Mercury(II) fulminate: Difference between revisions

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| IUPACName = Mercury(II) fulminate
| IUPACName = Mercury(II) fulminate
|SystematicName=Dioxycyanomercury
|SystematicName=Dioxycyanomercury
| OtherNames = Fulminated Mercury
| OtherNames = {{ubl
|Fulminated Mercury
|Bis(fulminato-kappaC)mercury
|Knallquecksilber (German)
|bis[(oxidoazanylidyne)methyl]mercury
}}
|Section1={{Chembox Identifiers
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
Line 29: Line 34:
}}
}}
|Section2={{Chembox Properties
|Section2={{Chembox Properties
| Formula = C<sub>2</sub>N<sub>2</sub>O<sub>2</sub>Hg
| Formula = {{chem2|Hg(CNO)2}}
| MolarMass = 284.624 g/mol
| C=2 |Hg=1 |N=2 |O=2
| Appearance = Grey, pale brown, or white crystalline solid
| Appearance = Grey, pale brown, or white crystalline solid
| Density = 4.42 g/cm<sup>3</sup>
| Density = {{val|4.42|u=g/cm3}}
| MeltingPtC = 160
| MeltingPtC = 160
| BoilingPtC = 356.6
| BoilingPtC = 356.6
| Solubility = slightly soluble
| Solubility = slightly soluble
| SolubleOther = soluble in [[ethanol]], [[ammonia]]
| Solubility1=soluble
| Solvent1=ethanol
| Solubility2=soluble
| Solvent2=ammonia
   }}
   }}
|Section3={{Chembox Explosive
|Section3={{Chembox Explosive
| Explosive_ref = <ref name="EncycExplosives">{{cite book |last1=Fedoroff |first1=Basil T. |last2=Sheffield |first2=Oliver E. |title=Encyclopedia of Explosives and Related Items |date=1 January 1974 |publisher=Picatinny Arsenal |location=Dover, NJ |pages=F220-221 |url=https://apps.dtic.mil/sti/pdfs/ADA011845.pdf |volume=6 |id=ADA011845, PATR2700 |access-date=5 November 2025 |chapter=F}}</ref>
| ShockSens = High
| ShockSens = High
| FrictionSens = High
{{ubl
| DetonationV = 4250 m/s
|{{val|5|u=cm}} ({{val|2|u=kg}} weight, {{val|20|u=mg}}, Bureau of Mines apparatus)
| REFactor =  
|{{val|4|u=in}} ({{val|1|u=lb}} weight, {{val|30|u=mg}}, Picatinny Arsenal apparatus)
}}
| FrictionSens = High (explodes with fiber & steel shoe tests)
| DetonationV = {{ubl
|{{val|3500|u=m/s}} (density = 2.0)
|{{val|4250|u=m/s}} (density = 3.0)
|{{val|5000|u=m/s}} (density = 4.0)
}}
| REFactor = {{val|37|to|50|u=%}} (Trauzl lead block)
}}
}}
|Section4={{Chembox Hazards
|Section4={{Chembox Hazards
| MainHazards = Highly toxic, shock sensitive explosive
| Hazards_ref = <ref>{{PubChem|11022444|Mercury(II) fulminate}}</ref>
| GHSPictograms = {{GHS01}}{{GHS06}}{{GHS08}}{{GHS09}}
| GHSSignalWord = Danger
| HPhrases = {{H-phrases|200|301|311|331|373|410}}
| PPhrases = {{P-phrases|201|202|260|261|262|264|270|271|273|280|281|301+316|302+352|304+340|316|319|321|330|361+364|372|373|380|391|401|403+233|405|501}}
| NFPA-H = 4
| NFPA-H = 4
| NFPA-F = 1
| NFPA-F = 1
Line 51: Line 72:
| AutoignitionPtC = 170
| AutoignitionPtC = 170
| AutoignitionPt_notes =  
| AutoignitionPt_notes =  
| TLV={{val|0.02|u=mg/m3}}
| TLV-TWA={{val|0.01|u=mg/m3}}
| TLV-STEL={{val|0.03|u=mg/m3}} (skin, 15 minute)
| PEL={{ubl
|{{val|0.01|u=mg/m3}} (TWA, 8h)
|{{val|0.04|u=mg/m3}} (ceiling)
}}
| REL={{ubl
|{{val|0.01|u=mg/m3}} (TWA, skin)
|{{val|0.03|u=mg/m3}} (STEL, skin)
}}
| IDLH={{val|2|u=mg/m3}} (as Hg)
| NIOSH_id=0384
   }}
   }}
|Section5={{Chembox Related
| Related_ref =
| OtherAnions = {{ubl
|[[Mercury(II) cyanide]]
|[[Mercury(II) thiocyanate]]
}}
| OtherCations = {{ubl
|[[Potassium fulminate]]
|[[Silver fulminate]]
}}
| OtherFunction =
| OtherFunction_label =
| OtherCompounds =
}}
}}
}}


