Fact-checked by Grok 2 weeks ago

Rubidium

Rubidium is a with the symbol and 37, classified as an in group 1 of the periodic table. It appears as a soft, silvery-white solid at , characterized by extreme reactivity that causes it to ignite spontaneously in air and react violently with water to produce hydrogen gas and heat. With a low of 39.3 °C and a density of 1.53 g/cm³, rubidium is one of the least dense metals and remains solid only slightly above . Discovered in 1861 by German scientists and through spectroscopic analysis of the mineral , rubidium was identified by its prominent red spectral lines, from which its name derives the Latin rubidus, meaning "deepest red." The element occurs naturally as two isotopes: stable ⁸⁵Rb (72.2% abundance) and weakly radioactive ⁸⁷Rb (27.8% abundance), with the latter being useful in for dating rocks via rubidium-strontium decay. Although rubidium does not form its own minerals, it is the 23rd most abundant element (16th among metals) in at 78 parts per million, primarily associated with lithium-bearing pegmatites such as and , and is extracted as a of production. Rubidium's high reactivity limits its handling to inert atmospheres, but its compounds find diverse applications due to unique electronic and optical properties. In , rubidium vapor is integral to precision atomic clocks, serving as a standard for GPS systems and . Rubidium salts produce a characteristic purple-violet color in and are used in specialty and ceramics to enhance durability and . Additionally, , a short-lived produced in cyclotrons, is employed in (PET) scans for to detect ischemia. Emerging uses include ion propulsion for , research in Bose-Einstein condensates for , and as of 2025, enhancing lithium-ion batteries.

Physical and Chemical Properties

Physical Properties

Rubidium is a soft, ductile, silvery-white that appears lustrous when freshly cut but tarnishes rapidly in air to a grayish-black color. It exists as a solid at standard (20–25 °C), though its low of 39.3 °C places it just above the liquid range under typical conditions, and it boils at 688 °C. The of rubidium is 1.532 g/cm³ at 20 °C, making it denser than the lighter alkali metals (0.534 g/cm³), sodium (0.968 g/cm³), and (0.862 g/cm³). Key physical properties of rubidium are summarized in the following table:
PropertyValueConditions
Melting point39.3 °CStandard pressure
688 °CStandard pressure
1.532 g/cm³20 °C
0.363 J/g·K
Thermal conductivity58 W/(m·K)20 °C
Electrical resistivity13.3 × 10⁻⁸ Ω·m20 °C
Mohs 0.3-
Rubidium's low arises from the weak characteristic of , where each atom contributes only a single to the sea, resulting in relatively low cohesive energy compared to transition metals./Descriptive_Chemistry/Elements_Organized_by_Group/Group_01:_Hydrogen_and_the_Alkali_Metals/1Group_1:_Properties_of_Alkali_Metals) In terms of mechanical properties, rubidium is softer than (Mohs hardness 0.4), consistent with the trend of decreasing hardness down the alkali metal group due to increasing atomic size and weaker interatomic forces.

Chemical Properties

Rubidium occupies (alkali metals) and period 5 of the periodic table, rendering it one of the most electropositive elements with an of 0.82 on the Pauling scale. This low electronegativity value underscores its strong tendency to donate electrons, characteristic of alkali metals, and contributes to its pronounced and reactivity. As a highly reactive alkali metal, rubidium ignites spontaneously upon exposure to air due to rapid oxidation. It also reacts violently with water, liberating hydrogen gas and forming rubidium hydroxide, often with explosive vigor from the heat generated: $2\text{Rb} + 2\text{H}_2\text{O} \rightarrow 2\text{RbOH} + \text{H}_2 In flame tests, rubidium imparts a distinctive red-violet color to the flame, arising from electronic transitions in its atoms or ions./Descriptive_Chemistry/Elements_Organized_by_Block/1_s-Block_Elements/Group__1:_The_Alkali_Metals/2Reactions_of_the_Group_1_Elements/Flame_Tests) The relatively low first ionization energy of 403 kJ/mol further explains its ease in losing the single valence electron to form the stable Rb⁺ cation. Rubidium demonstrates notable solubility in liquid , dissolving to produce a containing solvated electrons, which are electrons stabilized by the solvent's coordination. Additionally, it forms low-melting eutectic with , similar to the well-known sodium- (Na) , with phase diagrams showing eutectic points as low as 195 in certain compositions. These properties highlight rubidium's utility in applications requiring high reactivity and fluidity at reduced temperatures.

