TY - JOUR
T1 - Nanoscopic adhesion test for polymers by a light-lever system
AU - Narayama, Ifu
AU - Akabori, Keiichi
AU - Morita, Hiroshi
AU - Nagamura, Toshihiko
AU - Tanaka, Keiji
PY - 2009
Y1 - 2009
N2 - Polymer nano-adhesion between a cantilever tip coated with polymer and a flat polymer film was studied by a light-lever system using an atomic force microscope. The polymer interface was adhered at a temperature above the surface glass transition temperature for a given time. Nano-adhesion force (F nano), at which the tip was detached from the surface, was estimated from the deflection of the lever with a known spring constant. Nano-adhesion strength (GN) was simply obtained dividing Fnano by the contact area, which was estimated on the basis of Johnson-Kendall-Roberts theory. The time evolution of the interfacial thickness was independently examined by dynamic secondary ion mass spectrometry. Interestingly, G N increased with increasing interfacial thickness. However, it can be hardly judged whether GN is proportional to the interfacial thickness with the exponent of 1 or 2. Then, temperature dependence of G N was examined. Above the bulk glass transition temperature, the relation between temperature and GN was well expressed by a Williams-Landel-Ferry type equation. This means that the nano-adhesion strength is governed by friction between segments. Once this is accepted, GN should be proportional to the interfacial thickness with the exponent of 2.
AB - Polymer nano-adhesion between a cantilever tip coated with polymer and a flat polymer film was studied by a light-lever system using an atomic force microscope. The polymer interface was adhered at a temperature above the surface glass transition temperature for a given time. Nano-adhesion force (F nano), at which the tip was detached from the surface, was estimated from the deflection of the lever with a known spring constant. Nano-adhesion strength (GN) was simply obtained dividing Fnano by the contact area, which was estimated on the basis of Johnson-Kendall-Roberts theory. The time evolution of the interfacial thickness was independently examined by dynamic secondary ion mass spectrometry. Interestingly, G N increased with increasing interfacial thickness. However, it can be hardly judged whether GN is proportional to the interfacial thickness with the exponent of 1 or 2. Then, temperature dependence of G N was examined. Above the bulk glass transition temperature, the relation between temperature and GN was well expressed by a Williams-Landel-Ferry type equation. This means that the nano-adhesion strength is governed by friction between segments. Once this is accepted, GN should be proportional to the interfacial thickness with the exponent of 2.
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U2 - 10.1088/1742-6596/184/1/012032
DO - 10.1088/1742-6596/184/1/012032
M3 - Article
AN - SCOPUS:69649083584
SN - 1742-6588
VL - 184
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
M1 - 012032
ER -