Oxygen is the chemical element
with the symbol
O and atomic number
8. It is a member of the chalcogen group
in the periodic table
, a highly reactive nonmetal
, and an oxidizing agent
that readily forms oxide
s with most elements as well as with other compounds
. After hydrogen
, oxygen is the third-most abundant element
in the universe by mass. At standard temperature and pressure
, two atoms of the element bind
to form dioxygen
, a colorless and odorless diatomic gas
with the formula . Diatomic oxygen gas currently constitutes 20.95% of the Earth's atmosphere
, though this has changed considerably
over long periods of time. Oxygen makes up almost half of the Earth's crust
in the form of oxides.
[Atkins, P.; Jones, L.; Laverman, L. (2016).''Chemical Principles'', 7th edition. Freeman. ]
Dioxygen provides the energy released in combustion
and aerobic cellular respiration
[Schmidt-Rohr, K. (2020). "Oxygen Is the High-Energy Molecule Powering Complex Multicellular Life: Fundamental Corrections to Traditional Bioenergetics” ''ACS Omega'' 5: 2221-2233. http://dx.doi.org/10.1021/acsomega.9b03352]
and many major classes of organic molecule
s in living organism
s contain oxygen atoms, such as protein
s, nucleic acid
s, and fat
s, as do the major constituent inorganic compound
s of animal shells, teeth, and bone. Most of the mass of living organisms is oxygen as a component of water
, the major constituent of lifeforms. Oxygen is continuously replenished in Earth's atmosphere by photosynthesis
, which uses the energy of sunlight to produce oxygen from water and carbon dioxide. Oxygen is too chemically reactive to remain a free element in air without being continuously replenished by the photosynthetic action of living organisms. Another form (allotrope
) of oxygen, ozone
(), strongly absorbs ultraviolet UVB
radiation and the high-altitude ozone layer
helps protect the biosphere
from ultraviolet radiation
. However, ozone present at the surface is a byproduct of smog
and thus a pollutant.
Oxygen was isolated by Michael Sendivogius
before 1604, but it is commonly believed that the element was discovered independently by Carl Wilhelm Scheele
, in Uppsala
, in 1773 or earlier, and Joseph Priestley
, in 1774. Priority is often given for Priestley because his work was published first. Priestley, however, called oxygen "dephlogisticated air", and did not recognize it as a chemical element. The name ''oxygen'' was coined in 1777 by Antoine Lavoisier
, who first recognized oxygen as a chemical element and correctly characterized the role it plays in combustion.
Common uses of oxygen include production of steel
s and textile
s, brazing, welding and cutting
of steels and other metal
s, rocket propellant
, oxygen therapy
, and life support system
s in aircraft
History of study
One of the first known experiments on the relationship between combustion
and air was conducted by the 2nd century BCE Greek
writer on mechanics, Philo of Byzantium
. In his work ''Pneumatica'', Philo observed that inverting a vessel over a burning candle and surrounding the vessel's neck with water resulted in some water rising into the neck. Philo incorrectly surmised that parts of the air in the vessel were converted into the classical element fire
and thus were able to escape through pores in the glass. Many centuries later Leonardo da Vinci
built on Philo's work by observing that a portion of air is consumed during combustion and respiration
[Cook & Lauer 1968, p.499.]
In the late 17th century, Robert Boyle
proved that air is necessary for combustion. English chemist John Mayow
(1641–1679) refined this work by showing that fire requires only a part of air that he called ''spiritus nitroaereus''.
In one experiment, he found that placing either a mouse or a lit candle in a closed container over water caused the water to rise and replace one-fourteenth of the air's volume before extinguishing the subjects.
From this, he surmised that nitroaereus is consumed in both respiration and combustion.
Mayow observed that antimony
increased in weight when heated, and inferred that the nitroaereus must have combined with it.
He also thought that the lungs separate nitroaereus from air and pass it into the blood and that animal heat and muscle movement result from the reaction of nitroaereus with certain substances in the body.
Accounts of these and other experiments and ideas were published in 1668 in his work ''Tractatus duo'' in the tract "De respiratione".
, Ole Borch
, Mikhail Lomonosov
, and Pierre Bayen
all produced oxygen in experiments in the 17th and the 18th century but none of them recognized it as a chemical element
[Emsley 2001, p.299]
This may have been in part due to the prevalence of the philosophy of combustion and corrosion
called the ''phlogiston theory'', which was then the favored explanation of those processes.
Established in 1667 by the German alchemist J. J. Becher
, and modified by the chemist Georg Ernst Stahl
phlogiston theory stated that all combustible materials were made of two parts. One part, called phlogiston, was given off when the substance containing it was burned, while the dephlogisticated part was thought to be its true form, or calx
Highly combustible materials that leave little residue
, such as wood or coal, were thought to be made mostly of phlogiston; non-combustible substances that corrode, such as iron, contained very little. Air did not play a role in phlogiston theory, nor were any initial quantitative experiments conducted to test the idea; instead, it was based on observations of what happens when something burns, that most common objects appear to become lighter and seem to lose something in the process.
, and physician Michael Sendivogius
(Michał Sędziwój) in his work ''De Lapide Philosophorum Tractatus duodecim e naturae fonte et manuali experientia depromti'' (1604) described a substance contained in air, referring to it as 'cibus vitae' (food of life
), and this substance is identical with oxygen.
