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In this study, choline chloride/urea was used as a green deep eutectic solvent in the three-component reaction of hydrazine/phenylhydrazine, malononitrile, and aromatic aldehydes for synthesizing pyrazole derivatives, and in the four-component reaction of methyl/ethyl acetoacetate, hydrazine/phenylhydrazine, malononitrile, and aromatic aldehydes for synthesizing pyrano[2,3-c]pyrazole derivatives. Elemental analysis, ¹H, and 13C NMR spectroscopy were used to confirm the structure of the synthesized pyrazole and pyrano[2,3-c] pyrazole derivatives. The antimicrobial effects of the synthesized pyrazole and pyrano[2,3-c] pyrazole derivatives were investigated. In antimicrobial tests, instructions from clinical and laboratory standards institutes were used. Antimicrobial study was done on pathogenic gram-positive and gram-negative species, and specialized aquatic strains and fungal species. Using choline chloride/urea, novel pyrazole derivatives and pyrano[2,3-c]pyrazole derivatives were synthesized, and other derivatives were synthesized with higher efficiency in less time than some previously reported methods. MIC (minimum inhibitory concentration) and MBC (minimum bactericidal concentration) obtained for derivatives were higher than some antibiotic drugs. Synthesis and reports of new derivatives of pyrazole and pyrano[2,3-c]pyrazole, and investigation and reports of their antimicrobial properties on gram-positive, gram-negative, and specialized aquatic and fungal species are among the novel and important findings of this study. [ABSTRACT FROM AUTHOR]

Here we report a new synthetic approach to several intricate indoles and hydrazones starting with commercially available terpenes and steroids via Fischer indolization (FI) sequence under deep eutectic solvents (DES) conditions or by employing acetic acid reflux conditions. During the course of the reaction with pulegone 22 and pipertone 25 we observed Fischer indolization along with aromatization is occurring. In another instance, with thujone 32 we found cyclopropane ring is opening under thermal conditions leading to aromatized Fischer indole product. We also studied the FI sequence of some diketo derivatives to synthesize the corresponding bis indole derivatives, but instead we obtained mono hydrazone derivative which can be explained on the basis of steric reasons. In addition, we also modified other terpenes to study the FI sequence where we realized the formation of both hydrazone and indole derivatives. All the compounds synthesized here are well characterized by NMR and HRMS data. [ABSTRACT FROM AUTHOR]

In the present study, for the first time environmentally friendly deep eutectic solvents (DESs) are used as reaction media to perform an efficient, simple and straightforward photocatalytic amide synthesis at room temperature using thioacids and amines. This method features mild conditions, a broad substrate scope, high yields (≤99%) under ambient conditions with air and moisture tolerance. Moreover, the applied operationally mild reaction conditions tolerate the presence of several different functional group substituents on the amine counterpart. Finally, the developed approach allows the recycling of the reaction medium and catalyst for at least three consecutive cycles without a significant decrease in the reaction yield. [ABSTRACT FROM AUTHOR]

The study explored ferulic acid extraction from palm empty fruit bunch (EFB) fiber using deep eutectic solvent (DES) of chlorine chloride—acetic acid as the extraction medium and the way to recover and recycle the DES thereafter. Antisolvent was added to selectively precipitate the ferulic acid, which was recovered by filtration thereafter. Recycling the DES without further purification led to increased ferulic acid yield with each subsequent extraction, likely due to retained ferulic acid. The retained ferulic acid and other impurities could be removed by precipitation brought upon by the addition of a second antisolvent. 1H nuclear magnetic resonance revealed that there was no excess ferulic acid in the recycled DES‐treated with two types of antisolvents (ethanol and water). The yield of ferulic acid increased from 0.1367–0.1856 g/g when treated with only one antisolvent to 0.1368–0.2897 g/g with two antisolvent treatments. Oil droplets were also observed in the DES upon the addition of antisolvent 2, with recovered oil ranging from 0.6% to 3%. The study emphasized the significance of using DES as an extraction medium for ferulic acid from oil palm EFB fiber and the method to recycle the DES for subsequent processes. [ABSTRACT FROM AUTHOR]

This article discusses a new method for synthesizing benzimidazole derivatives using a deep eutectic solvent (DES) as the reaction medium. The researchers found that using choline chloride/glycerol/water as the solvent resulted in high yields of the desired products. The method was successful with various amines and aldehydes, and the products were obtained through simple work-up procedures. The article provides detailed information on the synthesis and characterization of the compounds, including their yields, physical properties, and spectroscopic data. This research offers a more sustainable and environmentally friendly approach to synthesizing benzimidazole derivatives. [Extracted from the article]

Tartary buckwheat green leaves are considered to be among the most important by-products in the buckwheat industry. Although Tartary buckwheat green leaves are abundant in pectic polysaccharides, their potential applications in the food industry are quite scarce. Therefore, to promote their potential applications as functional or fortified food ingredients, both deep-eutectic-solvent-assisted extraction (DESE) and high-pressure-assisted deep eutectic solvent extraction (HPDEE) were used to efficiently and selectively extract pectic polysaccharides from Tartary buckwheat green leaves (TBP). The results revealed that both the DESE and HPDEE techniques not only improved the extraction efficiency of TBP but also regulated its structural properties and beneficial effects. The primary chemical structures of TBP extracted using different methods were stable overall, mainly consisting of homogalacturonan and rhamnogalacturonan-I (RG-I) pectic regions. However, both the DESE and HPDEE methods could selectively extract RG-I-enriched TBP, and the proportion of the RG-I pectic region in TBP obviously improved. Additionally, both the DESE and HPDEE methods could improve the antioxidant and anti-glycosylation effects of TBP by increasing its proportion of free uronic acids and content of bound polyphenolics and reducing its molecular weight. Moreover, both the DESE and HPDEE methods could partially intensify the immunostimulatory effect of TBP by increasing its proportion of the RG-I pectic region. These findings suggest that DES-based extraction techniques, especially the HPDEE method, can be promising techniques for the efficient and selective extraction of RG-I-enriched TBP. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

