Uranium nitrides

Uranium nitride[1]

Names
IUPAC name

Uranium nitride

Identifiers

CAS Number

* UN: 25658-43-9 Y
* UN2: 12033-83-9

3D model (JSmol)

* UN: Interactive image
* UN2: Interactive image
* U2N3: Interactive image

ChemSpider |

* UN: 105089

PubChem CID

* UN: 117595

InChI

* InChI=1S/N.U

Key: MVXWAZXVYXTENN-UHFFFAOYSA-N

SMILES

* UN: U#N

* UN2: N#[U]#N

* U2N3: N#[U]=N([U]#N)

Properties

Chemical formula

| U2N3
Molar mass | 518.078 g/mol
Appearance  | crystalline solid
Density | 11300 kg·m−3, solid
Melting point | 900 to 1,100 °C (1,650 to 2,010 °F; 1,170 to 1,370 K) (decomposes to UN)
Boiling point | Decomposes

Solubility in water

| 0.08 g/100 ml (20 °C)
Structure

Crystal structure

| Hexagonal, hP5

Space group

| P-3m1, No. 164

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Y verify (what is YN ?)

Infobox references

Chemical compound

Uranium nitrides refers to any of a family of several ceramic materials: uranium mononitride (UN), uranium sesquinitride (U2N3) and uranium dinitride (UN2). The word nitride refers to the −3 oxidation state of the nitrogen bound to the uranium.

Uranium nitride has been considered as a potential nuclear fuel and will be used as such in the BREST-300 nuclear reactor currently under construction in Russia. It is said to be safer, stronger, denser, more thermally conductive and having a higher temperature tolerance. Challenges to implementation of the fuel include a complex conversion route from enriched UF6, the need to prevent oxidation during manufacturing and the need to define and license a final disposal route. The necessity to use expensive, highly isotopically enriched 15N is a significant factor to overcome. This is necessary due to the (relatively) high neutron capture cross-section of the far-more-common 14N, which affects the neutron economy of a reactor.[2]

## Synthesis

[edit]

### Carbothermic reduction

[edit]

The common technique for generating UN is carbothermic reduction of uranium oxide (UO2) in a 2 step method illustrated below.[3][4]

3UO2 \+ 6C → 2UC + UO2 \+ 4CO (in argon, > 1450 °C for 10 to 20 hours)
4UC + 2UO2 +3N2 → 6UN + 4CO

### Sol-gel

[edit]

Sol-gel methods and arc melting of pure uranium under nitrogen atmosphere can also be used.[5]

### Ammonolysis

[edit]

Another common technique for generating UN2 is the ammonolysis of uranium tetrafluoride. Uranium tetrafluoride is exposed to ammonia gas under high pressure and temperature, which replaces the fluorine with nitrogen and generates hydrogen fluoride.[6] Hydrogen fluoride is a colourless gas at this temperature and mixes with the ammonia gas.

### Hydriding-nitriding

[edit]

An additional method of UN synthesis employs fabrication directly from metallic uranium. By exposing metallic uranium to hydrogen gas at temperatures in excess of 280 °C, UH3 can be formed.[7] Furthermore, since UH3 has a higher specific volume than the metallic phase, hydridation can be used to physically decompose otherwise solid uranium. Following hydridation, UH3 can be exposed to a nitrogen atmosphere at temperatures around 500 °C, thereby forming U2N3. By additional heating to temperatures above 1150 °C, the sesquinitride can then be decomposed to UN.

2U + 3H2 → 2UH3
2UH3 \+ 1.5N2 → U2N3
U2N3 → UN + 0.5N2

Use of the isotope 15N (which constitutes around 0.37% of natural nitrogen) is preferable because the predominant isotope, 14N, has a significant neutron absorption cross section which affects neutron economy and, in particular, it undergoes an (n,p) reaction which produces significant amounts of radioactive 14C which would need to be carefully contained and sequestered during reprocessing or permanent storage.[8]

## Decomposition

[edit]

Each uranium dinitride complex is considered to have three distinct compounds present simultaneously because of decomposing of uranium dinitride (UN2) into uranium sesquinitride (U2N3), and then uranium mononitride (UN). Uranium dinitrides decompose to uranium mononitride by the following sequence of reactions:[9]

4UN2 → 2U2N3\+ N2
2U2N3 → 4UN +N2

Decomposition of UN2 is the most common method for isolating uranium sesquinitride (U2N3).

