Information about Sodium Sulfate









Sodium sulfate
Other namesSalt cake
Thenardite (mineral)
Glauber's salt (decahydrate)
Sal mirabilis (decahydrate)
Mirabilite (decahydrate)
Identifiers
CAS number7757-82-6
RTECS numberWE1650000 (anhydrous)
Properties
Molar mass142.04 g/mol (anhydrous)
268.15 g/mol (heptahydrate)
322.20 g/mol (decahydrate)
AppearanceWhite crystalline solid,
hygroscopic
Density2.68 g/cm³, anhydrous
(orthorhombic form)
1.464 g/cm³, decahydrate
Melting point 884 °C (1157 K) anhydrous
32.4 °C decahydrate
Solubility in water4.76 g/100 ml (0 °C)
42.7 g/100 ml (100 °C)
Structure
Crystal structuremonoclinic, orthorhombic or
hexagonal
Hazards
MSDSExternal MSDS
MSDSExternal MSDS
Main hazardsIrritant
NFPA 704
0
1
0
 
R/S statementNone
Related Compounds
Other anionsSodium hydrogen sulfate
Sodium sulfite
Sodium bisulfite
Sodium persulfate
Other cationsLithium sulfate
Potassium sulfate
Magnesium sulfate
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral dataUV, IR, NMR, MS
Except where noted otherwise, data are given for
materials in their standard state
(at 25 C, 100 kPa)

Sodium sulfate is the sodium salt of sulfuric acid. With an annual production of 6 million tonnes, it is one of the world's major commodity chemicals. Anhydrous, it is a white crystalline solid of formula Na2SO4; the decahydrate Na2SO4·10H2O has been known as Glauber's salt or, historically, sal mirabilis since the 17th century.

Sodium sulfate is mainly used for the manufacture of detergents and in the Kraft process of paper pulping. About two thirds of the world's production is from mirabilite, the natural mineral form of the decahydrate, and the remainder from by-products of chemical processes such as hydrochloric acid production.

History

Glauber's salt is named after Johann Rudolf Glauber, who discovered it in the 17th century in Hungarian spring water, and named it sal mirabilis (miraculous salt), because of its medicinal properties. The white or colourless crystals of Glauber's salt were used as a laxative until more sophisticated alternatives came about in 1900s.[1]

In the eighteenth century, Glauber's salt began to be used as a raw material for the production of soda ash, by reaction with potash. In the nineteenth century the Leblanc process became the principal method of soda production, and one of the world's major chemical processes, using synthetic sodium sulfate as a key intermediate.[2]

Physical and chemical properties

Sodium sulfate is chemically very stable, being unreactive toward most oxidising or reducing agents at normal temperatures. At high temperatures, it can be reduced to sodium sulfide.[3] It is a neutral salt, which forms aqueous solutions with pH of 7. The neutrality of such solutions reflects the fact that Na2SO4 is derived, formally speaking, from the strong acid sulfuric acid and a strong base sodium hydroxide. Sodium sulfate reacts with an equivalent amount of sulfuric acid to give an equilibrium concentration of the acid salt sodium hydrogen sulfate[4][5]:

Na2SO4(aq) + H2SO4(aq) 2 NaHSO4(aq)


In fact, the equilibrium is very complex, depending on concentration and temperature, with other acid salts being present.

Sodium sulfate is a typical ionic sulfate, containing Na+ ions and SO42− ions. Aqueous solutions can produce precipitates when combined with salts of Ba2+ or Pb2+, which form insoluble sulfates

Na2SO4(aq) + BaCl2(aq) → 2 NaCl(aq) + BaSO4(s)


Enlarge picture
Graph showing solubility of Na2SO4 vs. temperature
Sodium sulfate has unusual solubility characteristics in water.[6] Its solubility rises more than tenfold between 0 °C to 32.4 °C, where it reaches a maximum of 49.7 g Na2SO4 per 100 g water. At this point the solubility curve changes slope, and the solubility becomes almost independent of temperature. In the presence of NaCl, the solubility of sodium sulfate is markedly diminished. Such changes provide the basis for the use of sodium sulfate in passive solar heating systems, as well is in the preparation and purification of sodium sulfate. This nonconformity can be explained in terms of hydration, since 32.4 °C corresponds with the temperature at which the crystalline decahydrate (Glauber's salt) changes to give a sulfate liquid phase and an anhydrous solid phase.

