The Current Status of Iron Minerals in Indonesia
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Beneficiation of High Phosphorus Limonite Ore by Sodium- Carbonate-Added Carbothermic Reduction
ISIJ International, Vol. 52 (2012), No. 10, pp. 1757–1763 Beneficiation of High Phosphorus Limonite Ore by Sodium- carbonate-added Carbothermic Reduction Shaojun BAI,1) Shuming WEN,1,2)* Dianwen LIU,1) Wenbin ZHANG1) and Qinbo CAO1) 1) Faculty of Land Resources Engineering, Kunming University of Science and Technology, Kunming, Yunnan, 650093 PR China. E-mail: [email protected], [email protected], [email protected], [email protected] 2) Engineering Research Center and Ministry of Education for Efficient Utilization of Mineral Resources in Western of China, Kunming 650093, PR China. (Received on March 1, 2012; accepted on June 6, 2012) The characteristics of Huimin high phosphorus limonite ore and the beneficiation of this iron ore by sodium-carbonate-added carbothermic reduction, ultrafine grinding and magnetic separation were investi- gated. Iron particle size in reduced ore without Na2CO3 additive is tiny and the fayalite is abundant. It is indicated that the formation of fayalite is the main hindrance to accelerate the reduction of limonite. With a mass ratio of Na2O3 to ore of 10% additive, the reduction of limonite can be reinforced. The reinforcing affect may be caused by the increase of the reducing reaction activity of FeO and the acceleration of the carbon gasification reaction rate. Fluorapatite were not reduced in the low temperature reduction process and entered to gangue phases, after ultrafine grinding-magnetic separation process, a qualified iron con- centrate with 76.47% Fe, a recovery of 73.20% is obtained with simultaneous decrease in the phosphorus content down to 0.25%. KEY WORDS: iron ore; beneficiation; high phosphorus limonite ore; sodium carbonate; carbothermic reduc- tion; metallic iron; ultrafine grinding. -
Characterization of Soils A,\?) Saprolites from the Piedmont Region for M7aste Disposal Purposes
CHARACTERIZATION OF SOILS A,\?) SAPROLITES FROM THE PIEDMONT REGION FOR M7ASTE DISPOSAL PURPOSES Aziz Amoozegar, Philip J. Schoeneberger , and Michael J. Vepraskas Soil Science Department Agricultural Research Service College of Agriculture and Life Sciences North Carolina State University Raleigh, North Carolina 27695-7619 The activities on which this report is based were financed in part by the United States Department of the Interior, U. S. Geological Survey, through the Water Resources Research Institute of the University of North Carolina. Contents of this publication do not necessarily reflect the views and policies of the United States Department of the Interior, nor does mention of trade names or commercial products constitute their endorsement by the United States Government. Also, the use of trade names does not imply endorsement by the North Carolina Agricultural Research Service of the products named nor criticism of similar ones not mentioned. Agreement No. 14-08-0001-G1580 UWProject Number 70091 USGS Project No. 02(FY88) ACKNOWLEDGMENT Special recognition should be given to Ms. Barbara Pitman, former Agricultural Research Technician, Soil Science Department, who devoted long hours conducting the laboratory solute flow experiments and assisted with other field and laboratory investigations in this project. Thanks to Mr. Stewart J. Starr, College of Agriculture and Life Sciences, for providing land on Unit 1 Research Farm and for his patience with our research program. Appreciation is extended to Mr. Kevin Martin, president of Soil and Environmental Consultants, for his assistance in locating research sites, and to Mr. J. B. Hunt (Oak City Realty) and Mr. S. Dorsett (Dorsett and Associates) for allowing our research team to collect soil samples and conduct research on properties located in Franklin and Orange Counties, respectively. -
