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{{Elementbox_header | number=53 | symbol=I | name=iodine | left=[[tellurium]] | right=[[xenon]] | above=[[bromine|Br]] | below=[[astatine|At]] | color1=#ffff99 | color2=black }}
{{Elementbox_series | [[halogen]]s }}
{{Elementbox_groupperiodblock | group=17 | period=5 | block=p }}
{{Elementbox_appearance_img |Iodine-sample| violet-dark gray, lustrous }}
{{Elementbox_atomicmass_gpm | [[1 E-25 kg|126.90447]][[List of elements by atomic mass|(3)]] }}
{{Elementbox_econfig | &#91;[[krypton|Kr]]&#93; 4d<sup>10</sup> 5s<sup>2</sup> 5p<sup>5</sup> }}
{{Elementbox_epershell | 2, 8, 18, 18, 7 }}
{{Elementbox_section_physicalprop | color1=#ffff99 | color2=black }}
{{Elementbox_phase | [[solid]] }}
{{Elementbox_density_gpcm3nrt | 4.933 }}
{{Elementbox_meltingpoint | k=386.85 | c=113.7 | f=236.66 }}
{{Elementbox_boilingpoint | k=457.4 | c=184.3 | f=363.7 }}
{{Elementbox_criticalpoint | k=819 | mpa=11.7 }}
{{Elementbox_heatfusion_kjpmol | (I<sub>2</sub>) 15.52 }}
{{Elementbox_heatvaporiz_kjpmol | (I<sub>2</sub>) 41.57 }}
{{Elementbox_heatcapacity_jpmolkat25 | (I<sub>2</sub>) 54.44 }}
{{Elementbox_vaporpressure_katpa | 260 | 282 | 309 | 342 | 381 | 457 | comment=(rhombic) }}
{{Elementbox_section_atomicprop | color1=#ffff99 | color2=black }}
{{Elementbox_crystalstruct | orthorhombic }}
{{Elementbox_oxistates | ±1, 5, 7<br />(strongly [[acid]]ic oxide) }}
{{Elementbox_electroneg_pauling | 2.66 }}
{{Elementbox_ionizationenergies3 | 1008.4 | 1845.9 | 3180 }}
{{Elementbox_atomicradius_pm | [[1 E-10 m|140]] }}
{{Elementbox_atomicradiuscalc_pm | [[1 E-10 m|115]] }}
{{Elementbox_covalentradius_pm | [[1 E-10 m|133]] }}
{{Elementbox_vanderwaalsrad_pm | [[1 E-10 m|198]] }}
{{Elementbox_section_miscellaneous | color1=#ffff99 | color2=black }}
{{Elementbox_magnetic | nonmagnetic }}
{{Elementbox_eresist_ohmmat0 | 1.3×10<sup>7</sup> }}
{{Elementbox_thermalcond_wpmkat300k | 0.449 }}
{{Elementbox_bulkmodulus_gpa | 7.7 }}
{{Elementbox_cas_number | 7553-56-2 }}
{{Elementbox_isotopes_begin | color1=#ffff99 | color2=black }}
{{Elementbox_isotopes_stable | mn=127 | sym=I | na=100% | n=74 }}
{{Elementbox_isotopes_decay | mn=129 | sym=I
| na=[[synthetic radioisotope|syn]] | hl=15.7×10<sup>6</sup>[[year|y]]
| dm=[[beta emission|β<sup>-</sup>]] | de=0.194 | pn=129 | ps=[[xenon|Xe]] }}
{{Elementbox_isotopes_decay | mn=131 | sym=I
| na=[[synthetic radioisotope|syn]] | hl=8.02070 [[day|d]]
| dm=[[beta emission|β<sup>-</sup>]] | de=0.971 | pn=131 | ps=[[xenon|Xe]] }}
{{Elementbox_isotopes_end}}
{{Elementbox_footer | color1=#ffff99 | color2=black }}
'''Iodine''' ({{IPAEng|ˈaɪədaɪn, ˈaɪədɪn}}, or {{IPA|/ˈaɪədiːn/}}; from {{lang-el|''iodes''}} "violet"), is a [[chemical element]] that has the symbol '''I''' and [[atomic number]] 53. Iodine has 53 protons, 53 electrons, and 74 neutrons. Chemically, iodine is the least reactive of the [[halogen]]s, and the most [[electronegativity|electropositive]] halogen after [[astatine]]. Iodine is primarily used in [[medicine]], [[photography]] and [[dye]]s. It is required in trace amounts by most living [[organism]]s.

As with all other [[halogens]] (members of Group VII in the Periodic Table), iodine forms [[diatomic]] [[molecule]]s, and hence has the molecular formula of '''I<sub>2</sub>'''.

== Properties ==
Iodine is a dark-gray/purple-brown solid that can be seen [[sublimation (chemistry)|subliming]] at standard temperatures into a purple-pink gas that has an irritating odour. This halogen forms compounds with many elements, but is less reactive than the other members of its Group VII (halogens) and has some metallic-like properties. Iodine dissolves easily in [[chloroform]], [[carbon tetrachloride]]. The solubility of elementary iodine in water can be vastly increased by the addition of potassium iodide. The molecular iodine reacts reversibly with the negative ion, creating the [[triiodide]] anion, I<sub>3</sub><sup>−</sup>, which dissolves well in water. This is also the formulation of medicinal iodine of old. The deep blue color of [[starch]]-iodine complexes is produced only by the free element.

