Template:Short description Template:Cs1 config Template:See also Template:Redirect Template:Redirect Template:Distinguish Template:Use British English Template:Use dmy dates Template:Chembox
Nitrous oxide (dinitrogen oxide or dinitrogen monoxide), commonly known as laughing gas, nitrous, or factitious air, among others,<ref name="pubchem">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> is a chemical compound, an oxide of nitrogen with the formula Template:Chem. At room temperature, it is a colourless non-flammable gas, and has a slightly sweet scent and taste.<ref name=pubchem/> At elevated temperatures, nitrous oxide is a powerful oxidiser similar to molecular oxygen.<ref name=pubchem/>
Nitrous oxide has significant medical uses, especially in surgery and dentistry, for its anaesthetic and pain-reducing effects,<ref name="ACB 2020">Template:Cite journal</ref> and it is on the World Health Organization's List of Essential Medicines.<ref name="WHO21st">Template:Cite book</ref> Its colloquial name, "laughing gas", coined by Humphry Davy, describes the euphoric effects upon inhaling it, which cause it to be used as a recreational drug inducing a brief "high".<ref name="ACB 2020"/><ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> When abused chronically, it may cause neurological damage through inactivation of vitamin B12. It is also used as an oxidiser in rocket propellants and motor racing fuels, and as a frothing gas for whipped cream.
Nitrous oxide is also an atmospheric pollutant, with a concentration of 333 parts per billion (ppb) in 2020, increasing at 1 ppb annually.<ref name="agage" /><ref name="noaaesrl" /> It is a major scavenger of stratospheric ozone, with an impact comparable to that of CFCs.<ref name="sciozo"/> About 40% of human-caused emissions are from agriculture,<ref name="HTian">Template:Cite journal</ref><ref name=":0">Template:Cite journal</ref> as nitrogen fertilisers are digested into nitrous oxide by soil micro-organisms.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> As the third most important greenhouse gas, nitrous oxide substantially contributes to global warming.<ref name="ipccar5">Template:Cite book</ref><ref name="physorg">Template:Cite news</ref> Reduction of emissions is an important goal in the politics of climate change.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Discovery and early useEdit
The gas was first synthesised in 1772 by English natural philosopher and chemist Joseph Priestley who called it dephlogisticated nitrous air (see phlogiston theory)<ref name="Nitrous Oxide pioneers">Template:Cite journal</ref> or inflammable nitrous air.<ref>Template:Cite journal</ref> Priestley published his discovery in the book Experiments and Observations on Different Kinds of Air (1775), where he described how to produce the preparation of "nitrous air diminished", by heating iron filings dampened with nitric acid.<ref name="Joseph Priestley">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
The first important use of nitrous oxide was made possible by Thomas Beddoes and James Watt, who worked together to publish the book Considerations on the Medical Use and on the Production of Factitious Airs (1794). This book was important for two reasons. First, James Watt had invented a novel machine to produce "factitious airs" (including nitrous oxide) and a novel "breathing apparatus" to inhale the gas. Second, the book also presented the new medical theories by Thomas Beddoes, that tuberculosis and other lung diseases could be treated by inhalation of "Factitious Airs".<ref name="Drug discovery" />
The machine to produce "Factitious Airs" had three parts: a furnace to burn the needed material, a vessel with water where the produced gas passed through in a spiral pipe (for impurities to be "washed off"), and finally the gas cylinder with a gasometer where the gas produced, "air", could be tapped into portable air bags (made of airtight oily silk). The breathing apparatus consisted of one of the portable air bags connected with a tube to a mouthpiece. With this new equipment being engineered and produced by 1794, the way was paved for clinical trials,Template:Clarify which began in 1798 when Thomas Beddoes established the "Pneumatic Institution for Relieving Diseases by Medical Airs" in Hotwells (Bristol). In the basement of the building, a large-scale machine was producing the gases under the supervision of a young Humphry Davy, who was encouraged to experiment with new gases for patients to inhale.<ref name="Drug discovery" /> The first important work of Davy was examination of the nitrous oxide, and the publication of his results in the book: Researches, Chemical and Philosophical (1800). In that publication, Davy notes the analgesic effect of nitrous oxide at page 465 and its potential to be used for surgical operations at page 556.<ref name="Humphry Davy">Template:Cite book</ref> Davy coined the name "laughing gas" for nitrous oxide.<ref>Template:Cite book</ref>
Despite Davy's discovery that inhalation of nitrous oxide could relieve a conscious person from pain, another 44 years elapsed before doctors attempted to use it for anaesthesia. The use of nitrous oxide as a recreational drug at "laughing gas parties", primarily arranged for the British upper class, became an immediate success beginning in 1799. While the effects of the gas generally make the user appear stuporous, dreamy and sedated, some people also "get the giggles" in a state of euphoria, and frequently erupt in laughter.<ref name="Illicit drugs">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
One of the earliest commercial producers in the U.S. was George Poe, cousin of the poet Edgar Allan Poe, who also was the first to liquefy the gas.<ref name="wp">Template:Cite news</ref>
The first time nitrous oxide was used as an anaesthetic drug in the treatment of a patient was when dentist Horace Wells, with assistance by Gardner Quincy Colton and John Mankey Riggs, demonstrated insensitivity to pain from a dental extraction on 11 December 1844.<ref name="Discovery of Wells">Template:Cite journal</ref> In the following weeks, Wells treated the first 12 to 15 patients with nitrous oxide in Hartford, Connecticut, and, according to his own record, only failed in two cases.<ref name="Horace Wells">Template:Cite book</ref> In spite of these convincing results having been reported by Wells to the medical society in Boston in December 1844, this new method was not immediately adopted by other dentists. The reason for this was most likely that Wells, in January 1845 at his first public demonstration to the medical faculty in Boston, had been partly unsuccessful, leaving his colleagues doubtful regarding its efficacy and safety.<ref name="Discovery of anaesthesia">Template:Cite journal</ref> The method did not come into general use until 1863, when Gardner Quincy Colton successfully started to use it in all his "Colton Dental Association" clinics, that he had just established in New Haven and New York City.<ref name="Drug discovery" /> Over the following three years, Colton and his associates successfully administered nitrous oxide to more than 25,000 patients.<ref name="use in dentistry" /> Today, nitrous oxide is used in dentistry as an anxiolytic, as an adjunct to local anaesthetic.
