Ammonia

Ammonia is a compound of nitrogen and hydrogen with the formula NH3. A stable binary hydride, and the simplest pnictogen hydride, ammonia is a colourless gas with a characteristic pungent smell. It is a common nitrogenous waste, particularly among aquatic organisms, and it contributes significantly to the nutritional needs of terrestrial organisms by serving as a precursor to food and fertilizers. Ammonia, either directly or indirectly, is also a building block for the synthesis of many pharmaceutical products and is used in many commercial cleaning products. It is mainly collected by downward displacement of both air and water.

For NH4+, see Ammonium. For other uses, see Ammonia (disambiguation).

Ammonia
Ball-and-stick model of the ammonia molecule
Space-filling model of the ammonia molecule
Names
IUPAC names
Ammonia [1]
trihydridonitrogen
nitrogen trihydride
Other names
Azane (only intended for use in naming derivatives of ammonia)
Hydrogen nitride
Identifiers
3D model (JSmol)
3DMet
3587154
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.028.760
EC Number
  • 231-635-3
79
KEGG
MeSH Ammonia
RTECS number
  • BO0875000
UNII
UN number 1005
Properties
NH3
Molar mass 17.031 g/mol
Appearance Colourless gas
Odor strong pungent odour
Density 0.86 kg/m3 (1.013 bar at boiling point)

0.769  kg/m3 (STP)[2]
0.73 kg/m3 (1.013 bar at 15 °C)
681.9 kg/m3 at −33.3 °C (liquid)[3] See also Ammonia (data page)
817 kg/m3 at −80 °C (transparent solid)[4]

Melting point −77.73 °C (−107.91 °F; 195.42 K) (Triple point at 6.060 kPa, 195.4 K)
Boiling point −33.34 °C (−28.01 °F; 239.81 K)
Critical point (T, P) 132.4 °C (405.5 K), 111.3 atm (11,280 kPa)
47% w/w (0 °C)
31% w/w (25 °C)
18% w/w (50 °C)[5]
Solubility soluble in chloroform, ether, ethanol, methanol
Vapor pressure 857.3 kPa
Acidity (pKa) 32.5 (−33 °C),[6] 10.5 (DMSO)
Basicity (pKb) 4.75
Conjugate acid Ammonium
Conjugate base Azanide
−18.0·10−6 cm3/mol
1.3327
Viscosity
  • 10.07 µPa·s (25 °C)[7]
  • 0.276 mPa·s (−40 °C)
Structure
C3v
Trigonal pyramid
1.42 D
Thermochemistry
193 J·mol−1·K−1[8]
Std enthalpy of
formation (ΔfH⦵298)
 −46 kJ·mol−1[8]
Hazards
Safety data sheet See: data page
ICSC 0414 (anhydrous)
GHS pictograms [9]
GHS Signal word Danger
GHS hazard statements
 H290, H301, H311, H314, H330, H334, H336, H360, H362, H373, H400
P202, P221, P233, P261, P263, P271, P273, P280, P305+351+338, P310[9]
NFPA 704 (fire diamond)
Flash point 132
651 °C (1,204 °F; 924 K)
Explosive limits 15–28%
Lethal dose or concentration (LD, LC):
0.015 mL/kg (human, oral)
40,300 ppm (rat, 10 min)
28,595 ppm (rat, 20 min)
20,300 ppm (rat, 40 min)
11,590 ppm (rat, 1 hr)
7338 ppm (rat, 1 hr)
4837 ppm (mouse, 1 hr)
9859 ppm (rabbit, 1 hr)
9859 ppm (cat, 1 hr)
2000 ppm (rat, 4 hr)
4230 ppm (mouse, 1 hr)[10]
5000 ppm (mammal, 5 min)
5000 ppm (human, 5 min)[10]
NIOSH (US health exposure limits):[11]
PEL (Permissible)
 50 ppm (25 ppm ACGIH- TLV; 35 ppm STEL)
REL (Recommended)
 TWA 25 ppm (18 mg/m3) ST 35 ppm (27 mg/m3)
IDLH (Immediate danger)
 300 ppm
Related compounds
Other cations
 Phosphine
Arsine
Stibine
Bismuthine
Related nitrogen hydrides
 Hydrazine
Hydrazoic acid
Related compounds
 Ammonium hydroxide
Supplementary data page
Refractive index (n),
Dielectric constant (εr), etc.
Thermodynamic
data
 Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Although common in nature—both terrestrially and in the outer planets of the Solar System—and in wide use, ammonia is both caustic and hazardous in its concentrated form. It is classified as an extremely hazardous substance in the United States, and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[12]

The global industrial production of ammonia in 2018 was 175 million tonnes,[13] with no significant change relative to the 2013 global industrial production of 175 million tonnes.[14] Industrial ammonia is sold either as ammonia liquor (usually 28% ammonia in water) or as pressurized or refrigerated anhydrous liquid ammonia transported in tank cars or cylinders.[15]

NH3 boils at −33.34 °C (−28.012 °F) at a pressure of one atmosphere, so the liquid must be stored under pressure or at low temperature. Household ammonia or ammonium hydroxide is a solution of NH3 in water. The concentration of such solutions is measured in units of the Baumé scale (density), with 26 degrees Baumé (about 30% (by weight) ammonia at 15.5 °C or 59.9 °F) being the typical high-concentration commercial product.[16]

Etymology

Pliny, in Book XXXI of his Natural History, refers to a salt produced in the Roman province of Cyrenaica named hammoniacum, so called because of its proximity to the nearby Temple of Jupiter Amun (Greek Ἄμμων Ammon).[17] However, the description Pliny gives of the salt does not conform to the properties of ammonium chloride. According to Herbert Hoover's commentary in his English translation of Georgius Agricola's De re metallica, it is likely to have been common sea salt.[18] In any case, that salt ultimately gave ammonia and ammonium compounds their name.

Natural occurrence

Ammonia is a chemical found in trace quantities in nature, being produced from nitrogenous animal and vegetable matter. Ammonia and ammonium salts are also found in small quantities in rainwater, whereas ammonium chloride (sal ammoniac), and ammonium sulfate are found in volcanic districts; crystals of ammonium bicarbonate have been found in Patagonia guano.[19] The kidneys secrete ammonia to neutralize excess acid.[20] Ammonium salts are found distributed through fertile soil and in seawater.

Ammonia is also found throughout the Solar System on Mars, Jupiter, Saturn, Uranus, Neptune, and Pluto, among other places: on smaller, icy bodies such as Pluto, ammonia can act as a geologically important antifreeze, as a mixture of water and ammonia can have a melting point as low as 173 K (−100 °C; −148 °F) if the ammonia concentration is high enough and thus allow such bodies to retain internal oceans and active geology at a far lower temperature than would be possible with water alone.[21][22] Substances containing ammonia, or those that are similar to it, are called ammoniacal.

Properties

Ammonia is a colourless gas with a characteristically pungent smell. It is lighter than air, its density being 0.589 times that of air. It is easily liquefied due to the strong hydrogen bonding between molecules; the liquid boils at −33.3 °C (−27.94 °F), and freezes to white crystals[19] at −77.7 °C (−107.86 °F).

Ammonia may be conveniently deodorized by reacting it with either sodium bicarbonate or acetic acid. Both of these reactions form an odourless ammonium salt.

Solid
The crystal symmetry is cubic, Pearson symbol cP16, space group P213 No.198, lattice constant 0.5125 nm.[23]
Liquid
Liquid ammonia possesses strong ionising powers reflecting its high ε of 22. Liquid ammonia has a very high standard enthalpy change of vaporization (23.35 kJ/mol, cf. water 40.65 kJ/mol, methane 8.19 kJ/mol, phosphine 14.6 kJ/mol) and can therefore be used in laboratories in uninsulated vessels without additional refrigeration. See liquid ammonia as a solvent.
Solvent properties
Ammonia readily dissolves in water. In an aqueous solution, it can be expelled by boiling. The aqueous solution of ammonia is basic. The maximum concentration of ammonia in water (a saturated solution) has a density of 0.880 g/cm3 and is often known as '.880 ammonia'.
Combustion
Ammonia does not burn readily or sustain combustion, except under narrow fuel-to-air mixtures of 15–25% air. When mixed with oxygen, it burns with a pale yellowish-green flame. At high temperature and in the presence of a suitable catalyst, ammonia is decomposed into its constituent elements. Ignition occurs when chlorine is passed into ammonia, forming nitrogen and hydrogen chloride; if chlorine is present in excess, then the highly explosive nitrogen trichloride (NCl3) is also formed.

