Download the Scanned

Total Page:16

File Type:pdf, Size:1020Kb

Download the Scanned AmericanMineralogist, Volume64, pages 369-375, 1979 Newdata on hungchaoite,the second world occurrence, Death Valley region, California RtcHnRoC. Eno, Jluss F. McAlr-rsrER ANDG. DoNeln EsrnI-urN U.S. GeologicalSuruey Menlo Park, Califurnia 94025 Abstract Hungchaoiteoccurs with ginorite,mcallisterite, sborgite, sassolite, nobleite, ulexite, and, wheregypsum and ulexiteare abundant,with kurnakovite.inderite. and mcallisteritein surficialmatrix as productsfrom weatheredcolemanite and priceiteveins in late Tertiary rocks. Hungchaoiteis triclinic,space group PT;a :8.811(1), b : 10.644(2),c : 7.888(l)A;a : 103"23(l)',0 : 108o35(l)', 97.09(l), unit-cellvolume 666.2(l)Aa;Z 2[MgO.4BrOs.9HrO].Euhedral, tabular {100} to equant,colorless, untwinned crystals, up to 0.5mm, showl7 forms.The strongest lines in theX-ray powder pattern are, in A: 6.71(100), 3.3s6(92), 5.36(85 ), 4.093(78), 4.079(64), and 7.I 4(59). Hungchaoiteisoptically(-):*:1.445(2),0=1.485(2),7:l.a9}Q)(Nalight);2Il": ( -66.. 15(4)";r u,distinct; Xlta: +28",2Lb = 437",Y4 c = Good{lll}and {lll}and imperfect{010} cleavages. Hardness 2Yz. G (meas)1.706(5), p (calc)1.705 g cm-s. Hungchaoiteis metastablewith respectto inderite and mcallisteritein solution. Dehy- dration data are given. Introduction of DeathValley National Monument. The first local- ity is about 50 m southwestof the road in Twenty Hungchaoite,MgO.2BrO3.9H2O, was first de- Mule TeamCanyon, 2,140 m N25'W of U.S.mineral scribedby (1964a,b) Chu et al. from salinelacustrine monument40 on Monte Blanco(McAllister, 1970), sedimentsat an unspecified localityin Chinawhere it andis in thesoutheastern part of the Meridianclaim. reportedlyoccurs as fine-grained materialassociated The secondlocality is about 550m S30'E from the with ulexite,hydroboracite, and szaibelyitein gypsi- firstand is on the SouthMeridian claim. The third is feroussediments. It is identical in its chemicalcom- on the Hard Scrambleclaim (Erd et al., 1959,Fig. 1), positionand physicalproperties with the compound about l0 km southeastofthe first localityand 3 km MgO.2BzOr.9H2O, first synthesizedby Nikolaev N72oWof Ryan. and Chelishcheva( 1940). The hungchaoiteoccurs in a surficial sponge We presentdata here for the secondworld occur- formed by weatheringof fragmentalbasalt around renceof this mineraldiscovered by McAllister in the veinsof priceiteand colemanite.The basaltunit is in Death Valley region, (1970). California The larger lacustrinedeposits in the lower part of the Furnace sizeof the crystalsin the California occurrencehas Creek Formation that was assignedsomewhat in- enabledus to characterizemore completelythis min- conclusivelyto the earlyPliocene (Clarendonian) by eral and haspermitted the determinationof its crystal K. E. Lohman(in McAllister,1970, p. 6) on thebasis structure(Wan and Ghose,1977). of diatoms.The formation,which reaches a thickness of about 2,100m, extendsupward into clearlythe Occurrence(J.F.M.) middle Pliocene(Hemphillian), according to Loh- In the FurnaceCreek borate area hungchaoite has man. In a stratigraphicsequence measured (McAllis- beenfound at three placesin the northeasternfoot- ter, 1976)from the underlyingArtist Drive Forma- hillsof theBlack Mountains. The localities are on old tion acrossTwenty Mule Team Canyonsoutheast of