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Clay Mineralogy: Spectroscopic and Chemical Determinative Methods PDF

375 Pages·1994·14.453 MB·English
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Clay Mineralogy: Spectroscopic and Chemical Determinative Methods JOIN US ON THE INTERNET VIA WWW, GOPHER, FTP OR EMAil: WWW: http://www.thomson.com GOPHER: gopher.thomson.com A service of lOOP FTP: ftp.thomson.com EMAIL: [email protected] Clay Mineralogy: Spectroscopic and Chemical Determinative Methods Edited by J. M. Wilson FRSE Head, Division of Soils Macaulay Land Use Research Institute Craigiebuckler Aberdeen, UK SPRINGER-SCIENCE+BUSINESS MEDIA, B.V First edition 1994 Reprinted 1995,1996 © 1994 Springer Science+Business Media Dordrecht Origina1ly published by Chapman & HalI in 1994 Softcover reprint ofthe hardcover Ist edition1994 Typeset in 1O/12pt Palatino by Pure Tech Corporation, Pondicherry, India ISBN 978-94-010-4313-7 ISBN 978-94-011-0727-3 (eBook) DOI 10.1007/978-94-011-0727-3 Apart from any fair dealing for the purposes of research or private study, or criticism or review, as permitted under the UK Copyright Designs and Patents Act, 1988, this publication may not be reproduced, stored, or transmitted, in any form or by any means, without the prior permis sion in writing of the publishers, or in the case of reprographic reproduction only in accordance with the terms of the licences issued by the Copyright Licensing Agency in the UK, or in accordance with the terms of licences issued by the appropriate Reproduction Rights Organization outside the UK. Enquiries conceming reproduction outside the terms stated here should be sent to the publishers at the London address printed on this page, The publisher makes no representation, express or implied, with regard to the accuracy of the information contained in this book and cannot accept any legal responsibility or liability for any errors or omissions that may be made. A Catalogue record for this book is available from the British Library Library of Congress Catalog Card Number: 93-74207 §Printed on permanent acid-free text paper, manufactured in accordance with ANSI/NISO Z39.48-1992 (Permanence of Paper). Contents Preface ix List of contributors xi 1 Molecular spectroscopy: introduction and general 1 principles (B. A. Goodman) 1.1 Background 1 1.2 Absorption spectroscopy 3 1.3 Emission spectroscopy 4 1.4 Spectral intensity 4 1.5 Spectral peak widths 5 1.6 Spectral resolution 5 1.7 Signal-to-noise optimization 7 1.8 Spectral editing and analysis 8 Acknowledgement 10 2 Infrared methods 0. D. Russell and A. R. Fraser) 11 2.1 Introduction 11 2.2 Principles 11 2.3 Instrumental requirements 12 2.4 Preparative methods and pretreatments 15 2.5 Identification and characterization of clay minerals and associated minerals 18 2.6 Interpreting the IR spectra of clay materials 57 2.7 Quantitative analysis 61 2.8 Computer-aided methods 62 Acknowledgement 64 References 64 3 Mossbauer spectroscopy (B. A. Goodman) 68 3.1 Introduction 68 3.2 Principles of M6ssbauer spectroscopy 70 3.3 Instrumentation and experimental techniques 77 3.4 M6ssbauer spectroscopy of oxide minerals 82 3.5 M6ssbauer spectroscopy of aluminosilicate minerals 96 3.6 Phosphate minerals 110 VI Contents 3.7 Applications of M6ssbauer spectroscopy in archaeology and art 111 3.8 Conclusions 112 Acknowledgements 114 References 114 4 Nuclear magnetic resonance spectroscopy ( B. A. Goodman and J. A. Chudek) 120 4.1 Introduction 120 4.2 Principles of NMR spectroscopy 122 4.3 Experimental techniques 134 4.4 General features of MAS NMR spectra of minerals 142 4.5 High-resolution NMR spectroscopy of clay minerals 149 4.6 Clay surface studies 157 4.7 Structural distribution of paramagnetic ions 165 4.8 Conclusions 167 Acknowledgements 168 References 169 5 Electron paramagnetic resonance spectroscopy (B. A. Goodman and P. L. Hall) 173 5.1 Introduction to electron paramagnetic resonance 173 5.2 Electrons in transition metal ions 178 5.3 The case of two or more unpaired electrons: fine structure 183 5.4 Nuclear hyperfine coupling 193 5.5 Experimental procedures 195 5.6 Applications 200 5.7 Conclusions 219 Acknowledgements 221 References 221 6 X-ray photoelectron spectroscopy (E. Paterson and R. Swaffield) 226 6.1 Introduction 226 6.2 Fundamental aspects 227 6.3 Experimental aspects 230 6.4 Information content 240 6.5 Applications in clay mineralogy 247 6.6 Conclusions 255 Acknowledgements 255 References 255 7 X-ray fluorescence spectroscopy and microanalysis (D. C. Bain, W. J. McHardy and E. E. Lachowski) 260 7.1 Introduction 260 Contents vii 7.2 General principles 261 7.3 X-ray fluorescence spectrometry 265 7.4 Microanalysis with SEM 273 7.5 Analytical electron microscopy 281 7.6 Conclusions 294 Acknowledgement 294 References 294 8 Chemical analysis (D. C. Bain and B. F. L. Smith) 300 8.1 Introduction 300 8.2 Sample preparation 301 8.3 Methods of major elemental analysis 304 8.4 Analysis for ferrous iron 308 8.5 Exchange capacity 312 8.6 Determination of a structural formula 317 References 327 9 Characterization of poorly ordered minerals by selective chemical methods (B. F. L. Smith) 333 9.1 Introduction 333 9.2 Principles 334 9.3 Selective chemical methods 335 9.4 Comparison of methods 350 References 353 Index 359 Preface A knowledge of clay is important in many spheres of scientific endeav