Tobermorites: Their Real Structure and Order-Disorder (OD) Character
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Tobermorite Supergroup: a New Nomenclature
Mineralogical Magazine, April 2015, Vol. 79(2), pp. 485–495 The tobermorite supergroup: a new nomenclature CRISTIAN BIAGIONI*, STEFANO MERLINO AND ELENA BONACCORSI Dipartimento di Scienze della Terra, Universita` di Pisa, Via Santa Maria 53, 56126 Pisa, Italy [Received 10 July 2014; Accepted 30 September 2014; Associate Editor: S. J. Mills] ABSTRACT The name ‘tobermorites’ includes a number of calcium silicate hydrate (C-S-H) phases differing in their hydration state and sub-cell symmetry. Based on their basal spacing, closely related to the degree of hydration, 14, 11 and 9 A˚ compounds have been described. In this paper a new nomenclature scheme for these mineral species is reported. The tobermorite supergroup is defined. It is formed by the tobermorite group and the unclassified minerals plombie`rite, clinotobermorite and riversideite. Plombie`rite (‘14 A˚ tobermorite’) is redefined as a crystalline mineral having chemical composition Ca5Si6O16(OH)2·7H2O. Its type locality is Crestmore, Riverside County, California, USA. The tobermorite group consists of species having a basal spacing of ~11 A˚ and an orthorhombic sub-cell symmetry. Its general formula is Ca4+x(AlySi6Ày)O15+2xÀy·5H2O. Its endmember compositions correspond to tobermorite Ca5Si6O17·5H2O(x =1andy = 0) and the new species kenotobermorite, Ca4Si6O15(OH)2·5H2O(x =0andy = 0). The type locality of kenotobermorite is the N’Chwaning II mine, Kalahari Manganese Field, South Africa. Within the tobermorite group, tobermorite and kenotobermorite form a complete solid solution. Al-rich samples do not warrant a new name, because Al can only achieve a maximum content of 1/6 of the tetrahedral sites (y = 1). -
The Hydrated Calcium, Silicates Riversideite, Tobermorite, and Plombierite
293 The hydrated calcium, silicates riversideite, tobermorite, and plombierite. By J. D. C. McCoNNELL,M.Sc. 1)epartment of Mineralogy and Petrology, University of Cambridge. [Conmmnicated by Prof. C. E. Tilley, F.R.S., read March 26, 1953] ] NTRODUCTION. N a recent paper Taylor has shown that three distinct hydration I levels exist within the" calcium silicate hydrate (l)' group of artificial preparations (Taylor, 1953a, p. 168). The individual hydrates may be distinguished from the position of the 002 reflection in X-ray powder photographs. The d spacings corresponding to the three hydrates of this group examined during the present investigation are 1~'6, 11"3, and 9"6 ,A.. These hydrates have 1-[20 : SiO 2 molar ratios of approximately 2-0, 1.0, and 0"5 respectively. A recent examination of the minerals crestmoreite and riversideite (Taylor, 1953b) has shown that both these nfinerals are intimate inter- :growths of members of the above hydrate series with the mineral wilkeite. Both the artificial preparations and the crestmoreite-riversideite inter- growths have failed to provide material suitable for detailed optical study. During a mineralogical investigation of rocks from a dolerite-chalk contact at Ballycraigy, Larne, County Antrim, a mineral was examined and subsequently identified, from X-ray powder photographs, with the 11"3 .~. hydrate referred to above. Optical and X-ray studies on single crystals of this mineral were made and subsequently both the 14.6 and 9-6 A. hydrates were prepared from this material experimentally. X-ray powder photographs of a gelatinous material collected at Ballycraigy showed that this m~tteria] could also be identified with the 'calcium silicate hydrate (f)' group. -
Phillipsite and Al-Tobermorite Mineral Cements Produced Through Low-Temperature Water-Rock Reactions in Roman Marine Concrete Sean R
