General Chemical Resistance of a Fluoroelastomer Coatings & Sealants Fluoroelastomer
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Crown Chemical Resistance Chart
Crown Polymers, Corp. 11111 Kiley Drive Huntley, IL. 60142 USA www.crownpolymers.com 847-659-0300 phone 847-659-0310 facisimile 888-732-1270 toll free Chemical Resistance Chart Crown Polymers Floor and Secondary Containment Systems Products: CrownShield covers the following five (4) formulas: CrownShield 50, Product No. 320 CrownCote, Product No. 401 CrownShield 40-2, Product No. 323 CrownShield 28, Product No. 322 CrownPro AcidShield, Product No. 350 CrownCote AcidShield, Product No. 430 CrownPro SolventShield, Product No. 351 CrownCote SolventShield, Product No. 440 This chart shows chemical resistance of Crown Polymers foundational floor and secondary containment product line that would be exposed to chemical spill or immersion conditions. The chart was designed to provide general product information. For specific applications, contact your local Crown Polymers Floor and Secondary Containment Representative or call direct to the factory. ; Resistant to chemical immersion up to 7 days followed by wash down with water 6 Spillage environments that will be cleaned up within 72 hours after initial exposure. 9 Not Recommended Chemical CrownShield SolventShield AcidShield Chemical CrownShield SolventShield AcidShield 1, 4-Dichloro-2-butene 9 6 6 Aluminum Bromate ; ; ; 1, 4-Dioxane 9 6 6 Aluminum Bromide ; ; ; 1-1-1 Trichloroethane 9 ; ; Aluminum Chloride ; ; ; 2, 4-Pentanedione 6 ; 6 Aluminum Fluoride (25%) ; ; ; 3, 4-Dichloro-1-butene 6 6 6 Aluminum Hydroxide ; ; ; 4-Picoline (0-50%) 9 6 6 Aluminum Iodine ; ; ; Acetic Acid (0-15%) 9 6 6 -
Gasket Chemical Services Guide
Gasket Chemical Services Guide Revision: GSG-100 6490 Rev.(AA) • The information contained herein is general in nature and recommendations are valid only for Victaulic compounds. • Gasket compatibility is dependent upon a number of factors. Suitability for a particular application must be determined by a competent individual familiar with system-specific conditions. • Victaulic offers no warranties, expressed or implied, of a product in any application. Contact your Victaulic sales representative to ensure the best gasket is selected for a particular service. Failure to follow these instructions could cause system failure, resulting in serious personal injury and property damage. Rating Code Key 1 Most Applications 2 Limited Applications 3 Restricted Applications (Nitrile) (EPDM) Grade E (Silicone) GRADE L GRADE T GRADE A GRADE V GRADE O GRADE M (Neoprene) GRADE M2 --- Insufficient Data (White Nitrile) GRADE CHP-2 (Epichlorohydrin) (Fluoroelastomer) (Fluoroelastomer) (Halogenated Butyl) (Hydrogenated Nitrile) Chemical GRADE ST / H Abietic Acid --- --- --- --- --- --- --- --- --- --- Acetaldehyde 2 3 3 3 3 --- --- 2 --- 3 Acetamide 1 1 1 1 2 --- --- 2 --- 3 Acetanilide 1 3 3 3 1 --- --- 2 --- 3 Acetic Acid, 30% 1 2 2 2 1 --- 2 1 2 3 Acetic Acid, 5% 1 2 2 2 1 --- 2 1 1 3 Acetic Acid, Glacial 1 3 3 3 3 --- 3 2 3 3 Acetic Acid, Hot, High Pressure 3 3 3 3 3 --- 3 3 3 3 Acetic Anhydride 2 3 3 3 2 --- 3 3 --- 3 Acetoacetic Acid 1 3 3 3 1 --- --- 2 --- 3 Acetone 1 3 3 3 3 --- 3 3 3 3 Acetone Cyanohydrin 1 3 3 3 1 --- --- 2 --- 3 Acetonitrile 1 3 3 3 1 --- --- --- --- 3 Acetophenetidine 3 2 2 2 3 --- --- --- --- 1 Acetophenone 1 3 3 3 3 --- 3 3 --- 3 Acetotoluidide 3 2 2 2 3 --- --- --- --- 1 Acetyl Acetone 1 3 3 3 3 --- 3 3 --- 3 The data and recommendations presented are based upon the best information available resulting from a combination of Victaulic's field experience, laboratory testing and recommendations supplied by prime producers of basic copolymer materials. -
