Encyclopedia:
Methanol,
Talk:Methanol,
Liquid_fuels,
Methanol fuel,
Carbazol-9-yl-methanol,
Methanol economy,
Methanol reformer,
Direct-methanol fuel cell,
Image:Methanol acid base.gif,
Methanol (data page)
F)
Toxic (
T)
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NFPA 704| NFPA
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R-phrases| ,
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S-phrases| , , ,
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Flash point| 11 °C
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RTECS number
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Supplementary data page|-
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Structure & properties |
n,
εr, etc.
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Thermodynamic data | Phase behaviour
Solid, liquid, gas
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Spectral data|
UV,
IR,
NMR,
MS|-
! chembox | Related compounds
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alkanols
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ethanolbutanol|-
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chloromethanemethoxymethane|-
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Except where noted otherwise, data are given for
materials in their standard state (at 25°C, 100 kPa)
Infobox disclaimer and references|-
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Methanol, also known as
methyl alcohol,
wood alcohol or
wood spirits, is a
chemical compound with
chemical formula CH3OH. It is the simplest
alcohol, and is a light,
volatile,
colourless,
flammable,
poisonous liquid with a distinctive odor that is somewhat milder and sweeter than
ethanol (
ethyl alcohol). It is used as an
antifreeze,
solvent,
fuel, and as a
denaturant for
ethyl alcohol.
Methanol is produced naturally in the
anaerobic metabolism of many varieties of bacteria. As a result, there is a small fraction of methanol vapor in the atmosphere. Over the course of several days, atmospheric methanol is
oxidized by oxygen with the help of sunlight to carbon dioxide and water.
Methanol burns in air forming
carbon dioxide and
water:
:2 CH
3OH + 3 O
2 → 2 CO
2 + 4 H
2O
A methanol flame is almost colorless. Care should be exercised around burning methanol to avoid burning oneself on the almost invisible fire.
Because of its poisonous properties, methanol is frequently used as a denaturant additive for ethanol manufactured for industrial uses— this addition of a
poison economically exempts industrial ethanol from the rather significant 'liquor' taxes that would otherwise be levied as it is the essence of all potable alcoholic beverages. Methanol is often called wood alcohol because it was once produced chiefly as a byproduct of the destructive distillation of wood. It is now produced synthetically by a multi-step process. In short,
natural gas and steam are reformed in a furnace to produce hydrogen and carbon monoxide; then, hydrogen and carbon monoxide gases react under pressure in the presence of a catalyst. The reforming step is endothermic and the synthesis step is exothermic.
History
In their
embalming process, the ancient Egyptians used a mixture of substances, including methanol, which they obtained from the
pyrolysis of wood. Pure methanol, however, was first isolated in
1661 by
Robert Boyle, who called it
spirit of box, because he produced it via the distillation of
boxwood. It later became known as
pyroxylic spirit. In
1834, the
French chemists
Jean-Baptiste Dumas and
Eugene Peligot determined its elemental composition. They also introduced the word
methylene to organic chemistry, forming it from
Greek methy = "
wine" +
hŷlē =
wood (patch of trees). Its intended origin was "
alcohol made from
wood (substance)", but it has Greek language errors. The term "methyl" was derived in about
1840 by
back-formation from
methylene, and was then applied to describe "methyl alcohol". This was shortened to "methanol" in
1892 by the International Conference on Chemical Nomenclature. The
suffix -yl used in
organic chemistry to form names of
radicals, was extracted from the word "methyl".
In
1923, the
German chemist
Matthias Pier, working for
BASF developed a means to convert
synthesis gas (a mixture of
carbon oxides and
hydrogen) into methanol. This process used a
zinc chromate catalyst, and required extremely vigorous conditions—pressures ranging from 30–100 MPa (300–1000
atm), and temperatures of about 400 °
C. Modern methanol production has been made more efficient through use of catalysts (commonly
copper) capable of operating at lower pressures.
The use of methanol as a motor fuel received attention during the oil crises of the 1970s due to its availability and low cost. Problems occurred early in the development of gasoline-methanol blends. As a result of its low price some gasoline marketers over blended. Others used improper blending and handling techniques. This led to consumer and media problems and the last time out of methanol blends. However, there is still a great deal of interest in using methanol as a neat fuel. The flexible-fuel vehicles currently being manufactured by General Motors, Ford and Chrysler can run on any combination of ethanol, methanol and/or gasoline. Neat alcohol fuels will become more widespread as more flexible-fuel automobiles are manufactured.
In 2006 astronomers using the
MERLIN array of radio telescopes at
Jodrell Bank Observatory discovered a huge cloud of methanol in space. The cloud measures 300 billion miles across, and is emitted from stars as they form.