patentedmining claims of the U.S. Borax& Chem- the Meridian localities,this basaltunit is about 300m ical Corporation,which are now within the boundarv abovethe baseof the FurnaceCreek Formation and 00/03-004x / 79 / 0304-0369$02.00 369 ERD ET AL.: HUNGCHAOITE Hungchaoite on the Hard Scrambleclaim, in con- trast to the other localities, occurs in a surficial aggre- gate that containsmuch gypsum and ulexite,at veins of priceite and colemanite. It is closely associated with kurnakovite, inderite, and mcallisterite,and is within a few meters of an assemblagecontaining riv- adavite, mcallisterite, ulexite, gypsum, and con- spicuousquantities of thenardite and mirabilite. Eu- hedral crystalsof hungchaoite(specimen no. JFM69- 5-5G7) for this report are from the Hard Scramble Y I locality. Three other specimensfrom the same gfab sample show the following mineral relations. (l) Nodules of hungchaoitecoalesce on a gypsum-kur- Fig. l. Tabular r,unl.nuoit. crystal in isometric p.B.rp".tiu", 1e; Standard orientation (with axial cross); (B) Viewed along Y nakovite intergrowth on corroded vein colemanite. Computer drawing by K. L. Keester using the computer program The oppositeside of the colemaniteis encrustedwith of Keesterand Giddings (1971). finer grained inderite and ulexite. (2) An irregular veinlet of hungchaoite penetrates an aggregate of about 100m abovethe colemanite-ulexite-probertite gypsum and weatheredbasalt on a core of coleman- ore zone. ite. Fine-grained inderite was depositedon a some- veinlet and Although the rocks enclosingthe priceite and co- what corroded surfaceofthe hungchaoite gyp- lemanite veins are of late Tertiary age, the hung- as nodules next to nodules of hungchaoiteon chaoite and associatedminerals around the veins are sum. (3) Ulexite, inderite, and hungchaoite occur Holocene and still form in the presentdesert environ- separately in nodules or crusts on an aggregate of grained ment, as shown by the fragile, ephemeralnature of gypsum and kurnakovite. Clots of very fine at- puffed ground in which the hungchaoiteoccurs and mcallisteriteare in a matrix of weatheredbasalt by encrustationsof some of the minerals on man- tached to the aggregate. made surfacesin prospectand mine workings (Erd et al.,196l,p.562; McAllister,1961, p.8300). Boron of CrystallograPhY the hungchaoite,which was releasedfrom weathered Morphology priceite and colemanite, apparently migrated much earlier from bedded ulexite in the ore zone. Hungchaoiteoccurs as euhedral to anhedral,tabu- Hungchaoite on the Meridian claim was collected lar {100}to equant,untwinned crystals (Fig. l) up to (specimenJFM58-l-8C) from a small pad of puffed 0.5mm in largestdimension. The formsobserved are ground that was not in contact with any of the ex- listedin Tablel. A numericaldescription of thehabit posed veins of colemaniteor priceite. Anhedral and developmentis providedby column D of Table l, subhedral hungchaoite or exceedingly fine textured whichlists the normaldistance of the form from the ulexiteforms commonly l- to 2-mm clots in a porous, origin.These data were obtained by Dr. KennethL. scarcelycoherent aggregateof montmorillonite and Keesterusing a computerprogram (Keester and Gid- residualanalcime. Gowerite. nobleite.and mcallister- dings,197 l) which exactlysimulates the realcrystal ite are very minor constituents. On the South (Fig. I ) andthus