Sodium sulfate decahydrate is also unusual among hydrated salts in having a measureable residual entropy (entropy at absolute zero) of 6.32 J·K-1·mol-1. This is ascribed to its ability to distribute water much more rapidly compared to most hydrates.[7]

Sodium sulfate displays a moderate tendency to form double salts. The only alums formed with common trivalent metals are NaAl(SO4)2 (unstable above 39 °C) and NaCr(SO4)2, in contrast to potassium sulfate and ammonium sulfate which form many stable alums.[8] Double salts with some other alkali metal sulfates are known, including Na2SO4.3K2SO4 which occurs naturally as the mineral glaserite. Formation of glaserite by reaction of sodium sulfate with potassium chloride has been used as the basis of a method for producing potassium sulfate, a fertiliser.[9] Other double salts include 3Na2SO4.CaSO4, 3Na2SO4.MgSO4 (vanthoffite) and NaF.Na2SO4.[10]

Production

The world production of sodium sulfate, mostly in the form of the decahydrate amounts to approximately 5.5 to 6 million tonnes annually (Mt/a). In 1985, production was 4.5 Mt/a, half from natural sources, and half from chemical production. After 2000, at a stable level until 2006, natural production had increased to 4 Mt/a, and chemical production decreased to 1.5 to 2 Mt/a, with a total of 5.5 to 6 Mt/a.[11][12][13][14] For all applications, naturally produced and chemically produced sodium sulfate are practically interchangeable.

Natural sources

Two thirds of the world's production of the decahydrate (Glauber's salt) is from the natural mineral form mirabilite, for example as found in lake beds in southern Saskatchewan. In 1990, Mexico and Spain were the world's main producers of natural sodium sulfate (each around 500,000 tonnes), with Russia, USA and Canada around 350,000 tonnes each.[12] Estimatedly, natural resources amount to over 1 billion tonnes.[11][12]

Major producers of 200–1500 Mt/a in 2006 include Searles Valley Minerals (California, USA), Airborne Industrial Minerals (Saskatchewan, Canada), Química del Rey (Coahuila, Mexico), Criaderos Minerales Y Derivados and Minera de Santa Marta, also known as Grupo Crimidesa (Burgos, Spain), FMC Foret (Toledo, Spain), Sulquisa (Madrid, Spain), and in China Chengdu Sanlian Tianquan Chemical (Sichuan), Hongze Yinzhu Chemical Group (Jiangsu), Nafine Chemical Industry Group (Shanxi), and Sichuan Province Chuanmei Mirabilite (Sichuan), and Kuchuksulphat JSC (Altai Krai, Siberia, Russia).[11][13]

Anhydrous sodium sulfate occurs in arid environments as the mineral thenardite. It slowly turns to mirabilite in damp air. Sodium sulfate is also found as glauberite, a calcium sodium sulfate mineral. Both minerals are less common than mirabilite.

Chemical industry

About one third of the world's sodium sulfate is produced as by-product of other processes in chemical industry. Most of this production is chemically inherent to the primary process, and only marginally economical. By effort of the industry, therefore, sodium sulfate production as by-product is declining.

The most important chemical sodium sulphate production is during hydrochloric acid production, either from sodium chloride (salt) and sulfuric acid, in the Mannheim process, or from sulfur dioxide in the Hargreaves process.[15][16] The resulting sodium sulfate from these processes are known as salt cake.
Mannheim: 2 NaCl + H2SO4 → 2 HCl + Na2SO4
Hargreaves: 4 NaCl + 2 SO2 + O2 + 2 H2O → 4 HCl + 2 Na2SO4


The second major production of sodium sulfate are the processes where surplus sulfuric acid is neutralised by sodium hydroxide, as applied on a large scale in the production of rayon. This method is also a regularly applied and convenient laboratory preparation.
2 NaOH(aq) + H2SO4(aq) → Na2SO4(aq) + 2 H2O(l)


Formerly, sodium sulfate was also a by-product of the manufacture of sodium dichromate, where sulfuric acid is added to sodium chromate solution forming sodium dichromate, or subsequently chromic acid. Alternatively, sodium sulfate is or was formed in the production of lithium carbonate, chelating agents, resorcinol, ascorbic acid, silica pigments, nitric acid, and phenol.[11]

Bulk sodium sulfate is usually purified via the decahydrate form, since the anhydrous form tends to attract iron compounds and organic compounds. The anhydrous form is easily produced from the hydrated form by gentle warming.

