Direct identification of 103–107Mo by a rapid chemical separation procedure

Tittel, G.; Kaffrell, Ν.; Trautmann, Ν.; Herrmann, G.

doi:10.1016/0022-1902(77)80376-x

Cited by 21 publications

(3 citation statements)

References 3 publications

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“…The discovery of 123 Rh, 124 Rh, 125 Rh, and 126 Rh was reported in the 2010 article "Identification of 45 new neutronrich isotopes produced by in-flight fission of a 238 U beam at 345 MeV/nucleon," by Ohnishi et al [65]. The experiment was performed at the RI Beam Factory at RIKEN, where the new isotopes were created by in-flight fission of a 345…”

Section: −126 Rhmentioning

confidence: 99%

“…The results for the new isotopes discovered in this study were summarized in a table. 933 counts for 123 Rh, 94 counts for 124 Rh, 13 counts for 125 Rh, and 1 count for 126 Rh were recorded.…”

Section: −126 Rhmentioning

confidence: 99%

“…The half-life of 108 Mo, 1.5±0.4 sec, agrees within the errors with a value of 0.86±0.39 sec recently reported by Wilhelmy et al" These measured values are consistent with the presently adopted values of 3.5(5) s and 1.09(2) s for107 Mo and 108 Mo, respectively. The accepted half-life for107 Mo corresponds to a later measurement by the same group[125]. The 108 Mo reference was an internal report[126].4.22.…”

mentioning

confidence: 99%

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Discovery of rubidium, strontium, molybdenum, and rhodium isotopes

Parker

Thoennessen

2012

Atomic Data and Nuclear Data Tables

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Section: −126 Rhmentioning

confidence: 99%

Section: −126 Rhmentioning

confidence: 99%

mentioning

confidence: 99%

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Discovery of rubidium, strontium, molybdenum, and rhodium isotopes

Parker

Thoennessen

2012

Atomic Data and Nuclear Data Tables

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A gas-jet system for the study of short-lived, light fission products

Rengan

Griffin

1986

Journal of Radioanalytical and Nuclear Chemistry, Articles

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For the study of short-lived fission products, a gas jet system has been set up in a beam port of the Ford Nuclear Reactor at the University of Michigan. The system consists of a target chamber joined to three polyethylene tubes which serve as gas inlet, fission product outlet and an outlet for pressure monitoring. The target chamber is housed in a 7.6 cm (ID) aluminum tube supported inside a radial beam port. This tube can be withdrawn by ~l m, allowing the target chamber to be positioned either close to or ~1 m from the core. The aluminum tube is surrounded by water, which provides shielding and protects the target when not in use (at ~1 m position). The target is ~1 mg of 23Su, chemically plated on an aluminum planchett. The uranium is covered with 2.7 mg'cm-2 of aluminum. The aluminum covering stops most of the heavy fission fragments; the light fission fragments pass through the foil and are thermalized in a gaseous mixture of nitrogen and ethylene. The transport time of fission products from the target chamber to the detector position was measured to be 970 msec. Preliminary experiments indicate that the transport time can be reduced further. The gas jet system is being utilized for the development of fast, gas-phase chemistry for the separation of bromine from fission products.

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Fractional independent yields of 104Tc and 105Tc from thermal-neutron-induced fission of 235U and of 239Pu

Vine

Wahl

1981

Journal of Inorganic and Nuclear Chemistry

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Direct identification of 103–107Mo by a rapid chemical separation procedure

Cited by 21 publications

References 3 publications

Discovery of rubidium, strontium, molybdenum, and rhodium isotopes

Discovery of rubidium, strontium, molybdenum, and rhodium isotopes

A gas-jet system for the study of short-lived, light fission products

Fractional independent yields of 104Tc and 105Tc from thermal-neutron-induced fission of 235U and of 239Pu

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