List of Refrigerants
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Effect of Insulations on Cop in Vapor Compression Refrigeration System
International Journal of Mechanical Engineering and Technology (IJMET) Volume 10, Issue 01, January 2019, pp. 1201-1208, Article ID: IJMET_10_01_122 Available online at http://www.iaeme.com/ijmet/issues.asp?JType=IJMET&VType=10&IType= 01 ISSN Print: 0976-6340 and ISSN Online: 0976-6359 © IAEME Publication Scopus Indexed EFFECT OF INSULATIONS ON COP IN VAPOR COMPRESSION REFRIGERATION SYSTEM Anusha Peyyala Assistant Professor P V P Siddhartha Institute of Technology, Research Scholar, Acharya Nagarjuna University, India. Dr N V V S Sudheer Associate Professor, R V R & J C College of Engineering, Guntur India ABSTRACT In this project, experimentation is done on Vapour Compression Refrigeration System [VCRS] as the COP is high for this system and it is the present trend of the HVAC in the domestic industry. This study presents investigation of best suited refrigerant and insulation combination for gas pipeline and liquid pipeline of a split air conditioning system. Analysis are performed for R22-Chlorodiflouromethane, a HydroChloroFlouro Carbon refrigerant, which has been using in the present world that cause both global warming and ozone layer depletion and R410a, mixture of di- flouromethane and pentaflouroethane, a Hydroflouro carbon refrigerant, which is future of HVAC which reduces the effect of ozone layer depletion [ODP] and Global Warming Potential [GWP].For these two refrigerants, we had found out the best insulation suitable as insulation also affects the COP of air conditioner, which has been observed from the literature. Minimizing the temperature of refrigerant in suction line helps condensing unit work more effectively intern the system performance increases. This reduces the overall power required for working of air conditioner, thereby reducing the maintenance cost of system. -
New and Improved Infrared Absorption Cross Sections for Chlorodifluoromethane (HCFC-22)
Atmos. Meas. Tech., 9, 2593–2601, 2016 www.atmos-meas-tech.net/9/2593/2016/ doi:10.5194/amt-9-2593-2016 © Author(s) 2016. CC Attribution 3.0 License. New and improved infrared absorption cross sections for chlorodifluoromethane (HCFC-22) Jeremy J. Harrison1,2 1Department of Physics and Astronomy, University of Leicester, University Road, Leicester, LE1 7RH, UK 2National Centre for Earth Observation, University of Leicester, University Road, Leicester, LE1 7RH, UK Correspondence to: Jeremy J. Harrison ([email protected]) Received: 10 December 2015 – Published in Atmos. Meas. Tech. Discuss.: 18 January 2016 Revised: 3 May 2016 – Accepted: 6 May 2016 – Published: 17 June 2016 Abstract. The most widely used hydrochlorofluorocarbon 1 Introduction (HCFC) commercially since the 1930s has been chloro- difluoromethane, or HCFC-22, which has the undesirable The consumer appetite for safe household refrigeration led effect of depleting stratospheric ozone. As this molecule to the commercialisation in the 1930s of dichlorodifluo- is currently being phased out under the Montreal Pro- romethane, or CFC-12, a non-flammable and non-toxic re- tocol, monitoring its concentration profiles using infrared frigerant (Myers, 2007). Within the next few decades, other sounders crucially requires accurate laboratory spectroscopic chemically related refrigerants were additionally commer- data. This work describes new high-resolution infrared ab- cialised, including chlorodifluoromethane, or a hydrochlo- sorption cross sections of chlorodifluoromethane over the rofluorocarbon known as HCFC-22, which found use in a spectral range 730–1380 cm−1, determined from spectra wide array of applications such as air conditioners, chillers, recorded using a high-resolution Fourier transform spectrom- and refrigeration for food retail and industrial processes. -
1,1,1,2-Tetrafluoroethane
