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Redox reactions of polyaniline films doped with d,l-camphor sulfonic acid

机译:d,l-樟脑磺酸掺杂的聚苯胺薄膜的氧化还原反应

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摘要

Simplified comparison of standard redox potentials demonstrates that redox reactions of d,l-camphor sulfonic acid (CSA) doped polyaniline (PANI) films with aqueous solutions of FeCl_3 and K_3Fe(CN)_6 should not take place. Nevertheless the reactions are possible and described here. The initial rate of 0.01 M Fe~(3+) reduction is higher than that obtained with HC1 doped PANI film at similar conditions. Films doped with CSA stay active at neutral pH with K_3Fe(CN)_6 as the oxidizing agent, which is different from depressed electroactivity of PANI-HCl films in these conditions. The redox processes are not limited by simple surface reaction and have two kinetically different steps (the initial, fast and the second, slower). A new mechanism is suggested according to which two redox half reactions (oxidation of the polymer fragments and reduction of ions in the solution) are separated in space and are coupled by counter transport of electrons and Cl~- anions into the opposite direction. A new phenomenon is demonstrated where the gradient of Cl~- activity in the film changes the equilibrium state of the redox process in aqueous solution.
机译:标准氧化还原电势的简化比较表明,d,l-樟脑磺酸(CSA)掺杂的聚苯胺(PANI)膜与FeCl_3和K_3Fe(CN)_6的水溶液之间不应发生氧化还原反应。然而,反应是可能的并且在此描述。 0.01 M Fe〜(3+)还原的初始速率高于在相同条件下用HC1掺杂的PANI膜获得的速率。掺杂CSA的薄膜在K_3Fe(CN)_6作为氧化剂的中性pH下保持活性,这与这些条件下PANI-HCl薄膜的电活性降低有关。氧化还原过程不受简单的表面反应的限制,并具有两个动力学上不同的步骤(初始,快速和慢速)。提出了一种新的机理,根据该机理,两个氧化还原半反应(聚合物碎片的氧化和溶液中离子的还原)在空间上分开,并通过电子和Cl-阴离子向相反方向的反向传输而耦合。证实了一种新现象,其中薄膜中Cl〜-活性的梯度改变了水溶液中氧化还原过程的平衡状态。

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