Helium-3: Difference between revisions
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| symbol =He | | symbol =He | ||
| mass_number =3 | | mass_number =3 | ||
| mass =3. | | mass ={{val|3.016029322}}<ref>{{AME2020 II}}</ref> | ||
| num_neutrons =1 | | num_neutrons =1 | ||
| num_protons =2 | | num_protons =2 | ||
| abundance =0.000137% ( | | abundance =0.000137% (atmosphere)<ref name="CIAAWhelium">[http://www.ciaaw.org/helium.htm "Standard Atomic Weights: Helium"]. [[CIAAW]]. 1983.</ref><br/>0.01% ([[Solar System]]) | ||
| halflife =stable | | halflife =stable | ||
| error_halflife = | | error_halflife = | ||
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| parent_mass =3 | | parent_mass =3 | ||
| parent_decay =[[beta decay]] of tritium | | parent_decay =[[beta decay]] of tritium | ||
| spin ={{ | | spin ={{sfrac|1|2}} [[reduced Planck constant|''ħ'']] | ||
}} | }} | ||
'''Helium-3''' ('''<sup>3</sup>He'''<ref name=csaga>{{cite arXiv |last=Galli |first=D. |title=The cosmic saga of <sup>3</sup>He |date=September 2004 |eprint=astro-ph/0412380v1}}</ref><ref name="ley196610">{{Cite magazine|last=Ley |first=Willy |date=October 1966 |title=The Delayed Discovery |department=For Your Information |url=https://archive.org/stream/Galaxy_v25n01_1966-10#page/n115/mode/2up |magazine=Galaxy Science Fiction |pages=116–127 }}</ref> see also [[helion (chemistry)|helion]]) is a light, [[stable isotope|stable]] [[isotope]] of [[helium]] with two [[proton]]s and one [[neutron]]. (In contrast, the most common isotope, [[helium-4]], has two protons and two neutrons.) Helium-3 and [[Isotopes of hydrogen#Hydrogen-1 (Protium)|hydrogen-1]] are the only stable [[nuclide]]s with more protons than neutrons. It was discovered in 1939. Helium-3 atoms are [[fermionic]] and become a [[superfluid]] at the temperature of 2.491 mK. | '''Helium-3''' ('''<sup>3</sup>He'''<ref name=csaga>{{cite arXiv |last=Galli |first=D. |title=The cosmic saga of <sup>3</sup>He |date=September 2004 |eprint=astro-ph/0412380v1}}</ref><ref name="ley196610">{{Cite magazine|last=Ley |first=Willy |date=October 1966 |title=The Delayed Discovery |department=For Your Information |url=https://archive.org/stream/Galaxy_v25n01_1966-10#page/n115/mode/2up |magazine=Galaxy Science Fiction |pages=116–127 }}</ref> see also [[helion (chemistry)|helion]]) is a light, [[stable isotope|stable]] [[isotope]] of [[helium]] with two [[proton]]s and one [[neutron]]. (In contrast, the most common isotope, [[helium-4]], has two protons and two neutrons.) Helium-3 and [[Isotopes of hydrogen#Hydrogen-1 (Protium)|hydrogen-1]] are the only stable [[nuclide]]s with more protons than neutrons. It was discovered in 1939. Helium-3 atoms are [[fermionic]] and become a [[superfluid]] at the temperature of 2.491 mK. | ||
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[[Nuclear fusion]] using helium-3 has long been viewed as a desirable future [[energy source]]. The fusion of two of its [[atom]]s would be [[Aneutronic fusion|aneutronic]], that is, it would not release the dangerous radiation of traditional fusion or require the much higher temperatures thereof.<ref>{{cite web |url=https://blogs.scientificamerican.com/news-blog/is-moons-sci-fi-vision-of-lunar-hel-2009-06-12/ |title=Is MOON's Sci-Fi Vision of Lunar Helium 3 Mining Based in Reality? |last=Matson |first=John |date=12 Jun 2009 |website=Scientific American – News Blog |access-date=29 Aug 2017 |archive-date=30 August 2017 |archive-url=https://web.archive.org/web/20170830062841/https://blogs.scientificamerican.com/news-blog/is-moons-sci-fi-vision-of-lunar-hel-2009-06-12/ |url-status=live }}</ref> The process may unavoidably create other reactions that themselves would cause the surrounding material to become radioactive.<ref>{{cite web |url=https://cds.cern.ch/record/1055767/files/CM-PRS00002036.pdf |title=Fears Over Factoids |last=Close |first=Frank |date=August 2007 |website=CERN Document Server |publisher=Physicsworld.com |access-date=8 July 2018 |archive-date=22 October 2017 |archive-url=https://web.archive.org/web/20171022191811/http://cds.cern.ch/record/1055767/files/CM-PRS00002036.pdf |url-status=live }}</ref> | [[Nuclear fusion]] using helium-3 has long been viewed as a desirable future [[energy source]]. The fusion of two of its [[atom]]s would be [[Aneutronic fusion|aneutronic]], that is, it would not release the dangerous radiation of traditional fusion or require the much higher temperatures thereof.<ref>{{cite web |url=https://blogs.scientificamerican.com/news-blog/is-moons-sci-fi-vision-of-lunar-hel-2009-06-12/ |title=Is MOON's Sci-Fi Vision of Lunar Helium 3 Mining Based in Reality? |last=Matson |first=John |date=12 Jun 2009 |website=Scientific American – News Blog |access-date=29 Aug 2017 |archive-date=30 August 2017 |archive-url=https://web.archive.org/web/20170830062841/https://blogs.scientificamerican.com/news-blog/is-moons-sci-fi-vision-of-lunar-hel-2009-06-12/ |url-status=live }}</ref> The process may unavoidably create other reactions that themselves would cause the surrounding material to become radioactive.<ref>{{cite web |url=https://cds.cern.ch/record/1055767/files/CM-PRS00002036.pdf |title=Fears Over Factoids |last=Close |first=Frank |date=August 2007 |website=CERN Document Server |publisher=Physicsworld.com |access-date=8 July 2018 |archive-date=22 October 2017 |archive-url=https://web.archive.org/web/20171022191811/http://cds.cern.ch/record/1055767/files/CM-PRS00002036.pdf |url-status=live }}</ref> | ||
Helium-3 is thought to be more abundant on the Moon than on Earth, having been deposited in the upper layer of [[regolith]] by the [[solar wind]] over billions of years,<ref>{{cite news |title=Global inventory of Helium-3 in lunar regoliths estimated by a multi-channel microwave radiometer on the Chang-E 1 lunar satellite |author1=Fa WenZhe |author2=Jin YaQiu |url=http://lunarnetworks.blogspot.in/2010/12/change-1-maps-moons-helium-3-inventory.html |date=December 2010 |access-date=2012-12-12 |archive-date=2017-10-11 |archive-url=https://web.archive.org/web/20171011021507/http://lunarnetworks.blogspot.in/2010/12/change-1-maps-moons-helium-3-inventory.html |url-status=live }}</ref> though still lower in abundance than in the Solar System's [[gas giant]]s.<ref>{{cite conference|first=E. N.|last=Slyuta|author2=Abdrakhimov, A. M.|author3=Galimov, E. M.|date=March 12–16, 2007|title=The Estimation of Helium-3 Probable Reserves in Lunar Regolith|conference=38th Lunar and Planetary Science Conference|pages=2175|url=http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf|access-date=2007-05-31|archive-date=2008-07-05|archive-url=https://web.archive.org/web/20080705122316/http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf|url-status=live}}</ref><ref name="F. H. Cocks 2010">{{cite journal|author=Cocks, F. H.|date=2010|title=<sup>3</sup>He in permanently shadowed lunar polar surfaces|journal= Icarus |volume=206 |issue=2 |pages=778–779 |doi=10.1016/j.icarus.2009.12.032 |bibcode=2010Icar..206..778C}}</ref> | Helium-3 is thought to be more abundant on the Moon than on Earth, having been deposited in the upper layer of [[regolith]] by the [[solar wind]] over billions of years,<ref>{{cite news |title=Global inventory of Helium-3 in lunar regoliths estimated by a multi-channel microwave radiometer on the Chang-E 1 lunar satellite |author1=Fa WenZhe |author2=Jin YaQiu |url=http://lunarnetworks.blogspot.in/2010/12/change-1-maps-moons-helium-3-inventory.html |date=December 2010 |access-date=2012-12-12 |archive-date=2017-10-11 |archive-url=https://web.archive.org/web/20171011021507/http://lunarnetworks.blogspot.in/2010/12/change-1-maps-moons-helium-3-inventory.html |url-status=live }}</ref> though still lower in abundance than in the Solar System's [[gas giant]]s.<ref>{{cite conference|first=E. N.|last=Slyuta|author2=Abdrakhimov, A. M.|author3=Galimov, E. M.|date=March 12–16, 2007 |title=The Estimation of Helium-3 Probable Reserves in Lunar Regolith|conference=38th Lunar and Planetary Science Conference|pages=2175|url=http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf|access-date=2007-05-31|archive-date=2008-07-05|archive-url=https://web.archive.org/web/20080705122316/http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf|url-status=live}}</ref><ref name="F. H. Cocks 2010">{{cite journal|author=Cocks, F. H.|date=2010|title=<sup>3</sup>He in permanently shadowed lunar polar surfaces|journal= Icarus |volume=206 |issue=2 |pages=778–779 |doi=10.1016/j.icarus.2009.12.032 |bibcode=2010Icar..206..778C}}</ref> | ||
== History == | == History == | ||
The existence of helium-3 was first proposed in 1934 by the Australian [[Nuclear physics|nuclear physicist]] [[Mark Oliphant]] while he was working at the [[University of Cambridge]] [[Cavendish Laboratory]]. Oliphant had performed experiments in which fast [[deuteron]]s collided with deuteron targets (incidentally, the first demonstration of [[nuclear fusion]]).<ref>{{cite journal|title=Transmutation Effects Observed with Heavy Hydrogen|first=M. L. E.|last=Oliphant|author2=Harteck, P. |author3=Rutherford, E. |journal=[[Proceedings of the Royal Society A]] | volume=144|issue=853|date=1934|pages=692–703|jstor=2935553| doi = 10.1098/rspa.1934.0077|bibcode=1934RSPSA.144..692O|doi-access=free}}</ref> Isolation of helium-3 was first accomplished by [[Luis Walter Alvarez|Luis Alvarez]] and [[Robert Cornog]] in 1939.<ref>{{cite journal|doi=10.1103/PhysRev.56.613|title=Helium and Hydrogen of Mass 3|date=1939|last1=Alvarez|first1=Luis|last2=Cornog|first2=Robert|journal=Physical Review|volume=56|issue=6|pages=613|bibcode = 1939PhRv...56..613A }}</ref><ref>{{cite book|url = https://archive.org/details/discoveringalvar0000alva|url-access = registration|pages =[https://archive.org/details/discoveringalvar0000alva/page/26 26]–30|title = Discovering Alvarez: selected works of Luis W. Alvarez, with commentary by his students and colleagues|publisher = University of Chicago Press|isbn = 978-0-226-81304-2|author1 = Alvarez, Luis W|author2 = Peter Trower, W|date = 1987}}</ref> Helium-3 was thought to be a [[radioactive isotope]] until it was also found in samples of natural helium, which is mostly [[helium-4]], taken both from the terrestrial atmosphere and from [[natural gas]] wells.<ref>{{cite web|date=1981|publisher=Newsmagazine Publication|url=http://www.lbl.gov/Science-Articles/Research-Review/Magazine/1981/81fepi1.html|title=Lawrence and His Laboratory: Episode: A Productive Error|access-date=2009-09-01|archive-date=2017-05-10|archive-url=https://web.archive.org/web/20170510110547/http://www2.lbl.gov/Science-Articles/Research-Review/Magazine/1981/81fepi1.html|url-status=dead}}</ref> | The existence of helium-3 was first proposed in 1934 by the Australian [[Nuclear physics|nuclear physicist]] [[Mark Oliphant]] while he was working at the [[University of Cambridge]] [[Cavendish Laboratory]]. Oliphant had performed experiments in which fast [[deuteron]]s collided with deuteron targets (incidentally, the first demonstration of [[nuclear fusion]]).<ref>{{cite journal|title=Transmutation Effects Observed with Heavy Hydrogen|first=M. L. E.|last=Oliphant|author2=Harteck, P. |author3=Rutherford, E. |journal=[[Proceedings of the Royal Society A]] | volume=144|issue=853|date=1934|pages=692–703|jstor=2935553| doi = 10.1098/rspa.1934.0077|bibcode=1934RSPSA.144..692O|doi-access=free}}</ref> Isolation of helium-3 was first accomplished by [[Luis Walter Alvarez|Luis Alvarez]] and [[Robert Cornog]] in 1939.<ref>{{cite journal|doi=10.1103/PhysRev.56.613 |title=Helium and Hydrogen of Mass 3|url=https://archive.org/details/sim_physical-review_1939-09-15_56_6/page/612 |date=1939|last1=Alvarez|first1=Luis|last2=Cornog|first2=Robert|journal=Physical Review|volume=56 |issue=6 |pages=613|bibcode = 1939PhRv...56..613A }}</ref><ref>{{cite book|url = https://archive.org/details/discoveringalvar0000alva|url-access = registration|pages =[https://archive.org/details/discoveringalvar0000alva/page/26 26]–30|title = Discovering Alvarez: selected works of Luis W. Alvarez, with commentary by his students and colleagues|publisher = University of Chicago Press|isbn = 978-0-226-81304-2|author1 = Alvarez, Luis W|author2 = Peter Trower, W|date = 1987}}</ref> Helium-3 was thought to be a [[radioactive isotope]] until it was also found in samples of natural helium, which is mostly [[helium-4]], taken both from the terrestrial atmosphere and from [[natural gas]] wells.<ref>{{cite web|date=1981|publisher=Newsmagazine Publication|url=http://www.lbl.gov/Science-Articles/Research-Review/Magazine/1981/81fepi1.html|title=Lawrence and His Laboratory: Episode: A Productive Error|access-date=2009-09-01|archive-date=2017-05-10|archive-url=https://web.archive.org/web/20170510110547/http://www2.lbl.gov/Science-Articles/Research-Review/Magazine/1981/81fepi1.html|url-status=dead}}</ref> | ||
== Physical properties == | == Physical properties == | ||
Due to its low atomic mass of 3.016 [[dalton (unit)| | Due to its low atomic mass of 3.016 [[dalton (unit)|Da]], helium-3 has some [[Physical property|physical properties]] different from those of helium-4, with a mass of 4.0026 Da. On account of the weak, induced [[dipole–dipole interaction]] between the helium atoms, their microscopic physical properties are mainly determined by their [[zero-point energy]]. Also, the microscopic properties of helium-3 cause it to have a higher zero-point energy than helium-4. This implies that helium-3 can overcome dipole–dipole interactions with less [[thermal energy]] than helium-4 can. | ||
The [[quantum mechanical]] effects on helium-3 and helium-4 are significantly different because with two [[proton]]s, two [[neutron]]s, and two [[electron]]s, helium-4 has an overall [[Spin (physics)|spin]] of zero, making it a [[boson]], but with one fewer neutron, helium-3 has an overall spin of one half, making it a [[fermion]]. | The [[quantum mechanical]] effects on helium-3 and helium-4 are significantly different because with two [[proton]]s, two [[neutron]]s, and two [[electron]]s, helium-4 has an overall [[Spin (physics)|spin]] of zero, making it a [[boson]], but with one fewer neutron, helium-3 has an overall spin of one half, making it a [[fermion]]. | ||
Pure helium-3 gas boils at 3.19 [[kelvin|K]] compared with helium-4 at 4.23 K, and its [[critical point (thermodynamics)|critical point]] is also lower at 3.35 K, compared with helium-4 at 5.2 K. Helium-3 has less than half the density of helium-4 when it is at its boiling point: 59 g/L compared to 125 g/L of helium-4 at a pressure of one atmosphere. Its latent heat of vaporization is also considerably lower at 0.026 [[kilojoule per mole|kJ/mol]] compared with the 0.0829 kJ/mol of helium-4.<ref>[http://www.trgn.com/database/cryogen.html Teragon's Summary of Cryogen Properties] {{Webarchive|url=https://web.archive.org/web/20170809013754/http://www.trgn.com/database/cryogen.html |date=2017-08-09 }} Teragon Research, 2005</ref><ref>{{cite journal|last=Chase|first=C. E.|author2=Zimmerman, G. O.|date=1973|title=Measurements of P-V-T and Critical Indices of He<sup>3</sup> |journal=[[Journal of Low Temperature Physics]]|volume=11|issue=5–6|pages=551|bibcode=1973JLTP...11..551C|doi=10.1007/BF00654447|s2cid=123038029}}</ref> | Pure helium-3 gas boils at 3.19 [[kelvin|K]] compared with helium-4 at 4.23 K, and its [[critical point (thermodynamics)|critical point]] is also lower at 3.35 K, compared with helium-4 at 5.2 K. Helium-3 has less than half the density of helium-4 when it is at its boiling point: 59 g/L compared to 125 g/L of helium-4 at a pressure of one atmosphere. Its latent heat of vaporization is also considerably lower at 0.026 [[kilojoule per mole|kJ/mol]] compared with the 0.0829 kJ/mol of helium-4.<ref>[http://www.trgn.com/database/cryogen.html Teragon's Summary of Cryogen Properties] {{Webarchive|url=https://web.archive.org/web/20170809013754/http://www.trgn.com/database/cryogen.html |date=2017-08-09 }} Teragon Research, 2005</ref><ref>{{cite journal|last=Chase|first=C. E.|author2=Zimmerman, G. O.|date=1973|title=Measurements of P-V-T and Critical Indices of He<sup>3</sup> |journal=[[Journal of Low Temperature Physics]]|volume=11|issue=5–6|pages=551|bibcode=1973JLTP...11..551C|doi=10.1007/BF00654447|s2cid=123038029}}</ref> | ||
=== Superfluidity === | === Superfluidity === | ||
[[File:Phase diagram of helium-3 (1975) 0.002 K region-en.svg|thumb|Phase diagram for | [[File:Phase diagram of helium-3 (1975) 0.002 K region-en.svg|thumb|Phase diagram for helium-3 ("bcc" indicates a [[body-centered cubic]] crystal lattice.)]] | ||
