Phase Extraction Method Research Articles

Synthesis of Magnetic Attapulgite Nanoparticles Via a Novel Surface Covalent Reaction Method and its Application in the Magnetic Solid Phase Extraction.

In this study, the attapulgite nanoparticle was immobilized on the surface of magnetic nanoparticle Fe3O4 via a novel surface covalent reaction method for the magnetic solid phase extraction (MSPE) for the first time. The surface covalent reaction method has the advantages of controllable steps, and can make the magnetic attapulgite nanoparticle (MANP) have good homogeneity and high stability. Field emission scanning electron microscopy, equipped with an energy dispersive spectrometer, Nitrogen adsorption BET, X-ray diffraction and Fourier transform infrared spectroscopy were applied to characterize the prepared MANP, confirming that the attapulgite nanoparticle could be effectively immobilized on the surface of magnetic nanoparticle Fe3O4 via covalent reactions. Under optimal conditions of the MSPE experiment based on the MANP, the limits of detection were found to be 10ng/mL for melamine and 3ng/mL for cyromazine with a relative standard deviation < 10% by a high-performance liquid chromatography system. Meanwhile, 0.1mg/mL melamine in milk and 0.1mg/mL cyromazine in cucumber can also be detected according to our MSPE procedure. More importantly, the MANP still has good magnetism and enrichment efficiency after several decades of use. These results showed that the MANP prepared by our method is a kind of promising material for the MSPE.

Simultaneous determination of picomolar level of dissolved silver with other key trace metals in seawater samples using solid phase extraction and isotope dilution methods

Simultaneous determination of dissolved silver (dAg) with other key GEOTRACES trace metals is difficult because dAg in seawater tends to form negatively charged chloride species that result in only 75% recovery efficiency with commonly used NOBIAS PA-1 chelating resins. In this study, we developed a method using solid phase extraction coupled with isotope dilution that enables full quantification (97.9 ± 2.1%) of dAg along with other major trace metals including cadmium (Cd), copper (Cu), manganese (Mn), nickel (Ni), and lead (Pb) (recovery efficiency = 100% to 102%) in seawater samples. Seawater samples were first spiked with Ag-109 and allowed to reach isotopic equilibrium before extraction using NOBIAS PA-1 chelating resin. Then, dAg isotope ratios (Ag-109/Ag-107) before and after solid phase extraction were determined and used to quantify dAg. Determination of dAg with dissolved Cd, Cu. Mn, Ni, and Pb in reference seawater material CASS-6 resulted in deviations of between 1.0% and 8.8% from the consensus values, which are well within the standard error of measurement. We then successfully determined the concentrations of dissolved Cd (0.05–0.2 nM), Cu (0.5–13 nM), Mn (10–140 nM), Ni (2–12 nM), Pb (5–110 nM), and Ag (10–40 pM) in Otsuchi Bay, Japan and its surrounding rivers. Evaluation of the behavior of dAg under a salinity gradient using estuarine samples collected from Samunsam River, Malaysia shows increasing dAg concentration with salinity (R2 = 0.68), which suggests release of sedimental Ag under high ambient chloride concentrations. Our new method enables rapid and simultaneous measurements of dAg with other key GEOTRACES trace metals in a single analysis, which is expected to expedite analysis and increase availability of oceanic dAg data globally.

Improved preconcentration workflow for organic explosive traces in aqueous samples using solvent-assisted dispersive solid-phase extraction

The present study deals with the development of a solvent-assisted dispersive solid phase extraction method for the extraction of HMX, RDX, and TNT from aqueous samples. Benzophenone and methanol were selected as explosives sorbent and dispersive solvent respectively. Extraction parameters like pH, extraction time, amount of sorbent, volume and type of the disperser solvent and centrifuge time were optimized. Dispersion of 0.5 mL dispersive solution (4% (w/v) benzophenone in methanol) was performed by injection into the 5 mL aqueous sample (pH=7) using a 1.0 mL syringe. After centrifuge, the extracted explosives were analyzed by high performance liquid chromatography with ultraviolet detection (HPLC-Uv). The results indicated that the linear ranges with the correlation coefficients of 0.99 ≤ R2 were 1.6–204.6 μg L−1, 1.4–213.7 μg L−1 and 1.3–225.9 μg L−1 for HMX, RDX and TNT respectively. The limit of detection and limit of quantification obtained for each explosive were: 0.3 μg L−1 and 0.8 μg L−1 for HMX, 0.3 μg L−1 and 0.9 μg L−1 for RDX and 0.2 μg L−1 and 0.7 μg L−1 for TNT. Finally, the practical applicability of the developed method was evaluated for the extraction of some organic explosives in water samples followed their determination by HPLC-Uv.