AbstractAs a typical genotoxic impurity (GTI), the concentration of benzo(a)pyrene (BaP) must be below the threshold of toxicological concern (TTC). However, achieving a trace BaP is a significant challenge by conventional separation media. Utilizing the unique recognition capabilities of surface molecular imprinting polymers (SMIPs), the versatility of N-vinyl-2-pyrrolidone deep eutectic solvents (NVP-DES), and the high surface area of two-dimensional nano-boron nitride (2D-nano-BN) sheets, a series of functionalized 2D-BN materials were prepared (NVP-DES-SMIP@2D-nano-BN) for the specific recognition and removal of BaP. Utilizing 2D-nano-BN sheets as the base, four NVP-DESs were employed as monomers, BaP as the template, EGDMA as the cross-linker, and BPO/DMA as the initiator to prepare NVP-DES-SMIP@2D-nano-BN. The free energy of DES was computed using Gaussian software, and characterization of NVP-DES-SMIP@2D-nano-BN was performed using Fourier transform infrared spectroscopy and transmission electron microscopy. Quantitative and qualitative determinations of BaP were conducted using high performance liquid chromatography and fluorescence. Using a recognition model, NVP-DES-SMIP@2D-nano-BN exhibited a Freundlich isotherm fit and second-order kinetics for BaP. [ABSTRACT FROM AUTHOR]

[Display omitted] • Deep eutectic solvent-catalyzed glycolysis of post-consumer PET is proposed. • ChCl–Zn(OAc) 2 affords complete conversion of PET with high BHET selectivity. • Degradation mechanism of PET glycolysis is examined through DFT calculations. • Machine learning is applied to construct a predictive model for PET glycolysis. To achieve a sustainable and circular economy, developing effective plastic recycling methods is essential. Despite advances in the chemical recycling of plastic waste, modern industries require highly efficient and sustainable solutions to address environmental problems. In this study, we propose an efficient glycolysis strategy for post-consumer polyethylene terephthalate (PET) using deep eutectic solvents (DESs) to produce bis(2-hydroxyethyl) terephthalate (BHET) with high selectivity. Choline chloride (ChCl)- and urea-based DESs were synthesized using various metal salts and were tested for the glycolysis of PET waste; ChCl–Zn(OAc) 2 exhibited the best performance. The DES-containing solvent system afforded a complete PET conversion, producing BHET at a high yield (91.6%) under optimal reaction conditions. The degradation mechanism of PET and its interaction with DESs were systematically investigated using density functional theory-based calculations. Furthermore, an intuitive machine learning model was developed to predict the PET conversion and BHET selectivity for different DES compositions. Our findings demonstrate that the DES-catalyzed glycolysis of post-consumer PET could enable the development of a sustainable chemical recycling process, providing insights to identify the new design of DESs for plastic decomposition. [ABSTRACT FROM AUTHOR]

In recent years, deep eutectic solvents (DESs) have attracted increasing attention due to their ionic liquid analogue. Compared with ionic liquids, deep eutectic solvents had more advantages such as low-cost, easy synthesis and wide application. In the present work. deep eutectic solvents were prepared from choline chloride and ethylene glycol, choline chloride and 1.3-propanediol, choline chloride and 1,4-butanediol, respectively. At the same time their hydrogen bonding interactions were investigated by the FTIR and 'H NMR. The effects of different temperatures (303.15~343.15 K), molar ratio and alkyl chain length on the physicochemical properties of deep eutectic solvents were researched. The results showed that the hydrogen bonding of choline chloride is weakened with the increase of polyol content in choline chloride/alcohol deep eutectic solvent, and the hydrogen bonding of polyol is enhanced. It can form suitable hydrogen bonds when the choline chloride to ethylene glycol molar ratio of is 1: 3. Also, with the increasing of temperature, the viscosity of deep eutectic solvent notably decreases while the conductivity increases. On the other hand, density is slight affected by the temperature change. Under the same temperature, the viscosity and polarity of the deep eutectic solvent increases, and the conductivity, surface tension, and pH decreases, as the length of the alkyl chain increases. As glycol content increases, the viscosity decreases, and the pH increases first and then decreases, while the polarity and surface tension does not change significantly. The results of this study reveal the hydrogen bonding interaction of deep eutectic solvents based on choline chloride and different glycol. Furthermore, the physicochemical properties of DESs can provide scientific guidance for its application in the extraction field, which is of great significance and value. [ABSTRACT FROM AUTHOR]

This study evaluates the ability of a choline chloride:ethylene glycol‐based deep eutectic solvent (DES) to dissolve lithium cobalt oxide (LCO) which is used as a cathode active material in Li‐ion batteries. Both a commercial powder and spent cathodes have been used. It was demonstrated that if HCl is added in a small proportion, a rapid and efficient LCO dissolution can be achieved. Indeed, if more than three protons are added per one cobalt atom present in the LCO structure, a complete dissolution of the material is accomplished within 2 h at 80 °C. This result might be considered as a viable alternative compared to the literature where much longer reaction times and higher temperatures are applied to achieve similar results with the same DES system used either pure or in presence of additional reducing agents. It was further demonstrated that Co and Li can be fully precipitated after Li2CO3 addition. This precipitation does neither pollute the DES nor leads to its degradation provided the pH does not exceed 10. Finally, it was shown that two additional reuse cycles can be carried out without any decrease of recovery efficiency, while no degradation products have been detected within the DES phase. [ABSTRACT FROM AUTHOR]

Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

In this study, the aim was to optimize the extraction conditions (molar ratio, time, temperature) in order to maximize the total individual amino acid (TAA) yield from bee bread, which is a fermented bee product, using choline chloride-acetic acid deep eutectic solvent (DES). In addition to the phenolic profile and amino acid profile investigated by LC-MS/MS, some spectrophotometric (total phenolic content, total flavonoid content, total proanthocyanidin content) and bioactivity (antioxidant/antimicrobial activity) tests were carried out on the extracts. Optimum conditions were determined as 1:2 for molar ratio, 15 min for time and 10 °C for temperature with optimization based on the TAA values of the different extracts (d: 0.99). Molar ratio and temperature were found to have statistically significant effects on TAA values. At optimum conditions, the amount of TAA obtained with DES (29.678 g/kg) was found to be approximately 35.2% and 54.4% higher than that obtained with ethanol and methanol extracts, respectively. All these results indicate that choline chloride-acetic acid DES can be chosen when preparing bee bread extracts, which are evaluated for different areas of use such as food and health due to active ingredient content. Higher active ingredients can be extracted by trying different DES combinations. [ABSTRACT FROM AUTHOR]

