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Chemical compound From Wikipedia, the free encyclopedia
Lithium carbonate is an inorganic compound, the lithium salt of carbonic acid with the formula Li
2CO
3. This white salt is widely used in processing metal oxides. It is on the World Health Organization's List of Essential Medicines[7] for its efficacy in the treatment of mood disorders such as bipolar disorder.[8][7]
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| Names | |
|---|---|
| IUPAC name
Lithium carbonate | |
| Other names
Dilithium carbonate, Carbolith, Cibalith-S, Duralith, Eskalith, Lithane, Lithizine, Lithobid, Lithonate, Lithotabs Priadel, Zabuyelite | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.008.239 |
| KEGG | |
PubChem CID |
|
| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) |
|
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| Properties | |
| Li 2CO 3 | |
| Molar mass | 73.89 g/mol |
| Appearance | Odorless white powder |
| Density | 2.11 g/cm3 |
| Melting point | 723 °C (1,333 °F; 996 K) |
| Boiling point | 1,310 °C (2,390 °F; 1,580 K) Decomposes from ~1300 °C |
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Solubility product (Ksp) |
8.15×10−4[2] |
| Solubility | Insoluble in acetone, ammonia, alcohol[3] |
| −27.0·10−6 cm3/mol | |
Refractive index (nD) |
1.428[4] |
| Viscosity |
|
| Thermochemistry | |
Heat capacity (C) |
97.4 J/mol·K[3] |
Std molar entropy (S⦵298) |
90.37 J/mol·K[3] |
Std enthalpy of formation (ΔfH⦵298) |
−1215.6 kJ/mol[3] |
Gibbs free energy (ΔfG⦵) |
−1132.4 kJ/mol[3] |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Irritant |
| GHS labelling: | |
 [5] | |
| Warning | |
| H302, H319[5] | |
| P305+P351+P338[5] | |
| Flash point | Non-flammable |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
525 mg/kg (oral, rat)[6] |
| Safety data sheet (SDS) | ICSC 1109 |
| Related compounds | |
Other cations |
Sodium carbonate Potassium carbonate Rubidium carbonate Caesium carbonate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Lithium carbonate is an important industrial chemical. Its main use is as a precursor to compounds used in lithium-ion batteries.
Glasses derived from lithium carbonate are useful in ovenware. Lithium carbonate is a common ingredient in both low-fire and high-fire ceramic glaze. It forms low-melting fluxes with silica and other materials. Its alkaline properties are conducive to changing the state of metal oxide colorants in glaze, particularly red iron oxide (Fe
2O
3). Cement sets more rapidly when prepared with lithium carbonate, and is useful for tile adhesives. When added to aluminium trifluoride, it forms LiF which yields a superior electrolyte for the processing of aluminium.[9]
Lithium carbonate-derived compounds are crucial to lithium-ion batteries. Lithium carbonate may be converted into lithium hydroxide as an intermediate. In practice, two components of the battery are made with lithium compounds: the cathode and the electrolyte. The electrolyte is a solution of lithium hexafluorophosphate, while the cathode uses one of several lithiated structures, the most popular of which are lithium cobalt oxide and lithium iron phosphate.
In 1843, lithium carbonate was used to treat stones in the bladder. In 1859, some doctors recommended a therapy with lithium salts for a number of ailments, including gout, urinary calculi, rheumatism, mania, depression, and headache.
In 1948, John Cade discovered the anti-manic effects of lithium ions.[10] This finding led to lithium carbonate's use as a psychiatric medication to treat mania, the elevated phase of bipolar disorder. Prescription lithium carbonate from a pharmacy is suitable for use as medicine in humans but industrial lithium carbonate is not since it may contain unsafe levels of toxic heavy metals or other toxicants. After ingestion, lithium carbonate is dissociated into pharmacologically active lithium ions (Li+) and (non-therapeutic) carbonate, with 300 mg of lithium carbonate containing approximately 8 mEq (8 mmol) of lithium ion.[8] According to the Food and Drug Administration (FDA), 300–600 mg of lithium carbonate taken two to three times daily is typical for maintenance of bipolar I disorder in adults,[8] where the exact dose given varies depending on factors such as the patient's serum lithium concentrations, which must be closely monitored by a physician to avoid lithium toxicity and potential kidney damage (or even kidney failure) from lithium-induced nephrogenic diabetes insipidus.[11][8] Dehydration and certain drugs, including NSAIDs such as ibuprofen, can increase serum lithium concentrations to unsafe levels whereas other drugs, such as caffeine, may decrease concentrations. In contrast to the elemental ions sodium, potassium, and calcium, there is no known cellular mechanism specifically dedicated to regulating intracellular lithium. Lithium can enter cells through epithelial sodium channels.[12] Lithium ions interfere with ion transport processes that relay and amplify messages carried to the cells of the brain.[13] Mania is associated with irregular increases in protein kinase C (PKC) activity within the brain. Lithium carbonate and sodium valproate, another drug traditionally used to treat the disorder, act in the brain by inhibiting PKC's activity and help to produce other compounds that also inhibit the PKC.[14] Lithium carbonate's mood-controlling properties are not fully understood.[15]
Taking lithium salts has risks and side effects. Extended use of lithium to treat mental disorders has been known to lead to acquired nephrogenic diabetes insipidus.[16] Lithium intoxication can affect the central nervous system and renal system and can be lethal.[17] Over a prolonged period, lithium can accumulate in the principal cells of the collecting duct and interfere with antidiuretic hormone (ADH), which regulates the water permeability of principal cells in the collecting tubule.[12] The medullary interstitium of the collecting duct system naturally has a high sodium concentration and attempts to maintain it. There is no known mechanism for cells to distinguish lithium ions from sodium ions, so damage to the kidney's nephrons may occur if lithium concentrations become too high as a result of dehydration, hyponatremia, an unusually low sodium diet, or certain drugs.
