Investigation of the hydrozincite structure by infrared and solid-state NMR spectroscopy

To better understand lattice disorder in hydrozincite, natural hydrozincite samples and synthetic analogues were investigated by XRD, FTIR, (super 13) C MAS, and (super 13) C CPMAS NMR. The size of coherent diffraction domains ranges between approximately 10 nm (Synth1) and approximately 30 nm (Synth2). FTIR peaks from the antisymmetric CO (sub 3) (super 2-) stretching nu 3 mode were observed at 1383 and 1515 cm (super -1) in all samples. Peaks due to OH vibrations were observed for all the samples at 3234, 3303, and 3363 cm (super -1) , and were sharp only for the samples having larger crystal domains. The (super 13) C MAS and CPMAS NMR spectra showed a main carbon signal at 164 ppm in the Synth2 sample, while two main signals were observed at approximately 164 and approximately 168 ppm in the Synth1 sample. The intensity ratio of the latter signals were found to be independent of contact time, in the investigated range between 0.2 and 30 ms. In addition, (super 13) C CPMAS dynamics indicates that the Synth1 sample has shorter T (sub 1rho ) with respect to Synth2. This indicates a more effective process of spin diffusion of proton magnetization in the former due to different structural properties of Synth1 and Synth2 samples. In addition, chemical shift anisotropy analysis was attributed to a structural change in the carbonate group or hydrogen bonding for Synth1 and Synth2. This was interpreted as a deviation from the ideal structure generated by linear and planar lattice defects and/or grain boundaries.