Type Of Solvent Research Articles

Antimicrobial Activity of Plant Extracts of Artemisia , Citrullus and Capparis

The current study shows the effectiveness of three plant extracts of Artemisia, Citrullus fruits and Capparis roots against the microbes of some common and important pathogens, which have become resistant to many antibiotics due to genetic mutations that occur in them, including Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Klebsiella pneumonia .The sensitivity of the studied isolates varied according to the type of extract and the type of solvent used, Alcoholic or Aqueous, as well as on the type of bacteria. While the effect of the effectiveness of the extracts of the fruits of the Citrullus plant and the roots of the capers plant showed a variation from one bacteria to another and from one extract to another.

Development of a green microextraction procedure for determining polyaromatic hydrocarbons in electronic equipment plastics

The global proliferation of electronic devices, driven by technological advancements, has led to the release of organic pollutants from the plastic components of these devices, particularly in indoor environments. Among these pollutants, polycyclic aromatic hydrocarbons (PAHs), which are emitted into the air from plastic components, play a critical role in the field of indoor environment pollution. Consequently, effectively monitoring the PAH content in plastics used in electronic equipment is crucial for preventing indoor contamination.In this study we aimed to develop a fast, inexpensive, easy, and environmentally friendly analysis method for determining PAH content in plastic equipment. A dispersive liquid liquid microextraction (DLLME) combined with solidified organic drop (SFO) microextraction technique was developed.Considering the eleven number of parameters that can affect the signal in the DLLME-SFO method, Plackett Burmann's design was applied to select the most three impactful parameters for 18 PAH species. A Box-Behnken experimental design was also applied to optimize the identified parameters. The optimal conditions for the most influential parameters such as solvent type, pH, and the sample weight were identified as 1-dodecanol, 12 and 0.24 g, respectively.The proposed method was validated under these optimized conditions, yielding low detection limits ranging from 0.004 to 0.11 ng mL−1. The calibration curves were linear with correlation coefficients above 0.98 and relative standard deviation (RSD) values ranging from 2.4% to 20%. This method was successfully applied to analyze PAH content in the plastic components of electronic devices. The extraction technique developed in this study is a newly developed technique and has not been previously used to analyze organic pollutants that may be present in electronic equipment plastic.

Synthesis of the modified SBA-15 mesoporous silica with TAN ligand to preconcentrate and determine trace amounts of Ni (II) ions in water and wastewater samples.

The synthesis of modified mesoporous silica (SBA-15), a powerful and highly effective adsorbent, was provided for the preconcentration, extraction, separation, and determination of trace amounts of Ni (II) ions. In this method, SBA-15 modified with 1-(2-thiazolylazo)-2-naphthol (TAN) was used as a suitable absorbent. The absorption of Ni (II) ions was studied using the FAAS technique. Transmission electron microscopy (TEM), thermogravimetric analysis (TGA), Brunauer-Emmett-Teller (BET), energy-dispersive spectroscopy (EDS), Fourier-transform infrared (FT-IR) spectroscopy, and CHNS elemental analysis techniques were used to assess the characteristics of SBA-15 and TAN/SBA-15. Effective parameters (pH, amount of nanocomposite, extraction time, and type of recovery solvent) for extracting Ni (II) ions via TAN/SBA-15 were investigated. The merit figures of the method were obtained with appropriate results, such as detection limit, accuracy, enrichment factor, and preconcentration factor. The calibration curve was linear within the range of 5.0-50ngmL-1 with a detection limit of 1.8ngmL-1. High preconcentration, small relative standard deviations, and enrichment factors (approximately 100) were represented by the statistical analysis. The proposed method for measuring Ni (II) ions was used at trace levels in real samples, such as seawater, river water, well water, and wastewater from a textile factory, an electrical power station, an MDF factory, and a food industrial company, with satisfactory results.

