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{{Short description|Nuclides with atomic number of 90 but with different mass numbers}}
{{Actinidesvsfissionproducts}}
{{Infobox thorium isotopes}}


Although '''[[thorium]]''' ('''Th'''), with atomic number 90, has 6 naturally occurring '''[[isotope]]s''', none of these isotopes are stable; however, one isotope, <sup>232</sup>Th, is ''relatively'' stable, with a half-life of 14.05 billion years, considerably longer than the [[age of the earth]], and even slightly longer than the generally accepted [[age of the universe]]. This isotope makes up nearly all natural thorium. As such, thorium is considered to be [[mononuclidic elements|mononuclidic]]. It has a characteristic terrestrial isotopic composition and thus an atomic mass can be given.
[[Thorium]] (<sub>90</sub>Th) has seven naturally occurring [[isotope]]s but none are stable. One isotope, [[thorium-232|<sup>232</sup>Th]], is ''relatively'' stable, with a half-life of 1.405×10<sup>10</sup> years, considerably longer than the [[age of the Earth]], and even slightly longer than the generally accepted [[age of the universe]]. This isotope makes up nearly all natural thorium, so thorium was considered to be [[mononuclidic elements|mononuclidic]]. However, in 2013, [[International Union of Pure and Applied Chemistry|IUPAC]] reclassified thorium as binuclidic, due to large amounts of <sup>230</sup>Th in deep seawater. Thorium has a characteristic terrestrial isotopic composition and thus a standard atomic weight can be given.
Standard atomic mass: 232.03806(2)&nbsp;[[atomic mass unit|u]].

Thirty [[radioisotope]]s have been characterized, with the most stable (after <sup>232</sup>Th) being <sup>230</sup>Th with a half-life of 75,380 years, <sup>229</sup>Th with a half-life of 7,340 years, and <sup>228</sup>Th with a half-life of 1.92 years. All of the remaining [[radioactive]] isotopes have half-lives that are less than thirty days and the majority of these have half-lives that are less than ten minutes. One isotope, <sup>229</sup>Th, has a [[nuclear isomer]] (or metastable state) with a remarkably low excitation energy,<ref name=Ruchowska>{{cite journal|author=E. Ruchowska|title=Nuclear structure of <sup>229</sup>Th |journal=Phys. Rev. C|volume= 73|pages=044326|year=2006 |doi=10.1103/PhysRevC.73.044326|issue=4 |bibcode = 2006PhRvC..73d4326R}}</ref> recently measured to be 7.6 ± 0.5&nbsp;eV.<ref name=Beck>{{cite journal|author=B. R. Beck|title=Energy splitting in the ground state doublet in the nucleus <sup>229</sup>Th |journal=[[Physical Review Letters]]|volume= 98|pages=142501|date=2007-04-06 |doi=10.1103/PhysRevLett.98.142501 |pmid=17501268 |bibcode=2007PhRvL..98n2501B|issue=14|display-authors=etal}}</ref>

The known isotopes of thorium range in [[mass number]] from 209<ref name=Ikezoe>{{cite journal|author=H. Ikezoe|title=alpha decay of a new isotope of <sup>209</sup>Th |year=1996| journal=[[Physical Review C]]| volume=54| issue=4| page=2043|doi=10.1103/PhysRevC.54.2043 |bibcode = 1996PhRvC..54.2043I |display-authors=etal}}</ref> to 238.

== Some notable isotopes ==

=== Thorium-228 ===
'''<sup>228</sup>Th''' is an [[isotope]] of [[thorium]] with 138 [[neutrons]]. It was once named Radiothorium, due to its occurrence in the [[disintegration chain]] of thorium-232. It has a [[half-life]] of 1.9116 years. It undergoes [[alpha decay]] to [[isotopes of radium|<sup>224</sup>Ra]]. Occasionally it decays by the unusual route of [[cluster decay]], emitting a nucleus of [[isotopes of oxygen|<sup>20</sup>O]] and producing stable [[isotopes of lead|<sup>208</sup>Pb]]. It is a daughter isotope of [[isotopes of uranium#Uranium-232|<sup>232</sup>U]].

Th-228 has an atomic weight of 228.0287411&nbsp;grams/mole. [[Uranium-232]] decays to this nuclide by alpha emission.

===Thorium-229===
'''<sup>229</sup>Th''' is a [[radioactive]] [[isotope]] of [[thorium]] that decays by [[alpha particle|alpha]] emission with a [[half-life]] of 7340 years.
<sup>229</sup>Th is produced by the decay of [[uranium-233]], and its principal use is for the production of the [[nuclear medicine|medical isotopes]] [[actinium-225]] and [[bismuth-213]].<ref>[http://www.ne.doe.gov/pdfFiles/U233RptConMarch2001.pdf Report to Congress on the extraction of medical isotopes from U-233]. U.S. Department of Energy. March 2001</ref>


Thirty-one [[radioisotope]]s have been characterized, with the most stable being <sup>232</sup>Th, <sup>230</sup>Th with a half-life of 75,380 years, <sup>229</sup>Th with a half-life of 7,917 years,<ref name="Varga14" /> and <sup>228</sup>Th with a half-life of 1.92 years. All of the remaining [[radioactive]] isotopes have half-lives that are less than thirty days and the majority of these have half-lives that are less than ten minutes. One isotope, <sup>229</sup>Th, has a [[nuclear isomer]] (or metastable state) with a remarkably low excitation energy,<ref name="Ruchowska">{{cite journal |author=E. Ruchowska|title=Nuclear structure of <sup>229</sup>Th |journal=[[Physical Review C]]|volume=73 |issue=4 |pages=044326 |year=2006 |doi=10.1103/PhysRevC.73.044326 |bibcode = 2006PhRvC..73d4326R |hdl=10261/12130 |hdl-access=free |url=https://cds.cern.ch/record/974608/files/PhysRevC.73.044326.pdf }}</ref> recently measured to be {{val|8.35574|u=eV}}{{^|Uncertainty omitted in lead for conciseness}}<ref name=Tiedau2024/> It has been proposed to perform laser spectroscopy of the <sup>229</sup>Th nucleus and use the low-energy transition for the development of a [[nuclear clock]] of extremely high accuracy.<ref name=PR-Tiedau2024/><ref name="Peik2003">{{cite journal
====Thorium-229m====
| first1 = E.
[[Gamma ray spectroscopy]] has indicated that <sup>229</sup>Th has a [[nuclear isomer]] <sup>229''m''</sup>Th with a remarkably low excitation energy. This would make it the lowest-energy nuclear isomer known, and it might be possible to excite this nuclear state using [[laser]]s with wavelengths in the [[vacuum ultraviolet]]. The isomer might have application for high density energy storage,<ref>
| last1 = Peik
{{cite conference
| first2 = Chr.
| last1=Poppe |first1=C. H. |last2=Weiss |first2=M. S. |last3=Anderson |first3=J. D.
| last2 = Tamm
| title = Nuclear isomers as ultra-high-energy-density materials
| booktitle = Air Force Meeting on High Energy Density Materials, Lancaster, CA
| year = 1992
| bibcode = 1992hedm.meet...23P
}}</ref> an accurate clock,<ref>{{cite journal
| first1=E. |last1=Peik
| first2=Chr. |last2=Tamm
| title = Nuclear laser spectroscopy of the 3.5&nbsp;eV transition in <sup>229</sup>Th
| title = Nuclear laser spectroscopy of the 3.5&nbsp;eV transition in <sup>229</sup>Th
| url = https://www.few.vu.nl/~wimu/Varying-Constants-Papers/Th-229-Peik-Tamm-EuLett-2003.pdf
| url = http://www.ptb.de/cms/fileadmin/internet/fachabteilungen/abteilung_4/4.4_zeit_und_frequenz/pdf/th001.pdf
| journal = Europhysics Letters
| journal = Europhysics Letters
| volume = 61
| volume = 61
Line 39: Line 18:
| doi = 10.1209/epl/i2003-00210-x
| doi = 10.1209/epl/i2003-00210-x
| bibcode = 2003EL.....61..181P
| bibcode = 2003EL.....61..181P
| s2cid = 250818523
| accessdate = 2013-12-14
| access-date = 2024-04-30
}}</ref> as a [[qubit]] for [[quantum computing]], or to test the effect of the chemical environment on nuclear decay rates.<ref name=Tkalya>{{cite journal
| archive-url = https://web.archive.org/web/20240414032917/http://www.few.vu.nl/~wimu/Varying-Constants-Papers/Th-229-Peik-Tamm-EuLett-2003.pdf
| last1=Tkalya |first1=Eugene V. |last2=Zherikhin |first2=Alexander N. |last3=Zhudov |first3=Valerii I.
| archive-date = 2024-04-14
| title = Decay of the low-energy nuclear isomer <sup>229</sup>Th<sup>''m''</sup> (3/2<sup>+</sup>, 3.5±1.0&nbsp;eV) in solids (dielectrics and metals): A new scheme of experimental research
| url-status = live
| journal = [[Physical Review C]]
}}</ref><ref name="Campbell2012">{{cite journal
| volume = 61
| first1=C.J. |last1=Campbell
| issue = 6
| first2=A.G. |last2=Radnaev
| year = 2000
| first3=A. |last3=Kuzmich
| pages = 064308
| first4=V.A. |last4=Dzuba
| doi = 10.1103/PhysRevC.61.064308
| first5=V.V. |last5=Flambaum
| bibcode = 2000PhRvC..61f4308T }}</ref>
| first6=A. |last6=Derevianko
| title = A single ion nuclear clock for metrology at the 19th decimal place
| journal = [[Physical Review Letters]]
| volume = 108 | issue = 12 | article-number = 120802
| date = 2012
|page=120802
| doi = 10.1103/PhysRevLett.108.120802
| pmid = 22540568
| arxiv = 1110.2490
| bibcode = 2012PhRvL.108l0802C
| s2cid = 40863227
| url = https://sites.lsa.umich.edu/kuzmich-lab/wp-content/uploads/sites/90/2014/05/229ThClock.pdf
| access-date=2024-04-30
}}</ref>


The known isotopes of thorium range in [[mass number]] from 207<ref name="Yang207"/> to 238.
The lifetime of the isomer has been measured to be 6±1&nbsp;hours. The measurement was done by collecting recoiled <sup>229m</sup>Th atoms in a MgF<sub>s</sub> crystal and measuring the light emission variation over time.<ref name="Zhao2012">{{cite journal|last=Zhao|first=Xinxin|coauthors=Yenny Natali Martinez de Escobar, Robert Rundberg, Evelyn M. Bond, Allen Moody, David J. Vieira|year=2012|title=Observation of the Deexcitation of the ^{229m}Th Nuclear Isomer|journal=Physical Review Letters|volume=109|issue=16|issn=0031-9007|doi=10.1103/PhysRevLett.109.160801}}</ref> If this isomer were to decay it would produce a [[gamma ray]] (defined by its origin, not its wavelength) in the ultraviolet range.


