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Sodium Chloride (Halite, Common Salt Or Table Salt, Rock Salt)
71376, 71386 Sodium chloride (Halite, Common Salt or Table Salt, Rock Salt) CAS number: 7647-14-5 Product Description: Molecular formula: NaCl Appearance: white powder (crystalline) Molecular weight: 58.44 g/mol Density of large crystals: 2.17 g/ml1 Melting Point: 804°C1 Density: 1.186 g/ml (5 M in water)2 2 Solubility: 1 M in H2O, 20°C, complete, clear, colorless 2 pH: 5.0-8.0 (1 M in H2O, 25°C) Store at room temperature Sodium chloride is geologically stable. If kept dry, it will remain a free-flowing solid for years. Traces of magnesium or calcium chloride in commercial sodium chloride adsorb moisture, making it cake. The trace moisture does not harm the material chemically in any way. 71378 BioUltra 71386 BioUltra for molecular biology, 5 M Solution The products are suitable for different applications like purification, precipitation, crystallisation and other applications which require tight control of elemental content. Trace elemental analyses have been performed for all qualities. The molecular biology quality is also tested for absence of nucleases. The Certificate of Analysis provides lot-specific results. Much of the sodium chloride is mined from salts deposited from evaporation of brine of ancient oceans, or recovered from sea water by solar evaporation. Due to the presence of trace hygroscopic minerals, food-grade salt has a small amount of silicate added to prevent caking; as a result, concentrated solutions of "table salt" are usually slightly cloudy in appearance. 71376 and 71386 do not contain any anti-caking agent. Applications: Sodium chloride is a commonly used chemical found in nature and in all body tissue, and is considered an essential nutrient. -
Volatility of Radiopharmacy-Prepared Sodium Iodide-131 Capsules
RADIATION SAFETY Volatility of Radiopharmacy-Prepared Sodium Iodide-131 Capsules James M. Bright, Trenton T. Rees, Louis E. Baca and Richard L. Green Pharmacy Services, Syncor International Corporation, Albuquerque, New Mexico; and Quality and Regulatory Department, Syncor International Corporation, Woodland Hills, California studied thyroid physiology using 128I in 1937 (1,2). In January Objective: The aims of this study were to quantify the extent 1941, Hertz and Roberts were the first to administer radioiodine of volatilization from 131I-NaI therapeutic capsules prepared in 131I for the treatment of hyperthyroid patients (3). Today, almost a centralized radiopharmacy and to quantify the amount of 60 y later, radioiodine therapy with 131I remains the primary volatile 131I released from a dispensing vial containing a compounded 131I-NaI therapy capsule. therapeutic agent used in nuclear medicine, and its use is firmly Methods: Therapy capsules were prepared by injecting 131I established in the 2 diseases first treated: hyperthyroidism and oral solution into capsules containing anhydrous dibasic thyroid carcinoma. sodium phosphate. Volatilized activity was obtained by filter- Initially the use of 131I was restricted to the only pharmaceu- ing air drawn across samples that were placed open on the tical dosage form then available—liquid oral solution. While 131 bottom of a sample holder cup. Volatile I was captured by liquid radioiodine proved to be beneficial to the patients to filtering it through 3 triethylenediamine-impregnated carbon whom it was administered, the frequency of contamination and cartridge filters, arranged in series. To quantify the amount of thyroid uptake activity in nuclear medicine personnel who volatile 131I released from a dispensing vial during a simulated patient administration, a vial containing a compounded 131I handled the material was noted with increasing alarm (4–7). -
Cyanide Poisoning and How to Treat It Using CYANOKIT (Hydroxocobalamin for Injection) 5G
