Potassium

Potassium — Material Page
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Potassium (K, atomic number 19) is the fourth alkali metal — a soft, silvery-white Group 1 element with a melting point of only 63.5 °C, a density of 0.86 g/cm³ (lighter than water), and the second most negative standard electrode potential of any element at –2.93 V vs. SHE. With a body-centered cubic (BCC) crystal structure, a single 4s¹ valence electron, and an atomic radius of 227 pm (the largest of the common alkali metals after caesium and rubidium), potassium is extraordinarily reactive — it ignites spontaneously in moist air, reacts violently with water (2K + 2H₂O → 2KOH + H₂↑, with the evolved hydrogen typically igniting), and must be stored under mineral oil or inert atmosphere. Potassium is the seventh most abundant element in Earth's crust (~2.1 wt%), occurring as potassium feldspar (orthoclase, KAlSi₃O₈), muscovite mica (KAl₂(AlSi₃)O₁₀(OH)₂), sylvite (KCl), and carnallite (KCl·MgCl₂·6H₂O). K⁺ is the dominant intracellular cation in all living cells — the K⁺ concentration inside mammalian cells is ~140 mM versus ~4 mM in extracellular fluid, a gradient maintained by the Na⁺/K⁺-ATPase pump that consumes ~30% of the ATP budget of neurons and ~20% of the total cellular ATP in the human body. Potassium is one of the three macronutrients (NPK — nitrogen, phosphorus, potassium) essential for plant growth, and global fertilizer-grade KCl (muriate of potash) and K₂SO₄ production (~45 million tonnes K₂O equivalent/year) dwarfs all other potassium chemistry combined.

The defining chemical characteristic of potassium metal is its combination of extreme reactivity and unique selectivity — K⁺ is the preferred cation in biological ion channels (K⁺ channels), the strongest flame colorant in analytical chemistry (766 nm violet emission), and the basis of the most important geochronological dating system for geological time. Potassium is a stronger reductant than sodium — it reduces water more vigorously, forms the superoxide KO₂ (rather than the peroxide Na₂O₂) on combustion in excess air, and reacts with liquid ammonia at –33 °C to give solvated electrons (deep blue solutions used in Birch reductions and dissolving metal reductions in organic synthesis). The Birch reduction (dissolving metal reduction with Li, Na, or K in liquid NH₃ with alcohol co-solvent) is an indispensable tool in synthetic organic chemistry for partial reduction of aromatic rings and selective reduction of conjugated systems — potassium in particular gives selectivity for 1,4-reduction of electron-rich aromatic systems. Potassium-sodium alloy (NaK, typically 78 wt% K, mp –12.6 °C) is liquid at room temperature and has been used as a nuclear reactor coolant (fast breeder reactors), heat transfer fluid in experimental systems, and as a highly reactive reagent in synthesis and pyrotechnic research.

Potassium's nuclear properties — specifically the natural radioactivity of ⁴⁰K and its branched decay to both ⁴⁰Ar and ⁴⁰Ca — underpin two of the most important quantitative tools in Earth science: K-Ar and ⁴⁰Ar/³⁹Ar geochronology, which together have dated virtually every major geological event and extraterrestrial sample from the Moon, Mars, and meteorites. ⁴⁰K (0.0117% natural abundance, t½ = 1.248 × 10⁹ yr) decays by branched β⁻ decay to ⁴⁰Ca (89.28%) and by electron capture/β⁺ to ⁴⁰Ar (10.72%) — the accumulation of radiogenic ⁴⁰Ar in minerals closed to argon loss records the time since the mineral cooled below its argon retention temperature (closure temperature), which ranges from ~150 °C (biotite) to >500 °C (hornblende) to >900 °C (K-feldspar). The ⁴⁰Ar/³⁹Ar variant (neutron irradiation converts ³⁹K to ³⁹Ar as a K proxy, enabling measurement of both ratios on a single aliquot by step-heating) provides better precision (±0.1–1%) and allows identification of argon loss from partially reset grains — it is the standard technique for dating volcanic eruptions, impact events, metamorphic terranes, and the timing of planetary differentiation in meteorites.