An important property of helium-3 atoms, which distinguishes them from the more common helium-4, is that they contain an odd number of spin {{frac|1|2}} particles, and are [[Fermion#Composite fermions|composite fermions]]. This is a direct result of the [[Angular momentum quantum number#Addition of quantized angular momenta|addition rules]] for quantized angular momentum. In contrast, helium-4 atoms are [[boson]]s, containing an even number of spin {{ | An important property of helium-3 atoms, which distinguishes them from the more common helium-4, is that they contain an odd number of spin {{frac|1|2}} particles, and therefore are [[Fermion#Composite fermions|composite fermions]]. This is a direct result of the [[Angular momentum quantum number#Addition of quantized angular momenta|addition rules]] for quantized angular momentum. In contrast, helium-4 atoms are [[boson]]s, containing an even number of spin-{{sfrac|1|2}} particles. At low temperatures (about 2.17 K), helium-4 undergoes a [[phase transition]]: A fraction of it enters a [[superfluid]] [[phase (matter)|phase]] that can be roughly understood as a type of [[Bose–Einstein condensate]]. Such a mechanism is not available for fermionic helium-3 atoms. Many speculated that helium-3 could also become a superfluid at much lower temperatures, if the atoms formed into ''pairs'' analogous to [[Cooper pair]]s in the [[BCS theory]] of [[superconductivity]]. Each Cooper pair, having integer spin, can be thought of as a boson. During the 1970s, [[David Lee (physicist)|David Lee]], [[Douglas Osheroff]] and [[Robert Coleman Richardson]] discovered two phase transitions along the melting curve, which were soon realized to be the two superfluid phases of helium-3.<ref>{{cite journal|last=Osheroff|first=D. D. |author2=Richardson, R. C. |author3=Lee, D. M. |date=1972|title=Evidence for a New Phase of Solid He<sup>3</sup> |journal=[[Physical Review Letters]]|volume=28|issue=14|pages=885–888|doi=10.1103/PhysRevLett.28.885|bibcode= 1972PhRvL..28..885O|doi-access=free}}</ref><ref>{{cite journal|last=Osheroff|first=D. D.|author2=Gully, W. J. |author3=Richardson, R. C. |author4= Lee, D. M. |date=1972|title=New Magnetic Phenomena in Liquid He<sup>3</sup> below 3 mK|journal=Physical Review Letters |volume=29|issue=14|pages=920–923|doi=10.1103/PhysRevLett.29.920|bibcode=1972PhRvL..29..920O}}</ref> The transition to a superfluid occurs at 2.491 millikelvins on the melting curve. They were awarded the 1996 [[Nobel Prize in Physics]] for their discovery. [[Alexei Alexeyevich Abrikosov|Alexei Abrikosov]], [[Vitaly Lazarevich Ginzburg|Vitaly Ginzburg]], and [[Anthony James Leggett|Tony Leggett]] won the 2003 Nobel Prize in Physics for their work on refining understanding of the superfluid phase of helium-3.<ref>{{cite journal|last=Leggett|first=A. J.|date=1972 |title=Interpretation of Recent Results on He<sup>3</sup> below 3 mK: A New Liquid Phase?|journal=Physical Review Letters |volume=29|issue=18|pages=1227–1230|doi=10.1103/PhysRevLett.29.1227|bibcode=1972PhRvL..29.1227L}}</ref> | ||
In a zero magnetic field, there are two distinct superfluid phases of <sup>3</sup>He, the A-phase and the B-phase. The B-phase is the low-temperature, low-pressure phase which has an isotropic energy gap. The A-phase is the higher temperature, higher pressure phase that is further stabilized by a magnetic field and has two point nodes in its gap. The presence of two phases is a clear indication that <sup>3</sup>He is an unconventional superfluid (superconductor), since the presence of two phases requires an additional symmetry, other than gauge symmetry, to be broken. In fact, it is a | In a zero magnetic field, there are two distinct superfluid phases of <sup>3</sup>He, the A-phase and the B-phase. The B-phase is the low-temperature, low-pressure phase which has an isotropic energy gap. The A-phase is the higher temperature, higher pressure phase that is further stabilized by a magnetic field and has two point nodes in its gap. The presence of two phases is a clear indication that <sup>3</sup>He is an unconventional superfluid (superconductor), since the presence of two phases requires an additional symmetry, other than gauge symmetry, to be broken. In fact, it is a p-wave superfluid, with spin one, {{nowrap|1='''S''' = 1 ''ħ''}}, and angular momentum one, {{nowrap|1='''L''' = 1 ''ħ''}}. The ground state corresponds to total angular momentum zero, {{nowrap|1='''J''' = '''S''' + '''L''' = 0}} (vector addition). Excited states are possible with non-zero total angular momentum, {{nowrap|'''J''' > 0}}, which are excited pair collective modes. These collective modes have been studied with much greater precision than in any other unconventional pairing system, because of the extreme purity of superfluid <sup>3</sup>He. This purity is due to all <sup>4</sup>He phase separating entirely and all other materials solidifying and sinking to the bottom of the liquid, making the A- and B-phases of <sup>3</sup>He the most pure condensed matter state possible. | ||
== Natural abundance == | == Natural abundance == | ||
=== Terrestrial abundance === | === Terrestrial abundance === | ||
{{ | {{main|Isotope geochemistry}} | ||
<sup>3</sup>He is a primordial substance in the Earth's [[mantle (geology)|mantle]], thought to have | <sup>3</sup>He is a primordial substance in the Earth's [[mantle (geology)|mantle]], thought to have been trapped during the planet's initial formation. The ratio of <sup>3</sup>He to <sup>4</sup>He within the Earth's crust and mantle is less than that in the solar disk (as estimated using meteorite and lunar samples), with terrestrial materials generally containing lower <sup>3</sup>He/<sup>4</sup>He ratios due to production of <sup>4</sup>He from radioactive decay. | ||
<sup>3</sup>He has a cosmological ratio of 300 atoms per million atoms of <sup>4</sup>He | <sup>3</sup>He has a cosmological ratio of 300 atoms per million atoms of <sup>4</sup>He,<ref name=Witt>[[#Witt|Wittenberg 1994]]</ref> leading to the assumption that the original ratio of these primordial gases in the mantle was around 200–300 ppm when Earth was formed. Over the course of Earth's history, a significant amount of <sup>4</sup>He has been generated by the [[Alpha decay|alpha decay]] of uranium, thorium and other radioactive isotopes, to the point that only around 7% of the helium now in the mantle is primordial helium,<ref name=Witt /> thus lowering the total <sup>3</sup>He:<sup>4</sup>He ratio to around 20 ppm. Ratios of <sup>3</sup>He:<sup>4</sup>He in excess of the atmospheric ratio are indicative of a contribution of <sup>3</sup>He from the mantle. Crustal sources are dominated by the [[helium-4|<sup>4</sup>He]] produced by radioactive decay. | ||
The ratio of helium-3 to helium-4 in natural Earth-bound sources varies greatly.<ref name=Aldrich>Aldrich, L.T.; Nier, Alfred O. Phys. Rev. 74, 1590 – 1594 (1948). The Occurrence of He3 in Natural Sources of Helium. Page 1592, Tables I and II.</ref><ref name=Holden>Holden, Normen E. 1993. Helium Isotopic Abundance Variation in Nature. [http://www.osti.gov/bridge/servlets/purl/10183304-ds0WIi/10183304.PDF copy of paper BNL-49331] "Table II. <sup>3</sup>He Abundance of Natural Gas ... <sup>3</sup>He in ppm ... Aldrich 0.05 – 0.5 ... Sano 0.46 – 22.7", "Table V. ... of Water ... <sup>3</sup>He in ppm ... 1.6 – 1.8 East Pacific ... 0.006 – 1.5 Manitoba Chalk River ... 164 Japan Sea" (Aldrich measured Helium from US wells, Sano that of Taiwan gas: {{ | The ratio of helium-3 to helium-4 in natural Earth-bound sources varies greatly.<ref name=Aldrich>Aldrich, L.T.; Nier, Alfred O. Phys. Rev. 74, 1590 – 1594 (1948). The Occurrence of He3 in Natural Sources of Helium. Page 1592, Tables I and II.</ref><ref name=Holden>Holden, Normen E. 1993. Helium Isotopic Abundance Variation in Nature. [http://www.osti.gov/bridge/servlets/purl/10183304-ds0WIi/10183304.PDF copy of paper BNL-49331] "Table II. <sup>3</sup>He Abundance of Natural Gas ... <sup>3</sup>He in ppm ... Aldrich 0.05 – 0.5 ... Sano 0.46 – 22.7", "Table V. ... of Water ... <sup>3</sup>He in ppm ... 1.6 – 1.8 East Pacific ... 0.006 – 1.5 Manitoba Chalk River ... 164 Japan Sea" (Aldrich measured Helium from US wells, Sano that of Taiwan gas: {{cite journal| doi = 10.1038/323055a0| issn = 1476-4687| volume = 323| issue = 6083| pages = 55–57| last1 = Sano| first1 = Yuji| last2 = Wakita| first2 = Hiroshi| last3 = Huang| first3 = Chin-Wang| title = Helium flux in a continental land area estimated from <sup>3</sup>He/<sup>4</sup>He ratio in northern Taiwan| journal = Nature| date = September 1986| bibcode = 1986Natur.323...55S| s2cid = 4358031}})</ref> Samples of the [[lithium]] ore [[spodumene]] from Edison Mine, South Dakota were found to contain 12 parts of helium-3 to a million parts of helium-4. Samples from other mines showed 2 parts per million.<ref name=Aldrich/> | ||
Helium is | Helium itself is present as up to 7% of some natural gas sources,<ref>[http://www.webelements.com/webelements/elements/text/He/key.html WebElements Periodic Table: Professional Edition: Helium: key information] {{Webarchive|url=https://web.archive.org/web/20080509100431/http://www.webelements.com/webelements/elements/text/He/key.html |date=2008-05-09 }}. Webelements.com. Retrieved on 2011-11-08.</ref> and large sources have over 0.5% (above 0.2% makes it viable to extract).<ref name=SmithDM>[[#Smith|Smith, D.M.]] "any concentration of helium above approximately 0.2 percent is considered worthwhile examining" ... "U.S. government still owns approximately 1 billion nm<sup>3</sup> of helium inventory", "Middle East and North Africa ... many very large, helium-rich (up to 0.5 percent) natural gas fields" (Smith uses nm<sup>3</sup> to mean "normal [[cubic metre]]", elsewhere called "cubic metre at [[normal temperature and pressure|NTP]])</ref> The fraction of <sup>3</sup>He in helium separated from natural gas in the U.S. was found to range from 70 to 242 parts per billion.<ref name=CRS/><ref name="BoM/DoI">{{cite report| first1=Thomas A. | last1=Davidson | first2=David E. | last2=Emerson| publisher=[[United States Bureau of Mines|Bureau of Mines]], [[US Department of the Interior]] | title= Method and Apparatus for Direct Determination of Helium-3 in Natural Gas and Helium | id=Report of Investigations 9302 | date=1990}}</ref> Hence the US 2002 stockpile of 1 billion normal m<sup>3</sup><ref name=SmithDM/> would have contained about {{convert|12 to 43|kg}} of helium-3. According to American physicist [[Richard Garwin]], about {{convert|26|m3}} or almost {{convert|5|kg}} of <sup>3</sup>He is available annually for separation from the US natural gas stream. If the process of separating out the <sup>3</sup>He could employ as feedstock the liquefied helium typically used to transport and store bulk quantities, estimates for the incremental energy cost range from {{val|34|to|300|u=$/l}} NTP, excluding the cost of infrastructure and equipment.<ref name=CRS/> Algeria's annual gas production is assumed to contain 100 million normal cubic metres<ref name=SmithDM/> and this would contain between {{val|7|and|24|u=m3}} of helium-3 (about {{val|1|to|4|u=kg}}) assuming a similar <sup>3</sup>He fraction. | ||
<sup>3</sup>He is also present in the [[Earth's atmosphere]]. The natural abundance of <sup>3</sup>He in | <sup>3</sup>He is also present in the [[Earth's atmosphere]]. The natural abundance of <sup>3</sup>He in atmospheric helium is {{val|1.37|e=-6}} (1.37 parts per million).<ref name="CIAAWhelium"/> The partial pressure of helium in the Earth's atmosphere is about {{val|0.52|u=Pa}}, and thus helium accounts for 5.2 parts per million of the total pressure ({{val|101325|u=Pa}}) in the Earth's atmosphere, and <sup>3</sup>He thus accounts for 7.2 parts per trillion of the atmosphere. Since the atmosphere of the Earth has a mass of about {{val|5.14|e=18|u=kg}},<ref>{{cite journal|doi = 10.1175/JCLI-3299.1|title = The Mass of the Atmosphere: A Constraint on Global Analyses|year = 2005|last1 = Smith|first1 = Lesley|last2 = Trenberth|first2 = Kevin E.|journal = Journal of Climate|volume = 18|issue = 6|pages = 864–875|bibcode = 2005JCli...18..864T| s2cid=16754900 |doi-access = free}}</ref> the mass of <sup>3</sup>He in the Earth's atmosphere is the product of these numbers and the molecular weight ratio of helium-3 to air (3.016 to 28.95), giving a mass of 3815 [[tonne]]s of helium-3 in the earth's atmosphere. | ||
<sup>3</sup>He is produced on Earth from three sources: lithium [[spallation]], [[cosmic rays]], and beta decay of tritium (<sup>3</sup>H). The contribution from cosmic rays is negligible within all except the oldest regolith materials, and lithium spallation reactions are a lesser contributor than the production of <sup>4</sup>He by [[alpha particle]] emissions. | <sup>3</sup>He is produced on Earth from three sources: lithium [[spallation]], [[cosmic rays]], and beta decay of tritium (<sup>3</sup>H). The contribution from cosmic rays is negligible within all except the oldest regolith materials, and lithium spallation reactions are a lesser contributor than the production of <sup>4</sup>He by [[alpha particle]] emissions. | ||
The total amount of helium-3 in the mantle may be in the range of | The total amount of helium-3 in the mantle may be in the range of 0.1–1 [[megatonne]]s. Some helium-3 finds its way up through deep-sourced [[Hotspot (geology)|hotspot]] volcanoes such as those of the [[Hawaiian Islands]], but only {{val|300|u=g}} per year is emitted to the atmosphere. [[Mid-ocean ridge]]s emit another 3 kg per year. Around [[subduction|subduction zone]]s, various sources produce helium-3 in [[natural gas]] deposits which possibly contain a thousand tonnes of helium-3 (although there may be 25 thousand tonnes if all ancient subduction zones have such deposits). Wittenberg estimated that United States crustal natural gas sources may have only half a tonne total.<ref>[[#Witt|Wittenberg 1994]] p. 3, Table 1; p. 9.</ref> Wittenberg cited Anderson's estimate of another 1200 tonnes in [[interplanetary dust]] particles on the ocean floors.<ref>[[#Witt|Wittenberg 1994]] Page A-1 citing Anderson 1993, "1200 metric tonne"</ref> In the 1994 study, extracting helium-3 from these sources consumes more energy than fusion would release.<ref>[[#Witt|Wittenberg 1994]] Page A-4 "1 kg (<sup>3</sup>He), pumping power would be {{val|1.13|e=6|u=MW⋅yr}} ... fusion power derived ... {{val|19|u=MW⋅yr}}"</ref> | ||
=== Lunar surface === | === Moon === | ||
{{Further|Lunar resources#Helium-3|Changesite-(Y)|In situ resource utilization#Moon}} | |||
Materials on the [[Moon]]'s surface contain helium-3 at concentrations between 1.4 and 15 [[Parts per billion|ppb]] in sunlit areas,<ref>[http://fti.neep.wisc.edu/Research/he3_pubs.html FTI Research Projects :: <sup>3</sup>He Lunar Mining] {{Webarchive|url=https://web.archive.org/web/20060904144943/http://fti.neep.wisc.edu/Research/he3_pubs.html|date=2006-09-04}}. Fti.neep.wisc.edu. Retrieved on 2011-11-08.</ref><ref>{{cite journal |author1=E. N. Slyuta |author2=A. M. Abdrakhimov |author3=E. M. Galimov |date=2007 |title=The estimation of helium-3 probable reserves in lunar regolith |url=http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf |url-status=live |journal=Lunar and Planetary Science XXXVIII |issue=1338 |pages=2175 |bibcode=2007LPI....38.2175S |archive-url=https://web.archive.org/web/20080705122316/http://www.lpi.usra.edu/meetings/lpsc2007/pdf/2175.pdf |archive-date=2008-07-05 |access-date=2007-05-31}}</ref> and may contain concentrations as much as 50 [[Parts per billion|ppb]] in permanently shadowed regions.<ref name="F. H. Cocks 2010" /> A number of people, starting with Gerald Kulcinski in 1986,<ref>{{cite news |author=Eric R. Hedman |date=January 16, 2006 |title=A fascinating hour with Gerald Kulcinski |url=http://www.thespacereview.com/article/536/1 |url-status=live |archive-url=https://web.archive.org/web/20110109082500/http://thespacereview.com/article/536/1 |archive-date=January 9, 2011 |access-date=August 30, 2007 |work=The Space Review}}</ref> have proposed to [[Exploration of the Moon|explore the Moon]], mine lunar [[regolith]] and use the helium-3 for [[Nuclear fusion|fusion]]. Because of the low concentrations of helium-3, any mining equipment would need to process extremely large amounts of regolith (over 150 tonnes of regolith to obtain one gram of helium-3).<ref>{{cite web |author=I.N. Sviatoslavsky |date=November 1993 |title=The challenge of mining He-3 on the lunar surface: how all the parts fit together |url=http://fti.neep.wisc.edu/pdf/wcsar9311-2.pdf |url-status=dead |archive-url=https://web.archive.org/web/20190120035522/http://fti.neep.wisc.edu/pdf/wcsar9311-2.pdf |archive-date=2019-01-20 |access-date=2008-03-04}} Wisconsin Center for Space Automation and Robotics Technical Report WCSAR-TR-AR3-9311-2.</ref> | |||
