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Munitions Constituents (EM) are chemicals used in formulations as propellants, pyrotechnics, and explosives in weapon systems, munitions, and blasting agents. This article introduces these materials, major physical and chemical properties, and fate in the environment. Important chemical groups include nitroaromatics (e.g. 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (2,4-DNT), nitramines (e.g. hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetreazocine (HMX)), nitrate esters (e.g. nitroglycerin (NG), pentaerythritol tetranitrate (PETN)), and nitrocellulose (NC).  Ammonium perchlorate (AP) is commonly used as a propellant in solid rock fuel and is addressed in a separate article on [[Perchlorate | perchlorate]].  Insensitive munitions (IM) are energetics in newer military explosives and are generally considered more stable than traditional explosives.
 
Munitions Constituents (EM) are chemicals used in formulations as propellants, pyrotechnics, and explosives in weapon systems, munitions, and blasting agents. This article introduces these materials, major physical and chemical properties, and fate in the environment. Important chemical groups include nitroaromatics (e.g. 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (2,4-DNT), nitramines (e.g. hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetreazocine (HMX)), nitrate esters (e.g. nitroglycerin (NG), pentaerythritol tetranitrate (PETN)), and nitrocellulose (NC).  Ammonium perchlorate (AP) is commonly used as a propellant in solid rock fuel and is addressed in a separate article on [[Perchlorate | perchlorate]].  Insensitive munitions (IM) are energetics in newer military explosives and are generally considered more stable than traditional explosives.
 
<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
 
<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
 
 
'''Related Article(s):'''
 
'''Related Article(s):'''
  
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*[[Metal(loid)s - Small Arms Ranges]]
 +
*[[Munitions Constituents - Abiotic Reduction]]
 +
*[[Munitions Constituents - Alkaline Degradation]]
 +
*[[Munitions Constituents - Composting]]
 
*[[Munitions Constituents - Deposition]]
 
*[[Munitions Constituents - Deposition]]
 
*[[Munitions Constituents - Dissolution]]
 
*[[Munitions Constituents - Dissolution]]
*[[Sorption of Munitions Constituents]]
 
 
*[[Munitions Constituents - IM Toxicology]]
 
*[[Munitions Constituents - IM Toxicology]]
*[[Modeling with TREECS™ for Predicting Fate and Environmental Risk of Munitions Constituents]]
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*[[Munitions Constituents – Photolysis]]
 +
*[[Munitions Constituents - Soil Sampling]]
 +
*[[Munitions Constituents - Sorption]]
 +
*[[Munitions Constituents- TREECS™ Fate and Risk Modeling |Munitions Constituents - TREECS™ Fate and Risk Modeling]]
 +
*[[Passive Sampling of Munitions Constituents]]
  
  
'''CONTRIBUTOR(S):''' [[Dr. Kevin Finneran]] and [[Dr. Robert Borden, P.E.]]
+
'''Contributor(s):''' [[Dr. Kevin Finneran]] and [[Dr. Robert Borden, P.E.]]
  
  
 
'''Key Resource(s)''':   
 
'''Key Resource(s)''':   
*[[Media:USEPA-2012-Site_characterization_for_munitions_constituents.pdf|EPA Federal Facilities Forum Issue Paper: Site Characterization for Munitions Constituents, EPA/505/S-11/001, 2012.]]<ref name= "USEPA2012FIP">U.S. Environmental Protection Agency (USEPA), 2012. EPA Federal Facilities Forum Issue Paper: Site Characterization for Munitions Constituents, EPA/505/S-11/001, 2012. [[Media:USEPA-2012-Site_characterization_for_munitions_constituents.pdf|Report pdf]]</ref>
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 +
*[//www.enviro.wiki/images/f/fd/USEPA-2012-Site_characterization_for_munitions_constituents.pdf EPA Federal Facilities Forum Issue Paper: Site Characterization for Munitions Constituents, EPA/505/S-11/001, 2012.]<ref name="USEPA2012FIP">U.S. Environmental Protection Agency (USEPA), 2012. EPA Federal Facilities Forum Issue Paper: Site Characterization for Munitions Constituents, EPA/505/S-11/001, 2012. [//www.enviro.wiki/images/f/fd/USEPA-2012-Site_characterization_for_munitions_constituents.pdf Report pdf]</ref>
  
 
==Explosives and Propellants==
 
==Explosives and Propellants==
[[File:KFinneran-Article 1-Table 1.PNG|500 px|thumbnail|left|Table 1. Common US military explosives, propellants, and IM formulations<ref name= "Thiboutot2002">Thiboutot, S., Ampleman, G. and Hewitt, A.D., 2002. Guide for characterization of sites contaminated with energetic materials (No. ERDC/CRREL-TR-02-1) U.S. Armu Environmental Center SFIM-AEC-TC-CR-200170. [[Media:Thiboutot-2002-Guide_for_charac_of_Sites_Contamianted.pdf|Report pdf]]</ref><ref>Jenkins, T.F., 2007. Energetic Munitions Constituents on DoD Training Ranges: Deposition, Accumulation, and Appropriate Characterization Technology, In: SERDP and ESTCP Technical Exchange Meeting on DoD Operational Range Assessment and Management Approaches, SERDP and ESTCP, Arlington, VA.</ref><ref>Fung, V., Schreiber, B., Patel, C., Samuels, P., Vinh, P. and Zhao, X.L., 2012. Process Improvement and Optimization of Insensitive Explosive IMX-101. In Insensitive Munitions & Munitions Constituents Technology Symposium (IMEMTS) & National Defense Industrial Association (NDIA): Las Vegas, NV, USA.</ref>.]]
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[[File:KFinneran-Article 1-Table 1.PNG|500 px|thumbnail|left|Table 1. Common US military explosives, propellants, and IM formulations<ref name="Thiboutot2002">Thiboutot, S., Ampleman, G. and Hewitt, A.D., 2002. Guide for characterization of sites contaminated with energetic materials (No. ERDC/CRREL-TR-02-1) U.S. Armu Environmental Center SFIM-AEC-TC-CR-200170. [//www.enviro.wiki/images/2/21/Thiboutot-2002-Guide_for_charac_of_Sites_Contamianted.pdf Report pdf]</ref><ref>Jenkins, T.F., 2007. Energetic Munitions Constituents on DoD Training Ranges: Deposition, Accumulation, and Appropriate Characterization Technology, In: SERDP and ESTCP Technical Exchange Meeting on DoD Operational Range Assessment and Management Approaches, SERDP and ESTCP, Arlington, VA.</ref><ref>Fung, V., Schreiber, B., Patel, C., Samuels, P., Vinh, P. and Zhao, X.L., 2012. Process Improvement and Optimization of Insensitive Explosive IMX-101. In Insensitive Munitions & Munitions Constituents Technology Symposium (IMEMTS) & National Defense Industrial Association (NDIA): Las Vegas, NV, USA.</ref>.]]
  