The paper reports the impact of anodic potentiostatic treatment of nickel in two representatives of a new type of eutectic ionic liquids (deep eutectic solvents), ethaline and reline, which are eutectic mixtures of choline chloride with ethylene glycol and urea, respectively. The influence of anodic treatment on surface morphology, roughness coefficients, and electrocatalytic activity towards the hydrogen evolution reaction is characterized. It is demonstrated that the current densities of nickel anodic dissolution in reline are approximately an order of magnitude lower than in ethaline under all other identical conditions. Significant differences in the kinetics of nickel anodic dissolution and passivation during anodic polarization in ethaline and reline have been established, which may be attributed to both a substantial difference in the viscosity of these solvents and differences in the chemical nature and composition of the ions present in them. It is found that anodic treatment in ethaline, at certain potentials, results in electrochemical polishing of the surface, confirmed by a decrease in measured roughness coefficients, while anodic treatment in reline does not allow effective electropolishing and only surface etching (increase in roughness coefficients) is observed. Anodic potentiostatic treatment of nickel in both investigated deep eutectic solvents at specific electrode potential values significantly enhances the electrocatalytic activity of the surface towards the hydrogen evolution reaction in an alkaline environment. This finding can be utilized in the development of electrocatalytic materials for the electrolytic synthesis of green hydrogen. [ABSTRACT FROM AUTHOR]

Copyright of Chemical Engineering (China) / Huaxue Gongcheng is the property of Hualu Engineering Science & Technology Co Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

In this work, an environmentally‐friendly deep eutectic solvent (DES) was employed as a catalyst to generate polyvinyl butyral (PVB) resins from polyvinyl alcohol (PVA) with a weakly acidic polymer (polyacrylic acid [PAA]) as an emulsifier. Finally, high viscosity PVB resins with molecular weight of 110,000–200,000 g · mol−1 and acetalization degree above 83% were successfully synthesized, which was found to satisfy the requirements for interlayer films between safety glass. Furthermore, it was well proved that the properties of PVB resins immensely depend on the molecular structures of the PVA. The molecular weight of the PVB, independent of alcoholic degrees of the PVA, indicated an upward trend with the increase of the molecular weight of the PVA. As for these four PVBs with high molecular weight, the Tg was sensitive to the content of hydroxyl and acetal groups rather than molecular weight, associated with the inter‐ or intra‐molecule hydrogen bond between OH. PVB‐1799 and PVB‐1797 had higher Ti and Tg than that of PVB‐1788 and PVB‐1795 because the former had low contents of vinyl acetate group (VAc) and alcohol hydroxyl group (VOH). The tensile strength of PVBs was all higher than 30 Mpa, and the elongation at break was about 300% due to their high molecular weights. [ABSTRACT FROM AUTHOR]

As an environmentally friendly solvent, deep eutectic solvent has become a research hotspot for fiber modification in recent years. In this paper, surface modification and functionalization of polyester fabrics (PET) were treated by the deep eutectic solvent of choline chloride/oxalic acid (ChCl/OA) and chitosan-dissolved ChCl/OA (ChCl/OA-CTS). The surface morphology, chemical structure, dimensional stability, mechanical properties, and antibacterial properties of PET before and after treatment were compared, and the results showed that PET fiber swelling occurred by ChCl/OA treatment, and fiber fineness increased by 15.92%. Scanning electron microscope (SEM) indicated that the surface roughness of the fiber increased and the surface etching occurred after washing and drying. Meanwhile, the adjacent fibers were "welded" to each other, resulting in increased friction between the fibers and improved stability of the fabric size. Fourier transform infrared (FTIR), energy dispersive spectrometers (EDS), and X-ray photoelectron spectroscopy (XPS) analysis showed that the chitosan was loaded on the surface of PET fiber after ChCl/OA-CTS treatment, the hydrophilicity of PET fiber was improved, and the inhibition rate of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) was 92.04% and 92.16%, respectively. In conclusion, the PET was physically etched and reproduced, and the chitosan can be embedded in the fiber with the swelling of the fiber. [ABSTRACT FROM AUTHOR]

Copyright of Basic Sciences Journal of Textile Universities / Fangzhi Gaoxiao Jichu Kexue Xuebao is the property of Basic Sciences Journal of Textile Universities and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of China Condiment is the property of China Condiment and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Pure cellulose nanofibers (CNFs) rapidly degrade in soil, limiting their prospective applications in agriculture. We incorporated lignin into CNFs as an antimicrobial and crosslinking agent to control the biodegradation rate. CNFs with different lignin concentrations were prepared by mechanochemical treatment in the presence of choline chloride-urea deep eutectic solvent. These were characterized using conductometric titration, scanning electron microscopy, and FT-IR. The fibers were applied to soil to determine the effect of lignin on soil respiration and nanocellulose degradation, and were used as a substrate for radish and cress seed germination. Modifying the lignin content of the fibers successfully modulated the biodegradation rate in soil. Fibers containing 35% lignin degraded 5.7% in 14 days, while fibers with 20% lignin degraded 20.8% in 14 days. Nanofiber suspensions showed low chemical inhibition for the germination of radish and cress seeds but higher lignin contents reduced the imbibition rate as a seed coating. This study presents the first use of lignin to control the biodegradation rate of cellulose nanofibers in a one-pot, scalable and sustainable system, allowing the advancement of lignocellulose nanofibers for applications such as seed coatings, mulches, and controlled release fertilizers. [ABSTRACT FROM AUTHOR]

