Fourier transform Raman spectroscopy of Syncrude Sweet Blend distillation fractions: the 200-1800 cm-1 region.

The fingerprint (200-1800 cm(-1)) region in FT-Raman spectra of Syncrude Sweet Blend (SSB) and its three constituent distillation fractions (naphtha, light gas oil and heavy gas oil) was analyzed in detail in this study. Approximately 50 bands were observed and assigned to functional groups in saturated (alkanes) and unsaturated (aromatics) species. Characteristic bands for mono-, bi-, and tricyclic aromatics were identified and used to quantify these groups in SSB and the distillation fractions.

FT-Raman and photoacoustic infrared spectroscopy of Syncrude heavy gas oil distillation fractions.

FT-Raman and photoacoustic (PA) infrared spectra of six distillation fractions derived from Syncrude heavy gas oil (HGO), which has a boiling range from 343 to 524 degrees C, were analyzed in detail in this study. Most of the information on the fingerprint region (200-1,800 cm(-1)) is provided by the FT-Raman spectra, which display approximately 30 bands that are assignable to functional groups in alkanes or aromatics. Monocyclic, bicyclic and tricyclic aromatics in the six fractions were also monitored using bands in this region.

Fourier transform Raman spectroscopy of Syncrude sweet blend distillation fractions derived from Athabasca bitumen.

The C-H stretching region in FT-Raman spectra of Syncrude sweet blend (SSB) and three distillation fractions (naphtha, light gas oil and heavy gas oil) was analyzed in detail in this investigation. The frequencies and intensities of the 11 aliphatic and three aromatic C-H bands used to fit the spectrum of SSB were equal to the averages (weighted sums) of the corresponding quantities in the spectra of the fractions. The additivity of the spectra, thought to be a consequence of the large number of discrete compounds contained in each fraction, makes it possible to estimate the composition of other SSB samples using the spectra of the fractions reported in this work.

Infrared Study of the Intercalation of Kaolinite by Caesium Bromide and Caesium Iodide.

CsBr- and CsI-kaolinite intercalation complexes were synthesized by gradually heating caesium halide disks of the DMSO-kaolinite intermediate up to 330 degreesC. Infrared spectroscopy revealed two types of complexes with the caesium salts: almost nonhydrous, obtained during thermal treatment of the DMSO complex, and hydrated, produced by regrinding the disk in air. Comparison of band positions for CsBr-kaolinite and CsI-kaolinite with those for the CsCl complex (observed in a previous study) shows that the strength of the hydrogen bond between the intercalated halide and the inner surface hydroxyl decreases on the order CsCl > CsBr > CsI.