K. Yumoto , Y. Cho , J.A. Ogura , S. Kameda , T. Niihara , T. Nakaoka , R. Kanemaru , H. Nagaoka , H. Tabata , Y. Nakauchi , M. Ohtake , H. Ueda , S. Kasahara , T. Morota , S. Sugita
{"title":"利用激光诱导击穿光谱对月球上的长岩至玄武岩土壤和岩石进行元素分析","authors":"K. Yumoto , Y. Cho , J.A. Ogura , S. Kameda , T. Niihara , T. Nakaoka , R. Kanemaru , H. Nagaoka , H. Tabata , Y. Nakauchi , M. Ohtake , H. Ueda , S. Kasahara , T. Morota , S. Sugita","doi":"10.1016/j.sab.2024.107049","DOIUrl":null,"url":null,"abstract":"<div><div>In-situ analysis of major elements using laser-induced breakdown spectroscopy (LIBS) is essential for future lunar landing missions, yet its performance under lunar conditions remains not fully understood. This uncertainty arises from the absence of an atmosphere and the diverse range of surface materials, which vary in chemical composition from anorthosites to basalts, and in physical properties from fine regolith to boulders. To address these challenges, we developed and cross-validated a multivariate LIBS calibration model by measuring 169 compressed fine powders of geologic samples under vacuum. These samples fully encompass the bulk composition range of lunar meteorites. We investigated the applicability of the model to a wider range of samples by measuring lunar meteorites, terrestrial anorthites, and lunar simulants in various physical forms, including rock chips and soils with different grain sizes and bulk densities. For powder samples, the quantification accuracy, assessed using root mean squared error (RMSE), resulted in 2.5 wt% SiO<sub>2</sub>, 0.25 wt% TiO<sub>2</sub>, 1.2 wt% Al<sub>2</sub>O<sub>3</sub>, 1.3 wt% MgO, 1.2 wt% CaO, 0.33 wt% Na<sub>2</sub>O, 0.47 wt% K<sub>2</sub>O (0.060 wt% K<sub>2</sub>O in the <1 wt% range), and 1.5 wt% T-Fe<sub>2</sub>O<sub>3</sub>. For rock chip samples, the RMSEs were 3.1 wt% SiO<sub>2</sub>, 0.32 wt% TiO<sub>2</sub>, 2.2 wt% Al<sub>2</sub>O<sub>3</sub>, 2.5 wt% MgO, 2.0 wt% CaO, 0.33 wt% Na<sub>2</sub>O, 0.089 wt% K<sub>2</sub>O, and 2.1 wt% T-Fe<sub>2</sub>O<sub>3</sub>. Despite significant differences in physical conditions between powders and rocks, their RMSEs remained consistent within a factor of two. Changes in grain size or bulk density of soils had relatively minor effects on the RMSE. These RMSEs confirm that the quantification accuracy of LIBS is sufficient to distinguish the subgroups within the lunar anorthosite suite (e.g., anorthosites vs. norites) and basalts (e.g., high-Ti vs. low-Ti) across a range of soil types, from coarse to fine and from loose to compact, as well as rocks. Furthermore, our analysis shows that LIBS can differentiate between “purest” and “pure” anorthosites (98 and 95 vol% plagioclase, respectively) based on the 3σ detection limits of Mg and Fe lines. These capabilities of LIBS align well with the goals of future lunar exploration, such as locating ilmenite-rich soils for resource extraction, detecting purest anorthosites to understand early lunar evolution, and identifying noritic impact melts to refine lunar chronology. Overall, our results demonstrate that LIBS serves as a versatile tool for rapid geochemical characterization on the Moon.</div></div>","PeriodicalId":21890,"journal":{"name":"Spectrochimica Acta Part B: Atomic Spectroscopy","volume":"221 ","pages":"Article 107049"},"PeriodicalIF":3.2000,"publicationDate":"2024-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Elemental analyses of feldspathic to basaltic soils and rocks on the moon using laser-induced breakdown spectroscopy\",\"authors\":\"K. Yumoto , Y. Cho , J.A. Ogura , S. Kameda , T. Niihara , T. Nakaoka , R. Kanemaru , H. Nagaoka , H. Tabata , Y. Nakauchi , M. Ohtake , H. Ueda , S. Kasahara , T. Morota , S. Sugita\",\"doi\":\"10.1016/j.sab.2024.107049\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In-situ analysis of major elements using laser-induced breakdown spectroscopy (LIBS) is essential for future lunar landing missions, yet its performance under lunar conditions remains not fully understood. This uncertainty arises from the absence of an atmosphere and the diverse range of surface materials, which vary in chemical composition from anorthosites to basalts, and in physical properties from fine regolith to boulders. To address these challenges, we developed and cross-validated a multivariate LIBS calibration model by measuring 169 compressed fine powders of geologic samples under vacuum. These samples fully encompass the bulk composition range of lunar meteorites. We investigated the applicability of the model to a wider range of samples by measuring lunar meteorites, terrestrial anorthites, and lunar simulants in various physical forms, including rock chips and soils with different grain sizes and bulk densities. For powder samples, the quantification accuracy, assessed using root mean squared error (RMSE), resulted in 2.5 wt% SiO<sub>2</sub>, 0.25 wt% TiO<sub>2</sub>, 1.2 wt% Al<sub>2</sub>O<sub>3</sub>, 1.3 wt% MgO, 1.2 wt% CaO, 0.33 wt% Na<sub>2</sub>O, 0.47 wt% K<sub>2</sub>O (0.060 wt% K<sub>2</sub>O in the <1 wt% range), and 1.5 wt% T-Fe<sub>2</sub>O<sub>3</sub>. For rock chip samples, the RMSEs were 3.1 wt% SiO<sub>2</sub>, 