Since that pathogenic bacteria are major threats to human health; this research describes the fabrication of an effective and sensitive platform based on graphene oxide/poly deep eutectic solvent/nickel oxide nano particles (GO/PDES/NiO NPs) nanocomposite at the surface of glassy carbon electrode for selective detection of Staphylococcus aureus (S. aureus). The DNA aptamers were immobilized on the modified electrode through the EDC/NHS chemistry. Each aptasensor modification step was checked by with cyclic voltammetry (CV) and electrochemical impedance spectra (EIS) techniques. The linear dynamic range of the proposed electrochemical aptasensor covered a large variation of S. aureus concentrations from 101 – 108 CFU.mL−1 and a detection limit of 10 CFU.mL−1 under optimum conditions was obtained. Analysis of spiked tap water, lake water and human serum samples revealed high potential of this aptasensor as a sensitive, effective, and label‐free promising tool for S. aureus detection. This is the first time that poly deep eutectic solvents used in live bacteria detection. [ABSTRACT FROM AUTHOR]

Hydrophilic deep eutectic solvents based on choline chloride, carboxylic acids, and water are studied as "green" extractants for the liquid–liquid microextraction of lead from vegetable oils. An automated method is proposed for the microextraction of lead from vegetable oils into a ternary deep eutectic solvent based on choline chloride, lactic acid, and water. The carboxylic acid in the extractant ensured the effective mass transfer of lead due to complexation. Water in the extractant made it possible to reduce its viscosity to automate liquid–liquid microextraction. The analytical capabilities of the developed method are demonstrated on an example of determining lead in vegetable oils by atomic absorption spectrometry with electrothermal atomization. The limit of detection (3σ) for lead is 0.3 μg/kg. The developed method does not require sample mineralization. [ABSTRACT FROM AUTHOR]

Propolis is a natural product created by honey bees with enzymes by process nectar, pollen, and resinous plant materials. Propolis is rich in bioactive content that is used in a multifunctional way in many different sectors such as health, food, and chemistry. However, propolis cannot be consumed in its raw form due to its resin-like structure which is less soluble in water. Therefore, it is challenging to separate the bioactive part from the apolar part due to the sticky structure of the raw propolis. Propolis has around 300 chemical compounds high in flavonoid and phenolic acids, and its composition varies depending on the climate, flora, and season. For this purpose, sustainable and environment-friendly extraction methods have been developed. In this review, conventional and novel extraction methods have been evaluated particularly in terms of extraction efficiency. Among the novel propolis extraction methods, ultrasound-assisted and green solvent extraction methods have gained great interest in terms of extraction efficiency, sustainability, and low operation cost. [ABSTRACT FROM AUTHOR]

Understanding the pyrolysis product distributions of deep eutectic solvent (DES)-isolated lignins (DESLs) from different types of biomass is of great significance for lignin valorization. The structure and pyrolysis properties of DESLs obtained from eucalyptus (E-DESL), pine (P-DESL), and rice straw (R-DESL) were studied through the use of various methods such as elemental analysis, GPC, HS-GC, and NMR techniques, and the pyrolysis characteristics and product distributions of the DESLs were also further investigated through the use of TGA, Py-GC/MS, and tubular furnace pyrolysis. DESLs with high purity (88.5–92.7%) can be efficiently separated from biomass while cellulose is retained. E-DESL has a relatively low molecular weight, and P-DESL has a relatively higher hydrogen–carbon effective ratio and a lower number of condensation structures. The Py-GC/MS results show that, during DESL pyrolysis, the monomeric aromatic hydrocarbons, p-hydroxyphenyl-type phenols, and catechol-type phenols are gradually released when the guaiacyl-type phenols and syringyl-type phenols decrease with the rising temperature. 4-methylguaiacol and 4-methylcatechol, derived from the guaiacyl-type structural units, are positively correlated with temperature, which causes a significant increase in products with a side-chain carbon number of 1 from P-DESL pyrolysis. 4-vinylphenol, as a representative product of the R-DESL, derived from p-hydroxyphenyl-type structural units, also gradually increased. In addition, the P-DESL produces more bio-oil during pyrolysis, while gases have the highest distribution in E-DESL pyrolysis. It is of great significance to study the characteristic product distribution of lignin isolated through the use of DES for lignin directional conversion into specific high-value aromatic compounds. [ABSTRACT FROM AUTHOR]

In this study, a hydroxyl‐rich ferrofluid was prepared by dispersing silica‐coated magnetic nanoparticles into a methyltrioctylammonium chloride‐glycerol deep eutectic solvent and then employed in the preconcentration of trace‐level of cinnamic acid derivatives (caffeic acid, p‐hydroxycinnamic acid, ferulic acid, and cinnamic acid) in traditional Chinese medicine prior to high‐performance liquid chromatography analysis. The structures of the synthesized materials were characterized by X‐ray diffraction and infrared spectroscopy. The experimental parameters affecting the extraction performance, such as deep eutectic solvent composition, dosage of ferrofluid, pH of aqueous sample solution, salt concentration, extraction time, type, and volume of desorption solvent, were studied and optimized. Under the optimum conditions, the enrichment factors of four cinnamic acid derivatives were in the range of 107–114. Low detection limits (0.2–0.9 ng/mL), good precisions (relative standard deviations 1.2%–9.5%), and satisfactory recoveries (96.0%–104.7%) were achieved. Subsequently, the possible microextraction mechanism of the proposed method was explored and elucidated. It showed that the prepared ferrofluid is easily dispersed in the aqueous sample and achieved recovery after the extraction. The developed approach is a simple, convenient, and efficient method for preconcentration and determination of cinnamic acid derivatives in complex matrices. [ABSTRACT FROM AUTHOR]

