Fluorimetric Determination of Eosin Y in Water Samples and Drinks Using Deep Eutectic Solvent-Based Liquid-Phase Microextraction
Open accessAbstract
An environmentally friendly and highly sensitive analytical method for the determination of the dye Eosin Y (EY) was developed utilizing vortex-assisted liquid–liquid microextraction based on deep eutectic solvents (DESs), combined with fluorescence detection (LPME-FLD). The extraction efficiencies of conventional solvents and various DES systems, composed of tetrabutylammonium bromide (TBAB) and alcohols (hexanol, octanol, and decanol) in different ratios, were systematically compared. DFT calculations provided insights into the most stable forms of EY in solvents of varying polarity. Theoretical Hansen solubility parameters and the COSMO-RS solvation model were applied to assess extraction efficiency. Hansen parameters were obtained via semiempirical PM7 calculations, while BP86/def2-TZVPD DFT computations were employed within the openCOSMO-RS framework. The developed method exhibited a linear calibration range between 0.1 and 130 µg·L−1, with a high correlation coefficient (R2 = 0.9982). The limit of detection (LOD) was established at 0.028 µg·L−1. Method precision and repeatability were confirmed over two days, with relative standard deviations (RSDs) ranging from 1.1% to 2.7% and with recoveries between 99.0% and 106.2%. The proposed analytical approach was successfully applied to the determination of EY in real water samples, demonstrating both its practical applicability and alignment with green chemistry principles.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Vortex-assisted DLLME uses mechanical agitation and offers a simple, economical, instrumentally minimal approach.
“In vortex-assisted DLLME, mechanical agitation is applied, offering a simple, economical, and instrumentally minimal approach [56,59,63,82,99].”
From Eco-Friendly Deep Eutectic Solvent-Based Extraction Technologies: A Comprehensive Review of Principles, Applications, and Comparative Insights (2026) · cites this paper as [99]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Density-functional thermochemistry. III. The role of exact exchange
Becke, A. D. (1993) · The Journal of Chemical Physics · doi:10.1063/1.464913 · Cited by 103,767 · see citing works
VMD: visual molecular dynamics
Humphrey, W., Dalke, A., & Schulten, K. (1996) · Journal of Molecular Graphics · doi:10.1016/0263-7855(96)00018-5 · Cited by 66,952 · see citing works
Weigend, F., & Ahlrichs, R. (2005) · Physical Chemistry Chemical Physics · doi:10.1039/b508541a · Cited by 30,761 · see citing works
Effect of the damping function in dispersion corrected density functional theory
Grimme, S., Ehrlich, S., & Goerigk, L. (2011) · Journal of Computational Chemistry · doi:10.1002/jcc.21759 · Cited by 28,221 · see citing works
Revealing Noncovalent Interactions
Johnson, E. R., Keinan, S., Mori‐Sánchez, P., Contreras‐García, J., Cohen, A. J., & Yang, W. (2010) · Journal of the American Chemical Society · doi:10.1021/ja100936w · Cited by 9,597 · see citing works
Klamt, A., & Schüürmann, G. (1993) · Journal of the Chemical Society Perkin Transactions 2 · doi:10.1039/p29930000799 · Cited by 9,449 · see citing works
Deep Eutectic Solvents (DESs) and Their Applications
