The Classification and Nomenclature of Clay Minerals

Total Page:16

File Type:pdf, Size:1020Kb

The Classification and Nomenclature of Clay Minerals THE CLASSIFICATION AND NOMENCLATURE OF CLAY MINERALS By R. C. MACKENZIE The Macaulay Institute for Soil Research, Craigiebuckler, Aberdeen [Received 21st April, 1959] ABSTRACT A report is given of the decisions reached at a meeting on the classifica- tion and nomenclature of clay minerals held under the auspices of Comit~ International pour l'Etude des Argiles at Brussels in July 1958. Tables of recently-proposed classification systems are included and some com- ments made on problems requiring agreement. The increasing interest in the classification and nomenclature of clay minerals over the last decade or so may be attributed largely to the development of investigational methods which enable a much more precise characterization of fine-grained minerals than was previously possible. In addition, however, the absence of any hard-and-fast rules as to new mineral nomenclature has led to a multiplicity of names through "new" minerals being described on the flimsiest of evidence, without regard as to whether they might be considered varieties of an already-established entity or indeed with- out, in many instances, adequate evidence of homogeneity. The resulting confusion is considerable, and the stage has now been reached when international agreement upon the main features of classification and nomenclature ought to be obtained. In an attempt to clarify the position representatives often countries met, under the" auspices of C.I.P.E.A., during the Journ6es Inter- nationales d'Etude des Argiles in Brussels in July, 1958.* Several decisions of interest were made at this meeting. (a) The following definition was adopted, subject to confirmation at the next meeting: Crystalline day minerals are hydrated silicates with layer or chain lattices consisting of sheets of silica tetrahedra arranged in hexagonal form condensed with octahedral layers; they are usually of small particle size. (b) A sound nomenclature is necessarily based on a satisfactory classification scheme. Accepting the above definition, and limiting attention to crystalline silicates a suitable initial division would appear to be (the names in brackets being alternatives): *A list of those attending is given in the Appendix. 52 CLAY MINERAL CLASSIFICATION 53. Crystalline silicates I Chain lattices Layer lattices I I L I 1 ~ I Palygorskite Sepiolite 1 : 1 2 : 1 2 : 2 (Diphormic) (Triphormic) (Tetraphormic). (c) It was agreed that recent classification systems be drawn up in tabular form and that these receive wide publicity so that individual clay mineralogists could compare the systems and express their preference, or suggest an alternative. A meeting of national repre- sentatives who would be aufait with opinion in their own countries would then be held in Copenhagen during the International Geolo- gical Congress in August 1960, when an attempt would be made to reach some agreement. Tables of the various classification schemes have now been drawn up (Tables 1-7) and are reproduced here in order to bring them to the attention of members of the Clay Minerals Group, who are invited to send comments to the author. A classification not tabulated is that of Konta (private com- munication) who has suggested that clay minerals be divided up on the basis of their crystal structure into 7 groups, each group to be named after the most abundant mineral of the group. This gives: 1. Allopane group (including hisingerite), 2. Kaolinite group, 3. Montmorillonite group, 4. Illite group, 5. Vermiculite group, 6. Chlorite group (including septechlorites), 7. Sepiolite and paly- gorskite group. This suffers from the disadvantage noted in (g) below--and, in addition, involves a decision upon the most abundant mineral in each group. In general, all Tables commence in the way recommended in paragraph (c) above, but after this there is considerable diversity. Nevertheless, the differences are sufficiently small to give rise to hope that agreement may soon be reached. The following notes upon features of the Tables may be of interest (they are lettered consecutively after the above paragraphs for ease of reference): (d) It is interesting to note that while shape factors are only considered in one classification (Table 1), swelling propetties are considered in four (Tables 1, 4, 5 and 6). (e) The most logical classification is undoubtedly that in Table 4, but difficulties arise in translation, and it is preferable that mineral names be international. For example, use of ferrtferous beidellite (beidellite ferrifOre) for nontronite is clumsy, 54 R. C. MACKENZIE G r~ I I O o O Q O t~ I I r.~ ;:::1 t7~ m., 6 t~ r..) = O r3 CLAY MINERAL CLASSIFICATION 55 TABLE 2--Tabulation of the classification proposal of Brindley (1955a). Chemical Structural Chemical Structural Category Groups Sub-Groups Species Varieties Halloysite Kaolin Minerals Kaolinite Dickite Nacrite Kaolin type Serpentine Chrysotile(s) Minerals Antigorite Chamosite Amesite Greenalite Cronstedtite, etc. Talc Pyrophyllite Muscovite Layer Sili- Phologopite Silicates cates Mica type Biotite Polymorphic Glauconite varieties ]llite(s) Montmorillonoids Vermiculite, etc, Penninite Clinochlore Chlorite Prochlorite Polymorphic type Daphnite, etc. varieties Mixed-layer Anauxite type Bravaisite, etc. Ch/oritoid Chain Palygorskite Silicates (attapulgite) Sepiolite TABLE 3--Tabulation of the classification proposals of Brown (1955) In view of the difference in emphasis of certain characteristics (e.g., the group name is subsidiary in the 1:1 Family and principal in 2:1 Family) it has been necessary to divide up the scheme into several discrete tables. A. DIPHORMIC FAMILY Population of General Class IF ly octahedral sheet Group Name Minerals L Nacrite Dioctahedral Kandites Dickite Kaolinite Halloysite J Layer Silicates 1:1 Serpentines Antigorite Chrysotile Trioctahedral Amesite Cronstedtite Berthierine B. TRIPHORMIC FAMILY Population of octahedral General Class Family Group Name sheet Minerals Beidellite* Dioctahedral Nontronite* Volkonskoite* Montmorillonite* Smectites Saporlite* Trioctahedral Sauconite* Hectorite Stevensite* Dioctahedral Dioct~hedral vermiculite Vermiculites Trioctahedral Jefferisite Ni-vermiculite Layer Silicates 2:1 Muscovite---~illite Dioctahedral Glauconite Paragonite Micas Phlogopite Trioctahcdral Biotite-. ledikite Lepidomelane Brittle Dioctahedral Margarite Micas Trioctahedral ? Talc Trioctahedral Talc Pyrophyllite Dioctahedral Pyrophyllite Interstratified Minerals *Chemical definitions as in Table 7. If stevensite is interstratified (Brindley, 1955b) it should be omitted--the same comments applies to Tables 4, 5 and 6--but see Faust, Hath- away and Millet (1959). CLAY MINERAL CLASSIFICATION 57 C. CHLORITE FAMILY General Population of octahedral Class Family Group Name sheets Minerals I ? Dioctahedral-Dioctahedral ? tI Leptochlorites Dioctahedral-Trioctahedral Cookeite, etc. Layer -- Silicates ? Unoxidized chlorites I Orthochlorites Trioctahedral-Trioctahedral Oxidized chlorites D. PALYGORSKITEAND SEPIOLITE F~ILY General Class Minerals Palygorskite Chain silicates Sepiolite E. AMORPHOUS* MINERALS Primary Distinction Group Mineral Chemical Formula t Opaline Silica SiO2.nH20 Oxides Limonite Fe2Oz.nH20 Kliachite AI~O3.nH~O Wad MnO2.nH20 Amorphous Silicates Allophane AI,,O3.2SiO2.nH20 Hisingerite Fe203.2SiO2.nH20 Phosphates Evansite A13PO4(OH)~.nH20 Azovskite Fe3PO4(OH) 6.nH~O *Amorphous is defined as "any material not shown by the method of investigation to be crystalline." 