The Mineral Fibers of Potential Concern in Talc
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Mineralogy and Geochemistry of Nephrite Jade from Yinggelike Deposit, Altyn Tagh (Xinjiang, NW China)
minerals Article Mineralogy and Geochemistry of Nephrite Jade from Yinggelike Deposit, Altyn Tagh (Xinjiang, NW China) Ying Jiang 1, Guanghai Shi 1,* , Liguo Xu 2 and Xinling Li 3 1 State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Beijing 100083, China; [email protected] 2 Geological Museum of China, Beijing 100034, China; [email protected] 3 Xinjiang Uygur Autonomous Region Product Quality Supervision and Inspection Institute, Xinjiang 830004, China; [email protected] * Correspondence: [email protected]; Tel.: +86-010-8232-1836 Received: 6 April 2020; Accepted: 6 May 2020; Published: 8 May 2020 Abstract: The historic Yinggelike nephrite jade deposit in the Altyn Tagh Mountains (Xinjiang, NW China) is renowned for its gem-quality nephrite with its characteristic light-yellow to greenish-yellow hue. Despite the extraordinary gemological quality and commercial significance of the Yinggelike nephrite, little work has been done on this nephrite deposit, due to its geographic remoteness and inaccessibility. This contribution presents the first systematic mineralogical and geochemical studies on the Yinggelike nephrite deposit. Electron probe microanalysis, X-ray fluorescence (XRF) spectrometry, inductively coupled plasma mass spectrometry (ICP-MS) and isotope ratio mass spectrometry were used to measure the mineralogy, bulk-rock chemistry and stable (O and H) isotopes characteristics of samples from Yinggelike. Field investigation shows that the Yinggelike nephrite orebody occurs in the dolomitic marble near the intruding granitoids. Petrographic studies and EMPA data indicate that the nephrite is mainly composed of fine-grained tremolite, with accessory pargasite, diopside, epidote, allanite, prehnite, andesine, titanite, zircon, and calcite. Geochemical studies show that all nephrite samples have low bulk-rock Fe/(Fe + Mg) values (0.02–0.05), as well as low Cr (0.81–34.68 ppm), Co (1.10–2.91 ppm), and Ni (0.52–20.15 ppm) contents. -
AMPHIBOLES: Crystal Chemistry, Occurrence, and Health Issues
AMPHIBOLES: Crystal Chemistry, Occurrence, and Health Issues 67 Reviews in Mineralogy and. Geochemistry 67 TABLE OF CONTENTS 1 Amphiboles: Crystal Chemistry Frank C. Hawthorne, Roberta Oberti INTRODUCTION 1 CHEMICAL FORMULA 1 SOMi : ASPECTS OF CHEMICAL ANALYSIS 1 Chemical composition 1 Summary 6 CALCULATION OF THE CHEMICAL FORMULA 7 24 (O, OH, F, CI) 7 23 (O) 8 13 cations 8 15 cations 8 16 cations 8 Summary 8 AMPIIIBOI I S: CRYSTAL STRUCTURE 8 Space groups 9 Cell dimensions 9 Site nomenclature 9 The C2/m amphibole structure 10 The P2/m amphibole structure 12 The P2/a amphibole structure 12 The Pnma amphibole structure 12 The Pnmn amphibole structure 14 The C1 amphibole structure 17 STACKING SEQUENCES AND SPACE GROUPS 18 BOND LENGTHS AND BOND VALENCES IN [4IA1-FREE AMPHIBOLES 19 THE DOUBLE-CHAIN OF TETRAHEDRA IN [4IA1 AMPHIBOLES 19 Variation in <T-0> bondlengths in C2/m amphiboles 21 Variation in <T-0> bondlengths in Pnma amphiboles 25 THE STEREOCHEMISTRY OF THE STRIP OF OCTAHEDRA 27 The C2/m amphiboles: variation in mean bondlengths 27 The Pnma amphiboles with B(Mg,Fe,Mn): variation in mean bondlengths 30 v Amphiboles - Table of Contents The Pnma amphiboles with BLi: variation in mean bondlengths 32 THE STEREOCHEMISTRY OF THE M (4) SITE 34 