ChemicalBook > Product Catalog > Organic Chemistry > Hydrocarbons and derivatives > Acyclic hydrocarbons > ETHYLENE
- Product Name:ETHYLENE
- Synonyms: ethylene,refrigeratedliquid(cryogenicliquid) etileno Liquid ethyene liquidethyene liquidethylene Olefiant gas olefiantgas R1150
- Product Categories: SCOTTY Gases Chemical Synthesis Specialty Gases Synthetic Reagents Analytical Standards Analytical/Chromatography Chromatography Environmental Standards Metabolites Pesticides & Pesticides Standards Plant growth regulators refrigerants Gas Standards Mixtures
- Mol File:74-85-1.mol
ETHYLENE Chemical Properties
- Melting point:−169 °C(lit.)
- Boiling point:−104 °C(lit.)
- Density 0.00126
- vapor density 0.97 (vs air)
- vapor pressure 35.04 atm ( 20 °C)
- refractive index 1.363
- Flash point:-100 °C
- explosive limit36%
- FreezingPoint -169.4℃
- Merck 13,3825
- BRN 1730731
- Stability:Stable. Highly flammable - note wide explosion limits. Incompatible with strong oxidizing agents. Readily forms explosive mixtures with air.
- CAS DataBase Reference74-85-1(CAS DataBase Reference)
- NIST Chemistry ReferenceEthylene(74-85-1)
- EPA Substance Registry SystemEthene(74-85-1)
- Hazard Codes F+,F
- Risk Statements 12-67
- Safety Statements 9-16-33-46-45
- RIDADR UN 1962 2.1
- WGK Germany -
- RTECS KU5340000
- F 4.5-31
- Autoignition Temperature842 °F
- HazardClass 2.1
- HS Code 29012100
- Hazardous Substances Data74-85-1(Hazardous Substances Data)
- ToxicityLC for mice in air: 950,000 ppm (Flury)
ETHYLENE Usage And Synthesis
- DescriptionEthylene is a colorless, odorless gas that is the simplest alkene hydrocarbon. It is a natural plant hormone and is produced synthetically from natural gas and petroleum. The double bond in ethylene makes this compound highly reactive, and the volume of ethylene used in the chemical industry is greater than any other organic compound.
- Chemical Propertiescolourless gas
- Chemical PropertiesEthylene, an alkene is a colorless gas (at room temperature). Sweet odor. Minimum detectable odor 5 260 ppm.
- UsesEthylene occurs in petroleum gases, in illuminatinggas, and in ripening fruits. It is made by dehydrating alcohol. It is used in oxyethyleneflame for welding and cutting metals; inthe manufacture of polyethylene, polystyrene,and other plastics; in making ethylene oxide;and as an inhalation anesthetic.
- UsesOxyethylene welding and cutting metals; manufacture of alcohol, mustard gas, and many other organics. manufacture of ethylene oxide (for plastics), "Polythene", polystyrene and other plastics. Plant growth regulator; used commercially to accelerate the ripening of various fruits.
- UsesEthylene is highly reactive and is one of the most important compounds for the chemical industry. The highest use of ethylene is in polymerization reactions. Polyethylene polymers are linear, but they contain side branchings of methyl groups. Among these are several groups defi ned by their density produced under different pressure regimens.
The second highest use of ethylene involves oxidation to ethylene oxide and its derivative ethylene glycol (HO-CH2-CH2-OH). Ethylene glycol is used mainly as antifreeze and in the production of polyesters. Other important compounds produced through oxidation of ethylene are acetaldehyde (H3C-CH = O) and vinyl acetate (CH2 = CH-O-CO-CH2). Ethylene may also be halogenated to produce a number of other compounds.
- Production MethodsEthylene is primarily obtained from the ethane and propane components of natural gas andfrom the naphtha, kerosene, and gas oil components of crude oil. It can also be synthesizedthrough the dehydration of ethanol (C2H5OH). The production of ethylene from hydrocarbonfeedstocks involves mixing with steam and then subjecting the hydrocarbons to thermalor catalytic cracking. Cracking is a process in which organic molecules are broken down intosmaller molecules. Thermal cracking involves the use of heat and pressure. Catalytic crackinguses various catalysts to reduce the amount of heat and pressure required in the process.Th ermal cracking of hydrocarbons to ethylene occurs between approximately 650°C and800°C (1200°F and 1500°F). After hydrocarbons are cracked, a mixture containing ethyleneand other gases such as methane, ethane, and propane is obtained. Ethylene is separated fromthese through physical processes such as fractional distillation, refrigeration, absorption, oradsorption.