Sendivogius, during his experiments performed between 1598 and 1604, properly recognized that the substance is equivalent to the gaseous byproduct released by the thermal decomposition
of potassium nitrate
. In Bugaj's view, the isolation
of oxygen and the proper association of the substance to that part of air which is required for life, lends sufficient weight to the discovery of oxygen by Sendivogius. This discovery of Sendivogius was however frequently denied by the generations of scientists and chemists which succeeded him.
It is also commonly claimed that oxygen was first discovered by Swedish pharmacist Carl Wilhelm Scheele
. He had produced oxygen gas by heating mercuric oxide
(HgO) and various nitrate
s in 1771–2.
Scheele called the gas "fire air" because it was then the only known agent
to support combustion. He wrote an account of this discovery in a manuscript titled ''Treatise on Air and Fire'', which he sent to his publisher in 1775. That document was published in 1777.
[Emsley 2001, p. 300]
In the meantime, on August 1, 1774, an experiment conducted by the British clergyman Joseph Priestley
focused sunlight on mercuric oxide contained in a glass tube, which liberated a gas he named "dephlogisticated air".
[Cook & Lauer 1968, p. 500]
He noted that candles burned brighter in the gas and that a mouse was more active and lived longer while breathing
it. After breathing the gas himself, Priestley wrote: "The feeling of it to my lungs was not sensibly different from that of common air
, but I fancied that my breast felt peculiarly light and easy for some time afterwards."
Priestley published his findings in 1775 in a paper titled "An Account of Further Discoveries in Air", which was included in the second volume of his book titled ''Experiments and Observations on Different Kinds of Air
Because he published his findings first, Priestley is usually given priority in the discovery.
The French chemist Antoine Laurent Lavoisier
later claimed to have discovered the new substance independently. Priestley visited Lavoisier in October 1774 and told him about his experiment and how he liberated the new gas. Scheele had also dispatched a letter to Lavoisier on September 30, 1774, which described his discovery of the previously unknown substance, but Lavoisier never acknowledged receiving it. (A copy of the letter was found in Scheele's belongings after his death.)
Lavoisier conducted the first adequate quantitative experiments on oxidation
and gave the first correct explanation of how combustion works.
He used these and similar experiments, all started in 1774, to discredit the phlogiston theory and to prove that the substance discovered by Priestley and Scheele was a chemical element
In one experiment, Lavoisier observed that there was no overall increase in weight when tin
and air were heated in a closed container.
He noted that air rushed in when he opened the container, which indicated that part of the trapped air had been consumed. He also noted that the tin had increased in weight and that increase was the same as the weight of the air that rushed back in. This and other experiments on combustion were documented in his book ''Sur la combustion en général'', which was published in 1777.
In that work, he proved that air is a mixture of two gases; 'vital air', which is essential to combustion and respiration, and ''azote'' (Gk. ' "lifeless"), which did not support either. ''Azote'' later became ''nitrogen
'' in English, although it has kept the earlier name in French and several other European languages.
Lavoisier renamed 'vital air' to ''oxygène'' in 1777 from the Greek
roots '' (oxys)'' (acid
, literally "sharp", from the taste of acids) and ''-γενής (-genēs)'' (producer, literally begetter), because he mistakenly believed that oxygen was a constituent of all acids.
Chemists (such as Sir Humphry Davy
in 1812) eventually determined that Lavoisier was wrong in this regard (hydrogen forms the basis for acid chemistry), but by then the name was too well established.
''Oxygen'' entered the English language despite opposition by English scientists and the fact that the Englishman Priestley had first isolated the gas and written about it. This is partly due to a poem praising the gas titled "Oxygen" in the popular book ''The Botanic Garden
'' (1791) by Erasmus Darwin
, grandfather of Charles Darwin
's original atomic hypothesis
presumed that all elements were monatomic and that the atoms in compounds would normally have the simplest atomic ratios with respect to one another. For example, Dalton assumed that water's formula was HO, leading to the conclusion that the atomic mass
of oxygen was 8 times that of hydrogen, instead of the modern value of about 16. In 1805, Joseph Louis Gay-Lussac
and Alexander von Humboldt
showed that water is formed of two volumes of hydrogen and one volume of oxygen; and by 1811 Amedeo Avogadro
had arrived at the correct interpretation of water's composition, based on what is now called Avogadro's law
and the diatomic elemental molecules in those gases.
[These results were mostly ignored until 1860. Part of this rejection was due to the belief that atoms of one element would have no chemical affinity towards atoms of the same element, and part was due to apparent exceptions to Avogadro's law that were not explained until later in terms of dissociating molecules.]
By the late 19th century scientists realized that air could be liquefied and its components isolated by compressing and cooling it. Using a cascade
method, Swiss chemist and physicist Raoul Pierre Pictet evaporated
liquid sulfur dioxide
in order to liquefy carbon dioxide, which in turn was evaporated to cool oxygen gas enough to liquefy it. He sent a telegram on December 22, 1877 to the French Academy of Sciences
in Paris announcing his discovery of liquid oxygen
Just two days later, French physicist Louis Paul Cailletet
announced his own method of liquefying molecular oxygen.
Only a few drops of the liquid were produced in each case and no meaningful analysis could be conducted. Oxygen was liquefied in a stable state for the first time on March 29, 1883 by Polish scientists from Jagiellonian University
, Zygmunt Wróblewski
and Karol Olszewski
In 1891 Scottish chemist James Dewar
was able to produce enough liquid oxygen for study.