Cyanide Poisoning and How to Treat It Using CYANOKIT (hydroxocobalamin for injection) 5g 1. CYANOKIT (single 5-g vial) [package insert]. Columbia, MD: Meridian Medical Technologies, Inc.; 2011. Please see Important Safety Information on slides 3-4 and full Prescribing Information for CYANOKIT starting on slide 33. CYANOKIT is a registered trademark of SERB Sarl, licensed by Meridian Medical Technologies, Inc., a Pfizer company. Copyright © 2015 Meridian Medical Technologies, Inc., a Pfizer company. All rights reserved. CYK783109-01 November/2015. Indication and Important Safety Information……………………………………………………………………………….………..…..3 . Identifying Cyanide Poisoning……………………………………………………………………………………………………………….…………….….5 . How CYANOKIT (hydroxocobalamin for injection) Works……………………………………………………………….12 . The Specifics of CYANOKIT…………………………………………………………………………………………………………………………….………17 . Administering CYANOKIT………………………………………………………………………………………………………………………………..……….21 . Storage and Disposal of CYANOKIT…................................................................................................................................26 . Grant Information for CYANOKIT……………………………………………………………………………………………………………………....30 . Full Prescribing Information………………………………………………………………………………………………….………………………………33 Please see Important Safety Information on slides 3-4 and full Prescribing Information for CYANOKIT starting on slide 33. CYANOKIT (hydroxocobalamin for injection) 5 g for intravenous infusion is indicated for the treatment of known or suspected cyanide poisoning. -
Self-Diffusion of Sodium, Chloride and Iodide Ions in Methanol-Water Mixture
Self-Diffusion of Sodium, Chloride and Iodide Ions in Methanol-Water Mixture E. Hawlicka* Institute of Applied Radiation Chemistry, Technical University, Wroblewskiego 15, 93-590, Lodz, Poland Z. Naturforsch. 41 a, 939-943 (1986); received April 25, 1986 The self-diffusion coefficients of Na+, C l- and I- in methanol-water solutions at 35 ± 0.01 °C have been measured in their dependence on the salt molarity in the range 1 • 10-4— 1 • 10-2 mol dm -3. The ionic self-diffusion coefficients in infinitely diluted solutions have been computed. The influence of the solvent composition on the solvation of the ions is discussed. A preferential hydration of Na+, Cl - and I “ ions in water-methanol mixtures has been found. In spite of the great interest in the porperties of aqueous solution with a Nal(Tl) scintillation crystal water-organic solvent electrolyte solutions, data on of the well-type (2 x 2"). the ionic mobilities in such systems are scarce. For the self-diffusion measurements the open-end Usually the ionic mobility is calculated from the capillary method was used. The details of the equivalent conductance and the transference num experimental procedure have been described in [6], ber. Ionic transference numbers have been reported The labelling of the sodium ions with 22Na or for water and 17 organic solvents [1], but only for a 24Na and the iodide ions with i25I or 1311, respective few water-organic solvents mixtures. ly, did not make any difference in the results. Similar information can be obtained from the ionic self-diffusion coefficients, which have been reported for a few water-organic solvent systems Results [2-5], The aim of the present work was to determine the All self-diffusion experiments have been carried self-diffusion coefficients of sodium, chloride and out at 25.0 ± 0.05 °C. -
Salt Effect on Vapor-Liquid Equilibria for Acetone-Water System'
SALT EFFECT ON VAPOR-LIQUID EQUILIBRIA FOR ACETONE-WATER SYSTEM' E1ZO SADA, TOSHIO OHNO** AND SHIGEHARU KITO Department of Chemical Engineering, Nagoya University, Nagoya, Japan Vapor-liquid equilibrium data of acetone-water system saturated with sodium chloride, potassium chloride, sodium nitrate, and calcium chloride dihydrate are determined under atmospheric pressure. These vapor-liquid equilibrium data are correlated by a method which gives approximately the behavior of salt in the liquid. The standard deviation of correlated results is 2.32%. To carry out this correlation, the vapor pressures of aqueous solutions saturated with salts are also determined. Investigations concerned with the effect of salt the portion between Cx and Hj is brought to the addition on the vapor-liquid equilibria of binary- vapor pressure of sample solution. Whenthe system systems are of theoretical and industrial importance, attains equilibrium (about one hour is needed), and not a little knowledge of vapor-liquid equilibrium the heights of Hl5 H2, and H3 aremeasured, and the