Lithium nitrite

Lithium nitrite
Names
Preferred IUPAC name
Lithium nitrite
Identifiers
13568-33–-7 Yes
EC number 23-976-1
Jmol-3D images Image
PubChem 23673709
Properties
LiNO2
Molar mass 52.9465 g/mol
Appearance white, hygroscopic crystals
Melting point 222 °C (432 °F; 495 K)
Thermochemistry
96 J/mol K
Std enthalpy of
formation (ΔfHo298)
 −372.4 kJ/mol
-302 kJ/mol
Hazards
EU Index Not listed
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Lithium nitrite is the lithium salt of nitrous acid, with formula LiNO2. This compound is hygroscopic and very soluble in water. It is used as a corrosion inhibitor in mortar.[1] It is also used in the production of explosives, due to its ability to nitrosate ketones under certain conditions.[2]

Properties

The following table lists a few of the physical and chemical properties of lithium nitrite:[3][4]

CAS # MW (g/mol) Description at 25 °C MP (°C) ΔfH° (kJ/mol) ΔfG° (kJ/mol) S° (J/deg*mol)
13568-33-7 52.947 Wh Hyg Cry 222 −372.4 −302.0 96.0

Preparation

Lithium nitrate (LiNO3) will undergo thermal decomposition above 500 °C to yield the evolution of lithium nitrite and oxygen as in the following reaction:[5]

2LiNO3 → 2LiNO2 + O2 (at ~500 °C)

Lithium nitrite can also be prepared by the reaction of nitric oxide (NO) with lithium hydroxide (LiOH) as shown below:[5]

4NO + 2LiOH → 2LiNO2 + N2O + H2O
6NO + 4LiOH → 4LiNO2 + N2 + 2H2O

Crystallization and crystal structure

Lithium nitrite crystals can be obtained most efficiently by reacting lithium sulfate and barium nitrite in an aqueous solution. However, these crystals can also be prepared by mixing equal amounts of lithium sulfate and potassium nitrite in highly concentrated aqueous solution. This is followed by considerable evaporation and filtration, which removes the resulting precipitate of potassium sulfate and lithium potassium sulfate after further evaporation and extraction with absolute alcohol.[6]

Lithium nitrite is exceptionally soluble in absolute alcohol. However, potassium nitrite is not very soluble. This makes absolute alcohol a choice solvent for the crystallization of lithium nitrite because the crystals can be extracted in a substantially pure state. The alcoholic solution will leave a white residue of small crystals upon evaporation. The addition of a small amount of water to this residue will yield the larger needle-shaped crystals of lithium nitrite monohydrate (LiNO2·H2O).[6]

The above methods will result in flat, needle-shaped crystals. These crystals are white and typically 1–2 cm. in length. Below 100 °C, these crystals will melt in their own water of crystallization and will tend to lose water slowly. Rapid dehydration will occur at temperatures above 160 °C as well as a minuscule loss of nitrogen oxide. This rapid dehydration leaves behind a residue which consists almost entirely of the anhydrous salt.[6] This anhydrous salt is extraordinarily soluble in water and will readily form a supersaturated solution. Monohydrate crystals will deposit from this supersaturated solution upon cooling or with the addition of ready formed salt crystals.[6]

Industrial uses

Reinforcement bars, ready mixed concrete materials, and repair materials are often subject to corrosion. These resources will rapidly degrade due to chloride attack and carbonatation. This not only affects the service lives of such materials, but it also requires a considerable cost for the repair of such defects. Lithium nitrite and calcium nitrite are generally used in the construction industry as a means to protect reinforced concrete structures from corrosion. Unlike calcium nitrite inhibitors, lithium nitrite is particularly valued for corrosion inhibition and resistance of carbonation when an accelerated hardening process is not used and when a high concentration of 10% or more cement is added by weight.[7]

Generally speaking, studying the effectiveness of such inhibitors has been done using destructive methods. These studies require placing specimens to accelerated corrosion and measuring the degree of corrosion. "However, it is extremely difficult to measure the effect of corrosion inhibitors in actual structures using a destructive method."

Recently, sensors that can measure changes in electrical resistance due to the corrosion in iron and thus indicate the degree of corrosion of a material have been developed. These sensors provide a non-destructive way to evaluate the degree of corrosion in concrete materials. Therefore, the effect of Lithium Nitrite as a corrosion inhibitor has also been studied by non-destructive means.[7]

A study was conducted in Korea to experimentally determine the most effective dose and performance of Lithium Nitrite corrosion inhibitors. This experiment employed the molar ratio of nitrite ions to chloride ions (NO2−/Cl−) as a test parameter. This study concluded that a lithium nitrite dosage of 0.6 in the nitrite-chloride ion molar ratio is a successful dosage for mortar containing chlorides.[7]

External links

References

  1. ↑ "Evaluation on the effect of lithium nitrite corrosion inhibitor by the corrosion sensors embedded in mortar"
  2. ↑ Nitrosation with Lithium Nitrite
  3. ↑ 6.) CRC handbook of chemistry and physics, 58th ed.; CRC press: Cleveland, 1978; Vol. 26.
  4. ↑ 7.) Lange's handbook of chemistry, 16th ed.; McGraw-Hill: New York, 2005.
  5. ↑ 5.0 5.1 Greenwood, N. N. and Earnshaw, A. Chemistry of the Elements, 2nd ed.; Reed Educational and Professional Publishing Ltd: Oxford, 1997.
  6. ↑ 6.0 6.1 6.2 6.3 Ball, W. "The nitrites of thallium, lithium, caesium, and rubidium". Journal of the Chemical Society, Transactions [Online] 1913, vol. 103, p 2130−2134. Royal Society of Chemistry. http://pubs.rsc.org/en/Journals (accessed Oct 28, 2011).
  7. ↑ 7.0 7.1 7.2 3.) Lee, Han-Seung and Shin, Sung-Woo. "Evaluation on the effect of lithium nitrite corrosion inhibitor by the corrosion sensors embedded in mortar". Construction and Building Materials [Online] Jan. 2007, vol. 21, pp. 1–6. Web of Knowledge. http://apps.webofknowledge.com (accessed Oct 28, 2011).