[Emsley 2001, p.303]
The first commercially viable process for producing liquid oxygen was independently developed in 1895 by German engineer Carl von Linde
and British engineer William Hampson. Both men lowered the temperature of air until it liquefied and then distilled
the component gases by boiling them off one at a time and capturing them separately.
Later, in 1901, oxyacetylene welding
was demonstrated for the first time by burning a mixture of acetylene
and compressed . This method of welding and cutting metal later became common.
In 1923, the American scientist Robert H. Goddard
became the first person to develop a rocket engine
that burned liquid fuel; the engine used gasoline
for fuel and liquid oxygen as the oxidizer
. Goddard successfully flew a small liquid-fueled rocket 56 m at 97 km/h on March 16, 1926 in Auburn, Massachusetts
In academic laboratories, oxygen can be prepared by heating together potassium chlorate mixed with a small proportion of manganese dioxide.
Oxygen levels in the atmosphere are trending slightly downward globally, possibly because of fossil-fuel burning.
Properties and molecular structure
At standard temperature and pressure
, oxygen is a colorless, odorless, and tasteless gas with the molecular formula
, referred to as dioxygen.
As ''dioxygen'', two oxygen atoms are chemically bound
to each other. The bond can be variously described based on level of theory, but is reasonably and simply described as a covalent double bond
that results from the filling of molecular orbitals
formed from the atomic orbital
s of the individual oxygen atoms, the filling of which results in a bond order
of two. More specifically, the double bond is the result of sequential, low-to-high energy, or Aufbau
, filling of orbitals, and the resulting cancellation of contributions from the 2s electrons, after sequential filling of the low σ and σ*
orbitals; σ overlap of the two atomic 2p orbitals that lie along the O-O molecular axis and overlap of two pairs of atomic 2p orbitals perpendicular to the O-O molecular axis, and then cancellation of contributions from the remaining two of the six 2p electrons after their partial filling of the lowest and *
[Jack Barrett, 2002, "Atomic Structure and Periodicity, (Basic concepts in chemistry, Vol. 9 of Tutorial chemistry texts), Cambridge, U.K.:Royal Society of Chemistry, p. 153, , se]
accessed January 31, 2015.
This combination of cancellations and σ and overlaps results in dioxygen's double bond character and reactivity, and a triplet electronic ground state
. An electron configuration
with two unpaired electrons, as is found in dioxygen orbitals (see the filled * orbitals in the diagram) that are of equal energy—i.e., degenerate
—is a configuration termed a spin triplet
state. Hence, the ground state of the molecule is referred to as triplet oxygen
[An orbital is a concept from quantum mechanics that models an electron as a wave-like particle that has a spatial distribution about an atom or molecule.]
The highest energy, partially filled orbitals are antibonding
, and so their filling weakens the bond order from three to two. Because of its unpaired electrons, triplet oxygen reacts only slowly with most organic molecules, which have paired electron spins; this prevents spontaneous combustion.
In the triplet form, molecules are paramagnetic
. That is, they impart magnetic character to oxygen when it is in the presence of a magnetic field, because of the spin magnetic moment
s of the unpaired electrons in the molecule, and the negative exchange energy
between neighboring molecules.
Liquid oxygen is so magnet
ic that, in laboratory demonstrations, a bridge of liquid oxygen may be supported against its own weight between the poles of a powerful magnet.
is a name given to several higher-energy species of molecular in which all the electron spins are paired. It is much more reactive with common organic molecules
than is normal (triplet) molecular oxygen. In nature, singlet oxygen is commonly formed from water during photosynthesis, using the energy of sunlight. It is also produced in the troposphere
by the photolysis of ozone by light of short wavelength
and by the immune system
as a source of active oxygen.
s in photosynthetic organisms (and possibly animals) play a major role in absorbing energy from singlet oxygen
and converting it to the unexcited ground state before it can cause harm to tissues.
The common allotrope
of elemental oxygen on Earth is called dioxygen
, , the major part of the Earth's atmospheric oxygen (see Occurrence
has a bond length of 121 pm
and a bond energy of 498 kJ/mol
, which is smaller than the energy of other double bonds or pairs of single bonds in the biosphere
and responsible for the exothermic
reaction of O2
with any organic molecule.
Due to its energy content, O2
is used by complex forms of life, such as animals, in cellular respiration
. Other aspects of are covered in the remainder of this article.
Trioxygen () is usually known as ozone
and is a very reactive allotrope of oxygen that is damaging to lung tissue.
Ozone is produced in the upper atmosphere
when combines with atomic oxygen made by the splitting of by ultraviolet
Since ozone absorbs strongly in the UV region of the spectrum
, the ozone layer
of the upper atmosphere functions as a protective radiation shield for the planet.