Structure

The ammonia molecule has a trigonal pyramidal shape as predicted by the valence shell electron pair repulsion theory (VSEPR theory) with an experimentally determined bond angle of 106.7°.[24] The central nitrogen atom has five outer electrons with an additional electron from each hydrogen atom. This gives a total of eight electrons, or four electron pairs that are arranged tetrahedrally. Three of these electron pairs are used as bond pairs, which leaves one lone pair of electrons. The lone pair repels more strongly than bond pairs, therefore the bond angle is not 109.5°, as expected for a regular tetrahedral arrangement, but 106.7°.[24] This shape gives the molecule a dipole moment and makes it polar. The molecule's polarity, and especially, its ability to form hydrogen bonds, makes ammonia highly miscible with water. The lone pair makes ammonia a base, a proton acceptor. Ammonia is moderately basic; a 1.0 M aqueous solution has a pH of 11.6, and if a strong acid is added to such a solution until the solution is neutral (pH = 7), 99.4% of the ammonia molecules are protonated. Temperature and salinity also affect the proportion of NH4+. The latter has the shape of a regular tetrahedron and is isoelectronic with methane.

The ammonia molecule readily undergoes nitrogen inversion at room temperature; a useful analogy is an umbrella turning itself inside out in a strong wind. The energy barrier to this inversion is 24.7 kJ/mol, and the resonance frequency is 23.79 GHz, corresponding to microwave radiation of a wavelength of 1.260 cm. The absorption at this frequency was the first microwave spectrum to be observed.[25]

Amphotericity

One of the most characteristic properties of ammonia is its basicity. Ammonia is considered to be a weak base. It combines with acids to form salts; thus with hydrochloric acid it forms ammonium chloride (sal ammoniac); with nitric acid, ammonium nitrate, etc. Perfectly dry ammonia will not combine with perfectly dry hydrogen chloride; moisture is necessary to bring about the reaction.[26][27] As a demonstration experiment, opened bottles of concentrated ammonia and hydrochloric acid produce clouds of ammonium chloride, which seem to appear "out of nothing" as the salt forms where the two diffusing clouds of molecules meet, somewhere between the two bottles.

NH3 + HCl → NH4Cl

The salts produced by the action of ammonia on acids are known as the ammonium salts and all contain the ammonium ion (NH4+).[26]

Although ammonia is well known as a weak base, it can also act as an extremely weak acid. It is a protic substance and is capable of formation of amides (which contain the NH2− ion). For example, lithium dissolves in liquid ammonia to give a solution of lithium amide:

2Li + 2NH3 → 2LiNH2 + H2

Self-dissociation

Like water, ammonia undergoes molecular autoionisation to form its acid and base conjugates:

2 NH
3 ⇌ NH+
4 + NH−
2

Ammonia often functions as a weak base, so it has some buffering ability. Shifts in pH will cause more or fewer ammonium cations (NH+
4) and amide anions (NH−
2) to be present in solution. At standard pressure and temperature, K=[NH+
4][NH−
2] = 10−30

Combustion

The combustion of ammonia to nitrogen and water is exothermic:

4 NH3 + 3 O2 → 2 N2 + 6 H2O (g) ΔH°r = −1267.20 kJ (or −316.8 kJ/mol if expressed per mol of NH3)

The standard enthalpy change of combustion, ΔH°c, expressed per mole of ammonia and with condensation of the water formed, is −382.81 kJ/mol. Dinitrogen is the thermodynamic product of combustion: all nitrogen oxides are unstable with respect to N2 and O2, which is the principle behind the catalytic converter. Nitrogen oxides can be formed as kinetic products in the presence of appropriate catalysts, a reaction of great industrial importance in the production of nitric acid:

4 NH3 + 5 O2 → 4 NO + 6 H2O

A subsequent reaction leads to NO2:

2 NO +O2 → 2 NO2

The combustion of ammonia in air is very difficult in the absence of a catalyst (such as platinum gauze or warm chromium(III) oxide), due to the relatively low heat of combustion, a lower laminar burning velocity, high auto-ignition temperature, high heat of vaporization, and a narrow flammability range. However, recent studies have shown that efficient and stable combustion of ammonia can be achieved using swirl combustors, thereby rekindling research interest in ammonia as a fuel for thermal power production.[28] The flammable range of ammonia in dry air is 15.15%-27.35% and in 100% relative humidity air is 15.95%-26.55%.[29] For studying the kinetics of ammonia combustion a detailed reliable reaction mechanism is required, however knowledge about ammonia chemical kinetics during combustion process has been challenging.[30]

Formation of other compounds

In organic chemistry, ammonia can act as a nucleophile in substitution reactions. Amines can be formed by the reaction of ammonia with alkyl halides, although the resulting -NH2 group is also nucleophilic and secondary and tertiary amines are often formed as byproducts. An excess of ammonia helps minimise multiple substitution and neutralises the hydrogen halide formed. Methylamine is prepared commercially by the reaction of ammonia with chloromethane, and the reaction of ammonia with 2-bromopropanoic acid has been used to prepare racemic alanine in 70% yield. Ethanolamine is prepared by a ring-opening reaction with ethylene oxide: the reaction is sometimes allowed to go further to produce diethanolamine and triethanolamine.

Amides can be prepared by the reaction of ammonia with carboxylic acid derivatives. Acyl chlorides are the most reactive, but the ammonia must be present in at least a twofold excess to neutralise the hydrogen chloride formed. Esters and anhydrides also react with ammonia to form amides. Ammonium salts of carboxylic acids can be dehydrated to amides so long as there are no thermally sensitive groups present: temperatures of 150–200 °C are required.

The hydrogen in ammonia is susceptible to replacement by myriad substituents. When heated with sodium it converts to sodamide, NaNH2.[26] With chlorine, monochloramine is formed.

Pentavalent ammonia is known as λ5-amine or, more commonly, ammonium hydride. This crystalline solid is only stable under high pressure and decomposes back into trivalent ammonia and hydrogen gas at normal conditions. This substance was once investigated as a possible solid rocket fuel in 1966.[31]

Ammonia as a ligand
Main article: Metal ammine complex
Ball-and-stick model of the tetraamminediaquacopper(II) cation, [Cu(NH3)4(H2O)2]2+

Ammonia can act as a ligand in transition metal complexes. It is a pure σ-donor, in the middle of the spectrochemical series, and shows intermediate hard-soft behaviour (see also ECW model). For historical reasons, ammonia is named ammine in the nomenclature of coordination compounds. Some notable ammine complexes include tetraamminediaquacopper(II) ([Cu(NH3)4(H2O)2]2+), a dark blue complex formed by adding ammonia to a solution of copper(II) salts. Tetraamminediaquacopper(II) hydroxide is known as Schweizer's reagent, and has the remarkable ability to dissolve cellulose. Diamminesilver(I) ([Ag(NH3)2]+) is the active species in Tollens' reagent. Formation of this complex can also help to distinguish between precipitates of the different silver halides: silver chloride (AgCl) is soluble in dilute (2M) ammonia solution, silver bromide (AgBr) is only soluble in concentrated ammonia solution, whereas silver iodide (AgI) is insoluble in aqueous ammonia.

Ammine complexes of chromium(III) were known in the late 19th century, and formed the basis of Alfred Werner's revolutionary theory on the structure of coordination compounds. Werner noted only two isomers (fac- and mer-) of the complex [CrCl3(NH3)3] could be formed, and concluded the ligands must be arranged around the metal ion at the vertices of an octahedron. This proposal has since been confirmed by X-ray crystallography.