58 R. C, MACKENZIE TABLE 4---Tabulation of the classification Population of General. Octahedral Class Fami~ Sheet Replacements Expansion Mineral None Non-swelling Kaolimte I Dioctahedral Sv,elling Halloysite Tetrahedral Donbassite (7) 7A None Non-swelling Antigorite (1:1) Tt-ioctahedral Magnesian Tetrahedral Non-swelling berthierine None Non-swelling Pyrophyllite Layer Octahedral Swelhng Montmorillonite silicates Tetrahedral Swelling Beidellite Dto,:tal'~dtal Tetrahedral and Dioctahedral Octahedral Swelling vermiculite Tetrahedrat Non-swelling lllite toA 12:D None Non-swelling Talc Octahedral Swelling Stevensite Tno,,."t .d~:dxa| Tel rahedral Swelling Sapphire Tetrahedral and Swelling Vet miculite Oetahedral Tetrahedral Non-swelling Ledikite ~4A Tnoctahedral Non-sv,elling Leptochlorite 12:2) Swelling Pseudochlorite Scmk. layer (AlSt between Trioctahedral layersj Non-~welling Chloritoid structure i ~oA Trioctahedral Tetrahedral and Non-swelling Palygorsk ite Chain Octahedral structurcs 12 A Trtoctahcdral Tetrahedral and Non-swelling Sepiolite Oetahcdral CLAY MINERAL CLASSIFICATION 59 proposal of Caill6re and H6nin (1957). Crystallographic and Formula Chemical Varieties and Replaccmr Textural Varieties Triclinic kaolinite Nacrite=monoclinic k., #=90"~ ~ Ai2Si~Os OH i Dickke = monociinJc k., fl = 96"8* Fireclay = pseudomonoclinic k. Mctahalloysite = pseudOhexagonal ~. AI2SizOs(OH)a.H:O All+ '~(Si~Lt:- -xAIx )Os(OH Noumeile-nickelifcrous :t INi lot Mg) Shrvsotile (Fibrous type) Mgz~si.zO~(OH) i Greenalite~ ferrd~:rous a. (Fc for Mg) )rti:toanligorlte =orthohexagonM a. and numerous other types Ferri~2"rous b. IFe:~for AJ, Fc z~ for Mg/ Oxidized fcrriterous b (More Fc 3~, less H § (AI~Mg3-D ISir Zinciferou~ b IZn for Mg) Grovcsite mang,).nifcrous b IMn for Mg) Cro,m;tedhte -fcrrofcrriferous b IFc for Mg,AI) AIzSi,~Oi0(OH)a xM+.(AIz_xMgx)SiiOlo(OH) z Nickeliferous nl (NI t'or Mg) xM+.AIz(Sil.xAIxJOlo(OH) 2 Volkonskoite =chromiferous b tCr for All Nolatrontle = ferrtferous b. I Fr for AI) (x'3y)M +.Ale ~. vlSq-xAIx)Olo(OH) ~ Brammallite =sodium i. (N,t for K) KxAI2(Sit.xAIx)Ql0
Recommended publications
  • High Dose Dosimetry Using Antigorite-Teflon Composite
    2011 International Nuclear Atlantic Conference - INAC 2011 Belo Horizonte,MG, Brazil, October 24-28, 2011 ASSOCIAÇÃO BRASILEIRA DE ENERGIA NUCLEAR - ABEN ISBN: 978-85-99141-04-5 HIGH DOSE DOSIMETRY USING ANTIGORITE-TEFLON COMPOSITE René R. Rocca 1, Sonia H. Tatumi 2 and Shigueo Watanabe 1 1 Instituto de Física Universidade de São Paulo Rua do Matão 187 – Travessa R. 05508-090 Butantã, SP [email protected][email protected] 2 Faculdade de Tecnologia de São Paulo CEETESP Pça. Cel. Fernando Prestes - Bom retiro, 30 01124-060 São Paulo, SP [email protected] ABSTRACT Pellets of antigorite crystals (Mg 3-x [Si 2O5] (OH) 4-2x ) and teflon powder were obtained in order to investigate the thermoluminescence (TL) dosimetric characteristics. ICP analysis was performed showing the presence of 0.25 mol% of Fe 2O3, 0.07 mol% of Al 2O3 and 0.006 mol% of MnO impurities. These pellets show two prominent TL peaks at 150 oC and another broad one at 250 oC observed in samples previously irradiated with gamma-rays from 60 Co source. The 150 oC peak increased up to 2 kGy and after this dose the intensity reaches a maximum then decreases gradually. However the 250 oC peak increased up even with a dose of 172 kGy. A good reproducibility of TL results was obtained showing that these pellets can be used for high dose measurements. An excellent theoretical fit using second order kinects model [10] was obtained for all the peaks; however the theoretical deconvolution [4] showed the presence of two additional peaks at 206 and 316 oC.
