- All Products
- Shop by Brands
- BW Technologies
- BW Technologies
- BW Technologies Monitors
- BW Clip
- BW Clip4
- GasAlertClip Extreme
- GasAlert Extreme
- GasAlertMicroClip XT
- GasAlertMicroClip XL
- GasAlertMicroClip X3
- GasAlertMax XT II
- GasAlertMicro 5 Series
- IntelliDox Docking System
- MicroDock II
- BW Ultra
- BW Solo
- Calibration Equipment
- Confined Space Kits
- GasAlertMicroClip XL Confined Space Kits
- GasAlertQuattro Confined Space Kits
- GasAlertMax XT II Confined Space Kits
- GasAlertMicro5 Confined Space Kits
- Sampling Equipment
- Sampling Accessories
- Gas Monitors
- Gas Monitor Manufacturers
- BW Technologies
- Gas Clip Technologies
- GfG Instruments
- Honeywell Analytics
- RAE Instruments
- RKI Instruments
- Gas Monitor Categories
- Single-Gas Monitors
- Multi-Gas Monitors
- Zero Maintenance Monitors
- Fixed System Gas Monitors
- Confined Space Kits
- Wireless Fixed Point Gas Detectors
- Hydrogen Sulfide (H2S) Monitors
- Calibration Gas
- Find By Instrument Brand
- Manufacturer Equivalent Cylinders
- *Ifyou are searching for a brand specific cylinder P/N# type it in thesearch box above, or navigate to the calibration section of yourinstrument brand
- Combustion Analyzers
- Water Quality
- Reliability Instruments
- All Categories
Oxygen is the element with atomic number 8 and represented by the symbol O. It is a member of the chalcogen group on the periodic table, and is a highly reactive nonmetallic period 2 element that readily forms compounds (notably oxides) with almost all other elements. At standard temperature and pressure two atoms of the element bind to form dioxygen, a colorless, odorless, tasteless diatomic gas with the formula O2. Oxygen is the third most abundant element in the universe by mass after hydrogen and helium and the most abundant element by mass in the Earth's crust. Diatomic oxygen gas constitutes 20.9% of the volume of air.
All major classes of structural molecules in living organisms, such as proteins, carbohydrates, and fats, contain oxygen, as do the major inorganic compounds that comprise animal shells, teeth, and bone. Oxygen in the form of O2 is produced from water by cyanobacteria, algae and plants during photosynthesis and is used in cellular respiration for all complex life. Oxygen is toxic to obligately anaerobic organisms, which were the dominant form of early life on Earth until O2 began to accumulate in the atmosphere 2.5 billion years ago. Another form (allotrope) of oxygen, ozone (O3), helps protect the biosphere from ultraviolet radiation with the high-altitude ozone layer, but is a pollutant near the surface where it is a by-product of smog.
Oxygen was independently discovered by Carl Wilhelm Scheele, in Uppsala, in 1773 or earlier, and Joseph Priestley in Wiltshire, in 1774, but Priestley is often given priority because his publication came out in print first. The name oxygen was coined in 1777 by Antoine Lavoisier, whose experiments with oxygen helped to discredit the then-popular phlogiston theory of combustion and corrosion. Oxygen is produced industrially by fractional distillation of liquefied air, use of zeolites to remove carbon dioxide and nitrogen from air, electrolysis of water and other means. Uses of oxygen include the production of steel, plastics and textiles; rocket propellant; oxygen therapy; and life support in aircraft, submarines, spaceflight and diving.
At standard temperature and pressure, oxygen is a colorless, odorless gas with the molecular formula O2, in which the two oxygen atoms are chemically bonded to each other with a spin triplet electron configuration. This bond has a bond order of two, and is often simplified in description as a double bond or as a combination of one two-electron bond and two three-electron bonds.
