Measurement of fission product gases in the atmosphere

被引:9
作者
Schell, WR [1 ]
Tobin, MJ [1 ]
Marsan, DJ [1 ]
Schell, CW [1 ]
VivesBatlle, J [1 ]
Yoon, SR [1 ]
机构
[1] UNIV PITTSBURGH,GRAD SCH PUBL HLTH,DEPT OCCUPAT HLTH,PITTSBURGH,PA 15261
关键词
D O I
10.1016/S0168-9002(96)00787-5
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The ability to quickly detect and assess the magnitude of releases of fission-produced radioactive material is of significant importance for ongoing operations of any conventional nuclear power plant or other activities with a potential for fission product release. In most instances, the control limits for the release of airborne radioactivity are low enough to preclude direct air sampling as a means of detection, especially for fission gases that decay by beta or electron emission. It is, therefore, customary to concentrate the major gaseous fission products (krypton, xenon and iodine) by cryogenic adsorption for subsequent separation and measurement. This study summarizes our initial efforts to develop an automated portable system for on-line separation and concentration with the potential for measuring environmental levels of radioactive gases, including Kr-85, Xe-131,Xe-133,Xe-135, C-14, H-3, S-35, I-125,I-131, etc., without using cryogenic fluids. Bench top and prototype models were constructed using the principle of heatless fractionation of the gases in a pressure swing system. This method removes the requirement for cryogenic fluids to concentrate gases and, with suitable electron and gamma ray detectors, provides for remote use under automatic computer control. Early results using Xe-133 tracer show that kinetic chromatography, i.e., high pressure adsorption of xenon and low pressure desorption of air, using specific types of molecular sieves, permits the separation and quantification of xenon isotopes from large volume air samples. We are now developing the ability to measure the presence and amounts of fission-produced xenon isotopes that decay by internal conversion electrons and beta radiation with short half-lives, namely Xe-131, 11.8d, Xe-133m, 2.2d, Xe-133, 5.2 d and Xe-135, 9.1 h. The ratio of the isotopic concentrations measured can be used to determine unequivocally the amount of fission gas and time of release of an air parcel many kilometers downwind from a nuclear activity where the fission products were discharged.
引用
收藏
页码:277 / 284
页数:8
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