allows quantitative determination of Meridian claim, hungchaoiteoccurs with more abun- relativegrowth velocities.Although D valueswere dant boron minerals(although very minor ulexite),in not determinedfor six forms(Table l), they are all puffed ground of clay and analcime, down a moder- smallerthan k {011}and haveD valuesin excessof ate slope 1.7 m from the nearestexposed colemanite 1.400.The crystalmorphology indicates that hung- vein. The closelyassociated minerals in irregularclots chaoiteis triclinicpinacoidal. Furthermore, both nat- or nodules,generally less than 5 mm in diameter,are ural etchpits and thoseproduced by attackof cold ginorite, mcallisterite, sborgite, sassolite,nobleite, water show paired facesin accordwith centricsym- and ulexite. Other borate minerals thus far identified metry. from gowerite, the South Meridian locality are ward- X-ray data smithite, and aristarainite. The aristarainite is the second known occurrence (McAllister, 1976) after Unit-cell dimensionswere determinedfrom pre- Salta, Argentina (Hurlbut and Erd, 1974). cessionphotographs (Mo radiation,Zr filter) of ERD ET AL.: HUNGCHAOITE 371 Table l. Angle table and morphological data for hungchaoite Triclinic; pinacoidal I a:b:c=0.8278:l:0.7411 o= 103.23t, B= 108.35', y=97.09' PotQo,to=0.8778:0.7079:1 ^=73" l5', p = 68'54r,r=77" 3Sl pof 0.9672, qo,= 0.7800, xo,= 0.3362, yo,= 0.3179 D* * Tabular Equant 001 46" 361 )Ao 501 68' 54' 73" l4l l . 000 0. 800 b 010 0" 00' 90' 00r 77" 35' 73" r4l 0.800 0.800 1 100 77" 351 90' 00 77" 351 68" 54' 0.125 0.125 f 410 89' l3' 90' 00t l1' 38' 89' l3' 72" 001 0.765 0.765 ' n 2ro 100" 55 90" 001 23" 201 100' 55' 75" 491 0.525 0.525 M rl0 t2l" l2l 90" 001 43" 361 I2I" 12' 83' 36' 0.4s0 0.450 | k 011 77" 021 48" 57 68" r5 ' 43" 521 29" 221 ]. 400 q 011 143' 58' 29" 4Sl 78" 321 ll3'59' 40" 251 not determined ' v 10r 67" 4Ll 54' l0 37" 00' 72" 041 31' 54' not deternined l0l -79" 451 37" 441 119' 02, 840 38' 50" ' 08, 0.97s 0.800 r l1 l0l" l4 52" 33'l 43" 20,, 98" 54' 41" 5l ' 0 . 950 0. 750 -63" z 414 221 34" 741 ll5'55' 75" 24' 47" 58' not deternined -50" x 212 35' 38" 13' tI2" 29' 66" 52' 47" 07 | not determined -34" u lll 271 47" 091 105" 54' s2" 45' 48" 16' 7.230 1.050 -13' S 131 57' 68" 23' 97" 261 25" 321 580 l5r not deternined p -737" 111 461 42" 091 723" tll 179" 47 | 66' 55' 0.975 0.975 -157' ' L2l 14 57" 331 l19" 05' 141" 05' 80" 37' not deternined *Values calculated from unit-cell paraneters showr in Table 2. **Distance from the origin. Determination by K. L, Keester singlecrystals from the Hard Scrambleclaim (speci- thesedata is 2.242g cffi-3,which is unlikelyfor a men no. JFM69-5-5G7).These data were refined by dimorph of hungchaoiteof specificgravity 1.703(5) least-squaresanalysis of the X-ray powder data and (Table2). Furthermore,Wan and Ghose(1977, p. areshown in Table2 comparedwith thoseobtained ll4l) have ques(ionedthe validity of the crystal from the syntheticcompound, MgO.2BrOs.9HrO. structureproposed for this phaseby Abdullaev and The crystalstructure of hungchaoitehas beendeter- Mamedovon the basisof ". .a numberof impos- minedby Wan and Ghose(1977) using our crystals sibly short (<2A) oxygen-oxygencontacts. ." On from the Hard Scramble occurrence.They show the other hand, Eyubovaet al. (1967)give X-ray hungchaoiteto be Mg[B,O'(OH)n].7HrO.Tung powder diffraction data for synthetic MgO.