Eg9601814 Supergene Alteration of Magnetite And
EG9601814 SUPERGENE ALTERATION OF MAGNETITE AND PYRITE AND THE ROLE OF THEIR ALTERATION PRODUCTS IN THE FIXATION OF URANIUM FROM THE CIRCULATING MEDIA. BY MA EL GEMMIZI Nuclear Materials A uthority Cairo- Egypt. ABSTRACT. In most of the Egyptian altered radioactive granites, highly magnetic heavy particles were found to be radioactive. They are a mixture of several iron oxide minerals which are products of supergene alteration of the pre-existing hypogene iron-bearing minerals especially magnetite and pyrite. The end products of this supergene alteration are mainly hydrated iron oxide minerals limonite hematite and geothite. During the alteration, deformation and defects in the minerals structure took place , thereby promoting diffusion of the substitutional and interstitial ions (uranium) to words these sites The mechanism of the alteration of the hypogene iron-bearing minerals; magnetite and pyrite to form the secondary minerals hematite, limonite and geothite; the role of these minerals in fixing uranium from the ciculating media as well as the applicability of these minerals as indicators to the radioactivity of the host rocks were discussed. INTRODUCTION It is quite common that in all the altered rocks magnetite and to some extent pyrite which are present as accessories are suffering from some degrees of alteration. Magnetite and pyrite in the altered granite of Wadi Nugrus, El Missikat and £1 Aradyia, Eastern Desert was found by (1 & 2) to possess several degrees of alteration and crystal deformation. This means that both minerals are sensitive to postdepositional environmental changes. The granites of the present study were described as altered granites overlained by metasediments and underlained by magmatic bodies which invaded the granites itself by sills. -
The Brown Iron Ores of West- Middle Tennessee
ORTONMFMORIAI LIBRARY Please do not destroy or throw away this publication. If you have no further use for it, write to the Geological Survey at Washington and ask for a frank to return It DEPARTMENT OF THE INTERIOR Hubert Work, Secretary U. S. GEOLOGICAL SURVEY George Otis Smith, Director Bulletin 795 D THE BROWN IRON ORES OF WEST- MIDDLE TENNESSEE BY ERNEST F. BURCHARD Prepared in cooperation with the Tennessee Geological Surrey Contributions to economic geology, 1927, Part I (Pages 63-112) Published October 20,1927 UNITED STATES GOVERNMENT PRINTING OFFICE WASHINGTON 1927 ADDITIONAL COPIES OF THIS PUBLICATION MAT BE PROCURED FROM THE SUPERINTENDENT OF DOCUMENTS GOVERNMENT PRINTING OFFICE WASHINGTON, D. C. AT 15 CENTS PEE COPY CONTENTS Page Introduction 53 Earlier geologic work _ _ _______ 55 The early iron industry 57 Geography _ 58 Geology. _ - 60 Stratigraphy - 60 Structure_ _ _ ._ 64 The iron ores _ . __ _ _ 65 Distribution ______________________________ 65 Occurrence and character- ____________:______ 66 Position and form of deposits____________________ 66 Types of ore 66 Mineral composition.. __ ____ ______________ ' 67 Chemical composition___________________,__ __ 69 Topographic relations _ _ _ _ 71 Geologic relations _' ____ 72 Suggestions as to origin ______ _______________ 74 Typical deposits _ ____ __ 77 Stewart County : _ 77 Deposits near Bear Spring _________________ 78 Deposits near Stribling _ _ __________ 80 Montgomery County __ _ ______________ 84 Deposits near Louise _ _ _ __ 84 Dickson County ___________________________ -
