Removal of Hazardous Oxyanions from the Environment Using Metal-Oxide-Based Materials
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Naming Polyatomic Ions and Acids Oxyanions
Oxyanions Naming Polyatomic Ions and Oxyanions Acids Oxyanions- negative ions containing Oxyanions may contain the prefix oxygen. “hypo-”, less than, or “per-”, more than. These have the suffix “-ate” or “-ite” For example - “-ate” means it has more oxygen atoms ClO4 Perchlorate bonded, “-ite” has less - ClO3 Chlorate For example - ClO2 Chlorite 2- SO4 sulfate ClO- Hypochlorite 2- SO3 sulfite Acids Naming acids Naming Acids Certain compounds produce H+ ions in Does it contain oxygen? water, these are called acids. If it does not, it gets the prefix “hydro-” and If it does contain an oxyanion, then the suffix “-ic acid” replace the ending. You can recognize them because the neutral compound starts with “H”. HCl If the ending was “–ate”, add “-ic acid” Hydrochloric acid If the ending was “–ite”, add “-ous acid” For example HCl, H2SO4, and HNO3. HF Don’t confuse a polyatomic ion with a H2SO4 Sulfuric Acid Hydrofluoric acid neutral compound. H2SO3 Sulfurous Acid HCN HCO - is hydrogen carbonate, not an acid. 3 Hydrocyanic acid Examples Examples Nomenclature (naming) of Covalent compounds HNO3 HNO3 Nitric Acid HI HI Hydroiodic acid H3AsO4 H3AsO4 Arsenic Acid HClO2 HClO2 Chlorous Acid 1 Determining the type of bond Covalent bonding is very Covalent bonding is very First, determine if you have an ionic different from ionic naming compound or a covalent compound. similar to ionic naming A metal and a nonmetal will form an You always name the one that is least Ionic names ignored the subscript ionic bond. electronegative first (furthest from because there was only one possible Compounds with Polyatomic ions form fluorine) ratio of elements. -
Molybdates: an Alternative to Hexavalent Chromates in Corrosion
Molybdates: An Alternative to Hexavalent Chromates 3ytzt7n2 in Corrosion Prevention and Control qz ,+ B3 F Stiles C. Thompson Sverdrup Technology, Inc. 626 Anchors St. NW Fort Walton Beach, FL 32548 (904) 833-7600 Introduction Hexavalent chromates have been the preferred corrosion inhibitor in military systems for years. Chromate conversion coatings are specified in MIL-STD-808, “Finishes, Materials and Processes for Corrosion Prevention and Control in Support Equipment ”, for aluminum, magnesium, and plated steel. A number of primers are formulated with zinc or strontium chromate. Passivation treatments for stainless steels frequently specify chromic acid. Some anodic coatings specify baths containing chromic and sulfuric acid and a pcst treatment or rinse with aqueous sodium dichromate. Even water-based primers formulated for volatile organic I compound (VOC) compliance in such areas as southern California contain chromate-based corrosion inhibitors. Chromates are decreasing in industrial use, however, as concerns about their environmental risks and toxicity increase. One pollution prevention approach is to substitute analogs of chromates in similar applications. Molybdate is one such analog of lower toxicity. Federal Environmental Regulations A number of environmental regulations now control hexavalent chromate. Toxic Substances Control Act (TSCA). Under TSCA, the Environmental Protection Agency @PA) must be notified 90 days prior to manufacture. EPA may restrict or prohibit manufacture where there is unreasonable risk to the environment. EPA also has the authority to require testing for health or environmental effects. No current regulation specifies molybdate. Resource Conservation and Recovery Act (RCRA). RCRA regulates the treatment, storage, transportation, and disposal of hazardous waste (HW). The EPA HW number for hexavalent chromium is D007. -
And Inter-Protein Couplings of Backbone Motions Underlie