## Uses

[edit]

Uranium mononitride is being considered as a potential fuel for generation IV reactors such as the Hyperion Power Module reactor created by Hyperion Power Generation.[10] It has also been proposed as nuclear fuel in some fast neutron nuclear test reactors. UN is considered superior because of its higher fissionable density, thermal conductivity, and melting temperature than the most common nuclear fuel, uranium oxide (UO2), while also demonstrating lower release of fission product gases and swelling, and decreased chemical reactivity with cladding materials.[11] It also has a superior mechanical, thermal, and radiation stability compared to standard metallic uranium fuel.[9][12] The thermal conductivity is on the order of 4–8 times higher than that of uranium dioxide, the most commonly used nuclear fuel, at typical operating temperatures. Increased thermal conductivity results in a smaller thermal gradient between inner and outer sections of the fuel,[8] potentially allowing for higher operating temperatures and reducing macroscopic restructuring of the fuel, which limits fuel lifetime.[4]

## Molecular and crystal structure

[edit]

The uranium dinitride (UN2) compound has a face-centered cubic crystal structure of the calcium fluoride (CaF2) type with a space group of Fm3m.[13] Nitrogen forms triple bonds on each side of uranium forming a linear structure.[14][15]

α-(U2N3) has a body-centered cubic crystal structure of the (Mn2O3) type with a space group of Ia3 .[13]

UN has a face-centered cubic crystal structure of the NaCl type.[14][16] The metal component of the bond uses the 5f orbital of the uranium but forms a relatively weak interaction but is important for the crystal structure. The covalent portion of the bonds forms from the overlap between the 6d orbital and 7s orbital on the uranium and the 2p orbitals on the nitrogen.[14][17] N forms a triple bond with uranium creating a linear structure.[15]

* Uranium dinitride

* Uranium sesquinitride

* Uranium mononitride

## Uranium nitrido derivatives

[edit]

Recently, there have been many developments in the synthesis of complexes with terminal uranium nitride (–U≡N) bonds. In addition to radioactive concerns common to all uranium chemistry, production of uranium nitrido complexes has been slowed by harsh reaction conditions and solubility challenges. Nonetheless, syntheses of such complexes have been reported in the past few years, for example the three shown below among others.[18][19] Other U≡N compounds have also been synthesized or observed with various structural features, such as bridging nitride ligands in di-/polynuclear species, and various oxidation states.[20][21]

[N(n-Bu)4] [(C6F5)3B−N≡U(Nt-BuAr)3][22] | N≡UF3[23] | [Na(12-crown-4)2] [N≡U−N(CH2CH2Ntips)3][24]

|
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## See also

[edit]

* List of energy densities
* Nuclear fuel cycle
* Nuclear reactor
* Uranium carbide
* Uranium oxide

## References

[edit]

