Pulsed N.M.R. studies of radiation-induced crosslinking and gel formation in linear polydimethy siloxane

R. Folland, A. Charlesby
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引用次数: 41

Abstract

Pulsed N.M.R. measurements of the proton spin-lattice, T1, and spin-spin, T2, relaxation times for γ-irradiated linear polydimethylsiloxane (Mw = 0.6 × 104) as a function of dose up to 200 Mrad are reported. The dependences of T1 and T2 on dose are discussed in terms of the effects of the introduction of intermolecular crosslinks on the molecular motion. Above the gel point the spin-spin relaxation exhibits a double exponential decay characteristic of two-phase system. This behaviour is attributed to the heterogeneous phase separation of the material into gel and sol fractions. The value of T2 for each phase provides information regarding the differing molecular mobilities of the gel and sol phases and their dependence on radiation dose. The sol fractions determined from the N.M.R. T2 measurements are compared with those obtained using the conventional sol extraction technique and are shown to be reasonable quantitative agreement. The applicability of N.M.R. as a quantitative method for the determination of gel points and gel fractions is demonstrated and discussed.

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线性聚二甲基硅氧烷辐射诱导交联和凝胶形成的脉冲核磁共振研究
本文报道了γ辐照线性聚二甲基硅氧烷(Mw = 0.6 × 104)的质子自旋晶格T1和自旋自旋T2弛豫时间随剂量(200mrad)变化的脉冲核磁共振测量结果。根据分子间交联的引入对分子运动的影响,讨论了T1和T2对剂量的依赖性。在凝胶点以上,自旋-自旋弛豫表现出两相体系的双指数衰减特征。这种行为归因于材料的非均相分离成凝胶和溶胶馏分。每个相的T2值提供了关于凝胶和溶胶相的不同分子迁移率及其对辐射剂量的依赖的信息。用核磁共振T2测定的溶胶组分与传统的溶胶萃取技术测定的溶胶组分进行了比较,结果表明两者在定量上是一致的。论证和讨论了核磁共振作为测定凝胶点和凝胶组分的定量方法的适用性。
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