Smith, E. L., Abbott, A. P., & Ryder, K. S. (2014) · Chemical Reviews · doi:10.1021/cr300162p · Cited by 7,378 · see citing works
A comprehensive electron wavefunction analysis toolbox for chemists, Multiwfn
Lu, T. (2024) · The Journal of Chemical Physics · doi:10.1063/5.0216272 · Cited by 5,551 · see citing works
Software update: The ORCA program system—Version 5.0
Neese, F. (2022) · Wiley Interdisciplinary Reviews Computational Molecular Science · doi:10.1002/wcms.1606 · Cited by 5,009 · see citing works
AGREE─Analytical GREEnness Metric Approach and Software
Pena‐Pereira, F., Wojnowski, W., & Tobiszewski, M. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c01887 · Cited by 4,002 · see citing works
Lu, T., & Chen, Q. (2022) · Journal of Computational Chemistry · doi:10.1002/jcc.26812 · Cited by 3,991 · see citing works
Hansen, C. M. (2007) · CRC Press eBooks · doi:10.1201/9781420006834 · Cited by 3,167 · see citing works
MOPAC: A semiempirical molecular orbital program
Stewart, J. J. P. (1990) · Journal of Computer-Aided Molecular Design · doi:10.1007/bf00128336 · Cited by 2,901 · see citing works
Stewart, J. J. P. (2012) · Journal of Molecular Modeling · doi:10.1007/s00894-012-1667-x · Cited by 2,028 · see citing works
Manousi, N., Wojnowski, W., Płotka-Wasylka, J., & Samanidou, V. (2023) · Green Chemistry · doi:10.1039/d3gc02347h · Cited by 1,685 · see citing works
The COSMO and COSMO‐RS solvation models
Klamt, A. (2017) · Wiley Interdisciplinary Reviews Computational Molecular Science · doi:10.1002/wcms.1338 · Cited by 393 · see citing works
The role of water in deep eutectic solvent-base extraction
Vilková, M., Płotka‐Wasylka, J., & Andruch, V. (2020) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2020.112747 · Cited by 324 · see citing works
Liquid-phase microextraction – The different principles and configurations
Yamini, Y., Rezazadeh, M., & Seidi, S. (2019) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2018.06.010 · Cited by 309 · see citing works
Deep eutectic solvents. The new generation of green solvents in analytical chemistry
Santana‐Mayor, Á., Rodríguez‐Ramos, R., Herrera‐Herrera, A. V., Socas‐Rodríguez, B., & Rodríguez‐Delgado, M. Á. (2020) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2020.116108 · Cited by 302 · see citing works
The possible mechanism of eco-friendly synthesized nanoparticles on hazardous dyes degradation
Nandhini, N. T., Rajeshkumar, S., & Sathiavelu, M. (2019) · Biocatalysis and Agricultural Biotechnology · doi:10.1016/j.bcab.2019.101138 · Cited by 223 · see citing works
The hype with ionic liquids as solvents
Kunz, W., & Häckl, K. (2016) · Chemical Physics Letters · doi:10.1016/j.cplett.2016.07.044 · Cited by 176 · see citing works
Batistela, V. R., Pellosi, D. S., de Souza, F. D., da Costa, W. F., Santin, S. M. D. O., de Souza, V. R., Caetano, W., de Oliveira, H. P. M., Scarmínio, I. S., & Hioka, N. (2011) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2011.03.027 · Cited by 166 · see citing works
Wojeicchowski, J. P., Ferreira, A. M., Abranches, D. O., Mafra, M. R., & Coutinho, J. A. P. (2020) · ACS Sustainable Chemistry & Engineering · doi:10.1021/acssuschemeng.0c03553 · Cited by 150 · see citing works
García‐Ratés, M., & Neese, F. (2019) · Journal of Computational Chemistry · doi:10.1002/jcc.25833 · Cited by 140 · see citing works
In situ decomposition of deep eutectic solvent as a novel approach in liquid-liquid microextraction
