Ammonium nitrate

{{short description|Chemical compound with formula NH4NO3}}

{{Use dmy dates|date=August 2020}}

{{chembox

| Watchedfields = changed

| verifiedrevid = 476998591

| ImageFile = Ammonium-nitrate-2D.svg

| ImageAlt = Structural formula

| ImageName = Structural formula of ammonium cation (left) and nitrate anion (right)

| ImageFile1 = Ammonium-nitrate-xtal-3D-balls-A.png

| ImageAlt1 = Ammonium nitrate crystal structure

| ImageName1 = H=white, N=blue, O=red

| ImageFile2 = Ammonium_Nitrate.jpg

| ImageAlt2 = Sample of white powder and spherules

| IUPACName = Ammonium nitrate

|Section1={{Chembox Identifiers

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| ChemSpiderID = 21511

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = T8YA51M7Y6

| ChEBI = 63038

| ChEMBL = 1500032

| InChI = 1/NO3.H3N/c2-1(3)4;/h;1H3/q-1;/p+1

| InChIKey = DVARTQFDIMZBAA-IKLDFBCSAH

| SMILES = [O-][N+]([O-])=O.[NH4+]

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChI = 1S/NO3.H3N/c2-1(3)4;/h;1H3/q-1;/p+1

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = DVARTQFDIMZBAA-UHFFFAOYSA-O

| CASNo = 6484-52-2

| CASNo_Ref = {{cascite|correct|CAS}}

| UNNumber = 0222with > 0.2% combustible substances
1942with ≤ 0.2% combustible substances
2067fertilizers
2426liquid

| RTECS = BR9050000

| PubChem = 22985

| EC_number = 229-347-8

}}

|Section2={{Chembox Properties

| Formula = NH4NO3

| MolarMass = 80.043 g/mol

| Appearance = white crystalline solid

| Density = 1.725 g/cm3 (20 °C)

| Solubility = 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)Pradyot Patnaik. Handbook of Inorganic Chemicals. McGraw-Hill, 2002, {{ISBN|0-07-049439-8}}

| MeltingPtC = 169.6

| MeltingPt_notes =

| BoilingPt = approx.

| BoilingPtC = 210

|BoilingPt_notes = decomposes

| MagSus = {{val|-33.6e-6|u=cm3/mol}}

}}

|Section3={{Chembox Structure

| Coordination =

| CrystalStruct = orthorhombic{{Cite journal |last1=Kaniewski |first1=Maciej |last2=Huculak-Mączka |first2=Marta |last3=Zieliński |first3=Jakub |last4=Biegun |first4=Marcin |last5=Hoffmann |first5=Krystyna |last6=Hoffmann |first6=Józef |date=2021 |title=Crystalline Phase Transitions and Reactivity of Ammonium Nitrate in Systems Containing Selected Carbonate Salts |journal=Crystals |language=en |volume=11 |issue=10 |pages=1250 |doi=10.3390/cryst11101250 |doi-access=free |bibcode=2021Cryst..11.1250K |issn=2073-4352}}

}}

|Section6={{Chembox Explosive

| ShockSens = very low

| FrictionSens = very low

| DetonationV = 2500 m/s

| REFactor = }}

|Section7={{Chembox Hazards

| GHSPictograms = {{GHS07}} {{GHS03}} {{GHS01}}

| GHSSignalWord = Danger

| HPhrases = {{H-phrases|201|271|319}}

| PPhrases = {{P-phrases|220|221|271|280|264|372}}

| MainHazards = Explosive, Oxidizer

| NFPA-H = 1

| NFPA-F = 0

| NFPA-R = 3

| NFPA-S = OX

| LD50 = 2085–5300 mg/kg (oral in rats, mice){{cite book |author1=Martel, B. |author2=Cassidy, K. |title=Chemical Risk Analysis: A Practical Handbook |publisher=Butterworth–Heinemann |year=2004 |page=362 |isbn=1-903996-65-1}}

