اکسیژن بهعنوان اکساینده کاربرد بسیار زیادی داشته، و تنها فلوئور از آن الکترونگاتیوتر است. اکسیژن مایع بهعنوان اکسیدکننده در نیروی حرکتی موشکها استفاده میشود. از آنجا که اکسیژن برای تنفس ضروری است در پزشکی کاربرد دارد. گاهی اوقات کسانی که کوهنوردی میکنند یا در هواپیما پرواز میکنند، مخازن اکسیژن همراه دارند (بهعنوان هوا). اکسیژن در جوشکاری و ساخت فولاد و همچنین متانول نیز کاربرد دارد.
اکسیژن به عنوان یک ماده آرامش بخش، سابقه کاربرد دارد که تا زمان حال نیز ادامه دارد و بارهای اکسیژن در مهمانیها و بزمهای امروزی وجود دارد. در سده ۱۹ اکسیژن معمولاً با اکسید نیترات ترکیب میشد که اثر تسکین دهنده دارد.
اکسیژن فراوانترین عنصر در پوسته کره زمین است و برآوردهایی در این زمینه وجود دارد که مقدار آن را ۴۶٫۷٪ ذکر میکنند. اکسیژن ۸۷٪ اقیانوسها (به صورت آب ،H۲O)و ۲۰٪ درصد جو زمین (به صورت اکسیژن مولکولی، O۲، یا O۳، ازن) را به خود اختصاص میدهد. ترکیبات اکسیژن به ویژه اکسیدفلزات و سیلیکاتها (SiO۴۴-) و کربناتها (CO۳۲-)معمولاً در خاک و تخته سنگها یافت میشوند. آب یخ زده یک جسم سخت متداول بر روی سیارات دیگر و ستارههای دنباله دار میباشد. کلاهکهای یخ کره مریخ از دیاکسید کربن منجمد تولید شدهاند. ترکیبات اکسیژن در سراسر کهکشان یافت میشوند و طیف نور اکسیژن اغلب در ستارهها دیده میشود.
الکترون به خاطر وجود الکترونگاتیوی، اکسیژن تقریباً با تمام عناصر دیگر پیوند شیمیایی تشکیل میدهد (که این مطلب منشأ تعریف اصلی اکسید شدن میباشد). تنها عناصری که تحت عمل اکسایش قرار نمیگیرند گازهای اصیل هستند. یکی از معروفترین این اکسیدها اکسید هیدروژن یا آب است H۲O. سایر اکسیدهای معروف دیگر ترکیبات کربن و اکسیژن هستند مانند دیاکسید کربن (CO۲)، الکلها (R-OH)، آلدئیدها (R-CHO) و کربوکسیلیک اسیدها (R-COOH). رادیکالهای اکسیژن مانند کلراتها (ClO۳-)، پرکلراتها (ClO۴-)، کروماتها (CrO۴۲-)، دی کروماتها (Cr۲O۷۲-)، پرمنگناتها (MnO۴-)، و نیتراتها (NO۳-)، اکسایندههای قوی هستند. خیلی از فلزات مانند آهن با اتم اکسیژن پیوند برقرار میکنند اکسید آهن(Fe۲O۳). ازن (O۳)، با عمل تخلیه برق ایستایی (الکترواستاتیکی) در حضور مولکول اکسیژن شکل میگیرد. مولکول اکسیژن دوتایی (O۲)۲ نیز شناخته شده، که از جزء کمی از اکسیژن مایع را تشکیل میدهد. اپوکسیدها و اترها موادی هستند که در آن اتم اکسیژن قسمتی از یک حلقه سه اتمی هستند.
قرارگرفتن طولانی در معرض اکسیژن خالص میتواند برای شش و سامانه عصبی سمی باشد. تأثیرات ریوی شامل آماس شش (ورم ریه) کاهش ظرفیت شش و آسیب به بافتهای ششی میباشد. تأثیرات بر سامانه عصبی شامل کاهش بینایی، تشنج و اغما میشود.
همچنین مشتقات خاصی از اکسیژن، مانند ازون (O۳)، پروکسید هیدروژن و رادیکالهای هیدروکسیل و سواکسیدها بسیار سمی میباشند. بدن سازوکارهایی را برای مقابله با اینگونهها توسعه داده. برای نمونه، عامل طبیعی گلوتاتیون (glutathione) و بیلی روبین که فراورده بخش شدن طبیعی هموگلوبین است، میتوانند به عنوان یک پاداکسید (ضد اکسید) عمل کنند. منابع تمرکزیافته اکسیژن باعث احتراق سریع شده و بنابراین، در کنار فراوردههای سوختی خطر گسترش سریع آتشسوزی و انفجار وجود دارد.
آتشی که در مخازن اکسیژن آپولو ۱۳ رخ داد به این دلیل سریع گسترش پیدا کرد، که فشار جوی اکسیژن در حالت معمولی بود[نیازمند منبع]، درحالیکه هنگام عملیات پرتاب این فشار باید یک سوم فشار جوی معمولی باشد).
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 Wiltshire, 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.
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 elementfire 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.
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".
