Printed from https://www.webqc.org

Properties of KIO3

Properties of KIO3 (Potassium iodate):

Compound NamePotassium iodate
Chemical FormulaKIO3
Molar Mass214.00097 g/mol

Chemical structure
KIO3 (Potassium iodate) - Chemical structure
Lewis structure
3D molecular structure
Physical properties
Appearancewhite crystalline powder
Odorodorless
Solubility47.4 g/100mL
Density3.8900 g/cm³
Helium 0.0001786
Iridium 22.562
Melting560.00 °C
Helium -270.973
Hafnium carbide 3958

Alternative Names

Iodic acid, potassium salt

Elemental composition of KIO3
ElementSymbolAtomic weightAtomsMass percent
PotassiumK39.0983118.2702
IodineI126.90447159.3009
OxygenO15.9994322.4290
Mass Percent CompositionAtomic Percent Composition
K: 18.27%I: 59.30%O: 22.43%
K Potassium (18.27%)
I Iodine (59.30%)
O Oxygen (22.43%)
K: 20.00%I: 20.00%O: 60.00%
K Potassium (20.00%)
I Iodine (20.00%)
O Oxygen (60.00%)
Mass Percent Composition
K: 18.27%I: 59.30%O: 22.43%
K Potassium (18.27%)
I Iodine (59.30%)
O Oxygen (22.43%)
Atomic Percent Composition
K: 20.00%I: 20.00%O: 60.00%
K Potassium (20.00%)
I Iodine (20.00%)
O Oxygen (60.00%)
Identifiers
CAS Number7758-05-6
SMILES[K+].[O-]I(=O)=O
Hill formulaIKO3

Related compounds
FormulaCompound name
KIO4Potassium periodate

Sample reactions for KIO3
EquationReaction type
BaCl2 + KIO3 = Ba(IO3)2 + KCldouble replacement
KIO3 = KI + O2decomposition
KIO3 + AgNO3 = KNO3 + AgIO3double replacement
KIO3 + H2SO3 = KI + H2SO4double replacement
Sr(NO3)2 + KIO3 = Sr(IO3)2 + KNO3double replacement

Related
Molecular weight calculator
Oxidation state calculator

Potassium iodate (KIO₃): Chemical Compound

Scientific Review Article | Chemistry Reference Series

Abstract

Potassium iodate (KIO₃) represents an inorganic ionic compound characterized by its white crystalline appearance and solubility in aqueous media. With a molar mass of 214.001 grams per mole, this compound demonstrates a density of 3.89 grams per cubic centimeter. Potassium iodate decomposes at 560 degrees Celsius and exhibits significant solubility variations with temperature, ranging from 4.74 grams per 100 milliliters at 0 degrees Celsius to 32.3 grams per 100 milliliters at 100 degrees Celsius. The compound serves as a strong oxidizing agent with applications spanning from food fortification to radiation protection protocols. Its crystalline structure adopts a trigonal configuration with space group R3m, featuring iodine in the +5 oxidation state. Potassium iodate finds extensive industrial utilization due to its stability compared to iodide salts and its predictable oxidative behavior.

Introduction

Potassium iodate constitutes an important inorganic compound classified as an iodate salt. This compound holds significant industrial and chemical relevance due to its oxidative properties and stability in various environmental conditions. Unlike potassium iodide, potassium iodate demonstrates superior stability in humid environments, making it particularly valuable for applications requiring long-term storage. The compound exists as a white, odorless crystalline powder that exhibits characteristic decomposition behavior upon heating. Potassium iodate finds primary application in iodine supplementation programs, where it serves as a reliable source of dietary iodine in salt fortification initiatives. The compound's oxidative capabilities also render it useful in analytical chemistry and various industrial processes requiring controlled oxidation reactions.

Molecular Structure and Bonding

Molecular Geometry and Electronic Structure

The potassium iodate molecule consists of potassium cations (K⁺) and iodate anions (IO₃⁻). The iodate ion exhibits trigonal pyramidal geometry according to VSEPR theory, with iodine as the central atom surrounded by three oxygen atoms. The iodine atom in IO₃⁻ demonstrates sp³ hybridization, resulting in bond angles of approximately 100 degrees between oxygen atoms. This geometry arises from the presence of one lone pair of electrons on the iodine atom. The I-O bond length measures 1.82 angstroms, consistent with partial double bond character due to resonance stabilization within the iodate ion. The electronic configuration of iodine in the +5 oxidation state is [Kr]4d¹⁰5s²5p⁰, with the empty 5p orbitals participating in bonding with oxygen atoms.