Many students who have seen the classroom demonstration where iodine crystals are gently heated in a test tube come away with the impression that liquid iodine does not exist at atmospheric pressure. This misconception arises because the small amount of vapour produced has such a deep colour that the iodine liquid appears not to form. In fact, if iodine crystals are heated carefully to just above their melting point of 113.7 °C, the crystals melt into a liquid, which will be present under a dense blanket of the vapour.

== History ==
Iodine was discovered by [[Bernard Courtois]] in 1811. He was born to a manufacturer of [[Potassium nitrate|saltpeter]] (a vital part of gunpowder). At the time of the [[Napoleonic Wars]], [[France]] was at war and saltpeter was in great demand. Saltpeter produced from French [[niter]] beds required sodium carbonate, which could be isolated from [[seaweed]] washed up on the coasts of [[Normandy]] and [[Brittany]]. To isolate the sodium carbonate, seaweed was burned and the ash then washed with water. The remaining waste was destroyed by adding [[sulfuric acid]]. One day Courtois added too much sulfuric acid and a cloud of purple vapor rose. Courtois noted that the vapor crystallized on cold surfaces making dark crystals. Courtois suspected that this was a new element but lacked the money to pursue his observations.

However he gave samples to his friends, [[Charles Bernard Desormes]] (1777 - 1862) and [[Nicolas Clément]] (1779 - 1841), to continue research. He also gave some of the substance to [[Joseph Louis Gay-Lussac]] (1778 - 1850), a well-known chemist at that time, and to [[André-Marie Ampère]] (1775 - 1836). On [[29 November]] [[1813]], Dersormes and Clément made public Courtois’ discovery. They described the substance to a meeting of the [[Imperial Institute of France]]. On December 6, Gay-Lussac announced that the new substance was either an element or a compound of oxygen. Ampère had given some of his sample to [[Humphry Davy]] (1778 - 1829). Davy did some experiments on the substance and noted its similarity to [[chlorine]]. Davy sent a letter dated December 10 to the [[Royal Society of London]] stating that he had identified a new element. A large argument erupted between Davy and Gay-Lussac over who identified iodine first but both scientists acknowledged Courtois as the first to isolate the chemical element.

== Applications ==
Iodine is used in pharmaceuticals, antiseptics, medicine, food supplements, dyes, catalysts, halogen lights, photography, water purifying, and starch detection.

* [[Tincture of iodine]] (10% elemental iodine in ethanol base) is an essential component of any emergency survival kit, used both to disinfect wounds and to sanitize surface water for drinking (3 drops per litre, let stand for 30 minutes). Alcohol-free iodine solutions such as [[Lugol's iodine]], as well as other [[iodophor]] type antiseptics, are also available as effective elemental iodine sources for this purpose.
* Iodine compounds are important in the field of [[organic chemistry]]
* Iodine, as a heavy element, is quite [[radio-opaque]]. Organic compounds of a certain type (typically iodine-substituted benzene derivatives) are thus used in [[medicine]] as X-ray [[radiocontrast]] agents for intravenous injection. This is often in conjunction with advanced X-ray techniques such as [[angiography]] and [[CT scan]]ning
* [[Silver iodide]] is used in photography.
* [[Tungsten]] iodide is used to stabilize the filaments in [[light bulb]]s.

== Occurrence on earth ==
Iodine naturally occurs in the environment chiefly as dissolved [[iodide]] in [[seawater]], although it is also found in some minerals and soils. The element may be prepared in an ultrapure form through the reaction of [[potassium iodide]] with [[copper(II) sulfate]]. There are also a few other methods of isolating this element. Although the element is actually quite rare, [[kelp]] and certain other plants have some ability to concentrate iodine, which helps introduce the element into the [[food chain]] as well as keeping its cost down.

== Sources ==
[[Image:Iodine.PNG|thumb|right|Iodine output in 2005]]
Iodine is found in the mineral [[Caliche (mineral)|caliche]], found in [[Chile]], between the [[Andes]] and the sea. It can also be found in some seaweeds as well as extracted from seawater, however extracting iodine from the mineral is the only economical way to extract the substance.{{Fact|date=February 2007}}

Extraction from seawater involves electrolysis. The brine is first purified and acidified using sulphuric acid and is then reacted with chlorine. An iodine solution is produced but it is yet too dilute and has to be concentrated. To do this air is blown into the solution which causes the iodine to evaporate, then it is passed into an absorbing tower containing acid where sulfur dioxide is added to reduce the iodine. The solution is then added to chlorine again to concentrate the solution more, and the final solution is at a level of about 99%.{{Fact|date=April 2007}}

Another source is from [[kelp]]. This source was used in the 18th and 19th centuries but is no longer economically viable.

In 2005, Chile was the top producer of iodine with almost two-thirds world share followed by Japan and the USA, reports the [[British Geological Survey]].

== Prices ==
The average price for iodine in 2005 was $7.03 [[US dollar]]s per [[kilogram]]. In 2006 this suddenly rose to $17.03 US dollars per kilogram. In [[Chile]], the world’s largest producer of iodine, prices dramatically changed too (2005 $16.97 US dollars 2006 $20.00 US dollars for one kilogram). The DNSC (Defence National Stockpile Center) claims that in 2005 they sold each kilogram of iodine for $18.36 US dollars and by 2006 they reported that each kilogram yielded $21.29. <ref>DNSC, 2006</ref>

== Descriptive chemistry ==
Elemental iodine is poorly soluble in water, with one gram dissolving in 3450 ml at 20 °C and 1280 ml at 50 °C. By contrast with [[chlorine]], the formation of the hypohalite ion (IO<sup>–</sup>) in neutral aqueous solutions of iodine is negligible.

