International Standards for Drinking-Water
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Old Time Chemical Names
Old Time Chemical Names 1080------------------------------------------------Sodium fluroacetate 2-Propanone-------------------------------------Acetone Absinthe-------------------------------------------Distillate of worm wood Abstinthium--------------------------------------Distillate of worm wood Acarcia gum-------------------------------------Gum arabic Acetaldehyde------------------------------------Acetic aldehyde Acetate of alumina-----------------------------Aluminium acetate Acetate of ammonia---------------------------Ammonium acetate Acetate of amyl---------------------------------Amyl acetate Acetate of baryta-------------------------------Barium acetate Acetate of cobalt-------------------------------Cobalt acetate Acetate of copper------------------------------Copper acetate Acetate of ethyl---------------------------------Ethyl acetate Acetate of iron----------------------------------Iron acetate Acetate of lead----------------------------------Lead acetate Acetate of lime----------------------------------Calcium acetate Acetate of manganese------------------------Manganous acetate Acetate of oxide of ethyl---------------------Ethyl acetate Acetate of potassa-----------------------------Potassium acetate Acetate of potassium--------------------------Potassium acetate Acetate of protoxide of Manganese-------Manganous acetate Acetate of soda---------------------------------Sodium acetate Acetate of zinc----------------------------------Zinc acetate Acetic aid basic bismuth---------------------Bismuth subacetate CH3COOBiO Acetic -
1 Abietic Acid R Abrasive Silica for Polishing DR Acenaphthene M (LC
1 abietic acid R abrasive silica for polishing DR acenaphthene M (LC) acenaphthene quinone R acenaphthylene R acetal (see 1,1-diethoxyethane) acetaldehyde M (FC) acetaldehyde-d (CH3CDO) R acetaldehyde dimethyl acetal CH acetaldoxime R acetamide M (LC) acetamidinium chloride R acetamidoacrylic acid 2- NB acetamidobenzaldehyde p- R acetamidobenzenesulfonyl chloride 4- R acetamidodeoxythioglucopyranose triacetate 2- -2- -1- -β-D- 3,4,6- AB acetamidomethylthiazole 2- -4- PB acetanilide M (LC) acetazolamide R acetdimethylamide see dimethylacetamide, N,N- acethydrazide R acetic acid M (solv) acetic anhydride M (FC) acetmethylamide see methylacetamide, N- acetoacetamide R acetoacetanilide R acetoacetic acid, lithium salt R acetobromoglucose -α-D- NB acetohydroxamic acid R acetoin R acetol (hydroxyacetone) R acetonaphthalide (α)R acetone M (solv) acetone ,A.R. M (solv) acetone-d6 RM acetone cyanohydrin R acetonedicarboxylic acid ,dimethyl ester R acetonedicarboxylic acid -1,3- R acetone dimethyl acetal see dimethoxypropane 2,2- acetonitrile M (solv) acetonitrile-d3 RM acetonylacetone see hexanedione 2,5- acetonylbenzylhydroxycoumarin (3-(α- -4- R acetophenone M (LC) acetophenone oxime R acetophenone trimethylsilyl enol ether see phenyltrimethylsilyl... acetoxyacetone (oxopropyl acetate 2-) R acetoxybenzoic acid 4- DS acetoxynaphthoic acid 6- -2- R 2 acetylacetaldehyde dimethylacetal R acetylacetone (pentanedione -2,4-) M (C) acetylbenzonitrile p- R acetylbiphenyl 4- see phenylacetophenone, p- acetyl bromide M (FC) acetylbromothiophene 2- -5- -
Chemical Reagents Their Purity & Tests