== List of isotopes ==
The isomer transition energy of <sup>229</sup>Th is currently derived from indirect measurements of the gamma-ray spectrum resulting from the decay of <sup>233</sup>U. In 1989–1993 first measurements were performed using high-quality germanium detectors, resulting in an estimate of E = 3.5±1.0&nbsp;eV for the <sup>229</sup>Th isomer transition energy.<ref name=Helmer1990>
{{Isotopes table
{{cite journal
|symbol=Th
| title = Energy separation of the doublet of intrinsic states at the ground state of <sup>229</sup>Th
|refs=<!-- not NUBASE2016 yet (2019-07-14) -->
| author = Reich, C. W. and Helmer, R. G.
|notes=m, histname, unc(), mass#, hl-nst, spin(), spin#, EC, CD, IT, daughter-st
| journal = Phys. Rev. Lett.
| volume = 64
| issue = 3
| pages = 271–273
|date=Jan 1990
| doi = 10.1103/PhysRevLett.64.271
| url = http://link.aps.org/doi/10.1103/PhysRevLett.64.271
| publisher = American Physical Society
|bibcode = 1990PhRvL..64..271R }}
</ref><ref name=Helmer1994>
{{cite journal
| journal=[[Physical Review C]]
| volume=49 | pages=1845–1858
| year=1994
| author=Helmer, R. G.; Reich, C. W.
| title = An Excited State of Th-229 at 3.5&nbsp;eV
| doi=10.1103/PhysRevC.49.1845
| issue=4
|bibcode = 1994PhRvC..49.1845H }}
</ref> This unnaturally low value triggered a multitude of investigations, both theoretical and experimental, trying to determine the transition energy precisely and to specify other properties of the isomer state of <sup>229</sup>Th (such as the lifetime and the magnetic moment). However, searches for direct photon emission from the low-lying excited state have failed to report an unambiguous signal. New indirect measurements with an advanced high-resolution x-ray microcalorimeter were carried out in 2007<ref name=Beck/> yielding a new value for the transition energy of E = 7.6±0.5&nbsp;eV, corrected to E = 7.8±0.5&nbsp;eV in 2009.<ref name=BeckReview>
{{cite conference
| title = Improved value for the energy splitting of the ground-state doublet in the nucleus <sup>229</sup>Th
| author = Beck B R, Wu C Y, Beiersdorfer P, Brown G V, Becker J A, Moody K J, Wilhelmy J B, Porter F S, Kilbourne C A and Kelley R L
| date = 2009-07-30
| conference = 12th Int. Conf. on Nuclear Reaction Mechanisms (Varenna, Italy)
| id = LLNL-PROC-415170
| url = https://e-reports-ext.llnl.gov/pdf/375773.pdf
}}
}}
</ref> This value is currently the most accepted one in the community but cannot be considered definite until a direct measurement is made successfully. The shift into the VUV domain probably explains why previous attempts to directly observe the transition were unsuccessful.

===Thorium-230===
'''<sup>230</sup>Th''' is a [[radioactive]] [[isotope]] of [[thorium]] that can be used to date [[coral]]s and determine [[ocean current]] flux. '''Ionium''' was a name given early in the study of radioactive elements to the <sup>230</sup>Th [[isotope]] produced in the [[decay chain]] of [[Uranium-238|<sup>238</sup>U]] before it was realized that ionium and [[thorium]] are chemically identical. The symbol '''Io''' was used for this supposed element. (The name is still used in [[ionium-thorium dating]].)

===Thorium-231===
'''<sup>231</sup>Th''' has 141 [[neutrons]]. It is the decay product of [[uranium-235]]. It is found in very small amounts on the [[earth]] and has a [[half-life]] of 25.5 hours. When it decays it emits a [[beta ray]] and forms [[protactinium-231]]. It has a decay energy of 0.39&nbsp;MeV. It has a mass of 231.0363043&nbsp;grams/mole.

===Thorium-232===
''As Thorium is [[Mononuclidic elements|mononuclidic]], the [[Thorium|main article on thorium]] effectively discusses this isotope.''

'''<sup>232</sup>Th''' is the only [[primordial isotope]] of [[thorium]] and makes up effectively all of natural thorium, with other isotopes of thorium appearing only in trace amounts as relatively short-lived [[decay product]]s of [[uranium]] and thorium.<ref>{{cite web |url=http://ie.lbl.gov/education/parent/Th_iso.htm |title=Isotopes of Thorium (Z=90) |author=Isotopes Project Home Page, [[Lawrence Berkeley National Laboratory]] |accessdate=2010-01-18}}</ref>

<sup>232</sup>Th decays by [[alpha decay]] with a [[half-life]] of 1.405{{E|10}} years, over three times the [[age of the earth]] and more than the [[age of the universe]]. Its [[decay chain]] is the [[thorium series]] eventually ending in [[lead-208]]. The remainder of the chain is quick; the longest half-lives in it are 5.75 years for [[radium-228]] and 1.91 years for [[thorium-228]], with all other half-lives totaling less than 5 days.<ref>{{cite web |url=http://hepwww.rl.ac.uk/ukdmc/Radioactivity/Th_chain/Th_chain.html |title=Th-232 Decay Chain |author=[[Rutherford Appleton Laboratory]] |accessdate=2010-01-25}}</ref>

<sup>232</sup>Th is a [[fertile material]] able to [[neutron capture|absorb]] a [[neutron]] and undergo [[Nuclear transmutation|transmutation]] into the [[fissile]] [[nuclide]] [[uranium-233]], which is the basis of the [[thorium fuel cycle]].<ref>{{cite web |url=http://www.world-nuclear.org/info/inf62.html |title=Thorium |author=[[World Nuclear Association]] |accessdate=2010-01-25}}</ref>

In the form of [[Thorotrast]], a [[thorium dioxide]] [[suspension (chemistry)|suspension]], it was used as [[contrast medium]] in early [[X-ray]] diagnostics. Thorium-232 is now classified as [[carcinogen]]ic.<ref>{{cite journal |last1= Krasinskas |first1= Alyssa M |last2= Minda |first2= Justina |last3= Saul |first3= Scott H |last4= Shaked |first4= Abraham |last5= Furth |first5= Emma E |title=Redistribution of thorotrast into a liver allograft several years following transplantation: a case report |journal= [[Nature (journal)|Nature]] |volume= 17 |pages= 117–120 |year= 2004 |doi= 10.1038/modpathol.3800008 |pmid=14631374 |issue=1}}</ref>

===Thorium-233===
'''<sup>233</sup>Th''' is an isotope of [[thorium]] that decays into [[protactinium-233]] through beta decay. It has a half-life of 21.83 minutes.<ref name="NUBASE">{{cite journal| first = Audi| last = Georges|title = The NUBASE Evaluation of Nuclear and Decay Properties| journal = Nuclear Physics A| volume = 729| pages = 3–128| publisher = Atomic Mass Data Center| year = 2003| doi=10.1016/j.nuclphysa.2003.11.001| bibcode=2003NuPhA.729....3A}}</ref>

===Thorium-234===
'''<sup>234</sup>Th''' is an [[isotope]] of [[thorium]] whose [[Atomic nucleus|nuclei]] contain 144 [[neutron]]s. Th-234 has a [[half-life]] of 24.1 days, and when it decays, it emits a [[beta particle]], and in so doing, it [[Nuclear transmutation|transmutes]] into [[protactinium]]-234. Th-234 has a mass of 234.0436 [[atomic mass unit]]s (amu), and it has a decay energy of about 270&nbsp;keV (kilo[[electron-volt]]s). [[Uranium]]-238 usually decays into this isotope of thorium. (It can undergo [[spontaneous fission]].)