Triplet oxygen is the ground state of the O2 molecule. The electron configuration of the molecule has two unpaired electrons occupying two degenerate molecular orbitals. These orbitals are classified as antibonding , so the diatomic oxygen bond is weaker than the diatomic nitrogen triple bond in which all bonding molecular orbitals are filled, but some antibonding orbitals are not.
In normal triplet form, O2 molecules are paramagnetic—they form a magnet in the presence of a magnetic field—because of the spin magnetic moments of the unpaired electrons in the molecule, and the negative exchange energy between neighboring O2 molecules. Liquid oxygen is attracted to a magnet to a sufficient extent that, in laboratory demonstrations, a bridge of liquid oxygen may be supported against its own weight between the poles of a powerful magnet.
Singlet oxygen, a name given to several higher-energy species of molecular O2 in which all the electron spins are paired, is much more reactive towards common organic molecules. 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. Carotenoids in photosynthetic organisms (and possibly also in 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, O2. It has a bond length of 121 pm and a bond energy of 498 kJ·mol-1. This is the form that is used by complex forms of life, such as animals, in cellular respiration and is the form that is a major part of the Earth's atmosphere. Other aspects of O2 are covered in the remainder of this article.
Trioxygen (O3) 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 O2 combines with atomic oxygen made by the splitting of O2 by ultraviolet (UV) radiation. 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, however, it is a pollutant formed as a by-product of automobile exhaust.
The metastable molecule tetraoxygen (O4) was discovered in 2001, and was assumed to exist in one of the six phases of solid oxygen. It was proven in 2006 in that phase, created by pressurizing O2 to 20 GPa, is in fact a rhombohedral O8 cluster. This cluster has the potential to be a much more powerful oxidizer than either O2 or O3 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.
Oxygen is more soluble in water than nitrogen; water contains approximately 1 molecule of O2 for every 2 molecules of N2, compared to 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 1 atm of air, freshwater contains about 6.04 milliliters (mL) of oxygen per liter, whereas 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 and solid O2 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 O2 is usually obtained by the fractional distillation of liquefied air; Liquid oxygen may also be produced by condensation out of air, using liquid nitrogen as a coolant. It is a highly-reactive substance and must be segregated from combustible materials.
Isotopes and stellar origin
Naturally occurring oxygen is composed of three stable isotopes, 16O,17O, and 18O, with 16O being the most abundant (99.762% natural abundance). Oxygen isotopes range in mass number from 12 to 28.
Most 16O is synthesized at the end of the helium fusion process in stars but some is made in the neon burning process. 17O 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. Most 18O is produced when 14N (made abundant from CNO burning) captures a 4He nucleus, making 18O common in the helium-rich zones of stars.
Fourteen radioisotopes have been characterized, the most stable being 15O with a half-life of 122.24 seconds (s) and 14O with a half-life of 70.606 s. 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 16O is electron capture to yield nitrogen, and the most common mode for the isotopes heavier than 18O is beta decay to yield fluorine.
Oxygen is the most abundant chemical element, by mass, in our biosphere, air, sea and land. Oxygen is the third most abundant chemical element in the universe, after hydrogen and helium. About 0.9% of the Sun's mass is oxygen. Oxygen constitutes 49.2% of the Earth's crust by mass and is 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 21.0% of its volume and 23.1% of its mass (some 1015 tonnes). 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% O2 by volume) and Venus have far lower concentrations. However, the O2 surrounding these other planets is produced solely by ultraviolet radiation impacting 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 decay remove it from the atmosphere. In the present equilibrium, production and consumption occur at the same rate of roughly 1/2000th of the entire atmospheric oxygen per year.
Free oxygen also occurs in solution in the world's water bodies. The increased solubility of O2 at lower temperatures has important implications for ocean life, as polar oceans support a much higher density of life due to their higher oxygen content. Polluted water may have reduced amounts of O2 in it, depleted by decaying algae and other biomaterials. Scientists assess this aspect of water quality by measuring the water's biochemical oxygen demand, or the amount of O2 needed to restore it to a normal concentration.
