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DYNAMIC PROPERTIES OF HOMOPOLYMER LAYERS ADSORBED ON A SOLID SURFACE

机译:吸附在固体表面上的均聚物层的动态特性

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Dynamic properties of homopolymer layers adsorbed on a solid surface from a dilute solution are examined through dynamic Monte Carlo simulations over a range of surface/segment interaction energies and at different bulk concentrations. In particular, we studied the relationship between the detachment rate of adsorbed polymers and the first Rouse relaxation rate of adsorbed chains. The power-law dependence of the detachment rate on the chain length which we have reported earlier [Phys. Rev. Lett. 74, 2503 (1995)] is seen to correspond to the power-law dependence of the first Rouse relaxation rate of the adsorbed chains, which is also the same as the power-law dependence of the first Rouse relaxation rate of the free chains (nonadsorbed chains). However, the detachment rate is usually much slower than the first Rouse relaxation rate of adsorbed chains. Increasing the surface/segment interaction energy (e in units of k(B)T) increases the difference between the two. More interestingly, when e-1.0 or higher, the detachment rate decreases significantly as one lowers the bulk concentration, but the first Rouse relaxation rate does not decrease significantly. The results seem to suggest that the detachment rate may become effectively zero (i.e., detachment time goes to infinite) as one continuously decreases the bulk concentration in the strong adsorption limit (e greater than or equal to 1.0). (C) 1996 American Institute of Physics. [References: 54]
机译:通过动态蒙特卡罗模拟,在一定范围的表面/链段相互作用能和不同的堆积浓度下,通过稀有溶液吸附在固体表面上的均聚物层的动力学性质。特别地,我们研究了吸附的聚合物的脱离速率与吸附的链的第一劳斯弛豫速率之间的关系。脱离速率对链长的幂律依赖性,我们早先已经报道过[Phys。牧师74,2503(1995)]对应于吸附链的第一Rouse弛豫率的幂律相关性,也与自由链的第一Rouse弛豫率的幂律相关性相同(非吸附链)。但是,脱离速度通常比吸附链的第一劳斯弛豫速度慢得多。增加表面/段相互作用能(以k(B)T为单位的e)会增加两者之间的差异。更有趣的是,当e-1.0或更高时,随着人们降低整体浓度,分离速率显着降低,但是第一Rouse松弛速率却没有显着降低。结果似乎表明,随着在强吸附极限下(e大于或等于1.0)连续降低体积浓度,分离速率实际上可以变为零(即,分离时间变为无穷大)。 (C)1996年美国物理研究所。 [参考:54]

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