1. ^ R. B. Matthews; K. M. Chidester; C. W. Hoth; R. E. Mason; R. L. Petty (1988). "Fabrication and testing of uranium nitride fuel for space power reactors". Journal of Nuclear Materials. 151 (3): 345. Bibcode:1988JNuM..151..345M. doi:10.1016/0022-3115(88)90029-3.
2. ^ Chaudri, Khurrum Saleem (2013). "Coupled analysis for new fuel design using UN and UC for SCWR". Progress in Nuclear Energy. 63: 57–65\. Bibcode:2013PNuE...63...57C. doi:10.1016/j.pnucene.2012.11.001.
3. ^ Minato, Kazuo; Akabori, Mitsuo; Takano, Masahide; Arai, Yasuo; Nakajima, Kunihisa; Itoh, Akinori; Ogawa, Toru (2003). "Fabrication of nitride fuels for transmutation of minor actinides". Journal of Nuclear Materials. 320 (1–2): 18–24\. Bibcode:2003JNuM..320...18M. doi:10.1016/S0022-3115(03)00163-6. ISSN 0022-3115.1–2&rft.pages=18-24&rft.date=2003&rft.issn=0022-3115&rft_id=info:doi/10.1016/S0022-3115(03)00163-6&rft_id=info:bibcode/2003JNuM..320...18M&rft.aulast=Minato&rft.aufirst=Kazuo&rft.au=Akabori,+Mitsuo&rft.au=Takano,+Masahide&rft.au=Arai,+Yasuo&rft.au=Nakajima,+Kunihisa&rft.au=Itoh,+Akinori&rft.au=Ogawa,+Toru&rfr_id=info:sid/en.wikipedia.org:Uranium+nitrides" class="Z3988">
4. ^ a b Carmack, W. J. (2004). "Internal Gelation as Applied to the Production of Uranium Nitride Space Nuclear Fuel". AIP Conference Proceedings. 699: 420–425\. Bibcode:2004AIPC..699..420C. doi:10.1063/1.1649601. ISSN 0094-243X.
5. ^ Ganguly, C.; Hegde, P. J. Sol-Gel Sci. Technol.. 1997, 9, 285.
6. ^ Silva, G. W. C.; Yeamans, C. B.; Ma, L.; Cerefice, G. S.; Czerwinski, K. R.; Sarrelberger, A. P. Chem. Mater.. 2008, 20, 3076.
7. ^ urn:nbn:se:kth:diva-35249: Manufacturing methods for (U-Zr)N-fuels
8. ^ a b Matthews, R. B.; Chidester, K. M.; Hoth, C. W.; Mason, R. E.; Petty, R. L. Journal of Nuclear Materials. '1988, 151(3), 345.
9. ^ a b Silva, G. W. Chinthaka; Yeamans, Charles B.; Sattelberger, Alfred P.; Hartmann, Thomas; Cerefice, Gary S.; Czerwinski, Kenneth R. (2009). "Reaction Sequence and Kinetics of Uranium Nitride Decomposition". Inorganic Chemistry. 48 (22): 10635–10642\. doi:10.1021/ic901165j. ISSN 0020-1669. PMID 19845318.
10. ^ Staff (2009-11-20). "Hyperion launches U2N3-fuelled, Pb-Bi-cooled fast reactor". Nuclear Engineering International. Global Trade Media, a division of Progressive Media Group Ltd.
11. ^ "Simple method for producing a stable form of uranium nitride". Advanced Ceramics Report. International Newsletters. August 1, 2012. "[R]esearcher ... Stephen Liddle, says: '... it could help... extract and separate the 2-3% of the highly radioactive material in nuclear waste.'"
12. ^ Mizutani, A.; Sekimoto, H. Ann. Nucl. Energy. 2005, 25(9), 623–638.
13. ^ a b Rundle, R. E.; Baenziger, N. C.; Wilson, A. S.; McDonald, R. A. J. Am. Chem Soc.. 1948, 70, 99.
14. ^ a b c Weck P. F., Kim E., Balakrishnan N., Poineau F., Yeamans C. B., and Czerwinski K. R. Chem. Phys. Lett.. 2007, 443, 82. doi:10.1016/j.cplett.2007.06.047
15. ^ a b Wang, X.; Andrews, L.; Vlaisavljevich, B.; Gagliardi, L. Inorganic Chemistry. 2011, 50(8), 3826–3831. doi:10.1021/ic2003244
16. ^ Mueller, M. H.; Knott, H. W.Acta Crystallogr.. 1958, 11, 751–752. doi:10.1107/S0365110X58002061
17. ^ Évarestov, R. A., Panin, A. I., & Losev, M. V. Journal of Structural Chemistry. 2008, 48, 125–135.
18. ^ Nocton, G.; Pécaut, J.; Mazzanti, M. A Nitrido-Centered Uranium Azido Cluster Obtained from a Uranium Azide. Angew. Chem. Int. Ed. 2008, 47 (16), 3040–3042. doi:10.1002/anie.200705742
19. ^ Thomson, R. K.; Cantat, T.; Scott, B. L.; Morris, D. E.; Batista, E. R.; Kiplinger, J. L. Uranium azide photolysis results in C–H bond activation and provides evidence for a terminal uranium nitride. Nature Chemistry 2010, 2, 723–729. doi:10.1038/nchem.705
20. ^ Fox, A. R.; Arnold, P. L.; Cummins, C. C. Uranium−Nitrogen Multiple Bonding: Isostructural Anionic, Neutral, and Cationic Uranium Nitride Complexes Featuring a Linear U═N═U Core. J. Am. Chem. Soc. 2010, 132 (10), 3250–3251. doi:10.1021/ja910364u
21. ^ Evans, W. J.; Kozimor, S. A.; Ziller, J. W. Molecular Octa-Uranium Rings with Alternating Nitride and Azide Bridges. Science 2005, 309 (5742), 1835–1838. doi:10.1126/science.1116452
22. ^ Fox, A.; Cummins, C. Uranium−Nitrogen Multiple Bonding: The Case of a Four-Coordinate Uranium(VI) Nitridoborate Complex. J. Am. Chem. Soc., 2009, 131 (16), 5716–5717. doi:10.1021/ja8095812
23. ^ Andrew, L.; Wang, X.; Lindh, R.; Roos, B.; Marsden, C. Simple N≡UF3 and P≡UF3 Molecules with Triple Bonds to Uranium. Angew. Chem. Int. Ed. 2008, 47 (29), 5366-5370. doi:10.1002/anie.200801120
24. ^ King, D.; Tuna, F.; McInnes, E.; McMaster, J.; Lewis, W.; Blake, A.; Liddle, S. T. Synthesis and Structure of a Terminal Uranium Nitride Complex. Science 2012, 337 (6095), 717–720. doi:10.1126/science.1223488

