Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with
In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL de...
Ausführliche Beschreibung
Autor*in: |
Qiao, Lizhen [verfasserIn] Tao, Yuan [verfasserIn] Qin, Honglin [verfasserIn] Niu, Ruiting [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2022 |
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Schlagwörter: |
Dispersive liquid-liquid extraction |
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Übergeordnetes Werk: |
Enthalten in: Journal of chromatography / A - New York, NY [u.a.] : Science Direct, 1958, 1689 |
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Übergeordnetes Werk: |
volume:1689 |
DOI / URN: |
10.1016/j.chroma.2022.463771 |
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Katalog-ID: |
ELV009105425 |
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520 | |a In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. | ||
650 | 4 | |a Dispersive liquid-liquid extraction | |
650 | 4 | |a Multi-magnetic center magnetic ionic liquids | |
650 | 4 | |a Back-extraction | |
650 | 4 | |a Parabens | |
700 | 1 | |a Tao, Yuan |e verfasserin |4 aut | |
700 | 1 | |a Qin, Honglin |e verfasserin |4 aut | |
700 | 1 | |a Niu, Ruiting |e verfasserin |4 aut | |
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2022 |
allfields |
10.1016/j.chroma.2022.463771 doi (DE-627)ELV009105425 (ELSEVIER)S0021-9673(22)00962-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Qiao, Lizhen verfasserin (orcid)0000-0002-3290-9070 aut Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. Dispersive liquid-liquid extraction Multi-magnetic center magnetic ionic liquids Back-extraction Parabens Tao, Yuan verfasserin aut Qin, Honglin verfasserin aut Niu, Ruiting verfasserin aut Enthalten in Journal of chromatography / A New York, NY [u.a.] : Science Direct, 1958 1689 Online-Ressource (DE-627)302467416 (DE-600)1491247-8 (DE-576)094950253 1873-3778 nnns volume:1689 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1689 |
spelling |
10.1016/j.chroma.2022.463771 doi (DE-627)ELV009105425 (ELSEVIER)S0021-9673(22)00962-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Qiao, Lizhen verfasserin (orcid)0000-0002-3290-9070 aut Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. Dispersive liquid-liquid extraction Multi-magnetic center magnetic ionic liquids Back-extraction Parabens Tao, Yuan verfasserin aut Qin, Honglin verfasserin aut Niu, Ruiting verfasserin aut Enthalten in Journal of chromatography / A New York, NY [u.a.] : Science Direct, 1958 1689 Online-Ressource (DE-627)302467416 (DE-600)1491247-8 (DE-576)094950253 1873-3778 nnns volume:1689 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1689 |
allfields_unstemmed |
10.1016/j.chroma.2022.463771 doi (DE-627)ELV009105425 (ELSEVIER)S0021-9673(22)00962-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Qiao, Lizhen verfasserin (orcid)0000-0002-3290-9070 aut Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. Dispersive liquid-liquid extraction Multi-magnetic center magnetic ionic liquids Back-extraction Parabens Tao, Yuan verfasserin aut Qin, Honglin verfasserin aut Niu, Ruiting verfasserin aut Enthalten in Journal of chromatography / A New York, NY [u.a.] : Science Direct, 1958 1689 Online-Ressource (DE-627)302467416 (DE-600)1491247-8 (DE-576)094950253 1873-3778 nnns volume:1689 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1689 |
allfieldsGer |
10.1016/j.chroma.2022.463771 doi (DE-627)ELV009105425 (ELSEVIER)S0021-9673(22)00962-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Qiao, Lizhen verfasserin (orcid)0000-0002-3290-9070 aut Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. Dispersive liquid-liquid extraction Multi-magnetic center magnetic ionic liquids Back-extraction Parabens Tao, Yuan verfasserin aut Qin, Honglin verfasserin aut Niu, Ruiting verfasserin aut Enthalten in Journal of chromatography / A New York, NY [u.a.] : Science Direct, 1958 1689 Online-Ressource (DE-627)302467416 (DE-600)1491247-8 (DE-576)094950253 1873-3778 nnns volume:1689 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1689 |
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10.1016/j.chroma.2022.463771 doi (DE-627)ELV009105425 (ELSEVIER)S0021-9673(22)00962-1 DE-627 ger DE-627 rda eng 540 DE-600 35.00 bkl Qiao, Lizhen verfasserin (orcid)0000-0002-3290-9070 aut Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with 2022 nicht spezifiziert zzz rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. Dispersive liquid-liquid extraction Multi-magnetic center magnetic ionic liquids Back-extraction Parabens Tao, Yuan verfasserin aut Qin, Honglin verfasserin aut Niu, Ruiting verfasserin aut Enthalten in Journal of chromatography / A New York, NY [u.a.] : Science Direct, 1958 1689 Online-Ressource (DE-627)302467416 (DE-600)1491247-8 (DE-576)094950253 1873-3778 nnns volume:1689 GBV_USEFLAG_U SYSFLAG_U GBV_ELV SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 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_150 GBV_ILN_151 GBV_ILN_224 GBV_ILN_370 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2027 GBV_ILN_2034 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2056 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2190 GBV_ILN_2336 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4313 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4338 GBV_ILN_4393 35.00 Chemie: Allgemeines AR 1689 |
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Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with |
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title_full |
Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with |
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Qiao, Lizhen |
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Journal of chromatography / A |
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Qiao, Lizhen Tao, Yuan Qin, Honglin Niu, Ruiting |
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Elektronische Aufsätze |
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Qiao, Lizhen |
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10.1016/j.chroma.2022.463771 |
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(ORCID)0000-0002-3290-9070 |
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multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with |
title_auth |
Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with |
abstract |
In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. |
abstractGer |
In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. |
abstract_unstemmed |
In this paper, several new multi-magnetic center magnetic ionic liquids (MMILs) were prepared with paramagnetic component simultaneously contained in both the cation and anion and used as extractants to establish a dispersive liquid-liquid microextraction (DLLME) approach followed by in-situ MMIL decomposition based back-extraction for the enrichment and determination of four parabens in beverages. The appropriate MMIL was selected by investigating the extraction performances of the obtained MMILs combined with high performance liquid chromatography-ultraviolet detection (HPLC-UV), and some other experimental factors were explored. Under the optimized DLLME conditions, the four parabens exhibited coefficients of determination (R2) above 0.9987 in the linear range of 0.1-500 ng·mL−1 for ethylparaben, propylparaben and butylparaben and 0.2-500 ng·mL−1 for methylparaben. The limits of detection (LODs) and limits of quantification (LOQs) were respectively within 0.03-0.06 ng·mL−1 and 0.1-0.2 ng·mL−1, and the relative standard deviations (RSDs) for intra-day and inter-day precision were below 10.8%. Moreover, the application of the developed MMIL-based DLLME method in beverage samples exhibited recoveries within 81.3%-112.1% with RSDs of 0.3%-13.1% at three different spiked levels. |
collection_details |
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title_short |
Multi-magnetic center ionic liquids for dispersive liquid-liquid microextraction coupled with |
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Tao, Yuan Qin, Honglin Niu, Ruiting |
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up_date |
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