Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications
Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is pe...
Ausführliche Beschreibung
Autor*in: |
Borojovich, Eitan J. C. [verfasserIn] Moyal, Amiram [verfasserIn] Nikolski, Andrey [verfasserIn] Assulin, Maor [verfasserIn] Shamish, Zorik [verfasserIn] Elish, Eyal [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Anmerkung: |
© Akadémiai Kiadó, Budapest, Hungary 2021 |
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Übergeordnetes Werk: |
Enthalten in: Journal of radioanalytical and nuclear chemistry - Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968, 329(2021), 1 vom: 02. Juni, Seite 179-190 |
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Übergeordnetes Werk: |
volume:329 ; year:2021 ; number:1 ; day:02 ; month:06 ; pages:179-190 |
Links: |
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DOI / URN: |
10.1007/s10967-021-07788-8 |
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Katalog-ID: |
SPR044445369 |
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520 | |a Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. | ||
650 | 4 | |a Nuclear forensics |7 (dpeaa)DE-He213 | |
650 | 4 | |a Phosphate rocks |7 (dpeaa)DE-He213 | |
650 | 4 | |a Uranium |7 (dpeaa)DE-He213 | |
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700 | 1 | |a Moyal, Amiram |e verfasserin |4 aut | |
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700 | 1 | |a Assulin, Maor |e verfasserin |4 aut | |
700 | 1 | |a Shamish, Zorik |e verfasserin |4 aut | |
700 | 1 | |a Elish, Eyal |e verfasserin |4 aut | |
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10.1007/s10967-021-07788-8 doi (DE-627)SPR044445369 (SPR)s10967-021-07788-8-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Borojovich, Eitan J. C. verfasserin aut Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2021 Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 Moyal, Amiram verfasserin aut Nikolski, Andrey verfasserin aut Assulin, Maor verfasserin aut Shamish, Zorik verfasserin aut Elish, Eyal verfasserin aut Enthalten in Journal of radioanalytical and nuclear chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968 329(2021), 1 vom: 02. Juni, Seite 179-190 (DE-627)320578011 (DE-600)2017242-4 1588-2780 nnns volume:329 year:2021 number:1 day:02 month:06 pages:179-190 https://dx.doi.org/10.1007/s10967-021-07788-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 329 2021 1 02 06 179-190 |
spelling |
10.1007/s10967-021-07788-8 doi (DE-627)SPR044445369 (SPR)s10967-021-07788-8-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Borojovich, Eitan J. C. verfasserin aut Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2021 Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 Moyal, Amiram verfasserin aut Nikolski, Andrey verfasserin aut Assulin, Maor verfasserin aut Shamish, Zorik verfasserin aut Elish, Eyal verfasserin aut Enthalten in Journal of radioanalytical and nuclear chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968 329(2021), 1 vom: 02. Juni, Seite 179-190 (DE-627)320578011 (DE-600)2017242-4 1588-2780 nnns volume:329 year:2021 number:1 day:02 month:06 pages:179-190 https://dx.doi.org/10.1007/s10967-021-07788-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 329 2021 1 02 06 179-190 |
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10.1007/s10967-021-07788-8 doi (DE-627)SPR044445369 (SPR)s10967-021-07788-8-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Borojovich, Eitan J. C. verfasserin aut Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2021 Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 Moyal, Amiram verfasserin aut Nikolski, Andrey verfasserin aut Assulin, Maor verfasserin aut Shamish, Zorik verfasserin aut Elish, Eyal verfasserin aut Enthalten in Journal of radioanalytical and nuclear chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968 329(2021), 1 vom: 02. Juni, Seite 179-190 (DE-627)320578011 (DE-600)2017242-4 1588-2780 nnns volume:329 year:2021 number:1 day:02 month:06 pages:179-190 https://dx.doi.org/10.1007/s10967-021-07788-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 329 2021 1 02 06 179-190 |
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10.1007/s10967-021-07788-8 doi (DE-627)SPR044445369 (SPR)s10967-021-07788-8-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Borojovich, Eitan J. C. verfasserin aut Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2021 Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 Moyal, Amiram verfasserin aut Nikolski, Andrey verfasserin aut Assulin, Maor verfasserin aut Shamish, Zorik verfasserin aut Elish, Eyal verfasserin aut Enthalten in Journal of radioanalytical and nuclear chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968 329(2021), 1 vom: 02. Juni, Seite 179-190 (DE-627)320578011 (DE-600)2017242-4 1588-2780 nnns volume:329 year:2021 number:1 day:02 month:06 pages:179-190 https://dx.doi.org/10.1007/s10967-021-07788-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 329 2021 1 02 06 179-190 |
