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Isotopes of technetium

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Summary

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Technetium (43Tc) is one of the two elements with {{nowrap|Z 99Tc per gram of pitchblende) or neutron capture by molybdenum. The element was first obtained in 1936 from bombarded molybdenum, the first artificial element to be produced. The most stable radioisotopes are 97Tc (half-life of 4.21 million years), 98Tc (half-life: 4.2 million years), and 99Tc (half-life: 211,100 years). Given that their stated uncertainties are 16 and 30 times their difference, the half-lives of 97Tc and 98Tc are statistically indistinguishable.

Thirty-three other radioisotopes have been characterized with atomic masses ranging from 85Tc to 120Tc. Those with half-lives more than an hour have masses 93 to 96.

Technetium also has numerous meta states. 97mTc is the most stable, with a half-life of 91.1 days (0.097 MeV), followed by 95mTc (half-life: 62.0 days, 0.039 MeV) and 99mTc (half-life: 6.01 hours, 0.143 MeV). 99mTc emits only gamma rays while decaying to 99Tc.

For isotopes lighter than 98Tc, the primary decay mode is electron capture to isotopes of molybdenum. For the heavier isotopes, the primary mode is beta emission to isotopes of ruthenium, with the exception that 98Tc and 100Tc can decay both by beta emission and electron capture.

Technetium-99m is the technetium isotope employed in the nuclear medicine industry. Its low-energy isomeric transition, which yields a gamma-ray at ~140.5 keV, is ideal for imaging using Single Photon Emission Computed Tomography (SPECT). Several technetium isotopes, such as 94mTc, 95Tc, and 96Tc, which are produced via (p,n) reactions using a cyclotron on molybdenum targets, have also been identified as potential Positron Emission Tomography (PET) or gamma-emitting agents for medical imaging. Technetium-101 has been produced using a D-D fusion-based neutron generator from the 100Mo(n,γ)101Mo reaction on natural molybdenum and subsequent beta-minus decay of 101Mo to 101Tc. Despite its shorter half-life (14.22 minutes), 101Tc exhibits unique decay characteristics suitable for radioisotope diagnostic or therapeutic procedures, where it has been proposed that its implementation, as a supplement for dual-isotopic imaging or replacement for 99mTc, could be performed by on-site production and dispensing at the point of patient care.

Technetium-99 is the most common and most readily available isotope, as it is a major fission product from fission of actinides like uranium and plutonium with a fission product yield of 6% or more, and in fact the most significant long-lived fission product. Lighter isotopes of technetium are almost never produced in fission because the initial fission products normally have a higher neutron/proton ratio than is stable for their mass range, and therefore undergo beta decay until reaching the ultimate product. Beta decay of fission products of mass 98 and lower, or 100, stops at stable (or very long-lived) isotopes of lower atomic number and does not reach technetium. For greater masses, the technetium isotopes are very short-lived and quickly undergo further beta decay. Therefore, the technetium in spent nuclear fuel is practically all 99Tc. In the presence of fast neutrons a small amount of will be produced by (n,2n) "knockout" reactions. If nuclear transmutation of fission-derived technetium, or technetium wastes from medical applications, is desired, fast neutrons are therefore not desirable as the long lived increases rather than reducing the longevity of the radioactivity in the material.

One gram of 99Tc produces disintegrations a second (that is, 0.62 GBq/g).

Technetium has no primordial isotopes and does not occur in nature in significant quantities, and thus a standard atomic weight cannot be given.

List of isotopes

Technetium-83 |-id=Technetium-86 | 86Tc | 85.94464(32)# | 55(7) ms | β+ | 86Mo | (0+) | |-id=Technetium-86m | 1.10(12) μs | IT | 86Tc | (6+) | |-id=Technetium-87 | β+

