Rubidium
minor Rubidium is potassium's heavier shadow. It substitutes for potassium in feldspars and micas, weathers out of them as Rb⁺, and then behaves as that ion and nothing else: no hydrolysis, no complexation of note, no redox chemistry, and no solid that would take it back out of solution. Conventional treatment leaves it where it is, and no drinking water or effluent standard consulted for this chapter sets a chemical value for it, though WHO gives rubidium-86 a radionuclide guidance level, so there is no treatment role to describe. What rubidium is good for is measurement. Blood and urine are rubidium rich relative to strontium, so sewage effluent leaves a works with a dissolved Rb to Sr ratio unlike that of the river it enters, and because both ions are conservative that ratio survives downstream and traces the plume.
Typical wastewaters
- municipal sewageRb⁺, conservative and enriched relative to Sr²⁺ because blood and urine are rubidium rich; the dissolved Rb to Sr ratio traces the effluent plume
- geothermal brine and lithium mica processingRb⁺, the hydrated ion, no complexation or hydrolysisnamed as industrial sources by the element chapter
1 · Identity
- Symbol, number
- Rb, 37
- Oxidation states in water
- +1 only, the hydrated Rb⁺ ion; no hydrolysis, no complexation of note, no redox chemistry
- Note
- The element chapter covers the metal and its violent reaction with water; dissolved rubidium is simply the ion left behind.
2 · Occurrence in water
- Natural sources
- Weathering of potassium feldspars and micas, in which rubidium substitutes for potassium; potash brines and evaporites (element chapter). It stays in solution like potassium and is taken up by plants and animals with it.
- Anthropogenic sources
- Sewage effluent carries rubidium enriched relative to strontium because blood and urine are Rb enriched; the dissolved Rb to Sr ratio traced the Blue Plains outfall plume in the tidal Potomac. Geothermal brines and lithium mica processing are the industrial sources (element chapter).
| matrix | typical range | note |
|---|---|---|
| seawater | 0.12 mg/L | PubChem figure carried in the element chapter |
| municipal wastewater effluent | not recordedabstract only | the tracer paper's abstract gives the Rb to Sr enrichment, not concentrations |
3 · Speciation
Rb⁺ throughout; no hydrolysis, no significant ion pairing, no redox change. It follows potassium through water treatment and the environment and is taken up by ion exchange onto clays somewhat more strongly than potassium, by analogy with caesium.
| condition | dominant species | note |
|---|---|---|
| all natural waters | Rb⁺ | conservative |
- Solubility
- All common salts are freely soluble.
- Hydrolysis
- None.
- Complexation
- Negligible.
- Precipitates
- None.
4 · Role in treatment
Not relevant or not given for this element.
5 · Removal and control
- Efficiency
- not recorded
- Interferences
- potassium and sodium compete on every exchanger
6 · Analytics
| method | standard | detection limit | note |
|---|---|---|---|
| ICP-MS | not recorded | not recorded | rubidium is routinely measured in ICP-MS trace element suites and was used as an interference monitor in the PGE isopod study (see Pd) |
- Sampling pitfalls
- Rb is conservative and easy; only the Rb to Sr ratio, not the concentration, carries the sewage signal, so measure both on the same filtered, acidified sample.
7 · Regulatory limits
Limits change, and many are set locally. Treat these as the published values to start from, not as your compliance target: check the standard in force at your site and the numbers written into your own permit.
