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Ammonium nitrate

From Wikipedia, the free encyclopedia
Chemical compound with formula NH4NO3

Ammonium nitrate
Structural formula
Structural formula of ammonium cation (left) and nitrate anion (right)
Ammonium nitrate crystal structure
H=white, N=blue, O=red
Sample of white powder and spherules
Names
IUPAC name
Ammonium nitrate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.026.680Edit this at Wikidata
EC Number
  • 229-347-8
RTECS number
  • BR9050000
UNII
UN number0222with > 0.2% combustible substances
1942with ≤ 0.2% combustible substances
2067fertilizers
2426liquid
  • InChI=1S/NO3.H3N/c2-1(3)4;/h;1H3/q-1;/p+1 checkY
    Key: DVARTQFDIMZBAA-UHFFFAOYSA-O checkY
  • InChI=1/NO3.H3N/c2-1(3)4;/h;1H3/q-1;/p+1
    Key: DVARTQFDIMZBAA-IKLDFBCSAH
  • [O-][N+]([O-])=O.[NH4+]
Properties
NH4NO3
Molar mass80.043 g/mol
Appearancewhite crystalline solid
Density1.725 g/cm3 (20 °C)
Melting point169.6 °C (337.3 °F; 442.8 K)
Boiling pointapprox. 210 °C (410 °F; 483 K) decomposes
Endothermic
118 g/100 ml (0 °C)
150 g/100 ml (10 °C)
192 g/100 ml (20 °C)
297 g/100 ml (40 °C)
410 g/100 ml (60 °C)
576 g/100 ml (80 °C)
1024 g/100 ml (100 °C)[1]
−33.6×10−6 cm3/mol
Structure
orthorhombic[2]
Explosive data
Shock sensitivityvery low
Friction sensitivityvery low
Detonation velocity2500m/s
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Explosive, Oxidizer
GHS labelling:
GHS07: Exclamation markGHS03: OxidizingGHS01: Explosive
Danger
H201,H271,H319
P220,P221,P264,P271,P280,P372
NFPA 704 (fire diamond)
Lethal dose or concentration (LD, LC):
2085–5300 mg/kg (oral in rats, mice)[3]
Related compounds
Otheranions
Ammonium nitrite
Othercations
Sodium nitrate
Potassium nitrate
Hydroxylammonium nitrate
Related compounds
Ammonium perchlorate
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Ammonium nitrate is achemical compound with the formulaNH4NO3. It is a white crystalline salt consisting ofions ofammonium andnitrate. It is highly soluble in water andhygroscopic as a solid, but does not formhydrates. It is predominantly used inagriculture as a high-nitrogenfertilizer.[5]

Its other major use is as a component ofexplosive mixtures used in mining, quarrying, and civil construction. It is the major constituent ofANFO, an industrial explosive which accounts for 80% of explosives used in North America; similar formulations have been used inimprovised explosive devices.

Many countries are phasing out its use in consumer applications due to concerns over its potential for misuse.[6]Accidental ammonium nitrate explosions have killed thousands of people since the early 20th century.[6][7] Global production was estimated at 21.6 million tonnes in 2017.[8] By 2021, global production of ammonium nitrate was down to 16.7 million tonnes.[7]

Occurrence

[edit]

Ammonium nitrate is found as the natural mineralgwihabaite (formerly known as nitrammite)[9] – the ammonium analogue ofsaltpetre (mineralogical name: niter)[10][11] – in the driest regions of theAtacama Desert inChile, often as a crust on the ground or in conjunction with other nitrate,iodate, andhalide minerals. Ammonium nitrate was mined there until theHaber–Bosch process made it possible to synthesize nitrates from atmospheric nitrogen, rendering nitrate mining obsolete.

Production, reactions and crystalline phases

[edit]

The industrial production of ammonium nitrate entails theacid-base reaction ofammonia withnitric acid:[12]

HNO3 + NH3 → NH4NO3

The ammonia required for this process is obtained by theHaber process from nitrogen and hydrogen. Ammonia produced by the Haber process can be oxidized to nitric acid by theOstwald process. Ammonia is used in itsanhydrous form (a gas) and the nitric acid is concentrated. The reaction is violent owing to its highlyexothermic nature. After the solution is formed, typically at about 83% concentration, the excess water is evaporated off to leave an ammonium nitrate (AN) content of 95% to 99.9% concentration (AN melt), depending on grade. The AN melt is then made into "prills" or small beads in aspray tower, or into granules by spraying and tumbling in a rotating drum. The prills or granules may be further dried, cooled, and then coated to prevent caking. These prills or granules are the typical AN products in commerce.

