Sulfur Trioxide Interim AEGL Document
Total Page:16
File Type:pdf, Size:1020Kb

Load more
Recommended publications
-
SULFUR TRIOXIDE -- Chemical Fact Sheet
OLEUM/SULFUR TRIOXIDE -- Chemical Fact Sheet 1 What is it? Oleum is a cloudy, gray, fuming, oily, corrosive liquid with a sharp, penetrating odor. When Oleum comes into contact with air following a spill, it releases Sulfur Trioxide. Sulfur Trioxide is a white gas having the appearance of fog. It also has a sharp, penetrating odor that is detectable at low concentrations. Because of the tendency to liberate Sulfur Trioxide on contact with air, Oleum is also known as “fuming Sulfuric Acid”. Where does it Oleum is made by dissolving Sulfur Trioxide into Sulfuric Acid. Sulfur come from? Trioxide is made from Sulfur Dioxide in the presence of a catalyst. What are the It is used in the oil refining process to make crude oil distillates into higher quality materials. common uses for it? Manufacture of soap Manufacture of high purity Sulfuric Acid for the electronic industry Manufacture of catalyst used in production of Sulfuric Acid. How is it Oleum is shipped by truck and pipeline. transported in CCC? How is it stored Oleum is stored in covered tanks. in CCC? Health Hazards from Exposure Exposure Route Symptoms First Aid Inhalation Irritates nose, throat and Remove to fresh air. Seek (low concentrations) lungs medical attention if Burning Sensation symptoms persist. Sneezing, coughing Inhalation Burning sensation Remove to fresh air, get (high concentrations & prolonged exposure) Coughing, gagging medical attention including Chest tightness and pain, oxygen administration. Fluid in lungs Initiate CPR if breathing has Suffocation, death stopped. Eyes Severely irritates eyes Rinse eyes with water for at Burning/discomfort least 5 minutes. -
Source Test Method ST-20 SULFUR DIOXIDE, SULFUR TRIOXIDE
Source Test Method ST-20 SULFUR DIOXIDE, SULFUR TRIOXIDE, SULFURIC ACID MIST (Adopted January 20, 1982) REF: Regulations 6-320, 6-330, 9-1-302, 9-1-304 thru 310, 10-1-301, 12-6-301 1. APPLICABILITY 1.1 This method is used to quantify emissions of s ulfur dioxide, sulfur trioxide and sulfuric acid mist. It determines compliance with Regulations 6-320 and 6-330 for SULFUR TRIOXIDE and SULFURIC ACID MIST, and 9-1-302, 9- 1-304 thru 310 and 10-1-301 and 12-6-301 for SULFUR DIOXIDE. 1.2 This method, modified with a glass fiber disc filter as the back-up SO 3 filter, has been given alternate status by the EPA to EPA Method 8. It may be used to determine compliance with oxides of sulfur regulations under Regulation 9. 2. PRINCIPLE 2.1 Sulfuric acid mist, sulfur trioxide and sulfur dioxide are collected in a single extractive sampling train. Acid mist is trapped in a quartz wool plug in the sample probe and is subsequently analyzed with an acid-base titration. Sulfur trioxide is absorbed in an 80% isopropyl alcohol (IPA)/water solution with a quartz wool back-up filter and is analyzed using analytical procedure Lab-12. Sulfur dioxide is absorbed in an aqueous hydrogen peroxide solution and is analyzed using analytical procedure Lab-12. 3. RANGE 3.1 The minimum measurable concentration using this method listed below are: 3 3.1.1 Acid mist - 0.0002 gr/ft as H2SO4 3.1.2 Sulfur trioxide - 7 ppm 3.1.3 Sulfur dioxide - 7 ppm 3.2 The maximum measurable concentrations using this method listed below are: 3.2.1 Acid mist - undetermined 3.2.2 Sulfur trioxide - 350 ppm 3.2.3 Sulfur dioxide - 2.5 % 4. -
(VI) and Chromium (V) Oxide Fluorides
Portland State University PDXScholar Dissertations and Theses Dissertations and Theses 1976 The chemistry of chromium (VI) and chromium (V) oxide fluorides Patrick Jay Green Portland State University Follow this and additional works at: https://pdxscholar.library.pdx.edu/open_access_etds Part of the Chemistry Commons Let us know how access to this document benefits ou.y Recommended Citation Green, Patrick Jay, "The chemistry of chromium (VI) and chromium (V) oxide fluorides" (1976). Dissertations and Theses. Paper 4039. https://doi.org/10.15760/etd.5923 This Thesis is brought to you for free and open access. It has been accepted for inclusion in Dissertations and Theses by an authorized administrator of PDXScholar. Please contact us if we can make this document more accessible: [email protected]. All ABSTRACT OF