Retention Index Mixture for GC (R8769)
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Section 13. Disposal Considerations Disposal Methods : the Generation of Waste Should Be Avoided Or Minimized Wherever Possible
SAFETY DATA SHEET Flammable Liquid Mixture: Docosane / Dodecane / Dotriacontane / Eicosane / Heptane / Hexacosane / Hexadecane / Hexane / N-Decane / N-Nonane / N- Octadecane / Octacosane / Octane / Tetracosane / Tetradecane / Triacontane Section 1. Identification GHS product identifier : Flammable Liquid Mixture: Docosane / Dodecane / Dotriacontane / Eicosane / Heptane / Hexacosane / Hexadecane / Hexane / N-Decane / N-Nonane / N-Octadecane / Octacosane / Octane / Tetracosane / Tetradecane / Triacontane Other means of : Not available. identification Product use : Synthetic/Analytical chemistry. SDS # : 019981 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 24-hour telephone : 1-866-734-3438 Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : FLAMMABLE LIQUIDS - Category 1 substance or mixture SKIN CORROSION/IRRITATION - Category 2 SERIOUS EYE DAMAGE/ EYE IRRITATION - Category 2A TOXIC TO REPRODUCTION (Fertility) - Category 2 TOXIC TO REPRODUCTION (Unborn child) - Category 2 SPECIFIC TARGET ORGAN TOXICITY (SINGLE EXPOSURE) (Narcotic effects) - Category 3 SPECIFIC TARGET ORGAN TOXICITY (REPEATED EXPOSURE) - Category 2 AQUATIC HAZARD (ACUTE) - Category 2 AQUATIC HAZARD (LONG-TERM) - Category 1 GHS label elements Hazard pictograms : Signal word : Danger Hazard statements : Extremely flammable liquid and vapor. May form explosive mixtures in Air. Causes serious eye irritation. Causes skin irritation. Suspected of damaging fertility or the unborn child. May cause drowsiness and dizziness. May cause damage to organs through prolonged or repeated exposure. Very toxic to aquatic life with long lasting effects. Precautionary statements General : Read label before use. Keep out of reach of children. If medical advice is needed, have product container or label at hand. -
Catalytic Pyrolysis of Plastic Wastes for the Production of Liquid Fuels for Engines
Electronic Supplementary Material (ESI) for RSC Advances. This journal is © The Royal Society of Chemistry 2019 Supporting information for: Catalytic pyrolysis of plastic wastes for the production of liquid fuels for engines Supattra Budsaereechaia, Andrew J. Huntb and Yuvarat Ngernyen*a aDepartment of Chemical Engineering, Faculty of Engineering, Khon Kaen University, Khon Kaen, 40002, Thailand. E-mail:[email protected] bMaterials Chemistry Research Center, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand Fig. S1 The process for pelletization of catalyst PS PS+bentonite PP ) t e PP+bentonite s f f o % ( LDPE e c n a t t LDPE+bentonite s i m s n HDPE a r T HDPE+bentonite Gasohol 91 Diesel 4000 3500 3000 2500 2000 1500 1000 500 Wavenumber (cm-1) Fig. S2 FTIR spectra of oil from pyrolysis of plastic waste type. Table S1 Compounds in oils (%Area) from the pyrolysis of plastic wastes as detected by GCMS analysis PS PP LDPE HDPE Gasohol 91 Diesel Compound NC C Compound NC C Compound NC C Compound NC C 1- 0 0.15 Pentane 1.13 1.29 n-Hexane 0.71 0.73 n-Hexane 0.65 0.64 Butane, 2- Octane : 0.32 Tetradecene methyl- : 2.60 Toluene 7.93 7.56 Cyclohexane 2.28 2.51 1-Hexene 1.05 1.10 1-Hexene 1.15 1.16 Pentane : 1.95 Nonane : 0.83 Ethylbenzen 15.07 11.29 Heptane, 4- 1.81 1.68 Heptane 1.26 1.35 Heptane 1.22 1.23 Butane, 2,2- Decane : 1.34 e methyl- dimethyl- : 0.47 1-Tridecene 0 0.14 2,2-Dimethyl- 0.63 0 1-Heptene 1.37 1.46 1-Heptene 1.32 1.35 Pentane, -
