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This research explores the potential of ionic liquids (ILs) in restoring paper artifacts, particularly an aged book sample. Three distinct ILs—1-ethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide, 1-methyl-3-pentylimidazolium bis(trifluoromethylsulfonyl)imide, and 1-methyl-3-heptylimidazolium bis(trifluoromethylsulfonyl)imide —both in their pure form and isopropanol mixtures, were examined for their specific consumption in conjunction with paper, with 1-ethyl-3-propylimidazolium bis(trifluoromethylsulfonyl)imide displaying the highest absorption. Notably, the methyl-3-heptylimidazolium ionic liquid displayed pronounced deacidification capabilities, elevating the paper pH close to a neutral 7. The treated paper exhibited significant color enhancements, particularly with 1-heptyl-3-methylimidazolium and 1-pentyl-3-methylimidazolium ILs, as evidenced by CIE-Lab* parameters. An exploration of ILs as potential UV stabilizers for paper unveiled promising outcomes, with 1-heptyl-3-methylimidazolium IL demonstrating minimal yellowing post-UV irradiation. FTIR spectra elucidated structural alterations, underscoring the efficacy of ILs in removing small-molecular additives and macromolecules. The study also addressed the preservation of inked artifacts during cleaning, showcasing ILs' ability to solubilize iron gall ink, particularly the one with the 1-ethyl-3-propylimidazolium cation. While exercising caution for prolonged use on inked supports is still recommended, ILs are shown here to be valuable for cleaning ink-stained surfaces, establishing their effectiveness in paper restoration and cultural heritage preservation. [ABSTRACT FROM AUTHOR]

This study explores the efficacy of 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide and 1-hexyl-3-methylimidazolium chloride as cleaning agents for aged cellulosic artifacts. A 10% v/v acetone solution of these ionic liquids (ILs) effectively removes the brownish-yellow color of aged paper in a 10 min immersion treatment. Colorimetric analysis shows a remarkable increase in lightness (L*) by up to 40% and a decrease in red/brownish tones (b*) after IL treatment. The cleaning process also deacidifies the paper, shifting the pH to neutral-slightly basic levels and enhancing its long-term stability. Optimal pH outcomes are achieved, with ionic liquid consumption values of 0.4–0.6 g/g of paper. The FTIR analysis revealed structural changes in cellulose induced by the washing step, which is mainly due to the reorganization effect imparted by the ionic liquids. Furthermore, ILs mobilized degraded compounds and acidic species, aiding in their extraction during the restoration process. Mechanical testing indicated an enhancement in the overall tensile strength and strain at break values for IL-treated papers by up to 33%. This study demonstrates the multiple benefits of alkylimidazolium ionic liquids for preserving and restoring cultural heritage artifacts made of cellulosic materials. [ABSTRACT FROM AUTHOR]

Disposable paper cups are usually composed of high-grade paper board and an inner polyethylene coatings and are extensively used in daily life. However, most disposable paper cups are only used for a short time and then incinerated or accumulated in landfill at the end of their service due to the difficulty in separating the components, leading to a serious threat to our ecosystem. Therefore, developing a facile and green method to recycle and reuse disposable paper cups is vital. By using ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl) as a solvent, transparent and homogenous cellulose/polyethylene composite films were successfully prepared from used bamboo-based disposable paper cups through the "one-pot method", without any pre-treatment. It was found that there was a transformation of cellulose I to II after the dissolution and regeneration processes, and the crystallinity degree of the regenerated cellulose-based materials decreased significantly, resulting in a change in thermal properties. Meanwhile, compared to traditional pure cellulose films, the composite films possessed good UV-shielding properties and hydrophobicity. Moreover, they also displayed good mechanical properties. Additionally, the size of the ground PE coatings displayed obvious effects on the structures and properties of the composite films, where the CPE100 (sieved with 100–200 mesh) possessed the most homogeneous texture and the highest tensile strength (82 Mpa), higher than that of commercial polyethylene film (9–12 MPa), showing superiority as packaging or wrapping materials. Consequently, the goals to fabricate uniform cellulose/polyethylene composite films and valorize the solid waste from disposable paper cups were simultaneously achieved by a facile and green "one-pot method". [ABSTRACT FROM AUTHOR]