Near the Earth's surface, it is a pollutant
formed as a by-product of automobile exhaust
At low earth orbit
altitudes, sufficient atomic oxygen is present to cause corrosion of spacecraft
() was discovered in 2001,
and was assumed to exist in one of the six phases of solid oxygen
. It was proven in 2006 that this phase, created by pressurizing to 20 GPa
, is in fact a rhombohedral cluster
. This cluster has the potential to be a much more powerful oxidizer
than either or and may therefore be used in rocket fuel
A metallic phase was discovered in 1990 when solid oxygen is subjected to a pressure of above 96 GPa and it was shown in 1998 that at very low temperatures, this phase becomes superconducting
more readily in water than nitrogen, and in freshwater more readily than seawater. Water in equilibrium with air contains approximately 1 molecule of dissolved for every 2 molecules of (1:2), compared with an atmospheric ratio of approximately 1:4. The solubility of oxygen in water is temperature-dependent, and about twice as much (14.6 mg·L−1
) dissolves at 0 °C than at 20 °C (7.6 mg·L−1
At 25 °C and of air, freshwater contains about 6.04 milliliters
(mL) of oxygen per liter
, and seawater
contains about 4.95 mL per liter. At 5 °C the solubility increases to 9.0 mL (50% more than at 25 °C) per liter for water and 7.2 mL (45% more) per liter for sea water.
Oxygen condenses at 90.20 K
(−182.95 °C, −297.31 °F), and freezes at 54.36 K (−218.79 °C, −361.82 °F). Both liquid
are clear substances with a light sky-blue
color caused by absorption in the red (in contrast with the blue color of the sky, which is due to Rayleigh scattering
of blue light). High-purity liquid is usually obtained by the fractional distillation
of liquefied air. Liquid oxygen may also be condensed from air using liquid nitrogen as a coolant.
Liquid oxygen is a highly reactive substance and must be segregated from combustible materials.
The spectroscopy of molecular oxygen is associated with the atmospheric processes of aurora
The absorption in the Herzberg continuum
and Schumann–Runge bands
in the ultraviolet produces atomic oxygen that is important in the chemistry of the middle atmosphere.
Excited state singlet molecular oxygen is responsible for red chemiluminescence in solution.
Isotopes and stellar origin
Naturally occurring oxygen is composed of three stable isotope
, and 18O
, with 16
O being the most abundant (99.762% natural abundance
O is synthesized
at the end of the helium fusion
process in massive star
s but some is made in the neon burning process
O is primarily made by the burning of hydrogen into helium
during the CNO cycle
, making it a common isotope in the hydrogen burning zones of stars.
O is produced when 14N
(made abundant from CNO burning) captures a 4He
nucleus, making 18
O common in the helium-rich zones of evolved, massive stars
s have been characterized. The most stable are 15
O with a half-life
of 122.24 seconds and 14
O with a half-life of 70.606 seconds.
All of the remaining radioactive
isotopes have half-lives that are less than 27 s and the majority of these have half-lives that are less than 83 milliseconds.
The most common decay mode
of the isotopes lighter than 16
O is β+ decay
to yield nitrogen, and the most common mode for the isotopes heavier than 18
O is beta decay
to yield fluorine
Oxygen is the most abundant chemical element by mass in the Earth's biosphere
, air, sea and land. Oxygen is the third most abundant chemical element in the universe, after hydrogen and helium.
[Emsley 2001, p.297]
About 0.9% of the Sun
's mass is oxygen.
Oxygen constitutes 49.2% of the Earth's crust
as part of oxide compounds such as silicon dioxide
and is the most abundant element by mass in the Earth's crust
. It is also the major component of the world's oceans (88.8% by mass).
Oxygen gas is the second most common component of the Earth's atmosphere
, taking up 20.8% of its volume and 23.1% of its mass (some 1015
[Emsley 2001, p.298] [Figures given are for values up to above the surface]
Earth is unusual among the planets of the Solar System
in having such a high concentration of oxygen gas in its atmosphere: Mars
(with 0.1% by volume) and Venus
have much less. The surrounding those planets is produced solely by the action of ultraviolet radiation on oxygen-containing molecules such as carbon dioxide.
The unusually high concentration of oxygen gas on Earth is the result of the oxygen cycle
. This biogeochemical cycle
describes the movement of oxygen within and between its three main reservoirs on Earth: the atmosphere, the biosphere, and the lithosphere
. The main driving factor of the oxygen cycle is photosynthesis
, which is responsible for modern Earth's atmosphere. Photosynthesis releases oxygen into the atmosphere, while respiration
, and combustion remove it from the atmosphere. In the present equilibrium, production and consumption occur at the same rate.
Free oxygen also occurs in solution in the world's water bodies. The increased solubility of at lower temperatures (see Physical properties
) has important implications for ocean life, as polar oceans support a much higher density of life due to their higher oxygen content. Water polluted
with plant nutrients such as nitrate
s or phosphate
s may stimulate growth of algae by a process called eutrophication
and the decay of these organisms and other biomaterials may reduce the content in eutrophic water bodies. Scientists assess this aspect of water quality by measuring the water's biochemical oxygen demand
, or the amount of needed to restore it to a normal concentration.
[Emsley 2001, p.301]
measure the ratio of oxygen-18 and oxygen-16 in the shells
s of marine organisms to determine the climate millions of years ago (see oxygen isotope ratio cycle
molecules that contain the lighter isotope
, oxygen-16, evaporate at a slightly faster rate than water molecules containing the 12% heavier oxygen-18, and this disparity increases at lower temperatures.
[Emsley 2001, p.304]
During periods of lower global temperatures, snow and rain from that evaporated water tends to be higher in oxygen-16, and the seawater left behind tends to be higher in oxygen-18. Marine organisms then incorporate more oxygen-18 into their skeletons and shells than they would in a warmer climate.