Recommended publications
  • A Multi-Methodological Study of Kurnakovite: a Potential B-Rich 2 Aggregate 3 4 G
    1 A multi-methodological study of kurnakovite: a potential B-rich 2 aggregate 3 4 G. Diego Gatta1, Alessandro Guastoni2, Paolo Lotti1, Giorgio Guastella3, 5 Oscar Fabelo4 and Maria Teresa Fernandez-Diaz4 6 7 1Dipartimento di Scienze della Terra, Università degli Studi di Milano, 8 Via Botticelli 23, I-20133 Milano, Italy 9 2Dipartmento di Geoscienze, Università degli Studi di Padova, 10 Via G. Gradenigo 6, I-35131, Padova, Italy 11 3Agenzia delle Dogane e dei Monopoli, Direzione Regionale per la Lombardia, 12 Laboratorio e Servizi Chimici, Via Marco Bruto 14, I-20138 Milan, Italy 13 4Institut Laue-Langevin, 71 Avenue des Martyrs, F-38000 Grenoble, France 14 15 16 Abstract 17 The crystal structure and crystal chemistry of kurnakovite from Kramer Deposit (Kern 18 County, California), ideally MgB3O3(OH)5·5H2O, was investigated by single-crystal neutron 19 diffraction (data collected at 293 and 20 K) and by a series of analytical techniques aimed to determine 20 its chemical composition. The concentration of more than 50 elements was measured. The empirical 21 formula of the sample used in this study is: Mg0.99(Si0.01B3.00)Σ3.01O.3.00(OH)5·4.98H2O. The fraction 22 of rare earth elements (REE) and other minor elements is, overall, insignificant. Even the fluorine 23 content, as potential OH-group substituent, is insignificant (i.e., ~ 0.008 wt%). The neutron structure 24 model obtained in this study, based on intensity data collected at 293 and 20 K, shows that the 25 structure of kurnakovite contains: [BO2(OH)]-groups in planar-triangular coordination (with the B- 2 26 ions in sp electronic configuration), [BO2(OH)2]-groups in tetrahedral coordination (with the B-ions 3 27 in sp electronic configuration), and Mg(OH)2(H2O)4-octahedra, connected in (neutral) 28 Mg(H2O)4B3O3(OH)5 units forming infinite chains running along [001].
    [Show full text]
  • Trace Elements and Minerals in Fumarolic Sulfur: the Case of Ebeko Volcano, Kuriles
    Hindawi Geofluids Volume 2018, Article ID 4586363, 16 pages https://doi.org/10.1155/2018/4586363 Research Article Trace Elements and Minerals in Fumarolic Sulfur: The Case of Ebeko Volcano, Kuriles E. P. Shevko,1 S. B. Bortnikova,2 N. A. Abrosimova,2 V. S. Kamenetsky ,3,4 S. P. Bortnikova,2 G. L. Panin,2 and M. Zelenski 3 1 Sobolev Institute of Geology and Mineralogy, SBRAS, Novosibirsk 630090, Russia 2Trofmuk Institute of Petroleum Geology and Geophysics, SBRAS, No. 3, Novosibirsk 630090, Russia 3Institute of Experimental Mineralogy RAS, Chernogolovka 142432, Russia 4EarthSciencesandCODES,UniversityofTasmania,PrivateBag79,Hobart,TAS7001,Australia Correspondence should be addressed to M. Zelenski; [email protected] Received 25 June 2017; Revised 13 October 2017; Accepted 14 December 2017; Published 20 March 2018 Academic Editor: Joerg Goettlicher Copyright © 2018 E. P. Shevko et al. Tis is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Native sulfur deposits on fumarolic felds at Ebeko volcano (Northern Kuriles, Russia) are enriched in chalcophile elements (As- Sb-Se-Te-Hg-Cu) and contain rare heavy metal sulfdes (Ag2S, HgS, and CuS), native metal alloys (Au2Pd), and some other low- solubility minerals (CaWO4, BaSO4). Sulfur incrustations are impregnated with numerous particles of fresh and altered andesite groundmass and phenocrysts (pyroxene, magnetite) as well as secondary minerals, such as opal, alunite, and abundant octahedral pyrite crystals. Te comparison of elemental abundances in sulfur and unaltered rocks (andesite) demonstrated that rock-forming elements (Ca, K, Fe, Mn, and Ti) and other lithophile and chalcophile elements are mainly transported by fumarolic gas as aerosol particles, whereas semimetals (As, Sb, Se, and Te), halogens (Br and I), and Hg are likely transported as volatile species, even ∘ at temperatures slightly above 100 C.