Established in 1667 by the German alchemist J. J. Becher, and modified by the chemist Georg Ernst Stahl by 1731, 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.
Polish alchemist, philosopher, and physicianMichael Sendivogius 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 and various nitrates 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.
In the meantime, on August 1, 1774, an experiment conducted by the British clergyman Joseph Priestley focused sunlight on mercuric oxide (HgO) contained in a glass tube, which liberated a gas he named "dephlogisticated air". 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 also dispatched a letter to Lavoisier on September 30, 1774, that 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. ἄζωτον "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 ὀξύς (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.
John Dalton'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.[a]
In 1891 Scottish chemist James Dewar was able to produce enough liquid oxygen for study. 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 O 2. This method of welding and cutting metal later became common.
Oxygen levels in the atmosphere are trending slightly downward globally, possibly because of fossil-fuel burning.
Properties and molecular structure
Orbital diagram, after Barrett (2002), showing the participating atomic orbitals from each oxygen atom, the molecular orbitals that result from their overlap, and the aufbau filling of the orbitals with the 12 electrons, 6 from each O atom, beginning from the lowest energy orbitals, and resulting in covalent double bond character from filled orbitals (and cancellation of the contributions of the pairs of σ and σ* and π and π* orbital pairs).
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 orbitals 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 π 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 π and π* orbitals.
This combination of cancellations and σ and π 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 π* 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 O 2 molecule is referred to as triplet oxygen.[b] 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.
Liquid oxygen, temporarily suspended in a magnet owing to its paramagnetism
In the triplet form, O 2 molecules are paramagnetic. That is, they impart magnetic character to oxygen when it is in the presence of a magnetic field, because of the spinmagnetic moments of the unpaired electrons in the molecule, and the negative exchange energy between neighboring O 2 molecules. Liquid oxygen is so magnetic that, in laboratory demonstrations, a bridge of liquid oxygen may be supported against its own weight between the poles of a powerful magnet.[c]
Singlet oxygen is a name given to several higher-energy species of molecular O 2 in which all the electron spins are paired. It is much more reactive with common organic molecules than is molecular oxygen per se. 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 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, O 2, the major part of the Earth's atmospheric oxygen (see Occurrence). O2 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 O 2 are covered in the remainder of this article.
The metastable molecule tetraoxygen (O 4) 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 O 2 to 20 GPa, is in fact a rhombohedralO 8cluster. This cluster has the potential to be a much more powerful oxidizer than either O 2 or O 3 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 dissolves more readily in water than nitrogen, and in freshwater more readily than seawater. Water in equilibrium with air contains approximately 1 molecule of dissolved O 2 for every 2 molecules of N 2 (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 1 standard atmosphere (101.3 kPa) 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 gas dissolved in water at sea-level
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 solidO 2 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 O 2 is usually obtained by the fractional distillation of liquefied air. Liquid oxygen may also be condensed from air using liquid nitrogen as a coolant.
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 and airglow. 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.
Fourteen radioisotopes have been characterized. The most stable are 15O with a half-life of 122.24 seconds and 14O 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 16O is β+ decay 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 the Earth's 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 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 tonnes).[d] 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% O 2 by volume) and Venus have much less. The O 2 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, decay, and combustion remove it from the atmosphere. In the present equilibrium, production and consumption occur at the same rate.
Cold water holds more dissolved O 2.
Free oxygen also occurs in solution in the world's water bodies. The increased solubility of O 2 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 nitrates or phosphates may stimulate growth of algae by a process called eutrophication and the decay of these organisms and other biomaterials may reduce the O 2 content in eutrophic water bodies. Scientists assess this aspect of water quality by measuring the water's biochemical oxygen demand, or the amount of O 2 needed to restore it to a normal concentration.
Paleoclimatologists measure the ratio of oxygen-18 and oxygen-16 in the shells and skeletons of marine organisms to determine the climate millions of years ago (see oxygen isotope ratio cycle). Seawater 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. 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.
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.
Photosynthesis splits water to liberate O 2 and fixes CO 2 into sugar in what is called a Calvin cycle.
In nature, free oxygen is produced by the light-driven splitting of water during oxygenic photosynthesis. According to some estimates, 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. 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:
O 2 build-up in Earth's atmosphere: 1) no O 2 produced; 2) O 2 produced, but absorbed in oceans & seabed rock; 3) O 2 starts to gas out of the oceans, but is absorbed by land surfaces and formation of ozone layer; 4–5) O 2 sinks filled and the gas accumulates
Free oxygen gas was almost nonexistent in Earth's atmosphere before photosynthetic archaea and bacteria 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). For the first billion years, any free oxygen produced by these organisms combined with dissolved iron in the oceans to form banded iron formations. When such oxygen sinks became saturated, 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.
Since the beginning of the Cambrian period 540 million years ago, atmospheric O 2 levels have fluctuated between 15% and 30% by volume. Towards the end of the Carboniferous period (about 300 million years ago) atmospheric O 2 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 O 2 in the present atmosphere.
One hundred million tonnes of O 2 are extracted from air for industrial uses annually by two primary methods. The most common method is fractional distillation of liquefied air, with N 2distilling as a vapor while O 2 is left as a liquid.
