Pub Date : 2024-12-31DOI: 10.1007/s10967-024-09920-w
E. Wong, H. J. Tan, J. A. Corcho-Alvarado, E. Loh, J. Ong, C. Y. Ong, D. Toh, S. Röllin, R. Gosteli, H. Sahli, V. Furrer, S. Kradolfer, J. Ossola, C. Von Gunten, M. Stauffer
This paper provides insights into the radioactivity levels in soils and marine sediments from selected monitoring sites in Singapore. The environmental samples were measured for naturally occurring (e.g., 40K, 238U, 235U, 234U and 232Th) and anthropogenic (e.g., 90Sr, 137Cs, 239Pu and 240Pu) radionuclides. Additionally, the 137Cs activity in surface seawater was analysed. In soil, the decay series of 232Th and 238U are the highest contributors to the total radioactivity, while in sediments, 40K is the main contributor to the total radioactivity. The massic activities of anthropogenic radionuclides in soil (90Sr: 0.24–0.34 Bq kg−1; 137Cs: < 0.3–0.65 Bq kg−1; 239+240Pu: 0.002–0.057 Bq kg−1) and sediment (90Sr: 0.15–0.17 Bq kg−1; 137Cs: < 0.46–0.54 Bq kg−1; 239+240Pu: 0.239–0.294 Bq kg−1), and the activity concentration of 137Cs in seawater (137Cs: 1.1 mBq kg−1), are low and comparable to the values reported for the region. The Pu isotope data demonstrates that the main source of anthropogenic radionuclides in soil (240Pu/239Pu atom ratios: 0.17–0.19) is the global fallout from nuclear weapons testings (NWTs); in sediments (240Pu/239Pu atom ratios: 0.24–0.26), contributions from the Pacific Proving Grounds (PPG) have also been identified. This study also highlights significant differences in radioactivity levels in soils between the northern and central regions of Singapore, which are attributed to soil disturbances in the northern region as a result of intensive anthropogenic activities carried out in the 1980s.
{"title":"Natural and anthropogenic radionuclides in selected environmental radioactivity monitoring sites in Singapore","authors":"E. Wong, H. J. Tan, J. A. Corcho-Alvarado, E. Loh, J. Ong, C. Y. Ong, D. Toh, S. Röllin, R. Gosteli, H. Sahli, V. Furrer, S. Kradolfer, J. Ossola, C. Von Gunten, M. Stauffer","doi":"10.1007/s10967-024-09920-w","DOIUrl":"10.1007/s10967-024-09920-w","url":null,"abstract":"<div><p>This paper provides insights into the radioactivity levels in soils and marine sediments from selected monitoring sites in Singapore. The environmental samples were measured for naturally occurring (e.g., <sup>40</sup>K, <sup>238</sup>U, <sup>235</sup>U, <sup>234</sup>U and <sup>232</sup>Th) and anthropogenic (e.g., <sup>90</sup>Sr, <sup>137</sup>Cs, <sup>239</sup>Pu and <sup>240</sup>Pu) radionuclides. Additionally, the <sup>137</sup>Cs activity in surface seawater was analysed. In soil, the decay series of <sup>232</sup>Th and <sup>238</sup>U are the highest contributors to the total radioactivity, while in sediments, <sup>40</sup>K is the main contributor to the total radioactivity. The massic activities of anthropogenic radionuclides in soil (<sup>90</sup>Sr: 0.24–0.34 Bq kg<sup>−1</sup>; <sup>137</sup>Cs: < 0.3–0.65 Bq kg<sup>−1</sup>; <sup>239+240</sup>Pu: 0.002–0.057 Bq kg<sup>−1</sup>) and sediment (<sup>90</sup>Sr: 0.15–0.17 Bq kg<sup>−1</sup>; <sup>137</sup>Cs: < 0.46–0.54 Bq kg<sup>−1</sup>; <sup>239+240</sup>Pu: 0.239–0.294 Bq kg<sup>−1</sup>), and the activity concentration of <sup>137</sup>Cs in seawater (<sup>137</sup>Cs: 1.1 mBq kg<sup>−1</sup>), are low and comparable to the values reported for the region. The Pu isotope data demonstrates that the main source of anthropogenic radionuclides in soil (<sup>240</sup>Pu/<sup>239</sup>Pu atom ratios: 0.17–0.19) is the global fallout from nuclear weapons testings (NWTs); in sediments (<sup>240</sup>Pu/<sup>239</sup>Pu atom ratios: 0.24–0.26), contributions from the Pacific Proving Grounds (PPG) have also been identified. This study also highlights significant differences in radioactivity levels in soils between the northern and central regions of Singapore, which are attributed to soil disturbances in the northern region as a result of intensive anthropogenic activities carried out in the 1980s.</p></div>","PeriodicalId":661,"journal":{"name":"Journal of Radioanalytical and Nuclear Chemistry","volume":"334 2","pages":"1433 - 1443"},"PeriodicalIF":1.5,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10967-024-09920-w.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143481138","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-31DOI: 10.1007/s10967-024-09878-9
P. Costa, J. L. Weaver, M. P. Raele, K. Pritchard, J. B. Leão, C. Domienikan, N. C. Maliszewskyj, F. S. da Silva, W. W. Pereira, F. A. Genezini