The calcic, sodic-calcic and sodic amphiboles 35 Amphiboles with small B cations (magnesium-iron-manganese- lithium, magnesium-sodium and lithium-sodium) 36 The C2/m amphiboles: variation in <M(4)-0> bondlengths 36 The Pnma amphiboles: variation in <MA-0> bondlengths 36 I III! STEREOCHEMISTRY OF THE A SITE 37 The C2/m amphiboles 37 The PU a amphibole 40 The Pnma amphiboles 40 The Pnmn amphiboles 41 THE STEREOCHEMISTRY OF THE 0(3) SITE 41 The C2/m amphiboles 41 UNIT-CELL PARAMETERS AND COMPOSITION IN C2/m AMPHIBOLES 42 SUMMARY 46 ACKNOWLEDGMENTS 46 REFERENCES 47 APPENDIX 1: CRYSTAL-STRUCTURE REFINEMENTS OF AMPHIBOLE 51 Z Classification of the Amphiboles Frank C. -
Depositional Setting of Algoma-Type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok
Depositional Setting of Algoma-type Banded Iron Formation Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok To cite this version: Blandine Gourcerol, P Thurston, D Kontak, O Côté-Mantha, J Biczok. Depositional Setting of Algoma-type Banded Iron Formation. Precambrian Research, Elsevier, 2016. hal-02283951 HAL Id: hal-02283951 https://hal-brgm.archives-ouvertes.fr/hal-02283951 Submitted on 11 Sep 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Accepted Manuscript Depositional Setting of Algoma-type Banded Iron Formation B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok PII: S0301-9268(16)30108-5 DOI: http://dx.doi.org/10.1016/j.precamres.2016.04.019 Reference: PRECAM 4501 To appear in: Precambrian Research Received Date: 26 September 2015 Revised Date: 21 January 2016 Accepted Date: 30 April 2016 Please cite this article as: B. Gourcerol, P.C. Thurston, D.J. Kontak, O. Côté-Mantha, J. Biczok, Depositional Setting of Algoma-type Banded Iron Formation, Precambrian Research (2016), doi: http://dx.doi.org/10.1016/j.precamres. 2016.04.019 This is a PDF file of an unedited manuscript that has been accepted for publication. -
Riebeckite Na2[(Fe2+,Mg)3Fe 2 ]Si8o22(OH)
2+ 3+ Riebeckite Na2[(Fe ; Mg)3Fe2 ]Si8O22(OH)2 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Monoclinic. Point Group: 2=m: As prismatic crystals, to 20 cm. Commonly ¯brous, asbestiform; earthy, massive. Twinning: Simple or multiple twinning 100 . k f g Physical Properties: Cleavage: Perfect on 110 , intersecting at 56 and 124 ; partings f g ± ± on 100 , 010 . Fracture: [Conchoidal to uneven.] Tenacity: Brittle. Hardness = 6 f g f g D(meas.) = 3.28{3.44 D(calc.) = 3.380 Optical Properties: Semitransparent. Color: Black, dark blue; dark blue to yellow-green in thin section. Luster: Vitreous to silky. Optical Class: Biaxial (+) or ({). Pleochroism: X = blue, indigo; Y = yellowish green, yellow- brown; Z = dark blue. Orientation: Y = b; X c = 8 to 7 ; Z c = 6 {7 . Dispersion: ^ ¡ ± ¡ ± ^ ± ± Strong. ® = 1.656{1.697 ¯ = 1.670{1.708 ° = 1.665{1.740 2V(meas.) = 50±{90±. Cell Data: Space Group: C2=m: a = 9.822 b = 18.07 c = 5.334 ¯ = 103:52± Z = 2 X-ray Powder Pattern: Doubrutscha [Dobrudja], Romania. (ICDD 19-1061). 8.40 (100), 3.12 (55), 2.726 (40), 2.801 (18), 4.51 (16), 2.176 (16), 3.27 (14) Chemistry: (1) (2) (1) (2) SiO2 52.90 50.45 CaO 0.12 0.08 TiO2 0.57 0.14 Li2O 0.54 Al2O3 0.12 1.96 Na2O 6.85 6.80 Fe2O3 17.20 17.52 K2O 0.03 1.48 Cr2O3 0.04 F 2.58 + FeO 17.95 17.90 H2O 0.87 MnO 0.00 1.40 O = F 1.09 ¡ 2 MgO 2.96 0.05 Total 98.74 100.68 (1) Dales Gorge Iron Formation, Western Australia; by electron microprobe, corresponds to 2+ 3+ (Na2:00Ca0:02K0:01)§=2:03(Fe2:26Mg0:66Ti0:06)§=2:98Fe1:95(Si7:98Al0:02)§=8:00O22(OH)2: (2) Pikes 2+ Peak area, Colorado, USA; corresponds to (Na2:02K0:29Ca0:01)§=2:32(Fe2:30Li0:33Mn0:18Al0:10 3+ Ti0:02Mg0:01)§=2:94Fe2:02(Si7:75Al0:25)§=8:00O22[F1:25(OH)0:89]§=2:14: Polymorphism & Series: Forms a series with magnesioriebeckite. -