The primary objective of [[Indian Space Research Organisation]]'s first lunar probe called [[Chandrayaan-1]], launched on October 22, 2008, was reported in some sources to be mapping the Moon's surface for helium-3-containing minerals.<ref>{{cite news |date=2008-09-19 |title=With He-3 on mind, India gets ready for lunar mission |url=http://economictimes.indiatimes.com/News/News_By_Industry/ET_Cetera/With_He-3_on_mind_India_gets_ready_for_lunar_mission/articleshow/3500270.cms |url-status=live |archive-url=https://web.archive.org/web/20080921212710/http://economictimes.indiatimes.com/News/News_By_Industry/ET_Cetera/With_He-3_on_mind_India_gets_ready_for_lunar_mission/articleshow/3500270.cms |archive-date=2008-09-21 |access-date=2008-09-21 |work=The Times Of India}}</ref> No such objective is mentioned in the project's official list of goals, though many of its scientific payloads have held helium-3-related applications.<ref>[http://www.isro.org/chandrayaan/htmls/objective_scientific.htm Scientific] {{webarchive|url=https://web.archive.org/web/20091012110215/http://www.isro.org/Chandrayaan/htmls/objective_scientific.htm|date=2009-10-12}}. Isro.org (2008-11-11). Retrieved on 2011-11-08.</ref><ref>[http://luna-ci.blogspot.com/2008/11/chandrayaan-1-payload-feature-2-sub-kev.html Luna C/I:: Chandrayaan-1 Payload Feature #2: Sub KeV Atom Reflecting Analyser (SARA)] {{Webarchive|url=https://web.archive.org/web/20190720000332/http://luna-ci.blogspot.com/2008/11/chandrayaan-1-payload-feature-2-sub-kev.html|date=2019-07-20}}. Luna-ci.blogspot.com (2008-11-12). Retrieved on 2011-11-08.</ref> | |||
[[Cosmochemistry|Cosmochemist]] and [[geochemist]] [[Ouyang Ziyuan]] from the [[Chinese Academy of Sciences]] who is now in charge of the [[Chang'e program|Chinese Lunar Exploration Program]] has already stated on many occasions that one of the main goals of the program would be the mining of helium-3, from which operation "each year, three space shuttle missions could bring enough fuel for all human beings across the world".<ref>[http://www.chinadaily.com.cn/cndy/2006-07/26/content_649325.htm He asked for the moon-and got it] {{Webarchive|url=https://web.archive.org/web/20230615211000/http://www.chinadaily.com.cn/cndy/2006-07/26/content_649325.htm|date=2023-06-15}}. Chinadaily.com.cn (2006-07-26). Retrieved on 2011-11-08.</ref> | |||
In January 2006, the Russian space company [[RKK Energiya]] announced that it considers lunar helium-3 a potential economic resource to be mined by 2020,<ref>[https://web.archive.org/web/20080809210848/http://www.space.com/news/ap_060126_russia_moon.html Russian Rocket Builder Aims for Moon Base by 2015, Reports Say]. Associated Press (via space.com). 26 January 2006</ref> if funding can be found.<ref>{{cite web |author=James Oberg |date=February 6, 2006 |title=Moonscam: Russians try to sell the Moon for foreign cash |url=http://www.thespacereview.com/article/551/1 |url-status=live |archive-url=https://web.archive.org/web/20230615211006/https://www.thespacereview.com/article/551/1 |archive-date=June 15, 2023 |access-date=August 30, 2007}}</ref><ref>{{cite web |author=Dwayne A. Day |author-link=Dwayne A. Day |date=March 5, 2007 |title=Death throes and grand delusions |url=http://www.thespacereview.com/article/824/1 |url-status=live |archive-url=https://web.archive.org/web/20230615211002/https://www.thespacereview.com/article/824/1 |archive-date=June 15, 2023 |access-date=August 30, 2007 |work=[[The Space Review]]}}</ref> | |||
Not all writers feel the extraction of lunar helium-3 is feasible, or even that there will be a demand for it for fusion. [[Dwayne A. Day|Dwayne Day]], writing in ''[[The Space Review]]'' in 2015, characterises helium-3 extraction from the Moon for use in fusion as magical thinking about an unproven technology, and questions the feasibility of lunar extraction, as compared to production on Earth.<ref>{{cite news |last1=Day |first1=Dwayne |author-link=Dwayne A. Day |date=September 28, 2015 |title=The helium-3 incantation |url=http://www.thespacereview.com/article/2834/1 |url-status=live |archive-url=https://web.archive.org/web/20181227075502/http://www.thespacereview.com/article/2834/1 |archive-date=27 December 2018 |access-date=11 January 2019 |work=The Space Review |quote=The belief in helium-3 mining is a great example of a myth that has been incorporated into the larger enthusiasm for human spaceflight, a magical incantation that is murmured, but rarely actually discussed.}}</ref> | |||
=== Gas giants === | |||
Mining [[gas giant]]s for helium-3 has also been proposed.<ref>{{cite web |author=Bryan Palaszewski |title=Atmospheric Mining in the Outer Solar System |url=http://gltrs.grc.nasa.gov/reports/2006/TM-2006-214122.pdf |url-status=dead |archive-url=https://web.archive.org/web/20090327051914/http://gltrs.grc.nasa.gov/reports/2006/TM-2006-214122.pdf |archive-date=2009-03-27}} NASA Technical Memorandum 2006-214122. AIAA–2005–4319. Prepared for the 41st Joint Propulsion Conference and Exhibit cosponsored by AIAA, ASME, SAE, and ASEE, Tucson, Arizona, July 10–13, 2005.</ref> The [[British Interplanetary Society]]'s hypothetical [[Project Daedalus]] interstellar probe design was fueled by helium-3 mines in the atmosphere of [[Jupiter]], for example. | |||
=== Solar nebula (primordial) abundance === | === Solar nebula (primordial) abundance === | ||
One early estimate of the primordial ratio of <sup>3</sup>He to <sup>4</sup>He in the solar nebula has been the measurement of their ratio in the atmosphere of Jupiter, measured by the mass spectrometer of the Galileo atmospheric entry probe. This ratio is about 1: | One early estimate of the primordial ratio of <sup>3</sup>He to <sup>4</sup>He in the solar nebula has been the measurement of their ratio in the atmosphere of Jupiter, measured by the mass spectrometer of the Galileo atmospheric entry probe. This ratio is about 1:10000,<ref>{{Cite journal | bibcode = 1996Sci...272..846N | title = The Galileo Probe Mass Spectrometer: Composition of Jupiter's Atmosphere | last1 = Niemann | first1 = Hasso B. | last2 = Atreya | first2 = Sushil K. | last3 = Carignan | first3 = George R. | last4 = Donahue | first4 = Thomas M. | last5 = Haberman | first5 = John A. | last6 = Harpold | first6 = Dan N. | last7 = Hartle | first7 = Richard E. | last8 = Hunten | first8 = Donald M. | last9 = Kasprzak | first9 = Wayne T. | display-authors = 8| volume = 272 | date = 1996 | pages = 846–9 | journal = Science | doi = 10.1126/science.272.5263.846 | pmid = 8629016 | issue = 5263| s2cid = 3242002 }}</ref> or 100 parts of <sup>3</sup>He per million parts of <sup>4</sup>He. This is roughly the same ratio of the isotopes as in [[lunar regolith]], which contains 28 ppm helium-4 and 2.8 ppb helium-3 (which is at the lower end of actual sample measurements, which vary from about 1.4 to 15 ppb). Terrestrial ratios of the isotopes are lower by a factor of 100, mainly due to enrichment of helium-4 stocks in the mantle by billions of years of [[alpha decay]] from [[uranium]], [[thorium]] as well as their [[decay product]]s and [[extinct radionuclide]]s. | ||
== Human production == | == Human production == | ||
=== Tritium decay === | === Tritium decay === | ||
{{ | {{see also|Tritium}} | ||
Virtually all helium-3 used in industry today is produced from the radioactive decay of [[tritium]], given its very low natural abundance and its very high cost. | Virtually all helium-3 used in industry today is produced from the radioactive decay of [[tritium]], given its very low natural abundance and its very high cost. | ||
Production, sales and distribution of helium-3 in the United States are managed by the [[US Department of Energy]] (DOE) [[DOE Isotope Program]].<ref>{{cite web |title=Isotope Development & Production for Research and Applications (IDPRA) |url=http://science.energy.gov/np/research/idpra/ |website=US Department of Energy Office of Science |date=18 October 2018 |access-date=11 January 2019 |archive-date=19 October 2011 |archive-url=https://web.archive.org/web/20111019074945/http://science.energy.gov/np/research/idpra/ |url-status=live }}</ref> | Production, sales and distribution of helium-3 in the United States are managed by the [[US Department of Energy]] (DOE) [[DOE Isotope Program]].<ref>{{cite web |title=Isotope Development & Production for Research and Applications (IDPRA) |url=http://science.energy.gov/np/research/idpra/ |website=US Department of Energy Office of Science |date=18 October 2018 |access-date=11 January 2019 |archive-date=19 October 2011 |archive-url=https://web.archive.org/web/20111019074945/http://science.energy.gov/np/research/idpra/ |url-status=live }}</ref> | ||
While tritium has several different experimentally determined values of its [[half-life]], [[National Institute of Standards and Technology|NIST]] lists {{val|4500|8|u=days | While tritium has several different experimentally determined values of its [[half-life]], [[National Institute of Standards and Technology|NIST]] lists {{val|4500|8|u=days}} ({{val|12.32|0.02|u=years}}).<ref> | ||
{{Cite journal | {{Cite journal | ||
|author = Lucas, L. L. | |author = Lucas, L. L. | ||
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<!-- simpler | <!-- simpler | ||
:<chem>^3_1H \to ^3_2{He^+} + {e^-} + \bar{\nu}_e + 18.6 keV</chem> | : <chem>^3_1H \to ^3_2{He^+} + {e^-} + \bar{\nu}_e + 18.6 keV</chem> | ||
--> | --> | ||
Among the total released energy of {{val|18.6|u=keV}}, the part taken by [[electron]]'s kinetic energy varies, with an average of {{val|5.7|u=keV}}, while the remaining energy is carried off by the nearly undetectable [[electron antineutrino]]. | Among the total released energy of {{val|18.6|u=keV}}, the part taken by [[electron]]'s kinetic energy varies, with an average of {{val|5.7|u=keV}}, while the remaining energy is carried off by the nearly undetectable [[electron antineutrino]]. | ||
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Tritium is a critical component of [[nuclear weapons]] and historically it was produced and stockpiled primarily for this application. The decay of tritium into helium-3 reduces the explosive power of the fusion warhead, so periodically the accumulated helium-3 must be removed from warhead reservoirs and tritium in storage. Helium-3 removed during this process is marketed for other applications. | Tritium is a critical component of [[nuclear weapons]] and historically it was produced and stockpiled primarily for this application. The decay of tritium into helium-3 reduces the explosive power of the fusion warhead, so periodically the accumulated helium-3 must be removed from warhead reservoirs and tritium in storage. Helium-3 removed during this process is marketed for other applications. | ||
For decades this has been, and remains, the principal source of the world's helium-3.<ref>{{Cite web |url=http://www.srs.gov/general/news/factsheets/tritium_esrs.pdf |title=Savannah River Tritium Enterprise: Fact Sheet |access-date=2016-03-01 |archive-date=2016-12-22 |archive-url=https://web.archive.org/web/20161222012847/http://www.srs.gov/general/news/factsheets/tritium_esrs.pdf |url-status=live }}</ref> Since the signing of the [[START I]] Treaty in 1991 the number of nuclear warheads that are kept ready for use has decreased.<ref>Charmian Schaller [https://web.archive.org/web/20061029124748/http://afci.lanl.gov/aptnews/aptnews.mar1_98.html Accelerator Production of Tritium – That Could Mean 40 Years of Work]. Los Alamos Monitor. March 1, 1998</ref><ref>[http://www.ieer.org/sdafiles/vol_5/5-1/tritium.html Science for Democratic Action Vol. 5 No. 1] {{Webarchive|url=https://web.archive.org/web/20060927015706/http://www.ieer.org/sdafiles/vol_5/5-1/tritium.html |date=2006-09-27 }}. IEER. Retrieved on 2011-11-08;</ref> This has reduced the quantity of helium-3 available from this source. Helium-3 stockpiles have been further diminished by increased demand,<ref name=CRS>{{cite report | first1=Dana A. | last1=Shea | first2=Daniel | last2=Morgan | publisher=[[Congressional Research Service]] | title=The Helium-3 Shortage: Supply, Demand, and Options for Congress | id=7-5700 | url=https://www.fas.org/sgp/crs/misc/R41419.pdf | date=22 December 2010 | access-date=23 December 2015 | archive-date=4 March 2016 | archive-url=https://web.archive.org/web/20160304003156/http://www.fas.org/sgp/crs/misc/R41419.pdf | url-status=live }}</ref> primarily for use in neutron radiation detectors and medical diagnostic procedures. US industrial demand for helium-3 reached a peak of {{ | For decades this has been, and remains, the principal source of the world's helium-3.<ref>{{Cite web |url=http://www.srs.gov/general/news/factsheets/tritium_esrs.pdf |title=Savannah River Tritium Enterprise: Fact Sheet |access-date=2016-03-01 |archive-date=2016-12-22 |archive-url=https://web.archive.org/web/20161222012847/http://www.srs.gov/general/news/factsheets/tritium_esrs.pdf |url-status=live }}</ref> Since the signing of the [[START I]] Treaty in 1991 the number of nuclear warheads that are kept ready for use has decreased.<ref>Charmian Schaller [https://web.archive.org/web/20061029124748/http://afci.lanl.gov/aptnews/aptnews.mar1_98.html Accelerator Production of Tritium – That Could Mean 40 Years of Work]. Los Alamos Monitor. March 1, 1998</ref><ref>[http://www.ieer.org/sdafiles/vol_5/5-1/tritium.html Science for Democratic Action Vol. 5 No. 1] {{Webarchive|url=https://web.archive.org/web/20060927015706/http://www.ieer.org/sdafiles/vol_5/5-1/tritium.html |date=2006-09-27 }}. IEER. Retrieved on 2011-11-08;</ref> This has reduced the quantity of helium-3 available from this source. Helium-3 stockpiles have been further diminished by increased demand,<ref name="CRS">{{cite report | first1=Dana A. | last1=Shea | first2=Daniel | last2=Morgan | publisher=[[Congressional Research Service]] | title=The Helium-3 Shortage: Supply, Demand, and Options for Congress | id=7-5700 | url=https://www.fas.org/sgp/crs/misc/R41419.pdf | date=22 December 2010 | access-date=23 December 2015 | archive-date=4 March 2016 | archive-url=https://web.archive.org/web/20160304003156/http://www.fas.org/sgp/crs/misc/R41419.pdf | url-status=live }}</ref> primarily for use in neutron radiation detectors and medical diagnostic procedures. US industrial demand for helium-3 reached a peak of {{val|70,000}} litres (approximately {{val|8|u=kg}}) per year in 2008. Price at auction, historically about $100 per litre, reached as high as $2000 per litre.<ref>[https://spectrum.ieee.org/physics-projects-deflate-for-lack-of-helium3 Physics Projects Deflate for Lack of Helium-3] . Spectrum.ieee.org. Retrieved on 2011-11-08.</ref> Since then, demand for helium-3 has declined to about 6000 [[litre]]s per year due to the high cost and efforts by the DOE to recycle it and find substitutes. Assuming a density of {{val|114|u=g/m3}} at $100/L helium-3 would be about a thirtieth as expensive as tritium (roughly $880/g vs. roughly ${{val|30000}} per gram) while at $2000 per litre, helium-3 would be about half as expensive as tritium (${{val|17540}}/g vs. ${{val|30000}}/g). | ||
The DOE recognized the developing shortage of both tritium and helium-3, and began producing tritium by lithium irradiation at the [[Tennessee Valley Authority]]'s [[Watts Bar Nuclear Generating Station]] in 2010.<ref name=CRS/> In this process tritium-producing burnable absorber rods (TPBARs) containing lithium in a ceramic form are inserted into the reactor in place of the normal boron control rods<ref>[http://pbadupws.nrc.gov/docs/ML0325/ML032521359.pdf Tritium Production] {{ | The DOE recognized the developing shortage of both tritium and helium-3, and began producing tritium by lithium irradiation at the [[Tennessee Valley Authority]]'s [[Watts Bar Nuclear Generating Station]] in 2010.<ref name="CRS" /> In this process tritium-producing burnable absorber rods (TPBARs) containing lithium in a ceramic form are inserted into the reactor in place of the normal boron control rods<ref>[http://pbadupws.nrc.gov/docs/ML0325/ML032521359.pdf Tritium Production] {{webarchive|url=https://web.archive.org/web/20160827030415/http://pbadupws.nrc.gov/docs/ML0325/ML032521359.pdf |date=2016-08-27 }} Nuclear Regulatory Commission, 2005.</ref> Periodically the TPBARs are replaced and the tritium extracted. | ||
Currently only two commercial nuclear reactors (Watts Bar Nuclear Plant Units 1 and 2) are being used for tritium production but the process could, if necessary, be vastly scaled up to meet any conceivable demand simply by utilizing more of the nation's power reactors{{ | Currently only two commercial nuclear reactors (Watts Bar Nuclear Plant Units 1 and 2) are being used for tritium production but the process could, if necessary, be vastly scaled up to meet any conceivable demand simply by utilizing more of the nation's power reactors{{citation needed|reason=It is not obvious that any reactor could use TPBARs|date=February 2024}}. | ||
Substantial quantities of tritium and helium-3 could also be extracted from the heavy water moderator in [[CANDU]] nuclear reactors.<ref name=CRS/><ref name=D2O>{{cite patent | Substantial quantities of tritium and helium-3 could also be extracted from the heavy water moderator in [[CANDU]] nuclear reactors.<ref name="CRS" /><ref name="D2O">{{cite patent | ||