THE TllESIS OF Patrick Jay Green for the Master of Science in Chemistry presented April 16, 1976. Title: Chemistry of Chromium(VI) and Chromium(V) Oxide Fluorides. APPROVEO BY MEMBERS OF THE THESIS CO'"o\l TIEE: y . • Ii . ' I : • • • • • New preparative routes to chromyl fluoride were sought. It was found that chlorine ironofluoride reacts with chromium trioxide and chromyl chlo ride to produce chromyl fluoride. Attempts were ~ade to define a mechan ism for the reaction of ClF and Cr0 in light of by-products observed 3 and previous investigations. Carbonyl fluoride and chromium trioxide react to fom chro·yl fluoride and carbo:i dioxide. A mechanism was also proposed for this react10n. Chromium trioxide 11itl\ l~F6 or WF5 reacts to produce chromyl fluoride and the respective oxide tetrafluoride. 2 Sulfur hexafluoride did not react with Cr03. -
Oxidation of Sulfur Dioxide to Sulfur Trioxide Over Supported Vanadia Catalysts
Applied Catalysis B: Environmental 19 (1998) 103±117 Oxidation of sulfur dioxide to sulfur trioxide over supported vanadia catalysts Joseph P. Dunn, Prashanth R. Koppula, Harvey G. Stenger, Israel E. Wachs* Zettlemoyer Center for Surface Studies, Department of Chemical Engineering, Lehigh University, Bethlehem, PA 18015, USA Accepted 2 June 1998 Abstract The objectives of this research are to establish the fundamental kinetics and mechanism of sulfur dioxide oxidation over supported vanadia catalysts and use these insights to facilitate the design of SCR DeNOx catalysts with minimal sulfur dioxide oxidation activity. A series of supported vanadia catalysts were prepared on various metal-oxide supports: ceria, zirconia, titania, alumina and silica. Raman spectroscopy was used to determine the coordination of surface species. At low vanadia 5 loadings, vanadia preferentially exists on oxide support surfaces as isolated tetrahedrally coordinated (M±O)3V O species. 5 At higher vanadia loadings, the isolated (M±O)3V O species polymerize on the oxide support surface breaking two V±O±M bonds and forming two V±O±V bridging bonds. The turnover frequency for sulfur dioxide oxidation was very low, 104 to 106 s1 at 4008C, and was independent of vanadia coverage suggesting that only one vanadia site is required for the oxidation reaction. As the support was varied, sulfur dioxide oxidation activity of the supported vanadia catalysts varied by one order of magnitude (Ce>Zr, Ti>Al>Si). The basicity of the bridging V±O±M oxygen appears to be responsible for in¯uencing the adsorption and subsequent oxidation of the acidic sulfur dioxide molecule. Over the range of conditions studied, the rate of sulfur dioxide oxidation is zero-order in oxygen, ®rst-order in sulfur dioxide and inhibited by sulfur trioxide. -
Sulfur (IV) Isotopic Exchange Reaction in Aqueous and Concentrated Acid
THE KINETICS OF THE SULFtJR(IV) - suLFuR(vI) ISOTOPIC EXCHANGE REACTION IN AQUEOUS AND CONCTRATED ACID )LUTIONS by RAY LOCKE McDONALD A THESIS submitted to OHEGON STATE COLLEGE In parti1 fulfillment of the requirements for the degree of DOCTOR 0F PHW)SOPHY June 196]. flIiY1i$IT Redacted for Privacy Professor of Chemistry In Charge of Major Red acted f or P rivacy Chairman of Department of Cnemistry Redacted for Privacy Chairman of School Graduate Committee Redacted for Privacy Dean of Graduate School nate thesis is presented Typed by LeAnna kiarris tffi*ffimffi Fcar rdsrmo ad mflss. dte rU egestr d lilt rretc Mlr1 tb lutEm'rprm [ilr;r* dffi tldr te EufUe ?. E. I*1ill. TABLE OF CONTENTS Page I. INTRODUCTION ...................... i II. E(PERIMENTAL ...................... 7 A. General Procedure ................. 7 B. Radioactivity Analysis ............... 9 C. Chemical Analysis ................ il D, Preparation of Materials and Reactant Solutions 13 1. General ................. 13 2. Sulfur Dioxide ................ 1.3 3. Labeled Aqueous Sulfuric Acid ......... i1 )4. Labeled Concentrated Sulfuric cid ....... 15 ;. Labeled 100% Sulfuric Acid ........... 16 6. Labeled Fuming Sulfuric Acid .......... 16 7. Labeled Aqueous Sodium Bisulfate ........ 16 8. Lat.ed Sodium Bisulfate in Aqueous Sulfuric Acid .................. 17 9. Labeled Sodium Bisulfate in Concentrated . Sulfuric Acid .................. 17 10. Labeled Sodium Sulfate ............. 17 li. Labeled Sodium Sulfate in Aqueous Sodium Bisulfate ................ 18 12. Labeled Elemental Sulfur ............ 18 III. RUN PROCEDURE AND DATA ................ 19 A. Sulfur(IV) - Sulfur(VI) Exchange in Basic Media . 19 B, - Sulfur(IV) Sulfur(VI) Exchange in Acidic Media . .23 1. Radiosulfur Ecchsuge Experiments Between Sulfur Dioxìe and Aqueous Sulfuric Acid of High Specific Activity ........... -