::I<sub>2</sub>+ H<sub>2</sub>O ↔ H<sup>+</sup> + I<sup>–</sup> + HIO &nbsp; (''K'' = 2.0×10<sup>-13</sup>) <ref name="cw">Advanced Inorganic Chemistry by Cotton and Wilkinson, 2nd ed.</ref>
Solubility in water is greatly improved if the solution contains dissolved [[iodide]]s such as [[hydroiodic acid]], [[potassium iodide]], or [[sodium iodide]]. Dissolved [[bromide]]s also improve water solubility of iodine. Iodine is soluble in a number of organic solvents, including [[ethanol]] (20.5 g/100 ml at 15 °C, 21.43 g/100 ml at 25 °C), [[diethyl ether]] (20.6 g/100 ml at 17 °C, 25.20 g/100 ml at 25 °C), [[chloroform]], [[acetic acid]], [[glycerol]], [[benzene]] (14.09 g/100 ml at 25 °C), [[carbon tetrachloride]] (2.603 g/100 ml at 35 °C), and [[carbon disulfide]] (16.47 g/100 ml at 25 °C)<ref>Merck Index of Chemicals and Drugs, 9th ed.</ref>. Aqueous and ethanol solutions are brown. Solutions in chloroform, carbon tetrachloride, and carbon disulfide are violet.

Elemental iodine can be prepared by oxidizing [[iodide]]s with chlorine:

::2I<sup>–</sup> + Cl<sub>2</sub> → I<sub>2</sub> + 2Cl<sup>–</sup>

or with [[manganese dioxide]] in acid solution:<ref name="cw"/>

::2I<sup>–</sup> + 4H<sup>+</sup> + MnO<sub>2</sub> → I<sub>2</sub> + 2H<sub>2</sub>O + Mn<sup>2+</sup>

Iodine is reduced to [[hydroiodic acid]] by [[hydrogen sulfide]]:<ref name="glinka">General Chemistry (volume 2) by N.L. Glinka, Mir Publishing 1981</ref>

::I<sub>2</sub> + H<sub>2</sub>S → 2HI + S↓

or by [[hydrazine]]:
::2I<sub>2</sub> + N<sub>2</sub>H<sub>4</sub> → 4HI + N<sub>2</sub>

Iodine is oxidized to [[iodate]] by [[nitric acid]]:<ref name="pauling">General Chemistry by Linus Pauling, 1947 ed.</ref>

::I<sub>2</sub> + 10HNO<sub>3</sub> → 2HIO<sub>3</sub> + 10NO<sub>2</sub> + 4H<sub>2</sub>O

or by [[chlorate]]s:<ref name="pauling"/>

::I<sub>2</sub> + 2ClO<sub>3</sub><sup>–</sup> → 2IO<sub>3</sub><sup>–</sup> + Cl<sub>2</sub>

Iodine is converted in a two stage reaction to [[iodide]] and [[iodate]] in solutions of alkali hydroxides (such as [[sodium hydroxide]]):<ref name="cw"/>

::{|
|I<sub>2</sub> + 2OH<sup>–</sup> → I<sup>–</sup> + IO<sup>–</sup> + H<sub>2</sub>O
|
| (''K'' = 30)
|-
|3IO<sup>–</sup> → 2I<sup>–</sup> + IO<sub>3</sub><sup>–</sup>
|
| (''K'' = 10<sup>20</sup>)
|}

== Notable inorganic iodine compounds ==
<div style="-moz-column-count:4; column-count:4;">
{{Iodides}}</div>
''See also [[:category:Iodine compounds|iodine compounds]]''

== Stable iodine in biology ==
Iodine is an essential [[trace element]]; its only known roles in biology are as constituents of the [[thyroid]] [[hormone]]s, ''[[thyroxine]]'' (T4) and ''[[triiodothyronine]]'' (T3). These are made from addition condensation products of the amino acid [[tyrosine]], and are stored prior to release in a protein-like molecule called thryroglobulin. T4 and T3 contain four and three atoms of iodine per molecule, respectively. The [[thyroid gland]] actively absorbs iodide from the blood to make and release these hormones into the blood, actions which are regulated by a second hormone [[TSH]] from the pituitary. Thyroid hormones are phylogenetically very old molecules which are synthesized by most multicellular organisms, and which even have some effect on unicellular organisms.

Thyroid hormones play a very basic role in biology, acting on gene transcription to regulate the basal metabolic rate. The total deficiency of thyroid hormones can reduce basal metabolic rate up to 50%, while in excessive production of thyroid hormones the basal metabolic rate can be increased by 100%. T4 acts largely as a precursor to T3, which is (with some minor exceptions) the biologically active hormone.

=== Human dietary intake ===
The United States [[Food and Drug Administration]] recommends 150 [[Kilogram#SI multiples|micrograms]] of iodine per day for both men and women.<ref>[[21 CFR]] 101.9 (c)(8)(iv)</ref> This is necessary for proper production of thyroid hormone.{{Fact|date=April 2007}} Natural sources of iodine include sea life, such as kelp and certain seafood, as well as plants grown on iodine-rich soil.{{Fact|date=April 2007}} Salt for human consumption is often fortified with iodine and is referred to as [[iodized salt]].

