Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation
Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotop...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Ko, P. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013transfer abstract |
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| Umfang: |
4 |
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| Übergeordnetes Werk: |
Enthalten in: Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy - Li, Qiang ELSEVIER, 2021, Amsterdam [u.a.] |
|---|---|
| Übergeordnetes Werk: |
volume:90 ; year:2013 ; day:1 ; month:12 ; pages:68-71 ; extent:4 |
| Links: |
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| DOI / URN: |
10.1016/j.sab.2013.10.008 |
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| 520 | |a Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. | ||
| 520 | |a Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. | ||
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10.1016/j.sab.2013.10.008 doi GBVA2013013000029.pica (DE-627)ELV022012354 (ELSEVIER)S0584-8547(13)00268-1 DE-627 ger DE-627 rakwb eng 540 530 540 DE-600 530 DE-600 540 VZ 42.15 bkl Ko, P. verfasserin aut Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation 2013transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Jovanovic, I. oth Enthalten in Elsevier Li, Qiang ELSEVIER Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy 2021 Amsterdam [u.a.] (DE-627)ELV005740053 volume:90 year:2013 day:1 month:12 pages:68-71 extent:4 https://doi.org/10.1016/j.sab.2013.10.008 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 42.15 Zellbiologie VZ AR 90 2013 1 1201 68-71 4 045F 540 |
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10.1016/j.sab.2013.10.008 doi GBVA2013013000029.pica (DE-627)ELV022012354 (ELSEVIER)S0584-8547(13)00268-1 DE-627 ger DE-627 rakwb eng 540 530 540 DE-600 530 DE-600 540 VZ 42.15 bkl Ko, P. verfasserin aut Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation 2013transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Jovanovic, I. oth Enthalten in Elsevier Li, Qiang ELSEVIER Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy 2021 Amsterdam [u.a.] (DE-627)ELV005740053 volume:90 year:2013 day:1 month:12 pages:68-71 extent:4 https://doi.org/10.1016/j.sab.2013.10.008 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 42.15 Zellbiologie VZ AR 90 2013 1 1201 68-71 4 045F 540 |
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10.1016/j.sab.2013.10.008 doi GBVA2013013000029.pica (DE-627)ELV022012354 (ELSEVIER)S0584-8547(13)00268-1 DE-627 ger DE-627 rakwb eng 540 530 540 DE-600 530 DE-600 540 VZ 42.15 bkl Ko, P. verfasserin aut Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation 2013transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Jovanovic, I. oth Enthalten in Elsevier Li, Qiang ELSEVIER Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy 2021 Amsterdam [u.a.] (DE-627)ELV005740053 volume:90 year:2013 day:1 month:12 pages:68-71 extent:4 https://doi.org/10.1016/j.sab.2013.10.008 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 42.15 Zellbiologie VZ AR 90 2013 1 1201 68-71 4 045F 540 |
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10.1016/j.sab.2013.10.008 doi GBVA2013013000029.pica (DE-627)ELV022012354 (ELSEVIER)S0584-8547(13)00268-1 DE-627 ger DE-627 rakwb eng 540 530 540 DE-600 530 DE-600 540 VZ 42.15 bkl Ko, P. verfasserin aut Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation 2013transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Jovanovic, I. oth Enthalten in Elsevier Li, Qiang ELSEVIER Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy 2021 Amsterdam [u.a.] (DE-627)ELV005740053 volume:90 year:2013 day:1 month:12 pages:68-71 extent:4 https://doi.org/10.1016/j.sab.2013.10.008 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 42.15 Zellbiologie VZ AR 90 2013 1 1201 68-71 4 045F 540 |
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10.1016/j.sab.2013.10.008 doi GBVA2013013000029.pica (DE-627)ELV022012354 (ELSEVIER)S0584-8547(13)00268-1 DE-627 ger DE-627 rakwb eng 540 530 540 DE-600 530 DE-600 540 VZ 42.15 bkl Ko, P. verfasserin aut Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation 2013transfer abstract 4 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. Jovanovic, I. oth Enthalten in Elsevier Li, Qiang ELSEVIER Dual stimuli-responsive polypeptide-calcium phosphate hybrid nanoparticles for co-delivery of multiple drugs in cancer therapy 2021 Amsterdam [u.a.] (DE-627)ELV005740053 volume:90 year:2013 day:1 month:12 pages:68-71 extent:4 https://doi.org/10.1016/j.sab.2013.10.008 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 42.15 Zellbiologie VZ AR 90 2013 1 1201 68-71 4 045F 540 |
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Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. 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boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation |
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Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation |
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Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. |
| abstractGer |
Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. |
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Spectral analysis of molecular emissions from laser-produced plasmas can augment laser-induced breakdown spectroscopy measurements, in which only atomic spectra are typically considered. Molecular isotopic shifts can be significantly greater than the respective atomic isotope shifts, enabling isotopic measurements with lower spectral resolution and in atmospheric pressure conditions. Successful isotopic measurements using molecular spectra have been made in the past by gating off the atomic emissions, or by the use of a femtosecond laser in conjunction with a non-gated detector. We report that it is possible to make accurate isotopic measurements by use of molecular emissions from non-gated spectral data even when nanosecond lasers are used. We demonstrate this capability by measuring the isotopic composition of boron-containing samples using 10-ns, 1064-nm pulses from an Nd:YAG laser and a non-gated detector. We investigate how the accuracy and precision of the multivariate calibration model used in the isotopic reconstruction is influenced by the spectral data analysis. The effect of the selection of the spectral region of interest for analysis and the optimization of a numerical spectral filter is studied. It is shown that the accuracy of isotopic reconstruction can be greatly improved by spectral filtering, and that it is relatively insensitive to laser pulse duration. |
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Boron isotopic measurements from spectrally filtered non-gated molecular spectra induced by laser ablation |
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