This study aimed to investigate the ultrasound‐assisted extraction of bioactive compounds from persimmon (Diospyros kaki) calyx by deep eutectic solvents (DES) with different molar ratios. For this reason, the prepared DES extracts' total phenolic–flavonoid compounds and antioxidant activities (1,1‐diphenyl‐2‐picrilhydrazyl radical scavenging activity [DPPH•], Cupric Reducing Antioxidant Capacity (CUPRAC), and ferric reducing antioxidant power [FRAP]) were investigated as a result of the experimental design and optimization study conducted for this purpose. A sonication time of 20 min was determined as the optimal condition. Under these conditions, a molar ratio of 1.9:1 (lactic acid:choline chloride) and a water ratio of 70% provided the highest phenolic/flavonoid compounds and antioxidative activity. Correlations among water ratio, molar ratio, and sonication time were determined using principal component analysis (PCA). In conditions where total flavonoid compound, FRAP, and DPPH• are high due to PCA, it can be concluded that the sonication time is at high level; on the contrary, the water and molar ratios are at low level. In conclusion, ultrasound‐assisted extraction using DES proved effective in persimmon calyx. Therefore, it can be recommended to use these environmentally friendly green solvents as an alternative to organic solvents in preparing extracts in various fields. Practical Application: This study shows the effectiveness of the ultrasound‐assisted green extraction method using persimmon calyx specified as waste. These findings are compelling in the food industry in terms of consumers being now aware of green technology and the discovery that calyx is a good source of bioactive compounds. [ABSTRACT FROM AUTHOR]

Protein-templated molecularly imprinted polymers have limitations such as poor mass transfer, slow recognition kinetics, and difficulties in isolation and purification due to their large molecular sizes, complex structures, and flexible conformations. To address these limitations and obtain lysozyme (Lyz)-imprinted polymers, a molecularly imprinted polymer (UiO66@DES-MIPs) was prepared for the first time by using Lyz as a template molecule, a metal–organic framework (UiO66-NH2) as a matrix, and a water-compatible deep eutectic solvent (DES) as a functional monomer. The introduction of UiO66-NH2 by the solvothermal method with a large specific surface area and favorable stability and resistance to environmental disturbances into the MIPs can reduce the "embedding" phenomenon and acquire a higher binding capacity and fast mass transfer. In addition, a water-soluble binary DES (1:2 molar ratio of choline chloride to 1,3 dimethylurea) prepared by a hydrothermal method as a functional monomer generates multiple forces with Lyz, increasing the hydrophilicity of UiO66@DES-MIPs and contributing to the formation and stabilization of the imprinted sites. Consequently, UiO66@DES-MIPs exhibited good selectivity, water compatibility, and fast adsorption equilibrium (the adsorption equilibrated at 243.87 ± 4.88 mg g−1 in 90 min). Besides, reusability experiments indicated that the UiO66@DES-MIPs could be recycled six times without obvious loss of adsorption capacity. The imprinting factor of UiO66@DES-MIPs is 3.67. The isolation and purification of Lyz from egg white confirmed the practicability of UiO66@DES-MIPs. The high adsorption capacity and specific recognition make this polymer a promising candidate for the isolation and purification of biological macromolecules. [ABSTRACT FROM AUTHOR]

The solvothermal synthesis of covalent organic framework (COF) modified silica gel usually requires the use of harmful organic solvents, tedious steps, and harsh reaction conditions. In pursuit of green chemistry, a new strategy for the facile preparation of COF@SiO2 composite material was realized in this work by using a low-toxicity and low-cost deep eutectic solvent as the reaction medium. Additionally, a flexible polyacrylic acid (PAA) was introduced for the purpose of improving the hydrophilic selectivity and separation efficiency of COF@SiO2. Based on the above ideas, a novel PAA/COF@SiO2 composite was successfully developed as a liquid chromatographic packing material. Performance evaluation of the slurry-packed PAA/COF@SiO2 column showed that diverse types of analytes were effectively separated, and the retention behavior of polar nucleosides showed a U-shaped trend, indicating mixed-mode of hydrophobic/hydrophilic retention mechanisms. Thermodynamic studies revealed that the separation mechanism was largely independent of temperature. This work verifies the feasibility of synthesizing polymer/COF@SiO2 composite material in the deep eutectic solvent. This strategy provides a theoretical reference for the green and facile preparation of COF@SiO2 as an efficient liquid chromatographic stationary phase. [ABSTRACT FROM AUTHOR]

This study focuses on modeling of deep eutectic solvents (DESs) assisted liquid-liquid-extraction of Am(III), U(VI), Eu(III). In the present work, DESs are having tri – n octyl phosphine oxide (TOPO) and choline chloride acetate as hydrogen bond acceptor and malonic acid, oxalic acid and glycolic acid as hydrogen bond donor. The UNIQUAC-extended-PDH* model is used in the extraction formulation incorporating weak long-range interactions and short-range interactions. Metaheuristic algorithm, such as genetic algorithm, is employed for the determination of thermodynamically consistent binary interaction parameters using a pool of 40 tielines across six systems. The estimation of efficiency evaluation and extraction quantification contributes to a deeper understanding of the behavior of deep eutectic solvents in the extraction of lanthanides and actinides. Accurate modeling: UNIQUAC-ext-PDH* model effectively predicts DES extraction properties, aiding process development. Extraction optimization: Variations in extraction efficiency observed among DESs based on different acids, suggesting potential for optimization strategies. DES as co-solvent vs. extractant: Comparison reveals differences in extraction behavior, providing insights for selecting the more favorable option in lanthanide and actinide extraction. [ABSTRACT FROM AUTHOR]

Cellulose nanofibers (CNFs) are extensively utilized as affordable, renewable materials. The conventional technique for making CNFs is time‐consuming, requires hazardous toxic chemicals, and consumes enormous amounts of energy. CNFs from empty fruit bunches (EFB) were produced via deep eutectic solvent (DES) and ultrasonication. The DES treatment conditions were optimized using the central composite design (CCD) approach of response surface methodology (RSM). Analysis of variance (ANOVA) revealed that the reaction time, DES molar ratio, and temperature were all significant variables. The experimental results closely correspond to the theoretical model of CNFs yield. X‐ray diffraction (XRD) studies demonstrated that the crystallinity index of the CNFs increased significantly after sonication. It could be stated that DES treatment and ultrasonication were effective ways to successfully generate CNFs from EFB. This study may serve as foundation for high‐yield, industrial‐scale synthesis of nanocellulose using DES treatment. [ABSTRACT FROM AUTHOR]