## External links

[edit]

* New Uranium Bond at The Periodic Table of Videos (University of Nottingham)
* Uranium Mononitride (UN) Handbook (Los Alamos National Laboratory)

* v
* t
* e

Uranium compounds

U(II)|

* UB2
* US

U(III)|

* UF3
* UCl3
* UBr3
* UI3
* UP
* U(OH)3
* UH3
* UN

| Organouranium(III) compounds|

* U(C5H5)3

|

U(IV)|

* U(BH4)4
* UC
* UCl4
* UF4
* UBr4
* UI4
* UO2
* U(OH)4
* UH4
* USi2
* US2
* USe2
* UTe2
* U(SO4)2

| Organouranium(IV) compounds|

* U(C8H8)2
* U(C5H5)4
* U(C5H5)3Cl

|

U(IV,V)|

* U2N3

U(V)|

* UCl5
* UF5
* UBr5
* UI5
* U2O5

U(V,VI)|

* U3O8

U(VI)|

* (NH4)2U2O7
* Na2U2O7
* MgU2O7
* UCl6
* UF6
* U(PO4)2
* UO3
* UN2

| Uranyl compounds|

* Na4UO2(CO3)3
* U2O7
* UO4
* UO2(CH3COO)2
* UO2(CHO2)2
* UO2CO3
* UO2C2O4
* UO2CO3·2(NH4)2CO3
* UO2Cl2
* UO2F2
* UO2(NO3)2
* UO2(OH)2
* (UO2)2(OH)4
* UO2(PO3)2
* UO2(SO4)2
* ZnUO2(CH3COO)4

|

U(XII)|

* UO6 (hypothetical)

* v
* t
* e

Salts and covalent derivatives of the nitride ion

| NH3
N2H4

HN2−
H2N− |  |  |  | He(N2)11

|
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|
|

Li3N
LiN3 | Be3N2
Be(N3)2 | BN
-B | C4N2
C2N2
β-C3N4
g-C3N4
CxNy | N2 | NxOy
+O | N3F
N2F2
N2F4
NF3
+F | Ne
Na3N
NaN3 | Mg3N2
Mg(N3)2 | AlN | Si3N4
-Si | PN
P3N5
-P | SxNy

S2N2
S4N4
SN2H2 | NCl3
ClN3
+Cl | Ar
K3N
KN3 | Ca3N2
Ca(N3)2 |  | ScN | TiN
Ti3N4 | VN | CrN
Cr2N | MnxNy | FexNy | Co3N | Ni3N | Cu3N | Zn3N2 | GaN | Ge3N4
-Ge | AsN
+As | Se4N4 | Br3N
BrN3
+Br | Kr
RbN3 | Sr3N2
Sr(N3)2 |  | YN | ZrN | NbN | β-Mo2N | Tc  | Ru  | Rh  | PdN | Ag3N | Cd3N2 | InN | Sn  | SbN | Te4N4?  | I3N
IN3
+I | Xe
CsN3 | Ba3N2
Ba(N3)2 | *  | LuN | HfN
Hf3N4 | TaN | WN | RexNy | Os  | Ir  | Pt  | Au  | Hg3N2 | Tl3N | (PbNH) | BiN | Po  | At  | Rn
Fr  | Ra3N2 | **  | Lr  | Rf  | Db  | Sg  | Bh  | Hs  | Mt  | Ds  | Rg  | Cn  | Nh  | Fl  | Mc  | Lv  | Ts  | Og

*  | LaN | CeN | PrN | NdN | PmN | SmN | EuN | GdN | TbN | DyN | HoN | ErN | TmN | YbN
**  | Ac  | ThxNy | PaN | UxNy | NpN | PuN | AmN | CmN | BkN | Cf  | Es  | Fm  | Md  | No
*[CID]: Compound ID
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