Nora M. Bernet, Cleo Soldini, Timo M. O. Felder, Kristýna Lapčíková, Cajetan Neubauer, Wendy L. Queen, Ralf Kaegi, Federica Tamburini, Thomas B. Hofstetter
{"title":"电喷雾电离轨道阱质谱法分析磷酸盐和有机磷化合物的氧同位素","authors":"Nora M. Bernet, Cleo Soldini, Timo M. O. Felder, Kristýna Lapčíková, Cajetan Neubauer, Wendy L. Queen, Ralf Kaegi, Federica Tamburini, Thomas B. Hofstetter","doi":"10.1021/acs.analchem.5c04367","DOIUrl":null,"url":null,"abstract":"Orbitrap mass spectrometry with electrospray ionization (ESI-Orbitrap MS) enables <sup>18</sup>O/<sup>16</sup>O ratio measurements in phosphate and organophosphorus compounds, which offers promising avenues for the study of metabolic, biogeochemical, and environmental processes. While the instrumental feasibility of such <sup>18</sup>O/<sup>16</sup>O ratio measurements has been shown, the applicability of such analyses in aqueous matrices on multipurpose mass spectrometers remains unaddressed. Here, we (i) evaluated the interplay between instrument parameters and the long-term accuracy and precision of ESI-Orbitrap MS for the determination of δ<sup>18</sup>O(PO<sub>4</sub>) from H<sub>2</sub>PO<sub>4</sub><sup>–</sup> vs PO<sub>3</sub><sup>–</sup> fragments of phosphate, (ii) identified properties of methanolic sample solutions that are critical for accurate and precise measurements, and (iii) propose a sample purification procedure for the elimination of matrix-based interferences. In 10 measurement campaigns over two years, we observed a long-term reproducibility of δ<sup>18</sup>O(PO<sub>4</sub>) within ±2.8‰. Results of in-source fragmentation experiments of H<sub>2</sub>PO<sub>4</sub><sup>–</sup> to PO<sub>3</sub><sup>–</sup> show excellent agreement of δ<sup>18</sup>O and offer promising opportunities to probe for <sup>18</sup>O/<sup>16</sup>O ratios in organophosphorus compounds. By investigating the effect of the aqueous matrix and interfering anions on <sup>18</sup>O/<sup>16</sup>O ratio measurements, we found that a water content exceeding 50 vol % and the presence of oxyanions such as nitrate and sulfate limit measurement accuracy due to interferences of matrix constituents in the ESI source. To overcome these challenges, we evaluated selective phosphate extraction with a zirconium-based metal–organic framework (MOF) as sorbent. The resulting purification procedure allowed for successful extraction and recovery of phosphate from nitrate- and sulfate-containing aqueous solutions, resulting in methanolic phosphate samples that enabled accurate analyses of δ<sup>18</sup>O(PO<sub>4</sub>) by ESI-Orbitrap MS.","PeriodicalId":27,"journal":{"name":"Analytical Chemistry","volume":"6 1","pages":""},"PeriodicalIF":6.7000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Oxygen Isotope Analyses of Phosphate and Organophosphorus Compounds by Electrospray Ionization Orbitrap Mass Spectrometry\",\"authors\":\"Nora M. Bernet, Cleo Soldini, Timo M. O. Felder, Kristýna Lapčíková, Cajetan Neubauer, Wendy L. Queen, Ralf Kaegi, Federica Tamburini, Thomas B. Hofstetter\",\"doi\":\"10.1021/acs.analchem.5c04367\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Orbitrap mass spectrometry with electrospray ionization (ESI-Orbitrap MS) enables <sup>18</sup>O/<sup>16</sup>O ratio measurements in phosphate and organophosphorus compounds, which offers promising avenues for the study of metabolic, biogeochemical, and environmental processes. While the instrumental feasibility of such <sup>18</sup>O/<sup>16</sup>O ratio measurements has been shown, the applicability of such analyses in aqueous matrices on multipurpose mass spectrometers remains unaddressed. Here, we (i) evaluated the interplay between instrument parameters and the long-term accuracy and precision of ESI-Orbitrap MS for the determination of δ<sup>18</sup>O(PO<sub>4</sub>) from H<sub>2</sub>PO<sub>4</sub><sup>–</sup> vs PO<sub>3</sub><sup>–</sup> fragments of phosphate, (ii) identified properties of methanolic sample solutions that are critical for accurate and precise measurements, and (iii) propose a sample purification procedure for the elimination of matrix-based interferences. In 10 measurement campaigns over two years, we observed a long-term reproducibility of δ<sup>18</sup>O(PO<sub>4</sub>) within ±2.8‰. Results of in-source fragmentation experiments of H<sub>2</sub>PO<sub>4</sub><sup>–</sup> to PO<sub>3</sub><sup>–</sup> show excellent agreement of δ<sup>18</sup>O and offer promising opportunities to probe for <sup>18</sup>O/<sup>16</sup>O ratios in organophosphorus compounds. By investigating the effect of the aqueous matrix and interfering anions on <sup>18</sup>O/<sup>16</sup>O ratio measurements, we found that a water content exceeding 50 vol % and the presence of oxyanions such as nitrate and sulfate limit measurement accuracy due to interferences of matrix constituents in the ESI source. To overcome these challenges, we evaluated selective phosphate extraction with a zirconium-based metal–organic framework (MOF) as sorbent. 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Oxygen Isotope Analyses of Phosphate and Organophosphorus Compounds by Electrospray Ionization Orbitrap Mass Spectrometry
Orbitrap mass spectrometry with electrospray ionization (ESI-Orbitrap MS) enables 18O/16O ratio measurements in phosphate and organophosphorus compounds, which offers promising avenues for the study of metabolic, biogeochemical, and environmental processes. While the instrumental feasibility of such 18O/16O ratio measurements has been shown, the applicability of such analyses in aqueous matrices on multipurpose mass spectrometers remains unaddressed. Here, we (i) evaluated the interplay between instrument parameters and the long-term accuracy and precision of ESI-Orbitrap MS for the determination of δ18O(PO4) from H2PO4– vs PO3– fragments of phosphate, (ii) identified properties of methanolic sample solutions that are critical for accurate and precise measurements, and (iii) propose a sample purification procedure for the elimination of matrix-based interferences. In 10 measurement campaigns over two years, we observed a long-term reproducibility of δ18O(PO4) within ±2.8‰. Results of in-source fragmentation experiments of H2PO4– to PO3– show excellent agreement of δ18O and offer promising opportunities to probe for 18O/16O ratios in organophosphorus compounds. By investigating the effect of the aqueous matrix and interfering anions on 18O/16O ratio measurements, we found that a water content exceeding 50 vol % and the presence of oxyanions such as nitrate and sulfate limit measurement accuracy due to interferences of matrix constituents in the ESI source. To overcome these challenges, we evaluated selective phosphate extraction with a zirconium-based metal–organic framework (MOF) as sorbent. The resulting purification procedure allowed for successful extraction and recovery of phosphate from nitrate- and sulfate-containing aqueous solutions, resulting in methanolic phosphate samples that enabled accurate analyses of δ18O(PO4) by ESI-Orbitrap MS.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.