Beryllium nitride
Beryllium nitride, Be3N2, is a nitride of beryllium. It can be prepared from the elements at high temperature (1100–1500 °C),[2] unlike Beryllium azide or BeN6, it decomposes in vacuum into beryllium and nitrogen.[2] It is readily hydrolysed forming beryllium hydroxide and ammonia.[2] It has two polymorphic forms cubic α-Be3N2 with a defect anti-fluorite structure, and hexagonal β-Be3N2.[2] It reacts with silicon nitride, Si3N4 in a stream of ammonia at 1800–1900 °C to form BeSiN2.[2]
Identifiers | |
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ECHA InfoCard | 100.013.757 |
EC Number |
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UNII | |
Properties | |
Be3N2 | |
Molar mass | 55.06 g/mol |
Appearance | yellow or white powder |
Density | 2.71 g/cm3 |
Melting point | 2,200 °C (3,990 °F; 2,470 K) |
Boiling point | 2,240 °C (4,060 °F; 2,510 K) (decomposes) |
decomposes | |
Solubility in [[acids, bases]] | hydrolyzes |
Structure | |
Cubic, cI80, SpaceGroup = Ia-3, No. 106 (α form) | |
Hazards | |
NIOSH (US health exposure limits): | |
PEL (Permissible) |
TWA 0.002 mg/m3 C 0.005 mg/m3 (30 minutes), with a maximum peak of 0.025 mg/m3 (as Be)[1] |
REL (Recommended) |
Ca C 0.0005 mg/m3 (as Be)[1] |
IDLH (Immediate danger) |
Ca [4 mg/m3 (as Be)][1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Preparation
Beryllium nitride is prepared by heating beryllium metal powder with dry nitrogen in an oxygen-free atmosphere in temperatures between 700 and 1400 °C.
Uses
It is used in refractory ceramics[3] as well as in nuclear reactors and to produce radioactive carbon-14 for tracer applications.
Reactions
Beryllium nitride reacts with mineral acids producing ammonia and the corresponding salts of the acids:
- Be3N2 + 6 HCl → 3 BeCl2 + 2 NH3
In strong alkali solutions, a beryllate forms, with evolution of ammonia:
- Be3N2 + 6 NaOH → 3 Na2BeO2 + 2 NH3
Both the acid and alkali reactions are brisk and vigorous. Reaction with water, however, is very slow:
- Be3N2 + 6 H2O → 3 Be(OH)2 + 2 NH3
Reactions with oxidizing agents are likely to be violent. It is oxidized when heated at 600 °C in air.
References
- NIOSH Pocket Guide to Chemical Hazards. "#0054". National Institute for Occupational Safety and Health (NIOSH).
- Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5
- Hugh O. Pierson, 1996, Handbook of Refractory Carbides and Nitrides: Properties, Characteristics, Processing, and Applications, William Andrew Inc.,ISBN 0-8155-1392-5
NH3 N2H4 |
He(N2)11 | ||||||||||||||||
Li3N | Be3N2 | BN | β-C3N4 g-C3N4 CxNy |
N2 | NxOy | NF3 | Ne | ||||||||||
Na3N | Mg3N2 | AlN | Si3N4 | PN P3N5 |
SxNy SN S4N4 |
NCl3 | Ar | ||||||||||
K | Ca3N2 | ScN | TiN | VN | CrN Cr2N |
MnxNy | FexNy | CoN | Ni3N | CuN | Zn3N2 | GaN | Ge3N4 | As | Se | NBr3 | Kr |
Rb | Sr3N2 | YN | ZrN | NbN | β-Mo2N | Tc | Ru | Rh | PdN | Ag3N | CdN | InN | Sn | Sb | Te | NI3 | Xe |
Cs | Ba3N2 | Hf3N4 | TaN | WN | Re | Os | Ir | Pt | Au | Hg3N2 | TlN | Pb | BiN | Po | At | Rn | |
Fr | Ra3N2 | Rf | Db | Sg | Bh | Hs | Mt | Ds | Rg | Cn | Nh | Fl | Mc | Lv | Ts | Og | |
↓ | |||||||||||||||||
La | CeN | Pr | Nd | Pm | Sm | Eu | GdN | Tb | Dy | Ho | Er | Tm | Yb | Lu | |||
Ac | Th | Pa | UN | Np | Pu | Am | Cm | Bk | Cf | Es | Fm | Md | No | Lr |