Nitrous oxide was not found to be a strong enough anaesthetic for use in major surgery in hospital settings, however. Instead, diethyl ether, being a stronger and more potent anaesthetic, was demonstrated and accepted for use in October 1846, along with chloroform in 1847.<ref name="Drug discovery" /> When Joseph Thomas Clover invented the "gas-ether inhaler" in 1876, however, it became a common practice at hospitals to initiate all anaesthetic treatments with a mild flow of nitrous oxide, and then gradually increase the anaesthesia with the stronger ether or chloroform. Clover's gas-ether inhaler was designed to supply the patient with nitrous oxide and ether at the same time, with the exact mixture being controlled by the operator of the device. It remained in use by many hospitals until the 1930s.<ref name="use in dentistry" /> Although hospitals today use a more advanced anaesthetic machine, these machines still use the same principle launched with Clover's gas-ether inhaler, to initiate the anaesthesia with nitrous oxide, before the administration of a more powerful anaesthetic.
Colton's popularisation of nitrous oxide led to its adoption by a number of less than reputable quacksalvers, who touted it as a cure for consumption, scrofula, catarrh and other diseases of the blood, throat and lungs. Nitrous oxide treatment was administered and licensed as a patent medicine by the likes of C. L. Blood and Jerome Harris in Boston and Charles E. Barney of Chicago.<ref name="alleged">Template:Cite news</ref><ref name="man">Template:Cite news</ref>
Chemical properties and reactionsEdit
Nitrous oxide is a colourless gas with a faint, sweet odour.
Nitrous oxide supports combustion by releasing the dipolar bonded oxygen radical, and can thus relight a glowing splint.
Template:Chem is inert at room temperature and has few reactions. At elevated temperatures, its reactivity increases. For example, nitrous oxide reacts with Template:Chem at Template:Convert to give Template:Chem:
This reaction is the route adopted by the commercial chemical industry to produce azide salts, which are used as detonators.<ref name="InorgChem">Template:Cite book</ref>
Mechanism of actionEdit
The pharmacological mechanism of action of inhaled Template:Chem is not fully known. However, it has been shown to directly modulate a broad range of ligand-gated ion channels, which likely plays a major role. It moderately blocks NMDAR and [[CHRNB2|β
- redirect Template:Smallsub-subunit]]-containing nACh channels, weakly inhibits AMPA, kainate, [[GABAA-rho receptor|GABA
- redirect Template:Smallsub]] and [[5-HT3 receptor|5-HT
- redirect Template:Smallsub receptors]], and slightly potentiates [[GABAA receptor|GABA
- redirect Template:Smallsub]] and glycine receptors.<ref name="pmid11020766">Template:Cite journal</ref><ref name="pmid9822732">Template:Cite journal</ref> It also has been shown to activate [[Two-pore-domain potassium channel|two-pore-domain Template:Chem channels]].<ref name="pmid14742687">Template:Cite journal</ref> While Template:Chem affects several ion channels, its anaesthetic, hallucinogenic and euphoriant effects are likely caused mainly via inhibition of NMDA receptor-mediated currents.<ref name="pmid11020766" /><ref name="pmid17352529">Template:Cite journal</ref> In addition to its effects on ion channels, Template:Chem may act similarly to nitric oxide (NO) in the central nervous system.<ref name="pmid17352529" /> Nitrous oxide is 30 to 40 times more soluble than nitrogen.
The effects of inhaling sub-anaesthetic doses of nitrous oxide may vary unpredictably with settings and individual differences;<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> however, Jay (2008)<ref name="Mike Jay 22–25">Template:Cite journal</ref> suggests that it reliably induces the following states and sensations:
- Intoxication
- Euphoria/dysphoria
- Spatial disorientation
- Temporal disorientation
- Reduced pain sensitivity
A minority of users also experience uncontrolled vocalisations and muscular spasms. These effects generally disappear minutes after removal of the nitrous oxide source.<ref name="Mike Jay 22–25"/>
Anxiolytic effectEdit
In behavioural tests of anxiety, a low dose of Template:Chem is an effective anxiolytic. This anti-anxiety effect is associated with enhanced activity of GABA
- redirect Template:Smallsub receptors, as it is partially reversed by benzodiazepine receptor antagonists. Mirroring this, animals that have developed tolerance to the anxiolytic effects of benzodiazepines are partially tolerant to Template:Chem.<ref name="emmanouil">Template:Cite journal</ref> Indeed, in humans given 30% Template:Chem, benzodiazepine receptor antagonists reduced the subjective reports of feeling "high", but did not alter psychomotor performance.<ref name="zacny">Template:Cite journal</ref><ref>Template:Cite journal</ref>
Analgesic effectEdit
The analgesic effects of Template:Chem are linked to the interaction between the endogenous opioid system and the descending noradrenergic system. When animals are given morphine chronically, they develop tolerance to its pain-killing effects, and this also renders the animals tolerant to the analgesic effects of Template:Chem.<ref>Template:Cite journal</ref> Administration of antibodies that bind and block the activity of some endogenous opioids (not β-endorphin) also block the antinociceptive effects of Template:Chem.<ref name="branda">Template:Cite journal</ref> Drugs that inhibit the breakdown of endogenous opioids also potentiate the antinociceptive effects of Template:Chem.<ref name="branda" /> Several experiments have shown that opioid receptor antagonists applied directly to the brain block the antinociceptive effects of Template:Chem, but these drugs have no effect when injected into the spinal cord.
