Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-24T02:21:52.895Z Has data issue: false hasContentIssue false

Preparation and properties of a basic lead carbonate–montmorillonite complex

Published online by Cambridge University Press:  09 July 2018

S. Tsutsumi
Affiliation:
Institute of Earth Science, School of Education, Waseda University, 1-6-1 Nishiwaseda, Shinjuku-ku, Tokyo 169-50
A. Yamazaki
Affiliation:
Department of Mineral Resources Engineering, School of Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku-ku, Tokyo 169, Japan
M. Uehara
Affiliation:
Institute of Earth Science, School of Education, Waseda University, 1-6-1 Nishiwaseda, Shinjuku-ku, Tokyo 169-50
R. Otsuka
Affiliation:
Department of Mineral Resources Engineering, School of Science and Engineering, Waseda University, 3-4-1 Ohkubo, Shinjuku-ku, Tokyo 169, Japan

Abstract

A basic lead carbonate-montmorillonitec omplexw as prepared by treating a natural montmorillonite hydrothermally for 120 h at 250°C with lead powder, dry ice and lead nitrate solution. The product is a non-swelling material showing well-outlined, hexagonal, thin plates <1 µm in size; the symmetry is pseudo-orthorhombic, a = 5·141(7) Å, b = 9·005(5) Å, c = 17·420(4) Å, and Z = 2. The X-ray powder pattern is characterized by a 17·4 Å reflection and an integral series to the 14th order. The TG-DTA curves of this 17 Å-mineral showed one endotherm around 400°C accompanied by weight loss and two exthotherms at about 680 and 780°C By applying hightemperature X-ray diffractometry (XRD) and infrared (IR) spectroscopy, it was found that the endotherm is due to decomposition of carbonate hydroxide in the interlayer, while the two exthotherms are caused by crystallization of a hexagonal phase of PbAl2Si2O8 and by the conversion of this phase into lead feldspar, respectively. The crystal structure of the 17 Å-mineral was determined and refined as a 2:1 dioctahedral smectite interlayered with a hydrocerussite-like layer by a one-dimensional Fourier synthesis method.

Type
Research Article
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 1993

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Appleman, A. & Evans, H.T. (1973) Indexing and Least-Square Refinement of Powder Diffraction Data. P.B. Rep. No. 216 188, National Technical Information Services, Springfield.Google Scholar
Ball, M.C. & Casson, M.J. (1977) Thermal studies on lead(II) salts-II, J. Inorg. Nucl. Chem. 39, 19491951.Google Scholar
Cowley, J.M. (1956) Electron-diffraction study of the structure of basic lead carbonate, 2Pbco3·Pb(OH)2 . Acta Cryst. 9, 391396.Google Scholar
Flemming, N.J., Lopata, V.L, Sanipelli, B.L. & Taylor, P. (1984) Thermal decomposition of basic lead carbonates: A comparison of hydrocerussite and plumbonacraite. Thermochim. Acta. 81, 18.CrossRefGoogle Scholar
Hayase, K., Dristas, J.A., Tsutsum1 S., Otsuka, R., Tanabe, S., Sudo, T. & Nishiyama, T. (1978) Surite, A new Pbrich layer silicate mineral. Am. Miner. 63, 11751181.Google Scholar
Katz, G. & Reed, L. (1957) The unit cell and space group of basic lead carbonate. Acta Cryst. 10, 142.Google Scholar
Kotama, R., Nishi, Y. & Kano, M. (1969) Thermal decomposition of lead hydroxide carbonate. Nippon Kagaku Zasshi, 90, 3034.Google Scholar
Sorrell, C.A. (1962) Solid state formation of barium, Strontium and lead feldspars in clay-sulfate mixture. Am. Miner. 47, 291309.Google Scholar
White, W.B. (1974) Carbonate. Pp. 227-284 in: The Infrared Spectra of Minerals (V.C. Farmer, Editor), Mineralogical Society, London.Google Scholar