Isotopes of zirconium

(Redirected from Zirconium-92)

Naturally occurring zirconium (40Zr) is composed of four stable isotopes (of which one may in the future be found radioactive), and one very long-lived radioisotope (96Zr), a primordial nuclide that decays via double beta decay with an observed half-life of 2.0×1019 years;[5] it can also undergo single beta decay, which is not yet observed, but the theoretically predicted value of t1/2 is 2.4×1020 years.[6] The second most stable radioisotope is 93Zr, which has a half-life of 1.53 million years. Thirty other radioisotopes have been observed. All have half-lives less than a day except for 95Zr (64.02 days), 88Zr (83.4 days), and 89Zr (78.41 hours). The primary decay mode is electron capture for isotopes lighter than 92Zr, and the primary mode for heavier isotopes is beta decay.

Isotopes of zirconium (40Zr)
Main isotopes[1]Decay
abun­dancehalf-life (t1/2)modepro­duct
88Zrsynth83.4 dε88Y
γ
89Zrsynth78.4 hε89Y
β+89Y
γ
90Zr51.5%stable
91Zr11.2%stable
92Zr17.1%stable
93Zrtrace1.53×106 yβ93Nb
94Zr17.4%stable
96Zr2.80%2.0×1019 y[2]ββ96Mo
Standard atomic weight Ar°(Zr)

List of isotopes

Nuclide
[n 1]
ZNIsotopic mass (Da)
[n 2][n 3]
Half-life
[n 4][n 5]
Decay
mode

Daughter
isotope

[n 6]
Spin and
parity
[n 7][n 5]
Natural abundance (mole fraction)
Excitation energyNormal proportionRange of variation
78Zr403877.95523(54)#50# ms
[>170 ns]
0+
79Zr403978.94916(43)#56(30) msβ+, p78Sr5/2+#
β+79Y
80Zr404079.9404(16)4.6(6) sβ+80Y0+
81Zr404180.93721(18)5.5(4) sβ+ (>99.9%)81Y(3/2−)#
β+, p (<.1%)80Sr
82Zr404281.93109(24)#32(5) sβ+82Y0+
83Zr404382.92865(10)41.6(24) sβ+ (>99.9%)83Y(1/2−)#
β+, p (<.1%)82Sr
84Zr404483.92325(21)#25.9(7) minβ+84Y0+
85Zr404584.92147(11)7.86(4) minβ+85Y7/2+
85mZr292.2(3) keV10.9(3) sIT (92%)85Zr(1/2−)
β+ (8%)85Y
86Zr404685.91647(3)16.5(1) hβ+86Y0+
87Zr404786.914816(9)1.68(1) hβ+87Y(9/2)+
87mZr335.84(19) keV14.0(2) sIT87Zr(1/2)−
88Zr[n 8]404887.910227(11)83.4(3) dEC88Y0+
89Zr404988.908890(4)78.41(12) hβ+89Y9/2+
89mZr587.82(10) keV4.161(17) minIT (93.77%)89Zr1/2−
β+ (6.23%)89Y
90Zr[n 9]405089.9047044(25)Stable0+0.5145(40)
90m1Zr2319.000(10) keV809.2(20) msIT90Zr5-
90m2Zr3589.419(16) keV131(4) ns8+
91Zr[n 9]405190.9056458(25)Stable5/2+0.1122(5)
91mZr3167.3(4) keV4.35(14) μs(21/2+)
92Zr[n 9]405291.9050408(25)Stable0+0.1715(8)
93Zr[n 10]405392.9064760(25)1.53(10)×106 yβ (73%)93mNb5/2+
β (27%)93Nb
94Zr[n 9]405493.9063152(26)Observationally stable[n 11]0+0.1738(28)
95Zr[n 9]405594.9080426(26)64.032(6) dβ95Nb5/2+
96Zr[n 12][n 9][n 13]405695.9082734(30)2.0(4)×1019 yββ[n 14]96Mo0+0.0280(9)
97Zr405796.9109531(30)16.744(11) hβ97mNb1/2+
98Zr405897.912735(21)30.7(4) sβ98Nb0+
99Zr405998.916512(22)2.1(1) sβ99mNb1/2+
100Zr406099.91776(4)7.1(4) sβ100Nb0+
101Zr4061100.92114(3)2.3(1) sβ101Nb3/2+
102Zr4062101.92298(5)2.9(2) sβ102Nb0+
103Zr4063102.92660(12)1.3(1) sβ103Nb(5/2−)
104Zr4064103.92878(43)#1.2(3) sβ104Nb0+
105Zr4065104.93305(43)#0.6(1) sβ (>99.9%)105Nb
β, n (<.1%)104Nb
106Zr4066105.93591(54)#200# ms
[>300 ns]
β106Nb0+
107Zr4067106.94075(32)#150# ms
[>300 ns]
β107Nb
108Zr4068107.94396(64)#80# ms
[>300 ns]
β108Nb0+
109Zr4069108.94924(54)#60# ms
[>300 ns]
110Zr4070109.95287(86)#30# ms
[>300 ns]
0+
111Zr[8]4071
112Zr[8]40720+
113Zr[9]4073
114Zr[10]40740+
This table header & footer:

Zirconium-88

88Zr is a radioisotope of zirconium with a half-life of 83.4 days. In January 2019, this isotope was discovered to have a neutron capture cross section of approximately 861,000 barns; this is several orders of magnitude greater than predicted, and greater than that of any other nuclide except xenon-135.[11]

Zirconium-89

89Zr is a radioisotope of zirconium with a half-life of 78.41 hours. It is produced by proton irradiation of natural yttrium-89. Its most prominent gamma photon has an energy of 909 keV.

Zirconium-89 is employed in specialized diagnostic applications using positron emission tomography[12] imaging, for example, with zirconium-89 labeled antibodies (immuno-PET).[13] For a decay table, see Maria Vosjan. "Zirconium-89 (89Zr)". Cyclotron.nl.

Zirconium-93

Yield, % per fission[14]
ThermalFast14 MeV
232Thnot fissile6.70 ± 0.405.58 ± 0.16
233U6.979 ± 0.0986.94 ± 0.075.38 ± 0.32
235U6.346 ± 0.0446.25 ± 0.045.19 ± 0.31
238Unot fissile4.913 ± 0.0984.53 ± 0.13
239Pu3.80 ± 0.033.82 ± 0.033.0 ± 0.3
241Pu2.98 ± 0.042.98 ± 0.33?
Nuclidet12YieldQ[a 1]βγ
(Ma)(%)[a 2](keV)
99Tc0.2116.1385294β
126Sn0.2300.10844050[a 3]βγ
79Se0.3270.0447151β
135Cs1.336.9110[a 4]269β
93Zr1.535.457591βγ
107Pd6.5  1.249933β
129I15.7  0.8410194βγ

93Zr is a radioisotope of zirconium with a half-life of 1.53 million years, decaying through emission of a low-energy beta particle. 73% of decays populate an excited state of niobium-93, which decays with a halflife of 14 years and a low-energy gamma ray to the stable ground state of 93Nb, while the remaining 27% of decays directly populate the ground state.[15] It is one of only 7 long-lived fission products. The low specific activity and low energy of its radiations limit the radioactive hazards of this isotope.

Nuclear fission produces it at a fission yield of 6.3% (thermal neutron fission of 235U), on a par with the other most abundant fission products. Nuclear reactors usually contain large amounts of zirconium as fuel rod cladding (see zircaloy), and neutron irradiation of 92Zr also produces some 93Zr, though this is limited by 92Zr's low neutron capture cross section of 0.22 barns. Indeed, one of the primary reasons for using zirconium in fuel rod cladding is its low cross section.

93Zr also has a low neutron capture cross section of 0.7 barns.[16][17] Most fission zirconium consists of other isotopes; the other isotope with a significant neutron absorption cross section is 91Zr with a cross section of 1.24 barns. 93Zr is a less attractive candidate for disposal by nuclear transmutation than are 99Tc and 129I. Mobility in soil is relatively low, so that geological disposal may be an adequate solution. Alternatively, if the effect on the neutron economy of 93
Zr
's higher cross section is deemed acceptable, irradiated cladding and fission product Zirconium (which are mixed together in most current nuclear reprocessing methods) could be used to form new zircalloy cladding. Once the cladding is inside the reactor, the relatively low level radioactivity can be tolerated, but transport and manufacturing might require special precautions.

References