Synthetic Turf Scientific Advisory Panel Meeting Materials
California Environmental Protection Agency Office of Environmental Health Hazard Assessment Synthetic Turf Study Synthetic Turf Scientific Advisory Panel Meeting May 31, 2019 MEETING MATERIALS THIS PAGE LEFT BLANK INTENTIONALLY Office of Environmental Health Hazard Assessment California Environmental Protection Agency Agenda Synthetic Turf Scientific Advisory Panel Meeting May 31, 2019, 9:30 a.m. – 4:00 p.m. 1001 I Street, CalEPA Headquarters Building, Sacramento Byron Sher Auditorium The agenda for this meeting is given below. The order of items on the agenda is provided for general reference only. The order in which items are taken up by the Panel is subject to change. 1. Welcome and Opening Remarks 2. Synthetic Turf and Playground Studies Overview 4. Synthetic Turf Field Exposure Model Exposure Equations Exposure Parameters 3. Non-Targeted Chemical Analysis Volatile Organics on Synthetic Turf Fields Non-Polar Organics Constituents in Crumb Rubber Polar Organic Constituents in Crumb Rubber 5. Public Comments: For members of the public attending in-person: Comments will be limited to three minutes per commenter. For members of the public attending via the internet: Comments may be sent via email to [email protected]. Email comments will be read aloud, up to three minutes each, by staff of OEHHA during the public comment period, as time allows. 6. Further Panel Discussion and Closing Remarks 7. Wrap Up and Adjournment Agenda Synthetic Turf Advisory Panel Meeting May 31, 2019 THIS PAGE LEFT BLANK INTENTIONALLY Office of Environmental Health Hazard Assessment California Environmental Protection Agency DRAFT for Discussion at May 2019 SAP Meeting. Table of Contents Synthetic Turf and Playground Studies Overview May 2019 Update ..... -
Sampling Dynamics for Volatile Organic Compounds Using Headspace Solid-Phase Microextraction Arrow for Microbiological Samples
separations Communication Sampling Dynamics for Volatile Organic Compounds Using Headspace Solid-Phase Microextraction Arrow for Microbiological Samples Kevin E. Eckert 1, David O. Carter 2 and Katelynn A. Perrault 1,* 1 Laboratory of Forensic and Bioanalytical Chemistry, Forensic Sciences Unit, Division of Natural Sciences and Mathematics, Chaminade University of Honolulu, 3140 Waialae Ave., Honolulu, HI 96816, USA; [email protected] 2 Laboratory of Forensic Taphonomy, Forensic Sciences Unit, Division of Natural Sciences and Mathematics, Chaminade University of Honolulu, 3140 Waialae Avenue, Honolulu, HI 96816, USA; [email protected] * Correspondence: [email protected] Received: 10 August 2018; Accepted: 27 August 2018; Published: 10 September 2018 Abstract: Volatile organic compounds (VOCs) are monitored in numerous fields using several commercially-available sampling options. Sorbent-based sampling techniques, such as solid-phase microextraction (SPME), provide pre-concentration and focusing of VOCs prior to gas chromatography–mass spectrometry (GC–MS) analysis. This study investigated the dynamics of SPME Arrow, which exhibits an increased sorbent phase volume and improved durability compared to traditional SPME fibers. A volatile reference mixture (VRM) and saturated alkanes mix (SAM) were used to investigate optimal parameters for microbiological VOC profiling in combination with GC–MS analysis. Fiber type, extraction time, desorption time, carryover, and reproducibility were characterized, in addition to a comparison with traditional SPME fibers. The developed method was then applied to longitudinal monitoring of Bacillus subtilis cultures, which represents a ubiquitous microbe in medical, forensic, and agricultural applications. The carbon wide range/polydimethylsiloxane (CWR/PDMS) fiber was found to be optimal for the range of expected VOCs in microbiological profiling, and a statistically significant increase in the majority of VOCs monitored was observed. -