The Institute of Paper Chemistry
The Institute of Paper Chemistry Appleton, Wisconsin Doctor's Dissertation Reaction Products of Lignin Model Compounds and Sodium Hydrosulfide Thomas G. Zentner June, 1953 A STUDY OF THE REACTION PRODUCTS OF LIGNIN MODEL COMPOUNDS AND SODIUM HYDROSULFIDE A thesis submitted by Thomas G. Zentner B.S. 1948, Texas A & M College M.S. 1950, Lawrence College in partial fulfillment of the requirements of The Institute of Paper Chemistry for the degree of Doctor of Philosophy from Lawrence College, Appleton, Wisconsin June, 1952 TABLE OF CONTENTS INTRODUCTION 1 HISTORICAL REVIEW 2 PRESENTATION OF THE PROBLEM 8 EXPERIMENTAL PROCEDURES 10 Synthesis of Compounds 10 Synthesis of 1-(4-Hydroxy-3-methoxyphenyl)-l-propanol 10 Synthesis of 1-(4-Benzoxy-3-methoxyphenyl)-l-propanol 11 Reaction of 1-(4-Benzoxy-3-methoxyphenyl) l-propanol with Benzyl Chloride 12 Synthesis of Propiovanillone 14 Synthesis of (-(4-Acetyl-2-methoxyphenoxy)acetovanillone 17 Attempted Synthesis of a-(2-Methoxy-4-methylphehoxy)- propiovanillone 17 Attempted Synthesis of 4-[l-(2-Methoxy-4-methylphenoxy)- l-propyl]guaiacol 21 Synthesis of 2t,4-Dihydroxy-3-methoxychalcone 23 Synthesis of 4,4'-Dihydroxy-3,3 -dimethoxychalcone 24 Synthesis of 4-Propionylpyrocatechol 24 Synthesis of Bis[l-(4-hydroxy-3-methoxyphenyl)-1- propyl] Disulfide 26 Reaction of Isolated Native Lignin with Potassium Hydrosulfide 27 Sodium Hydrosulfide Cooks 28 Cooking Liquor 28 General Procedures 30 Propiovanillone' 32 iii 2 ,4-Dihydroxy-3-methoxychalcone 34 4,4'-Dihydroxy-3,3 '-methoxychalcohe 37 4'-Hydroxy-3t-methoxyflavanone 39 2-Vanillylidene-3-coumaranone 41 Vanillin 44 G- (4-Acetyl-2-methoxyphenoxy)acetovanillone 45 1-(4-Hydroxy-3-methoxyphenyl)-1-propanol 49 DISCUSSION 58 SUMMARY AND CONCLUSIONS 69 LITERATURE CITED 71 INTRODUCTION Although the kraft process has been in use for many years, there is no sound explanation of the role played by the sulfide ion in the cook. -
Chemical Resistance 100% SOLIDS EPOXY SYSTEMS
Chemical Resistance 100% SOLIDS EPOXY SYSTEMS CHEMICAL 8300 SYSTEM 8200 SYSTEM 8000 SYSTEM OVERKOTE PLUS HD OVERKOTE HD OVERKRETE HD BASED ON ONE YEAR IMMERSION TESTING –––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– Acetic Acid (0-15%) G II Acetonitrile LLG L Continuous Immersion Acetone (0-20%) LLL Acetone (20-30%) Suitable for continuous immersion in that chemical (based on LLG Acetone (30-50%) L G I ONE YEAR testing) to assure unlimited service life. Acetone (50-100%) G II Acrylamide (0-50%) LLL G Short-Term Exposure Adipic Acid Solution LLL Alcohol, Isopropyl LLL Suitable for short-term exposure to that chemical such as Alcohol, Ethyl LLG secondary containment (72 hours) or splash and spill Alcohol, Methyl LLI (immediate clean-up). Allyl Chloride LLI Allylamine (0-20%) L L I Allylamine (20-30%) L G I I Not Suitable Allylamine (30-50%) GGI Not suitable for any exposure to that chemical. Aluminum Bromide LL– Aluminum Chloride L L – Aluminum Fluoride (0-25%) L L – This chart shows chemical resistance of our various Aluminum Hydroxide LLL 1 topping materials (90 mils – ⁄4"). These ratings are based on Aluminum Iodide LL– temperatures being ambient. At higher temperatures, chemical Aluminum Nitrate LL– resistance may be effected. When chemical exposure is Aluminum Sodium Chloride L L – minimal to non-existent, a 9000 System–FlorClad™ HD or Aluminum Sulfate LLL 4600 System– BriteCast™ HD may be used. Alums L L L 2-Aminoethoxyethanol Resistance data is listed with the assumption that the material GGG has properly cured for at least four days, at recommended Ammonia – Wet L L – temperatures, prior to any chemical exposure. -