This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the United Nations Environment Programme, the International Labour Organisation, or the World Health Organization. Concise International Chemical Assessment Document 11 1,1,1,2-Tetrafluoroethane First draft prepared by Mrs P. Barker and Mr R. Cary, Health and Safety Executive, Liverpool, United Kingdom, and Dr S. Dobson, Institute of Terrestrial Ecology, Huntingdon, United Kingdom Please not that the layout and pagination of this pdf file are not identical to the printed CICAD Published under the joint sponsorship of the United Nations Environment Programme, the International Labour Organisation, and the World Health Organization, and produced within the framework of the Inter-Organization Programme for the Sound Management of Chemicals. World Health Organization Geneva, 1998 The International Programme on Chemical Safety (IPCS), established in 1980, is a joint venture of the United Nations Environment Programme (UNEP), the International Labour Organisation (ILO), and the World Health Organization (WHO). The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. The Inter-Organization -
SAFETY DATA SHEET Difluoromethane (R32) SECTION 1
SAFETY DATA SHEET Difluoromethane (R32) Issue Date: 16.01.2013 Version: 1.1 SDS No.: 000010021734 Last revised date: 26.11.2018 1/14 SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1 Product identifier Product name: Difluoromethane (R32) Other Name: HFC-32 Additional identification Chemical name: Difluoromethane Chemical formula: CH2F2 INDEX No. - CAS-No. 75-10-5 EC No. 200-839-4 REACH Registration No. 01-2119471312-47 1.2 Relevant identified uses of the substance or mixture and uses advised against Identified uses: Industrial and professional. Perform risk assessment prior to use. Refrigerant. Use as an Intermediate (transported, on-site isolated). Use for electronic component manufacture. Using gas alone or in mixtures for the calibration of analysis equipment. Formulation of mixtures with gas in pressure receptacles. Uses advised against Consumer use. 1.3 Details of the supplier of the safety data sheet Supplier Linde Gas GmbH Telephone: +43 50 4273 Carl-von-Linde-Platz 1 A-4651 Stadl-Paura E-mail: [email protected] 1.4 Emergency telephone number: Emergency number Linde: + 43 50 4273 (during business hours), Poisoning Information Center: +43 1 406 43 43 SECTION 2: Hazards identification 2.1 Classification of the substance or mixture Classification according to Regulation (EC) No 1272/2008 as amended. Physical Hazards Flammable gas Category 1 H220: Extremely flammable gas. Gases under pressure Liquefied gas H280: Contains gas under pressure; may explode if heated. SDS_AT - 000010021734 SAFETY DATA SHEET Difluoromethane (R32) Issue Date: 16.01.2013 Version: 1.1 SDS No.: 000010021734 Last revised date: 26.11.2018 2/14 2.2 Label Elements Signal Words: Danger Hazard Statement(s): H220: Extremely flammable gas. -
Kinetic Modeling for PAH Formation in a Counterflow Diffusion Flame of Isobutane
27th ICDERS July 28th – August 2nd, 2019 Beijing, China Kinetic modeling for PAH formation in a counterflow diffusion flame of isobutane Wei-Kai Chiua, Hairong Taob, Kuang C. Linc,* aDepartment of Mechanical and Electro-Mechanical Engineering,Kaohsiung 80424, National Sun Yat-Sen University, Taiwan bCollege of Chemistry, Beijing Normal University, Beijing 100875, China cEngineering and System Science,Hsinchu 30013, National Tsing Hua University, Taiwan 1 Abstract In the purpose of understanding the complex chemistry of aromatic hydrocarbon formation in diffusion flames of isobutane oxidation, mechanism that consists of 300 species and 11790 reactions is employed for verifying experimental measurements. The kinetic mechanism is incorporated into a 1-D axisymmetric laminar finite-rate model of a counterflow flame to compute the species profiles. Furthermore, the reaction pathway diagram produced by rate of production analysis illustrates the correlation between the decomposition of isobutane and formation of the target species. Keywords: isobutane, counterflow diffusion flame, paromatic hydrocarbon, chemical kinetic modeling 2 Introduction Isobutane (iC4H10) is an isomer of butane and flammable gas. Although it is not ideal fuel on its own, this species plays a role in the oxidation of large hydrocarbon fuels and is used in liquified natural gas (LNG) [1]. The detailed kinetic mechanism of isobutane combustion contains dozens of species and hundreds of reactions. When a kinetic mechanism is applied to a reaction source term of species transport equations, the computational solutions can be used to describe reactive flows and species distribution in multidimensional reactors. This kind of numerical modeling permits designers and analysts to evaluate emissions and performance of fuels in reactors or combustors. -