Biorefinery of flavonoid aglycones by natural deep eutectic solvents (NADESs) is a green approach for the valorization of agro-food wastes. Using rutin/quercetin as a model system, this work studies the role of Bronsted acids in deglycosylation of flavonoid glycosides and the sustainable approach to producing aglycone-rich extracts by acidic NADESs. Different NADESs were tested, and the effects of Bronsted acids in catalysis and Hammett acidities were determined. The deglycosylation kinetics of rutin in the choline chloride-citric acid was measured and followed a first-order model with a half-life time (t1/2) of 0.16 h at 90 °C and an activation energy (Ea) of 140.3 kJ mol-1. A two-step one-pot approach was valid to produce quercetin-rich extracts from Sophora japonica buds waste. The quercetin-to-rutin ratio in the acidic NADES extracts was adjustable by changing the heating time. The acidic NADES of ChCl-Citric and quercetin-rich extracts showed low cytotoxicity to Caco-2 cells with EC50 greater than 2000 mg L-1, and the cytotoxicity was mainly determined by citric acid. The study provides a new perspective for the valorization of bioproducts into ready-to-use flavonoid aglycone-rich extracts using acidic NADES. [ABSTRACT FROM AUTHOR]

Sulfated polysaccharides are important promising biologically active substances with anticoagulant properties. Biological activity is affected by the method of preparation, as well as the type of the polysaccharide and its molecular structure. In this work, we have considered various methods for the synthesis of promising anticoagulants – polysaccharide sulfates using the example of obtaining agarose sulfate. We compared various sulfating agents: chlorosulfonic acid, sulfamic acid, with various activators, and a deep eutectic solvent mixture of sulfamic acid with urea (in the melt). It has been shown that when urea is used as an activator of the process of sulfation of agarose with sulfamic acid in 1,4-dioxane, agarose sulfate with a high sulfur content (up to 14.5 wt%) is formed, which is close to the use of chlorosulfonic acid as a sulfating agent (with the production of agarose sulfate with 15.0 wt% sulfur). The use of solid catalysts in the process of sulfation of agarose with sulfamic acid leads to the production of agarose sulfate with a sulfur content of up to 14.1 wt% (for a catalyst based on the oxidized carbonaceous material Sibunit-4®). Sulfation of agarose in a deep eutectic solvent – a mixture of sulfamic acid with urea – leads to the production of agarose sulfate with a sulfur content of up to 13.7 wt%. The resulting agarose sulfates were characterized by FTIR spectroscopy, X-ray diffraction, elemental analysis, atomic force microscopy and DFT. [ABSTRACT FROM AUTHOR]

Copyright of Science & Technology of Food Industry is the property of Science & Technology of Food Industry Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

CO2 capture from biogas is an effective route to facilitate the utilization of biogas by improving its CH4 purity. In this work, choline chloride-monoethanolamine deep eutectic solvent (ChCl-MEA DES), was employed as a promising absorbent for CO2 capture. The effects of absorption pressure and temperature, and water content in DES, on CO2 absorption capacity, rates, and selectivity were experimentally evaluated. The experimental data were analyzed by analysis of variance (ANOVA) and response surface method (RSM). The absorption behavior of CO2 by DES mainly conformed to the laws of physical absorption. The highest CO2 absorption capacity of ChCl-MEA DES was 0.608 mol-CO2/mol-DES, and the best CO2/CH4 selectivity factor was 25. Regression equations of CO2 absorption capacity and rate were established to evaluate the results under different operating conditions. [ABSTRACT FROM AUTHOR]

BACKGROUND: Carbon dioxide is not only a major greenhouse gas but also an important carbon resource, which is abundant, renewable, low cost and non‐toxic. The coupling reaction of CO2 with epoxides has shown great potential in the field of chemical carbon fixation due to its 100% atomic utilization efficiency. Deep eutectic solvents (DESs) based on tetrabutylammonium bromide (TBAB) were evaluated for cycloaddition reaction of CO2 with propylene oxide (PO) to propylene carbonate (PC). Density functional theory (DFT) was used to calculate the catalytic performance of DES in CO2 cycloaddition reaction. RESULTS: The utilization of DES containing triethanolamine (TEA) as hydrogen bond donor significantly shortened the reaction time. Under optimal reaction conditions (30 mmol PO, 5 mol% TBAB/TEA (1:1) DES, 1.0 MPa CO2, 90 °C, 2 h), high PC yield (98%) was obtained. DFT calculations revealed that TBAB/TEA (1:1) DES was used as the catalyst for the coupling reaction between PO and CO2, with the ring‐opening process serving as the rate‐determining step and energy barrier of 17.9 kcal mol−1. TBAB/TEA (1:1) DES exhibited excellent recyclability and could be reused more than five times. CONCLUSION: TBAB/TEA (1:1) DES is a highly efficient homogeneous catalyst for the synthesis of cyclic carbonates through the cycloaddition reaction of CO2 and epoxides. The synergistic catalytic effect of the double hydrogen bonds between DES and Br anions is the reason for its high efficiency. © 2023 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

A renewed understanding of eco-friendly principles is moving the industrial sector toward a shift in the utilization of less harmful solvents as a main strategy to improve manufacturing. Green analytical chemistry (GAC) has definitely paved the way for this transition by presenting green solvents to a larger audience. Among the most promising, surely DESs (deep eutectic solvents), NaDESs (natural deep eutectic solvents), HDESs (hydrophobic deep eutectic solvents), and HNaDESs (hydrophobic natural deep eutectic solvents), with their unique features, manifest a wide-range of applications, including their use as a means for the extraction of small bioactive compounds. In examining recent advancements, in this review, we want to focus our attention on some of the most interesting and novel 'solvent-free' extraction techniques, such as microwave-assisted extraction (MAE) and ultrasound-assisted extraction (UAE) in relation to the possibility of better exploiting DESs and NaDESs as plausible extracting solvents of the phenolic compounds (PCs) present in different matrices from olive oil components, such as virgin olive pomace, olive leaves and twigs, virgin and extra virgin olive oil (VOO and EVOO, respectively), and olive cake and olive mill wastewaters (OMWW). Therefore, the status of DESs and NaDESs is shown in terms of their nature, efficacy and selectivity in the extraction of bioactive phytochemicals such as secoiridoids, lignans, phenolic acids and alcohols. Related studies on experimental design and processes' optimization of the most promising DESs/NaDESs are also reviewed. In this framework, an extensive list of relevant works found in the literature is described to consider DESs/NaDESs as a suitable alternative to petrochemicals in cosmetics, pharmaceutical, or food applications. [ABSTRACT FROM AUTHOR]

