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PORE-SPANNING PPY(DBS) AS A VOLTAGE-GATED SYNTHETIC MEMBRANE ION CHANNEL

机译:孔跨越PPY(DBS)作为电压门合成膜离子通道

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The transport of monovalent cations across a suspended PPy(DBS) polymer membrane in an aqueous solution as a function of its redox state is investigated. Maximum ion transport is found to occur when PPy(DBS) is in the reduced state, and minimum transport in the oxidized state. No deviation in the dynamics of ion transport based on the direction of the applied electrical field is observed. Additionally, it is found that ion transport rates linearly increased proportional to the state of reduction until a steady state is reached when the polymer is fully reduced. Therefore controlled, bidirectional ion transport is for the first time demonstrated. The effect of aqueous Li~+ concentration on ion transport in the fully reduced state of the polymer is studied. It is found that ion transport concentration dependence follows Michaelis-Menten kinetics (which models protein reaction rates, such as those forming ion channels in a cell membrane) with an r~2 value of 0.99. For the given PPy(DBS) polymer charge density and applied potential across the membrane, the maximum possible ion transport rate per channel is found to be 738 ions per second and the Michaelis constant, representing the concentration at which half the maximum ion transport rate occurs, is 619.5mM
机译:一价阳离子的跨悬浮聚吡咯的传输(DBS)聚合物在水溶液中作为其氧化还原状态的功能的膜进行了研究。最大离子迁移是发现当聚吡咯(DBS)是在还原态发生,并且最小传输以氧化态。在离子传输的基础上所施加的电场的方向的动力学没有偏差是观察。此外,已经发现,直到当聚合物完全还原达到稳定状态下的离子迁移率线性增加成比例减少的状态。因此控制,双向离子迁移是首次证明。水性锂〜+浓度对聚合物的完全还原的状态离子迁移的效果进行了研究。据发现,离子迁移浓度依赖性如下的Michaelis-Menten动力学(其模型蛋白的反应速率,如那些在细胞膜形成离子通道),用0.99的R〜2的值。对于穿过膜的给定的聚吡咯(DBS)聚合物的电荷密度与施加的电位,每信道的最大可能的离子迁移率被发现是每秒738根离子和米氏常数,表示在其中最大离子迁移率的一半时的浓度,是619.5mM

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