Chemical Bonding and Intermolecular Forces

Potassium iodate features ionic bonding between potassium cations and iodate anions, with a lattice energy of approximately 650 kilojoules per mole. The iodate ion itself contains covalent bonds with significant double bond character resulting from pπ-dπ bonding between iodine and oxygen atoms. This bonding configuration gives rise to a formal charge distribution where each oxygen atom carries a -0.5 charge and iodine carries a +1 formal charge. Intermolecular forces in solid potassium iodate primarily consist of electrostatic interactions between ions, with additional dipole-dipole interactions between iodate ions. The compound crystallizes in a rhombohedral structure with space group R3m, where each potassium ion is coordinated to six oxygen atoms from adjacent iodate ions. The molecular dipole moment of the iodate ion measures 2.7 Debye, contributing to the compound's solubility in polar solvents.

Physical Properties

Phase Behavior and Thermodynamic Properties

Potassium iodate appears as a white crystalline solid with no observable odor. The compound melts with decomposition at 560 degrees Celsius, undergoing thermal breakdown to potassium iodide and oxygen. The density of crystalline potassium iodate measures 3.89 grams per cubic centimeter at 25 degrees Celsius. Solubility in water demonstrates significant temperature dependence, increasing from 4.74 grams per 100 milliliters at 0 degrees Celsius to 32.3 grams per 100 milliliters at 100 degrees Celsius. The compound exhibits limited solubility in ethanol and remains insoluble in liquid ammonia and concentrated nitric acid. The specific heat capacity of potassium iodate is 0.866 joules per gram per degree Celsius, while its standard enthalpy of formation measures -500.4 kilojoules per mole. The entropy of formation stands at 150.5 joules per mole per degree Kelvin.

Spectroscopic Characteristics

Infrared spectroscopy of potassium iodate reveals characteristic vibrational modes corresponding to the iodate ion. The asymmetric stretching vibration of I-O bonds appears at 780 centimeters⁻¹, while symmetric stretching occurs at 680 centimeters⁻¹. Bending vibrations are observed at 340 centimeters⁻¹ and 290 centimeters⁻¹. Raman spectroscopy shows strong bands at 810 centimeters⁻¹ and 710 centimeters⁻¹, corresponding to symmetric and asymmetric stretching modes respectively. Ultraviolet-visible spectroscopy demonstrates absorption maxima at 285 nanometers with molar absorptivity of 9000 liters per mole per centimeter, attributed to charge transfer transitions within the iodate ion. X-ray photoelectron spectroscopy confirms the +5 oxidation state of iodine with binding energies of 619.5 electronvolts for I 3d₅/₂ and 631.0 electronvolts for I 3d₃/₂.

Chemical Properties and Reactivity

Reaction Mechanisms and Kinetics

Potassium iodate functions as a strong oxidizing agent with a standard reduction potential of +1.08 volts for the IO₃⁻/I⁻ couple in acidic media. The compound decomposes thermally according to first-order kinetics with an activation energy of 150 kilojoules per mole, producing potassium iodide and oxygen gas. In acidic solutions, potassium iodate oxidizes iodide ions to iodine in a reaction that follows second-order kinetics with respect to hydrogen ion concentration. The rate constant for this reaction measures 2.5 × 10⁻³ liters per mole per second at 25 degrees Celsius. Potassium iodate reacts with reducing agents such as sulfur dioxide, hydrogen sulfide, and organic compounds through electron transfer mechanisms. The compound demonstrates stability in neutral and alkaline conditions but becomes increasingly reactive in acidic environments due to the formation of iodic acid.

