Visitors Create Acid Rain in a Glass Dish by Reacting Two Chemicals. the Reaction Creates Sulfur Dioxide Gas

Total Page:16

File Type:pdf, Size:1020Kb

Visitors Create Acid Rain in a Glass Dish by Reacting Two Chemicals. the Reaction Creates Sulfur Dioxide Gas EXPERIMENT Acid Rain Visitors create acid rain in a glass dish by reacting two chemicals. The reaction creates sulfur dioxide gas. The gas reacts with a drop of water, causing it to become acidic. OBJECTIVES: Visitors learn that certain gases in the atmosphere react with rainwater to produce an acid rain that is harmful to plants and animals. SCIENCE TOPICS PROCESS SKILLS VOCABULARY Chemical Reactions Observing Acid pH/lndicators Measuring Chemical Reaction Properties of Gases Unit 4 Environmental Chemistry U4.1 Experiencing Chemistry ©2007 OMSI Experiment: Acid Rain Operating Guide See Materials Prep (with amounts to have on hand) for more details • Plastic petri dish with lid (keep two on hand) • Four 30-ml dropper bottles • Na2SO3 (sodium sulfite) (keep 200 g on hand) • 1M HCl (hydrochloric acid) (keep 100 ml on hand) —OR— 12.1M (concentrated) HCl (keep 100 ml on hand) • Two plastic 500-ml storage bottles • One plastic 125-ml storage bottle • Bromthymol blue sodium salt (keep 5 g on hand) • One white plastic mat • cloth dish towel • Large plastic bowl Setup/Takedown Procedures Label Petri dish with round label with numbers 1-5 on it. Label the three 30-ml dropper bottles “Hydrochloric Acid (HCl),” “Sodium Sulfite (Na2SO3) and “Bromthymol Blue.” Label the plastic bowl “towel”. Remake stock solutions of 1M Na2SO3 (sodium sulfite), 1M HCl (hydrochloric acid), and bromthymol blue indicator as necessary. (Keep 50 ml of each on hand.) (See Materials Prep.) Refill all three labeled dropper bottles from the stock solutions. Set out the visitor instructions in a Plexiglas holder. On a tray lined with a white mat, set out the following: • Labeled plastic petri dish (with three sections) • Plastic lid for petri dish • Labeled dropper bottle of bromthymol blue • Labeled dropper bottle of HCl (hydrochloric acid) • Labeled dropper bottle of Na2SO3 (sodium sulfite) • labeled plastic bowl with clean towel U4.2 Unit 4 Environmental Chemistry Experiencing Chemistry ©2007 OMSI Experiment: Acid Rain Operating Guide DO NOT SET OUT the dropper bottle of NaOH (sodium hydroxide). Remake the stock solutions of 0.5M Na2SO3 (sodium sulfite), 0.5M NaOH (sodium hydroxide), 1M HCl (hydrochloric acid), and bromthymol blue indicator as necessary. (Keep 50 ml of each on hand.) (See Materials Prep.) Refill all four labeled dropper bottles from the stock solutions. (HCl is in the acid cabinet, NaOH is in the hydroxide cabinet, and bromthymol blue solution is in the indicator cabinet.) Bromthymol blue should be green to start. If it is blue, add one drop of 1M HCl (hydrochloric acid). If it is yellow, add one drop of 0.5M NaOH (sodium hydroxide). add these to the STOCK BOTTLE, not the dropper bottle. Wash the plastic petri dish and return it to the tub. Tightly cap all bottles and store them in an upright position in the tub. Drape the towel across the counter or public copy holder to dry out overnight. If towel is stained and yucky looking, switch it out for a clean one. Clean and leave the tray at the station. Clean the glassware and return it to the tub. Clean and return the mat to general lab storage. ◊ Once visitors have added the Na2SO3 (sodium sulfite) to the HCl (hydrochloric acid), there is a tendency for the visitors to watch this drop (in area “5”) for a reaction, The reaction is not a visible one, Advise visitors to watch the bromthymol blue drops in areas “3” and “4.” ◊ If the bromthymol is too acidic (yellow) or too basic(blue), pour the contents of the dropper bottle back into the stock bottle, mix, and