Explosive materials are commonly classified according to the speed of the chemical reaction wave that propagates through the material. If the wave velocity is greater than the speed of sound ([[wikipedia::Supersonic speed |supersonic]]), the material is said to undergo detonation and is considered an [[wikipedia:Explosive material | explosive]]. If the wave propagation velocity is less than the speed of sound, the material is considered to undergo deflagration (rapid burning) and is often used as a [[wikipedia:Propellant |propellant]]<ref name= "USEPA2012FIP"/>.
+
Explosive materials are commonly classified according to the speed of the chemical reaction wave that propagates through the material. If the wave velocity is greater than the speed of sound ([[wikipedia::Supersonic speed |supersonic]]), the material is said to undergo detonation and is considered an [[wikipedia:Explosive material | explosive]]. If the wave propagation velocity is less than the speed of sound, the material is considered to undergo deflagration (rapid burning) and is often used as a [[wikipedia:Propellant |propellant]]<ref name="USEPA2012FIP" />.
  
 
Common military explosives are mixtures consisting of one or more explosive compounds including [[wikipedia:Trinitrotoluene |trinitrotoluene]] (TNT), 1,3,5-hexahydro-1,3,5-trinitrotriazine or [[wikipedia:RDX | Research Development Explosive (RDX)]], octrahydro-1,3,5,7- tetranitro-1,3,5,7-tetrazocine or [[wikipedia:HMX |High Melting Explosive (HMX)]], and 2,4,6- trinitro-phenylmethylnitramine ([[wikipedia:Tetryl |tetryl]]) and [[wikipedia:Dunnite | ammonium picrate]]. However, the US military is replacing many of these materials with [[wikipedia:Insensitive munition | insensitive munitions]] (IM) to reduce risks of accidental detonation. IM materials will burn, rather than explode, when subjected to fast or slow heating, bullets, shrapnel, shaped charges, or the detonation of another nearby munition. Important components of IM include [[wikipedia:2,4-Dinitroanisole |2,4-dinitroanisole (DNAN)]], [[wikipedia:Nitroguanidine | nitroguanidine]] (NQ), 3-nitro-1,2,4-triazol-5-one (NTO) and other traditional munitions components (RDX, HMX). We highlight common military explosives, propellants, and IM formulations in Table 1.
 
Common military explosives are mixtures consisting of one or more explosive compounds including [[wikipedia:Trinitrotoluene |trinitrotoluene]] (TNT), 1,3,5-hexahydro-1,3,5-trinitrotriazine or [[wikipedia:RDX | Research Development Explosive (RDX)]], octrahydro-1,3,5,7- tetranitro-1,3,5,7-tetrazocine or [[wikipedia:HMX |High Melting Explosive (HMX)]], and 2,4,6- trinitro-phenylmethylnitramine ([[wikipedia:Tetryl |tetryl]]) and [[wikipedia:Dunnite | ammonium picrate]]. However, the US military is replacing many of these materials with [[wikipedia:Insensitive munition | insensitive munitions]] (IM) to reduce risks of accidental detonation. IM materials will burn, rather than explode, when subjected to fast or slow heating, bullets, shrapnel, shaped charges, or the detonation of another nearby munition. Important components of IM include [[wikipedia:2,4-Dinitroanisole |2,4-dinitroanisole (DNAN)]], [[wikipedia:Nitroguanidine | nitroguanidine]] (NQ), 3-nitro-1,2,4-triazol-5-one (NTO) and other traditional munitions components (RDX, HMX). We highlight common military explosives, propellants, and IM formulations in Table 1.
  
 
Propellant formulations often contain several components. The primary component is often nitrocellulose (NC), which is combined with other EM compounds including nitroglycerin (NG), NQ, DNT, HMX, burn rate modifiers, binders or plasticizers, and stabilizers.  Gun propellants usually are single component based (e.g., NC), double based (e.g., NC and NG), or triple based (e.g., NC, NG, and NQ).  
 
Propellant formulations often contain several components. The primary component is often nitrocellulose (NC), which is combined with other EM compounds including nitroglycerin (NG), NQ, DNT, HMX, burn rate modifiers, binders or plasticizers, and stabilizers.  Gun propellants usually are single component based (e.g., NC), double based (e.g., NC and NG), or triple based (e.g., NC, NG, and NQ).  
 
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<BR clear="left">
 
==Physical and Chemical Properties==
 
==Physical and Chemical Properties==
 
The structure (e.g., Fig. 1), as well as physical and chemical properties of explosive materials control their fate and transport in the environment (Table 2).
 
The structure (e.g., Fig. 1), as well as physical and chemical properties of explosive materials control their fate and transport in the environment (Table 2).
[[File:KFinneran-Article 1-Figure 1.PNG|550 px|thumbnail|center]]
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[[File:KFinneran-Article 1-Figure 1.PNG|440 px|thumbnail|left]]
  
 
With the exception of NG, the major EM are solids at ambient temperatures (Table 2). Table 2 provides the molecular mass, aqueous solubility, Log octanol-water partition coefficient (Log K<sub>ow</sub>), and vapor pressure of common explosive materials. Although NG is a liquid, it is commonly used as a component of double- and triple-base propellants, with the solid polymeric NC. Aqueous solubility of EM varies dramatically between the different materials and can have an important influence on their mobility in the environment. Organic compounds with a high K<sub>ow</sub> are more likely to sorb to organic carbon in soil or bioaccumulate; however, EM tend to be high in nitrogen, and by definition, are strong oxidizing agents. EM materials tend to form crystals. The vapor pressure of these materials is relatively low, so volatilization is not an important removal mechanism for most EM.
 
With the exception of NG, the major EM are solids at ambient temperatures (Table 2). Table 2 provides the molecular mass, aqueous solubility, Log octanol-water partition coefficient (Log K<sub>ow</sub>), and vapor pressure of common explosive materials. Although NG is a liquid, it is commonly used as a component of double- and triple-base propellants, with the solid polymeric NC. Aqueous solubility of EM varies dramatically between the different materials and can have an important influence on their mobility in the environment. Organic compounds with a high K<sub>ow</sub> are more likely to sorb to organic carbon in soil or bioaccumulate; however, EM tend to be high in nitrogen, and by definition, are strong oxidizing agents. EM materials tend to form crystals. The vapor pressure of these materials is relatively low, so volatilization is not an important removal mechanism for most EM.
 
<br />
 
<br />
{| class="wikitable" style="text-align: center; margin-right: auto; border: none;"
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 +
<BR clear="left">
 +
{| class="wikitable" style="text-align: center; margin-right: auto; border: none; width=100%;"
 +
|+<div align="left">Table 2. Physical and chemical characteristics of explosive materials</div>
 
|-
 
|-
! style="background-color:#CEE0F2;"|'''Explosive'''!!style="background-color:#CEE0F2;"| '''CAS'''!! style="background-color:#CEE0F2;"|'''Formula'''!!style="background-color:#CEE0F2;"|'''Molecular Weight [g/mol]'''!!style="background-color:#CEE0F2;"|'''Aqueous Solubility at 25°C [mg/L]'''!!style="background-color:#CEE0F2;"|''' Log K<sub>ow</sub>'''!!style="background-color:#CEE0F2;"|'''Vapor Pressure at 20°C
+
! style="background-color:#CEE0F2;" |'''Explosive'''!! style="background-color:#CEE0F2;" |'''CAS'''!! style="background-color:#CEE0F2;" |'''Formula'''!! style="background-color:#CEE0F2;" |'''Molecular Weight [g/mol]'''!! style="background-color:#CEE0F2;" |'''Aqueous Solubility at 25°C [mg/L]'''!! style="background-color:#CEE0F2;" |''' Log K<sub>ow</sub>'''!! style="background-color:#CEE0F2;" |'''Vapor Pressure at 20°C'''
[mm Hg]'''
+
[mm Hg]
  