Copyright of Biomass Chemical Engineering is the property of Editorial Office of Biomass Chemical Engineering and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Thermal conductivity of 77 choline chloride-based deep eutectic solvents (DESs) has been estimated at 1.01325 bar and 298.15–333.15 K temperature range in the framework of geometric similitude concept incorporated in the Redlich–Kwong equation of state. The dataset consists of the choline chloride class of hydrogen bond acceptor and alcohol, organic acid, carbohydrate, amide-based hydrogen bond donors of which 17 DESs are used to estimate the model parameters in the Genetic Algorithm paradigm with a root mean square deviation of 4.37%. A priori estimation of thermal conductivity is further reported for the remaining 60 DESs over the same temperature range, and the framework is established as a theoretical framework for estimating the thermal conductivity of DES. [ABSTRACT FROM AUTHOR]

Designing and developing low-cost, high-efficiency catalysts to reduce the overpotential and improve the efficiency of hydrogen energy conversion are current research hotspots. In this work, CoNi2S4 nanosheets on carbon cloth (CoNi2S4/CC) were prepared to use one-step pyrolysis of the deep eutectic solvent (DES) precursor. It is feasible to cover carbon cloth evenly with DES due to its intense adherence and liquid conditions at ambient temperature. The CoNi2S4 nanosheet's coupling a CC substrate increases the electron transport efficiency and prevents the catalyst from agglomeration and corrosion during catalytic processes. Self-supported CoNi2S4/CC exhibited excellent hydrogen evolution reaction (155 mV at 50 mA cm–2 and 30 mV at 10 mA cm–2) and oxygen evolution reaction (372 mV at 100 mA cm–2 and 153 mV at 10 mA cm–2) activities. Serving as a bifunctional catalyst, CoNi2S4/CC requires cell voltages of only 1.42 and 1.86 V to achieve 10 mA cm–2 and 100 mA cm–2 current density, respectively, in overall water splitting in 1.0 M KOH, exhibiting extraordinary durability. Moreover, CoNi2S4/CC exhibits excellent overall water-splitting activity in simulated seawater, which significantly advances the development of seawater electrolysis. [ABSTRACT FROM AUTHOR]

A cold-induced homogenous liquid–liquid microextraction method combined with solidification of floating organic droplets effervescent-assisted dispersive liquid–liquid microextraction has been developed for simultaneous extraction of several pyrethroid and carbamate pesticides from edible oils. The extracted analytes were determined by high performance liquid chromatography-diode array detector. For this purpose, 5 mL of edible oil sample was transferred into a glass test tube and it was mixed with 150 µL α-terpineol: acetic acid deep eutectic solvent. After vortexing (for 5 min), the mixture was placed into an ice: sodium chloride bath to adjust the solution temperature at −16℃. In this step, the oil sample was solidified, and the deep eutectic solvent was collected on top of the oil. Thus, it was collected and dispersed into 5.0 mL sodium carbonate solution at a concentration of 1.0 mol/L containing 2.5% w/v sodium chloride. In this step, the deep eutectic solvent was decomposed in the solution and α-terpineol dispersed in the sample solution. To obtain high extraction efficiency the effective parameters were optimised and under optimal conditions, the method showed broad linear ranges (2.6–500 ng/mL) with good coefficient of determinations ≥0.994. The extraction recoveries and enrichment factors of the method were in the ranges of 78–93% and 98–116%, respectively. The limits of detection and quantification were within the range of 0.2–0.8 and 0.6–2.6 ng/mL, respectively. The method was successfully used for the determination of the analytes in different edible oil samples. [ABSTRACT FROM AUTHOR]

The development of efficient derivatization methods of chitin, such as acylation, has been identified to confer new properties and functions to chitin. In this study, we investigate the synthesis of mixed chitin esters via the acylation of chitin in deep eutectic solvents (DESs) comprising 1-allyl-3-methylimidazolum chloride and 1,1,3,3-tetramethylguanidine based on a previous study that reported the development of efficient acylation of chitin in the DES to obtain single chitin esters. A stearoyl group was selected as the first substituent, which was combined with several bulky acyl and long oleoyl groups as the second substituents. After dissolution of chitin in the DES (2 wt%), the acylation reactions were conducted using stearoyl and the desired acyl chlorides for 1 h + 24 h at 100 °C in the resulting solutions. The IR and 1H NMR spectra of the isolated products confirmed the structures of mixed chitin esters with two different substituents. The substituent ratios in the derivatives, which were estimated via the 1H NMR analysis, were changed according to the feed ratios of two acyl chlorides. [ABSTRACT FROM AUTHOR]

The present methodology explored the effectiveness and versatility of deep eutectic solvent with ultrasonic energy as an eco-friendly protocol for the synthesis of bisthioglycolic acid derivatives. Bisthioglycolic moiety holds its role as a potent scaffold in sulfur-containing drugs. The presented strategy offers significant advantages such as green catalyst as well as solvent, excellent yield, short reaction time, and simple reaction workup. This methodology shows a wide range of substrate scope that contain both electron-donating as well as electron-withdrawing groups. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