Atomic Structure and Isotopes

Electron Configuration

Rubidium, with 37, has a ground state electron configuration of [Kr] 5s¹, where the noble gas core corresponds to the configuration of ( 36) and a single occupies the 5s orbital. This arrangement places rubidium in group 1 of the periodic table, classifying it as an with high reactivity due to the loosely bound . The is characterized by the principal n = 5 and the l = 0 (s orbital). The empirical of a rubidium atom is 248 pm, reflecting its position in the periodic table where atomic size increases down due to additional electron shells. Upon to form the Rb⁺ ion, the is 152 pm for a of 6, consistent with the loss of the 5s and the resulting smaller effective size in ionic compounds. Rubidium predominantly exhibits a +1 in its compounds, as the single is readily lost to achieve a stable configuration. The spectroscopic properties of rubidium arise from transitions involving the , producing prominent emission lines in the , particularly around 780 nm and 794 nm, which give rise to the characteristic coloration observed in tests.

Isotopes

Rubidium occurs naturally with two isotopes: ^{85}Rb, which is stable and constitutes 72.2% of natural rubidium, and ^{87}Rb, which makes up the remaining 27.8%. ^{85}Rb has a nuclear spin of 5/2 and is non-radioactive, while ^{87}Rb, with a nuclear spin of 3/2, is weakly radioactive. ^{87}Rb undergoes to stable ^{87}Sr, with a of 4.96 \times 10^{10} years. The decay constant for this process is \lambda = 1.40 \times 10^{-11} \mathrm{year}^{-1}, enabling the ^{87}Rb-^{87}Sr method for , which dates geological materials by measuring the accumulation of radiogenic ^{87}Sr relative to stable isotopes. Several artificial isotopes of rubidium have been produced, primarily through nuclear reactions in reactors or accelerators. For example, ^{82}Rb decays primarily by with a of 1.26 minutes and is employed in for due to its short and suitable decay properties. Another notable artificial , ^{86}Rb, has a of 18.7 days and primarily undergoes to ^{86}Sr; it has been used as a tracer in biological studies to mimic transport. The mass difference between ^{87}Rb and ^{85}Rb leads to observable isotope effects in diffusion processes, such as kinetic fractionation during ion desolvation in aqueous solutions, where lighter isotopes diffuse slightly faster, influencing fractionation factors around -1.1 \permil for ^{87}Rb/^{85}Rb.

Occurrence and Production

Natural Occurrence

Rubidium is primarily produced through the slow neutron capture process (s-process) during nucleosynthesis in the helium- and carbon-burning phases of asymptotic giant branch stars. This stellar process accounts for the majority of rubidium isotopes heavier than iron in the cosmos. In the Earth's crust, rubidium has an average concentration of 90 parts per million (ppm), ranking it as the 16th most abundant element. The element's concentration in seawater averages 0.12 ppm (120 parts per billion, ppb), reflecting its conservative behavior in ocean cycles with a residence time of approximately 800,000 years. Rubidium seldom forms its own minerals but substitutes for potassium in a variety of silicate and evaporite minerals due to their closely similar ionic radii (Rb⁺: 1.52 Å; K⁺: 1.38 Å). Key sources include lepidolite, a mica mineral that can contain up to 3.2% rubidium by weight, pollucite (a zeolite) with up to 1.4% rubidium, and carnallite (a halide) where rubidium replaces part of the potassium content. It is also prevalent in potassium feldspars like orthoclase and microcline, comprising 0.5–2% of such minerals in granitic rocks. In the , rubidium occurs at trace levels, typically around 20 in tissues on a dry weight basis, where it mimics in physiological roles such as activation and . Concentrations can be higher in marine algae, reaching up to 7.4 , facilitating from . Naturally occurring rubidium exhibits an isotopic ratio of ^{85}Rb/^{87}Rb ≈ 2.6 (72.17% ^{85}Rb and 27.83% ^{87}Rb), which varies modestly with geological age owing to the of the radioactive ^{87}Rb .

