Kinetics of Selenium and Tellurium Removal with Cuprous Ion from Copper Sulfate-Sulfuric Acid Solution
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Inorganic Selenium and Tellurium Speciation in Aqueous Medium of Biological Samples
1 INORGANIC SELENIUM AND TELLURIUM SPECIATION IN AQUEOUS MEDIUM OF BIOLOGICAL SAMPLES ________________________ A Thesis Presented to The Faculty of the Department of Chemistry Sam Houston State University ________________________ In Partial fulfillment Of the Requirements for the Degree of Master of Science ________________________ by Rukma S. T. Basnayake December, 2001 2 INORGANIC SELENIUM AND TELLURIUM SPECIATION IN AQUEOUS MEDIUM OF BIOLOGICAL SAMPLES by Rukma S.T. Basnayake _______________________________ APPROVED: ________________________________ Thomas G. Chasteen, Thesis Director ________________________________ Paul A. Loeffler ________________________________ Benny E. Arney Jr. APPROVED: _____________________________ Dr. Brian Chapman, Dean College of Arts and Sciences 3 ABSTRACT Basnayake, Rukma ST, Inorganic Selenium and Tellurium Speciation in Aqueous Medium of Biological Samples, Master of Science (Chemistry), December 2001, Sam Houston State University, Huntsville, Texas, 60 pp. Purpose The purpose of this research was to develop methods to study the ability of bacteria, Pseudomonas fluorescens K27 to detoxify tellurium and selenium salts by biotransformation processes under anaerobic conditions. Another purpose was to make an effort to separate biologically produced Se0 from cells. Methods Pseudomonas fluorescens K27 was grown in TSN3 medium (tryptic soy broth with 0.3% nitrate) under anaerobic conditions and the production of elemental tellurium and elemental selenium was observed when amended with inorganic tellurium salts and selenium salts, respectively. The amount of soluble tellurium species in the culture medium also was determined. Samples from a 2.75 L bioreactor were taken after cultures had reached the stationary growth phase and were centrifuged in order to separate insoluble species (elemental tellurium, elemental selenium) from soluble species (oxyanions of tellurium, oxyanions of selenium). -
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Preparation of Telluric Acid from Tellurium Dioxide by Oxidation with Potassium Permanganate Frank C. Mathers, Charles M. Rice, Howard Broderick, and Robert Forney, Indiana University General Statement Tellurium dioxide, Te0 2 , although periodically similar to sulfur dioxide, cannot be oxidized by nitric acid to the valence of six, i.e., to telluric acid, H 2 Te04.2H 2 0. Among the many stronger oxidizing agents that will produce this oxidation, potassium permanganate in a nitric acid solution is quite satisfactory. This paper gives directions and data for the preparation of telluric acid by this reaction. The making of telluric acid is a desirable laboratory experiment because (1) tellurim dioxide is available in large quantities and is easily obtained, (2) the telluric acid is a stable compound, easily purified, easily crystallized, and non-corrosive, and (3) students are interested in experimenting with the rarer elements. The small soluibility of telluric acid and the high solubility of both manganese and potassium nitrates in nitric acidi gives a sufficient differ- ence in properties for successful purification by crystallization of the telluric acid. Methods of Analyses Tellurium dioxide can be volumetrically 2 titrated in a sulfuric acid solution by an excess of standard potassium permanganate, followed by enough standard oxalic acid to decolorize the excess of permanganate. The excess of oxalic acid must then be titrated by more of the perman- ganate. The telluric acid can be titrated, like any ordinary monobasic acid, 3 (1911). with standard sodium hydroxide using phenolphthalein as an indicator, if an equal volume of glycerine is added. If any nitric acid is present, it must be neutralized first with sodium hydroxide, using methyl orange as indicator. -