Paleoclimatologists also directly measure this ratio in the water molecules of ice core
samples as old as hundreds of thousands of years.
have measured the relative quantities of oxygen isotopes in samples from the Earth
, the Moon
, and meteorite
s, but were long unable to obtain reference values for the isotope ratios in the Sun
, believed to be the same as those of the primordial solar nebula
. Analysis of a silicon
wafer exposed to the solar wind
in space and returned by the crashed Genesis spacecraft
has shown that the Sun has a higher proportion of oxygen-16 than does the Earth. The measurement implies that an unknown process depleted oxygen-16 from the Sun's disk of protoplanetary material
prior to the coalescence of dust grains that formed the Earth.
Oxygen presents two spectrophotometric absorption band
s peaking at the wavelengths 687 and 760 nm
. Some remote sensing
scientists have proposed using the measurement of the radiance coming from vegetation canopies in those bands to characterize plant health status from a satellite
platform. This approach exploits the fact that in those bands it is possible to discriminate the vegetation's reflectance
from its fluorescence
, which is much weaker. The measurement is technically difficult owing to the low signal-to-noise ratio
and the physical structure of vegetation; but it has been proposed as a possible method of monitoring the carbon cycle
from satellites on a global scale.
Biological production and role of O2
Photosynthesis and respiration
In nature, free oxygen is produced by the light-driven splitting
of water during oxygenic photosynthesis
. According to some estimates, green algae
in marine environments provide about 70% of the free oxygen produced on Earth, and the rest is produced by terrestrial plants. Other estimates of the oceanic contribution to atmospheric oxygen are higher, while some estimates are lower, suggesting oceans produce ~45% of Earth's atmospheric oxygen each year.
A simplified overall formula for photosynthesis is:
:: 6 + 6 + photon
s → + 6
:: carbon dioxide
+ water + sunlight → glucose
Photolytic oxygen evolution
occurs in the thylakoid membrane
s of photosynthetic organisms and requires the energy of four photon
[Thylakoid membranes are part of chloroplasts in algae and plants while they simply are one of many membrane structures in cyanobacteria. In fact, chloroplasts are thought to have evolved from cyanobacteria that were once symbiotic partners with the progenitors of plants and algae.]
Many steps are involved, but the result is the formation of a proton
gradient across the thylakoid membrane, which is used to synthesize adenosine triphosphate
(ATP) via photophosphorylation
[Raven 2005, 115–27]
The remaining (after production of the water molecule) is released into the atmosphere.
[Water oxidation is catalyzed by a manganese-containing enzyme complex known as the oxygen evolving complex (OEC) or water-splitting complex found associated with the lumenal side of thylakoid membranes. Manganese is an important cofactor, and calcium and chloride are also required for the reaction to occur. (Raven 2005)]
The chemical energy of oxygen is released in mitochondria
to generate ATP during oxidative phosphorylation
The reaction for aerobic respiration is essentially the reverse of photosynthesis and is simplified as:
:: + 6 → 6 + 6 + 2880 kJ/mol
through membranes in the lungs and into red blood cell
binds , changing color from bluish red to bright red
( is released from another part of hemoglobin through the Bohr effect
). Other animals use hemocyanin
and some arthropod
s) or hemerythrin
s and lobster
A liter of blood can dissolve 200 cm3
Until the discovery of anaerobic metazoa
oxygen was thought to be a requirement for all complex life.
Reactive oxygen species
, such as superoxide
ion () and hydrogen peroxide
(), are reactive by-products of oxygen use in organisms.
Parts of the immune system
of higher organisms create peroxide, superoxide, and singlet oxygen to destroy invading microbes. Reactive oxygen species also play an important role in the hypersensitive response
of plants against pathogen attack.
Oxygen is damaging to obligately anaerobic organisms
, which were the dominant form of early life
on Earth until began to accumulate in the atmosphere
about 2.5 billion years ago during the Great Oxygenation Event
, about a billion years after the first appearance of these organisms.
An adult human at rest inhales
1.8 to 2.4 grams of oxygen per minute. This amounts to more than 6 billion tonnes of oxygen inhaled by humanity per year.
[(1.8 grams/min/person)×(60 min/h)×(24 h/day)×(365 days/year)×(6.6 billion people)/1,000,000 g/t=6.24 billion tonnes]
The free oxygen partial pressure
in the body of a living vertebrate organism is highest in the respiratory system
, and decreases along any arterial system
, peripheral tissues, and venous system
, respectively. Partial pressure is the pressure that oxygen would have if it alone occupied the volume.
Build-up in the atmosphere
Free oxygen gas was almost nonexistent in Earth's atmosphere
before photosynthetic archaea
evolved, probably about 3.5 billion years ago. Free oxygen first appeared in significant quantities during the Paleoproterozoic
eon (between 3.0 and 2.3 billion years ago).
Even if there was much dissolved iron
in the oceans when oxygenic photosynthesis was getting more common, it appears the banded iron formation
s were created by anoxyenic or micro-aerophilic iron-oxidizing bacteria which dominated the deeper areas of the photic zone
, while oxygen-producing cyanobacteria covered the shallows. Free oxygen began to outgas
from the oceans 3–2.7 billion years ago, reaching 10% of its present level around 1.7 billion years ago.