Major sodium sulfate by-product producers of 50–80 Mt/a in 2006 include Elementis Chromium (chromium industry, Castle Hayne, NC, USA), Lenzing AG (200 Mt/a, rayon industry, Lenzing, Austria), Addiseo (formerly Rhodia, methionine industry, Les Roches-Roussillon, France), Elementis (chromium industry, Stockton-on-Tees, UK), Shikoku Chemicals (Tokushima, Japan) and Visko-R (rayon industry, Russia).[11]

Applications

Commodity industries

With USA pricing at $30 per metric tonne in 1970, in 2006 up to $90 per metric tonne for salt cake quality and $130 for better grades, sodium sulfate is a very cheap material. The largest use is as filler in powdered home laundry detergents, consuming approx. 50% of world production. This use is waning as domestic consumers are increasingly switching to compact or liquid detergents that do not include sodium sulfate.[11]

Another formerly major use for sodium sulfate, notably in the USA and Canada, is in the Kraft process for the manufacture of wood pulp. Organics present in the "black liquor" from this process are burnt to produce heat, needed to drive the reduction of sodium sulfate to sodium sulfide. However, this process is being replaced by newer processes; use of sodium sulfate in the USA and Canadian pulp industry declined from 1.4 Mt/a in 1970 to only approx. 150,000 tonnes in 2006.[11]

The glass industry provides another significant application for sodium sulfate, as second largest application in Europe. Sodium sulfate is used as a fining agent, to help remove small air bubbles from molten glass. It fluxes the glass, and prevents scum formation of the glass melt during refining. The glass industry in Europe has been consuming from 1970 to 2006 a stable 110,000 tonnes annually.[11]

Sodium sulfate is important in the manufacture of textiles, particularly in Japan, where it is the largest application. Sodium sulfate helps in "levelling", reducing negative charges on fibres so that dyes can penetrate evenly. Unlike the alternative sodium chloride, it does not corrode the stainless steel vessels used in dyeing. This application in Japan and USA consumed in 2006 approximately 100,000 tonnes.[11]

Thermal storage

The high heat storage capacity in the phase change from solid to liquid, and the advantageous phase change temperature of 32 degrees Celsius (90 degrees Fahrenheit) makes this material especially appropriate for storing low grade solar heat for later release in space heating applications. In some application the material is incorporated into thermal tiles that are placed in an attic space while in other applications the salt is incorporated into cells surrounded by solar–heated water. The phase change allows a substantial reduction in the mass of the material required for effective heat storage (83 calories per gram stored across the phase change, versus one calorie per gram per degree Celsius using only water), with the further advantage of a consistency of temperature as long as sufficient material in the appropriate phase is available.

Small scale applications

Sodium sulfate as a drying agent(1)

Drying a wet organic phase using sodium sulfate, which clumps, indicating that more sodium sulfate is needed.

In case of problems, see Wikipedia:Media help.
Sodium sulfate as a drying agent(2)

Drying a fairly dry organic phase using sodium sulfate, which does not clump, indicating that the solution is dry.

In case of problems, see Wikipedia:Media help.

In the laboratory, anhydrous sodium sulfate is widely used as an inert drying agent, for removing traces of water from organic solutions.[17] It is more efficient, but slower-acting, than the similar agent magnesium sulfate. It is only effective below about 30 °C, but it can used with a variety of materials since it is chemically fairly inert. Sodium sulfate is added to the solution until the crystals no longer clump together; the two video clips (see above) demonstrate how the crystals clump when still wet, but some crystals flow freely once a sample is dry.

Glauber's salt, the decahydrate, was historically used as a laxative. It is effective for the removal of certain drugs such as acetaminophen from the body, for example, after an overdose.[18][19]

In 1953, sodium sulfate was proposed for heat storage in passive solar heating systems. This takes advantage of its unusual solubility properties, and the high heat of crystallisation (78.2 kJ/mol).[20]

Other uses for sodium sulfate include de-frosting windows, in carpet fresheners, starch manufacture, and as an additive to cattle feed.

Lately, sodium sulfate has been found effective in dissolving very finely electroplated micron gold that is found in gold electroplated hardware on electronic products such as pins, and other connectors and switches. It is safer and cheaper than other reagents used for gold recovery, with little concern for adverse reactions or health effects.

Safety

Although sodium sulfate is generally regarded as non-toxic,[21] it should be handled with care. The dust can cause temporary asthma or eye irritation; this risk can be prevented by using eye protection and a paper mask. Transport is not limited, and no Risk Phrase or Safety Phrase apply.[22]

