Vinyl chloride monomer
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||62.50 g·mol−1|
|Melting point||−153.8 °C (−244.8 °F; 119.3 K)|
|Boiling point||−13.4 °C (7.9 °F; 259.8 K)|
|2.7 g/L (0.0432 mol/L)|
|Vapor pressure||2580 mm. of mercury 20 °C (68 °F)|
Heat capacity (C)
|0.8592 J/K/g (gas)|
0.9504 J/K/g (solid)
Std enthalpy of
|−94.12 kJ/mol (solid)|
|R-phrases (outdated)||R12, R45|
|S-phrases (outdated)||S45, S53|
|NFPA 704 (fire diamond)|
|Flash point||−61 °C (−78 °F; 212 K)|
|NIOSH (US health exposure limits):|
|TWA 1 ppm C 5 ppm [15-minute]|
IDLH (Immediate danger)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Vinyl chloride is an organochloride with the formula H2C=CHCl that is also called vinyl chloride monomer (VCM) or chloroethene. This colorless compound is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). About 13 billion kilograms are produced annually. VCM is among the top twenty largest petrochemicals (petroleum-derived chemicals) in world production. The United States currently remains the largest VCM manufacturing region because of its low-production-cost position in chlorine and ethylene raw materials. China is also a large manufacturer and one of the largest consumers of VCM. Vinyl chloride is a gas with a sweet odor. It is highly toxic, flammable, and carcinogenic. It can be formed in the environment when soil organisms break down chlorinated solvents. Vinyl chloride that is released by industries or formed by the breakdown of other chlorinated chemicals can enter the air and drinking water supplies. Vinyl chloride is a common contaminant found near landfills. In the past VCM was used as a refrigerant.
Vinyl chloride is a chemical intermediate, not a final product. Due to the hazardous nature of vinyl chloride to human health there are no end products that use vinyl chloride in its monomer form. Polyvinyl chloride (PVC) is very stable, storable, and nowhere near as acutely toxic as the vinyl chloride monomer (VCM).
Vinyl chloride liquid is fed to polymerization reactors where it is converted from a monomeric VCM to a polymeric PVC. The final product of the polymerization process is PVC in either a flake or pellet form. From its flake or pellet form PVC is sold to companies that heat and mold the PVC into end products such as PVC pipe and bottles. Several million tons of PVC are sold on the global market each year.
Until 1974, vinyl chloride was used in aerosol spray propellant. Vinyl chloride was briefly used as an inhalational anaesthetic, in a similar vein to ethyl chloride, though its toxicity forced this practice to be abandoned.
Smaller amounts of vinyl chloride are used in furniture and automobile upholstery, wall coverings, housewares, and automotive parts. Vinyl chloride has also been used in the past as a refrigerant.
Vinyl chloride was first produced in 1835 by Justus von Liebig and his student Henri Victor Regnault. They obtained it by treating 1,2-dichloroethane with a solution of potassium hydroxide in ethanol.
In 1912, Fritz Klatte, a German chemist working for Griesheim-Elektron, patented a means to produce vinyl chloride from acetylene and hydrogen chloride using mercuric chloride as a catalyst. While this method was widely used during the 1930s and 1940s in the West, it has since been superseded by more economical processes based on ethylene in the United States and Europe. It remains the main production method in China.
Vinyl chloride is produced on a substantial scale—approximately 31.1 million tons were produced in 2000. Two methods are employed, the hydrochlorination of acetylene and the dehydrochlorination of ethylene dichloride (1,2-dichloroethane). Numerous attempts have been made to convert ethane directly to vinyl chloride.
Vinyl chloride can also be obtained as a byproduct in the synthesis of chlorofluorocarbons when saturated chlorofluorocarbons are catalytically dechlorinated by ethylene. Ethane sulfochlorination has been proposed as a route to produce vinyl chloride using sulfur instead of oxygen.
1,2-Dichloroethane ("dichloroethane", (C2H4Cl2)) is cheaply produced from inexpensive ethane. When heated to 500 °C at 15–30 atm (1.5 to 3 MPa) pressure, dichloroethane decomposes to produce vinyl chloride and anhydrous HCl.
Due to the relatively low cost of dichloroethane compared to acetylene, most vinyl chloride has been produced via this technique since the late 1950s.
The thermal cracking reaction is highly endothermic, and is generally carried out in a fired heater. Even though residence time and temperature are carefully controlled, it produces significant quantities of chlorinated hydrocarbon side products. In practice, EDC conversion is relatively low (50 to 60 percent). The furnace effluent is immediately quenched with cold EDC to stop undesirable side reactions. The resulting vapor-liquid mixture then goes to a purification system. Some processes use an absorber-stripper system to separate HCl from the chlorinated hydrocarbons, while other processes use a refrigerated continuous distillation system.
The reaction is exothermic and highly selective. Product purity and yields are generally very high.