In recent years, there has been a steady increase in the interest in changing lignocellulose processing technologies from harmful and nonecological to more ecological and sustainable. Deep eutectic solvents (DESs) and ionic liquids (ILs) are green, efficient solvents/catalysts for biomass pretreatment as well as its further transformation. In many cases, they are used together with biocatalysts. Additionally, in processes where DESs and ILs are used for the pretreatment of biomass, before enzymatic transformation, traces of these solvents can influence the activity of biocatalysts. For this reason, it is important to evaluate the effect of novel, green solvents on the activity of enzymes widely applied in the biomass valorization processes. In this work, we present the impact of chosen DESs and ILs, most often applied in biomass pretreatment and transformation, on the enzymatic activity of popular cellulolytic enzymes and enzymatic preparations (namely, cellulases from Aspergillus niger, Trichoderma reesei, and Viscozyme L). The enzymatic activity was investigated in the process of transformation of cellulose or biomass to glucose. The results showed that many of the solvents tested had a negative effect on enzymatic activity, suggesting a separation of pretreatment and enzymatic processes. [ABSTRACT FROM AUTHOR]

The effect of ethylenediaminetetraacetic acid (EDTA) on the electrochemical behavior of copper in choline chloride-ethylene glycol (ChCl-EG) deep eutectic solvent (DES) and the electrocrystallization mechanism of copper under different potential steps as well as on the micromorphology and phase composition of copper deposit was studied by ultraviolet-visible spectrophotometry (UV), cyclic voltammetry (CV), chronoamperometry (CA), scanning electron microscopy (SEM), and X-ray diffraction (XRD) techniques. The results showed that the addition of EDTA led to a change in the form of copper complexes in the DES. The Cl- in [CuCl4]2- was replaced by EDTA, making the copper species more stable. The addition of EDTA did not affect the nucleation mode of copper, but made the micromorphology of copper deposit from a large and irregular particulate structure to a uniform and fine spherical one. [ABSTRACT FROM AUTHOR]

An ultrasonic-assisted demulsified dispersive liquid–liquid microextraction based on solidification of floating organic droplet (UA-DE-DLLME-SFO) technique was considered for the preconcentration of Co and Ni before their determination by micro sampling flame atomic absorption spectrometry (FAAS). In this method, the sample solution was mixed with 1-dodecanol as an extractant and a deep eutectic solvent (tetrabutylammonium bromide: acetic acid) as a dispersive solvent. The dispersion of extraction solvent was performed through the decomposition of deep eutectic solvent in the sample solution. Ultrasonication promoted the dispersion of the extraction solvent into the sample solution. After dispersing, acetonitrile as a demulsifier was introduced to break down the emulsion quickly without centrifugation. The influence of the experimental variables on the extraction recoveries was optimised. The limits of detection were found to be 0.2 µg L−1 and 0.4 µg L−1 with the preconcentration factors of100 for Co and Ni, respectively. The relative standard deviations (RSDs, %) (50 µg L−1, n = 10) were 2.5% and 3.4%, for Co and Ni, respectively. The accuracy of the method was checked through the analysis of certified reference materials namely NIST SRM 1643bof water sample, SRM 1568aof rice flour, and FAPAS QC material of brown rice (T07370 QC). The recoveries of Co and Ni added in water and food samples were obtained in the range of 92.6–98.5% and 92.9–101.5% respectively. [ABSTRACT FROM AUTHOR]

The catalytic alkoxycarbonylation of alkenes is an attractive, atom‐efficient method for producing value‐added carboxylic esters. However, the conventional catalyst system for this reaction needs coordination with a noble metal, sensitive ligands and proton acid additives. Therefore, the design of a simple and efficient catalyst system without any acid additives under mild conditions is still a major challenge. In this work, a simple ruthenium/deep eutectic solvent catalytic system was developed to effectively catalyse the alkoxycarbonylation reaction without any sensitive ligands or acid additives under mild conditions. The conversion of 1‐hexene reached 99.0 %, and the ester selectivity was 99.1 %, much higher than that of Ruthenium carbonyl without deep eutectic solvent. The excellent performance of the catalytic system could be ascribed to the form of the ruthenium active species [Ru(CO)2Br3]− in the deep eutectic solvent. This innovative catalyst system presents a significant advancement in the alkoxycarbonylation reaction, eliminating the use of acid additives and delicate ligands. [ABSTRACT FROM AUTHOR]

Supported metal catalysts have attracted considerable attention because of their remarkably high catalytic activity and thermal stability. In this work, we report a facile and eco‐friendly method to synthesize porous Au/TiO2 nanocomposites with tunable size and different loading of Au nanoparticles. Porous TiO2 particles with average size of 20 nm were obtained using deep eutectic solvent‐assisted solvothermal method, in which Au NPs were immobilized by citrate reduction process. By adjusting the molar ratio of citrate and gold precursor, the size and loading of Au particles could be effectively controlled. The optimized nanocomposite with maximum Au loading and smallest particle size of 9 nm manifested the best catalytic activity in the 4‐nitrophenol reduction and excellent reusability. The superior catalytic performance can be ascribed to the strong interfacial interaction between small Au NPs and porous TiO2 support together with the high concentration of active sites at the interface. [ABSTRACT FROM AUTHOR]

Hydrophilic deep eutectic solvents are actively positioned as efficient extractants for removing heterocyclic compounds from light hydrocarbon fractions. Of particular interest is the subclass of natural deep eutectic solvents (NaDESs), since they contain substances of exclusively natural origin. However, these processes have not been systematically studied to date in extraction equipment. To study the process of countercurrent extraction of pyridine, quinoline, and indole from a model solution of light hydrocarbon fractions using commercial equipment, a series of NaDESs based on citric and malic acids, xylitol, and water was used for the first time in this work. The high extraction capacity of these NaDES was demonstrated in laboratory experiments, and the extraction mechanism was determined. A detailed study of the efficiency of extraction of heterocycles with varying process conditions allowed us to move on to studying the process using extractors of the mixer–settler type. From the model solution of light hydrocarbon fractions, pyridine, quinoline, and indole were removed to concentrations <1 ppm by countercurrent extraction using a cascade of six mixer–settlers. [ABSTRACT FROM AUTHOR]