A Simple Dispersive Liquid-Liquid Microextraction for the Determination of Copper II in the Water Samples of the Halfaya Oil Field in Maysan

Background: Copper, an important trace element for life on Earth, is crucial to many metabolic processes. This includes its role in the production and breakdown of nucleic acids and the metabolism of proteins, lipids, and carbohydrates. Objective: We aim to integrate DLLME with a spectrophotometric method to establish a novel approach for quantifying trace amounts of copper in water samples. Methods: In this study, a new ligand known as a 2-(4 aminophenol) benzimidazole azo derivative was successfully synthesized. This ligand was created by converting 2-(4-aminophenyl) benzimidazole into a diazonium salt and coupling it with 8-hydroxyquinoline in an alkaline environment. The resulting product was a brown azo dye, which served as the ligand for detecting copper (II) in aqueous samples. Results: To analyze copper (II) in both pure and aqueous samples, we developed and validated micro-extraction techniques combined with UV-Vis measurement. Specifically, we used the DLLME (dispersive liquid-liquid microextraction) method to separate, enrich, and assess copper (II) in both its pure form and in aqueous samples. UV-Vis spectroscopy at a wavelength of 503 nm was used for this purpose. We considered several variables during the experiment, including the type and volume of the dispersive solvent, the extraction solvents, the temperature, the reaction duration, and the centrifuging time. By optimizing these conditions, we achieved linear procedures within the concentration range of (1.0–25.0) and (2.0–25.0) μg/mL for spectroscopy and DLLME methods, respectively. For the spectroscopic and DLLME approaches, the coefficient of determination (R2) was found to be 0.9963 and 0.9979 for the spectrophotometric and DLLME methods, respectively. The limit of detection (LOD) for copper (II) was found to be 0.23 and 0.04 μg/mL, respectively. Moreover, the recovery of the target analyte in aqueous samples was found to be between 95.6% and 101% for the spectroscopy method and between 102.4% and 108.2% for the DLLME method. Conclusions: These results demonstrate the effectiveness and accuracy of both methods in analyzing copper (II) in aqueous samples.

Constraining the Excessive Aggregation of Non-Fullerene Acceptor Molecules Enables Organic Solar Modules with the Efficiency >16.

Translating high-performance organic solar cell (OSC) materials from spin-coating to scalable processing is imperative for advancing organic photovoltaics. For bridging the gap between laboratory research and industrialization, it is essential to understand the structural formation dynamics within the photoactive layer during printing processes. In this study, two typical printing-compatible solvents in the doctor-blading process are employed to explore the intricate mechanisms governing the thin-film formation in the state-of-the-art photovoltaic system PM6:L8-BO. Our findings highlight the synergistic influence of both the donor polymer PM6 and the solvent with a high boiling point on the structural dynamics of L8-BO within the photoactive layer, significantly influencing its morphological properties. The optimized processing strategy effectively suppresses the excessive aggregation of L8-BO during the slow drying process in doctor-blading, enhancing thin-film crystallization with preferential molecular orientation. These improvements facilitate more efficient charge transport, suppress thin-film defects and charge recombination, and finally enhance the upscaling potential. Consequently, the optimized PM6:L8-BO OSCs demonstrate power conversion efficiencies of 18.42% in small-area devices (0.064 cm2) and 16.02% in modules (11.70 cm2), respectively. Overall, this research provides valuable insights into the interplay among thin-film formation kinetics, structure dynamics, and device performance in scalable processing.

Efficient ultrasonic extraction of alkaloids and glycosides from Camptotheca acuminata Decne via deep eutectic solvents: Kinetics and mechanisms

The study investigated the extraction of alkaloids and glycosides from the Camptotheca acuminata Decne using deep eutectic solvent (DES). 18 types of deep eutectic solvents (DESs) were prepared, and it was found that the extraction performance of choline chloride (ChCl)-formic acid (FA) was optimal, surpassing traditional solvents such as methanol/70 % methanol. In comparison to methanol, the extracted amount of compounds by DES was 2–3 times higher. The extraction processes involving the molar ratio of ChCl-FA, pH, DES/H2O mass ratio, solid/liquid ratio, as well as ultrasonic power were optimized. A mathematical model for solid/liquid extraction kinetics from Camptotheca acuminata Decne was developed. The extraction mechanism was investigated using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), and 1H nuclear magnetic resonance(1H NMR). The results revealed that the DES caused dissociation in Camptotheca acuminata Decne and formed hydrogen bonds with Camptothecin (CPT). Meanwhile, density functional theory (DFT) calculations verified that FA-based exhibited the highest extracted amount for CPT. In addition, this study investigated the recovery rate of DES, and the results showed that after 10 cycles, the DES system remained effective for the extraction of alkaloids and glycosides.