| inventor1-last = Sur | | inventor1-last = Sur | ||
| inventor1-first = Bhaskar | | inventor1-first = Bhaskar | ||
| Line 126: | Line 139: | ||
}} {{Webarchive|url=https://web.archive.org/web/20151223142855/http://www.ic.gc.ca/opic-cipo/cpd/eng/patent/2810716/summary.html?type=number_search&tabs1Index=tabs1_1 |date=23 December 2015 }}</ref> India and Canada, the two countries with the largest [[heavy water reactor]] fleet, are both known to extract tritium from moderator/coolant heavy water, but those amounts are not nearly enough to satisfy global demand of either tritium or helium-3. | }} {{Webarchive|url=https://web.archive.org/web/20151223142855/http://www.ic.gc.ca/opic-cipo/cpd/eng/patent/2810716/summary.html?type=number_search&tabs1Index=tabs1_1 |date=23 December 2015 }}</ref> India and Canada, the two countries with the largest [[heavy water reactor]] fleet, are both known to extract tritium from moderator/coolant heavy water, but those amounts are not nearly enough to satisfy global demand of either tritium or helium-3. | ||
As tritium is also produced inadvertently in various processes in [[light water reactor]]s (see | As tritium is also produced inadvertently in various processes in [[light water reactor]]s (see ''[[Tritium]]'' for details), extraction from those sources could be another source of helium-3. If the annual discharge of tritium (per 2018 figures) at [[La Hague reprocessing facility]] is taken as a basis, the amounts discharged ({{val|31.2|u=g}} at La Hague) are not nearly enough to satisfy demand, even if 100% recovery is achieved. | ||
{{Annual discharge of tritium from nuclear facilities}} | {{Annual discharge of tritium from nuclear facilities}} | ||
==Uses== | == Uses == | ||
===Helium-3 spin echo=== | === Helium-3 spin echo === | ||
Helium-3 can be used to do [[Helium-3 surface spin echo|spin echo experiments of surface dynamics]], which are underway at the Surface Physics Group at [[Cavendish Laboratory|the Cavendish Laboratory]] in Cambridge and in the Chemistry Department at [[Swansea University]]. | Helium-3 can be used to do [[Helium-3 surface spin echo|spin echo experiments of surface dynamics]], which are underway at the Surface Physics Group at [[Cavendish Laboratory|the Cavendish Laboratory]] in Cambridge and in the Chemistry Department at [[Swansea University]]. | ||
===Neutron detection=== | === Neutron detection === | ||
Helium-3 is an important isotope in instrumentation for [[neutron detection]]. It has a high absorption cross section for thermal [[neutron radiation|neutron]] beams and is used as a converter gas in neutron detectors. The neutron is converted through the nuclear reaction | Helium-3 is an important isotope in instrumentation for [[neutron detection]]. It has a high absorption cross section for thermal [[neutron radiation|neutron]] beams and is used as a converter gas in neutron detectors. The neutron is converted through the nuclear reaction | ||
:n + <sup>3</sup>He → <sup>3</sup>H + <sup>1</sup>H + 0.764 MeV | :n + <sup>3</sup>He → <sup>3</sup>H + <sup>1</sup>H + 0.764 MeV | ||
into charged particles [[tritium]] ions (T, <sup>3</sup>H) and [[Hydrogen ions]], or protons (p, <sup>1</sup>H) which then are detected by creating a charge cloud in the stopping gas of a [[proportional counter]] or a [[Geiger–Müller tube]].<ref>[http://www.lanl.gov/quarterly/q_sum03/neutron_detect.shtml A Modular Neutron Detector | Summer 2003| Los Alamos National Laboratory] {{Webarchive|url=https://web.archive.org/web/20080503051236/http://www.lanl.gov/quarterly/q_sum03/neutron_detect.shtml |date=2008-05-03 }}. Lanl.gov. Retrieved on 2011-11-08.</ref> | into charged particles [[tritium]] ions (T, <sup>3</sup>H) and [[Hydrogen ions]], or protons (p, <sup>1</sup>H) which then are detected by creating a charge cloud in the stopping gas of a [[proportional counter]] or a [[Geiger–Müller tube]].<ref>[http://www.lanl.gov/quarterly/q_sum03/neutron_detect.shtml A Modular Neutron Detector | Summer 2003| Los Alamos National Laboratory] {{Webarchive|url=https://web.archive.org/web/20080503051236/http://www.lanl.gov/quarterly/q_sum03/neutron_detect.shtml |date=2008-05-03 }}. Lanl.gov. Retrieved on 2011-11-08.</ref> | ||
Furthermore, the absorption process is strongly [[Spin (physics)|spin]]-dependent, which allows a [[Spin polarization|spin-polarized]] helium-3 volume to transmit neutrons with one spin component while absorbing the other. This effect is employed in [[Polarized neutron scattering|neutron polarization analysis]], a technique which probes for magnetic properties of matter.<ref>[http://www.ncnr.nist.gov/AnnualReport/FY2002_html/pages/neutron_spin.htm NCNR Neutron Spin Filters] {{ | Furthermore, the absorption process is strongly [[Spin (physics)|spin]]-dependent, which allows a [[Spin polarization|spin-polarized]] helium-3 volume to transmit neutrons with one spin component while absorbing the other. This effect is employed in [[Polarized neutron scattering|neutron polarization analysis]], a technique which probes for magnetic properties of matter.<ref>[http://www.ncnr.nist.gov/AnnualReport/FY2002_html/pages/neutron_spin.htm NCNR Neutron Spin Filters] {{webarchive|url=https://web.archive.org/web/20070520100431/http://www.ncnr.nist.gov/AnnualReport/FY2002_html/pages/neutron_spin.htm |date=2007-05-20 }}. Ncnr.nist.gov (2004-04-28). Retrieved on 2011-11-08.</ref><ref>[http://www.ill.eu/science-technology/neutron-technology-at-ill/optics/ <sup>3</sup>He-spin-filters/ ILL <sup>3</sup>He spin filters]{{dead link|date=September 2023 |bot=InternetArchiveBot |fix-attempted=yes }}. Ill.eu (2010-10-22). Retrieved on 2011-11-08.</ref><ref>{{cite journal|url= http://www.ncnr.nist.gov/staff/hammouda/publications/2000_gentile_j_appl_cryst.pdf|title= SANS polarization analysis with nuclear spin-polarized <sup>3</sup>He|doi= 10.1107/S0021889800099817|journal= J. Appl. Crystallogr.|date= 2000|volume= 33|issue= 3|pages= 771–774|last1= Gentile|first1= T.R.|last2= Jones|first2= G.L.|last3= Thompson|first3= A.K.|last4= Barker|first4= J.|last5= Glinka|first5= C.J.|last6= Hammouda|first6= B.|last7= Lynn|first7= J.W.|bibcode= 2000JApCr..33..771G|access-date= 2011-11-08|archive-date= 2012-04-02|archive-url= https://web.archive.org/web/20120402004050/http://www.ncnr.nist.gov/staff/hammouda/publications/2000_gentile_j_appl_cryst.pdf|url-status= live}}</ref><ref>[http://www.ncnr.nist.gov/equipment/he3nsf/index.html Neutron Spin Filters: Polarized <sup>3</sup>He] {{Webarchive|url=https://web.archive.org/web/20111016142515/http://ncnr.nist.gov/equipment/he3nsf/index.html |date=2011-10-16 }}. NIST.gov</ref> | ||
The United States [[Department of Homeland Security]] had hoped to deploy detectors to spot smuggled plutonium in shipping containers by their neutron emissions, but the worldwide shortage of helium-3 following the drawdown in nuclear weapons production since the [[Cold War]] has to some extent prevented this.<ref>{{Cite news |last=Wald |first=Matthew L. |date=2009-11-22 |title=Shortage Slows a Program to Detect Nuclear Bombs |url=https://www.nytimes.com/2009/11/23/us/23helium.html |access-date=2025-05-11 |work=The New York Times |language=en-US |issn=0362-4331}}</ref> As of 2012, DHS determined the commercial supply of [[boron-10]] would support converting its neutron detection infrastructure to that technology.<ref>{{ | The United States [[Department of Homeland Security]] had hoped to deploy detectors to spot smuggled plutonium in shipping containers by their neutron emissions, but the worldwide shortage of helium-3 following the drawdown in nuclear weapons production since the [[Cold War]] has to some extent prevented this.<ref>{{Cite news |last=Wald |first=Matthew L. |date=2009-11-22 |title=Shortage Slows a Program to Detect Nuclear Bombs |url=https://www.nytimes.com/2009/11/23/us/23helium.html |access-date=2025-05-11 |work=The New York Times |language=en-US |issn=0362-4331}}</ref> As of 2012, DHS determined the commercial supply of [[boron-10]] would support converting its neutron detection infrastructure to that technology.<ref>{{cite web |url=http://science.energy.gov/~/media/np/pdf/research/idpra/workshop-on-isotope-federal-supply-and-demand/presentations/Slovik_He3_Alternative_Isotopes_DOE_IP_Workshop_Jan_11_2012.pdf |title=Office of Science |access-date=2014-07-18 |archive-url=https://web.archive.org/web/20140726214826/http://science.energy.gov/~/media/np/pdf/research/idpra/workshop-on-isotope-federal-supply-and-demand/presentations/Slovik_He3_Alternative_Isotopes_DOE_IP_Workshop_Jan_11_2012.pdf |archive-date=2014-07-26 |url-status=dead }}</ref> | ||
===Cryogenics=== | === Cryogenics === | ||
Helium-3 refrigerators are devices used in experimental physics for obtaining temperatures down to about 0.2 [[kelvin]].<ref name="liquidseas">{{cite web |title=Workings of a 3He refrigerator |website=Harvard X-Ray Group Home Page |url=https://liquids.seas.harvard.edu/penanen/workings.html |access-date=2025-04-17}}</ref> By [[evaporative cooling]] of helium-4, a [[1-K pot]] liquefies a small amount of helium-3 in a small vessel called a helium-3 pot. Evaporative cooling at low pressure of the liquid helium-3, usually driven by [[adsorption]] since due to its high price the helium-3 is usually contained in a closed system to avoid losses, cools the helium-3 pot to a fraction of a kelvin. | Helium-3 refrigerators are devices used in experimental physics for obtaining temperatures down to about 0.2 [[kelvin]].<ref name="liquidseas">{{cite web |title=Workings of a 3He refrigerator |website=Harvard X-Ray Group Home Page |url=https://liquids.seas.harvard.edu/penanen/workings.html |access-date=2025-04-17}}</ref> By [[evaporative cooling]] of helium-4, a [[1-K pot]] liquefies a small amount of helium-3 in a small vessel called a helium-3 pot. Evaporative cooling at low pressure of the liquid helium-3, usually driven by [[adsorption]] since, due to its high price, the helium-3 is usually contained in a closed system to avoid losses, cools the helium-3 pot to a fraction of a kelvin. | ||
A [[dilution refrigerator]] uses a mixture of helium-3 and helium-4 to reach [[cryogenics|cryogenic]] temperatures as low as a few thousandths of a kelvin.<ref name="cerndilution">{{cite web |title=Dilution Refrigeration |website=na47sun05.cern.ch |date=2009-02-07 |url=http://na47sun05.cern.ch/target/outline/dilref.html |archive-url=https://web.archive.org/web/20100208194054/http://na47sun05.cern.ch/target/outline/dilref.html |archive-date=2010-02-08 |url-status=dead |access-date=2025-04-17}}</ref> | A [[dilution refrigerator]] uses a mixture of helium-3 and helium-4 to reach [[cryogenics|cryogenic]] temperatures as low as a few thousandths of a kelvin.<ref name="cerndilution">{{cite web |title=Dilution Refrigeration |website=na47sun05.cern.ch |date=2009-02-07 |url=http://na47sun05.cern.ch/target/outline/dilref.html |archive-url=https://web.archive.org/web/20100208194054/http://na47sun05.cern.ch/target/outline/dilref.html |archive-date=2010-02-08 |url-status=dead |access-date=2025-04-17}}</ref> | ||
===Nuclear magnetic resonance=== | === Nuclear magnetic resonance === | ||
Helium-3 nuclei have an intrinsic [[nuclear spin]] of {{ | Helium-3 nuclei have an intrinsic [[nuclear spin]] of {{sfrac|1|2}} ''ħ'', and a relatively high [[gyromagnetic ratio]]. Because of this, it is possible to use [[Nuclear magnetic resonance]] (NMR) to observe helium-3. This analytical technique, usually called <sup>3</sup>He-NMR, can be used to identify helium-containing compounds. It is however limited by the low abundance of helium-3 in comparison to helium-4, which is itself not NMR-active. | ||
Helium-3 can be [[Hyperpolarization (physics)|hyperpolarized]] using non-equilibrium means such as spin-exchange optical pumping.<ref>{{cite journal|title = Hyperpolarized <sup>3</sup>He Gas Production and MR Imaging of the Lung|first1 = Jason C.|last1 = Leawoods|first2 = Dmitriy A.|last2 = Yablonskiy|first3 = Brian|last3 = Saam|first4 = David S.|last4 = Gierada|first5 = Mark S.|last5 = Conradi|date =2001|journal =Concepts in Magnetic Resonance|volume =13|issue = 5|pages =277–293|doi=10.1002/cmr.1014|citeseerx = 10.1.1.492.8128}}</ref> During this process, [[circular polarization|circularly polarized]] infrared laser light, tuned to the appropriate wavelength, is used to excite electrons in an [[alkali metal]], such as [[caesium]] or [[rubidium]] inside a sealed glass vessel. The [[angular momentum]] is transferred from the alkali metal electrons to the noble gas nuclei through collisions. In essence, this process effectively aligns the nuclear spins with the magnetic field in order to enhance the NMR signal. | Helium-3 can be [[Hyperpolarization (physics)|hyperpolarized]] using non-equilibrium means such as spin-exchange optical pumping.<ref>{{cite journal|title = Hyperpolarized <sup>3</sup>He Gas Production and MR Imaging of the Lung|first1 = Jason C.|last1 = Leawoods|first2 = Dmitriy A.|last2 = Yablonskiy|first3 = Brian|last3 = Saam|first4 = David S.|last4 = Gierada|first5 = Mark S.|last5 = Conradi|date =2001|journal =Concepts in Magnetic Resonance|volume =13|issue = 5|pages =277–293|doi=10.1002/cmr.1014|citeseerx = 10.1.1.492.8128}}</ref> During this process, [[circular polarization|circularly polarized]] infrared laser light, tuned to the appropriate wavelength, is used to excite electrons in an [[alkali metal]], such as [[caesium]] or [[rubidium]] inside a sealed glass vessel. The [[angular momentum]] is transferred from the alkali metal electrons to the noble gas nuclei through collisions. In essence, this process effectively aligns the nuclear spins with the magnetic field in order to enhance the NMR signal. | ||
The hyperpolarized gas may then be stored at pressures of 10 atm, for up to 100 hours. Following inhalation, gas mixtures containing the hyperpolarized helium-3 gas can be imaged with an MRI scanner to produce anatomical and functional images of lung ventilation. This technique is also able to produce images of the airway tree, locate unventilated defects, measure the [[pulmonary gas pressures|alveolar oxygen partial pressure]], and measure the [[ventilation/perfusion ratio]]. This technique may be critical for the diagnosis and treatment management of chronic respiratory diseases such as [[chronic obstructive pulmonary disease|chronic obstructive pulmonary disease (COPD)]], [[emphysema]], [[cystic fibrosis]], and [[asthma]].<ref>{{cite journal|title = Hyperpolarized Gas Imaging of the Lung|first1 = Talissa|last1 = Altes|first2 = Michael|last2 = Salerno|date =2004|journal =J Thorac Imaging|volume =19|issue = 4|pages =250–258|doi=10.1097/01.rti.0000142837.52729.38|pmid = 15502612}}</ref> | The hyperpolarized gas may then be stored at pressures of 10 atm, for up to 100 hours. Following inhalation, gas mixtures containing the hyperpolarized helium-3 gas can be imaged with an MRI scanner to produce anatomical and functional images of lung ventilation. This technique is also able to produce images of the airway tree, locate unventilated defects, measure the [[pulmonary gas pressures|alveolar oxygen partial pressure]], and measure the [[ventilation/perfusion ratio]]. This technique may be critical for the diagnosis and treatment management of chronic respiratory diseases such as [[chronic obstructive pulmonary disease|chronic obstructive pulmonary disease (COPD)]], [[emphysema]], [[cystic fibrosis]], and [[asthma]].<ref>{{cite journal|title = Hyperpolarized Gas Imaging of the Lung|first1 = Talissa|last1 = Altes|first2 = Michael|last2 = Salerno|date =2004|journal =J Thorac Imaging|volume =19|issue = 4|pages =250–258|doi=10.1097/01.rti.0000142837.52729.38|pmid = 15502612}}</ref> | ||