Another production method is a variant of thenitrophosphate process:

Ca(NO3)2 +2 NH3 +CO2 + H2O → 2 NH4NO3 + CaCO3

The products,calcium carbonate and ammonium nitrate, may be separately purified or sold combined ascalcium ammonium nitrate.

Ammonium nitrate can also be made viametathesis reactions:

(NH4)2SO4 +Ba(NO3)2 → 2 NH4NO3 +BaSO4
(NH4)2SO4 +Ca(NO3)2 → 2 NH4NO3 +CaSO4
NH4Cl +AgNO3 → NH4NO3 +AgCl

Reactions

[edit]

As ammonium nitrate is asalt, both the cation,NH+4, and the anion,NO3, may take part in chemical reactions.

Solid ammonium nitrate decomposes on heating. At temperatures below around 300 °C, the decomposition mainly producesnitrous oxide and water:

NH4NO3 → N2O + 2 H2O

At higher temperatures, the following reaction predominates.[13]

2 NH4NO3 → 2 N2 + O2 + 4 H2O

Both decomposition reactions areexothermic and their products are gases. Under certain conditions, this can lead to arunaway reaction, with the decomposition process becoming explosive.[14] See§ Disasters for details. Manyammonium nitrate disasters, with loss of lives, have occurred.

The red–orange colour in an explosion cloud is due tonitrogen dioxide, a secondary reaction product.[14]

Crystalline phases

[edit]

Several crystalline phases of ammonium nitrate have been observed. The following occur under atmospheric pressure.

PhaseTemperature (°C)Symmetry
(liquid)(above 169.6)
I169.6 to 125.2cubic
II125.2 to 84.2tetragonal
III84.2 to 32.3α-rhombic
IV32.3 to −16.8β-rhombic
Vbelow −16.8tetragonal[15]

The transition between β-rhombic to α-rhombic forms (at 32.3 °C) occurs at ambient temperature in many parts of the world. These forms have a 3.6% difference in density and hence transition between them causes a change in volume. One practical consequence of this is that ammonium nitrate cannot be used as asolid rocket motor propellant, as it develops cracks. Stabilized ammonium nitrate (PSAN) was developed as a solution to this and incorporates metal halides stabilisers, which prevent density fluctuations.[16]

Applications

[edit]

Fertilizer

[edit]

Ammonium nitrate is an important fertilizer withNPK rating 34-0-0 (34% nitrogen).[17] Whilst less concentrated thanurea (46-0-0), ammonium nitrate is more stable and does not rapidly lose nitrogen to the atmosphere.

Explosives

[edit]
See also:List of ammonium nitrate disasters

Ammonium nitrate readily forms explosive mixtures with varying properties when combined with explosives such as TNT or with fuels likealuminium powder or fuel oil. Examples of explosives containing ammonium nitrate include:

Mixture with fuel oil

[edit]
Main article:ANFO

ANFO is a mixture of 94% ammonium nitrate ("AN") and 6%fuel oil ("FO") widely used as a bulk industrialexplosive.[18]: 1  It is used incoal mining,quarrying, metalmining, and civil construction in undemanding applications where the advantages of ANFO's low cost, relative safety, and ease of use matter more than the benefits offered by conventional industrial explosives, such as water resistance,oxygen balance, high detonation velocity, and performance in small diameters.[18]: 2 

Terrorism

[edit]

Ammonium nitrate-based explosives were used in theSterling Hall bombing in Madison, Wisconsin, 1970, theOklahoma City bombing in 1995, the2011 Delhi bombings, the2011 bombing in Oslo, theMyyrmanni bombing and the2013 Hyderabad blasts.

In November 2009, the government of theKPK (previously termed as NWFP) ofPakistan imposed a ban onammonium sulfate, ammonium nitrate, andcalcium ammonium nitrate fertilizers in the formerMalakand Division – comprising theUpper Dir,Lower Dir,Swat,Chitral, andMalakand districts of the NWFP – following reports that those chemicals were used by militants to make explosives. Due to these bans, "Potassium chlorate – the material which allowssafety matches to catch fire – has surpassed fertilizer as the explosive of choice for insurgents."[19]

On 14 Nov 2025, 2500 kg Ammonium Nitrate captured from white collar Doctor's Terrorists Network was exploded in Nogaon Police Station in Jammu Kashmir state of India, killing 12 officials[20].