Photosynthesis and respiration
In nature, free oxygen is produced by the light-driven splitting of water during oxygenic photosynthesis. Green algae and cyanobacteria in marine environments provide about 70% of the free oxygen produced on earth and the rest is produced by terrestrial plants.
A simplified overall formula for photosynthesis is:
6CO2 + 6H2O + photons → C6H12O6 + 6O2
Photolytic oxygen evolution occurs in the thylakoid membranes of photosynthetic organisms and requires the energy of four photons. Many steps are involved, but the result is the formation of a proton gradient across the thylakoid membrane, which is used to synthesize ATP via photophosphorylation. The O2 remaining after oxidation of the water molecule is released into the atmosphere.
Molecular dioxygen, O2, is essential for cellular respiration in all aerobic organisms. Oxygen is used in mitochondria to help generate adenosine triphosphate (ATP) during oxidative phosphorylation. The reaction for aerobic respiration is essentially the reverse of photosynthesis and is simplified as:
C6H12O6 + 6O2 → 6CO2 + 6H2O + 2880 kJ·mol-1
In vertebrates, O2 is diffused through membranes in the lungs and into red blood cells. Hemoglobin binds O2, changing its color from bluish red to bright red. Other animals use hemocyanin (molluscs and some arthropods) or hemerythrin (spiders and lobsters). A liter of blood can dissolve 200 cc of O2.
Reactive oxygen species, such as superoxide ion (O2-) and hydrogen peroxide (H2O2), are dangerous by-products of oxygen use in organisms. Parts of the immune system of higher organisms, however, 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.
An adult human in 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.
Build-up in the atmosphere
Free oxygen gas was almost nonexistent in Earth's atmosphere before photosynthetic archaea and bacteria evolved. Free oxygen first appeared in significant quantities during the Paleoproterozoic era (between 2.5 and 1.6 billion years ago). At first, the oxygen combined with dissolved iron in the oceans to form banded iron formations. Free oxygen started to gas out of the oceans 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 anaerobic organisms then living to extinction during the oxygen catastrophe about 2.4 billion years ago. However, cellular respiration using O2 enables aerobic organisms to produce much more ATP than anaerobic organisms, helping the former to dominate Earth's biosphere. Photosynthesis and cellular respiration of O2 allowed for the evolution of eukaryotic cells and ultimately complex multicellular organisms such as plants and animals.
Since the beginning of the Cambrian era 540 million years ago, O2 levels have fluctuated between 15% and 30% by volume. Towards the end of the Carboniferous era (about 300 million years ago) atmospheric O2 levels reached a maximum of 35% by volume, allowing insects and amphibians to grow much larger than today's species. Human activities, including the burning of 7 billion tonnes of fossil fuels each year have had very little effect on the amount of free oxygen in the atmosphere. At the current rate of photosynthesis it would take about 2,000 years to regenerate the entire O2 in the present atmosphere.
Two major methods are employed to produce 100 million tonnes of O2 extracted from air for industrial uses annually. The most common method is to fractionally-distill liquefied air into its various components, with nitrogen N2 distilling as a vapor while oxygen O2 is left as a liquid.
The other major method of producing O2 gas involves 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% O2. 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.
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. Contrary to popular belief, the 2:1 ratio observed in the DC electrolysis of acidified water does not prove that the empirical formula of water is H2O unless certain assumptions are made about the molecular formulae of hydrogen and oxygen themselves.
A similar method is the electrocatalytic O2 evolution from oxides and oxoacids. Chemical catalysts can be used as well, such as in chemical oxygen generators 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 technology involves forcing air to dissolve through ceramic membranes based on zirconium dioxide by either high pressure or an electric current, to produce nearly pure O2 gas.