Geology and Mineralogy of the Ape.X Washington County, Utah
Geology and Mineralogy of the Ape.x Germanium-Gallium Mine, Washington County, Utah Geology and Mineralogy of the Apex Germanium-Gallium Mine, Washington County, Utah By LAWRENCE R. BERNSTEIN U.S. GEOLOGICAL SURVEY BULLETIN 1577 DEPARTMENT OF THE INTERIOR DONALD PAUL HODEL, Secretary U.S. GEOLOGICAL SURVEY Dallas L. Peck, Director UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON: 1986 For sale by the Distribution Branch, Text Products Section U.S. Geological Survey 604 South Pickett St. Alexandria, VA 22304 Library of Congress Cataloging-in-Publication Data Bernstein, Lawrence R. Geology and mineralogy of the Apex Germanium Gallium mine, Washington County, Utah (U.S. Geological Survey Bulletin 1577) Bibliography: p. 9 Supt. of Docs. no.: I 19.3:1577 1. Mines and mineral resources-Utah-Washington County. 2. Mineralogy-Utah-Washington County. 3. Geology-Utah-Wasington County. I. Title. II. Series: United States. Geological Survey. Bulletin 1577. QE75.B9 no. 1577 557.3 s 85-600355 [TN24. U8] [553' .09792'48] CONTENTS Abstract 1 Introduction 1 Germanium and gallium 1 Apex Mine 1 Acknowledgments 3 Methods 3 Geologic setting 3 Regional geology 3 Local geology 3 Ore geology 4 Mineralogy 5 Primary ore 5 Supergene ore 5 Discussion and conclusions 7 Primary ore deposition 7. Supergene alteration 8 Implications 8 References 8 FIGURES 1. Map showing location of Apex Mine and generalized geology of surrounding region 2 2. Photograph showing main adit of Apex Mine and gently dipping beds of the Callville Limestone 3 3. Geologic map showing locations of Apex and Paymaster mines and Apex fault zone 4 4. Scanning electron photomicrograph showing plumbian jarosite crystals from the 1,601-m level, Apex Mine 6 TABLES 1. -
Virginia Division of Mineral Resources Minerals Of
VIRGINIA DIVISION OF MINERAL RESOURCES PUBLICATION 89 MINERALS OF ALBEMARLE COUNTY, VIRGINIA Richard S. Mitchell and William F. Giannini COMMONWEALTH OF VIRGINIA DEPARTMENT OF MINES, MINERALS AND ENERGY DIVISION OF MINERAL RESOURCES Robert C. Milici, Commissioner of Mineral Resources and State Geologist CHARLOTTESVILLE, VIRG INIA 1988 VIRGINIA DIVISION OF MINERAL RESOURCES PUBLICATION 89 MINERALS OF ALBEMARLE COUNTY, VIRGINIA Richard S. Mitchell and William F. Giannini COMMONWEALTH OF VIRGINIA DEPARTMENT OF MINES, MINERALS AND ENERGY DIVISION OF MINERAL RESOURCES Robert C. Milici, Commissioner of Mineral Resources and State Geologist CHARLOTTESVILLE. VIRGINIA 1 988 VIRGINIA DIVISION OF MINERAL RESOURCES PUBLICATION 89 MINERALS OF ALBEMARLE COUNTY, VIRGINIA Richard S. Mitchell and William F. Giannini COMMONWEALTH OF VIRGINIA DEPARTMENT OF MINES, MINERALS AND ENERGY DIVISION OF MINERAL RESOURCES Robert C. Milici, Commissioner of Mineral Resources and State Geologist CHARLOTTESVILLE, VIRGINIA 19BB DEPARTMENT OF MINES, MINERALS AND ENERGY RICHMOND, VIRGIMA O. Gene Dishner, Director COMMONWEALTH OF VIRGIMA DEPARTMENT OF PURCHASES AND SUPPLY RICHMOND Copyright 1988, Commonwealth of Virginia Portions of this publication may be quoted if credit is given to the Virginia Division of Mineral Resources. CONTENTS Page I I I 2 a J A Epidote 5 5 5 Halloysite through 8 9 9 9 Limonite through l0 Magnesite through muscovite l0 ll 1l Paragonite ll 12 l4 l4 Talc through temolite-acti 15 15 l5 Teolite group throug l6 References cited l6 ILLUSTRATIONS Figure Page 1. Location map of I 2. 2 A 4. 6 5. Goethite 6 6. Sawn goethite pseudomorph with unreplaced pyrite center .......... 7 7. 1 8. 8 9. 10. 11. -
Chemical Mass Balance of Calcrete Genesis on the Toledo Granite (Spain)