'''Mercury(II) fulminate''', or '''Hg(CNO)<sub>2</sub>''', is a [[primary explosive]]. It is highly sensitive to [[friction]], heat and [[shock (mechanics)|shock]] and is mainly used as a trigger for other explosives in [[percussion cap]]s and [[detonator]]s. Mercury(II) cyanate, though its chemical formula is identical, has a different atomic arrangement, making the [[cyanate]] and [[fulminate]] [[Ion#Anions and cations|anionic]] [[isomer]]s.
'''Mercury(II) fulminate''' is a [[primary explosive]] with the chemical formula {{chem2|Hg(CNO)2}}. When recrystallized from water it exists as the [[hemihydrate]] {{chem2|2 Hg(CNO)2*H2O}}. The anyhydrous form is obtained by recrystallization from ethanol.<ref name="EncycExplosives"/>{{rp|F217}} It is highly sensitive to [[friction]], heat and [[shock (mechanics)|shock]] and is mainly used as a trigger for other explosives in [[percussion cap]]s and [[detonator]]s. Mercury(II) cyanate, though its chemical formula is identical, has a different atomic arrangement, making the [[cyanate]] and [[fulminate]] [[Ion#Anions and cations|anionic]] [[isomer]]s.


First used as a [[priming composition]] in small copper caps beginning in the 1820s, mercury fulminate quickly replaced [[flint]]s as a means to ignite [[black powder]] charges in [[Muzzleloader|muzzle-loading]] [[firearm]]s. Later, during the late 19th century and most of the 20th century, mercury fulminate  became widely used in [[Primer (firearms)|primers]] for [[Cartridge (firearms)|self-contained rifle and pistol ammunition]]; it was the only practical detonator for firing projectiles until the early 20th century.<ref name=wisniak/> Mercury fulminate has the distinct advantage over [[potassium chlorate]] of being non-corrosive, but it is known to weaken with time, by decomposing into its constituent elements. The reduced mercury which results forms amalgams with cartridge brass, weakening it, as well. Today, mercury fulminate has been replaced in primers by more efficient chemical substances. These are non-corrosive, less toxic, and more stable over time; they include [[lead azide]], [[lead styphnate]], and [[Tetrazene explosive|tetrazene]] derivatives. In addition, none of these compounds requires [[Mercury (element)|mercury]] for manufacture, supplies of which can be unreliable in wartime.
First used as a [[priming composition]] in small copper caps beginning in the 1820s, mercury fulminate quickly replaced [[flint]]s as a means to ignite [[black powder]] charges in [[Muzzleloader|muzzle-loading]] [[firearm]]s. Later, during the late 19th century and most of the 20th century, mercury fulminate  became widely used in [[Primer (firearms)|primers]] for [[Cartridge (firearms)|self-contained rifle and pistol ammunition]]; it was the only practical detonator for firing projectiles until the early 20th century.<ref name=wisniak/>  
 
Mercury fulminate has the distinct advantage over [[potassium chlorate]] of being non-corrosive, but it is known to attack aluminum and magnesium strongly, and brass, bronze, copper, and zinc slowly when dry; when wet it immediately reacts with aluminum and magnesium and strongly attacks brass, bronze, copper and zinc when.<ref name="EncycExplosives"/> Today, mercury fulminate has been replaced in primers by more efficient chemical substances. These are non-corrosive, less toxic, and more stable over time; they include [[lead azide]], [[lead styphnate]], and [[Tetrazene explosive|tetrazene]] derivatives. In addition, none of these compounds requires mercury for manufacture, supplies of which can be unreliable in wartime.<ref name="Weingart">{{cite book |last1=Weingart |first1=George W. |title=Pyrotechnics |pages=10 |edition=2nd |url=https://archive.org/details/Pyrotechnics_by_G._Weingart_2nd_ed._Corrected/page/n23/mode/2up |access-date=5 November 2025 |date=1947 |quote=Calomel [Hg<sub>2</sub>Cl<sub>2</sub>] is made in this country and sold in normal times at about 65 cents a pound, but due to the scarcity of mercury and the great demand for it in the manufacture of detonating caps the price has recently advanced to several dollars per pound.}}</ref> 