=== Iodine deficiency ===
{{main|Iodine deficiency}}
In areas where there is little iodine in the diet&mdash;typically remote inland areas and semi-arid equatorial climates where no marine foods are eaten&mdash;[[iodine deficiency]] gives rise to hypothyroidism, symptoms of which are extreme fatigue, [[goitre]], mental slowing, depression, weight gain, and low basal body temperatures.{{Fact|date=April 2007}}

Iodine deficiency is also the leading cause of preventable [[mental retardation]], an effect which happens primarily when babies and small children are made [[hypothyroid]] by lack of the element. The addition of iodine to table salt has largely eliminated this problem in the wealthier nations, but iodine deficiency remains a serious public health problem in the developing world.{{Fact|date=April 2007}}

== Radioiodine and biology ==
=== Radioiodine and the thyroid ===
The artificial [[radioisotope]] <sup>131</sup>I (a beta emitter), also known as [[radioiodine]] which has a [[half-life]] of 8.0207 days, has been used in treating [[cancer]] and other pathologies of the [[thyroid]] [[gland]]s. <sup>123</sup>I is the radioisotope most often used in nuclear imaging of the [[kidney]] and thyroid as well as thyroid uptake scans (used for the evaluation of [[Graves' Disease]]). The most common compounds of iodine are the iodides of [[sodium]] and [[potassium]] ([[potassium iodide|KI]]) and the iodates (KIO<sub>3</sub>).

<sup>129</sup>I ([[half-life]] 15.7 million years) is a product of <sup>130</sup>[[xenon|Xe]] [[spallation]] in the [[Earth's atmosphere|atmosphere]] and [[uranium]] and [[plutonium]] fission, both in subsurface rocks and nuclear reactors. Nuclear processes, in particular nuclear fuel reprocessing and atmospheric nuclear weapons tests have now swamped the natural signal for this isotope. <sup>129</sup>I was used in rainwater studies following the [[Chernobyl accident]]. It also has been used as a ground-water tracer and as an indicator of nuclear waste dispersion into the natural environment.

If humans are exposed to radioactive iodine, the thyroid gland will absorb it as if it were non-radioactive iodine, leading to elevated chances of thyroid cancer. Isotopes with shorter half-lives such as <sup>131</sup>I present a greater risk than those with longer half-lives since they generate more radiation per unit of time. Taking large amounts of regular iodine will saturate the thyroid and prevent uptake. Iodine pills are sometimes distributed to persons living close to nuclear establishments, for use in case of accidents that could lead to releases of radioactive iodine.
* [[Iodine-123]] and [[iodine-125]] are used in medicine as tracers for imaging and evaluating the function of the thyroid.
* [[Iodine-131]] is used in medicine for treatment of thyroid cancer and Graves' Disease.
* Uncombined (elemental) iodine is mildly toxic to all living things.
* [[Potassium iodide]] (KI tablets, or "SSKI" = "Saturated Solution of KI" liquid drops) can be given to people in a nuclear disaster area when [[Nuclear fission|fission]] has taken place, to flush out the radioactive iodine-131 fission product. The half-life of iodine-131 is only eight days, so the treatment would need to continue only a couple of weeks. In cases of leakage of certain nuclear materials without fission, or certain types of [[dirty bomb]] made with other than radioiodine, this precaution would be of no avail.

=== Radioiodine and the kidney ===
In the 1970s imaging techniques were developed in [[California]] to utilize radioiodine in diagnostics for [[renal]] [[hypertension]].

== Isotopes ==
{{main|isotopes of iodine}}
There are 37 [[isotope]]s of iodine and only one, <sup>127</sup>I, is stable.

In many ways, <sup>129</sup>I is similar to [[chlorine-36|<sup>36</sup>Cl]]. It is a soluble halogen, fairly non-reactive, exists mainly as a non-sorbing [[anion]], and is produced by cosmogenic, thermonuclear, and in-situ reactions. In hydrologic studies, <sup>129</sup>I concentrations are usually reported as the ratio of <sup>129</sup>I to total I (which is virtually all <sup>127</sup>I). As is the case with <sup>36</sup>Cl/Cl, <sup>129</sup>I/I ratios in nature are quite small, 10<sup>−14</sup> to 10<sup>−10</sup> (peak thermonuclear <sup>129</sup>I/I during the 1960s and 1970s reached about 10<sup>−7</sup>). <sup>129</sup>I differs from <sup>36</sup>Cl in that its half-life is longer (15.7 vs. 0.301 million years), it is highly biophilic, and occurs in multiple [[ion]]ic forms (commonly, I<sup>−</sup> and [[Iodate|IO<sub>3</sub><sup>−</sup>]]) which have different chemical behaviors. This makes it fairly easy for <sup>129</sup>I to enter the biosphere as it becomes incorporated into vegetation, soil, milk, animal tissue, etc.

Excesses of stable <sup>129</sup>Xe in meteorites have been shown to result from decay of "primordial" <sup>129</sup>I produced newly by the supernovas which created the dust and gas from which the solar system formed. <sup>129</sup>I was the first [[extinct radionuclide]] to be identified as present in the early [[solar system]]. Its decay is the basis of the I-Xe [[radiometric dating]] scheme, which covers the first 83 million years of [[solar system]] evolution.

Effects of various radioiodine isotopes in biology are discussed below.

== Toxicity of iodine ==
Excess iodine has symptoms similar to those of iodine deficiency. Commonly encountered symptoms are abnormal growth of the thyroid gland and disorders in functioning and growth of the organism as a whole. Elemental iodine, I<sub>2</sub>, is a deadly poison if taken in larger amounts; if 2-3 grams of it is consumed, it is fatal to humans. Iodides are similar in toxicity to bromides.