General Properties

PropertyValueNotes
Atomic Number19Group 1 (alkali metals), Period 4; 4s¹ electron configuration; sits below sodium (11) and above rubidium (37) in Group 1; standard electrode potential –2.93 V vs. SHE — second most negative of the common alkali metals (Li: –3.04 V, Na: –2.71 V, K: –2.93 V, Rb: –2.98 V, Cs: –3.03 V); the anomalous trend (K more negative than Na) reflects the lower hydration energy of K⁺ relative to the ionization energy difference
Atomic Mass39.098 uThree naturally occurring isotopes: ³⁹K (93.258%), ⁴⁰K (0.0117% — naturally radioactive), ⁴¹K (6.730%); the low abundance of ⁴⁰K belies its geological importance — despite being only 117 ppm of natural K, its 1.248 Gyr half-life and 10.72% branching to ⁴⁰Ar makes it the basis of K-Ar geochronology; δ⁴¹K isotope ratios (MC-ICP-MS) are an emerging tracer for K cycling in ocean chemistry, weathering, and biological fractionation
Density (20 °C)0.862 g/cm³Less dense than water — potassium floats on water while reacting violently with it; the second-lowest density of any solid element at room temperature after lithium (0.534 g/cm³); sodium (0.971 g/cm³) and potassium (0.862 g/cm³) are both less dense than water, a direct consequence of the large atomic radii of Period 3–4 alkali metals relative to their modest atomic masses
Melting Point63.5 °C (336.7 K)Low enough to melt in hot water (>63.5 °C); the NaK eutectic alloy (78 wt% K) melts at –12.6 °C, enabling liquid-metal operation at and below room temperature; the low melting point reflects the weak metallic bonding of the single large 4s electron in a very large unit cell; within the alkali metal group, melting points decrease monotonically: Li (180.5 °C), Na (97.7 °C), K (63.5 °C), Rb (39.3 °C), Cs (28.4 °C)
Boiling Point759 °C (1,032 K)Wide liquid range (696 °C); K vapor is monatomic and absorbs strongly at the D-line doublet (766.5/769.9 nm, violet) — the flame photometry K emission at 766 nm is the most sensitive and selective optical detection method for K⁺ in clinical and agricultural analysis; potassium vapor pressure is significant above ~500 °C, requiring care in high-temperature operations
Thermal Conductivity102.5 W/m·KExcellent thermal conductivity relative to its density — higher than iron (80 W/m·K) despite being only 10.9% as dense; the NaK liquid metal alloy (78K-22Na) has thermal conductivity ~25 W/m·K in the liquid state, and the excellent heat transfer properties of liquid alkali metals have driven their use as fast breeder reactor coolants (sodium) and heat transfer fluids in experimental high-temperature systems; the high thermal conductivity of solid K facilitates rapid heat dissipation from exothermic reactions during synthesis operations
Electrical Resistivity72 nΩ·m (20 °C)Low resistivity for a metal — comparable to lithium (92.8 nΩ·m) and sodium (47.7 nΩ·m); reflects the free-electron metallic structure of alkali metals; the high electrical conductivity of alkali metals combined with their extreme reactivity and low density has prompted theoretical interest in K as a potential low-temperature electride conductor and in K-graphite intercalation compounds (KC₈) as superconductors (Tc ~0.55 K)
Crystal StructureBCC; a = 5.321 Å (room temperature)BCC structure at room temperature; transforms to FCC below –73 °C under some conditions; the very large BCC unit cell (5.321 Å vs. iron 2.866 Å) reflects the large atomic radius of K (227 pm); the BCC structure collapses under high pressure through a complex sequence of phases (fcc, tI19, oC16, tI4...) — K under pressure exhibits superconductivity up to Tc ~20 K and a "transparent" high-pressure phase; at ambient conditions the BCC structure accounts for K's softness, low melting point, and high compressibility

