Synthesis of Knowledge on Tremolite in Talc
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June 19, 2020 Mr. Joe Bhatia President and CEO American
June 19, 2020 Mr. Joe Bhatia President and CEO American National Standards Institute 1899 L Street, NW, 11th Fl. Washington, DC 20036 Dear Mr. Bhatia, The U.S. Council for International Business (USCIB) writes to strongly encourage ANSI to reject the AFNOR proposal to revise ISO 26000, develop one or more implementation guidelines or standards and create a new Technical Committee (TC) on Social Responsibility. Our concerns echo those expressed in statements to ISO from the International Labor Organization (ILO) Secretary-General Guy Ryder (Annex 1), the International Labor Office (Annex 2), and the joint statement from the International Organization of Employers (IOE) and the International Trade Union Confederation (ITUC) (Annex 3). Further development of the AFNOR proposal would break hard-won consensus and jeopardize the impact of ISO 26000; require unnecessary output of resources among stakeholders that would be better used for implementation and innovation in the field of social responsibility; and create divergence with authoritative international standards. ISO 26000 has provided companies of all sizes valuable guidance on the underlying principles of social responsibility. The scope of subject-matter within ISO 26000, and that it is not intended or appropriate for certification purposes or for regulatory or contractual use, were carefully and painstakingly negotiated features of the guidance. Re-starting a years-long and bureaucratic process to revise ISO 26000 would damage its impact by reversing the consensus reached in its initial drafting. In particular, establishing a TC would enable a proliferation of standards with provisions that may not be appropriate for businesses, nor useful for advancing human rights. -
Current Best Practices for Vermiculite Attic Insulation
What is vermiculite insulation? What if I occasionally have to go into Vermiculite is a naturally occurring mineral that has my attic? the unusual property of expanding into worm-like EPA and ATSDR strongly recommend that accordion shaped pieces when heated. The homeowners make every effort not to disturb expanded vermiculite is a light-weight, fire- vermiculite insulation in their attics. If you resistant, absorbent, and odorless material. These occasionally have to go into your attic, current best properties allow vermiculite to be used to make practices state you should: numerous products, including attic insulation. 1. Make every effort to stay on the floored part Do I have vermiculite insulation? of your attic and to not disturb the Vermiculite can be purchased in various forms for insulation. various uses. Sizes of vermiculite products range 2. If you must perform activities that may from very fine particles to large (coarse) pieces disturb the attic insulation such as moving nearly an inch long. Vermiculite attic insulation is a boxes (or other materials), do so as gently pebble-like, pour-in product and is usually light- as possible to minimize the disturbance. brown or gold in color. The pictures in the center of What should I do if I have 3. Leave the attic immediately after the this pamphlet and on the cover show several disturbance. samples of vermiculite attic insulation. vermiculite attic insulation? 4. If you need work done in your attic such as DO NOT DISTURB IT. Any disturbance has the the installation of cable or utility lines, hire trained and certified professionals who can Is vermiculite insulation a problem? potential to release asbestos fibers into the air. -
Wollastonite–A Versatile Industrial Mineral
Industrial Minerals of the United States Wollastonite–A Versatile Industrial Mineral What is Wollastonite? Wollastonite is a chemically simple mineral named in honor of English mineralogist and chemist Sir W.H. Wollaston (1766–1828). It is composed of calcium (Ca) and silicon and oxygen (SiO2, silica) with the chemical formula CaSiO3. Although much wollastonite is relatively pure CaSiO3, it can contain some iron, magnesium, (Above and right) Hand specimens of manganese, aluminum, potassium, wollastonite showing acicular crystal clusters. sodium, or strontium substituting for calcium in the mineral structure. Pure wollastonite is bright white; the geologic conditions during formation What Makes Wollastonite and host rock composition. The type and amount