Low-frequency anharmonic couplings in crystalline bromoform: Theory.

Theoretical calculations of the low-frequency anharmonic couplings of the ß-phase of crystalline bromoform are presented based on density functional theory quantum chemistry calculations. The electrical and mechanical anharmonicities between intra- and intermolecular modes are calculated, revealing that the electrical anharmonicity dominates the cross-peak intensities in the 2D Raman-THz response and crystalline, as well as liquid, bromoform. Furthermore, the experimentally observed difference in relative cross-peak intensities between the two intramolecular modes of bromoform and the intermolecular modes can be explained by the C3v-symmetry of bromoform in combination with orientational averaging. The good agreement with the experimental results provides further evidence for our interpretation that the 2D Raman-THz response of bromoform is, indeed, related to the anharmonic coupling between the intra- and intermolecular modes.

Low-frequency anharmonic couplings in bromoform revealed from 2D Raman-THz spectroscopy: From the liquid to the crystalline phase.

Two-dimensional (2D) Raman-THz spectroscopy in the frequency of up to 7 THz has been applied to study the crystalline ß-phase of bromoform (CHBr3). As for liquid CHBr3, cross peaks are observed, which, however, sharpen up in the crystalline sample and split into assignable sub-contributions. In the Raman dimension, the frequency positions of these cross peaks coincide with the intramolecular bending modes of the CHBr3 molecules and in the THz dimension with the IR-active lattice modes of the crystal. This work expands the applicability of this new 2D spectroscopic technique to solid samples at cryogenic temperatures. Furthermore, it provides new experimental evidence that the cross peaks, indeed, originate from the coupling between intra- and intermolecular vibrational modes.

Approach for determination of detonation performance and aluminum percentage of aluminized-based explosives by laser-induced breakdown spectroscopy.

Energetic materials containing aluminum powder are hazardous compounds, which have wide applications as propellants, explosives, and pyrotechnics. This work introduces a new method on the basis of the laser-induced breakdown spectroscopy technique in air and argon atmospheres to investigate determination of aluminum content and detonation performance of 1,3,5-trinitro-1,3,5-triazine (RDX)-based aluminized explosives. Plasma emission of aluminized RDX explosives are recorded where atomic lines of Al, C, H, N, and O, as well as molecular bands of AlO and CN are identified. The formation mechanism of AlO and CN molecular bands is affected by the aluminum percentage and oxygen content present in the composition and plasma. Relative intensity of the Al/O is used to determine detonation velocity and pressure of the RDX/Al samples. The released energy in the laser-induced plasma of aluminized RDX composition is related to the heat of explosion and percentage of aluminum.