Rubidium and cesium: properties, deposits, and applications
Rubidium and cesium belong to the group of rare alkali metals characterized by high chemical reactivity and distinctive physical properties. Their content in the Earth’s crust is low; however, these elements are present in many minerals, mainly as isomorphic impurities substituting for potassium and lithium. Both metals are of strategic importance due to their rarity, the complexity of their extraction, and their unique applications—ranging from electro-optical industries and precision measuring instruments to defense systems and advanced energy technologies.
They are considered together because they belong to the same chemical group, have similar physicochemical properties, often form common mineral associations, and are enriched under the same geological conditions. In nature, rubidium and cesium are mainly concentrated in rare-metal pegmatites, apogranites, greisens, metasomatites, salt deposits, brines, and thermal waters.
Rubidium and cesium ores is included in the list of minerals of national importance, approved by Resolution of the Cabinet of Ministers of Ukraine No. 827 of December 12, 1994, as rare metal ores.
List of minerals of national importance
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Go to the listGeneral information
Rubidium (Latin: Rubidium, Rb) is a chemical element of Group I of the periodic table with atomic number 37 and atomic mass 85.47. It belongs to the alkali metals. It was discovered in 1861 by R. Bunsen and G. Kirchhoff. The name derives from the Latin rubidus (“dark red”). In nature, it occurs as a mixture of two stable isotopes: ^85Rb (72.15%) and ^87Rb (27.85%). The latter is radioactive, with a half-life of about 5×10¹⁰ years, which allows the ^87Rb/^87Sr ratio to be used for determining the radiometric age of rocks. In addition, 19 artificially synthesized isotopes of rubidium are known.
In its natural state, rubidium is a soft, silvery-white alkali metal with a density of 1.525 g/cm³ and a melting point of 39.5 °C. Its oxidation state is +1. The metal is extremely reactive: it ignites easily in air, reacts explosively with water, and actively interacts with all inorganic acids. Its Clarke value is 1.5×10⁻²%. Rubidium belongs to dispersed elements and typically occurs as an isomorphic impurity in minerals of alkali metals, mainly potassium and lithium, such as pollucite, lepidolite, zinnwaldite, amazonite, biotite, spodumene, and carnallite. The highest concentrations are found in low-temperature pegmatite veins, where Rb content can reach 1–3%.
Cesium (Latin: Caesium, Cs) is also a Group I element with atomic number 55 and atomic mass 132.9. It belongs to alkali metals as well. Its name comes from the Latin caesius (“sky blue”). In nature, it is represented by one stable isotope, ^133Cs; numerous artificial radioactive isotopes are also known. Cesium is a low-melting, soft metal with a yellowish-golden hue, a density of 1.9 g/cm³, and a melting point of 28.5 °C. Like rubidium, it oxidizes instantly in air and reacts explosively with water. Its Clarke value is 3.7×10⁻³%. It is a rare element that forms its own mineral—pollucite (Cs[AlSi₂O₆])—and is also found in spodumene, lepidolite, zinnwaldite, cesium-bearing astrophyllite, kupletskite, cesium biotite, and other minerals.
Applications and raw material requirements
Rubidium and cesium are widely used in high-tech industries. They are applied in the electro-optical industry, including vacuum radio tubes, thermistors, lasers, masers, luminescent screens and tubes, for manufacturing photocell cathodes, as well as in special ceramics, glass, and enamels. Rubidium salts are used in gas-discharge tubes and serve as catalysts in organic synthesis. The isotope ^133Cs is used as the basis for quantum frequency standards.
Cesium is also used in magnetohydrodynamic (MHD) generators, plasma amplifiers for ultra-high frequencies, automatic control systems, missile guidance systems, long-distance communication technologies, and missile defense systems.
Rubidium salts are usually obtained as a by-product during the production of lithium, magnesium, and potassium compounds. Metallic rubidium is produced by reducing its salts with metallic calcium, followed by purification through rectification and vacuum distillation.
Economic overview
Global reserves of rubidium are estimated at approximately 1,150 thousand tons, while cesium reserves are about 100 thousand tons. Their main concentration is associated with rare-metal pegmatite deposits in the United States, Canada, Zimbabwe, China, Namibia, Brazil, and Argentina, as well as with rare-metal brines of salt lakes in the United States.
