|Unit system||SI base unit|
|Unit of||Amount of substance|
The mole (symbol: mol) is the unit of measurement for amount of substance in the International System of Units (SI). It is defined as exactly 6.02214076×1023 constitutive particles, which may be atoms, molecules, ions, or electrons.
The definition was adopted in November 2018 as one of the seven SI base units, revising the previous definition that specified it as the number of atoms in 12 grams of carbon-12 (12C), an isotope of carbon.
The number 6.02214076×1023 (the Avogadro number) was chosen so that the mass of one mole of a chemical compound, in grams, is numerically equal (for all practical purposes) to the average mass of one molecule of the compound, in daltons. Thus, for example, one mole of water contains 6.02214076×1023 molecules, whose total mass is about 18.015 grams – and the mean mass of one molecule of water is about 18.015 daltons.
The mole is widely used in chemistry as a convenient way to express amounts of reactants and products of chemical reactions. For example, the chemical equation 2H2 + O2 → 2H2O can be interpreted to mean that 2 mol dihydrogen (H2) and 1 mol dioxygen (O2) react to form 2 mol water (H2O). The mole may also be used to represent the number of atoms, ions, or other entities in a given sample of a substance. The concentration of a solution is commonly expressed by its molarity, defined as the amount of dissolved substance per unit volume of solution, for which the unit typically used is moles per litre (mol/l), commonly abbreviated M.
The term gram-molecule (g mol) was formerly used for "mole of molecules", and gram-atom (g atom) for "mole of atoms". For example, 1 mole of MgBr2 is 1 gram-molecule of MgBr2 but 3 gram-atoms of MgBr2.
Nature of the particles
The mole is essentially a count of particles. Usually the particles counted are chemically identical entities, individually distinct. For example, a solution may contain a certain number of dissolved molecules that are more or less independent of each other. However, in a solid the constituent particles are fixed and bound in a lattice arrangement, yet they may be separable without losing their chemical identity. Thus the solid is composed of a certain number of moles of such particles. In yet other cases, such as diamond, where the entire crystal is essentially a single molecule, the mole is still used to express the number of atoms bound together, rather than a count of multiple molecules. Thus, common chemical conventions apply to the definition of the constituent particles of a substance, in other cases exact definitions may be specified.
The molar mass of a substance is the mass of a sample, in multiples of the gram, divided by the amount of substance in that sample. The amount of substance is the number of moles in the sample. It is a characteristic property of the substance. For most practical purposes, its magnitude is numerically the same as that of the mean mass of one molecule, expressed in daltons. For example, the molar mass of water is 18.015 g/mol. Other methods include the use of the molar volume or the measurement of electric charge.
The number of moles of a substance in a sample is obtained by dividing the mass of the sample by the molar mass of the compound. For example, 100 g of water is about 5.551 mol of water.
The molar mass of a substance depends not only on its molecular formula, but also on the distribution of isotopes of each chemical element present in it. For example, the mass of one mole of calcium-40 is 39.96259098±0.00000022 grams, whereas the mass of one mole of calcium-42 is 41.95861801±0.00000027 grams, and of one mole of calcium with the normal isotopic mix is 40.078±0.004 grams.
The molar concentration, also called molarity, of a solution of some substance is the number of moles per unit of volume of the final solution. In the SI its standard unit is mol/m3, although more practical units, such as mol/litre are used.
The molar fraction or mole fraction of a substance in a mixture (such as a solution) is the number of moles of the compound in one sample of the mixture, divided by the total number of moles of all components. For example, if 20 g of NaCl is dissolved in 100 g of water, the amounts of the two substances in the solution will be (20 g)/(58.443 g/mol) = 0.34221 mol and (100 g)/(18.015 g/mol) = 5.5509 mol, respectively; and the molar fraction of NaCl will be 0.34221/(0.34221 + 5.5509) = 0.05807.
In a mixture of gases, the partial pressure of each component is proportional to its molar ratio.
The first table of standard atomic weight (atomic mass) was published by John Dalton (1766–1844) in 1805, based on a system in which the relative atomic mass of hydrogen was defined as 1. These relative atomic masses were based on the stoichiometric proportions of chemical reaction and compounds, a fact that greatly aided their acceptance: It was not necessary for a chemist to subscribe to atomic theory (an unproven hypothesis at the time) to make practical use of the tables. This would lead to some confusion between atomic masses (promoted by proponents of atomic theory) and equivalent weights (promoted by its opponents and which sometimes differed from relative atomic masses by an integer factor), which would last throughout much of the nineteenth century.
Jöns Jacob Berzelius (1779–1848) was instrumental in the determination of relative atomic masses to ever-increasing accuracy. He was also the first chemist to use oxygen as the standard to which other masses were referred. Oxygen is a useful standard, as, unlike hydrogen, it forms compounds with most other elements, especially metals. However, he chose to fix the atomic mass of oxygen as 100, which did not catch on.