== Precautions for stable iodine ==
Direct contact with skin can cause lesions, so it should be handled with care. Iodine vapor is very irritating to the [[eye]] and to mucous membranes. Concentration of iodine in the air should not exceed 1 [[milligram|mg]]/[[cubic metre|m³]] (eight-hour time-weighted average). When mixed with [[ammonia]], it can form [[nitrogen triiodide]] which is extremely sensitive and can explode unexpectedly.

== Clandestine use ==
In the United States, the [[Drug Enforcement Agency]] (DEA) regards iodine and compounds containing iodine (ionic iodides, iodoform, ethyl iodide, and so on) as reagents useful for the clandestine manufacture of [[methamphetamine]]. Persons who attempt to purchase significant quantities of such chemicals without establishing a legitimate use are likely to find themselves the target of a DEA investigation. Persons selling such compounds without doing [[due diligence]] to establish that the materials are not being diverted to clandestine use may be subject to stiff penalties, such as expensive fines or even imprisonment.<ref name="dea1">[http://www.usdoj.gov/dea/pubs/csa/872.htm 21 USC Sec. 872 01/22/02]</ref><ref name="dea2">[http://www.usdoj.gov/dea/pubs/states/newsrel/sanfran032205.html Chemical Supplier Convicted of Diversion of Iodine]</ref>

== See also ==
{{diatomicelements}}
* [[Iodide as an antioxidant]]
* [[Iodised salt]]
* [[Chemical Oxygen Iodine Laser]]

== References ==
<references/>

== External links ==
{{Commons|Iodine}}
{{wiktionary|iodine}}
* [http://www.atsdr.cdc.gov/csem/iodine/ ATSDR - CSEM: Radiation Exposure from Iodine 131] U.S. Department of Health and Human Services (public domain)
* [http://www.chemicalelements.com/elements/i.html ChemicalElements.com - Iodine]
* [http://whqlibdoc.who.int/publications/2004/9241592001.pdf who.int - WHO Global Database on Iodine Deficiency]
* [http://www.iodinenetwork.net/ Network for Sustained Elimination of Iodine Deficiency]
* [http://www.organic-chemistry.org/chemicals/oxidations/iodine.shtm Oxidizing Agents > Iodine]
* [http://periodic.lanl.gov/elements/53.html Los Alamos National Laboratory - Iodine]
* [[21 CFR]] 101.9 (c)(8)(iv) ([http://a257.g.akamaitech.net/7/257/2422/01apr20051500/edocket.access.gpo.gov/cfr_2005/aprqtr/21cfr101.9.htm Text] [http://a257.g.akamaitech.net/7/257/2422/01apr20051500/edocket.access.gpo.gov/cfr_2005/aprqtr/pdf/21cfr101.9.pdf PDF]) &mdash; [[Food and Drug Administration|FDA]] [[nutrition facts label]] information for vitamins and minerals



[[Category:Dietary minerals]]
[[Category:Iodine| ]]
[[Category:Halogens]]
[[Category:DEA List I chemicals]]

[[af:Jodium]]
[[ar:يود]]
[[bn:আয়োডিন]]
[[be:Ёд]]
[[bs:Jod]]
[[bg:Йод]]
[[ca:Iode]]
[[cs:Jód]]
[[co:Iodiu]]
[[da:Jod]]
[[de:Iod]]
[[et:Jood]]
[[el:Ιώδιο]]
[[es:Yodo]]
[[eo:Jodo]]
[[eu:Iodo]]
[[fa:ید]]
[[fr:Iode]]
[[fur:Jodi]]
[[gl:Iodo (elemento)]]
[[ko:아이오딘]]
[[hy:Յոդ]]
[[hr:Jod]]
[[io:Iodo]]
[[id:Yodium]]
[[is:Joð]]
[[it:Iodio]]
[[he:יוד]]
[[sw:Iodini]]
[[ht:Yòd]]
[[la:Iodium]]
[[lv:Jods (elements)]]
[[lb:Iod]]
[[lt:Jodas]]
[[jbo:zirkliru]]
[[hu:Jód]]
[[mk:Јод]]
[[mr:आयोडिन]]
[[nl:Jodium]]
[[ja:ヨウ素]]
[[no:Jod]]
[[nn:Jod]]
[[oc:Iòde]]
[[uz:Yod]]
[[nds:Jod]]
[[pl:Jod]]
[[pt:Iodo]]
[[ro:Iod]]
[[qu:Yudu]]
[[ru:Иод]]
[[sq:Jodi]]
[[scn:Iodiu]]
[[simple:Iodine]]
[[sk:Jód]]
[[sl:Jod]]
[[sr:Јод]]
[[sh:Jod]]
[[fi:Jodi]]
[[sv:Jod]]
[[ta:அயோடின்]]
[[th:ไอโอดีน]]
[[vi:Iốt]]
[[tg:Йод]]
[[tr:İyot]]
[[uk:Йод]]
[[zh-yue:碘]]
[[zh:碘]]