In situ-generated mononuclear half-sandwich [(η6‐p‐cymene)RuCl(amide)] complexes as efficient catalysts in the selective oxidation of benzyl alcohol to benzaldehyde

The application of in situ-generated mononuclear Ru(II)-organometallic complexes (1–7) i.e., [(η6-p-cymene)RuCl(L)], produced by the interaction of Ru dimer [(p-cymene)RuCl2]2 with some polyfunctional amide ligands(L) as highly efficient catalystsin the oxidation of various benzyl alcohols (B-OLs) by tert-butyl hydroperoxide (TBHP) oxidant to produce selectively the benzaldehydes (B-ALs) in high yields in CH3CN is described. The in situ-generated catalysts were found to be highly active than the [(p-cymene)RuCl2]2 precursor (dimer) in the oxidation of B-OL to B-AL. The influence of various reaction parameters such as type of catalyst, reaction temperature, oxidant and solvent during the B-OL oxidation was systematically monitored to optimize the catalytic conditions. In order to confirm the formation of predicted in situ-generated mononuclear Ru(II) complex catalysts during the oxidation of B-OL, one of the Ru(II) complex (1) was synthesized and characterized by Elemental analysis (EA), Infrared (IR), Proton-NMR and Mass spectral techniques and its mono nuclear structure is proposed. Further, it was observed that the activity of in-situ generated and pre-synthesized Ru(II) catalyst was almost same in the oxidation of B-OL to B-AL.

Greener analysis of eleven basic drugs in blood and urine using carbowax 20M based biofluid sampler (BFS) device

For the first time, a novel biofluid sampler (BFS) and sample preparation deviceis applied for the analysis of 11 basic drugs (i.e., pheniramine, chlorpheniramine, fluoxetine, tramadol, amitriptyline, ketamine, diazepam, chlordiazepoxide, clozapine, chlorpromazine, dothiepin) in biological matrices (i.e., blood and urine). BFS utilizes advanced, highly effective sorbents derived from sol-gel sorbent coating technology onto cellulose fabric substrate, improving sample collection and retention. BFS has the capability to retain a biological sample from 10 to 1000 µL without requiring any dilution or pre-treatmentof the sample. The biological samples were pipetted onto the BFS device and dried at room temperature. Subsequently, adsorbed analytes were back-extracted into 1000 µL of methanol without requiring any imposed external diffusion process andthen analyzed by gas chromatography-mass spectrometry (GC-MS). A one-factor-at-a-time (OFAT) screening procedure was used to extensively screen and optimize several parameters, including sample volume, elution time, solvent volume, and solvent type. Under the optimal conditions of the study, the method was found to be linear within the range 0.1–10 µg mL−1 for both blood and urine. Quantification limits were established for blood samples within the range of 0.084 to 0.099 μg mL−1 and for urine samples within the range of 0.060 to 0.078 μg mL−1. The precisions within and between days were less than 7 % and 10 %, respectively. The target analytes showed good recoveries utilizing the recommended protocol, with ranges of 45.1 % − 103.4 %. Furthermore, the methodology has been effectively implemented in forensic toxicology case work. Moreover, the green characteristics and applicability of the suggested methodology was evaluated using softwares i.e., AGREE and BAGI.

Occupational Exposures, Chronic Obstructive Pulmonary Disease and Tomographic Findings in the Spanish Population.

Self-reported occupational exposure was previously associated with COPD in the Spanish population. This study aimed to analyse the relationship between occupational exposure to various chemical and biological agents, COPD, emphysema, and the bronchial wall area, which was determined by lung computed tomography (CT) in 226 individuals with COPD and 300 individuals without COPD. Lifetime occupational exposures were assessed using the ALOHA(+) job exposure matrix, and CT and spirometry were also performed. COPD was associated with high exposure to vapours, gases, dust and fumes (VGDF) (OR 2.25 95% CI 1.19-4.22), biological dust (OR 3.01 95% CI 1.22-7.45), gases/fumes (OR 2.49 95% CI 1.20-5.17) and with exposure to various types of solvents. High exposure to gases/fumes, chlorinated solvents and metals (coefficient 8.65 95% CI 1.21-16.09, 11.91 95%CI 0.46- 23.36, 14.45 95% CI 4.42-24.49, respectively) and low exposure to aromatic solvents (coefficient 8.43 95% CI 1.16-15.70) were associated with a low 15th percentile of lung density indicating emphysema. We conclude that occupational exposure to several specific agents is associated with COPD and emphysema in the Spanish population.