Apart from an indirect action, nitrous oxide, like morphine<ref>Gillman M.A. [1986a]. Minireview: Analgesic [sub anaesthetic] nitrous oxide interacts with the endogenous opioid system : A review of the evidence. Life Sciences 39: 1209-1221</ref> also interacts directly with the endogenous opioid system by binding at opioid receptor binding sites.<ref>(Daras, C., Cantrill, R. C., Gillman, M. A. [1983]. 3[H]-Naloxone displacement: evidence for nitrous oxide as an opioid agonist. European Journal of Pharmacology 89: 177-8.</ref><ref>Ori, C., Ford-Rice, F., London, E. D. [1989]. Effects of nitrous oxide and halothane on mu and kappa opioid receptors in guinea-pig brain. Anesthesiology 70: 541-544.)</ref>
Conversely, [[alpha-2 adrenergic receptor|α
- redirect Template:Smallsub-adrenoceptor]] antagonists block the pain-reducing effects of Template:Chem when given directly to the spinal cord, but not when applied directly to the brain.<ref name="guo">Template:Cite journal</ref> Indeed, [[alpha-2B adrenergic receptor|α
- redirect Template:Smallsub-adrenoceptor]] knockout mice or animals depleted in norepinephrine are nearly completely resistant to the antinociceptive effects of Template:Chem.<ref>Template:Cite journal</ref> Apparently Template:Chem-induced release of endogenous opioids causes disinhibition of brainstem noradrenergic neurons, which release norepinephrine into the spinal cord and inhibit pain signalling.<ref name="pmid10781114">Template:Cite journal</ref> Exactly how Template:Chem causes the release of endogenous opioid peptides remains uncertain.
ProductionEdit
Various methods of producing nitrous oxide are used.<ref name=CatalysisToday2005>Template:Cite journal</ref>
Industrial methodsEdit
Nitrous oxide is prepared on an industrial scale by carefully heating ammonium nitrate<ref name=CatalysisToday2005 /> at about 250 °C, which decomposes into nitrous oxide and water vapour.<ref>Template:Cite book</ref>
The addition of various phosphate salts favours formation of a purer gas at slightly lower temperatures. This reaction may be difficult to control, resulting in detonation.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Laboratory methodsEdit
The decomposition of ammonium nitrate is also a common laboratory method for preparing the gas. Equivalently, it can be obtained by heating a mixture of sodium nitrate and ammonium sulfate:<ref>"Nitrogen Family" Template:Webarchive. chemistry.tutorvista.com</ref>
Another method involves the reaction of urea, nitric acid and sulfuric acid:<ref>"Preparation of Nitrous Oxide from Urea, Nitric Acid and Sulfuric Acid".</ref>
Direct oxidation of ammonia with a manganese dioxide-bismuth oxide catalyst has been reported:<ref>Template:Cite journal</ref> cf. Ostwald process.
Hydroxylammonium chloride reacts with sodium nitrite to give nitrous oxide. If the nitrite is added to the hydroxylamine solution, the only remaining by-product is salt water. If the hydroxylamine solution is added to the nitrite solution (nitrite is in excess), however, then toxic higher oxides of nitrogen also are formed:
Treating Template:Chem with Template:Chem and HCl also has been demonstrated:
Hyponitrous acid decomposes to N
- redirect Template:SmallsubO and water with a half-life of 16 days at 25 °C at pH 1–3.<ref name="Wiberg&Holleman">Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier Template:ISBN</ref>
Atmospheric occurrenceEdit
Nitrous oxide is a minor component of Earth's atmosphere and is an active part of the planetary nitrogen cycle. Based on analysis of air samples gathered from sites around the world, its concentration surpassed 330 ppb in 2017.<ref name="agage">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> The growth rate of about 1 ppb per year has also accelerated during recent decades.<ref name="noaaesrl">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Nitrous oxide's atmospheric abundance has grown more than 20% from a base level of about 270 ppb in 1750.<ref name="tar">Template:Cite book</ref> Important atmospheric properties of Template:Chem are summarized in the following table:
| Property | Value |
|---|---|
| Ozone depletion potential (ODP) | 0.017<ref name=Ravishankara>Template:Citation</ref> (CCl3F = 1) |
| Global warming potential (GWP: 100-year) | 273<ref name="ar5">Template:Cite book</ref> (CO2 = 1) |
| Atmospheric lifetime | 116 ± 9 years<ref name="ar6"/> |
In 2022 the IPCC reported that: "The human perturbation of the natural nitrogen cycle through the use of synthetic fertilizers and manure, as well as nitrogen deposition resulting from land-based agriculture and fossil fuel burning has been the largest driver of the increase in atmospheric N2O of 31.0 ± 0.5 ppb (10%) between 1980 and 2019."<ref name="ar6">Template:Cite report</ref>
Emissions by sourceEdit
17.0 (12.2 to 23.5) million tonnes total annual average nitrogen in Template:Chem was emitted in 2007–2016.<ref name="ar6"/> About 40% of Template:Chem emissions are from humans and the rest are part of the natural nitrogen cycle.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> The Template:Chem emitted each year by humans has a greenhouse effect equivalent to about 3 billion tonnes of carbon dioxide: for comparison humans emitted 37 billion tonnes of actual carbon dioxide in 2019, and methane equivalent to 9 billion tonnes of carbon dioxide.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Most of the Template:Chem emitted into the atmosphere, from natural and anthropogenic sources, is produced by microorganisms such as denitrifying bacteria and fungi in soils and oceans.<ref name="Sloss1992">Template:Cite book</ref> Soils under natural vegetation are an important source of nitrous oxide, accounting for 60% of all naturally produced emissions. Other natural sources include the oceans (35%) and atmospheric chemical reactions (5%).<ref name="inputs">U.S. Environmental Protection Agency (2010), "Methane and Nitrous Oxide Emissions from Natural Sources". Report EPA 430-R-10-001.</ref> Wetlands can also be emitters of nitrous oxide.<ref name=":4">Template:Cite journal</ref><ref name=":3">Template:Cite journal</ref> Emissions from thawing permafrost may be significant, but as of 2022 this is not certain.<ref name="ar6" />