The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy”
chemengineering Article Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy” Robert J. Meier Pro-Deo Consultant, 52525 Heinsberg, North-Rhine Westphalia, Germany; [email protected] Abstract: Group contribution (GC) methods to predict thermochemical properties are of eminent importance to process design. Compared to previous works, we present an improved group contri- bution parametrization for the heat of formation of organic molecules exhibiting chemical accuracy, i.e., a maximum 1 kcal/mol (4.2 kJ/mol) difference between the experiment and model, while, at the same time, minimizing the number of parameters. The latter is extremely important as too many parameters lead to overfitting and, therewith, to more or less serious incorrect predictions for molecules that were not within the data set used for parametrization. Moreover, it was found to be important to explicitly account for common chemical knowledge, e.g., geminal effects or ring strain. The group-related parameters were determined step-wise: first, alkanes only, and then only one additional group in the next class of molecules. This ensures unique and optimal parameter values for each chemical group. All data will be made available, enabling other researchers to extend the set to other classes of molecules. Keywords: enthalpy of formation; thermodynamics; molecular modeling; group contribution method; quantum mechanical method; chemical accuracy; process design Citation: Meier, R.J. Group Contribution Revisited: The Enthalpy of Formation of Organic Compounds with “Chemical Accuracy”. 1. Introduction ChemEngineering 2021, 5, 24. To understand chemical reactivity and/or chemical equilibria, knowledge of thermo- o https://doi.org/10.3390/ dynamic properties such as gas-phase standard enthalpy of formation DfH gas is a necessity. -
Certificate of Analysis
National Institute of Standards & Technology Certificate of Analysis Standard Reference Material 2285 Ignitable Liquids Test Mixture This Standard Reference Material (SRM) is intended primarily for use in the calibration of chromatographic instrumentation used for the classification of an ignitable liquid residue. SRM 2285 is a solution of 15 compounds, including even carbon number aliphatic hydrocarbons from hexane to tetracosane, toluene, p-xylene, 2-ethyltoluene, 3-ethyltoluene, and 1,2,4-trimethylbenzene in methylene chloride. A unit of SRM 2285 consists of five 2 mL ampoules, each containing approximately 1.2 mL of solution. Certified Mass Fraction Values: The certified values for the 15 constituents are given in Table 1. These values are based on results obtained from the gravimetric preparation of this solution and from the analytical results determined by using gas chromatography. A NIST certified value is a value for which NIST has the highest confidence in its accuracy in that all known or suspected sources of uncertainty have been investigated or taken into account [1]. Information Concentration Values: Information values for concentrations, expressed as percent volume fractions, are provided in Table 2 for the components. An information value is considered to be a value that will be of interest and use to the SRM user, but insufficient information is available to assess adequately the uncertainty associated with the value or only a limited number of analyses were performed [1]. Expiration of Certification: The certification of SRM 2285 is valid, within the measurement uncertainty specified, until 30 March 2023, provided the SRM is handled and stored in accordance with the instructions given in this certificate (see “Instructions for Handling, Storage, and Use”). -
