INTERDIFFUSION KINETICS OF MISCIBLE POLYMER/POLYMER LAMINATES INVESTIGATED BY ATOMIC FORCE MICROSCOPY
Special Issue: In Honor of the 80th Birthday of Professor Fosong Wang (Part II)|Updated:2023-01-03
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INTERDIFFUSION KINETICS OF MISCIBLE POLYMER/POLYMER LAMINATES INVESTIGATED BY ATOMIC FORCE MICROSCOPY
Chinese Journal of Polymer ScienceVol. 31, Issue 6, Pages: 870-878(2013)
Affiliations:
a.Key Laboratory for Large-Format Battery Materials and System, Ministry of Education, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074, China
b.Wuhan National High Magnetic Field Center, Huazhong University of Science and Technology, Wuhan 430074, China
Yong-gui Liao, Meng-jun Peng, Feng-zhen Liu, et al. INTERDIFFUSION KINETICS OF MISCIBLE POLYMER/POLYMER LAMINATES INVESTIGATED BY ATOMIC FORCE MICROSCOPY[J]. Chinese Journal of Polymer Science, 2013, 31(6): 870-878.
DOI:
Yong-gui Liao, Meng-jun Peng, Feng-zhen Liu, et al. INTERDIFFUSION KINETICS OF MISCIBLE POLYMER/POLYMER LAMINATES INVESTIGATED BY ATOMIC FORCE MICROSCOPY[J]. Chinese Journal of Polymer Science, 2013, 31(6): 870-878.DOI: 10.1007/s10118-013-1268-x.
INTERDIFFUSION KINETICS OF MISCIBLE POLYMER/POLYMER LAMINATES INVESTIGATED BY ATOMIC FORCE MICROSCOPY
BMA) blend and the interdiffusion kinetics of PVC/PnBMA laminates have been investigated by differential scanning calorimetry (DSC) and atomic force microscopy (AFM)
respectively. This blend exhibited a lower critical solution temperature behavior. Below 120℃
DSC results showed each blend with different PVC contents exhibited only a single glass transition temperature which increased with PVC content
indicating that PVC and P
n
BMA were miscible. After PVC/P
n
BMA laminates were annealed at different temperature for different time
a smooth cross-section across interface was prepared by ultramicrotoming. Combined with topography and phase images of tapping mode AFM
the relative concentration profile
interface width and the relationship between interface width and annealing time could be obtained. In a regime of rubbery/rubbery interdiffusion
the diffusion obeyed a typical Fickian Case-I behavior where the interface width was proportional to the square root of annealing time. The mutual diffusion coefficient was in good agreement with that obtained from DSC and positron annihilation lifetime spectroscopy. However
in the regime of glassy/rubbery interdiffusion
the diffusion followed a typical Case-II behavior where the interface width was proportional to annealing time. These results imply that AFM is a reliable and powerful tool for the investigation of polymer/polymer interdiffusion at a level of polymer chain size.
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