CHEMICAL REAGENTS THEIR PURITY AND TESTS A NEW AND IMPROVED TEXT BASED ON AND REPLACING THE LATEST EDITION OF KRAUCH ' DIE PRUFUNG DER CHEMISCHEN REAGENTIEN AUF REINHEIT' BY E. MERCK AUTHORIZED TRANSLATION BY HENRY SCHENCK, A.B. (HARVARD) LONDON ARCHIBALD CONSTABLE & CO., LTD. 10 ORANGE STREET, LEICESTER SQUARE, W.C. ••' 1907 DR. As long ago as the early seventies 1 fell, (ho need of a treatise on Chemical Reagents, and thought of compiling such a. work. I was I hen an assistant in Mir chemical laboratory of the (Jovernment Agricultural Kxporiment Station at. Minister, and in my chemical work (here met with constant difficulties on account, of the great variations in the chemicals which were graded as *'(•. I\M "puriss," cic. If was my aim to fix uniform standards for such chemicals as are used in analytical work, such standards to define closely the decree of purity of the chemicals and yet to be possible of attainment, in practice by the manufacturer. Not until ISSN, however, did my work in this direction take the tangible form of a. book, " I)ic l*ntvjuu<j dcr (1hvun~ srhcti h't'(t(fcntic?i ituj licinlicil.'1 A second revised and enlarged edition was published in lN'.M. In INiMi a. third edition, carefully revised and still further enlarged, was pub- lished. Since thai time a ^ood many changes have taken place, so that my book ajcain needed revision. As I was unable to undertake this work, Mr. 10. Merck, appreciating the usefulness of such a. work as mine, published in MM).r) what might be considered its up-to-date revision. -
Listed Toxic Air Contaminants and Common Chemicals
Listed Toxic Air Contaminants and Common Chemicals (sorted by Chemical name) CHEMICAL NAME CAS # Listed Air Toxic 1,1,1,2-Tetrachloroethane 630206 Y 1,1,1,2-Tetrafluoroethane 811972 Y 1,1,2,2-Tetrachloroethane 79345 Y 1,1,2-Trichloroethane 79005 Y 1,1-Difluoroethane (HCFC 152a) 75376 Y 1,1-Dimethyl hyrazine 57147 Y 1,2,4 Trimethylbenzene 95636 N 1,2,4-Trichlorobenzene 120821 Y 1,2-Dibromo-3-chloropropane 96128 Y 1,2-Dichlorobenzene 95501 Y 1,2-Dimethyl hyrazine 540738 Y 1,2-Diphenylhydrazine (Hydrazobenzene) 122667 Y 1,2-Epoxybutane 106887 Y 1,2-Propylenimine (2-Methyl aziridine) 75558 Y 1,3-Butadiene 106990 Y 1,3-Dichloropropene 542756 Y 1,3-Propane sultone 1120714 Y 1,4-Dichlorobenzene (p-Dichlorobenzene) 106467 Y 1,4-Dioxane (1,4-Diethyleneoxide) 123911 Y 1-Chloro-1,1-difluoroethane (CFC 142B) 75683 Y 2,2,4-Trimethylpentane 540841 Y 2,4,5-Trichlorophenol 95954 Y 2,4,6-Trichlorophenol 88062 Y 2,4-and 2,6-Toluene diisocyanateh 26471625 Y 2,4-Diaminoanisole 615054 Y 2,4-Diaminotoluene 95807 Y 2,4-Dichlorophenoxyacetic acid, salts & esters 94757 Y (2,4-D) 2,4-Dimethylphenol 105679 Y 2,4-Dinitrophenol 51285 Y 2,4-Dinitrotoluene 121142 Y 2,4-Toluene diamine (2,4-Diaminotoluene) 95807 Y 2-Acetylaminofluorene 53963 Y 2-Aminoanthraquinone 117793 Y CHEMICAL NAME CAS # Listed Air Toxic 2-Chloroacetophenone 532274 Y 2-Chlorophenol 95578 Y 2-Nitropropane 79469 Y 3,3'-Dichlorobenzidene 91941 Y 3,3'-Dimethoxybenzidine 119904 Y 3,3'-Dimethyl benzidine 119937 Y 4,4-Methylene bis (2-chloroaniline) 101144 Y 4,4-Methylenedianiline 101779 Y 4,6-Dinitro-o-cresol -
Sulfuric Acid Aerosol Is Formed by the Oxidation of SO in Standard, NH /N ) Diluted to 2 RELATIVE HUMIDITY (RH) 3 2 Gas/Aqueous/Aerosol Phase
