Radiocarbon Dispersion around Canadian Nuclear Facilities

Canadian deuterium uranium (CANDU) pressurized heavy-water reactors produce 14C by neutron activation of trace quantities of nitrogen in annular gas and reactor components (14N(n,p)14C), and from 170 in the heavy water moderator by (17O(n,a)14C). The radiocarbon produced in the moderator is removed on ion exchange resins incorporated in the water purification systems; however, a much smaller gaseous portion is vented from reactor stacks at activity levels considerably below 1% of permissible derived emission limits. Early measurements of the carbon speciation indicated that >90% of the 14C emitted was in the form of CO2. We conducted surveys of the atmospheric dispersion of 14CO2 at the Chalk River Laboratories and at the Pickering Nuclear Generating Station. We analyzed air, vegetation, soils and tree rings to add to the historical record of 14C emissions at these sites, and to gain an understanding of the relative importance of the various carbon pools that act as sources/sinks within the total 14C budget. Better model parameters than those currently available for calculating the dose to the critical group can be obtained in this manner. Global dose estimates may require the development of techniques for estimating emissions occurring outside the growing season.This material was digitized as part of a cooperative project between Radiocarbon and the University of Arizona Libraries.The Radiocarbon archives are made available by Radiocarbon and the University of Arizona Libraries. Contact [email protected] for further information.Migrated from OJS platform February 202

Radiocarbon Dispersion Around Canadian Nuclear Facilities

Canadian deuterium uranium (CANDU) pressurized heavy-water reactors produce 14C by neutron activation of trace quantities of nitrogen in annular gas and reactor components (14N(n,p)14C), and from 170 in the heavy water moderator by (17O(n,a)14C). The radiocarbon produced in the moderator is removed on ion exchange resins incorporated in the water purification systems; however, a much smaller gaseous portion is vented from reactor stacks at activity levels considerably below 1% of permissible derived emission limits. Early measurements of the carbon speciation indicated that >90% of the 14C emitted was in the form of CO2. We conducted surveys of the atmospheric dispersion of 14CO2 at the Chalk River Laboratories and at the Pickering Nuclear Generating Station. We analyzed air, vegetation, soils and tree rings to add to the historical record of 14C emissions at these sites, and to gain an understanding of the relative importance of the various carbon pools that act as sources/sinks within the total 14C budget. Better model parameters than those currently available for calculating the dose to the critical group can be obtained in this manner. Global dose estimates may require the development of techniques for estimating emissions occurring outside the growing season.This material was digitized as part of a cooperative project between Radiocarbon and the University of Arizona Libraries.The Radiocarbon archives are made available by Radiocarbon and the University of Arizona Libraries. Contact [email protected] for further information.Migrated from OJS platform February 202