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Fusion Science and Technology
Latest News
First astatine-labeled compound shipped in the U.S.
The Department of Energy’s National Isotope Development Center (NIDC) on March 31 announced the successful long-distance shipment in the United States of a biologically active compound labeled with the medical radioisotope astatine-211 (At-211). Because previous shipments have included only the “bare” isotope, the NIDC has described the development as “unleashing medical innovation.”
H. W. Kugel, Y. Hirooka, J. Timberlake, R. Bell, A. England, R. Isler, S. Jones, R. Kaita, S. Kaye, M. Khandagle, M. Okabayashi, S. Paul, H. Takahashi, W. Tighe, S. Von Goeler, A. Post-Zwicker
Fusion Science and Technology | Volume 25 | Number 4 | July 1994 | Pages 377-387
Technical Paper | Plasma Engineering | doi.org/10.13182/FST94-A30244
Articles are hosted by Taylor and Francis Online.
Boronization was performed by plasma ablation of two solid boronized target probes. Probe-1, in a mushroom shape, consisted of a 10.7% boronized two-dimensional carbon-carbon composite containing 3.6g of boron in a B4C binder. Probe-2, in a rectangular shape, consisted of an 86% boronized graphite felt composite containing 19.5 g of 40-μm boron particles. Probe-1 boronization deposited ∼26 monolayers of boron. After boronization with Probe-1, the loop voltage in 1-MW neutral-beam-heated plasmas decreased 27%, and volt-second consumption decreased 20%. Strong peripheral spectral lines from low-Z elements decreased by factors of ∼5. The central oxygen density decreased 15 to 20%. Carbon levels initially increased during boronization but were significantly reduced after boronization. The total radiated power during neutral beam injection decreased by 43%. Probe-2 boronization deposited ∼70 monolayers. Probe-2 boronization exhibited similar improved plasma conditions, but for some parameters, a smaller percentage change occurred because of the previous boronization with Probe-1. The ablation rates of both probes were consistent with front-face temperatures above the boron melting point. The results demonstrate the performance of two different boronized probe materials and the relative simplicity and effectiveness of solid target boronization as a convenient, real-time impurity control technique.