Corrosion-2020) (461 Event of the European Federation of Corrosion)
European Federation of Corrosion National Academy of Sciences of Ukraine Ministry of Education and Science of Ukraine Ukrainian Association of Corrosionists Karpenko Physico-Mechanical Institute Ivan Franko Lviv National University Ivano-Frankivsk National Technical University of Oil and Gas ХV International Conference «Problems of corrosion and corrosion protection of materials» (Corrosion-2020) (461 event of the European Federation of Corrosion) ABSTRACT BOOK October 15–16, 2020 Lviv, Ukraine UДC 539.3, 620.193, 620.194, 620.179, 620.197, 621.181:669.018, 621.785. XV International Conference “Problems of Corrosion and Corrosion Protection of Materials“ (Corrosion-2020). October 15-16, 2020, Lviv, Ukraine: Book of Abstract / Karpenko Physico-Mechanical Institute of NAS of Ukraine; S. Korniy, М.-О. Danyliak, Yu. Maksishko (Eds.). – Lviv, 2020. – 121 p. XV International Conference “Problems of Corrosion and Corrosion Protection of Materials“ (Corrosion-2020) was held at Lviv Palace of Arts on October 15-16, 2020. This Book of Abstract contains the results of studies are devoted to fundamentals of corrosion and corrosion assisted mechanical fracture; hydrogen and gas corrosion; new corrosion resistant materials; thermal spray, electroplated and other coatings; inhibitor, biocidal and electrochemical protection; testing methods and corrosion control; corrosion protection of oil and gas industry and chemical equipment. In the authors edition. Editorial board: S. Korniy, М.-О. Danyliak, Yu. Maksishko ©Karpenko Physico-Mechanical Institute of NAS of Ukraine, Lviv, 2020 CONFERENCE TOPICS: fundamentals of corrosion and corrosion assisted mechanical fracture; hydrogen and gas corrosion; new corrosion resistant materials and coatings; inhibitor and biocidal protection; electrochemical protection; testing methods and corrosion control; corrosion protected equipment of the oil and gas, chemical and energy industries. -
Thermal-Chem Corp. High Performance Epoxy Topcoats Products
Polyurethane Thermal-Chem Corp. High Performance Epoxy Topcoats Products Chemical Resistance Chart E56 E = Excellent G = Good F = Fair Clear surfacer Plus 3.0 DecoTop < = Occasional Spillage U = Do Not Use AcidGard VersiGard ArmorTred Resurfacer Resurfacer ArmorClad Resurfacer Re DecoThane ArmorBond SolventGard DecoTop P92 Chemical 750 755 757 728 731 736 705 748 1056 1060 Polyurethane Thermal-Chem Corp. High Performance Epoxy Topcoats Products Chemical Resistance Chart E56 E = Excellent G = Good F = Fair Clear surfacer Plus 3.0 DecoTop < = Occasional Spillage U = Do Not Use AcidGard VersiGard ArmorTred Resurfacer Resurfacer ArmorClad Resurfacer Re DecoThane ArmorBond SolventGard DecoTop P92 Chemical 750 755 757 728 731 736 705 748 1056 1060 1, 4-Dichloro-2-butene U E E U U U U U U U 1, 4-Dioxane U < < U U U U U U U 1-1-1 Trichloroethane E E E F F G G F G G 2, 4-Pentanedione F E E < < < < < F F 3, 4-Dichloro-1-butene < E E U U U U U U U 4-Picoline (0-50%) U < < U U U U U U V Acetic Acid (0-5%) E E E G G G G G G G Acetic Acid (5-15%) < E E < < < < < F F Acetone(0-20%) E E E F G G G G E F Acetone (20-30% < E E < < < < < < < Acetone (30-50%) < E E < < < < < < < Acetone (50-100%) < F F < < < < < E < Acetonitrile F E E < < < < < < < Acrylamide (0-50%) E E E F G G G G E F Adipic Acid Solution E E E E E E E E E G Alcohol, Ethyl E E E F F F F F G F Alcohol, Isopropyl E E E F F F F F G F Alcohol, Methyl < E E < < < < < < < Allyl Chloride < E E U U U U U < < Allylamine (0-20%) < E E U U U U U < < Allylamine (20-30%) < E E U U U U U < < Allylamine (30-50%) U < < U U U U U U U Aluminum Bromate E E E F G G G G E E Aluminum Bromide E E E E E E E E E E Aluminum Chloride E E E E E E E E E E Aluminum Fluoride (25%) E E E E E E E E E E Polyurethane Thermal-Chem Corp. -
BOSC Review of US EPA ORD Research Programs
May 8, 2017 Robert Kavlock, Ph.D. Acting Assistant Administrator Office of Research and Development U.S. Environmental Protection Agency Dear Dr. Kavlock: On behalf of the Board of Scientific Counselors (BOSC), I am pleased to provide you a collection of reports addressing Charge Questions posed by five of the National Research Program areas and the four cross- cutting Roadmap programs. In general, we have found these programs to be on track to meet the objectives in their current Strategic Research Action Plans (StRAPs) and Roadmaps. We provide a series of recommendations to continue to strengthen the excellent research being done in ORD, and look forward to working with you in the future on these programs. Sincerely, Deborah L. Swackhamer, Ph.D. Chair, BOSC Cc: Bruce Rodan, Associate Director of Science REVIEW OF U.S. EPA OFFICE OF RESEARCH AND DEVELOPMENT’S RESEARCH PROGRAMS BOSC EXECUTIVE COMMITTEE Chair Deborah L. Swackhamer, Ph.D. James N. Galloway, Ph.D. I. Leslie Rubin, M.D. University of Minnesota University of Virginia Developmental Pediatric Specialists Viney Aneja, Ph.D. Earthea A. Nance, Ph.D., P.E. Sandra Smith, M.S. North Carolina State University Texas Southern University AECOM Shahid Chaudhry Paula Olsiewski, Ph.D., P.E. Gina Solomon, M.D., M.P.H. California Energy Commission Alfred P. Sloan Foundation California EPA Elizabeth Corley, Ph.D. Diane E. Pataki, Ph.D. Ponisseril Somasundaran, Ph.D. Arizona State University The University of Utah Columbia University Susan E. Cozzens, Ph.D. Robert Richardson, Ph.D. Tammy P. Taylor, Ph.D. Georgia Institute of Technology Michigan State University Pacific Northwest National Laboratory Courtney Flint, Ph.D. -
Traumatic Shock. Ii. the Preparation of Cystine, Methionine, and Homocystine Containing Radioactive Sulfur
TRAUMATIC SHOCK. II. THE PREPARATION OF CYSTINE, METHIONINE, AND HOMOCYSTINE CONTAINING RADIOACTIVE SULFUR Arnold M. Seligman, … , Alexander M. Rutenburg, Henry Banks J Clin Invest. 1943;22(2):275-279. https://doi.org/10.1172/JCI101393. Research Article Find the latest version: https://jci.me/101393/pdf TRAUMATIC SHOCK. II. THE PREPARATION OF CYSTINE, METHIONINE, AND HOMOCYSTINE CONTAINING RADIOACTIVE SULFUR By ARNOLD M. SELIGMAN, ALEXANDER M. RUTENBURG, AND HENRY BANKS 1 (From the Surgical Research Department of the Beth Israel Hospital and the Department of Surgery, Harvard Medical School, Boston) (Received for publication November 12, 1942) In order to prepare, from radioactive sulfur, the benzyl mercaptan (I) (0.6 moles), reported by sulfur-containing amino acids of a high order of Wood and du Vigneaud (4) in 23 per cent yield, specific activity for biological experiments such was found to give a 21.5 per cent yield when 0.06 as those described in the foregoing publication, it mole was used. Reduction of benzylcysteine was necessary (owing to the cost of radioactive (VIII) to cysteine with sodium