Paper cups are widely employed in daily life with many advantages, but most of the used paper cups are incinerated or landfilled, due to the great challenge of separating the thin inner polyethylene (PE) coating, causing the waste of energy and the pollution of our environment. Therefore, recycling and converting the used paper cups into high-value materials is meaningful and important. In this work, transparent cellulose-based films were successfully prepared from the used paper cups via 1-allyl-3-methylimidazolium chloride ionic liquid after simple pretreatment. Additionally, the difference in properties and structures of cellulose-based films regenerated in different coagulation baths (water or ethanol) was also explored. It was found that the cellulose-based film possessed good thermal property and displayed better hydrophobicity than the traditional pure cellulose film. Moreover, they also demonstrated good mechanical property and the tensile strength of cellulose-based film regenerated in water can reach 31.5 Mpa, higher than those of cellulose-based film regenerated in ethanol (25.5 Mpa) and non-degradable polyethylene film (9–12 MPa), indicating their great potential as the packaging materials. Consequently, valorization of the low cost used paper cups and preparation of high-valve cellulose-based films were realized simultaneously by a facile and green process. [ABSTRACT FROM AUTHOR]

The article announces the winners of "Materials" journal's Best Paper Award for 2015 which include the papers "Optical Properties of ZnO Nanoparticles Capped With Polymers" by Shingo Tachikawa et al., "Thermotropic Ionic Liquid Crystals" by Kirill V. Axenov and Sabine Laschat, and "Progress in Nano-Engineered Anodic Aluminum Oxide Membrane Development" by Gerrard Eddy Jai Poinern et al.

Hydrothermal hydrolysis in hot pressurized liquid water (HPLW) is attractive for biomass conversion into valuable products because it achieves high reaction rates without catalysts and additives. The hydrothermal hydrolysis of high crystalline cellulose requires higher reaction temperature than polysaccharides having low crystallinity. It can be expected to increase the reaction rate or decrease temperature by decreasing the crystallinity. In the present study ashless filter paper as a fibrous pure cellulose sample was pretreated with ionic liquids (ILs) such as imidazolium chloride ILs containing alkyl side chains ranging from two to six carbons, and with an aqueous solution of bis(ethylenediamine ammonium) copper (BEDC). Herein, the pretreatment with ILs was to regenerate filter paper: dissolving in ILs at 373 K for 120 min or in an aqueous BEDC solution at room temperature, precipitating by adding water, washing the solid, and then drying. Subsequently, the pretreated filter paper samples were hydrolyzed at 533 K and 5.0 MPa in HPLW in a small semi-batch reactor, and the effects of the pretreatment with ILs or BEDC on reaction rates and product yields were examined. While the crystallinity indexes with all ILs and BEDC after the pretreatments decreased to 44 to 47 from the original sample of 87, the reaction rates and product yields were significantly affected by the IL species. At 533 K and 5.0 MPa, the dissolution rate with [AMIM][Cl] was nine times as fast as that for untreated sample.

CO2 is not only the main gas that causes the greenhouse effect but also a resource with abundant reserves, low price, and low toxicity. It is expected to become an important "carbon source" to replace oil and natural gas in the future. The efficient and clean resource utilization of CO2 has shown important scientific and economic value. Making full use of abundant CO2 resources is in line with the development direction of green chemistry and has attracted the attention of scientists. Environmentally friendly ionic liquids show unique advantages in the capture and conversion of CO2 due to their non-volatilization, designable structure, and good solubility, and show broad application prospects. The purpose of this paper is to discuss the research on the use of an ionic liquid as a catalyst to promote the synthesis of various value-added chemicals in CO2, hoping to make full use of CO2 resources while avoiding the defects of the traditional synthesis route, such as the use of highly toxic raw materials, complicated operation, or harsh reaction conditions. The purpose of this paper is to provide reference for the application and development of ionic liquids in CO2 capture and conversion. [ABSTRACT FROM AUTHOR]