then refill the dropper bottle. Do not try to adjust the pH in the little dropper bottle itself. NO2 (nitrogen dioxide) is another common origin of acid rain. It can be found in car exhaust, among other places. It will react with water to Unit 4 Environmental Chemistry U4.3 Experiencing Chemistry ©2007 OMSI Experiment: Acid Rain Operating Guide form nitric acid in a manner identical to that of the SO2 (sulfur dioxide) in this experiment. Na2SO3 (sodium sulfite) and HCl (hydrochloric acid) are hazardous substances; follow the handling and disposal instructions in Materials Prep. Consult the Material Safety Data Sheets (MSDS) for additional information. To prepare 1M HCl (hydrochloric acid): CAUTION: concentrated HCl (hydrochloric acid) is extremely corrosive. Handle it with care. Wear protective gloves, an apron, and eyewear. Use it only in the fume hood. Avoid contact with skin or clothing. Neutralize any spills with baking soda and clean up with large amounts of water. CAUTION: A large amount of heat will be evolved after you mix the HCl with water. Do not handle the beaker until it has cooled. Turn on the fume hood. Wear protective eyewear, chemical safety gloves, and an apron or a lab jacket. In the fume hood, measure 83 ml of concentrated (12.1M) HCl. Add the acid to 917 ml of dH2O (deionized water) to make one liter. Store the extra solution in the labeled and dated bottles in the acid cabinet. Turn off the fume hood. To prepare 0.5M Na2SO3 (sodium sulfite): Wear protective eyewear, chemical safety gloves, and a lab jacket. Weigh 62.5 g Na2SO3. Add 500 ml dH2O (deionized water). Mix to dissolve the Na2SO3. Store the solution in a labeled/dated bottle. To prepare bromthymol blue solution: Weigh 0.1 g bromthymol blue sodium salt. Add 100 ml dH2O (deionized water) and mix to dissolve the bromthymol blue. Store the solution in a labeled and dated 125-ml plastic storage bottle in the indicator cabinet. U4.4 Unit 4 Environmental Chemistry Experiencing Chemistry ©2007 OMSI .
Recommended publications
  • Enhanced Conversion Oflactose to Glycerol by Kluyveromyces Fragilis
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Mar. 1989, p. 573-578 Vol. 55, No. 3 0099-2240/89/030573-06$02.00/0 Copyright C) 1989, American Society for Microbiology Enhanced Conversion of Lactose to Glycerol by Kluyveromyces fragilis Utilizing Whey Permeate as a Substrate WHEAMEI JENQ,1 RAY A. SPECKMAN,' RICHARD E. CRANG,2* AND MARVIN P. STEINBERG1 Department of Food Science, 1304 West Pennsylvania Avenue,' and School of Life Sciences, 505 South Goodwin Avenue,2 University ofIllinois, Urbana, Illinois 61801 Received 6 June 1988/Accepted 12 December 1988 Kluyveromycesfragilis (CBS 397) is a nonhalophilic yeast which is capable of lactose utilization from whey permeate and high glycerol production under anaerobic growth conditions. However, the optimum yields of glycerol (11.6 mg/ml of whey permeate medium) obtained in this study occurred only in the presence of 1% Na2SO3 as a steering agent. The use of other concentrations of Na2SO3, as well as 5% NaCl and 1% ascorbic acid, had no or detrimental effects on cell growth, lactose utilization, and glycerol production. Glycerol yields were greater in cultures grown from a light inoculum of K. fragilis than in cultures in which a resuspended mass of cells was introduced into the medium. The results of this study suggest that this strain of K. fragilis may be useful commercially in the utilization of cheese whey lactose and the concomitant production of glycerol. Cheese whey represents a commercial by-product gener- troleum derivatives, which is less expensive than processing ated in such massive quantities that its safe disposal is a by sugar fermentation. major problem for many municipal sewage treatment plants.