 
|-
 
|-
| TNT|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=118-96-7 118-96-7]|| C<sub>7</sub>H<sub>5</sub>N<sub>3</sub>O<sub>6</sub>|| 227.13<sup>c</sup>|| 130<sup>c</sup>|| 1.60<sup>c</sup>|| 1.99 E-4<sup>c</sup>
+
|TNT||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=118-96-7 118-96-7]||C<sub>7</sub>H<sub>5</sub>N<sub>3</sub>O<sub>6</sub>||227.13<sup>c</sup>||130<sup>c</sup>||1.60<sup>c</sup>||1.99 E-4<sup>c</sup>
 
|-
 
|-
| RDX|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=121-82-4 121-82-4]|| C<sub>3</sub>H<sub>6</sub>N<sub>6</sub>O<sub>6</sub>|| 222.26<sup>d</sup>|| 56.4<sup>i</sup> || 0.87<sup>d</sup>|| 1 to 4 E-9<sup>d</sup>
+
|RDX||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=121-82-4 121-82-4]||C<sub>3</sub>H<sub>6</sub>N<sub>6</sub>O<sub>6</sub>||222.26<sup>d</sup>||56.4<sup>i</sup>||0.87<sup>d</sup>||1 to 4 E-9<sup>d</sup>
 
|-
 
|-
| HMX|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=2691-41-0&terms=hmx 2691-41-0]|| C<sub>4</sub>H<sub>8</sub>N<sub>8</sub>O<sub>8</sub>|| 296.16<sup>a</sup>|| 4.5<sup>i</sup>|| 0.165<sup>i</sup>|| 3.3E-14<sup>a</sup>
+
|HMX||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=2691-41-0&terms=hmx 2691-41-0]||C<sub>4</sub>H<sub>8</sub>N<sub>8</sub>O<sub>8</sub>||296.16<sup>a</sup>||4.5<sup>i</sup>||0.165<sup>i</sup>||3.3E-14<sup>a</sup>
 
|-
 
|-
| Tetryl || [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=479-45-8&terms=tetryl 479-45-8]|| C<sub>7</sub>H<sub>5</sub>N<sub>5</sub>O<sub>8</sub>|| 287.14<sup>a</sup>|| 80<sup>a</sup>|| || 5.7E-9 (25°C)<sup>a</sup>
+
|Tetryl||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=479-45-8&terms=tetryl 479-45-8]||C<sub>7</sub>H<sub>5</sub>N<sub>5</sub>O<sub>8</sub>||287.14<sup>a</sup>||80<sup>a</sup>|| ||5.7E-9 (25°C)<sup>a</sup>
 
|-
 
|-
| 2,4-DNT|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=121-14-2&terms=2%2c4-DNT 121-14-2]|| C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>4</sub>|| 182.15<sup>a</sup>|| 300 (22°C) <sup>f</sup>|| 1.98<sup>f</sup>|| 1.47E-4<sup>f</sup>
+
|2,4-DNT||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=121-14-2&terms=2%2c4-DNT 121-14-2]||C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>4</sub>||182.15<sup>a</sup>||300 (22°C) <sup>f</sup>||1.98<sup>f</sup>||1.47E-4<sup>f</sup>
 
|-
 
|-
| 2,6-DNT|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=606-20-2&terms=2%2c6-DNT 606-20-2]|| C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>4</sub>|| 182.15<sup>a</sup>|| 180 (22°C)<sup>f</sup>|| 1.72 or 2.10<sup>f</sup>|| 5.67E-4<sup>f</sup>
+
|2,6-DNT||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=606-20-2&terms=2%2c6-DNT 606-20-2]||C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>4</sub>||182.15<sup>a</sup>||180 (22°C)<sup>f</sup>||1.72 or 2.10<sup>f</sup>||5.67E-4<sup>f</sup>
 
|-
 
|-
| 2-ADNT|| 35572-78-2|| C<sub>7</sub>H<sub>7</sub>N<sub>3</sub>O<sub>4</sub>|| 197.17<sup>a</sup>|| 2800<sup>a</sup>|| || 4.0E-5<sup>a</sup>
+
|2-ADNT||35572-78-2||C<sub>7</sub>H<sub>7</sub>N<sub>3</sub>O<sub>4</sub>||197.17<sup>a</sup>||2800<sup>a</sup>|| ||4.0E-5<sup>a</sup>
 
|-
 
|-
| 4-ADNT|| 19406-51-0|| C<sub>7</sub>H<sub>7</sub>N<sub>3</sub>O<sub>4</sub>|| 197.17<sup>a</sup>|| 2800<sup>a</sup>|| || 2.0E-5<sup>a</sup>
+
|4-ADNT||19406-51-0||C<sub>7</sub>H<sub>7</sub>N<sub>3</sub>O<sub>4</sub>||197.17<sup>a</sup>||2800<sup>a</sup>|| ||2.0E-5<sup>a</sup>
 
|-
 
|-
| NTO|| 932-64-9|| C<sub>2</sub>H<sub>2</sub>N<sub>4</sub>O3|| 130.08|| 2000<sup>m</sup>|| 0.858<sup>m</sup>||  
+
|NTO||932-64-9||C<sub>2</sub>H<sub>2</sub>N<sub>4</sub>O<sub>3</sub>||130.08||2000<sup>m</sup>||0.858<sup>m</sup>||
 
|-
 
|-
| DNAN|| 119-27-7|| C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>5</sub>|| 198.13<sup>j</sup>|| 213<sup>o, p</sup>|| 1.58<sup>o, p</sup>|| 1.E-4 (25°C)<sup>j</sup>
+
|DNAN||119-27-7||C<sub>7</sub>H<sub>6</sub>N<sub>2</sub>O<sub>5</sub>||198.13<sup>j</sup>||213<sup>o, p</sup>||1.58<sup>o, p</sup>||1.E-4 (25°C)<sup>j</sup>
 
|-
 
|-
| NQ|| [http://www.commonchemistry.org/ChemicalDetail.aspx?ref=556-88-7 556-88-7]|| CH<sub>4</sub>N<sub>4</sub>O<sub>2</sub>|| 104.07|| 4,400<sup>n</sup>||-0.89<sup>j</sup>
+
|NQ||[http://www.commonchemistry.org/ChemicalDetail.aspx?ref=556-88-7 556-88-7]||CH<sub>4</sub>N<sub>4</sub>O<sub>2</sub>||104.07||4,400<sup>n</sup>||-0.89<sup>j</sup>
 