Production
Today, synthesis gas is most commonly produced from the
methane component in
natural gas rather than from coal. Three processes are commercially practiced. At moderate pressures of 1 to 2 MPa (10–20 atm) and high temperatures (around 850 °C), methane
reacts with
steam on a nickel catalyst to produce
syngas according to the
chemical equation:
:
CH4 +
H2O →
CO + 3
H2This reaction, commonly called steam-methane reforming or SMR, is endothermic and the heat transfer limitations place limits on the size of the catalytic reactors used. Methane can also undergo partial oxidation with molecular oxygen to produce syngas, as the following equation shows:
:2
CH4 +
O2 → 2
CO + 4
H2this reaction is exothermic and the heat given off can be used
in-situ to drive the steam-methane reforming reaction. When the two processes are combined, it is referred to as autothermal reforming. The ratio of CO and H
2 can be adjusted by using the water-gas shift reaction,
:
CO +
H2O →
CO2 +
H2,
to provide the appropriate stoichiometry for methanol synthesis.
The carbon monoxide and hydrogen then react on a second catalyst to produce methanol. Today, the most widely used catalyst is a mixture of
copper,
zinc oxide, and
alumina first used by
ICI in
1966. At 5–10 MPa (50–100 atm) and 250 °C, it can catalyze the production of methanol from carbon monoxide and hydrogen with high selectivity
:
CO + 2
H2 → CH
3OH
It is worth noting that the production of synthesis gas from methane produces 3
moles of hydrogen for every mole of carbon monoxide, while the methanol synthesis consumes only 2 moles of hydrogen for every mole of carbon monoxide. One way of dealing with the excess hydrogen is to inject
carbon dioxide into the methanol synthesis reactor, where it, too, reacts to form methanol according to the
chemical equation:
CO2 + 3
H2 → CH
3OH +
H2OAlthough natural gas is the most economical and widely used feedstock for methanol production, other feedstocks can be used. Where natural gas is unavailable, light
petroleum products can be used in its place. The
South African firm
Sasol produces methanol using synthesis gas from
coal.
Uses
Methanol is used on a limited basis to fuel
internal combustion engines, mainly by virtue of the fact that it is not nearly as
flammable as
gasoline. Methanol blends are the fuel of choice in
open wheel racing circuits like
Champcars, as well as in
radio controlled model airplanes (required in the "
glow-plug" engines that primarily power them), cars and trucks. Dirt circle track racecars such as Sprint cars, Late Models, and Modifieds use methanol to fuel their engines.
Drag racers and mud racers also use methanol as their primary fuel source. Methanol is required with a supercharged engine in a
Top Alcohol Dragster and, until the end of the 2005 season, all vehicles in the
Indianapolis 500 had to run methanol.
Mud racers have mixed methanol with gasoline and nitrous oxide to produce more power than gasoline and nitrous oxide alone.
Methanol is a traditional ingredient in
methylated spirit or
denatured alcohol.
During
World War II, methanol was used as a fuel in several Nazi Germany military rocket designs, under name
M-Stoff, and in a mixture as
C-Stoff.
One of the drawbacks of methanol as a fuel is its
corrosivity to some metals, including
aluminium. Methanol, although a weak acid, attacks the oxide coating that normally protects the aluminium from corrosion:
:6 CH
3OH + Al
2O
3 → 2 Al(OCH
3)
3 + 3 H
2O
The resulting
methoxide salts are soluble in methanol, resulting in clean aluminium surface, which is readily oxidised by some dissolved
oxygen. Also the methanol can act as a oxidiser:
:6 CH
3OH + 4 Al → 2 Al
2(OCH
3)
3 + 3 H
2So the corrosion continues until the metal is eaten away.reference
When produced from wood or other organic materials, the resulting organic methanol (
bioalcohol) has been suggested as renewable alternative to petroleum-based
hydrocarbons. However, one cannot use BA100 (100% bioalcohol) in modern petroleum cars without modification.
Methanol is also used as a
solvent and as an
antifreeze in
pipelines. The largest use of methanol by far, however, is in making other chemicals. About 40% of methanol is converted to
formaldehyde, and from there into products as diverse as
plastics,
plywood,
paints,
explosives, and
permanent press textiles.
In some
wastewater treatment plants, a small amount of methanol is added to
wastewater to provide a food source of carbon for the
denitrification bacteria, which convert
nitrates to
nitrogen.
In the
1990s, large amounts of methanol were used in the
United States to produce the gasoline additive
methyl tert-butyl ether (MTBE). The
1990 Clean Air Act required certain major cities to use MTBE in their gasoline to reduce
photochemical smog. However, by the late 1990s, it was found that MTBE had leaked out of gasoline storage tanks and into the
groundwater in sufficient amounts to affect the taste of municipal drinking water in many areas. Moreover, MTBE was found to be a
carcinogen in animal studies. In the resulting backlash, several states banned the use of MTBE, and its future production remains uncertain.
Direct-methanol fuel cells are unique in their low temperature, atmospheric pressure operation, allowing them to be miniaturized to an unprecedented degree. This, combined with the relatively easy and safe storage and handling of methanol may open the possibility of fuel cell-powered
consumer electronics.