0.32 wt% TiO<sub>2</sub>, 2.2 wt% Al<sub>2</sub>O<sub>3</sub>, 2.5 wt% MgO, 2.0 wt% CaO, 0.33 wt% Na<sub>2</sub>O, 0.089 wt% K<sub>2</sub>O, and 2.1 wt% T-Fe<sub>2</sub>O<sub>3</sub>. Despite significant differences in physical conditions between powders and rocks, their RMSEs remained consistent within a factor of two. Changes in grain size or bulk density of soils had relatively minor effects on the RMSE. These RMSEs confirm that the quantification accuracy of LIBS is sufficient to distinguish the subgroups within the lunar anorthosite suite (e.g., anorthosites vs. norites) and basalts (e.g., high-Ti vs. low-Ti) across a range of soil types, from coarse to fine and from loose to compact, as well as rocks. Furthermore, our analysis shows that LIBS can differentiate between “purest” and “pure” anorthosites (98 and 95 vol% plagioclase, respectively) based on the 3σ detection limits of Mg and Fe lines. These capabilities of LIBS align well with the goals of future lunar exploration, such as locating ilmenite-rich soils for resource extraction, detecting purest anorthosites to understand early lunar evolution, and identifying noritic impact melts to refine lunar chronology. 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Elemental analyses of feldspathic to basaltic soils and rocks on the moon using laser-induced breakdown spectroscopy
In-situ analysis of major elements using laser-induced breakdown spectroscopy (LIBS) is essential for future lunar landing missions, yet its performance under lunar conditions remains not fully understood. This uncertainty arises from the absence of an atmosphere and the diverse range of surface materials, which vary in chemical composition from anorthosites to basalts, and in physical properties from fine regolith to boulders. To address these challenges, we developed and cross-validated a multivariate LIBS calibration model by measuring 169 compressed fine powders of geologic samples under vacuum. These samples fully encompass the bulk composition range of lunar meteorites. We investigated the applicability of the model to a wider range of samples by measuring lunar meteorites, terrestrial anorthites, and lunar simulants in various physical forms, including rock chips and soils with different grain sizes and bulk densities. For powder samples, the quantification accuracy, assessed using root mean squared error (RMSE), resulted in 2.5 wt% SiO2, 0.25 wt% TiO2, 1.2 wt% Al2O3, 1.3 wt% MgO, 1.2 wt% CaO, 0.33 wt% Na2O, 0.47 wt% K2O (0.060 wt% K2O in the <1 wt% range), and 1.5 wt% T-Fe2O3. For rock chip samples, the RMSEs were 3.1 wt% SiO2, 0.32 wt% TiO2, 2.2 wt% Al2O3, 2.5 wt% MgO, 2.0 wt% CaO, 0.33 wt% Na2O, 0.089 wt% K2O, and 2.1 wt% T-Fe2O3. Despite significant differences in physical conditions between powders and rocks, their RMSEs remained consistent within a factor of two. Changes in grain size or bulk density of soils had relatively minor effects on the RMSE. These RMSEs confirm that the quantification accuracy of LIBS is sufficient to distinguish the subgroups within the lunar anorthosite suite (e.g., anorthosites vs. norites) and basalts (e.g., high-Ti vs. low-Ti) across a range of soil types, from coarse to fine and from loose to compact, as well as rocks. Furthermore, our analysis shows that LIBS can differentiate between “purest” and “pure” anorthosites (98 and 95 vol% plagioclase, respectively) based on the 3σ detection limits of Mg and Fe lines. These capabilities of LIBS align well with the goals of future lunar exploration, such as locating ilmenite-rich soils for resource extraction, detecting purest anorthosites to understand early lunar evolution, and identifying noritic impact melts to refine lunar chronology. Overall, our results demonstrate that LIBS serves as a versatile tool for rapid geochemical characterization on the Moon.
期刊介绍:
Spectrochimica Acta Part B: Atomic Spectroscopy, is intended for the rapid publication of both original work and reviews in the following fields:
Atomic Emission (AES), Atomic Absorption (AAS) and Atomic Fluorescence (AFS) spectroscopy;
Mass Spectrometry (MS) for inorganic analysis covering Spark Source (SS-MS), Inductively Coupled Plasma (ICP-MS), Glow Discharge (GD-MS), and Secondary Ion Mass Spectrometry (SIMS).
Laser induced atomic spectroscopy for inorganic analysis, including non-linear optical laser spectroscopy, covering Laser Enhanced Ionization (LEI), Laser Induced Fluorescence (LIF), Resonance Ionization Spectroscopy (RIS) and Resonance Ionization Mass Spectrometry (RIMS); Laser Induced Breakdown Spectroscopy (LIBS); Cavity Ringdown Spectroscopy (CRDS), Laser Ablation Inductively Coupled Plasma Atomic Emission Spectroscopy (LA-ICP-AES) and Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICP-MS).
X-ray spectrometry, X-ray Optics and Microanalysis, including X-ray fluorescence spectrometry (XRF) and related techniques, in particular Total-reflection X-ray Fluorescence Spectrometry (TXRF), and Synchrotron Radiation-excited Total reflection XRF (SR-TXRF).
Manuscripts dealing with (i) fundamentals, (ii) methodology development, (iii)instrumentation, and (iv) applications, can be submitted for publication.