Molecular interaction of polyimide films probed by using soft-pulse dynamic compression ATR time-resolved infrared and double Fourier-transform based 2D-IR spectroscopy

2014 ◽  
Vol 72 ◽  
pp. 79-89 ◽  
Author(s):  
Yuji Nishikawa ◽  
Tatsuhiko Nakano ◽  
Isao Noda
2009 ◽  
Vol 63 (11) ◽  
pp. 1204-1210 ◽  
Author(s):  
Yuji Nishikawa ◽  
Tatsuhiko Nakano ◽  
Isao Noda

A time-resolved soft-pulse dynamic compression attenuated total reflection (ATR) step-scan Fourier transform rheo-optical system has been developed. This system was used to observe different viscoelastic properties of polyethyleneterephthalate (PET) and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBHx). Resonance features were observed in the dynamic compression ATR spectrum of PHBHx with 625 Hz soft-pulse frequency. In contrast, the dynamic compression ATR spectrum of PET showed no resonance features. The resonance feature of PHBHx was found at 1723 cm−1, which corresponds to the structural or morphological reorganization of a less ordered (Type II) crystalline form under compressive perturbation. The time-resolved evolution of infrared (IR) spectra was effectively analyzed by conventional generalized two-dimensional (2D) correlation analysis. The 2D-IR results indicate that the dynamic response of the well-ordered Type I crystalline state (1289 and 1261 cm−1) is faster than that of the Type II (1723, 1277, and 1228 cm−1). The present method shows promise for characterizing a wide variety of viscoelastic materials, including polymer alloys, blends, composites, and copolymers, and semicrystalline polymers.


2008 ◽  
Vol 36 (6) ◽  
pp. 1165-1168 ◽  
Author(s):  
Amandine Maréchal ◽  
W. John Ingledew ◽  
Peter R. Rich

Vibrational changes associated with CO recombination to ferrous horseradish peroxidase were investigated by rapid-scan FTIR (Fourier-transform IR) spectroscopy in the 1200–2200 cm−1 range. At pH 6.0, two conformers of bound CO are present that appear as negative bands at 1905 and 1934 cm−1 in photolysis spectra. Their recombination rate constants are identical, confirming that they arise from two substates of bound CO that are in rapid thermal equilibrium, rather than from heterogeneous protein sites. A smaller positive band at 2134 cm−1 also appears on photolysis and decays with the same rate constant, indicative of an intraprotein geminate site involved in recombination or, possibly, a weak-affinity surface CO-binding site. Other signals arising from protein and haem in the 1700–1200 cm−1 range can also be time-resolved with similar kinetics.


1993 ◽  
Vol 47 (9) ◽  
pp. 1376-1381 ◽  
Author(s):  
T. J. Johnson ◽  
A. Simon ◽  
J. M. Weil ◽  
G. W. Harris

The step-scan technique in Fourier transform infrared (FT-IR) spectroscopy is employed in new applications of time resolved spectroscopy (TRS). Results are demonstrated on time-resolved laser emissions and photolytically generated chemical reactions using both emission and absorption modes. New achievements in FT-IR temporal resolution are demonstrated, as well as the complementary nature of step-scan and rapid-scan time-resolved spectroscopy.


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