== Table ==
{| class="wikitable" style="font-size:95%; white-space:nowrap"
! rowspan="2" | nuclide<br />symbol
! rowspan="2" | historic<br>name
! Z([[proton|p]])
! N([[neutron|n]])
! &nbsp;<br />isotopic mass (u)<br />&nbsp;
! rowspan="2" | half-life<ref group="n">Bold for nuclides with half-lives longer than the age of the universe (nearly stable)</ref>
! rowspan="2" | decay<br>mode(s)<ref>{{cite web |url=http://www.nucleonica.net/unc.aspx |title=Universal Nuclide Chart |publisher=nucleonica |registration=yes}}</ref><ref group="n">Abbreviations:<br>CD: [[Cluster decay]]<br>EC: [[Electron capture]]<br>IT: [[Isomeric transition]]<br>SF: [[Spontaneous fission]]</ref>
! rowspan="2" | daughter<br>isotope(s)<ref group="n">Bold for stable isotopes</ref>
! rowspan="2" | nuclear<br />spin
! rowspan="2" | representative<br />isotopic<br />composition<br />(mole fraction)
! rowspan="2" | range of natural<br />variation<br />(mole fraction)
|-
|-
| <sup>207</sup>Th<ref name="Yang207">{{cite journal |title=New isotope <sup>207</sup>Th and odd-even staggering in α-decay energies for nuclei with ''Z''&nbsp;>&nbsp;82 and ''N''&nbsp;<&nbsp;126 |last=Yang |first=H. B. |display-authors=et al. |journal=Physical Review C |year=2022 |volume=105 |number=L051302 |doi=10.1103/PhysRevC.105.L051302|bibcode=2022PhRvC.105e1302Y |s2cid=248935764 }}</ref>
! colspan="3" | excitation energy
|
| style="text-align:right" | 90
| style="text-align:right" | 117
|
| 9.7(+46.6−4.4) ms
| [[alpha decay|α]]
| <sup>203</sup>Ra
|
|
|
|-
| <sup>208</sup>Th<ref name="Cardona">{{cite web|url=https://tel.archives-ouvertes.fr/tel-01139498/document|last=Cardona|first=J.A.H.|title=Production and decay properties of neutron deficient isotopes with N < 126 and 74 ≤ Z ≤ 92 at SHIP |date=2012 |publisher=Goethe Universität Frankfury Allemagne}}</ref>
|
| style="text-align:right" | 90
| style="text-align:right" | 118
| 208.01791(4)
| 1.7(+1.7-0.6) ms
| α
| <sup>204</sup>Ra
| 0+
|
|
|-
|-
| <sup>209</sup>Th<ref name="Ikezoe">{{cite journal|author=H. Ikezoe|title=alpha decay of a new isotope of <sup>209</sup>Th |year=1996| journal=[[Physical Review C]]| volume=54| issue=4|pages=2043–2046 |doi=10.1103/PhysRevC.54.2043 |pmid=9971554 |bibcode = 1996PhRvC..54.2043I |display-authors=etal}}</ref>
| <sup>209</sup>Th
|
|
| style="text-align:right" | 90
| style="text-align:right" | 90
Line 132: Line 83:
| 209.01772(11)
| 209.01772(11)
| 7(5)&nbsp;ms<br>[3.8(+69−15)]
| 7(5)&nbsp;ms<br>[3.8(+69−15)]
|
| α
| <sup>205</sup>Ra
|
| 5/2−#
| 5/2−#
|
|
Line 144: Line 95:
| rowspan=2|210.015075(27)
| rowspan=2|210.015075(27)
| rowspan=2|17(11)&nbsp;ms<br>[9(+17−4)&nbsp;ms]
| rowspan=2|17(11)&nbsp;ms<br>[9(+17−4)&nbsp;ms]
| α
| [[alpha decay|α]]
| <sup>206</sup>Ra
| <sup>206</sup>Ra
| rowspan=2|0+
| rowspan=2|0+
Line 240: Line 191:
|
|
| colspan="3" style="text-indent:2em" | 2042(13)&nbsp;keV
| colspan="3" style="text-indent:2em" | 2042(13)&nbsp;keV
| 137(4)&nbsp;µs
| 137(4)&nbsp;μs
|
|
|
|
Line 262: Line 213:
| style="text-align:right" | 127
| style="text-align:right" | 127
| 217.013114(22)
| 217.013114(22)
| 240(5)&nbsp;µs
| 240(5)&nbsp;μs
| α
| α
| <sup>213</sup>Ra
| <sup>213</sup>Ra
Line 281: Line 232:
|
|
|-
|-
| rowspan=2|<sup>219</sup>Th
| <sup>219</sup>Th
|
| rowspan=2|
| rowspan=2 style="text-align:right" | 90
| style="text-align:right" | 90
| rowspan=2 style="text-align:right" | 129
| style="text-align:right" | 129
| rowspan=2|219.01554(5)
| 219.01554(5)
| rowspan=2|1.05(3)&nbsp;µs
| 1.05(3)&nbsp;μs
| α{{refn|group=n|Theoretically capable of β<sup>+</sup> decay to <sup>219</sup>Ac{{NUBASE2020|ref}}}}
| α
| <sup>215</sup>Ra
| <sup>215</sup>Ra
| rowspan=2|9/2+#
| 9/2+#
|
| rowspan=2|
|
| rowspan=2|
|-
|-
| β<sup>+</sup> (10<sup>−7</sup>%)
| <sup>220</sup>Th
|
| <sup>219</sup>Ac
| style="text-align:right" | 90
|-
| style="text-align:right" | 130
| rowspan=2|<sup>220</sup>Th
| 220.015748(24)
| rowspan=2|
| 9.7(6)&nbsp;μs
| rowspan=2 style="text-align:right" | 90
| α{{refn|group=n|Theoretically capable of electron capture to <sup>220</sup>Ac{{NUBASE2020|ref}}}}
| rowspan=2 style="text-align:right" | 130
| rowspan=2|220.015748(24)
| rowspan=2|9.7(6)&nbsp;µs
| α
| <sup>216</sup>Ra
| <sup>216</sup>Ra
| rowspan=2|0+
| 0+
|
| rowspan=2|
|
| rowspan=2|
|-
| [[Electron capture|EC]] (2&times;10<sup>−7</sup>%)
| <sup>220</sup>Ac
|-
|-
| <sup>221</sup>Th
| <sup>221</sup>Th
Line 323: Line 268:
|
|
|-
|-
| rowspan=2|<sup>222</sup>Th
| <sup>222</sup>Th
|
| rowspan=2|
| rowspan=2 style="text-align:right" | 90
| style="text-align:right" | 90
| rowspan=2 style="text-align:right" | 132
| style="text-align:right" | 132
| rowspan=2|222.018468(13)
| 222.018468(13)
| rowspan=2|2.237(13)&nbsp;ms
| 2.237(13)&nbsp;ms
| α{{refn|group=n|Theoretically capable of electron capture to <sup>222</sup>Ac{{NUBASE2020|ref}}}}
| α
| <sup>218</sup>Ra
| <sup>218</sup>Ra
| rowspan=2|0+
| 0+
|
| rowspan=2|
|
| rowspan=2|
|-
| EC (1.3&times;10<sup>−8</sup>%)
| <sup>222</sup>Ac
|-
|-
| <sup>223</sup>Th
| <sup>223</sup>Th
Line 362: Line 304:
| rowspan=2|
| rowspan=2|
|-
|-
| β<sup>+</sup>β<sup>+</sup> (rare)
| CD (rare)
| <sup>224</sup>Ra
| '''<sup>208</sup>Pb'''<br>'''<sup>16</sup>O'''
|-
|-
| rowspan=2|<sup>225</sup>Th
| rowspan=2|<sup>225</sup>Th
Line 377: Line 319:
| rowspan=2|
| rowspan=2|
|-
|-
| EC (10%)
| [[Electron capture|EC]] (10%)
| <sup>225</sup>Ac
| <sup>225</sup>Ac
|-
|-
Line 413: Line 355:
| <sup>224</sup>Ra
| <sup>224</sup>Ra
| rowspan=2|0+
| rowspan=2|0+
| rowspan=2|Trace<ref group="n">Intermediate decay product of <sup>232</sup>Th</ref>
| rowspan=2|Trace<ref group="n">Intermediate decay product of [[thorium-232|<sup>232</sup>Th]]</ref>
| rowspan=2|
| rowspan=2|
|-
|-
| [[Cluster decay|CD]] (1.3&times;10<sup>−11</sup>%)
| [[Cluster decay|CD]] (1.3×10<sup>−11</sup>%)
| '''<sup>208</sup>Pb'''<br><sup>20</sup>O
| '''<sup>208</sup>Pb'''<br><sup>20</sup>O
|-
|-
Line 424: Line 366:
| style="text-align:right" | 139
| style="text-align:right" | 139
| 229.031762(3)
| 229.031762(3)
| 7.34(16)&times;10<sup>3</sup>&nbsp;y
| 7.916(17)×10<sup>3</sup>&nbsp;y
| α
| α
| <sup>225</sup>Ra
| <sup>225</sup>Ra
| 5/2+
| 5/2+
| Trace<ref group=n>Intermediate decay product of [[neptunium-237|<sup>237</sup>Np]]</ref>
|
|
|
|-
|-
| style="text-indent:1em" | <sup>229m</sup>Th
| style="text-indent:1em" | <sup>229m</sup>Th
|
|
| colspan="3" style="text-indent:2em" | 0.0076(5)&nbsp;keV
| colspan="3" style="text-indent:2em" | 8.355733(10) eV<ref name=Elwell2024 />
| 70(50)&nbsp;h
| 7(1)&nbsp;μs<ref name="Seiferle2017" />
| [[Isomeric transition|IT]]
| [[Isomeric transition|IT]]
| <sup>229</sup>Th
| <sup>229</sup>Th
Line 441: Line 383:
|
|
|-
|-
| rowspan=3|<sup>230</sup>Th<ref group="n">Used in [[Uranium-thorium dating]]</ref>
| rowspan=3|<sup>230</sup>Th<ref group="n">Used in [[Uranium–thorium dating]]</ref>
| rowspan=3|Ionium
| rowspan=3|Ionium
| rowspan=3 style="text-align:right" | 90
| rowspan=3 style="text-align:right" | 90
| rowspan=3 style="text-align:right" | 140
| rowspan=3 style="text-align:right" | 140
| rowspan=3|230.0331338(19)
| rowspan=3|230.0331338(19)
| rowspan=3|7.538(30)&times;10<sup>4</sup>&nbsp;y
| rowspan=3|7.538(30)×10<sup>4</sup>&nbsp;y
| α
| α
| <sup>226</sup>Ra
| <sup>226</sup>Ra
| rowspan=3|0+
| rowspan=3|0+
| rowspan=3|Trace <ref group="n" name="us">Intermediate decay product of [[Uranium-238|<sup>238</sup>U]]</ref>
| rowspan=3|0.0002(2)<ref group="n" name="us">Intermediate decay product of [[Uranium-238|<sup>238</sup>U]]</ref>
| rowspan=3|
| rowspan=3|
|-
|-
| CD (5.6&times;10<sup>−11</sup>%)
| CD (5.6×10<sup>−11</sup>%)
| <sup>206</sup>Hg<br><sup>24</sup>Ne
| <sup>206</sup>Hg<br><sup>24</sup>Ne
|-
|-
| [[Spontaneous fission|SF]] (5&times;10<sup>−11</sup>%)
| [[Spontaneous fission|SF]] (5×10<sup>−11</sup>%)
| (Various)
| (Various)
|-
|-
Line 474: Line 416:
| <sup>227</sup>Ra
| <sup>227</sup>Ra
|-
|-
| rowspan=4|<sup>232</sup>Th<ref group="n">[[Primordial nuclide|Primordial]] [[radionuclide]]</ref>
| rowspan=3|[[Thorium-232|<sup>232</sup>Th]]<ref group="n">[[Primordial nuclide|Primordial]] [[radionuclide]]</ref>
| rowspan=4|Thorium
| rowspan=3|Thorium
| rowspan=4 style="text-align:right" | 90
| rowspan=3 style="text-align:right" | 90
| rowspan=4 style="text-align:right" | 142
| rowspan=3 style="text-align:right" | 142
| rowspan=4|232.0380553(21)
| rowspan=3|232.0380553(21)
| rowspan=4|'''1.405(6)&times;10<sup>10</sup>&nbsp;y'''
| rowspan=3|'''1.405(6)×10<sup>10</sup>&nbsp;y'''
| α<ref group="n">Theorized to also undergo β<sup>−</sup>β<sup>−</sup> decay to <sup>232</sup>U</ref>
| α
| <sup>228</sup>Ra
| <sup>228</sup>Ra
| rowspan=4|0+
| rowspan=3|0+
| rowspan=4|1.0000
| rowspan=3|0.9998(2)
| rowspan=4|
| rowspan=3|
|-
|-
| β<sup></sup>β<sup>−</sup> (rare)
| SF (1.1×10<sup>−9</sup>%)
| <sup>232</sup>U
|-
| SF (1.1&times;10<sup>−9</sup>%)
| (various)
| (various)
|-
|-
| CD (2.78&times;10<sup>−10</sup>%)
| CD (2.78×10<sup>−10</sup>%)
| <sup>182</sup>Yb<br><sup>26</sup>Ne<br><sup>24</sup>Ne
| <sup>182</sup>Yb<br><sup>26</sup>Ne<br><sup>24</sup>Ne
|-
|-
Line 504: Line 443:
| <sup>233</sup>Pa
| <sup>233</sup>Pa
| 1/2+
| 1/2+
| Trace<ref group="n">Produced in neutron capture by <sup>232</sup>Th</ref>
|
|
|
|-
|-
| <sup>234</sup>Th
| <sup>234</sup>Th
| Uranium X1
| Uranium X<sub>1</sub>
| style="text-align:right" | 90
| style="text-align:right" | 90
| style="text-align:right" | 144
| style="text-align:right" | 144
Line 566: Line 505:
|
|
|
|
{{Isotopes table/footer}}
|}
<references group="n" />

=== Notes ===
* Geologically exceptional samples are known in which the isotopic composition lies outside the reported range. The uncertainty in the atomic mass may exceed the stated value for such specimens.
* Values marked # are not purely derived from experimental data, but at least partly from systematic trends. Spins with weak assignment arguments are enclosed in parentheses.
* Uncertainties are given in concise form in parentheses after the corresponding last digits. Uncertainty values denote one standard deviation, except isotopic composition and standard atomic mass from IUPAC, which use expanded uncertainties.


== Uses ==
== Uses ==
Thorium has been suggested for use as a source of nuclear energy. Presumably, it would need to be exposed to neutrons in a nuclear reactor, to convert the common isotope to some species that is fissionable.
Thorium has been suggested for use in [[thorium-based nuclear power]].

In many countries the use of thorium in consumer products is banned or discouraged because it is radioactive.


It is currently used in cathodes of vacuum tubes, for a combination of physical stability at high temperature and a low work energy required to remove an electron from its surface.
It is currently used in cathodes of vacuum tubes, for a combination of physical stability at high temperature and a low work energy required to remove an electron from its surface.

It has, for about a century, been used in [[Gas mantle|mantle]]s of gas and vapor lamps such as [[Gas lighting|gas lights]] and camping lanterns.
It has, for about a century, been used in [[Gas mantle|mantle]]s of gas and vapor lamps such as [[Gas lighting|gas lights]] and camping lanterns.
Its radioactivity is a consideration for its non-nuclear uses but is too small to rule it out.


===Low dispersion lenses===
Thorium was also used in certain glass elements of Aero-Ektar lenses made by Kodak during World War II. Thus they are mildly radioactive. Two of the glass elements in the f/2.5 Aero-Ektar lenses are 11 and 13% thorium by weight. The Thorium-containing glasses were used because they have a high refractive index with a low dispersion (variation of index with wavelength), a highly desirable property. Many surviving Aero-Ektar lenses have a tea colored tint, possibly due to radiation damage to the glass.
Thorium was also used in certain glass elements of '''Aero-Ektar''' lenses made by Kodak during World War II. Thus they are mildly radioactive.<ref>[http://new55project.blogspot.co.uk/2012/02/f25-aero-ektar-lenses.html f2.5 Aero Ektar Lenses ]{{Dead link|date=February 2023 |bot=InternetArchiveBot |fix-attempted=yes }} Some images.</ref> Two of the glass elements in the f/2.5 Aero-Ektar lenses are 11% and 13% thorium by weight. The thorium-containing glasses were used because they have a high refractive index with a low dispersion (variation of index with wavelength), a highly desirable property. Many surviving Aero-Ektar lenses have a tea colored tint, possibly due to radiation damage to the glass.