Developing a Method for Determining the Mass Balance of Selenium and Tellurium Bioprocessed by a Selenium-Resistant Bacterium Grown in The
Developing a Method for Determining the Mass Balance of Selenium and Tellurium Bioprocessed by a Selenium-Resistant Bacterium Grown in the Presence of Selenite or Tellurite __________________ A Thesis Presented to The Faculty of the Department of Chemistry Sam Houston State University ____________________ In Partial Fulfillment Of the Requirements for the Degree of Master of Science ____________________ by Janet Horton Bius December, 2001 Developing a Method for Determining the Mass Balance of Selenium and Tellurium Bioprocessed by a Selenium-Resistant Bacterium Grown in the Presence of Selenite or Tellurite by Janet Horton Bius ____________________ Approved: _____________________________ Thomas G. Chasteen ____________________________ Mary F. Plishker ____________________________ Rick C. White Approved: ____________________________ Brian Chapman, Dean College of Arts and Sciences II ABSTRACT Bius, Janet Horton, Developing a Method for Determining the Mass Balance of Selenium and Tellurium Bioprocessed by a Selenium-Resistant Bacterium Grown in the Presence of Selenite or Tellurite, Master of Science (Chemistry), December, 2001. Sam Houston State University, Hunts- ville, Texas, 68 pp. Purpose The purpose of this investigation was to determine: (1) the mass balance of selenium or tellurium that was bioreduced when a selenium-resistant facultative anaerobe was amended with either selenium or tellurium; and (2) methods to analyze for these metalloids in biological samples. Methods Analytical methods were developed for the determination of -
A Review of the Structural Architecture of Tellurium Oxycompounds
Mineralogical Magazine, May 2016, Vol. 80(3), pp. 415–545 REVIEW OPEN ACCESS A review of the structural architecture of tellurium oxycompounds 1 2,* 3 A. G. CHRISTY ,S.J.MILLS AND A. R. KAMPF 1 Research School of Earth Sciences and Department of Applied Mathematics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA [Received 24 November 2015; Accepted 23 February 2016; Associate Editor: Mark Welch] ABSTRACT Relative to its extremely low abundance in the Earth’s crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. -
(%.(Zwj-2Mk Date
The behavior of tellurium during copper ore processing at the American Smelting and Refining Company (Tucson, AZ) Item Type Thesis Authors Josephson, Amy E. Download date 10/10/2021 10:50:30 Link to Item http://hdl.handle.net/11122/6826 THE BEHAVIOR OF TELLURIUM DURING COPPER ORE PROCESSING AT THE AMERICAN SMELTING AND REFINING COMPANY (TUCSON, AZ) By Amy E. Josephson RECOMMENDED: \k/ — Dr. Rainer J. Newberry Dr. Thomas P. Trainor Dr. Sarah M. Hayes Advisory Committee Chair Dr. Thomas K. Green Chair, Department of Chemistry and Biochemistry APPROVED: Dr. Paul W. Layer Dean, College of Nat and Mathematics Dean of the Graduate School ... (%.(ZwJ-2Mk Date / THE BEHAVIOR OF TELLURIUM DURING COPPER ORE PROCESSING AT THE AMERICAN SMELTING AND REFINING COMPANY (TUCSON, AZ) By Amy E. Josephson, B.S. A Thesis Submitted in Partial Fulfillment of the Requirements for the Degree of Master of Science in Environmental Chemistry University of Alaska Fairbanks August 2016 APPROVED: Sarah M. Hayes, Committee Chair Rainer J. Newberry, Committee Member Thomas P. Trainor, Committee Member Thomas K. Green, Chair Department of Chemistry and Biochemistry Paul W. Layer, Dean College of Natural Science and Mathematics Michael A. Castellini, Dean of the Graduate School Abstract Essentially all tellurium (Te), an element used in solar panels and other high technology devices, is recovered as a byproduct of copper mining. Recent increases in demand have sparked questions of long-term supplies of Te (crustal abundance ~3 pg-kg"1). As part of a larger study investigating Te resources, this project examines the behavior of Te during Cu ore mining, smelting, and refining at the American Smelting and Refining Company (Tucson, AZ) as a first step toward optimizing Te recovery. -
List of Lists