Application of continuous magnetic solid phase extraction in the extraction of tetracycline antibiotics from honey samples

This study aimed to develop a continuous magnetic solid phase extraction method in a narrow bore tube for the extraction of tetracycline antibiotics from honey samples before their determination with high performance liquid chromatography–diode array detector. In this work, a magnetic covalent organic framework is used as the sorbent. The extraction method is performed in a narrow bore tube by adding 25 mg of a magnetic sorbent prepared from melamine, barbituric acid, and Fe3O4 into the diluted honey sample solution. By using a magnet, the sorbent is moved up and down through the narrow bore tube for five times to improve extraction efficiency. After adsorption the analytes, they are eluted from the sorbent surface using 2,2–dimethoxypropane under vortexing. Then, by using a magnet, the eluent containing the extracted analytes are taken and evaporated with continuous flow of nitrogen. Finally, the residue containing the enriched analytes is reconstituted in microliter–level of mobile phase and injected into chromatographic system for quantitative analysis. Based on the outcomes, the method demonstrated good linearity (0.37–1000 ng g−1), high enrichment factors (175–203), good extraction recoveries (70–81 %), low LODs (0.11–0.18 ng g−1) and LOQs (0.37–0.60 ng g−1). The proposed method is effectively applied for quantification of tetracyclines in twenty–four honey samples. Considering the results, none of the honey samples was contaminated with the studied antibiotics. Regarding to the above–mentioned analytical advantages of the proposed method, its simplicity and rapidity, and green synthesis of the magnetic sorbent particles, the suggested method can be used as a routine method for the extraction of tetracyclines from honey samples.

Development of a dispersive micro-solid phase extraction method based on using cobalamin as a green adsorbent for the extraction of Cd(II) and Pb(II) from oil samples

ABSTRACT A dispersive micro-solid phase extraction procedure using cobalamin as a green sorbent has been developed for the extraction of Cd(II) and Pb(II) ions from oil samples. At first, a desired amount of oil sample was dissolved in chloroform. Then, the specified amount of cobalamin was added and vortexed. After centrifuging, the separated solid particles were dissolved in nitric acid solution. Finally, the analytes were analysed by flame atomic absorption spectrometry. Effects of different analytical parameters such as amounts of sample and cobalamin, vortex time, complexing agent amount, type and volume of dissolving solvent, and temperature on the extraction efficiency of Pb(II) and Cd(II) ions were investigated and optimised. Under optimised conditions, calibration curves were established with the linear ranges of 1.5–150 μg Kg−1 for Cd(II) and 1–150 μg Kg−1 for Pb(II). The detection limits were found to be 0.48 and 0.34 µg Kg−1 along with extraction recoveries of 89.1% and 94.8% for Cd(II) and Pb(II) ions, respectively. The proposed method demonstrated good repeatability, with the relative standard deviation ranging from 3.8% to 4.1% (n = 6, C = 10 μg Kg−1 of each cation). Finally, the method was successfully applied to determine the concentrations of Cd(II) and Pb(II) ions in various oil samples.

Adaptive double PCA method of phase extraction in fringe projection profilometry

Adaptive double PCA method of phase extraction in fringe projection profilometry

Application of cobalt-cerium-iron ternary layered double hydroxide for extraction of perfluorooctane sulfonate followed by HPLC-MS/MS analysis