www.nature.com/scientificreports OPEN Intra- and inter-protein couplings of backbone motions underlie protein thiol-disulfde exchange cascade Received: 26 July 2018 Wenbo Zhang1,3, Xiaogang Niu2,3, Jienv Ding1,3,5, Yunfei Hu2,3,6 & Changwen Jin1,2,3,4 Accepted: 6 October 2018 The thioredoxin (Trx)-coupled arsenate reductase (ArsC) is a family of enzymes that catalyzes the Published: xx xx xxxx reduction of arsenate to arsenite in the arsenic detoxifcation pathway. The catalytic cycle involves a series of relayed intramolecular and intermolecular thiol-disulfde exchange reactions. Structures at diferent reaction stages have been determined, suggesting signifcant conformational fuctuations along the reaction pathway. Herein, we use two state-of-the-art NMR methods, the chemical exchange saturation transfer (CEST) and the CPMG-based relaxation dispersion (CPMG RD) experiments, to probe the conformational dynamics of B. subtilis ArsC in all reaction stages, namely the enzymatic active reduced state, the intra-molecular C10–C82 disulfde-bonded intermediate state, the inactive oxidized state, and the inter-molecular disulfde-bonded protein complex with Trx. Our results reveal highly rugged energy landscapes in the active reduced state, and suggest global collective motions in both the C10–C82 disulfde-bonded intermediate and the mixed-disulfde Trx-ArsC complex. Protein thiol-disulfde exchange reactions play fundamental roles in living systems, represented by the thiore- doxin (Trx) and glutaredoxin (Grx) systems that maintain the cytoplasmic reducing environment, the protein DsbA that catalyzes the formation of protein disulfde bonds in bacterial periplasm, as well as the protein disulfde isomerase (PDI) proteins that facilitate correct disulfde bonding1–5. -
A Titrimetric Determination of Thorium John J
Ames Laboratory ISC Technical Reports Ames Laboratory 6-1954 A titrimetric determination of thorium John J. Ford Iowa State College James S. Fritz Iowa State College Follow this and additional works at: http://lib.dr.iastate.edu/ameslab_iscreports Part of the Chemistry Commons Recommended Citation Ford, John J. and Fritz, James S., "A titrimetric determination of thorium" (1954). Ames Laboratory ISC Technical Reports. 92. http://lib.dr.iastate.edu/ameslab_iscreports/92 This Report is brought to you for free and open access by the Ames Laboratory at Iowa State University Digital Repository. It has been accepted for inclusion in Ames Laboratory ISC Technical Reports by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. A titrimetric determination of thorium Abstract A rapid, accurate method for thorium is proposed in which thorium is titrated with a standard solution of ethylenediaminetetraacetic acid (EDTA). Alizarin Red S serves as the indicator, a sharp change from pink to yellow marking the end point of the titration. The method is selective for thorium although several cations and anions interfere. A preliminary extraction of thorium nitrate by mentyl oxide provides an excellent separation of thorium from most interfering ions. Keywords Ames Laboratory Disciplines Chemistry This report is available at Iowa State University Digital Repository: http://lib.dr.iastate.edu/ameslab_iscreports/92 Physical 'cieuccs Re· dmg Room UNITED STATES ATOMIC ENERGY COMMISSION ISC-520 A TITRIMETRIC DETERMINATION OF THORIUM By John J. Ford James S. Fritz June 1954 Technical Information Service, Oak Ridge, Tennessee J Subject Category, CHEMISTRY. Work performed under Contract No. -
Evidence Against Stabilization of the Transition State Oxyanion by a Pka-Perturbed RNA Base in the Peptidyl Transferase Center
Evidence against stabilization of the transition state oxyanion by a pKa-perturbed RNA base in the peptidyl transferase center K. Mark Parnell*, Amy C. Seila†, and Scott A. Strobel*‡§ Departments of *Molecular Biophysics and Biochemistry, †Genetics, and ‡Chemistry, Yale University, 260 Whitney Avenue, New Haven, CT 06520-8114 Edited by Harry F. Noller, University of California, Santa Cruz, CA, and approved July 16, 2002 (received for review April 8, 2002) The crystal structure of the ribosomal 50S subunit from Haloarcula activity, suggesting that 23S and 5S rRNA may constitute the marismortui in complex with the transition state analog CCdA- bulk of the peptidyl transferase center (8). phosphate-puromycin (CCdApPmn) led to a mechanistic proposal The most unambiguous evidence that the active site of the wherein the universally conversed A2451 in the ribosomal active ribosome is comprised of RNA came from the 2.4-Å crystal site acts as an ‘‘oxyanion hole’’ to promote the peptidyl transferase structure of the Haloarcula marismortui 50S ribosomal subunit reaction [Nissen, P., Hansen, J., Ban, N., Moore, P.B., and Steitz, T.A. reported by Ban et al. (9) and Nissen et al. (10). The structure of the (2000) Science 289, 920–929]. In the model, close proximity (3 Å) 50S subunit complexed with the transition-state analog CCdA- between the A2451 N3 and the nonbridging phosphoramidate phosphate-puromycin (CCdApPmn) was vital to this structural oxygen of CCdApPmn suggested that the carbonyl oxyanion identification. CCdApPmn includes the minimal components of formed during the tetrahedral transition state is stabilized by both peptidyl transferase substrates (11). CCdA binds the P site, and hydrogen bonding to the protonated A2451 N3, the pKa of which puromycin binds the A site (Fig. -
Naming Compounds
Naming Compounds Naming compounds is an important part of chemistry. Most compounds fall in to one of three categories- ionic compounds, molecular compounds, or acids. Part One: Naming Ionic Compounds Identifying Ionic Compounds Ionic compounds consist of combinations of positively charged ions called cations (usually metals), and negatively charged ions called anions (usually non-metals). In general, you can identify an ionic compound because it contains a metal (these are usually found in the left and center areas of the periodic table) and a non-metal (these are generally found in the right hand area of the periodic table). Also, a compound will have no charge. For example, NaCl and Fe2O3 are ionic compounds; they each contain a metal (Na and Fe) and a non-metal (Cl - and O), and they do not have charges. MnO4 is NOT an ionic compound; it does contain a metal (Mn) and a non-metal (O), but it has a charge. Thus, it is a polyatomic ion, not a compound. A compound will NEVER have a charge! Naming Ionic Compounds There are three steps involved in naming ionic compounds- naming the cation, naming the anion, and naming the entire compound. 1. Name the cation. i. Cations formed from metal atoms have the same name as the metal. Examples: Na+= sodium ion; Al3+= aluminum ion ii. If a metal can form ions of different charges (i.e., is one of the central transition metals), specify the charge with Roman numerals in parentheses. Examples: Fe+= iron (I) ion; Fe2+= iron (II) ion; Fe3+= iron (III) ion iii. -
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). -
FALL2015.Pdf
Introducing… In Meso In Situ Serial Crystallography mitegen.com/imisx Easy Crystallizaon in LCP • Simple in situ X-ray Diffracon • Standard Goniometer Compable • Serial Crystallography Enabling • Advanced Dual-Sandwich Design Rethink what your LCP crystallizaon plate is capable of. EZ-Cut LCP LCP Tools Easy Access LCP Crystallizaon Plate Starter Kits, Syringes, Lipids & More Take your crystallizaon in LCP to the next level with MiTeGen’s new LCP line mitegen.com/lcp ACA - Structure Matters www.AmerCrystalAssn.org Table of Contents 2 President’s Column 2-4 News from Canada 4 From the Editor's Desk 5-6 Update on Structural Dynamics Chris Cahill 7 What's on the Cover ACA President 8-11 Poster Prizes in Philadelphia 12 Undergraduate Student Reception in Philadelphia Contributors to this Issue What's on the Cover 13-51 Philadelphia ACA Meeting Page 7 21 Index of Advertisers 53-54 2015 ACA Summer Course 56 What's New on the ACA History Website Spotlight on Stamps Juanma García-Ruiz Net RefleXions 15 Plenary Lecturer in Philadelphia 58-59 Puzzle Corner 59 YSSIG Activities 60-61 48th Erice International School of Crystallography 61-62 Updates from 2014-2015 AIP Science & Technology Fellows 62 CSD50 Symposium Daniel Rabinovich 64-65 News & Awards Spotlight on Stamps 65-66 Book Reviews 66-67 2015 Wisconsin Crystal-Growing Competition 68 Net RefleXions 69 CCDC Data Deposition Service Enhancement 70-71 ACA 2016 Denver Preview 72 Future Meetings Anastasiya Vinokur Net RefleXions Contributions to ACA RefleXions may be sent to either of the Editors: Please address matters pertaining to advertisements, membership Judith L. -