0.21<sup>l</sup>
 
0.21<sup>l</sup>
|| 1.00E-9 (est)<sup>j</sup>
+
||1.00E-9 (est)<sup>j</sup>
 
|-
 
|-
| colspan="12" style="color:black;text-align:left;"|
+
| colspan="12" style="color:black;text-align:left;" |
a = Thiboutout et al. (2002)<ref name= "Thiboutot2002"/>,  
+
a = Thiboutout et al. (2002)<ref name="Thiboutot2002" />,  
b = Pennington et al. (2006) Final Report<ref>Pennington, J.C., Jenkins, T.F., Ampleman G., Thiboutot, S., Brannon, J.M., Hewitt, A.D., Lewis, J., Brochu, S., Diaz, E., Walsh, M.R., Walsh, M.E., Taylor, S., Lynch, J.C., Clausen, J., Ranney, T.A., Ramsey, C.A., Hayes, C.A., Grant, C.L., Collins, C.M., Bigl, S.R., Yost, S., Dontsova, K., 2006.  Distribution and fate of energetics on DoD test and training ranges: Final Report. ERDC TR-06-13. Vicksburg, MS: U.S. Army Engineer Research and Development Center. [[Media:Pennington-2006-Distribution_and_Fate...Final_Report.pdf|Report pdf]]</ref>,
+
b = Pennington et al. (2006) Final Report<ref>Pennington, J.C., Jenkins, T.F., Ampleman G., Thiboutot, S., Brannon, J.M., Hewitt, A.D., Lewis, J., Brochu, S., Diaz, E., Walsh, M.R., Walsh, M.E., Taylor, S., Lynch, J.C., Clausen, J., Ranney, T.A., Ramsey, C.A., Hayes, C.A., Grant, C.L., Collins, C.M., Bigl, S.R., Yost, S., Dontsova, K., 2006.  Distribution and fate of energetics on DoD test and training ranges: Final Report. ERDC TR-06-13. Vicksburg, MS: U.S. Army Engineer Research and Development Center. [//www.enviro.wiki/images/0/07/Pennington-2006-Distribution_and_Fate...Final_Report.pdf Report pdf]</ref>,
c = EPA Technical Fact Sheet for TNT<ref name= "USEPA2014TNT">U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet - 2,4,6-Trinitrotoluene (TNT).  [[Media:USEPA-2014-TNT_Technical_Fact_Sheet_Final_Report.pdf|Report pdf]]</ref>,
+
c = EPA Technical Fact Sheet for TNT<ref name="USEPA2014TNT">U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet - 2,4,6-Trinitrotoluene (TNT).  [//www.enviro.wiki/images/e/ec/USEPA-2014-TNT_Technical_Fact_Sheet_Final_Report.pdf Report pdf]</ref>,
d = EPA Technical Fact Sheet for RDX<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for RDX.  [[Media:USEPA-2014-RDX_Technical_fact_sheet_contaminant_final_Report.pdf|Report pdf]]</ref>,
+
d = EPA Technical Fact Sheet for RDX<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for RDX.  [//www.enviro.wiki/images/f/f8/USEPA-2014-RDX_Technical_fact_sheet_contaminant_final_Report.pdf Report pdf]</ref>,
f = EPA Technical Fact Sheet for DNT<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for DNT.  [[Media:USEPA-2014-DNT_Technical_fact_sheet-contaminant-final_Report.pdf|Report pdf]]</ref>,
+
f = EPA Technical Fact Sheet for DNT<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for DNT.  [//www.enviro.wiki/images/c/c5/USEPA-2014-DNT_Technical_fact_sheet-contaminant-final_Report.pdf Report pdf]</ref>,
g = EPA Technical Fact Sheet for Perchlorate<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for Perchlorate. [[Media:USEPA-2014-Technical_fact_sheet_contaminant_perchlorate_final.pdf|Report pdf]]</ref>,
+
g = EPA Technical Fact Sheet for Perchlorate<ref>U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for Perchlorate. [//www.enviro.wiki/images/0/0a/USEPA-2014-Technical_fact_sheet_contaminant_perchlorate_final.pdf Report pdf]</ref>,
h = McGrath (1995)<ref>McGrath, C.J. 1995. Review of formulations for processes affecting the subsurface transport of explosives. IRRP-95-2, U.S. Army Engineer Waterways Experiment Station, Vicksburg, MS. [[Media:IRRP_95_2.pdf|Report pdf]]</ref>,
+
h = McGrath (1995)<ref>McGrath, C.J. 1995. Review of formulations for processes affecting the subsurface transport of explosives. IRRP-95-2, U.S. Army Engineer Waterways Experiment Station, Vicksburg, MS. [//www.enviro.wiki/images/a/a2/IRRP_95_2.pdf Report pdf]</ref>,
 
i = Monteil-Rivera et al. (2004)<ref>Monteil-Rivera, F., Paquet, L., Deschamps, S., Balakrishnan, V.K., Beaulieu, C. and Hawari, J., 2004. Physico-chemical measurements of CL-20 for environmental applications: Comparison with RDX and HMX. Journal of Chromatography A, 1025(1), 125-132. [http://dx.doi.org/10.1016/j.chroma.2003.08.060 doi: 10.1016/j.chroma.2003.08.060]</ref>,
 
i = Monteil-Rivera et al. (2004)<ref>Monteil-Rivera, F., Paquet, L., Deschamps, S., Balakrishnan, V.K., Beaulieu, C. and Hawari, J., 2004. Physico-chemical measurements of CL-20 for environmental applications: Comparison with RDX and HMX. Journal of Chromatography A, 1025(1), 125-132. [http://dx.doi.org/10.1016/j.chroma.2003.08.060 doi: 10.1016/j.chroma.2003.08.060]</ref>,
j = DNAN WEEL FINAL<ref>OARS, 2014. Workplace environmental exposure level (WEEL) 2,4-Dinitroanisole (DNAN). OARS, Cincinnati, OH. [[Media:OARS_WHEEL-2014-DNAN_WEEL_FINAL_2014.pdf|Report pdf]]</ref>,
+
j = DNAN WEEL FINAL<ref>OARS, 2014. Workplace environmental exposure level (WEEL) 2,4-Dinitroanisole (DNAN). OARS, Cincinnati, OH. [//www.enviro.wiki/images/e/e6/OARS_WHEEL-2014-DNAN_WEEL_FINAL_2014.pdf Report pdf]</ref>,
 
l = DRDC 2011<ref name="DRDC2011">DRDC, 2011. Annual Report 2010-2011. Environmental fate and ecological impact of emerging energetic chemicals (DNAN and its Amino-Derivatives, NTO, NQ, FOX-7, and FOX-12).  Prepared by J. Hawari. NRC# 53363, Defense Research and Development Canada, National Research Council of Canada,  Montréal, Québec.</ref>,
 