| body | limit | note |
|---|---|---|
| WHO GDWQ 4th ed. with addenda (2022) | no guideline | not in Table A₃.3 (guideline values) nor in Table A₃.2 (chemicals considered but not given a value) |
| EU DWD 2020/2184 | not set | not an Annex I parameter |
| US EPA NPDWR | not regulated | no MCL |
| WHO GDWQ Table A₆.1 (radionuclides) | 100 Bq/L | rubidium-86; guidance level at 0.1 mSv per year |
| body | limit | note |
|---|---|---|
| EU CWW BREF BAT-AEL 1, BAT 12 | not set | Tables 1 to 3 carry TOC, COD, TSS, TN, Ninorg, TP, AOX, Cr, Cu, Ni and Zn only |
8 · Health and environmental effects
- Toxicity
- No drinking water guideline. The US EPA provisional (PPRTV, 2016) assessment derived only a screening subchronic reference dose of 5 x 10⁻3 mg/kg per day for rubidium chloride (human LOAEL 5.3 mg/kg per day in small antidepressant trials: weight gain, diarrhoea, nausea, polyuria, confusion, agitation; uncertainty factor 1000), no chronic value, and found no IRIS, HEAST or drinking water health advisory value. Rats given 1,200 mg/L rubidium chloride in drinking water (167 mg/kg per day) for 10 days showed altered saliva flow and composition; mice at 299 to 896 mg/kg per day in drinking water for 3 weeks developed sound-induced convulsive seizures and deaths, worse when dietary potassium and magnesium were deficient. Rat studies indicated that lower doses take longer to produce toxicity, so no chronic value was derived.
- Bioaccumulation
- Taken up with potassium by all organisms; blood and urine are Rb enriched relative to Sr, which is the basis of the effluent tracer.
Read these with care
- The PPRTV screening value is a Superfund risk assessment number, not a limit, and the document itself labels it as carrying considerably more uncertainty than a full provisional value.
- No river or groundwater concentration was read; the Gaillardet world river average and the Turkish spring range seen in search summaries are not written.
What this chapter does not cover
- No river, groundwater, drinking water or effluent concentration was read from a primary source.
- No aquatic ecotoxicity data were read.
- No GCC discharge standard was read.
- The clay ion exchange selectivity for Rb⁺ over K⁺ is asserted from the caesium analogy, not read.
- Ecotoxicity: No aquatic ecotoxicity value is quoted for rubidium.
Notes
- Decision 2016/902
Sources
Dissolved rubidium to strontium ratio as a conservative tracer for wastewater effluent-sourced contaminant inputs near a major urban wastewater treatment plant, Water Research (2021), doi 10.1016/j.watres.2021.117691 (abstract, PubMed 34619608)
WHO Guidelines for Drinking-water Quality, 4th ed. incorporating the first and second addenda (2022), Annex 3 chemical summary tables: Table A3.2 chemicals for which guideline values have not been established and Table A3.3 guideline values for chemicals of health significance
WHO Guidelines for Drinking-water Quality, 4th ed. incorporating the first and second addenda (2022), Annex 6 Table A6.1 guidance levels for radionuclides in drinking-water (individual dose criterion 0.1 mSv per year, levels rounded to the nearest order of magnitude)
Directive (EU) 2020/2184 on the quality of water intended for human consumption (recast), Annex I Parts B, C and D (annexes read on legislation.gov.uk)
US EPA, National Primary Drinking Water Regulations (table of MCLs; inorganic chemicals and radionuclides; beta particle and photon emitters 4 millirem per year)
Commission Implementing Decision (EU) 2016/902 establishing BAT conclusions for common waste water and waste gas treatment/management systems in the chemical sector (CWW), BAT 12 Tables 1 to 3 (TOC, COD, TSS, TN, Ninorg, TP, AOX, Cr, Cu, Ni, Zn) (annex read on legislation.gov.uk)
The Element Book, element chapter and reference text for Rb (alkali metal chemistry, reaction with water, potassium mineral hosts, crust and seawater abundance)
Identity
- Name and symbol
- Rubidium, Rb
- Atomic number
- 37 protons
- Position
- group 1 · period 5 · s-block · alkali metal
- CAS number
- 7440-17-7
Atomic structure
- Atomic mass
- 85.4678 u
- Electron configuration
- 1s² 2s² 2p⁶ 3s² 3p⁶ 4s² 3d¹⁰ 4p⁶ 5s¹
[Kr] 5s¹ - Electrons per shell
- 2, 8, 18, 8, 1
- Valence electrons
- 1 outer shell
| isotope | mass (u) | abundance |
|---|---|---|
| 85Rb | 84.911 789 74(3) | 72.17 % |
| 87Rb | 86.909 180 53(4) | 27.83 % |
Physical properties
- State at room temperature
- Solid
- Melting point
- 312.46 K (39.31 °C)
- Boiling point
- 961 K (687.85 °C)
- Density
- 1.53 g/cm3
- Appearance
- grey white
- Thermal conductivity
- 58.2 W/(m·K)
- Electrical resistivity
- 128 nΩ·m at 20 °C
- Electrical conductivity
- 7.81 MS/m
- Crystal structure
- body-centered cubic
- Molar heat capacity
- 31.06 J/(mol·K)
Chemical properties
- Oxidation states
- +1
- Electronegativity
- 0.82 (Pauling Scale)
- Ionisation energy
- 4.177 eV
1st 403, 2nd 2,633, 3rd 3,860 kJ/mol - Electron affinity
- 0.468 eV
- Atomic radius
- empirical 220, covalent 220, van der Waals 303 pm
- Ionic radius
- Rb⁺ 152 pm
- Reactivity
- A soft alkali metal, the second most electropositive element after caesium: one loosely held 5s electron makes it ignite spontaneously in air and react violently with water, so it is stored under dry mineral oil or in an inert atmosphere.
