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Phase Evolution of Ancient and Historical Ceramics
EMU Notes in Mineralogy, Vol. 20 (2019), Chapter 6, 233–281 The struggle between thermodynamics and kinetics: Phase evolution of ancient and historical ceramics 1 2 ROBERT B. HEIMANN and MARINO MAGGETTI 1Am Stadtpark 2A, D-02826 Go¨rlitz, Germany [email protected] 2University of Fribourg, Department of Geosciences, Earth Sciences, Chemin du Muse´e 6, CH-1700 Fribourg, Switzerland [email protected] This contribution is dedicated to the memory of Professor Ursula Martius Franklin, a true pioneer of archaeometric research, who passed away at her home in Toronto on July 22, 2016, at the age of 94. Making ceramics by firing of clay is essentially a reversal of the natural weathering process of rocks. Millennia ago, potters invented simple pyrotechnologies to recombine the chemical compounds once separated by weathering in order to obtain what is more or less a rock-like product shaped and decorated according to need and preference. Whereas Nature reconsolidates clays by long-term diagenetic or metamorphic transformation processes, potters exploit a ‘short-cut’ of these processes that affects the state of equilibrium of the system being transformed thermally. This ‘short-cut’ is thought to be akin to the development of mineral-reaction textures resulting from disequilibria established during rapidly heated pyrometamorphic events (Grapes, 2006) involving contact aureoles or reactions with xenoliths. In contrast to most naturally consolidated clays, the solidified rock-like ceramic material inherits non-equilibrium and statistical states best described as ‘frozen-in’. The more or less high temperatures applied to clays during ceramic firing result in a distinct state of sintering that is dependent on the firing temperature, the duration of firing, the firing atmosphere, and the composition and grain-size distribution of the clay. -
Marinellite, a New Feldspathoid of the Cancrinite-Sodalite Group
Eur. J. Mineral. 2003, 15, 1019–1027 Marinellite, a new feldspathoid of the cancrinite-sodalite group ELENA BONACCORSI* and PAOLO ORLANDI Dipartimento di Scienze della Terra, Universita` di Pisa, Via S. Maria 53, I-56126 Pisa, Italy * Corresponding author, e-mail: [email protected] Abstract: Marinellite, [(Na,K)42Ca6](Si36Al36O144)(SO4)8Cl2·6H2O, cell parameters a = 12.880(2) Å, c = 31.761(6) Å, is a new feldspathoid belonging to the cancrinite-sodalite group. The crystal structure of a twinned crystal was preliminary refined in space group P31c, but space group P62c could also be possible. It was found near Sacrofano, Latium, Italy, associated with giuseppettite, sanidine, nepheline, haüyne, biotite, and kalsilite. It is anhedral, transparent, colourless with vitreous lustre, white streak and Mohs’ hardness of 5.5. The mineral does not fluoresce, is brittle, has conchoidal fracture, and presents poor cleavage on {001}. Dmeas is 3 3 2.405(5) g/cm , Dcalc is 2.40 g/cm . Optically, marinellite is uniaxial positive, non-pleochroic, = 1.495(1), = 1.497(1). The strongest five reflections in the X-ray powder diffraction pattern are [d in Å (I) (hkl)]: 3.725 (100) (214), 3.513 (80) (215), 4.20 (42) (210), 3.089 (40) (217), 2.150 (40) (330). The electron microprobe analysis gives K2O 7.94, Na2O 14.95, CaO 5.14, Al2O3 27.80, SiO2 32.73, SO3 9.84, Cl 0.87, (H2O 0.93), sum 100.20 wt %, less O = Cl 0.20, (total 100.00 wt %); H2O calculated by difference. The corresponding empirical formula, based on 72 (Si + Al), is (Na31.86K11.13Ca6.06) =49.05(Si35.98Al36.02)S=72O144.60(SO4)8.12Cl1.62·3.41H2O. -
26 May 2021 Aperto
