Salamatgharamaleki Saeed, Atespare Asu Ece, Behroozi Kohlan Taha, Yildiz Mehmet, Menceloglu Yusuf Ziya, Unal Serkan, Dizman Bekir
Integrated Manufacturing Technologies Research and Application Center & Composite Technologies Center of Excellence, Sabanci University, Istanbul 34906, Turkey.
Faculty of Engineering and Natural Sciences, Materials Science and Nano Engineering, Sabanci University, Istanbul 34956, Turkey.
ACS Omega. 2025 Feb 14;10(7):6753-6767. doi: 10.1021/acsomega.4c08659. eCollection 2025 Feb 25.
Poly(2-alkyl/aryl-2-oxazoline)-polyethylenimine (POZ-PEI) copolymers resulting from the partial hydrolysis of poly(2-alkyl/aryl-2-oxazoline)s (POZs) offer highly tunable properties. The amine groups on the PEI units are suitable for a range of postpolymerization modifications such as ring-opening of epoxides, acylation, and coupling. The reactivity of these amines can be controlled by altering the available structural variables of the copolymer. This makes these copolymers promising candidates as thermal latent curing agents (TLCs) for cross-linking of epoxides. In this paper, a range of POZ homopolymers with different alkyl/aryl pendant groups (ethyl/propyl/pentyl/phenyl) and molar masses (1000, 2000, and 5000 g/mol) were hydrolyzed at different hydrolysis ratios (25%, 50%, and 75%) to synthesize POZ-PEI copolymers. The effects of these parameters on the thermal and structural properties of the copolymers were analyzed using H NMR, FTIR, DSC, and TGA. The POZ-PEI copolymers exhibited lower glass transition temperature ( ) and decomposition temperature ( ) values in contrast to their precursor homopolymers. TLCs based on the obtained POZ-PEI copolymers were prepared and mixed with bisphenol A diglycidyl ether (DGEBA) to obtain one-component epoxy resins (OCERs). The effect of the mentioned variables on the curing behavior of the prepared OCERs was studied in terms of the enthalpy of curing, left limit temperature, and conversion. POZ-PEI-based TLCs with more hydrophobic side chains, at low hydrolysis ratios and with low molar masses, showed the best latency. PPhOZ-PEI-1 copolymer, with a of 52 °C was chosen as the optimal TLC providing mainly chemical latency though steric effects and physical latency by remaining solid at room temperature. Isothermal DSC tests were performed at different temperatures to examine the stability of the resulting OCER. The results showed that this sample was stable at 40 °C for 3 h and partially cured at 60 °C. Also, the viscoelastic properties of the chosen OCER were investigated by rheology studies, namely, amplitude, frequency, and temperature sweeps. The linear viscoelastic region of the PPhOZ-PEI-1-DGEBA OCER extended up to 10% shear strain. The lowest viscosity for this OCER was observed at 104 °C, and a crossover point was seen at 118 °C. Lastly, the thermomechanical properties of the cured sample were analyzed using DMA, which showed a tan δ peak at 87.6 °C.
由聚(2-烷基/芳基-2-恶唑啉)(POZ)部分水解得到的聚(2-烷基/芳基-2-恶唑啉)-聚乙烯亚胺(POZ-PEI)共聚物具有高度可调节的性能。PEI单元上的胺基适用于一系列后聚合修饰,如环氧化物的开环、酰化和偶联。这些胺的反应活性可以通过改变共聚物的可用结构变量来控制。这使得这些共聚物有望成为用于环氧化物交联的热潜伏固化剂(TLC)。在本文中,一系列具有不同烷基/芳基侧基(乙基/丙基/戊基/苯基)和摩尔质量(1000、2000和500 g/mol)的POZ均聚物在不同水解率(25%、50%和75%)下进行水解以合成POZ-PEI共聚物。使用核磁共振氢谱(H NMR)、傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)和热重分析法(TGA)分析了这些参数对共聚物热性能和结构性能的影响。与它们的前体均聚物相比,POZ-PEI共聚物表现出更低的玻璃化转变温度( )和分解温度( )值。制备了基于所得POZ-PEI共聚物的TLC,并将其与双酚A二缩水甘油醚(DGEBA)混合以获得单组分环氧树脂(OCER)。从固化焓、下限温度和转化率方面研究了上述变量对所制备OCER固化行为的影响。具有更多疏水侧链、低水解率和低摩尔质量的基于POZ-PEI的TLC表现出最佳的潜伏性。玻璃化转变温度为52℃的PPhOZ-PEI-1共聚物被选为最佳TLC,它主要通过空间效应提供化学潜伏性,并通过在室温下保持固态提供物理潜伏性。在不同温度下进行等温DSC测试以检查所得OCER的稳定性。结果表明,该样品在40℃下稳定3小时,并在6℃下部分固化。此外,通过流变学研究,即振幅、频率和温度扫描,研究了所选OCER的粘弹性性能。PPhOZ-PEI-1-DGEBA OCER的线性粘弹性区域扩展到10%的剪切应变。该OCER在104℃下观察到最低粘度,并在118℃下出现一个交叉点。最后,使用动态热机械分析(DMA)分析了固化样品的热机械性能,结果显示在87.6℃处有一个损耗角正切(tan δ)峰。