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Potassium nitrate[1]
Identifiers
CAS number 7757-79-1 Yes check.svgY
PubChem 24434
ChemSpider 22843
UN number 1486
RTECS number TT3700000
Properties
Molecular formula KNO3
Molar mass 101.103 g/mol
Appearance white solid
Odor odorless
Density 2.109 g/cm3 (16 °C)
Melting point

334 °C

Boiling point

400 °C decomp.

Solubility in water 13.3 g/100 mL (0 °C)
36 g/100 mL (25 °C)
247 g/100 mL (100 °C)
Solubility slightly soluble in ethanol
soluble in glycerol, ammonia
Structure
Crystal structure Orthorhombic, Aragonite
Hazards
MSDS External MSDS
EU Index Not listed
Main hazards Oxidant
NFPA 704
NFPA 704.svg
0
1
0
OX
Flash point Non-flammable
LD50 3750 mg/kg
Related compounds
Other anions Potassium nitrite
Other cations Lithium nitrate
Sodium nitrate
Rubidium nitrate
Caesium nitrate
Related compounds Potassium sulfate
Potassium chloride
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references
The crystal structure of KNO3

Potassium nitrate is a chemical compound with the chemical formula KNO3. A naturally occurring mineral source of nitrogen, KNO3 constitutes a critical oxidizing component of black powder/gunpowder. In the past it was also used for several kinds of burning fuses, including slow matches. Potassium nitrate readily precipitates from mixtures of salts, and decomposing urine was the main commercial source of the nitrate ion, through various means, from the Late Middle Ages and Early Modern era through the 19th century.

Its common names include saltpetre (saltpeter in American English), from Medieval Latin sal petræ: "stone salt" or possibly "Salt of Petra", nitrate of potash, and nitre (American niter). For specific information about the naturally occurring mineral, see niter. The name Peru saltpetre or Chile saltpetre (American "Peru saltpeter" or "Chile saltpeter") is applied to sodium nitrate, a similar nitrogen compound that is also used in explosives and fertilizers. The major problem of using the cheaper sodium nitrate in gunpowder is its tendency to go damp.

Contents

Description

Potassium nitrate is the oxidising component of black powder. Before the large-scale industrial fixation of nitrogen through the Haber process, major sources of potassium nitrate were the deposits crystallizing from cave walls and the draining of decomposing organic material.[citation needed] Dung-heaps were a particularly common source: ammonia from the decomposition of urea and other nitrogenous materials would undergo bacterial oxidation to produce nitrates. These often contained calcium nitrate, which could be converted to potassium nitrate by the addition of potash from wood ashes. It was and is also used as a component in some fertilizers. Potassium nitrate when used by itself as a fertilizer has an NPK rating of 13-0-44. Potassium nitrate was once thought to induce impotence, and is still falsely rumored to be in institutional food (such as military fare) as an anaphrodisiac; these uses would be ineffective, since potassium nitrate has no such properties.[2] However, potassium nitrate successfully combats high blood pressure and was once used as a hypotensive. Other nitrates and nitrites such as glyceryl trinitrate (nitroglycerin), amyl nitrite and isosorbide derivatives are still used to relieve angina.

History of production

Historically, niter-beds were prepared by mixing manure with either mortar or wood ashes, common earth and organic materials such as straw to give porosity to a compost pile typically 1.5 meters high by 2 meters wide by 5 meters long.[3] The heap was usually under a cover from the rain, kept moist with urine, turned often to accelerate the decomposition and leached with water after approximately one year. The liquid containing various nitrates was then converted with wood ashes to potassium nitrate, crystallized and refined for use in gunpowder.

Urine has also been used in the manufacture of saltpetre for gunpowder. In this process, stale urine placed in a container of straw hay is allowed to sour for many months, after which water is used to wash the resulting chemical salts from the straw. The process is completed by filtering the liquid through wood ashes and air-drying in the sun.[3] Saltpetre crystals can then be collected and added to sulfur and charcoal to create black powder.[4] Potassium nitrate could also be harvested from accumulations of bat guano in caves. This was the traditional method used in Laos for the manufacture of gunpowder for Bang Fai rockets.