and butyl alcohol sulfur) to investigate the efficiency of utilization did not give good yields; therefore, sodium and of small amounts of sulfur. The synthetic meth- liquid ammonia were used. Since radioactive ods utilized are not novel, but are described be- benzyl mercaptan is necessary for the synthesis of low because of the data obtained on yields in all three amino acids, a method of preparation of numerous small scale preparations. Since pres- the mercaptan from hydrogen sulfide, other than ent methods of preparing radioactive sulfur from that described by Tarver and Schmidt, in 70 per neutron bombardment of carbon tetrachloride in- cent yield, was investigated. -
WO 2017/116773 Al 6 July 2017 (06.07.2017) W P O P C T
(12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2017/116773 Al 6 July 2017 (06.07.2017) W P O P C T (51) International Patent Classification: 85008-3279 (US). SHULT, Nicholas S.; 2255 North 44th C23F 1/14 (2006.01) H05K 3/38 (2006.01) Street, Suite 300, Phoenix, Arizona 85008-3279 (US). C01B 15/08 (2006.01) C09G 1/00 (2006.01) GOLDSMITH, Adam T.; 2255 North 44th Street, Suite 300, Phoenix, Arizona 85008-3279 (US). (21) International Application Number: PCT/US20 16/0673 13 (74) Agent: ROSENFIELD, Susan Stone; Fennemore Craig, 2394 East Camelback Road, Suite 600, Phoenix, Arizona (22) International Filing Date: 85016 (US). 16 December 2016 (16. 12.2016) (81) Designated States (unless otherwise indicated, for every (25) Filing Language: English kind of national protection available): AE, AG, AL, AM, (26) Publication Language: English AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, (30) Priority Data: DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, 62/273,389 30 December 201 5 (30. 12.2015) US HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KH, KN, 15/380,702 15 December 201 6 (15. 12.2016) US KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, (71) Applicant: TESSENDERLO KERLEY, INC. [US/US]; MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, 2255 North 44th Street, Suite 300, Phoenix, Arizona NI, NO, NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, 85008-3279 (US). -
Working with Hazardous Chemicals
A Publication of Reliable Methods for the Preparation of Organic Compounds Working with Hazardous Chemicals The procedures in Organic Syntheses are intended for use only by persons with proper training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011; the full text can be accessed free of charge at http://www.nap.edu/catalog.php?record_id=12654). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices. In some articles in Organic Syntheses, chemical-specific hazards are highlighted in red “Caution Notes” within a procedure. It is important to recognize that the absence of a caution note does not imply that no significant hazards are associated with the chemicals involved in that procedure. Prior to performing a reaction, a thorough risk assessment should be carried out that includes a review of the potential hazards associated with each chemical and experimental operation on the scale that is planned for the procedure. Guidelines for carrying out a risk assessment and for analyzing the hazards associated with chemicals can be found in Chapter 4 of Prudent Practices. The procedures described in Organic Syntheses are provided as published and are conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein. -
Chemical Resistance Chart