An ammine ligand bound to a metal ion is markedly more acidic than a free ammonia molecule, although deprotonation in aqueous solution is still rare. One example is the Calomel reaction, where the resulting amidomercury(II) compound is highly insoluble.

HgCl2 + 2 NH3 → HgCl(NH2) + NH4Cl

Detection and determination
This section is about detection in the laboratory. For detection in astronomy, see § In astronomy.

Ammonia in solution
Main article: Ammonia solution

Ammonia and ammonium salts can be readily detected, in very minute traces, by the addition of Nessler's solution, which gives a distinct yellow colouration in the presence of the slightest trace of ammonia or ammonium salts. The amount of ammonia in ammonium salts can be estimated quantitatively by distillation of the salts with sodium or potassium hydroxide, the ammonia evolved being absorbed in a known volume of standard sulfuric acid and the excess of acid then determined volumetrically; or the ammonia may be absorbed in hydrochloric acid and the ammonium chloride so formed precipitated as ammonium hexachloroplatinate, (NH4)2PtCl6.[32]

Gaseous ammonia

Sulfur sticks are burnt to detect small leaks in industrial ammonia refrigeration systems. Larger quantities can be detected by warming the salts with a caustic alkali or with quicklime, when the characteristic smell of ammonia will be at once apparent.[32] Ammonia is an irritant and irritation increases with concentration; the permissible exposure limit is 25 ppm, and lethal above 500 ppm.[33] Higher concentrations are hardly detected by conventional detectors, the type of detector is chosen according to the sensitivity required (e.g. semiconductor, catalytic, electrochemical). Holographic sensors have been proposed for detecting concentrations up to 12.5% in volume.[34]

Ammoniacal nitrogen (NH3-N)

Ammoniacal nitrogen (NH3-N) is a measure commonly used for testing the quantity of ammonium ions, derived naturally from ammonia, and returned to ammonia via organic processes, in water or waste liquids. It is a measure used mainly for quantifying values in waste treatment and water purification systems, as well as a measure of the health of natural and man-made water reserves. It is measured in units of mg/L (milligram per litre).

History
This high-pressure reactor was built in 1921 by BASF in Ludwigshafen and was re-erected on the premises of the University of Karlsruhe in Germany.

The ancient Greek historian Herodotus mentioned that there were outcrops of salt in an area of Libya that was inhabited by a people called the "Ammonians" (now: the Siwa oasis in northwestern Egypt, where salt lakes still exist).[35][36] The Greek geographer Strabo also mentioned the salt from this region. However, the ancient authors Dioscorides, Apicius, Arrian, Synesius, and Aëtius of Amida described this salt as forming clear crystals that could be used for cooking and that were essentially rock salt.[37] Hammoniacus sal appears in the writings of Pliny,[38] although it is not known whether the term is identical with the more modern sal ammoniac (ammonium chloride).[19][39][40]

The fermentation of urine by bacteria produces a solution of ammonia; hence fermented urine was used in Classical Antiquity to wash cloth and clothing, to remove hair from hides in preparation for tanning, to serve as a mordant in dying cloth, and to remove rust from iron.[41]

In the form of sal ammoniac (نشادر, nushadir), ammonia was important to the Muslim alchemists as early as the 8th century, first mentioned by the Persian-Arab chemist Jābir ibn Hayyān,[42] and to the European alchemists since the 13th century, being mentioned by Albertus Magnus.[19] It was also used by dyers in the Middle Ages in the form of fermented urine to alter the colour of vegetable dyes. In the 15th century, Basilius Valentinus showed that ammonia could be obtained by the action of alkalis on sal ammoniac.[43] At a later period, when sal ammoniac was obtained by distilling the hooves and horns of oxen and neutralizing the resulting carbonate with hydrochloric acid, the name "spirit of hartshorn" was applied to ammonia.[19][44]

Gaseous ammonia was first isolated by Joseph Black in 1756 by reacting sal ammoniac (Ammonium Chloride) with calcined magnesia (Magnesium Oxide).[45][46] It was isolated again by Peter Woulfe in 1767,[47][48] by Carl Wilhelm Scheele in 1770[49] and by Joseph Priestley in 1773 and was termed by him "alkaline air".[19][50] Eleven years later in 1785, Claude Louis Berthollet ascertained its composition.[51][19]

The Haber–Bosch process to produce ammonia from the nitrogen in the air was developed by Fritz Haber and Carl Bosch in 1909 and patented in 1910. It was first used on an industrial scale in Germany during World War I,[52] following the allied blockade that cut off the supply of nitrates from Chile. The ammonia was used to produce explosives to sustain war efforts.[53]

Before the availability of natural gas, hydrogen as a precursor to ammonia production was produced via the electrolysis of water or using the chloralkali process.

With the advent of the steel industry in the 20th century, ammonia became a byproduct of the production of coking coal.

Uses

Fertilizer

In the US as of 2019, approximately 88% of ammonia was used as fertilizers either as its salts, solutions or anhydrously.[13] When applied to soil, it helps provide increased yields of crops such as maize and wheat.[54] 30% of agricultural nitrogen applied in the US is in the form of anhydrous ammonia and worldwide 110 million tonnes are applied each year.[55]

Precursor to nitrogenous compounds

Ammonia is directly or indirectly the precursor to most nitrogen-containing compounds. Virtually all synthetic nitrogen compounds are derived from ammonia. An important derivative is nitric acid. This key material is generated via the Ostwald process by oxidation of ammonia with air over a platinum catalyst at 700–850 °C (1,292–1,562 °F), ≈9 atm. Nitric oxide is an intermediate in this conversion:[56]

NH3 + 2 O2 → HNO3 + H2O

Nitric acid is used for the production of fertilizers, explosives, and many organonitrogen compounds.

Ammonia is also used to make the following compounds:

Ammonia can also be used to make compounds in reactions which are not specifically named. Examples of such compounds include: ammonium perchlorate, ammonium nitrate, formamide, dinitrogen tetroxide, alprazolam, ethanolamine, ethyl carbamate, hexamethylenetetramine, and ammonium bicarbonate.

As a cleaner

Household ammonia is a solution of NH3 in water, and is used as a general purpose cleaner for many surfaces. Because ammonia results in a relatively streak-free shine, one of its most common uses is to clean glass, porcelain and stainless steel. It is also frequently used for cleaning ovens and soaking items to loosen baked-on grime. Household ammonia ranges in concentration by weight from 5 to 10% ammonia.[57] United States manufacturers of cleaning products are required to provide the product's material safety data sheet which lists the concentration used.[58]

Fermentation

Solutions of ammonia ranging from 16% to 25% are used in the fermentation industry as a source of nitrogen for microorganisms and to adjust pH during fermentation.

Antimicrobial agent for food products

As early as in 1895, it was known that ammonia was "strongly antiseptic ... it requires 1.4 grams per litre to preserve beef tea."[59] In one study, anhydrous ammonia destroyed 99.999% of zoonotic bacteria in 3 types of animal feed, but not silage.[60][61] Anhydrous ammonia is currently used commercially to reduce or eliminate microbial contamination of beef.[62][63] Lean finely textured beef (popularly known as "pink slime") in the beef industry is made from fatty beef trimmings (c. 50–70% fat) by removing the fat using heat and centrifugation, then treating it with ammonia to kill E. coli. The process was deemed effective and safe by the US Department of Agriculture based on a study that found that the treatment reduces E. coli to undetectable levels.[64] There have been safety concerns about the process as well as consumer complaints about the taste and smell of beef treated at optimal levels of ammonia.[65] The level of ammonia in any final product has not come close to toxic levels to humans.

Minor and emerging uses

Refrigeration – R717

Because of ammonia's vaporization properties, it is a useful refrigerant.[52] It was commonly used before the popularisation of chlorofluorocarbons (Freons). Anhydrous ammonia is widely used in industrial refrigeration applications and hockey rinks because of its high energy efficiency and low cost. It suffers from the disadvantage of toxicity, and requiring corrosion resistant components, which restricts its domestic and small-scale use. Along with its use in modern vapor-compression refrigeration it is used in a mixture along with hydrogen and water in absorption refrigerators. The Kalina cycle, which is of growing importance to geothermal power plants, depends on the wide boiling range of the ammonia–water mixture. Ammonia coolant is also used in the S1 radiator aboard the International Space Station in two loops which are used to regulate the internal temperature and enable temperature dependent experiments.[66][67]

The potential importance of ammonia as a refrigerant has increased with the discovery that vented CFCs and HFCs are extremely potent and stable greenhouse gases.[68] The contribution to the greenhouse effect of CFCs and HFCs in current use, if vented, would match that of all CO2 in the atmosphere.