This industrial route to vinyl chloride was common before ethylene became widely distributed. When vinyl chloride producers shifted to using the thermal cracking of EDC described above, some used byproduct HCl in conjunction with a colocated acetylene-based unit. The hazards of storing and shipping acetylene meant that the vinyl chloride facility needed to be located very close to the acetylene generating facility. China still uses this method to produce vinyl chloride due to the large reserves of coal from which acetylene is produced.
Ethane is readily available, particularly on the U.S. gulf coast. Ethylene is made from ethane by cracking ethane and then ethylene is used for production of vinyl chloride. Hence, to save the processing cost for manufacturing ethylene, numerous attempts have been made to convert ethane directly to vinyl chloride. The direct feed of ethane to vinyl chloride plants could thus considerably decrease the raw material costs and make the plants less dependent on cracker capacity. The conversion of ethane to vinyl chloride can be performed by various routes:
High-temperature oxidative chlorination:
A major drawback to the use of ethane are the forcing conditions required for its use, which can be attributed to its lack of molecular functionality. In contrast to ethylene, which easily undergoes chlorine addition, ethane must first be functionalized by substitution reactions, which gives rise to a variety of consecutive and side-chain reactions. The reaction must, therefore, be kinetically controlled in order to obtain a maximal vinyl chloride yield. Vinyl chloride yields average 20–50% per pass. Ethylene, ethyl chloride, and 1,2-dichloroethane are obtained as major byproducts. With special catalysts and at optimized conditions, however, ethane conversions of greater than 96% have been reported from oxychlorination reactions. The ethylene formed can either be recycled or oxychlorinated and cracked in a conventional manner. Many such ethane-based processes have been and are being developed.
Vinyl chloride is stored as a liquid. The presently accepted upper limit of safety as a health hazard is 500 ppm. Often, the storage containers for the product vinyl chloride are high capacity spheres. The spheres have an inside sphere and an outside sphere. Several inches of empty space separate the inside sphere from the outside sphere. This void area between the spheres is purged with an inert gas such as nitrogen. As the nitrogen purge gas exits the void space it passes through an analyzer that is designed to detect if any vinyl chloride is leaking from the internal sphere. If vinyl chloride starts to leak from the internal sphere or if a fire is detected on the outside of the sphere then the contents of the sphere are automatically dumped into an emergency underground storage container. Containers used for handling vinyl chloride at atmospheric temperature are always under pressure. Inhibited vinyl chloride may be stored at normal atmospheric conditions in suitable pressure vessel. Uninhibited vinyl chloride may be stored either under refrigeration or at normal atmospheric temperature in the absence of air or sunlight but only for a duration of a few days. If for longer periods, regular checks should be made for the presence of polymers.
Transporting VCM presents the same risks as transporting other flammable gases such as propane, butane (LPG) or natural gas (for which the same safety regulations apply). The equipment used for VCM transport is specially designed to be impact and corrosion resistant.
In the U.S., OSHA lists vinyl chloride as a Class IA Flammable Liquid, with a National Fire Protection Association Flammability Rating of 4. Because of its low boiling point, liquid VCM will undergo flash evaporation (i.e., autorefrigerate) upon its release to atmospheric pressure. The portion vaporized will form a dense cloud (more than twice as heavy as the surrounding air). The risk of subsequent explosion or fire is significant. According to OSHA, the flash point of vinyl chloride is −78 °C (−108.4 °F). Its flammable limits in air are: lower 3.6 volume% and upper 33.0 volume%. The explosive limits are: lower 4.0%, upper 22.05 by volume in air. Fire may release toxic hydrogen chloride (HCl) and carbon monoxide (CO). VCM can polymerise rapidly due to heating and under the influence of air, light and contact with a catalyst, strong oxidisers and metals such as copper and aluminium, with fire or explosion hazard. As a gas mixed with air, VCM is a fire and explosion hazard. On standing VCM can form peroxides, which may then explode. VCM will react with iron and steel in the presence of moisture. Vinyl chloride is a gas at normal atmospheric temperature and pressure.
It is flammable, emitting hydrogen chloride.
Vinyl chloride finds its major application in the production of PVC. It is volatile, so the primary exposure is via inhalation as against food or water with occupational hazards being highest. Prior to 1974, workers were commonly exposed to 1,000 ppm vinyl chloride, causing "vinyl chloride illness" such as acroosteolysis and Raynaud's Phenomenon. The symptoms of vinyl chloride exposure are classified by ppm levels in ambient air with 4,000 ppm having a threshold effect. The intensity of symptoms varies from acute (1,000-8,000 ppm), including dizziness, nausea, visual disturbances, headache, and ataxia, to chronic (above 12,000 ppm), including narcotic effect, cardiac arrhythmias, and fatal respiratory failure. RADS (Reactive Airway Dysfunction Syndrome) may be caused by acute exposure to vinyl chloride.