As these lenses were used for aerial reconnaissance, the radiation level is not high enough to fog film over a short period. This would indicate the radiation level is reasonably safe. However. when not in use, it would be prudent to store these lenses as far as possible from normally inhabited areas; allowing the inverse square relationship to attenuate the radiation.<ref>{{Cite web|title = Aero-Ektar Lenses|url = http://home.earthlink.net/~michaelbriggs/aeroektar/aeroektar.html |author=Michael S. Briggs |date=January 16, 2002 |accessdate = 2015-08-28}}</ref>
These lenses were used for aerial reconnaissance because the radiation level is not high enough to fog film over a short period. This would indicate the radiation level is reasonably safe. However, when not in use, it would be prudent to store these lenses as far as possible from normally inhabited areas; allowing the inverse square relationship to attenuate the radiation.<ref>{{Cite web|title = Aero-Ektar Lenses|url = http://home.earthlink.net/~michaelbriggs/aeroektar/aeroektar.html|author = Michael S. Briggs|date = January 16, 2002|access-date = 2015-08-28|archive-url = https://web.archive.org/web/20150812205035/http://home.earthlink.net/~michaelbriggs/aeroektar/aeroektar.html|archive-date = August 12, 2015|url-status = dead}}</ref>

==Actinides vs. fission products==
{{Actinidesvsfissionproducts}}
{{Clear}}

== Notable isotopes ==

=== Thorium-228 ===
'''<sup>228</sup>Th''' is an [[isotope]] of [[thorium]] with 138 [[neutrons]]. It was once named Radiothorium, due to its occurrence in the [[disintegration chain]] of thorium-232. It has a [[half-life]] of 1.9116 years. It undergoes [[alpha decay]] to [[isotopes of radium|<sup>224</sup>Ra]]. Occasionally it decays by the unusual route of [[cluster decay]], emitting a nucleus of [[isotopes of oxygen|<sup>20</sup>O]] and producing stable [[isotopes of lead|<sup>208</sup>Pb]]. It is a daughter isotope of [[Uranium-232|<sup>232</sup>U]] in the thorium decay series.

<sup>228</sup>Th has an atomic weight of 228.0287411&nbsp;grams/mole.

Together with its decay product <sup>224</sup>Ra it is used for alpha particle radiation therapy.<ref>{{cite web | url=https://www.scatecinnovation.no/artikler/thor-medical-production-of-alpha-emitters-for-cancer-treatment | title=Thor Medical – production of alpha emitters for cancer treatment | date=May 2023}}</ref>

===Thorium-229===
'''<sup>229</sup>Th''' is a [[radioactive]] [[isotope]] of [[thorium]] that decays by [[alpha particle|alpha]] emission with a [[half-life]] of 7917 years.<ref name="Varga14" />
<sup>229</sup>Th is produced by the decay of [[uranium-233]], and its principal use is for the production of the [[nuclear medicine|medical isotopes]] [[actinium-225]] and [[bismuth-213]].<ref>[http://www.ne.doe.gov/pdfFiles/U233RptConMarch2001.pdf Report to Congress on the extraction of medical isotopes from U-233] {{webarchive|url=https://web.archive.org/web/20110927225711/http://www.ne.doe.gov/pdfFiles/U233RptConMarch2001.pdf |date=2011-09-27 }}. U.S. Department of Energy. March 2001</ref>

===Thorium-229m===
<sup>229</sup>Th has a [[nuclear isomer]], {{SimpleNuclide|Th|229|m}}, with a remarkably low excitation energy of {{val|8.355733|(10)|u=eV}}, corresponding to a photon frequency of {{val|2020407|3|u=GHz}} (wavelength {{val|148382.2|0.2|u=pm}}).<!--These values are from the Elwell preprint which has tighter bounds, although completely consistent with the Tiedau paper-->{{r|Thirolf2024|Tiedau2024|Elwell2024}} Although in the very high frequency [[Ultraviolet#Subtypes|vacuum ultraviolet]] frequency range, this is the only known opportunity for direct laser excitation of a nuclear state,<ref>{{cite journal
| first1=E.V. |last1=Tkalya
| first2=V.O. |last2=Varlamov
| first3=V.V. |last3=Lomonosov
| first4=S.A. |last4=Nikulin
| title=Processes of the nuclear isomer <sup>229m</sup>Th(3/2<sup>+</sup>, 3.5±1.0 eV) Resonant excitation by optical photons
| journal=Physica Scripta
| volume=53 | issue=3
| pages=296–299
| date=1996
| doi=10.1088/0031-8949/53/3/003
| bibcode=1996PhyS...53..296T
| s2cid=250744766
}}</ref> which could have applications like a [[nuclear clock]] of very high accuracy<ref name="Peik2003" /><ref name="Campbell2012" /><ref>{{cite journal
| title=Towards a <sup>229</sup>Th-based nuclear clock
| first1=Lars |last1=von der Wense
| first2=Benedict |last2=Seiferle
| first3=Peter G. |last3=Thirolf
| journal=Measurement Techniques |volume=60 |issue=12 |pages=1178–1192 |date=March 2018
| doi=10.1007/s11018-018-1337-1
| arxiv=1811.03889
| bibcode=2018arXiv181103889V | s2cid=119359298
}}</ref><ref name=Thirolf2020>{{cite conference
|title='Phase Transition' in the 'Thorium-Isomer Story'
|first=Peter G. |last=Thirolf |display-authors=etal
|journal=[[Acta Physica Polonica B]]
|volume=51 |issue=3 |pages=561–570
|date=March 2020
|url=https://www.actaphys.uj.edu.pl/R/51/3/561/pdf
|conference=XXXVI Mazurian Lakes Conference on Physics (1–7 November 2019)
|conference-url=https://mazurian.fuw.edu.pl/wp-content/uploads/2019/09/2019Program.pdf
|location=[[Piaski, Pisz County]], Poland<!--Damn, there are a lot of places names "Piaski" in Poland!-->
|doi=10.5506/APhysPolB.51.561 |doi-access=free
|arxiv=2108.13388
}} Originally presented as ''Characterization of the elusive <sup>229m</sup>Th isomer – milestones towards a nuclear clock''.</ref> or as a [[qubit]] for [[quantum computing]].<ref>{{cite journal
| first1=S. |last1=Raeder
| first2=V. |last2=Sonnenschein
| first3=T. |last3=Gottwald
| first4=I.D. |last4=Moore
| first5=M. |last5=Reponen
| first6=S. |last6=Rothe
| first7=N. |last7=Trautmann
| first8=K. |last8=Wendt
| title = Resonance ionization spectroscopy of thorium isotopes - towards a laser spectroscopic identification of the low-lying 7.6 eV isomer of <sup>229</sup>Th
| journal = [[J. Phys. B: At. Mol. Opt. Phys.]]
| volume = 44
|issue=16
| pages = 165005
| date = 2011
| doi = 10.1088/0953-4075/44/16/165005
| arxiv=1105.4646
|bibcode=2011JPhB...44p5005R
|s2cid=118379032
}}</ref>

These applications were for a long time impeded by imprecise measurements of the isomeric energy, as laser excitation's exquisite precision makes it difficult to use to search a wide frequency range. There were many investigations, both theoretical and experimental, trying to determine the transition energy precisely and to specify other properties of the isomeric state of <sup>229</sup>Th (such as the lifetime and the magnetic moment) before the frequency was accurately measured in 2024.{{r|Tiedau2024|Thirolf2024|Elwell2024}}

====History====
Early measurements were done by producing the {{val|29.5855|u=keV}} excited state of <sup>229</sup>Th, and measuring the difference in emitted gamma ray energies as it decays to either the <sup>229m</sup>Th (90%) or <sup>229</sup>Th (10%) isomeric states.

In 1976, [[gamma ray spectroscopy]] first indicated that <sup>229</sup>Th has a [[nuclear isomer]], <sup>229m</sup>Th, with a remarkably low excitation energy.<ref>{{cite journal
| first1=L.A. |last1=Kroger
| first2=C.W. |last2=Reich
| title = Features of the low energy level scheme of <sup>229</sup>Th as observed in the α-decay of <sup>233</sup>U
| journal = [[Nuclear Physics A]]
| volume = 259
| issue=1
| pages = 29–60
| date = 1976
| doi = 10.1016/0375-9474(76)90494-2
|bibcode=1976NuPhA.259...29K
}}</ref> At that time the energy was inferred to be below 100 eV, purely based on the non-observation of the isomer's direct decay. However, in 1990, further measurements led to the conclusion that the energy is almost certainly below 10 eV,<ref name="Helmer1990">{{cite journal
| title = Energy separation of the doublet of intrinsic states at the ground state of <sup>229</sup>Th
| last1=Reich |first1=C. W. |author2=Helmer, R. G.
| journal = [[Physical Review Letters]]
| volume = 64
| issue = 3
| pages = 271–273
|date=Jan 1990
| doi = 10.1103/PhysRevLett.64.271
|pmid=10041937 | publisher = American Physical Society
|bibcode = 1990PhRvL..64..271R |url=https://zenodo.org/record/1233878 }}
</ref> making the isomer to be the one of lowest known excitation energy. In the following years, the energy was further constrained to {{val|3.5|1.0|u=eV}}, which was for a long time the accepted energy value.<ref name="Helmer1994">{{cite journal
| journal=[[Physical Review C]]
| volume=49 | issue=4| pages=1845–1858
| date=April 1994
| last1=Helmer |first1=R. G. |last2=Reich |first2=C. W.
| title = An Excited State of <sup>229</sup>Th at 3.5&nbsp;eV
| doi=10.1103/PhysRevC.49.1845
| pmid=9969412 | bibcode = 1994PhRvC..49.1845H
| url=https://zenodo.org/record/1233767}}</ref>