AperTO - Archivio Istituzionale Open Access dell'Università di Torino The crystal structure of sacrofanite, the 74 Å phase of the cancrinite–sodalite supergroup This is the author's manuscript Original Citation: Availability: This version is available http://hdl.handle.net/2318/90838 since Published version: DOI:10.1016/j.micromeso.2011.06.033 Terms of use: Open Access Anyone can freely access the full text of works made available as "Open Access". Works made available under a Creative Commons license can be used according to the terms and conditions of said license. Use of all other works requires consent of the right holder (author or publisher) if not exempted from copyright protection by the applicable law. (Article begins on next page) 05 October 2021 This Accepted Author Manuscript (AAM) is copyrighted and published by Elsevier. It is posted here by agreement between Elsevier and the University of Turin. Changes resulting from the publishing process - such as editing, corrections, structural formatting, and other quality control mechanisms - may not be reflected in this version of the text. The definitive version of the text was subsequently published in MICROPOROUS AND MESOPOROUS MATERIALS, 147, 2012, 10.1016/j.micromeso.2011.06.033. You may download, copy and otherwise use the AAM for non-commercial purposes provided that your license is limited by the following restrictions: (1) You may use this AAM for non-commercial purposes only under the terms of the CC-BY-NC-ND license. (2) The integrity of the work and identification of the author, copyright owner, and publisher must be preserved in any copy. -
Preprint American Mineralogist 407
This is a preprint, the final version is subject to change, of the American Mineralogist (MSA) Cite as Authors (Year) Title. American Mineralogist, in press. (DOI will not work until issue is live.) DOI: http://dx.doi.org/10.2138/am.2012.4189 7/11 1 Semi-quantitative determination of the Fe/Mg ratio in synthetic cordierite using 2 Raman spectroscopy 3 REVISION 1 4 Authors: Udo Haefeker1, Reinhard Kaindl2, Peter Tropper1 5 6 1Institute of Mineralogy and Petrography, University Innsbruck, Innrain 52, A-6020 7 Innsbruck, Austria. 8 E-mail: [email protected] 9 2Present address: MATERIALS – Institute for Surface Technologies and Photonics, 10 Functional Surfaces, JOANNEUM RESEARCH Forschungsgesellschaft mbH, 11 Leobner Straße 94, A-8712 Niklasdorf, Austria. 12 13 ABSTRACT 14 Investigations of H2O-bearing synthetic well-ordered Mg-Fe-cordierites (XFe = 0-1) 15 with micro-Raman spectroscopy revealed a linear correlation between the Fe/Mg 16 ratio and the position of certain Raman peaks. In the range between 100 and 1250 17 cm-1 all peaks except for three peaks shift towards lower wavenumbers with 18 increasing XFe as a consequence of the substitution of the lighter Mg by the heavier 19 Fe atom on the octahedral sites and the associated structural changes. Selected 20 medium and strong peaks show a shift of 5 to 13 cm-1, respectively. Based on recent 21 quantum-mechanicalPreprint calculations American (Kaindl et al. 2011) Mineralogist these shifts can be attributed to 22 specific vibrational modes in the cordierite structure, thus showing that the Mg-Fe 23 exchange affects the vibrational modes of tetrahedral, octahedral and mixed sites. -
Andalusite and Na- and Li-Rich Cordierite in the La Costa Pluton, Sierras Pampeanas, Argentina: Textural and Chemical Evidence for a Magmatic Origin