Canada is the largest producer of pollucite concentrate (about 45 t/year), where the Bernic Lake deposit is in operation. Significant mining activities are also carried out in Zimbabwe (Bikita) and Namibia (Karibib). Despite having substantial reserves, Russia primarily extracts cesium from imported concentrate. Deposits are considered large if reserves exceed 1,000 tons of Rb₂O and 5,000 tons of Cs₂O. However, in complex deposits, even the first hundreds of tons may be of industrial interest.
Genetic and Geological-Industrial Types of Deposits
Rubidium and cesium deposits are divided into endogenous and exogenous types, which are usually closely associated with lithium deposits. Endogenous types include:
- rare-metal granite pegmatites (Kings Mountain, Black Hills, Pala-Men — USA; Preissac-Lacorne, Bernic Lake — Canada; Goltsovskoye — Russia; Lalin — Spain; Sencekourou — Mali; Fu-Zep — China; Munaki, Karibib — Namibia; Darang-Peak — Afghanistan; Bikita, Bun — Zimbabwe);
- rare-metal metasomatites;
- agpaitic nepheline syenites;
- rare-metal volcanogenic and volcanogenic-sedimentary formations (Henou-Kamb Hills — USA).
Among exogenous types, elevated concentrations of Rb and Cs are associated with:
- deposits of intracontinental salt seas (Wienburg — Germany);
- large marine salt bays;
- modern salt lakes (Searles, Great Salt Lake — USA);
- formation and artesian waters (Pripyat Depression, Angara-Lena and Tunguska basins);
- mineralized waters of mountainous regions (Azatavan — Lesser Caucasus; Karamadon, Karobi, Baksan — Greater Caucasus; Bakhmir — Pamir);
- thermal waters of modern volcanic zones (Wairakei — New Zealand; Kunashir — Kamchatka; Salsko — Italy; Tokanu — New Zealand; Arima — Japan).
The most important ore types for endogenous deposits include spodumene ores, spodumene-lepidolite with pollucite, lepidolite with petalite, pure pollucite ores, holmquistite–cesium-biotite, lepidolite–microcline–albite, astrophyllite fenites, cesium-bearing volcanic glasses, etc. For exogenous deposits, significant materials include carnallites, various types of brines (sodium chloride, carbonate-chloride sodium, sulfate-chloride sodium-magnesium), as well as chloride, bicarbonate-chloride, and other mineralized waters.
Deposits in Ukraine
On the Ukrainian Shield, rare-metal pegmatites with pollucite are known only on the southern flank of the Zhovtorichenske deposit in the Dnipropetrovsk region. They were identified during uranium ore exploration between 1960 and 1991. The pegmatite bodies are confined to metasomatic diopside quartzites of the Hdantsivka suite.
Series of veins with a thickness of 0.1–0.5 m have been identified, exhibiting a zonal structure enriched in pollucite. The central zones consist of coarse-grained aggregates of microcline, spodumene, and pollucite; the endocontacts are composed of fine-grained formations with apatite and rubellite. Apophyses and branches (up to 5 cm thick and 1.5 m long) composed of albite-polucite aggregates with microcline and apatite are common.
The pegmatites contain quartz, microcline, albite, grains of spodumene, pollucite, rubellite, apatite, columbite, arsenopyrite, and muscovite. Spodumene occurs as short prismatic crystals up to 4×1 cm; pollucite is fine-grained, white or bluish with a metallic luster. Apatite and rubellite reach up to 1 cm, while columbite and arsenopyrite are up to 3 mm.
At the Stankuvatske deposit, Rb and Cs are associated with zones of biotitization and phlogopitization at the contacts of pegmatites with amphibolites and ultrabasic rocks. The thickness of these zones ranges from a few centimeters to 8 m. Contents: up to 1.80% Rb₂O and up to 0.50% Cs₂O. The main concentrator is phlogopite (on average 0.76% Rb₂O and 0.83% Cs₂O).
At the Polokhivske deposit, industrial concentrations are recorded in recrystallized garnet-biotite and garnet-biotite-cordierite gneisses: average contents are 0.11% Rb₂O and 0.04% Cs₂O. The main carrier of rare alkalis is biotite.
Additionally, elevated concentrations have been identified:
- in zones of phlogopitization at the contact of the Novomoskovsk granite massif with ultrabasic rocks;
- in small granite intrusions of the Volyn and Azov blocks;
- in hydrothermally altered granites of the Perzhanske ore field (Zhytomyr region), up to 2000 g/t Rb₂O;
- in groundwater of Donbas (Rb up to 1.25 mg/L, Cs up to 0.08 mg/L);
- in groundwater of the Kerch–Taman region (Rb up to 4 mg/L).