Niche uses

[edit]

Ammonium nitrate is used in someinstant cold packs, as its dissolution in water is highlyendothermic. In 2021,King Abdullah University of Science and Technology in Saudi Arabia conducted experiments to study the potential for dissolving ammonium nitrate in water foroff-grid cooling systems and as a refrigerant. They suggested that the water could be distilled and reused using solar energy to avoid water wastage in severe environments.[21]

It was once used, in combination with independently explosive "fuels" such asguanidine nitrate,[22][23] as a cheaper (but less stable) alternative to5-aminotetrazole in the inflators ofairbags manufactured byTakata Corporation, which were recalled as unsafe after killing 14 people.[24] The current USA death total is 27.[25]

Safety, handling, and storage

[edit]

Numerous safety guidelines are available for storing and handling ammonium nitrate. Health and safety data are shown on thesafety data sheets available from suppliers and from various governments.[26][27][28]

Pure ammonium nitrate does not burn, but as a strong oxidizer, it supports and accelerates the combustion of organic (and some inorganic) material.[26][29][30] It should not be stored near combustible substances.

While ammonium nitrate is stable at ambient temperature and pressure under many conditions, it may detonate from a strong initiation charge. It should not be stored near high explosives or blasting agents.

Molten ammonium nitrate is very sensitive to shock and detonation, particularly if it becomes contaminated with incompatible materials such as combustibles, flammable liquids, acids, chlorates, chlorides, sulfur, metals, charcoal and sawdust.[31][26]

Contact with certain substances such aschlorates,mineral acids andmetal sulfides, can lead to vigorous or even violent decomposition capable of igniting nearby combustible material or detonating.[32][33]

Ammonium nitrate begins decomposition after melting, releasingNOx,HNO3,NH
3
andH2O. It should not be heated in a confined space.[26] The resulting heat and pressure from decomposition increases the sensitivity to detonation and increases the speed of decomposition. Detonation may occur at 80atmospheres. Contamination can reduce this to 20 atmospheres.[31]

Ammonium nitrate has acritical relative humidity of 59.4% at 30 °C. At higher humidity it will absorb moisture from the atmosphere. Therefore, it is important to store ammonium nitrate in a tightly sealed container. Otherwise, it can coalesce into a large, solid mass. Ammonium nitrate can absorb enough moisture to liquefy. Blending ammonium nitrate with certain other fertilizers can lower the critical relative humidity.[34]

The potential for use of the material as an explosive has prompted regulatory measures. For example, in Australia, the Dangerous Goods Regulations came into effect in August 2005 to enforce licensing in dealing with such substances.[35] Licenses are granted only to applicants (industry) with appropriate security measures in place to prevent any misuse.[36] Additional uses such as education and research purposes may also be considered, but individual use will not. Employees of those with licenses to deal with the substance are still required to be supervised by authorized personnel and are required to pass a security and national police check before a license may be granted.

Health hazards

[edit]

Ammonium nitrate is not hazardous to health and is usually used in fertilizer products.[37][38][39]

Ammonium nitrate has anLD50 of 2217 mg/kg,[40] which for comparison is about two-thirds that oftable salt.

Disasters

[edit]
Main article:List of ammonium nitrate disasters

Ammonium nitrate decomposes, non-explosively, into thegasesnitrous oxide andwater vapor when heated. However, it can be induced to decompose explosively bydetonation.[41] Large stockpiles of the material can also be a major fire risk due to their supportingoxidation, a situation which can easily escalate to detonation. Explosions are not uncommon: relatively minor incidents occur most years, and several large and devastating explosions have also occurred. Examples include theOppau explosion of 1921 (one of thelargest artificial non-nuclear explosions), theTexas City disaster of 1947, the2015 Tianjin explosions in China, and the2020 Beirut explosion.[42]

Ammonium nitrate can explode through two mechanisms:

See also

[edit]