of impurities can Useful? produce gray, cream, brown, pale- Lewis Deposit, mined by NYCO green, or red colors. Minerals, Inc., in the Adirondack Wollastonite has several physical Mountains in Essex County, was properties that make it useful as an formed by the recrystallization of industrial mineral: Geology of U.S. Precambrian carbonate rocks inter- Wollastonite Deposits layered with high-grade metamor- ∑ Wollastonite is largely inert, phic rocks. Nearby reserves are although it will dissolve in concen- Wollastonite is formed by two contained in the Oak Hill and trated hydrochloric acid. It will not processes. The first occurs when Deerhead deposits. The ore bodies react with other components of silica and limestone are raised to a consist of the minerals wollastonite, manufactured products either during temperature of 400°–450°C, either garnet, and diopside with as much as or after the manufacturing process. because of deep burial (regional 60 percent of the bodies being ∑ During crushing, wollastonite metamorphism) or by being baked wollastonite. -
Greensand.Pdf
www.natureswayresources.com GREENSAND Greensand is a naturallyoccurring mineral mined from ocean deposits from a sedimentary rock known as “Glauconite”. It is often an olive-green colored sandstonerock found in layers in many sedimentary rock formations. Origin of Greensand Greensand forms in anoxic (without oxygen) marine environments that are rich in organic detritus and low in sedimentary inputs. Some greensands contain marine fossils (i.e. New Jersey Greensand). Greensand has been found in deposits all over the world. The greenish color comes from the mineral glauconite and iron potassiumsilicate that weathers and breaks down releasing the stored minerals. The color may range from a dark greenish gray, green-black to blue-green dependingon the minerals and water content. It often weatherseasilyand forms nodules that have been oxidized with iron bearing minerals that has a reddish brown or rust color. +3 The major chemical description is ((K,Na)(Fe , Al, Mg)2(Si,Al)4O10(OH)2) General chemical information: Iron (Fe) 12-19% Potassium (K) 5-7 % Silicon (Si) 25.0% Oxygen (O) 45% Magnesium (Mg) 2-3 % Aluminum (Al) 1.9 % Sodium (Na) 0.27% Hydrogen (H) 0.47% Over 30 other trace minerals and many micronutrients. Types of Greensand Glauconite is the namegiven to a group of naturally occurring iron rich silica minerals that may be composed of pellets or grains. When glauconite is mined the upper layers that have weathered and become oxidizedand minerals are released.These sometimes form pyrite a iron sulfide (FeS2) when oxygen is www.natureswayresources.com absent. In the deeper layers or reduced zone pyrite crystals often form. -
Yellowish Green Diopside and Tremolite from Merelani, Tanzania
YELLOWISH GREEN DIOPSIDE AND TREMOLITE FROM MERELANI, TANZANIA Eric A. Fritz, Brendan M. Laurs, Robert T. Downs, and Gelu Costin tion (typical of diopside, which is a pyroxene) shown by other crystals in the parcels. Four similar-appearing yellowish green samples Mr. Ulatowski loaned one example of both types of from Block D at Merelani, Tanzania, were identified crystals to GIA for examination (figure 1), and we also as diopside and tremolite. The gems are identical in color, but their standard gemological properties are typical for calcic pyroxene and amphibole. The identification of the diopside was made with Raman Figure 1. These yellowish green crystals were recov- spectroscopy, while single-crystal X-ray diffraction ered from Block D at Merelani in the latter part of and electron-microprobe analyses were used to 2005. A blocky morphology is shown by the diopside confirm the amphibole species as tremolite. crystal (1.6 cm tall; left and bottom), whereas the Absorption spectroscopy (in the visible–mid-infrared tremolite crystal has a flattened, diamond-shaped range) revealed that the two gem materials are col- cross-section. Photos by Robert Weldon. ored by V3+, Cr3+, or both. t the 2006 Tucson gem shows, Steve Ulatowski A showed one of the authors (BML) some yellowish green crystals that he purchased as diopside while on buy- ing trips to Tanzania in August and November 2005. The material was reportedly produced during this time period from Block D at Merelani, in the same area that yielded some large tsavorite gem rough (see Laurs, 2006). Mr. Ula- towski obtained 1,200 grams of the green crystals, mostly as broken pieces ranging from 0.1 to 50 g (typically 1–5 g). -