INVESTIGATIONS OF THE HETEROGENEOUS REACTION BETWEEN AMMONIA AND SULFURIC/SULFUROUS ACID AEROSOLS Thomas Townsend, Colette Noonan and John R. Sodeau Centre for Research into Atmospheric Chemistry, Department of Chemistry, University College Cork, and Environmental Research Institute, Cork, Ireland. [email protected] INTRODUCTION EXPERIMENTAL SET-UP AMMONIA (100ppm Sulfuric acid aerosol is formed by the oxidation of SO in standard, NH /N ) diluted to 2 RELATIVE HUMIDITY (RH) 3 2 gas/aqueous/aerosol phase. The preferred form of sulfuric acid tuned between 1% and 70%. ppb range. Admitted to flow AEROSOL GENERATION tube via a 6mm diameter in the aerosol phase is ammonium sulfate (NH4)2SO4. If there H2SO4 /C2H2O4 aerosol Dilution Unit movable, glass injector. is not enough ammonia present, sulfuric acid exists either as generated by passing a flow (200-500 ccm) of air over a P H2SO4(aq) or NH4HSO4. heated solution or via a nebuliser. AEROSOL FLOW-REACTOR Aerosols AerosolAerosol Humidifier Generator Made of glass, ID: 10cm, maximal ….are tiny particles suspended in the air. Those larger than reactive length Z: 80cm. Aerosol Flow Carrier Flow Operated at room temperature and Soluble trace gases such as Ammonia, about 1μm in size are mainly produced by windblown dust Comp. Air atmospheric pressure. NH3, are produced from agricultural and sea-spray. Aerosols smaller than 1μm are mostly formed Unit by condensation processes e.g. conversion of SO gas released PARTICLE SIZER (SMPS) sources and represents a significant 2 from volcanic eruptions to sulfate-type particles. Monitors aerosol fraction, NH3/N2 atmospheric pollutant in Ireland. particle size, mass, surface SMPS CHEMILUMINESCENCE area, volume. -
Orca Corrosion Chart
Unsaturated Polyester Vinylster (Epoxy Acrylate Resins) CHEMICAL Conc Resins NO ISO BIS Novolac Bromine ENVIRONMENT % 511/512 301 585 570 545/555 A 1 Acetaldehyde 20 NR 40 40 40 2 Acetic Acid 10 80 100 100 100 3 Acetic Acid 15 60 100 100 100 4 Acetic Acid 25 60 100 100 100 5 Acetic Acid 50 - 80 80 80 6 Acetic Acid 75 NR 65 65 65 7 Acetic Acid, Glacial 100 NR NR 40 NR 8 Acetic Anhydride 100 NR NR 40 NR 9 Acetone 10 NR NR 80 80 10 Acetone 100 NR NR NR NR 11 Acetonitrile 20 - 40 40 40 12 Acetyl Acetone 20 - 40 50 40 13 Acrolein (Acrylaldehyde) 20 - 40 40 40 14 Acrylamide 50 NR 40 40 40 15 Acrylic Acid 25 NR 40 40 40 16 Acrylic Latex All - 80 80 80 17 Acrylonitrile Latex Dispersion 2 NR 25 25 25 Activated Carbon Beds, Water 18 - 80 100 80 Treatment Adipic Acid(1.5g solution in 19 23 - 80 80 80 water at 25℃, sol in hot water) 20 ALAMINE amines - 65 80 65 21 Alkyl(C8-10) Dimethyl Amine 100 - 80 100 80 22 Alkyl(C8-10) Chloride All - 80 100 95 23 Alkyl Benzene Sulfonic Acid 90 NR 50 50 50 Alkyl Tolyl Trimethyl 24 - - 40 50 40 Ammonium Chloride 25 Allyl Alcohol 100 NR NR 25 NR 26 Allyl Chloride All NR 25 25 25 27 Alpha Methylstyrene 100 NR 25 50 25 28 Alpha Oleum Sulfates 100 NR 50 50 50 29 Alum Sat'd 80 100 120 100 30 Aluminum Chloride Sat'd 80 100 120 100 31 Aluminum Chlorohydrate All - 100 100 100 32 Aluminum Chlorohydroxide 50 - 100 100 100 33 Aluminum Fluoride All - 25 25 25 34 Aluminum Hydroxide 100 80 80 95 80 35 Aluminum Nitrate All 80 100 100 100 36 Aluminum Potassium Sulfate Sat'd 80 100 120 100 37 Aluminum Sulfate Sat'd 80 100 120 100 -
United States Patent (19) (11 3,954,955 Furkert (45) *May 4, 1976
United States Patent (19) (11 3,954,955 Furkert (45) *May 4, 1976 54 PROCESS FOR WORKING UP THE WASH Engineering, Duan Nostrand Co., N.Y., N.Y., 1932, SOLUTION OBTAINED IN THE WASHING pp. 1-3. OF SOCONTAINING OFF-GASES 75) Inventor: Herbert Furkert, Grosskonigsdorf, Primary Examiner-Oscar R. Vertiz Germany Assistant Examiner-Gary P. Straub 73) Assignee: Davy Powergas GmbH, Attorney, Agent, or Firm-Millen, Raptes & White Cologne-Braunsfeld, Germany * Notice: The portion of the term of this patent subsequent to Mar. 5, 1991, 57 ABSTRACT has been disclaimed. In a process which comprises scrubbing an SO 22 Filed: Aug. 