Commercial Production

Rubidium is commercially produced primarily as a during the extraction of from and cesium from ores, with these minerals serving as the main sources in operations tied to and cesium . The low concentration of rubidium in these ores—typically 1-3.5% as rubidium oxide in and up to 2% in —necessitates efficient recovery processes integrated into larger-scale production. As of 2025, occurs in , with known output from other countries having ceased in the past two decades (e.g., Tanco mine in ceased operations; Bikita in depleted in 2018). Emerging projects include Namibia's Rubidium Hills (targeting start in 2026) and Australian sites like the Seymour Project (8.3 million tonnes Rb resource at 0.27% Rb₂O). The U.S. remains 100% import reliant. The extraction process typically begins with acid leaching of the crushed using a mixture of (HF) and (H₂SO₄) under controlled temperature and pressure conditions to solubilize rubidium along with other metals into a mixed solution. This undergoes purification through fractional , where rubidium salts precipitate selectively based on differences, or ion resins that preferentially bind rubidium ions for separation from , sodium, and contaminants. These steps yield rubidium (RbCl) or as intermediates, with recovery efficiencies often exceeding 80% in optimized industrial flows. Metallic rubidium is then obtained by reducing the purified rubidium chloride, either via of the in a controlled inert atmosphere or through thermal reduction with calcium metal at elevated temperatures around 800°C, following the reaction: $2\text{RbCl} + \text{Ca} \rightarrow 2\text{Rb} + \text{CaCl}_2 The thermal method is more commonly used industrially due to its and lower energy demands compared to . Resulting rubidium vapor or distillate is collected and further purified by to remove trace impurities like residual calcium or metals. Commercial-grade rubidium metal achieves 99.5% purity, sufficient for most applications, while research-grade material reaches 99.99% through multiple passes under high . Global annual production of rubidium metal remains limited, estimated at 5-10 metric tons as of , reflecting its niche demand, byproduct status, and unreported output from . This modest scale underscores rubidium's role as a minor commodity, with production closely tied to fluctuations in and cesium markets.

History

Discovery

Rubidium was first identified spectroscopically in 1861 by German chemists and at the University of , using their newly developed flame spectroscopy technique on samples of the mineral . While analyzing these samples, they observed two prominent lines in the spectrum, appearing as deep ruby red, which were distinct from known elements. These lines, later precisely measured at wavelengths of 794.8 nm and 780.2 nm, indicated the presence of a new . The was named rubidium, derived from the Latin word rubidus, meaning "deepest red," in reference to the characteristic color of these lines observed when its salts were heated in a . Early investigations also revealed traces of the in samples of the lepidolite, a lithium-bearing , where it appeared as an impurity during spectroscopic examination. Chemical confirmation of rubidium came in 1863 when Bunsen isolated pure rubidium chloride (RbCl) through repeated recrystallization of residues from and mineral water concentrates, separating it from contaminating and sodium salts based on differences. This process yielded the first pure compound of the element, verifying its distinct chemical identity as an . The metallic element was first isolated in 1882 by Carl Setterberg through of molten rubidium chloride, under Bunsen's supervision.