The earliest known complete purification process for potassium nitrate is described in 1270 by the Arab chemist and engineer Hasan al-Rammah of Syria in his book al-Furusiyya wa al-Manasib al-Harbiyya ('The Book of Military Horsemanship and Ingenious War Devices'), where he first described the use of potassium carbonate (in the form of wood ashes) to remove calcium and magnesium salts from the potassium nitrate.[5]

During the 19th century and until around World War I, potassium nitrate was produced on an industrial scale, first by the Birkeland–Eyde process in 1905, and then later from ammonia produced by the much more efficient Haber process. Today practically all nitrates are produced from the oxidation of ammonia made by the Haber process.

Uses

Potassium nitrate is also used as a fertilizer, in amateur rocket propellants, and in several fireworks such as smoke bombs.

In the process of food preservation, potassium nitrate has been a common ingredient of salted meat since the Middle Ages,[6] but its use has been mostly discontinued due to inconsistent results compared to more modern nitrate and nitrite compounds. Even so, saltpetre is still used in some food applications, such as charcuterie and the brine used to make corned beef.[7] Sodium nitrate (and nitrite) have mostly supplanted potassium nitrate's culinary usage, as they are more reliable in preventing bacterial infection than saltpetre. All three give cured salami and corned beef their characteristic pink hue.

In the European Union, the compound is referred to as E252.

It is commonly used in pre-rolled cigarettes to maintain an even burn of the tobacco.[8]

As a fertilizer, it is used as a source of nitrogen and potassium, two of the macro nutrients for plants.

Potassium nitrate is also the main component (usually about 98%) of tree stump remover, as it accelerates the natural decomposition of the stump.[9]

Potassium nitrate is also commonly used in the heat treatment of metals as a solvent in the post-wash. The oxidizing, water solubility and low cost make it an ideal short-term rust inhibitor.

It has also been used in the manufacture of ice cream and can be found in some toothpastes for sensitive teeth.[10] Recently, the use of potassium nitrate in toothpastes for treating sensitive teeth has increased dramatically, despite the fact that it has not been conclusively shown to reduce dentine hypersensitivity.[11]

Potassium nitrate is also one of the three components of black powder, along with powdered charcoal (substantially carbon) and sulfur, where it acts as an oxidizer. When subjected to the flame test it produces a lilac flame due to the presence of potassium.[12]

Saltpetre is thought to decrease sex drive, but there is no scientific evidence to support that the substance causes such an effect.[13]

See also

References

  1. ^ Record of Potassium nitrate in the GESTIS Substance Database from the IFA, accessed on 2007-03-09.
  2. ^ "The Straight Dope: Does saltpeter suppress male ardor?". 1989-06-16. http://www.straightdope.com/classics/a3_221.html. Retrieved 2007-10-19. 
  3. ^ a b LeConte, Joseph (1862). Instructions for the Manufacture of Saltpeter. Columbia, S.C.: South Carolina Military Department. pp. 14. http://docsouth.unc.edu/imls/lecontesalt/leconte.html. Retrieved 2007-10-19. 
  4. ^ The Foxfire Fund (1979). The Foxfire Book, Volume 5. Doubleday Books. ISBN 0385143087. (excerpt)
  5. ^ Ahmad Y Hassan, Potassium Nitrate in Arabic and Latin Sources, History of Science and Technology in Islam.
  6. ^ "Meat Science", University of Wisconsin
  7. ^ Corned Beef, Food Network
  8. ^ Inorganic Additives for the Improvement of Tobacco, TobaccoDocuments.org
  9. ^ Stump Remover MSDS, spectracide.com
  10. ^ "Sensodyne Toothpaste for Sensitive Teeth". 2008-08-03. http://us.sensodyne.com/products_freshmint.aspx. Retrieved 2008-08-03. 
  11. ^ "Potassium containing toothpastes for dentine hypersensitivity". 2006-05-23. http://www.cochrane.org/reviews/en/ab001476.html. Retrieved 2007-10-19. 
  12. ^ Amthyst Galleries, Inc.
  13. ^ Jones, Richard E.; Kristin H. López (2006). Human Reproductive Biology, Third Edition. Elsevier/Academic Press. p. 226. ISBN 0120884658, 9780120884650. 