Charles Frédéric Gerhardt (1816–56), Henri Victor Regnault (1810–78) and Stanislao Cannizzaro (1826–1910) expanded on Berzelius' works, resolving many of the problems of unknown stoichiometry of compounds, and the use of atomic masses attracted a large consensus by the time of the Karlsruhe Congress (1860). The convention had reverted to defining the atomic mass of hydrogen as 1, although at the level of precision of measurements at that time—relative uncertainties of around 1%—this was numerically equivalent to the later standard of oxygen = 16. However the chemical convenience of having oxygen as the primary atomic mass standard became ever more evident with advances in analytical chemistry and the need for ever more accurate atomic mass determinations.
The name mole is an 1897 translation of the German unit Mol, coined by the chemist Wilhelm Ostwald in 1894 from the German word Molekül (molecule). However, the related concept of equivalent mass had been in use at least a century earlier.
The oxygen-16 definition was replaced with one based on carbon-12 during the 1960s. The mole was defined by International Bureau of Weights and Measures as "the amount of substance of a system which contains as many elementary entities as there are atoms in 0.012 kilogram of carbon-12." Thus, by that definition, one mole of pure 12C had a mass of exactly 12 g. The four different definitions were equivalent to within 1%.
|Scale basis||Scale basis
relative to 12C = 12
from the 12C = 12 scale
|Atomic mass of hydrogen = 1||1.00794(7)||−0.788%|
|Atomic mass of oxygen = 16||15.9994(3)||+0.00375%|
|Relative atomic mass of 16O = 16||15.9949146221(15)||+0.0318%|
Since the definition of the gram was not mathematically tied to that of the dalton, the number of molecules per mole NA (the Avogadro constant) had to be determined experimentally. The experimental value adopted by CODATA in 2010 is NA = (6.02214129±0.00000027)×1023 mol−1. In 2011 the measurement was refined to (6.02214078±0.00000018)×1023 mol−1.
2019 redefinition of SI base units
On 16 November 2018, after a meeting of scientists from more than 60 countries at the CGPM in Versailles, France, all SI base units were defined in terms of physical constants. This meant that each SI unit, including the mole, would not be defined in terms of any physical objects but rather they would be defined by constants that are, in their nature, exact.
- the number of molecules, etc. in a given amount of material is a fixed dimensionless quantity that can be expressed simply as a number, not requiring a distinct base unit;
- the SI thermodynamic mole is irrelevant to analytical chemistry and could cause avoidable costs to advanced economies;
- the mole is not a true metric (i.e. measuring) unit, rather it is a parametric unit and amount of substance is a parametric base quantity;
- the SI defines numbers of entities as quantities of dimension one, and thus ignores the ontological distinction between entities and units of continuous quantities.
In chemistry, it has been known since Proust's law of definite proportions (1794) that knowledge of the mass of each of the components in a chemical system is not sufficient to define the system. Amount of substance can be described as mass divided by Proust's "definite proportions", and contains information that is missing from the measurement of mass alone. As demonstrated by Dalton's law of partial pressures (1803), a measurement of mass is not even necessary to measure the amount of substance (although in practice it is usual). There are many physical relationships between amount of substance and other physical quantities, the most notable one being the ideal gas law (where the relationship was first demonstrated in 1857). The term "mole" was first used in a textbook describing these colligative properties.
Like chemists, chemical engineers use the unit mole extensively, but different unit multiples may be more suitable for industrial use. For example, the SI unit for volume is the cubic metre, a much larger unit than the commonly used litre in the chemical laboratory. When amount of substance is also expressed in kmol (1000 mol) in industrial-scaled processes, the numerical value of molarity remains the same.
For convenience in avoiding conversions in the imperial (or American customary units), some engineers adopted the pound-mole (notation lb-mol or lbmol), which is defined as the number of entities in 12 lb of 12C. One lb-mol is equal to 453.59237 mol, which value is the same as the number of grams in an international avoirdupois pound.
In the metric system, chemical engineers once used the kilogram-mole (notation kg-mol), which is defined as the number of entities in 12 kg of 12C, and often referred to the mole as the gram-mole (notation g-mol), when dealing with laboratory data.
Late 20th-century chemical engineering practice came to use the kilomole (kmol), which is numerically identical to the kilogram-mole, but whose name and symbol adopt the SI convention for standard multiples of metric units – thus, kmol means 1000 mol. This is analogous to the use of kg instead of g. The use of kmol is not only for "magnitude convenience" but also makes the equations used for modelling chemical engineering systems coherent. For example, the conversion of a flowrate of kg/s to kmol/s only requires the molecular mass without the factor 1000 unless the basic SI unit of mol/s were to be used.
Greenhouse and growth chamber lighting for plants is sometimes expressed in micromoles per square metre per second, where 1 mol photons = 6.02×1023 photons.
October 23, denoted 10/23 in the US, is recognized by some as Mole Day. It is an informal holiday in honor of the unit among chemists. The date is derived from the Avogadro number, which is approximately 6.022×1023. It starts at 6:02 a.m. and ends at 6:02 p.m. Alternatively, some chemists celebrate June 2, June 22, or February 6, a reference to the 6.02 part of the constant.