Revision as of 22:07, 21 January 2008

Template:Elementbox header Template:Elementbox series Template:Elementbox groupperiodblock Template:Elementbox appearance img Template:Elementbox atomicmass gpm Template:Elementbox econfig Template:Elementbox epershell Template:Elementbox section physicalprop Template:Elementbox phase Template:Elementbox density gpcm3nrt Template:Elementbox meltingpoint Template:Elementbox boilingpoint Template:Elementbox criticalpoint Template:Elementbox heatfusion kjpmol Template:Elementbox heatvaporiz kjpmol Template:Elementbox heatcapacity jpmolkat25 Template:Elementbox vaporpressure katpa Template:Elementbox section atomicprop Template:Elementbox crystalstruct Template:Elementbox oxistates Template:Elementbox electroneg pauling Template:Elementbox ionizationenergies3 Template:Elementbox atomicradius pm Template:Elementbox atomicradiuscalc pm Template:Elementbox covalentradius pm Template:Elementbox vanderwaalsrad pm Template:Elementbox section miscellaneous Template:Elementbox magnetic Template:Elementbox eresist ohmmat0 Template:Elementbox thermalcond wpmkat300k Template:Elementbox bulkmodulus gpa Template:Elementbox cas number Template:Elementbox isotopes begin Template:Elementbox isotopes stable |- ! style="text-align:right;" | 129I | style="text-align:center;" | syn | style="text-align:right;" | 15.7×106y | β- | style="text-align:right;" | 129Xe |- ! style="text-align:right;" | 131I | style="text-align:center;" | syn | style="text-align:right;" | 8.02070 d | β- | style="text-align:right;" | 131Xe Template:Elementbox isotopes end Template:Elementbox footer Iodine (/ˈaɪədaɪn, ˈaɪədɪn/, or /ˈaɪədiːn/; from Template:Lang-el "violet"), is a chemical element that has the symbol I and atomic number 53. Iodine has 53 protons, 53 electrons, and 74 neutrons. Chemically, iodine is the least reactive of the halogens, and the most electropositive halogen after astatine. Iodine is primarily used in medicine, photography and dyes. It is required in trace amounts by most living organisms.

As with all other halogens (members of Group VII in the Periodic Table), iodine forms diatomic molecules, and hence has the molecular formula of I2.

Properties

Iodine is a dark-gray/purple-brown solid that can be seen subliming at standard temperatures into a purple-pink gas that has an irritating odour. This halogen forms compounds with many elements, but is less reactive than the other members of its Group VII (halogens) and has some metallic-like properties. Iodine dissolves easily in chloroform, carbon tetrachloride. The solubility of elementary iodine in water can be vastly increased by the addition of potassium iodide. The molecular iodine reacts reversibly with the negative ion, creating the triiodide anion, I3, which dissolves well in water. This is also the formulation of medicinal iodine of old. The deep blue color of starch-iodine complexes is produced only by the free element.

Many students who have seen the classroom demonstration where iodine crystals are gently heated in a test tube come away with the impression that liquid iodine does not exist at atmospheric pressure. This misconception arises because the small amount of vapour produced has such a deep colour that the iodine liquid appears not to form. In fact, if iodine crystals are heated carefully to just above their melting point of 113.7 °C, the crystals melt into a liquid, which will be present under a dense blanket of the vapour.

History

Iodine was discovered by Bernard Courtois in 1811. He was born to a manufacturer of saltpeter (a vital part of gunpowder). At the time of the Napoleonic Wars, France was at war and saltpeter was in great demand. Saltpeter produced from French niter beds required sodium carbonate, which could be isolated from seaweed washed up on the coasts of Normandy and Brittany. To isolate the sodium carbonate, seaweed was burned and the ash then washed with water. The remaining waste was destroyed by adding sulfuric acid. One day Courtois added too much sulfuric acid and a cloud of purple vapor rose. Courtois noted that the vapor crystallized on cold surfaces making dark crystals. Courtois suspected that this was a new element but lacked the money to pursue his observations.

However he gave samples to his friends, Charles Bernard Desormes (1777 - 1862) and Nicolas Clément (1779 - 1841), to continue research. He also gave some of the substance to Joseph Louis Gay-Lussac (1778 - 1850), a well-known chemist at that time, and to André-Marie Ampère (1775 - 1836). On 29 November 1813, Dersormes and Clément made public Courtois’ discovery. They described the substance to a meeting of the Imperial Institute of France. On December 6, Gay-Lussac announced that the new substance was either an element or a compound of oxygen. Ampère had given some of his sample to Humphry Davy (1778 - 1829). Davy did some experiments on the substance and noted its similarity to chlorine. Davy sent a letter dated December 10 to the Royal Society of London stating that he had identified a new element. A large argument erupted between Davy and Gay-Lussac over who identified iodine first but both scientists acknowledged Courtois as the first to isolate the chemical element.

Applications

Iodine is used in pharmaceuticals, antiseptics, medicine, food supplements, dyes, catalysts, halogen lights, photography, water purifying, and starch detection.

  • Tincture of iodine (10% elemental iodine in ethanol base) is an essential component of any emergency survival kit, used both to disinfect wounds and to sanitize surface water for drinking (3 drops per litre, let stand for 30 minutes). Alcohol-free iodine solutions such as Lugol's iodine, as well as other iodophor type antiseptics, are also available as effective elemental iodine sources for this purpose.
  • Iodine compounds are important in the field of organic chemistry
  • Iodine, as a heavy element, is quite radio-opaque. Organic compounds of a certain type (typically iodine-substituted benzene derivatives) are thus used in medicine as X-ray radiocontrast agents for intravenous injection. This is often in conjunction with advanced X-ray techniques such as angiography and CT scanning
  • Silver iodide is used in photography.
  • Tungsten iodide is used to stabilize the filaments in light bulbs.

Occurrence on earth

Iodine naturally occurs in the environment chiefly as dissolved iodide in seawater, although it is also found in some minerals and soils. The element may be prepared in an ultrapure form through the reaction of potassium iodide with copper(II) sulfate. There are also a few other methods of isolating this element. Although the element is actually quite rare, kelp and certain other plants have some ability to concentrate iodine, which helps introduce the element into the food chain as well as keeping its cost down.