Bibliography

  • Dennis W. Barnum. (2003). "Some History of Nitrates." Journal of Chemical Education. v. 80, p. 1393-. link.
  • Alan Williams: The production of saltpeter in the Middle Ages, Ambix, 22 (1975), pp. 125-33. Maney Publishing, ISSN 0002-6980.

External links


1911 encyclopedia

Up to date as of January 14, 2010

From LoveToKnow 1911

SALTPETRE (from the Lat. sal, salt, petra, a rock), the commercial name given to three naturally occurring nitrates, distinguished as (1) ordinary saltpetre, nitre, or potassium nitrate, (2) Chile saltpetre, cubic nitre, or sodium nitrate, (3) wall-saltpetre or calcium nitrate. These nitrates generally occur as efflorescences caused by the oxidation of nitrogenous matter in the presence of the alkalies and alkaline earths.

1. Ordinary Saltpetre or Potassium Nitrate, KN03, occurs, mingled with other nitrates, on the surface and in the superficial layers of the soil in many countries, especially in certain parts of India, Persia, Arabia and Spain. The deposits in the great limestone caves of Kentucky, Virginia and Indiana have been probably derived from the overlying soil and accumulated by percolating water; they are of no commercial value. The actual formation of this salt is not quite clear; but it is certainly conditioned by the simultaneous contact of decaying nitrogenous matter, alkalies, air and moisture. The demand for saltpetre as an ingredient of gunpowder led to the formation of saltpetre plantations or nitriaries, which at one time were common in France, Germany, and other countries; the natural conditions were simulated by exposing heaps of decaying organic matter mixed with alkalies (lime, &c.) to atmospheric action. The salt is obtained from the soil in which it occurs naturally, or from the heaps in which it is formed artificially, by extracting with water, and adding to the solution wood-ashes or potassium carbonate. The liquid is filtered and then crystallized. Since potassium nitrate is generally more serviceable than the sodium salt, whose deliquescent properties inhibit its use for gunpowder manufacture, the latter salt, of which immense natural deposits occur (see below (2) Chile saltpetre), is converted into ordinary saltpetre in immense quantities. This is generally effected by adding the calculated amount of potassium chloride (of which immense quantities are obtained as a by-product in the Stassfurt salt industry) dissolved in hot water to a saturated boiling solution of sodium nitrate; the common salt, which separates on boiling down the solution, is removed from the hot solution, and on cooling the potassium nitrate crystallizes out and is separated and dried.

As found in nature, saltpetre generally forms aggregates of delicate acicular crystals, and sometimes silky tufts; distinctly developed crystals are not found in nature. When crystallized from water, crystals belonging to the orthorhombic system, and having a prism angle of 61 0 10', are obtained; they are often twinned on the prism planes, giving rise to pseudo-hexagonal groups resembling aragonite. There are perfect cleavages parallel to the dome (oiI). The hardness is 2, and the specific gravity 2 I. It is fairly soluble in water; too parts at o° dissolving 13.3 parts of the salt, and about 30 parts at 20°; the most saturated solution contains 327.4 parts of the salt in too of water; this solution boils at 114.1°. It fuses at 339° to a colourless liquid, which solidifies on cooling to a white fibrous mass, known in pharmacy as sal prunelia. It is an energetic oxidizing agent, and on this property its most important applications depend. At a red heat it evolves oxygen with the formation of potassium nitrite, which, in turn, decomposes at a higher temperature. Heated with many metals it converts them into oxides, and with combustible substances, such as charcoal, sulphur, &c., a most intense conflagration occurs. Its chief uses are in glass-making to promote fluidity, in metallurgy to oxidize impurities, as a constituent of gunpowder and in pyrotechny; it is also used in the manufacture of nitric acid.