The main components of anthropogenic emissions are fertilised agricultural soils and livestock manure (42%), runoff and leaching of fertilisers (25%), biomass burning (10%), fossil fuel combustion and industrial processes (10%), biological degradation of other nitrogen-containing atmospheric emissions (9%) and human sewage (5%).<ref name="denman">K. L. Denman, G. Brasseur, et al. (2007), "Couplings Between Changes in the Climate System and Biogeochemistry". In Fourth Assessment Report of the Intergovernmental Panel on Climate Change, Cambridge University Press.</ref><ref>Template:Cite book</ref><ref name="epaUpdated">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref name="epa">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>IPCC. 2013. Climate change: the physical basis (WG I, full report). p. 512.</ref> Agriculture enhances nitrous oxide production through soil cultivation, the use of nitrogen fertilisers and animal waste handling.<ref>Template:Cite journal</ref> These activities stimulate naturally occurring bacteria to produce more nitrous oxide. Nitrous oxide emissions from soil can be challenging to measure as they vary markedly over time and space,<ref>Template:Cite journal</ref> and the majority of a year's emissions may occur when conditions are favorable during "hot moments"<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> and/or at favorable locations known as "hotspots".<ref>Template:Cite journal</ref>
Among industrial emissions, the production of nitric acid and adipic acid are the largest sources of nitrous oxide emissions. The adipic acid emissions specifically arise from the degradation of the nitrolic acid intermediate derived from the nitration of cyclohexanone.<ref name="denman"/><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>
Biological processesEdit
Microbial processes that generate nitrous oxide may be classified as nitrification and denitrification. Specifically, they include:
- aerobic autotrophic nitrification, the stepwise oxidation of ammonia (Template:Chem) to nitrite (Template:Chem) and to nitrate (Template:Chem)
- anaerobic heterotrophic denitrification, the stepwise reduction of Template:Chem to Template:Chem, nitric oxide (NO), Template:Chem and ultimately Template:Chem, where facultative anaerobe bacteria use Template:Chem as an electron acceptor in the respiration of organic material in the condition of insufficient oxygen (Template:Chem)
- nitrifier denitrification, which is carried out by autotrophic Template:Chem-oxidising bacteria and the pathway whereby ammonia (Template:Chem) is oxidised to nitrite (Template:Chem), followed by the reduction of Template:Chem to nitric oxide (NO), Template:Chem and molecular nitrogen (Template:Chem)
- heterotrophic nitrification
- aerobic denitrification by the same heterotrophic nitrifiers
- fungal denitrification
- non-biological chemodenitrification
These processes are affected by soil chemical and physical properties such as the availability of mineral nitrogen and organic matter, acidity and soil type, as well as climate-related factors such as soil temperature and water content.
The emission of the gas to the atmosphere is limited greatly by its consumption inside the cells, by a process catalysed by the enzyme nitrous oxide reductase.<ref>Template:Cite book</ref>
UsesEdit
Rocket motorsEdit
Nitrous oxide may be used as an oxidiser in a rocket motor. Compared to other oxidisers, it is much less toxic and more stable at room temperature, making it easier to store and safer to carry on a flight. Its high density and low storage pressure (when maintained at low temperatures) make it highly competitive with stored high-pressure gas systems.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
In a 1914 patent, American rocket pioneer Robert Goddard suggested nitrous oxide and gasoline as possible propellants for a liquid-fuelled rocket.<ref>Goddard, R. H. (1914) "Rocket apparatus" {{#if:1103503
|[{{#ifeq:|uspto|http://patft.uspto.gov/netacgi/nph-Parser?patentnumber=%7Chttps://patents.google.com/patent/US}}{{#iferror:{{#expr:1103503 }}|1103503}} U.S. patent {{#ifeq:Template:Replace|Template:Digits|Template:Replace|1103503}}]
|{{US patent|123456|link text}}}}</ref> Nitrous oxide has been the oxidiser of choice in several hybrid rocket designs (using solid fuel with a liquid or gaseous oxidiser). The combination of nitrous oxide with hydroxyl-terminated polybutadiene fuel has been used by SpaceShipOne and others. It also is notably used in amateur and high power rocketry with various plastics as the fuel.
Nitrous oxide may also be used as a monopropellant. In the presence of a heated catalyst at a temperature of Template:Convert, Template:Chem decomposes exothermically into nitrogen and oxygen.<ref>Nitrous Oxide Safety. Space Propulsion Group (2012)</ref> Because of the large heat release, the catalytic action rapidly becomes secondary, as thermal autodecomposition becomes dominant. In a vacuum thruster, this may provide a monopropellant specific impulse (I
- redirect Template:Smallsub) up to 180 s. While noticeably less than the I
- redirect Template:Smallsub available from hydrazine thrusters (monopropellant, or bipropellant with dinitrogen tetroxide), the decreased toxicity makes nitrous oxide a worthwhile option.
The ignition of nitrous oxide depends critically on pressure. It deflagrates at approximately Template:Convert at a pressure of 309 psi (21 atmospheres).<ref name="Munke">Munke, Konrad (2 July 2001) Nitrous Oxide Trailer Rupture, Report at CGA Seminar "Safety and Reliability of Industrial Gases, Equipment and Facilities", 15–17 October 2001, St. Louis, Missouri</ref> At 600 Template:Abbr, the required ignition energy is only 6 joules, whereas at 130 psi a 2,500-joule ignition energy input is insufficient.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref><ref>FR-5904. Pratt & Whitney Aircraft.</ref>
Internal combustion engineEdit
{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}}
In vehicle racing, nitrous oxide (often called "nitrous") increases engine power by providing more oxygen during combustion, thus allowing the engine to burn more fuel. It is an oxidising agent roughly equivalent to hydrogen peroxide, and much stronger than molecular oxygen. Nitrous oxide is not flammable at low pressure/temperature, but at about Template:Convert, its breakdown delivers more oxygen than atmospheric air. It often is mixed with another fuel that is easier to deflagrate.