C:\Documents and Settings\Alan Smithee\My Documents\MOTM
Rdosdladq1//6Lhmdq`knesgdLnmsg9@bshmnkhsd This month’s featured mineral has many interesting and unusual varieties: While our specimens have well-developed prismatic crystals, which is unusual for actinolite, a fibrous variety is a former ore of asbestos, and a microcrystalline variety is one of the two types of the gemstone jade. Read on! OGXRHB@K OQNODQSHDR 2+ Chemistry: GCa2(Mg,Fe )5Si8O22(OH)2 Basic Calcium Magnesium Iron Silicate (Calcium Magnesium Iron Silicate Hydroxide) Class: Silicates Subclass: Inosilicates (Double-Chain Silicates) Group: Tremolite (Amphibole Group) Crystal System: Monoclinic Crystal Habits: Usually long prismatic with diamond-shaped cross section; also bladed, columnar, acicular, divergent, fibrous (asbestiform), and radiating. A compact, microcrystalline form is known as nephrite jade. Color: Bright-to-dark green, grayish-green, and greenish-black. Luster: Vitreous; silky and pearly on cleavage surfaces. Transparency: Transparent to translucent Streak: Colorless to white Cleavage: Perfect in two directions lengthwise with intersecting cleavage planes. Fracture: Splintery, uneven; fibrous forms are flexible. Hardness: 5.0-6.0, nephrite variety is 6.5. Specific Gravity: 3.0-3.5 Luminescence: None Refractive Index: 1.63-1.66 Distinctive Features and Tests: Best field marks are the prismatic, often-radiating crystal habit and narrow cleavage-intersection angle. Can be confused with wollastonite, which is fluorescent; the tourmaline-group minerals, which lack cleavage; and epidote, which has a broader cleavage angle. Laboratory methods are necessary to differentiate actinolite from tremolite and ferro- actinolite, as explained in the box on Page 3. Dana Classification Number: 66.1.3a.2 M @L D The name “actinolite,” pronounced ack-TIH-no-lite, derives from the Greek aktino, meaning “ray,” a reference to the common radiate habit of its prismatic crystals. -
Chemographic Exploration of Amphibole Assemblages from Central Massachusetts and Southwestern New Hampshire
Mineral. Soc. Amer, Spec. Pap. 2, 251-274 (1969). CHEMOGRAPHIC EXPLORATION OF AMPHIBOLE ASSEMBLAGES FROM CENTRAL MASSACHUSETTS AND SOUTHWESTERN NEW HAMPSHIRE PETER ROBINSON AND HOWARD W. JAFFE Department of Geology, University of Massachusetts, Amherst, Massachusetts 01002 ABSTRACT Fourteen wet chemical and forty electron-probe analyses were made of amphiboles from critical assemblages in the kyanite and sillimanite zones of central Massachusetts and southwestern New Hampshire. The rocks studied in- clude plagioclase amphibolites that are metamorphosed mafic lavas and tuffs, aluminous anthophyllite rocks of uncertain derivation, quartz-garnet-amphibole granulites that are metamorphosed ferruginous cherts, and pods of ultramafic amphibolite. The rocks contain the following associations: hornblende-anthophyllite, hornblende-cummingtonite, anthophyllite-cummingtonite, hornblende-anthophyllite-cummingtonite, anthophyllite-cordierite, and anthophyllite- kyanite-sillimanite-staurolite_garnet. The following generalizations are made: 1) The cummingtonites are compositionally simple, containing neither sig- nificant AI/AI, NaJAI, nor Ca substitution. 