l = DRDC 2011<ref name="DRDC2011">DRDC, 2011. Annual Report 2010-2011. Environmental fate and ecological impact of emerging energetic chemicals (DNAN and its Amino-Derivatives, NTO, NQ, FOX-7, and FOX-12).  Prepared by J. Hawari. NRC# 53363, Defense Research and Development Canada, National Research Council of Canada,  Montréal, Québec.</ref>,
m = NTO WEEL FINAL<ref>OARS, 2014. Workplace environmental exposure level (WEEL) 3-Nitro-1,2,4-Triazol-5-One (NTO). OARS, Cincinnati, OH. [[Media:OARS-2014-NTO_OARS_WEEL.pdf|Report pdf]]</ref>,
+
m = NTO WEEL FINAL<ref>OARS, 2014. Workplace environmental exposure level (WEEL) 3-Nitro-1,2,4-Triazol-5-One (NTO). OARS, Cincinnati, OH. [//www.enviro.wiki/images/1/1d/OARS-2014-NTO_OARS_WEEL.pdf Report pdf]</ref>,
n = van der Schalie (1985)<ref>Schalie, W.H., 1985. The toxicity of nitroguanidine and photolyzed nitroguanidine to freshwater aquatic organisms (No. USAMBRDL-TR-8404). Army Medical Bioengineering Research and Development Laboratory, Fort Detrick, MD. [[Media:Van_der_Schalie-1985-The_Toxicity_of_Nitroguanidine_photolyzed_nitro.....pdf|Report pdf]]</ref>,
+
n = van der Schalie (1985)<ref>Schalie, W.H., 1985. The toxicity of nitroguanidine and photolyzed nitroguanidine to freshwater aquatic organisms (No. USAMBRDL-TR-8404). Army Medical Bioengineering Research and Development Laboratory, Fort Detrick, MD. [//www.enviro.wiki/images/4/42/Van_der_Schalie-1985-The_Toxicity_of_Nitroguanidine_photolyzed_nitro.....pdf Report pdf]</ref>,
o = Hawari (2014)<ref>Hawari, J., 2014. Annual Report 2013-2014. Environmental fate and ecological impact of emerging energetic chemicals (ADN, DNAN and its Amino-Derivatives, PETN, NTO, NQ, FOX-7, and FOX-12) and an insensitive formulation. Defense Research and Development Canada, National Research Council of Canada, Montréal, Québec. [[Media:Hawari-2014-Envl_fate_and_ecological_impact_of_emerging_energic_chemicals.pdf|Report pdf]]</ref>,
+
o = Hawari (2014)<ref>Hawari, J., 2014. Annual Report 2013-2014. Environmental fate and ecological impact of emerging energetic chemicals (ADN, DNAN and its Amino-Derivatives, PETN, NTO, NQ, FOX-7, and FOX-12) and an insensitive formulation. Defense Research and Development Canada, National Research Council of Canada, Montréal, Québec. [//www.enviro.wiki/images/8/8b/Hawari-2014-Envl_fate_and_ecological_impact_of_emerging_energic_chemicals.pdf Report pdf]</ref>,
 
p = Hawari et al. (2015)<ref>Hawari, J., Monteil-Rivera, F., Perreault, N.N., Halasz, A., Paquet, L., Radovic-Hrapovic, Z., Deschamps, S., Thiboutot, S. and Ampleman, G., 2015. Environmental fate of 2, 4-dinitroanisole (DNAN) and its reduced products. Chemosphere, 119, 16-23. [http://dx.doi.org/10.1016/j.chemosphere.2014.05.047 doi:10.1016/j.chemosphere.2014.05.047]</ref>.
 
p = Hawari et al. (2015)<ref>Hawari, J., Monteil-Rivera, F., Perreault, N.N., Halasz, A., Paquet, L., Radovic-Hrapovic, Z., Deschamps, S., Thiboutot, S. and Ampleman, G., 2015. Environmental fate of 2, 4-dinitroanisole (DNAN) and its reduced products. Chemosphere, 119, 16-23. [http://dx.doi.org/10.1016/j.chemosphere.2014.05.047 doi:10.1016/j.chemosphere.2014.05.047]</ref>.
  
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==Health and Environmental Impacts==
 
==Health and Environmental Impacts==
Exposure of humans to EM compounds can result in significant health issues. High oral or dermal exposures to TNT can cause liver and blood damage, anorexia, and anemia. High oral exposures to RDX can cause neurological affects such as convulsions.  Some EM can bioaccumulate in crop plants (e.g. RDX), leading to potential exposure by eating or direct contact<ref>Spain, J.C., Hughes, J.B. and Knackmuss, H.J. eds., 2000. Biodegradation of nitroaromatic compounds and explosives. CRC Press, 456 pgs.</ref><ref>Brannon, J.M. and Pennington, J.C., 2002. Environmental fate and transport process descriptors for explosives (No. ERDC/EL-TR-02-10). Engineer Research and development Center Vicksburg, MS Environmental Lab. [[Media:TR-02-10.pdf|Report pdf]]</ref>. TNT and 2,4-DNT are classified as possible human carcinogens by the U.S. EPA<ref name= "USEPA2014TNT"/>. In contrast, HMX is not currently classified as a human carcinogen, but has been shown to have adverse impacts on the liver and nervous system in some laboratory animals<ref>Agency for Toxic Substances and Disease Registry (ATSDR), 1997. HMX Fact Sheet. [[Media:ATSDR-1997-HMX-FAQ.PDF.pdf|Report pdf]]</ref>. The US military is replacing many of traditional explosives with IMs to reduce risks of accidental detonation.  Since IM materials including DNAN, NTO, and NQ have not been in common use, considerable effort has been focused on understanding the toxicity of these materials (see [[Munitions Constituents - IM Toxicology]]).
+
Exposure of humans to EM compounds can result in significant health issues. High oral or dermal exposures to TNT can cause liver and blood damage, anorexia, and anemia. High oral exposures to RDX can cause neurological affects such as convulsions.  Some EM can bioaccumulate in crop plants (e.g. RDX), leading to potential exposure by eating or direct contact<ref>Spain, J.C., Hughes, J.B. and Knackmuss, H.J. eds., 2000. Biodegradation of nitroaromatic compounds and explosives. CRC Press, 456 pgs.</ref><ref>Brannon, J.M. and Pennington, J.C., 2002. Environmental fate and transport process descriptors for explosives (No. ERDC/EL-TR-02-10). Engineer Research and development Center Vicksburg, MS Environmental Lab. [//www.enviro.wiki/images/9/9e/TR-02-10.pdf Report pdf]</ref>. TNT and 2,4-DNT are classified as possible human carcinogens by the U.S. EPA<ref name="USEPA2014TNT" />. In contrast, HMX is not currently classified as a human carcinogen, but has been shown to have adverse impacts on the liver and nervous system in some laboratory animals<ref>Agency for Toxic Substances and Disease Registry (ATSDR), 1997. HMX Fact Sheet. [//www.enviro.wiki/images/4/4f/ATSDR-1997-HMX-FAQ.PDF.pdf Report pdf]</ref>. The US military is replacing many of traditional explosives with IMs to reduce risks of accidental detonation.  Since IM materials including DNAN, NTO, and NQ have not been in common use, considerable effort has been focused on understanding the toxicity of these materials (see [[Munitions Constituents - IM Toxicology]]).
  
There are currently no federal maximum contaminant levels (MCLs) for TNT, RDX, and HMX. Life-time health advisory levels in drinking water vary from 400 µg/L for HMX, to 2 µg/L for RDX, and 2 µg/L for TNT<ref>United States Environmental Protection Agency (US EPA), 2009. Drinking water contaminant candidate list 3-final. Federal Register 74(194), 51850–51862. [[Media:drinking_water_contaminant_candidate_list.pdf|Report pdf]]</ref>.
+
There are currently no federal maximum contaminant levels (MCLs) for TNT, RDX, and HMX. Life-time health advisory levels in drinking water vary from 400 µg/L for HMX, to 2 µg/L for RDX, and 2 µg/L for TNT<ref>United States Environmental Protection Agency (US EPA), 2009. Drinking water contaminant candidate list 3-final. Federal Register 74(194), 51850–51862. [//www.enviro.wiki/images/5/5b/FR74-194DWCCL3.pdf Report pdf]</ref>.
  