Improved gamma ray spectroscopy measurements using an advanced high-resolution X-ray microcalorimeter were carried out in 2007, yielding a new value for the transition energy of {{val|7.6|0.5|u=eV}},<ref name="Beck">{{cite journal |author=B. R. Beck |title=Energy splitting in the ground state doublet in the nucleus <sup>229</sup>Th |journal=[[Physical Review Letters]] |volume=98 |issue=14 |pages=142501|date=2007-04-06 |doi=10.1103/PhysRevLett.98.142501 |pmid=17501268 |bibcode=2007PhRvL..98n2501B |s2cid=12092700 |url=https://zenodo.org/record/1233955 |display-authors=etal}}</ref> corrected to {{val|7.8|0.5|u=eV}} in 2009.<ref name="BeckReview">{{cite conference
| title = Improved value for the energy splitting of the ground-state doublet in the nucleus <sup>229</sup>Th
| vauthors = Beck BR, Wu CY, Beiersdorfer P, Brown GV, Becker JA, Moody KJ, Wilhelmy JB, Porter FS, Kilbourne CA, Kelley RL
| date = 2009-07-30
| conference = 12th Int. Conf. on Nuclear Reaction Mechanisms
| location = Varenna, Italy
| id = LLNL-PROC-415170
| url = https://e-reports-ext.llnl.gov/pdf/375773.pdf
| access-date = 2014-05-14
| archive-url = https://web.archive.org/web/20170127104504/https://e-reports-ext.llnl.gov/pdf/375773.pdf
| archive-date = 2017-01-27
| url-status = dead
}}</ref> This shift in isomeric energy from {{val|3.5|u=eV}} to {{val|7.8|u=eV}} possibly explains why several early attempts to directly observe the transition were unsuccessful.
Still, most of the searches in the 2010s for light emitted by the isomeric decay failed to observe any signal,<ref>{{Cite journal
|last1=Jeet |first1=Justin |first2=Christian |last2=Schneider |first3=Scott T. |last3=Sullivan
|first4=Wade G. |last4=Rellergert |first5=Saed |last5=Mirzadeh |first6=A. |last6=Cassanho
|first7=H. P. |last7=Jenssen |first8=Eugene V. |last8=Tkalya |first9=Eric R. |last9=Hudson
|display-authors=6
|title=Results of a Direct Search Using Synchrotron Radiation for the Low-Energy
|journal=[[Physical Review Letters]]
|volume=114 |issue=25 |pages=253001 |date=23 June 2015
|doi=10.1103/physrevlett.114.253001 |pmid=26197124 |arxiv=1502.02189 |bibcode=2015PhRvL.114y3001J
|s2cid=1322253 }}</ref><ref>{{Cite journal
|last1=Yamaguchi |first1=A. |last2=Kolbe |first2=M. |last3=Kaser |first3=H.
|last4=Reichel |first4=T. |last5=Gottwald |first5=A. |last6=Peik |first6=E.
|title=Experimental search for the low-energy nuclear transition in <sup>229</sup>Th with undulator radiation
|journal=New Journal of Physics |language=en
|volume=17 |issue=5 |pages=053053 |date=May 2015
|doi=10.1088/1367-2630/17/5/053053 |bibcode=2015NJPh...17e3053Y |doi-access=free
}}</ref><ref>{{cite thesis
| first = Lars | last = von der Wense
| degree = PhD
| title = On the direct detection of <sup>229m</sup>Th
| publisher = [[Ludwig Maximilian University of Munich]]
| date = 2016
| isbn=978-3-319-70461-6
| url = https://edoc.ub.uni-muenchen.de/20492/7/Wense_Lars_von_der.pdf
}}</ref><ref>{{cite journal
| title=On an attempt to optically excite the nuclear isomer in Th-229
| first1=S. |last1=Stellmer
| first2=G. |last2=Kazakov
| first3=M. |last3=Schreitl
| first4=H. |last4=Kaser
| first5=M. |last5=Kolbe
| first6=T. |last6=Schumm
| journal=[[Physical Review A]] |volume=97 |pages=062506 |date=2018
| issue=6 | doi= 10.1103/PhysRevA.97.062506
| arxiv=1803.09294 | bibcode=2018PhRvA..97f2506S| s2cid=4946329 }}</ref> pointing towards a potentially strong non-radiative decay channel. A direct detection of photons emitted in the isomeric decay was claimed in 2012<ref name="Zhao2012">{{cite journal
|last1=Zhao |first1=Xinxin
|date=18 October 2012
|title=Observation of the Deexcitation of the <sup>229m</sup>Th Nuclear Isomer
|journal=[[Physical Review Letters]] |volume=109 |issue=16 |article-number=160801
|doi=10.1103/PhysRevLett.109.160801
|first2=Yenny Natali |last2=Martinez de Escobar
|first3=Robert |last3=Rundberg
|first4=Evelyn M. |last4=Bond
|first5=Allen |last5=Moody
|first6=David J. |last6=Vieira
|page=160801
|bibcode=2012PhRvL.109p0801Z
|pmid=23215066
|doi-access=free
}}</ref> and again in 2018.<ref name=":1">{{Cite arXiv
|last1=Borisyuk|first1=P. V. |last2=Chubunova|first2=E. V. |last3=Kolachevsky|first3=N. N.
|last4=Lebedinskii|first4=Yu Yu |last5=Vasiliev|first5=O. S. |last6=Tkalya|first6=E. V.
|date=2018-04-01
|title=Excitation of <sup>229</sup>Th nuclei in laser plasma: the energy and half-life of the low-lying isomeric state
|eprint=1804.00299 |class=nucl-th
}}</ref> However, both reports were subject to controversial discussions within the community.<ref>{{Cite journal
|last1=Peik|first1=Ekkehard
|last2=Zimmermann|first2=Kai
|date=2013-07-03
|title=Comment on "Observation of the Deexcitation of the <sup>229m</sup>Th Nuclear Isomer"
|journal=[[Physical Review Letters]] |volume=111 |issue=1 |page=018901
|article-number=018901
|doi=10.1103/PhysRevLett.111.018901
|pmid=23863029 |bibcode=2013PhRvL.111a8901P
}}</ref><ref>{{Cite journal
|last1=Thirolf|first1=Peter G |last2=Seiferle|first2=Benedict |last3=von der Wense |first3=Lars
|date=2019-10-28
|title=The 229-thorium isomer: doorway to the road from the atomic clock to the nuclear clock
|journal=[[Journal of Physics B: Atomic, Molecular and Optical Physics]]
|volume=52 |issue=20 |article-number=203001
|doi=10.1088/1361-6455/ab29b8 |bibcode=2019JPhB...52t3001T |doi-access=free
}}</ref>

A direct detection of electrons being emitted in the [[internal conversion]] decay channel of <sup>229m</sup>Th was achieved in 2016.<ref name=":0">{{cite journal
| journal=[[Nature (journal)|Nature]]
| volume=533 | issue=7601 | pages=47–51
| date=5 May 2016
| title = Direct detection of the <sup>229</sup>Th nuclear clock transition
| first1=Lars | last1=von der Wense
| first2=Benedict | last2=Seiferle
| first3=Mustapha | last3=Laatiaoui
| first4=Jürgen B. | last4=Neumayr
| first5=Hans-Jörg | last5=Maier
| first6=Hans-Friedrich | last6=Wirth
| first7=Christoph | last7=Mokry
| first8=Jörg | last8=Runke
| first9=Klaus | last9=Eberhardt
| first10=Christoph E. | last10=Düllmann
| first11=Norbert G. | last11=Trautmann
| first12=Peter G. | last12=Thirolf
| display-authors=6
| doi=10.1038/nature17669
| pmid=27147026 | bibcode=2016Natur.533...47V| arxiv=1710.11398| s2cid=205248786 }}</ref> However, at the time the isomer's transition energy could only be weakly constrained to between 6.3 and 18.3&nbsp;eV. Finally, in 2019, non-optical electron spectroscopy of the internal conversion electrons emitted in the isomeric decay allowed for a determination of the isomer's excitation energy to {{val|8.28|0.17|u=eV}}<ref name="SeiferleEnergy">{{cite journal
| title = Energy of the <sup>229</sup>Th nuclear clock transition
| journal=[[Nature (journal)|Nature]]
| volume=573 | issue=7773 | pages=243–246
| date=12 September 2019
| first1=B. |last1=Seiferle
| first2=L. |last2=von der Wense
| first3=P.V. |last3=Bilous
| first4=I. |last4=Amersdorffer
| first5=C. |last5=Lemell
| first6=F. |last6=Libisch
| first7=S. |last7=Stellmer
| first8=T. |last8=Schumm
| first9=C.E. |last9=Düllmann
| first10=A. |last10=Pálffy
| first11=P.G. |last11=Thirolf
| doi=10.1038/s41586-019-1533-4
| pmid=31511684
| arxiv=1905.06308
| bibcode=2019Natur.573..243S
| s2cid=155090121
}}</ref> However, this value appeared at odds with the 2018 preprint showing that a similar signal as an {{val|8.4|u=eV}} xenon VUV photon can be shown, but with about {{val|1.3|0.2|0.1|u=eV}} less energy and an 1880&nbsp;s lifetime.<ref name=":1" /> In that paper, <sup>229</sup>Th was embedded in [[silicon dioxide|SiO<sub>2</sub>]], possibly resulting in an energy shift and altered lifetime, although the states involved are primarily nuclear, shielding them from electronic interactions.

As a peculiarity of its extremely low excitation energy, the lifetime of <sup>229m</sup>Th very much depends on the electronic environment of the nucleus. In neutral <sup>229</sup>Th, the isomer can decay by [[internal conversion]] within a few microseconds.<ref>{{cite journal
| last1=Karpeshin |first1=F.F. |last2=Trzhaskovskaya |first2=M.B.
| title = Impact of the electron environment on the lifetime of the <sup>229</sup>Th<sup>m</sup> low-lying isomer
| journal = [[Physical Review C]]
| volume = 76
| issue=5 | year = 2007
|page=054313 | article-number = 054313
| doi = 10.1103/PhysRevC.76.054313
|bibcode=2007PhRvC..76e4313K
}}</ref><ref name="Tkalya" /><ref name="Seiferle2017">{{cite journal
| last1=Seiferle |first1=B. |last2=von der Wense |first2=L. |last3=Thirolf |first3=P.G.
| title = Lifetime measurement of the <sup>229</sup>Th nuclear isomer
| journal = [[Physical Review Letters]]
| volume = 118
| issue=4 | year = 2017
|page=042501 | article-number = 042501
| doi = 10.1103/PhysRevLett.118.042501
| pmid=28186791 | arxiv=1801.05205
| bibcode=2017PhRvL.118d2501S |s2cid=37518294
| quote=A half-life of {{val|7|1|u=us}} has been measured
}}</ref> However, the isomeric energy is not enough to remove a second electron (thorium's second ionization energy is {{val|11.5|u=eV}}), so internal conversion is impossible in Th<sup>+</sup> ions. Radiative decay occurs with a half-life {{#expr:(ln(1740/7e-6)/ln10) round 1}} orders of magnitude longer, predicted to be between 1000–{{val|10000}} seconds.<ref name="Tkalya">{{cite journal
| last1=Tkalya |first1=Eugene V. |last2=Schneider |first2=Christian |last3=Jeet |first3=Justin |last4=Hudson |first4=Eric R.
| title = Radiative lifetime and energy of the low-energy isomeric level in <sup>229</sup>Th
| journal = [[Physical Review C]]
| volume = 92 | issue=5 | article-number = 054324
| date = 25 November 2015
|page=054324 | doi = 10.1103/PhysRevC.92.054324
| arxiv=1509.09101
| bibcode=2015PhRvC..92e4324T |s2cid=118374372
}}</ref><ref>{{cite journal
| last1=Minkov |first1=Nikolay |last2=Pálffy |first2=Adriana
| title = Reduced transition probabilities for the gamma decay of the 7.8 eV isomer in <sup>229m</sup>Th
| journal = [[Phys. Rev. Lett.]]
| volume = 118 | issue=21 | article-number = 212501
| date = 23 May 2017
|page=212501 | doi = 10.1103/PhysRevLett.118.212501
| arxiv = 1704.07919
| pmid = 28598657
| bibcode=2017PhRvL.118u2501M |s2cid=40694257
}}</ref> Embedded in [[ionic crystals]], ionization is not quite 100%, so a small amount of internal conversion occurs, leading to a recently measured lifetime of ≈{{val|600|u=s}},{{r|Tiedau2024|Elwell2024}}<!--Slightly different in different crystals--> which can be extrapolated to a lifetime for isolated ions of {{val|1740|50|u=s}}.{{r|Tiedau2024}}

In a 2018 experiment, it was possible to perform a first laser-spectroscopic characterization of the nuclear properties of <sup>229m</sup>Th.<ref>{{cite journal
| last1=Thielking |first1=J. |last2=Okhapkin |first2=M.V. |last3=Przemyslaw |first3=G.
| last4=Meier |first4=D.M. |last5=von der Wense |first5=L. |last6=Seiferle |first6=B.
| last7=Düllmann |first7=C.E. |last8=Thirolf |first8=P.G. |last9=Peik |first9=E.
| title = Laser spectroscopic characterization of the nuclear-clock isomer <sup>229m</sup>Th
| journal = Nature
| volume = 556
| issue=7701 | year = 2018
| pages = 321–325
| doi = 10.1038/s41586-018-0011-8
|pmid=29670266 | arxiv=1709.05325
|bibcode=2018Natur.556..321T |s2cid=4990345 }}</ref> In this experiment, [[laser spectroscopy]] of the <sup>229</sup>Th atomic shell was conducted using a <sup>229</sup>Th<sup>2+</sup> ion cloud with 2% of the ions in the nuclear excited state. This allowed probing for the hyperfine shift induced by the different nuclear spin states of the ground and the isomeric state. In this way, a first experimental value for the magnetic dipole and the electric quadrupole moment of <sup>229m</sup>Th could be inferred.

