Abstract

A pressure cell was constructed using a pair of type II diamonds for study of infrared spectra of solids in the 1- to 15-micron region. Using commercial infrared equipment, spectra can be studied routinely to calculated pressures as high as 30,000 atmospheres. Under pressure, bands generally shift to higher frequencies and decrease in intensity. The magnitude of both changes depends on the mode of vibration. Occasionally major changes in spectra occur. In calcite the carbon-oxygen symmetric stretching, mode v1, becomes active at elevated pressures while the doubly degenerate v3, stretching, and v4, bending, frequencies split. From the shift in frequency of v1 with pressure the “compressibility”, [(−1/Ro) (dR/dp)], of the C—O bond length, R, is calculated to be 2.8×10−7/atmosphere. Major spectral changes are not observed in the same pressure ranges in other carbonates having the calcite or aragonite structures. The results for calcite may be explained by a shift of the ion from the trigonal axis under pressure.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.