Nitrous oxide is stored as a compressed liquid. In an engine intake manifold, the evaporation and expansion of the liquid causes a large drop in intake charge temperature, resulting in a denser charge and allowing more air/fuel mixture to enter the cylinder. Sometimes nitrous oxide is injected into (or prior to) the intake manifold, whereas other systems directly inject it just before the cylinder (direct port injection).
The technique was used during World War II by Luftwaffe aircraft with the GM-1 system to boost the power output of aircraft engines. Originally meant to provide the Luftwaffe standard aircraft with superior high-altitude performance, technological considerations limited its use to extremely high altitudes. Accordingly, it was only used by specialised planes such as high-altitude reconnaissance aircraft, high-speed bombers and high-altitude interceptor aircraft. It sometimes could be found on Luftwaffe aircraft also fitted with another engine-boost system, MW 50, a form of water injection for aviation engines that used methanol for its boost capabilities.
One of the major problems of nitrous oxide oxidant in a reciprocating engine is excessive power: if the mechanical structure of the engine is not properly reinforced, it may be severely damaged or destroyed. It is important with nitrous oxide augmentation of petrol engines to maintain proper and evenly spread operating temperatures and fuel levels to prevent pre-ignition (also called detonation or spark knock).<ref>Cline, Allen W. (January 2000) "Engine Basics: Detonation and Pre-Ignition". CONTACT! Magazine</ref> However, most problems associated with nitrous oxide come not from excessive power but from excessive pressure, since the gas builds up a much denser charge in the cylinder. The increased pressure and temperature can melt, crack, or warp the piston, valve, and cylinder head.
Automotive-grade liquid nitrous oxide differs slightly from medical-grade. A small amount of sulfur dioxide (Template:Chem) is added to prevent substance abuse.<ref name="Automotive gas">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Aerosol propellant for foodEdit
The gas is approved for use as a food additive (E number: E942), specifically as an aerosol spray propellant. It is commonly used in aerosol whipped cream canisters and cooking sprays.
The gas is extremely soluble in fatty compounds. In pressurised aerosol whipped cream, it is dissolved in the fatty cream until it leaves the can, when it becomes gaseous and thus creates foam. This produces whipped cream four times the volume of the liquid, whereas whipping air into cream only produces twice the volume. Unlike air, nitrous oxide inhibits rancidification of the butterfat. Carbon dioxide cannot be used for whipped cream because it is acidic in water, which would curdle the cream and give it a seltzer-like "sparkle".
Extra-frothed whipped cream produced with nitrous oxide is unstable, and will return to liquid within half an hour to one hour.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Thus, it is not suitable for decorating food that will not be served immediately.
In December 2016, there was a shortage of aerosol whipped cream in the United States, with canned whipped cream use at its peak during the Christmas and holiday season, due to an explosion at the Air Liquide nitrous oxide facility in Florida in late August. The company prioritized the remaining supply of nitrous oxide to medical customers rather than to food manufacturing.<ref>Template:Cite news</ref>
Also, cooking spray, made from various oils with lecithin emulsifier, may use nitrous oxide propellant, or alternatively food-grade alcohol or propane.
MedicalEdit
{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}}
Nitrous oxide has been used in dentistry and surgery, as an anaesthetic and analgesic, since 1844.<ref name="Drug discovery">Template:Cite book</ref> In the early days, the gas was administered through simple inhalers consisting of a breathing bag made of rubber cloth.<ref name="use in dentistry">Template:Cite journal</ref> Today, the gas is administered in hospitals by means of an automated relative analgesia machine, with an anaesthetic vaporiser and a medical ventilator, that delivers a precisely dosed and breath-actuated flow of nitrous oxide mixed with oxygen in a 2:1 ratio.
Nitrous oxide is a weak general anaesthetic, and so is generally not used alone in general anaesthesia, but used as a carrier gas (mixed with oxygen) for more powerful general anaesthetic drugs such as sevoflurane or desflurane. It has a minimum alveolar concentration of 105% and a blood/gas partition coefficient of 0.46. The use of nitrous oxide in anaesthesia can increase the risk of postoperative nausea and vomiting.<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>
Dentists use a simpler machine which only delivers an Template:Chem/Template:Chem mixture for the patient to inhale while conscious but must still be a recognised purpose designed dedicated relative analgesic flowmeter with a minimum 30% of oxygen at all times and a maximum upper limit of 70% nitrous oxide. The patient is kept conscious throughout the procedure, and retains adequate mental faculties to respond to questions and instructions from the dentist.<ref>Template:Cite journal</ref>
Inhalation of nitrous oxide is used frequently to relieve pain associated with childbirth, trauma, oral surgery and acute coronary syndrome (including heart attacks). Its use during labour has been shown to be a safe and effective aid for birthing women.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Its use for acute coronary syndrome is of unknown benefit.<ref name="AHA10">Template:Cite journal</ref>
In Canada and the UK, Entonox and Nitronox are used commonly by ambulance crews (including unregistered practitioners) as rapid and highly effective analgesic gas.