Etymology and Recognition

The name "rubidium" originates from the Latin word rubidus, meaning "deepest red" or "dark red," a reference to the two prominent spectral lines observed in its during early spectroscopic studies. This nomenclature was proposed by the element's discoverers, German chemists and physicist , who identified rubidium spectroscopically in 1861 while analyzing mineral samples from . Following its identification, early efforts to determine rubidium's atomic weight relied on chemical analyses scaled to oxygen as the standard. In the 1880s, Frank W. Clarke's comprehensive recalculation estimated it at 85.53, with subsequent international atomic weight commissions refining values to approximately 85.4 by 1900. By the , improved measurements had narrowed it to 85.44, establishing a more precise foundation for its placement in chemical tables, though further isotopic studies in the mid-20th century adjusted it to the modern value of 85.4678. In Dmitri Mendeleev's revised periodic table of 1871, rubidium was positioned directly below in Group I (alkali metals), based on its atomic weight and analogous reactivity, which underscored its role as the next heavier homolog in the series. The chemical symbol "," derived from the element's name, was formally adopted during international standardization efforts in the , as documented in early atomic weight compilations by Clarke and others, facilitating consistent global use in . Rubidium's integration into scientific reached a significant milestone in the with its recognition in research, where the hyperfine transition in rubidium-87 atoms enabled the development of the first practical rubidium gas cell standards, marking a key advancement in timekeeping .

Compounds

Inorganic Compounds

Rubidium forms a variety of ionic inorganic compounds due to its position as an , primarily consisting of salts with the large Rb⁺ cation paired with various anions. These compounds exhibit high in and are typically prepared through neutralization or metathesis ( ) processes. For instance, can be synthesized by the of rubidium metal with : \ce{Rb + H2O -> RbOH + 1/2 H2}. Similarly, rubidium chloride is often obtained via metathesis, such as treating rubidium with followed by recrystallization. The large of Rb⁺ (approximately 1.52 ) influences the in these salts, leading to ionic lattices with coordination numbers of 6 or 8, depending on the anion size and .

Halides

The rubidium halides (RbX, where X = F, Cl, Br, I) are white to colorless crystalline solids that are highly hygroscopic and soluble in water, with solubility generally increasing down the group from fluoride to iodide due to decreasing lattice energy as the anion size increases. Rubidium chloride (RbCl) appears as a white, hygroscopic powder with a rock salt (NaCl-type) structure, crystallizing in the cubic space group Fm\bar{3}m, where Rb⁺ is octahedrally coordinated to six Cl⁻ ions. Its solubility in water is 77 g/100 mL at 0 °C, increasing to 130 g/100 mL at 100 °C. Rubidium fluoride (RbF) adopts a similar cubic rock salt structure (Fm\bar{3}m), with Rb⁺ coordinated to six F⁻ ions, and is less soluble than the other halides at about 130.6 g/100 mL in water at 20 °C. Rubidium bromide (RbBr) and rubidium iodide (RbI) also crystallize in the rock salt structure (Fm\bar{3}m), exhibiting octahedral coordination, with solubilities of 98 g/100 mL and 152 g/100 mL in water at 20 °C, respectively, reflecting the trend of increasing solubility with larger anions.

Oxides and Hydroxides

Rubidium oxide (Rb₂O) is a yellow to yellow-red solid that adopts the antifluorite structure, where oxide ions form a face-centered cubic with tetrahedral coordination of four Rb⁺ ions, resulting in a cubic arrangement that stabilizes the compound's . It reacts vigorously with to form . Rubidium hydroxide (RbOH) is a colorless, deliquescent solid and a strong base, capable of fully dissociating in to yield Rb⁺ and OH⁻ ions; its density is 3.20 g/cm³, and it melts at 301 °C. The hydroxide's high reactivity stems from the weak Rb–O bond, making it more basic than sodium or analogs.

Carbonates and Sulfates

Rubidium carbonate (Rb₂CO₃) is a white, hygroscopic powder soluble in (approximately 200 g/100 mL at 20 °C) and used in specialty to improve and reduce electrical by incorporating Rb⁺ into the matrix. It decomposes upon heating above °C to rubidium oxide and . Rubidium sulfate (Rb₂SO₄) forms colorless crystals with a solubility of about 48 g/100 mL in at 20 °C, adopting an orthorhombic structure where SO₄²⁻ tetrahedra are coordinated by eight Rb⁺ ions, influencing its use as a precursor for other rubidium salts.