Sources

File:Iodine.PNG
Iodine output in 2005

Iodine is found in the mineral caliche, found in Chile, between the Andes and the sea. It can also be found in some seaweeds as well as extracted from seawater, however extracting iodine from the mineral is the only economical way to extract the substance.[citation needed]

Extraction from seawater involves electrolysis. The brine is first purified and acidified using sulphuric acid and is then reacted with chlorine. An iodine solution is produced but it is yet too dilute and has to be concentrated. To do this air is blown into the solution which causes the iodine to evaporate, then it is passed into an absorbing tower containing acid where sulfur dioxide is added to reduce the iodine. The solution is then added to chlorine again to concentrate the solution more, and the final solution is at a level of about 99%.[citation needed]

Another source is from kelp. This source was used in the 18th and 19th centuries but is no longer economically viable.

In 2005, Chile was the top producer of iodine with almost two-thirds world share followed by Japan and the USA, reports the British Geological Survey.

Prices

The average price for iodine in 2005 was $7.03 US dollars per kilogram. In 2006 this suddenly rose to $17.03 US dollars per kilogram. In Chile, the world’s largest producer of iodine, prices dramatically changed too (2005 $16.97 US dollars 2006 $20.00 US dollars for one kilogram). The DNSC (Defence National Stockpile Center) claims that in 2005 they sold each kilogram of iodine for $18.36 US dollars and by 2006 they reported that each kilogram yielded $21.29. [1]

Descriptive chemistry

Elemental iodine is poorly soluble in water, with one gram dissolving in 3450 ml at 20 °C and 1280 ml at 50 °C. By contrast with chlorine, the formation of the hypohalite ion (IO) in neutral aqueous solutions of iodine is negligible.

I2+ H2O ↔ H+ + I + HIO   (K = 2.0×10-13) [2]

Solubility in water is greatly improved if the solution contains dissolved iodides such as hydroiodic acid, potassium iodide, or sodium iodide. Dissolved bromides also improve water solubility of iodine. Iodine is soluble in a number of organic solvents, including ethanol (20.5 g/100 ml at 15 °C, 21.43 g/100 ml at 25 °C), diethyl ether (20.6 g/100 ml at 17 °C, 25.20 g/100 ml at 25 °C), chloroform, acetic acid, glycerol, benzene (14.09 g/100 ml at 25 °C), carbon tetrachloride (2.603 g/100 ml at 35 °C), and carbon disulfide (16.47 g/100 ml at 25 °C)[3]. Aqueous and ethanol solutions are brown. Solutions in chloroform, carbon tetrachloride, and carbon disulfide are violet.

Elemental iodine can be prepared by oxidizing iodides with chlorine:

2I + Cl2 → I2 + 2Cl

or with manganese dioxide in acid solution:[2]

2I + 4H+ + MnO2 → I2 + 2H2O + Mn2+

Iodine is reduced to hydroiodic acid by hydrogen sulfide:[4]

I2 + H2S → 2HI + S↓

or by hydrazine:

2I2 + N2H4 → 4HI + N2

Iodine is oxidized to iodate by nitric acid:[5]

I2 + 10HNO3 → 2HIO3 + 10NO2 + 4H2O

or by chlorates:[5]

I2 + 2ClO3 → 2IO3 + Cl2

Iodine is converted in a two stage reaction to iodide and iodate in solutions of alkali hydroxides (such as sodium hydroxide):[2]

I2 + 2OH → I + IO + H2O (K = 30)
3IO → 2I + IO3 (K = 1020)

Notable inorganic iodine compounds

See also iodine compounds

Stable iodine in biology

Iodine is an essential trace element; its only known roles in biology are as constituents of the thyroid hormones, thyroxine (T4) and triiodothyronine (T3). These are made from addition condensation products of the amino acid tyrosine, and are stored prior to release in a protein-like molecule called thryroglobulin. T4 and T3 contain four and three atoms of iodine per molecule, respectively. The thyroid gland actively absorbs iodide from the blood to make and release these hormones into the blood, actions which are regulated by a second hormone TSH from the pituitary. Thyroid hormones are phylogenetically very old molecules which are synthesized by most multicellular organisms, and which even have some effect on unicellular organisms.

Thyroid hormones play a very basic role in biology, acting on gene transcription to regulate the basal metabolic rate. The total deficiency of thyroid hormones can reduce basal metabolic rate up to 50%, while in excessive production of thyroid hormones the basal metabolic rate can be increased by 100%. T4 acts largely as a precursor to T3, which is (with some minor exceptions) the biologically active hormone.

Human dietary intake

The United States Food and Drug Administration recommends 150 micrograms of iodine per day for both men and women.[6] This is necessary for proper production of thyroid hormone.[citation needed] Natural sources of iodine include sea life, such as kelp and certain seafood, as well as plants grown on iodine-rich soil.[citation needed] Salt for human consumption is often fortified with iodine and is referred to as iodized salt.