In large quantities, the price of liquid oxygen in 2001 was approximately $0.21/kg. Since the primary cost of production is the energy cost of liquefying the air, the production cost will change as energy cost varies.
For reasons of economy, oxygen is often transported in bulk as a liquid in specially-insulated tankers, since one litre of liquefied oxygen is equivalent to 840 liters of gaseous oxygen at atmospheric pressure and 20 °C. Such tankers are used to refill bulk liquid oxygen storage containers, which stand outside hospitals and other institutions with a need for large volumes of pure oxygen gas. Liquid oxygen is passed through heat exchangers, 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 O2 from the air is the essential purpose of respiration, so oxygen supplementation is used in medicine. Oxygen therapy is used to treat emphysema, pneumonia, some heart disorders, and any disease that impairs the body's ability to take up and use gaseous oxygen. Treatments are flexible enough to be used in hospitals, the patient's home, or increasingly by portable devices. Oxygen tents were once commonly used in oxygen supplementation, but have since been replaced mostly by the use of oxygen masks or nasal cannulas.
Hyperbaric (high-pressure) medicine uses special oxygen chambers to increase the partial pressure of O2 around the patient and, when needed, the medical staff. Carbon monoxide poisoning, gas gangrene, and decompression sickness (the 'bends') are sometimes treated using these devices. Increased O2 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 their blood. Increasing the pressure of O2 as soon as possible is part of the treatment.
Oxygen is also used medically for patients who require mechanical ventilation, often at concentrations above 21% found in ambient air.
Life support and recreational use
A notable application of O2 as a low-pressure breathing gas is in modern space suits, which surround their occupant's body with pressurized air. These devices use nearly pure oxygen at about one third normal pressure, resulting in a normal blood partial pressure of O2. This trade-off of higher oxygen concentration for lower pressure is needed to maintain flexible spacesuits.
Scuba divers and submariners also rely on artificially-delivered O2, but most often use normal pressure, and/or mixtures of oxygen and air. Pure or nearly pure O2 use in diving at higher-than-sea-level pressures is usually limited to rebreather, decompression, or emergency treatment use at relatively shallow depths (~ 6 meters depth, or less). Deeper diving requires significant dilution of O2 with other gases, such as nitrogen or helium, to help prevent oxygen toxicity.
People who climb mountains or fly in non-pressurized fixed-wing aircraft sometimes have supplemental O2 supplies. Passengers traveling in (pressurized) commercial airplanes have an emergency supply of O2 automatically supplied to them in case of cabin depressurization. Sudden cabin pressure loss activates chemical oxygen generators above each seat, causing oxygen masks to drop and forcing iron filings into the sodium chlorate inside the canister. A steady stream of oxygen gas is produced by the exothermic reaction. However, even this may pose a danger if inappropriately triggered: a ValuJet airplane crashed after use-date-expired O2 canisters, which were being shipped in the cargo hold, activated and caused fire. The canisters were mis-labeled as empty, and carried against dangerous goods regulations.
Oxygen, as a supposed mild euphoric, has a history of recreational use in oxygen bars and in sports. Oxygen bars are establishments, found in Japan, California, and Las Vegas, Nevada since the late 1990s that offer higher than normal O2 exposure for a fee. Professional athletes, especially in American football, also sometimes go off field between plays to wear oxygen masks in order to get a supposed "boost" in performance. However, the reality of a pharmacological effect is doubtful; a placebo or psychological boost being the most plausible explanation. Available studies support a performance boost from enriched O2 mixtures only if they are breathed during actual aerobic exercise. Other recreational uses include pyrotechnic applications, such as George Goble's five-second ignition of barbecue grills.
Smelting of iron ore into steel consumes 55% of commercially-produced oxygen. In this process, O2 is injected through a high-pressure lance into molten iron, which removes sulfur impurities and excess carbon as the respective oxides, SO2 and CO2. The reactions are exothermic, so the temperature increases to 1700 °C.