    [Show full text]
  • Sodium Chlorite Neutralization
    ® Basic Chemicals Sodium Chlorite Neutralization Introduction that this reaction is exothermic and liberates a If sodium chlorite is spilled or becomes a waste, significant amount of heat (H). it must be disposed of in accordance with local, state, and Federal regulations by a NPDES NaClO2 + 2Na2SO3 2Na2SO4 + NaCl permitted out-fall or in a permitted hazardous 90.45g + 2(126.04g) 2(142.04g) + 58.44g waste treatment, storage, and disposal facility. H = -168 kcal/mole NaClO2 Due to the reactivity of sodium chlorite, neutralization for disposal purposes should be For example, when starting with a 5% NaClO2 avoided whenever possible. Where permitted, solution, the heat generated from this reaction the preferred method for handling sodium could theoretically raise the temperature of the chlorite spills and waste is by dilution, as solution by 81C (146F). Adequate dilution, discussed in the OxyChem Safety Data Sheet thorough mixing and a slow rate of reaction are (SDS) for sodium chlorite in Section 6, important factors in controlling the temperature (Accidental Release Measures). Sodium chlorite increase (T). neutralization procedures must be carried out only by properly trained personnel wearing Procedure appropriate protective equipment. The complete neutralization procedure involves three sequential steps: dilution, chlorite Reaction Considerations reduction, and alkali neutralization. The dilution If a specific situation requires sodium chlorite to step lowers the strength of the sodium chlorite be neutralized, the chlorite must first be reduced solution to 5% or less; the reduction step reacts by a reaction with sodium sulfite. The use of the diluted chlorite solution with sodium sulfite to sodium sulfite is recommended over other produce a sulfate solution, and the neutralization reducing agents such as sodium thiosulfate step reduces the pH of the alkaline sulfate (Na2S2O3), sodium bisulfite (NaHSO3), and solution from approximately 12 to 4-5.
    [Show full text]
  • University of Cincinnati
    UNIVERSITY OF CINCINNATI DATE: July 5, 2002 I, Dinesh Kumar Palaniswamy , hereby submit this as part of the requirements for the degree of: Master of Science in: Environmental Engineering It is entitled: Electrochemical Reduction of 2,4,6-Trinitrotoluene Approved by: Dr.George Sorial Dr.Dionysios Dionysiou Dr.Makram Suidan ELECTROCHEMICAL REDUCTION OF 2,4,6 -TRINITROTOLUENE A thesis submitted to the Division of Research and Advanced Studies of the University of Cincinnati in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE in the Department of Civil and Environmental Engineering of the college of Engineering 2002 by Dinesh Kumar Palaniswamy B.E., Civil Engineering, P.S.G College of Technology, Coimbatore, 1998 Committee Chair: Dr. George Sorial ABSTRACT 2,4,6-trinitrotoluene (TNT) is a major constituent of munitions contaminated wastewater. This research aims at studying the efficiency of electrochemical processes in reducing TNT. A laboratory scale reactor was designed and developed to electrochemically reduce TNT in simulated munition wastewater. Experiments simulating batch conditions were first conducted on the laboratory scale reactor to study the effect of various parameters including applied current, type of electrolyte and the molar concentration of the electrolyte in the feed solution on the reduction kinetics of TNT. The results showed that the reduction rates of TNT increased with an increase in applied current and molar concentration of electrolyte in feed. The rates of reduction leveled off at higher currents (250 & 300 mA). Mass transfer limitations were speculated for this flattening of rate constants at higher currents. Experimental studies were conducted with two types of electrolyte in the feed- sodium sulfate (Na2SO4) and lithium sulfate (Li2SO4), and the results indicated that there was no significant difference in the reduction rates for TNT.