our, particularly in natural sciences such as geology, mineralogy and soil science, but also in more applied areas like environmental and mater ials science. Over the last two decades research into clay mineralogy has been strongly influenced by the development and application of a num ber of spectroscopic techniques which are now able to yield information about clay materials at a level of detail that previously would have seemed inconceivable. This information relates not only to the precise characterization of the individual clay components themselves, but also to the ways in which these components interact with a whole range of absorbate molecules. At present, however, the fruits of this research are to be found principally in a somewhat widely dispersed form in the scientific journals, and it was thus considered to be an appropriate time to bring together a compilation of these spectroscopic techniques in a way which would make them more accessible to the non-specialist. This is the primary aim of this book. The authors of the various chapters first describe the principles and instrumentation of the individual spectro scopic techniques, assuming a minimum of prior knowledge, and then go on to show how these methods have been usefully applied to clay mineralogy in its broadest context. The book concludes with two chap ters describing a purely chemical approach to the characterization of clays which, although somewhat traditional, is nevertheless considered to be a useful adjunct to the sophisticated physical techniques described beforehand. The philosophy throughout the book has been to try to strike a balance between an introductory text and a research compen dium so that it may be useful to scientists with no previous experience of clays as well as to those who are familiar with the problems of investigat ing these difficult materials. This approach is similar to that adopted in a previous book of this kind (A Handbook of Determinative Methods in Clay Mineralogy, 1987, edited by M. J. Wilson, Blackie, Glasgow) which is now out of print, and in fact Chapters 2, 8 and 9 are updated versions from this work. All other chapters are, however, completely new. Most of the authors are, or have been, associated with the Macaulay Land Use Research Institute in Aberdeen, which has had a long and distinguished history of research into soil mineralogy. Despite recent x Preface difficulties occasioned by financial constraints, soil mineralogy is identi fied in the Institute's mission statement as an area which it is regarded as important to develop in an international context. It is hoped that this book may be of some assistance in the fulfilment of this aspiration. Finally, we are most grateful to the Director of MLURI, Professor T. J. Maxwell, for allowing us to undertake and complete this book with the minimum of formalities. We also thank Mrs. Aileen Stewart for the time and effort she has devoted to processing the manuscript. M. J. Wilson Macaulay Land Use Research Institute Aberdeen Contributors D. C. Bain, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. J. A. Chudek, Department of Chemistry, University of Dundee, Dundee DD14HN A. R. Fraser, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. B. A. Goodman, Scottish Crops Research Institute, Invergowrie, Dundee DD25DA. P. L. Hall, Schlumberger, PO Box 153, Cambridge CB2 3BE. E. E. Lachowski, Department of Chemistry, University of Aberdeen AB92UE W. J. McHardy, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. E. Paterson, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. J. D. Russell, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. B. F. L. Smith, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. R. Swaffield, Macaulay Land Use Institute, Craigiebuckler, Aberdeen AB92QJ. CHAPTER 1 Molecular spectroscopy: introduction and general principles B. A. Goodman 1.1 BACKGROUND Molecular spectroscopy involves the interaction of electromagnetic radi ation with materials in order to produce an absorption pattern (i.e. a spectrum) from which structural or compositional information can be deduced. Electromagnetic radiation is conventionally, and rather arbi trarily, divided into a number of distinct regions, each of which covers a range of energies that corresponds to a different type of molecular pro cess (Figure 1.1). In order of increasing frequency these are: 1. Radiofrequency (c. 105 - 109 Hz). This corresponds to the energy in volved in changing the direction of spin of a nucleus (nuclear mag netic resonance, NMR). 2. Microwave (c. 109 to 3 X 1010 Hz). This range covers the energy in volved in changing the direction of electron spin (electron paramag netic resonance, EPR, also known as electron spin resonance, ESR) and the separations between rotational energy levels of gaseous molecules. 3. Infrared (c. 3 x 1010 to 3 X 1014 Hz). Separations between vibrational energy states occur in this region, in which the techniques of infrared absorption and Raman spectroscopy occur. 4. Visible and ultraviolet (c. 3 x 1014 to 3 X 1016 Hz). This region cor responds to the separations between the energy levels of valence electrons. Clay Mineralogy: Spectroscopic and Chemical Determinative Methods. Edited by M. J. Wilson. Published in 1994 by Chapman & Hall, London. ISBN 0 412 53380 4.

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