Herein, Ce-doped CoFe layered double hydroxide (LDH), noted as CoCeFe ternary LDH, was prepared using the co-precipitation route. Prosperous synthesis of CoFe LDH and successful partial replacement of iron cations with cerium cations in CoCeFe ternary LDH were confirmed by X-ray diffraction patterns, energy-dispersive X-ray spectroscopy, and elemental dot-mapping images. Nanosheet morphology was recognized for both CoFe LDH and CoCeFe ternary LDH from scanning electron microscopy and transmission electron microscopy micrographs. In the following, a dispersive solid phase extraction (DSPE) method was developed using the synthesized CoCeFe ternary LDH as a sorbent for extracting perfluorooctanesulfonic acid (PFOS) from wastewater samples. For the selective analysis of PFOS, high-performance liquid chromatography-tandem mass spectroscopy (HPLC-MS/MS) in multiple reaction monitoring mode was used. Analytical parameters such as the limit of detection equal to 0.02 μg/L, with a linear range of 0.05–300 μg/L, the limit of quantification equal to 0.05 μg/L, and an enrichment factor equal to 23.3 were achieved for PFOS at the optimized condition (sorbent: 5 mg of CoCeFe ternary LDH, eluent type and volume: 150 μL mobile phase, pH: 3, adsorption time: 3 min, and desorption time: 5 min). The developed strategy for the analysis of PFOS was tested in real wastewater samples, including copper mine and petrochemical wastewater. The amount of analytes in real samples was calculated using the standard addition method, and good relative recovery in the range of 86%–105% was obtained. The main novelty of this research is the application of CoCeFe ternary LDH to extract the PFOS from wastewater using the DSPE method for determination by HPLC-MS/MS.

Magnetic Poly(Amidoamine) Dendrimer for the Dispersive Solid Phase Extraction of Nitrophenols from Environmental Water Samples.

A fast and simple dispersive solid phase extraction method is described for nitrophenols determination in water samples by using gas chromatography-nitrogen phosphorous detector. Firstly, the Poly(amidoamine) grafted Fe3O4 magnetic nanoparticles were synthesized in different generations by successive addition of butyl acrylate and ethylenediamine. After characterization, the prepared dendrimer was utilized as an adsorbent for magnetic solid phase extraction of 2-nitrophenol, 3-nitrophenol, and 4-nitrophenol to benefit large number of surface amine interaction sites. The effects of the different parameters influencing the sample preparation efficiency were investigated. The proposed method showed linearity in the ranges of 0.04-700 and 0.05-700µg/dm3 for nitrophenols. The obtained limits of detection and quantification under optimized conditions were 0.01-0.02 and 0.04-0.05µg/dm3, respectively. The relative standard deviations (n = 5) were less than 3.8% (at 10µg/dm3). Moreover, the calculated enrichment factors were above 200. In addition, the relative recoveries for a spiked river water sample were satisfactory.

Comparison of Phase Extraction Methods on the Example of the PN-3 Microwave Interferometer

Comparison of Phase Extraction Methods on the Example of the PN-3 Microwave Interferometer

Development of a dispersive micro solid phase extraction-HPLC method for the simultaneous quantification of antiepileptic drugs in various matrices

Due to the widespread utilization of antiepileptic drugs for seizure control and patient well-being, it is crucial to determine their presence in biological and water samples. This is essential for optimizing therapy, comprehending drug behavior, identifying drug interactions, monitoring environmental contamination, and safeguarding public health and ecology. Hence, a novel method that combines dispersive micro solid phase extraction with HPLC-DAD was developed to simultaneously determine the presence of Lacosamide, Levetiracetam, and Phenytoin. To achieve this, a new sorbent was synthesized using the hydrothermal and sol–gel methods, which consisted of bimetallic MIL-100 (Fe, Ni) on MIL-100 (Mn), SiO2, and Fe3O4 nanoparticles. We compared the extraction capabilities of several sorbents in order to select the most effective one. The optimal ratio of components for the chosen sorbent was determined through the simplex lattice design to enhance its efficiency. The optimized values for SiO2, Fe3O4, and MIL-100 (Fe, Ni) on MIL-100 (Mn) were found to be 0.1, 0.34, and 0.56, respectively. The parameters that affected the dispersive micro solid phase extraction method were optimized using both experimental design and one factor at a time. Under the optimal conditions, the linear range for the detection of Lacosamide, Levetiracetam, and Phenytoin was determined to be 0.1–363.0, 0.3–372.0, and 0.4–435.0 ng mL−1, respectively, with low LODs below 0.13 ng mL−1. Additionally, a preconcentration factor of 492.6, 487.1, and 469.5 was achieved for measuring Lacosamide, Levetiracetam, and Phenytoin, respectively. The intra-day and inter-day relative standard deviations (RSDs) ranged from 3.8 % to 4.6 % and 4.2 % to 5.2 %, respectively. The recoveries and RSDs for analyzing real water, human urine, and serum samples were found to be between 89.6–97.0 % and 4.53–6.44 %, respectively.