Acid-Base and Redox Properties

The conjugate acid of iodate, iodic acid (HIO₃), exhibits weak acidic character with pKa values of 0.8 and 1.3 for successive protonation steps. Potassium iodate solutions demonstrate buffering capacity in the pH range of 2.5 to 4.5 due to the equilibrium between iodate and iodic acid. The compound maintains stability across a wide pH range from 5 to 9, with minimal decomposition observed under these conditions. Redox properties dominate the chemical behavior of potassium iodate, with the iodate ion capable of undergoing reduction to iodide, iodine, or various intermediate oxidation states depending on reaction conditions. Standard reduction potentials for relevant half-reactions include +1.195 volts for IO₃⁻/I₂ and +0.26 volts for IO₃⁻/I⁻ in acidic media. The compound demonstrates irreversible electrochemical behavior with reduction peaks observed at -0.8 volts versus standard hydrogen electrode.

Synthesis and Preparation Methods

Laboratory Synthesis Routes

Laboratory preparation of potassium iodate typically involves the neutralization of iodic acid with potassium hydroxide. This reaction proceeds quantitatively according to the equation: HIO₃ + KOH → KIO₃ + H₂O. The product crystallizes from aqueous solution upon cooling and evaporation. An alternative method employs the oxidation of iodine with potassium hydroxide in hot concentrated solutions: 3I₂ + 6KOH → KIO₃ + 5KI + 3H₂O. This reaction requires careful temperature control between 80 and 90 degrees Celsius to maximize iodate formation while minimizing side products. The resulting mixture undergoes fractional crystallization to separate potassium iodate from potassium iodide based on their differential solubility characteristics. Yields typically reach 85-90% with product purity exceeding 99% after recrystallization from water.

Industrial Production Methods

Industrial production of potassium iodate primarily utilizes the electrochemical oxidation of potassium iodide in divided cells. This process employs platinum or dimensionally stable anodes with current densities of 100-200 amperes per square meter and cell voltages of 3-4 volts. The electrochemical method offers advantages of high purity and minimal byproduct formation, with conversion efficiencies exceeding 95%. Alternative industrial routes involve the reaction of potassium hydroxide with iodine under controlled conditions, followed by purification through crystallization and centrifugation. Annual global production estimates approach 5000 metric tons, with major manufacturing facilities located in China, Japan, and Germany. Production costs primarily derive from raw material inputs, particularly iodine, which accounts for approximately 70% of total production expenses. Environmental considerations include the management of alkaline waste streams and the recovery of iodine from process residues.

Analytical Methods and Characterization

Identification and Quantification

Potassium iodate identification typically employs precipitation tests with silver nitrate, yielding white silver iodate (AgIO₃) that is insoluble in nitric acid but soluble in ammonia solution. Quantitative analysis commonly utilizes iodometric titration methods, where potassium iodate serves as its own standard in reactions with iodide ions in acidic media. The liberated iodine is titrated with standardized sodium thiosulfate solution using starch indicator. This method achieves detection limits of 0.1 milligrams per liter with relative standard deviations of 0.5%. Spectrophotometric methods based on the absorption characteristics of the iodate ion at 285 nanometers provide alternative quantification approaches with linear response ranges from 1 to 100 milligrams per liter. Ion chromatography with conductivity detection offers selective determination of iodate ions in complex matrices with detection limits of 0.01 milligrams per liter.

Purity Assessment and Quality Control

Pharmaceutical-grade potassium iodate must conform to purity specifications established in various pharmacopeias. The United States Pharmacopeia requires minimum purity of 99.0% with limits for heavy metals not exceeding 10 parts per million and arsenic not exceeding 3 parts per million. Loss on drying should not exceed 0.5% when determined by heating at 105 degrees Celsius for two hours. Residual solvent analysis by gas chromatography must demonstrate absence of organic solvents above detection limits of 100 parts per million. Microbiological testing confirms absence of pathogenic microorganisms with total aerobic microbial count not exceeding 1000 colony-forming units per gram. Stability testing under accelerated conditions (40 degrees Celsius and 75% relative humidity) demonstrates no significant decomposition over six months, supporting a typical shelf life of five years when stored in airtight containers protected from light.

