Polypropylene Chemical Resistance Guide Chemical Listing & Ratings
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Technical/Application Article 02 Version 1.10 22Nd January 2018 WRH/FD
Technical/Application Article 02 Version 1.10 22nd January 2018 WRH/FD Ion Science PID Response Factors PID Response Photoionisation Detectors (PIDs) respond to a broad range of organic and a few inorganic gaseous and volatile chemicals (‘volatiles’). In order for PID to respond to a volatile, the photon energy of the lamp must be greater than its ionisation energy (IE). Ion Science PIDs are available with lamps emitting light of maximum energy of 10.0 eV, 10.6 eV, and 11.7 eV. This Technical Article lists the response factors (‘RF’s’) for over 900 volatiles with PID incorporating these lamps. The RF relates the sensitivity of PID to a volatile to the sensitivity to the standard calibration gas isobutylene. The higher the RF, the lower the sensitivity. Isobutylene as Reference Gas Ideally, the PID response to a chemical volatile would be calibrated by using a low concentration of the chemical in air. However, this is often not practical. Isobutylene is then used to calibrate PID, and a Response Factor (RF) used to convert the isobutylene calibrated measurement to a measurement of the target volatile: Concentration of target chemical = isobutylene calibrated measurement x RF For example, the RF of anisole is 0.59 with a 10.6 eV lamp. Therefore, a reading of 10 ppm using an isobutylene-calibrated unit would indicate: Concentration of anisole = 10 ppm x 0.59 = 5.9 ppm In Ion Science detectors, RFs are pre-programmed into a compound library and can be called up to make the PID read out in units of the chemical of interest. -
CHEMICAL STORAGE SEGREGATION GUIDELINES Incompatible Chemicals Should Always Be Handled and Stored So That They Do Not Accidentally Come in Contact with Each Other
Laboratory Safety Reminders January 2007 ♦ Mount Holyoke College – Environmental Health and Safety CHEMICAL STORAGE SEGREGATION GUIDELINES Incompatible chemicals should always be handled and stored so that they do not accidentally come in contact with each other. This list is not complete, nor are all compatibilities shown. These materials can react to produce excessive heat, harmful vapors, and/or other deadly reactions. Always know the hazards and incompatibilities of a chemical before using it. Chemicals Avoid Accidental Contact With Acetic acid Chromic acid, nitric acid, permanganates, peroxides Hydroxyl-containing compounds such as perchloric acid, Acetic anhydride ethylene glycol Concentrated nitric acid and sulfuric acid mixtures, peroxides (i.e. Acetone peracetic acid solution, hydrogen peroxide) Acetylene Chlorine, bromine, copper, silver, fluorine, mercury Alkali, alkaline earth and strongly electropositive metals (powered Carbon dioxide, carbon tetrachloride and other chlorinated aluminum, magnesium, sodium, hydrocarbons potassium) Mercury, chlorine, calcium hypochlorite, iodine, bromine, hydrogen Ammonia (anhydrous) fluoride Acids, metal powders, flammable liquids, chlorates, nitrates, sulfur, Ammonium nitrate finely divided organics, combustibles Aniline Nitric acid, hydrogen peroxide Arsenical compounds Any reducing agent Azides Acids Ammonia, acetylene, butadiene, butane, other petroleum gases, Bromine sodium carbide, turpentine, benzene, finely divided metals Calcium oxide Water Carbon activated Calcium hypochlorite, other -
APPENDIX G Acid Dissociation Constants
