Abstract
The aim of this paper is the characterization of pure tobelite synthesized in the system (NH4)2O-Al2O3-SiO2-H2O, which is a first, indispensable step for accurately interpreting the data obtained in more complex chemical systems. Tobelite has been synthesized at hydrothermal conditions (200±3°C), using a solid:solution ratio (in weight)=1:15, and reaction times from 1 to 90days and has been characterized by X-ray diffraction; infrared and Raman spectroscopy; differential thermal analysis and thermogravimetry; and transmission-analytical electron microscopy. The average chemical composition of tobelite formed after 90days run time, determined by combining the analytical electron microscopy data with nitrogen determination in the solid products of the reaction by elemental analysis, was [NH4Al1.98(Si3.07Al0.93)O10(OH)2]. The refinement of the X-ray diffraction patterns indicated that the 1M polytype predominates, and the determined cell-parameters were: a=5.219 (0.004) Å; b=9.021 (0.007) Å; c=10.556 (0.009) Å; β=101.41° (0.08); V=487.23 (0.69) Å3. The infrared spectra indicated the presence of two υ4 bands (at 1403 and 1435cm−1), which can be related to the presence of two main tobelite populations with mean particle sizes of 400×60 and 2000×200Å. The thermal study by means of differential thermal analysis and thermogravimetry, combined with X-ray thermodiffraction suggested that the mechanisms of NH4 loss were different in the two differently-sized tobelite populations: the thinner particles showed a low thermal stability (between 380° and 440°C) and the NH4 loss was coupled with dehydroxylation, leading directly to the decrease of the tobelite content. Loss of NH4 from the thicker particles occurred between 440° and 500°C, causing a gradual contraction of the basal spacing, which was followed by dehydroxylation. There were no previous data of Raman spectroscopy of tobelite and this study presents its most characteristic features.
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