Bio-inspired copper complexes with Cu2S cores: (solvent) effects on oxygen reduction reactions.

The need for effective alternative energy sources and "green" industrial processes is a more crucial societal topic than ever. In this context, mastering oxygen reduction reactions (ORRs) is a key step to develop fuel cells or to propose alternatives to energy-intensive setups such as the anthraquinone process for hydrogen peroxide production. Achieving this goal using bio-inspired metal complexes based on abundant and non-toxic elements could provide an environmentally friendly option. Given the prevalence of Cu-containing active sites capable of reductive activation of dioxygen in nature, the development of Cu-based catalysts for the ORR thus appears to be a relevant approach. We herein report the preparation, full characterization and (TD)DFT investigation of a new dinuclear mixed-valent copper complex 6 exhibiting a Cu2S core and a bridging triflate anion. Its ORR activity was compared with that of its parent catalyst 1. Two types of solvents were used, acetonitrile and acetone, and various catalyst/Me8Fc (electron source) ratios were tested. Our results highlight a counterintuitive solvent effect for 1 and a drastic drop in the activity for 6 in coordinating acetonitrile together with the modification of its chemical structure.

Remediation of per- and polyfluoroalkyl substances (PFAS) contaminated soil via soil washing with various water-organic solvents

The feasibility of soil washing for remediating PFAS-contaminated clay soil using various water-organic solvents was systematically investigated based on the combination of batch and column tests. Batch tests using 22 types of solvents highlighted that 0 % (water) and 5 % solvents could effectively extract PFCAs (≤ C9), while long-chain PFCAs (≥ C10) and PFSAs required 80 % solvents for optimal extraction, with efficiency in the order of EtOH ≤ MeOH < Acetonitrile (ACN), suggesting a strong correlation with carbon chain lengths and functional head groups. Column tests with six selected washing solutions indicated rapid desorption of PFOA and PFOS initially, peaking at liquid-to-solid (L/S) ratios of 3–4 for 0 % and 5 % solutions, and at an L/S ratio of 1 for 80 % solutions. To remediate 1 kg-dry soil to meet the legislatively permissible levels for groundwater in Japan (PFOA + PFOS < 50 ng/L), 11 L of 0 % solution (water) or 5 L of 80 % ACN are required for washing out PFOA, while 62 L of 0 % solution (water) or 53 L of 80 % ACN for PFOS. Future research should address the treatment of PFAS-rich wastewater generated from washing PFAS-contaminated soils and the impacts of washing solutions on soil.

Re-evaluation of Microhardness of Mineral Trioxide Aggregate and Biodentine After Removal From Root Using Different Types of Solvents: An In Vitro Study.

Objective This study aimed to evaluate the effects of different solvents on the microhardness of mineral trioxide aggregate (MTA) and Biodentine, which are used in endodontic therapy for their biocompatibility and ability to create a hermetic seal. Methods A total of 150 extracted human single-rooted teeth were selected and sectioned into 4 mm slices. The samples were divided into two groups according to the material used: MTA and Biodentine. Then the samples were incubated at 37°C and 100% humidity for 28 days. After that, 15 MTA and Biodentinesampleseach were sent for microhardness test and the remaining samples were subdivided into four subgroups according to the solvent used, i.e., treated with normal saline, 5.25% sodium hypochlorite, 10% citric acid, or 40% hydrofluoric acid. The microhardness of the upper and lower surfaces of the samples was measured using a Vickers microhardness tester. Results The average microhardness values for Biodentine and MTA were found to be 74.4 HV and 69.9 HV, respectively. Treatment with sodium hypochlorite, citric acid, and hydrofluoric acid significantly reduced the microhardness of both materials. Hydrofluoric acid had the most pronounced effect, followed by citric acid and sodium hypochlorite. Statistical analysis using one-way analysis of variance (ANOVA) 'F' test showed highly significant differencesbetween the groups. Discussion The study demonstrated that solvents such as hydrofluoric acid, citric acid, and sodium hypochlorite effectively reduced the microhardness of MTA and Biodentine, facilitating their removal during retreatment. This reduction in microhardness is attributed to the chemical interactions of the solvents with the materials, leading to disintegration and reduced structural integrity. Conclusion Biodentine had greater microhardness compared to MTA, and hydroflouric acid reduced the microhardness to a greater extentcompared to other solvents.

