Title :
The Preparation of Stable and Actinide Nuclide Targets for Nuclear Measurements
Author :
Glover, K.M. ; Bint, L. ; Gayther, D.B. ; King, M. ; Whittaker, B. ; Wiltshire, R.A.P.
Author_Institution :
Chemistry Division,Bldg. 10.30, U.K.A.E.A., A.E.R.E., Harwell, Oxon, OX11 ORA, England
fDate :
4/1/1981 12:00:00 AM
Abstract :
Specifications for isotopic targets of both stable and actinide nuclides for nuclear measurements are very varied and individually very stringent. The majority of the targets are required to be of specified isotopic and chemical purity, well characterised and uniformly deposited over a precisely defined area. Mass assay of actinide targets may be requested to an accuracy of ± 0.1%, resolutions of <10 KeV FWHM may be requested for infinitely thin alpha sources and the Schmidt and Pleasonton criteria must be met for 252Cf fission fragment energy calibration sources. In order to cater for this wide range of requirements it is necessary to have available many preparation and calibration techniques. Actinide sources with activities in the range 0.01 ¿Ci to several hundred mCi and targets up to a few mg/cm2 are prepared by one of the following techniques, vacuum evaporation, painting, electrodeposition or the use of TEG as a spreading agent. These targets may be assayed quantitatively by absolute alpha counting and weighing and qualitatively by alpha spectrometry. Stable isotope targets with thickness varying from a few ¿g/cm2 to several hundred mg/cm2 are prepared primarily by vacuum evaporation and rolling. Mass assay is to ± 10% or better, the achievable accuracy being a function of substrate and target thickness.
Keywords :
Calibration; Chemical elements; Chemistry; Contamination; Energy resolution; Isotopes; Nuclear measurements; Painting; Pollution measurement; Vacuum technology;
Journal_Title :
Nuclear Science, IEEE Transactions on
DOI :
10.1109/TNS.1981.4331474