SAFETY DATA SHEET Chlorodifluoromethane (R 22) Issue Date: 16.01.2013 Version: 1.0 SDS No.: 000010021746 Last Revised Date: 18.06.2015 1/15
SAFETY DATA SHEET Chlorodifluoromethane (R 22) Issue Date: 16.01.2013 Version: 1.0 SDS No.: 000010021746 Last revised date: 18.06.2015 1/15 SECTION 1: Identification of the substance/mixture and of the company/undertaking 1.1 Product identifier Product name: Chlorodifluoromethane (R 22) Trade name: Gasart 503 R22 Additional identification Chemical name: Chlorodifluoromethane Chemical formula: CHClF2 INDEX No. - CAS-No. 75-45-6 EC No. 200-871-9 REACH Registration No. 01-2119517587-31 1.2 Relevant identified uses of the substance or mixture and uses advised against Identified uses: Industrial and professional. Perform risk assessment prior to use. Refrigerant. Using gas alone or in mixtures for the calibration of analysis equipment. Using gas as feedstock in chemical processes. Formulation of mixtures with gas in pressure receptacles. Uses advised against Consumer use. 1.3 Details of the supplier of the safety data sheet Supplier Linde Gas GmbH Telephone: +43 50 4273 Carl-von-Linde-Platz 1 A-4651 Stadl-Paura E-mail: [email protected] 1.4 Emergency telephone number: Emergency number Linde: + 43 50 4273 (during business hours), Poisoning Information Center: +43 1 406 43 43 SDS_AT - 000010021746 SAFETY DATA SHEET Chlorodifluoromethane (R 22) Issue Date: 16.01.2013 Version: 1.0 SDS No.: 000010021746 Last revised date: 18.06.2015 2/15 SECTION 2: Hazards identification 2.1 Classification of the substance or mixture Classification according to Directive 67/548/EEC or 1999/45/EC as amended. N; R59 The full text for all R-phrases is displayed in section 16. Classification according to Regulation (EC) No 1272/2008 as amended. -
Chlorofluorocarbons Chem 300A Tyler Jensen, Mackenzie Latimer, Jessie Luther, Jake Mcghee, Adeeb Noorani, Tyla Penner, & Maddy Springle
Chlorofluorocarbons Chem 300a Tyler Jensen, Mackenzie Latimer, Jessie Luther, Jake McGhee, Adeeb Noorani, Tyla Penner, & Maddy Springle 1.1: A Brief History of Chlorofluorocarbons Chlorofluorocarbons (CFCs), also known as Freons, were first synthesized in 1928 by Thomas Midgley Jr, who was working for General Motors trying to find a safe refrigerant to use in commercial applications. (Rosenbaum, n.d.). They are an anthropogenic compound containing fluorine, carbon, and chlorine atoms, and are classified as halocarbons. CFCs are a family of chemicals based upon hydrocarbon skeletons, where most hydrogens have been replaced with chlorine and/or fluorine atoms. They are chemically stable freons that are non-flammable, tasteless and odourless. CFCs are very volatile, which makes for ideal refrigerant gases, having a boiling point close to zero degrees (Rosenbaum, n.d) They were originally created to replace the toxic gases used in the late 1800’s and early 1900’s. Examples of the toxic gases replaced by CFCs as refrigerants are ammonia (NH3), methyl chloride (CH3Cl), and sulfur dioxide (SO2) (Wilkins, 1999). When first created dichlorodifloromethane was found to be less toxic than carbon dioxide, and as non-flammable as carbon tetrachloride (Midgley & Henne, 1930). The non-toxic, non-flammable, and non-reactive properties of CFCs made them ideal for use as refrigerants. CFCs were used in many developed countries for consumption and production as they were inflammable and non-toxic towards humanity. Chlorofluorocarbons can be used as refrigerants, cleaning agents, foaming agents, and propellants for aerosol sprays (Welch, n.d.). In 1974, Two University of California chemists, Professor F. Sherwood Rowland and Dr. -
UNITED STATES PATENT of FICE 2,640,086 PROCESS for SEPARATING HYDROGEN FLUORIDE from CHLORODFLUORO METHANE Robert H