Synthesis of 5-substituted-1H-tetrazoles by lemon juice as a homogeneous and natural catalyst under green reaction conditions

Tetrazole, as a heterocyclic compound, exhibits a wide spectrum of applications in various industries. This research focuses on utilizing a natural catalyst in the synthesis of tetrazole derivatives. Leveraging the acidic nature of lemon juice (LJ), we employed it as a potential catalyst in the synthesis of 5-substituted-1H-tetrazole. LJ would act as the reaction medium as well. This synthesis involves the cycloaddition reaction (3 + 2) of sodium azide to benzonitrile under solvent-free conditions. Optimization of the reaction conditions including temperature, reaction time, and solvent type was tuned towards the highest yield considering the mild reaction time. The best product yield (97 %) was obtained at 90 °C, 40 min, in the absence of additional solvent. Various benzonitrile derivatives were examined at the optimized reaction condition.

A Comparative Analysis of Flavonoid and Phenolic concentration from Diverse Varieties of Moringa oleifera Leaves Utilizing Methanol and Ethanol

Having its leaves abundant in nutrients such as vitamins and minerals, the moringa plant is highly regarded because of its nutritious and industrial usefulness. Despite its widespread utilisation, little is understood concerning the way various Moringa oleifera cultivars vary with regard to their phenolic and flavonoid concentration, particularly when extracting the compound utilising various solvents. To attempt to throw insight into the ways that various solvent types and environment variables affects the phytochemical compounds of Moringa oleifera leaves, this research investigation compared the efficacy of ethanol and methanol in removing phenolics as well as flavonoids from the leaves. The information gathered through this research could assist to identify the most appropriate methods for extraction that will maximize the medical and nutritional advantages associated with Moringa oleifera. New leaves of five different types of Moringa oleifera had been bought from the Winfred Thomas Agricultural Research Station in Alabama A&amp;M University. Upon being pulverised and dried, the resulting leaves had been preserved at room temperature. The leaves were immersed in a mixture of 70% ethanol as the solvent and 80% methanol all through the extraction method. The extracted samples had been then stirred, filtered, and freeze-dried. Following that, High-performance liquid chromatography was the technique employed to know the overall concentration of phenolic and flavonoid compounds. Descriptive and statistical analysis were performed using box plots, scatter plots, bar plots, and t-tests to evaluate the extent or degree to which both solvents removed phenolic and flavonoid compounds and estimated the total quantity of phenolic and flavonoids in the different cultivars. The findings from the descriptive study revealed the Nigerian variety had an increased phenolic content when extracted using methanol—roughly 822.3 µg/ml—than when removed using ethanol (80.6 µg/ml). The Indian type, on the contrary, had phenolic concentrations of 814.3 µg/ml as compared with 647.3 µg/ml in ethanol, revealing an important distinction in preference for methanol. The Nigerian cultivar possessed an increased extraction effectiveness of 1253.12 µg/ml using ethanol as opposed to methanol (1083.52 µg/ml) for flavonoids. The t-test results proved that though the difference was not statistically significant (t(28) = 0.608, p = 0.382), the average phenolic content obtained with methanol (M = 798.60, SD = 23.567) was slightly more than that obtained via ethanol (M = 790.60, SD = 45.183). In a similar vein extraction with methanol showed a smaller average flavonoid concentration (M = 1068.40, SD = 128.641) compared to the extraction with ethanol (M = 1129.40, SD = 166.018); nonetheless, this difference was not statistically significant (t(28) = 1.125, p = 0.334). The scatter diagram revealed a significant linear connection with both phenolic and flavonoid content, having a significant positive correlation (Pearson correlation coefficient = 0.95). Although some modifications depending on the variety, the research reveals that methanol and ethanol serve as suitable solvents for phenolic and flavonoid compound extraction from Moringa oleifera leaves. The usefulness of these developments in enhancing methods of extraction in manufacturing industries needs to be explored deeper.