Nitrates

Rubidium nitrate (RbNO₃) is a white, crystalline solid with high water solubility (65 g/100 mL at 25 °C) and a rhombohedral structure at room temperature, transitioning to cubic upon melting. It undergoes thermal decomposition at 310 °C to form rubidium nitrite and oxygen via the reaction \ce{2 RbNO3 -> 2 RbNO2 + O2}, a first-order process characteristic of alkali nitrates. This decomposition highlights the compound's role in pyrotechnics, though its primary chemical interest lies in its ionic lattice stability.

Organorubidium Compounds

Organorubidium compounds are a class of organometallic reagents featuring a direct carbon-rubidium bond, belonging to the broader family of organometallics. These compounds exhibit extreme reactivity due to the low of rubidium, making them powerful nucleophiles and bases in , though their handling requires inert atmospheres and low temperatures owing to high sensitivity to air and moisture. Unlike lighter analogs, organorubidium species often display enhanced aggregation tendencies influenced by the large of Rb⁺ (1.52 ), leading to unique structural motifs. Alkylrubidium compounds, such as methylrubidium (RbCH₃) and (trimethylsilyl)methylrubidium (RbCH₂SiMe₃), represent the simplest type and are typically colorless to white solids that ignite spontaneously in air, rendering them highly pyrophoric. Aryl rubidium compounds, including phenylrubidium derivatives, follow similar bonding patterns but are less commonly isolated due to competing elimination reactions; examples include those formed transiently in arene reductions. These types are distinguished from more stabilized carbanions like allyl or benzyl variants, which can be accessed under milder conditions. Preparation of organorubidium compounds commonly involves transmetallation reactions, such as the treatment of dialkylmercury compounds (e.g., (CH₃)₂Hg) with rubidium metal to alkylrubidium species like RbCH₃. Another route employs metal-halogen , where rubidium metal or preformed organorubidium react with alkyl or aryl halides, though this is more prevalent for aryl systems and requires careful control to avoid side reactions. For solvated variants, direct cleavage of ethers by rubidium metal can generate alkylrubidium intermediates, often in (THF) solution. These methods are adapted from those for lighter metals but necessitate specialized glassware due to the heightened reactivity of rubidium. In the solid state, organorubidium compounds frequently adopt polymeric structures, with Rb⁺ cations bridged by multiple ligands to satisfy coordination demands, as seen in the infinite chain motifs of alkylrubidium solvates. For instance, bis(trimethylsilyl)methylrubidium forms a dimeric unit in crystals, while unsolvated methylrubidium exhibits a polymeric akin to the nickel arsenide structure observed in heavier homologs. Solution structures are often solvated aggregates, such as THF-coordinated monomers or oligomers, which can influence reactivity by modulating accessibility of the Rb–C bond. These polymeric and solvated forms contrast with the more monomeric behaviors of organolithium compounds. Organorubidium compounds act as extremely strong bases, capable of deprotonating weakly acidic hydrocarbons like (pKₐ ≈ 41) to form carbanions for further synthetic elaboration. Their nucleophilicity enables initiation of anionic of dienes and styrenes, producing polymers with controlled microstructures, though cesium analogs are preferred for certain high-precision applications due to even greater reactivity. Exposure to air results in rapid decomposition, often with ignition, while protic solvents provoke explosive . In reductive processes, rubidium metal generates transient organorubidium species that mediate Birch-type reductions of fused arenes, such as converting 1,2-diphenylbenzene to a stabilized η⁵-bound . Compared to organolithium reagents, organorubidium compounds are less stable, decomposing more readily at ambient temperatures and showing increased tendency for β-hydride elimination in alkyl variants, which limits their storage to cryogenic conditions. However, they surpass organocesium counterparts in stability, as the larger Cs⁺ ion promotes even greater aggregation and reactivity, making rubidium derivatives a balanced choice for syntheses requiring moderate thermal tolerance. This trend aligns with the increasing metallic character down the alkali group, where bond polarity enhances but stability diminishes.