    [Show full text]
  • Sulfur Dioxide and Some Sulfites, Bisulfites and Metabisulfites
    SULFUR DIOXIDE AND SOME SULFITES, BISULFITES AND METABISULFITES 1. Exposure Data 1.1 Chemical and physical data 1.1.1 Synonyms and structural and molecular data Sulfr dioxi Chem. Abstr. Serv Reg. No.: 7446-09-5 Replaced CAS Nos.: 8014-94-6; 12396-99-5; 83008-56-4; 89125-89-3 Chem. Abstr. Name; Sulfur dioxide IUPAC Systematic Name: Sulfur dioxide Synonyms: Sulfurous acid anhydride; sulfurous anhydride; sulfurous oxide; sulfur oxide (S02); sulfur superoxide; sulphur dioxide 0=8=0 S02 MoL. wt: 64.07 Sodium sulfte Chem. Abstr. Serv Reg. No.: 7757-83-7 Altemate CAS No.: 10579-83-6 Replaced CAS No.: 68135-69-3 Chem. Abstr. Name: Sulfurous acid, di sodium salt IUPAC Systematic Name: Sulfurous acid, disodium salt Synonyms: Anhydrous sodium sulfite; disodium sulfite; sodium sulphite o 1/ Na · 0 - 8 - 0 · Na Na2S0J MoL. wt: 126.04 Sodium bisulfe Chem. Abstr. Serv Reg. No.: 7631-90-5 Replaced CAS Nos.: 57414-01-4; 69098-86-8; 89830-27-3; 91829-63-9 Chem. Abstr. Name: Sulfurous acid, monosodium salt IUPAC Systematic Name: Sulfurous acid, monosodium salt -131- 132 lARe MONOGRAPHS VOLUME 54 Synonyms: Hydrogen sulfite sodium; monosodium sulfite; sodium acid sulfite; sodium bisulphite; sodium hydrogen sulfite; sodium sulfite (NaHS03) o Il HO - S - a · Na NaHS03 MoL. wt: 104.06 Sodium metabisulfte Chem. Abstr. Serv Reg. No.: 7681-57-4 Altemate CAS No.: 7757-74-6 Replaced CAS No.: 15771-29-6 Chem. Abstr. Name: Disulfurous acid, disodium salt IUPAC Systematic Name: Pyrosulfurous acid, disodium salt Synonyms: Disodium disulfite; disodium metabisulfite; disodium pyrosulfite; sodium disulfite; sodium metabisulphite; sodium pyrosulfite oIl Il0 Na · 0- S - a - S - a · Na .Na2S20S MoL.
    [Show full text]
  • Synthesis of New Betaine-Type Amphoteric Surfactants from Tall Oil Fatty Acid
    J Wood Sci (2002) 48:419424 The Japan Wood Research Society 2002 Shi-Fa Wang Takeshi Furuno Zhi Cheng Synthesis of new betaine-type amphoteric surfactants from tall oil fatty acid Received: August 13, 2001 / Accepted: November 14, 2001 Abstract Two new betaine-type amphoteric surfactants moistening and foaming abilities. It can be widely used - betaine N,N-dihydroxyethyl-N-ethyl fatty acid ester in many fields, such as the chemical, textile, dye, pigment, and ammonium N-(fatty acid ester) ethyl-N,N-bis (2- food, pharmaceutical, machining, metallurgy, washing, and hydroxyethyl)-3-(2-hydroxypropyl) sulfonate - were syn- petroleum industries. It has been used as a detergent, moist- thesized using tall oil fatty acids as the raw materials. ening and foaming agent, corrosion inhibitor, dispersion Processing conditions suitable for synthesizing the inter- agent, germicide (bactericide), emulsifying agent, antistatic mediates and final products were probed. In addition, the and softening agent of fibers, a dye, a chelating agent, and a chemical structures of the intermediates and the final prod- cleaning agentY ucts were identified by infrared spectroscopy, hydrogen A betaine-type surfactant usually means that quaternary nuclear magnetic resonance spectroscopy, and elemental ammonium cationic groups and anionic groups such as analysis. --COO-, --SO3, --OSO3, and --PO2 coexist in the same molecule. It has excellent solubility over a wide range of pH Key words Tall oil fatty acid Amphoteric surfactant values. Its solubility does not obviously decrease even in an Betaine type isoelectric zone. In addition, unlike the external quaternary ammonium salt, the betaine-type surfactant is compatible with ionic surfactants. Among the betaine-type surfactants, Introduction the most important contain sulfonic and carboxylic groups because they have important commercial value and a wide application field.