}}{{cite web|url=http://www.ehs.neu.edu/laboratory_safety/general_information/nfpa_hazard_rating/documents/NFPAratingAC.htm |title=Hazard Rating Information for NFPA Fire Diamonds |access-date=13 March 2015 |url-status=dead |archive-url=https://web.archive.org/web/20150217114736/http://www.ehs.neu.edu/laboratory_safety/general_information/nfpa_hazard_rating/documents/NFPAratingAC.htm |archive-date=17 February 2015 }}

|Section8={{Chembox Related

| OtherAnions = Ammonium nitrite

| OtherCations = Sodium nitrate
Potassium nitrate
Hydroxylammonium nitrate

| OtherCompounds = Ammonium perchlorate

}}

}}

Ammonium nitrate is a chemical compound with the formula {{Chem2|NH4NO3}}. It is a white crystalline salt consisting of ions of ammonium and nitrate. It is highly soluble in water and hygroscopic as a solid, but does not form hydrates. It is predominantly used in agriculture as a high-nitrogen fertilizer.{{cite encyclopedia|first=Karl-Heinz |last=Zapp |title=Ammonium Compounds |encyclopedia=Ullmann's Encyclopedia of Industrial Chemistry |year=2012 |publisher=Wiley-VCH |location=Weinheim |doi=10.1002/14356007.a02_243|isbn=9783527303854 }}

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

Many countries are phasing out its use in consumer applications due to concerns over its potential for misuse.[https://www.dallasnews.com/news/news/2013/10/05/ammonium-nitrate-sold-by-ton-as-u.s.-regulation-is-stymied Ammonium nitrate sold by ton as U.S. regulation is stymied.] {{Webarchive|url=https://web.archive.org/web/20180228041244/https://www.dallasnews.com/news/news/2013/10/05/ammonium-nitrate-sold-by-ton-as-u.s.-regulation-is-stymied |date=28 February 2018 }} – The Dallas Morning News Accidental ammonium nitrate explosions have killed thousands of people since the early 20th century.{{Cite web|url=https://knoema.com//atlas/topics/Agriculture/Fertilizers-Production-Quantity-in-Nutrients/Ammonium-nitrate-production|title=Ammonium nitrate production by country, 2023 - knoema.com|website=Knoema}} Global production was estimated at 21.6 million tonnes in 2017.{{cite web|title=Ammonium nitrate production by country, 2019|url=https://knoema.com//atlas/topics/Agriculture/Fertilizers-Production-Quantity-in-Nutrients/Ammonium-nitrate-production|access-date=2020-08-14|website=Knoema|language=en-US}} By 2021, global production of ammonium nitrate was down to 16.7 million tonnes.

Occurrence

Ammonium nitrate is found as the natural mineral gwihabaite (formerly known as nitrammite){{cite web|url=https://www.mindat.org/min-6983.html|title=Gwihabaite|website=www.mindat.org}} – the ammonium analogue of saltpetre (mineralogical name: niter){{cite web|url=https://www.mindat.org/min-2917.html|title=Niter|website=www.mindat.org}}{{cite web|url=https://www.ima-mineralogy.org/Minlist.htm|title=List of Minerals|date=21 March 2011|website=www.ima-mineralogy.org}} – in the driest regions of the Atacama Desert in Chile, often as a crust on the ground or in conjunction with other nitrate, iodate, and halide minerals. Ammonium nitrate was mined there until the Haber–Bosch process made it possible to synthesize nitrates from atmospheric nitrogen, rendering nitrate mining obsolete.

Production, reactions and crystalline phases

The industrial production of ammonium nitrate entails the acid-base reaction of ammonia with nitric acid:{{cite patent |country=US|number=4927617|title=Process of producing concentrated solutions of ammonium nitrate|pubdate=1990-05-22|inventor1-last=Villard|inventor2-first=Yves|inventor2-last=Cotonea|inventor1-first=Alexandre|assign= Societe Chimique des Charbonnages S.A.}}

:HNO3 + NH3 → NH4NO3

The ammonia required for this process is obtained by the Haber process from nitrogen and hydrogen. Ammonia produced by the Haber process can be oxidized to nitric acid by the Ostwald process. Ammonia is used in its anhydrous form (a gas) and the nitric acid is concentrated. The reaction is violent owing to its highly exothermic 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 a spray 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 the nitrophosphate 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 as calcium ammonium nitrate.

Ammonium nitrate can also be made via metathesis reactions:

:(NH4)2SO4 + Ba(NO3)2 → 2 NH4NO3 + BaSO4

:(NH4)2SO4 + Ca(NO3)2 → 2 NH4NO3 + CaSO4

:NH4Cl + AgNO3 → NH4NO3 + AgCl

=Reactions=

As ammonium nitrate is a salt, both the cation, {{chem2|NH4+}}, and the anion, {{chem2|NO3-}}, may take part in chemical reactions.

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

: NH4NO3 → N2O + 2 H2O

At higher temperatures, the following reaction predominates.{{Greenwood&Earnshaw2nd|page=469}}

: 2 NH4NO3 → 2 N2 + O2 + 4 H2O

Both decomposition reactions are exothermic and their products are gases. Under certain conditions, this can lead to a runaway reaction, with the decomposition process becoming explosive. See {{section link||Disasters}} for details. Many ammonium nitrate disasters, with loss of lives, have occurred.