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10.1007/s10967-021-07788-8 doi (DE-627)SPR044445369 (SPR)s10967-021-07788-8-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Borojovich, Eitan J. C. verfasserin aut Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2021 Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 Moyal, Amiram verfasserin aut Nikolski, Andrey verfasserin aut Assulin, Maor verfasserin aut Shamish, Zorik verfasserin aut Elish, Eyal verfasserin aut Enthalten in Journal of radioanalytical and nuclear chemistry Dordrecht [u.a.] : Springer Science + Business Media B.V., 1968 329(2021), 1 vom: 02. Juni, Seite 179-190 (DE-627)320578011 (DE-600)2017242-4 1588-2780 nnns volume:329 year:2021 number:1 day:02 month:06 pages:179-190 https://dx.doi.org/10.1007/s10967-021-07788-8 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 329 2021 1 02 06 179-190 |
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C.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2021</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Akadémiai Kiadó, Budapest, Hungary 2021</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. 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Borojovich, Eitan J. C. |
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Borojovich, Eitan J. C. ddc 540 bkl 35.00 misc Nuclear forensics misc Phosphate rocks misc Uranium misc Chloride Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications |
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540 ASE 35.00 bkl Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications Nuclear forensics (dpeaa)DE-He213 Phosphate rocks (dpeaa)DE-He213 Uranium (dpeaa)DE-He213 Chloride (dpeaa)DE-He213 |
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ddc 540 bkl 35.00 misc Nuclear forensics misc Phosphate rocks misc Uranium misc Chloride |
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Borojovich, Eitan J. C. Moyal, Amiram Nikolski, Andrey Assulin, Maor Shamish, Zorik Elish, Eyal |
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halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications |
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Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications |
abstract |
Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. © Akadémiai Kiadó, Budapest, Hungary 2021 |
abstractGer |
Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. © Akadémiai Kiadó, Budapest, Hungary 2021 |
abstract_unstemmed |
Abstract An analytical approach for halides determination in uranium-bearing phosphate rocks, based on halides extraction from natural calcium phosphate by a metathesis reaction, followed by ion chromatography with conductivity detection analysis, is presented in this work. Chloride extraction is performed by mixing samples with sulfuric acid, causing an interchange between phosphate and sulfate ions towards calcium ions in the solid phase (metathesis). Addition of small amounts of calcium hydroxide improves the chromatographic determination by eliminating artifacts located in proximity to chloride retention time, and reducing phosphate peaks area. Limit of quantitation (LOQ) for chloride and bromide were found to be 25 mg/Kg and 50 mg/Kg, respectively. The metathesis reaction is proven by ED-XRF analysis of the precipitate produced during this reaction, showing the interchange between sulfate and phosphate ions. Chloride determination based on this approach was performed on several uranium-bearing phosphate rock samples from different sources. Since geolocation is one of the primary techniques needed for attribution, in a nuclear forensic investigation, this methodology may contribute to find new signatures, e.g. halides, in natural phosphate rocks deposits, to support that. The $ Cl^{−} $ content in 11 phosphate rock samples was determined after applying metathesis, and found to be in the range of 30–792 mg/Kg, supporting its relevance as nuclear forensic signature. The $ Br^{−} $ content was below the detection limit in all the samples. © Akadémiai Kiadó, Budapest, Hungary 2021 |
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container_issue |
1 |
title_short |
Halides as potential signatures for geolocation of uranium phosphate rocks for nuclear forensic applications |
url |
https://dx.doi.org/10.1007/s10967-021-07788-8 |
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author2 |
Moyal, Amiram Nikolski, Andrey Assulin, Maor Shamish, Zorik Elish, Eyal |
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Moyal, Amiram Nikolski, Andrey Assulin, Maor Shamish, Zorik Elish, Eyal |
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doi_str |
10.1007/s10967-021-07788-8 |
up_date |
2024-07-04T00:42:59.310Z |
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score |
7.4014397 |