The presence of large amounts of dissolved and free oxygen in the oceans and atmosphere may have driven most of the extant anaerobic organism
s to extinction
during the Great Oxygenation Event
(''oxygen catastrophe'') about 2.4 billion years ago. Cellular respiration
using enables aerobic organism
s to produce much more ATP
than anaerobic organisms.
Cellular respiration of occurs in all eukaryote
s, including all complex multicellular organisms such as plants and animals.
Since the beginning of the Cambrian
period 540 million years ago, atmospheric levels have fluctuated between 15% and 30% by volume.
Towards the end of the Carboniferous
period (about 300 million years ago) atmospheric levels reached a maximum of 35% by volume,
which may have contributed to the large size of insects and amphibians at this time.
Variations in atmospheric oxygen concentration have shaped past climates. When oxygen declined, atmospheric density dropped, which in turn increased surface evaporation, causing precipitation increases and warmer temperatures.
At the current rate of photosynthesis it would take about 2,000 years to regenerate the entire in the present atmosphere.
Extraterrestrial free oxygen
In the field of astrobiology
and in the search for extraterrestrial life
oxygen is a strong biosignature
. That said it might not be a definite biosignature, being possibly produced abiotically
on celestial bodies
with processes and conditions (such as a peculiar hydrosphere
) which allow free oxygen, like with Europa's
One hundred million tonnes of are extracted from air for industrial uses annually by two primary methods.
The most common method is fractional distillation
of liquefied air, with distilling
as a vapor while is left as a liquid.
The other primary method of producing is passing a stream of clean, dry air through one bed of a pair of identical zeolite
molecular sieves, which absorbs the nitrogen and delivers a gas stream that is 90% to 93% .
Simultaneously, nitrogen gas is released from the other nitrogen-saturated zeolite bed, by reducing the chamber operating pressure and diverting part of the oxygen gas from the producer bed through it, in the reverse direction of flow. After a set cycle time the operation of the two beds is interchanged, thereby allowing for a continuous supply of gaseous oxygen to be pumped through a pipeline. This is known as pressure swing adsorption
. Oxygen gas is increasingly obtained by these non-cryogenic
technologies (see also the related vacuum swing adsorption
Oxygen gas can also be produced through electrolysis of water
into molecular oxygen and hydrogen. DC electricity must be used: if AC is used, the gases in each limb consist of hydrogen and oxygen in the explosive ratio 2:1. A similar method is the electrocatalytic evolution from oxides and oxoacid
s. Chemical catalysts can be used as well, such as in chemical oxygen generator
s or oxygen candles that are used as part of the life-support equipment on submarines, and are still part of standard equipment on commercial airliners in case of depressurization emergencies. Another air separation method is forcing air to dissolve through ceramic
membranes based on zirconium dioxide
by either high pressure or an electric current, to produce nearly pure gas.
methods include high pressure oxygen tank
s, cryogenics and chemical compounds. For reasons of economy, oxygen is often transported in bulk as a liquid in specially insulated tankers, since one liter
of liquefied oxygen is equivalent to 840 liters of gaseous oxygen at atmospheric pressure and .
Such tankers are used to refill bulk liquid oxygen storage containers, which stand outside hospitals and other institutions that need large volumes of pure oxygen gas. Liquid oxygen is passed through heat exchanger
s, which convert the cryogenic liquid into gas before it enters the building. Oxygen is also stored and shipped in smaller cylinders containing the compressed gas; a form that is useful in certain portable medical applications and oxy-fuel welding and cutting
Uptake of from the air is the essential purpose of respiration
, so oxygen supplementation is used in medicine
. Treatment not only increases oxygen levels in the patient's blood, but has the secondary effect of decreasing resistance to blood flow in many types of diseased lungs, easing work load on the heart. Oxygen therapy
is used to treat emphysema
, some heart disorders (congestive heart failure
), some disorders that cause increased pulmonary artery pressure
, and any disease
that impairs the body's ability to take up and use gaseous oxygen.
[Cook & Lauer 1968, p.510]
Treatments are flexible enough to be used in hospitals, the patient's home, or increasingly by portable devices. Oxygen tent
s were once commonly used in oxygen supplementation, but have since been replaced mostly by the use of oxygen mask
s or nasal cannula
(high-pressure) medicine uses special oxygen chambers
to increase the partial pressure
of around the patient and, when needed, the medical staff.
Carbon monoxide poisoning
, gas gangrene
, and decompression sickness
(the 'bends') are sometimes addressed with this therapy. Increased concentration in the lungs helps to displace carbon monoxide
from the heme group of hemoglobin
Oxygen gas is poisonous to the anaerobic bacteria
that cause gas gangrene, so increasing its partial pressure helps kill them. Decompression sickness occurs in divers who decompress too quickly after a dive, resulting in bubbles of inert gas, mostly nitrogen and helium, forming in the blood. Increasing the pressure of as soon as possible helps to redissolve the bubbles back into the blood so that these excess gasses can be exhaled naturally through the lungs.
Normobaric oxygen administration at the highest available concentration is frequently used as first aid for any diving injury that may involve inert gas bubble formation in the tissues. There is epidemiological support for its use from a statistical study of cases recorded in a long term database.