    [Show full text]
  • Download PDF (402K)
    Geochemical Journal, Vol. 41, pp. 149 to 163, 2007 Boron isotope fractionation accompanying formation of potassium, sodium and lithium borates from boron-bearing solutions MAMORU YAMAHIRA, YOSHIKAZU KIKAWADA* and TAKAO OI Department of Chemistry, Sophia University, 7-1 Kioi-cho, Chiyoda-ku, Tokyo 102-8854, Japan (Received March 18, 2006; Accepted June 22, 2006) A series of experiments was conducted in which boron minerals were precipitated by water evaporation from solutions containing boron and potassium, sodium or lithium at 25°C, and boron isotope fractionation accompanying such mineral precipitation was investigated. In the boron-potassium ion system, K2[B4O5(OH)4]·2H2O, santite (K[B5O6(OH)4]·2H2O), KBO2·1.33H2O, KBO2·1.25H2O and sassolite (B(OH)3) were found deposited as boron minerals. Borax (Na2[B4O5(OH)4·8H2O) was found deposited in the boron-sodium ion system, and Li2B2O4·16H2O, Li2B4O7·5H2O, Li2B10O16·10H2O, LiB2O3(OH)·H2O and sassolite in the boron-lithium ion system. The boron isotopic analysis was con- 11 10 ducted for santite, K2[B4O5(OH)4]·2H2O, borax and Li2B2O4·16H2O. The separation factor, S, defined as the B/ B isotopic ratio of the precipitate divided by that of the solution, ranged from 0.991 to 1.012. Computer simulations for modeling boron mineral formations, in which polyborates were decomposed into three coor- dinated BO3 unit and four coordinated BO4 unit for the purpose of calculation of their boron isotopic reduced partition function ratios, were attempted to estimate the equilibrium constant, KB, of the boron isotope exchange between the boric – acid molecule (B(OH)3) and the monoborate anion (B(OH)4 ).
    [Show full text]
  • Inyoite Cab3o3(OH)5 • 4H2O C 2001-2005 Mineral Data Publishing, Version 1
    Inyoite CaB3O3(OH)5 • 4H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Typically as crystals, short prismatic along [001], tabular on {001}, exhibiting prominent {110} and {001} and a dozen other minor forms, to 2.5 cm; in cockscomb aggregates of pseudorhombohedral crystals; also coarse spherulitic, granular. Physical Properties: Cleavage: {001}, good; {010}, distinct. Fracture: Irregular. Tenacity: Brittle. Hardness = 2 D(meas.) = 1.875 D(calc.) = 1.87 Soluble in H2O. Optical Properties: Transparent, translucent on dehydration. Color: Colorless, white on dehydration. Luster: Vitreous. Optical Class: Biaxial (–). Orientation: Y = b; X ∧ c =37◦; Z ∧ c = –53◦. Dispersion: r< v, slight. α = 1.490–1.495 β = 1.501–1.505 γ = 1.516–1.520 2V(meas.) = 70◦–86◦ Cell Data: Space Group: P 21/a. a = 10.621(1)) b = 12.066(1) c = 8.408(1) β = 114◦1.2◦ Z=4 X-ray Powder Pattern: Monte Azul mine, Argentina. 7.67 (100), 2.526 (25), 3.368 (22), 1.968 (22), 2.547 (21), 3.450 (20), 2.799 (19) Chemistry: (1) (2) B2O3 37.44 37.62 CaO 20.42 20.20 + H2O 9.46 − H2O 32.46 H2O 42.18 rem. 0.55 Total 100.33 100.00 • (1) Hillsborough, Canada; remnant is gypsum. (2) CaB3O3(OH)5 4H2O. Occurrence: Along fractures and nodular in sedimentary borate deposits; may be authigenic in playa sediments. Association: Meyerhofferite, colemanite, priceite, hydroboracite, ulexite, gypsum. Distribution: In the USA, in California, from an adit on Mount Blanco, Furnace Creek district, Death Valley, Inyo Co., and in the Kramer borate deposit, Boron, Kern Co.