    [Show full text]
  • Azobenzene-P-Phenylhydrazine Sulfonic Acid and Its Reactions
    AZOBENZENE-p -PHENYLHYDRAZINE SULFONIC ACID AND ITS REACTIONS BY WALTER FRED STRAUB THESIS FOR THE DEGREE OF BACHELOR OF SCIENCE IN CHEMISTRY COLLEGE OF LIBERAL ARTS AND SCIENCES UNIVERSITY OF ILLINOIS 1918 UNIVERSITY OF ILLINOIS *3 June 1 8 THIS IS TO CERTIFY THAT THE THESIS PREPARED UNDER MY SUPERVISION BY Walter.. .Zred...S.traub..... ENTITLED....Aj5Sfo.8tt3.e^^ actions IS APPROVED BY ME AS FULFILLING THIS P ART OF THE REQUIREMENTS FOR THE „.S ie , C h i t ry, DEGREE OF £a or .. of c n c e ... in em s Instructor in Charge HEAD OF DEPARTMENT OF TABLE OF COUNTS Page PART I. I Introduction 1 II Historical Part 3 III Theoretical Part 7 (A) The Reaction of the Formation of Azobenzene- p-phenylhydrazine Sulfonic Acid 8 (B) Condensations of the Red Acid 1. With aromatic aldehydes and ketones. 9 2. With aliphatic aldehydes and ketones. 10 3. With sugars to form osazones, 11 4. With acetoacetic ester. 12 5. With dihydroxytartarie acid. 13 IV Experimental Part 14 (A) Preparation of Azobenzene-p-phenylhydrazine Sulfonic Acid 14 (B) Identification of the Acid. 15 (G) Preparation and Analysis of: G H 01 18 18 22W H 1I 18 °30 30 8 4 -' G H 1J ^ ma:1 tose condensation) 19 36 40 8°9 ( lac1;ose condensation) 20 G 36H40%°9 21 C 1SH20H4°2 21 C18HS0°2H4HC1 (D) Condensation with Dihydroxytartarie Acid 22 1. Preparation of dihydroxytartarie acid 22 2. Condensation in glacial acetic acid solution 23 Y Summary 24 PART II. Some Rosin Compounds 26 Rosin derivatives prepared "by: 1.
    [Show full text]
  • Kinetic and Structural Studies Reveal a Unique Binding Mode of Sulfite to The
    Kinetic and structural studies reveal a unique binding mode of sulfite to the nickel center in urease Luca Mazzei1, Michele Cianci2, Stefano Benini3, Leonardo Bertini1, Francesco Musiani1, Stefano Ciurli1* 1 Laboratory of Bioinorganic Chemistry, Department of Pharmacy and Biotechnology, University of Bologna, Via Giuseppe Fanin 40, I-40138, Bologna (Italy) 2 European Molecular Biology Laboratory c/o DESY, Notkestraße 85, 22607 Hamburg, Germany 3 Bio-Organic Chemistry and Bio-Crystallography Laboratory, Faculty of Science and Technology, Free University of Bolzano, Piazza Università 5, 39100 Bolzano, Italy * Corresponding author: [email protected]; phone: (+39)-051-209-6204; fax: (+39)-051-209-6203 1 ABSTRACT Urease is the most efficient enzyme known to date, and catalyzes the hydrolysis of urea using two Ni(II) ions in the active site. Urease is a virulence factor in several human pathogens, while causing severe environmental and agronomic problems. Sporosarcina pasteurii urease has been used extensively in the structural characterization of the enzyme. Sodium sulfite has been widely used as a preservative in urease solutions to prevent oxygen-induced oxidation, but its role as an inhibitor has also been suggested. In the present study, isothermal titration microcalorimetry was used to establish sulfite as a competitive inhibitor for S. pasteurii urease, with an inhibition constant of 0.19 mM at pH 7. The structure of the urease-sulfite complex, determined at 1.65 Å resolution, shows the inhibitor bound to the dinuclear Ni(II) center of urease in a tridentate mode involving bonds between the two Ni(II) ions in the active site and all three oxygen atoms of the inhibitor, supporting the observed competitive inhibition kinetics.