data in this field is already available2}. However, vapor pressure is calculated from the following most investigations are limited to presentation of equation. P '---(Hi-H,W+(Hg-H,W experimental data with no attempt to develop a cor- LO -% r relation. Among these, only a few correlations />*" (1) are proposed, for example, by Johnson and Furter5), As the density of sample solution is usually an order and Hashitani and Hirata3). In this paper, the vapor-liquid equilibrium data of magnitude lower than for mercury, it does not decrease the accuracy of measurementto use the for the acetone-water system saturated with each density of pure water at measuring temperature in of four kinds of salt, i.e. -
The Summer Assignment Will Receive a GRADE on the First Day of Class – August 9
Bishop Moore AP Chemistry Summer Assignment June 2017 Future AP Chemistry Student, Welcome to AP Chemistry. In order to ensure the best start for everyone next fall, I have prepared a summer assignment that reviews basic chemistry concepts some of which you may have forgotten you learned. For those topics you need help with there are a multitude of tremendous chemistry resources available on the Internet. With access to hundreds of websites either in your home or at the local library, I am confident that you will have sufficient resources to prepare adequately for the fall semester. The reference text book as part of AP course is “Chemistry: The Central Science” by Brown LeMay 14th Edition for AP. Much of the material in this summer packet will be familiar to you. It will be important for everyone to come to class the first day prepared. While I review throughout the course, extensive remediation is not an option as we work towards our goal of being 100% prepared for the AP Exam in early May. There will be a test covering the basic concepts included in the summer packet during the first or second week of school. You may contact me by email: ([email protected]) this summer. I will do my best to answer your questions ASAP. I hope you are looking forward to an exciting year of chemistry. You are all certainly excellent students, and with plenty of motivation and hard work you should find AP Chemistry a successful and rewarding experience. Finally, I recommend that you spread out the summer assignment. -
Action of Ammonium Chloride Upon Silicates
Bulletin No. 207 Series E, Chemistry and Physics, 36 DEPARTMENT OF TEiE INTERIOR UNITED STATES GEOLOGICAL SURVEY CHARLES D. WALCOTT, DIRECTOR THE ACTION OF AMMONIUM CHLORIDE UPON SILICATES BY AND GKKOKG-IE Srj::ir, WASHINGTON GOVERNMEN.T PllINTING OFFICE 1902 CONTENTS. Page. Introductory statement......--..-..---.--.------.--.-..--.-.-----------. 7 Analcite-.....-.-.-.--.-.....-.--.'--------....--.-.--..._.-.---.-...---.--. 8 Leucite .....................'.................-....................^-..... 16 The constitution of analcite and leucite.........-..--.-..--...--.---------. 17 Pollucite---. ............................................................ 21 Natrolite--------------------------..-..-----------------.------ --------- 22 Scolecite ................,.:............-.....-.................--.--.... 24 Prehnite .....--.-............--.------------------------------ --------- 25 The trisilicic acids-.--.-.--..---..........-._-----...-.........-...----.- 26 Stilbite.............-..................-....-.-.-----...--.---.......... 29 Henlandite .......... .......................---.-..-.-..-...-----.--..--.. 81 Chabazite............................................................... 32 Thoinsonite...-.-.-..-...._.................---...-.-.-.----..-----..--.. 34 Lanmontite -.-.------.-..-------------.-..-.-..-.-------.-.-----........ 35 Pectolite ......:......... ......................................'.......;.., 36 Wollastonite ....'............................ ................:........... 39 Apophyllite. _.--._..._-....__.....:......___-------------....----..-...._ -
POTASSIUM CYANIDE -- Chemical Fact Sheet What Is It? 1 Potassium Cyanide Is a White Granular Solid with a Bitter Almond Odor
