Spectroscopic Identification of Amber Imitations: Different Pressure and Temperature Treatments of Copal Resins

Copal resins can be treated with heat and/or pressure to imitate ambers in the gem market. To explore the effects of different modification conditions on post-treatment spectral changes, five experimental methods with different temperature–pressure parameters were designed to modify two types of copal resins. The treated copal resins were examined by infrared, Raman and nuclear magnetic resonance spectroscopy. Results indicate that all the treatment methods simulate the maturation process, with spectral characteristics becoming more similar to those of ambers. Multi-stage heat–pressure treatment has the most significant effect on Colombia and Madagascar copal resins, with their spectra being similar to those of Dominican and Mexican ambers. Rapid high-temperature treatment at 180 °C modified the Borneo copal resin, with its infrared spectrum developing a “Baltic shoulder” resembling that of heat-treated Baltic amber. Even though there are many similarities between treated copal resins and natural ambers, they can still be distinguished by spectroscopic methods.

Spectroscopic Identification of Hydrogen Bond Vibrations and Quasi-Isostructural Polymorphism in N-Salicylideneaniline

The ortho-hydroxy aryl Schiff base 2-[(E)-(phenylimino)methyl]phenol and its deutero-derivative have been studied by the inelastic incoherent neutron scattering (IINS), infrared (IR) and Raman experimental methods, as well as by Density Functional Theory (DFT) and Density-Functional Perturbation Theory (DFPT) simulations. The assignments of vibrational modes within the 3500–50 cm−1 spectral region made it possible to state that the strong hydrogen bond in the studied compound can be classified as the so-called quasi-aromatic bond. The isotopic substitution supplemented by the results of DFT calculations allowed us to identify vibrational bands associated with all five major hydrogen bond vibrations. Quasi-isostructural polymorphism of 2-[(E)-(phenylimino)methyl]phenol (SA) and 2-[(E)-(phenyl-D5-imino)methyl]phenol (SA-C6D5) has been studied by powder X-ray diffraction in the 20–320 K temperature range.

Spectroscopic Identification on CO2 Separation from CH4 + CO2 Gas Mixtures Using Hydroquinone Clathrate Formation

The formation of hydroquinone (HQ) clathrate and the guest behaviors of binary (CH4 + CO2) gas mixtures were investigated by focusing on an application to separate CO2 from landfill gases. Spectroscopic measurements show that at two experimental pressures of 20 and 40 bar, CO2 molecules are preferentially captured in HQ clathrates regardless of the gas composition. In addition, preferential occupation by CO2 is observed more significantly when the formation pressure and the CH4 concentration are lower. Because the preferential occupation of CO2 is found with binary (CH4 + CO2) gas mixtures regardless of the composition of the feed gas, a clathrate-based process can be applied to CO2 separation or concentration from landfill gases or (CH4 + CO2) mixed gases.