The red–orange colour in an explosion cloud is due to nitrogen dioxide, a secondary reaction product.{{Cite web|url=https://cen.acs.org/safety/industrial-safety/chemistry-behind-Beirut-explosion/98/web/2020/08|title=The chemistry behind the Beirut explosion|website=Chemical & Engineering News}}

=Crystalline phases=

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

:

class="wikitable"
Phase

! Temperature (°C)

! Symmetry

(liquid)

| (above 169.6)

|

I

| 169.6 to 125.2

| cubic

II

| 125.2 to 84.2

| tetragonal

III

| 84.2 to 32.3

| α-rhombic

IV

| 32.3 to −16.8

| β-rhombic

V

| below −16.8

| tetragonal{{cite journal |first1=C. S. |last1=Choi |first2=H. J. |last2=Prask |title=The structure of ND4NO3 phase V by neutron powder diffraction |journal=Acta Crystallographica B |year=1983 |volume=39 |issue=4 |pages=414–420 |doi=10.1107/S0108768183002669 |doi-access=free |bibcode=1983AcCrB..39..414C }}

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 a solid 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.{{cite journal |last1=Kumar |first1=Pratim |title=Advances in phase stabilization techniques of AN using KDN and other chemical compounds for preparing green oxidizers |journal=Defence Technology |date=December 2019 |volume=15 |issue=6 |pages=949–957 |doi=10.1016/j.dt.2019.03.002|doi-access=free |bibcode=2019DeTe...15..949K }}

Applications

=Fertilizer=

Ammonium nitrate is an important fertilizer with NPK rating 34-0-0 (34% nitrogen).{{cite web |url=http://www.caes.uga.edu/commodities/fieldcrops/forages/events/SHC12/03%20Fertilization%20Outlook%20for%20Hay%20Producers/Nutrient%20Content%20of%20Fertilizer%20Materials.pdf |title=Nutrient Content of Fertilizer Materials |access-date=27 June 2012 |archive-url=https://web.archive.org/web/20121224131002/http://www.caes.uga.edu/commodities/fieldcrops/forages/events/SHC12/03%20Fertilization%20Outlook%20for%20Hay%20Producers/Nutrient%20Content%20of%20Fertilizer%20Materials.pdf |archive-date=24 December 2012 |url-status=dead }} It is less concentrated than urea (46-0-0), giving ammonium nitrate a slight transportation disadvantage. Ammonium nitrate's advantage over urea is that it is more stable and does not rapidly lose nitrogen to the atmosphere.

=Explosives=

{{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 like aluminium powder or fuel oil.

Examples of explosives containing ammonium nitrate include:

==Mixture with fuel oil==

{{main|ANFO}}

ANFO is a mixture of 94% ammonium nitrate ("AN") and 6% fuel oil ("FO") widely used as a bulk industrial explosive.{{cite book |last=Cook |first=Melvin A. |title=The Science of Industrial Explosives |publisher=IRECO Chemicals |year=1974 |page=1 |asin=B0000EGDJT}}{{rp|1}} It is used in coal mining, quarrying, metal mining, 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.{{rp|2}}

==Terrorism==

Ammonium nitrate-based explosives were used in the Sterling Hall bombing in Madison, Wisconsin, 1970, the Oklahoma City bombing in 1995, the 2011 Delhi bombings, the 2011 bombing in Oslo, the Myyrmanni bombing and the 2013 Hyderabad blasts.

In November 2009, the government of the KPK (previously termed as NWFP) of Pakistan imposed a ban on ammonium sulfate, ammonium nitrate, and calcium ammonium nitrate fertilizers in the former Malakand Division{{Snd}}comprising the Upper Dir, Lower Dir, Swat, Chitral, and Malakand districts of the NWFP – following reports that those chemicals were used by militants to make explosives. Due to these bans, "Potassium chlorate{{Snd}}the material which allows safety matches to catch fire{{Snd}}has surpassed fertilizer as the explosive of choice for insurgents."{{cite web|url=https://www.usatoday.com/story/news/world/2013/06/25/ammonium-nitrate-potassium-chlorate-ieds-afghanistan/2442191/|title=Afghan bomb makers shifting to new explosives for IEDs|first=Tom Vanden|last=Brook|website=USA TODAY}}