87Mo
β+, p (
86Nb
-id=Technetium-87m
647(24) ns
IT
87Tc
7/2+#

| |-id=Technetium-88 | 88Tc | 87.9337942(44) | 6.4(8) s | β+ | 88Mo | (2+) | |-id=Technetium-88m1 | 5.8(2) s | β+ | 88Mo | (6+) | |-id=Technetium-88m2 | 146(12) ns | IT | 88Tc | (4+) | |-id=Technetium-89 | 89Tc | 88.9276486(41) | 12.8(9) s | β+ | 89Mo | (9/2+) | |-id=Technetium-89m | 12.9(8) s | β+ | 89Mo | (1/2−) | |-id=Technetium-90 | 90Tc | 89.9240739(11) | 49.2(4) s | β+ | 90Mo | (8+) | |-id=Technetium-90m | 8.7(2) s | β+ | 90Mo | 1+ | |-id=Technetium-91 | 91Tc | 90.9184250(25) | 3.14(2) min | β+ | 91Mo | (9/2)+ | |-id=Technetium-91m | 3.3(1) min | β+ (99%) | 91Mo | (1/2)− | |-id=Technetium-92 | 92Tc | 91.9152698(33) | 4.25(15) min | β+ | 92Mo | (8)+ | |-id=Technetium-92m1 | 1.03(6) μs | IT | 92Tc | (4+) | |-id=Technetium-92m2 | | IT | 92Tc | (3+) | |-id=Technetium-92m3 | | IT | 92Tc | 1+ | |-id=Technetium-93 | 93Tc | 92.9102451(11) | 2.75(5) h | β+ | 93Mo | 9/2+ | |-id=Technetium-93m1 | IT (77.4%)

93Tc
β+ (22.6%)
93Mo
-id=Technetium-93m2
10.2(3) μs
IT
93Tc
(17/2)−

| |-id=Technetium-94 | 94Tc | 93.9096523(44) | 293(1) min | β+ | 94Mo | 7+ | |-id=Technetium-94m | β+ (99.82%)

94Mo
IT (
94Tc
-id=Technetium-95
95Tc
94.9076523(55)
19.258(26) h
β+
95Mo
9/2+

| |-id=Technetium-95m | β+ (96.1%)

95Mo
IT (3.9%)
95Tc
-id=Technetium-96
96Tc
95.9078667(55)
4.28(7) d
β+
96Mo
7+

| |-id=Technetium-96m | IT (98.0%)

96Tc
β+ (2.0%)
96Mo
-id=Technetium-97
97Tc
96.9063607(44)

| | EC | 97Mo | 9/2+ | |-id=Technetium-97m | IT (96.06%)

97Tc
EC (3.94%)
97Mo
-id=Technetium-98
β− (99.71%)
98Ru
-
EC (0.29%)
98Mo
-id=Technetium-98m
14.7(5) μs
IT
98Tc
(2,3)−

| |- | 99TcLong-lived fission product | 98.90624968(97) | | β− | 99Ru | 9/2+

trace
IT
99Tc
-
β− (0.0037%)
99Ru
-id=Technetium-100
β−
100Ru
-
EC (0.0018%)
100Mo
-id=Technetium-100m1
8.32(14) μs
IT
100Tc
(4)+

| |-id=Technetium-100m2 | 3.2(2) μs | IT | 100Tc | (6)+ | |-id=Technetium-101 | 101Tc | 100.907305(26) | 14.22(1) min | β− | 101Ru | 9/2+ | |-id=Technetium-101m | 636(8) μs | IT | 101Tc | 1/2− | |-id=Technetium-102 | 102Tc | 101.9092072(98) | 5.28(15) s | β− | 102Ru | 1+ | |-id=Technetium-102m | 4.35(7) min | β− | 102Ru | (4+) | |-id=Technetium-103 | 103Tc | 102.909174(11) | 54.2(8) s | β− | 103Ru | 5/2+ | |-id=Technetium-104 | 104Tc | 103.911434(27) | 18.3(3) min | β− | 104Ru | (3−) | |-id=Technetium-104m1 | 3.5(3) μs | IT | 104Tc | (5−) | |-id=Technetium-104m2 | 400(20) ns | IT | 104Tc | 4# | |-id=Technetium-105 | 105Tc | 104.911662(38) | 7.64(6) min | β− | 105Ru | (3/2−) | |-id=Technetium-106 | 106Tc | 105.914357(13) | 35.6(6) s | β− | 106Ru | (1,2)(+#) | |-id=Technetium-107 | 107Tc | 106.9154584(93) | 21.2(2) s | β− | 107Ru | (3/2−) | |-id=Technetium-107m1 | 3.85(5) μs | IT | 107Tc | (1/2+) | |-id=Technetium-107m2 | 184(3) ns | IT | 107Tc | (5/2+) | |-id=Technetium-108 | 108Tc | 107.9184935(94) | 5.17(7) s | β− | 108Ru | (2)+ | |-id=Technetium-109 | β− (99.92%)

109Ru
β−, n (0.08%)
108Ru
-id=Technetium-110
β− (99.96%)
110Ru
-
β−, n (0.04%)
109Ru
-id=Technetium-111
β− (99.15%)
111Ru
-
β−, n (0.85%)
110Ru
-id=Technetium-112
β− (98.5%)
112Ru
-
β−, n (1.5%)
111Ru
-id=Technetium-112m
150(17) ns
IT
112Tc

| | |-id=Technetium-113 | β− (97.9%)