Because a helium atom, or even [[Helium dimer#Cage|two helium atoms]], can be encased in [[fullerene]]-like cages, the NMR spectroscopy of this element can be a sensitive probe for changes of the carbon framework around it.<ref>{{cite journal |title= <sup>3</sup>He NMR: A Powerful New Tool for Following Fullerene Chemistry |first1= Martin |last1= Saunders |first2= Hugo A. |last2= Jimenez-Vazquez |first3= Benedict W. |last3= Bangerter |first4= R. James |last4= Cross |first5= Stanley |last5= Mroczkowski |first6= Daron I. |last6= Freedberg |first7= Frank A. L. |last7= Anet |journal= Journal of the American Chemical Society |year= 1994 |volume= 116 |issue= 8 |pages= 3621–3622 |doi= 10.1021/ja00087a067 }}</ref><ref>{{cite web |url= http://chem.ch.huji.ac.il/nmr/techniques/1d/row1/he.html |title= (3He) Helium NMR |author= Institute of Chemistry, The [[Hebrew University of Jerusalem]] }}</ref> Using [[carbon-13 NMR]] to analyze fullerenes themselves is complicated by so many subtle differences among the carbons in anything but the simplest, highly | Because a helium atom, or even [[Helium dimer#Cage|two helium atoms]], can be encased in [[fullerene]]-like cages, the NMR spectroscopy of this element can be a sensitive probe for changes of the carbon framework around it.<ref>{{cite journal |title= <sup>3</sup>He NMR: A Powerful New Tool for Following Fullerene Chemistry |first1= Martin |last1= Saunders |first2= Hugo A. |last2= Jimenez-Vazquez |first3= Benedict W. |last3= Bangerter |first4= R. James |last4= Cross |first5= Stanley |last5= Mroczkowski |first6= Daron I. |last6= Freedberg |first7= Frank A. L. |last7= Anet |journal= Journal of the American Chemical Society |year= 1994 |volume= 116 |issue= 8 |pages= 3621–3622 |doi= 10.1021/ja00087a067 |bibcode= 1994JAChS.116.3621S }}</ref><ref>{{cite web |url= http://chem.ch.huji.ac.il/nmr/techniques/1d/row1/he.html |title= (3He) Helium NMR |author= Institute of Chemistry, The [[Hebrew University of Jerusalem]] }}</ref> Using [[carbon-13 NMR]] to analyze fullerenes themselves is complicated by so many subtle differences among the carbons in anything but the simplest, highly symmetric structures. | ||
===Radio energy absorber for tokamak plasma experiments=== | === Radio energy absorber for tokamak plasma experiments === | ||
Both MIT's [[Alcator C-Mod]] tokamak and the [[Joint European Torus]] (JET) have experimented with adding a little helium-3 to a H–D plasma to increase the absorption of radio-frequency (RF) energy to heat the hydrogen and deuterium ions, a "three-ion" effect.<ref>{{Cite web |url=https://www.popularmechanics.com/science/energy/a27961/mit-nuclear-fusion-experiment-increases-efficiency/ |title=''MIT Achieves Breakthrough in Nuclear Fusion'' Aug 2017 |date=28 August 2017 |access-date=2020-07-18 |archive-date=2020-08-01 |archive-url=https://web.archive.org/web/20200801123209/https://www.popularmechanics.com/science/energy/a27961/mit-nuclear-fusion-experiment-increases-efficiency/ |url-status=live }}</ref><ref>{{cite journal|url= https://www.nature.com/articles/nphys4167.epdf?author_access_token=kPYxN3CzZYD2LT4Si32eOdRgN0jAjWel9jnR3ZoTv0MmuIUEPmNcONMVzXjNf2zbVw9w-V0n8MdnZGKP1E4gbnnf8HWpVEg2srMePcKJH7P-Epjuig2d7CKPHhckCLXI|title= Efficient generation of energetic ions in multi-ion plasmas by radio-frequency heating|journal= Nature Physics|date= 19 June 2017|doi= 10.1038/nphys4167|last1= Kazakov|first1= Ye. O.|last2= Ongena|first2= J.|last3= Wright|first3= J. C.|last4= Wukitch|first4= S. J.|last5= Lerche|first5= E.|last6= Mantsinen|first6= M. J.|last7= Van Eester|first7= D.|last8= Craciunescu|first8= T.|last9= Kiptily|first9= V. G.|last10= Lin|first10= Y.|last11= Nocente|first11= M.|last12= Nabais|first12= F.|last13= Nave|first13= M. F. F.|last14= Baranov|first14= Y.|last15= Bielecki|first15= J.|last16= Bilato|first16= R.|last17= Bobkov|first17= V.|last18= Crombé|first18= K.|last19= Czarnecka|first19= A.|last20= Faustin|first20= J. M.|last21= Felton|first21= R.|last22= Fitzgerald|first22= M.|last23= Gallart|first23= D.|last24= Giacomelli|first24= L.|last25= Golfinopoulos|first25= T.|last26= Hubbard|first26= A. E.|last27= Jacquet|first27= Ph.|last28= Johnson|first28= T.|last29= Lennholm|first29= M.|last30= Loarer|first30= T.|volume= 13|issue= 10|pages= 973–978|bibcode= 2017NatPh..13..973K|hdl= 1721.1/114949|s2cid= 106402331|display-authors= 1|hdl-access= free|access-date= 18 July 2020|archive-date= 1 August 2020|archive-url= https://web.archive.org/web/20200801122526/https://www.nature.com/articles/nphys4167.epdf?author_access_token=kPYxN3CzZYD2LT4Si32eOdRgN0jAjWel9jnR3ZoTv0MmuIUEPmNcONMVzXjNf2zbVw9w-V0n8MdnZGKP1E4gbnnf8HWpVEg2srMePcKJH7P-Epjuig2d7CKPHhckCLXI|url-status= live}}</ref> | Both MIT's [[Alcator C-Mod]] tokamak and the [[Joint European Torus]] (JET) have experimented with adding a little helium-3 to a H–D plasma to increase the absorption of radio-frequency (RF) energy to heat the hydrogen and deuterium ions, a "three-ion" effect.<ref>{{Cite web |url=https://www.popularmechanics.com/science/energy/a27961/mit-nuclear-fusion-experiment-increases-efficiency/ |title=''MIT Achieves Breakthrough in Nuclear Fusion'' Aug 2017 |date=28 August 2017 |access-date=2020-07-18 |archive-date=2020-08-01 |archive-url=https://web.archive.org/web/20200801123209/https://www.popularmechanics.com/science/energy/a27961/mit-nuclear-fusion-experiment-increases-efficiency/ |url-status=live }}</ref><ref>{{cite journal|url= https://www.nature.com/articles/nphys4167.epdf?author_access_token=kPYxN3CzZYD2LT4Si32eOdRgN0jAjWel9jnR3ZoTv0MmuIUEPmNcONMVzXjNf2zbVw9w-V0n8MdnZGKP1E4gbnnf8HWpVEg2srMePcKJH7P-Epjuig2d7CKPHhckCLXI|title= Efficient generation of energetic ions in multi-ion plasmas by radio-frequency heating|journal= Nature Physics|date= 19 June 2017|doi= 10.1038/nphys4167|last1= Kazakov|first1= Ye. O.|last2= Ongena|first2= J.|last3= Wright|first3= J. C.|last4= Wukitch|first4= S. J.|last5= Lerche|first5= E.|last6= Mantsinen|first6= M. J.|last7= Van Eester|first7= D.|last8= Craciunescu|first8= T.|last9= Kiptily|first9= V. G.|last10= Lin|first10= Y.|last11= Nocente|first11= M.|last12= Nabais|first12= F.|last13= Nave|first13= M. F. F.|last14= Baranov|first14= Y.|last15= Bielecki|first15= J.|last16= Bilato|first16= R.|last17= Bobkov|first17= V.|last18= Crombé|first18= K.|last19= Czarnecka|first19= A.|last20= Faustin|first20= J. M.|last21= Felton|first21= R.|last22= Fitzgerald|first22= M.|last23= Gallart|first23= D.|last24= Giacomelli|first24= L.|last25= Golfinopoulos|first25= T.|last26= Hubbard|first26= A. E.|last27= Jacquet|first27= Ph.|last28= Johnson|first28= T.|last29= Lennholm|first29= M.|last30= Loarer|first30= T.|volume= 13|issue= 10|pages= 973–978|bibcode= 2017NatPh..13..973K|hdl= 1721.1/114949|s2cid= 106402331|display-authors= 1|hdl-access= free|access-date= 18 July 2020|archive-date= 1 August 2020|archive-url= https://web.archive.org/web/20200801122526/https://www.nature.com/articles/nphys4167.epdf?author_access_token=kPYxN3CzZYD2LT4Si32eOdRgN0jAjWel9jnR3ZoTv0MmuIUEPmNcONMVzXjNf2zbVw9w-V0n8MdnZGKP1E4gbnnf8HWpVEg2srMePcKJH7P-Epjuig2d7CKPHhckCLXI|url-status= live}}</ref> | ||
===Nuclear fuel=== | === Nuclear fuel === | ||
{{ | {{see also|Aneutronic fusion|Fusion rocket}} | ||
{| class="wikitable" | {| class="wikitable" | ||
|+ Comparison of [[neutronicity]] for different reactions<ref>{{cite web|url=http://members.tm.net/lapointe/IEC_Fusion.html|title=Inertial Electrostatic Confinement Fusion|access-date=2007-05-06|archive-date=2021-01-26|archive-url=https://web.archive.org/web/20210126172744/https://members.tm.net/lapointe/IEC_Fusion.html|url-status=live}}</ref><ref>{{cite web|url=http://www.lancs.ac.uk/ug/suttond1/#fusion|title = Nuclear Fission and Fusion|access-date=2007-05-06|archive-url=https://web.archive.org/web/20070404153838/http://www.lancs.ac.uk/ug/suttond1/#fusion <!-- Bot retrieved archive -->|archive-date=2007-04-04}}</ref><ref>{{cite web|url=http://library.thinkquest.org/28383/nowe_teksty/htmla/2_37a.html|title=The Fusion Reaction|access-date=2007-05-06|archive-date=2013-07-31|archive-url=https://web.archive.org/web/20130731134644/http://library.thinkquest.org/28383/nowe_teksty/htmla/2_37a.html|url-status=dead}}</ref><ref>{{cite web|url=http://fti.neep.wisc.edu/pdf/fdm1291.pdf|title=A Strategy for D – {{SimpleNuclide|Helium|3}} Development|author=John Santarius|date=June 2006|access-date=2007-05-06|archive-date=2007-07-03|archive-url=https://web.archive.org/web/20070703200058/http://fti.neep.wisc.edu/pdf/fdm1291.pdf|url-status=dead}}</ref><ref>{{cite web|url=http://hyperphysics.phy-astr.gsu.edu/hbase/nuclear/nucrea.html|title=Nuclear Reactions|access-date=2007-05-06|archive-date=2000-02-01|archive-url=https://web.archive.org/web/20000201210035/http://hyperphysics.phy-astr.gsu.edu/hbase/Nuclear/nucrea.html|url-status=live}}</ref> | |+ Comparison of [[neutronicity]] for different reactions<ref>{{cite web|url=http://members.tm.net/lapointe/IEC_Fusion.html|title=Inertial Electrostatic Confinement Fusion|access-date=2007-05-06|archive-date=2021-01-26|archive-url=https://web.archive.org/web/20210126172744/https://members.tm.net/lapointe/IEC_Fusion.html|url-status=live}}</ref><ref>{{cite web|url=http://www.lancs.ac.uk/ug/suttond1/#fusion|title = Nuclear Fission and Fusion|access-date=2007-05-06|archive-url=https://web.archive.org/web/20070404153838/http://www.lancs.ac.uk/ug/suttond1/#fusion <!-- Bot retrieved archive -->|archive-date=2007-04-04}}</ref><ref>{{cite web|url=http://library.thinkquest.org/28383/nowe_teksty/htmla/2_37a.html|title=The Fusion Reaction|access-date=2007-05-06|archive-date=2013-07-31|archive-url=https://web.archive.org/web/20130731134644/http://library.thinkquest.org/28383/nowe_teksty/htmla/2_37a.html|url-status=dead}}</ref><ref>{{cite web|url=http://fti.neep.wisc.edu/pdf/fdm1291.pdf|title=A Strategy for D – {{SimpleNuclide|Helium|3}} Development|author=John Santarius|date=June 2006|access-date=2007-05-06|archive-date=2007-07-03|archive-url=https://web.archive.org/web/20070703200058/http://fti.neep.wisc.edu/pdf/fdm1291.pdf|url-status=dead}}</ref><ref>{{cite web|url=http://hyperphysics.phy-astr.gsu.edu/hbase/nuclear/nucrea.html|title=Nuclear Reactions|access-date=2007-05-06|archive-date=2000-02-01|archive-url=https://web.archive.org/web/20000201210035/http://hyperphysics.phy-astr.gsu.edu/hbase/Nuclear/nucrea.html|url-status=live}}</ref> | ||
| Line 170: | Line 183: | ||
! scope="col" | n/MeV | ! scope="col" | n/MeV | ||
|- | |- | ||
! | ! rowspan="3" scope="row" |First-generation fusion fuels | ||
| {{chem2|[[Deuterium|^{2}D]] + ^{2}D}} | | {{chem2|[[Deuterium|^{2}D]] + ^{2}D}} | ||
| {{chem2|^{3}He}} + {{Physics particle|n|TL=1|BL=0}} | | {{chem2|^{3}He}} + {{Physics particle|n|TL=1|BL=0}} | ||
| Line 198: | Line 211: | ||
| 0.046 | | 0.046 | ||
|- | |- | ||
! | ! rowspan="2" scope="row" | Third-generation fusion fuels | ||
| class="nowrap" | {{chem2|^{3}He + ^{3}He}} | | class="nowrap" | {{chem2|^{3}He + ^{3}He}} | ||
| {{chem2|^{4}He}} + 2 {{Physics particle|p|TL=1|BL=1}} | | {{chem2|^{4}He}} + 2 {{Physics particle|p|TL=1|BL=1}} | ||
| Line 217: | Line 230: | ||
{{chem2|^{3}He}} can be produced by the low temperature fusion of {{overset|(D-p)|<sup>2</sup>H + <sup>1</sup>p}} → {{chem2|^{3}He}} + γ + 4.98 MeV. If the fusion temperature is below that for the helium nuclei to fuse, the reaction produces a high energy alpha particle which quickly acquires an electron producing a stable light helium ion which can be utilized directly as a source of electricity without producing dangerous neutrons. [[File:Fusion rxnrate.svg|right|300px|thumb|The fusion [[reaction rate]] increases rapidly with temperature until it maximizes and then gradually drops off. The DT rate peaks at a lower temperature (about 70 keV, or 800 million kelvins) and at a higher value than other reactions commonly considered for fusion energy.]] | {{chem2|^{3}He}} can be produced by the low temperature fusion of {{overset|(D-p)|<sup>2</sup>H + <sup>1</sup>p}} → {{chem2|^{3}He}} + γ + 4.98 MeV. If the fusion temperature is below that for the helium nuclei to fuse, the reaction produces a high energy alpha particle which quickly acquires an electron producing a stable light helium ion which can be utilized directly as a source of electricity without producing dangerous neutrons. [[File:Fusion rxnrate.svg|right|300px|thumb|The fusion [[reaction rate]] increases rapidly with temperature until it maximizes and then gradually drops off. The DT rate peaks at a lower temperature (about 70 keV, or 800 million kelvins) and at a higher value than other reactions commonly considered for fusion energy.]] | ||
{{chem2|^{3}He}} can be used in fusion reactions by either of the reactions {{chem2|^{2}H + ^{3}He -> ^{4}He + ^{1}p}} + 18.3 [[electronvolt|MeV]], or {{chem2|^{3}He + ^{3}He -> ^{4}He + 2 ^{1}p}} + 12.86 MeV. | {{chem2|^{3}He}} can be used in fusion reactions by either of the reactions {{chem2|^{2}H + ^{3}He -> ^{4}He + ^{1}p}} + 18.3 [[electronvolt|MeV]], or {{chem2|^{3}He + ^{3}He -> ^{4}He + 2 ^{1}p}} + 12.86 MeV. | ||
The conventional [[deuterium]] + [[tritium]] ("[[deuterium–tritium fusion|D–T]]") fusion process produces energetic neutrons which render reactor components [[radioactive]] with [[activation product]]s. The appeal of helium-3 fusion stems from the [[aneutronic fusion|aneutronic]] nature of its reaction products. Helium-3 itself is non-radioactive. The lone high-energy by-product, the [[proton]], can be contained by means of electric and magnetic fields. The momentum energy of this proton (created in the fusion process) will interact with the containing electromagnetic field, resulting in direct net electricity generation.<ref>{{cite web|url=http://fti.neep.wisc.edu/presentations/jfs_ieee0904.pdf|title=Lunar {{SimpleNuclide|Helium|3}} and Fusion Power|author=John Santarius|date=September 28, 2004|access-date=2007-05-06|archive-date=2007-07-03|archive-url=https://web.archive.org/web/20070703200103/http://fti.neep.wisc.edu/presentations/jfs_ieee0904.pdf|url-status=dead}}</ref> | The conventional [[deuterium]] + [[tritium]] ("[[deuterium–tritium fusion|D–T]]") fusion process produces energetic neutrons which render reactor components [[radioactive]] with [[activation product]]s. The appeal of helium-3 fusion stems from the [[aneutronic fusion|aneutronic]] nature of its reaction products. Helium-3 itself is non-radioactive. The lone high-energy by-product, the [[proton]], can be contained by means of electric and magnetic fields. The momentum energy of this proton (created in the fusion process) will interact with the containing electromagnetic field, resulting in direct net electricity generation.<ref>{{cite web |url=http://fti.neep.wisc.edu/presentations/jfs_ieee0904.pdf |title=Lunar {{SimpleNuclide|Helium|3}} and Fusion Power |author=John Santarius |date=September 28, 2004 |access-date=2007-05-06 |archive-date=2007-07-03 |archive-url=https://web.archive.org/web/20070703200103/http://fti.neep.wisc.edu/presentations/jfs_ieee0904.pdf |url-status=dead }}</ref> | ||
Because of the higher [[Coulomb barrier]], the temperatures required for {{chem2|^{2}H + ^{3}He}} fusion are much higher than those of conventional [[deuterium–tritium fusion|D–T fusion]]. Moreover, since both reactants need to be mixed together to fuse, reactions between nuclei of the same reactant will occur, and the D–D reaction ({{chem2|^{2}H + ^{2}H}}) does produce a [[neutron]]. Reaction rates vary with temperature, but the D–{{chem2|^{3}He}} reaction rate is never greater than 3.56 times the D–D reaction rate (see graph). Therefore, fusion using D–{{chem2|^{3}He}} fuel at the right temperature and a D-lean fuel mixture, can produce a much lower neutron flux than D–T fusion, but is not clean, negating some of its main attraction. | Because of the higher [[Coulomb barrier]], the temperatures required for {{chem2|^{2}H + ^{3}He}} fusion are much higher than those of conventional [[deuterium–tritium fusion|D–T fusion]]. Moreover, since both reactants need to be mixed together to fuse, reactions between nuclei of the same reactant will occur, and the D–D reaction ({{chem2|^{2}H + ^{2}H}}) does produce a [[neutron]]. Reaction rates vary with temperature, but the D–{{chem2|^{3}He}} reaction rate is never greater than 3.56 times the D–D reaction rate (see graph). Therefore, fusion using D–{{chem2|^{3}He}} fuel at the right temperature and a D-lean fuel mixture, can produce a much lower neutron flux than D–T fusion, but is not clean, negating some of its main attraction. | ||
| Line 225: | Line 238: | ||
The second possibility, fusing {{chem2|^{3}He}} with itself ({{chem2|^{3}He + ^{3}He}}), requires even higher temperatures (since now both reactants have a +2 charge), and thus is even more difficult than the D-{{chem2|^{3}He}} reaction. It offers a theoretical reaction that produces no neutrons; the charged protons produced can be contained in electric and magnetic fields, which in turn directly generates electricity. {{chem2|^{3}He + ^{3}He}} fusion is feasible as demonstrated in the laboratory and has immense advantages, but commercial viability is many years in the future.<ref>{{cite journal|url=http://www.technologyreview.com/energy/19296/|title=Mining the Moon: Lab experiments suggest that future fusion reactors could use helium-3 gathered from the moon|author=Mark Williams|journal=MIT Technology Review|date=August 23, 2007|access-date=2011-01-25|archive-date=2010-12-30|archive-url=https://web.archive.org/web/20101230224725/http://www.technologyreview.com/Energy/19296/|url-status=live}}</ref> | The second possibility, fusing {{chem2|^{3}He}} with itself ({{chem2|^{3}He + ^{3}He}}), requires even higher temperatures (since now both reactants have a +2 charge), and thus is even more difficult than the D-{{chem2|^{3}He}} reaction. It offers a theoretical reaction that produces no neutrons; the charged protons produced can be contained in electric and magnetic fields, which in turn directly generates electricity. {{chem2|^{3}He + ^{3}He}} fusion is feasible as demonstrated in the laboratory and has immense advantages, but commercial viability is many years in the future.<ref>{{cite journal|url=http://www.technologyreview.com/energy/19296/|title=Mining the Moon: Lab experiments suggest that future fusion reactors could use helium-3 gathered from the moon|author=Mark Williams|journal=MIT Technology Review|date=August 23, 2007|access-date=2011-01-25|archive-date=2010-12-30|archive-url=https://web.archive.org/web/20101230224725/http://www.technologyreview.com/Energy/19296/|url-status=live}}</ref> | ||