Notes and references
-  IUPAC: "On the revision of the International System of Units."
- International Bureau of Weights and Measures (2006), The International System of Units (SI) (PDF) (8th ed.), pp. 114–15, ISBN 92-822-2213-6, archived (PDF) from the original on 2017-08-14
- Wang, Yuxing; Bouquet, Frédéric; Sheikin, Ilya; Toulemonde, Pierre; Revaz, Bernard; Eisterer, Michael; Weber, Harald W; Hinderer, Joerg; Junod, Alain; et al. (2003). "Specific heat of MgB2 after irradiation". Journal of Physics: Condensed Matter. 15 (6): 883–893. arXiv:cond-mat/0208169. Bibcode:2003JPCM...15..883W. doi:10.1088/0953-8984/15/6/315.
- Lortz, R.; Wang, Y.; Abe, S.; Meingast, C.; Paderno, Yu.; Filippov, V.; Junod, A.; et al. (2005). "Specific heat, magnetic susceptibility, resistivity and thermal expansion of the superconductor ZrB12". Phys. Rev. B. 72 (2): 024547. arXiv:cond-mat/0502193. Bibcode:2005PhRvB..72b4547L. doi:10.1103/PhysRevB.72.024547.
- International Bureau of Weights and Measures. "Realising the mole Archived 2008-08-29 at the Wayback Machine." Retrieved 25 September 2008.
- Helm, Georg (1897). "The Principles of Mathematical Chemistry: The Energetics of Chemical Phenomena". transl. by Livingston, J.; Morgan, R. New York: Wiley: 6. Cite journal requires
- Some sources place the date of first usage in English as 1902. Merriam–Webster proposes Archived 2011-11-02 at the Wayback Machine an etymology from Molekulärgewicht (molecular weight).
- Ostwald, Wilhelm (1893). Hand- und Hilfsbuch zur Ausführung Physiko-Chemischer Messungen [Handbook and Auxiliary Book for Conducting Physical-Chemical Measurements]. Leipzig, Germany: Wilhelm Engelmann. p. 119. From p. 119: "Nennen wir allgemein das Gewicht in Grammen, welches dem Molekulargewicht eines gegebenen Stoffes numerisch gleich ist, ein Mol, so ... " (If we call in general the weight in grams, which is numerically equal to the molecular weight of a given substance, a "mol", then ... )
- mole, n.8, Oxford English Dictionary, Draft Revision Dec. 2008
- de Bièvre, Paul; Peiser, H. Steffen (1992). "'Atomic Weight' — The Name, Its History, Definition, and Units" (PDF). Pure and Applied Chemistry. 64 (10): 1535–43. doi:10.1351/pac199264101535.
- physics.nist.gov/ Archived 2015-06-29 at the Wayback Machine Fundamental Physical Constants: Avogadro Constant
- Andreas, Birk; et al. (2011). "Determination of the Avogadro Constant by Counting the Atoms in a 28Si Crystal". Physical Review Letters. 106 (3): 30801. arXiv:1010.2317. Bibcode:2011PhRvL.106c0801A. doi:10.1103/PhysRevLett.106.030801. PMID 21405263.
- "BIPM – Resolution 3 of the 14th CGPM". www.bipm.org. Archived from the original on 9 October 2017. Retrieved 1 May 2018.
- CIPM Report of 106th Meeting Archived 2018-01-27 at the Wayback Machine Retrieved 7 April 2018
- "Redefining the Mole". NIST. NIST. 2018-10-23. Retrieved 24 October 2018.
- Price, Gary (2010). "Failures of the global measurement system. Part 1: the case of chemistry". Accreditation and Quality Assurance. 15 (7): 421–427. doi:10.1007/s00769-010-0655-z..
- Johansson, Ingvar (2010). "Metrological thinking needs the notions of parametric quantities, units, and dimensions". Metrologia. 47 (3): 219–230. Bibcode:2010Metro..47..219J. doi:10.1088/0026-1394/47/3/012.
- Cooper, G; Humphry, S (2010). "The ontological distinction between units and entities". Synthese. 187 (2): 393–401. doi:10.1007/s11229-010-9832-1.
- Himmelblau, David (1996). Basic Principles and Calculations in Chemical Engineering (6 ed.). pp. 17–20. ISBN 978-0-13-305798-0.
- "Lighting Radiation Conversion". Archived from the original on March 11, 2016. Retrieved March 10, 2016.
- History of National Mole Day Foundation, Inc Archived 2010-10-23 at the Wayback Machine
- Happy Mole Day! Archived 2014-07-29 at the Wayback Machine, Mary Bigelow. SciLinks blog, National Science Teachers Association. October 17, 2013.
- What Is Mole Day? – Date and How to Celebrate Archived 2014-07-30 at Wikiwix, Anne Marie Helmenstine. About.com
- The Perse School (Feb 7, 2013), The Perse School celebrates moles of the chemical variety, Cambridge Network, archived from the original on 2015-02-11, retrieved Feb 11, 2015,
As 6.02 corresponds to 6th February, the School has adopted the date as their 'Mole Day'.