References

1. ^ Szydlo, Zbigniew (1994). Water which does not wet hands: The Alchemy of Michael Sendivogius. London-Warsaw: Polish Academy of Sciences. 
2. ^ Aftalion, Fred (1991). A History of the International Chemical Industry. Philadelphia: University of Pennsylvania Press, 11–16. ISBN 0-8122-1297-5. 
3. ^ (1990) Handbook of Chemistry and Physics, 71st edition, Ann Arbor, Michigan: CRC Press.Michigan"> 
4. ^ (1960) The Merck Index, 7th edition, Rahway, New Jersey, USA: Merck & Co.. 
5. ^ Nechamkin, H. (1968). The Chemistry of the Elements. New York: McGraw-Hill.McGraw-Hill&rft.place=New%20York"> 
6. ^ Linke, W.F.; A. Seidell (1965). Solubilities of Inorganic and Metal Organic Compounds, 4th edition, Van Nostrand. 
7. ^ Brodale, G.; Giauque, W. F. (1958). "The Heat of Hydration of Sodium Sulfate. Low Temperature Heat Capacity and Entropy of Sodium Sulfate Decahydrate". Journal of the American Chemical Society 80: 2042–2044. 
8. ^ Lipson, H.; Beevers, C.A. (1935). "The Crystal Structure of the Alums". Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences 148 (865): 664-680. Retrieved on 2007-07-21. 
9. ^ Garrett, Donald E. (2001). Sodium sulfate : handbook of deposits, processing, properties, and use. San Diego: Academic Press. ISBN 9780122761515. 
10. ^ Mellor, J. W. (1961 (new impression)). Mellor's Comprehensive Treatise on Inorganic and Theoretical Chemistry, Volume II. London: Longmans, 656-673. 
11. ^ Suresh, Bala; Kazuteru Yokose (May 2006). Sodium sulfate. Zurich: Chemical Economic Handbook SRI Consulting, 771.1000A–771.1002J. 
12. ^ Statistical compendium Sodium sulfate. US Geological Survey, Minerals Information (1997). Retrieved on 2007-04-22.
13. ^ (1999) The economics of sodium sulphate, Eighth edition, London: Roskill Information Services, 195 pages and appendices. 
14. ^ (Nov 1984) The sodium sulphate business. London: Chem Systems International. 
15. ^ Butts, D. (1997). Kirk-Othmer Encyclopedia of Chemical Technology, 4th edition. 
16. ^ Hargreaves, J. (1873). "". Chem. News 27: p183. 
17. ^ Vogel, A.I., Smith, B.V., Waldron, N.M. (1980). Vogel's Elementary Practical Organic Chemistry 1 Preparations, 3rd Edition, London: Longman Scientific & Technical. 
18. ^ Cocchetto, D.M.; Levy, G. (1981). "Absorption of orally administered sodium sulfate in humans.". J Pharm Sci 70 (3): 331–3. DOI:10.1002/jps.2600700330. Retrieved on 2007-06-06. 
19. ^ Prescott, L. F.; Critchley, J. A. J. H. (1979). "The Treatment of Acetaminophen Poisoning". Annual Review of Pharmacology and Toxicology 23: 87–101. DOI:10.1146/annurev.pa.23.040183.000511. 
20. ^ Telkes, Maria (1953). Improvements in or relating to a device and a composition of matter for the storage of heat. 
21. ^ Sodium sulfate (WHO Food Additives Series 44). World Health Organization (2000). Retrieved on 2007-06-06.
22. ^ MSDS Sodium Sulfate Anhydrous. James T Baker (2006). Retrieved on 2007-04-21.

External links

Thenardite is an anhydrous sodium sulfate mineral, Na2SO4 which occurs in arid evaporite environments. It also occurs in dry caves and old mine workings as an efflorescence and as a crusty deposit around fumaroles. It occurs in volcanic caves on Mt.
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Mirabilite, also known as "Glauber's salt", is a hydrous sodium sulfate mineral: Na2SO4·10H2O. It is a vitreous, colorless to white monoclinic mineral which forms as an evaporite from sodium sulfate bearing brines.
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CAS registry numbers are unique numerical identifiers for chemical compounds, polymers, biological sequences, mixtures and alloys. They are also referred to as CAS numbers, CAS RNs or CAS #s.
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Molar mass, symbol M,[1] is the mass of one mole of a substance (chemical element or chemical compound).[2] It is a physical property which is characteristic of each pure substance.
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As a general term, a substance is said to be anhydrous if it contains no water. The way of achieving the anhydrous form differs from one substance to another.

Solvents

In many cases, the presence of water can prevent a reaction from happening, or form undesirable products.
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Hygroscopy is the ability of a substance to attract water molecules from the surrounding environment through either absorption or adsorption.