Measurements of Higher Alkanes Using NO Chemical Ionization in PTR-Tof-MS
Atmos. Chem. Phys., 20, 14123–14138, 2020 https://doi.org/10.5194/acp-20-14123-2020 © Author(s) 2020. This work is distributed under the Creative Commons Attribution 4.0 License. Measurements of higher alkanes using NOC chemical ionization in PTR-ToF-MS: important contributions of higher alkanes to secondary organic aerosols in China Chaomin Wang1,2, Bin Yuan1,2, Caihong Wu1,2, Sihang Wang1,2, Jipeng Qi1,2, Baolin Wang3, Zelong Wang1,2, Weiwei Hu4, Wei Chen4, Chenshuo Ye5, Wenjie Wang5, Yele Sun6, Chen Wang3, Shan Huang1,2, Wei Song4, Xinming Wang4, Suxia Yang1,2, Shenyang Zhang1,2, Wanyun Xu7, Nan Ma1,2, Zhanyi Zhang1,2, Bin Jiang1,2, Hang Su8, Yafang Cheng8, Xuemei Wang1,2, and Min Shao1,2 1Institute for Environmental and Climate Research, Jinan University, 511443 Guangzhou, China 2Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality, 511443 Guangzhou, China 3School of Environmental Science and Engineering, Qilu University of Technology (Shandong Academy of Sciences), 250353 Jinan, China 4State Key Laboratory of Organic Geochemistry and Guangdong Key Laboratory of Environmental Protection and Resources Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 Guangzhou, China 5State Joint Key Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, 100871 Beijing, China 6State Key Laboratory of Atmospheric Boundary Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese -
Advanced Separation Techniques Combined with Mass Spectrometry for Difficult Analytical Tasks - Isomer Separation and Oil Analysis
FINNISH METEOROLOGICAL INSTITUTE Erik Palménin aukio 1 P.O. Box 503 FI-00101 HELSINKI 131 CONTRIBUTIONS tel. +358 29 539 1000 WWW.FMI.FI FINNISH METEOROLOGICAL INSTITUTE CONTRIBUTIONS No. 131 ISBN 978-952-336-016-7 (paperback) ISSN 0782-6117 Erweko Helsinki 2017 ISBN 978-952-336-017-4 (pdf) Helsinki 2017 ADVANCED SEPARATION TECHNIQUES COMBINED WITH MASS SPECTROMETRY FOR DIFFICULT ANALYTICAL TASKS - ISOMER SEPARATION AND OIL ANALYSIS JAAKKO LAAKIA Department of Chemistry University of Helsinki Finland Advanced separation techniques combined with mass spectrometry for difficult analytical tasks – isomer separation and oil analysis Jaakko Laakia Academic Dissertation To be presented, with the permission of the Faculty of Science of the University of Helsinki, for public criticism in Auditorium A129 of the Department of Chemistry (A.I. Virtasen aukio 1, Helsinki) on May 12th, 2017, at 12 o’clock noon. Helsinki 2017 1 TABLE OF CONTENTS ABSTRACT 4 Supervisors Professor Tapio Kotiaho TIIVISTELMÄ 5 Department of Chemistry LIST OF ORIGINAL PAPERS 6 Faculty of Science ACKNOWLEDGEMENTS 7 ABBREVIATIONS 8 and 1. INTRODUCTION 10 Division of Pharmaceutical Chemistry and Technology 1.1.1 Basic operation principles of ion mobility 12 spectrometry 11 Faculty of Pharmacy 1.1.2 Applications of ion mobility spectrometry 16 University of Helsinki 1.2 Basic operation principles and applications of two-dimensional gas 19 chromatography – time-of-flight mass spectrometry Docent Tiina Kauppila 1.3 Aims of study 23 Division of Pharmaceutical Chemistry and Technology -