Potassium nitrate was used at one time in many different diseased conditions, but it is now never administered internally, as its extremely depressant action upon the heart is not compensated for by any useful properties which are not possessed by many other drugs. One most valuable use it has, however, in the treatment of asthma. All nitrites (e.g. sodium nitrite, ethyl nitrite, amyl nitrite) cause relaxation of involuntary muscular fibre and therefore relieve the asthmatic attacks, which depend upon spasm of the involuntary muscles in the bronchial tubes. Saltpetre may be made to act as a nitrite by dissolving it in water in the strength of about fifty grains to the ounce, soaking blotting-paper in the solution and letting the paper dry. Pieces about 2 in. square are then successively put into a jar and lighted. The patient inhales the fumes, which contain a considerable proportion of nitrogen oxides. This treatment is frequently very successful indeed in relaxing the bronchial spasm upon which the most obvious features of an attack depend.

2. Chile saltpetre, cubic nitre or sodium nitrate, NaNO,, occurs under the same conditions as ordinary saltpetre in deposits covering immense areas in South America, which are known locally as caliche or terra salitrosa, and abound especially in the provinces of Tarapaca and Antofagasta in Chile. The nitrate fields are confined to a narrow strip of country, averaging 21 m. in width, situated on the eastern slopes of the coast ranges and extending from north to south for 260 geographical miles, between the latitudes 25° 45' and 19° 12' S. The nitrate forms beds, varying in thickness from 6 in. to 12 ft., under a covering of conglomerate locally known as lostra, which is itself overlain by a loose sandy soil. The conglomerate consists of rock fragments, sodium chloride and various sulphates, cemented together by gypsum to form a hard compact mass 6 to 10 ft. in thickness. The caliche has often a granular structure, and is yellowishwhite, bright lemon-yellow, brownish or violet in colour. It contains from 48 to 75% of sodium nitrate and from 20 to 40% of common salt, which are associated with various minor saline components, including sodium iodate and more or less insoluble mineral, and also some organic matter, e.g. guano, which suggests the idea that the nitrate was formed by the nitrification of this kind of excremental matter. The caliche is worked up in loco for crude nitrate by extracting the salts with hot water, allowing the suspended earth to settle, and then transferring the clarified liquor, first to a cistern where it deposits part of its sodium chloride at a high temperature, and then to another where, on cooling, it yields a crop of crystals of purified nitrate. The nitre thus refined is exported chiefly from Valparaiso, whence the name of "Chile saltpetre." The mother liquors used to be thrown away, but are now utilized for the extraction of their iodine.

Chemically pure sodium nitrate can be obtained by repeated recrystallization of Chile saltpetre or by synthesis. It forms colourless, transparent rhombohedra, like those of Iceland spar; the angles are nearly equal to right angles, being 73° 30', so that the crystals look like cubes: hence the name of "cubic saltpetre." There are perfect cleavages parallel to the rhombohedral faces, and the crystals exhibit a strong negative double refraction, like calcite. One hundred parts of water at o° and at Ioo° dissolve 72.9 and 180 parts of the salt; at 120° the boiling-point of the saturated solution, 216 parts. The salt fuses at 316°; at higher temperatures it loses oxygen (more readily than the corresponding potassium salt) with the formation of nitrite which, at very high temperatures, is reduced ultimately to a mixture of peroxide, Na202, and oxide, Na 2 0. The chief applications of Chile saltpetre are in the nitric acid industry, and in the manufacture of ordinary saltpetre for making gunpowder, ordinary Chile saltpetre being unsuitable by reason of its deliquescent nature, a property, however, not exhibited by the perfectly pure salt. It is also employed as a manure. For references to memoirs descriptive of the Chilian nitrate deposits, see G. P. Merrill, The Non-Metallic Minerals (New York, 1904). 1904).

3. Wall-saltpetre or lime saltpetre, calcium nitrate, Ca(N03)2, is found as an efflorescence on the walls of stables; it is now manufactured in large quantities by fixing atmospheric nitrogen, i.e. by passing a powerful electric arc discharge through moist air and absorbing the nitric acid formed by lime. Its chief applications are as a manure and in the nitric acid industry.


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