.4%, respectively, compared with neat EP. Moreover, the results from cone calorimetry tests showed that the char yield of EP-PMAIL6 was enhanced by 162% from 9.5 to 24.9% compared with neat EP, resulting in a strong intumescent char layer structure with outstanding fire retardance and mechanical properties. The thermo-oxidative stable protective layer retarded the transfer of heat and flammable volatiles during combustion and protected the epoxy matrix from further degradation. In conclusion, our results might provide a new perspective for producing composites with excellent flame retardancy and smoke suppression properties using ionic liquid-based metal-organic hybrid.
引用
收藏
页码:10135 / 10146
页数:12
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