2) The hornblendes are high in AI/AI substitution. Those coexisting with cummingtonite in the kyanite zone or in retrograded rocks have a higher Al content than those coexisting with cum- mingtonite in the sillimanite zone, in close agreement with the prograde reaction tschermakitic hornblende -7 cumming- tonite + plagioclase + H20 proposed by Shido. The Na content of hornblende is considerably less than that of the theoretical edenite end member and is relatively insensitive to variation in the Na content of coexisting plagioclase. 3) Anthophyllites coexisting with hornblende contain about 1as much AI/AI substitution and 1as much Na substitution as coexisting hornblendes. Ca is negligible. Anthophyllites with cordierite, aluminosilicates, or garnet equal or surpass hornblende in AI/AI and Na substitution. -
Crystal Structure of Protoamphibole
Mineral. Soc. Amer. Spec. Pap. 2, 101-109 (1969). CRYSTAL STRUCTURE OF PROTOAMPHIBOLE G. V. GIBBS Department of Geological Sciences, Virginia Polytechnic Institute Blacksburg, Virginia 24061 ABSTRACT The structure proposed for protoamphibole (Gibbs et al., 1960) has been verified and refined by three-dimensional Fourier and least-squares methods using data collected with a Weissenberg single crystal counter-diffractometer. The symmetry is Pnmn with a = 9.330, b = 17.879 and c = 5.288 A and the unit-cell content is 2(Nao.03Li",oMg, ••) (Si r. ,.Alo.040,1.71) (OHo.15F,.14). The structure consists of layers of interlocking chains of fluorine-centered hexagonal rings of SiO. groups. The layers are bound together by Mg.Li cations which are coordinated between the chains, the coordination being effected by a ~(cI3) stagger between adjacent layers. An additional stagger of ~(-cI3) in the sequence along a gives an overall displacement of zero between alternate layers, accounting for the 9.33 A a cell edge and the orthogonal geometry. The direction of stagger can be related to the placement of the cations in the octahedral layer. The M -cation coordination groups are nearly regular octahedra with the exception of M(4) which is similar to Mg(l) in protoenstatite. The M(3), M(1) and M(2) sites are occupied principally by Mg. In addition to being randomly distributed around the cavity walls of the A-site, Li ions are also segregated in about 25% of the M(4) sites, the others being occupied by Mg ions. The individual Si-O bond distances in the chains are consistent with Cruickshank's d-p -n: bonding model: Si-O(non- bridging) bonds [Si(1)-O(1) = 1.592; Si(2)-0(4) = 1.592; Si(2)-0(2) = 1.605 AJ are significantly shorter, on the average, than the Si-O(bridging) bonds [Si(1)-0(5) = 1.616; Si(1)-0(6) = 1.623; Si(1)-0(7) = 1.624; Si(2)-0(5) = 1.626; Si(2)-0(6) = 1.655 AJ. -
ANTHOPHYLLITE Revised: Published by A.E
FROM: Robinson, G.W., 2004 Mineralogy of Michigan by E.W. Heinrich updated and ANTHOPHYLLITE revised: published by A.E. Seaman Mineral Mg7Si8O22(OH)2 Museum, Houghton, MI, 252p. The only common orthorhombic member of the amphibole group; forms a solid solution series with ferro-anthophyllite. Anthophyllite is a metamorphic mineral, occurring in various schists, gneisses, and some iron formations. It also occurs as a hydrothermal mineral species in altered peridotites. The Marquette County localities cited below were reported by Brooks (1873). The identity of his anthophyllites has never been verified or supported by optical data. It is suspected that some, if not all, of the amphibole he reported as anthophyllite