Shishov, A., Chromá, R., Vakh, C., Kuchár, J., Simon, A., Andruch, V., & Bulatov, A. (2019) · Analytica Chimica Acta · doi:10.1016/j.aca.2019.03.038 · Cited by 97 · see citing works
Shishov, A. Y., Makoś‐Chełstowska, P., Bulatov, A. V., & Andruch, V. (2022) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.2c00858 · Cited by 94 · see citing works
Switchable-hydrophilicity solvent liquid-liquid microextraction
Alshana, U., Hassan, M., Al-Nidawi, M., Yilmaz, E., & Soylak, M. (2020) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2020.116025 · Cited by 90 · see citing works
COSMO-RS based screening of ionic liquids for extraction of phenolic compounds from aqueous media
Khan, A. S., Ibrahim, T. H., Rashid, Z., Khamis, M. I., Nancarrow, P., & Jabbar, N. A. (2021) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2021.115387 · Cited by 88 · see citing works
Derayea, S. M., & Nagy, D. M. (2018) · Reviews in Analytical Chemistry · doi:10.1515/revac-2017-0020 · Cited by 82 · see citing works
Homogeneous liquid-liquid microextraction based on deep eutectic solvents
Ramezani, A. M., Ahmadi, R., & Yamini, Y. (2022) · TrAC Trends in Analytical Chemistry · doi:10.1016/j.trac.2022.116566 · Cited by 76 · see citing works
Switchable hydrophilicity solvents in analytical chemistry. Five years of achievements
Bazel, Y., Rečlo, M., & Chubirka, Y. (2020) · Microchemical Journal · doi:10.1016/j.microc.2020.105115 · Cited by 72 · see citing works
Self-citationInvestigation on the pH-dependent binding of Eosin Y and bovine serum albumin by spectral methods
Gao, D., Tian, Y., Liang, F., Jin, D., Chen, Y., Zhang, H., & Yu, A. (2007) · Journal of Luminescence · doi:10.1016/j.jlumin.2007.02.062 · Cited by 69 · see citing works
Mchedlov‐Petrossyan, N. O., & Kleshchevnikova, V. N. (1994) · Journal of the Chemical Society Faraday Transactions · doi:10.1039/ft9949000629 · Cited by 68 · see citing works
Multiple approaches for achieving drug solubility: an in silico perspective
Das, T., Mehta, C. H., & Nayak, U. Y. (2020) · Drug Discovery Today · doi:10.1016/j.drudis.2020.04.016 · Cited by 57 · see citing works
Vodolazkaya, N. A., Gurina, Y. A., Salamanova, N. V., & Mchedlov‐Petrossyan, N. O. (2008) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2008.11.007 · Cited by 51 · see citing works
Hansen Solubility Parameters Applied to the Extraction of Phytochemicals
Novaes, F. J. M., de Faria, D. C., Ferraz, F. Z., & Neto, F. R. D. A. (2023) · Plants · doi:10.3390/plants12163008 · Cited by 48 · see citing works
Soylak, M., Uzcan, F., & Göktaş, O. (2023) · Journal of Food Composition and Analysis · doi:10.1016/j.jfca.2023.105287 · Cited by 47 · see citing works
Narayanan, V. A., Stokes, D. L., & Vo‐Dinh, T. (1994) · Journal of Raman Spectroscopy · doi:10.1002/jrs.1250250607 · Cited by 44 · see citing works
Tamburello-Luca, A. A., Hébert, P., Antoine, R., Brevet, P., & Girault, H. H. (1997) · Langmuir · doi:10.1021/la9621271 · Cited by 43 · see citing works
pH-Dependence of the Absorption and Fluorescent Properties of Fluorone Dyes in Aqueous Solutions
Slyusareva, E. A., & Gerasimova, M. A. (2014) · Russian Physics Journal · doi:10.1007/s11182-014-0188-8 · Cited by 42 · see citing works
Andruch, V., Kalyniukova, A., Płotka‐Wasylka, J., Jatkowska, N., Snigur, D. V., Zaruba, S., Płatkiewicz, J., Zgoła‐Grześkowiak, A., & Werner, J. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.108509 · Cited by 42 · see citing works