For remediation of gaseous emissions

Ammonia is used to scrub SO2 from the burning of fossil fuels, and the resulting product is converted to ammonium sulfate for use as fertilizer. Ammonia neutralizes the nitrogen oxide (NOx) pollutants emitted by diesel engines. This technology, called SCR (selective catalytic reduction), relies on a vanadia-based catalyst.[69]

Ammonia may be used to mitigate gaseous spills of phosgene.[70]

As a fuel
Ammoniacal Gas Engine Streetcar in New Orleans drawn by Alfred Waud in 1871.
The X-15 aircraft used ammonia as one component fuel of its rocket engine

The raw energy density of liquid ammonia is 11.5 MJ/L,[71] which is about a third that of diesel. There is the opportunity to convert ammonia back to hydrogen, where it can be used to power hydrogen fuel cells or directly within high-temperature fuel cells.[72] The conversion of ammonia to hydrogen via the sodium amide process,[73] either for combustion or as fuel for a proton exchange membrane fuel cell,[71] is possible. Conversion to hydrogen would allow the storage of hydrogen at nearly 18 wt% compared to ≈5% for gaseous hydrogen under pressure.

Ammonia engines or ammonia motors, using ammonia as a working fluid, have been proposed and occasionally used.[74] The principle is similar to that used in a fireless locomotive, but with ammonia as the working fluid, instead of steam or compressed air. Ammonia engines were used experimentally in the 19th century by Goldsworthy Gurney in the UK and the St. Charles Avenue Streetcar line in New Orleans in the 1870s and 1880s,[75] and during World War II ammonia was used to power buses in Belgium.[76]

Ammonia is sometimes proposed as a practical alternative to fossil fuel for internal combustion engines.[76][77][78] Its high octane rating of 120[79] and low flame temperature[80] allows the use of high compression ratios without a penalty of high NOx production. Since ammonia contains no carbon, its combustion cannot produce carbon dioxide, carbon monoxide, hydrocarbons, or soot.

Even though ammonia production currently creates 1.8% of global CO2 emissions, the Royal Society report[81] claims that "green" ammonia can be produced by using low-carbon hydrogen (blue hydrogen and green hydrogen). Total decarbonization of ammonia production and the accomplishment of net-zero targets are possible by 2050.

However ammonia cannot be easily used in existing Otto cycle engines because of its very narrow flammability range, and there are also other barriers to widespread automobile usage. In terms of raw ammonia supplies, plants would have to be built to increase production levels, requiring significant capital and energy sources. Although it is the second most produced chemical (after sulfuric acid), the scale of ammonia production is a small fraction of world petroleum usage. It could be manufactured from renewable energy sources, as well as coal or nuclear power. The 60 MW Rjukan dam in Telemark, Norway produced ammonia for many years from 1913, providing fertilizer for much of Europe.

Despite this, several tests have been done. In 1981, a Canadian company converted a 1981 Chevrolet Impala to operate using ammonia as fuel.[82][83] In 2007, a University of Michigan pickup powered by ammonia drove from Detroit to San Francisco as part of a demonstration, requiring only one fill-up in Wyoming.[84]

Compared to hydrogen as a fuel, ammonia is much more energy efficient, and could be produced, stored, and delivered at a much lower cost than hydrogen which must be kept compressed as a cryogenic liquid.[71][85]

Rocket engines have also been fueled by ammonia. The Reaction Motors XLR99 rocket engine that powered the X-15 hypersonic research aircraft used liquid ammonia. Although not as powerful as other fuels, it left no soot in the reusable rocket engine, and its density approximately matches the density of the oxidizer, liquid oxygen, which simplified the aircraft's design.

As a stimulant
Anti-meth sign on tank of anhydrous ammonia, Otley, Iowa. Anhydrous ammonia is a common farm fertilizer that is also a critical ingredient in making methamphetamine. In 2005, Iowa used grant money to give out thousands of locks to prevent criminals from getting into the tanks.[86]

Ammonia, as the vapor released by smelling salts, has found significant use as a respiratory stimulant. Ammonia is commonly used in the illegal manufacture of methamphetamine through a Birch reduction.[87] The Birch method of making methamphetamine is dangerous because the alkali metal and liquid ammonia are both extremely reactive, and the temperature of liquid ammonia makes it susceptible to explosive boiling when reactants are added.[88]

Textile

Liquid ammonia is used for treatment of cotton materials, giving properties like mercerisation, using alkalis. In particular, it is used for prewashing of wool.[89]

Lifting gas

At standard temperature and pressure, ammonia is less dense than atmosphere and has approximately 45-48% of the lifting power of hydrogen or helium. Ammonia has sometimes been used to fill weather balloons as a lifting gas. Because of its relatively high boiling point (compared to helium and hydrogen), ammonia could potentially be refrigerated and liquefied aboard an airship to reduce lift and add ballast (and returned to a gas to add lift and reduce ballast).

Woodworking
See also: Ammonia fuming

Ammonia has been used to darken quartersawn white oak in Arts & Crafts and Mission-style furniture. Ammonia fumes react with the natural tannins in the wood and cause it to change colours.[90]

Energy carrier

In early August 2018, scientists from Australia's Commonwealth Scientific and Industrial Research Organisation (CSIRO) announced the success of developing a process to release hydrogen from ammonia and harvest that at ultra-high purity as a fuel for cars. This uses a special membrane. Two demonstration fuel cell vehicles have the technology, a Hyundai Nexo and Toyota Mirai.[91]

Safety precautions
The world's longest ammonia pipeline (roughly 2400 km long),[92] running from the TogliattiAzot plant in Russia to Odessa in Ukraine

The U.S. Occupational Safety and Health Administration (OSHA) has set a 15-minute exposure limit for gaseous ammonia of 35 ppm by volume in the environmental air and an 8-hour exposure limit of 25 ppm by volume.[93] The National Institute for Occupational Safety and Health (NIOSH) recently reduced the IDLH (Immediately Dangerous to Life and Health, the level to which a healthy worker can be exposed for 30 minutes without suffering irreversible health effects) from 500 to 300 based on recent more conservative interpretations of original research in 1943. Other organizations have varying exposure levels. U.S. Navy Standards [U.S. Bureau of Ships 1962] maximum allowable concentrations (MACs): continuous exposure (60 days): 25 ppm / 1 hour: 400 ppm.[94] Ammonia vapour has a sharp, irritating, pungent odour that acts as a warning of potentially dangerous exposure. The average odour threshold is 5 ppm, well below any danger or damage. Exposure to very high concentrations of gaseous ammonia can result in lung damage and death.[93] Ammonia is regulated in the United States as a non-flammable gas, but it meets the definition of a material that is toxic by inhalation and requires a hazardous safety permit when transported in quantities greater than 13,248 L (3,500 gallons).[95]

Liquid ammonia is dangerous because it is hygroscopic and because it can cause caustic burns. See Gas carrier § Health effects of specific cargoes carried on gas carriers for more information.

Toxicity

The toxicity of ammonia solutions does not usually cause problems for humans and other mammals, as a specific mechanism exists to prevent its build-up in the bloodstream. Ammonia is converted to carbamoyl phosphate by the enzyme carbamoyl phosphate synthetase, and then enters the urea cycle to be either incorporated into amino acids or excreted in the urine.[96] Fish and amphibians lack this mechanism, as they can usually eliminate ammonia from their bodies by direct excretion. Ammonia even at dilute concentrations is highly toxic to aquatic animals, and for this reason it is classified as dangerous for the environment.