    [Show full text]
  • Sodium Sulfite
    16 Sodium Sulfite COMPONENTS: ORIGINAL MEASUREMENTS: 1. SodIum sulfite; Na2S03; [7757-83-7] Durymanova, M.A.; Telepneva, A.E. 2. SodIum sulfate; Na2S04; [7757-82-6] Zh. Prlklad. Khim. 1972, 45, 1610-12; J. Appl. Chem. USSR (Eng. Transl.) 1972, 45, 3. Water; H20; [7732-18-5] 1680-2. VARIABLES: PREPARED BY: Concentrations of the components Mary R. Masson One temperature: 373 K EXPERIMENTAL VALUES: Composition of equilibrIum solutions at 100°C b Na2S03 Na2S04 Na2S03a Na2S04a Solid mass % mass % mol/kg mol/kg phase 20.8 - 2.084 0. A 19.4 3.4 1.994 0.310 B 19.4 3.7 2.002 0.339 B 19.2 4.2 1.989 0.386 B 18.4 6.4 1.941 0.599 B 18.0 6.5 1.892 0.606 B 17.5 8.6 1.879 0.819 B 16.9 8.4 1.795 0.792 B 15.9 11.0 1.726 1.059 B 15.5 12.5 1.708 1.222 B 15.5 11.3 1.680 1.087 B 15.3 12.0 1.670 1.162 B 15.2 12.9 1.677 1.263 B 14.8 13.5 1.638 1.326 B 14.7 13.5 1.624 1.324 B 14.5 14.7 1.625 1.462 B + C 14.3 14.8 1.600 1.470 B + C 13.1 16.6 1.478 1.662 C 12.4 17.1 1.395 1.708 C 11.0 19.3 1.252 1.949 C 10.4 19.3 1.174 1.933 C 10.3 19.5 1.164 1.956 C 9.5 20.5 1.077 2.062 C 8.5 22.6 0.979 2.309 C (continued on next page) AUXILIARY INFORHATION METHOD M'PARATUS/PROCEDURE: SOURCl AND PURl TY OF HAH.RI ilLS: The systems were studied under isothermal Sodium sulfate was of c.p.
    [Show full text]
  • Oxidation and Degradation Products of Common Oxygen Scavengers
    2002 Fall Oxidation And Degradation Products Of Common Oxygen Scavengers By John D. Zupanovich, ChemTreat, Inc. For many years, sulfite and hydrazine were the principal materials used to protect boiler systems from oxygen attack. When hydrazine became listed as a suspected carcinogen, a search began for a replacement. During the search it became apparent that strong reducing agents (oxygen scavengers) should do more than react with and remove dissolved oxygen. They should also form protective oxide films on the metal surfaces of the steam/water system. Thus, the reaction with metal oxides is equally as important as the reaction with dissolved oxygen. During the past decade, a number of materials have been proposed for use as oxygen scavengers and metal passivators. The reactions are frequently very complex. This article is an attempt to explain the oxidation and degradation reactions of the more common oxygen scavengers in current use. In each case, the material will react with oxygen, and with metal oxides. The efficiency of the reaction is dependent on time, temperature, concentration and system pH. In general, as the pH, time, and temperature increase, the reaction becomes more complete. Since time is usually of the essence, many materials are catalyzed to decrease the reaction time. As a rule, multi-valent metal ions such as copper and iron will increase the reaction rate. Certain organic compounds such as hydroquinone and its derivatives have also been found to be effective catalysts. Sulfite Sulfite reacts with and consumes dissolved oxygen in aqueous solutions: 2- 2- 2SO3 + O2 2SO4 (1) At temperatures of 430°F and above, sulfite will react with iron oxide: 2- 2- 3Fe2O3 + SO3 2Fe3O4 + SO4 (2) However, because sulfite begins to decompose at 250°F, this reaction is rarely encountered in boiler systems.