Iodine deficiency

In areas where there is little iodine in the diet—typically remote inland areas and semi-arid equatorial climates where no marine foods are eaten—iodine deficiency gives rise to hypothyroidism, symptoms of which are extreme fatigue, goitre, mental slowing, depression, weight gain, and low basal body temperatures.[citation needed]

Iodine deficiency is also the leading cause of preventable mental retardation, an effect which happens primarily when babies and small children are made hypothyroid by lack of the element. The addition of iodine to table salt has largely eliminated this problem in the wealthier nations, but iodine deficiency remains a serious public health problem in the developing world.[citation needed]

Radioiodine and biology

Radioiodine and the thyroid

The artificial radioisotope 131I (a beta emitter), also known as radioiodine which has a half-life of 8.0207 days, has been used in treating cancer and other pathologies of the thyroid glands. 123I is the radioisotope most often used in nuclear imaging of the kidney and thyroid as well as thyroid uptake scans (used for the evaluation of Graves' Disease). The most common compounds of iodine are the iodides of sodium and potassium (KI) and the iodates (KIO3).

129I (half-life 15.7 million years) is a product of 130Xe spallation in the atmosphere and uranium and plutonium fission, both in subsurface rocks and nuclear reactors. Nuclear processes, in particular nuclear fuel reprocessing and atmospheric nuclear weapons tests have now swamped the natural signal for this isotope. 129I was used in rainwater studies following the Chernobyl accident. It also has been used as a ground-water tracer and as an indicator of nuclear waste dispersion into the natural environment.

If humans are exposed to radioactive iodine, the thyroid gland will absorb it as if it were non-radioactive iodine, leading to elevated chances of thyroid cancer. Isotopes with shorter half-lives such as 131I present a greater risk than those with longer half-lives since they generate more radiation per unit of time. Taking large amounts of regular iodine will saturate the thyroid and prevent uptake. Iodine pills are sometimes distributed to persons living close to nuclear establishments, for use in case of accidents that could lead to releases of radioactive iodine.

  • Iodine-123 and iodine-125 are used in medicine as tracers for imaging and evaluating the function of the thyroid.
  • Iodine-131 is used in medicine for treatment of thyroid cancer and Graves' Disease.
  • Uncombined (elemental) iodine is mildly toxic to all living things.
  • Potassium iodide (KI tablets, or "SSKI" = "Saturated Solution of KI" liquid drops) can be given to people in a nuclear disaster area when fission has taken place, to flush out the radioactive iodine-131 fission product. The half-life of iodine-131 is only eight days, so the treatment would need to continue only a couple of weeks. In cases of leakage of certain nuclear materials without fission, or certain types of dirty bomb made with other than radioiodine, this precaution would be of no avail.

Radioiodine and the kidney

In the 1970s imaging techniques were developed in California to utilize radioiodine in diagnostics for renal hypertension.

Isotopes

There are 37 isotopes of iodine and only one, 127I, is stable.

In many ways, 129I is similar to 36Cl. It is a soluble halogen, fairly non-reactive, exists mainly as a non-sorbing anion, and is produced by cosmogenic, thermonuclear, and in-situ reactions. In hydrologic studies, 129I concentrations are usually reported as the ratio of 129I to total I (which is virtually all 127I). As is the case with 36Cl/Cl, 129I/I ratios in nature are quite small, 10−14 to 10−10 (peak thermonuclear 129I/I during the 1960s and 1970s reached about 10−7). 129I differs from 36Cl in that its half-life is longer (15.7 vs. 0.301 million years), it is highly biophilic, and occurs in multiple ionic forms (commonly, I and IO3) which have different chemical behaviors. This makes it fairly easy for 129I to enter the biosphere as it becomes incorporated into vegetation, soil, milk, animal tissue, etc.

Excesses of stable 129Xe in meteorites have been shown to result from decay of "primordial" 129I produced newly by the supernovas which created the dust and gas from which the solar system formed. 129I was the first extinct radionuclide to be identified as present in the early solar system. Its decay is the basis of the I-Xe radiometric dating scheme, which covers the first 83 million years of solar system evolution.

Effects of various radioiodine isotopes in biology are discussed below.

Toxicity of iodine

Excess iodine has symptoms similar to those of iodine deficiency. Commonly encountered symptoms are abnormal growth of the thyroid gland and disorders in functioning and growth of the organism as a whole. Elemental iodine, I2, is a deadly poison if taken in larger amounts; if 2-3 grams of it is consumed, it is fatal to humans. Iodides are similar in toxicity to bromides.

Precautions for stable iodine

Direct contact with skin can cause lesions, so it should be handled with care. Iodine vapor is very irritating to the eye and to mucous membranes. Concentration of iodine in the air should not exceed 1 mg/ (eight-hour time-weighted average). When mixed with ammonia, it can form nitrogen triiodide which is extremely sensitive and can explode unexpectedly.

Clandestine use

In the United States, the Drug Enforcement Agency (DEA) regards iodine and compounds containing iodine (ionic iodides, iodoform, ethyl iodide, and so on) as reagents useful for the clandestine manufacture of methamphetamine. Persons who attempt to purchase significant quantities of such chemicals without establishing a legitimate use are likely to find themselves the target of a DEA investigation. Persons selling such compounds without doing due diligence to establish that the materials are not being diverted to clandestine use may be subject to stiff penalties, such as expensive fines or even imprisonment.[7][8]

See also

References

  1. ^ DNSC, 2006
  2. ^ a b c Advanced Inorganic Chemistry by Cotton and Wilkinson, 2nd ed.
  3. ^ Merck Index of Chemicals and Drugs, 9th ed.
  4. ^ General Chemistry (volume 2) by N.L. Glinka, Mir Publishing 1981
  5. ^ a b General Chemistry by Linus Pauling, 1947 ed.
  6. ^ 21 CFR 101.9 (c)(8)(iv)
  7. ^ 21 USC Sec. 872 01/22/02
  8. ^ Chemical Supplier Convicted of Diversion of Iodine