This study demonstrates the construction and operation of a portable, solid-state thermal neutron sensor that utilizes a photodiode coated with a thin layer of boron-10 (10B). The boron layer was created using pulsed laser deposition and analyzed with neutron depth profiling (NDP) and scanning electron microscopy (SEM). The sensor's response to both thermal and cold neutrons was evaluated under varying neutron fluence rates. Additionally, the impact of the angles between the neutron beam and the sensor surface was examined. SEM results showed a porous 10B film structure, while NDP indicated a nearly uniform distribution of the isotope throughout the film. The electronic signal generated by the sensor exhibited a linear response to neutron fluence rates. However, the measured intrinsic efficiencies were lower than those of commercially available gas-phase detectors, with thermal neutrons yielding an efficiency of (1.17 ± 0.01) % and cold neutrons at (1.78 ± 0.01) %. Potential design upgrades that could increase the sensor's efficiency in the future are also discussed.
{"title":"Development and performance of a low-cost, solid-state, thermal neutron sensor with a 10B converter","authors":"P. Costa, J. L. Weaver, M. P. Raele, K. Pritchard, J. B. Leão, C. Domienikan, N. C. Maliszewskyj, F. S. da Silva, W. W. Pereira, F. A. Genezini","doi":"10.1007/s10967-024-09878-9","DOIUrl":"10.1007/s10967-024-09878-9","url":null,"abstract":"<div><p>This study demonstrates the construction and operation of a portable, solid-state thermal neutron sensor that utilizes a photodiode coated with a thin layer of boron-10 (<sup>10</sup>B). The boron layer was created using pulsed laser deposition and analyzed with neutron depth profiling (NDP) and scanning electron microscopy (SEM). The sensor's response to both thermal and cold neutrons was evaluated under varying neutron fluence rates. Additionally, the impact of the angles between the neutron beam and the sensor surface was examined. SEM results showed a porous <sup>10</sup>B film structure, while NDP indicated a nearly uniform distribution of the isotope throughout the film. The electronic signal generated by the sensor exhibited a linear response to neutron fluence rates. However, the measured intrinsic efficiencies were lower than those of commercially available gas-phase detectors, with thermal neutrons yielding an efficiency of (1.17 ± 0.01) % and cold neutrons at (1.78 ± 0.01) %. Potential design upgrades that could increase the sensor's efficiency in the future are also discussed.</p></div>","PeriodicalId":661,"journal":{"name":"Journal of Radioanalytical and Nuclear Chemistry","volume":"334 2","pages":"1333 - 1342"},"PeriodicalIF":1.5,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143481157","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-31DOI: 10.1007/s10967-024-09925-5
Zhaoying Zhang, He Cai, Zhenjiang Tian, Chuanying Liu, Chengliang Xiao
99mTc, as the most widely used radioactive nuclide in diagnostic imaging, whose supply heavily relies on the 99Mo. Neutron activation technology, as an alternative to uranium fission technique, has become a pivotal route for producing 99Mo. A critical aspect of its practical application lies in enhancing the sorption capacity of the column chromatography packing materials for the low specific activity molybdenum product. This study synthesizes two types of iron-cerium bimetallic composite materials, iron-cerium alkoxide (ICA) and iron-cerium oxide (ICO), as novel column chromatography packing materials compatible with low specific activity 99Mo. Characterization techniques such as TEM, XRD, and BET were employed to reveal the surface morphology and mesoporous structure of ICA and ICO. An evaluation of their sorption performance showed that both ICA and ICO exhibited rapid sorption kinetics (< 10 min) and excellent sorption selectivity. Notably, ICA demonstrated a static sorption capacity of 207 mg Mo/g and a dynamic sorption capacity of 180 mg Mo/g, surpassing most reported adsorbents. Mechanistic studies using XPS, FT-IR, and zeta potential measurement suggest that the sorption of Mo onto both ICA and ICO is primarily governed by electrostatic interactions. Additionally, the sorption mechanism for ICA also includes ion exchange and surface complexation. With Re being the most common non-radioactive substitute for 99mTc, desorption separation experiments revealed that ICA has a Re elution rate of over 75%, confirming its potential as a promising candidate material in low specific activity 99Mo/99mTc generators.