The other primary method of producing O 2 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% O 2. 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 O 2 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 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 O 2 gas.
Oxygen and MAPP gas compressed gas cylinders with regulators
Oxygen storage methods include high pressure oxygen tanks, 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 20 °C (68 °F). 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 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 O 2 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, pneumonia, 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.
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 O 2 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 O 2 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 O 2 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.
An application of O 2 as a low-pressure breathing gas is in modern space suits, 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 O 2. This trade-off of higher oxygen concentration for lower pressure is needed to maintain suit flexibility.
People who climb mountains or fly in non-pressurized fixed-wing aircraft sometimes have supplemental O 2 supplies.[h] Pressurized commercial airplanes have an emergency supply of O 2 automatically supplied to the passengers in case of cabin depressurization. Sudden cabin pressure loss activates chemical oxygen generators above each seat, causing oxygen masks 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 reaction.
Oxygen, as a mild euphoric, has a history of recreational use in oxygen bars and in sports. Oxygen bars are establishments found in the United States since the late 1990s that offer higher than normal O 2 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 duringaerobic exercise.
Smelting of iron ore into steel consumes 55% of commercially produced oxygen. In this process, O 2 is injected through a high-pressure lance into molten iron, which removes sulfur impurities and excess carbon as the respective oxides, SO 2 and CO 2. The reactions are exothermic, so the temperature increases to 1,700 °C.
Water (H 2O) 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 bonds between water molecules hold them approximately 15% closer than what would be expected in a simple liquid with just van der Waals forces.[i]
Oxides, such as iron oxide or rust, form when oxygen combines with other elements.
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 (O 2) can be toxic at elevated partial pressures, leading to convulsions and other health problems.[j] 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 O 2 partial pressure of about 21 kPa. This is not a problem except for patients on mechanical ventilators, since gas supplied through oxygen masks in medical applications is typically composed of only 30%–50% O 2 by volume (about 30 kPa at standard pressure).
At one time, premature babies were placed in incubators containing O 2-rich air, but this practice was discontinued after some babies were blinded by the oxygen content being too high.
Breathing pure O 2 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 O 2 partial pressure in the breathing gas is, in general, about 30 kPa (1.4 times normal), and the resulting O 2 partial pressure in the astronaut's arterial blood is only marginally more than normal sea-level O 2 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 O 2 partial pressure more than 60 kPa can eventually lead to permanent pulmonary fibrosis. Exposure to a O 2 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% O 2 at 66 m (217 ft) or more of depth; the same thing can occur by breathing 100% O 2 at only 6 m (20 ft).
Combustion and other hazards
The interior of the Apollo 1 Command Module. Pure O 2 at higher than normal pressure and a spark led to a fire and the loss of the Apollo 1 crew.
Highly concentrated sources of oxygen promote rapid combustion. Fire and explosion hazards exist when concentrated oxidants and fuels 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 O 2 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 O 2 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 O 2 but at slightly more than atmospheric pressure, instead of the 1⁄3 normal pressure that would be used in a mission.[k]
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.
^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.
^Figures given are for values up to 50 miles (80 km) above the surface
^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.
^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 reason is that increasing the proportion of oxygen in the breathing gas at low pressure acts to augment the inspired O 2 partial pressure nearer to that found at sea-level.
^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.
^Since O 2's partial pressure is the fraction of O 2 times the total pressure, elevated partial pressures can occur either from high O 2 fraction in breathing gas or from high breathing gas pressure, or a combination of both.
^No single ignition source of the fire was conclusively identified, although some evidence points to an arc from an electrical spark.
^Weast, Robert (1984). CRC, Handbook of Chemistry and Physics. Boca Raton, Florida: Chemical Rubber Company Publishing. pp. E110. ISBN0-8493-0464-4.
^ abJack 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, ISBN0854046577, see  accessed January 31, 2015.
^"Oxygen Facts". Science Kids. February 6, 2015. Retrieved November 14, 2015.
^Evans, David Hudson; Claiborne, James B. (2005). The Physiology of Fishes (3rd ed.). CRC Press. p. 88. ISBN978-0-8493-2022-4.
^Lide, David R. (2003). "Section 4, Properties of the Elements and Inorganic Compounds; Melting, boiling, and critical temperatures of the elements". CRC Handbook of Chemistry and Physics (84th ed.). Boca Raton, Florida: CRC Press. ISBN978-0-8493-0595-5.
^From The Chemistry and Fertility of Sea Waters by H.W. Harvey, 1955, citing C.J.J. Fox, "On the coefficients of absorption of atmospheric gases in sea water", Publ. Circ. Cons. Explor. Mer, no. 41, 1907. Harvey notes that according to later articles in Nature, the values appear to be about 3% too high.
^Webb JT; Olson RM; Krutz RW; Dixon G; Barnicott PT (1989). "Human tolerance to 100% oxygen at 9.5 psia during five daily simulated 8-hour EVA exposures". Aviat Space Environ Med. 60 (5): 415–21. doi:10.4271/881071. PMID2730484.