Mechanical Properties

PropertyValueNotes
Yield Strength~2 MPaAmong the lowest yield strengths of any solid element — potassium is so soft it can be cut with a butter knife and deforms plastically under its own weight at room temperature; the extremely low strength reflects the minimal cohesive energy of a single large s-electron per atom in a very large unit cell with weak metallic bonding; potassium has no engineering structural applications whatsoever — it is used exclusively as a chemical reagent, heat transfer medium (as NaK alloy), or in compound form
Young's Modulus3.53 GPaOne of the lowest elastic moduli of any solid element — comparable to soft rubber (1–10 MPa), roughly 60× lower than aluminum (70 GPa) and 60× lower than iron (211 GPa); reflects the extreme compressibility of the large, loosely bound BCC lattice; the compressibility of alkali metals makes them important model systems for equation-of-state studies at high pressure
HardnessMohs ~0.4One of the softest of all elements — softer than lithium (Mohs ~0.6) and sodium (~0.5); can be cut with a fingernail; the softness reflects the near-absence of directional bonding and the very large atomic radius; pure K is also highly ductile — it flows plastically without fracture, which is relevant to handling pellets and ingots under inert atmosphere

Chemical Properties

PropertyValue / BehaviorNotes
Reactivity with WaterViolently exothermic; ignites H₂ evolved; produces KOH solution2K + 2H₂O → 2KOH + H₂↑ (ΔH = –392 kJ/mol K); the hydrogen generated ignites immediately from the heat of the reaction — K burns with a violet/lilac flame (766 nm K* emission); more violent than sodium (which may or may not ignite the H₂) but less violent than rubidium and caesium (which detonate even on surface contact); Class D metal fire — water, CO₂, and halogenated extinguishants are all contraindicated; extinguish with dry sand or Met-L-X Class D powder
Reactivity with AirForms K₂O immediately; forms KO₂ (superoxide) in excess O₂; tarnishes within secondsUnlike sodium (Na₂O₂ peroxide in excess O₂), potassium preferentially forms the superoxide KO₂ (yellow solid) in excess air — KO₂ is a strong oxidant that reacts violently with water (4KO₂ + 2H₂O → 4KOH + 3O₂) and with organic materials; aged K metal that has formed a KO₂ crust is especially hazardous and must be destroyed by specialist disposal rather than attempting to cut through the crust; storage under paraffin oil or in inert atmosphere (Ar, N₂) is mandatory for laboratory K metal
Oxidation State+1 exclusively (K⁺)K⁺ ionic radius 138 pm (octahedral) — significantly larger than Na⁺ (102 pm), which is the structural basis for K⁺ channel selectivity: the selectivity filter of K⁺ channels (GYGF motif) coordinates K⁺ at a precisely optimal distance that is energetically unfavorable for the smaller Na⁺, providing ~1,000:1 K⁺/Na⁺ selectivity in the most discriminating channels; K⁺ in negative oxidation states exists only in electrides (K⁺ e⁻ compounds such as K in liquid ammonia, K-cryptand compounds)
