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Acidic Buffer Mechanism of Cyclotriphosphazene and Melamine Cyanurate Synergism System Flame Retardant Epoxy Resin

机译:环三磷腈与三聚氰胺三聚氰胺协同体系阻燃环氧树脂的酸性缓冲机理

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In this research, a new synergistic mechanism based on an acid-buffer action for cyclotriphosphazene (CPZ)/melamine cyanurate (MCA) flame retardant epoxy resin (EP) was proposed. This mechanism broke through the conventional well-recognized phosphorus-nitrogen interaction one. It revealed that CPZ had not only acid-catalytic charring but also acid-catalytic degrading effect on EP. The former that occurs in higher temperature range to improve the flame resistance in the condensed phase is a mechanism generally accepted for the phosphorus flame retardant, but the later that occurs in lower temperature range to deteriorate the flame retardance is usually ignored by the people. For CPZ/MCA flame retardant EP, the produced organic base from decomposed MCA can neutralize the acids from CPZ. Decline of the acidity effectively weakened the acid-catalytic effect, and reduced the volatiles release rate of the degraded resin in the initial stage, thus slowing down the combustion in the gaseous phase. With increasing temperature, the neutralized products were converted to the phosphorus-containing acids again to promote the formation of the chars. A series of characterizations such as vertical burning test, X-ray photoelectron spectra, micro-scale combustion calorimetry, thermogravimetric, and differential thermogravimetric analysis of the flame retardant materials and the pH value detection of the corresponding carbonation products were performed to investigate the acid-buffer mechanism. The experimental results including no NP forms in the condensed phase obviously improved flame retardance and increased degradation temperature of CPZ/MCA/EP compared with CPZ/EP, as well as the enhanced pH value of the former carbonation residue confirmed the above mechanism. POLYM. ENG. SCI., 55:1046-1051, 2015. (c) 2014 Society of Plastics Engineers
机译:在这项研究中,提出了一种基于酸缓冲作用的环三磷腈(CPZ)/三聚氰胺氰尿酸酯(MCA)阻燃环氧树脂(EP)的新协同机理。这一机理突破了公认的传统的磷氮相互作用。揭示了CPZ不仅具有酸催化炭化作用,而且具有对EP的酸催化降解作用。前者在较高温度范围内发生以提高在冷凝相中的阻燃性是磷阻燃剂普遍接受的机制,但后者在较低温度范围内发生以使阻燃性劣化通常被人们所忽略。对于CPZ / MCA阻燃剂EP,由分解的MCA产生的有机碱可以中和CPZ的酸。酸度的下降有效地减弱了酸催化作用,并且在初始阶段降低了降解树脂的挥发物释放速率,从而减慢了气相燃烧。随着温度升高,中和的产物再次转化为含磷的酸,以促进炭的形成。进行了一系列表征,例如垂直燃烧测试,X射线光电子能谱,微尺度燃烧量热法,热重分析和差示热重分析,以及阻燃剂材料的pH值检测,以检测相应的碳酸化产物。缓冲机制。与CPZ / EP相比,在冷凝相中不包含NP形式的实验结果明显改善了CPZ / MCA / EP的阻燃性并提高了其降解温度,并且前者碳酸化残基的pH值提高证实了上述机理。 POLYM。 ENG。 SCI。,55:1046-1051,2015.(c)2014年塑料工程师学会

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