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. -
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. -
VERMICULITE by Michael J
VERMICULITE By Michael J. Potter Domestic survey data and tables were prepared by Nicholas Muniz, statistical assistant, and the world production table was prepared by Glenn J. Wallace, international data coordinator. +2 Vermiculite is a hydrated magnesium-aluminum-iron silicate, with a suggested formula of (Mg,Fe ,Al)3(Al,Si)4O10(OH)2·4H2O (Fleisher and Mandarino, 1991, p. 211). Flakes of raw vermiculite concentrate are mica-like in appearance and contain water molecules within their internal structure. When the flakes are heated rapidly at a temperature of 900º C or higher, the water flashes into steam, and the flakes expand into accordion-like particles. The color, which can range from black and various shades of brown to yellow for the raw flakes, changes upon expansion to gold or bronze. This expansion process is called exfoliation, and the resulting lightweight material is chemically inert, fire resistant, and odorless. In lightweight plaster and concrete, vermiculite provides good thermal insulation. Vermiculite can absorb such liquids as fertilizers, herbicides, and insecticides, which can then be transported as free-flowing solids (Harben and Kuzvart, 1996). Production Domestic production (sold or used) data for vermiculite were collected by the U.S. Geological Survey (USGS) from two voluntary canvasses—one for mine-mill (concentrator) operations and the other for exfoliation plants. Data were not available for the three mine-mill operations. The two U.S. producers of vermiculite concentrate were Virginia Vermiculite Ltd. with operations near Woodruff, SC, and in Louisa County, VA; and W.R. Grace & Co. from its operation at Enoree, SC. Vermiculite concentrate was shipped to exfoliating plants for conversion into lightweight material. -
Wollastonite
Strictly private and confidential Wollastonite A versatile mineral which can support sustainable farming 07 June 2019 Business Risk Analysis – Visionary Execution Strictly private and confidential 2 Disclaimer & Forward-Looking Statements Cautionary Statement on Forward-Looking Information & Statements: This presentation contains certain forward-looking information and statements which may not be based on fact, including without limitation, statements regarding the Company’s expectations in respect of its future financial position, business strategy, future exploration and production, mineral resource potential, exploration drilling, permitting, access to capital, events or developments that the Company expects to take place in the future. All statements, other than statements of historical facts, are forward-looking information and statements. The words “believe”, “expect”, “anticipate”, “contemplate”, “target”, “plan”, “intends”, “continue”, “budget”, “estimate”, “may”, “will”, “aim”, “goal” and similar expressions identify forward-looking information and statements. In addition to the forward-looking information and statements noted above, this presentation includes those that relate to: the expected results of exploration activities; the estimation of mineral resources; the ability to identify new mineral resources and convert mineral resources into mineral reserves; ability to raise additional capital and complete future financings; capital expenditures and costs, including forecasted costs; the ability of the Company to comply with -
The Conversion of Wollastonite to Caco3 Considering Its Use for CCS Application As Cementitious Material
applied sciences Article The Conversion of Wollastonite to CaCO3 Considering Its Use for CCS Application as Cementitious Material Kristoff Svensson *, Andreas Neumann, Flora Feitosa Menezes, Christof Lempp and Herbert Pöllmann Institute for Geosciences and Geography, Martin-Luther-University of Halle-Wittenberg, Von-Seckendorff-Platz 3, 06120 Halle (Saale), Germany; [email protected] (A.N.); fl[email protected] (F.F.M.); [email protected] (C.L.); [email protected] (H.P.) * Correspondence: [email protected]; Tel.: +49-345-55-26138 Received: 21 December 2017; Accepted: 8 February 2018; Published: 20 February 2018 Featured Application: Building materials and CCS. Abstract: The reaction of wollastonite (CaSiO3) with CO2 in the presence of aqueous solutions (H2O) and varied temperature conditions (296 K, 323 K, and 333 K) was investigated. The educts (CaSiO3) and the products (CaCO3 and SiO2) were analyzed by scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), and differential scanning calorimetry with thermogravimetry coupled with a mass spectrometer and infrared spectrometer (DSC-TG/MS/IR). The reaction rate increased significantly at higher temperatures and seemed less dependent on applied pressure. It could be shown that under the defined conditions wollastonite can be applied as a cementitious material for sealing wells considering CCS applications, because after 24 h the degree of conversion from CaSiO3 to CaCO3 at 333 K was very high (>90%). As anticipated, the most likely application of wollastonite as a cementitious material in CCS would be for sealing the well after injection of CO2 in the reservoir. -
X-Ray Structure Refinements of Tremolite at 140 and 295 K: Crystal Chemistry and Petrologic Implications
American Mineralogist, Volume 81, pages 1117-1125,1996 X-ray structure refinements of tremolite at 140 and 295 K: Crystal chemistry and petrologic implications HEXIONG YANG1.. ANDBERNARD W. EVANS2 'Department of Geological Sciences. Campus Box 250, University of Colorado, Boulder, Colorado 80309-0250, U.S.A. 2Department of Geological Sciences, Box 351310, University of Washington, Seattle, Washington 98195-1310, U.S.A. ABSTRACT A near-end-member natural tremolite, N!lo.o,Ca1.97M~.9sFeo.Q3Alo.oISis.oo022(OH)2'was studied by single-crystal X-ray diffraction at 140 and 295 K to seek a possible crystal- chemical explanation for the typically low CaI~ M ratios, relative to the ideal ratio of 2/5, observed in both natural and synthetic tremolite samples. Difference-Fourier maps re- vealed the presence of a residual electron density close to the M4 site along the diad axis toward the octahedral strip. Structure refinements indicated that the M4 and M4' sites are occupied by Ca + Na and M(Fe + Mg), respectively. In comparison with the configuration of the M2 coordination polyhedron in diopside, the degree of distortion and the volume of the M4 coordination polyhedron in tremolite are relatively large and the M4 cation is slightly underbonded. These two factors contribute to an energetic drive toward M-en- riched tremolite. The average unit-cell volume of 906.6(2) A3 determined at 295 K for nearly pure tremolite in this study suggests an end-member reference-state volume for tremolite of907 A3. This indicates that cell volumes of synthetic tremolite of 904.2(4) A3 reflect 8-10% cummingtonite solid solution, as previous authors have claimed. -
Experimental Study of Mineral Carbonation of Wollastonite For
DEGREE PROJECT IN TECHNOLOGY, FIRST CYCLE, 15 CREDITS STOCKHOLM, SWEDEN 2019 Experimental Study of Mineral Carbonation of Wollastonite for Increased CO2 Uptake DINA BABIKER MATILDA AHLSTRAND KTH ROYAL INSTITUTE OF TECHNOLOGY SCHOOL OF ARCHITECTURE AND THE BUILT ENVIRONMENT TRITA TRITA-ABE-MBT-19533 www.kth.se Abstract The cement and concrete industry stand for approximately 8% of the global CO2 emissions. The demand of concrete and cement is expected to increase rapidly with the growing world population and increased urbanization. This makes it of the utmost importance for the industry to try to mitigate its emissions. One way to reduce the industry’s environmental impact is by mineral carbonation curing through which CO2 can be sequestered in the concrete. This investigation studied the CO2 uptake of wollastonite (CaSiO3) which can be used for mineral carbonation. The CO2 uptake of different brands of wollastonite powders for different temperatures, pressures and water to solid ratios were tested through carbonation, and the samples were then analyzed through XRD, SEM and particle size analysis. The results showed large differences in CO2 uptake between the brands of wollastonite powders. They also indicate that lower temperatures lead to higher CO2 uptake but also possibly slow down the reaction rate and that higher CO2 pressures seem to increase CO2 uptake though the effect is small. There was significant variation of the effects of the water to solid ratios on CO2 uptake between the tested brands. The morphology of the powders also seemed to be of little relevance as an amorphous and crystalline powder were the two best performing powders, similarly particle size is not indicated by the result to have a large effect on CO2 uptake, though further studies are required to fully determine the effect of the morphology and particle size.