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MOOMMH03 | First Results At 24 GHz With The Superconducting Source For Ions (SuSI) | 1 |
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The superconducting ECR ion source SuSI at Michigan State University was designed to operate primarily at 18GHz and has demonstrated very good performance at this frequency especially when coupling two klystrons to the plasma [1]. Following a period of training, SuSI has been able to reach the magnetic field needed for operation in the high-B mode at 24 GHz. SuSI has several interesting features. First the axial magnetic profile is defined using 6 solenoids which provide some flexibility to adjust parameters such as field gradient at the resonance, Bminimum or plasma length. Second with a diameter of only 101mm, SuSI plasma chamber has a nominal volume of about 3.5 l. Therefore, power density in excess of 2kW/l could be reach and lead potentially to new insight on the maximum performance achievable with an ECR. In January 2014, a 10 kW 24 GHz Gyrotron obtained from the Russian company GYCOM was commissioned at MSU on a dummy load and then connected to SuSI. We report here on the first measurements done with SuSI at 24 GHz.
* L.T. Sun, J. Brandon, D.G. Cole, M. Doleans, G. Machicoane, D. Morris, T. Ropponen, L. Tobos., ECRIS 2010 (MOCOAK02) |
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Slides MOOMMH03 [3.591 MB] | |
MOPPH019 | Metallic Beam Development with an ECR Ion Source at Michigan State University (MSU) | 79 |
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Funding: Supported by Michigan State University, National Science Foundation: NSF Award Number PHY-1102511 Electron Cyclotron Resonance (ECR) ion sources have been used at MSU to provide metal ion beams to the coupled cyclotron facility (CCF), and in the future, for The Facility for Rare Isotope Beams (FRIB). The challenges of metallic beam production with ECR are in production, efficiency, stability and contamination. Future facilities such as FRIB will add the challenge of intensity. We report development of two rare earth metals and the conversion from the oxidized state into metal. The enriched isotopes of 144 Sm, and 176 Yb are commonly available in the sesquioxide form which is unsuitable for use in our standard ovens. We report here results from the off-line chemical reduction of samarium, and ytterbium oxides into metal. We were able to demonstrate efficiencies of up to 90 % throughout the conversion process. The samples were then run on our ECR ion sources to confirm the products of the reduction. In addition we report the development of cadmium metal by passing vapor though over 3/4 m of heated stainless steel tubing and observed 4.3 euA of Cd 20+ with an average consumption of 1 mg/hr. |
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