harxxxxx_App-G.qxd 3/8/10 1:34 PM Page AP11 APPENDIX G Acid Dissociation Constants § ϭ 0.1 M 0 ؍ (Ionic strength ( † ‡ † Name Structure* pKa Ka pKa ϫ Ϫ5 Acetic acid CH3CO2H 4.756 1.75 10 4.56 (ethanoic acid) N ϩ H3 ϫ Ϫ3 Alanine CHCH3 2.344 (CO2H) 4.53 10 2.33 ϫ Ϫ10 9.868 (NH3) 1.36 10 9.71 CO2H ϩ Ϫ5 Aminobenzene NH3 4.601 2.51 ϫ 10 4.64 (aniline) ϪO SNϩ Ϫ4 4-Aminobenzenesulfonic acid 3 H3 3.232 5.86 ϫ 10 3.01 (sulfanilic acid) ϩ NH3 ϫ Ϫ3 2-Aminobenzoic acid 2.08 (CO2H) 8.3 10 2.01 ϫ Ϫ5 (anthranilic acid) 4.96 (NH3) 1.10 10 4.78 CO2H ϩ 2-Aminoethanethiol HSCH2CH2NH3 —— 8.21 (SH) (2-mercaptoethylamine) —— 10.73 (NH3) ϩ ϫ Ϫ10 2-Aminoethanol HOCH2CH2NH3 9.498 3.18 10 9.52 (ethanolamine) O H ϫ Ϫ5 4.70 (NH3) (20°) 2.0 10 4.74 2-Aminophenol Ϫ 9.97 (OH) (20°) 1.05 ϫ 10 10 9.87 ϩ NH3 ϩ ϫ Ϫ10 Ammonia NH4 9.245 5.69 10 9.26 N ϩ H3 N ϩ H2 ϫ Ϫ2 1.823 (CO2H) 1.50 10 2.03 CHCH CH CH NHC ϫ Ϫ9 Arginine 2 2 2 8.991 (NH3) 1.02 10 9.00 NH —— (NH2) —— (12.1) CO2H 2 O Ϫ 2.24 5.8 ϫ 10 3 2.15 Ϫ Arsenic acid HO As OH 6.96 1.10 ϫ 10 7 6.65 Ϫ (hydrogen arsenate) (11.50) 3.2 ϫ 10 12 (11.18) OH ϫ Ϫ10 Arsenious acid As(OH)3 9.29 5.1 10 9.14 (hydrogen arsenite) N ϩ O H3 Asparagine CHCH2CNH2 —— —— 2.16 (CO2H) —— —— 8.73 (NH3) CO2H *Each acid is written in its protonated form. -
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. -
Fullerene-Acene Chemistry
University of New Hampshire University of New Hampshire Scholars' Repository Doctoral Dissertations Student Scholarship Spring 2007 Fullerene-acene chemistry: Part I Studies on the regioselective reduction of acenes and acene quinones; Part II Progress toward the synthesis of large acenes and their Diels-Alder chemistry with [60]fullerene Andreas John Athans University of New Hampshire, Durham Follow this and additional works at: https://scholars.unh.edu/dissertation Recommended Citation Athans, Andreas John, "Fullerene-acene chemistry: Part I Studies on the regioselective reduction of acenes and acene quinones; Part II Progress toward the synthesis of large acenes and their Diels-Alder chemistry with [60]fullerene" (2007). Doctoral Dissertations. 363. https://scholars.unh.edu/dissertation/363 This Dissertation is brought to you for free and open access by the Student Scholarship at University of New Hampshire Scholars' Repository. It has been accepted for inclusion in Doctoral Dissertations by an authorized administrator of University of New Hampshire Scholars' Repository. For more information, please contact [email protected]. FULLERENE-ACENE CHEMISTRY: PART I: STUDIES ON THE REGIOSELECTIVE REDUCTION OF ACENES AND ACENE QUINONES; PART II: PROGRESS TOWARD THE SYNTHESIS OF LARGE ACENES AND THEIR DIELS- ALDER CHEMISTRY WITH [60]FULLERENE VOLUME 1 CHAPTERS 1-5 BY ANDREAS JOHN ATHANS B.S. University of New Hampshire, 2001 DISSERTATION Submitted to the University of New Hampshire in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy m Chemistry May, 2007 Reproduced with permission of the copyright owner. Further reproduction prohibited without permission. UMI Number: 3 2 6 0 5 8 6 INFORMATION TO USERS The quality of this reproduction is dependent upon the quality of the copy submitted. -
Hazard Summary Identification Reason For
Common Name: CHROMIC ACID CAS Number: 7738-94-5 DOT Number: NA 1463 (Solid) RTK Substance number: 0429 UN 1755 (Solution) Date: September 1996 Revision: July 2002 ------------------------------------------------------------------------- ------------------------------------------------------------------------- HAZARD SUMMARY * Chromic Acid can affect you when breathed in and by * Exposure to hazardous substances should be routinely passing through your skin. evaluated. This may include collecting personal and area * Chromic Acid should be handled as a CARCINOGEN-- air samples. You can obtain copies of sampling results WITH EXTREME CAUTION. from your employer. You have a legal right to this * Chromic Acid can cause reproductive damage. Handle information under OSHA 1910.1020. with