United States Office of Solid Waste EPA 550-B-10-001 Environmental Protection and Emergency Response May 2010 Agency www.epa.gov/emergencies LIST OF LISTS Consolidated List of Chemicals Subject to the Emergency Planning and Community Right- To-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act • EPCRA Section 302 Extremely Hazardous Substances • CERCLA Hazardous Substances • EPCRA Section 313 Toxic Chemicals • CAA 112(r) Regulated Chemicals For Accidental Release Prevention Office of Emergency Management This page intentionally left blank. TABLE OF CONTENTS Page Introduction................................................................................................................................................ i List of Lists – Conslidated List of Chemicals (by CAS #) Subject to the Emergency Planning and Community Right-to-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act ................................................. 1 Appendix A: Alphabetical Listing of Consolidated List ..................................................................... A-1 Appendix B: Radionuclides Listed Under CERCLA .......................................................................... B-1 Appendix C: RCRA Waste Streams and Unlisted Hazardous Wastes................................................ C-1 This page intentionally left blank. LIST OF LISTS Consolidated List of Chemicals -
Laboratory and Chemical Storage Areas Must Be Kept Locked When Not in Use
CHEMICAL HYGIENE PLAN AND HAZARDOUS MATERIALS SAFETY MANUAL FOR LABORATORIES This is the Chemical Hygiene Plan specific to the following areas: Laboratory name or room number(s): ___________________________________ Building: __________________________________________________________ Supervisor: _______________________________________________________ Department: _______________________________________________________ EMERGENCY TELEPHONE NUMBERS: 911 for Emergency and urgent consultation 3-2035 MSU Police; 3-2066 Facilities Management 3-2179 or (606) 207-0629 Eddie Frazier, Director of Risk Management 3-2584 or (606) 207-9425 Holly Niehoff, Environmental Health & Safety Specialist 3-2099 Derek Lewis, Environmental Health & Safety Technician 3-______ Building Supervisor State 24-hour warning point for HAZMAT Spill Notification If you need to report a spill in accordance with SARA Title III Section 304 and KRS 39E.190, please contact the Duty Officer at the Commonwealth Emergency Operations Center at 800.255.2587 which serves as the twenty-four (24) hour warning point and contact for the Commonwealth Emergency Response Commission. Updated 2018 All laboratory chemical use areas must maintain a work-area specific Chemical Hygiene Plan which conforms to the requirements of the OSHA Laboratory Standard 29 CFR 19190.1450. Morehead State UniversityMorehead laboratories State may Chemical use this document Hygiene Plan as a starting point for creating their work area specific Chemical Hygiene Plan (CHP). MSU Laboratory Awareness Certification For CHP of (Professor, Building, Room)________________________ The Occupational Safety and Health Administration (OSHA) requires that laboratory employees be made aware of the Chemical Hygiene Plan at their place of employment (29 CFR 1910.1450). The Morehead State University Chemical Hygiene Plan and Hazardous Materials Safety Manual serves as the written Chemical Hygiene Plan (CHP) for laboratories using chemicals at Morehead State University. -
Metals-10-01176.Pdf
metals Article Selective Recovery of Tellurium from the Tellurium-Bearing Sodium Carbonate Slag by Sodium Sulfide Leaching Followed by Cyclone Electrowinning Zhipeng Xu 1,2,3, Zoujiang Li 1,2, Dong Li 1,2, Xueyi Guo 1,2,*, Ying Yang 1,2, Qinghua Tian 1,2,* and Jun Li 1,2 1 School of Metallurgy and Environment, Central South University, Changsha 410083, China; [email protected] (Z.X.); [email protected] (Z.L.); [email protected] (D.L.); [email protected] (Y.Y.); [email protected] (J.L.) 2 National & Regional Joint Engineering Research Center of Nonferrous Metal Resource Recycling, Changsha 410083, China 3 First