Natural deep eutectic based dispersive liquid-liquid microextraction and solidified floating organic drop for cadmium determination by electrothermal atomic absorption spectrometry with multivariate optimization (DLLME-SFOD-NADES-ETAAS)

A novel method was developed for cadmium determination based on dispersive liquid-liquid microextraction and solidified floating organic drop by multivariate optimization with electrothermal atomic absorption spectrometric detection using a natural deep eutectic solvent (NADES) of (L)-menthol and formic acid. Important factors, including pH, final concentration of PAN, mole ratio of formic acid, volume of NADES, type of dispersive solvent, and vortex time, were assessed using two-level fractional factorial design (FFD), and circumscribed central composite design (CCC). The analytical performance parameters, encompassing linearity range, limit of detection (LOD), limit of quantification (LOQ), and precision, were evaluated. The linearity range ranged from 0.72 to 2.50 ng/L, with corresponding LOD and LOQ values of 0.22 and 0.72 ng/L, respectively. Precision was evaluated by conducting three replicates of the three concentration levels, resulting in %RSD values of 11.8 %, 5.1 %, and 3.9 %, respectively. An enrichment factor (EF) of 112 was achieved. The optimized method was applied for cadmium determination in various matrices, including drinking water, environmental water, seafoods, yielding %recovery in the ranges of 78.05–102.41 %. Finally, comparison of t-values between the developed method and CRMs demonstrated satisfactory results at a 95 % confidence level.

Separation of oil from rapeseed protein rich extracts by microfiltration using hydrophilic ceramic membranes

Rapeseed, containing up to 40 % protein along with a well-balanced profile of essential amino acids, stands out as a promising novel plant-based protein source. Yet, protein extraction faces challenges, due to adverse effects of oil extraction on protein properties and down-stream processing. In this work was explored the potential of using hydrophilic silicon carbide ceramic (SiC) membranes to separate oil from a protein rich extract and produce permeates rich in protein and retentates containing oleosomes. Various solvents including water, sodium chloride, alkaline (pH 8.5) and a complex alkaline salt solvent were used to obtain a variety of protein and oil extracts from the whole rapeseeds. The type of solvent significantly affected the composition and colloidal structure of the feed which has minor effect on the oil separation but significant effect on filtration performance and composition of the permeates and retentates obtained. The membrane filtration process achieved significant oil separation, with permeates exhibiting minimal oil content ranging from 0.1 to 1.3 % (w/w), for water and alkaline solvents respectively. Assessment of the filtration performance showed fluxes from 23 to 50 L·h−1·m−2 and final volume concentration ratios of 1.3, 1.4, 1.6 and 1.9 for salt, alkaline-salt, alkaline and water solvents. The retentate, composed of 11.8–19.8 % protein and 23.6–28.7 % w/w dry matter, is a relevant and innovative ingredient for plant food formulations. These findings show the potential of membrane filtration with SiC in enabling removal of oil and producing streams with potential for diverse applications in the food industry.

Integrative process of extraction and purification of tagitinin C using ethanolic two-phase system based on protic ionic liquids

Tithonia diversifolia is a tropical plant composed of several compounds with medicinal properties. This study aimed to design a sequential process for the extraction of tagitinin C from T. diversifolia using organic solvents (acetone, acetonitrile, methanol, and ethanol) and purification in the ethanolic two-phase system (ETPS) formed by protic ionic liquids (PILs), polypropylene glycol 2000 (PPG-2000) and ethanol, reported here for the first time. The extraction process variables such as type of solvent, solid–liquid ratio, temperature, and process time were evaluated. Ethanol was the best tagitinin C extracting agent (702.1 µg/mL). Phase diagrams were constructed using PPG-2000, PIL, and ethanol at 298.15 K. The sequencing with the purification process occurred by adding the other constituents directly into the ethanol extract. Tagitinin C preferentially migrated to the top phase (rich in PPG-2000), while phenolic compounds (contaminants) were partitioned mainly to the opposite phase (PIL-rich phase). ETPS formed by [2HEA][Ac] (15.52 wt%) + PPG 2000 (49.91 wt%) + ethanol (34.57 wt%) at 298.15 K presented the highest selectivity (S = 18.3), extraction efficiency in the top phase (EE% = 86 %) and purification factor (3.4-fold), demonstrating the ability of ETPS to selectively and sequentially extract and purify tagitinin C.

