|Jmol 3D model||Interactive image|
|Molar mass||7.95 g/mol|
|Appearance||colorless to gray solid|
|Melting point||688.7 °C (1,271.7 °F; 961.9 K)|
|Boiling point||decomposes at 900–1000 °C|
|Solubility||slightly soluble in dimethylformamide
reacts with ammonia, diethyl ether, ethanol
Refractive index (nD)
a = 0.40834 nm:56
|170.8 J/mol K|
Std enthalpy of
Gibbs free energy (ΔfG˚)
|Safety data sheet||ICSC 0813|
|200 °C (392 °F; 473 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|77.5 mg/kg (oral, rat)|
LC50 (median concentration)
|22 mg/m3 (rat, 4 hr)|
|US health exposure limits (NIOSH):|
|TWA 0.025 mg/m3|
|TWA 0.025 mg/m3|
IDLH (Immediate danger)
Lithium aluminium hydride
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Lithium hydride is the inorganic compound with the formula LiH. This alkali metal hydride is a colorless solid, although commercial samples are grey. Characteristic of a salt-like, or ionic, hydride, it has a high melting point and is not soluble but reactive with all organic and protic solvents; it is soluble and non-reactive with certain molten salts such as lithium fluoride, lithium borohydride, and sodium hydride. With a molecular mass of slightly less than 8, it is the lightest ionic compound.
LiH is a diamagnetic and an ionic conductor with a conductivity gradually increasing from ×10−5 Ω−1cm−1 at 443 °C to 0.18 Ω−1cm−1 at 754 °C; there is no discontinuity in this increase through the melting point. 2:36 The dielectric constant of LiH decreases from 13.0 (static, low frequencies) to 3.6 (visible light frequencies).:35 LiH is a soft material with a Mohs hardness of 3.5.:42 Its compressive creep (per 100 hours) rapidly increases from < 1% at 350 °C to > 100% at 475 °C meaning that LiH can't provide mechanical support when heated.:39
The thermal conductivity of LiH decreases with temperature and depends on morphology: the corresponding values are 0.125 W/(cm·K) for crystals and 0.0695 W/(cm·K) for compacts at 50 °C, and 0.036 W/(cm·K) for crystals and 0.0432 W/(cm·K) for compacts at 500 °C.:60 The linear thermal expansion coefficient is 4.2×10−5/°C at room temperature.:49
Synthesis and processing
- 2 Li + H2 → 2 LiH
This reaction is especially rapid at temperatures above 600 °C. Addition of 0.001–0.003% carbon, or/and increasing temperature or/and pressure, increases the yield up to 98% at 2-hour residence time.:147 However, the reaction proceeds at temperatures as low as 29 °C. The yield is 60% at 99 °C and 85% at 125 °C, and the rate depends significantly on the surface condition of LiH.:5
Less common ways of LiH synthesis include thermal decomposition of lithium aluminium hydride (200 °C), lithium borohydride (300 °C), n-butyllithium (150 °C), or ethyllithium (120 °C), as well as several reactions involving lithium compounds of low stability and available hydrogen content.:144–145
Chemical reactions yield LiH in the form of lumped powder, which can be compressed into pellets without a binder. More complex shapes can be produced by casting from the melt.:160 ff. Large single crystals (about 80 mm long and 16 mm in diameter) can be then grown from molten LiH powder in hydrogen atmosphere by the Bridgman–Stockbarger technique. They often have bluish color owing to the presence of colloidal Li. This color can be removed by post-growth annealing at lower temperatures (~550 °C) and lower thermal gradients.:154 Major impurities in these crystals are Na (20–200 parts per million, ppm), O (10–100 ppm), Mg (0.5–6 ppm), Fe (0.5-2 ppm) and Cu (0.5-2 ppm).:155
LiH powder reacts rapidly with air of low humidity, forming LiOH, Li
2O and Li
3. In moist air the powder ignites spontaneously, forming a mixture of products including some nitrogenous compounds. The lump material reacts with humid air forming a superficial coating which is a viscous fluid. This inhibits further reaction, although the appearance of a film of 'tarnish' is quite evident. Little or no nitride is formed on exposure to humid air. The lump material, contained in a metal dish, may be heated in air to slightly below 200 °C, without igniting, although it ignites readily when touched by an open flame. The surface condition of LiH, presence of oxides on the metal dish, etc., have a considerable effect on the ignition temperature. Dry oxygen does not react with crystalline LiH unless heated strongly, when an almost explosive combustion occurs.:6
LiH is highly reactive toward water and other protic reagents::7
- LiH + H2O → Li+ + H2 + OH−
LiH is less reactive with water than Li and thus is a much less powerful reducing agent for water, alcohols, and other media containing reducible solutes. This is true of all the binary saline hydrides.:22
LiH pellets slowly expand in moist air forming LiOH; however, the expansion rate is below 10% within 24 hours in a pressure of 2 mm of water vapor.:7 If moist air contains carbon dioxide then the product is lithium carbonate.:8 LiH reacts with ammonia, slowly at room temperature, but the reaction accelerates significantly above 300 °C.:10 LiH reacts slowly with higher alcohols and phenols but vigorously with lower alcohols.:14
LiH reacts with sulfur dioxide:
- 2 LiH + 2 SO2 → Li2S2O4 + H2
though above 50 °C the product is lithium sulfide.:9
LiH reacts with acetylene to form lithium carbide and hydrogen. With anhydrous organic acids, phenols and acid anhydrides LiH reacts slowly producing hydrogen gas and the lithium salt of the acid. With water-containing acids, LiH reacts faster than with water.:8 Many reactions of LiH with oxygen-containing species yield LiOH which in turn irreversibly reacts with LiH at temperatures above 300 °C::10
- LiH + LiOH → Li2O + H2
Hydrogen storage and fuel
With a hydrogen content three times that of NaH, LiH has the highest hydrogen content of any hydride. LiH is periodically of interest for hydrogen storage, but applications have been thwarted by its stability to decomposition. Thus removal of H2 requires temperatures above the 700 °C used for its synthesis, such temperatures are expensive to create and maintain. The compound was once tested as a fuel component in a model rocket.