 
==Fate and Transport in the Environment==
 
==Fate and Transport in the Environment==
Much of the early work on environmental issues related to EM focused on concentrated sources including manufacturing facilities and locations where off-specification, unserviceable, and obsolete munitions were destroyed<ref>Spalding, R. and Fulton, J., 1988. Groundwater Munition Residues and Nitrate near Grand Island, Nebraska, USA. Journal of Contaminant Hydrology, 2(2), 139-153 [https://doi.org/10.1016/0169-7722(88)90004-6 doi:10.1016/0169-7722(88)90004-6]</ref> . More recently, attention has focused on potential contamination from military training when partial detonations deposit EM particles on range soils (see [[Munitions Constituents - Deposition]]). Once deposited on a range, the EM dissolves over time, a process thought to be the rate-limiting step for aqueous transport of these compounds to soil and groundwater. The mass of EM dissolved is a function of the aqueous solubility of the compound, the mass of explosive residues deposited on the soil, the size of individual residues, and the three-dimensional (3D) structure of formulations that have multiple constituents (see [[Munitions Constituents - Dissolution]]). During transport through the subsurface, EM migration is influenced by sorption to the solid phase (see [[Sorption of Munitions Constituents]]), as well as chemical transformation and biodegradation.
+
Much of the early work on environmental issues related to EM focused on concentrated sources including manufacturing facilities and locations where off-specification, unserviceable, and obsolete munitions were destroyed<ref>Spalding, R. and Fulton, J., 1988. Groundwater Munition Residues and Nitrate near Grand Island, Nebraska, USA. Journal of Contaminant Hydrology, 2(2), 139-153 [https://doi.org/10.1016/0169-7722(88)90004-6 doi:10.1016/0169-7722(88)90004-6]</ref> . More recently, attention has focused on potential contamination from military training when partial detonations deposit EM particles on range soils (see [[Munitions Constituents - Deposition]]). Once deposited on a range, the EM dissolves over time, a process thought to be the rate-limiting step for aqueous transport of these compounds to soil and groundwater. The mass of EM dissolved is a function of the aqueous solubility of the compound, the mass of explosive residues deposited on the soil, the size of individual residues, and the three-dimensional (3D) structure of formulations that have multiple constituents (see [[Munitions Constituents - Dissolution]]). During transport through the subsurface, EM migration is influenced by sorption to the solid phase (see [[Munitions Constituents - Sorption]]), as well as chemical transformation and biodegradation.
  
 
However, the Department of Defense (DoD) has invested considerable resources to understand how these factors can be influenced, or how they operate in natural settings, to limit transport of EM in surface or groundwater.  In addition, a number of remediation strategies have been developed that address EM, and applied both in situ and ex situ at DoD facilities.   
 
However, the Department of Defense (DoD) has invested considerable resources to understand how these factors can be influenced, or how they operate in natural settings, to limit transport of EM in surface or groundwater.  In addition, a number of remediation strategies have been developed that address EM, and applied both in situ and ex situ at DoD facilities.   
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==References==
 
==References==
  
<references/>
+
<references />
  
 
==See Also==
 
==See Also==
 +
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1043 Natural Attenuation of Explosives in Soil and Water Systems at DoD Sites]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1043 Natural Attenuation of Explosives in Soil and Water Systems at DoD Sites]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1159 A Predictive Capability for the Source Terms of Residual Munitions Constituents from Burning and/or Detonation Activities]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1159 A Predictive Capability for the Source Terms of Residual Munitions Constituents from Burning and/or Detonation Activities]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1176 In-Situ Remediation of Explosives Contaminated Groundwater with Sequential Reactive Treatment Zones]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1176 In-Situ Remediation of Explosives Contaminated Groundwater with Sequential Reactive Treatment Zones]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1212 Bacterial Degradation of DNT and TNT Mixtures]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1212 Bacterial Degradation of DNT and TNT Mixtures]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1213 Microbial Degradation of RDX and HMX]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1213 Microbial Degradation of RDX and HMX]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1214 Novel Pathways of Nitroaromatic Metabolism: Hydroxylamine Formation, Reactivity and Potential for Ring Fission for Destruction of TNT]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1214 Novel Pathways of Nitroaromatic Metabolism: Hydroxylamine Formation, Reactivity and Potential for Ring Fission for Destruction of TNT]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1231 Fe0-Based Bioremediation of RDX-Contaminated Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1231 Fe0-Based Bioremediation of RDX-Contaminated Groundwater]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1232 Remediation of Explosives Contaminated Groundwater with Zero-Valent Iron]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1232 Remediation of Explosives Contaminated Groundwater with Zero-Valent Iron]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1254 Environmental Fate and Transport of a New Energetic Material, CL-20]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-1254 Environmental Fate and Transport of a New Energetic Material, CL-20]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1256 Environmental Fate and Transport of a New Energetic Material, CL-20]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1256 Environmental Fate and Transport of a New Energetic Material, CL-20]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1297 Integrated Automated Analyzer for Monitoring of Explosives in Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1297 Integrated Automated Analyzer for Monitoring of Explosives in Groundwater]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1298 Long-Term Monitoring for Explosives-Contaminated Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-1298 Long-Term Monitoring for Explosives-Contaminated Groundwater]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1376 Enhancement of In Situ Bioremediation of Energetic Compounds by Coupled Abiotic/Biotic Processes]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1376 Enhancement of In Situ Bioremediation of Energetic Compounds by Coupled Abiotic/Biotic Processes]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1377 Biodegradation of Nitroaromatic Compounds by Stimulating Humic Substance- and Fe(III)-Reduction]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1377 Biodegradation of Nitroaromatic Compounds by Stimulating Humic Substance- and Fe(III)-Reduction]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1378 Groundwater Chemistry and Microbial Ecology Effects on Explosives Biodegradation]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1378 Groundwater Chemistry and Microbial Ecology Effects on Explosives Biodegradation]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1606 Development of Biomarkers for Assessing In Situ RDX Biodegradation Potential]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Protecting-Groundwater-Resources/ER-1606 Development of Biomarkers for Assessing In Situ RDX Biodegradation Potential]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1607 New Approaches to Evaluate the Biological Degradation of RDX in Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1607 New Approaches to Evaluate the Biological Degradation of RDX in Groundwater]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1609 Identification of Microbial Gene Biomarkers for In Situ RDX Biodegradation]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminants-on-Ranges/Characterizing-Fate-and-Transport/ER-1609 Identification of Microbial Gene Biomarkers for In Situ RDX Biodegradation]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-199518 Monitored Natural Attenuation of Explosives in Groundwater]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-199518 Monitored Natural Attenuation of Explosives in Groundwater]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-199520 Phytoremediation of Explosives-Contaminated Groundwater in Constructed Wetlands]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-199520 Phytoremediation of Explosives-Contaminated Groundwater in Constructed Wetlands]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-199917 Portable SERS Instrument for Explosives Monitoring]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Monitoring/ER-199917 Portable SERS Instrument for Explosives Monitoring]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200110 Biologically Active Zone Enhancement (BAZE) for In Situ RDX Degradation in Ground Water]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200110 Biologically Active Zone Enhancement (BAZE) for In Situ RDX Degradation in Ground Water]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200112 Electrically Induced Redox Barriers for In Situ Treatment of Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200112 Electrically Induced Redox Barriers for In Situ Treatment of Groundwater]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200223 Remediation of TNT and RDX in Groundwater Using Zero-Valent Iron Permeable Reactive Barriers and Zero-Valent Iron In Situ Treatment Wells]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200223 Remediation of TNT and RDX in Groundwater Using Zero-Valent Iron Permeable Reactive Barriers and Zero-Valent Iron In Situ Treatment Wells]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200425 In Situ Bioremediation of Energetic Compounds in Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200425 In Situ Bioremediation of Energetic Compounds in Groundwater]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200426 Treatment of RDX and HMX Plumes Using Mulch Biowalls]
 