The amounts of helium-3 needed as a replacement for [[fossil fuel|conventional fuel]]s are substantial by comparison to amounts currently available. The total amount of energy produced in the {{chem2|^{2}D + ^{3}He}} reaction is 18.4 M[[electronvolt|eV]], which corresponds to some 493 [[watt-hour|megawatt-hour]]s (4.93×10<sup>8</sup> W·h) per three [[gram]]s (one [[mole (chemistry)|mole]]) of {{chem2|^{3}He}}. If the total amount of energy could be converted to electrical power with 100% efficiency (a physical impossibility), it would correspond to about 30 minutes of output of a gigawatt electrical plant per mole of {{chem2|^{3}He}}. Thus, a year's production (at 6 grams for each operation hour) would require 52.5 kilograms of helium-3. The amount of fuel needed for large-scale applications can also be put in terms of total consumption: electricity consumption by 107 million U.S. households in 2001<ref>Date from the US Energy Information Administration</ref> totaled 1,140 billion kW·h (1. | The amounts of helium-3 needed as a replacement for [[fossil fuel|conventional fuel]]s are substantial by comparison to amounts currently available. The total amount of energy produced in the {{chem2|^{2}D + ^{3}He}} reaction is 18.4 M[[electronvolt|eV]], which corresponds to some 493 [[watt-hour|megawatt-hour]]s (4.93×10<sup>8</sup> W·h) per three [[gram]]s (one [[mole (chemistry)|mole]]) of {{chem2|^{3}He}}. If the total amount of energy could be converted to electrical power with 100% efficiency (a physical impossibility), it would correspond to about 30 minutes of output of a gigawatt electrical plant per mole of {{chem2|^{3}He}}. Thus, a year's production (at 6 grams for each operation hour) would require 52.5 kilograms of helium-3. The amount of fuel needed for large-scale applications can also be put in terms of total consumption: electricity consumption by 107 million U.S. households in 2001<ref>Date from the US Energy Information Administration</ref> totaled 1,140 billion kW·h ({{val|1.14|e=15|u=W.h}}). Again assuming 100% conversion efficiency, 6.7 [[tonne]]s per year of helium-3 would be required for that segment of the energy demand of the United States, 15 to 20 tonnes per year given a more realistic end-to-end conversion efficiency.{{citation needed|date=January 2011}} | ||
A second-generation approach to controlled [[nuclear fusion|fusion]] power involves combining helium-3 and [[deuterium|deuterium, {{chem2|^{2}D}}]]. This reaction produces an [[alpha particle]] and a high-energy [[proton]]. The most important potential advantage of this fusion reaction for power production as well as other applications lies in its compatibility with the use of [[electrostatic]] fields to control fuel [[ion]]s and the fusion protons. High speed protons, as positively charged particles, can have their kinetic energy converted directly into [[electricity]], through use of [[Solid-state chemistry|solid-state]] conversion materials as well as other techniques. Potential conversion efficiencies of 70% may be possible, as there is no need to convert proton energy to heat in order to drive a [[turbine]]-powered [[Electric generator|electrical generator]].{{ | A second-generation approach to controlled [[nuclear fusion|fusion]] power involves combining helium-3 and [[deuterium|deuterium, {{chem2|^{2}D}}]]. This reaction produces an [[alpha particle]] and a high-energy [[proton]]. The most important potential advantage of this fusion reaction for power production as well as other applications lies in its compatibility with the use of [[electrostatic]] fields to control fuel [[ion]]s and the fusion protons. High speed protons, as positively charged particles, can have their kinetic energy converted directly into [[electricity]], through use of [[Solid-state chemistry|solid-state]] conversion materials as well as other techniques. Potential conversion efficiencies of 70% may be possible, as there is no need to convert proton energy to heat in order to drive a [[turbine]]-powered [[Electric generator|electrical generator]].{{citation needed|date=April 2012}} | ||
====He-3 power plants==== | ==== He-3 power plants ==== | ||
There have been many claims about the capabilities of helium-3 power plants. According to proponents, fusion power plants operating on [[deuterium]] and helium-3 would offer lower capital and [[operating cost]]s than their competitors due to less technical complexity, higher conversion efficiency, smaller size, the absence of radioactive fuel, no air or water [[pollution]], and only low-level [[radioactive]] waste disposal requirements. Recent estimates suggest that about $6 billion in [[Investment (macroeconomics)|investment]] [[Capital (economics)|capital]] will be required to develop and construct the first helium-3 fusion [[power plant]]. Financial break even at today's wholesale [[electricity]] prices (5 US cents per [[kilowatt-hour]]) would occur after five 1-[[gigawatt]] plants were on line, replacing old conventional plants or meeting new demand.<ref>{{cite news|url=http://www.popularmechanics.com/science/air_space/1283056.html?page=4|title=Mining The Moon|author=Paul DiMare|date=October 2004|work=Popular Mechanics|access-date=2007-05-06|archive-url=https://web.archive.org/web/20070814162104/http://www.popularmechanics.com/science/air_space/1283056.html?page=4|archive-date=2007-08-14|url-status=dead}}</ref> | There have been many claims about the capabilities of helium-3 power plants. According to proponents, fusion power plants operating on [[deuterium]] and helium-3 would offer lower capital and [[operating cost]]s than their competitors due to less technical complexity, higher conversion efficiency, smaller size, the absence of radioactive fuel, no air or water [[pollution]], and only low-level [[radioactive]] waste disposal requirements. Recent estimates suggest that about $6 billion in [[Investment (macroeconomics)|investment]] [[Capital (economics)|capital]] will be required to develop and construct the first helium-3 fusion [[power plant]]. Financial break even at today's wholesale [[electricity]] prices (5 US cents per [[kilowatt-hour]]) would occur after five 1-[[gigawatt]] plants were on line, replacing old conventional plants or meeting new demand.<ref>{{cite news |url=http://www.popularmechanics.com/science/air_space/1283056.html?page=4 |title=Mining The Moon |author=Paul DiMare |date=October 2004 |work=Popular Mechanics |access-date=2007-05-06 |archive-url=https://web.archive.org/web/20070814162104/http://www.popularmechanics.com/science/air_space/1283056.html?page=4 |archive-date=2007-08-14 |url-status=dead }}</ref> | ||
The reality is not so clear-cut. The most advanced fusion programs in the world are [[inertial confinement fusion]] (such as [[National Ignition Facility]]) and [[magnetic confinement fusion]] (such as [[ITER]] and [[Wendelstein 7-X]]). In the case of the former, there is no solid roadmap to power generation. In the case of the latter, commercial power generation is not expected until around 2050.<ref>{{cite news|url=http://www.iter.org/proj/Pages/ITERAndBeyond.aspx |title=ITER & Beyond |access-date=2009-08-04 |url-status=dead |archive-url=https://web.archive.org/web/20090520151601/http://www.iter.org/PROJ/Pages/ITERAndBeyond.aspx |archive-date=2009-05-20 }}</ref> In both cases, the type of fusion discussed is the simplest: D–T fusion. The reason for this is the very low [[Coulomb barrier]] for this reaction; for D+<sup>3</sup>He, the barrier is much higher, and it is even higher for <sup>3</sup>He–<sup>3</sup>He. The immense cost of reactors like [[ITER]] and [[National Ignition Facility]] are largely due to their immense size, yet to scale up to higher plasma temperatures would require reactors far larger still. The 14.7 MeV proton and 3.6 MeV alpha particle from D–<sup>3</sup>He fusion, plus the higher conversion efficiency, means that more electricity is obtained per kilogram than with [[deuterium–tritium fusion|D–T fusion]] (17.6 MeV), but not that much more. As a further downside, the rates of reaction for [[Aneutronic fusion#Candidate reactions|helium-3 fusion reactions]] are not particularly high, requiring a reactor that is larger still or more reactors to produce the same amount of electricity. | The reality is not so clear-cut. The most advanced fusion programs in the world are [[inertial confinement fusion]] (such as [[National Ignition Facility]]) and [[magnetic confinement fusion]] (such as [[ITER]] and [[Wendelstein 7-X]]). In the case of the former, there is no solid roadmap to power generation. In the case of the latter, commercial power generation is not expected until around 2050.<ref>{{cite news |url=http://www.iter.org/proj/Pages/ITERAndBeyond.aspx |title=ITER & Beyond |access-date=2009-08-04 |url-status=dead |archive-url=https://web.archive.org/web/20090520151601/http://www.iter.org/PROJ/Pages/ITERAndBeyond.aspx |archive-date=2009-05-20 }}</ref> In both cases, the type of fusion discussed is the simplest: D–T fusion. The reason for this is the very low [[Coulomb barrier]] for this reaction; for D+<sup>3</sup>He, the barrier is much higher, and it is even higher for <sup>3</sup>He–<sup>3</sup>He. The immense cost of reactors like [[ITER]] and [[National Ignition Facility]] are largely due to their immense size, yet to scale up to higher plasma temperatures would require reactors far larger still. The 14.7 MeV proton and 3.6 MeV alpha particle from D–<sup>3</sup>He fusion, plus the higher conversion efficiency, means that more electricity is obtained per kilogram than with [[deuterium–tritium fusion|D–T fusion]] (17.6 MeV), but not that much more. As a further downside, the rates of reaction for [[Aneutronic fusion#Candidate reactions|helium-3 fusion reactions]] are not particularly high, requiring a reactor that is larger still or more reactors to produce the same amount of electricity. | ||
In 2022, [[Helion Energy]] claimed that their 7th fusion prototype (Polaris; fully funded and under construction as of September 2022) will demonstrate "net electricity from fusion", and will demonstrate "helium-3 production through deuterium–deuterium fusion" by means of a "patented high-efficiency closed-fuel cycle".<ref>{{cite web |url=https://www.helionenergy.com/faq/ |title=Helion FAQ |accessdate=29 September 2022}}</ref> | In 2022, [[Helion Energy]] claimed that their 7th fusion prototype (Polaris; fully funded and under construction as of September 2022) will demonstrate "net electricity from fusion", and will demonstrate "helium-3 production through deuterium–deuterium fusion" by means of a "patented high-efficiency closed-fuel cycle".<ref>{{cite web |url=https://www.helionenergy.com/faq/ |title=Helion FAQ |accessdate=29 September 2022}}</ref> | ||
====Alternatives to He-3==== | ==== Alternatives to He-3 ==== | ||
To attempt to work around this problem of massively large power plants that may not even be economical with D–T fusion, let alone the far more challenging D–<sup>3</sup>He fusion, a number of other reactors have been proposed – the [[Fusor]], [[Polywell]], [[Focus fusion]], and many more, though many of these concepts have fundamental problems with achieving a net energy gain, and generally attempt to achieve fusion in thermal disequilibrium, something that could potentially prove impossible,<ref>{{cite news|title=A general critique of inertial-electrostatic confinement fusion systems|author= Todd Rider|hdl = 1721.1/29869}}</ref> and consequently, these long-shot programs tend to have trouble garnering funding despite their low budgets. Unlike the "big" and "hot" fusion systems, if such systems worked, they could scale to the higher barrier [[aneutronic fusion|aneutronic]] fuels, and so their proponents tend to promote [[Aneutronic fusion#Boron|p-B fusion]], which requires no exotic fuel such as helium-3 | To attempt to work around this problem of massively large power plants that may not even be economical with D–T fusion, let alone the far more challenging D–<sup>3</sup>He fusion, a number of other reactors have been proposed – the [[Fusor]], [[Polywell]], [[Focus fusion]], and many more, though many of these concepts have fundamental problems with achieving a net energy gain, and generally attempt to achieve fusion in thermal disequilibrium, something that could potentially prove impossible,<ref>{{cite news |title=A general critique of inertial-electrostatic confinement fusion systems |author=Todd Rider |hdl=1721.1/29869 }}</ref> and consequently, these long-shot programs tend to have trouble garnering funding despite their low budgets. Unlike the "big" and "hot" fusion systems, if such systems worked, they could scale to the higher barrier [[aneutronic fusion|aneutronic]] fuels, and so their proponents tend to promote [[Aneutronic fusion#Boron|p-B fusion]], which requires no exotic fuel such as helium-3. | ||
== See also == | == See also == | ||
| Line 303: | Line 298: | ||
|title=Return to the Moon: Exploration, Enterprise, and Energy in the Human Settlement of Space | |title=Return to the Moon: Exploration, Enterprise, and Energy in the Human Settlement of Space | ||
|publisher=Springer | |publisher=Springer | ||
|ref=Schmitt}} | |ref=Schmitt}} | ||
* {{cite book | * {{cite book | ||
|author=J. Wilks | |author=J. Wilks | ||
| Line 309: | Line 304: | ||
|title=The properties of liquid and solid helium | |title=The properties of liquid and solid helium | ||
|publisher=Oxford University Press | |publisher=Oxford University Press | ||
|ref=Wilks}} | |ref=Wilks}} | ||
* {{cite book | * {{cite book | ||
|author=E. R. Dobbs | |author=E. R. Dobbs | ||
| Line 315: | Line 310: | ||
|title=Helium three | |title=Helium three | ||
|publisher=Oxford University Press | |publisher=Oxford University Press | ||
|ref=Dobbs}} | |ref=Dobbs}} | ||
* {{cite book | * {{cite book | ||
|author=G. E. Volovik | |author=G. E. Volovik | ||
| Line 333: | Line 328: | ||
|title=Helium three: proceedings of the Second Symposium on Liquid and Solid Helium Three, held at the Ohio State University, August 23--25, 1960 | |title=Helium three: proceedings of the Second Symposium on Liquid and Solid Helium Three, held at the Ohio State University, August 23--25, 1960 | ||
|publisher=Ohio State University Press | |publisher=Ohio State University Press | ||
|ref=Daunt}} | |ref=Daunt}} | ||
== External links == | == External links == | ||
* [http://nobelprize.org/physics/laureates/2003/presentation-speech.html The Nobel Prize in Physics 2003, presentation speech] {{Webarchive|url=https://web.archive.org/web/20080723225703/http://nobelprize.org/physics/laureates/2003/presentation-speech.html |date=2008-07-23 }} | * [http://nobelprize.org/physics/laureates/2003/presentation-speech.html The Nobel Prize in Physics 2003, presentation speech] {{Webarchive|url=https://web.archive.org/web/20080723225703/http://nobelprize.org/physics/laureates/2003/presentation-speech.html |date=2008-07-23 }} | ||
* [http://www.bbc.co.uk/sn/tvradio/programmes/horizon/broadband/tx/moonsale/ ''Moon for Sale'': A BBC Horizon documentary on the possibility of lunar mining of Helium-3] | * [https://web.archive.org/web/20070712123222/http://www.bbc.co.uk/sn/tvradio/programmes/horizon/broadband/tx/moonsale/ ''Moon for Sale'': A BBC Horizon documentary on the possibility of lunar mining of Helium-3] | ||
{{ | {{isotope sequence | ||
|element=helium | |element=helium | ||
|lighter=[[diproton]] | |lighter=[[diproton]] | ||
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|after=Stable | |after=Stable | ||
}} | }} | ||
{{Authority control}} | {{Authority control}} | ||
Latest revision as of 18:47, 19 November 2025
Template:Short description Script error: No such module "about". Script error: No such module "Infobox".Template:Template otherScript error: No such module "Check for unknown parameters". Helium-3 (3He[1][2] see also helion) is a light, stable isotope of helium with two protons and one neutron. (In contrast, the most common isotope, helium-4, has two protons and two neutrons.) Helium-3 and hydrogen-1 are the only stable nuclides with more protons than neutrons. It was discovered in 1939. Helium-3 atoms are fermionic and become a superfluid at the temperature of 2.491 mK.