==Preparation==
==Preparation==
Mercury(II) fulminate is prepared by dissolving [[mercury (element)|mercury]] in [[nitric acid]] and adding [[ethanol]] to the solution. [[Edward Charles Howard]] is credited with first preparing it in 1800.<ref>{{cite journal
Mercury(II) fulminate is prepared by dissolving mercury in [[nitric acid]] and adding [[ethanol]] to the solution. [[Edward Charles Howard]] is credited with first preparing it in 1800.<ref>{{cite journal |title=On a New Fulminating Mercury |author=Edward Howard |journal=[[Philosophical Transactions of the Royal Society of London]] |year=1800 |volume=90 |issue=1 |pages=204–238 |doi=10.1098/rstl.1800.0012 |s2cid=138658702}}</ref><ref name=wisniak>{{cite journal | last=Wisniak | first=Jaime | title=Edward Charles Howard. Explosives, meteorites, and sugar | journal=Educación Química | publisher=Universidad Nacional Autonoma de Mexico | volume=23 | issue=2 | year=2012 |language=en| issn=0187-893X | doi=10.1016/s0187-893x(17)30114-3 | pages=230–239| doi-access=free }}</ref> However, [[Johann Kunckel]] had discovered the compound more than a century before in the [[17th century]].<ref>{{cite web |title=300 years after discovery, structure of mercury fulminate finally determined |url=https://phys.org/news/2007-08-years-discovery-mercury-fulminate.html |website=Phys.org |access-date=19 February 2025 |date=August 24, 2007}}</ref> The [[crystal structure]] of this compound was determined only in 2007.<ref>{{cite journal |author1=W. Beck |author2=J. Evers |author3=M. Göbel |author4=G. Oehlinger |author5=T. M. Klapötke | title = The Crystal and Molecular Structure of Mercury Fulminate (Knallquecksilber) | year = 2007 | journal = [[Zeitschrift für anorganische und allgemeine Chemie]] | volume = 633 | issue = 9 | pages = 1417–1422 | doi = 10.1002/zaac.200700176| doi-access = free }}</ref>
| title = On a New Fulminating Mercury
 
| author = Edward Howard
[[Silver fulminate]] can be prepared in a similar way, but this salt is even more unstable than mercury fulminate; it can explode even under water and is impossible to accumulate in large amounts because it detonates under its own weight.<ref>{{Cite web |title=The Sciences - Fulminating Substances |author= |website=Scientific American |date=11 June 1853 |url= https://www.scientificamerican.com/article/fulminating-substances-1853-06-11/}}</ref>
| journal = [[Philosophical Transactions of the Royal Society of London]]
 
| year = 1800
Another preparation method is through reaction of the sodium salt of nitromethane with an aqueous solution of [[mercury(II) chloride]] ({{chem2|HgCl2}}) at {{convert|0|C|F}} to form a white precipitate of mercuric nitromethanate. This is digested with warm, dilute [[hydrochloric acid]] (HCl) to produce mercury(II) fulminate.<ref name="EncycExplosives"/>{{rp|F219}}
| volume = 90
| issue = 1
| pages = 204–238
| doi = 10.1098/rstl.1800.0012
| s2cid = 138658702
| doi-access =
}}</ref><ref name=wisniak>{{cite journal | last=Wisniak | first=Jaime | title=Edward Charles Howard. Explosives, meteorites, and sugar | journal=Educación Química | publisher=Universidad Nacional Autonoma de Mexico | volume=23 | issue=2 | year=2012 |language=en| issn=0187-893X | doi=10.1016/s0187-893x(17)30114-3 | pages=230–239| doi-access=free }}</ref> However, [[Johann Kunckel]] had discovered the compound more than a century before in the [[17th century]].<ref>{{cite web |title=300 years after discovery, structure of mercury fulminate finally determined |url=https://phys.org/news/2007-08-years-discovery-mercury-fulminate.html |website=Phys.org |access-date=19 February 2025 |date=August 24, 2007}}</ref> The [[crystal structure]] of this compound was determined only in 2007.<ref>{{cite journal |author1=W. Beck |author2=J. Evers |author3=M. Göbel |author4=G. Oehlinger |author5=T. M. Klapötke | title = The Crystal and Molecular Structure of Mercury Fulminate (Knallquecksilber) | year = 2007 | journal = [[Zeitschrift für anorganische und allgemeine Chemie]] | volume = 633 | issue = 9 | pages = 1417–1422 | doi = 10.1002/zaac.200700176| doi-access = free }}</ref>