may actually be grunerite, inasmuch as some of Brooks’ localities are underlain by Bijiki or Negaunee Iron Formation which in the Marquette district includes grunerite- magnetite schists (Van Hise and Leith, 1911; Richarz, 1927a, b, c; 1932). Northern Peninsula. Baraga County: Spurr Mountain: “Anthophylite” containing 1.78% Mn is reported by Brooks (1873). Dickinson County: 1. Metronite quarry near Felch: Lamey (1934) reports, along with other silicates, the presence of “feranthophyllite” (=ferro-anthophyllite). This has not been verified and is very doubtful (Heinrich, 1962b). 2. NE ¼ NE ¼, section 23, T42N, R29W: In the Skunk Creek Member of the Solberg Schist, actinolite(?) fringed by an amphibole that “may be anthophyllite” was found in a hornblende- magnetite schist (James et al., 1961). 3. Vulcan Iron Formation: One variant consists of grunerite with magnetite, quartz, and anthophyllite (James et al., 1961). Marquette County: 1. Washington mine: Anthophyllite-quartz-magnetite schist. 2. South of New England mine: In slaty magnetite schist. -
Arts of the Indus Valley
2 ARTS OF THE INDUS VALLEY HE arts of the Indus Valley Civilisation emerged during Tthe second half of the third millennium BCE. The forms of art found from various sites of the civilisation include sculptures, seals, pottery, jewellery, terracotta figures, etc. The artists of that time surely had fine artistic sensibilities and a vivid imagination. Their delineation of human and animal figures was highly realistic in nature, since the anatomical details included in them were unique, and, in the case of terracotta art, the modelling of animal figures was done in an extremely careful manner. The two major sites of the Indus Valley Civilisation, along the Indus river—the cities of Harappa in the north and Mohenjodaro in the south—showcase one of earliest examples of civic planning. Other markers were houses, markets, storage facilities, offices, public baths, etc., arranged in a grid-like pattern. There was also a highly developed drainage system. While Harappa and Mohenjodaro are situated in Pakistan, the important sites excavated in India are Lothal and Dholavira in Gujarat, Rakhigarhi in Haryana, Bust of a bearded priest Ropar in Punjab, Kalibangan in Rajasthan, etc. Stone Statues Statues whether in stone, bronze or terracotta found in Harappan sites are not abundant, but refined. The stone statuaries found at Harappa and Mohenjodaro are excellent examples of handling three-dimensional volumes. In stone are two male figures—one is a torso in red sandstone and the other is a bust of a bearded man in soapstone—which are extensively discussed. The figure of the bearded man, interpreted as a priest, is draped in a shawl coming under the right arm and covering the left shoulder. -
A Review of the Structural Architecture of Tellurium Oxycompounds
Mineralogical Magazine, May 2016, Vol. 80(3), pp. 415–545 REVIEW OPEN ACCESS A review of the structural architecture of tellurium oxycompounds 1 2,* 3 A. G. CHRISTY ,S.J.MILLS AND A. R. KAMPF 1 Research School of Earth Sciences and Department of Applied Mathematics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA [Received 24 November 2015; Accepted 23 February 2016; Associate Editor: Mark Welch] ABSTRACT Relative to its extremely low abundance in the Earth’s crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. -
Cordierite-Anthophyllite Rocks at Rat Lake, Manitoba