CHEMICAL GEOLOGY i\mirise ISOTOPE GEOSCIE.\'CE Chemical Geology 170 (2000) 19-35 \vww.elsevirr.coni/locate/chemgeo Chemical mass balance of calcrete genesis on the Toledo granite (Spain) Arnaud Chiquet a. * , Fabric olili b, Bruno Hamelin a, Annie Michard a, miel Nahon a UP O.!+ CEREGE. UiWR 6536. CiYRS/ UttiivrsiiG Ai.r-n-lor.veillr111, SO. 13535 Ai.r-c~ti-Pivi.eiice,cet le.^ Frotlce " CEREGE, UAIR 6336. ORSTOM/ UiiiLw.yi/8 Ai.r-Mntrri/lr 111. BI' SO. 135-35Ai.r-etr-Plvi~rricc~. Cedes 0-3, France Received 15 April 199s; acceptcd 12 Slay I999 Abstract The chernical mass balance of cnlcrete genesis is studied on a typical sequence developed in granite, in the Toledo mountains. Central Spain. Field evidence and petrographic observations indicate that the texture and the bulk volume of the parent rock are strictly preserved all along the studied cnlcrete profile. hlicroscopic observations indicate that the calcitizatinn process starts within the saprolite, superimposed on the usual nieclianisnis of granite weathering: the fresh rock is first weathered to secondary clays. mainly smectites, \vhicli are then pseudoniorphically replaced by calcite. Based on this evidence. chemical inass tiansfers are calculated. assuming ¡so-volume transformation from the parent rock to the calcrete. The mass balance results show the increasing loss of matter due to weathering of the primary phases, from the saprolite towards the calcrete layers higher in the sequence. Zr, Ti or Th, which are classically considered as immobile during weuthering, are also depleted along the profile, especially in the calcrete layer. This results from the prevailing highly alkaline conditions, which could account for the simultaneous precipitation of CaCO, and silicate dissolution. -
Weathering Profiles and Clay Mineralogical Developments, Bornholm, Denmark
Weathering profiles and clay mineralogical developments, Bornholm, Denmark Pingchuan Tan1, 2, Nikolas Oberhardt1, Henning Dypvik1,2, Lars Riber1, Ray E. Ferrell Jr3. 1 Department of Geoscience, University of Oslo, P.O.BOX 1047, Blindern, NO-0316 Oslo, Norway 2 Centre for Earth Evolution and Dynamics, University of Oslo, P.O.BOX 1028, Blindern, NO-0315 Oslo, Norway 3 Department of Geology & Geophysics, Louisiana State University, Baton Rouge, LA, 70803, USA Corresponding author – Pingchuan Tan: [email protected] ABSTRACT Saprock-saprolite associations were studied by field and laboratory methods (optical microscopy, X-ray powder diffraction, scanning electron microscopy, electron microprobe) in order to describe regolith development in the crystalline rocks of the Nygård kaolin pit (Bornholm, Denmark). The clay sequences and stages of porosity development are similar to those observed for reservoir rocks from the Utsira High (Riber, L., Dypvik, H., Sørlie, R. and Ferrell, R. (2016) Clay minerals in deeply buried paleoregolith profiles, Norwegian North Sea. Clays and Clay Minerals, in press). The weathering of the parent granite began before the end of the Mesozoic. Two stages of syn- /pre-burial alteration, followed by diagenesis during burial, and then post-uplift weathering have been recognized. In stage Ι, plagioclase and some biotite (biotite-vermiculite-kaolinite) reacted to form elongate booklets of highly-ordered kaolinite or smaller, blocky pseudohexagonal crystals. Stage II represented more extreme weathering developed along local fracture systems. The higher potential for fluid flow in the fractures caused highly-ordered kaolinite to alter to halloysitic, poorly- ordered kaolinite. Plagioclase, biotite, and K-feldspar continued to interact with formation water and formed additional quantities of secondary clay minerals. -
Landslides and the Weathering of Granitic Rocks
