Analysis of Noise for Rapid-Scan and Step-Scan Methods of FT-IR Difference Spectroscopy

2001 ◽  
Vol 55 (9) ◽  
pp. 1161-1165 ◽  
Author(s):  
Steven S. Andrews ◽  
Steven G. Boxer
2007 ◽  
Vol 111 (7) ◽  
pp. 1517-1522 ◽  
Author(s):  
Baokang Jin ◽  
Peng Liu ◽  
Ye Wang ◽  
Zipin Zhang ◽  
Yupeng Tian ◽  
...  

2009 ◽  
Vol 394 (8) ◽  
pp. 2277-2277
Author(s):  
Michael Schleeger ◽  
Christoph Wagner ◽  
Michiel J. Vellekoop ◽  
Bernhard Lendl ◽  
Joachim Heberle

1987 ◽  
Vol 41 (7) ◽  
pp. 1147-1151 ◽  
Author(s):  
J. T. Cronin ◽  
T. B. Brill

Rapid-scan infrared spectroscopy (RSFT-IR) with better than 100-ms temporal resolution has been used to quantify the gas decomposition products of energetic materials in real time at various heating rates up to 800°C/s and under buffer gas pressures of 1 to 1000 psi. A new method is described that permits simultaneous real-time recording of the temperature of the condensed phase and of the IR spectra of the gaseous products under the above conditions. Endothermic and exothermic events in the condensed phase can now be correlated with the evolved gases under conditions approaching those of combustion. The design and procedure for using the cell are given and are applied to the thermolysis of 1,7-diazido-2,4,6-trinitro-2,4,6-triazaheptane (DATH) and pentaery-thrityltetrammonium nitrate (PTTN).


2009 ◽  
Vol 394 (7) ◽  
pp. 1869-1877 ◽  
Author(s):  
Michael Schleeger ◽  
Christoph Wagner ◽  
Michiel J. Vellekoop ◽  
Bernhard Lendl ◽  
Joachim Heberle

1994 ◽  
Vol 48 (3) ◽  
pp. 316-319 ◽  
Author(s):  
Michael G. Sowa ◽  
Henry H. Mantsch

Rapid-scan- and step-scan-based Fourier transform infrared photoacoustic depth profiling results of an extracted but intact human tooth are compared. The effects of various data processing methods are examined. Analysis of the phase dispersion of the photothermal signal along with spectral linearization is used to access the extent of photoacoustic saturation in the photoacoustic spectra. Phase-modulated/phase-resolved depth profiling methods are less prone to photoacoustic saturation and provide superior localization of the surface and subsurface absorbers distributed in the tooth enamel. Mid-infrared depth profiling studies of calcified tissues can aid in the understanding of degenerative bone diseases, bone growth, and modeling, as well as tissue mineralization.


1992 ◽  
Vol 46 (6) ◽  
pp. 900-911 ◽  
Author(s):  
T. B. Brill ◽  
P. J. Brush ◽  
K. J. James ◽  
J. E. Shepherd ◽  
K. J. Pfeiffer

The interface of a Pt filament pyrolysis control unit and a rapid-scan FT-IR spectrometer is described that enables the thermal decomposition of a thin film of material to be studied isothermally after heating at 2000°C/s. A model of the heat transfer of the Pt filament as a function of gas atmosphere and pressure is developed to help understand the instrument response. The control voltage of the Pt filament is highly sensitive to the thermochemistry of the thin film of sample. By simultaneously recording the control voltage and the rapid-scan IR spectra of the near-surface gas products, one learns considerable detail about chemical mechanisms relevant to combustion of a bulk material. The application of T-jump/FT-IR spectroscopy is illustrated with rapid thermolysis data for the energetic organoazide polymers azidomethyl-methyloxetane (AMMO), bis(azidomethyl)oxetane (BAMO), and glycidylazide polymer (GAP); the cyclic nitramine, octahydro-1,3,5,7-tetranitro-1,3,5,7-tetraazacine (HMX); and the nitroaromatic 1,3,5-triamino-2,4,6-trinitrobenzene (TATB).


2021 ◽  
Vol 8 ◽  
Author(s):  
Victor A. Lorenz-Fonfria ◽  
Kiyoshi Yagi ◽  
Shota Ito ◽  
Hideki Kandori

Fundamental vibrations of the chromophore in the membrane protein bacteriorhodopsin (BR), a protonated Schiff base retinal, have been studied for decades, both by resonance Raman and by infrared (IR) difference spectroscopy. Such studies started comparing vibrational changes between the initial BR state (all-trans retinal) and the K intermediate (13-cis retinal), being later extended to the rest of intermediates. They contributed to our understanding of the proton-pumping mechanism of BR by exploiting the sensitivity of fundamental vibrational transitions of the retinal to its conformation. Here, we report on new bands in the 2,500 to 1,800 cm−1 region of the K-BR difference FT-IR spectrum. We show that the bands between 2,500 and 2,300 cm−1 originate from overtone and combination transitions from C-C stretches of the retinal. We assigned bands below 2,300 cm−1 to the combination of retinal C-C stretches with methyl rocks and with hydrogen-out-of-plane vibrations. Remarkably, experimental C-C overtone bands appeared at roughly twice the wavenumber of their fundamentals, with anharmonic mechanical constants ≤3.5 cm−1, and in some cases of ∼1 cm−1. Comparison of combination and fundamental bands indicates that most of the mechanical coupling constants are also very small. Despite the mechanical quasi-harmonicity of the C-C stretches, the area of their overtone bands was only ∼50 to ∼100 times smaller than of their fundamental bands. We concluded that electrical anharmonicity, the second mechanism giving intensity to overtone bands, must be particularly high for the retinal C-C stretches. We corroborated the assignments of negative bands in the K-BR difference FT-IR spectrum by ab initio anharmonic vibrational calculations of all-trans retinal in BR using a quantum-mechanics/molecular mechanics approach, reproducing reasonably well the small experimental anharmonic and coupling mechanical constants. Yet, and in spite accounting for both mechanical and electrical anharmonicities, the intensity of overtone C-C transitions was underestimated by a factor of 4–20, indicating room for improvement in state-of-the-art anharmonic vibrational calculations. The relatively intense overtone and combination bands of the retinal might open the possibility to detect retinal conformational changes too subtle to significantly affect fundamental transitions but leaving a footprint in overtone and combination transitions.


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