Ammonia is a constituent of tobacco smoke.[97]

Coking wastewater

Ammonia is present in coking wastewater streams, as a liquid by-product of the production of coke from coal.[98] In some cases, the ammonia is discharged to the marine environment where it acts as a pollutant. The Whyalla steelworks in South Australia is one example of a coke-producing facility which discharges ammonia into marine waters.[99]

Aquaculture

Ammonia toxicity is believed to be a cause of otherwise unexplained losses in fish hatcheries. Excess ammonia may accumulate and cause alteration of metabolism or increases in the body pH of the exposed organism. Tolerance varies among fish species.[100] At lower concentrations, around 0.05 mg/L, un-ionised ammonia is harmful to fish species and can result in poor growth and feed conversion rates, reduced fecundity and fertility and increase stress and susceptibility to bacterial infections and diseases.[101] Exposed to excess ammonia, fish may suffer loss of equilibrium, hyper-excitability, increased respiratory activity and oxygen uptake and increased heart rate.[100] At concentrations exceeding 2.0 mg/L, ammonia causes gill and tissue damage, extreme lethargy, convulsions, coma, and death.[100][102] Experiments have shown that the lethal concentration for a variety of fish species ranges from 0.2 to 2.0 mg/l.[102]

During winter, when reduced feeds are administered to aquaculture stock, ammonia levels can be higher. Lower ambient temperatures reduce the rate of algal photosynthesis so less ammonia is removed by any algae present. Within an aquaculture environment, especially at large scale, there is no fast-acting remedy to elevated ammonia levels. Prevention rather than correction is recommended to reduce harm to farmed fish[102] and in open water systems, the surrounding environment.

Storage information

Similar to propane, anhydrous ammonia boils below room temperature when at atmospheric pressure. A storage vessel capable of 250 psi (1.7 MPa) is suitable to contain the liquid.[103] Ammonia is used in numerous different industrial application requiring carbon or stainless steel storage vessels. Ammonia with at least 0.2 percent by weight water content is not corrosive to carbon steel. NH3 carbon steel construction storage tanks with 0.2 percent by weight or more of water could last more than 50 years in service.[104] Ammonium compounds should never be allowed to come in contact with bases (unless in an intended and contained reaction), as dangerous quantities of ammonia gas could be released.

Household use

Solutions of ammonia (5–10% by weight) are used as household cleaners, particularly for glass. These solutions are irritating to the eyes and mucous membranes (respiratory and digestive tracts), and to a lesser extent the skin. Caution should be used that the chemical is never mixed into any liquid containing bleach, as a toxic gas may result. Mixing with chlorine-containing products or strong oxidants, such as household bleach, can generate chloramines.[105]

Laboratory use of ammonia solutions
Hydrochloric acid sample releasing HCl fumes, which are reacting with ammonia fumes to produce a white smoke of ammonium chloride.

The hazards of ammonia solutions depend on the concentration: "dilute" ammonia solutions are usually 5–10% by weight (<5.62 mol/L); "concentrated" solutions are usually prepared at >25% by weight. A 25% (by weight) solution has a density of 0.907 g/cm3, and a solution that has a lower density will be more concentrated. The European Union classification of ammonia solutions is given in the table.

Concentration
by weight (w/w)		 Molarity Concentration
mass/volume (w/v)		 Classification R-phrases
5–10% 2.87–5.62 mol/L 48.9–95.7 g/L Irritant (Xi) R36/37/38
10–25% 5.62–13.29 mol/L 95.7–226.3 g/L Corrosive (C) R34
>25% >13.29 mol/L >226.3 g/L
  • Corrosive (C)
  • Dangerous for
    the environment (N)
 R34, R50
S-Phrases: (S1/2), S16, S36/37/39, S45, S61.

The ammonia vapour from concentrated ammonia solutions is severely irritating to the eyes and the respiratory tract, and these solutions should only be handled in a fume hood. Saturated ("0.880" – see #Properties) solutions can develop a significant pressure inside a closed bottle in warm weather, and the bottle should be opened with care; this is not usually a problem for 25% ("0.900") solutions.

Ammonia solutions should not be mixed with halogens, as toxic and/or explosive products are formed. Prolonged contact of ammonia solutions with silver, mercury or iodide salts can also lead to explosive products: such mixtures are often formed in qualitative inorganic analysis, and should be lightly acidified but not concentrated (<6% w/v) before disposal once the test is completed.

Laboratory use of anhydrous ammonia (gas or liquid)

Anhydrous ammonia is classified as toxic (T) and dangerous for the environment (N). The gas is flammable (autoignition temperature: 651 °C) and can form explosive mixtures with air (16–25%). The permissible exposure limit (PEL) in the United States is 50 ppm (35 mg/m3), while the IDLH concentration is estimated at 300 ppm. Repeated exposure to ammonia lowers the sensitivity to the smell of the gas: normally the odour is detectable at concentrations of less than 50 ppm, but desensitised individuals may not detect it even at concentrations of 100 ppm. Anhydrous ammonia corrodes copper- and zinc-containing alloys, and so brass fittings should not be used for handling the gas. Liquid ammonia can also attack rubber and certain plastics.

Ammonia reacts violently with the halogens. Nitrogen triiodide, a primary high explosive, is formed when ammonia comes in contact with iodine. Ammonia causes the explosive polymerisation of ethylene oxide. It also forms explosive fulminating compounds with compounds of gold, silver, mercury, germanium or tellurium, and with stibine. Violent reactions have also been reported with acetaldehyde, hypochlorite solutions, potassium ferricyanide and peroxides.

Synthesis and production
This section is about industrial synthesis. For synthesis in certain organisms, see § Biosynthesis.
See also: Ammonia production
Production trend of ammonia between 1947 and 2007

Ammonia is one of the most produced inorganic chemicals, with global production reported at 175 million tonnes in 2018.[13] China accounted for 28.5% of that, followed by Russia at 10.3%, the United States at 9.1%, and India at 6.7%.[13]

Before the start of World War I, most ammonia was obtained by the dry distillation[106] of nitrogenous vegetable and animal waste products, including camel dung, where it was distilled by the reduction of nitrous acid and nitrites with hydrogen; in addition, it was produced by the distillation of coal, and also by the decomposition of ammonium salts by alkaline hydroxides[107] such as quicklime:[108]

2 NH4Cl + 2 CaO → CaCl2 + Ca(OH)2 + 2 NH3(g)

For small scale laboratory synthesis, one can heat urea and calcium hydroxide:

(NH2)2CO + Ca(OH)2 → CaCO3 + 2 NH3

Haber-Bosch process

Mass production of ammonia mostly uses the Haber–Bosch process, a gas phase reaction between hydrogen (H2) and nitrogen (N2) at a moderately-elevated temperature (450 °C) and high pressure (100 standard atmospheres (10 MPa)):[109]

This reaction is both exothermic and results in decreased entropy, meaning that the reaction is favoured at lower temperatures[110] and higher pressures.[111] This makes it difficult and expensive to achieve, as lower temperatures result in slower reaction kinetics (hence a slower reaction rate)[112] and high pressure requires high-strength pressure vessels[113] that aren't weakened by hydrogen embrittlement. In addition, diatomic nitrogen is bound together by an exceptionally strong triple bond, which makes it rather inert.[114] Both the yield and efficiency of the Haber-Bosch Process are low, meaning that ammonia produced must be continuously separated and extracted for the reaction to proceed at an appreciable pace.[115] Combined with the energy needed to produce hydrogen[note 1] and purified atmospheric nitrogen, ammonia production is a very energy-intensive process, consuming 1 to 2% of global energy, 3% of global carbon emissions,[117] and 3 to 5% of natural gas consumption.[118]

Liquid ammonia as a solvent
See also: Inorganic nonaqueous solvent

Liquid ammonia is the best-known and most widely studied nonaqueous ionising solvent. Its most conspicuous property is its ability to dissolve alkali metals to form highly coloured, electrically conductive solutions containing solvated electrons. Apart from these remarkable solutions, much of the chemistry in liquid ammonia can be classified by analogy with related reactions in aqueous solutions. Comparison of the physical properties of NH3 with those of water shows NH3 has the lower melting point, boiling point, density, viscosity, dielectric constant and electrical conductivity; this is due at least in part to the weaker hydrogen bonding in NH3 and because such bonding cannot form cross-linked networks, since each NH3 molecule has only one lone pair of electrons compared with two for each H2O molecule. The ionic self-dissociation constant of liquid NH3 at −50 °C is about 10−33.

