Abstract

Isochronous mass spectrometry (IMS) in storage rings is a successful technique for accurate mass measurements of short-lived nuclides with relative precision of about 10−5−10−710^{-5}-10^{-7}. Instabilities of the magnetic fields in storage rings are one of the major contributions limiting the achievable mass resolving power, which is directly related to the precision of the obtained mass values. A new data analysis method is proposed allowing one to minimise the effect of such instabilities. The masses of the previously measured at the CSRe 41^{41}Ti, 43^{43}V, 47^{47}Mn, 49^{49}Fe, 53^{53}Ni and 55^{55}Cu nuclides were re-determined with this method. An improvement of the mass precision by a factor of ∼1.7\sim 1.7 has been achieved for 41^{41}Ti and 43^{43}V. The method can be applied to any isochronous mass experiment irrespective of the accelerator facility. Furthermore, the method can be used as an on-line tool for checking the isochronous conditions of the storage ring.

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