    [Show full text]
  • UCLA Electronic Theses and Dissertations
    UCLA UCLA Electronic Theses and Dissertations Title Use of Boron in Detergents and its Impact on Reclamation Permalink https://escholarship.org/uc/item/2rw7k2r7 Author Ghavanloughajar, Maryam Publication Date 2015 Peer reviewed|Thesis/dissertation eScholarship.org Powered by the California Digital Library University of California UNIVERSITY OF CALIFORNIA Los Angeles Use of Boron in Detergents and its Impact on Reclamation A thesis submitted in partial satisfaction of the requirements for the degree Master of Science in Civil Engineering by Maryam Ghavanloughajar 2015 ABSTRACT OF THE THESIS Use of Boron in Detergents and its Impact on Reclamation By Maryam Ghavanloughajar Master of Science in Civil Engineering University of California, Los Angeles, 2015 Professor Michael K. Stenstrom, Chair Many parts of the world are experiencing severe water drought and it affects societies both economically and environmentally. Therefore, conservation practices are essential to balance water supply and demand. Greywater or wastewaters from showers and luandries, if treated well can be a reliable source for activities such as irrigation, toilet flushing and car washing. Greywaters are not as contaminated as sewage but still may require treatment before reuse. The application of insufficiently treated water for irrigation can cause harm to plants and animals. Pollutant such as boron in greywater is of particular interest because many plants are sensitive to even low concentrations. High concentrations of boron can induce toxicity, reduce growth rate and yield in plants. Therefore, proposed greywater treatment systems need to consider the sensitivity of plant species and boron concentrations and potential removal. This thesis reviews boron chemistry, its effect on plants and currently available boron removal technologies.
    [Show full text]
  • Design Rules for Discovering 2D Materials from 3D Crystals
    Design Rules for Discovering 2D Materials from 3D Crystals by Eleanor Lyons Brightbill Collaborators: Tyler W. Farnsworth, Adam H. Woomer, Patrick C. O'Brien, Kaci L. Kuntz Senior Honors Thesis Chemistry University of North Carolina at Chapel Hill April 7th, 2016 Approved: ___________________________ Dr Scott Warren, Thesis Advisor Dr Wei You, Reader Dr. Todd Austell, Reader Abstract Two-dimensional (2D) materials are championed as potential components for novel technologies due to the extreme change in properties that often accompanies a transition from the bulk to a quantum-confined state. While the incredible properties of existing 2D materials have been investigated for numerous applications, the current library of stable 2D materials is limited to a relatively small number of material systems, and attempts to identify novel 2D materials have found only a small subset of potential 2D material precursors. Here I present a rigorous, yet simple, set of criteria to identify 3D crystals that may be exfoliated into stable 2D sheets and apply these criteria to a database of naturally occurring layered minerals. These design rules harness two fundamental properties of crystals—Mohs hardness and melting point—to enable a rapid and effective approach to identify candidates for exfoliation. It is shown that, in layered systems, Mohs hardness is a predictor of inter-layer (out-of-plane) bond strength while melting point is a measure of intra-layer (in-plane) bond strength. This concept is demonstrated by using liquid exfoliation to produce novel 2D materials from layered minerals that have a Mohs hardness less than 3, with relative success of exfoliation (such as yield and flake size) dependent on melting point.
    [Show full text]
  • Alphabetical List
    LIST L - MINERALS - ALPHABETICAL LIST Specific mineral Group name Specific mineral Group name acanthite sulfides asbolite oxides accessory minerals astrophyllite chain silicates actinolite clinoamphibole atacamite chlorides adamite arsenates augite clinopyroxene adularia alkali feldspar austinite arsenates aegirine clinopyroxene autunite phosphates aegirine-augite clinopyroxene awaruite alloys aenigmatite aenigmatite group axinite group sorosilicates aeschynite niobates azurite carbonates agate silica minerals babingtonite rhodonite group aikinite sulfides baddeleyite oxides akaganeite oxides barbosalite phosphates akermanite melilite group barite sulfates alabandite sulfides barium feldspar feldspar group alabaster barium silicates silicates albite plagioclase barylite sorosilicates alexandrite oxides bassanite sulfates allanite epidote group bastnaesite carbonates and fluorides alloclasite sulfides bavenite chain silicates allophane clay minerals bayerite oxides almandine garnet group beidellite clay minerals alpha quartz silica minerals beraunite phosphates alstonite carbonates berndtite sulfides altaite tellurides berryite sulfosalts alum sulfates berthierine serpentine group aluminum hydroxides oxides bertrandite sorosilicates aluminum oxides oxides beryl ring silicates alumohydrocalcite carbonates betafite niobates and tantalates alunite sulfates betekhtinite sulfides amazonite alkali feldspar beudantite arsenates and sulfates amber organic minerals bideauxite chlorides and fluorides amblygonite phosphates biotite mica group amethyst