30, 1972 containing gas with an aqueous ammonia solution to form ammonium sulfite and ammonium bisulfite as re (21) Appl. No.: 284,709 action products, neutralizing said reaction products Related U.S. Application Data with sulfuric acid to form SO, and aqueous ammo nium sulfate, and concentrating the resultant aqueous 63 Continuation-in-part of Ser. No. 228,258, Feb. 22, ammonium sulfate by evaporation, the improvement 1972, Pat. No. 3,795,731. which comprises: 30 Foreign Application Priority Data a heating the concentrated aqueous ammonium sulfate to a temperature of 900-1250°C in a Aug. 31, 197 Germany............................ 2143444 combustion chamber burning a carbon or sulfur containing fuel, in the presence of sufficient 52 U.S. Cl.............................. 423/541 A; 423/242 oxygen to maintain an oxygen content of 1-10 vol (5) Int. Cl..................... C01B 17160; C01B 17/50 % in the gas exiting from the combustion (58) Field of Search........... 423/522,539, 541, 542, chamber, to form a hot split gas consisting 4231544, 545, 547, 550, 242, 523 essentially of sulfur dioxide, sulfur trioxide, molecular nitrogen, molecular oxygen and water (56) References Cited vapor; and UNITED STATES PATENTS b. -
Circular of the Bureau of Standards No. 26
DEPARTMENT OF COMMERCE AND LABOR Circular Bureau of Standards ANALYZED IRON AND MANGANESE ORES METHODS OF ANALYSIS WASHINGTON GOVERNMENT PRINTING OFFICE 1910 / / * -z « DEPARTMENT OF COMMERCE AND LABOR Circular OF THE Bureau of Standards S. W. STRATTON, Director No. 26 ANALYZED IRON AND MANGANESE ORES METHODS OF ANALYSIS [1st Edition] Issued June 2 5, IOIO WASHINGTON GOVERNMENT PRINTING OFFICE 1910 $ d) 1 ANALYZED IRON AND MANGANESE ORES—METHODS OF ANALYSIS CONTENTS Page. I. Introduction 3 1. Mixing 4 2. Drying 4 3. Reagents 4 4. Apparatus 5 II. Methods of analysis at the Bureau of Standards . 5 1. Silica 5 2. Phosphorus 5 3. Aluminum 6 (a) Phosphate (Peters’s) method 6 ( b Ether separation 6 (c) Phenylhydrazine precipitation 6 (d) Electrolytic separation 6 4. Titanium 7 (a) Gravimetric 7 ( b Colorimetric 7 5. Standardization of permanganate solutions 7 6. Iron 8 (a) Gravimetric 8 ( b Jones reductor 8 (c) Stannous chloride method 9 7. Available oxygen 9 (a) Ferrous sulphate 9 10. (b) Oxalic acid 9 (c) Sodium oxalate 9 ( ) Distillation 10 8. Manganese 10 (a) Ford 10 (b) Ford, modified 10 (c) Acetate 10 (d) Volhard 10 1 ( e ) Ford- Williams (/) von Knorre 1 1 ( g ) Bismuthate (h) Persulphate colorimetric 1 9. Lime 12 Magnesia 12 III. Methods used by other analysts 12 1. Commercial chemists 12 2. Works chemists 13 3. Mine chemists 14 I. INTRODUCTION General information regarding standard samples, including a description of the methods used in their preparation, is published in Circular No. 25. The information and methods given in this circular have special reference to samples Nos. -
Investigation of the Solar Hybrid Photo-Thermochemical Sulfur-Ammonia Water Splitting Cycle for Hydrogen Production Agni E
361 A publication of CHEMICAL ENGINEERING TRANSACTIONS The Italian Association VOL. 45, 2015 of Chemical Engineering www.aidic.it/cet Guest Editors: Petar Sabev Varbanov, Jiří Jaromír Klemeš, Sharifah Rafidah Wan Alwi, Jun Yow Yong, Xia Liu Copyright © 2015, AIDIC Servizi S.r.l., ISBN 978-88-95608-36-5; ISSN 2283-9216 DOI: 10.3303/CET1545061 Investigation of the Solar Hybrid Photo-Thermochemical Sulfur-Ammonia Water Splitting Cycle for Hydrogen Production Agni E. Kalyvaa, Ekaterini Ch. Vagiaa, Athanasios G. Konstandopoulosb, Arun R. Srinivasac, Ali