Supporting Information for Modeling the Formation and Composition Of
Supporting Information for Modeling the Formation and Composition of Secondary Organic Aerosol from Diesel Exhaust Using Parameterized and Semi-explicit Chemistry and Thermodynamic Models Sailaja Eluri1, Christopher D. Cappa2, Beth Friedman3, Delphine K. Farmer3, and Shantanu H. Jathar1 1 Department of Mechanical Engineering, Colorado State University, Fort Collins, CO, USA, 80523 2 Department of Civil and Environmental Engineering, University of California Davis, Davis, CA, USA, 95616 3 Department of Chemistry, Colorado State University, Fort Collins, CO, USA, 80523 Correspondence to: Shantanu H. Jathar ([email protected]) Table S1: Mass speciation and kOH for VOC emissions profile #3161 3 -1 - Species Name kOH (cm molecules s Mass Percent (%) 1) (1-methylpropyl) benzene 8.50×10'() 0.023 (2-methylpropyl) benzene 8.71×10'() 0.060 1,2,3-trimethylbenzene 3.27×10'(( 0.056 1,2,4-trimethylbenzene 3.25×10'(( 0.246 1,2-diethylbenzene 8.11×10'() 0.042 1,2-propadiene 9.82×10'() 0.218 1,3,5-trimethylbenzene 5.67×10'(( 0.088 1,3-butadiene 6.66×10'(( 0.088 1-butene 3.14×10'(( 0.311 1-methyl-2-ethylbenzene 7.44×10'() 0.065 1-methyl-3-ethylbenzene 1.39×10'(( 0.116 1-pentene 3.14×10'(( 0.148 2,2,4-trimethylpentane 3.34×10'() 0.139 2,2-dimethylbutane 2.23×10'() 0.028 2,3,4-trimethylpentane 6.60×10'() 0.009 2,3-dimethyl-1-butene 5.38×10'(( 0.014 2,3-dimethylhexane 8.55×10'() 0.005 2,3-dimethylpentane 7.14×10'() 0.032 2,4-dimethylhexane 8.55×10'() 0.019 2,4-dimethylpentane 4.77×10'() 0.009 2-methylheptane 8.28×10'() 0.028 2-methylhexane 6.86×10'() -
Safety Data Sheet
SAFETY DATA SHEET Flammable Liquid Mixture: Docosane / Dodecane / Eicosane / Hexacosane / Hexadecane / Hexane / N-Decane / N-Heptane / N-Nonane / N-Octadecane / N- Octane / Octacosane / Tetracosane / Tetradecane Section 1. Identification GHS product identifier : Flammable Liquid Mixture: Docosane / Dodecane / Eicosane / Hexacosane / Hexadecane / Hexane / N-Decane / N-Heptane / N-Nonane / N-Octadecane / N-Octane / Octacosane / Tetracosane / Tetradecane Other means of : Not available. identification Product use : Synthetic/Analytical chemistry. SDS # : 019735 Supplier's details : Airgas USA, LLC and its affiliates 259 North Radnor-Chester Road Suite 100 Radnor, PA 19087-5283 1-610-687-5253 24-hour telephone : 1-866-734-3438 Section 2. Hazards identification OSHA/HCS status : This material is considered hazardous by the OSHA Hazard Communication Standard (29 CFR 1910.1200). Classification of the : FLAMMABLE LIQUIDS - Category 1 substance or mixture SKIN CORROSION/IRRITATION - Category 2 SERIOUS EYE DAMAGE/ EYE IRRITATION - Category 2A TOXIC TO REPRODUCTION (Fertility) - Category 2 TOXIC TO REPRODUCTION (Unborn child) - Category 2 SPECIFIC TARGET ORGAN TOXICITY (SINGLE EXPOSURE) (Respiratory tract irritation) - Category 3 SPECIFIC TARGET ORGAN TOXICITY (SINGLE EXPOSURE) (Narcotic effects) - Category 3 SPECIFIC TARGET ORGAN TOXICITY (REPEATED EXPOSURE) - Category 2 AQUATIC HAZARD (ACUTE) - Category 2 AQUATIC HAZARD (LONG-TERM) - Category 1 GHS label elements Hazard pictograms : Signal word : Danger Hazard statements : Extremely flammable liquid and vapor. May form explosive mixtures in Air. Causes serious eye irritation. Causes skin irritation. May cause respiratory irritation. Suspected of damaging fertility or the unborn child. May cause drowsiness and dizziness. May cause damage to organs through prolonged or repeated exposure. Very toxic to aquatic life with long lasting effects. Precautionary statements General : Read label before use. -
