pH controlled condensation of polysiloxane networks at the water-air interface

被引:1
|
作者
Wieland, D. C. Florian [1 ,2 ]
Degen, Patrick [3 ]
Paulus, Michael [2 ]
Schroer, Martin A. [2 ,4 ]
Rehage, Heinz [3 ]
Tolan, Metin [2 ]
机构
[1] Helmholtz Zentrum Geesthacht, D-21502 Geesthacht, Germany
[2] DELTA, Fak Phys, D-44221 Dortmund, Germany
[3] Fak Chem, D-44227 Dortmund, Germany
[4] DESY, D-22607 Hamburg, Germany
关键词
Liquid-air interface; Controllable membranes; In situ; Rheology; Langmuir; SELF-ASSEMBLED MONOLAYERS; POLYMER NANOCAPSULES; AIR/WATER INTERFACE; MICROCAPSULES; NANOPARTICLES; FILMS; DEFORMATION; APPARATUS; SURFACE;
D O I
10.1016/j.colsurfa.2014.03.099
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Structural and mechanical properties of molecularly thick polysiloxane membranes were studied on different liquid subphases to investigate the impact of the subphase's pH value on the cross-linking process. The lateral structure of these films was studied in-situ by grazing incidence diffraction while torsions pendulum experiments reveal the response of the system to mechanical stress. The results show a hindered cross-linking on acidic subphases. At alkaline and neutral pH conditions the cross-linking process was not effected. The data revealed that the degree of polymerization can be tuned by regulating the subphase's pH value, which opens the opportunity to build complex polysiloxane membranes in a controlled manner. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:44 / 48
页数:5
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