extreme caution. * If you think you are experiencing any work-related health * Chromic Acid is a CORROSIVE CHEMICAL and problems, see a doctor trained to recognize occupational contact can severely irritate and burn the skin and eyes diseases. Take this Fact Sheet with you. with possible eye damage. * Breathing Chromic Acid can irritate the nose, throat and WORKPLACE EXPOSURE LIMITS lungs causing coughing, wheezing and/or shortness of The following exposure limits are for Chromic Acid breath. (measured as Chromium VI): * Chromic Acid can cause a sore and/or hole in the “bone” dividing the inner nose, sometimes with bleeding, OSHA: The legal airborne permissible exposure limit discharge or formation of a crust. (PEL) is 0.1 mg/m3, not to be exceeded at any * Chromic Acid may cause a skin allergy. If allergy time. develops, very low future exposure can cause itching and a skin rash. NIOSH: The recommended airborne exposure limit is * High exposure may affect the liver. -
Conductivity and Density of Chromic Acid Solutions
; RP198 CONDUCTIVITY AND DENSITY OF CHROMIC ACID SOLU- TIONS By H. R. Moore and W. Blum ABSTRACT The conductivity and density of chromic acid solutions were determined (<*r concentrations to molar up 10 (1,000 g/1 of Cr03 ). The density is practically a linear function of concentration. The conductivity increases to a maximum at about 5 molar and then decreases. CONTENTS Page I. Introduction 255 II. Preparation of solutions 256 1. Purification of chromic acid 256 2. Methods of analysis 257 (a) Preparation of samples 257 (6) Insoluble 257 (c) Sulphate 258 (d) Alkali salts 258 (e) Chromic acid 258 (/) Trivalent chromium 258 (1) Differential titration 258 (2) Direct precipitation 259 III. Conductivity measurements 259 1. Apparatus and method 259 2. Determination of cell constants 260 IV. Density measurements 260 V. Results obtained 261 VI. Conclusions 263 I. INTRODUCTION This study is a step in an investigation of the theory of chromium plating. The solutions used in this process have chromic acid as their principal constituent. In addition, they contain some other anion, such as the sulphate ion, which is introduced as sulphuric acid or as a sulphate. During operation there is always formed in the bath some trivalent chromium, commonly supposed to exist as "chromium chromates" of undefined composition. The ultimate purpose of this research is to determine the form and function of the sulphate and trivalent chromium in such solutions. The effects of these constituents upon the density and conductivity of chromic acid will they throw light on this problem. ; be measured to see whether First, however, it was necessary to determine the density and con- ductivity of pure chromic-acid solutions to serve as a basis of refer- ence. -
Increte Stain-Crete
Version: 4.0 Revision Date: 08/23/2019 SAFETY DATA SHEET 1. Identification Material name: OB - STAIN-CRETE CHEM STAIN - 5 GL BLACK Material: CSCR G005 080 Recommended use and restriction on use Recommended use : Additive Restrictions on use: Not known. Manufacturer/Importer/Supplier/Distributor Information EUCLID CHEMICAL COMPANY 19218 REDWOOD ROAD CLEVELAND OH 44110 US Contact person : EH&S Department Telephone : 216-531-9222 Emergency telephone number : 1-800 -424 -9300 (US); 1 -613 -996 -6666 (Canada) 2. Hazard(s) identification Hazard Classification Health Hazards Acute toxicity (Oral) Category 4 Acute toxicity (Inhalation - dust and Category 2 mist) Skin Corrosion/Irritation Category 1A Serious Eye Damage/Eye Irritation Category 1 Respiratory sensitizer Category 1 Skin sensitizer Category 1 Germ Cell Mutagenicity Category 1B Carcinogenicity Category 1A Toxic to reproduction Category 1B Unknown toxicity - Health Acute toxicity, oral 