Andalusite and Na- and Li-rich cordierite in the La Costa pluton, Sierras Pampeanas, Argentina: textural and chemical evidence for a magmatic origin Pablo H. Alasino . Juan A. Dahlquist . Carmen Galindo · Cesar Casquet · Julio Saavedra Abstraet The La Costa pluton in the Sierra de Velasco Keywords Andalusite· Na- and Li-rich cormerite . (NW Argentina) consists of S-type granitoids that can be S-type granite . La Costa pluton . Sierras Pampeanas grouped into three igneous facies: the alkali-rich Santa Cruz facies (SCF, Si02 ",67 wt%) mstinguished by the presence of andalusite and Na- and Li-rich cormerite Introduetion (Na20 = 1.55-1.77 wt% and LhO = 0.14---0.66 wt%), the Anillaco facies (Si02 '" 74 wt%) with a significant pro Andalusite and cormerite are important and common rock portion of Mn-rich garnet, and the Anjullón facies (Si02 forming mineral s in metapelitic rocks and may also be '" 7 5 wt%) with abundant albitic plagioc1ase. The petrog abundant in felsic peralurninous igneous rocks such as raphy, mineral chemistry and whole-rock geochemistry of granites, pegmatites, aplites and rhyolites. A fundamental the SCF are compatible with magmatic crystallization of question conceming the presence of andalusite and corm Na- and Li-rich cormerite, andalusite and muscovite from erite in peraluminous rocks is how they formed, i.e. whe the peraluminous magma under moderate P-T conditions ther they crystallized from the magma or were trapped as ('" 1.9 kbar and ca. 735°C). The high Li content of cor xenocrysts (e.g. Flood and Shaw 1975 ; Clarke et al. 1976, merite in the SCF is unusual for granitic rocks of inter 2005; Bellido and Barrera 1979; Phillips et al. -
Structural Characteristics of Gas Hydrates Within the Framework of Generalized Crystallography A
Crystallography Reports, Vol. 48, No. 3, 2003, pp. 347–350. Translated from Kristallografiya, Vol. 48, No. 3, 2003, pp. 391–394. Original Russian Text Copyright © 2003 by Talis. THEORY OF CRYSTAL STRUCTURES Structural Characteristics of Gas Hydrates within the Framework of Generalized Crystallography A. L. Talis Russian Institute of Synthesis of Mineral Raw Materials, Aleksandrov, Vladimir oblast, 601650 Russia e-mail: [email protected] Received September 16, 2002 Abstract—It is shown that the symmetry of the {5, 3, 3} polytope (four-dimensional dodecahedron) embedded into E4 enables one to derive all the polyhedra–cavities that make up gas hydrates from the {5, 3} dodecahedron. Consideration is given to the allomorphic embedding of the {5, 3} subgraph into the incidence graph of the Desargues configuration 103, which determines the mechanism of incorporation of guest molecules into the polyhedra–cavities of gas hydrates and their escape from these polyhedra at the symmetry level. The relation- ships obtained may be considered as a basis for an a priori derivation of the determined (periodic and aperiodic) structures of gas hydrates. © 2003 MAIK “Nauka/Interperiodica”. The impossibility of dividing the three-dimensional pentagonal “cap” of the icosahedron into a hexagonal Euclidean space E3 into regular tetrahedra determines 2π one (if a wedge with an angle ------ is inserted), with the the structural characteristics of tetrahedrally coordi- 5 nated aqueous frameworks of gas hydrates that cannot disclination interactions being determined by the prod- be adequately reflected within the framework of classi- uct of the corresponding elements of group Y'. The cal crystallography. For example, the polyhedra–cavi- 2π introduction of two, three, and four Ð------ disclinations ties D, T, P, and H (dodecahedron, tetra-, penta-, and 5 hexadecahedra), the constituent fragments of the struc- into an icosahedron along its fivefold axes results in the tures of gas hydrates, are determined as dual to the Z12, formation of the Z14, Z15, and Z16 polyhedra [2]. -
