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Synthesis of Carbon-Rich Hybrid Foam from GAP-Modified Polyurethane

机译:用GAP改性聚氨酯合成富碳杂化泡沫

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4,4'-Diisocyanato diphenylmethane(MDI)-based polyur-ethanes melt and start to burn at 150-200°C.Mainly H2O,CO2,CO,HCN,and N2 are formed.The new modified polyurethane shows a different pyrolysis behavior.GAP-diol(glycidyl azide polymer),which was used as a modifying agent,is a well-known energetic binder with a high burning velocity and a very low adiabatic flame temperature.The modified polyurethane starts to burn at approximately 190°C because of the emitted burnable gases,but it does not melt.The PU foam shrinks slightly and a black,solid,carbon-rich hybrid foam remains.TGA and EGA-FTIR revealed a three-step decomposition mechanism of pure GAP-diol,the isocyanate-GAP-diol,and PU-GAP-diol formulations.The first decomposition step is caused by an exothermic reaction of the azido group of the GAP-diol.This decomposition reaction is independent of the oxygen content in the atmosphere.In the range of 190-240°C the azido group spontaneously decomposes to nitrogen and ammonia.This decomposition is assumed to take place partly via the intermediate hydrogen azide that decomposes spontaneously to nitrogen and ammonia in the range of 190-240°C.The second decomposition step was attributed to the depolymerization of the urethane and bisub-stituted urea groups.The third decomposition step in the range of 500-750°C was attributed to the carbonization process of the polymer backbone,which yielded solid,carbon-rich hybrid foams at 900°C.In air,the second and the third decomposition step shifted to lower temperatures while no solid carbon hybrid foam was left.Samples of PU-GAP-diol,which were not heated by a temperature program but ignited by a bunsen burner,formed a similar carbon-rich hybrid foam.It was therefore concluded that the decomposition products of the hydrogen azide,ammonia and mainly nitrogen act as an inert atmosphere.FTIR,solid-state ~(13)C-NMR,XRD,and heat conductivity measurements revealed a high content of sp~2-hybridized,aromatic structures in the hybrid foam.The carbon-rich foam shows a considerable hardness coupled with high temperature resistance and large specific surface area of 2.1 m~2·g~(-1).
机译:4,4'-二异氰酸根合二苯甲烷(MDI)基聚氨酯在150-200°C熔化并开始燃烧,主要形成H2O,CO2,CO,HCN和N2。新的改性聚氨酯表现出不同的热解行为用作改性剂的GAP-二醇(缩水甘油叠氮化物聚合物)是一种众所周知的高能粘合剂,具有很高的燃烧速度和非常低的绝热火焰温度。改性的聚氨酯在大约190°C时开始燃烧聚氨酯泡沫略微收缩,剩下黑色,固体,富含碳的混合泡沫。TGA和EGA-FTIR揭示了纯GAP-二醇(异氰酸酯)的三步分解机理-GAP-二醇和PU-GAP-二醇配方。第一步分解是由GAP-二醇的叠氮基团放热反应引起的,该分解反应与大气中的氧含量无关。 190-240°C时叠氮基自发分解为氮和氨。假定部分反应是通过中间叠氮化氢在190-240°C范围内自发分解为氮和氨而发生的。第二个分解步骤归因于氨基甲酸酯和双取代尿素基团的解聚。在500-750°C范围内的分解步骤归因于聚合物主链的碳化过程,该过程在900°C下产生了固体,富碳的混合泡沫。在空气中,第二个和第三个分解步骤转移到较低的温度没有经过温度程序加热但被本生灯点燃的PU-GAP-二醇样品形成了类似的富碳杂化泡沫,因此得出结论: FTIR,固态〜(13)C-NMR,XRD和热导率测量表明杂化泡沫中sp〜2杂化的芳族结构含量高。富碳泡沫具有显着的硬度,并具有耐高温性和2.1 m〜2·g〜(-1)的大比表面积。

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