Geological Society of America Reviews in Engineering Geology, Volume III © 1977 7 Landslides and the weathering of granitic rocks PHILIP B. DURGIN Pacific Southwest Forest and Range Experiment Station, Forest Service, U.S. Department of Agriculture, Berkeley, California 94701 (stationed at Arcata, California 95521) ABSTRACT decomposition, so they commonly occur as mountainous ero- sional remnants. Nevertheless, granitoids undergo progressive Granitic batholiths around the Pacific Ocean basin provide physical, chemical, and biological weathering that weakens examples of landslide types that characterize progressive stages the rock and prepares it for mass movement. Rainstorms and of weathering. The stages include (1) fresh rock, (2) core- earthquakes then trigger slides at susceptible sites. stones, (3) decomposed granitoid, and (4) saprolite. Fresh The minerals of granitic rock weather according to this granitoid is subject to rockfalls, rockslides, and block glides. sequence: plagioclase feldspar, biotite, potassium feldspar, They are all controlled by factors related to jointing. Smooth muscovite, and quartz. Biotite is a particularly active agent in surfaces of sheeted fresh granite encourage debris avalanches the weathering process of granite. It expands to form hydro- or debris slides in the overlying material. The corestone phase biotite that helps disintegrate the rock into grus (Wahrhaftig, is characterized by unweathered granitic blocks or boulders 1965; Isherwood and Street, 1976). The feldspars break down within decomposed rock. Hazards at this stage are rockfall by hyrolysis and hydration into clays and colloids, which may avalanches and rolling rocks. Decomposed granitoid is rock migrate from the rock. Muscovite and quartz grains weather that has undergone granular disintegration. Its characteristic slowly and usually form the skeleton of saprolite. -
Limonite Deposits Near Scappoose Columbia County Oregon
Limonite Deposits Near Scappoose Columbia County Oregon By PRESTON E. HOTZ A CONTRIBUTION TO ECONOMIC GEOLOGY GEOLOGICAL SURVEY BULLETIN 982-C A description of low-grade iron * deposits of economic interest UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1953 UNITED STATES DEPARTMENT OF THE INTERIOR DOUGLAS McKAY, Secretary GEOLOGICAL SURVEY W. E. WRATHER, Director For sale by the Superintendent of Documents, U. S. Government Printing Office Washington 25, D. C. - Price 65 cents CONTENTS Page Abstract_ _______________________________________________________ 75 Introduction ______________________________________________________ 75 Purpose and scope____-_____.__-_____________._________________ 75 Acknowledgments__ __________________________________________ 76 History.______.___-__-_-____---_--_-_-_--_____-_-_____________ 76 Previous work_______________________________________________ 76 Geography.._ __________--_---_-_-_--___--__--_-___________________ 77 Geology..._-__-__--__-------_---------_---------------__--____. 78 Stratigraphy. _________ ^ . ______________________________________ 78 Oligocene sedimentary rocks._______________________________ 78 Columbia River basalt--___________________________________ 79 Troutdale formation _______________________________________ 80 Terrace deposits.._________________________________________ 81 Recent alluvium.__________________________________________ 81 Structure..___________________________________________________ 81 Ore deposits. _-______---___--____-__--_-________-___________ 81 Distribution__ -
Data of Geochemistry
