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Hydration and conductivity studies of polymer-water interactions in polyacrylamide hydrogels

机译:聚丙烯酰胺水凝胶中聚合物与水相互作用的水化和电导率研究

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The conductivity and hydration mechanisms of polyacrylamide (PAA) hydrogels have been investigated by means of (a) equilibrium and dynamic water sorption isotherms, (b) thermally stimulated depolarization currents (TSDC) techniques in the temperature range 77 to 300 K and (c) broad band dielectric relaxation spectroscopy (DRS) in the frequency range 10~(-2) to 10~6 Hz and the temperature range 230 to 330 K. A systematic analysis of our combined results indicates that water molecules up to a critical hydration value, h_c, of about 0.15 g of water/g of dry weight are irrotationally bound to primary hydration sites and do not contribute themselves to the dielectric spectra. This h_c value is in accordance with equilibrium isothermal measurements on the same samples. Moreover, a reorganization of water in the hydrogels seems to take place for h greater than or equal 0.8. The Arrhenius behaviour of DC-conductivity, σ_(dc), as well as of the loss tangent, tan δ, and electric modulus, M double prime , dispersions, with an activation energy of the order of 0.8 eV, suggests that the observed phenomena have a common origin and that the conductivity mechanism is not governed by the co-operative motion of the polymeric chains, the charge carriers (protons) motion occurring probably through the water-filled micropores of the hydrogel.
机译:聚丙烯酰胺(PAA)水凝胶的电导率和水合机理已通过以下方法进行了研究:(a)平衡和动态水吸附等温线,(b)在77至300 K温度范围内的热激发去极化电流(TSDC)技术,以及(c)宽带介电弛豫谱(DRS)的频率范围为10〜(-2)至10〜6 Hz,温度范围为230至330K。对我们综合结果的系统分析表明,水分子达到了临界水化值, h_c,约0.15 g水/ g干重不旋转地结合到一级水合位点上,并且对介电谱没有贡献。该h_c值与相同样品上的平衡等温测量值一致。此外,水凝胶中的水似乎在h大于或等于0.8时发生了重组。直流电导率σ_(dc)的Arrhenius行为以及损耗正切tanδ和电模量M doubleprime分散体的活化能为0.8 eV左右,表明观察到的现象具有共同的起源并且电导率机制不受聚合物链的协同运动支配,电荷载体(质子)的运动可能通过水凝胶中充满水的微孔发生。

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