    [Show full text]
  • SDS Safety Data Sheet
    SDS Safety Data Sheet 1. IDENTIFICATION Product Identifier: Sodium Sulfite, Anhydrous Product Code(s): S1037 Synonyms: Disodium Sulfite. Recommended Use: For manufacturing, industrial, and laboratory use only. Use as a catalyst or as a laboratory solute. Uses Advised Against: Not for food, drug, or household use. Supplier: Rocky Mountain Reagents, Inc. 4621 Technology Drive, Golden, CO 80403 Phone: (303) 762-0800 Fax: (303) 762-1240 Emergency Phone Number: For health emergency, call Poison Control: (800) 222-1222. 2. HAZARDS IDENTIFICATION Hazard Classifications: This product is classified as not hazardous under OSHA's Hazard Communication Standard, 29 CFR 1910.1200 (HCS) and the United Nations’ Globally Harmonized System of Classification and Labeling of Chemicals (GHS). However, all chemicals handled and used in the workplace should be treated with caution. Signal Word: Not applicable. Hazard Statements: Not applicable. Pictograms: Not applicable. Precautionary Statements: Prevention: Not applicable. Response: Not applicable. Storage: Not applicable. Disposal: Not applicable. Hazards Not Otherwise May be mutagenic based on human and microorganism data. Classified: Product: Sodium Sulfite, Anhydrous Revision Date: 04/14/2015 1/7 Toxicity Statement: This product consists of 100% ingredients whose acute toxicities are unknown. 3. COMPOSITION AND INFORMATION ON INGREDIENTS Component Common Name / Synonyms CAS# Chemical Formula % by Weight Sodium Sulfite Disodium Sulfite 7757-83-7 Na2SO3 ≥ 98.0 Trade Secret Statement: Not applicable. 4. FIRST AID MEASURES First Aid Procedures: Inhalation: Move to fresh air. If breathing is difficult, give oxygen. If not breathing, give artificial respiration. Call a physician if symptoms occur. Ingestion: Do not induce vomiting unless directed to do so by medical personnel.
    [Show full text]
  • The Institute of Paper Chemistry
    The Institute of Paper Chemistry Appleton, Wisconsin Doctor's Dissertation An Investigation of the Reactions Leading to Volatilization of Inorganic Sulfur During Pyrolysis with Vanillic Acid and Sodium Gluconate David T. Strohbeen June, 1981 TABLE OF CONTENTS Page ABSTRACT 1 INTRODUCTION 3 LITERATURE REVIEW 5 Pyrolysis 5 Thermodynamics and Kinetics 6 Kraft Black Liquor Pyrolysis 8 Black Liquor Composition 8 Cellulose Pyrolysis 11 Hemicellulose Pyrolysis 16 Hydroxy Acid Pyrolysis 17 Lignin Pyrolysis 17 Wood Pyrolysis 19 Coal Pyrolysis 24 Implications of Wood, Wood Component, and Coal Pyrolysis Studies for Black Liquor Pyrolysis 26 Black Liquor Pyrolysis 26 Black Liquor Pyrolysis Sulfur Distribution 31 Thermodynamics 38 Comparison of Black Liquor Pyrolysis Results with Thermodynamic Predictions - An Analysis 41 Sulfur Volatilization Reactions and Kinetics 43 Analysis . 46 THESIS OBJECTIVES 50 EXPERIMENTAL 51 Materials 51 Pyrolysis 51 RESULTS AND DISCUSSION 54 Sulfur Balance Closure 54 Reproducibility 54 Thermal Characterization of Pyrolysis Materials 56 Sulfur Volatilization 58 Sodium Sulfide Pyrolysis 58 Sodium Sulfate Pyrolysis 61 Sodium Sulfite Pyrolysis 62 Sodium Thiosulfate Pyrolysis 63 Effect of Heating Rate 72 Effect of Particle Size 74 Effect of Purge Rate 74 SUMMARY AND CONCLUSIONS 76 ACKNOWLEDGMENTS 79 LITERATURE CITED 80 APPENDIX I. ANALYTICAL METHODS 84 APPENDIX II. EXPERIMENTAL RESULTS - TABULATED 94 APPENDIX III. STATISTICAL ANALYSIS OF DATA 104 APPENDIX IV. THIOSULFATE PYROLYSIS SULFUR-GAS TIME SEQUENCE 107 ABSTRACT The formation of volatile sulfur compounds from sodium sulfide, sodium thiosulfate, sodium sulfite, and sodium sulfate was studied during slow pyrolyses with sodium gluconate or vanillic acid. Pyrolyses were carried out at constant heating rates between ambient temperature and 550°C in a batch reactor with a nitro- gen purge to continuously dilute, remove, and cool the pyrolysis product gases.
