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Photopolymerization-induced phase separation in binary blends of photocurable/linear polymers

机译:光固化/线性聚合物的二元共混物中的光聚合诱导相分离

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Phase separation behavior and morphology of polymer blends induced by photopolymerization have been investigated in a binary blend of photocurable polymer (2,2-bis(4-(acryloxy diethoxy)phenyl)propane; BPE4) and linear polymer (polysulfone; PSU) using electron microscopy techniques. A ternary phase diagram of mono-BPE4/poly-BPE4/PSU exhibits a lower critical solution temperature (LOST) behavior. In situ polymerization of BPE4 over a wide range of PSU compositions (5-70 wt%) results in network-like bicontinuous phase separated structures at high temperatures, while semi-interpenetrating polymer network (IPN) structures are cured at low temperatures. Even at 10 wt% PSU, the PSU-rich phase is a continuous network-like phase. BPE4-rich domains in the network-like structures are controlled from the nanoscale (30 nm) to the microscale (1 mum) by varying the composition, curing temperature and irradiation intensity. By means of time-evolution study of the phase structure, it is found that BPE4-rich domains appeared in a PSU-rich matrix after the induction time. These domains quickly grow in size up to the sub-micron level, but further growth appears to be slow. The PSU-rich matrix develops into the network-like pattern by the increase in the number and growth of the BPE4-rich domains. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 31]
机译:在光固化聚合物(2,2-双(4-(丙烯酰二乙氧基)苯基)丙烷; BPE4)和线性聚合物(聚砜; PSU)的二元共混物中,研究了由光聚合引发的聚合物共混物的相分离行为和形态。显微镜技术。 mono-BPE4 / poly-BPE4 / PSU的三元相图显示出较低的临界溶液温度(LOST)行为。在宽范围的PSU组合物(5-70 wt%)上进行BPE4的原位聚合,可在高温下形成网状双连续相分离结构,而在低温下固化半互穿聚合物网络(IPN)结构。即使在PSU含量为10 wt%时,富含PSU的阶段仍是连续的网络状阶段。通过改变组成,固化温度和辐照强度,可将网络状结构中富含BPE4的域控制在纳米级(30 nm)到微米级(1 mum)之间。通过对相结构的时间演化研究,发现在诱导时间之后,富含BPE4的域出现在富含PSU的基质中。这些域的大小迅速增长到亚微​​米级别,但是进一步的增长似乎很缓慢。富含PSU的基质通过富含BPE4的域的数量和增长而发展为类似网络的模式。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:31]

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