Applications and Uses

Industrial and Commercial Applications

Potassium iodate finds extensive application in the food industry as an iodine fortification agent for table salt. This usage capitalizes on the compound's stability in humid conditions compared to potassium iodide, particularly in tropical climates. The typical incorporation rate ranges from 20 to 40 milligrams per kilogram of salt, providing adequate dietary iodine supplementation. In baking technology, potassium iodate serves as a dough conditioner and improving agent at concentrations of 10-50 parts per million flour basis, where it strengthens gluten networks through oxidative cross-linking. The compound functions as an analytical reagent in iodometric titrations, providing a primary standard for thiosulfate solutions due to its high purity and stability. Additional industrial applications include use as an oxidizing agent in organic synthesis, particularly in the preparation of iodine-containing compounds, and as a component in radiation protection protocols.

Research Applications and Emerging Uses

Research applications of potassium iodate encompass its use as a model compound for studying iodate chemistry and crystallization behavior. The compound serves as a precursor for the synthesis of various metal iodates through metathesis reactions, yielding materials with interesting nonlinear optical properties. Recent investigations explore potassium iodate as an oxidizing agent in sustainable chemical processes, particularly in green oxidation reactions where it offers advantages of selectivity and minimal environmental impact. Emerging applications include utilization in electrochemical energy storage systems, where potassium iodate demonstrates potential as a cathode material in potassium-ion batteries due to its high theoretical capacity of 300 milliampere-hours per gram. Patent activity surrounding potassium iodate primarily focuses on improved production methods, stabilization techniques for food applications, and novel formulations for radiation protection.

Historical Development and Discovery

The discovery of potassium iodate parallels the broader investigation of iodine compounds in the early 19th century. Initial reports of iodate salts appeared following the discovery of iodine by Bernard Courtois in 1811. Systematic study of potassium iodate began in the 1820s with the work of Joseph Louis Gay-Lussac, who characterized its composition and oxidative properties. The compound's stability compared to iodide salts was recognized early, leading to its proposed use in various chemical applications. Industrial production methods developed throughout the late 19th century, particularly electrochemical processes that enabled large-scale manufacture. The recognition of iodine deficiency disorders in the early 20th century prompted investigation of various iodine compounds for supplementation purposes, with potassium iodate emerging as the preferred compound for salt fortification in many regions due to its stability. Continued research has refined production methods and expanded applications into diverse chemical and industrial fields.

Conclusion

Potassium iodate represents a chemically significant compound with diverse applications stemming from its unique combination of stability and oxidative power. The compound's ionic structure featuring the trigonal pyramidal iodate ion confers distinctive physical and chemical properties that differentiate it from related halogenates. Its role in iodine supplementation programs demonstrates the practical importance of inorganic chemistry in addressing nutritional deficiencies. The well-characterized decomposition behavior and redox chemistry of potassium iodate provide model systems for studying reaction mechanisms and kinetics. Future research directions likely include development of more sustainable production methods, exploration of novel applications in energy storage, and refinement of analytical techniques for iodate determination in complex matrices. The compound continues to serve as an important industrial chemical and research material with ongoing relevance in both applied and fundamental chemistry.

Chemical Compound Properties Database

This database contains physical properties and alternative names for thousands of chemical compounds. In chemical formula you may use:
  • Any chemical element. Capitalize the first letter in chemical symbol and use lower case for the remaining letters: Ca, Fe, Mg, Mn, S, O, H, C, N, Na, K, Cl, Al.
  • Functional groups: D, T, Ph, Me, Et, Bu, AcAc, For, Tos, Bz, TMS, tBu, Bzl, Bn, Dmg
  • parenthesis () or brackets [].
  • Common compound names.
Examples: H2O, CO2, CH4, NH3, NaCl, CaCO3, H2SO4, C6H12O6, water, carbon dioxide, methane, ammonia, sodium chloride, calcium carbonate, sulfuric acid, glucose.

The database includes melting points, boiling points, densities, and alternative names collected from various chemical sources.

What are compound properties?

Chemical compound properties include physical characteristics such as melting point, boiling point, and density, which are important for chemical identification and applications. Alternative names help identify the same compound when referenced by different naming conventions.

How to use this tool?

Enter a chemical formula (like H2O) or compound name (like water) to look up available properties and alternative names. The tool will search through the database and display any available physical properties and known alternative names for the compound.
Please let us know how we can improve this web app.
Menu Balance Molar mass Gas laws Units Chemistry tools Periodic table Chemical forum Symmetry Constants Contribute Contact us
How to cite?