    [Show full text]
  • Washington State Minerals Checklist
    Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite
    [Show full text]
  • Mineral Processing
    Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19
    [Show full text]
  • First-Principles Modeling of the Infrared Spectrum of Antigorite
    Eur. J. Mineral., 33, 389–400, 2021 https://doi.org/10.5194/ejm-33-389-2021 © Author(s) 2021. This work is distributed under the Creative Commons Attribution 4.0 License. First-principles modeling of the infrared spectrum of antigorite Etienne Balan1, Emmanuel Fritsch1,2, Guillaume Radtke1, Lorenzo Paulatto1, Farid Juillot1,2, and Sabine Petit3 1Sorbonne Université, CNRS, MNHN, Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie (IMPMC), 4 place Jussieu, 75252 Paris CEDEX 05, France 2Institut de Recherche pour le Développement (IRD), Centre de Nouméa, 101 Promenade Roger Laroque, Anse Vata, 98848 Nouméa, New Caledonia 3Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), CNRS UMR 7285, Université de Poitiers, 6 rue Michel Brunet, 86073, Poitiers CEDEX 9, France Correspondence: Etienne Balan ([email protected]) Received: 22 March 2021 – Revised: 14 June 2021 – Accepted: 22 June 2021 – Published: 19 July 2021 Abstract. The infrared absorption spectrum of a natural antigorite sample from New Caledonia is compared to its theoretical counterpart computed for the pristine antigorite m D 17 polysome within the density functional perturbation theory framework. The theoretical model reproduces most of the bands related to Si-O stretching −1 −1 in the 800–1300 cm range, OH libration, hindered OH translation and SiO4 bending in the 400–800 cm range, and OH stretching in the 3500–3700 cm−1 range. Most of the observed bands have a composite nature involving several vibrational modes contributing to their intensity, except the apical and one of the basal Si-O stretching bands whose intensity is carried by a single mode.
    [Show full text]
  • Mapping Phyllosilicates and Aqueous Alteration Products at Tyrrhena Terra, Mars
    52nd Lunar and Planetary Science Conference 2021 (LPI Contrib. No. 2548) 1323.pdf MAPPING PHYLLOSILICATES AND AQUEOUS ALTERATION PRODUCTS AT TYRRHENA TERRA, MARS. F. H. Grant1 and J. L. Bishop2, 1University of California, Los Angeles (Los Angeles, CA; [email protected]), 2SETI Institute (Mountain View, CA). Summary: Outcrops of phyllosilicates and small sites of less common aqueous alteration minerals were mapped at Tyrrhena Terra on Mars using CRISM pa- rameters, and CRISM spectral data were collected to more closely analyze the mineralogy in this region. Fe- and Mg-rich smectite and chlorite group phyllosilicates are both detected at Tyrrhena Terra, including sapo- nite, chamosite, and clinochlore. Zeolites and car- bonates are among the rarer alteration minerals also observed at Tyrrhena Terra that further constrain the alteration history in this region. More chlorite than smectite is observed, indicating higher temperature alteration processes occurred at Tyrrhena Terra. Introduction: Tyrrhena Terra is a region in the southern hemisphere of Mars, between the Isidis and Hellas impact basins and south of Libya Montes. The selected study site (Fig. 1) is of particular interest be- cause it has a large concentration of phyllosilicate minerals exposed on the surface, among small outcrops of rarer aqueous alteration minerals [1]. Phyllosilicates are a crucial mineral group to study when striving to understand the aqueous alteration history of a region. Less common aqueous alteration minerals, including zeolite, carbonate, and hydrated sulfates, are also im- portant to further constrain the alteration history of a region [2]. For this research project, we focused pri- marily on identifying the phyllosilicate minerals smec- tite and chlorite.