Reactions in Liquid AmmoniaSolvated electrons (blue solution at low K); bronze metallic solution at high KPotassium dissolves in liquid NH₃ (–33 °C) to give a brilliant deep blue solution of solvated electrons (K⁺ + e⁻ₛₒₗᵥ) — the deepest blue color achievable by any chemistry; at higher K concentrations the solution turns bronze-metallic as solvated electron pairs form; these solutions are extremely powerful reductants (E° ≈ –2.87 V) used in Birch reductions (partial reduction of aromatic rings, e.g. benzene to 1,4-cyclohexadiene), dissolving metal synthesis of strained ring systems, and reductive cleavage reactions in complex molecule synthesis; K in NH₃ gives selectivity for 1,4-reduction of electron-rich aromatics (vs. Na which preferentially reduces electron-poor systems)
IdentifierValue
SymbolK
Atomic Number19
CAS Number7440-09-7
UN NumberUN2257 (potassium metal, solid)
EINECS Number231-119-8
IsotopeTypeNotes
³⁹K Stable 93.258% natural abundance; I = 3/2, NMR-active (moderate quadrupole moment); ³⁹K NMR is used to characterize K⁺ coordination in ionic liquids, potassium-ion battery electrolytes, ion-exchange membranes, and zeolite frameworks; ³⁹K(p,n)³⁹Ca and ³⁹K(d,p)⁴⁰K reactions studied for accelerator-based isotope production; δ⁴¹K/³⁹K isotope ratios used to trace K biogeochemical cycling — this uses ³⁹K as the denominator isotope in the standard three-isotope notation
⁴⁰K Radioactive* 0.01170% natural abundance; t½ = 1.248 × 10⁹ yr; branched decay: β⁻ to ⁴⁰Ca (89.28%, Emax = 1.311 MeV) and electron capture/β⁺ to ⁴⁰Ar (10.72%, EC to excited ⁴⁰Ar* emitting 1,460.8 keV gamma — the strongest natural gamma-ray line in the environment); ⁴⁰K is the dominant source of natural radioactivity in the human body (~4,400 Bq/70 kg person) and the dominant natural gamma emitter in soils and building materials; the accumulation of radiogenic ⁴⁰Ar from ⁴⁰K decay in minerals is the basis of K-Ar geochronology (t½ known to ±0.2%) and the ⁴⁰Ar/³⁹Ar method — together, these techniques have dated virtually every major geological event, lunar sample, Martian meteorite, and impact crater on Earth; ⁴⁰K also contributes to the natural radioactivity of seawater (~12 Bq/L) and to the internal radiation dose from food (bananas and other K-rich foods contain ~14 Bq/100 g from ⁴⁰K); the 1,460.8 keV line is a standard energy calibration reference for high-purity germanium (HPGe) gamma-ray detectors
⁴¹K Stable 6.730% natural abundance; I = 3/2, NMR-active (larger quadrupole moment than ³⁹K; less receptive but used in complementary solid-state NMR studies); enriched ⁴¹K is used as an IDMS spike for high-precision K concentration measurements in geological reference materials, seawater, and biological samples; δ⁴¹K measurements (MC-ICP-MS, ±0.05‰) trace K isotope fractionation in continental weathering (K-feldspar dissolution), marine sediments (K⁺ uptake in clay minerals), plant uptake (biological fractionation –0.6 to –1.5‰ per mass unit relative to rock), and potassium-ion battery electrode reactions where slight isotopic fractionation during K⁺ intercalation into graphite anodes has been reported