Applications

Industrial Uses

Rubidium finds limited but specialized industrial applications, primarily due to its chemical reactivity and ability to modify material properties in niche manufacturing processes. The leading use is in the production of specialty , where rubidium (Rb₂O) or (Rb₂CO₃) is incorporated to enhance optical and electrical characteristics. Specifically, it reduces the electrical conductivity of glass, improving the stability and durability of fiber optic cables for . Additionally, rubidium compounds are added to used in photocells, where they contribute to higher sensitivity and performance. In , rubidium salts serve as promoters or components in various chemical reactions, leveraging their ability to facilitate . Rubidium carbonate, for instance, is employed in the of and rubbers, enhancing reaction efficiency and product quality. Other applications include its use as a catalyst in , , oxidation processes, and the production of , where small amounts improve yield and selectivity. Rubidium forms alloys, notably with , that exhibit low melting points and high thermal conductivity, making them suitable for applications. Rubidium-potassium mixtures have been investigated for use as coolants in experimental reactors, where their liquid state at operational temperatures allows efficient dissipation without solidification issues. In , rubidium is utilized in vacuum tubes as a getter to absorb residual gases, thereby maintaining integrity and extending device lifespan. It also shows promise in ion systems for , where its ease of enables efficient thrust generation, though commercial adoption remains limited. Global production of rubidium remains minor, with no official data reported for 2024, though estimates suggest annual output of 2 to 7 metric tons as of projections for 2025, primarily directed toward manufacturing and . High-purity rubidium metal commands an economic value of approximately $128 per gram for small quantities (1 g, 99.75% purity) as of 2024, reflecting its and specialized processing requirements.

Scientific and Technological Uses

Rubidium plays a pivotal role in atomic clocks, particularly through the use of its isotope ⁸⁷Rb in vapor cells for high-precision standards. These clocks rely on the hyperfine transition between the ground states of ⁸⁷Rb atoms, which occurs at a frequency of 6.835 GHz, providing exceptional stability for timekeeping applications such as GPS satellites and . Compact rubidium-based designs, including chip-scale versions, achieve fractional frequency uncertainties below 10⁻¹¹ over times of seconds, enabling portable and robust standards for and . In , the rubidium-strontium (Rb-Sr) dating method utilizes the of ⁸⁷Rb to ⁸⁷Sr, with a of approximately 48.8 billion years, to determine the ages of ancient rocks and meteorites. This technique has dated lunar basaltic samples from Apollo missions to around 3.9 billion years and meteorites to up to 4.5 billion years, providing key insights into the early solar system's formation. By analyzing isochrons from multiple minerals, Rb-Sr dating reveals ages and thermal histories, as demonstrated in studies of Martian meteorites like ALH 84001. Optically pumped rubidium magnetometers exploit the in ⁸⁷Rb vapor to detect with sensitivities down to femtoteslas, making them ideal for geomagnetic surveys and geophysical exploration. These devices polarize Rb atoms using light and measure frequencies in Earth's field, achieving resolutions better than 0.1 for mapping subsurface structures. In airborne applications, such as those by , rubidium magnetometers have contributed to satellite missions like Magsat for global modeling. Rubidium atoms were instrumental in the first realization of Bose-Einstein condensates (BECs) in 1995, achieved through and evaporative cooling techniques that reduced temperatures to nanokelvins. At , a dilute gas of ⁸⁷Rb atoms was cooled to 170 nK, forming a coherent where atoms occupy the lowest energy level collectively, enabling studies of and quantum vortices. This breakthrough, awarded the 2001 , has since advanced ultracold atom research for simulating complex . In , ⁸²Rb serves as a tracer in () for assessing myocardial blood flow. Produced via a strontium-82 with a short of 76 seconds, ⁸²Rb allows dynamic of cardiac uptake, quantifying stress-induced ischemia with higher accuracy than SPECT methods and lower doses around 1-2 mSv per scan. Clinical protocols recommend 1,100-1,500 MBq doses for rest/stress studies, improving diagnosis of . Rubidium atoms are employed in neutral-atom quantum computing platforms, where they are trapped in optical lattices or to serve as qubits. Researchers manipulate ⁸⁷Rb hyperfine states with lasers to perform entangling gates, achieving fidelities above 99% in arrays of up to 50 atoms, as demonstrated in Harvard's programmable . As of 2025, advancements continue in scaling these systems for practical and computing applications.