Helium-3 occurs as a primordial nuclide, escaping from Earth's crust into its atmosphere and into outer space over millions of years. It is also thought to be a natural nucleogenic and cosmogenic nuclide, one produced when lithium is bombarded by natural neutrons, which can be released by spontaneous fission and by nuclear reactions with cosmic rays. Some found in the terrestrial atmosphere is a remnant of atmospheric and underwater nuclear weapons testing.
Nuclear fusion using helium-3 has long been viewed as a desirable future energy source. The fusion of two of its atoms would be aneutronic, that is, it would not release the dangerous radiation of traditional fusion or require the much higher temperatures thereof.[3] The process may unavoidably create other reactions that themselves would cause the surrounding material to become radioactive.[4]
Helium-3 is thought to be more abundant on the Moon than on Earth, having been deposited in the upper layer of regolith by the solar wind over billions of years,[5] though still lower in abundance than in the Solar System's gas giants.[6][7]
History
The existence of helium-3 was first proposed in 1934 by the Australian nuclear physicist Mark Oliphant while he was working at the University of Cambridge Cavendish Laboratory. Oliphant had performed experiments in which fast deuterons collided with deuteron targets (incidentally, the first demonstration of nuclear fusion).[8] Isolation of helium-3 was first accomplished by Luis Alvarez and Robert Cornog in 1939.[9][10] Helium-3 was thought to be a radioactive isotope until it was also found in samples of natural helium, which is mostly helium-4, taken both from the terrestrial atmosphere and from natural gas wells.[11]
Physical properties
Due to its low atomic mass of 3.016 Da, helium-3 has some physical properties different from those of helium-4, with a mass of 4.0026 Da. On account of the weak, induced dipole–dipole interaction between the helium atoms, their microscopic physical properties are mainly determined by their zero-point energy. Also, the microscopic properties of helium-3 cause it to have a higher zero-point energy than helium-4. This implies that helium-3 can overcome dipole–dipole interactions with less thermal energy than helium-4 can.
The quantum mechanical effects on helium-3 and helium-4 are significantly different because with two protons, two neutrons, and two electrons, helium-4 has an overall spin of zero, making it a boson, but with one fewer neutron, helium-3 has an overall spin of one half, making it a fermion.
Pure helium-3 gas boils at 3.19 K compared with helium-4 at 4.23 K, and its critical point is also lower at 3.35 K, compared with helium-4 at 5.2 K. Helium-3 has less than half the density of helium-4 when it is at its boiling point: 59 g/L compared to 125 g/L of helium-4 at a pressure of one atmosphere. Its latent heat of vaporization is also considerably lower at 0.026 kJ/mol compared with the 0.0829 kJ/mol of helium-4.[12][13]
Superfluidity
An important property of helium-3 atoms, which distinguishes them from the more common helium-4, is that they contain an odd number of spin <templatestyles src="Fraction/styles.css" />1⁄2 particles, and therefore are composite fermions. This is a direct result of the addition rules for quantized angular momentum. In contrast, helium-4 atoms are bosons, containing an even number of spin-Template:Sfrac particles. At low temperatures (about 2.17 K), helium-4 undergoes a phase transition: A fraction of it enters a superfluid phase that can be roughly understood as a type of Bose–Einstein condensate. Such a mechanism is not available for fermionic helium-3 atoms. Many speculated that helium-3 could also become a superfluid at much lower temperatures, if the atoms formed into pairs analogous to Cooper pairs in the BCS theory of superconductivity. Each Cooper pair, having integer spin, can be thought of as a boson. During the 1970s, David Lee, Douglas Osheroff and Robert Coleman Richardson discovered two phase transitions along the melting curve, which were soon realized to be the two superfluid phases of helium-3.[14][15] The transition to a superfluid occurs at 2.491 millikelvins on the melting curve. They were awarded the 1996 Nobel Prize in Physics for their discovery. Alexei Abrikosov, Vitaly Ginzburg, and Tony Leggett won the 2003 Nobel Prize in Physics for their work on refining understanding of the superfluid phase of helium-3.[16]
In a zero magnetic field, there are two distinct superfluid phases of 3He, the A-phase and the B-phase. The B-phase is the low-temperature, low-pressure phase which has an isotropic energy gap. The A-phase is the higher temperature, higher pressure phase that is further stabilized by a magnetic field and has two point nodes in its gap. The presence of two phases is a clear indication that 3He is an unconventional superfluid (superconductor), since the presence of two phases requires an additional symmetry, other than gauge symmetry, to be broken. In fact, it is a p-wave superfluid, with spin one, S = 1 ħ, and angular momentum one, L = 1 ħ. The ground state corresponds to total angular momentum zero, J = S + L = 0 (vector addition). Excited states are possible with non-zero total angular momentum, J > 0, which are excited pair collective modes. These collective modes have been studied with much greater precision than in any other unconventional pairing system, because of the extreme purity of superfluid 3He. This purity is due to all 4He phase separating entirely and all other materials solidifying and sinking to the bottom of the liquid, making the A- and B-phases of 3He the most pure condensed matter state possible.
Natural abundance
Terrestrial abundance
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3He is a primordial substance in the Earth's mantle, thought to have been trapped during the planet's initial formation. The ratio of 3He to 4He within the Earth's crust and mantle is less than that in the solar disk (as estimated using meteorite and lunar samples), with terrestrial materials generally containing lower 3He/4He ratios due to production of 4He from radioactive decay.
3He has a cosmological ratio of 300 atoms per million atoms of 4He,[17] leading to the assumption that the original ratio of these primordial gases in the mantle was around 200–300 ppm when Earth was formed. Over the course of Earth's history, a significant amount of 4He has been generated by the alpha decay of uranium, thorium and other radioactive isotopes, to the point that only around 7% of the helium now in the mantle is primordial helium,[17] thus lowering the total 3He:4He ratio to around 20 ppm. Ratios of 3He:4He in excess of the atmospheric ratio are indicative of a contribution of 3He from the mantle. Crustal sources are dominated by the 4He produced by radioactive decay.
The ratio of helium-3 to helium-4 in natural Earth-bound sources varies greatly.[18][19] Samples of the lithium ore spodumene from Edison Mine, South Dakota were found to contain 12 parts of helium-3 to a million parts of helium-4. Samples from other mines showed 2 parts per million.[18]
Helium itself is present as up to 7% of some natural gas sources,[20] and large sources have over 0.5% (above 0.2% makes it viable to extract).[21] The fraction of 3He in helium separated from natural gas in the U.S. was found to range from 70 to 242 parts per billion.[22][23] Hence the US 2002 stockpile of 1 billion normal m3[21] would have contained about Template:Convert of helium-3. According to American physicist Richard Garwin, about Template:Convert or almost Template:Convert of 3He is available annually for separation from the US natural gas stream. If the process of separating out the 3He could employ as feedstock the liquefied helium typically used to transport and store bulk quantities, estimates for the incremental energy cost range from Template:Val NTP, excluding the cost of infrastructure and equipment.[22] Algeria's annual gas production is assumed to contain 100 million normal cubic metres[21] and this would contain between Template:Val of helium-3 (about Template:Val) assuming a similar 3He fraction.
3He is also present in the Earth's atmosphere. The natural abundance of 3He in atmospheric helium is Template:Val (1.37 parts per million).[24] The partial pressure of helium in the Earth's atmosphere is about Template:Val, and thus helium accounts for 5.2 parts per million of the total pressure (Template:Val) in the Earth's atmosphere, and 3He thus accounts for 7.2 parts per trillion of the atmosphere. Since the atmosphere of the Earth has a mass of about Template:Val,[25] the mass of 3He in the Earth's atmosphere is the product of these numbers and the molecular weight ratio of helium-3 to air (3.016 to 28.95), giving a mass of 3815 tonnes of helium-3 in the earth's atmosphere.
3He is produced on Earth from three sources: lithium spallation, cosmic rays, and beta decay of tritium (3H). The contribution from cosmic rays is negligible within all except the oldest regolith materials, and lithium spallation reactions are a lesser contributor than the production of 4He by alpha particle emissions.
The total amount of helium-3 in the mantle may be in the range of 0.1–1 megatonnes. Some helium-3 finds its way up through deep-sourced hotspot volcanoes such as those of the Hawaiian Islands, but only Template:Val per year is emitted to the atmosphere. Mid-ocean ridges emit another 3 kg per year. Around subduction zones, various sources produce helium-3 in natural gas deposits which possibly contain a thousand tonnes of helium-3 (although there may be 25 thousand tonnes if all ancient subduction zones have such deposits). Wittenberg estimated that United States crustal natural gas sources may have only half a tonne total.[26] Wittenberg cited Anderson's estimate of another 1200 tonnes in interplanetary dust particles on the ocean floors.[27] In the 1994 study, extracting helium-3 from these sources consumes more energy than fusion would release.[28]
Moon
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Materials on the Moon's surface contain helium-3 at concentrations between 1.4 and 15 ppb in sunlit areas,[29][30] and may contain concentrations as much as 50 ppb in permanently shadowed regions.[7] A number of people, starting with Gerald Kulcinski in 1986,[31] have proposed to explore the Moon, mine lunar regolith and use the helium-3 for fusion. Because of the low concentrations of helium-3, any mining equipment would need to process extremely large amounts of regolith (over 150 tonnes of regolith to obtain one gram of helium-3).[32]
The primary objective of Indian Space Research Organisation's first lunar probe called Chandrayaan-1, launched on October 22, 2008, was reported in some sources to be mapping the Moon's surface for helium-3-containing minerals.[33] No such objective is mentioned in the project's official list of goals, though many of its scientific payloads have held helium-3-related applications.[34][35]
Cosmochemist and geochemist Ouyang Ziyuan from the Chinese Academy of Sciences who is now in charge of the Chinese Lunar Exploration Program has already stated on many occasions that one of the main goals of the program would be the mining of helium-3, from which operation "each year, three space shuttle missions could bring enough fuel for all human beings across the world".[36]
In January 2006, the Russian space company RKK Energiya announced that it considers lunar helium-3 a potential economic resource to be mined by 2020,[37] if funding can be found.[38][39]
Not all writers feel the extraction of lunar helium-3 is feasible, or even that there will be a demand for it for fusion. Dwayne Day, writing in The Space Review in 2015, characterises helium-3 extraction from the Moon for use in fusion as magical thinking about an unproven technology, and questions the feasibility of lunar extraction, as compared to production on Earth.[40]
Gas giants
Mining gas giants for helium-3 has also been proposed.[41] The British Interplanetary Society's hypothetical Project Daedalus interstellar probe design was fueled by helium-3 mines in the atmosphere of Jupiter, for example.
Solar nebula (primordial) abundance
One early estimate of the primordial ratio of 3He to 4He in the solar nebula has been the measurement of their ratio in the atmosphere of Jupiter, measured by the mass spectrometer of the Galileo atmospheric entry probe. This ratio is about 1:10000,[42] or 100 parts of 3He per million parts of 4He. This is roughly the same ratio of the isotopes as in lunar regolith, which contains 28 ppm helium-4 and 2.8 ppb helium-3 (which is at the lower end of actual sample measurements, which vary from about 1.4 to 15 ppb). Terrestrial ratios of the isotopes are lower by a factor of 100, mainly due to enrichment of helium-4 stocks in the mantle by billions of years of alpha decay from uranium, thorium as well as their decay products and extinct radionuclides.
Human production
Tritium decay
Script error: No such module "Labelled list hatnote". Virtually all helium-3 used in industry today is produced from the radioactive decay of tritium, given its very low natural abundance and its very high cost.
Production, sales and distribution of helium-3 in the United States are managed by the US Department of Energy (DOE) DOE Isotope Program.[43]
While tritium has several different experimentally determined values of its half-life, NIST lists Template:Val (Template:Val).[44] It decays into helium-3 by beta decay as in this nuclear equation:
Among the total released energy of Template:Val, the part taken by electron's kinetic energy varies, with an average of Template:Val, while the remaining energy is carried off by the nearly undetectable electron antineutrino. Beta particles from tritium can penetrate only about Template:Convert of air, and they are incapable of passing through the dead outermost layer of human skin.[45] The unusually low energy released in the tritium beta decay makes the decay (along with that of rhenium-187) appropriate for absolute neutrino mass measurements in the laboratory (the most recent experiment being KATRIN).
The low energy of tritium's radiation makes it difficult to detect tritium-labeled compounds except by using liquid scintillation counting.
Tritium is a radioactive isotope of hydrogen and is typically produced by bombarding lithium-6 with neutrons in a nuclear reactor. The lithium nucleus absorbs a neutron and splits into helium-4 and tritium. Tritium decays into helium-3 with a half-life of Template:Val, so helium-3 can be produced by simply storing the tritium until it undergoes radioactive decay. As tritium forms a stable compound with oxygen (tritiated water) while helium-3 does not, the storage and collection process could continuously collect the material that outgasses from the stored material.