Mid-Infrared (2.1-25 Urn) Spectra of Minerals: First Edition
DEPARTMENT OF THE INTERIOR U.S. GEOLOGICAL SURVEY Mid-Infrared (2.1-25 urn) Spectra of Minerals: First Edition by John W. Salisbury . U.S. Geological Survey1 Louis S. Walter NASA Goddard Space Flight Center2 Norma Vergo U.S. Geological Survey1 Open-File Report 87-263 This report 1s preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards. Stop 927 laboratory for Terrestrial Physics Reston, VA 22092 Greenbelt, MD 20771 Contents 1.0 Abstract 2.0 Introduction 3.0 Experimental Technique 3.1 Sample Acquisition and Preparation 3.2 Sample Characterization 3.3 Acquisition of Spectra 3.4 Data Storage and Retrieval 4.0 Discussion of Spectra 4.1 Major Spectral Features of Minerals 4.2 Effect of Particle Size 4.21 Role of surface and volume scattering 4.22 Changes in spectral contrast 4.23 Transparency peaks 4.24 Christiansen frequency 4.3 Effect of Crystal!ographic Orientation 4.4 Effect of Packing 4.5 Effect of Atmospheric Gases 4.6 Effect of Impurities 4.7 Using Laboratory Spectra to Predict Remote Sensing Measurements 5.0 Acknowledgements 6.0 Appendix 1: Mineral spectra and description sheets are presented in alphabetical order. Minerals are listed alphabetically and by mineral class, subclass and group at the beginning of the appendix. 7.0 Appendix 2. Making a KBr Pellet 1.0 ABSTRACT Almost all libraries of mineral spectra 1n the mid-Infrared are 1n the form of transmittance spectra. Although useful In a laboratory setting, such spectra are of limited benefit for Interpreting remote sensing observations because they do not include the effects of scattering. -
The Erystal Strueture of Bieehulite, Ca2[Ai2si06](OH)2
Zeitsclll'ift fiir Kristallographie, Bd, 146, S. 35-41 (1977) ~ by Akademische Verlagsgesellschaft, vViesbaden 1977 The erystal strueture of bieehulite, Ca2[AI2Si06](OH)2 By Knt'l' SARI, and NmA:-I.IAN DEH CRA'l"fl<,RJEE Institut fiir Mineralogie, Ruhr- U niversitiit, Boehum (Received 29 .January 1977) Auszug Die Kristallstruktur von synthetiscllOm Bicchulit wurde mit Rontgen- Einkristallmethoden bestimmt (R = 0,07 fUr aile 65 beobachteten Reflexe). Bicchulit hat eine Geruststruktur vom Sodalith-Typ. Al und Si sind statistisch auf die Tetraederpliitze verteilt und nul' von Sauorstoffatomen koordiniert. Calcium ist von drei Sauerstoffatomen und drei OR-Gruppen oktaedrisch umgeben. .1eweils vier wIehe Oktaeder sind libel' gemeinsame OR-OR-Kanten zu einer Vierergruppe verkniipft. Diese Vierergruppen sind in die Hohlriiume des Geriists eingelagcrt. Abstract The crystal structure of synthetic bicchulite was determined with single- crystal x-ray methods (R = 0.07 for all 65 observed reflections). Bicchulite has a sodalite-type framework structure with Al and Si distributed statistically in the tetrahedral sites, coordinated solely by oxygen atoms. Calcium is coordinated octahedrally by three oxygen atoms and three OR groups. Four such octahedra are linked to a group by OR -OR edges. ThesE' octahedra groups occupy the cavities within the fntm8work. Introduetion Single crystals of synthetic bicchulite, Ca2[AhSi06](OH)2 were grown under hydrothermal conditions by GUPTA and CHATTERJEE (1977). The crystals were more or less equidimensional but very small (at most (J.()5mm in diameter). GUPTA and CHATTERJEE (1977) deter- mined the lattice constants of bicchulite from powder patterns (Guinier and powder diffractometer method, Cu radiation). They indexed the powder patterns on the basis of a body-centered cubic cell, as sug- gested by HENMI et al. -
Foitite: Formation During Late Stages of Evolution of Complex Granitic Pegmatites at Dobrá Voda, Czech Republic, and Pala, California, U.S.A