Life support and recreational use
An application of as a low-pressure breathing gas
is in modern space suit
s, which surround their occupant's body with the breathing gas. These devices use nearly pure oxygen at about one-third normal pressure, resulting in a normal blood partial pressure of . This trade-off of higher oxygen concentration for lower pressure is needed to maintain suit flexibility.
and surface-supplied underwater divers
rs also rely on artificially delivered . Submarines, submersibles and atmospheric diving suits
usually operate at normal atmospheric pressure. Breathing air is scrubbed of carbon dioxide by chemical extraction and oxygen is replaced to maintain a constant partial pressure. Ambient pressure
divers breathe air or gas mixtures with an oxygen fraction suited to the operating depth. Pure or nearly pure use in diving at pressures higher than atmospheric is usually limited to rebreathers
, or decompression
at relatively shallow depths (~6 meters depth, or less),
or medical treatment in recompression chambers
at pressures up to 2.8 bar, where acute oxygen toxicity can be managed without the risk of drowning. Deeper diving requires significant dilution of with other gases, such as nitrogen or helium, to prevent oxygen toxicity
People who climb mountains or fly in non-pressurized fixed-wing aircraft
sometimes have supplemental supplies.
[The reason is that increasing the proportion of oxygen in the breathing gas at low pressure acts to augment the inspired partial pressure nearer to that found at sea-level.]
Pressurized commercial airplanes have an emergency supply of automatically supplied to the passengers in case of cabin depressurization. Sudden cabin pressure loss activates chemical oxygen generator
s above each seat, causing oxygen mask
s to drop. Pulling on the masks "to start the flow of oxygen" as cabin safety instructions dictate, forces iron filings into the sodium chlorate
inside the canister.
A steady stream of oxygen gas is then produced by the exothermic
Oxygen, as a mild euphoric
, has a history of recreational use in oxygen bar
s and in sport
s. Oxygen bars are establishments found in the United States since the late 1990s that offer higher than normal exposure for a minimal fee.
Professional athletes, especially in American football
, sometimes go off-field between plays to don oxygen masks to boost performance. The pharmacological effect is doubted; a placebo
effect is a more likely explanation.
Available studies support a performance boost from oxygen enriched mixtures only if it is breathed ''during'' aerobic exercise
Other recreational uses that do not involve breathing include pyrotechnic
applications, such as George Goble
's five-second ignition of barbecue
of iron ore
consumes 55% of commercially produced oxygen.
In this process, is injected through a high-pressure lance into molten iron, which removes sulfur
impurities and excess carbon
as the respective oxides, and . The reactions are exothermic
, so the temperature increases to 1,700 °C
Another 25% of commercially produced oxygen is used by the chemical industry.
is reacted with to create ethylene oxide
, which, in turn, is converted into ethylene glycol
; the primary feeder material used to manufacture a host of products, including antifreeze
polymers (the precursors of many plastic
s and fabric
Large quantities of oxygen or air is used in oxy-cracking process and for the production of acrylic acid, diformyl-furane, and benzylic acid. On the other hand, the electrochemical synthesis of hydrogen peroxide from oxygen is a promising technology to replace the currently used hydroquinone-process. Last but not least, catalytic oxidation is used in afterburners to get rid of hazardous gases.
Most of the remaining 20% of commercially produced oxygen is used in medical applications, metal cutting and welding
, as an oxidizer in rocket fuel
, and in water treatment
Oxygen is used in oxyacetylene welding
, burning acetylene
with to produce a very hot flame. In this process, metal up to thick is first heated with a small oxy-acetylene flame and then quickly cut by a large stream of .
[Cook & Lauer 1968, p.508]
The oxidation state
of oxygen is −2 in almost all known compounds of oxygen. The oxidation state −1 is found in a few compounds such as peroxide
s. Compounds containing oxygen in other oxidation states are very uncommon: −1/2 (superoxide
s), −1/3 (ozonide
s), 0 (elemental
, hypofluorous acid
), +1/2 (dioxygenyl
), +1 (dioxygen difluoride
), and +2 (oxygen difluoride
Oxides and other inorganic compounds
() is an oxide of hydrogen
and the most familiar oxygen compound. Hydrogen atoms are covalently bonded
to oxygen in a water molecule but also have an additional attraction (about 23.3 kJ/mol per hydrogen atom) to an adjacent oxygen atom in a separate molecule. These hydrogen bond
s between water molecules hold them approximately 15% closer than what would be expected in a simple liquid with just van der Waals force
[Also, since oxygen has a higher electronegativity than hydrogen, the charge difference makes it a polar molecule. The interactions between the different dipoles of each molecule cause a net attraction force.]
Due to its electronegativity
, oxygen forms chemical bond
s with almost all other elements to give corresponding oxide
s. The surface of most metals, such as aluminium
, are oxidized in the presence of air and become coated with a thin film of oxide that passivates
the metal and slows further corrosion
. Many oxides of the transition metal
s are non-stoichiometric compound
s, with slightly less metal than the chemical formula
would show. For example, the mineral FeO
) is written as
, where ''x'' is usually around 0.05.