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200426 Treatment of RDX and HMX Plumes Using Mulch Biowalls]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200519 Field Demonstration/Validation of Electrolytic Barriers for Energetic Compounds at Pueblo Chemical Depot]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/ER-200519 Field Demonstration/Validation of Electrolytic Barriers for Energetic Compounds at Pueblo Chemical Depot]
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201207 Bioaugmentation for Aerobic Bioremediation of RDX-Contaminated Groundwater]
+
*[https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201207 Bioaugmentation for Aerobic Bioremediation of RDX-Contaminated Groundwater]

Latest revision as of 21:18, 30 October 2024

Munitions Constituents (EM) are chemicals used in formulations as propellants, pyrotechnics, and explosives in weapon systems, munitions, and blasting agents. This article introduces these materials, major physical and chemical properties, and fate in the environment. Important chemical groups include nitroaromatics (e.g. 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (2,4-DNT), nitramines (e.g. hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetreazocine (HMX)), nitrate esters (e.g. nitroglycerin (NG), pentaerythritol tetranitrate (PETN)), and nitrocellulose (NC). Ammonium perchlorate (AP) is commonly used as a propellant in solid rock fuel and is addressed in a separate article on perchlorate. Insensitive munitions (IM) are energetics in newer military explosives and are generally considered more stable than traditional explosives.

Related Article(s):


Contributor(s): Dr. Kevin Finneran and Dr. Robert Borden, P.E.


Key Resource(s):

Explosives and Propellants

Table 1. Common US military explosives, propellants, and IM formulations[2][3][4].

Explosive materials are commonly classified according to the speed of the chemical reaction wave that propagates through the material. If the wave velocity is greater than the speed of sound (supersonic), the material is said to undergo detonation and is considered an explosive. If the wave propagation velocity is less than the speed of sound, the material is considered to undergo deflagration (rapid burning) and is often used as a propellant[1].

Common military explosives are mixtures consisting of one or more explosive compounds including trinitrotoluene (TNT), 1,3,5-hexahydro-1,3,5-trinitrotriazine or Research Development Explosive (RDX), octrahydro-1,3,5,7- tetranitro-1,3,5,7-tetrazocine or High Melting Explosive (HMX), and 2,4,6- trinitro-phenylmethylnitramine (tetryl) and ammonium picrate. However, the US military is replacing many of these materials with insensitive munitions (IM) to reduce risks of accidental detonation. IM materials will burn, rather than explode, when subjected to fast or slow heating, bullets, shrapnel, shaped charges, or the detonation of another nearby munition. Important components of IM include 2,4-dinitroanisole (DNAN), nitroguanidine (NQ), 3-nitro-1,2,4-triazol-5-one (NTO) and other traditional munitions components (RDX, HMX). We highlight common military explosives, propellants, and IM formulations in Table 1.

Propellant formulations often contain several components. The primary component is often nitrocellulose (NC), which is combined with other EM compounds including nitroglycerin (NG), NQ, DNT, HMX, burn rate modifiers, binders or plasticizers, and stabilizers. Gun propellants usually are single component based (e.g., NC), double based (e.g., NC and NG), or triple based (e.g., NC, NG, and NQ).

Physical and Chemical Properties

The structure (e.g., Fig. 1), as well as physical and chemical properties of explosive materials control their fate and transport in the environment (Table 2).

KFinneran-Article 1-Figure 1.PNG

With the exception of NG, the major EM are solids at ambient temperatures (Table 2). Table 2 provides the molecular mass, aqueous solubility, Log octanol-water partition coefficient (Log Kow), and vapor pressure of common explosive materials. Although NG is a liquid, it is commonly used as a component of double- and triple-base propellants, with the solid polymeric NC. Aqueous solubility of EM varies dramatically between the different materials and can have an important influence on their mobility in the environment. Organic compounds with a high Kow are more likely to sorb to organic carbon in soil or bioaccumulate; however, EM tend to be high in nitrogen, and by definition, are strong oxidizing agents. EM materials tend to form crystals. The vapor pressure of these materials is relatively low, so volatilization is not an important removal mechanism for most EM.


Table 2. Physical and chemical characteristics of explosive materials

Explosive CAS Formula Molecular Weight [g/mol] Aqueous Solubility at 25°C [mg/L] Log Kow Vapor Pressure at 20°C

[mm Hg]

TNT 118-96-7 C7H5N3O6 227.13c 130c 1.60c 1.99 E-4c
RDX 121-82-4 C3H6N6O6 222.26d 56.4i 0.87d 1 to 4 E-9d
HMX 2691-41-0 C4H8N8O8 296.16a 4.5i 0.165i 3.3E-14a
Tetryl 479-45-8 C7H5N5O8 287.14a 80a 5.7E-9 (25°C)a
2,4-DNT 121-14-2 C7H6N2O4 182.15a 300 (22°C) f 1.98f 1.47E-4f
2,6-DNT 606-20-2 C7H6N2O4 182.15a 180 (22°C)f 1.72 or 2.10f 5.67E-4f
2-ADNT 35572-78-2 C7H7N3O4 197.17a 2800a 4.0E-5a
4-ADNT 19406-51-0 C7H7N3O4 197.17a 2800a 2.0E-5a
NTO 932-64-9 C2H2N4O3 130.08 2000m 0.858m
DNAN 119-27-7 C7H6N2O5 198.13j 213o, p 1.58o, p 1.E-4 (25°C)j
NQ 556-88-7 CH4N4O2 104.07 4,400n -0.89j

0.21l

1.00E-9 (est)j

a = Thiboutout et al. (2002)[2], b = Pennington et al. (2006) Final Report[5], c = EPA Technical Fact Sheet for TNT[6], d = EPA Technical Fact Sheet for RDX[7], f = EPA Technical Fact Sheet for DNT[8], g = EPA Technical Fact Sheet for Perchlorate[9], h = McGrath (1995)[10], i = Monteil-Rivera et al. (2004)[11], j = DNAN WEEL FINAL[12], l = DRDC 2011[13], m = NTO WEEL FINAL[14], n = van der Schalie (1985)[15], o = Hawari (2014)[16], p = Hawari et al. (2015)[17].

Table 2. Physical and chemical properties of important explosives and propellants.

Health and Environmental Impacts

Exposure of humans to EM compounds can result in significant health issues. High oral or dermal exposures to TNT can cause liver and blood damage, anorexia, and anemia. High oral exposures to RDX can cause neurological affects such as convulsions. Some EM can bioaccumulate in crop plants (e.g. RDX), leading to potential exposure by eating or direct contact[18][19]. TNT and 2,4-DNT are classified as possible human carcinogens by the U.S. EPA[6]. In contrast, HMX is not currently classified as a human carcinogen, but has been shown to have adverse impacts on the liver and nervous system in some laboratory animals[20]. The US military is replacing many of traditional explosives with IMs to reduce risks of accidental detonation. Since IM materials including DNAN, NTO, and NQ have not been in common use, considerable effort has been focused on understanding the toxicity of these materials (see Munitions Constituents - IM Toxicology).