0 % Acute toxicity, dermal 19.51 % Acute toxicity, inhalation, vapor 32.98 % Acute toxicity, inhalation, dust 19.51 % or mist Environmental Hazards Acute hazards to the aquatic Category 1 environment 1/17 000000013822 Version: 4.0 Revision Date: 08/23/2019 Unknown toxicity - Environment Acute hazards to the aquatic 73.06 % environment Chronic hazards to the aquatic 100 % environment Label Elements Hazard Symbol : Signal Word: Danger Hazard Statement: Fatal if inhaled. Harmful if swallowed. Causes severe skin burns and eye damage. May cause allergy or asthma symptoms or breathing difficulties if inhaled. May cause an allergic skin reaction. May cause genetic defects. May cause cancer. May damage fertility or the unborn child. Very toxic to aquatic life. Precautionary Statements Prevention: Do not breathe dust/fume/gas/mist/vapors/spray. -
Hydrogenation of 2-Methylnaphthalene in a Trickle Bed Reactor Over Bifunctional Nickel Catalysts
The University of Maine DigitalCommons@UMaine Electronic Theses and Dissertations Fogler Library Fall 12-2020 Hydrogenation of 2-methylnaphthalene in a Trickle Bed Reactor Over Bifunctional Nickel Catalysts Matthew J. Kline University of Maine, [email protected] Follow this and additional works at: https://digitalcommons.library.umaine.edu/etd Part of the Catalysis and Reaction Engineering Commons, and the Petroleum Engineering Commons Recommended Citation Kline, Matthew J., "Hydrogenation of 2-methylnaphthalene in a Trickle Bed Reactor Over Bifunctional Nickel Catalysts" (2020). Electronic Theses and Dissertations. 3284. https://digitalcommons.library.umaine.edu/etd/3284 This Open-Access Thesis is brought to you for free and open access by DigitalCommons@UMaine. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of DigitalCommons@UMaine. For more information, please contact [email protected]. HYDROGENATION OF 2-METHYLNAPHTHALENE IN A TRICKLE BED REACTOR OVER BIFUNCTIONAL NICKEL CATALYSTS By Matthew J. Kline B.S. Seton Hill University, 2018 A THESIS Submitted in Partial Fulfillment of the Requirements For the Degree of Master oF Science (in Chemical Engineering) The Graduate School The University of Maine December 2020 Advisory Committee: M. Clayton Wheeler, Professor of Chemical Engineering, Advisor Thomas J. Schwartz, Assistant ProFessor oF Chemical Engineering William J. DeSisto, ProFessor oF Chemical Engineering Brian G. Frederick, ProFessor oF Chemistry -
Carboxylic Acids
13 Carboxylic Acids The active ingredients in these two nonprescription pain relievers are derivatives of arylpropanoic acids. See Chemical Connections 13A, “From Willow Bark to Aspirin and Beyond.” Inset: A model of (S)-ibuprofen. (Charles D. Winters) KEY QUESTIONS 13.1 What Are Carboxylic Acids? HOW TO 13.2 How Are Carboxylic Acids Named? 13.1 How to Predict the Product of a Fischer 13.3 What Are the Physical Properties of Esterification Carboxylic Acids? 13.2 How to Predict the Product of a B-Decarboxylation 13.4 What Are the Acid–Base Properties of Reaction Carboxylic Acids? 13.5 How Are Carboxyl Groups Reduced? CHEMICAL CONNECTIONS 13.6 What Is Fischer Esterification? 13A From Willow Bark to Aspirin and Beyond 13.7 What Are Acid Chlorides? 13B Esters as Flavoring Agents 13.8 What Is Decarboxylation? 13C Ketone Bodies and Diabetes CARBOXYLIC ACIDS ARE another class of organic compounds containing the carbonyl group. Their occurrence in nature is widespread, and they are important components of foodstuffs such as vinegar, butter, and vegetable oils. The most important chemical property of carboxylic acids is their acidity. Furthermore, carboxylic acids form numerous important derivatives, including es- ters, amides, anhydrides, and acid halides. In this chapter, we study carboxylic acids themselves; in Chapters 14 and 15, we study their derivatives. 457 458 CHAPTER 13 Carboxylic Acids 13.1 What Are Carboxylic Acids? Carboxyl group A J COOH The functional group of a carboxylic acid is a carboxyl group, so named because it is made group. up of a carbonyl group and a hydroxyl group (Section 1.7D). -
