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Time-domain dynamic opto-rheology study of polymer films using step-scan FTIR time-resolved spectroscopy (S[sup 2]FTIR TRS)
Author(s) -
Haochuan Wang,
Richard A. Palmer,
Christopher J. Manning,
Jon R. Schoonover
Publication year - 1998
Publication title -
aip conference proceedings
Language(s) - English
Resource type - Conference proceedings
SCImago Journal Rank - 0.177
H-Index - 75
eISSN - 1551-7616
pISSN - 0094-243X
DOI - 10.1063/1.55726
Subject(s) - fourier transform infrared spectroscopy , materials science , polymer , copolymer , rheology , tacticity , spectroscopy , infrared spectroscopy , polypropylene , polymer chemistry , elastomer , composite material , chemical engineering , chemistry , organic chemistry , polymerization , physics , quantum mechanics , engineering
Step-scan Fourier transform infrared spectroscopy in conjunction with impulse stress on polymer films has been used to monitor dynamic rheological responses in real time. A novel piezo-electrically-driven polymer microrheometer was employed to apply repetitive impulses to the polymer sample while time-domain spectra were recorded. Recent results include the study of both semi-crystalline polymers such as isotactic polypropylene (iPP) and elastomers such as Estane polyester/polyurethane copolymer and Kraton tri-block copolymer. The spectral changes of iPP are consistent with frequency-domain results. For iPP at room temperature, large differences in the response times of different absorption bands are not seen. However, the orientation response of the CH{sub 3} rocking mode is slightly slower than the responses of the backbone modes. To the authors` knowledge, this is the first reported successful step-scan FTIR time-domain dynamic polymer opto-rheology experiment. The advantages of the time-domain experiment over the frequency-domain experiment are also discussed briefly. This technique appears to be applicable to a variety of polymer samples, and examples from additional results are illustrated.

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