- Definitionethylene: A colourlessflammable gaseous hydrocarbon,C2H4; m.p. –169°C; b.p. –103.7°C. It isthe first member of the alkene seriesof hydrocarbons. It is made bycracking hydrocarbons from petroleumand is now a major raw materialfor making other organicchemicals (e.g. ethanal, ethanol,ethane-1,2-diol). It can be polymerizedto polyethene. It occurs naturallyin plants, in which it acts as agrowth substance promoting theripening of fruits.
- General DescriptionA colorless gas with a sweet odor and taste. ETHYLENE is lighter than air. ETHYLENE is easily ignited and a flame can easily flash back to the source of the leak. Under prolonged exposure to fire or heat the containers may rupture violently and rocket. Can cause explosion.
- Air & Water ReactionsHighly flammable.
- Reactivity ProfilePeroxidizable monomer may initiate exothermic polymerization of the bulk material [Bretherick 1979. p. 160]. ETHYLENE in the presence of aluminum chloride may undergo a violent reaction [J. Inst. Pet. 33:254. 1947]. Ozone and ETHYLENE react explosively [Berichte 38:3837]. ETHYLENE can polymerize at low pressure if catalyzed by titanium halides. (Sundaram, K. M, M. M. Shreehan, E. F. Olszewski. thylene. Kirk-Othmer Encyclopedia of Chemical Technology. John Wiley & Sons, Inc. 2001.)
- HazardHighly flammable, dangerous fire and explosion risk; explosive limits in air 3–36% by volume. Simple asphyxiant; questionable carcinogen.
- Health HazardModerate concentration in air causes drowsiness, dizziness, and unconsciousness. Overexposure causes headache, drowsiness, muscular weakness.
- Health HazardExposure to ethylene atmosphere can causeasphyxiation. At high concentrations it is anarcotic and can cause unconsciousness.
- Fire HazardFlammable gas; burns with a luminous flame;
autoignition temperature 490°C (914°F)
(NFPA 1997), 543°C (1009°F) (Merck
1996); fire-extinguishing measure: shut off
the flow of gas; use a water spray to keep
fire-exposed containers cool.
Ethylene forms explosive mixtures in air; the LEL and UEL values are 2.7% and 36% by volume of air, respectively. Its reaction with fluorine is explosively violent (△H=- 112 kcal/mol), and violent with chlorine (△H=- 36 kcal/mol). In the presence of sunlight or UV light, an ethylene– chlorine mixture will explode spontaneously. The reaction is explosive at room temperature over the oxides of mercury or silver (Mellor 1946, Suppl. 1956). Ethylene reacts vigorously with oxidizing substances. It reacts with ozone to form ethylene ozonide, H2C(O3)CH2, which is unstable and explodes on mechanical shock. Acidcatalyzed addition of hydrogen peroxide may produce ethyl hydroperoxide, which is unstable and explodes on heat or shock:.
- Industrial usesEthylene, also called ethane, is a colorless,inflammable gas, CH2:CH2, produced in thecracking of petroleum. Ethylene liquefies at–68.2°C. Ethylene is the largest-volume organicchemical produced today, and is the basic buildingblock of the petrochemical industry. Polymerizationof ethylene is its largest use. Whenethylene is reacted in the presence of transitionmetal catalysts, such as Mo2O5 or Cr2O3, at highpressures, it forms low-density polyethylene(LDPE); at lower pressures, high-density polyethylene(HDPE) is produced. Recently, lowpressures have been employed for making a newvariant, linear low-density polyethylene(LLDPE). Ethylene is now used to produce ethylalcohol, acrylic acid, and styrene, and it is thebasis for many types of reactive chemicals.
Trichloroethylene is a colorless liquid ofpleasant odor of the composition CHCl:CCl2,also known as westrosol. Its boiling point is87°C and its specific gravity 1.471. It is insolublein water and is unattacked by dilute acidsand alkalis. It is non flammable and is less toxicthan tetrachlorethane. Trichloroethylene is apowerful solvent for fats, waxes, resins, rubber,and other organic substances, and is employedfor the extraction of oils and fats, for cleaningfabrics, and for degreasing metals preparatoryto plating. The freezing point is –88°C, and itis also used as a refrigerant. It is also used insoaps employed in the textile industry fordegreasing.