Oxygen is present in the atmosphere in trace quantities in the form of carbon dioxide
(). The Earth's crust
is composed in large part of oxides of silicon
, as found in granite
), aluminium (aluminium oxide
, in bauxite
), iron (iron(III) oxide
, in hematite
), and calcium carbonate
). The rest of the Earth's crust is also made of oxygen compounds, in particular various complex silicate
s (in silicate minerals
). The Earth's mantle, of much larger mass than the crust, is largely composed of silicates of magnesium and iron.
silicates in the form of , , and are used as detergent
s and adhesive
[Cook & Lauer 1968, p.507]
Oxygen also acts as a ligand
for transition metals, forming transition metal dioxygen complexes
, which feature metal–. This class of compounds includes the heme
. An exotic and unusual reaction occurs with
, which oxidizes oxygen to give O2+
, dioxygenyl hexafluoroplatinate
[Cook & Lauer 1968, p.505]
Among the most important classes of organic compounds that contain oxygen are (where "R" is an organic group): alcohol
s (R-OH); ether
s (R-O-R); ketone
s (R-CO-R); aldehyde
s (R-CO-H); carboxylic acid
s (R-COOH); ester
s (R-COO-R); acid anhydrides
(R-CO-O-CO-R); and amide
s (). There are many important organic solvent
s that contain oxygen, including: acetone
, diethyl ether
, ethyl acetate
, acetic acid
, and formic acid
. Acetone () and phenol
() are used as feeder materials in the synthesis of many different substances. Other important organic compounds that contain oxygen are: glycerol
, citric acid
, acetic anhydride
, and acetamide
s are ethers in which the oxygen atom is part of a ring of three atoms. The element is similarly found in almost all biomolecule
s that are important to (or generated by) life.
Oxygen reacts spontaneously with many organic
compounds at or below room temperature in a process called autoxidation
[Cook & Lauer 1968, p.506]
Most of the organic compound
s that contain oxygen are not made by direct action of . Organic compounds important in industry and commerce that are made by direct oxidation of a precursor include ethylene oxide
and peracetic acid
Safety and precautions
The NFPA 704
standard rates compressed oxygen gas as nonhazardous to health, nonflammable and nonreactive, but an oxidizer. Refrigerated liquid oxygen (LOX) is given a health hazard rating of 3 (for increased risk of hyperoxia
from condensed vapors, and for hazards common to cryogenic liquids such as frostbite), and all other ratings are the same as the compressed gas form.
Oxygen gas () can be toxic
at elevated partial pressure
s, leading to convulsion
s and other health problems.
[Since 's partial pressure is the fraction of times the total pressure, elevated partial pressures can occur either from high fraction in breathing gas or from high breathing gas pressure, or a combination of both.] [Cook & Lauer 1968, p.511]
Oxygen toxicity usually begins to occur at partial pressures more than 50 kilopascals
(kPa), equal to about 50% oxygen composition at standard pressure or 2.5 times the normal sea-level partial pressure of about 21 kPa. This is not a problem except for patients on mechanical ventilator
s, since gas supplied through oxygen mask
s in medical applications is typically composed of only 30%–50% by volume (about 30 kPa at standard pressure).
At one time, premature babies
were placed in incubators containing -rich air, but this practice was discontinued after some babies were blinded by the oxygen content being too high.
Breathing pure in space applications, such as in some modern space suits, or in early spacecraft such as Apollo
, causes no damage due to the low total pressures used.
In the case of spacesuits, the partial pressure in the breathing gas is, in general, about 30 kPa (1.4 times normal), and the resulting partial pressure in the astronaut's arterial blood is only marginally more than normal sea-level partial pressure.
Oxygen toxicity to the lungs and central nervous system
can also occur in deep scuba diving
and surface supplied diving
Prolonged breathing of an air mixture with an partial pressure more than 60 kPa can eventually lead to permanent pulmonary fibrosis
Exposure to an partial pressures greater than 160 kPa (about 1.6 atm) may lead to convulsions (normally fatal for divers). Acute oxygen toxicity (causing seizures, its most feared effect for divers) can occur by breathing an air mixture with 21% at or more of depth; the same thing can occur by breathing 100% at only .
Combustion and other hazards
Highly concentrated sources of oxygen promote rapid combustion. Fire
hazards exist when concentrated oxidants and fuel
s are brought into close proximity; an ignition event, such as heat or a spark, is needed to trigger combustion.
Oxygen is the oxidant, not the fuel, but nevertheless the source of most of the chemical energy released in combustion.
Concentrated will allow combustion to proceed rapidly and energetically.
pipes and storage vessels used to store and transmit both gaseous and liquid oxygen
will act as a fuel; and therefore the design and manufacture of systems requires special training to ensure that ignition sources are minimized.
The fire that killed the Apollo 1
crew in a launch pad test spread so rapidly because the capsule was pressurized with pure but at slightly more than atmospheric pressure, instead of the normal pressure that would be used in a mission.
Liquid oxygen spills, if allowed to soak into organic matter, such as wood
s, and asphalt
can cause these materials to detonate
unpredictably on subsequent mechanical impact.
* Geological history of oxygen
* Hypoxia (environmental)
for depletion in aquatic ecology
* Ocean deoxygenation
* Hypoxia (medical)
, a lack of oxygen
* Limiting oxygen concentration
* Oxygen compounds
* Oxygen plant
* Oxygen sensor
at ''The Periodic Table of Videos
'' (University of Nottingham)
Oxidizing Agents > OxygenRoald Hoffmann article on "The Story of O"
Scripps Institute: Atmospheric Oxygen has been dropping for 20 years
Category:Chemical substances for emergency medicine
Category:Biology and pharmacology of chemical elements