1989
DOI: 10.1016/0168-9002(89)90117-4
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Preparation of actinide targets by electrodeposition

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Cited by 60 publications
(24 citation statements)
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“…In most of the measurements, our data reaches into the energy window relevant in the γ process. on tantalum backings (see [25] for a sketch of the electrolysis cell), but these layers did not properly adhere to the backings. Instead, the samples were made by careful and uniform deposition of 100 µl of the PdCl 2 solution within the area of the beam spot (12 mm in diameter) and subsequent drying.…”
Section: Experimental Techniquementioning
confidence: 99%
“…In most of the measurements, our data reaches into the energy window relevant in the γ process. on tantalum backings (see [25] for a sketch of the electrolysis cell), but these layers did not properly adhere to the backings. Instead, the samples were made by careful and uniform deposition of 100 µl of the PdCl 2 solution within the area of the beam spot (12 mm in diameter) and subsequent drying.…”
Section: Experimental Techniquementioning
confidence: 99%
“…However, the solution that did not adhere to the surface can be collected and reused resulting in minimal loss of a precious metal, with the overall deposition efficiency approaching 100%. Molecular plating has ~90% efficiency for the deposition of metal out of solution [1,2] comparable to PAD. Thus, the PAD method is likely a robust route to create metal oxide films suitable for nuclear science applications which require film uniformity and controlled film thickness.…”
Section: Methods Advantagesmentioning
confidence: 99%
“…Molecular plating has been used by Trautmann et al [1] and Mullen et al [2] to create uranium, plutonium and curium oxide films. Their films ranged from 150 to 550 nm in thickness, which are typical for nuclear science applications.…”
Section: Methods Advantagesmentioning
confidence: 99%
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“…[108]. Within the ECHo collaboration, the Institute for Nuclear Chemistry at the Johannes Gutenberg University Mainz, which has decade-long experience with high-performance chemical separation of substantial amounts of radionuclides, see, e.g., [109][110][111], performs the chemical separation. The mass separation is performed at the RISIKO mass separator [112,113] operated at the Institute of Physics at the Johannes Gutenberg University Mainz or at the General Purpose Separator at the ISOLDE facility at CERN [60] to further purify the initial 163 Ho samples by an efficient and selective suppression of the 166m Ho contamination.…”
Section: Reactor Production Of 163 Homentioning
confidence: 99%