Hydration in Weak Polyelectrolyte Brushes

被引:29
作者
Deodhar, Chaitra [1 ]
Soto-Cantu, Erick [1 ]
Uhrig, David [2 ]
Bonnesen, Peter [2 ]
Lokitz, Bradley S. [2 ]
Ankner, John F. [3 ]
Kilbey, S. Michael, II [1 ,2 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
[3] Oak Ridge Natl Lab, Spallat Neutron Source, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
POLY(METHACRYLIC ACID) BRUSHES; GRAFTING DENSITY; BEHAVIOR; POLYMERIZATION; REFLECTIVITY; LUBRICATION; EQUILIBRIUM; NEUTRONS; SURFACES; PROFILE;
D O I
10.1021/mz300615v
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Weak polyelectrolytes (PEs) are complex because intertwined connections between conformation and charge are regulated by the local dielectric environment. While end-tethered PE chains so-called PE "brushes"-are archetypal systems for comprehending structure property relationships, it is revealed that the reference state nominally referred to as "dry" is, in fact, a situation in which the chains are hydrated by water vapor in the ambient. Using charge-negative PE homopolymer brushes based on methacrylic acid and copolymer brushes that incorporate methacrylic acid and 2-hydroxyethylmethacrylate, we determine self-consistently the water content of PE films using neutron reflectometry under different hydration conditions. Modeling multiple data sets, we obtain dry polymer mass density and layer thickness, independent of adsorbed water, and PE brush profiles into different pH solutions. We show that hydration of the chains distorts, here by as much as 30%, the quantification of these important physical parameters benchmarked to films in ambient conditions.
引用
收藏
页码:398 / 402
页数:5
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