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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. -
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. -
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). -
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 -
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. -
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. -
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. -
Chrysotile Asbestos
This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Environmental Health Criteria 203 CHRYSOTILE ASBESTOS First draft prepared by Dr G. Gibbs, Canada (Chapter 2), Mr B.J. Pigg, USA (Chapter 3), Professor W.J. Nicholson, USA (Chapter 4), Dr A. Morgan, UK and Professor M. Lippmann, USA (Chapter 5), Dr J.M.G. Davis, UK and Professor B.T. Mossman, USA (Chapter 6), Professor J.C. McDonald, UK, Professor P.J. Landrigan, USA and Professor W.J. Nicholson, USA (ChapterT), Professor H. Schreier, Canada (Chapter 8). Published under the joint sponsorship of the United Nations Environment Progralnme, the International Labour Organisation, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 1998 The International Programme on chemicat safety (Ipcs), esrablished in 1980, is a joint venture of the united Nations Environment programme (uNEp), the International l-abour organisation (ILo), and the world ueatttr orginization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure rc chemicals, through international peer review processes, as a prerequisiie for the promotion of chemical safety, and to provide technical assistance -
Chrysotile Asbestos As a Cause of Mesothelioma: Application of the Hill Causation Model
Commentary Chrysotile Asbestos as a Cause of Mesothelioma: Application of the Hill Causation Model RICHARD A. LEMEN, PHD Chrysotile comprises over 95% of the asbestos used this method, researchers are asked to evaluate nine today. Some have contended that the majority of areas of consideration: strength of association, tempo- asbestos-related diseases have resulted from exposures rality, biologic gradient, consistency, specificity, bio- to the amphiboles. In fact, chrysotile is being touted as logic plausibility, coherence, experimental evidence, the form of asbestos which can be used safely. Causa- and analogy. None of these considerations, in and of tion is a controversial issue for the epidemiologist. How itself, is determinative for establishing a causal rela- much proof is needed before causation can be estab- tionship. As Hill himself noted, “[n]one of my nine lished? This paper examines one proposed model for establishing causation as presented by Sir Austin Brad- view points can bring indisputable evidence for or ford Hill in 1965. Many policymakers have relied upon against the cause and effect hypothesis, and none can this model in forming public health policy as well as be required as a sine qua non.” In the same vein, it is deciding litigation issues. Chrysotile asbestos meets not necessary for all nine considerations to be met Hill’s nine proposed criteria, establishing chrysotile before causation is established. Instead, Hill empha- asbestos as a cause of mesothelioma. Key words: sized that the responsibility for making causal judg- asbestos; chrysotile; amphiboles; causation; mesothe- ments rested with a scientific evaluation of the totality lioma; Hill model. of the data. -
List of Abbreviations
List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote -
Nepouite Isomorphous Series
N¶epouite Ni3Si2O5(OH)4 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Orthorhombic, probable. Point Group: n.d. As crude pseudohexagonal vermiform crystals, to 1 cm; massive. Physical Properties: Hardness = 2.5 D(meas.) = 3.24 D(calc.) = [3.07{3.40] Optical Properties: Semitransparent. Color: Intense dark green to dull green. Optical Class: Biaxial ({). Pleochroism: Weak; X = dark green; Z = yellow-green. ® = 1.622 ¯ = 1.576{1.579 ° = 1.645 2V(meas.) = n.d. Cell Data: Space Group: n.d. a = 5.27{5.31 b = 9.14{9.20 c = 7.24{7.28 Z = [2] X-ray Powder Pattern: Letovice, Czech Republic. 7.31 (100), 3.63 (90), 2.501 (70), 2.894 (60), 1.530 (60), 4.55 (50b), 2.321 (40) Chemistry: (1) (2) (3) SiO2 32.84 37.0 31.60 Al2O3 0.97 0.21 Fe2O3 0.22 FeO 1.90 NiO 49.05 44.9 58.92 MgO 3.64 5.95 CaO 0.50 0.22 Na2O 0.10 K2O 0.07 + H2O 9.64 11.9 9.48 Total 98.54 100.6 100.00 (1) N¶epoui, New Caledonia. (2) Nakety, New Caledonia. (3) Ni3Si2O5(OH)4: Polymorphism & Series: Dimorphous with pecoraite; forms a series with lizardite. Mineral Group: Kaolinite-serpentine group. Occurrence: An alteration product of nickel-rich ultrama¯c rocks. Association: Serpentine, chlorite, hydrous nickel silicates, iron oxides. Distribution: From the Reis II mine, N¶epoui; near Nakety, and at Thio, New Caledonia. In the 132 North nickel mine, Widgiemooltha district, Western Australia. From Pavlos, Greece.