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Rheology of poly(methyl methacrylate) Langmuir monolayers: Percolation transition to a soft glasslike system
被引:28
|作者:
Maestro, A.
[1
]
Ortega, F.
[1
]
Rubio, R. G.
[1
]
Rubio, M. A.
[2
]
Kraegel, J.
[3
]
Miller, R.
[3
]
机构:
[1] Univ Complutense, Fac Quim, Dept Quim Fis 1, E-28040 Madrid, Spain
[2] Univ Nacl Educ Distancia, Fac Ciencias, Dept Fis Teor, Madrid 28040, Spain
[3] Max Planck Inst Colloids & Interfaces, D-14476 Potsdam, Germany
关键词:
AIR-WATER-INTERFACE;
SURFACE LIGHT-SCATTERING;
MOLECULAR-WEIGHT DEPENDENCE;
POLYMER MONOLAYERS;
SUPERCOOLED LIQUIDS;
SYNTHETIC-POLYMER;
RELAXATION;
DYNAMICS;
BEHAVIOR;
FILMS;
D O I:
10.1063/1.3560612
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:
An experimental study of the equilibrium properties and of the surface rheology of Langmuir monolayers of poly(methyl methacrylate) (PMMA) at the air/water interface has been carried out as a function of polymer concentration (Gamma) and molecular weight (M-w). Dilational and shear complex elasticity moduli covering a frequency range from 10(-3) to 0.2 Hz have been discussed. It was found that the air/water interface behaves as a poor solvent for PMMA monolayers, thus suggesting that the polymer coils take collapsed soft-disks (pancakes) shape at the interface. The equilibrium and dynamic results suggest a fluid-to-soft-glass transition as the polymer concentration increases above a critical packing fraction at constant temperature. This two-dimensional transition is in agreement with results previously discussed for the dilational rheology of poly(4-hydroxystyrene) [F. Monroy, F. Ortega, R.G. Rubio, H. Ritacco, and D. Langevin, J. Chem. Phys. 95, 056103 (2005)]. Furthermore, the Gamma-dependence of the relaxation dynamics of the monolayers suggests that the gel state may be considered as a fragile soft glass. (C) 2011 American Institute of Physics. [doi:10.1063/1.3560612]
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