Incompatible Chemical Groups.Pdf
Incompatible Chemical Hazard Groups (and some common examples) Mineral Acids Do NOT Store with… Hydrochloric acid Hydrogen peroxide Acetone Sulfuric Acid Sodium hydroxide Methanol Phosphoric Acid Calcium hydroxide Nitric Acid (keep separate) Chloroform Acetic Acid Strong Organic Acids Do NOT Store with… Acetic Acid3, 4 Hydrogen peroxide Acetone Acetonitrile Formic Acid Sodium hydroxide Methanol Benzene Sulfuric Acid Chloroform Special 1. Organic acids are varied and may be incompatible with each other. Notes: Check MSDSs for specifics 2. Store nitric acid separately in its own secondary container. It is a strong oxidizer. 3. Store acetic acid away from oxidizing agents — especially nitric acid. 4. Acetic acid may be stored with some inorganic acids and most flammable solvents but keep in a separate secondary container. (>70% acetic acid is combustible). Weak These are typically not corrosive and not strongly reactive and can be Organic Acids stored with general liquid lab chemicals. Examples include butyric, maleic, and benzoic acids. Non-Flammable Do NOT Store with… Chlorinated Solvents Methylene chloride Acetone Hexane Chloroform Methanol Nitric Acid Trichloroethane Ethanol Hydrogen Peroxide Carbon tetrachloride Organic Solvents Do NOT Store with… Acetone Hydrogen peroxide Nitric Acid Methanol Sodium hydroxide Chromic Acid Phenol Calcium hydroxide Sulfuric Acid Xylene Trichlorfluoromethane Hydrochloric Acid Oxidizers Do NOT Store with… Nitric Acid Sodium metal Paper and oily rags Hydrogen peroxide Isopropyl Alcohol Xylene Chromic Acid Acetone Sodium nitrate Perchloric Acid Ethyl ether Bromate salts . -
Reactions of Alcohols
Reactions of Alcohols Alcohols are versatile organic compounds since they undergo a wide variety of transformations – the majority of which are either oxidation or reduction type reactions. Normally: Oxidation is a loss of electrons; Reduction is a gain of electrons. But in organic terms: Oxidation: loss of H2; addition of O or O2; addition of X2 (halogens). Reduction: - addition of H2 or H ; loss of O or O2; loss of X2. Neither an oxidation nor reduction: Addition or loss of H+, H2O, HX. Ch11 Reacns of Alcohols (landscape).docx Page 1 Oxidation of Alcohols Primary and secondary alcohols are easily oxidized by a variety of reagents. Secondary Alcohols The most common reagent used for oxidation of secondary alcohols to ketones is chromic acid, H2CrO4. Chromic acid is produced in situ by reaction of sodium dichromate, sulfuric acid and water. Na2Cr2O7 + H2O + 2H2SO4 2 H2CrO4 + 2 NaHSO4 Ch11 Reacns of Alcohols (landscape).docx Page 2 Mechanism of oxidation The alcohol and chromic acid produce a chromate ester, which then reductively eliminates the Cr species. The Cr is reduced (VI IV), the alcohol is oxidized. Oxidation of Primary Alcohols Primary alcohols are easily oxidized just like secondary alcohols, and the INITIAL product of oxidation is an aldehyde. Ch11 Reacns of Alcohols (landscape).docx Page 3 However, the aldehyde can also be easily oxidized to an acid, and this ‘over-oxidation’ is a practical problem. E.g. A common reagent that selectively oxidizes a primary alcohol to an aldehyde (and no further) is pyridinium chlorochromate, PCC. N: CrO3, HCl (PCC) E.g. Tertiary Alcohols These are resistant to oxidation because they have no hydrogen atoms attached to the oxygen bearing carbon (carbinol carbon).