Another 25% of commercially-produced oxygen is used by the chemical industry. Ethylene is reacted with O2 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 and polyester polymers (the precursors of many plastics and fabrics).
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 O2 to produce a very hot flame. In this process, metal up to 60 cm thick is first heated with a small oxy-acetylene flame and then quickly cut by a large stream of O2. Rocket propulsion requires a fuel and an oxidizer. Larger rockets use liquid oxygen as their oxidizer, which is mixed and ignited with the fuel for propulsion.
Paleoclimatologists measure the ratio of oxygen-18 and oxygen-16 in the shells and skeletons of marine organisms to determine what the climate was like millions of years ago. Seawater molecules that contain the lighter isotope, oxygen-16, evaporate at a slightly faster rate than water molecules containing the 12% heavier oxygen-18; this disparity increases at lower temperatures. 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 that are up to several hundreds of thousands of years old.
Planetary geologists have measured different abundances of oxygen isotopes in samples from the Earth, the Moon, Mars, and meteorites, 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. However, 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 bands 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.
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 peroxides. Compounds containing oxygen in other oxidation states are very uncommon: -1/2 (superoxides), -1/3 (ozonides), 0 (elemental, hypofluorous acid), +1/2 (dioxygenyl), +1 (dioxygen difluoride), and +2 (oxygen difluoride).
Oxides and other inorganic compounds
Water (H2O) is the 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-1 per hydrogen atom) to an adjacent oxygen atom in a separate molecule. These hydrogen bonds between water molecules hold them approximately 15% closer than what would be expected in a simple liquid with just Van der Waals forces.
Due to its electronegativity, oxygen forms chemical bonds with almost all other elements at elevated temperatures to give corresponding oxides. However, some elements readily form oxides at standard conditions for temperature and pressure; the rusting of iron is an example. The surface of metals like aluminium and titanium are oxidized in the presence of air and become coated with a thin film of oxide that passivates the metal and slows further corrosion. Some of the transition metal oxides are found in nature as non-stoichiometric compounds, with a slightly less metal than the chemical formula would show. For example, the natural occurring FeO is actually written as Fe1−xO, where x is usually around 0.05.
Oxygen as a compound is present in the atmosphere in trace quantities in the form of carbon dioxide (CO2). The earth's crustal rock is composed in large part of oxides of silicon (silica SiO2, found in granite and sand), aluminium (aluminium oxide Al2O3, in bauxite and corundum), iron (iron(III) oxide Fe2O3, in hematite and rust) and other metals.
The rest of the Earth's crust is also made of oxygen compounds, in particular calcium carbonate (in limestone) and silicates (in feldspars). Water-soluble silicates in the form of Na4SiO4, Na2SiO3, and Na2Si2O5 are used as detergents and adhesives.
Oxygen also acts as a ligand for transition metals, forming metal–O2 bonds with the iridium atom in Vaska's complex, with the platinum in PtF6, and with the iron center of the heme group of hemoglobin.
Organic compounds and biomolecules
Among the most important classes of organic compounds that contain oxygen are (where "R" is an organic group): alcohols (R-OH); ethers (R-O-R); ketones (R-CO-R); aldehydes (R-CO-H); carboxylic acids (R-COOH); esters (R-COO-R); acid anhydrides (R-CO-O-CO-R); and amides (R-C(O)-NR2). There are many important organic solvents that contain oxygen, including: acetone, methanol, ethanol, isopropanol, furan, THF, diethyl ether, dioxane, ethyl acetate, DMF, DMSO, acetic acid, and formic acid. Acetone ((CH3)2CO) and phenol (C6H5OH) are used as feeder materials in the synthesis of many different substances. Other important organic compounds that contain oxygen are: glycerol, formaldehyde, glutaraldehyde, citric acid, acetic anhydride, and acetamide. Epoxides are ethers in which the oxygen atom is part of a ring of three atoms.