Patented May 26, 1953 2,640,086 UNITED STATES PATENT of FICE 2,640,086 PROCESS FOR SEPARATING HYDROGEN FLUORIDE FROM CHLORODFLUORO METHANE Robert H. Baldwin, Chadds Ford, Pa., assignor to E. H. du Pont de Nemours and Company, Wi inington, Del, a corporation of Delaware No Drawing. Application December 15, 1951, Serial No. 261,929 9 Claims. (C. 260-653) 2 This invention relates to a process for Sep These objects are accomplished essentially by arating hydrogen fluoride from monochlorodi Subjecting a mixture of hydrogen fluoride and fluoronethane, and more particularly, separat Inonochlorodifluoromethane in the liquid phase ing these components from the reaction mixture to temperatures below 0° C., preferably at about obtained in the fluorination of chloroform with -30° C. to -50° C., at either atmospheric or hydrogen fluoride, Super-atmospheric pressures, together with from In the fluorination of chloroform in the prest about 0.25 mol to about 2.5 mols of chloroform ence Of a Catalyst, a reaction mixture is pro per mol of chlorodifluoronethane contained in duced which consists essentially of HCl, HF, the mixture and separating an upper layer rich CHCIF2, CHCl2F, CHCls, and CHF3. A method O in HF from a lower organic layer. The proceSS of Separating these components is disclosed in is operative with mixtures containing up to 77% U. S. Patent No. 2,450,414 which involves sep by weight of HF. arating the components by a special fractional It has been found that chloroform is substan distillation under appropriate temperatures and tially immiscible With EIF at temperatures be pressures. -
HFO-1234Yf) Combustion
Kinetic Mechanism of 2,3,3,3-Tetrafluoropropene (HFO-1234yf) Combustion V.I. Babushok, G.T Linteris Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD, USA Short communication To be submitted to “Journal of Fluorine Chemistry” Corresponding author: Valeri I. Babushok Engineering Laboratory National Institute of Standards and Technology Gaithersburg, MD, USA E-mail: [email protected] Phone: 301-975-8975 Keywords: R-1234yf; Refrigerant flammability, Burning velocity, Low ODP/GWP refrigerants, kinetic model. 1 Kinetic Mechanism of 2,3,3,3-Tetrafluoropropene (HFO-1234yf) Combustion V.I. Babushok, G.T Linteris Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD, USA Abstract A kinetic model for 2,3,3,3-tetrafluoropropene (HFO-1234yf) high temperature oxidation and combustion is proposed. It is combined with the GRI-Mech-3.0 model, with the previously developed model for 2-bromo-3,3,3-trifluoropropene (2-BTP), and with the NIST C1-C2 hydrofluorocarbon model. The model includes 909 reactions and 101 species. Combustion equilibrium calculations indicate a maximum combustion temperature of 2076 K for an HFO- 1234yf volume fraction of 0.083 in air for standard conditions (298 K, 0.101 MPa). Modeling of flame propagation in mixtures of 2,3,3,3-tetrafluoropropene with oxygen- enriched air demonstrates that the calculated maximum burning velocity reproduces the experimentally observed maximum burning velocity within about ___%reasonably well. However, the calculated maximum is observed in lean mixtures in contrast to the experimental results showing the maximum burning velocity shifted to the rich mixtures of HFO-1234yf. Keywords: R-1234yf; rRefrigerant flammability; bBurning velocity; lLow ODP/GWP refrigerants; kinetic model. -
CHAPTER12 Atmospheric Degradation of Halocarbon Substitutes
CHAPTER12 AtmosphericDegradation of Halocarbon Substitutes Lead Author: R.A. Cox Co-authors: R. Atkinson G.K. Moortgat A.R. Ravishankara H.W. Sidebottom Contributors: G.D. Hayman C. Howard M. Kanakidou S .A. Penkett J. Rodriguez S. Solomon 0. Wild CHAPTER 12 ATMOSPHERIC DEGRADATION OF HALOCARBON SUBSTITUTES Contents SCIENTIFIC SUMMARY ......................................................................................................................................... 12.1 12.1 BACKGROUND ............................................................................................................................................... 12.3 12.2 ATMOSPHERIC LIFETIMES OF HFCS AND HCFCS ................................................................................. 12.3 12.2. 