The Determination of Sulfate and Sulfide Sulfur in Rocks Or Minerals
The Determination of Sulfate and Sulfide Sulfur in Rocks or Minerals By ANGELINA C. VLISIDIS CONTRIBUTIONS TO GEOCHEMISTRY GEOLOGICAL SURVEY BULLETIN 1214-D UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1966 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretary GEOLOGICAL SURVEY William T. Pecora, Director For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 - Price 15 cents (paper cover) CONTENTS Page Abstract_____--__-___-_______-__---____,__-_-__-_---_-_______-_- Dl Introduction. ______________________________________________________ 1 Preparations. _________._.-.__-_-.__.._-_---__----.________._.._____ 2 Standard samples____________________________________________ 2 Reagents. _______________.-_-___-____-__-_-__-_-___-_______-_- 2 Procedure._______________________________________________________ 2 Results__ __________-______-_____----__--_--_----_-_-_-___-___--_ 3 References.._ _____________________________________________________ 5 TABLE Page TABLE 1. Results of sulfide and sulfate sulfur analyses in which varying amounts of a sulfate standard were added to sulfide minerals.. _ D4 m 209-517 66 CONTRIBUTIONS TO GEOCHEMISTRY THE DETERMINATION OF SULFATE AND SULFIDE SULFUR IN ROCKS OR MINERALS By ANGELINA C. VLISEDIS , ABSTRACT A method for the determination of sulfate and sulfide sulfur that occur together in rocks or minerals is presented. All the sulfate sulfur is converted to barium sulfate in an inert atmosphere to prevent oxidation of any sulfide sulfur. Cadmium chloride is added to precipitate any sulfide ion that may be liberated. The sulfate sulfur is then measured indirectly by the determination of the barium and is therefore unaffected by any. subsequent oxidation of the sulfide sulfur. -
Sulfur and Tennessee Row Crops
W 435 SULFUR AND TENNESSEE ROW CROPS Sulfur (S) deficiencies have become more common in recent years. This publication outlines the importance and role of S in higher plants, summarizes recent research, and defines the University of Tennessee’s current S recommendations for row crops. Tyson B. Raper1, Angela T. McClure2, Frank Yin3 and Blake Brown4 1Assistant Professor, Cotton and Small Grains Specialist, Department of Plant Sciences 2Associate Professor, Corn and Soybean Specialist, Department of Plant Sciences 3Associate Professor, Cropping Systems Agronomist, Department of Plant Sciences 4Director, AgResearch and Education Center at Milan INTRODUCTION Sulfur (S) deficiencies have become more common in recent years due to a reduction in S deposition. Research at the University of Tennessee has begun to answer several key questions on crop response to applications of this nutrient. The objective of this publication is to outline the importance of S and the role it plays within higher plants, describe why the deficiencies are becoming more common, summarize recent research and define the University of Tennessee’s current S recommendations for Tennessee row crops. THE ROLE AND IMPORTANCE OF SULFUR IN HIGHER PLANTS Sulfur is an important nutrient in living systems; it is contained within four common amino acids that assist in the synthesis, structure and function of proteins (Brosnan & Brosnan, 2006). In plant nutrition, S is classified as a macronutrient since it is required in quantities much larger than most micronutrients. Within the macronutrient classification, S falls within the secondary nutrient subclassification along with calcium and magnesium. Although S isn’t a primary macronutrient, it is occasionally referred to as the fourth major nutrient (Stewart, 2010), and if contained within a fertilizer, the S percentage is commonly listed as the fourth Figure 1: Most S containing fertilizers have four number in the fertilizer analysis or grade numbers reported in the analysis or grade, with the first (Figure 1). -
United States Patent Office Patented Jan
