Effect of Chemical State on the Decay Constant ofU235m

Abstract
Experimental investigation of the influence of chemical forms on the decay constant of U235m has been performed. The U235m atoms from a very thin Pu239 source were collected by the recoil method on platinum, carbon, and silicon plates in a pure argon atmosphere. Applying the differential method with two identical, specially designed 12-stage secondary electron multipliers, emission rates of the internal-conversion electrons of very weak energy from the isomer in different chemical states have been compared. Stability and sensitivity of the whole measuring system have been checked using C14 and metallic U235m sources. We used metallic uranium (U) and uranium atoms slightly diffused into carbon (UC) or silicon (USi) base for the different chemical states. The results are: λ(U)λ(UC)=(3.18±0.50)×103λ(U), λ(U)λ(USi)=(2.21±0.36)×103λ(U), and λ(USi)λ(UC)=(0.97±0.43)×103λ(USi). Errors are standard deviations. We also determined the half-life of U235m to be T12=26.05±0.05 min by using a low-background 2π gas-flow counter. Furthermore, diffusion of the isomer into the base materials, carbon and silicon, was investigated in some detail.