{"title":"Iron-cerium composites with high molybdenum sorption capability: potential application in low specific activity 99Mo/99mTc generators","authors":"Zhaoying Zhang, He Cai, Zhenjiang Tian, Chuanying Liu, Chengliang Xiao","doi":"10.1007/s10967-024-09925-5","DOIUrl":"10.1007/s10967-024-09925-5","url":null,"abstract":"<div><p> <sup>99m</sup>Tc, as the most widely used radioactive nuclide in diagnostic imaging, whose supply heavily relies on the <sup>99</sup>Mo. Neutron activation technology, as an alternative to uranium fission technique, has become a pivotal route for producing <sup>99</sup>Mo. A critical aspect of its practical application lies in enhancing the sorption capacity of the column chromatography packing materials for the low specific activity molybdenum product. This study synthesizes two types of iron-cerium bimetallic composite materials, iron-cerium alkoxide (ICA) and iron-cerium oxide (ICO), as novel column chromatography packing materials compatible with low specific activity <sup>99</sup>Mo. Characterization techniques such as TEM, XRD, and BET were employed to reveal the surface morphology and mesoporous structure of ICA and ICO. An evaluation of their sorption performance showed that both ICA and ICO exhibited rapid sorption kinetics (< 10 min) and excellent sorption selectivity. Notably, ICA demonstrated a static sorption capacity of 207 mg Mo/g and a dynamic sorption capacity of 180 mg Mo/g, surpassing most reported adsorbents. Mechanistic studies using XPS, FT-IR, and zeta potential measurement suggest that the sorption of Mo onto both ICA and ICO is primarily governed by electrostatic interactions. Additionally, the sorption mechanism for ICA also includes ion exchange and surface complexation. With Re being the most common non-radioactive substitute for <sup>99m</sup>Tc, desorption separation experiments revealed that ICA has a Re elution rate of over 75%, confirming its potential as a promising candidate material in low specific activity <sup>99</sup>Mo/<sup>99m</sup>Tc generators.</p></div>","PeriodicalId":661,"journal":{"name":"Journal of Radioanalytical and Nuclear Chemistry","volume":"334 2","pages":"1263 - 1273"},"PeriodicalIF":1.5,"publicationDate":"2024-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143481156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-20DOI: 10.1007/s10967-024-09912-w
Taha Yaseen Wais, Barivan Farooq Namq, Laith Ahmed Najam, Hyam Nazmy Badr Khalaf, Abbasher M. Gismelseed, Howaida Mansour, Mostafa Yuness Abdelfatah Mostafa
Using a high-purity germanium detector (HPGe), the natural and artificial radioactivity in soil samples taken from agricultural regions near the Al-Kasak oil refinery were examined. According to estimates, the average specific activities of 226Ra, 232Th, 40K, and 137Cs were 20, 15, 283, and 3.6 Bq kg−1, respectively. The specific activities of 226Ra, 232Th, 40K, and 137Cs in the soil samples were comparatively lower than the average values of these radionuclides worldwide. The investigation also analyzed several radiological hazard indices. The hazard indices calculated in this study were utilized to assess the potential health risks associated with radiation in the soil. The results indicate that these indices are significantly below their permissible limits. Therefore, the soil in the study area does not pose any excessive radiation exposure to the inhabitants and can be safely used as construction material without presenting an immediate radiological threat to the public.