In 2019, the isomer's excitation energy was constrained to {{val|8.28|0.17|u=eV}} based on the direct detection of internal conversion electrons<ref name="SeiferleEnergy" /> and a secure population of <sup>229m</sup>Th from the nuclear ground state was achieved by excitation of the {{val|29|u=keV}} nuclear excited state via synchrotron radiation.<ref name="Masuda2019">{{cite journal
| title = X-ray pumping of the <sup>229</sup>Th nuclear clock isomer
| journal=[[Nature (journal)|Nature]]
| volume=573 | issue=7773 | pages=238–242
| date=12 September 2019
| first1=T. |last1=Masuda
| first2=A. |last2=Yoshimi
| first3=A. |last3=Fujieda
| first4=H. |last4=Fujimoto
| first5=H. |last5=Haba
| first6=H. |last6=Hara
| first7=T. |last7=Hiraki
| first8=H. |last8=Kaino
| first9=Y. |last9=Kasamatsu
| first10=S. |last10=Kitao
| first11=K. |last11=Konashi
| first12=Y. |last12= Miyamoto
| first13=K. |last13=Okai
| first14=S. |last14=Okubo
| first15=N. |last15=Sasao
| first16=M. |last16=Seto
| first17=T. |last17=Schumm
| first18=Y. |last18=Shigekawa
| first19=K. |last19=Suzuki
| first20=S. |last20=Stellmer
| first21=K. |last21=Tamasaku
| first22=S. |last22=Uetake
| first23=M. |last23=Watanabe
| first24=T. |last24=Watanabe
| first25=Y. |last25=Yasuda
| first26=A. |last26=Yamaguchi
| first27=Y. |last27=Yoda
| first28=T. |last28=Yokokita
| first29=M. |last29=Yoshimura
| first30=K. |last30=Yoshimura
| display-authors=6
| doi=10.1038/s41586-019-1542-3
| pmid=31511686
| arxiv=1902.04823
| bibcode=2019Natur.573..238M
| s2cid=119083861
}}</ref> Additional measurements by a different group in 2020 produced a figure of {{val|8.10|0.17|u=eV}} ({{val|153.1|3.2|u=nm}} wavelength).<ref>{{cite journal
|first1=Tomas |last1=Sikorsky |first2=Jeschua |last2=Geist |first3=Daniel |last3=Hengstler
|first4=Sebastian |last4=Kempf |first5=Loredana |last5=Gastaldo |first6=Christian |last6=Enss
|first7=Christoph |last7=Mokry |first8=Jörg |last8=Runke |first9=Christoph E. |last9=Düllmann
|first10=Peter |last10=Wobrauschek |first11=Kjeld |last11=Beeks |first12=Veronika |last12=Rosecker
|first13=Johannes H. |last13=Sterba |first14=Georgy |last14=Kazakov |first15=Thorsten |last15=Schumm
|first16=Andreas |last16=Fleischmann
|display-authors=6
|title=Measurement of the <sup>229</sup>Th Isomer Energy with a Magnetic Microcalorimeter
|journal=[[Physical Review Letters]]
|volume=125 |issue=14 |article-number=142503 |date=2 October 2020
|page=142503 |doi=10.1103/PhysRevLett.125.142503 |pmid=33064540 |arxiv=2005.13340
|bibcode=2020PhRvL.125n2503S |s2cid=218900580
}}</ref> Combining these measurements, the expected transition energy is {{val|8.12|0.11|u=eV}}.<ref>{{cite news
|first=Lars |last=von der Wense
|title=Ticking Toward a Nuclear Clock
|journal=[[Physics (magazine)|Physics]] |volume=13 |article-number=152 |date=28 September 2020
|url=https://physics.aps.org/articles/v13/152
}}</ref>

In April 2024, two separate groups finally reported precision laser excitation Th<sup>4+</sup> cations doped into [[ionic crystals]] (of [[Calcium fluoride|CaF<sub>2</sub>]] and LiSrAlF<sub>6</sub> with additional interstitial [[Fluoride|F<sup>−</sup> anions]] for charge compensation), giving a precise measurement of the transition energy.<ref name=Thirolf2024>{{cite news
|title=Shedding Light on the Thorium-229 Nuclear Clock Isomer
|first=Peter |last=Thirolf
|date=April 29, 2024
|journal=[[Physics (magazine)|Physics]] |volume=17 |article-number=71
|doi=10.1103/Physics.17.71
|url=https://physics.aps.org/articles/v17/71
}}</ref><ref name=PR-Tiedau2024>{{cite press release
|title=Atomic Nucleus Excited with Laser: A Breakthrough after Decades
|date=29 April 2024
|publisher=[[TU Wien]]
|url=https://www.tuwien.at/en/tu-wien/news/news-articles/news/lange-erhoffter-durchbruch-erstmals-atomkern-mit-laser-angeregt
|access-date=29 April 2024
}}</ref><ref name=Tiedau2024>{{cite journal
|title=Laser Excitation of the Th-229 Nucleus
|first1=J. |last1=Tiedau |first2=M. V. |last2=Okhapkin |first3=K. |last3=Zhang
|first4=J. |last4=Thielking |first5=G. |last5=Zitzer |first6=E. |last6=Peik
|first7=F. |last7=Schaden |first8=T. |last8=Pronebner |first9=I. |last9=Morawetz
|first10=L. |last10=Toscani De Col |first11=F. |last11=Schneider |first12=A. |last12=Leitner
|first13=M. |last13=Pressler |first14=G.A. |last14=Kazakov |first15=K. |last15=Beeks
|first16=T. |last16=Sikorsky |first17=T. |last17=Schumm
|display-authors=6
|journal=[[Physical Review Letters]] |volume=132 |article-number=182501
|date=29 April 2024
|issue=18 |page=182501 |doi=10.1103/PhysRevLett.132.182501
|bibcode=2024PhRvL.132r2501T |url=https://www.tuwien.at/fileadmin/Assets/tu-wien/News/2024/Thorium_Preprint.pdf
|quote=The nuclear resonance for the Th<sup>4+</sup> ions in Th:CaF<sub>2</sub> is measured at the wavelength {{val|148.3821|(5)|u=nm}}, frequency {{val|2020.409|(7)|u=THz}}, and the fluorescence lifetime in the crystal is {{val|630|(15)|u=s}}, corresponding to an isomer half-life of {{val|1740|(50)|u=s}} for a nucleus isolated in vacuum.
}}</ref><ref name=Elwell2024>{{cite arXiv
|title=Laser excitation of the <sup>229</sup>Th nuclear isomeric transition in a solid-state host
|first1=R. |last1=Elwell |first2=Christian |last2=Schneider |first3=Justin |last3=Jeet
|first4=J. E. S. |last4=Terhune |first5=H. W. T. |last5=Morgan |first6=A. N. |last6=Alexandrova
|first7=Hoang Bao |last7=Tran Tan |first8=Andrei |last8=Derevianko |first9=Eric R. |last9=Hudson
|eprint=2404.12311 |class=physics.atom-ph
|date=18 April 2024
|quote=a narrow, laser-linewidth-limited spectral feature at {{val|148.38219|(4)|errend=<sub>stat</sub>(20)<sub>sys</sub>|u=nm}} ({{val|2020407.3|(5)|errend=<sub>stat</sub>(30)<sub>sys</sub>|u=GHz}}) that decays with a lifetime of {{val|568|(13)|errend=<sub>stat</sub>(20)<sub>sys</sub>|u=s}}. This feature is assigned to the excitation of the <sup>229</sup>Th nuclear isomeric state, whose energy is found to be {{val|8.355733|(2)|errend=<sub>stat</sub>(10)</sys>|u=eV}} in <sup>229</sup>Th:LiSrAlF<sub>6</sub>.
}}</ref> This enables the construction of high-precision lasers which will measure the frequency up to the accuracy of the best [[atomic clock]]s.{{r|Campbell2012|Thirolf2020}}

===Thorium-230===
'''<sup>230</sup>Th''' is a [[radioactive]] [[isotope]] of [[thorium]] that can be used to date [[coral]]s and determine [[ocean current]] flux. '''Ionium''' was a name given early in the study of radioactive elements to the <sup>230</sup>Th isotope produced in the [[decay chain]] of [[Uranium-238|<sup>238</sup>U]] before it was realized that ionium and thorium are chemically identical. The symbol '''Io''' was used for this supposed element. (The name is still used in [[ionium–thorium dating]].)

===Thorium-231===
'''<sup>231</sup>Th''' has 141 [[neutrons]]. It is the decay product of [[uranium-235]]. It is found in very small amounts on the [[earth]] and has a [[half-life]] of 25.5 hours.<ref>{{cite journal|first1=G. B.|last1=Knight|first2=R. L.|last2=Macklin|title=Radiations of Uranium Y|journal=Physical Review|date=1 January 1949|pages=34–38|volume=75|issue=1|doi=10.1103/PhysRev.75.34|bibcode=1949PhRv...75...34K}}</ref> When it decays, it emits a [[beta ray]] and forms [[protactinium-231]]. It has a decay energy of 0.39&nbsp;MeV. It has a mass of 231.0363043&nbsp;grams/mole.

===Thorium-232===
{{main|Thorium-232}}
'''<sup>232</sup>Th''' is the only [[primordial nuclide]] of [[thorium]] and makes up effectively all of natural thorium, with other isotopes of thorium appearing only in trace amounts as relatively short-lived [[decay product]]s of [[uranium]] and thorium.<ref>{{cite web |url=http://ie.lbl.gov/education/parent/Th_iso.htm |title=Isotopes of Thorium (Z=90) |work=Isotopes Project |publisher=[[Lawrence Berkeley National Laboratory]] |access-date=2010-01-18 |url-status=dead |archive-url=https://web.archive.org/web/20100203162843/http://ie.lbl.gov/education/parent/Th_iso.htm |archive-date=2010-02-03 }}</ref>
The isotope decays by [[alpha decay]] with a [[half-life]] of 1.405{{E|10}} years, over three times the [[age of the Earth]] and approximately the [[age of the universe]].
Its [[decay chain]] is the [[thorium series]], eventually ending in [[lead-208]]. The remainder of the chain is quick; the longest half-lives in it are 5.75 years for [[radium-228]] and 1.91 years for [[thorium-228]], with all other half-lives totaling less than 15 days.<ref>{{cite web |url=http://hepwww.rl.ac.uk/ukdmc/Radioactivity/Th_chain/Th_chain.html |title=Th-232 Decay Chain |author=Rutherford Appleton Laboratory |access-date=2010-01-25 |author-link=Rutherford Appleton Laboratory |archive-url=https://web.archive.org/web/20120319190834/http://hepwww.rl.ac.uk/ukdmc/Radioactivity/Th_chain/Th_chain.html |archive-date=2012-03-19 |url-status=dead }}</ref>

<sup>232</sup>Th is a [[fertile material]] able to [[neutron capture|absorb]] a [[neutron]] and undergo [[Nuclear transmutation|transmutation]] into the [[fissile]] [[nuclide]] [[uranium-233]], which is the basis of the [[thorium fuel cycle]].<ref>{{cite web |url=http://www.world-nuclear.org/info/inf62.html |title=Thorium |author=World Nuclear Association |access-date=2010-01-25 |author-link=World Nuclear Association |archive-date=2013-02-16 |archive-url=https://web.archive.org/web/20130216102005/http://www.world-nuclear.org/info/inf62.html |url-status=dead }}</ref>
In the form of [[Thorotrast]], a [[thorium dioxide]] [[suspension (chemistry)|suspension]], it was used as a [[contrast medium]] in early [[X-ray]] diagnostics. Thorium-232 is now classified as [[carcinogen]]ic.<ref>{{cite journal |last1= Krasinskas |first1= Alyssa M |last2= Minda |first2= Justina |last3= Saul |first3= Scott H |last4= Shaked |first4= Abraham |last5= Furth |first5= Emma E |title=Redistribution of thorotrast into a liver allograft several years following transplantation: a case report |journal= Mod. Pathol. |volume= 17 |pages= 117–120 |year= 2004 |doi= 10.1038/modpathol.3800008 |pmid=14631374 |issue=1|doi-access= free }}</ref>

===Thorium-233===
'''<sup>233</sup>Th''' is an isotope of [[thorium]] that decays into [[protactinium-233]] through beta decay. It has a half-life of 21.83 minutes.{{NUBASE2020|ref}} Traces occur in nature as the result of natural [[neutron activation]] of <sup>232</sup>Th.<ref name=4n1>{{cite journal |last1=Peppard |first1=D. F. |last2=Mason |first2=G. W. |last3=Gray |first3=P. R. |last4=Mech |first4=J. F. |title=Occurrence of the (4n + 1) series in nature |journal=Journal of the American Chemical Society |date=1952 |volume=74 |issue=23 |pages=6081–6084 |doi=10.1021/ja01143a074 |url=https://digital.library.unt.edu/ark:/67531/metadc172698/m2/1/high_res_d/metadc172698.pdf |archive-url=https://web.archive.org/web/20190429182951/https://digital.library.unt.edu/ark:/67531/metadc172698/m2/1/high_res_d/metadc172698.pdf |archive-date=2019-04-29 |url-status=live }}</ref>

===Thorium-234===
'''<sup>234</sup>Th''' is an [[isotope]] of [[thorium]] whose [[Atomic nucleus|nuclei]] contain 144 [[neutron]]s. <sup>234</sup>Th has a [[half-life]] of 24.1 days, and when it decays, it emits a [[beta particle]], and in doing so, it [[Nuclear transmutation|transmutes]] into [[protactinium]]-234. <sup>234</sup>Th has a mass of 234.0436 [[atomic mass unit]]s (amu), and it has a decay energy of about 270&nbsp;keV ([[electronvolt|kiloelectronvolts]]). [[Uranium]]-238 usually decays into this isotope of thorium (although in rare cases it can undergo [[spontaneous fission]] instead).