Western Washington University Western CEDAR Geology Faculty Publications Geology 2017 Phillipsite and Al-tobermorite Mineral Cements Produced through Low-Temperature Water-Rock Reactions in Roman Marine Concrete Sean R. Mulcahy Western Washington University, [email protected] Marie D. Jackson University of Utah, Salt Lake City Heng Chen Southeast University, Nanjing Yao Li Xi'an Jiaotong University, Xi'an Piergiulio Cappelletti Università degli Studi di Napoli Federico II, Naples See next page for additional authors Follow this and additional works at: https://cedar.wwu.edu/geology_facpubs Part of the Geology Commons Recommended Citation Mulcahy, Sean R.; Jackson, Marie D.; Chen, Heng; Li, Yao; Cappelletti, Piergiulio; and Wenk, Hans-Rudolf, "Phillipsite and Al- tobermorite Mineral Cements Produced through Low-Temperature Water-Rock Reactions in Roman Marine Concrete" (2017). Geology Faculty Publications. 67. https://cedar.wwu.edu/geology_facpubs/67 This Article is brought to you for free and open access by the Geology at Western CEDAR. It has been accepted for inclusion in Geology Faculty Publications by an authorized administrator of Western CEDAR. For more information, please contact [email protected]. Authors Sean R. Mulcahy, Marie D. Jackson, Heng Chen, Yao Li, Piergiulio Cappelletti, and Hans-Rudolf Wenk This article is available at Western CEDAR: https://cedar.wwu.edu/geology_facpubs/67 American Mineralogist, Volume 102, pages 1435–1450, 2017 Phillipsite and Al-tobermorite mineral cements produced through low-temperature k water-rock reactions in Roman marine concrete MARIE D. JACKSON1,*, SEAN R. MULCAHY2, HENG CHEN3, YAO LI4, QINFEI LI5, PIERGIULIO CAppELLETTI6, 7 AND HANS-RUDOLF WENK 1Department of Geology and Geophysics, University of Utah, Salt Lake City, Utah 84112, U.S.A. -
Atomistic Modeling of Crystal Structure of Ca1.67Sihx
Cement and Concrete Research 67 (2015) 197–203 Contents lists available at ScienceDirect Cement and Concrete Research journal homepage: http://ees.elsevier.com/CEMCON/default.asp Atomistic modeling of crystal structure of Ca1.67SiHx Goran Kovačević a, Björn Persson a, Luc Nicoleau b, André Nonat c, Valera Veryazov a,⁎ a Theoretical Chemistry, P.O.B. 124, Lund University, Lund 22100, Sweden b BASF Construction Solutions GmbH, Advanced Materials & Systems Research, Albert Frank Straße 32, 83304 Trostberg, Germany c Laboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS-Université de Bourgogne, BP 47870, F-21078 Dijon Cedex, France article info abstract Article history: The atomic structure of calcium-silicate-hydrate (C1.67-S-Hx) has been investigated by theoretical methods in Received 13 February 2014 order to establish a better insight into its structure. Three models for C-S-H all derived from tobermorite are pro- Accepted 12 September 2014 posed and a large number of structures were created within each model by making a random distribution of silica Available online xxxx oligomers of different size within each structure. These structures were subjected to structural relaxation by ge- ometry optimization and molecular dynamics steps. That resulted in a set of energies within each model. Despite Keywords: an energy distribution between individual structures within each model, significant energy differences are Calcium-Silicate-Hydrate (C-S-H) (B) Crystal Structure (B) observed between the three models. The C-S-H model related to the lowest energy is considered as the most Atomistic simulation probable. It turns out to be characterized by the distribution of dimeric and pentameric silicates and the absence of monomers. -
Brownmillerite Ca2(Al, Fe )2O5 C 2001-2005 Mineral Data Publishing, Version 1
3+ Brownmillerite Ca2(Al, Fe )2O5 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Orthorhombic. Point Group: mm2. As square platelets, to about 60 µm; massive. Physical Properties: Hardness = n.d. D(meas.) = 3.76 D(calc.) = 3.68–3.73 Optical Properties: Semitransparent. Color: Reddish brown. Optical Class: Biaxial (–). Pleochroism: Distinct; X = Y = yellow-brown; Z = dark brown. Orientation: Y and Z lie in the plane of the platelets; extinction in that plane is diagonal. α = < 2.02 β = > 2.02 γ = > 2.02 2V(meas.) = n.d. Cell Data: Space Group: Ibm2. a = 5.584(5) b = 14.60(1) c = 5.374(5) Z = 2 X-ray Powder Pattern: Near Mayen, Germany. 2.65 (vs), 7.19 (s), 2.78 (s), 1.93 (s), 2.05 (ms), 3.65 (m), 1.82 (m) Chemistry: (1) (2) (3) TiO2 1.5 1.9 Al2O3 17.2 22.3 13.1 Fe2O3 30.5 27.6 41.9 Cr2O3 0.1 n.d. MgO n.d. n.d. CaO 46.2 44.8 43.7 insol. 