Hygroscopic substances include honey, glycerin, ethanol, methanol, concentrated sulfuric acid, methamphetamine, and concentrated
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In physics, density is mass m per unit volume V—how heavy something is compared to its size. A small, heavy object, such as a rock or a lump of lead, is denser than a lighter object of the same size or a larger object of the same weight, such as pieces of
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The melting point of a crystalline solid is the temperature range at which it changes state from solid to liquid. Although the phrase would suggest a specific temperature and is commonly and incorrectly used as such in most textbooks and literature, most crystalline compounds
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Solubility is a physical property referring to the ability for a given substance, the solute, to dissolve in a solvent.[1] It is measured in terms of the maximum amount of solute dissolved in a solvent at equilibrium. The resulting solution is called a saturated solution.
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Water is a common chemical substance that is essential to all known forms of life.[1] In typical usage, water refers only to its liquid form or state, but the substance also has a solid state, ice, and a gaseous state, water vapor.
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crystal structure is a unique arrangement of atoms in a crystal. A crystal structure is composed of a motif, a set of atoms arranged in a particular way, and a lattice. Motifs are located upon the points of a lattice, which is an array of points repeating periodically in three
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monoclinic crystal system is one of the 7 lattice point groups. A crystal system is described by three vectors. In the monoclinic system, the crystal is described by vectors of unequal length, as in the orthorhombic system. They form a rectangular prism with a parallelogram as base.
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orthorhombic crystal system is one of the 7 lattice point groups. Orthorhombic lattices result from stretching a cubic lattice along two of its lattice vectors by two different factors, resulting in a rectangular prism with a rectangular base (a by b
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In geometry, a hexagon is a polygon with six edges and six vertices. A regular hexagon has Schläfli symbol .

Regular hexagon



The internal angles of a regular hexagon (one where all sides and all angles are equal) are all 120° and the hexagon has 720 degrees.
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material safety data sheet (MSDS) is a form containing data regarding the properties of a particular substance. An important component of product stewardship and workplace safety, it is intended to provide workers and emergency personnel with procedures for handling or
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Occupational safety and health (OSH) is a cross-disciplinary area concerned with protecting the safety, health and welfare of people engaged in work or employment. As a secondary effect, OSH may also protect co-workers, family members, employers, customers, suppliers, nearby
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NFPA 704 is a standard maintained by the U.S. National Fire Protection Association. It defines the colloquial "fire diamond" used by emergency personnel to quickly and easily identify the risks posed by nearby hazardous materials.
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Risk and Safety Statements, also known as R/S statements, R/S numbers, R/S phrases, and R/S sentences, is a system of hazard codes and phrases for labeling dangerous chemicals and compounds.
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ion is an atom or molecule which has lost or gained one or more electrons, making it positively or negatively charged. A negatively charged ion, which has more electrons in its electron shells than it has protons in its nuclei, is known as an anion
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Sodium bisulfate, also sodium hydrogen sulfate, has the chemical formula NaHSO4.

Production

Sodium bisulfate is produced by two methods. One method involves mixing stoichiometric quantities of sodium hydroxide and sulfuric acid which react to form
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Sodium sulfite (sodium sulphite) is a soluble compound of sodium. Its chemical formula is Na2SO3. It has a molecular weight of 126.04. It is a product of SO2 scrubbing, a part of the flue gas desulfurization process.
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Sodium hydrogen sulfite or sodium bisulfite is a chemical compound with the chemical formula NaHSO3. Sodium bisulfite is a food additive with E-number E-222. Sodium bisulfite can be prepared by bubbling sulfur dioxide in a solution of sodium carbonate in water.
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Sodium persulfate (Na2S2O8) is a chemical compound. It is a strong oxidizer. Its risk and safety phrases are
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ion is an atom or molecule which has lost or gained one or more electrons, making it positively or negatively charged. A negatively charged ion, which has more electrons in its electron shells than it has protons in its nuclei, is known as an anion
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Lithium sulfate is a white inorganic salt used to treat bipolar disorder (see Lithium pharmacology). It is soluble in water, though it does not follow the usual trend of solubility versus temperature — its solubility in water decreases with increasing temperature.
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Potassium sulfate (K2SO4) (in British English potassium sulphate or archaically known as potash of sulfur) is a non-flammable white crystalline salt which is soluble in water.
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Magnesium sulfate (or sulphate) is a chemical compound containing magnesium and sulfate, with the formula MgSO4. It is often encountered as the heptahydrate, MgSO4·7H2O, commonly called Epsom salts.
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This page provides supplementary chemical data on sodium sulfate.

Material Safety Data Sheet

The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet (MSDS) for this chemical from a reliable
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The refractive index (or index of refraction) of a medium is a measure for how much the speed of light (or other waves such as sound waves) is reduced inside the medium. For example, typical glass has a refractive index of 1.
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The relative static permittivity (or static relative permittivity) of a material under given conditions is a measure of the extent to which it concentrates electrostatic lines of flux.
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