[[Silver fulminate]] can be prepared in a similar way, but this [[salt (chemistry)|salt]] is even more unstable than mercury fulminate; it can explode even under water and is impossible to accumulate in large amounts because it detonates under its own weight.<ref>{{Cite web |title=The Sciences - Fulminating Substances |author= |website=Scientific American |date=11 June 1853 |url= https://www.scientificamerican.com/article/fulminating-substances-1853-06-11/}}</ref>
===Intermediates===
The oxidation and nitration of ethanol with nitric acid proceeds through a multitude of intermediate compounds before reaching mercury fulminate; [[acetaldehyde]] ({{chem2|CH3CHO}}), [[nitroso]]acetaldehyde ({{chem2|CH2(NO)\sCHO)}}, isonitrosoacetaldehyde ({{chem2|CH(\dNOH)\sCHO}}), isonitrosoacetic acid ({{chem2|CH(\dNOH)\sCOOH}}), nitroisonitrosoacetic acid ({{chem2|C(NO2)(\dNOH)\sCOOH}}), formo[[nitrolic acid]] ({{chem2|O2H\sCH\dNOH}}), and fulminic acid ({{chem2|C\dNOH}}) are first formed. The last reacts with mercury to produce the fulminate.<ref name="EncycExplosives"/>{{rp|F219}}


==Decomposition==
==Decomposition==
The thermal decomposition of mercury(II) fulminate can begin at temperatures as low as 100&nbsp;°C, though it proceeds at a much higher rate with increasing temperature.<ref>{{cite journal|doi=10.1098/rspa.1933.0040|title=Thermal decomposition and detonation of mercury fulminate|author1=W. E. Garner|author2=H. R. Hailes|name-list-style=amp|journal=Proceedings of the Royal Society of London|volume=139|issue=1–3|year=1933|pages=1–40|bibcode=1933CP....334..128S|doi-access=free}}</ref>
The thermal decomposition of mercury(II) fulminate can begin at temperatures as low as {{convert|100|C|F}}, though it proceeds at a much higher rate with increasing temperature.<ref>{{cite journal|doi=10.1098/rspa.1933.0040|title=Thermal decomposition and detonation of mercury fulminate|first1=W. E. |last1=Garner|first2=H. R. |last2=Hailes |journal=Proceedings of the Royal Society of London|volume=139|issue=1–3|year=1933|pages=1–40|bibcode=1933CP....334..128S|doi-access=free}}</ref>


A possible reaction for the decomposition of mercury(II) fulminate yields [[carbon dioxide]] gas, [[nitrogen]] gas, and a combination of relatively stable mercury salts.
It may be decomposed with relative safety by reaction with ten times its weight of 20% [[sodium thiosulfate]] solution. This may evolve some toxic [[cyanogen]] gas.<ref name="EncycExplosives"/>
:4 Hg(CNO)<sub>2</sub> → 2 CO<sub>2</sub> + N<sub>2</sub> + HgO + 3 Hg(OCN)CN
 
:Hg(CNO)<sub>2</sub> 2 CO + N<sub>2</sub> +   Hg
A possible reaction for the decomposition of mercury(II) fulminate yields [[carbon dioxide]] gas, [[nitrogen]] gas, and a combination of relatively stable mercury salts.{{cn|date=November 2025}}
:Hg(CNO)<sub>2</sub> → :Hg(OCN)<sub>2</sub> ([[cyanate]] or / and [[isocyanate]])
:{{chem2|4 Hg(CNO)2 -> 2 CO2 + N2 + HgO + 3 Hg(OCN)CN}}
:2 Hg(CNO)<sub>2</sub> → 2 CO<sub>2</sub> + N<sub>2</sub> + Hg + Hg(CN)<sub>2</sub> ([[mercury(II) cyanide]])
:{{chem2|Hg(CNO)2 -> 2 CO + N2 + Hg}}
:{{chem2|Hg(CNO)2 -> Hg([[cyanate|O\sC\tN]])2 or Hg([[isocyanate|N\dC\dO]])2}}
:{{chem2|2 Hg(CNO)2 -> 2 CO2 + N2 + Hg + [[mercury(II) cyanide|Hg(CN)2]]}}