A train carrying Anhydrous Ammonia.

Solubility of salts
Solubility (g of salt per 100 g liquid NH3)
Ammonium acetate 253.2
Ammonium nitrate 389.6
Lithium nitrate 243.7
Sodium nitrate 97.6
Potassium nitrate 10.4
Sodium fluoride 0.35
Sodium chloride 157.0
Sodium bromide 138.0
Sodium iodide 161.9
Sodium thiocyanate 205.5

Liquid ammonia is an ionising solvent, although less so than water, and dissolves a range of ionic compounds, including many nitrates, nitrites, cyanides, thiocyanates, metal cyclopentadienyl complexes and metal bis(trimethylsilyl)amides.[119] Most ammonium salts are soluble and act as acids in liquid ammonia solutions. The solubility of halide salts increases from fluoride to iodide. A saturated solution of ammonium nitrate (Divers' solution, named after Edward Divers) contains 0.83 mol solute per mole of ammonia and has a vapour pressure of less than 1 bar even at 25 °C (77 °F).

Solutions of metals
See also: Solvated electron

Liquid ammonia will dissolve all of the alkali metals and other electropositive metals such as Ca,[120] Sr, Ba, Eu, and Yb (also Mg using an electrolytic process[121]). At low concentrations (<0.06 mol/L), deep blue solutions are formed: these contain metal cations and solvated electrons, free electrons that are surrounded by a cage of ammonia molecules.

These solutions are very useful as strong reducing agents. At higher concentrations, the solutions are metallic in appearance and in electrical conductivity. At low temperatures, the two types of solution can coexist as immiscible phases.

Redox properties of liquid ammonia
See also: Redox
E° (V, ammonia) E° (V, water)
Li+ + e− ⇌ Li −2.24 −3.04
K+ + e− ⇌ K −1.98 −2.93
Na+ + e− ⇌ Na −1.85 −2.71
Zn2+ + 2e− ⇌ Zn −0.53 −0.76
NH4+ + e− ⇌ ½ H2 + NH3 0.00 —
Cu2+ + 2e− ⇌ Cu +0.43 +0.34
Ag+ + e− ⇌ Ag +0.83 +0.80

The range of thermodynamic stability of liquid ammonia solutions is very narrow, as the potential for oxidation to dinitrogen, E° (N2 + 6NH4+ + 6e− ⇌ 8NH3), is only +0.04 V. In practice, both oxidation to dinitrogen and reduction to dihydrogen are slow. This is particularly true of reducing solutions: the solutions of the alkali metals mentioned above are stable for several days, slowly decomposing to the metal amide and dihydrogen. Most studies involving liquid ammonia solutions are done in reducing conditions; although oxidation of liquid ammonia is usually slow, there is still a risk of explosion, particularly if transition metal ions are present as possible catalysts.

Ammonia's role in biological systems and human disease
Main symptoms of hyperammonemia (ammonia reaching toxic concentrations).[122]

Ammonia is both a metabolic waste and a metabolic input throughout the biosphere. It is an important source of nitrogen for living systems. Although atmospheric nitrogen abounds (more than 75%), few living creatures are capable of using this atmospheric nitrogen in its diatomic form, N2 gas. Therefore, nitrogen fixation is required for the synthesis of amino acids, which are the building blocks of protein. Some plants rely on ammonia and other nitrogenous wastes incorporated into the soil by decaying matter. Others, such as nitrogen-fixing legumes, benefit from symbiotic relationships with rhizobia that create ammonia from atmospheric nitrogen.[123]

Biosynthesis

In certain organisms, ammonia is produced from atmospheric nitrogen by enzymes called nitrogenases. The overall process is called nitrogen fixation. Intense effort has been directed toward understanding the mechanism of biological nitrogen fixation; the scientific interest in this problem is motivated by the unusual structure of the active site of the enzyme, which consists of an Fe7MoS9 ensemble.[124]

Ammonia is also a metabolic product of amino acid deamination catalyzed by enzymes such as glutamate dehydrogenase 1. Ammonia excretion is common in aquatic animals. In humans, it is quickly converted to urea, which is much less toxic, particularly less basic. This urea is a major component of the dry weight of urine. Most reptiles, birds, insects, and snails excrete uric acid solely as nitrogenous waste.

In physiology

Ammonia also plays a role in both normal and abnormal animal physiology. It is biosynthesised through normal amino acid metabolism and is toxic in high concentrations. The liver converts ammonia to urea through a series of reactions known as the urea cycle. Liver dysfunction, such as that seen in cirrhosis, may lead to elevated amounts of ammonia in the blood (hyperammonemia). Likewise, defects in the enzymes responsible for the urea cycle, such as ornithine transcarbamylase, lead to hyperammonemia. Hyperammonemia contributes to the confusion and coma of hepatic encephalopathy, as well as the neurologic disease common in people with urea cycle defects and organic acidurias.[125]

Ammonia is important for normal animal acid/base balance. After formation of ammonium from glutamine, α-ketoglutarate may be degraded to produce two molecules of bicarbonate, which are then available as buffers for dietary acids. Ammonium is excreted in the urine, resulting in net acid loss. Ammonia may itself diffuse across the renal tubules, combine with a hydrogen ion, and thus allow for further acid excretion.[126]

Excretion
Main article: Excretion

Ammonium ions are a toxic waste product of metabolism in animals. In fish and aquatic invertebrates, it is excreted directly into the water. In mammals, sharks, and amphibians, it is converted in the urea cycle to urea, because it is less toxic and can be stored more efficiently. In birds, reptiles, and terrestrial snails, metabolic ammonium is converted into uric acid, which is solid, and can therefore be excreted with minimal water loss.[127]

Reference ranges for blood tests, comparing blood content of ammonia (shown in yellow near middle) with other constituents

In astronomy
Ammonia occurs in the atmospheres of the outer giant planets such as Jupiter (0.026% ammonia), Saturn (0.012% ammonia), and in the atmospheres and ices of Uranus and Neptune.

Ammonia has been detected in the atmospheres of the giant planets, including Jupiter, along with other gases like methane, hydrogen, and helium. The interior of Saturn may include frozen crystals of ammonia.[128] It is naturally found on Deimos and Phobos – the two moons of Mars.

Interstellar space

Ammonia was first detected in interstellar space in 1968, based on microwave emissions from the direction of the galactic core.[129] This was the first polyatomic molecule to be so detected. The sensitivity of the molecule to a broad range of excitations and the ease with which it can be observed in a number of regions has made ammonia one of the most important molecules for studies of molecular clouds.[130] The relative intensity of the ammonia lines can be used to measure the temperature of the emitting medium.

The following isotopic species of ammonia have been detected:

NH3, 15NH3, NH2D, NHD2, and ND3

The detection of triply deuterated ammonia was considered a surprise as deuterium is relatively scarce. It is thought that the low-temperature conditions allow this molecule to survive and accumulate.[131]

Since its interstellar discovery, NH3 has proved to be an invaluable spectroscopic tool in the study of the interstellar medium. With a large number of transitions sensitive to a wide range of excitation conditions, NH3 has been widely astronomically detected – its detection has been reported in hundreds of journal articles. Listed below is a sample of journal articles that highlights the range of detectors that have been used to identify ammonia.

The study of interstellar ammonia has been important to a number of areas of research in the last few decades. Some of these are delineated below and primarily involve using ammonia as an interstellar thermometer.

