Gerald A. Simiele, Robert A. Fjeld, Carlton Robertson
{"title":"Radioactive decontamination of waste oil by filtration, centrifugation, and chelation","authors":"Gerald A. Simiele, Robert A. Fjeld, Carlton Robertson","doi":"10.1016/0191-815X(87)90070-2","DOIUrl":null,"url":null,"abstract":"<div><p>Laboratory studies were conducted on select physical and chemical processes for decontamination of a composite waste lubricating oil from a boiling water reactor. Physical treatments included successive filtration through 25, 8 and 1 μm filters to remove particulate matter and centrifugation to remove water. Chemical treatment consisted of mixing the oil with an aqueous solution of the chelating agent ethylenediaminetetraacetic acid (EDTA) and centrifuging the resulting emulsion. The effectiveness of the treatment processes was evaluated by measuring radionuclide concentrations in the oil following each treatment step and calculating decontamination factors.</p><p>The total activity of the oil was dominated by <sup>60</sup>Co, <sup>54</sup>Mn, and <sup>137</sup>Cs, although <sup>51</sup>Cr, <sup>58</sup>Co, <sup>59</sup>Fe, and <sup>134</sup>Cs were also present. Filtration consistently achieved decontamination factors of approximately 200, 100, and 40 for <sup>137</sup>Cs, <sup>54</sup>Mn, and <sup>60</sup>Co, respectively, and reduced concentrations of the other radionuclides below their detection limits. Following filtration, centrifugation reduced <sup>137</sup>Cs concentrations below the detection limit and reduced <sup>54</sup>Mn and <sup>60</sup>Co concentrations by approximately 40% and 20%, respectively. Subsequent chemical treatment with EDTA reduced the <sup>54</sup>Mn concentration to below the detection limit and removed approximately 95% of the remaining <sup>60</sup>Co activity. The overall decontamination factor for successive filtration, centrifugation, and chelation was in excess of 10,000 for <sup>54</sup>Mn and <sup>137</sup>Cs and on the order of 1000 for <sup>60</sup>Co.</p></div>","PeriodicalId":100966,"journal":{"name":"Nuclear and Chemical Waste Management","volume":"7 3","pages":"Pages 257-263"},"PeriodicalIF":0.0000,"publicationDate":"1987-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0191-815X(87)90070-2","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nuclear and Chemical Waste Management","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0191815X87900702","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Laboratory studies were conducted on select physical and chemical processes for decontamination of a composite waste lubricating oil from a boiling water reactor. Physical treatments included successive filtration through 25, 8 and 1 μm filters to remove particulate matter and centrifugation to remove water. Chemical treatment consisted of mixing the oil with an aqueous solution of the chelating agent ethylenediaminetetraacetic acid (EDTA) and centrifuging the resulting emulsion. The effectiveness of the treatment processes was evaluated by measuring radionuclide concentrations in the oil following each treatment step and calculating decontamination factors.
The total activity of the oil was dominated by 60Co, 54Mn, and 137Cs, although 51Cr, 58Co, 59Fe, and 134Cs were also present. Filtration consistently achieved decontamination factors of approximately 200, 100, and 40 for 137Cs, 54Mn, and 60Co, respectively, and reduced concentrations of the other radionuclides below their detection limits. Following filtration, centrifugation reduced 137Cs concentrations below the detection limit and reduced 54Mn and 60Co concentrations by approximately 40% and 20%, respectively. Subsequent chemical treatment with EDTA reduced the 54Mn concentration to below the detection limit and removed approximately 95% of the remaining 60Co activity. The overall decontamination factor for successive filtration, centrifugation, and chelation was in excess of 10,000 for 54Mn and 137Cs and on the order of 1000 for 60Co.