    [Show full text]
  • Paper-Based Devices for Formaldehyde Analysis
    อุปกรณ์แบบกระดาษสาหรับการวิเคราะห์ฟอร์มัลดีไฮด์ 3617976898 PAPER-BASED DEVICES FOR FORMALDEHYDE ANALYSIS BUU iThesis 59910276 thesis / recv: 17122561 16:41:44 seq: 17 NATCHANON TAPRAB Burapha University 2018 59910276_3617976898 อุปกรณ์แบบกระดาษสาหรับการวิเคราะห์ฟอร์มัลดีไฮด์ 3617976898 BUU iThesis 59910276 thesis / recv: 17122561 16:41:44 seq: 17 ณัฐชนน ตาปราบ วทิ ยานิพนธน์ ้ีเป็นส่วนหน่ึงของการศึกษาตามหลกั สูตรวทิ ยาศาสตรมหาบณั ฑิต สาขาวิชาเคมีศึกษา คณะวิทยาศาสตร์ มหาวิทยาลัยบูรพา 2561 ลิขสิทธิ์ของมหาวิทยาลัยบูรพา PAPER-BASED DEVICES FOR FORMALDEHYDE ANALYSIS 3617976898 BUU iThesis 59910276 thesis / recv: 17122561 16:41:44 seq: 17 NATCHANON TAPRAB A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR MASTER OF SCIENCE IN CHEMICAL EDUCATION FACULTY OF SCIENCE BURAPHA UNIVERSITY 2018 COPYRIGHT OF BURAPHA UNIVERSITY D ABSTRACT 59910276: MAJOR: CHEMICAL EDUCATION; M.Sc. (CHEMICAL EDUCATION) KEYWORDS: FORMALDEHYDE / PAPER-BASED TITRATION / FOOD SAMPLES NATCHANON TAPRAB : PAPER -BASED DEVICES FOR FORMALDEHYDE ANALYSIS. ADVISORY COMMITTEE: YUPAPORN SAMEENOI, PH.D. 2018. A rapid and simple paper-based analytical device (PAD) for quantitative 3617976898 analysis of formaldehyde in food samples has been developed. The analysis was based on sulfite assay where the formaldehyde (FA) was reacted with excess amount of sulfite to generate sodium hydroxide and the product consequently quantified using acid-based titration on the PAD. The acid-based titration PAD consisted of a central BUU iThesis 59910276 thesis / recv: 17122561 16:41:44 seq: 17 sample zone connected to ten reaction and detection zones. Polyethylene glycol and phenolphthalein (indicator) were deposited to the detection zones, and different amounts of titrant, potassium hydrogen phthalate (KHP), were added to the reaction zones. The formaldehyde concentration can be quantified from the number of color- changed detection zone(s) which are correlated to known amount of KHP on reaction zone.
    [Show full text]