Oxygen reacts spontaneously with many organic compounds at or below room temperature in a process called autoxidation. Most of the organic compounds that contain oxygen are not made by direct action of O2. Organic compounds important in industry and commerce that are made by direct oxidation of a precursor include ethylene oxide and peracetic acid.
The element is found in almost all biomolecules that are important to (or generated by) life. Only a few common complex biomolecules, such as squalene and the carotenes, contain no oxygen. Of the organic compounds with biological relevance, carbohydrates contain the largest proportion by mass of oxygen. All fats, fatty acids, amino acids, and proteins contain oxygen (due to the presence of carbonyl groups in these acids and their ester residues). Oxygen also occurs in phosphate (PO43-) groups in the biologically important energy-carrying molecules ATP and ADP, in the backbone and the purines (except adenine) and pyrimidines of RNA and DNA, and in bones as calcium phosphate and hydroxylapatite.
Oxygen gas (O2) can be toxic at elevated partial pressures, leading to convulsions and other health problems. Oxygen toxicity usually begins to occur at partial pressures more than 50 kilopascals (kPa), or 2.5 times the normal sea-level O2 partial pressure of about 21 kPa. Therefore, air supplied through oxygen masks in medical applications is typically composed of 30% O2 by volume (about 30 kPa at standard pressure). At one time, premature babies were placed in incubators containing O2-rich air, but this practice was discontinued after some babies were blinded by it.
Breathing pure O2 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 O2 partial pressure in the breathing gas is, in general, about 30 kPa (1.4 times normal), and the resulting O2 partial pressure in the astronaut's arterial blood is only marginally more than normal sea-level O2 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 O2 partial pressure more than 60 kPa can eventually lead to permanent pulmonary fibrosis. Exposure to a O2 partial pressures greater than 160 kPa may lead to convulsions (normally fatal for divers). Acute oxygen toxicity can occur by breathing an air mixture with 21% O2 at 66 m or more of depth while the same thing can occur by breathing 100% O2 at only 6 m.
Combustion and other hazards
Highly-concentrated sources of oxygen promote rapid combustion. Fire and explosion hazards exist when concentrated oxidants and fuels are brought into close proximity; however, an ignition event, such as heat or a spark, is needed to trigger combustion. Oxygen itself is not the fuel, but the oxidant. Combustion hazards also apply to compounds of oxygen with a high oxidative potential, such as peroxides, chlorates, nitrates, perchlorates, and dichromates because they can donate oxygen to a fire.
Concentrated O2 will allow combustion to proceed rapidly and energetically. Steel 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 O2 systems requires special training to ensure that ignition sources are minimized. The fire that killed the Apollo 1 crew on a test launch pad spread so rapidly because the capsule was pressurized with pure O2 but at slightly more than atmospheric pressure, instead of the 1/2 normal pressure that would be used in a mission.
Liquid oxygen spills, if allowed to soak into organic matter, such as wood, petrochemicals, and asphalt can cause these materials to detonate unpredictably on subsequent mechanical impact. As with other cryogenic liquids, on contact with the human body it can cause burns to the skin and the eyes.
Effects of Various O2 Levels
|Concentration Of Oxygen||Resulting Conditions on Humans|
|23.5% Volume||Maximum “Safe Level”; OSHA|
|21%||Oxygen Concentration of AIR (20.954)|
|19.5%||Minimum “Safe Level”; OSHA, NIOSH|
|17%||Impairment of judgment starts to be evident|
|16%||First signs of anoxia appears|
|16-12%||Breathing and pulse rate increases, muscular co-ordination is slightly impaired|
|14-10%||Consciousness continuous; emotional upsets, abnormal fatigue upon exertion, disturbed respiration|
|10-6%||Nausea and vomiting, inability to move freely and loss of consciousness may occur|
|<6%||Convulsive movements and gasping respiration occurs; respiration stops and a few minutes later heart action ceases|