Other chemical derivatives of methanol include
dimethyl ether, which has replaced
chlorofluorocarbons as an
aerosol spray propellant, and
acetic acid.
There are now plans to use the chemical in eco-friendly fuel cells for laptop computers, the cells will break down methanol via an electrochemical process.
[http://newsimg.bbc.co.uk/media/images/41687000/jpg/_41687194_t_fuelcell01_203.jpg] Health and safety
Methanol is
intoxicating but not directly poisonous. It is
toxic by its breakdown (
toxication) by the
enzyme alcohol dehydrogenase in the
liver by forming
formic acid and
formaldehyde which cause
blindness by destruction of the
optic nerve.
http://www.newton.dep.anl.gov/askasci/chem03/chem03561.htm Methanol ingestion can also be fatal due to its
CNS depressant properties in the same manner as
ethanol poisoning. It enters the body by
ingestion,
inhalation, or
absorption through the
skin. Fetal tissue will not tolerate methanol. Dangerous doses will build up if a person is regularly exposed to vapors or handles liquid without skin protection. If methanol has been ingested, a doctor should be contacted immediately. The usual fatal dose: 100–125 mL (4 fl oz). Toxic effects take hours to start, and effective antidotes can often prevent permanent damage. This is treated using
ethanol or
fomepizole.
[http://pediatrics.aappublications.org/cgi/content/full/107/1/170] Either of these drugs acts to slow down the action of
alcohol dehydrogenase on methanol by means of
competitive inhibition, so that it is excreted by the
kidneys rather than being transformed into toxic metabolites. Though it is miscible with water, methanol is very hard to wash off the skin; it is best to treat methanol like
gasoline.
The initial symptoms of methanol intoxication are those of
central nervous system depression: headache, dizziness, nausea, lack of coordination, confusion, drowsiness, and with suffiently large doses, unconsciousness and death. The initial symptoms of methanol exposure are usually less severe than the symptoms resulting from the ingestion of a similar quantity of
ethyl alcohol.
Once the initial symptoms have passed, a second set of symptoms arises 10–30 hours after the initial exposure to methanol: blurring or complete loss of vision, together with
acidosis. These symptoms result from the accumulation of toxic levels of
formate in the bloodstream, and may progress to death by
respiratory failure. The
ester derivatives of methanol do not share this toxicity.
Ethanol is sometimes denatured (adulterated), and thus made undrinkable, by the addition of methanol. The result is known as
methylated spirit or "meths" (UK use). (The latter should not be confused with
meth, a common abbreviation for
methamphetamine.)
Pure methanol has been used in
open wheel racing since the mid-1960s. Unlike petroleum fires, methanol fires can be extinguished with plain water (while methanol is less dense than water, they are miscible, and the addition of water will cause the fire to use its heat to boil the water). In addition, a methanol-based fire burns invisibly, unlike gasoline, which burns with thick black smoke. If a fire occurs on the track, there is no smoke to obstruct the view of fast approaching drivers. The decision to permanently switch to methanol in American
Indycar racing is directly linked to a devastating crash and explosion at the
1964 Indianapolis 500 which killed drivers
Eddie Sachs and
Dave MacDonald.
One concern with the addition of methanol to automotive fuels is highlighted by recent groundwater impacts from the fuel additive
methyl tert-butyl ether (MTBE). Leaking underground gasoline storage tanks created MTBE plumes in groundwater that eventually adulterated well water. Methanol's high solubility in water raises concerns that similar well water contamination could arise from the widespread use of methanol as an automotive fuel.
See also
*
Liquid fuels
*
List of Stoffs*
Methanol (data page)*
Methanol economy*
Aspartame*
TBA References
*
Robert Boyle,
The Sceptical Chymist (
1661) – contains account of distillation of wood alcohol.
External links
*
http://methanol.org The Methanol Institute Industry trade group, lots of information on methanol's use in fuel cells and as an alternative fuel.
*
http://www.npi.gov.au/database/substance-info/profiles/54.html National Pollutant Inventory - Methanol Fact Sheet*
http://www.bluerhinos.co.uk/molview/indv.php?id=1 Molview from bluerhinos.co.uk See Methanol in 3D
*
http://www.labnews.co.uk/new_labnews/article.php?artid=1017&categoryid=2&scheme=2 Methanol Discovered in SpaceCategory:AlcoholsCategory:BiofuelsCategory:Solventsar:ميثانولbg:Метанолbs:Metanolca:Metanolcs:Methanolda:Metanolde:Methanolet:Metanoolel:Μεθανόληes:Metanoleo:Metanoloeu:Metanolfr:Méthanolko:메탄올it:Metanolohe:מתנולla:Methanollt:Metanolislv:Metanolslb:Methanolhu:Metanolnl:Methanolja:メタノールno:Metanolnn:Metanolpl:Alkohol metylowypt:Metanolru:Метанолsk:Metanolsl:Metanolfi:Metanolisv:Metanolth:เมทานอลtr:Metanoluk:Метанолzh:甲醇category:anatomical preservation