Predicting solvation free energies for neutral molecules in any solvent with openCOSMO-RS
Müller, S., Nevolianis, T., García‐Ratés, M., Riplinger, C., Leonhard, K. O., & Smirnova, I. V. (2024) · Fluid Phase Equilibria · doi:10.1016/j.fluid.2024.114250 · Cited by 41 · see citing works
Levillain, P., & Fompeydie, D. (1985) · Analytical Chemistry · doi:10.1021/ac00290a029 · Cited by 40 · see citing works
Namlı, H., & Bişgin, A. T. (2024) · Journal of Food Composition and Analysis · doi:10.1016/j.jfca.2024.105980 · Cited by 40 · see citing works
Almahri, A., Abdel-Lateef, M. A.-K., Samir, E., Derayea, S. M., & Hamd, M. A. E. (2020) · Luminescence · doi:10.1002/bio.3983 · Cited by 39 · see citing works
Modelling solubility in semi-crystalline polymers: a critical comparative review
Atiq, O., Ricci, E., Baschetti, M. G., & Angelis, M. G. D. (2022) · Fluid Phase Equilibria · doi:10.1016/j.fluid.2022.113412 · Cited by 39 · see citing works
Darwish, A. S., Lemaoui, T., AlYammahi, J., Taher, H., Benguerba, Y., BANAT, F. A., & AlNashef, I. M. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.121631 · Cited by 39 · see citing works
Lazović, M. Č., Cvijetić, I., Jankov, M. S., Milojković‐Opsenica, D., Trifković, J., & Ristivojević, P. M. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.122649 · Cited by 35 · see citing works
Assessment of Hansen solubility parameters in deep eutectic solvents for solubility predictions
Otárola-Sepúlveda, J., Cea‐Klapp, E., Aravena, P., Ormazábal-Latorre, S., Canales, R. I., Garrido, J. M., & Valerio, O. (2023) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2023.122669 · Cited by 35 · see citing works
Abdel-Lateef, M. A.-K., Almahri, A., Derayea, S. M., & Samir, E. (2020) · Reviews in Analytical Chemistry · doi:10.1515/revac-2020-0120 · Cited by 31 · see citing works
Mahnashi, M. H., Mahmoud, A. M., El‐Wekil, M. M., & Shahin, R. Y. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.109062 · Cited by 26 · see citing works
Amat‐Guerri, F., López‐González, M., Sastre, R., & Martinez-Utrilla, T. L. R. (1990) · Dyes and Pigments · doi:10.1016/0143-7208(90)80021-g · Cited by 25 · see citing works
Fizer, O. I., Fizer, M. M., Sidey, V. I., Studenyak, Y., & Mariychuk, R. T. (2018) · Journal of Molecular Modeling · doi:10.1007/s00894-018-3692-x · Cited by 25 · see citing works
Self-citationFernandes, C. C., Paiva, A., Haghbakhsh, R., & Duarte, A. R. C. (2025) · Scientific Reports · doi:10.1038/s41598-025-87050-3 · Cited by 25 · see citing works
A Study on the Fluorescence Quenching of Eosin by certain Organic Dyes
Kathiravan, A., Anbazhagan, V., Jhonsi, M. A., & Renganathan, R. (2008) · Zeitschrift für Physikalische Chemie · doi:10.1524/zpch.2008.5267 · Cited by 23 · see citing works
Fizer, O. I., Fizer, M. M., Sidey, V. I., & Studenyak, Y. (2020) · Microchemical Journal · doi:10.1016/j.microc.2020.105758 · Cited by 21 · see citing works
Self-citationde Freitas, C. F., Estevão, B. M., Pellosi, D. S., Scarmínio, I. S., Caetano, W., Hioka, N., & Batistela, V. R. (2020) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2020.114794 · Cited by 21 · see citing works
Nagar, B., & Dhar, B. B. (2022) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.1c02924 · Cited by 21 · see citing works