Lithium carbonate is used to impart a red color to fireworks.[18]
Unlike sodium carbonate, which forms at least three hydrates, lithium carbonate exists only in the anhydrous form. Its solubility in water is low relative to other lithium salts. The isolation of lithium from aqueous extracts of lithium ores capitalizes on this poor solubility. Its apparent solubility increases 10-fold under a mild pressure of carbon dioxide; this effect is due to the formation of the metastable lithium bicarbonate, which is more soluble:[9][19]
The extraction of lithium carbonate at high pressures of CO
2 and its precipitation upon depressurizing is the basis of the Quebec process.
Lithium carbonate can also be purified by exploiting its diminished solubility in hot water. Thus, heating a saturated aqueous solution causes crystallization of Li
2CO
3.[20]
Lithium carbonate, and other carbonates of group 1, do not decarboxylate readily. Li
2CO
3 decomposes at temperatures around 1300 °C.
Lithium is extracted from primarily two sources: spodumene in pegmatite deposits, and lithium salts in underground brine pools. About 82,000 tons were produced in 2020, showing significant and consistent growth.[21]
In the Salar de Atacama in the Atacama Desert of Northern Chile, lithium carbonate and hydroxide are produced from brine.[22][23]
The process pumps lithium rich brine from below ground into shallow pans for evaporation. The brine contains many different dissolved ions, and as their concentration increases, salts precipitate out of solution and sink. The remaining supernatant liquid is used for the next step. The sequence of pans may vary depending on the concentration of ions in a particular source of brine.
In the first pan, halite (sodium chloride or common salt) crystallises. This has little economic value and is discarded. The supernatant, with ever increasing concentration of dissolved solids, is transferred successively to the sylvinite (sodium potassium chloride) pan, the carnalite (potassium magnesium chloride) pan and finally a pan designed to maximise the concentration of lithium chloride. The process takes about 15 months. The concentrate (30-35% lithium chloride solution) is trucked to Salar del Carmen. There, boron and magnesium are removed (typically residual boron is removed by solvent extraction and/or ion exchange and magnesium by raising the pH above 10 with sodium hydroxide)[24] then in the final step, by addition of sodium carbonate, the desired lithium carbonate is precipitated out, separated, and processed.
Some of the by-products from the evaporation process may also have economic value.
There is considerable attention to the use of water in this water poor region. SQM commissioned a life-cycle analysis (LCA) which concluded that water consumption for SQM's lithium hydroxide and carbonate is significantly lower than the average consumption by production from the main ore-based process, using spodumene. A more general LCA suggests the opposite for extraction from reservoirs.[25]
The majority of brine based production is in the "lithium triangle" in South America.
A potential source of lithium is the leachates of geothermal wells, carried to the surface.[26] Recovery of lithium has been demonstrated in the field; the lithium is separated by simple precipitation and filtration.[27] The process and environmental costs are primarily those of the already-operating well; net environmental impacts may thus be positive.[28]
The brine of United Downs Deep Geothermal Power project near Redruth is claimed by Cornish Lithium to be valuable due to its high lithium concentration (220 mg/L) with low magnesium (<5 mg/L) and total dissolved solids content of <29g/L,[29] and a flow rate of 40-60l/s.[25]
α-spodumene is roasted at 1100 °C for 1h to make β-spodumene, then roasted at 250 °C for 10 minutes with sulphuric acid.[30][22]
As of 2020, Australia was the world's largest producer of lithium intermediates,[31] all based on spodumene.
In recent years mining companies have begun exploration of lithium projects throughout North America, South America and Australia to identify economic deposits that can potentially bring new supplies of lithium carbonate online to meet the growing demand for the product.[32]
In 2020 Tesla Motors announced a revolutionary process to extract lithium from clay in Nevada using only salt and no acid. This was met with scepticism.[33]
A few small companies are recycling spent batteries, focusing on recovering copper and cobalt. Some recover lithium carbonate alongside the compound Li2Al4(CO3)(OH)12⋅3H2O also.[34][35][36][37]
In April 2017 MGX Minerals reported it had received independent confirmation of its rapid lithium extraction process to recover lithium and other valuable minerals from oil and gas wastewater brine. [38]
Electrodialysis has been proposed to extract lithium from seawater, but it is not commercially viable.[39]
Natural lithium carbonate is known as zabuyelite.[40] This mineral is connected with deposits of some salt lakes and some pegmatites.[41]
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