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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Polyelectrolyte Multilayer Films of Different Charge Density Copolymers with Synergistic Nonelectrostatic Interactions Prepared by the Layer-by-Layer Technique
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Polyelectrolyte Multilayer Films of Different Charge Density Copolymers with Synergistic Nonelectrostatic Interactions Prepared by the Layer-by-Layer Technique

机译:分层法制备的具有不同电荷协同作用的不同电荷密度共聚物的聚电解质多层膜

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摘要

Random copolymers composed of diallyldimethylammonium chloride (DADMAC)and acrylamide with varying contents (8-100 mol %)of the cationic DAD MAC component were alternated with polyanionic,fully charged poly(styrenesulfonate)to form multilayer thin films.UV-vis spectrophotometry,FTIR spectroscopy,and quartz-crystal microgravimetry (QCM)were employed to follow multilayer buildup.Atomic force microscopy was used to obtain structural information.Layer thicknesses have been determined with small-angle X-ray scattering and ellipsometry,in addition to values calculated from QCM.While in previous work,a critical charge density limit could be observed,below which no layer growth is possible;in this system,multilayer formation takes place with copolymers with charge densities as low as 8 mol %.Instead of a continuous increase of adsorbed amounts with decreasing charge density above the critical charge density,as found in previous work,similar layer thicknesses for films with 100 and 8 mol % charged polyelectrolytes and maximally adsorbed amounts for copolymers in an intermediate charge density region have been found.This adsorption behavior is explained in terms of synergistic nonelectrostatic interactions between the polyelectrolytes used.
机译:将由二烯丙基二甲基氯化铵(DADMAC)和丙烯酰胺组成的无规共聚物与阳离子DAD MAC组分的不同含量(8-100 mol%)与聚阴离子,完全带电的聚(苯乙烯磺酸盐)交替形成多层薄膜。紫外可见分光光度法,FTIR分光光度法和石英晶体微重力法(QCM)跟踪多层积层。使用原子力显微镜获得结构信息。除了通过QCM计算得出的值外,还通过小角度X射线散射和椭偏法确定了层厚度在以前的工作中,可以观察到一个临界的电荷密度极限,在此极限之下不可能发生层增长;在该系统中,多层结构是在电荷密度低至8 mol%的共聚物下发生的,而不是吸附的连续增加在先前的工作中发现,电荷密度降低到高于临界电荷密度时的量,对于具有100 mol%和8 mol%炭的薄膜,层厚度相似已发现在中间电荷密度区域中存在老化的聚电解质和共聚物的最大吸附量。这种吸附行为通过所用聚电解质之间的协同非静电相互作用来解释。

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