Fifty percent nitrous oxide can be considered for use by trained non-professional first aid responders in prehospital settings, given the relative ease and safety of administering 50% nitrous oxide as an analgesic. The rapid reversibility of its effect would also prevent it from precluding diagnosis.<ref>Template:Cite journal</ref>
RecreationalEdit
{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}}
Recreational inhalation of nitrous oxide, to induce euphoria and slight hallucinations, began with the British upper class in 1799 in gatherings known as "laughing gas parties".<ref>Template:Cite book</ref>
From the 19th century, the widespread availability of the gas for medical and culinary purposes allowed for recreational use to greatly expand globally. In the UK as of 2014, nitrous oxide was estimated to be used by almost half a million young people at nightspots, festivals and parties.<ref>Template:Cite news</ref>
Widespread recreational use of the drug throughout the UK was featured in the 2017 Vice documentary Inside The Laughing Gas Black Market, in which journalist Matt Shea met with dealers of the drug who stole it from hospitals.<ref>Template:CitationTemplate:Cbignore</ref>
A significant issue cited in London's press is the effect of nitrous oxide canister littering, which is highly visible and causes significant complaints from communities.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Prior to 8 November 2023 in the UK, nitrous oxide was subject to the Psychoactive Substances Act 2016, making it illegal to produce, supply, import or export nitrous oxide for recreational use. The updated law prohibited possession of nitrous oxide, classifying it as a Class C drug under the Misuse of Drugs Act 1971.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
While nitrous oxide is understood by most recreational users to give a "safe high", many are unaware that excessive consumption may cause neurological harm which, if left untreated, can cause permanent neurological damage.<ref name="bbc.co.uk">Template:Cite news</ref> In Australia, recreation use became a public health concern following a rise in reports of neurotoxicity and emergency room admissions. In the state of South Australia, legislation was passed in 2020 to restrict canister sales.<ref name=nangs/>
In 2024, under the street name "Galaxy Gas", nitrous oxide has exploded in popularity among young people for recreational use. Most of the popularity has been fostered through TikTok.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
SafetyEdit
Nitrous oxide is a significant occupational hazard for surgeons, dentists and nurses. Because the gas is minimally metabolised in humans (with a rate of 0.004%), it retains its potency when exhaled into the room by the patient, and can intoxicate the clinic staff if the room is poorly ventilated, with potential chronic exposure. A continuous-flow fresh-air ventilation system or Template:Chem scavenger system may be needed to prevent waste-gas buildup.Template:Citation needed The National Institute for Occupational Safety and Health recommends that workers' exposure to nitrous oxide should be controlled during the administration of anaesthetic gas in medical, dental and veterinary operators.<ref>CDC.gov NIOSH Alert: Controlling Exposures to Nitrous Oxide During Anesthetic Administration. Cincinnati, OH: U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control, National Institute for Occupational Safety and Health, DHHS (NIOSH) Publication No. 94-100</ref> It set a recommended exposure limit (REL) of 25 ppm (46 mg/m3) to escaped anaesthetic.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Exposure to nitrous oxide causes short-term impairment of cognition, audiovisual acuity, and manual dexterity, as well as spatial and temporal disorientation,<ref>Criteria for a recommended standard: occupational exposure to waste anesthetic gases and vapors. Cincinnati, OH: U.S. Department of Health, Education, and Welfare, Public Health Service, Center for Disease Control, National Institute for Occupational Safety and Health, DHEW (NIOSH) Publication No. 77B140.</ref> putting the user at risk of accidental injury.<ref name="Mike Jay 22–25"/>
Nitrous oxide is neurotoxic, and medium or long-term habitual consumption of significant quantities can cause neurological harm with the potential for permanent damage if left untreated.<ref name=nangs>Template:Cite journal</ref><ref name="bbc.co.uk"/> It is believed that, like other NMDA receptor antagonists, Template:Chem produces Olney's lesions in rodents upon prolonged (several hour) exposure.<ref name="pmid14622904">Template:Cite journal</ref><ref name="pmid12854473">Template:Cite journal</ref><ref name="pmid10928976">Template:Cite journal</ref><ref name="pmid15718054">Template:Cite journal</ref> However, because it is normally expelled from the body rapidly, it is less likely to be neurotoxic than other NMDAR antagonists.<ref name="pmid16179534">Template:Cite journal</ref> In rodents, short-term exposure results in only mild injury that is rapidly reversible, and neuronal death occurs only after constant and sustained exposure.<ref name="pmid14622904" /> Nitrous oxide may also cause neurotoxicity after extended exposure because of hypoxia. This is especially true of non-medical formulations such as whipped-cream chargers ("whippits" or "nangs"),<ref>Template:Cite journal</ref> which contain no oxygen gas.<ref name="Middleton 2012 p.">Template:Cite book</ref>
In reports to poison control centers, heavy users (≥400 g or ≥200 L of Template:N2O gas in one session) or frequent users (regular, i.e., daily or weekly) have developed signs of peripheral neuropathy: ataxia (gait abnormalities) or paresthesia (perception of sensations such as tingling, numbness, or prickling, mostly in the extremities). Such early signs of neurological damage indicate chronic toxicity.<ref>Template:Cite journal</ref>
Nitrous oxide might have therapeutic use in treating stroke. In a rodent model, nitrous oxide at 75% by volume reduced ischemia-induced neuronal death induced by occlusion of the middle cerebral artery, and decreased NMDA-induced Ca2+ influx in neuronal cell cultures, a cause of excitotoxicity.<ref name="pmid16179534" />
Occupational exposure to ambient nitrous oxide has been associated with DNA damage, due to interruptions in DNA synthesis.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> This correlation is dose-dependent<ref>Template:Cite journal</ref><ref>Template:Cite journal</ref> and does not appear to extend to casual recreational use; however, further research is needed to confirm the level of exposure needed to cause damage.