Protolytic equilibria of fluorescein halo derivatives in aqueous-organic systems
Mchedlov‐Petrossyan, N. O., Kukhtik, V. I., & Egorova, S. I. (2006) · Russian Journal of General Chemistry · doi:10.1134/s1070363206100197 · Cited by 19 · see citing works
Pierau, L., Andaloussi, S. A., Chiappone, A., Lajnef, S., Peyrot, F., Malval, J., Steffen Jockusch, B., & Versace, D. (2024) · European Polymer Journal · doi:10.1016/j.eurpolymj.2024.113143 · Cited by 18 · see citing works
Erdinç, N., & Göktürk, S. (2014) · Analytical Chemistry Letters · doi:10.1080/22297928.2014.960534 · Cited by 15 · see citing works
Sabatini, F., Degano, I., & Colombini, M. P. (2020) · Separation Science Plus · doi:10.1002/sscp.202000002 · Cited by 15 · see citing works
Homogeneous Liquid–Liquid Microextraction
Bedair, A., & Mansour, F. R. (2024) · Integrated analytical systems · doi:10.1007/978-3-031-50527-0_10 · Cited by 14 · see citing works
Salim, M. M., Marie, A. A., Kamal, A. H., Hammad, S. F., & Elkhoudary, M. M. (2022) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2022.121919 · Cited by 13 · see citing works
Kakalejčíková, S., Bazeľ, Y., Thi, V. A. L., & Fizer, M. M. (2024) · Molecules · doi:10.3390/molecules29143397 · Cited by 13 · see citing works
Self-citationDeep eutectic solvents in microextraction
Alshana, U., & Soylak, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-822139-6.00019-5 · Cited by 12 · see citing works
Vodolazkaya, N. A., Kleshchevnikova, Y. A., & Mchedlov‐Petrossyan, N. O. (2013) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2013.08.018 · Cited by 12 · see citing works
Brumley, W. C., & Farley, J. W. (2003) · Electrophoresis · doi:10.1002/elps.200305514 · Cited by 11 · see citing works
Photophysical and antibacterial activity of light-activated quaternary eosin Y
Staneva, D., Yordanova, S., Vasileva−Tonkova, E., Stoyanov, S., & Grabchev, I. K. (2019) · Open Chemistry · doi:10.1515/chem-2019-0135 · Cited by 11 · see citing works
Tóth, J., Bazeľ, Y., & Balogh, I. S. (2021) · Talanta · doi:10.1016/j.talanta.2021.122185 · Cited by 9 · see citing works
Self-citationRíos, M. D. D. L., & Belmonte, R. M. (2022) · SN Applied Sciences · doi:10.1007/s42452-022-04959-4 · Cited by 8 · see citing works
Wang, J., Chen, L., Li, Y., Shen, W., & Manley‐Harris, M. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.109588 · Cited by 8 · see citing works
Kakalejčíková, S., Harenčár, D., Bazeľ, Y., & Fizer, M. M. (2025) · Processes · doi:10.3390/pr13041051 · Cited by 8 · see citing works
Self-citationDhasarathan, R., Kavitha, B., Aswathaman, H., Senthilkumar, N., & Rani, S. (2021) · Materials Today Proceedings · doi:10.1016/j.matpr.2021.08.150 · Cited by 7 · see citing works
Kakalejčíková, S., & Bazeľ, Y. (2024) · Microchemical Journal · doi:10.1016/j.microc.2024.110226 · Cited by 7 · see citing works
Self-citationFernandes, C. C., Paiva, A., Haghbakhsh, R., & Duarte, A. R. C. (2025) · Journal of Molecular Liquids · doi:10.1016/j.molliq.2025.127544 · Cited by 7 · see citing works
Liedekerke, B. M. V., Nelis, H. J. C. F., Wittekind, D. H., & Leenheer, A. P. D. (1991) · The Histochemical Journal · doi:10.1007/bf01046590 · Cited by 5 · see citing works
Application of Eosin Y as a Probe for Spectroscopic Determination of Aripiprazole in Human Plasma
Saeed, M. A., Mostafa, N. S., Mahmoud, A. M., & El-Sayed, M. A. (2025) · Luminescence · doi:10.1002/bio.70131 · Cited by 5 · see citing works