    [Show full text]
  • NMAM 9000: Asbestos, Chrysotile By
    ASBESTOS, CHRYSOTILE by XRD 9000 MW: ~283 CAS: 12001-29-5 RTECS: CI6478500 METHOD: 9000, Issue 3 EVALUATION: FULL Issue 1: 15 May 1989 Issue 3: 20 October 2015 EPA Standard (Bulk): 1% by weight PROPERTIES: Solid, fibrous mineral; conversion to forsterite at 580 °C; attacked by acids; loses water above 300 °C SYNONYMS: Chrysotile SAMPLING MEASUREMENT BULK TECHNIQUE: X-RAY POWDER DIFFRACTION SAMPLE: 1 g to 10 g ANALYTE: Chrysotile SHIPMENT: Seal securely to prevent escape of asbestos PREPARATION: Grind under liquid nitrogen; wet-sieve SAMPLE through 10 µm sieve STABILITY: Indefinitely DEPOSIT: 5 mg dust on 0.45 µm silver membrane BLANKS: None required filter ACCURACY XRD: Copper target X-ray tube; optimize for intensity; 1° slit; integrated intensity with RANGE STUDIED: 1% to 100% in talc [1] background subtraction BIAS: Negligible if standards and samples are CALIBRATION: Suspensions of asbestos in 2-propanol matched in particle size [1] RANGE: 1% to 100% asbestos OVERALL PRECISION ( ): Unknown; depends on matrix and ESTIMATED LOD: 0.2% asbestos in talc and calcite; 0.4% concentration asbestos in heavy X-ray absorbers such as ferric oxide ACCURACY: ±14% to ±25% PRECISION ( ): 0.07 (5% to 100% asbestos); 0.10 (@ 3% asbestos); 0.125 (@ 1% asbestos) APPLICABILITY: Analysis of percent chrysotile asbestos in bulk samples. INTERFERENCES: Antigorite (massive serpentine), chlorite, kaolinite, bementite, and brushite interfere. X-ray fluorescence and absorption is a problem with some elements; fluorescence can be circumvented with a diffracted beam monochromator, and absorption is corrected for in this method. OTHER METHODS: This is NIOSH method P&CAM 309 [2] applied to bulk samples only, since the sensitivity is not adequate for personal air samples.
    [Show full text]
  • State County Historic Site Name As Reported Development Latitude
    asbestos_sites.xls. Summary of information of reported natural occurrences of asbestos found in geologic references examined by the authors. Dataset is part of: Van Gosen, B.S., and Clinkenbeard, J.P., 2011, Reported historic asbestos mines, historic asbestos prospects, and other natural occurrences of asbestos in California: U.S. Geological Survey Open-File Report 2011-1188, available at http://pubs.usgs.gov/of/2011/1188/. Data fields: State, ―CA‖ indicates that the site occurs in California. County, Name of the county in which the site is located. Historic site name as reported, The name of the former asbestos mine, former asbestos prospect, or reported occurrence, matching the nomenclature used in the source literature. Development, This field indicates whether the asbestos site is a former asbestos mine, former prospect, or an occurrence. "Past producer" indicates that the deposit was mined and produced asbestos ore for commercial uses sometime in the past. "Past prospect" indicates that the asbestos deposit was once prospected (evaluated) for possible commercial use, typically by trenching and (or) drilling, but the deposit was not further developed. "Occurrence" indicates that asbestos was reported at this site. The occurrence category includes (1) sites where asbestos-bearing rock is described in a geologic map or report and (2) asbestos noted as an accessory mineral or vein deposit within another type of mineral deposit. Latitude, The latitude of the site's location in decimal degrees, measured using the North American Datum of
    [Show full text]
  • Iron.Rich Amesite from the Lake Asbestos Mine. Black
    Canodian Mineralogist Yol.22, pp. 43742 (1984) IRON.RICHAMESITE FROM THE LAKE ASBESTOS MINE. BLACKLAKE. OUEBEC MEHMET YEYZT TANER,* AND ROGER LAURENT DAporternentde Gdologie,Universitd Loval, Qudbec,Qudbec GIK 7P4 ABSTRACT o 90.02(1l)', P W.42(12)',1 89.96(8)'.A notreconnais- sance,c'est la premibrefois qu'on ddcritune am6site riche Iron-rich amesite is found in a metasomatically altered enfer. Elles'ct form€ependant l'altdration hydrothermale granite sheet20 to 40 cm thick emplacedin serpentinite of du granitedans la serpentinite,dans les m€mes conditions the Thetford Mi[es ophiolite complex at the Lake Asbestos debasses pression et temperaturequi ont prdsid6d la for- mine (z16o01'N,11"22' W) ntheQuebec Appalachians.The mation de la rodingite dansle granite et de I'amiante- amesiteis associatedsdth 4lodingife 6semblage(grossu- chrysotiledans la serpentinite. lar + calcite t diopside t clinozoisite) that has replaced the primary minerals of