Inhalation of pure nitrous oxide causes oxygen deprivation, resulting in low blood pressure, fainting, and even heart attacks. This can occur if the user inhales large quantities continuously, as with a strap-on mask connected to a gas canister or other inhalation system, or prolonged breath-holding.Template:Citation needed
Long-term exposure to nitrous oxide may cause [[Vitamin B12 deficiency|vitamin B
- redirect Template:Smallsub deficiency]]. This can cause serious neurotoxicity if the user has preexisting vitamin B
- redirect Template:Smallsub deficiency.<ref>Template:Cite journal</ref> It inactivates the cobalamin form of vitamin B
- redirect Template:Smallsub by oxidation. Symptoms of vitamin B
- redirect Template:Smallsub deficiency, including sensory neuropathy, myelopathy and encephalopathy, may occur within days or weeks of exposure to nitrous oxide anaesthesia in people with subclinical vitamin B
- redirect Template:Smallsub deficiency. Symptoms are treated with high doses of vitamin B
- redirect Template:Smallsub, but recovery can be slow and incomplete.<ref>Template:Cite book</ref> People with normal vitamin B
- redirect Template:Smallsub levels have stores to make the effects of nitrous oxide insignificant, unless exposure is repeated and prolonged (nitrous oxide abuse). Vitamin B
- redirect Template:Smallsub levels should be checked in people with risk factors for vitamin B
- redirect Template:Smallsub deficiency prior to using nitrous oxide anaesthesia.<ref>{{#invoke:citation/CS1|citation
|CitationClass=web }}</ref>
Several experimental studies in rats indicate that chronic exposure of pregnant females to nitrous oxide may have adverse effects on the developing fetus.<ref name="Vieira1980">Template:Cite journal</ref><ref>Template:Cite journal</ref><ref>Template:Cite journal</ref>
At room temperature (Template:Convert) the saturated vapour pressure is 50.525 bar, rising up to 72.45 bar at Template:Convert—the critical temperature. The pressure curve is thus unusually sensitive to temperature.<ref>Nitrous oxide Template:Webarchive. Air Liquide Gas Encyclopedia.</ref> As with many strong oxidisers, contamination of parts with fuels have been implicated in rocketry accidents, where small quantities of nitrous/fuel mixtures explode due to "water hammer"-like effects (sometimes called "dieseling"—heating due to adiabatic compression of gases can reach decomposition temperatures).<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Some common building materials such as stainless steel and aluminium can act as fuels with strong oxidisers such as nitrous oxide, as can contaminants that may ignite due to adiabatic compression.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> There also have been incidents where nitrous oxide decomposition in plumbing has led to the explosion of large tanks.<ref name="Munke" />
Environmental impactEdit
Global accounting of Template:Chem sources and sinks over the decade ending 2016 indicates that about 40% of the average 17 TgN/yr (teragrams, or million metric tons, of nitrogen per year) of emissions originated from human activity, and shows that emissions growth chiefly came from expanding agriculture.<ref name="HTian" /><ref name=":0" />
Nitrous oxide has significant global warming potential as a greenhouse gas. On a per-molecule basis, considered over a 100-year period, nitrous oxide has 265 times the atmospheric heat-trapping ability of carbon dioxide (Template:Chem).<ref name="ar5" /> However, because of its low concentration (less than 1/1,000 of that of Template:Chem), its contribution to the greenhouse effect is less than one third that of carbon dioxide, and also less than methane.<ref name="clim">US Environmental Protection Agency, "Climate Change Indicators: Atmospheric Concentrations of Greenhouse Gases" Web document, accessed on 2017-02-14</ref> On the other hand, since about 40% of the Template:Chem entering the atmosphere is the result of human activity,<ref name="denman" /> control of nitrous oxide is part of efforts to curb greenhouse gas emissions.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Most human caused nitrous oxide released into the atmosphere is a greenhouse gas emission from agriculture, when farmers add nitrogen-based fertilizers onto the fields, and through the breakdown of animal manure. Reduction of emissions can be a hot topic in the politics of climate change.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
Nitrous oxide is also released as a by-product of burning fossil fuel, though the amount released depends on which fuel was used. It is also emitted through the manufacture of nitric acid, which is used in the synthesis of nitrogen fertilizers. The production of adipic acid, a precursor to nylon and other synthetic clothing fibres, also releases nitrous oxide.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
A rise in atmospheric nitrous oxide concentrations has been implicated as a possible contributor to the extremely intense global warming during the Cenomanian-Turonian boundary event.<ref>Template:Cite journal</ref>
Nitrous oxide has also been implicated in thinning the ozone layer. A 2009 study suggested that Template:Chem emission was the single most important ozone-depleting emission and it was expected to remain the largest throughout the 21st century.<ref name="sciozo">Template:Cite journal</ref><ref>Template:Cite magazine</ref>
LegalityEdit
{{#invoke:Labelled list hatnote|labelledList|Main article|Main articles|Main page|Main pages}}
In India transfer of nitrous oxide from bulk cylinders to smaller, more transportable E-type, 1,590-litre-capacity tanks<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> is legal when intended for medical anaesthesia.
The New Zealand Ministry of Health has warned that nitrous oxide is a prescription medicine whose sale or possession without a prescription is an offense under the Medicines Act.<ref>Template:Cite news</ref> This would seemingly prohibit all non-medicinal uses of nitrous oxide, although it is implied that only recreational use will be targeted.
In August 2015, the Council of the London Borough of Lambeth (UK) banned the use of the drug for recreational purposes, making offenders liable to an on-the-spot fine of up to £1,000.<ref>Template:Cite news</ref> In September 2023, the UK Government announced that nitrous oxide would be made illegal by the end of the year, with possession potentially carrying up to a two-year prison sentence or an unlimited fine.<ref>Template:Cite news</ref>
Possession of nitrous oxide is legal under United States federal law and is not subject to DEA purview.<ref name="ccle">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> It is, however, regulated by the Food and Drug Administration under the Food Drug and Cosmetics Act; prosecution is possible under its "misbranding" clauses, prohibiting the sale or distribution of nitrous oxide for the purpose of human consumption without a proper medical license. Many states have laws regulating the possession, sale and distribution of nitrous oxide. Such laws usually ban distribution to minors or limit the amount that may be sold without special license.Template:Citation needed For example, in California, possession for recreational use is prohibited and qualifies as a misdemeanor.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>
See alsoEdit
ReferencesEdit
Further readingEdit
External linksEdit
- Occupational Safety and Health Guideline for Nitrous Oxide
- Paul Crutzen Interview Freeview video of Paul Crutzen Nobel Laureate for his work on decomposition of ozone talking to Harry Kroto Nobel Laureate by the Vega Science Trust.