Scientific & Research Applications

Use CaseForm Typically UsedDescription
Birch Reduction & Dissolving Metal SynthesisK metal pellets (99.97%), Na metal (alternative); liquid NH₃ solventPotassium dissolved in liquid ammonia (–33 °C) generates solvated electrons — powerful reductants used in Birch reductions (partial reduction of arenes to unconjugated cyclohexadienes: benzene → 1,4-cyclohexadiene; anisole → 2,5-dihydroanisole), reductive cleavage of C-O bonds (benzylic deprotection, PMB ether cleavage), and reduction of alkynes to trans-alkenes. K in NH₃ is preferred over Na for electron-rich aromatic systems where regioselectivity favors the unsubstituted positions; Na is preferred for electron-poor systems. Birch reductions are widely used in pharmaceutical synthesis (e.g. prostaglandin intermediates, steroid synthesis, natural product total synthesis).
Potassium-Ion Battery ResearchK metal foil (anode), KPF₆/KFSI electrolyte salts, K₂CO₃ precursorsPotassium-ion batteries (KIBs) are studied as potential alternatives to lithium-ion batteries for large-scale stationary energy storage, exploiting potassium's earth abundance (K: 2.1 wt% crust vs. Li: 20 ppm), lower cost, and favorable K⁺/K electrode potential (–2.93 V, close to Li⁺/Li –3.04 V, enabling high cell voltages). K⁺ intercalation into graphite (KC₈, theoretical capacity 279 mAh/g) and hard carbon anodes, and into Prussian blue analogue cathodes, has been demonstrated. Key research challenges include K metal's extreme reactivity with electrolytes (SEI formation), K dendrite growth on K metal anodes, and finding electrolytes with wide electrochemical windows compatible with K metal.
Chemical Synthesis & Strong Base ReactionsK metal pellets; KOH, KNH₂, K-selectride (derived from K)Potassium metal is a primary precursor for extremely strong bases used in organic synthesis: potassium amide (KNH₂, prepared by K + NH₃) is a superbase (pKa ~38) used to deprotonate weakly acidic C-H bonds and for directed ortho-metalation; potassium hydride (KH, from K + H₂) is a powerful non-nucleophilic base used for enolate formation, alcohol deprotonation, and as a base/reducing agent for transition metal chemistry; potassium tert-butoxide (KOtBu, from K + tBuOH) is a bulky strong base for elimination reactions, Wittig reaction, and directed metalation. KHMDS (potassium hexamethyldisilazide) is the most widely used K-based non-nucleophilic strong base in asymmetric synthesis.
Ion Channel & Biological Transport StudiesKCl solutions; K-selective electrodes; ³⁶Cl/⁴²K radiotracer historicallyThe K⁺/Na⁺ selectivity of ion channels — fundamentally determined by the geometry and chemistry of the selectivity filter — is studied using patch-clamp electrophysiology, crystallography of KcsA and other K⁺ channels, and molecular dynamics simulation. K⁺ flux across cell membranes determines resting membrane potential (–70 mV in neurons), action potential repolarization, and cell volume regulation. Research with potassium compounds (KCl, K₂SO₄ gradients) simulates physiological K⁺ concentrations; synthetic K⁺ channel mimics (valinomycin K⁺ carrier, crown ether 18-crown-6 selective for K⁺ over Na⁺) are studied as ion transport models and antibiotic mechanisms.
Geochronology Standards & K-Ar DatingK-bearing standards (sanidine Fish Canyon Tuff, MMhb-1 hornblende), enriched ³⁸Ar or ³⁷Ar spike⁴⁰Ar/³⁹Ar geochronology (a variant of K-Ar) is the gold-standard dating technique for volcanic rocks, metamorphic minerals, and extraterrestrial samples — the method irradiates samples with fast neutrons in a research reactor (converting ³⁹K to ³⁹Ar as a K proxy), then measures ⁴⁰Ar/³⁹Ar ratios by step-heating in a mass spectrometer. This enables plateau age spectra that identify argon loss from partially reset samples, integration ages for well-behaved systems, and isochron ages that constrain initial ⁴⁰Ar/³⁶Ar. Precision routinely reaches ±0.1–0.5% (±0.1–1 Ma for Cenozoic rocks), enabling dating of individual volcanic eruptions, orbital forcing correlations, and calibration of the geological time scale.
Spectroscopy Calibration & Laser CoolingK vapor cell, enriched ³⁹K or ⁴¹K atomic beamPotassium atomic lines at 766.5 nm and 769.9 nm (4s → 4p D-line doublet) are standard emission lines for flame photometry calibration and for diode laser wavelength referencing. In ultracold physics, ⁴⁰K (the fermionic isotope) is used alongside ⁸⁷Rb (bosonic) to study mixtures of Fermi and Bose superfluids, interspecies Feshbach resonances, and polaronic physics in ultracold Fermi-Bose mixtures; ⁴¹K is used for Bose-Einstein condensate experiments. The accessible 767/770 nm cooling wavelengths (GaAlAs diode lasers) make K a convenient atomic physics workhorse; ⁴⁰K Fermi gases are used to study BCS-BEC crossover and superfluidity analogous to neutron stars.