Technical and Regulatory Guidance for Constructed Treatment Wetlands
Technical/Regulatory Guideline Technical and Regulatory Guidance Document for Constructed Treatment Wetlands December 2003 Prepared by The Interstate Technology & Regulatory Council Wetlands Team ABOUT ITRC Established in 1995, the Interstate Technology & Regulatory Council (ITRC) is a state-led, national coalition of personnel from the environmental regulatory agencies of some 40 states and the District of Columbia; three federal agencies; tribes; and public and industry stakeholders. The organization is devoted to reducing barriers to, and speeding interstate deployment of, better, more cost-effective, innovative environmental techniques. ITRC operates as a committee of the Environmental Research Institute of the States (ERIS), a Section 501(c)(3) public charity that supports the Environmental Council of the States (ECOS) through its educational and research activities aimed at improving the environment in the United States and providing a forum for state environmental policy makers. More information about ITRC and its available products and services can be found on the Internet at www.itrcweb.org. DISCLAIMER This document is designed to help regulators and others develop a consistent approach to their evaluation, regulatory approval, and deployment of specific technologies at specific sites. Although the information in this document is believed to be reliable and accurate, this document and all material set forth herein are provided without warranties of any kind, either express or implied, including but not limited to warranties of the accuracy or completeness of information contained in the document. The technical implications of any information or guidance contained in this document may vary widely based on the specific facts involved and should not be used as a substitute for consultation with professional and competent advisors. -
Investigation Into the Effect of Sulfate and Borate Incorporation on the Structure and Properties of Srfeo3-Δ
crystals Article Investigation into the Effect of Sulfate and Borate Incorporation on the Structure and Properties of SrFeO3-δ Abbey Jarvis and Peter Raymond Slater * School of Chemistry, University of Birmingham, Birmingham B15 2TT, UK; [email protected] * Correspondence: [email protected]; Tel.: +44-121-414-8906 Academic Editor: Stevin Pramana Received: 28 April 2017; Accepted: 3 June 2017; Published: 7 June 2017 Abstract: In this paper, we demonstrate the successful incorporation of sulfate and borate into SrFeO3-δ, and characterise the effect on the structure and conductivity, with a view to possible utilisation as a cathode material in Solid Oxide Fuel Cells. The incorporation of low levels of sulfate/borate is sufficient to cause a change from a tetragonal to a cubic cell. Moreover, whereas heat treatment of undoped SrFeO3-δ under N2 leads to a transformation to brownmillerite Sr2Fe2O5 with oxygen vacancy ordering, the sulfate/borate-doped samples remain cubic under the same conditions. Thus, sulfate/borate doping appears to be successful in introducing oxide ion vacancy disorder in this system. Keywords: solid oxide fuel cell; cathode; perovskite; sulfate; borate 1. Introduction Research into solid oxide fuel cells (SOFCs) as alternate energy materials has grown due to their high efficiency and consequent reduction in greenhouse gas emissions. Specifically, research into perovskite materials has attracted significant interest for potential SOFC materials including cathode, electrolyte and anode materials (see, for example, the review articles [1,2]). Traditionally, doping strategies for perovskite materials has involved the introduction of cations of a similar size e.g., Sr2+ for 3+ 2+ 3+ La , Mg for Ga to give the oxide ion conducting electrolyte La1−xSrxGa1−yMgyO3−x/2−y/2 [3]. -
