Michael Schubert , Juergen Kopitz , Sabine Taeglich , Christian Lucks , Kay Knoeller
{"title":"作为地下水停留时间示踪剂的放射性硫--针对富含硫酸盐的水样调整 35S 提取方法。","authors":"Michael Schubert , Juergen Kopitz , Sabine Taeglich , Christian Lucks , Kay Knoeller","doi":"10.1016/j.jenvrad.2024.107553","DOIUrl":null,"url":null,"abstract":"<div><div>Cosmogenic radio-sulphur (<sup>35</sup>S) is applicable as aqueous environmental tracer for investigating sub-yearly groundwater residence times. For the purpose <sup>35</sup>SO<sub>4</sub> has to be extracted from large-volume water samples (ca. 20 l) and measured by liquid scintillation counting (LSC). Publications that discuss sample preparation approaches focus on waters with low or moderate sulphate concentrations based on sulphate extraction using an ion-exchange resin. However, sulphate extraction by ion-exchange is not feasible for water samples that contain total sulphate loads of over about 1500 mg. Our paper presents an approach for the preparation of water samples with sulphate loads of up to 6000 mg based on BaSO<sub>4</sub> precipitation directly from the sample. The key challenge of this approach is the co-precipitation of interfering natural radionuclides (<sup>226</sup>Ra, short-lived progeny of <sup>222</sup>Rn, <sup>210</sup>Pb + progeny, <sup>32/33</sup>P), which complicates LSC measurement of <sup>35</sup>S. Two options are discussed to allow either pre-precipitating the unwanted radionuclides before, or keeping them in solution during Ba<sup>35</sup>SO<sub>4</sub> precipitation.</div></div>","PeriodicalId":15667,"journal":{"name":"Journal of environmental radioactivity","volume":"280 ","pages":"Article 107553"},"PeriodicalIF":1.9000,"publicationDate":"2024-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Radio-sulphur as groundwater residence time tracer – Adapting the 35S extraction approach for water samples rich in sulphate\",\"authors\":\"Michael Schubert , Juergen Kopitz , Sabine Taeglich , Christian Lucks , Kay Knoeller\",\"doi\":\"10.1016/j.jenvrad.2024.107553\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cosmogenic radio-sulphur (<sup>35</sup>S) is applicable as aqueous environmental tracer for investigating sub-yearly groundwater residence times. For the purpose <sup>35</sup>SO<sub>4</sub> has to be extracted from large-volume water samples (ca. 20 l) and measured by liquid scintillation counting (LSC). Publications that discuss sample preparation approaches focus on waters with low or moderate sulphate concentrations based on sulphate extraction using an ion-exchange resin. However, sulphate extraction by ion-exchange is not feasible for water samples that contain total sulphate loads of over about 1500 mg. Our paper presents an approach for the preparation of water samples with sulphate loads of up to 6000 mg based on BaSO<sub>4</sub> precipitation directly from the sample. The key challenge of this approach is the co-precipitation of interfering natural radionuclides (<sup>226</sup>Ra, short-lived progeny of <sup>222</sup>Rn, <sup>210</sup>Pb + progeny, <sup>32/33</sup>P), which complicates LSC measurement of <sup>35</sup>S. Two options are discussed to allow either pre-precipitating the unwanted radionuclides before, or keeping them in solution during Ba<sup>35</sup>SO<sub>4</sub> precipitation.</div></div>\",\"PeriodicalId\":15667,\"journal\":{\"name\":\"Journal of environmental radioactivity\",\"volume\":\"280 \",\"pages\":\"Article 107553\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2024-10-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of environmental radioactivity\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0265931X24001851\",\"RegionNum\":3,\"RegionCategory\":\"环境科学与生态学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of environmental radioactivity","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0265931X24001851","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Radio-sulphur as groundwater residence time tracer – Adapting the 35S extraction approach for water samples rich in sulphate
Cosmogenic radio-sulphur (35S) is applicable as aqueous environmental tracer for investigating sub-yearly groundwater residence times. For the purpose 35SO4 has to be extracted from large-volume water samples (ca. 20 l) and measured by liquid scintillation counting (LSC). Publications that discuss sample preparation approaches focus on waters with low or moderate sulphate concentrations based on sulphate extraction using an ion-exchange resin. However, sulphate extraction by ion-exchange is not feasible for water samples that contain total sulphate loads of over about 1500 mg. Our paper presents an approach for the preparation of water samples with sulphate loads of up to 6000 mg based on BaSO4 precipitation directly from the sample. The key challenge of this approach is the co-precipitation of interfering natural radionuclides (226Ra, short-lived progeny of 222Rn, 210Pb + progeny, 32/33P), which complicates LSC measurement of 35S. Two options are discussed to allow either pre-precipitating the unwanted radionuclides before, or keeping them in solution during Ba35SO4 precipitation.
期刊介绍:
The Journal of Environmental Radioactivity provides a coherent international forum for publication of original research or review papers on any aspect of the occurrence of radioactivity in natural systems.
Relevant subject areas range from applications of environmental radionuclides as mechanistic or timescale tracers of natural processes to assessments of the radioecological or radiological effects of ambient radioactivity. Papers deal with naturally occurring nuclides or with those created and released by man through nuclear weapons manufacture and testing, energy production, fuel-cycle technology, etc. Reports on radioactivity in the oceans, sediments, rivers, lakes, groundwaters, soils, atmosphere and all divisions of the biosphere are welcomed, but these should not simply be of a monitoring nature unless the data are particularly innovative.