=Niche uses=

Ammonium nitrate is used in some instant cold packs, as its dissolution in water is highly endothermic. In 2021, King Abdullah University of Science and Technology in Saudi Arabia conducted experiments to study the potential for dissolving ammonium nitrate in water for off-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.{{cite news |last1=Coxworth |first1=Ben |title=Sunlight and salt water join forces in electricity-free cooling system |url=https://newatlas.com/good-thinking/sunlight-salt-water-electricity-free-cooling-system/ |access-date=21 September 2021 |work=New Atlas |publisher=Gizmag Pty Ltd. |date=20 September 2021}}

It was once used, in combination with independently explosive "fuels" such as guanidine nitrate,{{cite patent|country=US|number=5531941|title=Process for preparing azide-free gas generant composition|inventor1-last=Poole|inventor1-first=Donald R.|assign= Automotive Systems Laboratory|pubdate=1996-07-02}}[https://www.nytimes.com/2014/12/10/business/compound-in-takata-airbags-is-inquirys-focus.html Airbag Compound Has Vexed Takata for Years] – The New York Times as a cheaper (but less stable) alternative to 5-aminotetrazole in the inflators of airbags manufactured by Takata Corporation, which were recalled as unsafe after killing 14 people.[https://www.nytimes.com/2016/08/27/business/takata-airbag-recall-crisis.html?hpw&rref=automobiles&action=click&pgtype=Homepage&module=well-region®ion=bottom-well&WT.nav=bottom-well A Cheaper Airbag, and Takata's Road to a Deadly Crisis.] – The New York Times The current USA death total is 27.{{cite web |title=Takata Spotlight |url=https://www.nhtsa.gov/vehicle-safety/takata-recall-spotlight |website=NHTSA.gov |access-date=31 May 2024}}

Safety, handling, and storage

Numerous safety guidelines are available for storing and handling ammonium nitrate. Health and safety data are shown on the safety data sheets available from suppliers and from various governments.[https://purl.fdlp.gov/GPO/gpo45474 Chemical Advisory: Safe Storage, Handling, and Management of Ammonium Nitrate] United States Environmental Protection Agency{{cite web|url=http://www.hse.gov.uk/pubns/indg230.pdf|title=Storing and handling ammonium nitrate|access-date=22 March 2006|archive-url=https://web.archive.org/web/20110704142701/http://www.hse.gov.uk/pubns/indg230.pdf|archive-date=4 July 2011|url-status=live}}{{cite web|url=http://www.sciencelab.com/msds.php?msdsId=9927336|title=Ammonium nitrate MSDS|access-date=25 January 2012|archive-date=18 August 2011|archive-url=https://web.archive.org/web/20110818021106/http://www.sciencelab.com/msds.php?msdsId=9927336|url-status=dead}}

Pure ammonium nitrate does not burn, but as a strong oxidizer, it supports and accelerates the combustion of organic (and some inorganic) material.{{cite book| author= Pradyot Patnaik| title= Handbook of Inorganic Chemicals| publisher= McGraw-Hill| year= 2002| isbn= 0-07-049439-8}}{{cite web|title=Ammonium nitrate|url=https://pubchem.ncbi.nlm.nih.gov/compound/Ammonium-nitrate|access-date=2020-08-06|website=PubChem}} 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.{{cite web|date=2012-04-01|title=Report for Kooragang Island Update PHA MOD1 Report|url=http://www.orica.com/ArticleDocuments/493/2012_Orica-KI_revised_PHA.pdf.aspx |archive-url=https://web.archive.org/web/20140812063130/http://www.orica.com/ArticleDocuments/493/2012_Orica-KI_revised_PHA.pdf.aspx |archive-date=2014-08-12 |url-status=live|access-date=2020-08-06|website=Orica Mining Services}}

Contact with certain substances such as chlorates, mineral acids and metal sulfides, can lead to vigorous or even violent decomposition capable of igniting nearby combustible material or detonating.{{cite web|url=http://www.aidic.it/lp2013/webpapers/141cagnina.pdf|archive-url=https://web.archive.org/web/20160414164158/http://www.aidic.it/lp2013/webpapers/141cagnina.pdf|url-status=dead|title=Chemical Engineering Transactions|archive-date=14 April 2016}}{{cite web|title=Ammonium Nitrate|url=https://webwiser.nlm.nih.gov/substance?substanceId=453&identifier=Ammonium%20Nitrate&identifierType=name&menuItemId=7&catId=64|access-date=2020-08-06|website=webwiser.nlm.nih.gov|language=en}}

Ammonium nitrate begins decomposition after melting, releasing {{NOx}}, HNO3, Ammonia and H2O. It should not be heated in a confined space. The resulting heat and pressure from decomposition increases the sensitivity to detonation and increases the speed of decomposition. Detonation may occur at 80 atmospheres. Contamination can reduce this to 20 atmospheres.