- Safety ProfileSuspected carcinogen. A simple asphyxiant. High concentrations cause anesthesia. A common air contaminant. It is phytotoxic. A very dangerous fire hazard when exposed to heat or flame. Moderate explosion hazard when exposed to flame. A flammable gas. To figh fire, stop flow of gas, use Co2, dry chemical, or fine water spray. Mixtures with aluminum chloride explode in the presence of nickel catalysts, methyl chloride, or nitromethane. Explosive reaction with bromotrichloromethane (at 120℃/51 bar), carbon tetrachloride (25-100°C/30 bar). Explosive reaction with chlorine catalyzed by sunlight or UV light or in the presence of mercury(I) oxide, mercury(Ⅱ) oxide, or silver oxide. Mixtures with chlorotrifluoroethylene polymerize explosively when exposed to 50 kV gamma rays at 308 krad/hr. Has been involved in industrial accidents. Violent polymerization is catalyzed by copper above 4OO0C/54 bar. Incompatible with AlCl3, (CC4 + benzoyl peroxide), (bromotrichloromethane + NCh), 03, CCl4, Cl2, NOx, tetrafluoroethylene trifluorohypofluorite. When heated to decomposition it emits acrid smoke and irritating fumes
- Potential ExposureEthylene is used in production of fabricated plastics, antifreeze; making fibers; to manufacture ethylene oxide, polyethylene for plastics, alcohol, mustard gas and other organics. It is used to accelerate ripening of fruit; as an anesthetic; and for oxyethylene welding and cutting of metals
- storageEthylene is stored in a cool, well-ventilatedarea isolated from oxygen, chlorine, andflammable and oxidizing substances. It isprotected against lightning, statical electricity,heat, and physical damage. It is shippedin steel pressure cylinders and tank barges.
- ShippingUN1962 Ethylene, Hazard Class: 2.1; Labels: 2.1-Flammable gas; UN1038 Ethylene, refrigerated liquid (cryogenic liquid), Hazard Class: 2.1; Labels: 2.1- Flammable gas. Cylinders must be transported in a secure upright position, in a well-ventilated truck. Protect cylinder and labels from physical damage. The owner of the compressed gas cylinder is the only entity allowed by federal law (49CFR) to transport and refill them. It is a violation of transportation regulations to refill compressed gas cylinders without the express written permission of the owner.
- Purification MethodsPurify ethylene by passage through a series of towers containing molecular sieves or anhydrous CaSO4 or a cuprous ammonia solution, then conc H2SO4, followed by KOH pellets. Alternatively, it has been condensed in liquid nitrogen, with melting, freezing and pumping to remove air before passage through an activated charcoal trap, followed by a further condensation in liquid air. A sputtered sodium trap was used to remove oxygen. [Beilstein 1 IV 677.]
- IncompatibilitiesA highly flammable gas at room temperature. Contact with oxidizers may cause explosive polymerization and fire. May be spontaneously explosive in sunlight or ultraviolet light when mixed with chlorine. Reacts violently with mixtures of carbon tetrachloride and benzoyl peroxide; bromotrichloromethane; aluminum chloride and ozone. Incompatible with acids, halogens, nitrogen oxides; hydrogen bromide; aluminum chloride; chlorine dioxide; nitrogen dioxide. May accumulate static electrical charges, and may cause ignition of its vapors.
- Waste DisposalReturn refillable compressed gas cylinders to supplier
ETHYLENE Preparation Products And Raw materials
- PROPYLENE ETHANE Vanadyl acetylacetonate LANTHANUM ACETYLACETONATE Titanium diisopropoxide bis(acetylacetonate) Manganic acetylacetonate Ruthenium acetylacetonate VANADIUM(III) ACETYLACETONATE TRIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)YTTERBIUM Platinum bis(acetylacetonate) Cupric acetylacetonate CHROMIUM(III) ACETYLACETONATE TRIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)DYSPROSIUM(III) MANGANESE(II) ACETYLACETONATE COBALT(II) ACETYLACETONATE TRIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)EUROPIUM(III) PR(TMHD)3 Bis(2,4-pentanediono)nickel
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