Industrial & Commercial Applications

SectorForm / Compound UsedDescription
Fertilizer Industry (Potassium Compounds)KCl (muriate of potash, MOP), K₂SO₄ (sulfate of potash, SOP), KNO₃Potassium is one of the three primary macronutrients for plant growth (N-P-K), essential for stomatal regulation, enzyme activation, protein synthesis, and sugar transport in phloem. Global KCl production is ~45 million tonnes/year (K₂O equivalent), mined from evaporite deposits (sylvinite, carnallite) in Canada (Saskatchewan, the world's largest reserves), Russia, Belarus, and Germany. The K metal is not used directly — K compounds (KCl, K₂SO₄, KNO₃) are the fertilizer forms. K₂SO₄ (chloride-free) is preferred for sensitive crops (tobacco, fruits, potatoes); KNO₃ provides both K and N for fertigation.
NaK Alloy (Coolant & Heat Transfer)NaK alloy (typically 78 wt% K, 22 wt% Na; mp –12.6 °C)NaK (sodium-potassium alloy, ~78K-22Na by weight) is liquid from –12.6 °C to ~785 °C and provides excellent heat transfer properties (thermal conductivity ~25 W/m·K liquid) for experimental nuclear reactors, concentrated solar power secondary loops, and high-temperature electronics cooling. It was used as the secondary coolant in the EBR-II and Dounreay fast breeder reactors. NaK's low melting point (vs. sodium's 98 °C) eliminates the freeze-up risk that limits sodium cooled systems. Extreme reactivity with water and air requires complete system inertisation with argon; NaK disposal requires specialized alkoxide/alcohol treatment and is a registered hazardous waste stream.
Pyrotechnics & Signal FlaresKNO₃ (oxidizer), KClO₄ (perchlorate oxidizer), K metal (reducing, limited use)Potassium compounds are the standard oxidizers in fireworks and signal flares: KNO₃ (black powder: 75% KNO₃, 15% charcoal, 10% S) has been used since the 9th century; KClO₄ (potassium perchlorate) is the dominant modern oxidizer in colored signal flares and star compositions — it is preferred over KClO₃ for stability and lower sensitivity to friction and impact; K metal vapor produces the characteristic violet/lilac flame (766.5 nm K atomic emission) used in colored fire compositions. Potassium compounds also produce the violet flame in theatrical pyrotechnics and theatrical special effects.
Glass & Ceramics ManufacturingK₂O (from K₂CO₃, potassium carbonate), K-feldspar mineral as batch materialPotassium oxide (K₂O, added as K₂CO₃ flux) in glass compositions increases chemical durability, raises the refractive index, and improves working properties vs. Na₂O glasses — potassium crystal glass (full lead crystal replacements using K₂O-BaO-ZnO compositions, 24% K₂O) achieves high refractive index (n ~1.53) and sparkle for high-quality tableware. K₂O additions to borosilicate glass improve chemical resistance; K-aluminosilicate glass-ceramics (Corning Gorilla Glass: ion-exchange strengthening by replacing Na⁺ in surface with larger K⁺ from KNO₃ melt at 410 °C) creates a compressive surface stress layer of ~700–900 MPa that provides scratch and impact resistance in smartphone screens.
KOH Electrolyte (Alkaline Electrolysis)KOH solution (25–30 wt%) as alkaline electrolyzer electrolyteConcentrated KOH (30 wt%, ~6 M) is the standard electrolyte in alkaline water electrolyzers for hydrogen production — KOH is preferred over NaOH due to its higher ionic conductivity at equivalent concentration (~0.625 S/cm vs. ~0.34 S/cm for NaOH at 25 °C, because K⁺ has lower hydration energy and higher mobility than Na⁺ in concentrated solution). Industrial alkaline electrolyzers (Thyssenkrupp, Nel Hydrogen, McPhy) consuming up to 300 MW of renewable electricity use KOH electrolyte in Zirfon-membrane separated cells producing green hydrogen at <4 kWh/Nm³ efficiency targets. KOH is also the electrolyte in alkaline fuel cells (AFCs) used in the Apollo spacecraft and early submarine applications.
PurityMain Use
99.97%High-purity potassium for controlled laboratory reactions and sensitive applications — the standard grade for Birch reductions and dissolving metal synthesis (where Na/K impurities could alter regioselectivity), potassium-ion battery research (K metal anode fabrication under inert atmosphere, electrolyte compatibility studies), strong base synthesis (KH, KNH₂, KOtBu preparation), spectroscopy standards and calibration references, and prototype energy system development where impurity-driven side reactions must be minimized
Synonym / Alternative NameContext
KChemical symbol; from Latin/New Latin Kalium (from Arabic al-qalyah, "plant ash" — the traditional source of potassium carbonate K₂CO₃); Humphry Davy isolated potassium in 1807 by electrolysis of molten potash (KOH), naming it "potassium" from "potash"; the Latin name Kalium (adopted by Jöns Jacob Berzelius) gave the symbol K, still used universally in scientific notation
Potassium metalStandard commercial and regulatory designation for the elemental form; used in UN dangerous goods classification (UN2257, Class 4.3 water-reactive flammable solid), REACH/CLP safety data sheets, laboratory supply catalogues, and research purchasing documentation; distinguished from potassium compounds (KCl, KOH, KNO₃, K₂CO₃, KPF₆) in all safety and regulatory contexts
KaliumLatin/German/Nordic language name; the official element name in German (Kalium), Dutch (Kalium), Swedish (Kalium), and several other European languages; used in all European pharmacopoeia drug specifications (serum kalium level rather than serum potassium), in German chemical literature, and in older international scientific texts; gives the standard symbol K universally retained in the chemical symbol despite the English/French name change to potassium