the granite. The Quebec amesite Mots-clds:am6site, rodingite, granite, complexeophio- occurs as subhedral grains 2@ to 6@ pm.in diameter that litique, Thetford Mines, Qu6bec. have a tabular habit. It is optically positive with a small 2V, a 1.612,1 1.630,(t -'o = 0.018).Its structuralfor- INTRoDUc"iloN mula, calculated from electron-microprobe data, is: (Mg1.1Fe6.eA1s.e)(Alo.esil.df Os(OH)r.2. X-ray powder- Amesite is a raxehydrated aluminosilicate of mag- diffraction yield data dvalues that are systematicallygreater nesium in which some ferrous iron usually is found than those of amesitefrom Chester, Massachusetts,prob- replacingmapesium. The extent of this replacement ably becauseof the partial replacement of Mg by Fe.
    [Show full text]
  • The Properties of Moulding Sand with Halloysite
    ARCHIVES of ISSN (2299-2944) FOUNDRY ENGINEERING Volume 12 Issue 2/2012 DOI: 10.2478/v10266-012-0062-5 Published quarterly as the organ of the Foundry Commission of the Polish Academy of Sciences 205 – 210 The Properties of Moulding Sand with Halloysite M. Cholewa, Ł. Kozakiewicz* Silesian University of Technology, Foundry Department, Towarowa 7, 44-100 Gliwice, PL *Corresponding author: E-mail address: [email protected] Received 25-05-2012; accepted in revised form 31-05-2012 Abstract Until now, the mould sand in general use in the foundry industry are based on bentonite, which resulted from the fact that a good recognition properties and phenomena associated with this material. Come to know and normalized content of montmorillonite and carbonates and their important role in the construction of bentonite, and mass properties of the participation of compressive strength or scatter. Halloysite is widely used in industry and beyond them. However, little is known about its use in the foundry in Poland and abroad. This article presents preliminary research conducted at the Foundry Department of Silesian University of Technology on this material. Will raise the question of the representation of this two materials, which contains information connected with history and formation of materials, their structure and chemical composition. In the research, the results of compressive strength tests in wet masses of quartz matrix, where as a binder is used halloysite and bentonite in different proportions. Keywords: Halloysite, Bentonite, Moulding Sand Automation in the previous period concerned the processes 1. Introduction related mainly to the implementation of form, hence the early arrangements are known as automatic molding lines (ALF).
    [Show full text]
  • Minerals-10-00395-V2.Pdf
    minerals Article Slatecalculation—A Practical Tool for Deriving Norm Minerals in the Lowest-Grade Metamorphic Pelites and Roof Slates Hans Wolfgang Wagner 1,* , Dieter Jung 2, Jean-Frank Wagner 3 and Matthias Patrick Wagner 4 1 Lehrstuhl für Geologie, Universität Trier, Im Nettetal 4, D 56727 Mayen, Germany 2 Mineralogisch-Petrographisches Institut Universität Hamburg, Grindelallee 48, D 20146 Hamburg, Germany; [email protected] 3 Lehrstuhl für Geologie, Universität Trier, Behringstrasse 21, D 54296 Trier, Germany; [email protected] 4 Institute of Geography, Kiel University, D 24118 Kiel, Germany; [email protected] * Correspondence: [email protected] Received: 3 March 2020; Accepted: 26 April 2020; Published: 29 April 2020 Abstract: Roof and wall slates are fine-grained rocks with slaty cleavage, and it is often difficult to determine their mineral composition. A new norm mineral calculation called slatecalculation allows the determination of a virtual mineral composition based on full chemical analysis, including the amounts of carbon dioxide (CO2), carbon (C), and sulfur (S). Derived norm minerals include feldspars, carbonates, micas, hydro-micas, chlorites, ore-minerals, and quartz. The mineral components of the slate are assessed with superior accuracy compared to the petrographic analysis based on the European Standard EN 12326. The inevitable methodical inaccuracies in the calculations are limited and transparent. In the present paper, slates, shales, and phyllites from worldwide occurrences were examined. This also gives an overview of the rocks used for discontinuous roofing and external cladding. Keywords: mineralogy; roof slates; shales; phyllites; norm mineral calculation; hydro-micas; illite 1. Introduction Under the term “roof and wall slates”, rocks that have good cleavage and high suitability for overlapping and discontinuous roofing as well as external cladding.