T-Raissid, Nazim Muradovd, Konstantinos E. Kakosimos*,a aTexas A&M University at Qatar, Chemical Engineering Department, Sustainable Energy Research Laboratory (SERL), PO Box 23874, Doha, Qatar bChemical Process Engineering Research Institute, Aerosol and Particle Technology Laboratory (APTL), Center for Research and Technology-Hellas (CERTH/CPERI), P.O. Box 361, 57001 Thermi-Thessaloniki, Greece cTexas A&M University, Department of Mechanical Engineering, College Station, TX 77843-3123, USA dFlorida Solar Energy Center, University of Central Florida, Cocoa, FL 32922, USA [email protected] Hydrogen is currently being used in many industries, from chemical and refining to metallurgical, glass and electronics, while being at the same time a promising energy carrier. Therefore the need for hydrogen is experiencing a very rapid growth. At the same time, the traditional hydrogen production methods (e.g., steam methane reforming, water electrolysis) are energy and resources intensive. Thus, research focus is on sustainable technologies that can produce hydrogen in an economic and environmental friendly way. Hydrogen production via a solar driven hybrid sulfur-ammonia water splitting cycle (HySA) developed at Florida Solar Energy Center is such a promising technology. -
Thermodynamic Properties of Isoprene- and Monoterpene-Derived Organosulfates Estimated with Cosmotherm
Atmos. Chem. Phys., 20, 5679–5696, 2020 https://doi.org/10.5194/acp-20-5679-2020 © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License. Thermodynamic properties of isoprene- and monoterpene-derived organosulfates estimated with COSMOtherm Noora Hyttinen1, Jonas Elm2, Jussi Malila1, Silvia M. Calderón1, and Nønne L. Prisle1 1Nano and Molecular Systems Research Unit, University of Oulu, P.O. Box 3000, 90014 Oulu, Finland 2Department of Chemistry and iClimate, Aarhus University, Langelandsgade 140, 8000 Aarhus C, Denmark Correspondence: Noora Hyttinen (noora.hyttinen@oulu.fi), and Nønne L. Prisle (nonne.prisle@oulu.fi) Received: 25 November 2019 – Discussion started: 17 December 2019 Revised: 9 April 2020 – Accepted: 10 April 2020 – Published: 13 May 2020 Abstract. Organosulfates make significant contributions 1 Introduction to atmospheric secondary organic aerosol (SOA), but lit- tle is known about the thermodynamic properties of at- mospherically relevant organosulfates. We have used the Organosulfates (R−OSO3H, OS) have been identified as COSMOtherm program to calculate both the gas- and components of atmospheric secondary organic aerosol condensed-phase properties of previously identified at- (SOA) from a variety of environments (Surratt et al., 2007; mospherically relevant monoterpene- and isoprene-derived Glasius et al., 2018a,b). In the Amazon, the contribution organosulfates. Properties include solubilities, activities and of organic sulfate was found to be 3 %–42 % of the total saturation vapor pressures, which are critical to the aerosol- aerosol sulfate for the compounds measured using aerosol phase stability and atmospheric impact of organosulfate mass spectrometry (Glasius et al., 2018a). In Atlanta, Geor- SOA. Based on the estimated saturation vapor pressures, the gia, organosulfates accounted for 16.5 % of the total organic organosulfates of this study can all be categorized as semi- carbon of fine particulate matter (PM2:5)(Hettiyadura et al., volatile or low-volatile, with saturation vapor pressures 4 2019). -
Inorganic Chemistry Practical