POTASSIUM CYANIDE -- Chemical Fact Sheet What is it? 1 Potassium Cyanide is a white granular solid with a bitter almond odor. It is similar in appearance to sugar. Potassium Cyanide has been used to extract metals from ore and as a rat poison. Where does it Potassium Cyanide is the product of reacting potassium with hydrogen cyanide. come from? What are the Rat Poison common uses for Metal Plating it? Semiconductor Manufacturing How is it Potassium Cyanide is shipped by truck transported in CCC? How is it stored Potassium Cyanide is stored in tightly closed containers. in CCC? Health Hazards from Exposure Exposure Route Symptoms First Aid Inhalation Irritates nose, throat and lungs Remove to fresh air. Seek (low concentrations) Headache or Dizziness medical attention. DO NOT Nausea ATTEMPT CPR. Inhalation Burning sensation Remove to fresh air. Get (high concentrations & prolonged exposure) Unconsciousness medical attention Convulsions immediately. DO NOT Coma ATTEMPT CPR. Death Ingestion Digestive tract burn DO NOT INDUCE Abdominal pain VOMITING. Seek medical Vomiting attention. Large doses can cause death Eyes Severe eye irritant Rinse eyes with water for at Blurred Vision least 15 minutes. Seek Redness, swelling, eye burns medical attention. Skin Skin irritant Wash skin with water for 15 Burning/discomfort minutes. Remove Ulcers contaminated clothing and Skin burns shoes. Seek medical attention . Contra Costa RMP/CalARP Companies that Use, Store or Manufacture this Chemical 2 Electroforming Company Web Sites on the Internet US Environmental -
Activation Analysis
26 August 1967 Leading Articles MEDIBALJOURNAL 509 her patients or the hospital midwife to undertake the home lation has been found between arsenic level in the blood and visiting of them after discharge. degree of renal insufficiency as indicated by blood creatinine Br Med J: first published as 10.1136/bmj.3.5564.509 on 26 August 1967. Downloaded from From the Bradford reports it can be seen that the final measurements. But speculative inquiries of this kind are decision to permit a mother and baby home after 48 hours worth while because they may sometimes provide the first must be made by someone at least of registrar status. It clue to the solution of an intractable problem. Information would also be of considerable value if the general practitioner of a more immediately useful kind can be expected from and district midwife in charge of such a case could freely using activation analysis in problems where the underlying obtain an opinion by domiciliary consultation from either the biochemical and physiological considerations are better hospital obstetric or paediatric department on any puerperal understood. or neonatal complication before readmission of the woman Thyroid metabolism, much studied by radioactive isotopes, after she has returned home. offers interesting problems for attack by activation analysis. When early discharge was discussed in these columns three Semi-automatic methods for the routine determination of years ago' the conclusion was drawn that, though it might protein-bound stable iodine have been elaborated, notably be suitable in emergency conditions, it had little part in in France,2 where the establishment of a laboratory to carry long-term planning. -
Kinetics of the Self-Decomposition of Ozone and the Ozonation of Cyanide Ion and Dyes in Aqueous Solutions
KINETICS OF THE SELF-DECOMPOSITION OF OZONE AND THE OZONATION OF CYANIDE ION AND DYES IN AQUEOUS SOLUTIONS Masaaki TERAMOTO,Seiichiro IMAMURA,Naoyuki YATAGAI, Yoshio NISHIKAWA and Hiroshi TERANISHI Department of Industrial Chemistry, Kyoto Institute of Technology, Matsugasaki, Kyoto 606 Kinetic studies on the self-decomposition of ozone in water, the decomposition of CN~and CNO~,and the decolorization of several dyes by ozone were performed over a wide range of pHusing a stopped-flow apparatus under homogeneousconditions at 298 K. The rate of self- decomposition of ozone was measured in the pH range from 1 to 13.5, and it was found that in the pH range above 8 the rate was expressed by -dlOs]/dt=374 [O3] [OH-]0-88 while in the acidic region the concentration dependence of the rate was complicated, and a simple rate expression could not be obtained. The rate of decomposition of CN~by ozone was expressed by -d[CN-]/dt=310 [O3]° 8 [CN-]° 55 (9.4<pH<11.6) and the rate of decomposition of CNO~was found to be much slower than that of CN~. The decolorization rates of naphthol yellow and methylene blue followed second-order kinetics. Rate constants are presented. The purpose of this paper is to obtain the intrinsic Intr oduction reaction kinetics of the ozonation of several typical Ozone is a powerful oxidizing agent, and it has contaminants such as cyanide and cyanate ions and been recognized as very effective for disinfection, dyes in water using a stopped-flow technique under decolorization, deodorization and the decomposition homogeneous conditions. -