Sacrificial template synthesis of hollow sulfonate group functionalized microporous organic network for efficient solid phase extraction of sulfonamide antibiotics from milk and honey samples

The highly conjugated and hydrophobic characteristics of microporous organic networks (MONs) have largely impeded their broad applications in sample pretreatment especially for the polar or ionic analytes. In this work, a novel uniform hollow shaped sulfonate group functionalized MON (H-MON-SO3H-2) was synthesized via the sacrificial template method for the efficient solid phase extraction (SPE) of sulfonamides (SAs) from environmental water, milk, and honey samples prior to HPLC analysis. H-MON-SO3H-2 exhibited large specific surface area, penetrable space, good stability, and numerous hydrogen bonding, electrostatic, hydrophobic and π-π interaction sites, allowing sensitive SPE of SAs with wide linear range (0.150-1000 μg L−1), low limit of detection (0.045-0.188 μg L−1), good precisions (intra-day and inter-day RSD < 7.3%, n = 5), large enrichment factors (95.7-98.5), high adsorption capacities (250.4-545.0 mg g−1), and satisfactory reusability (more than 80 times). Moreover, the established method was successfully applied to extract SAs from spiked samples with the recoveries of 86.1-104.3%. This work demonstrated the great potential of H-MON-SO3H-2 in the efficient SPE of trace SAs in complex environmental water and food samples and revealed the prospect of hollow MONs in sample pretreatment.

Multi-wavelength pinhole point diffraction interferometry for optics metrology with interferometric intensity based phase retrieval method

In this paper, we propose a multi-wavelength pinhole point diffraction interferometry (MPPDI) and a two-step phase extraction method based on the interferometric intensity information. MPPDI is mainly used to extend the dynamic measurement range of traditional pinhole point diffraction interferometry (PPDI) to realize the measurement of large-aperture and high-order aspheric surface. Spherical/aspherical optics will be test under three different wavelengths, and the corresponding interferograms are recoded by 3CMOS detector at the same moment. By combining different wavelengths, MPPDI can obtain a synthetic wavelength with a larger measuring range and greater flexibility. In interferometry, the choice of the wavelength of the light source has a great influence on the measurement range and accuracy. In MPPDI, we can choose different wavelength combinations to select the most suitable synthetic wavelength according to the asphericity of the tested mirror. To enhance efficiency and reduce the impact of air disturbances during phase shifts, we propose a new phase extraction method based on interferometric intensity to interpret the phase map of surface information. The background intensity of diffraction wavefront is firstly pre-recorded by 3CMOS, then phase-shift interferograms of test mirror is acquired with two-step piezoelectric ceramic driver (PZT) movement. From the analysis, it can be found that fringe modulation has tiny influence on the interferograms intensity. Therefore, based on global intensity distribution of fringe pattern and grayscale information, phase map can be retrieval using proposed two-step processing method (only single phase-shift). The two-step phase extraction method can reduce the number of phase shifts from 9 to 3, which improves the efficiency and reduces errors due to multiple phase shifts. MPPDI and two-step phase extraction we proposed have a larger measurement while reducing the number of phase shifts and avoiding error accumulation due to too many phase shifts. Suitable for large-aperture and high-order aspheric surface measurement.

Zn-doped MoO3 nanorods for dispersive solid phase extraction of trace Pb(II) from water and food samples

A rapid, and environmentally friendly dispersive solid phase extraction method based on Zn-doped MoO3 nanorods for efficient extraction of trace level of Pb(II) from water and food samples was established before high-resolution continuum source flame atomic absorption spectrometric detection. The sorbent characterization studies were carried out using BET, FE-SEM, XRD, and FT-IR techniques. To achieve effective phase separation and accurate analytical data, the adsorption and desorption procedures have been precisely adjusted. The presented approach demonstrated a wide working range (9.3–500 µg L−1), a relatively low detection limit (3.1 µg L−1), and very good extraction recoveries (90–104%) under optimum conditions. The matrix effect was investigated by the addition of interference ions. The presence of many different anions and cations in the environment did not lead to negative results and selectivity towards the analyte was observed. The method was validated by the analysis of certified reference materials (TMDA - 64.3 and INCT-OBTL-5). The enhancement factor has been determined as 10.9. The suggested method worked efficiently to extract and determine Pb(II) from water, tea, and oil samples.