Vapor Pressures and Vaporization Enthalpies of the N-Alkanes from 2 C21 to C30 at T ) 298.15 K by Correlation Gas Chromatography
BATCH: je1a04 USER: jeh69 DIV: @xyv04/data1/CLS_pj/GRP_je/JOB_i01/DIV_je0301747 DATE: October 17, 2003 1 Vapor Pressures and Vaporization Enthalpies of the n-Alkanes from 2 C21 to C30 at T ) 298.15 K by Correlation Gas Chromatography 3 James S. Chickos* and William Hanshaw 4 Department of Chemistry and Biochemistry, University of MissourisSt. Louis, St. Louis, Missouri 63121 5 6 The temperature dependence of gas chromatographic retention times for n-heptadecane to n-triacontane 7 is reported. These data are used to evaluate the vaporization enthalpies of these compounds at T ) 298.15 8 K, and a protocol is described that provides vapor pressures of these n-alkanes from T ) 298.15 to 575 9 K. The vapor pressure and vaporization enthalpy results obtained are compared with existing literature 10 data where possible and found to be internally consistent. Sublimation enthalpies for n-C17 to n-C30 are 11 calculated by combining vaporization enthalpies with fusion enthalpies and are compared when possible 12 to direct measurements. 13 14 Introduction 15 The n-alkanes serve as excellent standards for the 16 measurement of vaporization enthalpies of hydrocarbons.1,2 17 Recently, the vaporization enthalpies of the n-alkanes 18 reported in the literature were examined and experimental 19 values were selected on the basis of how well their 20 vaporization enthalpies correlated with their enthalpies of 21 transfer from solution to the gas phase as measured by gas 22 chromatography.3 A plot of the vaporization enthalpies of 23 the n-alkanes as a function of the number of carbon atoms 24 is given in Figure 1. -
Table 2. Chemical Names and Alternatives, Abbreviations, and Chemical Abstracts Service Registry Numbers
Table 2. Chemical names and alternatives, abbreviations, and Chemical Abstracts Service registry numbers. [Final list compiled according to the National Institute of Standards and Technology (NIST) Web site (http://webbook.nist.gov/chemistry/); NIST Standard Reference Database No. 69, June 2005 release, last accessed May 9, 2008. CAS, Chemical Abstracts Service. This report contains CAS Registry Numbers®, which is a Registered Trademark of the American Chemical Society. CAS recommends the verification of the CASRNs through CAS Client ServicesSM] Aliphatic hydrocarbons CAS registry number Some alternative names n-decane 124-18-5 n-undecane 1120-21-4 n-dodecane 112-40-3 n-tridecane 629-50-5 n-tetradecane 629-59-4 n-pentadecane 629-62-9 n-hexadecane 544-76-3 n-heptadecane 629-78-7 pristane 1921-70-6 n-octadecane 593-45-3 phytane 638-36-8 n-nonadecane 629-92-5 n-eicosane 112-95-8 n-Icosane n-heneicosane 629-94-7 n-Henicosane n-docosane 629-97-0 n-tricosane 638-67-5 n-tetracosane 643-31-1 n-pentacosane 629-99-2 n-hexacosane 630-01-3 n-heptacosane 593-49-7 n-octacosane 630-02-4 n-nonacosane 630-03-5 n-triacontane 638-68-6 n-hentriacontane 630-04-6 n-dotriacontane 544-85-4 n-tritriacontane 630-05-7 n-tetratriacontane 14167-59-0 Table 2. Chemical names and alternatives, abbreviations, and Chemical Abstracts Service registry numbers.—Continued [Final list compiled according to the National Institute of Standards and Technology (NIST) Web site (http://webbook.nist.gov/chemistry/); NIST Standard Reference Database No.