3,297,748 United States Patent Office Patented Jan. 10, 1967 1. 2 was found to have superior odor qualities, based upon 3,297,748 ALKYLBENZENE SULFONATE COLOR AND odor ratings made by subjective panel testing. ODOR INHIBITION By sulfonation is meant the treatment of alkylbenzenes John B. Wilkes, Albany, Calif., assignor to Chevron Re with concentrated sulfuric acid, and particularly with search Company, a corporation of Delaware concentrated sulfuric acid-sulfur trioxide mixtures, there No Drawing. Filed June 13, 1963, Ser. No. 287,489 by to produce the corresponding alkylbenzene sulfonic 2 Claims. (CI. 260-505) acids. Preferably, the present process contemplates the use of oleum having from about 5 to 28 percent sulfur This invention relates to an improved method for the trioxide content, by weight. In general, sulfonation reac preparation of branched-chain alkylbenzene sulfonate de 0 tion temperatures useful in the process range from about tergents. More specifically, this invention relates to the 50 to 150 F.; and, as is known in the art, from about a preparation of branched side-chain alkylbenzene sulfo stoichiometric amount to about a 20 percent excess of nate detergent by the sulfonation of branched-chain alkyl the sulfonating agent, based upon the alkylbenzene, is benzenes with oleum in the presence of color and odor preferably used. Usually, the sulfur trioxide in the oleum inhibiting amounts of acetic acid and a lower alkylben mixture is the sulfonation agent consumed, although the ZCle. sulfuric acid may also be consumed to the point where The active ingredient in most detergents in household the residual sulfuric acid medium has been reduced use are alkylated aryl sulfonates. -
Determination of Sulfuric Acid and Oleum Concentration Relevant For: Chemical Industry / Sulfuric Acid Production
Determination of Sulfuric Acid and Oleum Concentration Relevant for: Chemical industry / Sulfuric acid production Sulfuric acid is widely used in the chemical industry, plastics industry and petrochemistry, for the production of phosphoric acid as a starting material for fertilizers, in the metal industry (e.g. in etching baths), and in accumulators. Dissolving sulfur trioxide, SO3, in concentrated sulfuric acid results in a fuming solution called oleum (or "fuming sulfuric acid"). Oleum is used in the chemical industry, for example for the production of intermediate materials or chemical fibers. 2.2. Conventional: Titration - a tedious method The conventional method for determination of sulfuric acid concentration is titration. However, titration is not only time-consuming and hazardous, but also includes a range of error prone operation steps even for skilled 1. Quality control in sulfuric acid production laboratory staff. The titration of sulfuric acid or oleum is carried out Sulfuric acid (H2SO4) is a high production volume with a base, commonly sodium hydroxide, NaOH. The chemical and plays an important role in various acid sample has to be diluted prior to titration - a time- industries. Sulfuric acid is a colorless and odorless consuming and hazardous operation. The accuracy of oily liquid which is highly hygroscopic. Depending on the results is influenced by several factors such as the its concentration the acid is used for different skill of the operator, the quality of the standard base purposes. solution, the precision of the burettes, the quality of The production of sulfuric acid proceeds in several the indicator used, etc. In routine analysis accuracies of 0.1 % w/w to 0.5 % w/w H SO can be attained. -
Introduction to Chemistry
Introduction to Chemistry Author: Tracy Poulsen Digital Proofer Supported by CK-12 Foundation CK-12 Foundation is a non-profit organization with a mission to reduce the cost of textbook Introduction to Chem... materials for the K-12 market both in the U.S. and worldwide. Using an open-content, web-based Authored by Tracy Poulsen collaborative model termed the “FlexBook,” CK-12 intends to pioneer the generation and 8.5" x 11.0" (21.59 x 27.94 cm) distribution of high-quality educational content that will serve both as core text as well as provide Black & White on White paper an adaptive environment for learning. 