References

[edit]
  1. ^Pradyot Patnaik.Handbook of Inorganic Chemicals. McGraw-Hill, 2002,ISBN 0-07-049439-8
  2. ^Kaniewski, Maciej; Huculak-Mączka, Marta; Zieliński, Jakub; Biegun, Marcin; Hoffmann, Krystyna; Hoffmann, Józef (2021)."Crystalline Phase Transitions and Reactivity of Ammonium Nitrate in Systems Containing Selected Carbonate Salts".Crystals.11 (10): 1250.Bibcode:2021Cryst..11.1250K.doi:10.3390/cryst11101250.ISSN 2073-4352.
  3. ^Martel, B.; Cassidy, K. (2004).Chemical Risk Analysis: A Practical Handbook. Butterworth–Heinemann. p. 362.ISBN 1-903996-65-1.
  4. ^"Hazard Rating Information for NFPA Fire Diamonds". Archived fromthe original on 17 February 2015. Retrieved13 March 2015.
  5. ^Zapp, Karl-Heinz (2012). "Ammonium Compounds".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a02_243.ISBN 9783527303854.
  6. ^abAmmonium nitrate sold by ton as U.S. regulation is stymied.Archived 28 February 2018 at theWayback MachineThe Dallas Morning News
  7. ^ab"Ammonium nitrate production by country, 2023 - knoema.com".Knoema.
  8. ^"Ammonium nitrate production by country, 2019".Knoema. Retrieved14 August 2020.
  9. ^"Gwihabaite".www.mindat.org.
  10. ^"Niter".www.mindat.org.
  11. ^"List of Minerals".www.ima-mineralogy.org. 21 March 2011.
  12. ^US 4927617, Villard, Alexandre & Cotonea, Yves, "Process of producing concentrated solutions of ammonium nitrate", published 22 May 1990, assigned to Societe Chimique des Charbonnages S.A. 
  13. ^Greenwood, Norman N.; Earnshaw, Alan (1997).Chemistry of the Elements (2nd ed.).Butterworth-Heinemann. p. 469.doi:10.1016/C2009-0-30414-6.ISBN 978-0-08-037941-8.
  14. ^ab"The chemistry behind the Beirut explosion".Chemical & Engineering News. 21 January 2025.
  15. ^Choi, C. S.; Prask, H. J. (1983)."The structure of ND4NO3 phase V by neutron powder diffraction".Acta Crystallographica B.39 (4):414–420.Bibcode:1983AcCrB..39..414C.doi:10.1107/S0108768183002669.
  16. ^Kumar, Pratim (December 2019)."Advances in phase stabilization techniques of AN using KDN and other chemical compounds for preparing green oxidizers".Defence Technology.15 (6):949–957.Bibcode:2019DeTe...15..949K.doi:10.1016/j.dt.2019.03.002.
  17. ^"Nutrient Content of Fertilizer Materials"(PDF). Archived fromthe original(PDF) on 24 December 2012. Retrieved27 June 2012.
  18. ^abCook, Melvin A. (1974).The Science of Industrial Explosives. IRECO Chemicals. p. 1.ASIN B0000EGDJT.
  19. ^Brook, Tom Vanden."Afghan bomb makers shifting to new explosives for IEDs".USA TODAY.
  20. ^https://www.hindustantimes.com/india-news/there-was-lot-of-smoke-and-dead-bodies-locals-recount-aftermath-of-accidental-explosion-in-nowgam-101763187975875.html
  21. ^Coxworth, Ben (20 September 2021)."Sunlight and salt water join forces in electricity-free cooling system".New Atlas. Gizmag Pty Ltd. Retrieved21 September 2021.
  22. ^US 5531941, Poole, Donald R., "Process for preparing azide-free gas generant composition", published 2 July 1996, assigned to Automotive Systems Laboratory 
  23. ^Airbag Compound Has Vexed Takata for YearsThe New York Times
  24. ^A Cheaper Airbag, and Takata's Road to a Deadly Crisis.The New York Times
  25. ^"Takata Spotlight".NHTSA.gov. Retrieved31 May 2024.
  26. ^abcdChemical Advisory: Safe Storage, Handling, and Management of Ammonium NitrateUnited States Environmental Protection Agency
  27. ^"Storing and handling ammonium nitrate"(PDF).Archived(PDF) from the original on 4 July 2011. Retrieved22 March 2006.
  28. ^"Ammonium nitrate MSDS". Archived fromthe original on 18 August 2011. Retrieved25 January 2012.
  29. ^Pradyot Patnaik (2002).Handbook of Inorganic Chemicals. McGraw-Hill.ISBN 0-07-049439-8.
  30. ^"Ammonium nitrate".PubChem. Retrieved6 August 2020.
  31. ^ab"Report for Kooragang Island Update PHA MOD1 Report".Orica Mining Services. 1 April 2012.Archived from the original on 12 August 2014. Retrieved6 August 2020.
  32. ^"Chemical Engineering Transactions"(PDF). Archived fromthe original(PDF) on 14 April 2016.
  33. ^"Ammonium Nitrate".webwiser.nlm.nih.gov. Archived fromthe original on 22 August 2020. Retrieved6 August 2020.
  34. ^Fertilizers Europe (2006)."Guidance for Compatibility of Fertilizer Blending Materials"(PDF).Archived(PDF) from the original on 8 June 2015.
  35. ^"Dangerous Goods (HCDG) Regulations"(PDF).Archived(PDF) from the original on 23 March 2012.
  36. ^Ammonium Nitrate-Regulating its use, Balancing Access & Protection from"Worksafe Victoria". Archived fromthe original on 11 March 2011.
  37. ^CF Industries."Ammonium nitrate MSDS"(PDF). Archived fromthe original(PDF) on 27 March 2014.
  38. ^"Chemicalland21 – Ammonium Nitrate". Archived fromthe original on 10 January 2012.
  39. ^"Ammonium Nitrate". Paton Fertilizers Pty Ltd. 2005.
  40. ^"Material Safety Data Sheet, Ammonium nitrate MSDS". Archived fromthe original on 18 August 2011. Retrieved25 January 2012.
  41. ^Chaturvedi, Shalini; Dave, Pragnesh N. (January 2013). "Review on Thermal Decomposition of Ammonium Nitrate".Journal of Energetic Materials.31 (1):1–26.Bibcode:2013JEnM...31....1C.doi:10.1080/07370652.2011.573523.S2CID 94427830.
  42. ^"Lebanon's president calls for two-week state of emergency in Beirut after blast".Reuters. Beirut. 4 August 2020. Retrieved4 August 2020.Aoun, in remarks published on the Presidency Twitter account, said it was "unacceptable" that 2,750 tonnes of ammonium nitrate was stored in a warehouse for six years without safety measures and vowed that those responsible would face the "harshest punishments".