==References==
==References==
{{Reflist}}
{{Reflist}}
* Isotope masses from:
* Isotope masses from:
**{{NUBASE 2003}}
**{{cite journal |author=G. Audi |author2=A. H. Wapstra |author3=C. Thibault |author4=J. Blachot |author5=O. Bersillon |year=2003 |title=The NUBASE evaluation of nuclear and decay properties |url=http://www.nndc.bnl.gov/amdc/nubase/Nubase2003.pdf |journal=[[Nuclear Physics A]] |volume=729 |issue= |pages=3–128 |doi=10.1016/j.nuclphysa.2003.11.001 |bibcode=2003NuPhA.729....3A}}
* Isotopic compositions and standard atomic masses from:
* Isotopic compositions and standard atomic masses from:
**{{CIAAW2003}}
**{{cite journal |author=J. R. de Laeter |author2=J. K. Böhlke |author3=P. De Bièvre |author4=H. Hidaka |author5=H. S. Peiser |author6=K. J. R. Rosman |author7=P. D. P. Taylor |year=2003 |title=Atomic weights of the elements. Review 2000 (IUPAC Technical Report) |url=http://www.iupac.org/publications/pac/75/6/0683/pdf/ |journal=[[Pure and Applied Chemistry]] |volume=75 |issue=6 |pages=683–800 |doi=10.1351/pac200375060683}}
**{{CIAAW 2005}}
**{{cite journal |author=M. E. Wieser |year=2006 |title=Atomic weights of the elements 2005 (IUPAC Technical Report) |url=http://iupac.org/publications/pac/78/11/2051/pdf/ |journal=[[Pure and Applied Chemistry]] |volume=78 |issue=11 |pages=2051–2066 |doi=10.1351/pac200678112051 |laysummary=http://old.iupac.org/news/archives/2005/atomic-weights_revised05.html}}
* Half-life, spin, and isomer data selected from the following sources. See editing notes on [[Talk:Isotopes of thorium|this article's talk page]].
* Half-life, spin, and isomer data selected from the following sources.
**{{cite journal |author=G. Audi |author2=A. H. Wapstra |author3=C. Thibault |author4=J. Blachot |author5=O. Bersillon |year=2003 |title=The NUBASE evaluation of nuclear and decay properties |url=http://amdc.in2p3.fr/nubase/Nubase2003.pdf |journal=[[Nuclear Physics A]] |volume=729 |issue= |pages=3–128 |doi=10.1016/j.nuclphysa.2003.11.001 |bibcode=2003NuPhA.729....3A}}
**{{cite journal |author=G. Audi |author2=A. H. Wapstra |author3=C. Thibault |author4=J. Blachot |author5=O. Bersillon |year=2003 |title=The NUBASE evaluation of nuclear and decay properties |url=http://amdc.in2p3.fr/nubase/Nubase2003.pdf |journal=[[Nuclear Physics A]] |volume=729 |issue=1 |pages=3–128 |doi=10.1016/j.nuclphysa.2003.11.001 |bibcode=2003NuPhA.729....3A |url-status=dead |archive-url=https://web.archive.org/web/20110720233206/http://amdc.in2p3.fr/nubase/Nubase2003.pdf |archive-date=2011-07-20 }}
**{{NNDC}}
**{{cite web |author=[[National Nuclear Data Center]] |title=NuDat 2.1 database |url=http://www.nndc.bnl.gov/nudat2/ |publisher=[[Brookhaven National Laboratory]] |accessdate=September 2005}}
**{{CRC85|chapter=11}}
**{{cite book |author=N. E. Holden |year=2004 |editor=D. R. Lide |chapter=Table of the Isotopes |title=[[CRC Handbook of Chemistry and Physics]] |page=Section 11 |nopp=yes |edition=85th |publisher=[[CRC Press]] |isbn=978-0-8493-0485-9}}


{{Navbox element isotopes}}
{{Isotope nav | element=thorium | lighter=Isotopes of actinium | heavier=Isotopes of protactinium }}
{{Authority control}}


[[Category:Thorium]]
[[Category:Isotopes of thorium| ]]
[[Category:Isotopes of thorium| ]]
[[Category:Thorium]]
[[Category:Lists of isotopes by element|Thorium]]
[[Category:Lists of isotopes by element|Thorium]]

Revision as of 20:08, 12 May 2024

Isotopes of thorium (90Th)
Main isotopes[1] Decay
abun­dance half-life (t1/2) mode pro­duct
227Th trace 18.68 d α 223Ra
228Th trace 1.9116 y α 224Ra
229Th trace 7917 y[2] α 225Ra
230Th 0.02% 75400 y α 226Ra
231Th trace 25.5 h β 231Pa
232Th 100.0% 1.405×1010 y α 228Ra
233Th trace 21.83 min β 233Pa
234Th trace 24.1 d β 234Pa
Standard atomic weight Ar°(Th)

Thorium (90Th) has seven naturally occurring isotopes but none are stable. One isotope, 232Th, is relatively stable, with a half-life of 1.405×1010 years, considerably longer than the age of the Earth, and even slightly longer than the generally accepted age of the universe. This isotope makes up nearly all natural thorium, so thorium was considered to be mononuclidic. However, in 2013, IUPAC reclassified thorium as binuclidic, due to large amounts of 230Th in deep seawater. Thorium has a characteristic terrestrial isotopic composition and thus a standard atomic weight can be given.

Thirty-one radioisotopes have been characterized, with the most stable being 232Th, 230Th with a half-life of 75,380 years, 229Th with a half-life of 7,917 years,[2] and 228Th with a half-life of 1.92 years. All of the remaining radioactive isotopes have half-lives that are less than thirty days and the majority of these have half-lives that are less than ten minutes. One isotope, 229Th, has a nuclear isomer (or metastable state) with a remarkably low excitation energy,[5] recently measured to be 8.35574 eV[6] It has been proposed to perform laser spectroscopy of the 229Th nucleus and use the low-energy transition for the development of a nuclear clock of extremely high accuracy.[7][8][9]

The known isotopes of thorium range in mass number from 207[10] to 238.

List of isotopes

Nuclide
[n 1]
Historic
name
Z N Isotopic mass (Da)
[n 2][n 3]
Half-life
[n 4]
Decay
mode

[n 5]
Daughter
isotope

[n 6]
Spin and
parity
[n 7][n 8]
Natural abundance (mole fraction)
Excitation energy Normal proportion Range of variation
207Th[10] 90 117 9.7(+46.6−4.4) ms α 203Ra
208Th[11] 90 118 208.01791(4) 1.7(+1.7-0.6) ms α 204Ra 0+
209Th[12] 90 119 209.01772(11) 7(5) ms
[3.8(+69−15)]
α 205Ra 5/2−#
210Th 90 120 210.015075(27) 17(11) ms
[9(+17−4) ms]
α 206Ra 0+
β+ (rare) 210Ac
211Th 90 121 211.01493(8) 48(20) ms
[0.04(+3−1) s]
α 207Ra 5/2−#
β+ (rare) 211Ac
212Th 90 122 212.01298(2) 36(15) ms
[30(+20-10) ms]
α (99.7%) 208Ra 0+
β+ (.3%) 212Ac
213Th 90 123 213.01301(8) 140(25) ms α 209Ra 5/2−#
β+ (rare) 213Ac
214Th 90 124 214.011500(18) 100(25) ms α 210Ra 0+
215Th 90 125 215.011730(29) 1.2(2) s α 211Ra (1/2−)
216Th 90 126 216.011062(14) 26.8(3) ms α (99.99%) 212Ra 0+
β+ (.006%) 216Ac
216m1Th 2042(13) keV 137(4) μs (8+)
216m2Th 2637(20) keV 615(55) ns (11−)
217Th 90 127 217.013114(22) 240(5) μs α 213Ra (9/2+)
218Th 90 128 218.013284(14) 109(13) ns α 214Ra 0+
219Th 90 129 219.01554(5) 1.05(3) μs α[n 9] 215Ra 9/2+#
220Th 90 130 220.015748(24) 9.7(6) μs α[n 10] 216Ra 0+
221Th 90 131 221.018184(10) 1.73(3) ms α 217Ra (7/2+)
222Th 90 132 222.018468(13) 2.237(13) ms α[n 11] 218Ra 0+
223Th 90 133 223.020811(10) 0.60(2) s α 219Ra (5/2)+
224Th 90 134 224.021467(12) 1.05(2) s α 220Ra 0+
CD (rare) 208Pb
16O
225Th 90 135 225.023951(5) 8.72(4) min α (90%) 221Ra (3/2)+
EC (10%) 225Ac
226Th 90 136 226.024903(5) 30.57(10) min α 222Ra 0+
227Th Radioactinium 90 137 227.0277041(27) 18.68(9) d α 223Ra 1/2+ Trace[n 12]
228Th Radiothorium 90 138 228.0287411(24) 1.9116(16) y α 224Ra 0+ Trace[n 13]
CD (1.3×10−11%) 208Pb
20O
229Th 90 139 229.031762(3) 7.916(17)×103 y α 225Ra 5/2+ Trace[n 14]
229mTh 8.355733(10) eV[13] 7(1) μs[14] IT 229Th 3/2+
230Th[n 15] Ionium 90 140 230.0331338(19) 7.538(30)×104 y α 226Ra 0+ 0.0002(2)[n 16]
CD (5.6×10−11%) 206Hg
24Ne
SF (5×10−11%) (Various)
231Th Uranium Y 90 141 231.0363043(19) 25.52(1) h β 231Pa 5/2+ Trace[n 12]
α (10−8%) 227Ra
232Th[n 17] Thorium 90 142 232.0380553(21) 1.405(6)×1010 y α[n 18] 228Ra 0+ 0.9998(2)
SF (1.1×10−9%) (various)
CD (2.78×10−10%) 182Yb
26Ne
24Ne
233Th 90 143 233.0415818(21) 21.83(4) min β 233Pa 1/2+ Trace[n 19]
234Th Uranium X1 90 144 234.043601(4) 24.10(3) d β 234mPa 0+ Trace[n 16]
235Th 90 145 235.04751(5) 7.2(1) min β 235Pa (1/2+)#
236Th 90 146 236.04987(21)# 37.5(2) min β 236Pa 0+
237Th 90 147 237.05389(39)# 4.8(5) min β 237Pa 5/2+#
238Th 90 148 238.0565(3)# 9.4(20) min β 238Pa 0+
This table header & footer:
  1. ^ mTh – Excited nuclear isomer.
  2. ^ ( ) – Uncertainty (1σ) is given in concise form in parentheses after the corresponding last digits.
  3. ^ # – Atomic mass marked #: value and uncertainty derived not from purely experimental data, but at least partly from trends from the Mass Surface (TMS).
  4. ^ Bold half-life – nearly stable, half-life longer than age of universe.
  5. ^ Modes of decay:
    CD: Cluster decay
    EC: Electron capture
    IT: Isomeric transition
  6. ^ Bold symbol as daughter – Daughter product is stable.
  7. ^ ( ) spin value – Indicates spin with weak assignment arguments.
  8. ^ # – Values marked # are not purely derived from experimental data, but at least partly from trends of neighboring nuclides (TNN).
  9. ^ Theoretically capable of β+ decay to 219Ac[1]
  10. ^ Theoretically capable of electron capture to 220Ac[1]
  11. ^ Theoretically capable of electron capture to 222Ac[1]
  12. ^ a b Intermediate decay product of 235U
  13. ^ Intermediate decay product of 232Th
  14. ^ Intermediate decay product of 237Np
  15. ^ Used in Uranium–thorium dating
  16. ^ a b Intermediate decay product of 238U
  17. ^ Primordial radionuclide
  18. ^ Theorized to also undergo ββ decay to 232U
  19. ^ Produced in neutron capture by 232Th

Uses

Thorium has been suggested for use in thorium-based nuclear power.