Heavy Metal(Loid) Transformations by Bacteria Isolated from Extreme Environments
Heavy Metal(loid) Transformations by Bacteria Isolated from Extreme Environments By Chris Maltman A Thesis Submitted to the Faculty of Graduate Studies in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Department of Microbiology University of Manitoba Winnipeg, Manitoba Canada Copyright © 2016 by Chris Maltman I Abstract The research presented here studied bacteria from extreme environments possessing strong resistance to highly toxic oxyanions of Te, Se, and V. The impact of tellurite on cells of aerobic anoxygenic phototrophs and heterotrophs from freshwater and marine habitats was 2- investigated. Physiological responses of cells to TeO3 varied. In its presence, biomass either increased, remained similar or decreased, with ATP production following the same trend. Four detoxification strategies were observed: 1) Periplasmic based reduction; 2) Reduction needing an intact cytoplasmic membrane; 3) Reduction involving an undisturbed whole cell; and 4) Membrane associated reduction. The first three require de novo protein synthesis, while the last was constitutively expressed. We also investigated two enzymes responsible for tellurite reduction. The first came from the periplasm of deep-ocean hydrothermal vent strain ER-Te-48 associated with tube worms. The second was a membrane associated reductase from Erythromonas ursincola, KR99. Both could also use tellurate as a substrate. ER-Te-48 also has a second periplasmic enzyme which reduced selenite. Additionally, we set out to find new organisms with the ability to resist and reduce Te, Se, and V oxyanions, as well as use them for anaerobic respiration. New strain CM-3, a Gram negative, rod shaped bacterium from gold mine tailings of the Central Mine in Nopiming Provincial Park, Canada, has very high level resistance and the capability to perform dissimilatory anaerobic reduction of tellurite, tellurate, and selenite. -
Tungsten Removal from Molybdate Solutions Using Chelating Ion-Exchange Resin: Equilibrium Adsorption Isotherm and Kinetics
J. Cent. South Univ. (2016) 23: 1052−1057 DOI: 10.1007/s11771-016-0354-y Tungsten removal from molybdate solutions using chelating ion-exchange resin: Equilibrium adsorption isotherm and kinetics ZHU Xian-zheng(朱先正), HUO Guang-sheng(霍广生), NI Jie(倪捷), SONG Qiong(宋琼) School of Metallurgy and Environment, Central South University, Changsha 410083, China © Central South University Press and Springer-Verlag Berlin Heidelberg 2016 Abstract: The equilibrium adsorption isotherm and kinetic of the sorption process for W and Mo on macro chelating resin D403 were investigated on single Na2MoO4 and Na2WO4 solutions. The sorption isotherm results show that the adsorption process of W obeys the Freundlich model very well whereas the exchange process with Mo approximately follows the Henry model. The kinetic experiments show that the intraparticle diffusion process was the rate-determining step for W sorption on the resin, and the corresponding activation energy is calculated to be 21.976 kJ/mol. Key words: tungsten; molybdate; ion-exchange resin; isotherms; kinetics tin (IV) oxide hydrate [14], that would preferentially 1 Introduction form precipitations with W under certain conditions. The separation was effective but a large number of The separation between W and Mo has been a precipitation agents were required and the impurity ions national difficulty due to their extremely similar accompanied with the added reagents were inevitable, physicochemical properties, resulting from the increasing the impurity-removal burden. lanthanide contraction [1]. Additionally, according to the Inspired by the different affinities towards O industrial requirement, WO3 impurity in final ammonium between W and Mo, we discovered a novel resin (D403) molybdate product should be restricted to below containing meglumine group which exhibited marvelous 150×10−6 (mass fraction) [2], making W removal from separation effects between Mo and W at pH above 8.0, at molybdate solutions particularly important.