250 pages ISBN-13: 9781478298601 Copyright © 2010, CK-12 Foundation, www.ck12.org ISBN-10: 147829860X Except as otherwise noted, all CK-12 Content (including CK-12 Curriculum Material) is made Please carefully review your Digital Proof download for formatting, available to Users in accordance with the Creative Commons Attribution/Non-Commercial/Share grammar, and design issues that may need to be corrected. Alike 3.0 Unported (CC-by-NC-SA) License (http://creativecommons.org/licenses/by-nc- sa/3.0/), as amended and updated by Creative Commons from time to time (the “CC License”), We recommend that you review your book three times, with each time focusing on a different aspect. which is incorporated herein by this reference. Specific details can be found at http://about.ck12.org/terms. Check the format, including headers, footers, page 1 numbers, spacing, table of contents, and index. 2 Review any images or graphics and captions if applicable. -
A Novel Exchange Method to Access Sulfated Molecules Jaber A
www.nature.com/scientificreports OPEN A novel exchange method to access sulfated molecules Jaber A. Alshehri, Anna Mary Benedetti & Alan M. Jones* Organosulfates and sulfamates are important classes of bioactive molecules but due to their polar nature, they are both difcult to prepare and purify. We report an operationally simple, double ion- exchange method to access organosulfates and sulfamates. Inspired by the novel sulfating reagent, TriButylSulfoAmmonium Betaine (TBSAB), we developed a 3-step procedure using tributylamine as the novel solubilising partner coupled to commercially available sulfating agents. Hence, in response to an increasing demand for complementary methods to synthesise organosulfates, we developed an alternative sulfation route based on an inexpensive, molecularly efcient and solubilising cation exchanging method using of-the-shelf reagents. The disclosed method is amenable to a range of diferentially substituted benzyl alcohols, benzylamines and aniline and can also be performed at low temperature for sensitive substrates in good to excellent isolated yield. Organosulfates and sulfamates contain polar functional groups that are important for the study of molecu- lar interactions in the life sciences, such as: neurodegeneration1; plant biology2; neural stem cells3; heparan binding4; and viral infection5. Recent total syntheses including 11-saxitoxinethanoic acid6, various saccharide assemblies7–10, and seminolipid11 have all relied on the incorporation of a highly polar organosulfate motif. Importantly, the frst in class organosulfate containing antibiotic, Avibactam12, has led to the discovery of other novel β-lactamase inhibitors 13,14. Despite the importance of the sulfate group, there remain difculties with the ease of their synthesis to enable further biological study. Our own interest in developing sulfated molecules resulted from a medicinal chemistry challenge to reliably synthesise sulfated glycomimetics 15–18. -
Utilization of Sulfur Dioxide in Organic Acids Recovery and Sulfur Trioxide Conversion with Iron Oxide As Catalyst Yonghui Shi Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 2006 Utilization of sulfur dioxide in organic acids recovery and sulfur trioxide conversion with iron oxide as catalyst Yonghui Shi Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Civil Engineering Commons, and the Environmental Engineering Commons Recommended Citation Shi, Yonghui, "Utilization of sulfur dioxide in organic acids recovery and sulfur trioxide conversion with iron oxide as catalyst " (2006). Retrospective Theses and Dissertations. 1486. https://lib.dr.iastate.edu/rtd/1486 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Utilization of sulfur dioxide in organic acids recovery and sulfur trioxide conversion with iron oxide as catalyst by Yonghui Shi A dissertation submitted to the graduate faculty in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Major: Civil Engineering (Environmental Engineering) Program of Study Committee: J. Hans van Leeuwen (Co-major Professor) Robert C. Brown (Co-major Professor) Shihwu Sung (Co-major Professor) Thomas D. Wheelock Roy Gu Iowa State University Ames, Iowa 2006 UMI Number: 3223019 UMI Microform 3223019 Copyright 2006 by ProQuest Information and Learning Company. All rights reserved. This microform edition is protected against unauthorized copying under Title 17, United States Code. ProQuest Information and Learning Company 300 North Zeeb Road P.O.