    [Show full text]
  • Industrial Minerals and Rocks in the 21St Century
    Industrial Minerals and Rocks in the 21st Century Milos Kuzvart Charles University, Prague NONMETALLICS: DEFINITION, CLASSIFICATION, OCCURENCE, ORIGIN, UTILIZATION The term 'industrial mineral' is not defined so strictly as the term 'ore' which is mostly a source of metal, or as that of 'fossil fuel' (coal, oil, natural gas), which is predominantly a source of energy. In both the latter cases the characteristic feature is the chemistry of the ore (besides the content of impurities, dressability, etc.) or fuel (besides the content of dirt bands, sulfur, etc.). The characteristic features of industrial minerals, however, líe in their physical properties (e.g., fibrosity of asbestos, insulatory properties of mica, the high specific gravity of barite). In this artiele raw materials of several types are considered under the term "industrial mineral s and rocks": 1. raw materials that are used in industry in variously prepared forms as minerals (e.g., talc, asbestos, diamond) or rocks (diatomite, bentonite, ochre); 2. raw material s that serve as a source of non-metallic elements (ftuorite for ftuori­ ne, apatite for phosphorus) or their simple compounds (e.g., borates for H3B03 or B 20 3); 3. raw materials of non-metallic habit that are source of metals, and also of their com­ pounds employed in other than metallurgical industries (e.g., beryl as a source of BeO, magnesite of MgO, bauxite or Al-rich laterite as a source of Alz03; all these three oxides are refractory materials); 4. building material s (rocks for aggregate, together with gravel and sand for concrete, decorative stone and roofing slate, limestone for cement and lime, brickloam).
    [Show full text]
  • The Calcination Behaviour of Fine-Sized Colemanite and Ulexite
    ISSN 2321 3361 © 2019 IJESC Research Article Volume 9 Issue No. 7 The Calcination Behaviour of Fine -Sized Colemanite and Ulexite Ore Under Conventional Heat Treatment Hoskan, Samil Graduate Student Department of Mining Engineering Dokuz Eylül University, İzmir, Turkey Abstract: Because waste material stroges and their enviromental problems are main problem in mining, re-use and evalaution of wastes are reasonable solutions. In this study, fine sized ( -3mm) waste Colemanite and Ulexite ores were exposured to conventional heat treatment in a spesific time (15-60 minute) to determine behaviour of ores under heat range bet ween 450C -600C. İn this study, beside measuring Boron calcination behaviour, it is targeted that seperating calcinated Boron minerals from unwanted minerals such as clay and calcite by screening. In order to make physical and chemical characterization of t he material to be used within the scope of experiments, 50 kg of Colemanite and Ulexite ore were taken and it was determined that 22,8% and 27,53% B2O3 grade respectively in chemical analysis. The sieve analysis of the samples were performed to determine c haracterization of the samples. The materials were dried and divided into 1 kg samples with cross -groove divider. After that, each 1 kg of samples were divided in to 125’gr of representative samples with small size cross -sectioned slicers and packaged for the planned experiments. Key words: Colemanite, Ulexite, Heat Treatment, Calcination, Boron . 1. INTRODUCTION were chosen on stock area and samples were taken from these locations. Boron combines with oxides and alkali ions in the earth crust to form minerals such as colemanite and ulexite.
    [Show full text]
  • Cal Poly Geology Club Death Valley Field Trip – 2004
    Cal Poly Geology Club Death Valley Field Trip – 2004 Guidebook by Don Tarman & Dave Jessey Field Trip Organizers Danielle Wall & Leianna Michalka DEATH VALLEY Introduction Spring 2004 Discussion and Trip Log Welcome to Death Valley and environs. During the next two days we will drive through the southern half of Death Valley and see some of the most spectacular geology and scenery in the United States. A detailed road log with mileages follows this short introductory section. We hope to keep the pace leisurely so that everyone can see as much as possible and have an opportunity to ask questions and enjoy the natural beauty of the region. IMPORTANT: WATER- carry and drink plenty. FUEL- have full tank upon leaving Stovepipe Wells or Furnace Creek (total driving distance approx. 150 miles). Participants must provide for their own breakfasts Saturday morning. Lunches will be prepared at the Stovepipe Wells campground before departing. We will make a brief stop at Furnace Creek visitor’s center and for fuel etc. Meeting Points Saturday morning meet in front at the Chevron station on the north side of the highway a short distance east of the campground (8:30 AM) Sunday morning (tentative- depending upon what our last stop is Saturday) meet at the Charles Brown highway intersection with 127 just at the south side of Shoshone. (8:30 AM). Get fuel before meeting. As you know we will be camping Saturday night between the hamlets of Shoshone and Tecopa. If for some reason you become separated from the main caravan during our journey Saturday – and this would be very difficult to accomplish- simply head for Shoshone/Tecopa.