==See also==
==See also==
Line 91: Line 138:


==External links==
==External links==
{{Commons category|Mercury(II) fulminate}}
* {{Commons inline|Mercury(II) fulminate}}
*[https://web.archive.org/web/20060425193836/http://www.npi.gov.au/database/substance-info/profiles/53.html National Pollutant Inventory - Mercury and compounds Fact Sheet]
 
*{{cite news | title = 300 years after discovery, structure of mercury fulminate finally determined | publisher = physorg.com | url = http://www.physorg.com/news107176552.html | date = 24 August 2007}}
{{Mercury compounds}}
{{Mercury compounds}}



Latest revision as of 19:02, 18 November 2025

Template:Chembox

Mercury(II) fulminate is a primary explosive with the chemical formula Template:Chem2. When recrystallized from water it exists as the hemihydrate Template:Chem2. The anyhydrous form is obtained by recrystallization from ethanol.[1]Template:Rp It is highly sensitive to friction, heat and shock and is mainly used as a trigger for other explosives in percussion caps and detonators. Mercury(II) cyanate, though its chemical formula is identical, has a different atomic arrangement, making the cyanate and fulminate anionic isomers.

First used as a priming composition in small copper caps beginning in the 1820s, mercury fulminate quickly replaced flints as a means to ignite black powder charges in muzzle-loading firearms. Later, during the late 19th century and most of the 20th century, mercury fulminate became widely used in primers for self-contained rifle and pistol ammunition; it was the only practical detonator for firing projectiles until the early 20th century.[2]

Mercury fulminate has the distinct advantage over potassium chlorate of being non-corrosive, but it is known to attack aluminum and magnesium strongly, and brass, bronze, copper, and zinc slowly when dry; when wet it immediately reacts with aluminum and magnesium and strongly attacks brass, bronze, copper and zinc when.[1] Today, mercury fulminate has been replaced in primers by more efficient chemical substances. These are non-corrosive, less toxic, and more stable over time; they include lead azide, lead styphnate, and tetrazene derivatives. In addition, none of these compounds requires mercury for manufacture, supplies of which can be unreliable in wartime.[3]

Preparation

Mercury(II) fulminate is prepared by dissolving mercury in nitric acid and adding ethanol to the solution. Edward Charles Howard is credited with first preparing it in 1800.[4][2] However, Johann Kunckel had discovered the compound more than a century before in the 17th century.[5] The crystal structure of this compound was determined only in 2007.[6]

Silver fulminate can be prepared in a similar way, but this salt is even more unstable than mercury fulminate; it can explode even under water and is impossible to accumulate in large amounts because it detonates under its own weight.[7]

Another preparation method is through reaction of the sodium salt of nitromethane with an aqueous solution of mercury(II) chloride (Template:Chem2) at Template:Convert to form a white precipitate of mercuric nitromethanate. This is digested with warm, dilute hydrochloric acid (HCl) to produce mercury(II) fulminate.[1]Template:Rp

Intermediates

The oxidation and nitration of ethanol with nitric acid proceeds through a multitude of intermediate compounds before reaching mercury fulminate; acetaldehyde (Template:Chem2), nitrosoacetaldehyde (Template:Chem2, isonitrosoacetaldehyde (Template:Chem2), isonitrosoacetic acid (Template:Chem2), nitroisonitrosoacetic acid (Template:Chem2), formonitrolic acid (Template:Chem2), and fulminic acid (Template:Chem2) are first formed. The last reacts with mercury to produce the fulminate.[1]Template:Rp

Decomposition

The thermal decomposition of mercury(II) fulminate can begin at temperatures as low as Template:Convert, though it proceeds at a much higher rate with increasing temperature.[8]

It may be decomposed with relative safety by reaction with ten times its weight of 20% sodium thiosulfate solution. This may evolve some toxic cyanogen gas.[1]

A possible reaction for the decomposition of mercury(II) fulminate yields carbon dioxide gas, nitrogen gas, and a combination of relatively stable mercury salts.Script error: No such module "Unsubst".

Template:Chem2
Template:Chem2
Template:Chem2
Template:Chem2

See also

References

Template:Reflist

External links

Template:Mercury compounds

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