- with water
- Reacts violently with water, sinking as it goes, to rubidium hydroxide and hydrogen, which the heat of reaction ignites: .
- with oxygen, air
- Ignites spontaneously in air; in excess oxygen it burns to the superoxide: , with Rb2O and suboxides formed in limited air.
- with acids
- Reacts explosively with dilute acids to the rubidium salt and hydrogen: .
- with halogens
- Burns in the halogens to the rubidium halides RbF, RbCl, RbBr and .
- Typical compounds
- RbOH rubidium hydroxidestrong base, starting point for rubidium chemistry
- RbCl rubidium chloridethe metal is made by reducing it with calcium
- RbO₂ rubidium superoxideproduct of burning the metal in oxygen
- Rb₂CO₃ rubidium carbonateused in optical glasses
- RbNO₃ rubidium nitratepurple colour in fireworks
- RbAg₄I₅ rubidium silver iodidehighest room-temperature conductivity of any ionic crystal
- RbOH rubidium hydroxide
Occurrence, production and use
- Crustal abundance
- 9.0×101 milligrams per kilogram
- Oceanic abundance
- 1.2×10-1 milligrams per liter
- Occurrence and sources
The element is much more abundant than was thought several years ago. It is now considered to be the 16th most abundant element in the earth's crust. Rubidium occurs in pollucite, leucite, and zinnwaldite, which contains traces up to 1%, in the form of the oxide. It is found in lepidolite to the extent of about 1.5%, and is recovered commercially from this source. Potassium minerals, such as those found at Searles Lake, California, and potassium chloride recovered from the brines in Michigan also contain the element and are commercial sources. It is also found along with cesium in the extensive deposits of pollucite at Bernic Lake, Manitoba.
- lepidolite (lithium mica, up to 3.5 percent Rb2O)zoned granite pegmatites; the commercial source as a by-product of lithium extraction
- pollucite (caesium aluminosilicate, up to 1.5 percent Rb2O)pegmatites; by-product of caesium mining (Bikita Zimbabwe depleted 2018, Sinclair Australia mined out 2019)
- carnallite, leucite, potash brines and evaporitesbrines in northern Chile and China; evaporites in New Mexico, Utah, France, Germany
- crustal and oceanic abundanceabout 90 ppm 1; 90 mg/kg crust and 0.12 mg/L seawater 2
- lepidolite (lithium mica, up to 3.5 percent Rb2O)
- Extraction, production
- By-product concentrate from lepidolite and pollucite processing
Rubidium concentrate is recovered while lithium or caesium is extracted from the ore and imported for chemical conversion; no official world production figure exists for 2024 and neither USGS nor RSC states a reaction for the separation or for making the metal
- Uses
Rubidium is used in vacuum tubes as a getter, a material that combines with and removes trace gases from vacuum tubes. It is also used in the manufacture of photocells and in special glasses. Since it is easily ionized, it might be used as a propellant in ion engines on spacecraft. Recent discoveries of large deposits of rubidium suggest that its usefulness will increase as its properties become better understood.