High enrichment and measurement of heterocyclic aromatic hydrocarbons from environmental waters with magnetic resorcinol-formaldehyde nanocomposites coupled with high performance liquid chromatography

Heterocyclic aromatic hydrocarbons are concerned pollutants with carcinogenic toxicity, which exist universally in various environmental matrices and have great harm to environmental and human health. In present work, magnetic resorcinol-formaldehyde composites (Fe3O4@SiO2@R–F) were fabricated via aldol condensation reaction under alkaline condition. The prepared magnetic materials were examined and analyzed with Fourier transform infrared spectroscopy and other related instruments. The Fe3O4@SiO2@R–F composites were utilized to develop an efficient magnetic solid phase extraction (MSPE) method for extracting six heteropolyclic aromatic hydrocarbons from environmental water samples including carbazole (CB), 7-methylquinoline (7-MQL), 9-methylcarbazole (9-MCB), dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MDBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT). The analytes were analyzed by high performance liquid chromatography-ultraviolet variable wavelength detector (HPLC-VWD). The main factors affecting MSPE were optimized. With the optimal parameters, 9-MCB and 4-MDBT have good linearity over the concentration range of 0.1–300 μg L−1, and 7-MQL, CB, DBT and 4,6-DMDBT have good linearity over the concentration range of 0.5–300 μg L−1. The limits of detection were over the concentration range of 0.012–0.031 μg L−1. This method was successfully employed to measure real waters, and the spiked recoveries ranged from 89.4% to 99.9%. The results confirmed that the developed method was reliable, robust and could be employed as a usefully alternate way for analyzing such pollutants in waters.

Trace Determination of Phenanthrene and Fluorene in Beverages Using D-μ-SPE and Liquid Chromatography Analysis

Dispersive micro solid phase extraction (D-μ-SPE) method using Graphene Oxide (GO) for the extraction and pre-concentration of selected polycyclic aromatic hydrocarbons (PAHs) from beverage samples prior to high-performance liquid chromatography - diode array detector (HPLC - DAD) is reported. Selected PAHs Fluorene (FLU) and Phenanthrene (PHE) were used as targeted analytes. An experimental design using Response Surface Methodology (RSM) and Box–Box–Behnken design (BBD) was performed to evaluate the interactive effects of three significant parameters: mass of sorbent, sample volume and extraction time. Under the optimum conditions, the method revealed good linearity (R2 = 0.9995 – 0.9998) over a concentration range of 0.5 – 5.0 mg L-1. The limit of detection (LOD) was in the range of 0.03 – 0.24 mg L-1 with satisfactory relative recoveries (81 – 99 %) and good relative standard deviation (RSD) of ≤ 3.80 % (n = 3). The method was successfully applied to tea, coffee, and milk samples and proved to be a simple, rapid, and reliable method with good extraction efficiencies for the detection of PAHs in beverage samples.

Development of a continuous magnetic dispersive solid phase extraction method for the extraction of seven widely used pesticides from fruit juices

Generally, food safety monitoring is vital issue to preserve human health and guarantee a longer lifespan. In present study, a continuous mode of magnetic dispersive solid phase extraction method based on using magnetic covalent organic framework@metal organic framework nanocomposite as sorbent has been proposed. The developed method has been tested for the extraction of some pesticides (pirimicarb, terbutryn, fenthion, triticonazole, hexaconazole, diniconazole, and haloxyfop-R-methyl) from commercial fruit juices prior to their analysis by high performance liquid chromatography–tandem mass spectrometry. In the current research, the properties of nanocomposite were characterized by scanning electron microscopy, Fourier–transform infrared spectrophotometry and X–ray diffraction techniques. In the next step, the synthesized nanocomposite was employed as an efficient sorbent in the developed extraction procedure that was done in a narrow bore tube. Under optimum extraction conditions, extraction recoveries were in the ranges of 67–83 %. Moreover, the limits of detection and quantification of the selected analytes were in the ranges of 17–43 and 56–143 ng L−1, respectively. Finally, the proposed method was successfully applied in the analysis of the opted pesticides in sixty fruit juice samples.