4.0 LOI 0.5 Total 94.4 100.3 100.6 (1) Near Mayen, Germany; by semiquantitative spectroscopy. (2) Hatrurim Formation, Israel; corresponds to Ca1.99(Al1.09Fe0.86Ti0.05)Σ=2.00O5. (3) Do.; corresponds to Ca1.95(Fe1.31Al0.64 Ti0.06)Σ=2.01O5. Occurrence: In thermally metamorphosed limestone blocks included in volcanic rocks (near Mayen, Germany); in high-temperature, thermally metamorphosed, impure limestones (Hatrurim Formation, Israel). Association: Calcite, ettringite, wollastonite, larnite, mayenite, gehlenite, diopside, pyrrhotite, grossular, spinel, afwillite, jennite, portlandite, jasmundite (near Mayen, Germany); melilite, mayenite, wollastonite, kalsilite, corundum (Kl¨och, Austria); spurrite, larnite, mayenite (Hatrurim Formation, Israel). -
Effect of Mineralogical Changes on Mechanical Properties of Well Cement
ARMA 19–1981 Well integrity of high temperature wells: Effect of mineralogical changes on mechanical properties of well cement TerHeege, J.H. and Wollenweber, J. TNO Applied Geosciences, Utrecht, the Netherlands Marcel Naumann Downloaded from http://onepetro.org/ARMAUSRMS/proceedings-pdf/ARMA19/All-ARMA19/ARMA-2019-1981/1133466/arma-2019-1981.pdf/1 by guest on 02 October 2021 Equinor ASA, Sandsli, Norway Pipilikaki, P. TNO Structural Reliability, Delft, the Netherlands Vercauteren, F. TNO Material Solutions, Eindhoven, the Netherlands This paper w as prepared for presentation at the 53rd US Rock Mechanics/Geomechanics Symposium held in New Y ork, NY , USA , 23–26 June 2019. This paper w as selected for presentation at the symposium by an ARMA Technical Program Committee based on a technical and critical review of the paper by a minimum of tw o technical reviewers. The material, as presented, does not necessarily reflect any position of ARMA, its of ficers, or members. ABSTRACT: Wells used for steam-assisted gravity drainage (SAGD), for cyclic steam stimulation (CSS), for hydrocarbon production in areas with anomalous high geothermal gradient, or for geothermal energy extraction all are operated in high temperature environments where maintaining long term wellbore integrity is one of the key challenges. Changes in cement mineralogy and associated mechanical properties may critically affect the integrity of high temperature wells. In this study, the relation between changes in mineralogy and mechanical properties of API class G cement with 40% silica flour was investigated by exposing samples for 1-4 weeks to temperatures of 60-420°C. The effect of mineralogical changes on mechanical properties was investigated using a combination of chemical and microstructural analysis and triaxial strength tests at confining pressures of 2-15 MPa. -
Bentorite Ca6(Cr, Al)2(SO4)3(OH)12 • 26H2O C 2001-2005 Mineral Data Publishing, Version 1
Bentorite Ca6(Cr, Al)2(SO4)3(OH)12 • 26H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6/m 2/m 2/m. As stout hexagonal prisms, {1010}, {1011}, {0001}, to 0.25 mm; commonly in fibrous masses, granular aggregates, and thin films. Twinning: On {1010} as composition plane. Physical Properties: Cleavage: {1010}, perfect; {0001}, distinct. Hardness = 2 D(meas.) = 2.025 D(calc.) = 2.021 Optical Properties: Transparent. Color: Bright violet. Streak: Very pale violet. Luster: Vitreous. Optical Class: Uniaxial (+). Pleochroism: O = nearly colorless; E = pale violet. Absorption: O < E. ω = 1.478(2) = 1.484(2) Cell Data: Space Group: P 63/mmc. a = 22.35 c = 21.41 Z = 8 X-ray Powder Pattern: Hatrurim Formation, Israel. 9.656 (100), 5.592 (40), 1.942 (20), 3.60 (10), 3.23 (10), 2.772 (10), 3.89 (8) Chemistry: (1) SO3 14.99 CO2 6.70 SiO2 2.50 Al2O3 1.01 Fe2O3 0.10 Cr2O3 7.48 MgO 0.00 CaO 29.90 H2O 37.70 Total 100.38 (1) Hatrurim Formation, Israel; by AA, SO3 by gravimetric analysis, CO2 and H2O by TGA; after deduction of CaO and CO2 as calcite and CaO, SiO2, H2O as truscottite, the remainder 3+ • (about 80%) corresponds to Ca5.88(Cr1.61Al0.32Fe0.02)Σ=1.95(S1.02O4)3.00(OH)11.97 28.06H2O. Mineral Group: Ettringite group. Occurrence: In low-temperature hydrothermal veins in black calcite–spurrite marble. Association: Calcite, thaumasite, truscottite, vaterite, jennite, tobermorite, brownmillerite, mayenite, melnikovite, “chlorite”. Distribution: In a marble quarry in the Hatrurim Formation, near the Arad-Sodom road, Negev Desert, Israel. -