Sources

[edit]
  • Properties: UNIDO and International Fertilizer Development Center (1998),Fertilizer Manual, Kluwer Academic Publishers,ISBN 0-7923-5032-4.

External links

[edit]
Ammonium salts
Inorganic salts
monatomic anions
oxyanions
other anions
Organic salts
Salts and covalent derivatives of thenitrate ion
HNO3He
LiNO3Be(NO3)2B(NO3)4RONO2
+CO3
+C2O4
NO3
NH4NO3
HOONO2FNO3
+F
Ne
NaNO3Mg(NO3)2Al(NO3)3
Al(NO3)4
SiP+SO4ClONO2
+Cl
Ar
KNO3Ca(NO3)2Sc(NO3)3Ti(NO3)4VO(NO3)3Cr(NO3)3Mn(NO3)2Fe(NO3)2
Fe(NO3)3
Co(NO3)2
Co(NO3)3
Ni(NO3)2CuNO3
Cu(NO3)2
Zn(NO3)2Ga(NO3)3GeAs+SeO3BrNO3
+Br
Kr
RbNO3Sr(NO3)2Y(NO3)3Zr(NO3)4NbO(NO3)3MoO2(NO3)2TcRu(NO3)3Rh(NO3)3Pd(NO3)2AgNO3Cd(NO3)2In(NO3)3Sn(NO3)4Sb4O4(OH)2(NO3)2TeINO3
+IO3
Xe(NO3)2
CsNO3Ba(NO3)2*Lu(NO3)3Hf(NO3)4TaO(NO3)3WO2(NO3)2ReO3NO3OsIr3O(NO3)10Pt(NO3)2
Pt(NO3)4
Au(NO3)4Hg2(NO3)2
Hg(NO3)2
TlNO3
Tl(NO3)3
Pb(NO3)2Bi(NO3)3
BiO(NO3)
Po(NO3)4AtRn
FrNO3Ra(NO3)2**LrRfDbSgBhHsMtDsRgCnNhFlMcLvTsOg
 
*La(NO3)3Ce(NO3)3
Ce(NO3)4
Pr(NO3)3Nd(NO3)3Pm(NO3)3Sm(NO3)3Eu(NO3)3Gd(NO3)3Tb(NO3)3Dy(NO3)3Ho(NO3)3Er(NO3)3Tm(NO3)3Yb(NO3)3
**Ac(NO3)3Th(NO3)4PaO(NO3)3U(NO3)4
UO2(NO3)2
Np(NO3)4
NpO(NO3)3
NpO2NO3
NpO2(NO3)2
Pu(NO3)3
Pu(NO3)4
PuO2(NO3)2
Am(NO3)3
AmO2(NO3)2
Cm(NO3)3Bk(NO3)3Cf(NO3)3Es(NO3)3FmMdNo
Nitrogen species
Hydrides
Organic
Oxides
Halides
Oxidation states
−3,−2,−1, 0,+1,+2,+3,+4,+5 (a stronglyacidic oxide)
National
Other
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