- National Pollutant Inventory – Oxide of nitrogen fact sheet
- National Institute for Occupational Safety and Health – Nitrous Oxide
- CDC – NIOSH Pocket Guide to Chemical Hazards – Nitrous Oxide
- Nitrous Oxide FAQ
- Erowid article on Nitrous Oxide
- Nitrous oxide fingered as monster ozone slayer Template:Webarchive, Science News
- Dental Fear Central article on the use of nitrous oxide in dentistry
- Altered States Database
Template:Drug use Template:General anesthetics {{#invoke:navbox|navbox
| name = Analgesics | title = Analgesics (N02A, N02B) | listclass = hlist | state = collapsed
| group1 = Opioids | list1 = {{#invoke:navbox|navbox|child
| group1 = Opiates/opium | list1 =
| group2 = Semisynthetic | list2 =
- Acetyldihydrocodeine
- Benzylmorphine
- BuprenorphineTemplate:Nbsp(+naloxone)
- Butorphanol
- Desomorphine
- DihydrocodeineTemplate:Nbsp(+paracetamol)
- Dihydromorphine
- Etorphine
- Ethylmorphine
- HydrocodoneTemplate:Nbsp(+paracetamol, +ibuprofen, +aspirin)
- Hydromorphinol
- Hydromorphone
- Levorphanol
- Metopon
- Nalbuphine
- Nicocodeine
- Nicodicodine
- Nicomorphine
- OxycodoneTemplate:Nbsp(+paracetamol, +aspirin, +ibuprofen, +naloxone, +naltrexone)
- Oxymorphone
- Papaveretum
- Thebacon
| group3 = Synthetic | list3 =
- Alfentanil
- Alphaprodine
- Anileridine
- Bezitramide
- Carfentanil
- Dextromoramide
- Dextropropoxyphene
- Dezocine
- Dimenoxadol
- Dipipanone
- Ethoheptazine
- Fentanyl# (+fluanisone)
- Ketobemidone
- Lofentanil
- Meptazinol
- Methadone#
- NFEPP
- Norpipanone
- Oliceridine
- Pentazocine
- Pethidine (meperidine)
- Phenadoxone
- Phenazocine
- Phenoperidine
- Piminodine
- Piritramide
- Proheptazine
- Propiram
- Remifentanil
- Sufentanil
- Tapentadol
- Tilidine
- TramadolTemplate:Nbsp(+celecoxib, +paracetamol)
- Viminol
}}
| group2 = Paracetamol-type | list2 =
- Acetanilide‡
- Bucetin‡
- Butacetin‡
- Paracetamol (acetaminophen)#
- Parapropamol‡
- Phenacetin‡
- Propacetamol‡
| group3 = NSAIDs | list3 = {{#invoke:navbox|navbox|child
| group1 = Propionates | list1 =
- Benoxaprofen ‡
- Fenoprofen
- Flurbiprofen
- Ibuprofen#Template:Nbsp(Dexibuprofen)Template:Nbsp(+paracetamol)
- KetoprofenTemplate:Nbsp(Dexketoprofen)
- Loxoprofen
- Naproxen
- Oxaprozin
- Suprofen
- Tiaprofenic acid
- Zaltoprofen
| group2 = Oxicams | list2 =
| group3 = Acetates | list3 =
- Acemetacin
- Bromfenac
- Diclofenac
- Etodolac
- IndometacinTemplate:Nbsp(Indometacin farnesil)
- Ketorolac
- Sulindac
- Tolmetin
- Zomepirac ‡
| group4 = COX-2 inhibitors | list4 =
| group5 = Fenamates | list5 =
| group6 = Salicylates | list6 =
- Aspirin (acetylsalicylic acid)# (+paracetamol/caffeine)
- Aloxiprin
- Benorylate
- Carbasalate calcium
- Choline salicylate
- Diflunisal
- Dipyrocetyl
- Ethenzamide
- Guacetisal
- Imidazole salicylate
- Magnesium salicylate
- Morpholine salicylate
- Potassium salicylate
- Salicin
- Salicylamide
- Salsalate
- Sodium salicylate
- WintergreenTemplate:Nbsp(methyl salicylate)
| group7 = Pyrazolones | list7 =
- Aminophenazone‡
- Ampyrone
- Metamizole (dipyrone)
- Nifenazone
- Phenazone
- PropyphenazoneTemplate:Nbsp(+paracetamol/caffeine)
| group8 = Others | list8 =
}}
| group4 = Cannabinoids | list4 =
| group5 = Ion channel
modulators | list5 = {{#invoke:navbox|navbox|child
| group1 = Calcium blockers | list1 =
| group2 = Sodium blockers | list2 =
- Carbamazepine
- Lacosamide
- Local anesthetics (e.g., cocaine, lidocaine)
- Mexiletine
- Nefopam
- Tricyclic antidepressants (e.g., amitriptyline#)
- Nav1.7/1.8-selective: DSP-2230§
- Funapide§
- PF-05089771§
- Suzetrigine
| group3 = Potassium openers | list3 =
}}
| group6 = Myorelaxants | list6 =
| group7 = Others | list7 =
- Analgecine
- Analgesic adjuvant
- Bedinvetmab
- Camphor
- Capsaicin
- Clonidine
- Frunevetmab
- Ketamine
- Menthol
- Methoxyflurane
- Phenazopyridine
- Proglumide
- Rimazolium
- Tanezumab
| list8 =
}} {{#invoke:Navbox|navbox}} Template:Navboxes Template:E number infobox 930-949 Template:Molecules detected in outer space Template:Nitrogen compounds Template:Oxygen compoundsTemplate:Portal bar