Abbas, F. S., Alaboodi, A. S., & Abojassim, A. A. (2023) · Cardiometry · doi:10.18137/cardiometry.2022.25.14631467 · Cited by 2 · see citing works
Studies on anionic dye Eosin Y in mixed anionic micellar medium
Sobika, M., Karunanithi, S., & Dash, S. (2023) · Results in Chemistry · doi:10.1016/j.rechem.2023.101220 · Cited by 2 · see citing works
Ferreira, S. C. R., Oliveira, M. C., Pais, A. A. C. C., & de Melo, J. S. S. (2024) · Talanta · doi:10.1016/j.talanta.2024.127409 · Cited by 2 · see citing works
H‐Point Standard Addition Method for Simultaneous Determination of Eosin and Erytrosine
Kaur, A., & Gupta, U. (2011) · Journal of Chemistry · doi:10.1155/2011/210259 · Cited by 2 · see citing works
Roslan, R., Kurnia, K. A., Hasanudin, N., Hilmy, N. I. M. F., & Ruslan, M. S. H. (2024) · AIP conference proceedings · doi:10.1063/5.0194883 · Cited by 1 · see citing works
Safe Food Coloring Agent as an Alternative to Eosin Stain
Kar, S., Kumar, H., Sangamesh, N., Mishra, S., Bajoria, A. A., & Saha, M. (2024) · Cureus · doi:10.7759/cureus.69817 · Cited by 1 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [7]Al-Behadili W.K.H. Jawad Y.M. Whaab W.S.A. Effect of solvent on intensity of absorption and fluorescence of Eosin Y dye and spectral properties of Eosin Y dye J. Med. Chem. Sci. 2023 6 322 334 10.26655/JMCHEMSCI.2023.2.13 · DOI
Cited by
Sorted by citations
Smirnova, S. V., Gorbovskaya, A. V., Vershinina, Y. S., Apyari, V. V., & Proskurnin, М. А. (2025) · Molecules · doi:10.3390/molecules30244769 · Cited by 5 · see citing works
Alahmadi, S. M., & Abu-Dief, A. M. (2026) · Sustainable Chemistry · doi:10.3390/suschem7030033 · Cited by 1 · see citing works
“In vortex-assisted DLLME, mechanical agitation is applied, offering a simple, economical, and instrumentally minimal approach [56,59,63,82,99].”
Gajdošová, A., & Šandrejová, J. (2026) · Analytica Chimica Acta · doi:10.1016/j.aca.2026.345413
Jaber, H., & Salman, R. (2026) · Ecological Chemistry and Engineering S · doi:10.2478/eces-2026-0005
- Authors
- Kakalejčíková, S., Bazeľ, Y., Drábiková, M., & Fizer, M.
- Affiliations
- University of Pavol Jozef Šafárik (SK)
- University of Nevada, Reno (US)
- Corresponding author
- Kakalejčíková, Sofia
- Bazeľ, Yaroslav
- Venue
- Molecules
- Publisher
- MDPI AG
- Published
- 2025-08-10
- Volume
- 30
- Issue
- 16
- Pages
- 3334
- ISSN
- 1420-3049 (ISSN-L)
- PMC
- PMC12388366
- OpenAlex
- W4413207769
- Cited by
- 4
- References
- 84
- Citations by year
- 2026: 3 · 2025: 1
- FWCI
- 1.50
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecules (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- VEGA (1/0177/23)
- Topics
- Physical Sciences › Chemistry › Analytical Chemistry › Analytical chemistry methods development
- Physical Sciences › Chemical Engineering › Catalysis › Ionic liquids properties and applications
- Physical Sciences › Chemistry › Spectroscopy › Analytical Chemistry and Chromatography
- Keywords
- eosin Y, deep eutectic solvents, liquid-phase microextraction, vortex-assisted liquid-liquid microextraction, fluorescence detection, tetrabutylammonium bromide, water samples, beverages, dye determination, extraction efficiency, Hansen solubility parameters, DFT calculations, green chemistry
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review