1 Tropospheric Loss Processes .............................................................................................................. 12.3 12.2.2 Stratospheric Loss Processes .............................................................................................................. 12.4 12.3 ATMOSPHERIC LIFETIMES OF OTHER CFC AND HALON SUBSTITUTES ......................................... 12.4 12.4 ATMOSPHERIC DEGRADATION OF SUBSTITUTES ................................................................................ 12.5 12.5 GAS PHASE DEGRADATION CHEMISTRY OF SUBSTITUTES .............................................................. 12.6 12.5.1 Reaction with NO .............................................................................................................................. -
Emissions from Small-Scale Combustion of Biomass Fuels - Extensive Quantification and Characterization
Emissions from small-scale combustion of biomass fuels - extensive quantification and characterization Christoffer Boman Anders Nordin Marcus Öhman Dan Boström Energy Technology and Thermal Process Chemistry Umeå University Roger Westerholm Analytical Chemistry, Arrhenius Laboratory Stockholm University _______________________________________________________________ Emissions from small-scale combustion of biomass fuels - extensive quantification and characterization Christoffer Boman1, Anders Nordin1, Roger Westerholm2, Marcus Öhman1, Dan Boström1 1Energy Technology and Thermal Process Chemistry, Umeå University, SE-901 87 Umeå, Sweden 2Analytical Chemistry, Arrhenius Laboratory, Stockholm University, SE-106 91 Stockholm, Sweden STEM-BHM (P12648-1 and P21906-1) Umeå, February 2005 SUMMARY This work was a part of the Swedish national research program concerning emissions and air quality ("Utsläpp och Luftkvalitet") with the sub-programme concerning biomass, health and environment ("Biobränlen, Hälsa, Miljö" - BHM). The main objective of the work was to systematically determine the quantities and characteristics of gaseous and particulate emissions from combustion in residential wood log and biomass fuel pellet appliances and report emission factors for the most important emission components. The specific focus was on present commercial wood and pellet stoves as well as to illustrate the potentials for future technology development. The work was divided in different sub- projects; 1) a literature review of health effects of ambient wood -
Liquefied Gas Conversion Chart
LIQUEFIED GAS CONVERSION CHART Cubic Feet / Pound Pounds / Gallon Product Name Column A Column B Acetylene UN/NA: 1001 14.70 4.90 CAS: 514-86-2 Air UN/NA: 1002 13.30 7.29 CAS: N/A Ammonia Anhydrous UN/NA: 1005 20.78 5.147 CAS: 7664-41-7 Argon UN/NA: 1006 9.71 11.63 CAS: 7440-37-1 Butane UN/NA: 1075 6.34 4.86 CAS: 106-97-8 Carbon Dioxide UN/NA: 2187 8.74 8.46 CAS: 124-38-9 Chlorine UN/NA: 1017 5.38 11.73 CAS: 7782-50-5 Ethane UN/NA: 1045 12.51 2.74 CAS: 74-84-0 Ethylene Oxide UN/NA: 1040 8.78 7.25 CAS: 75-21-8 Fluorine UN/NA: 1045 10.17 12.60 CAS: 7782-41-4 Helium UN/NA: 1046 97.09 1.043 CAS: 7440-59-7 Hydrogen UN/NA: 1049 192.00 0.592 CAS: 1333-74-0 1. Find the gas you want to convert. 2. If you know your quantity in cubic feet and want to convert to pounds, divide your amount by column A 3. If you know your quantity in gallons and want to convert to pounds, multiply your amount by column B 4. If you know your quantity in pounds and want to convert to gallons, divide your amount by column B If you have any questions, please call 1-800-433-2288 LIQUEFIED GAS CONVERSION CHART Cubic Feet / Pound Pounds / Gallon Product Name Column A Column B Hydrogen Chloride UN/NA: 1050 10.60 8.35 CAS: 7647-01-0 Krypton UN/NA: 1056 4.60 20.15 CAS: 7439-90-9 Methane UN/NA: 1971 23.61 3.55 CAS: 74-82-8 Methyl Bromide UN/NA: 1062 4.03 5.37 CAS: 74-83-9 Neon UN/NA: 1065 19.18 10.07 CAS: 7440-01-9 Mapp Gas UN/NA: 1060 9.20 4.80 CAS: N/A Nitrogen UN/NA: 1066 13.89 6.75 CAS: 7727-37-9 Nitrous Oxide UN/NA: 1070 8.73 6.45 CAS: 10024-97-2 Oxygen UN/NA: 1072 12.05 9.52 CAS: 7782-44-7 Propane UN/NA: 1075 8.45 4.22 CAS: 74-98-6 Sulfur Dioxide UN/NA: 1079 5.94 12.0 CAS: 7446-09-5 Xenon UN/NA: 2036 2.93 25.51 CAS: 7440-63-3 1.