Health and Safety

Biological Role

Rubidium is present as a in biological systems, where it mimics the behavior of due to their similar ionic radii and charges, allowing rubidium ions (Rb⁺) to enter cells primarily through potassium channels and the Na⁺/K⁺-ATPase pump. In humans, the total amount of rubidium in the body is approximately 0.36 g (equivalent to about 5 mg/kg or 5 ppm in a 70 kg adult), distributed across tissues such as muscles, bones, and endocrine glands, with the body treating Rb⁺ ions similarly to K⁺ by concentrating them intracellularly. The of rubidium in humans is 31–46 days. Although not , rubidium exhibits a slight stimulatory effect on , likely stemming from its potassium-like properties. Recent research as of 2025 has explored rubidium's potential associations with cardiovascular health, such as lowering , and anti-cancer effects like in treatment, though these roles remain under investigation. In various organisms, rubidium concentrations vary, with notably higher levels observed in ; for instance, macroalgae can accumulate up to about 1 ppm, reflecting environmental availability in . Rubidium can substitute for in enzymatic processes and cellular functions, such as in ion transport and metabolic pathways, without fulfilling a specific vital role. In mammals, rubidium is not required for survival or normal physiological processes, but elevated levels can interfere with nerve function by competing with , potentially leading to muscle semi-paralysis when rubidium dominates over in ion balances. Dietary exposure to rubidium occurs through common foods, with daily intake typically ranging from 1 to 5 mg, primarily from and fruits containing 0.6–8.5 mg/kg (such as tomatoes and cucumbers) and meats like at around 6–7 mg/kg. The radioisotope ⁸⁶Rb serves as a valuable tracer in plant nutrient studies, mimicking potassium uptake to assess , potassium status, and nutrient deficiencies in roots and tissues. In environmental cycling, rubidium exhibits low overall in food chains, attributed to its high reactivity and , which facilitate rapid and limit long-term retention in organisms despite some substitution for .

Precautions and Toxicity

Rubidium metal presents significant reactivity hazards due to its position as an . It ignites spontaneously upon exposure to air and reacts explosively with to produce gas and , potentially leading to or . These properties necessitate strict handling protocols to mitigate risks of ignition or explosion during storage and use. For safe storage, rubidium must be kept under or an such as to exclude and oxygen; glass containers should be avoided, as the metal attacks surfaces. including flame-resistant clothing, gloves, face shields, and respirators is essential during manipulation, with operations conducted in inert atmospheres or dry boxes. Regulatory guidelines treat rubidium compounds as not otherwise regulated (PNOR), with OSHA permissible exposure limits of 15 mg/m³ (total ) and 5 mg/m³ (respirable ). Toxicity from rubidium primarily arises from its compounds, particularly the formed upon reaction with moisture. The oral LD50 for in rats is 586 mg/kg, indicating moderate . or can lead to hyperkalemia-like effects due to rubidium's for in biological systems, manifesting as cardiac arrhythmias, , , and gastrointestinal disturbances. Direct skin or eye contact causes severe chemical burns from the caustic . Chronic exposure effects are limited, with no classification as a by IARC, NTP, or OSHA. In case of , involves immediate flushing of or eyes with copious for at least 15 minutes while removing contaminated clothing; acids should be avoided to prevent additional heat generation from . For , do not induce , and seek medical attention promptly. requires moving the individual to fresh air and monitoring for respiratory distress.