113Ru
β−, n (2.1%)
112Ru
-id=Technetium-113m
527(16) ns
IT
113Tc
5/2−#

| |-id=Technetium-114 | β− (98.7%)

114Ru
β−, n (1.3%)
113Ru
-id=Technetium-114m
β− (98.7%)
114Ru
-
β−, n (1.3%)
113Ru
-id=Technetium-115
115Tc
114.94010(21)#
78(2) ms
β−
115Ru
5/2+#

| |-id=Technetium-116 | 116Tc | 115.94502(32)# | 57(3) ms | β− | 116Ru | 2+# | |-id=Technetium-117 | 117Tc | 116.94832(43)# | 44.5(30) ms | β− | 117Ru | 5/2+# | |-id=Technetium-118 | 118Tc | 117.95353(43)# | 30(4) ms | β− | 118Ru | 2+# | |-id=Technetium-119 | 119Tc | 118.95688(54)# | 22(3) ms | β− | 119Ru | 5/2+# | |-id=Technetium-120 | 120Tc | 119.96243(54)# | 21(5) ms | β− | 120Ru | 3+# | |-id=Technetium-121 | 121Tc | 120.96614(54)# | 22(6) ms | β− | 121Ru | 5/2+# | |-id=Technetium-122 | 122Tc | 121.97176(32)# | 13# ms [550 ns] | | | 1+# |

Stability of technetium isotopes

Technetium and promethium are unusual light elements in that they have no stable isotopes. Using the liquid drop model for atomic nuclei, one can derive a semiempirical formula for the binding energy of a nucleus. This formula predicts a "valley of beta stability" along which nuclides do not undergo beta decay. Nuclides that lie "up the walls" of the valley tend to beta decay towards the center (by emitting an electron, emitting a positron, or capturing an electron). For a fixed number of nucleons A, the binding energies lie on one or more parabolas, with the most stable nuclide at the bottom. One can have more than one parabola because isotopes with an even number of protons and an even number of neutrons are more stable than isotopes with an odd number of neutrons and an odd number of protons. A single beta decay then transforms one into the other. When there is only one parabola, there can be only one stable isotope lying on that parabola. When there are two parabolas, that is, when the number of nucleons is even, it can happen (rarely) that there is a stable nucleus with an odd number of neutrons and an odd number of protons (although this happens only in five instances: 2H, 6Li, 10B, 14N and 180mTa). However, if this happens, there can be no stable isotope with an even number of neutrons and an even number of protons (180 is an exception, and 180mTa is suspected not to be truly stable).

For technetium (Z = 43), the valley of beta stability is centered at around 98 nucleons. However, for every number of nucleons from 94 to 102, there is already at least one stable nuclide of either molybdenum (Z = 42) or ruthenium (Z = 44), and the Mattauch isobar rule states that two adjacent isobars cannot both be stable. For the isotopes with odd numbers of nucleons, this immediately rules out a stable isotope of technetium, since there can be only one stable nuclide with a fixed odd number of nucleons. For the isotopes with an even number of nucleons, since technetium has an odd number of protons, any isotope must also have an odd number of neutrons. In such a case, the presence of a stable nuclide having the same number of nucleons and an even number of protons rules out the possibility of a stable nucleus.

References

References

  1. "Atomic weights of the elements 2011 (IUPAC Technical Report)". [[IUPAC]].
  2. (2008). "The Geochemistry of Technetium: A Summary of the Behavior of an Artificial Element in the Natural Environment". U.S. Department of Energy.
  3. (2001). "Production, processing and uses of 94mTc". Journal of Labelled Compounds and Radiopharmaceuticals.
  4. (2011-05-01). "Simple, rapid production of Tc-94m". Journal of Nuclear Medicine.
  5. (January 2018). "95g Tc and 96g Tc as alternatives to medical radioisotope 99m Tc". Heliyon.
  6. (September 2021). "Fusion-Based Neutron Generator Production of Tc-99m and Tc-101: A Prospective Avenue to Technetium Theranostics". Pharmaceuticals.
  7. ''The Encyclopedia of the Chemical Elements'', p. 693, "Toxicology", paragraph 2
  8. (2025). "Electron-capture decay of 98Tc". Physical Review C.
  9. (2017). "Technetium, the first radioelement on the periodic table". Journal of Chemical Education.
  10. ''Radiochemistry and Nuclear Chemistry''
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