Tritium is a critical component of nuclear weapons and historically it was produced and stockpiled primarily for this application. The decay of tritium into helium-3 reduces the explosive power of the fusion warhead, so periodically the accumulated helium-3 must be removed from warhead reservoirs and tritium in storage. Helium-3 removed during this process is marketed for other applications.
For decades this has been, and remains, the principal source of the world's helium-3.[46] Since the signing of the START I Treaty in 1991 the number of nuclear warheads that are kept ready for use has decreased.[47][48] This has reduced the quantity of helium-3 available from this source. Helium-3 stockpiles have been further diminished by increased demand,[22] primarily for use in neutron radiation detectors and medical diagnostic procedures. US industrial demand for helium-3 reached a peak of Template:Val litres (approximately Template:Val) per year in 2008. Price at auction, historically about $100 per litre, reached as high as $2000 per litre.[49] Since then, demand for helium-3 has declined to about 6000 litres per year due to the high cost and efforts by the DOE to recycle it and find substitutes. Assuming a density of Template:Val at $100/L helium-3 would be about a thirtieth as expensive as tritium (roughly $880/g vs. roughly $Template:Val per gram) while at $2000 per litre, helium-3 would be about half as expensive as tritium ($Template:Val/g vs. $Template:Val/g).
The DOE recognized the developing shortage of both tritium and helium-3, and began producing tritium by lithium irradiation at the Tennessee Valley Authority's Watts Bar Nuclear Generating Station in 2010.[22] In this process tritium-producing burnable absorber rods (TPBARs) containing lithium in a ceramic form are inserted into the reactor in place of the normal boron control rods[50] Periodically the TPBARs are replaced and the tritium extracted.
Currently only two commercial nuclear reactors (Watts Bar Nuclear Plant Units 1 and 2) are being used for tritium production but the process could, if necessary, be vastly scaled up to meet any conceivable demand simply by utilizing more of the nation's power reactorsScript error: No such module "Unsubst".. Substantial quantities of tritium and helium-3 could also be extracted from the heavy water moderator in CANDU nuclear reactors.[22][51] India and Canada, the two countries with the largest heavy water reactor fleet, are both known to extract tritium from moderator/coolant heavy water, but those amounts are not nearly enough to satisfy global demand of either tritium or helium-3.
As tritium is also produced inadvertently in various processes in light water reactors (see Tritium for details), extraction from those sources could be another source of helium-3. If the annual discharge of tritium (per 2018 figures) at La Hague reprocessing facility is taken as a basis, the amounts discharged (Template:Val at La Hague) are not nearly enough to satisfy demand, even if 100% recovery is achieved. Template:Annual discharge of tritium from nuclear facilities
Uses
Helium-3 spin echo
Helium-3 can be used to do spin echo experiments of surface dynamics, which are underway at the Surface Physics Group at the Cavendish Laboratory in Cambridge and in the Chemistry Department at Swansea University.
Neutron detection
Helium-3 is an important isotope in instrumentation for neutron detection. It has a high absorption cross section for thermal neutron beams and is used as a converter gas in neutron detectors. The neutron is converted through the nuclear reaction
- n + 3He → 3H + 1H + 0.764 MeV
into charged particles tritium ions (T, 3H) and Hydrogen ions, or protons (p, 1H) which then are detected by creating a charge cloud in the stopping gas of a proportional counter or a Geiger–Müller tube.[52]
Furthermore, the absorption process is strongly spin-dependent, which allows a spin-polarized helium-3 volume to transmit neutrons with one spin component while absorbing the other. This effect is employed in neutron polarization analysis, a technique which probes for magnetic properties of matter.[53][54][55][56]
The United States Department of Homeland Security had hoped to deploy detectors to spot smuggled plutonium in shipping containers by their neutron emissions, but the worldwide shortage of helium-3 following the drawdown in nuclear weapons production since the Cold War has to some extent prevented this.[57] As of 2012, DHS determined the commercial supply of boron-10 would support converting its neutron detection infrastructure to that technology.[58]
Cryogenics
Helium-3 refrigerators are devices used in experimental physics for obtaining temperatures down to about 0.2 kelvin.[59] By evaporative cooling of helium-4, a 1-K pot liquefies a small amount of helium-3 in a small vessel called a helium-3 pot. Evaporative cooling at low pressure of the liquid helium-3, usually driven by adsorption since, due to its high price, the helium-3 is usually contained in a closed system to avoid losses, cools the helium-3 pot to a fraction of a kelvin.
A dilution refrigerator uses a mixture of helium-3 and helium-4 to reach cryogenic temperatures as low as a few thousandths of a kelvin.[60]
Nuclear magnetic resonance
Helium-3 nuclei have an intrinsic nuclear spin of Template:Sfrac ħ, and a relatively high gyromagnetic ratio. Because of this, it is possible to use Nuclear magnetic resonance (NMR) to observe helium-3. This analytical technique, usually called 3He-NMR, can be used to identify helium-containing compounds. It is however limited by the low abundance of helium-3 in comparison to helium-4, which is itself not NMR-active.
Helium-3 can be hyperpolarized using non-equilibrium means such as spin-exchange optical pumping.[61] During this process, circularly polarized infrared laser light, tuned to the appropriate wavelength, is used to excite electrons in an alkali metal, such as caesium or rubidium inside a sealed glass vessel. The angular momentum is transferred from the alkali metal electrons to the noble gas nuclei through collisions. In essence, this process effectively aligns the nuclear spins with the magnetic field in order to enhance the NMR signal.
The hyperpolarized gas may then be stored at pressures of 10 atm, for up to 100 hours. Following inhalation, gas mixtures containing the hyperpolarized helium-3 gas can be imaged with an MRI scanner to produce anatomical and functional images of lung ventilation. This technique is also able to produce images of the airway tree, locate unventilated defects, measure the alveolar oxygen partial pressure, and measure the ventilation/perfusion ratio. This technique may be critical for the diagnosis and treatment management of chronic respiratory diseases such as chronic obstructive pulmonary disease (COPD), emphysema, cystic fibrosis, and asthma.[62]
Because a helium atom, or even two helium atoms, can be encased in fullerene-like cages, the NMR spectroscopy of this element can be a sensitive probe for changes of the carbon framework around it.[63][64] Using carbon-13 NMR to analyze fullerenes themselves is complicated by so many subtle differences among the carbons in anything but the simplest, highly symmetric structures.
Radio energy absorber for tokamak plasma experiments
Both MIT's Alcator C-Mod tokamak and the Joint European Torus (JET) have experimented with adding a little helium-3 to a H–D plasma to increase the absorption of radio-frequency (RF) energy to heat the hydrogen and deuterium ions, a "three-ion" effect.[65][66]
Nuclear fuel
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| Reactants | Products | Q | n/MeV | |
|---|---|---|---|---|
| First-generation fusion fuels | Template:Chem2 | Template:Chem2 + Template:Physics particle | 3.268 MeV | 0.306 |
| Template:Chem2 | Template:Chem2 + Template:Physics particle | 4.032 MeV | 0 | |
| Template:Chem2 | Template:Chem2 + Template:Physics particle | 17.571 MeV | 0.057 | |
| Second-generation fusion fuel | Template:Chem2 | Template:Chem2 + Template:Physics particle | 18.354 MeV | 0 |
| Net result of 2D burning (sum of first 4 rows) | Template:Chem2 | 2(Template:Chem2 + n + p) | 43.225 MeV | 0.046 |
| Third-generation fusion fuels | Template:Chem2 | Template:Chem2 + 2 Template:Physics particle | 12.86 MeV | 0 |
| Template:Chem2 + Template:Physics particle | 3 Template:Chem2 | 8.68 MeV | 0 | |
| Current nuclear fuel | Template:Chem2 | 2 FP+ 2.5n | ~200 MeV | 0.0075 |
Template:Chem2 can be produced by the low temperature fusion of Template:Overset → Template:Chem2 + γ + 4.98 MeV. If the fusion temperature is below that for the helium nuclei to fuse, the reaction produces a high energy alpha particle which quickly acquires an electron producing a stable light helium ion which can be utilized directly as a source of electricity without producing dangerous neutrons.
Template:Chem2 can be used in fusion reactions by either of the reactions Template:Chem2 + 18.3 MeV, or Template:Chem2 + 12.86 MeV.
The conventional deuterium + tritium ("D–T") fusion process produces energetic neutrons which render reactor components radioactive with activation products. The appeal of helium-3 fusion stems from the aneutronic nature of its reaction products. Helium-3 itself is non-radioactive. The lone high-energy by-product, the proton, can be contained by means of electric and magnetic fields. The momentum energy of this proton (created in the fusion process) will interact with the containing electromagnetic field, resulting in direct net electricity generation.[72]
Because of the higher Coulomb barrier, the temperatures required for Template:Chem2 fusion are much higher than those of conventional D–T fusion. Moreover, since both reactants need to be mixed together to fuse, reactions between nuclei of the same reactant will occur, and the D–D reaction (Template:Chem2) does produce a neutron. Reaction rates vary with temperature, but the D–Template:Chem2 reaction rate is never greater than 3.56 times the D–D reaction rate (see graph). Therefore, fusion using D–Template:Chem2 fuel at the right temperature and a D-lean fuel mixture, can produce a much lower neutron flux than D–T fusion, but is not clean, negating some of its main attraction.
The second possibility, fusing Template:Chem2 with itself (Template:Chem2), requires even higher temperatures (since now both reactants have a +2 charge), and thus is even more difficult than the D-Template:Chem2 reaction. It offers a theoretical reaction that produces no neutrons; the charged protons produced can be contained in electric and magnetic fields, which in turn directly generates electricity. Template:Chem2 fusion is feasible as demonstrated in the laboratory and has immense advantages, but commercial viability is many years in the future.[73]
The amounts of helium-3 needed as a replacement for conventional fuels are substantial by comparison to amounts currently available. The total amount of energy produced in the Template:Chem2 reaction is 18.4 MeV, which corresponds to some 493 megawatt-hours (4.93×108 W·h) per three grams (one mole) of Template:Chem2. If the total amount of energy could be converted to electrical power with 100% efficiency (a physical impossibility), it would correspond to about 30 minutes of output of a gigawatt electrical plant per mole of Template:Chem2. Thus, a year's production (at 6 grams for each operation hour) would require 52.5 kilograms of helium-3. The amount of fuel needed for large-scale applications can also be put in terms of total consumption: electricity consumption by 107 million U.S. households in 2001[74] totaled 1,140 billion kW·h (Template:Val). Again assuming 100% conversion efficiency, 6.7 tonnes per year of helium-3 would be required for that segment of the energy demand of the United States, 15 to 20 tonnes per year given a more realistic end-to-end conversion efficiency.Script error: No such module "Unsubst".
A second-generation approach to controlled fusion power involves combining helium-3 and [[deuterium|deuterium, Template:Chem2]]. This reaction produces an alpha particle and a high-energy proton. The most important potential advantage of this fusion reaction for power production as well as other applications lies in its compatibility with the use of electrostatic fields to control fuel ions and the fusion protons. High speed protons, as positively charged particles, can have their kinetic energy converted directly into electricity, through use of solid-state conversion materials as well as other techniques. Potential conversion efficiencies of 70% may be possible, as there is no need to convert proton energy to heat in order to drive a turbine-powered electrical generator.Script error: No such module "Unsubst".
He-3 power plants
There have been many claims about the capabilities of helium-3 power plants. According to proponents, fusion power plants operating on deuterium and helium-3 would offer lower capital and operating costs than their competitors due to less technical complexity, higher conversion efficiency, smaller size, the absence of radioactive fuel, no air or water pollution, and only low-level radioactive waste disposal requirements. Recent estimates suggest that about $6 billion in investment capital will be required to develop and construct the first helium-3 fusion power plant. Financial break even at today's wholesale electricity prices (5 US cents per kilowatt-hour) would occur after five 1-gigawatt plants were on line, replacing old conventional plants or meeting new demand.[75]
The reality is not so clear-cut. The most advanced fusion programs in the world are inertial confinement fusion (such as National Ignition Facility) and magnetic confinement fusion (such as ITER and Wendelstein 7-X). In the case of the former, there is no solid roadmap to power generation. In the case of the latter, commercial power generation is not expected until around 2050.[76] In both cases, the type of fusion discussed is the simplest: D–T fusion. The reason for this is the very low Coulomb barrier for this reaction; for D+3He, the barrier is much higher, and it is even higher for 3He–3He. The immense cost of reactors like ITER and National Ignition Facility are largely due to their immense size, yet to scale up to higher plasma temperatures would require reactors far larger still. The 14.7 MeV proton and 3.6 MeV alpha particle from D–3He fusion, plus the higher conversion efficiency, means that more electricity is obtained per kilogram than with D–T fusion (17.6 MeV), but not that much more. As a further downside, the rates of reaction for helium-3 fusion reactions are not particularly high, requiring a reactor that is larger still or more reactors to produce the same amount of electricity.
In 2022, Helion Energy claimed that their 7th fusion prototype (Polaris; fully funded and under construction as of September 2022) will demonstrate "net electricity from fusion", and will demonstrate "helium-3 production through deuterium–deuterium fusion" by means of a "patented high-efficiency closed-fuel cycle".[77]
Alternatives to He-3
To attempt to work around this problem of massively large power plants that may not even be economical with D–T fusion, let alone the far more challenging D–3He fusion, a number of other reactors have been proposed – the Fusor, Polywell, Focus fusion, and many more, though many of these concepts have fundamental problems with achieving a net energy gain, and generally attempt to achieve fusion in thermal disequilibrium, something that could potentially prove impossible,[78] and consequently, these long-shot programs tend to have trouble garnering funding despite their low budgets. Unlike the "big" and "hot" fusion systems, if such systems worked, they could scale to the higher barrier aneutronic fuels, and so their proponents tend to promote p-B fusion, which requires no exotic fuel such as helium-3.
See also
Notes and references
Bibliography
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External links
- The Nobel Prize in Physics 2003, presentation speech Template:Webarchive
- Moon for Sale: A BBC Horizon documentary on the possibility of lunar mining of Helium-3
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- ↑ Teragon's Summary of Cryogen Properties Template:Webarchive Teragon Research, 2005
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- ↑ a b Wittenberg 1994
- ↑ a b Aldrich, L.T.; Nier, Alfred O. Phys. Rev. 74, 1590 – 1594 (1948). The Occurrence of He3 in Natural Sources of Helium. Page 1592, Tables I and II.
- ↑ Holden, Normen E. 1993. Helium Isotopic Abundance Variation in Nature. copy of paper BNL-49331 "Table II. 3He Abundance of Natural Gas ... 3He in ppm ... Aldrich 0.05 – 0.5 ... Sano 0.46 – 22.7", "Table V. ... of Water ... 3He in ppm ... 1.6 – 1.8 East Pacific ... 0.006 – 1.5 Manitoba Chalk River ... 164 Japan Sea" (Aldrich measured Helium from US wells, Sano that of Taiwan gas: Script error: No such module "Citation/CS1".)
- ↑ WebElements Periodic Table: Professional Edition: Helium: key information Template:Webarchive. Webelements.com. Retrieved on 2011-11-08.
- ↑ a b c Smith, D.M. "any concentration of helium above approximately 0.2 percent is considered worthwhile examining" ... "U.S. government still owns approximately 1 billion nm3 of helium inventory", "Middle East and North Africa ... many very large, helium-rich (up to 0.5 percent) natural gas fields" (Smith uses nm3 to mean "normal cubic metre", elsewhere called "cubic metre at NTP)
- ↑ a b c d e Template:Cite report
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- ↑ Wittenberg 1994 p. 3, Table 1; p. 9.
- ↑ Wittenberg 1994 Page A-1 citing Anderson 1993, "1200 metric tonne"
- ↑ Wittenberg 1994 Page A-4 "1 kg (3He), pumping power would be Template:Val ... fusion power derived ... Template:Val"
- ↑ FTI Research Projects :: 3He Lunar Mining Template:Webarchive. Fti.neep.wisc.edu. Retrieved on 2011-11-08.
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- ↑ Luna C/I:: Chandrayaan-1 Payload Feature #2: Sub KeV Atom Reflecting Analyser (SARA) Template:Webarchive. Luna-ci.blogspot.com (2008-11-12). Retrieved on 2011-11-08.
- ↑ He asked for the moon-and got it Template:Webarchive. Chinadaily.com.cn (2006-07-26). Retrieved on 2011-11-08.
- ↑ Russian Rocket Builder Aims for Moon Base by 2015, Reports Say. Associated Press (via space.com). 26 January 2006
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- ↑ Script error: No such module "citation/CS1". NASA Technical Memorandum 2006-214122. AIAA–2005–4319. Prepared for the 41st Joint Propulsion Conference and Exhibit cosponsored by AIAA, ASME, SAE, and ASEE, Tucson, Arizona, July 10–13, 2005.
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- ↑ A Modular Neutron Detector | Summer 2003| Los Alamos National Laboratory Template:Webarchive. Lanl.gov. Retrieved on 2011-11-08.
- ↑ NCNR Neutron Spin Filters Template:Webarchive. Ncnr.nist.gov (2004-04-28). Retrieved on 2011-11-08.
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