In many countries the use of thorium in consumer products is banned or discouraged because it is radioactive.

It is currently used in cathodes of vacuum tubes, for a combination of physical stability at high temperature and a low work energy required to remove an electron from its surface.

It has, for about a century, been used in mantles of gas and vapor lamps such as gas lights and camping lanterns.

Low dispersion lenses

Thorium was also used in certain glass elements of Aero-Ektar lenses made by Kodak during World War II. Thus they are mildly radioactive.[15] Two of the glass elements in the f/2.5 Aero-Ektar lenses are 11% and 13% thorium by weight. The thorium-containing glasses were used because they have a high refractive index with a low dispersion (variation of index with wavelength), a highly desirable property. Many surviving Aero-Ektar lenses have a tea colored tint, possibly due to radiation damage to the glass.

These lenses were used for aerial reconnaissance because the radiation level is not high enough to fog film over a short period. This would indicate the radiation level is reasonably safe. However, when not in use, it would be prudent to store these lenses as far as possible from normally inhabited areas; allowing the inverse square relationship to attenuate the radiation.[16]

Actinides vs. fission products

Actinides[17] by decay chain Half-life
range (a)
Fission products of 235U by yield[18]
4n 4n + 1 4n + 2 4n + 3 4.5–7% 0.04–1.25% <0.001%
228Ra 4–6 a 155Euþ
244Cmƒ 241Puƒ 250Cf 227Ac 10–29 a 90Sr 85Kr 113mCdþ
232Uƒ 238Puƒ 243Cmƒ 29–97 a 137Cs 151Smþ 121mSn
248Bk[19] 249Cfƒ 242mAmƒ 141–351 a

No fission products have a half-life
in the range of 100 a–210 ka ...

241Amƒ 251Cfƒ[20] 430–900 a
226Ra 247Bk 1.3–1.6 ka
240Pu 229Th 246Cmƒ 243Amƒ 4.7–7.4 ka
245Cmƒ 250Cm 8.3–8.5 ka
239Puƒ 24.1 ka
230Th 231Pa 32–76 ka
236Npƒ 233Uƒ 234U 150–250 ka 99Tc 126Sn
248Cm 242Pu 327–375 ka 79Se
1.53 Ma 93Zr
237Npƒ 2.1–6.5 Ma 135Cs 107Pd
236U 247Cmƒ 15–24 Ma 129I
244Pu 80 Ma

... nor beyond 15.7 Ma[21]

232Th 238U 235Uƒ№ 0.7–14.1 Ga

Notable isotopes

Thorium-228

228Th is an isotope of thorium with 138 neutrons. It was once named Radiothorium, due to its occurrence in the disintegration chain of thorium-232. It has a half-life of 1.9116 years. It undergoes alpha decay to 224Ra. Occasionally it decays by the unusual route of cluster decay, emitting a nucleus of 20O and producing stable 208Pb. It is a daughter isotope of 232U in the thorium decay series.

228Th has an atomic weight of 228.0287411 grams/mole.

Together with its decay product 224Ra it is used for alpha particle radiation therapy.[22]

Thorium-229

229Th is a radioactive isotope of thorium that decays by alpha emission with a half-life of 7917 years.[2] 229Th is produced by the decay of uranium-233, and its principal use is for the production of the medical isotopes actinium-225 and bismuth-213.[23]

Thorium-229m

229Th has a nuclear isomer, 229m
Th
, with a remarkably low excitation energy of 8.355733(10) eV, corresponding to a photon frequency of 2020407±3 GHz (wavelength 148382.2±0.2 pm).[24][6][13] Although in the very high frequency vacuum ultraviolet frequency range, this is the only known opportunity for direct laser excitation of a nuclear state,[25] which could have applications like a nuclear clock of very high accuracy[8][9][26][27] or as a qubit for quantum computing.[28]

These applications were for a long time impeded by imprecise measurements of the isomeric energy, as laser excitation's exquisite precision makes it difficult to use to search a wide frequency range. There were many investigations, both theoretical and experimental, trying to determine the transition energy precisely and to specify other properties of the isomeric state of 229Th (such as the lifetime and the magnetic moment) before the frequency was accurately measured in 2024.[6][24][13]

History

Early measurements were done by producing the 29.5855 keV excited state of 229Th, and measuring the difference in emitted gamma ray energies as it decays to either the 229mTh (90%) or 229Th (10%) isomeric states.

In 1976, gamma ray spectroscopy first indicated that 229Th has a nuclear isomer, 229mTh, with a remarkably low excitation energy.[29] At that time the energy was inferred to be below 100 eV, purely based on the non-observation of the isomer's direct decay. However, in 1990, further measurements led to the conclusion that the energy is almost certainly below 10 eV,[30] making the isomer to be the one of lowest known excitation energy. In the following years, the energy was further constrained to 3.5±1.0 eV, which was for a long time the accepted energy value.[31]

Improved gamma ray spectroscopy measurements using an advanced high-resolution X-ray microcalorimeter were carried out in 2007, yielding a new value for the transition energy of 7.6±0.5 eV,[32] corrected to 7.8±0.5 eV in 2009.[33] This shift in isomeric energy from 3.5 eV to 7.8 eV possibly explains why several early attempts to directly observe the transition were unsuccessful. Still, most of the searches in the 2010s for light emitted by the isomeric decay failed to observe any signal,[34][35][36][37] pointing towards a potentially strong non-radiative decay channel. A direct detection of photons emitted in the isomeric decay was claimed in 2012[38] and again in 2018.[39] However, both reports were subject to controversial discussions within the community.[40][41]

A direct detection of electrons being emitted in the internal conversion decay channel of 229mTh was achieved in 2016.[42] However, at the time the isomer's transition energy could only be weakly constrained to between 6.3 and 18.3 eV. Finally, in 2019, non-optical electron spectroscopy of the internal conversion electrons emitted in the isomeric decay allowed for a determination of the isomer's excitation energy to 8.28±0.17 eV[43] However, this value appeared at odds with the 2018 preprint showing that a similar signal as an 8.4 eV xenon VUV photon can be shown, but with about 1.3+0.2
−0.1
 eV
less energy and an 1880 s lifetime.[39] In that paper, 229Th was embedded in SiO2, possibly resulting in an energy shift and altered lifetime, although the states involved are primarily nuclear, shielding them from electronic interactions.

As a peculiarity of its extremely low excitation energy, the lifetime of 229mTh very much depends on the electronic environment of the nucleus. In neutral 229Th, the isomer can decay by internal conversion within a few microseconds.[44][45][14] However, the isomeric energy is not enough to remove a second electron (thorium's second ionization energy is 11.5 eV), so internal conversion is impossible in Th+ ions. Radiative decay occurs with a half-life 8.4 orders of magnitude longer, predicted to be between 1000–10000 seconds.[45][46] Embedded in ionic crystals, ionization is not quite 100%, so a small amount of internal conversion occurs, leading to a recently measured lifetime of ≈600 s,[6][13] which can be extrapolated to a lifetime for isolated ions of 1740±50 s.[6]

In a 2018 experiment, it was possible to perform a first laser-spectroscopic characterization of the nuclear properties of 229mTh.[47] In this experiment, laser spectroscopy of the 229Th atomic shell was conducted using a 229Th2+ ion cloud with 2% of the ions in the nuclear excited state. This allowed probing for the hyperfine shift induced by the different nuclear spin states of the ground and the isomeric state. In this way, a first experimental value for the magnetic dipole and the electric quadrupole moment of 229mTh could be inferred.

In 2019, the isomer's excitation energy was constrained to 8.28±0.17 eV based on the direct detection of internal conversion electrons[43] and a secure population of 229mTh from the nuclear ground state was achieved by excitation of the 29 keV nuclear excited state via synchrotron radiation.[48] Additional measurements by a different group in 2020 produced a figure of 8.10±0.17 eV (153.1±3.2 nm wavelength).[49] Combining these measurements, the expected transition energy is 8.12±0.11 eV.[50]

In April 2024, two separate groups finally reported precision laser excitation Th4+ cations doped into ionic crystals (of CaF2 and LiSrAlF6 with additional interstitial F anions for charge compensation), giving a precise measurement of the transition energy.[24][7][6][13] This enables the construction of high-precision lasers which will measure the frequency up to the accuracy of the best atomic clocks.[9][27]

Thorium-230

230Th is a radioactive isotope of thorium that can be used to date corals and determine ocean current flux. Ionium was a name given early in the study of radioactive elements to the 230Th isotope produced in the decay chain of 238U before it was realized that ionium and thorium are chemically identical. The symbol Io was used for this supposed element. (The name is still used in ionium–thorium dating.)

Thorium-231

231Th has 141 neutrons. It is the decay product of uranium-235. It is found in very small amounts on the earth and has a half-life of 25.5 hours.[51] When it decays, it emits a beta ray and forms protactinium-231. It has a decay energy of 0.39 MeV. It has a mass of 231.0363043 grams/mole.

Thorium-232

232Th is the only primordial nuclide of thorium and makes up effectively all of natural thorium, with other isotopes of thorium appearing only in trace amounts as relatively short-lived decay products of uranium and thorium.[52] The isotope decays by alpha decay with a half-life of 1.405×1010 years, over three times the age of the Earth and approximately the age of the universe. Its decay chain is the thorium series, eventually ending in lead-208. The remainder of the chain is quick; the longest half-lives in it are 5.75 years for radium-228 and 1.91 years for thorium-228, with all other half-lives totaling less than 15 days.[53]

232Th is a fertile material able to absorb a neutron and undergo transmutation into the fissile nuclide uranium-233, which is the basis of the thorium fuel cycle.[54] In the form of Thorotrast, a thorium dioxide suspension, it was used as a contrast medium in early X-ray diagnostics. Thorium-232 is now classified as carcinogenic.[55]

Thorium-233

233Th is an isotope of thorium that decays into protactinium-233 through beta decay. It has a half-life of 21.83 minutes.[1] Traces occur in nature as the result of natural neutron activation of 232Th.[56]

Thorium-234

234Th is an isotope of thorium whose nuclei contain 144 neutrons. 234Th has a half-life of 24.1 days, and when it decays, it emits a beta particle, and in doing so, it transmutes into protactinium-234. 234Th has a mass of 234.0436 atomic mass units (amu), and it has a decay energy of about 270 keV (kiloelectronvolts). Uranium-238 usually decays into this isotope of thorium (although in rare cases it can undergo spontaneous fission instead).

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