Materials Co., Ltd., Qingyuan 511517, China * Correspondence: [email protected] (X.G.); [email protected] (Q.T.); Tel.: +86-731-8887-6255 (X.G.); +86-731-8887-7863 (Q.T.) Received: 27 July 2020; Accepted: 19 August 2020; Published: 1 September 2020 Abstract: The rigorous environmental requirements promote the development of new processes with short and clean technical routes for recycling tellurium from tellurium-bearing sodium carbonate slag. In this paper, a novel process for selective recovery of tellurium from the sodium carbonate slag by sodium sulfide leaching, followed by cyclone electrowinning, was proposed. 88% of tellurium was selectively extracted in 40 g/L Na2S solution at 50 ◦C for 60 min with a liquid to solid ratio of 8:1 mL/g, while antimony, lead and bismuth were enriched in the leaching residue. Tellurium in the leach liquor was efficiently electrodeposited by cyclone electrowinning without purification. The effects of current density, temperature and flow rate of the electrolyte on current efficiency, tellurium recovery, cell voltage, energy consumption, surface morphology, and crystallographic orientations were systematically investigated. -
Extreme Environments and High-Level Bacterial Tellurite Resistance
microorganisms Review Extreme Environments and High-Level Bacterial Tellurite Resistance Chris Maltman 1,* and Vladimir Yurkov 2 1 Department of Biology, Slippery Rock University, Slippery Rock, PA 16001, USA 2 Department of Microbiology, University of Manitoba, Winnipeg, MB R3T 2N2, Canada; [email protected] * Correspondence: [email protected]; Tel.: +724-738-4963 Received: 28 October 2019; Accepted: 20 November 2019; Published: 22 November 2019 Abstract: Bacteria have long been known to possess resistance to the highly toxic oxyanion tellurite, most commonly though reduction to elemental tellurium. However, the majority of research has focused on the impact of this compound on microbes, namely E. coli, which have a very low level of resistance. Very little has been done regarding bacteria on the other end of the spectrum, with three to four orders of magnitude greater resistance than E. coli. With more focus on ecologically-friendly methods of pollutant removal, the use of bacteria for tellurite remediation, and possibly recovery, further highlights the importance of better understanding the effect on microbes, and approaches for resistance/reduction. The goal of this review is to compile current research on bacterial tellurite resistance, with a focus on high-level resistance by bacteria inhabiting extreme environments. Keywords: tellurite; tellurite resistance; extreme environments; metalloids; bioremediation; biometallurgy 1. Introduction Microorganisms possess a wide range of extraordinary abilities, from the production of bioactive molecules [1] to resistance to and transformation of highly toxic compounds [2–5]. Of great interest are bacteria which can convert the deleterious oxyanion tellurite to elemental tellurium (Te) through reduction. Currently, research into bacterial interactions with tellurite has been lagging behind investigation of the oxyanions of other metals such as nickel (Ni), molybdenum (Mo), tungsten (W), iron (Fe), and cobalt (Co). -
Alternative Electrochemical Salt Waste Forms, Summary of FY11-FY12 Results
CRADA-PROTECTED INFORMATION Alternative Electrochemical Salt Waste Forms, Summary of FY11-FY12 Results Prepared for U.S. Department of Energy B.J. Riley, J.S. McCloy, J.V. Crum, W.C. Lepry, C.P. Rodriguez, C.F. Windisch Jr., J. Matyas, M.P. Westman, B.T. Rieck, J.B. Lang, M.J. Olszta, and D.A. Pierce Pacific Northwest National Laboratory January 17, 2014 FCRD-SWF-2013-000025, Rev.1 PNNL-22034 CRADA-PROTECTED INFORMATION CRADA-PROTECTED INFORMATION DISCLAIMER This information was prepared as an account of work sponsored by an agency of the U.S. Government. Neither the U.S. Government nor any agency thereof, nor any of their employees, makes any warranty, expressed or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness, of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. References herein to any specific commercial product, process, or service by trade name, trade mark, manufacturer, or otherwise, does not necessarily constitute or imply its endorsement, recommendation, or favoring by the U.S. Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the U.S. Government or any agency thereof. CRADA-PROTECTED INFORMATION Alternative Electrochemical Salt Waste Forms, Summary of FY11-FY12 Results January 17, 2014 iii SUMMARY The Fuel Cycle Research and Development Program, sponsored by the U.S. Department of Energy Office of Nuclear Energy, is currently investigating alternative waste forms for wastes generated from nuclear fuel processing. -
Study of the Preparation of Telluric Acid and Its Application in Analytical
A STUDY OF THE PRI-PARATION OP TELLURIC ACID A: r US APPLICATION IN ANALYTICAL CHE by . !£N HORNER B« S«, Franklin and Marshall College, 1949 A THESIS submitted in partial fulfillment of the requirements for the degree MAST Department of Chemistry KANSAS STA GB OF AGRICULTU L AND APPLIED SC 1951 &0<LUl~ ii ^1*8 T4 \<V$I Hlol TABLE OP CONTENTS I Oo i INTRODUCTION ft* 1 EXPERIMENTAL 5 Volumetric Determination of Tellurium Dioxide 5 Purification of Tellurium Dioxide . 13 Determination of the Solubility of Telluric Acid and Tellurixim Dioxide in Concentrated Ammonium Hydroxide ..... 13 Preparation of Telluric Acid ... 14 Determination of the Purity of Telluric Acid 20 The Determination of Barium by Homogeneous Precipitation as Barium Tollurate . 21 DISCUSSION 25 SUMMARY 27 ACK 29 LITERATURE CITED 30 INTRODUCTION The studies reported upon In this paper were directed towards (1) The preparation of telluric acid, and (2) the homogeneous precipitation of barium and similar Ions as tellurates. A review of the literature shows that there have been several methods of preparing telluric acid. Meyer and Franke (4) oxidized the elementary tellurium with a mixture of barium chlorate and sulfuric acid. Krepelka and Kubik (2) oxidized the elementary tellurium with 30 percent hydrogen peroxide, but their method necessitated using a 10-15 fold excess of the oxidizing agent. Staundenmaier (9) reacted a mixture of nitric and chromic acids with tellurium dioxide to effect oxidation to telluric acid. The procedure as developed by Mathers et al. (3) is the most widely used. Crude tellurium dioxide is purified and then oxidized by a slight excess of permanganate in a hot solution of about five molar nitric acid. -
Chemical Compatibility Storage Group
CHEMICAL SEGREGATION Chemicals are to be segregated into 11 different categories depending on the compatibility of that chemical with other chemicals The Storage Groups are as follows: Group A – Compatible Organic Acids Group B – Compatible Pyrophoric & Water Reactive Materials Group C – Compatible Inorganic Bases Group D – Compatible Organic Acids Group E – Compatible Oxidizers including Peroxides Group F– Compatible Inorganic Acids not including Oxidizers or Combustible Group G – Not Intrinsically Reactive or Flammable or Combustible Group J* – Poison Compressed Gases Group K* – Compatible Explosive or other highly Unstable Material Group L – Non-Reactive Flammable and Combustible, including solvents Group X* – Incompatible with ALL other storage groups The following is a list of chemicals and their compatibility storage codes. This is not a complete list of chemicals, but is provided to give examples of each storage group: Storage Group A 94‐75‐7 2,4‐D (2,4‐Dichlorophenoxyacetic acid) 94‐82‐6 2,4‐DB 609-99-4 3,5-Dinitrosalicylic acid 64‐19‐7 Acetic acid (Flammable liquid @ 102°F avoid alcohols, Amines, ox agents see SDS) 631-61-8 Acetic acid, Ammonium salt (Ammonium acetate) 108-24-7 Acetic anhydride (Flammable liquid @102°F avoid alcohols see SDS) 79‐10‐7 Acrylic acid Peroxide Former 65‐85‐0 Benzoic acid 98‐07‐7 Benzotrichloride 98‐88‐4 Benzoyl chloride 107-92-6 Butyric Acid 115‐28‐6 Chlorendic acid 79‐11‐8 Chloroacetic acid 627‐11‐2 Chloroethyl chloroformate 77‐92‐9 Citric acid 5949-29-1 Citric acid monohydrate 57-00-1 Creatine 20624-25-3