Mayenite Ca12al14o33 C 2001-2005 Mineral Data Publishing, Version 1
Mayenite Ca12Al14O33 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Cubic. Point Group: 43m (synthetic). In rounded anhedral grains, to 60 µm. Physical Properties: Hardness = n.d. D(meas.) = 2.85 D(calc.) = [2.67] Alters immediately to hydrated calcium aluminates on exposure to H2O. Optical Properties: Transparent. Color: Colorless. Optical Class: Isotropic. n = 1.614–1.643 Cell Data: Space Group: I43d (synthetic). a = 11.97–12.02 Z = 2 X-ray Powder Pattern: Near Mayen, Germany. 2.69 (vs), 4.91 (s), 2.45 (ms), 3.00 (m), 2.19 (m), 1.95 (m), 1.66 (m) Chemistry: (1) (2) (3) SiO2 0.4 Al2O3 45.2 49.5 51.47 Fe2O3 2.0 1.5 MnO 1.4 CaO 45.7 47.0 48.53 LOI 2.2 Total 95.1 99.8 100.00 (1) Near Mayen, Germany; by semiquantitative spectroscopy. (2) Hatrurim Formation, Israel; by electron microprobe, corresponding to (Ca11.7Mg0.5)Σ=12.2(Al13.5Fe0.25Si0.10)Σ=13.85O33. (3) Ca12Al14O33. Occurrence: In thermally metamorphosed limestone blocks included in volcanic rocks (near Mayen, Germany); common in high-temperature, thermally metamorphosed, impure limestones (Hatrurim Formation, Israel). Association: Calcite, ettringite, wollastonite, larnite, brownmillerite, gehlenite, diopside, pyrrhotite, grossular, spinel, afwillite, jennite, portlandite, jasmundite (near Mayen, Germany); melilite, wollastonite, kalsilite, brownmillerite, corundum (Kl¨och, Austria); spurrite, larnite, grossite, brownmillerite (Hatrurim Formation, Israel). Distribution: From the Ettringer-Bellerberg volcano, near Mayen, Eifel district, Germany. Found at Kl¨och, Styria, Austria. In the Hatrurim Formation, Israel. From Kopeysk, Chelyabinsk coal basin, Southern Ural Mountains, Russia. Name: For Mayen, Germany, near where the mineral was first described. -
Wollastonite Paper Revised -Symplectic.Pdf
This is a repository copy of Thermal stability of C-S-H phases and applicability of Richardson and Groves’ and Richardson C-(A)-S-H(I) models to synthetic C-S-H. White Rose Research Online URL for this paper: http://eprints.whiterose.ac.uk/109873/ Version: Accepted Version Article: Rodriguez, ET, Garbev, K, Merz, D et al. (2 more authors) (2017) Thermal stability of C-S-H phases and applicability of Richardson and Groves’ and Richardson C-(A)-S-H(I) models to synthetic C-S-H. Cement and Concrete Research, 93. pp. 45-56. ISSN 0008-8846 https://doi.org/10.1016/j.cemconres.2016.12.005 © 2016 Published by Elsevier Ltd. Licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ Reuse Unless indicated otherwise, fulltext items are protected by copyright with all rights reserved. The copyright exception in section 29 of the Copyright, Designs and Patents Act 1988 allows the making of a single copy solely for the purpose of non-commercial research or private study within the limits of fair dealing. The publisher or other rights-holder may allow further reproduction and re-use of this version - refer to the White Rose Research Online record for this item. Where records identify the publisher as the copyright holder, users can verify any specific terms of use on the publisher’s website. Takedown If you consider content in White Rose Research Online to be in breach of UK law, please notify us by emailing [email protected] including the URL of the record and the reason for the withdrawal request. -
Calcium-Aluminum-Silicate-Hydrate “
Cent. Eur. J. Geosci. • 2(2) • 2010 • 175-187 DOI: 10.2478/v10085-010-0007-6 Central European Journal of Geosciences Calcium-aluminum-silicate-hydrate “cement” phases and rare Ca-zeolite association at Colle Fabbri, Central Italy Research Article F. Stoppa1∗, F. Scordari2,E.Mesto2, V.V. Sharygin3, G. Bortolozzi4 1 Dipartimento di Scienze della Terra, Università G. d’Annunzio, Chieti, Italy 2 Dipartimento Geomineralogico, Università di Bari, Bari, Italy 3 Sobolev V.S. Institute of Geology and Mineralogy, Siberian Branch of the Russian Academy of Sciences, Novosibirsk 630090, Russia 4 Via Dogali, 20, 31100-Treviso Received 26 January 2010; accepted 8 April 2010 Abstract: Very high temperature, Ca-rich alkaline magma intruded an argillite formation at Colle Fabbri, Central Italy, producing cordierite-tridymite