Electron paramagnetic resonance, scanning electron microscopy with energy dispersion X-ray spectrometry, X-ray powder diffraction, and NMR characterization of iron-rich fired clays

被引:26
作者
Presciutti, F
Capitani, D [1 ]
Sgamellotti, A
Brunetti, BG
Costantino, F
Viel, S
Segre, A
机构
[1] CNR, Inst Chem Methodol, Res Area Rome, Monterotondo Staz, I-00016 Monterotondo, Italy
[2] Univ Perugia, Dept Chem, I-06123 Perugia, Italy
[3] Univ Perugia, Ctr SMAArt, I-06123 Perugia, Italy
[4] Univ Aix Marseille 1, F-13397 Marseille, France
[5] Univ Aix Marseille 3, F-13397 Marseille, France
关键词
D O I
10.1021/jp0536091
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The aim of this study is to clarify the structure of an iron-rich clay and the structural changes involved in the firing process as a preliminary step to get information on ancient ceramic technology. To this purpose, illite-rich clay samples fired at different temperatures were characterized using a multitechnique approach, i.e., by electron paramagnetic resonance, scanning electron microscopy with electron dispersion X-ray spectrometry, X-ray powder diffraction, magic angle spinning and multiple quantum magic angle spinning NMR. During firing, four main reaction processes occur: dehydration, dehydroxylation, structural breakdown, and recrystallization. When the results are combined from all characterization methods, the following conclusions could be obtained. Interlayer H2O is located close to aluminum in octahedral sites and is driven off at temperatures lower than 600 degrees C. Between 600 and 700 degrees C dehydroxylation occurs whereas, between 800 and 900 degrees C, the aluminum in octahedral sites disappears, due to the breakdown of the illite structure, and all iron present is oxidized to Fell. In samples fired at 1000 and 1100 degrees C iron clustering was observed as well as large single crystals of iron with the occurrence of ferro- or ferrimagnetic effects. Below 900 degrees C the aluminum in octahedral sites presents a continuous distribution of chemical shift, suggesting the presence of slightly distorted sites. Finally, over the whole temperature range, the presence of at least two tetrahedral aluminum sites was revealed, characterized by different values of the quadrupolar coupling constant.
引用
收藏
页码:22147 / 22158
页数:12
相关论文
共 43 条
[1]   Very fast MAS and MQMAS NMR studies of the spectroscopically challenging minerals kyanite and andalusite on 400, 500, and 800 MHz spectrometers [J].
Alemany, LB ;
Steuernagel, S ;
Amoureux, JP ;
Callender, RL ;
Barron, AR .
SOLID STATE NUCLEAR MAGNETIC RESONANCE, 1999, 14 (01) :1-18
[2]   EVIDENCE FROM SI-29 NMR FOR THE STRUCTURE OF MIXED-LAYER ILLITE SMECTITE CLAY-MINERALS [J].
ALTANER, SP ;
WEISS, CA ;
KIRKPATRICK, RJ .
NATURE, 1988, 331 (6158) :699-702
[3]  
Araujo HD., 2004, MAT RES, V7, P359
[4]   HETERONUCLEAR DECOUPLING IN ROTATING SOLIDS [J].
BENNETT, AE ;
RIENSTRA, CM ;
AUGER, M ;
LAKSHMI, KV ;
GRIFFIN, RG .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (16) :6951-6958
[5]   Comparison between the electron paramagnetic resonance spectra obtained in X- and W-bands on a fired clay: a preliminary study [J].
Bensimon, Y ;
Deroide, B ;
Zanchetta, JV .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1999, 60 (06) :813-818
[6]   QUANTITATIVE PHASE-ANALYSIS USING THE RIETVELD METHOD [J].
BISH, DL ;
HOWARD, SA .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1988, 21 (02) :86-91
[7]   Solid-state nuclear magnetic resonance study of the microporous aluminophosphate AlPO4-41 [J].
Caldarelli, S ;
Meden, A ;
Tuel, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (26) :5477-5487
[8]   Analysis of Fe segregation in the octahedral sheet of bentonitic illite-smectite by means of FTIR, 27Al MAS NMR and reverse Monte Carlo simulations [J].
Cuadros, J ;
Sainz-Díaz, CI ;
Ramírez, R ;
Hernández-Laguna, A .
AMERICAN JOURNAL OF SCIENCE, 1999, 299 (04) :289-308
[9]   ATOMIC COORDINATION AND THE DISTRIBUTION OF ELECTRIC-FIELD GRADIENTS IN AMORPHOUS SOLIDS [J].
CZJZEK, G ;
FINK, J ;
GOTZ, F ;
SCHMIDT, H ;
COEY, JMD ;
REBOUILLAT, JP ;
LIENARD, A .
PHYSICAL REVIEW B, 1981, 23 (06) :2513-2530
[10]  
Deer W. A., 1992, INTRO ROCK FORMING M, V696