    [Show full text]
  • Nature of Interlayer Material in Silicate Clays of Selected Oregon Soils
    AN ABSTRACT OF THE THESIS OF PAUL C, SINGLETON for the Ph.D. in Soils (Name) (Degree) (Major) Date thesis is presented July 28, 1965 Title NATURE OF INTERLAYER MATERIAL IN SILICATE CLAYS OF SELECTED OREGON SOILS - Redacted for Privacy Abstract approved = ajor professor) Ç A study was conducted to investigate the nature of hydroxy interlayers in the chlorite -like intergrade clays of three Oregon soils with respect to kind, amount, stability, and conditions of formation. The clays of the Hembre, Wren, and Lookout soils, selected to represent weathering products originating from basaltic materials under humid, subhumid, and semi -arid climatic conditions respectively, were subjected to a series of progressive treatments designed to effect a differential dissolution of the materials intimately asso- ciated with them. The treatments, chosen to represent a range of increasing severity of dissolution, were (1) distilled water plus mechanical stirring, (2) boiling 2% sodium carbonate, (3) buffered sodium citrate -dithionite, (4) boiling sodium hydroxide, and (5) preheating to 400 °C for 4 hours plus boiling sodium hydroxide. Extracts from the various steps of the dissolution procedure were chemically analyzed in order to identify the materials removed from the clays. X -ray diffraction analysis and cation exchange capacity determinations were made on the clays after each step, and any differences noted in the measured values were attributed to the removal of hydroxy interlayers from the clays. Hydroxy interlayers were found to occur more in the Hembre and Wren soils than in the Lookout soil, with the most stable interlayers occurring in the Wren. Soil reaction was one of the major differences between these soils.
    [Show full text]
  • Clay Minerals Soils to Engineering Technology to Cat Litter
    Clay Minerals Soils to Engineering Technology to Cat Litter USC Mineralogy Geol 215a (Anderson) Clay Minerals Clay minerals likely are the most utilized minerals … not just as the soils that grow plants for foods and garment, but a great range of applications, including oil absorbants, iron casting, animal feeds, pottery, china, pharmaceuticals, drilling fluids, waste water treatment, food preparation, paint, and … yes, cat litter! Bentonite workings, WY Clay Minerals There are three main groups of clay minerals: Kaolinite - also includes dickite and nacrite; formed by the decomposition of orthoclase feldspar (e.g. in granite); kaolin is the principal constituent in china clay. Illite - also includes glauconite (a green clay sand) and are the commonest clay minerals; formed by the decomposition of some micas and feldspars; predominant in marine clays and shales. Smectites or montmorillonites - also includes bentonite and vermiculite; formed by the alteration of mafic igneous rocks rich in Ca and Mg; weak linkage by cations (e.g. Na+, Ca++) results in high swelling/shrinking potential Clay Minerals are Phyllosilicates All have layers of Si tetrahedra SEM view of clay and layers of Al, Fe, Mg octahedra, similar to gibbsite or brucite Clay Minerals The kaolinite clays are 1:1 phyllosilicates The montmorillonite and illite clays are 2:1 phyllosilicates 1:1 and 2:1 Clay Minerals Marine Clays Clays mostly form on land but are often transported to the oceans, covering vast regions. Kaolinite Al2Si2O5(OH)2 Kaolinite clays have long been used in the ceramic industry, especially in fine porcelains, because they can be easily molded, have a fine texture, and are white when fired.
    [Show full text]