., , .,. '-'-' . MANlTiBA DEPARTMENJ Of MINES. RESOURCES & ENVIRONMENTAl MANIiGEMENT MINERAL BES(lJRCES DIvtSION OPEN FIIB REPORl' 76/1 OORDlERI'l'FI-ANTHOPHIWTE ROCKS AT RAT LAKE, MlNI'l'OBA; A METAMORPHOSED ALTERATION ZONE By D. A. Baldwin 19'16 Electronic Capture, 2011 The PDF file from which this document was printed was generated by scanning an original copy of the publication. Because the capture method used was 'Searchable Image (Exact)', it was not possible to proofread the resulting file to remove errors resulting from the capture process. Users should therefore verify critical information in an original copy of the publication. .. :., ,.' . .... .- .• I Tt'! OF CC!fl!fl'S .. ' i. -, Page Ifttraduct10n 1 ," Glael'll QeoloIJ 3 · ~ · " "'ell.e. ot unJcnom aft1DitJ (3, 4) 4 .' Coderite-AnthopbJlllte Roc1c1 6 ~I beU'.I.DI l'Ockl 6 .. " Quarts tree l'Ockl 6 ChIld..tl7 ot the Rat take Cordier1tWnthophJllite " BoGIe. 11 Oripn ot the Cord1.r1te-Antho~1l1tl Rocke 15 0I0phJ11ft81 IW'VI),' 18 '. :,(~, Airbome INPUT IVVi,Y 18 ..16 IUl'VI)' 20 OoIIalulonl IDCi Recoanendatianl 21 Iet.rtnael 2, Appendix "A" 25 Appendix "I" 27 \ , I .. ·. ~ . : . ~ . ·-. - 1-· IN'lRODUCTION -==ar=====:==s COrdierite-anthophyllite rocks containing disseminated sulphides of il'Onand copper, and traces of molybdn1te outcrop on the south shore of a small bay at Rat take, Manitoba (Location "5", Fig. 1). These rocks are siDdlar to those that occur in association with massive sulphide ore bodies at the Sherridon MLne, Manitoba, and the Coronation Mine, Saskatchewan. '!'he outcrops are found in an amphibolitic unit within cordierite s1 1limarrlte-anthophyll1te-biotite gneisses of ''unknown affinity" (Schledewitz, 1972). -
Talc, Soapstone & Steatite
TALC, SOAPSTONE AND STEATITE Indian Minerals Yearbook 2013 (Part- III : Mineral Reviews) 52nd Edition TALC, SOAPSTONE AND STEATITE (FINAL RELEASE) GOVERNMENT OF INDIA MINISTRY OF MINES INDIAN BUREAU OF MINES Indira Bhavan, Civil Lines, NAGPUR – 440 001 PHONE/FAX NO. (0712) 2565471 PBX : (0712) 2562649, 2560544, 2560648 E-MAIL : [email protected] Website: www.ibm.gov.in July, 2015 47-1 TALC, SOAPSTONE AND STEATITE 47 Talc, Soapstone and Steatite alc is a hydrous magnesium silicate. In trade EXPLORATION & DEVELOPMENT Tparlance, talc often includes: (i) the mineral No exploration was carried out during the talc in the form of flakes and fibres; (ii) steatite, year 2012-13. the massive compact cryptocrystalline variety of high-grade talc; and (iii) soapstone, the massive PRODUCTION, STOCKS & talcose rock containing variable talc (usually 50%), which is soft and soapy in nature. PRICES Commercial talc may contain other minerals like The production of steatite in 2012-13 was quartz, calcite, dolomite, magnesite, serpentine, 939 thousand tonnes which decreased by about chlorite, tremolite and anthophyllite as impurities. 6% as compared to that in the previous year. The properties of talc that enables its use in a There were 133 reporting mines in 2012-13 as wide variety of applications are its extreme against 138 in the previous year. Besides softness & smoothness, good lustre & sheen, production of steatite was reported by nine high slip & lubricating property, low moisture mines as associated mineral in 2012-13 as against content, ability to absorb oil & grease, chemical eight mines in previous year. Ten principal inertness, high fusion point, low electrical & heat producers accounted for nearly 70% of the total conductivity, high dielectric strength, good production during 2012-13.