Interstellar formation mechanisms
Ball-and-stick model of the diamminesilver(I) cation, [Ag(NH3)2]+

The interstellar abundance for ammonia has been measured for a variety of environments. The [NH3]/[H2] ratio has been estimated to range from 10−7 in small dark clouds[132] up to 10−5 in the dense core of the Orion Molecular Cloud Complex.[133] Although a total of 18 total production routes have been proposed,[134] the principal formation mechanism for interstellar NH3 is the reaction:

NH4+ + e− → NH3 + H·

The rate constant, k, of this reaction depends on the temperature of the environment, with a value of 5.2×10−6 at 10 K.[135] The rate constant was calculated from the formula . For the primary formation reaction, a = 1.05×10−6 and B = −0.47. Assuming an NH4+ abundance of 3×10−7 and an electron abundance of 10−7 typical of molecular clouds, the formation will proceed at a rate of 1.6×10−9 cm−3s−1 in a molecular cloud of total density 105 cm−3.[136]

All other proposed formation reactions have rate constants of between 2 and 13 orders of magnitude smaller, making their contribution to the abundance of ammonia relatively insignificant.[137] As an example of the minor contribution other formation reactions play, the reaction:

H2 + NH2 → NH3 + H

has a rate constant of 2.2×10−15. Assuming H2 densities of 105 and [NH2]/[H2] ratio of 10−7, this reaction proceeds at a rate of 2.2×10−12, more than 3 orders of magnitude slower than the primary reaction above.

Some of the other possible formation reactions are:

H− + NH4+ → NH3 + H2
PNH3+ + e− → P + NH3

Interstellar destruction mechanisms

There are 113 total proposed reactions leading to the destruction of NH3. Of these, 39 were tabulated in extensive tables of the chemistry among C, N, and O compounds.[138] A review of interstellar ammonia cites the following reactions as the principal dissociation mechanisms:[130]

NH3 + H3+ → NH4+ + H2

 

 

 

 

(1)

NH3 + HCO+ → NH4+ + CO

 

 

 

 

(2)

with rate constants of 4.39×10−9[139] and 2.2×10−9,[140] respectively. The above equations (1, 2) run at a rate of 8.8×10−9 and 4.4×10−13, respectively. These calculations assumed the given rate constants and abundances of [NH3]/[H2] = 10−5, [H3+]/[H2] = 2×10−5, [HCO+]/[H2] = 2×10−9, and total densities of n = 105, typical of cold, dense, molecular clouds.[141] Clearly, between these two primary reactions, equation (1) is the dominant destruction reaction, with a rate ≈10,000 times faster than equation (2). This is due to the relatively high abundance of H3+.

Single antenna detections

Radio observations of NH3 from the Effelsberg 100-m Radio Telescope reveal that the ammonia line is separated into two components – a background ridge and an unresolved core. The background corresponds well with the locations previously detected CO.[142] The 25 m Chilbolton telescope in England detected radio signatures of ammonia in H II regions, HNH2O masers, H-H objects, and other objects associated with star formation. A comparison of emission line widths indicates that turbulent or systematic velocities do not increase in the central cores of molecular clouds.[143]

Microwave radiation from ammonia was observed in several galactic objects including W3(OH), Orion A, W43, W51, and five sources in the galactic centre. The high detection rate indicates that this is a common molecule in the interstellar medium and that high-density regions are common in the galaxy.[144]

Interferometric studies

VLA observations of NH3 in seven regions with high-velocity gaseous outflows revealed condensations of less than 0.1 pc in L1551, S140, and Cepheus A. Three individual condensations were detected in Cepheus A, one of them with a highly elongated shape. They may play an important role in creating the bipolar outflow in the region.[145]

Extragalactic ammonia was imaged using the VLA in IC 342. The hot gas has temperatures above 70 K, which was inferred from ammonia line ratios and appears to be closely associated with the innermost portions of the nuclear bar seen in CO.[146] NH3 was also monitored by VLA toward a sample of four galactic ultracompact HII regions: G9.62+0.19, G10.47+0.03, G29.96-0.02, and G31.41+0.31. Based upon temperature and density diagnostics, it is concluded that in general such clumps are probably the sites of massive star formation in an early evolutionary phase prior to the development of an ultracompact HII region.[147]

Infrared detections

Absorption at 2.97 micrometres due to solid ammonia was recorded from interstellar grains in the Becklin-Neugebauer Object and probably in NGC 2264-IR as well. This detection helped explain the physical shape of previously poorly understood and related ice absorption lines.[148]

A spectrum of the disk of Jupiter was obtained from the Kuiper Airborne Observatory, covering the 100 to 300 cm−1 spectral range. Analysis of the spectrum provides information on global mean properties of ammonia gas and an ammonia ice haze.[149]

A total of 149 dark cloud positions were surveyed for evidence of 'dense cores' by using the (J,K) = (1,1) rotating inversion line of NH3. In general, the cores are not spherically shaped, with aspect ratios ranging from 1.1 to 4.4. It is also found that cores with stars have broader lines than cores without stars.[150]

Ammonia has been detected in the Draco Nebula and in one or possibly two molecular clouds, which are associated with the high-latitude galactic infrared cirrus. The finding is significant because they may represent the birthplaces for the Population I metallicity B-type stars in the galactic halo that could have been borne in the galactic disk.[151]

Observations of nearby dark clouds

By balancing and stimulated emission with spontaneous emission, it is possible to construct a relation between excitation temperature and density. Moreover, since the transitional levels of ammonia can be approximated by a 2-level system at low temperatures, this calculation is fairly simple. This premise can be applied to dark clouds, regions suspected of having extremely low temperatures and possible sites for future star formation. Detections of ammonia in dark clouds show very narrow lines—indicative not only of low temperatures, but also of a low level of inner-cloud turbulence. Line ratio calculations provide a measurement of cloud temperature that is independent of previous CO observations. The ammonia observations were consistent with CO measurements of rotation temperatures of ≈10 K. With this, densities can be determined, and have been calculated to range between 104 and 105 cm−3 in dark clouds. Mapping of NH3 gives typical clouds sizes of 0.1 pc and masses near 1 solar mass. These cold, dense cores are the sites of future star formation.

UC HII regions

Ultra-compact HII regions are among the best tracers of high-mass star formation. The dense material surrounding UCHII regions is likely primarily molecular. Since a complete study of massive star formation necessarily involves the cloud from which the star formed, ammonia is an invaluable tool in understanding this surrounding molecular material. Since this molecular material can be spatially resolved, it is possible to constrain the heating/ionising sources, temperatures, masses, and sizes of the regions. Doppler-shifted velocity components allow for the separation of distinct regions of molecular gas that can trace outflows and hot cores originating from forming stars.

Extragalactic detection

Ammonia has been detected in external galaxies,[152][153] and by simultaneously measuring several lines, it is possible to directly measure the gas temperature in these galaxies. Line ratios imply that gas temperatures are warm (≈50 K), originating from dense clouds with sizes of tens of pc. This picture is consistent with the picture within our Milky Way galaxy—hot dense molecular cores form around newly forming stars embedded in larger clouds of molecular material on the scale of several hundred pc (giant molecular clouds; GMCs).

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See also

Notes
  1. Hydrogen required for ammonia synthesis is most often produced through gasification of carbon-containing material, mostly natural gas, but other potential carbon sources include coal, petroleum, peat, biomass, or waste. As of 2012, the global production of ammonia produced from natural gas using the steam reforming process was 72 percent.[116] Hydrogen can also be produced from water and electricity using electrolysis: at one time, most of Europe's ammonia was produced from the Hydro plant at Vemork. Other possibilities include biological hydrogen production or photolysis, but at present, steam reforming of natural gas is the most economical means of mass-producing hydrogen.