Previtamin D2, vitamin D2, and vitamin D4 amounts in different mushroom species irradiated with ultraviolet (UV) light and occurrence of structurally related photoproducts

AbstractMushrooms are rich in ergosterol and ergosta‐5,7‐dienol, which can be partly converted into vitamin D2 and D4 through ultraviolet (UV) light exposure. Typically, mushrooms have very low vitamin D contents, but it can be increased by UV irradiation. This process generates additional photoisomers scarcely studied in mushrooms due to analytical challenges. Here, we developed a new solid phase extraction (SPE) method to separate vitamin D2, vitamin D4, and other tri‐ and pentacyclic photoisomers from the much higher abundant ergosterol. Subsequent GC/MS analysis enabled the detection of ten photoisomers in eight UV‐treated mushroom species, including vitamin D2 (previtamin D2, tachysterol2, two suprasterol2 and trans‐vitamin D2 isomers) and vitamin D4 (previtamin D4). Quantitated vitamin D2 contents of 10–540 µg/100 g dry weight agreed well with the sparse literature data available for the investigated mushroom species. In addition, previtamin D2 (nd–1950 µg/100 g dry weight) and vitamin D4 (10–140 µg/100 g dw) were quantified in the samples. The content and photoproduct compositions varied considerably between different mushroom species.Practical applications: The novel SPE method can be applied to study the vitamin D and photoisomer content of mushrooms.

Sensing analysis of self-mixing and Michelson interferometry with neural-network-based phase extraction

Self-mixing interference (SMI) and Michelson interference (MI) with the phase extraction method based on a neural network (NN) for sensing is analyzed in this work. Since MI and SMI signals are predominantly a cosine-like function of optical phase, the NN’s core task involves mapping the cosine function to phase values, which is solved by a tectonic characteristic function. Experimental results show that the movement information carried by MI and SMI signals can be accurately measured by the NN with a phase sensitivity of 10−3 rad, yielding outcomes that align with the simulations. Especially, algorithms are essential for extracting real-time motion direction of objects in MI. The simplicity of real-time motion direction extraction is the key advantage of SMI, while further utilization of variational mode decomposition is necessary to mitigate the impact of periodic optical frequency variation. This work offers a potentially valuable contribution to develop interferometry for engineering applications.

Deep Learning in the Phase Extraction of Electronic Speckle Pattern Interferometry

Electronic speckle pattern interferometry (ESPI) is widely used in fields such as materials science, biomedical research, surface morphology analysis, and optical component inspection because of its high measurement accuracy, broad frequency range, and ease of measurement. Phase extraction is a critical stage in ESPI. However, conventional phase extraction methods exhibit problems such as low accuracy, slow processing speed, and poor generalization. With the continuous development of deep learning in image processing, the application of deep learning in phase extraction from electronic speckle interferometry images has become a critical topic of research. This paper reviews the principles and characteristics of ESPI and comprehensively analyzes the phase extraction processes for fringe patterns and wrapped phase maps. The application, advantages, and limitations of deep learning techniques in filtering, fringe skeleton line extraction, and phase unwrapping algorithms are discussed based on the representation of measurement results. Finally, this paper provides a perspective on future trends, such as the construction of physical models for electronic speckle interferometry, improvement and optimization of deep learning models, and quantitative evaluation of phase extraction quality, in this field.

Application of magnetic dispersive solid phase extraction combined with solidification of floating organic droplet-based dispersive liquid–liquid microextraction and GC-MS in the extraction and determination of polycyclic aromatic hydrocarbons in honey

A magnetic dispersive solid phase extraction method combined with solidification of floating organic droplet-based dispersive liquid–liquid microextraction has been validated for the extraction of polycyclic aromatic hydrocarbons from honey samples. For this purpose, a carbonised cellulose–ferromagnetic nanocomposite was used as a sorbent through the magnetic dispersive solid phase extraction. For preparation of the sorbent, first, carbonised cellulose nanoparticles were created by treating cellulose filter paper with concentrated solution of sulfuric acid. Then, the prepared nanoparticles were loaded onto Fe3O4 nanoparticles through coprecipitation. In the extraction process, first, a few mg of the sorbent was added to the diluted honey solution and dispersed in it using vortex agitation. The particles were then separated and the adsorbed analytes were eluted with an organic solvent. The eluent was taken and after mixing with a water–immiscible extraction solvent was used in the following solidification of floating organic droplet-based dispersive liquid–liquid microextraction procedure. By performing the extraction process under the obtained optimum conditions, low limits of detection (0.08–0.17 ng g−1) and quantification (0.27–0.57 ng g−1), satisfactory precision (relative standard deviations ≤ 5.0%), and wide linear range (0.57–500 ng g−1) with great coefficients of determination (r2≥ 0.9986) were obtained.