Arxiv:1708.07449V1 [Nucl-Ex] 24 Aug 2017
August 25, 2017 0:18 WSPC/INSTRUCTION FILE cosmogenics-ijmpa International Journal of Modern Physics A c World Scientific Publishing Company Cosmogenic activation of materials Susana Cebri´an Grupo de F´ısica Nuclear y Astropart´ıculas, Universidad de Zaragoza, Calle Pedro Cerbuna 12, 50009 Zaragoza, Spain Laboratorio Subterr´aneo de Canfranc, Paseo de los Ayerbe s/n 22880 Canfranc Estaci´on, Huesca, Spain [email protected] Received Day Month Year Revised Day Month Year Experiments looking for rare events like the direct detection of dark matter particles, neutrino interactions or the nuclear double beta decay are operated deep underground to suppress the effect of cosmic rays. But the production of radioactive isotopes in ma- terials due to previous exposure to cosmic rays is an hazard when ultra-low background conditions are required. In this context, the generation of long-lived products by cosmic nucleons has been studied for many detector media and for other materials commonly used. Here, the main results obtained on the quantification of activation yields on the Earth’s surface will be summarized, considering both measurements and calculations following different approaches. The isotope production cross sections and the cosmic ray spectrum are the two main ingredients when calculating this cosmogenic activation; the different alternatives for implementing them will be discussed. Activation that can take place deep underground mainly due to cosmic muons will be briefly commented too. Presently, the experimental results for the cosmogenic production of radioisotopes are scarce and discrepancies between different calculations are important in many cases, but the increasing interest on this background source which is becoming more and more relevant can help to change this situation. -
Toxicological Profile for Cyanide
CYANIDE 141 5. PRODUCTION, IMPORT/EXPORT, USE, AND DISPOSAL 5.1 PRODUCTION The demand for hydrogen cyanide in the United States during 2000 was 1.615 billion pounds, up slightly from 1.605 billion pounds in 1999 (CMR 2001). Production of hydrogen cyanide in 2003 was 2.019 billion pounds in the United States (FAS 2005). The demand for hydrogen cyanide was projected to be 1.838 billion pounds in 2004 (CMR 2001; NYSDOH 2005). Major producers of hydrogen cyanide are Adisseo USA, Inc. (Institute, West Virginia); Cyanco Co. (Winnemucca, Nevada); Cytec Industries (Waggoman, Louisiana); Degussa Corp. (Theodora, Alabama); The Dow Chemical Company (Freeport, Texas); E.I. du Pont de Neumours and Company (Memphis, Tennessee; Beaumont, Texas); Innovene (Green Lake, Texas and Lima, Ohio); Invista, Inc. (Orange, Texas and Victoria, Texas); Rhom and Haas Texas Inc. (Deer Park, Texas); Solutia, Inc. (Alvin, Texas); Sterling Chemicals, Inc. (Texas City, Texas); and Syngenta Crop Protection (St. Garbiel, Louisiana) (SRI 2005). The combined annual production capacity of these plants is approximately 2.036 billion pounds (SRI 2005). As of February 2005, the following companies produced other cyanide compounds in the United States (SRI 2005): ammonium Crompton, Taft, Louisiana; and Mallinckrodt, Inc., St. Louis, Missouri thiocyanate: cyanogen: Matheson Gas Products, Inc., Gloucester, Massachusetts potassium cyanide: DuPont Chemical Company, Memphis, Tennessee; and The Dow Chemical Company, Nashua, New Hampshire potassium silver Engelhard Corporation, Union, New Jersey; and Metalor Technologies USA, North cyanide: Attleboro, Massachusetts Facilities in the United States producing sodium cyanide and their annual capacity (in millions of pounds) in 2005 include: Cyanco Co., Winnemucca, Nevada (86); and E.I.