Vinyl chloride is a mutagen having clastogenic effects which affect lymphocyte chromosomal structure. Vinyl chloride is a Group 1 human carcinogen posing elevated risks of rare angiosarcoma, brain and lung tumors, and malignant haematopoeitic lymphatic tumors. Chronic exposure leads to common forms of respiratory failure (emphysema, pulmonary fibrosis) and focused hepatotoxicity (hepatomegaly, hepatic fibrosis). Continuous exposure can cause CNS depression including euphoria and disorientation. Decreased male libido, spontaneous abortion, and birth defects are known major reproductive defects associated with vinyl chloride.
Vinyl chloride can have acute dermal and ocular effects. Dermal exposure effects are thickening of skin, edema, decreased elasticity, local frostbites, blistering, and irritation. The complete loss of skin elasticity expresses itself in Raynaud’s Phenomenon.
The US OSHA limits vinyl chloride exposure of workers to no more than 1 ppm for eight hours or 5 ppm for 15 minutes. The US EPA and FDA limit vinyl chloride in drinking water to 0.002 ppm. Food (ingestion) is a trivial source of exposure.
The hepatotoxicity of vinyl chloride has long been established since the 1930s when the PVC industry was just in its infant stages. In the very first study about the dangers of vinyl chloride, published by Patty in 1930, it was disclosed that exposure of test animals to just a single short-term high dose of vinyl chloride caused liver damage. In 1949, a Russian publication discussed the finding that vinyl chloride caused liver injury among workers. In 1954, B.F. Goodrich Chemical stated that vinyl chloride caused liver injury upon short-term exposures. Almost nothing was known about its long-term effects. They also recommended long-term animal toxicology studies. The study noted that if a chemical did justify the cost of testing, and its ill-effects on workers and the public were known, the chemical should not be made. In 1963, research paid for in part by Allied Chemical found liver damage in test animals from exposures below 500 parts per million (ppm). Also in 1963, a Romanian researcher published findings of liver disease in vinyl chloride workers. In 1968, Mutchler and Kramer, two Dow researchers, reported their finding that exposures as low as 300 ppm caused liver damage in vinyl chloride workers thus confirming earlier animal data in humans. In a 1969 presentation given in Japan, P. L. Viola, a European researcher working for the European vinyl chloride industry, indicated, "every monomer used in V.C. manufacture is hazardous....various changes were found in bone and liver. Particularly, much more attention should be drawn to liver changes. The findings in rats at the concentration of 4 to 10 ppm are shown in pictures." In light of the finding of liver damage in rats from just 4–10 ppm of vinyl chloride exposure, Viola added that he "should like some precautions to be taken in the manufacturing plants polymerizing vinyl chloride, such as a reduction of the threshold limit value of monomer …"
In 1970, Viola reported that test animals exposed to 30,000 ppm of vinyl chloride developed cancerous tumors. Viola began his research looking for the cause of liver and bone injuries found in vinyl chloride workers. Viola's findings in 1970 were a "red flag" to B.F. Goodrich and the industry. In 1972, Maltoni, another Italian researcher for the European vinyl chloride industry, found liver tumors (including angiosarcoma) from vinyl chloride exposures as low as 250 ppm for four hours a day.
In the late 1960s, the cancers that all of these studies warned of finally manifested themselves in workers. John Creech from B.F. Goodrich discovered angiosarcoma (a very rare cancer) in the liver of a worker at the B.F. Goodrich plant in Louisville, Kentucky. Then, finally, on January 23, 1974, B.F. Goodrich informed the government and issued a press release stating that it was "investigating whether the cancer deaths of three employees in the polyvinyl chloride operations at its Louisville, Ky. plant were related to occupational causes."
In 1997 the U.S. Centers for Disease Control and Prevention (CDC) concluded that the development and acceptance by the PVC industry of a closed loop polymerization process in the late 1970s "almost completely eliminated worker exposures" and that "new cases of hepatic angiosarcoma in vinyl chloride polymerization workers have been virtually eliminated."
The Houston Chronicle claimed in 1998 that the vinyl industry manipulated vinyl chloride studies to avoid liability for worker exposure and hid extensive and severe chemical spills in local communities.
According to the United States Environmental Protection Agency (EPA), "vinyl chloride emissions from polyvinyl chloride (PVC), ethylene dichloride (EDC), and vinyl chloride monomer (VCM) plants cause or contribute to air pollution that may reasonably be anticipated to result in an increase in mortality or an increase in serious irreversible, or incapacitating reversible illness. Vinyl chloride is a known human carcinogen that causes a rare cancer of the liver." EPA's 2001 updated Toxicological Profile and Summary Health Assessment for VCM in its Integrated Risk Information System (IRIS) database lowers EPA's previous risk factor estimate by a factor of 20 and concludes that "because of the consistent evidence for liver cancer in all the studies...and the weaker association for other sites, it is concluded that the liver is the most sensitive site, and protection against liver cancer will protect against possible cancer induction in other tissues."