Wiewióra, Andrzej

English

Wiewióra Andrzej

Petit Sabine

Martin F.

Prost R.

University of Szeged

Acta Mineralogica-Petrographica, Abstract Series 4, Szeged, 2004 CRYSTAL CHEMISTRY OF TALC: XRD AND SPECTROSCOPIC STUDIES WIEWIÔRA. A..1 PETIT, S.,2 MARTIN, F.,3 PROST, R.4 1 Institute o f Geological Sciences PAS [Instytut Nauk Geologycznyh PAN], Twarda 51 -55 , Warszawa, 00 818, Poland 2 HydrASA Laboratoire, Université de Poitiers, 40 av. du Recteur Pineau, Poitiers, 86022, France 3 HydrASA Laboratoire d'Analyse Structurale et Hydrothermalism, Université de Limoges, 123 av. Albert Thomas, Limoges, 87060, France 4 Laboratoire de Science du Sol INRA, r. de Saint-Cyr, Versailles, 78026, France E-mail: wiewiora@twarda.pan.pl In the monolithic (non powdered) samples of talc Wie-wiora (1997) determined superstructure, characterised by d(ooi) = 18.7 A with integral series of d(0oi// until / = 18, while X-ray tracings of powdered aggregates showed only all the talc common peaks. The strongest reflection for powder is 001, while it is 003 (006 of superstructure) for quasi single crystal sample. From intensities of the basal reflections, divided by Lorentz-polarisation factor for single crystal, a one-dimensional Fourier analysis was performed. It revealed increase in the electron density, right in the middle in the talc interlayer space (Fig. 1). This additional electron density band correlates rightly with a very strong vibration at 101 cm"' in the far infrared, for the first time obtained on monoli-thic sample, while this band is hardly visible in this position in the spectra from powdered sample. This band clearly indi-cates some Mg in the interlayer space of talc. There is no direct proof for the occupation of structural positions in talc by Ca, Na, K but positive correlation of Na with tetrahedral A1 (R2 = 0.71) may indicate that some Na may enter also the interlayer positions to enable charge balance due to tetrahedral substitution of Si by lower-valency cation, na-mely A1 and/or Fe3+. 1 I I I I r o d o o o o o o o Fig. 1: One-dimensional [001] electron density distribution for two layer structure of talc. Medium infrared Fourier spectroscopy revealed, in some samples of talc, vMg3OH (band present in all spectra), but also vMg2FeOH, vMgFe2OH, vFe3OH and for the first time vMg2A10H band. In the same samples 2vMg3OH, 2vMg2FeOH, 2vMgFe2OH, 2vFe3OH and 2vMg2A10H vib-rations were for the first time recorded in the near infrared spectral region. The spectra proved presence of Fe and A1 substituting Mg in the octahedral positions of talc and enabled their quantification (Petit et al., 2004). Mossbauer technique, as applied to study four samples, demonstrated that 62-68% of iron is as Fe2+ located in octahedral positions. Fe3+ is located in the octahedral and tetrahedral positions. The determined distributions of Fe2+ between M( l ) , M(2) and M(3) octahedral positions appear to depend on tempera-ture in which experiment was performed. At 80 K the two different octahedral occupancies of Fe were differentiated, but three occupation positions at 4 K. These XRD and spectroscopic data may mean that our understanding of talc structure as polytype 1 Aa—II FLVM). be-longing to C - l space group (more or less disordered) may be not adequate with real structure of some individual samples. In several samples of talc, originated by transformation of e.g. micas or chlorites, superstructure is quite evident. In the light of one-dimensional electron density by Fourier trans-forms analysis, the structure may be explained as two layer arrangement with the basal spacing d(00r> = 18.7 A. In each pair of layers, having different electron densities of octahed-ral sheets (possibly tetrahedral, also), the even (e) orientation of octahedral sheet, intra-layer displacement along <5> vec-tor and interlayer displacement of tetrahedral sheets belong-ing to adjacent layers along <1>, produce resultant layer dis-placement <0>. Such a structure (Fig. 1) gives superstructure reflections in XRD pattern. References PETIT, S. , MARTIN, F . , WIEWIORA, A . , D E PARSEVAL, P . , D E -CARREAU, A. (2004): American Mineralogist, 80, 319-326. WIEWIORA, A. (1997): Clays for our future: Proceedings of the 11th International Clay Conference, Ottawa, Canada, 443-449. 62 www. sei. u-szeged. hu/asvanytar>/acta. htm 116 

Chrystal chemistry of Talc : XRD and spectroscopic studies

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Chrystal chemistry of Talc: : XRD and spectroscopic studies

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