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  35. Herodotus with George Rawlinson, trans., The History of Herodotus (New York, New York: Tandy-Thomas Co., 1909), vol.2, Book 4, § 181, pp. 304–305.
  36. The land of the Ammonians is mentioned elsewhere in Herodotus' History and in Pausanias' Description of Greece:
    • Herodotus with George Rawlinson, trans., The History of Herodotus (New York, New York: Tandy-Thomas Co., 1909), vol. 1, Book 2, § 42, p. 245, vol. 2, Book 3, § 25, p. 73, and vol. 2, Book 3, § 26, p. 74.
    • Pausanias with W.H.S. Jones, trans., Description of Greece (London, England: William Heinemann Ltd., 1979), vol. 2, Book 3, Ch. 18, § 3, pp. 109 and 111 and vol. 4, Book 9, Ch. 16, § 1, p. 239.
  37. Kopp, Hermann, Geschichte der Chemie [History of Chemistry] (Braunschweig, (Germany): Friedrich Vieweg und Sohn, 1845), Part 3, p. 237. [in German]
  38. Chisholm 1911 cites Pliny Nat. Hist. xxxi. 39. See: Pliny the Elder with John Bostock and H. T. Riley, ed.s, The Natural History (London, England: H. G. Bohn, 1857), vol. 5, Book 31, § 39, p. 502.
  39. "Sal-ammoniac". Webmineral. Retrieved 7 July 2009.
  40. Pliny also mentioned that when some samples of what was purported to be natron (Latin: nitrum, impure sodium carbonate) were treated with lime (calcium carbonate) and water, the natron would emit a pungent smell, which some authors have interpreted as signifying that the natron either was ammonium chloride or was contaminated with it. See:
    • Pliny with W.H.S. Jones, trans., Natural History (London, England: William Heinemann Ltd., 1963), vol. 8, Book 31, § 46, pp. 448–449. From pp. 448–449: "Adulteratur in Aegypto calce, deprehenditur gusto. Sincerum enim statim resolvitur, adulteratum calce pungit et asperum [or aspersum] reddit odorem vehementer." (In Egypt it [i.e., natron] is adulterated with lime, which is detected by taste; for pure natron melts at once, but adulterated natron stings because of the lime, and emits a strong, bitter odour [or: when sprinkled [(aspersum) with water] emits a vehement odour])
    • Kidd, John, Outlines of Mineralogy (Oxford, England: N. Bliss, 1809), vol. 2, p. 6.
    • Moore, Nathaniel Fish, Ancient Mineralogy: Or, An Inquiry Respecting Mineral Substances Mentioned by the Ancients: ... (New York, New York: G. & C. Carvill & Co., 1834), pp. 96–97.
  41. See:
    • Forbes, R.J., Studies in Ancient Technology, vol. 5, 2nd ed. (Leiden, Netherlands: E.J. Brill, 1966), pp. 19, 48, and 65.
    • Moeller, Walter O., The Wool Trade of Ancient Pompeii (Leiden, Netherlands: E.J. Brill, 1976), p. 20.
    • Faber, G.A. (pseudonym of: Goldschmidt, Günther) (May 1938) "Dyeing and tanning in classical antiquity," Ciba Review, 9 : 277–312. Available at: Elizabethan Costume
    • Smith, William, A Dictionary of Greek and Roman Antiquities (London, England: John Murray, 1875), article: "Fullo" (i.e., fullers or launderers), pp. 551–553.
    • Rousset, Henri (31 March 1917) "The laundries of the Ancients," Scientific American Supplement, 83 (2152) : 197.
    • Bond, Sarah E., Trade and Taboo: Disreputable Professions in the Roman Mediterranean (Ann Arbor, Michigan: University of Michigan Press, 2016), p. 112.
    • Binz, Arthur (1936) "Altes und Neues über die technische Verwendung des Harnes" (Ancient and modern [information] about the technological use of urine), Zeitschrift für Angewandte Chemie, 49 (23) : 355–360. [in German]
    • Witty, Michael (December 2016) "Ancient Roman urine chemistry," Acta Archaeologica, 87 (1) : 179–191. Witty speculates that the Romans obtained ammonia in concentrated form by adding wood ash (impure potassium carbonate) to urine that had been fermented for several hours. Struvite (magnesium ammonium phosphate) is thereby precipitated, and the yield of struvite can be increased by then treating the solution with bittern, a magnesium-rich solution that is a byproduct of making salt from sea water. Roasting struvite releases ammonia vapors.
  42. Haq, Syed Nomanul (1995). Names, Natures and Things: The Alchemist Jabir Ibn Hayyan and His Kitab Al-Ahjar (Book of Stones). Springer. ISBN 978-0-7923-3254-1.
  43. Spiritus salis urinæ (spirit of the salt of urine, i.e., ammonium carbonate) had apparently been produced before Valentinus, although he presented a new, simpler method for preparing it in his book: Valentinus, Basilius, Vier Tractätlein Fr. Basilii Valentini ... [Four essays of Brother Basil Valentine ... ] (Frankfurt am Main, (Germany): Luca Jennis, 1625), "Supplementum oder Zugabe" (Supplement or appendix), pp. 80–81: "Der Weg zum Universal, damit die drei Stein zusammen kommen." (The path to the Universal, so that the three stones come together.). From p. 81: "Der Spiritus salis Urinæ nimbt langes wesen zubereiten / dieser proceß aber ist waß leichter unnd näher auß dem Salz von Armenia, ... Nun nimb sauberen schönen Armenischen Salz armoniac ohn alles sublimiren / thue ihn in ein Kolben / giesse ein Oleum Tartari drauff / daß es wie ein Muß oder Brey werde / vermachs baldt / dafür thu auch ein grosen vorlag / so lege sich als baldt der Spiritus Salis Urinæ im Helm an Crystallisch ... " (Spirit of the salt of urine [i.e., ammonium carbonate] requires a long method [i.e., procedure] to prepare; this [i.e., Valentine's] process [starting] from the salt from Armenia [i.e., ammonium chloride], however, is somewhat easier and shorter ... Now take clean nice Armenian salt, without sublimating all [of it]; put it in a [distillation] flask; pour oil of tartar [i.e., potassium carbonate that has dissolved only in the water that it has absorbed from the air] on it, [so] that it [i.e., the mixture] becomes like a mush or paste; assemble it [i.e., the distilling apparatus (alembic)] quickly; for that [purpose] connect a large receiving flask; then soon spirit of the salt of urine deposits as crystals in the "helmet" [i.e., the outlet for the vapors, which is atop the distillation flask] ...)
    See also: Kopp, Hermann, Geschichte der Chemie [History of Chemistry] (Braunschweig, (Germany): Friedrich Vieweg und Sohn, 1845), Part 3, p. 243. [in German]
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    • Priestley, Joseph, Experiments and Observations on Different Kinds of Air, vol. 1, 2nd ed. (London, England: 1775), Part 2, § 1: Observations on Alkaline Air, pp. 163–177.
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    • By 1775, Priestley had observed that electricity could decompose ammonia ("alkaline air"), yielding a flammable gas (hydrogen). See: Priestley, Joseph, Experiments and Observations on Different Kinds of Air, vol. 2 (London, England: J. Johnson, 1775), pp. 239–240.
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Works Cited

Further reading
  • Bretherick, L., ed. (1986). Hazards in the Chemical Laboratory (4th ed.). London: Royal Society of Chemistry. ISBN 978-0-85186-489-1. OCLC 16985764.
  • Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  • Housecroft, C. E.; Sharpe, A. G. (2000). Inorganic Chemistry (1st ed.). New York: Prentice Hall. ISBN 978-0-582-31080-3.
  • Weast, R. C., ed. (1972). Handbook of Chemistry and Physics (53rd ed.). Cleveland, OH: Chemical Rubber Co.
Salts and covalent derivatives of the nitride ion
NH3
N2H4		 He(N2)11
Li3N Be3N2 BN β-C3N4
g-C3N4
CxNy		 N2 NxOy NF3 Ne
Na3N Mg3N2 AlN Si3N4 PN
P3N5		 SxNy
SN
S4N4		 NCl3 Ar
K3N Ca3N2 ScN TiN VN CrN
Cr2N		 MnxNy FexNy CoN Ni3N CuN Zn3N2 GaN Ge3N4 As Se NBr3 Kr
Rb3N Sr3N2 YN ZrN NbN β-Mo2N Tc Ru Rh PdN Ag3N CdN InN Sn Sb Te NI3 Xe
Cs3N Ba3N2   Hf3N4 TaN WN Re Os Ir Pt Au Hg3N2 TlN Pb BiN Po At Rn
Fr3N Ra3N2   Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
↓
La CeN Pr Nd Pm Sm Eu GdN Tb Dy Ho Er Tm Yb Lu
Ac Th Pa UN Np Pu Am Cm Bk Cf Es Fm Md No Lr
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