{"title":"Natural and artificial radioactivity levels in the agricultural soil of lands near the Al-Kasak oil refinery, northern Iraq","authors":"Taha Yaseen Wais, Barivan Farooq Namq, Laith Ahmed Najam, Hyam Nazmy Badr Khalaf, Abbasher M. Gismelseed, Howaida Mansour, Mostafa Yuness Abdelfatah Mostafa","doi":"10.1007/s10967-024-09912-w","DOIUrl":"10.1007/s10967-024-09912-w","url":null,"abstract":"<div><p>Using a high-purity germanium detector (HPGe), the natural and artificial radioactivity in soil samples taken from agricultural regions near the Al-Kasak oil refinery were examined. According to estimates, the average specific activities of <sup>226</sup>Ra, <sup>232</sup>Th, <sup>40</sup>K, and <sup>137</sup>Cs were 20, 15, 283, and 3.6 Bq kg<sup>−1</sup>, respectively. The specific activities of <sup>226</sup>Ra, <sup>232</sup>Th, <sup>40</sup>K, and <sup>137</sup>Cs in the soil samples were comparatively lower than the average values of these radionuclides worldwide. The investigation also analyzed several radiological hazard indices. The hazard indices calculated in this study were utilized to assess the potential health risks associated with radiation in the soil. The results indicate that these indices are significantly below their permissible limits. Therefore, the soil in the study area does not pose any excessive radiation exposure to the inhabitants and can be safely used as construction material without presenting an immediate radiological threat to the public.</p></div>","PeriodicalId":661,"journal":{"name":"Journal of Radioanalytical and Nuclear Chemistry","volume":"334 2","pages":"1471 - 1484"},"PeriodicalIF":1.5,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143481269","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-20DOI: 10.1007/s10967-024-09895-8
Hani M. Hamed, Mohamed Soliman, Fatma S. Abdou, Sheldon Landsberger, A. H. Ali, Y. M. Khawassek, Akram Eldidamony, Abdullah M. Othman
A practical approach has been developed to estimate the thermal neutron self-shielding correction of Egyptian monazite sand, a primary source of rare earth elements (REEs), thorium (Th) and phosphorus (P) with uranium (U) quantity, consequently, the k0 Neutron Activation analysis (k0-NAA) method can be used to accurately quantify the elemental content. Assessment of neutron self-shielding correction was based on the optimization of the mass-specific count rate mathematical relationship by practical treatments including the using of inert diluting substance namely silicon dioxide (SiO2). It demonstrated that neutron self-shielding underestimated the elements' concentration in the sample by 59.2%. k0-NAA method detected REEs at 56.48%, Th at 5.67%, U at 0.381%. The approach was evaluated using synthetic monazite and also compared with ICP-MS and theoretical calculations. The overall performance of the method proved to be acceptable.
{"title":"A practical approach for estimation of thermal neutron self-shielding for quantification of REEs, Th and U in Egyptian monazite sand employing k0-NAA","authors":"Hani M. Hamed, Mohamed Soliman, Fatma S. Abdou, Sheldon Landsberger, A. H. Ali, Y. M. Khawassek, Akram Eldidamony, Abdullah M. Othman","doi":"10.1007/s10967-024-09895-8","DOIUrl":"10.1007/s10967-024-09895-8","url":null,"abstract":"<div><p>A practical approach has been developed to estimate the thermal neutron self-shielding correction of Egyptian monazite sand, a primary source of rare earth elements (REEs), thorium (Th) and phosphorus (P) with uranium (U) quantity, consequently, the <i>k</i><sub>0</sub> Neutron Activation analysis (k<sub><i>0</i></sub>-NAA) method can be used to accurately quantify the elemental content. Assessment of neutron self-shielding correction was based on the optimization of the mass-specific count rate mathematical relationship by practical treatments including the using of inert diluting substance namely silicon dioxide (SiO<sub>2</sub>). It demonstrated that neutron self-shielding underestimated the elements' concentration in the sample by 59.2%. <i>k</i><sub>0</sub>-NAA method detected REEs at 56.48%, Th at 5.67%, U at 0.381%. The approach was evaluated using synthetic monazite and also compared with ICP-MS and theoretical calculations. The overall performance of the method proved to be acceptable.</p></div>","PeriodicalId":661,"journal":{"name":"Journal of Radioanalytical and Nuclear Chemistry","volume":"334 2","pages":"1225 - 1246"},"PeriodicalIF":1.5,"publicationDate":"2024-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143481268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-12-16DOI: 10.1007/s10967-024-09894-9
Muhammad Yaruq Ali Khan, Xu Zhao, Zhiwu Lei, Yucheng Su, Hongqiang Wang, Eming Hu, Fang Hu, Adil Ejaz, Rida Fatima, Qingliang Wang
This study used oxidative pre-treatment and leaching methods to examine the extraction efficiency of uranium oxide (UO2) from UO2 ore. A 4-hour oxidative pre-treatment at 75 °C using a solution of 0.1 g of KMnO4, 3 mL of NaClO, and 12 mL of water at pH 0.3 was one of the ideal settings. After this treatment, 100 mL of deionized water at room temperature showed a leaching rate of 99.9% after 24 h. The results showed that leaching efficiency was much increased by acidic conditions. These findings providing insights to improve extraction in the uranium industry.