Rubidium forms a large number of compounds, although none of them has any significant commercial application. Some of the common rubidium compounds are: rubidium chloride (RbCl), rubidium monoxide (Rb2O) and rubidium copper sulfate Rb2SO4·CuSO4·6H20). A compound of rubidium, silver and iodine, RbAg4I5, has interesting electrical characteristics and might be useful in thin film batteries.
Because rubidium can be easily ionized, it has been considered for use in "ion engines" for space vehicles; however, cesium is somewhat more efficient for this purpose. It is also proposed for use as a working fluid for vapor turbines and for use in a thermoelectric generator using the magnetohydrodynamic principle where rubidium ions are formed by heat at high temperature and passed through a magnetic field. These conduct electricity and act like an amature of a generator thereby generating an electric current. Rubidium is used as a getter in vacuum tubes and as a photocell component. It has been used in making special glasses. RbAg4I5 is important, as it has the highest room conductivity of any known ionic crystal. At 20°C its conductivity is about the same as dilute sulfuric acid. This suggests use in thin film batteries and other applications.
- Glass and fibre optics: rubidium carbonate added to speciality glass to lower electrical conductivity and improve durability in fibre-optic networks; the leading market
- Electronics and timekeeping
- photoemissive cathodes in photocells, photomultipliers, night-vision and motion sensors
- rubidium atomic frequency standards for telecom synchronisation and GPS; rubidium fountain clocks in the US Naval Observatory timescale
- ultracold rubidium atoms in quantum-computing research
- oxygen getter in vacuum tubes
- Chemicals: catalyst or promoter in ammonia synthesis, sulfuric acid synthesis, hydrogenation, oxidation and polymerisation reactions
- Medicine
- rubidium-82 as a blood-flow tracer in PET imaging
- rubidium salts in antishock agents and research on epilepsy, thyroid disorder and depression
- Pyrotechnics: rubidium nitrate and hydroxide for violet colour and as oxidiser
- Safety, toxicity
- GHS classification, signal word Danger
- H260 In contact with water releases flammable gases which may ignite spontaneously Substances and mixtures which in contact with water, emit flammable gases
- H314 Causes severe skin burns and eye damage Skin corrosion/irritation
Discovery and name
- Discovered by
- Gustav Kirchhoff and Robert Bunsen
- Discovered
- 1861
- First isolated
- George de Hevesy
- Named by
- not in sources
- Origin of the name
- from Latin rubidus, 'deep red', for the color of its emission spectrum
Rubidium can be liquid at room temperature. It is a soft, silvery-white metallic element of the alkali group and is the second most electropositive and alkaline element. It ignites spontaneously in air and reacts violently in water, setting fire to the liberated hydrogen. As with other alkali metals, it forms amalgams with mercury and it alloys with gold, cesium, sodium, and potassium. It colors a flame yellowish violet. Rubidium metal can be prepared by reducing rubidium chloride with calcium, and by a number of other methods. It must be kept under a dry mineral oil or in a vacuum or inert atmosphere.
Notes
- BGS figure via RSC
- PubChem
Conventions
Valence electrons are counted by the usual convention: the outer shell for s- and p-block elements, ns and (n-1)d for the d-block, ns, (n-1)d and (n-2)f for the f-block. Lanthanides and actinides are placed in the f-block with no group number. Electrical conductivity is the reciprocal of the printed resistivity. Ionic radii are Shannon effective radii, six-coordinate unless noted. Where a field reads “not in sources” the value was not found; it is a gap, not a zero. Regulatory limits are the published values and change often, so check the standard in force at your site and the numbers written into your own permit before you design to them.
Data
Element records, isotopes, radii and the descriptive text come from PubChem (NCBI), the Los Alamos National Laboratory periodic table, IUPAC CIAAW and the IAEA Atomic Mass Data Center. Appearance, thermal conductivity, electrical resistivity, crystal structure, discovery and the origin of each name come from Wikipedia and Periodic-Table-JSON, used under CC BY-SA 4.0. Hazard classifications come from the ECHA C&L inventory via PubChem. Ionic radii follow R. D. Shannon (1976). The water chapters cite their own sources at the foot of each entry, and are written to the level of Snoeyink and Jenkins, Stumm and Morgan, MWH's Water Treatment and Metcalf and Eddy.