Using natural deep eutectic solvents for the extraction of antioxidant compounds from cornelian cherry (Cornus mas L.) fruits

Traditionally used extraction methods are usually based on toxic and/or flammable solvents. Therefore, currently, increased attention has been focused on environmentally friendly green extraction techniques. We aimed to develop a green extraction procedure by using natural deep eutectic solvents (NADES) to recover antioxidant compounds from cornelian cherry fruits (Cornus mas L.). Natural deep eutectic systems combined with maceration with shaking extraction were tested to recover of antioxidant compounds from cornelian cherry fruits. In this study, four different independent variables, namely solvent type (Glu-CA; Glu-Gly; LA-Glu), water concentration (30, 50, and 70 %; v/v), extraction time (30, 60, 90, and 120 min), and extraction temperature (25, 40, and 50 °C) were investigated. Glucose-glycerin (Glu-Gly; 1:1 M ratio) based solvent provided the best results. In addition, one-factor-at-a-time (OFAT) optimization showed that a temperature of 25 °C, 120 min of extraction time, and water concentration of 50 % (v/v) to be the best extraction parameters for Glu-Gly based NADES extraction. The developed method has been successfully applied for the extraction of antioxidant compounds from 13 different cornelian cherry cultivars. NADES can be used safely to extract phenolic compounds from cornelian cherry fruits compared to conventional extraction solvents (water and 80 % (v/v) ethanol).

Application of Ionic Liquids in Environmental and Food Fields

Abstract: As a new type of green solvent, ionic liquids have made rapid progress in the fields of organic synthesis, separation, and electrochemistry due to their unique physical and chemical properties. At the same time, the new fluorescence characteristics and good separation and adsorption functions of ionic liquids have gradually developed in the field of environment and food, showing a good application prospect. Based on the work of our research group and the progress and development of research technology, this article reviews the research results of ionic liquids in environmental monitoring and food detection and extraction in recent years. In the environmental field, ionic liquids have the ability of detection and remediation and they show the advantages of fast, efficient, green and recyclable in the detection of environmental pollutants. In the field of food, ionic liquids provide a new idea for the detection and extraction technology of food components. While ensuring green, safe and pollution-free, they show superior selectivity, repeatability and stability, and simplify the operation steps and costs to a certain extent, showing the capture vitality with life characteristics. As a potential smart material, the mechanism of ionic liquids as fluorescent probes and separation extractants was discussed. Finally, the future development and research directions of ionic liquids are prospected, and it is expected to realize the intelligentization of ionic liquid materials and the general integration of development.

One-pot fabrication of hydrophobic, superelastic, harakeke-derived nanocellulose aerogels with excellent shape recovery for oil adsorption and water-in-oil emulsion separation

Cellulose-based aerogels have attracted significant attention for oil/water separation due to their high porosity, large specific surface area and high adsorption capacity. However, their intrinsic hydrophilicity, and inadequate mechanical properties have often limited their practical applications. Traditional freeze-dried cellulose aerogels exhibit unsatisfactory elasticity and require a separate surface modification process to adjust the surface wettability. In this study, we present a novel one-pot fabrication strategy which simultaneously achieves the crosslinking of individual cellulose nanofibers and the hydrophobic modification of the surface wettability. Following directional freeze-drying, hydrophobic, superelastic, and anisotropic cellulose-based aerogel was prepared from the 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO)-oxidized cellulose nanofibers, isolated from harakeke (New Zealand native flax). The resulting aerogel exhibits a high water contact angle of 142°, good compressive recovery performance (85 % recovery of the original height after 100 compression cycles at 70 % strain), and outstanding adsorption capacity for various types of oil and organic solvents (80–105 g/g). Furthermore, the aerogel could also be used as a filter to separate surfactant stabilized water-in-oil emulsions with a high flux (782 L m−2 h−1) and a high separation efficiency (98.7–99.2 %). The novel aerogel prepared in this study is expected to have great potential for practical applications in oily wastewater remediation.