Data of Geochemistry ' * Chapter W. Chemistry of the Iron-rich Sedimentary Rocks GEOLOGICAL SURVEY PROFESSIONAL PAPER 440-W Data of Geochemistry MICHAEL FLEISCHER, Technical Editor Chapter W. Chemistry of the Iron-rich Sedimentary Rocks By HAROLD L. JAMES GEOLOGICAL SURVEY PROFESSIONAL PAPER 440-W Chemical composition and occurrence of iron-bearing minerals of sedimentary rocks, and composition, distribution, and geochemistry of ironstones and iron-formations UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1966 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretary GEOLOGICAL SURVEY William T. Pecora, Director For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price 45 cents (paper cover) CONTENTS Page Face Abstract. _ _______________________________ Wl Chemistry of iron-rich rocks, etc. Continued Introduction. _________ ___________________ 1 Oxide facies Continued Iron minerals of sedimentary rocks __ ______ 2 Hematitic iron-formation of Precambrian age__ W18 Iron oxides __ _______________________ 2 Magnetite-rich rocks of Mesozoic and Paleozoic Goethite (a-FeO (OH) ) and limonite _ 2 age___________-__-._____________ 19 Lepidocrocite (y-FeO(OH) )________ 3 Magnetite-rich iron-formation of Precambrian Hematite (a-Fe2O3) _ _ _ __ ___. _ _ 3 age._____-__---____--_---_-------------_ 21 Maghemite (7-Fe203) __ __________ 3 Silicate facies_________________________________ 21 Magnetite (Fe3O4) ________ _ ___ 3 Chamositic ironstone____--_-_-__----_-_---_- 21 3 Silicate iron-formation of Precambrian age_____ 22 Iron silicates 4 Glauconitic rocks__-_-____--------__-------- 23 4 Carbonate facies______-_-_-___-------_---------- 23 Greenalite. ________________________________ 6 Sideritic rocks of post-Precambrian age._______ 24 Glauconite____ _____________________________ 6 Sideritic iron-formation of Precambrian age____ 24 Chlorite (excluding chamosite) _______________ 7 Sulfide facies___________________________ 25 Minnesotaite. -
Study of the Calcination Process of Two Limonitic Iron Ores Between 250 °C and 950 °C
Lisbeth Longa-Avello - Cristina Pereyra-Zerpa - Julio Andrés Casal-Ramos - Pedro Delvasto Study of the calcination process of two limonitic iron ores between 250 °C and 950 °C Estudio del proceso de calcinación en dos minerales de hierro limoníticos entre 250 °C y 950 °C Estudo do processo de calcinação em dois minerais de ferro limoníticos entre 250 °C e 950 °C Lisbeth Longa-Avello* Cristina Pereyra-Zerpa** Fecha de recepción: 20 de septiembre de 2016 Julio Andrés Casal-Ramos*** Fecha de aprobación: 20 de marzo de 2017 Pedro Delvasto**** Abstract The dehydration process of two limonitic ores from Venezuela was studied between 250 °C and 950 °C by means of thermogravimetry, infrared spectroscopy, and x-ray diffraction. These techniques indicated for both minerals that the goethite-to-hematite transformation occurred in the range of 250-350 °C. In addition, the x-ray diffraction showed a structural re-arrangement within the orebody above 350 °C, temperature above which only the hematite structure is recognizable. Finally, infrared spectroscopy revealed that such transformation implies the loss of structural OH- functional groups, characteristic of the limonite. Keywords: Iron Ore; Limonite; Thermal Modification of Minerals. Resumen Se estudió el proceso de deshidratación de dos minerales limoníticos de Venezuela entre 250 °C y 950 °C, usando termogravimetría, espectroscopia infrarroja y difracción de rayos x. Para ambos materiales, estas técnicas indicaron que la transformación de goethita a hematita ocurrió en el rango de 250 °C a 350 °C. Adicionalmente, la difracción de rayos X mostró un rearreglo estructural dentro de la mena a una temperatura por encima de 350 °C; a temperaturas mayores, solo se reconoce la estructura de la hematita.