1399 The Canadian Mineralogist Vol. 38, pp. 1399-1408 (2000) FOITITE: FORMATION DURING LATE STAGES OF EVOLUTION OF COMPLEX GRANITIC PEGMATITES AT DOBRÁ VODA, CZECH REPUBLIC, AND PALA, CALIFORNIA, U.S.A. MILAN NOVÁK§ Department of Mineralogy, Petrology and Geochemistry, Masaryk University, Kotláøská 2, CZ-611 37 Brno, Czech Republic MATTHEW C. TAYLOR¶ Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada ABSTRACT Zoned crystals of tourmaline (elbaite–foitite) were found in pockets of the lepidolite-subtype granitic pegmatites at Dobrá Voda, western Moravia, Czech Republic, and the White Queen mine, Pala, San Diego County, California. Zoned crystals consist of pale pink, colorless and greenish Fe-poor elbaite, blue, violet or green Fe-rich elbaite, and dark violet to black foitite. Elbaite– foitite is associated with quartz, cookeite, albite and apatite at Dobrá Voda, and with albite, quartz, K-feldspar, beryl, and musco- vite at the White Queen mine. Chemical compositions of foitite and associated Fe-poor to Fe-rich elbaite are similar at both localities, and exhibit an X-site vacancy (≤0.78 apfu, in foitite), and variable amounts of Ca (≤0.05 apfu), Mn (≤0.47 apfu) and F (≤0.75 apfu, in elbaite), in contrast to foitite that in many cases is F-free. Two distinct stages of late Fe-enrichment in tourmaline were recognized, in contrast to Fe-depletion, noted in many granitic pegmatites. The first stage is generally characterized by increasing Fe and Na, and decreasing Al and Li contents; three substages show the following substitutions: (i) R2 (LiAl)–1, NaR2(OH) X ( ⅪAl2O)–1 and (OH) F–1 for elbaite containing <0.3 Fe apfu at Dobrá Voda (R = Fetot + Mn + Mg + Zn); (ii) Na R2(OH) X X ( ⅪAl2O)–1 or NaR ( ⅪAl)–1 and F (OH)–1 for Fe-rich elbaite with 0.5–1.0 Fe apfu; (iii) AlO2 [Li(OH)2]–1 and (OH) F–1, perhaps combined with R2 (LiAl)–1 for Fe-rich elbaite with 1.0–1.3 Fe apfu at the White Queen mine. -
Lithium in Sekaninaite from the Type Localitv, Dolni Bory. Czech Republic
167 Thz Canadian M incralo gist Vol. 35, pp.1,67-173(1997) LITHIUMIN SEKANINAITEFROM THE TYPE LOCALITV, DOLNIBORY. CZECH REPUBLIC PETR dERNfI anp RON CHAPMAN Departrnentof GeolagicalSciences, University of Manitoba, Winnipeg,Manitoba R3T2N2 WERNERSCHREYER Irutitut fir Mincralogie, Ruh.r-Uni'ttersitiltBoclun D44801 Bochwa Germary LIIISA OTTOLINI AND PIERO BOTTAZZI CNRCentro d.i Studio per la Cristallochimicae la Cristall.ografia I-27100 Pnia ltaly CATIIERINEA. MoCAMMON BayerischzsGeoinstitw, UniversbAtBayreutfu D-95440 Bayreuth. Germany ABSTRACI The (Si,Al)-orderedFe end-memberof the cordieritegroup, sekaninaite, from its type locality at Dohl Bory, CzechRepublic, was analyze4 and found to contain0.04 - 0.2ALi ard0,1.l -0,2-6Na apfu; (Fe + Mn)/(Mg + Fe + 1!tn) (at.) rangesfrom 0.74 to 0.97.Lithium is incorporatedby the substitutionchNavlli0\4gFe)-r . This sekaninaiteis the first memberof the cordieritegroup reportedto have substantialLi but negligible Be. All samplesof Na,Be-, NaJ-i'Be- and Nati-bearing cordierite-sekadnaite examinedto date show a minor deficit in the tetrahedralsite (0,237 in the literature, 0.036 in our data) and a slight excessof channelcations (NaKCa) over the proportion of (BeIi) (at.). The Li-bearing sekaninaitecomes from ralher simple granitic pegmatites,in which the only Li-bearing minerals are rare tiphylite and cookeite.Thus cordierite-groupminerals are crystal- 'Ihis chemicalsinks for U. ffnding stressesthe needto analyzefor tracelight elements,even in mineralsfrom poorly fractionated andrare-element-depleted environnents, provided the crystal chemistryis favorable. Keyvvords:sekaninaite, cordierite group, lithium, beryllium, CzechRepublic. SoMraans Nous avonsanalysd la sekaninalte,p61e ferrifbre ordonn6en Al,Si du groupede la cordi6rite,provenaat de sa localit6 type, i Dolnl Bory, en R6publiqueTch{ue. -