Ammonium nitrate has a critical 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.{{cite web

| url= http://www.productstewardship.eu/fileadmin/user_upload/user_upload_prodstew/documents/Guidance_for_compatibility2.pdf |archive-url=https://web.archive.org/web/20150608193905/http://www.productstewardship.eu/fileadmin/user_upload/user_upload_prodstew/documents/Guidance_for_compatibility2.pdf |archive-date=2015-06-08 |url-status=live

| title=Guidance for Compatibility of Fertilizer Blending Materials

| author= Fertilizers Europe

| date= 2006

}}

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.{{cite web|url=http://www.legislation.nsw.gov.au/sessionalview/sessional/subordleg/2005-531.pdf |archive-url=https://web.archive.org/web/20120323124216/http://www.legislation.nsw.gov.au/sessionalview/sessional/subordleg/2005-531.pdf |archive-date=2012-03-23 |url-status=live|title=Dangerous Goods (HCDG) Regulations}} Licenses are granted only to applicants (industry) with appropriate security measures in place to prevent any misuse.Ammonium Nitrate-Regulating its use, Balancing Access & Protection from {{cite web| url= http://www.worksafe.vic.gov.au/wps/wcm/connect/wsinternet/worksafe/home/forms+and+publications/publications/import_ammonium+nitrate+-+regulating+its+use%2C+balancing+access+_+protection| archive-url= https://web.archive.org/web/20110311054639/http://www.worksafe.vic.gov.au/wps/wcm/connect/wsinternet/worksafe/home/forms+and+publications/publications/import_ammonium+nitrate+-+regulating+its+use%2C+balancing+access+_+protection| url-status= dead| archive-date= 11 March 2011| title= Worksafe Victoria}} 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

Ammonium nitrate is not hazardous to health and is usually used in fertilizer products.{{cite web| url =http://www.cfindustries.com/pdf/Ammonium-Nitrate-Amtrate-MSDS.pdf| title =Ammonium nitrate MSDS| author =CF Industries| url-status =dead| archive-url =https://web.archive.org/web/20140327104129/http://www.cfindustries.com/pdf/Ammonium-Nitrate-Amtrate-MSDS.pdf| archive-date =27 March 2014}}{{cite web|url=http://chemicalland21.com/industrialchem/inorganic/ammonium%20nitrate.htm|title=Chemicalland21 – Ammonium Nitrate|url-status=dead|archive-url=https://web.archive.org/web/20120110035253/http://chemicalland21.com/industrialchem/inorganic/ammonium%20nitrate.htm|archive-date=10 January 2012}}{{cite news| title= Ammonium Nitrate| publisher= Paton Fertilizers Pty Ltd | year= 2005}}

Ammonium nitrate has an LD50 of 2217 mg/kg,{{cite web|url=http://www.sciencelab.com/msds.php?msdsId=9927336|title=Material Safety Data Sheet, Ammonium nitrate MSDS|access-date=25 January 2012|archive-date=18 August 2011|archive-url=https://web.archive.org/web/20110818021106/http://www.sciencelab.com/msds.php?msdsId=9927336|url-status=dead}} which for comparison is about two-thirds that of table salt.

Disasters

{{main|List of ammonium nitrate disasters}}

Ammonium nitrate decomposes, non-explosively, into the gases nitrous oxide and water vapor when heated. However, it can be induced to decompose explosively by detonation.{{cite journal |last1=Chaturvedi |first1=Shalini |last2=Dave |first2=Pragnesh N. |title=Review on Thermal Decomposition of Ammonium Nitrate |journal=Journal of Energetic Materials |date=January 2013 |volume=31 |issue=1 |pages=1–26 |doi=10.1080/07370652.2011.573523|bibcode=2013JEnM...31....1C |s2cid=94427830 }} Large stockpiles of the material can also be a major fire risk due to their supporting oxidation, 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 the Oppau explosion of 1921 (one of the largest artificial non-nuclear explosions), the Texas City disaster of 1947, the 2015 Tianjin explosions in China, and the 2020 Beirut explosion.{{cite news|date=4 August 2020|title=Lebanon's president calls for two-week state of emergency in Beirut after blast|language=en|work=Reuters|location=Beirut|url=https://www.reuters.com/article/us-lebanon-security-blast-president-idUSKCN2502TZ|access-date=4 August 2020|quote=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".}}

Ammonium nitrate can explode through two mechanisms:

See also

References

{{Reflist}}

=Sources=

{{refbegin}}

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

{{refend}}