metamorphism in the country rocks. An intense Ba-rich sulphate-carbonate- alkaline hydrothermal plume produced a zone of mineralization several meters thick around the igneous body. Reaction of hydrothermal fluids with country rocks formed calcium-silicate-hydrate (CSH), i.e., tobermorite- afwillite-jennite; calcium-aluminum-silicate-hydrate (CASH) – “cement” phases – i.e., thaumasite, strätlingite and an ettringite-like phase and several different species of zeolites: chabazite-Ca, willhendersonite, gismon- dine, three phases bearing Ca with the same or perhaps lower symmetry of phillipsite-Ca, levyne-Ca and the Ca-rich analogue of merlinoite. In addition, apophyllite-(KF) and/or apophyllite-(KOH), Ca-Ba-carbonates, portlandite and sulphates were present. A new polymorph from the pyrrhotite group, containing three layers of sphalerite-type structure in the unit cell, is reported for the first time. Such a complex association is unique. -
Tobermorite and Tobermorite-Like Calcium Silicate Hydrates: Their
TOBERMORITE AND TOBERMORITE-L/KE CALCIUM SILICATE HYDRATES: \ THEIR PROPERTIES AND RELATIONSHIPS TO CLAY MINERALS AUG. 1963 NO. 24 DIAMOND PURDUE UNIVERSITY LAFAYETTE INDIANA Final Report TOBERMDRITE AND TOBERMORITE-LIKE CALCIUM SILICATE HYDRATES: THEIR PROPERTIES AND RELATIONSHIPS TO CIAY MINERALS TO: K. B. Woods, Director Joint Highway Research Project August 2, 1963 PROM: H. L. Michael, Associate Director File: 4-6-9 Joint High-way Research Project Project: C=36-^7I Attached is a Final Report "by Mr. Sidney Diamond, Graduate Assistant on our staff, entitled "Tobermorite and Tobermorite-Like Calcium Silicate Hydrates: Their Properties and Relationships to Clay Minerals"., This research has been performed under the direction of Professors J. L. White of the Purdue University Agronomy Department and Professor W. L. Dolch of our staff. Mr. Diamond also used the report as his disertation for the Ph.D. Degree. The Plan of Study for this research was approved by the Board on May 22, 1962, and it subsequently was approved by the Indiana State Highway Commission and the Bureau of Public Roads as an HPS research project. This is the final report on this project and it will be submitted to the sponsoring organization for review. Several papers from the research are anticipated and each will be submitted to the Board and the sponsors for review and approval prior to publication. The report is submitted to the Board for information and for the record. Respectfully submitted, Harold L. Michael, Secretary HLM:bc Attachment Copies: F. L. Ashbaucher J. F. McLaughlin J. R. Cooper R. D. Miles W. L. -
Thermal Decomposition of 14 a Tobermorite from Crestmore V
Thermal Decomposition of 14 A Tobermorite From Crestmore V. C. FARMER, Macaulay Institute for Soil Research, Aberdeen, Scotland; and J. JEEVARATNAM, K. SPEAKMAN, and H. F. W. TAYLOR, Department of Chemistry, University of Aberdeen, Scotland The thermal decomposition of 14 A tobermorite from Crest- more has been studied using weight and CO2 loss curves, X- ray fiber rotation photographs, and infrared absorption spec- tra. The initial mineral has the approximate composition 5 CaO 6 SiO2 9 H20 with small amounts of CO2 and B203. Part of the water is present in molecular form, and SiOH groups may also be present; this is compatible with the idealized con- stitutional formula Ca5Si6018H2 8 H20. At 55 C, there is a sharp change to 11.3 A tobermorite, Ca5Si6O18H2 4H20. The 11 .3 A tobermorite loses most of its water gradually, at 55 to 200 C, apparently without undergoing fundamental change in structure. At 200 to 450 C, a 9.35 A tobermorite is formed; this has the approximate composition CaESi60I8H2. At 450 to 650 C, most of the remaining water is lost, as well as the CO2. This process appears to be a gradual one, in which some essential features of the structure are retained; the layer thick- ness increases to 9.7 A. The process may occur through con- densation between adjacent SiOH groups, as suggested pre- viously (). At 730 to 775 C a wollastonite-like intermediate phase is formed, which at 850 to 900 C gives place to wollas- tonite itself. Infrared absorption spectra are given for each of the main stages.