EXPERIMENTAL INORGANIC CHEMISTRY For B.Sc. and M.Sc. Students As per new Syllabus Dr. M.K.Shah 2 Dedicated to all our beloved graduates & post graduate students 3 INORGANIC PREPARATION 4 1. TETRAMINE CUPRIC SULPHATE, [Cu(NH3)4 ]SO4H2O (A) REAGENTS Cupric sulphate, Ammonia, Ethyl alcohol, Nitric acid, Distilled water, Sulphuric acid. (B) REACTION CuSO45H2O(aq) + 4NH3(aq) [Cu (NH3)4]SO4H2O + 4H2O (C) PROCEDURE Take 5 gm crystalline cupric sulphate in a 250 ml beaker. Dissolve it in minimum quantity of water and then add few drops of diluted sulphuric acid. Add concentrated ammonia solution to the beaker with constant stirring, until the blue precipitate of cupric hydroxide, first formed completely dissolve to yield a clear, deep blue solution and there should be smell of ammonia in the beaker. Now add 20 ml alcohol dropwise from the dropping funnel to the beaker with constant stirring until the blue precipitates settled and clear solution is obtained. Heat it to 60o 70oC in the water bath for about 10-15 minutes. Then stop heating and remove the beaker from the water bath and allow it to stand. Long needle shaped blue crystals of tetramine cupric sulphate separates out. Filter and wash the crystals with a few drops of alcohol. Dry the crystals on a porous plate or in a desiccator. Weigh the dry crystal and find out the percentage yield followed by percentage purity by usual methods. 2. TRI (THIOUREA)-CUPROUS SULPHATE, [Cu (NH2CSNH2)3]2 SO4 2H2O] (A) REAGENTS Cupric sulphate, Ethyl alcohol, Nitric acid, Thiourea, Distilled water, Ammonia. -
Membrane Separation of Ammonium Bisulfate from Ammonium Sulfate in Aqueous Solutions for CO2 Mineralisation
Article Membrane Separation of Ammonium Bisulfate from Ammonium Sulfate in Aqueous Solutions for CO2 Mineralisation Evelina Koivisto and Ron Zevenhoven * Thermal and Flow Engineering Laboratory, Åbo Akademi University, Piispankatu 8, 20500 Turku, Finland; [email protected] * Correspondence: [email protected]; Tel.: +358-2-215-3223 Received: 24 February 2018; Accepted: 2 April 2018; Published: 4 April 2018 Abstract: The separation of ammonium bisulfate (ABS) from ammonium sulfate (AS) in aqueous solutions by monovalent ion selective membranes was studied. Optimised usage of these chemicals is both an important and challenging step towards a more efficient CO2 mineralisation process route developed at Åbo Akademi University (ÅA). The membranes were placed in a three or five- compartment electrodialysis stack. Silver, stainless steel and platinum electrodes were tested, of which a combination of Pt (anode) and stainless steel (cathode) electrodes were found to be most suitable. Separation efficiencies close to 100% were reached based on ABS concentrations in the feed solution. The tests were performed with an initial voltage of either 10 V–20 V, but limitations in the electrical power supply equipment eventually resulted in a voltage drop as separation proceeded. Exergy calculations for energy efficiency assessment show that the input exergy (electrical power) is many times higher than the reversible mixing exergy, which indicates that design modifications must be made. Further work will focus on the possibilities to make the separation even more efficient and to develop the analysis methods, besides the use of another anode material. Keywords: ammonium (bi)sulfate; CCS; CO2 mineralisation; electrodialysis; ion selective membranes 1. Introduction CO2 mineralisation is one method to sequester CO2, especially at locations where underground storage is impossible or where the market potential of the solid products is recognised.