Polyurethane Thermal-Chem Corp. High Performance Epoxy Topcoats Products Chemical Resistance Chart E56 E = Excellent G = Good F = Fair Clear surfacer Plus 3.0 DecoTop < = Occasional Spillage U = Do Not Use AcidGard VersiGard ArmorTred Resurfacer Resurfacer ArmorClad Resurfacer Re DecoThane ArmorBond SolventGard DecoTop P92 Chemical 750 755 757 728 731 736 705 748 1056 1060 Polyurethane Thermal-Chem Corp. High Performance Epoxy Topcoats Products Chemical Resistance Chart E = Excellent G = Good F = Fair Clear surfacer Plus 3.0 DecoTop < = Occasional Spillage U = Do Not Use AcidGard VersiGard ArmorTred Resurfacer Resurfacer ArmorClad Resurfacer Re ThermalCrete ArmorBond SolventGard DecoFinish P81 Chemical 750 755 757 728 731 736 705 748 1030 1062 1, 4-Dichloro-2-butene U E E U U U U U U U 1, 4-Dioxane U < < U U U U U U U 1-1-1 Trichloroethane E E E F F G G F G G < < < < < 2, 4-Pentanedione F E E F F 3, 4-Dichloro-1-butene < E E U U U U U U U 4-Picoline (0-50%) U < < U U U U U V V Acetic Acid (0-5%) E E E G G G G G E G < < < < < < Acetic Acid (5-15%) E E E F Acetone(0-20%) E E E F G G G G E F Acetone (20-30% < E E < < < < < E < Acetone (30-50%) < E E < < < < < E < Acetone (50-100%) < F F < < < < < E < Acetonitrile F E E < < < < < E < Acrylamide (0-50%) E E E F G G G G F Adipic Acid Solution E E E E E E E E G Alcohol, Ethyl E E E F F F F F F Alcohol, Isopropyl E E E F F F F F G F Alcohol, Methyl < E E < < < < < < < Allyl Chloride < E E U U U U U E < Allylamine (0-20%) < E E U U U U U < Allylamine (20-30%) < E E U U U U U < Allylamine (30-50%) U < < U U U U U U Aluminum Bromate E E E F G G G G E Aluminum Bromide E E E E E E E E E Aluminum Chloride E E E E E E E E E Aluminum Fluoride (25%) E E E E E E E E E Polyurethane Thermal-Chem Corp. -
Photolysis of Frozen Iodate Salts As a Source of Active Iodine in the Polar Environment
Atmos. Chem. Phys., 16, 12703–12713, 2016 www.atmos-chem-phys.net/16/12703/2016/ doi:10.5194/acp-16-12703-2016 © Author(s) 2016. CC Attribution 3.0 License. Photolysis of frozen iodate salts as a source of active iodine in the polar environment Óscar Gálvez1,a, M. Teresa Baeza-Romero2, Mikel Sanz2,b, and Alfonso Saiz-Lopez3 1Departamento de Física Molecular, Instituto de Estructura de la Materia, IEM-CSIC, 28006 Madrid, Spain 2Escuela de Ingeniería Industrial, Universidad de Castilla-La Mancha, 45071 Toledo, Spain 3Department of Atmospheric Chemistry and Climate, Institute of Physical Chemistry Rocasolano, CSIC, 28006 Madrid, Spain anow at: Departamento de Física Interdisciplinar, Facultad de Ciencias, Universidad Nacional de Educación a Distancia, 28040 Madrid, Spain bnow at: Institute of Physical Chemistry Rocasolano, CSIC, 28006 Madrid, Spain Correspondence to: Óscar Gálvez ([email protected], [email protected]) Received: 15 September 2015 – Published in Atmos. Chem. Phys. Discuss.: 15 October 2015 Revised: 22 September 2016 – Accepted: 26 September 2016 – Published: 12 October 2016 Abstract. Reactive halogens play a key role in the oxida- 1 Introduction tion capacity of the polar troposphere. However, sources and mechanisms, particularly those involving active iodine, are still poorly understood. In this paper, the photolysis of an Atmospheric iodine compounds are present in the marine atmospherically relevant frozen iodate salt has been experi- and polar boundary layers (Saiz-Lopez et al., 2012), where mentally studied using infrared (IR) spectroscopy. The sam- they play a relevant role in catalytic ozone destruction (Saiz- ples were generated at low temperatures in the presence of Lopez et al., 2007b; Read et al., 2008), and they could also different amounts of water.