Precursor to complex metal hydrides
LiH is not usually a hydride-reducing agent except in the synthesis of hydrides of certain metalloids. For example, silane is produced by the reaction of lithium hydride and silicon tetrachloride via the Sundermeyer process:
- 4 LiH + SiCl4 → 4 LiCl + SiH4
Lithium hydride is used in the production of a variety of reagents for organic synthesis, such as lithium aluminium hydride (LiAlH4) and lithium borohydride (LiBH4). Triethylborane reacts to give superhydride (LiBHEt3).
In nuclear chemistry and physics
LiH, especially lithium-7 deuteride, is a good moderator for nuclear reactors. The right isotopes help. Deuterium has a lower neutron absorption cross-section than aneutronic hydrogen, decreasing neutron absorption in a reactor. Lithium-7 is preferred for a moderator because it has a lower neutron cross-section and also forms less tritium under neutron bombardment.
The corresponding lithium-6 deuteride, formula 6Li2H or 6LiD, is the fusion fuel in thermonuclear weapons. In warheads of the Teller-Ulam design, a fission trigger explosion heats, compresses and bombards 6LiD with neutrons to produce tritium in an exothermic reaction. The deuterium and tritium (both isotopes of hydrogen) then fuse to produce helium-4, a neutron and 17.59 MeV of energy.
Before the Castle Bravo nuclear test it was thought that only the less common lithium-6 isotope would breed tritium when struck with fast neutrons. The test showed that the more plentiful lithium-7 also does so, albeit by an endothermic reaction.
As discussed above, LiH reacts explosively with water to give hydrogen gas and LiOH, which is caustic. Consequently, LiH dust can explode in humid air, or even in dry air due to static electricity. At concentrations of 5–55 mg/m3 in air the dust is extremely irritating to the mucous membranes and skin and may cause an allergic reaction. Because of the irritation, LiH is normally rejected rather than accumulated by the body.:182:157
Some lithium salts, which can be produced in LiH reactions, are toxic. LiH fire should not be extinguished using carbon dioxide, carbon tetrachloride, or aqueous fire extinguishers; they should be smothered by covering with a metal object or graphite or dolomite powder. Sand is less suitable as it can explode when mixed with burning LiH, especially if not dry. LiH is normally transported in oil, using containers made of ceramic, certain plastics or steel, and is handled in an atmosphere of dry argon or helium.:156 Nitrogen can be used, but not at elevated temperatures as it reacts with lithium.:157 LiH normally contains some metallic Li, which corrodes steel or silica containers at elevated temperatures.:173–174, 179
- Lide, D. R., ed. (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. p. 4.70. ISBN 0-8493-0486-5.
- David Arthur Johnson; Open University (12 August 2002). Metals and chemical change. Royal Society of Chemistry. pp. 167–. ISBN 978-0-85404-665-2. Retrieved 1 November 2011.
- Smith, R. L.; Miser, J. W. (1963). Compilation of the properties of lithium hydride. NASA.
- "NIOSH Pocket Guide to Chemical Hazards #0371". National Institute for Occupational Safety and Health (NIOSH).
- "Lithium hydride". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
- Lex. Astronautix.com (1964-04-25). Retrieved on 2011-11-01.
- Empirical laws for hybrid combustion of lithium hydride with fluorine in small rocket engines. Ntrs.nasa.gov. Retrieved on 2011-11-01.
- Peter Rittmeyer, Ulrich Wietelmann "Hydrides" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a13_199
- Peter J. Turchi (1998). Propulsion techniques: action and reaction. AIAA. pp. 339–. ISBN 978-1-56347-115-5. Retrieved 2 November 2011.
- Welch, Frank H. (February 1974). "Lithium hydride: A space age shielding material". Nuclear Engineering and Design. 26 (3): 440–460. doi:10.1016/0029-5493(74)90082-X.
- Massie, Mark; Dewan, Leslie C. "US 20130083878 A1, April 4, 2013, NUCLEAR REACTORS AND RELATED METHODS AND APPARATUS". U.S. Patent Office. U.S. Government. Retrieved 2 June 2016.
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