There are currently no federal maximum contaminant levels (MCLs) for TNT, RDX, and HMX. Life-time health advisory levels in drinking water vary from 400 µg/L for HMX, to 2 µg/L for RDX, and 2 µg/L for TNT[21].

Fate and Transport in the Environment

Much of the early work on environmental issues related to EM focused on concentrated sources including manufacturing facilities and locations where off-specification, unserviceable, and obsolete munitions were destroyed[22] . More recently, attention has focused on potential contamination from military training when partial detonations deposit EM particles on range soils (see Munitions Constituents - Deposition). Once deposited on a range, the EM dissolves over time, a process thought to be the rate-limiting step for aqueous transport of these compounds to soil and groundwater. The mass of EM dissolved is a function of the aqueous solubility of the compound, the mass of explosive residues deposited on the soil, the size of individual residues, and the three-dimensional (3D) structure of formulations that have multiple constituents (see Munitions Constituents - Dissolution). During transport through the subsurface, EM migration is influenced by sorption to the solid phase (see Munitions Constituents - Sorption), as well as chemical transformation and biodegradation.

However, the Department of Defense (DoD) has invested considerable resources to understand how these factors can be influenced, or how they operate in natural settings, to limit transport of EM in surface or groundwater. In addition, a number of remediation strategies have been developed that address EM, and applied both in situ and ex situ at DoD facilities.

References

  1. ^ 1.0 1.1 U.S. Environmental Protection Agency (USEPA), 2012. EPA Federal Facilities Forum Issue Paper: Site Characterization for Munitions Constituents, EPA/505/S-11/001, 2012. Report pdf
  2. ^ 2.0 2.1 Thiboutot, S., Ampleman, G. and Hewitt, A.D., 2002. Guide for characterization of sites contaminated with energetic materials (No. ERDC/CRREL-TR-02-1) U.S. Armu Environmental Center SFIM-AEC-TC-CR-200170. Report pdf
  3. ^ Jenkins, T.F., 2007. Energetic Munitions Constituents on DoD Training Ranges: Deposition, Accumulation, and Appropriate Characterization Technology, In: SERDP and ESTCP Technical Exchange Meeting on DoD Operational Range Assessment and Management Approaches, SERDP and ESTCP, Arlington, VA.
  4. ^ Fung, V., Schreiber, B., Patel, C., Samuels, P., Vinh, P. and Zhao, X.L., 2012. Process Improvement and Optimization of Insensitive Explosive IMX-101. In Insensitive Munitions & Munitions Constituents Technology Symposium (IMEMTS) & National Defense Industrial Association (NDIA): Las Vegas, NV, USA.
  5. ^ Pennington, J.C., Jenkins, T.F., Ampleman G., Thiboutot, S., Brannon, J.M., Hewitt, A.D., Lewis, J., Brochu, S., Diaz, E., Walsh, M.R., Walsh, M.E., Taylor, S., Lynch, J.C., Clausen, J., Ranney, T.A., Ramsey, C.A., Hayes, C.A., Grant, C.L., Collins, C.M., Bigl, S.R., Yost, S., Dontsova, K., 2006. Distribution and fate of energetics on DoD test and training ranges: Final Report. ERDC TR-06-13. Vicksburg, MS: U.S. Army Engineer Research and Development Center. Report pdf
  6. ^ 6.0 6.1 U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet - 2,4,6-Trinitrotoluene (TNT). Report pdf
  7. ^ U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for RDX. Report pdf
  8. ^ U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for DNT. Report pdf
  9. ^ U.S. Environmental Protection Agency (USEPA), 2014. EPA Technical Fact Sheet for Perchlorate. Report pdf
  10. ^ McGrath, C.J. 1995. Review of formulations for processes affecting the subsurface transport of explosives. IRRP-95-2, U.S. Army Engineer Waterways Experiment Station, Vicksburg, MS. Report pdf
  11. ^ Monteil-Rivera, F., Paquet, L., Deschamps, S., Balakrishnan, V.K., Beaulieu, C. and Hawari, J., 2004. Physico-chemical measurements of CL-20 for environmental applications: Comparison with RDX and HMX. Journal of Chromatography A, 1025(1), 125-132. doi: 10.1016/j.chroma.2003.08.060
  12. ^ OARS, 2014. Workplace environmental exposure level (WEEL) 2,4-Dinitroanisole (DNAN). OARS, Cincinnati, OH. Report pdf
  13. ^ DRDC, 2011. Annual Report 2010-2011. Environmental fate and ecological impact of emerging energetic chemicals (DNAN and its Amino-Derivatives, NTO, NQ, FOX-7, and FOX-12). Prepared by J. Hawari. NRC# 53363, Defense Research and Development Canada, National Research Council of Canada, Montréal, Québec.
  14. ^ OARS, 2014. Workplace environmental exposure level (WEEL) 3-Nitro-1,2,4-Triazol-5-One (NTO). OARS, Cincinnati, OH. Report pdf
  15. ^ Schalie, W.H., 1985. The toxicity of nitroguanidine and photolyzed nitroguanidine to freshwater aquatic organisms (No. USAMBRDL-TR-8404). Army Medical Bioengineering Research and Development Laboratory, Fort Detrick, MD. Report pdf
  16. ^ Hawari, J., 2014. Annual Report 2013-2014. Environmental fate and ecological impact of emerging energetic chemicals (ADN, DNAN and its Amino-Derivatives, PETN, NTO, NQ, FOX-7, and FOX-12) and an insensitive formulation. Defense Research and Development Canada, National Research Council of Canada, Montréal, Québec. Report pdf
  17. ^ Hawari, J., Monteil-Rivera, F., Perreault, N.N., Halasz, A., Paquet, L., Radovic-Hrapovic, Z., Deschamps, S., Thiboutot, S. and Ampleman, G., 2015. Environmental fate of 2, 4-dinitroanisole (DNAN) and its reduced products. Chemosphere, 119, 16-23. doi:10.1016/j.chemosphere.2014.05.047
  18. ^ Spain, J.C., Hughes, J.B. and Knackmuss, H.J. eds., 2000. Biodegradation of nitroaromatic compounds and explosives. CRC Press, 456 pgs.
  19. ^ Brannon, J.M. and Pennington, J.C., 2002. Environmental fate and transport process descriptors for explosives (No. ERDC/EL-TR-02-10). Engineer Research and development Center Vicksburg, MS Environmental Lab. Report pdf
  20. ^ Agency for Toxic Substances and Disease Registry (ATSDR), 1997. HMX Fact Sheet. Report pdf
  21. ^ United States Environmental Protection Agency (US EPA), 2009. Drinking water contaminant candidate list 3-final. Federal Register 74(194), 51850–51862. Report pdf
  22. ^ Spalding, R. and Fulton, J., 1988. Groundwater Munition Residues and Nitrate near Grand Island, Nebraska, USA. Journal of Contaminant Hydrology, 2(2), 139-153 doi:10.1016/0169-7722(88)90004-6

See Also