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首页> 外文期刊>Journal of Elastomers & Plastics >Azomethine ether-based potential curing agent for epoxy resin (diglycidyl ether of bisphenol A): Synthesis and characterization
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Azomethine ether-based potential curing agent for epoxy resin (diglycidyl ether of bisphenol A): Synthesis and characterization

机译:环氧树脂的基于氮杂甲酸乙烯醚基潜在固化剂(双酚A的二缩水甘油醚A):合成和表征

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Novel azomethine ether-based compounds (A:N-((4-(9-(4-(phenylimino)methyl)phenoxy)nonyloxy)benzylidene)bezenamine and B:N-((4-(9-(4-(p-hydroxyphenylimino)methyl)phenoxy)nonyloxy)benzylidene)-4-hydroxybenzenamine) were synthesized by condensation reaction of dialdehyde, 4,4-(1,9-nonandiyle)bis(oxy)dibenzaldehyde with aromatic amines. Structures of synthesized compounds were successfully characterized by Fourier transform infrared (FTIR), ultraviolet-visible, proton nuclear magnetic resonance imaging and photoluminescence (PL) spectroscopy. The PL spectral analysis revealed that emission maxima of compounds A and B are at 475 and 500 nm, respectively, indicate blue and green light emission with large Stokes shift range (Delta lambda(ST), 109-138 nm). Two series of polymers: one azomethine-based polymers (C1-C5) and other without azomethine (H1-H4) were prepared by curing diglycidyl ether of bisphenol A with a synthesized curing agent (B) and commercial curing agent, respectively, in various proportions. The structural characterization of the resulting polymers was carried out by FTIR spectral analysis. Thermal properties revealed that azomethine-based polymers (C1-C5) were thermally stable up to 400 degrees C as compared to H1-H4. The glass transition temperature of the polymers, determined by differential scanning calorimetry, was in the range 121-123 degrees C.
机译:通过双醛、4,4-(1,9-壬二酰)双(氧)二苯甲醛与芳香胺的缩合反应,合成了新的偶氮甲醚基化合物(A:N-((4-(9-(4-(苯基亚氨基)甲基)苯氧基)壬氧基)苯氧基)苯胺和B:N-((4-(4-(对羟基苯基亚氨基)甲基)苯氧基)苯氧基)苯胺)。利用傅里叶变换红外光谱(FTIR)、紫外可见光谱、质子核磁共振成像和光致发光光谱(PL)对合成化合物的结构进行了表征。PL光谱分析表明,化合物A和B的发射最大值分别为475和500 nm,表明蓝色和绿色光发射具有较大的斯托克斯位移范围(δlambda(ST),109-138 nm)。用合成的固化剂(B)和市售固化剂分别以不同比例固化双酚A的二缩水甘油醚,制备了两个系列的聚合物:一个基于偶氮甲基的聚合物(C1-C5)和另一个不含偶氮甲基的聚合物(H1-H4)。通过FTIR光谱分析对所得聚合物的结构进行了表征。热性能表明,与H1-H4相比,甲亚胺基聚合物(C1-C5)在400℃下具有热稳定性。通过差示扫描量热法测定聚合物的玻璃化转变温度,其范围为121-123℃。

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