    [Show full text]
  • Death Valley National Monument
    DEATH VALLEY NATIONAL MONUMENT CALIFORNIA NEVADA UNITED STATES DEPARTMENT OF THE INTERIOR DEATH VALLEY NATIONAL PARK SERVICE NATIONAL MONUMENT Contents DEATH VALLEY FROM BREAKFAST CANYON Cover Open all year • Regular season, October 15 to May 15 BEFORE WHITE MEN CAME 3 THE HISTORICAL DRAMA 4 cipitation at headquarters during the past TALES WRITTEN IN ROCK AND LANDSCAPE 5 DEATH VALLEY National Monument is distinguished by its desert scenery— 15 years has been 2.03 inches. DESERT WILDLIFE 10 a combination of unusual geology, flora, Summer daytime temperatures in the DESERT PLANTLIFE 11 fauna, and climate. Famed as a scene of valley itself are quite high. The maxi­ suffering in the gold-rush drama of mum air temperature of 134° F. in the INTERPRETIVE SERVICES 12 1849, Death Valley has long been shade recorded in Death Valley was a WHAT TO SEE AND DO WHILE IN THE MONUMENT 12 known to scientist and layman alike as world record until 1922 when 136.4° F. HOW TO REACH DEATH VALLEY 13 a region rich in scientific and human was reported from El Azizia, Libya. interest. The monument was established Higher locations on the mountains in the MONUMENT SEASON 14 in 1933 and covers almost 3,000 square monument have comfortable daytime WHAT TO WEAR 14 miles. temperatures and cool nights. ACCOMMODATIONS 14 The monument is in the rugged desert From late October until May, the val­ ADMINISTRATION 15 region east of the Sierra Nevada in east­ ley climate is usually very pleasant. ern California and southwestern Nevada. Days are often warm and sunny, nights PLEASE HELP PROTECT THIS MONUMENT 15 The valley itself is about 140 miles long, cool and invigorating, with the temper­ with the forbidding Panamint Range ature seldom below freezing.
    [Show full text]
  • Borax: History & Uses Borax Belongs to a Group of Boron Minerals Called Borates Resembling Quartz Crystals, Fibrous Cottonballs Or Earthy White Powders
    Borax: History & Uses Borax belongs to a group of boron minerals called borates resembling quartz crystals, fibrous cottonballs or earthy white powders. They originated in hot springs or vapors associated with the outpouring of volcanic rocks such as the colorful formations of Artists Drive. Seeping groundwater formed glassy borate veins in the extinct lakebeds of Furnace Creek and has moved soluble borates to modern salt flats such as the floor of Death Valley. There, evaporation has left a mixed white crust of salt, borax and alkalies. The history of borax in America began in earnest with the borax boom of the 1870s, when many California and Nevada salt flats were claimed by prospectors. One was Aaron Winters, who used the famous green-flame test to locate borax on a Death Valley salt marsh in 1881. His claims were soon purchased by W.T. Coleman, builder of Harmony Borax Works, where marsh muds were refined until 1889. The contemporary Eagle Borax Works folded in 1882 because of poor depos-its, summer heat and remoteness. Coleman’s company beat the heat by moving summer operation to the Amargosa Works near less- torrid Shoshone. The transportation problem was solved by hitching 20-mule teams to gigantic borax wagons with a payload in tandem of over 20 tons. By 1890, salt marsh operations were obsolete and F.M. “Borax” 20 Mule Team Wagon. Photo Courtesy of NPS. Smith consolidated most claims in the Pacific Coast Borax Company. He concentrated on mining glassy veins of a rich new borate in the Calico Mountains, south of Death Valley.
    [Show full text]