Bicchulite Ca2al2sio6(OH)2 C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Cubic
Bicchulite Ca2Al2SiO6(OH)2 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Cubic. Point Group: 43m: As an extremely ¯ne powder. Physical Properties: Hardness = n.d. D(meas.) = n.d. D(calc.) = 2.813 (synthetic). Optical Properties: Semitransparent. Color: White or gray; colorless in thin section. Luster: Powdery, earthy. Optical Class: Isotropic. n = 1.625 Cell Data: Space Group: I43m: a = 8.82{8.83 Z = 4 X-ray Powder Pattern: Fuka, Japan. 2.786 (100), 2.753 (95), 3.60 (90), 2.597 (50), 1.559 (50), 3.04 (40), 2.96 (40) Chemistry: (1) (2) (3) SiO2 28.51 23.77 20.56 TiO2 0.09 0.92 Al2O3 21.79 23.59 34.89 Fe2O3 2.66 6.72 FeO 0.25 0.20 MnO 0.03 0.02 MgO 2.72 2.00 CaO 35.26 36.89 38.38 Na2O 0.25 0.14 K2O 0.18 0.11 + H2O 8.03 4.79 6.17 H2O¡ 0.43 0.40 P2O5 0.02 0.02 Total 100.22 99.57 100.00 (1) Fuka, Japan; mixed with vesuvianite. (2) Do.; contaminated by small amounts of gehlenite, vesuvianite, and hydrogrossular. (3) Ca2Al2SiO6(OH)2: Polymorphism & Series: Dimorphous with kamaishilite. Occurrence: In skarns in limestones, formed through alteration of gehlenite subjected to later retrograde hydration reactions. Association: Vesuvianite, hydrogrossular, gehlenite, melilite, calcite. Distribution: From Fuka, near Bicchu, Okayama Prefecture, and in the Akagan¶e mine, Iwate Prefecture, Japan. At Carneal, Co. Antrim, Ireland. Name: For Bicchu, the town encompassing the Japanese type locality. Type Material: Department of Earth Sciences, Okayama University, Okayama, Japan, ONM-01; Institute of Geological Sciences, London, England. -
Boromullite, Al9bsi2o19, a New Mineral from Granulite-Facies Metapelites, Mount Stafford, Central Australia: a Natural Analogue of a Synthetic “Boron-Mullite”
Eur. J. Mineral. Fast Track Article Fast Track DOI: 10.1127/0935-1221/2008/0020-1809 This paper is dedicated to the memory of Werner Schreyer Boromullite, Al9BSi2O19, a new mineral from granulite-facies metapelites, Mount Stafford, central Australia: a natural analogue of a synthetic “boron-mullite” Ian S. BUICK1,Edward S. GREW2,*, Thomas ARMBRUSTER3,Olaf MEDENBACH4,Martin G. YATES2, Gray E. BEBOUT5 and Geoffrey L. CLARKE6 1 Research School of Earth Sciences, The Australian National University, Canberra, ACT 0200, Australia 2 Department of Earth Sciences, University of Maine, 5790 Bryand Research Center, Orono, Maine 04469-5790, USA *Corresponding author, e-mail: [email protected] 3 Institut für Geologie, Gruppe Mineralogie-Kristallographie, Universität Bern, Freiestrasse 3, 3012 Bern, Switzerland 4 Institut für Geowissenschaften/Mineralogie, Ruhr-Universität Bochum, 44780 Bochum, Germany 5 Department of Earth & Environmental Sciences, Lehigh University, 31 Williams Drive, Bethelem, PA 18015, USA 6 School of Geosciences, University of Sydney, NSW 2006, Australia Abstract: Boromullite is a new mineral corresponding to a 1:1 polysome composed of Al5BO9 and Al2SiO5 modu- les. Electron-microprobe analysis of the holotype prism is SiO2 19.01(1.12), TiO2 0.01(0.02), B2O3 6.52(0.75), Al2O3 74.10(0.95), MgO 0.07(0.03), CaO 0.00(0.02), MnO 0.01(0.04), FeO 0.40(0.08), Sum 100.12 wt.%, which gives Mg0.01Fe0.03Al8.88Si1.93B1.14O18.94 (normalised to 12 cations), ideally Al9BSi2O19. Overall, in the type specimen, it ranges in composition from Mg0.01Fe0.03Al8.72Si2.44B0.80O19.20 to Mg0.01Fe0.03Al9.22Si1.38B1.35O18.67.