Based on the environmental concerns, the utilisation of hemicelluloses in food packaging has become a sustainable alternative to synthetic polymers and an important method for the efficient utilisation of biomass resources. After cellulose, hemicellulose is a second component of agricultural and forestry biomass that is being taken advantage of given its abundant source, biodegradability, nontoxicity and good biocompatibility. However, due to its special molecular structure and physical and chemical characteristics, the mechanical and barrier properties of hemicellulose films and coatings are not sufficient for food packaging applications and modification for performance enhancement is needed. Even though there are many studies on improving the hydrophobic properties of hemicelluloses, most do not meet environmental requirements and the chemical modification of these biopolymers is still a challenge. The present review examines emerging and green alternatives to acetylation for xylan hemicellulose in order to improve its performance, especially when it is used as biopolymer in paper coatings or films for food packaging. Ionic liquids (ILs) and enzymatic modification are environmentally friendly methods used to obtain xylan derivatives with improved thermal and mechanical properties as well as hydrophobic performances that are very important for food packaging materials. Once these novel and green methodologies of hemicellulose modifications become well understood and with validated results, their production on an industrial scale could be implemented. This paper will extend the area of hemicellulose applications and lead to the implementation of a sustainable alternative to petroleum-based products that will decrease the environmental impact of packaging materials. [ABSTRACT FROM AUTHOR]

Fire is a typical disaster in the processing industry. Ionic liquids, as a type of green flame retardant, play an important role in process safety. In order to grasp the current research status, hotspots, and frontiers in the field of ionic liquids in flame retardancy, the bibliometric mapping method is applied to study the relevant literature in Web of Science datasets from 2000–2022 in this paper. The results show that the research on ionic liquids in flame retardancy is multidisciplinary and involves some disciplines such as energy science, material science, and environmental protection. Journal of Power Sources, Polymer Degradation and Stability, ACS Applied Materials and Interfaces, and Chemical Engineering Journal are the core journals in the field. The results of keyword co-occurrence indicate that the hotspots of research can be divided into five components: the improvement and application of pure ionic liquids electrolytes, the research of gel polymer electrolytes, applying ionic liquids to enhance the polymer materials' flame retardancy properties, utilizing ionic liquids and inorganic materials to synergize flame retardant polymers, and using ionic liquids flame retardant to improve material's multiple properties. The burst terms and time zone diagram's results point out the combination of computational quantum chemistry to study the flame retardancy mechanism of ionic liquids, the study of fluorinated electrolytes, ionic liquids for smoke suppression, phosphorus-containing ionic liquids for flame retardant, and machine learning-assisted design of ILs flame retardants are the research frontiers and future research trends. [ABSTRACT FROM AUTHOR]

With increasingly stringent emission limits on sulfur and sulfur-containing substances, the reduction and removal of sulfur compounds from fuels has become an urgent task. Emissions of sulfur-containing compounds pose a significant threat to the environment and human health. Ionic liquids (ILs) have attracted much attention in recent years as green solvents and functional materials, and their unique properties make them useful alternatives to conventional desulfurization organic solvents. This paper reviews the advantages and disadvantages of traditional desulfurization technologies such as hydrodesulfurization, oxidative desulfurization, biological desulfurization, adsorptive desulfurization, extractive desulfurization, etc. It focuses on the synthesis of ionic liquids and their applications in oxidative desulfurization, extractive desulfurization, extractive oxidative desulfurization, and catalytic oxidative desulfurization, and it analyzes the problems of ionic liquids that need to be solved urgently in desulfurization, looking forward to the development of sulfuric compounds as a kind of new and emerging green solvent in the field of desulfurization.

A compact, multi-channel ionic liquid-gated graphene field-effect transistor (FET) has been proposed and developed in our work for on-field continuous monitoring of nitrate nitrogen and other nitrogen fertilizers to achieve sustainable and efficient farming practices in agriculture. However, fabricating graphene FETs with easy filling of ionic liquids, minimal graphene defects, and high process yields remains challenging, given the sensitivity of these devices to processing conditions and environmental factors. In this work, two approaches for the fabrication of our graphene FETs were presented, evaluated, and compared for high yields and easy filling of ionic liquids. The process difficulties, major obstacles, and improvements are discussed herein in detail. Both devices, those fabricated using a 3 μm-thick CYTOP® layer for position restriction and volume control of the ionic liquid and those using a ~20 nm-thick photosensitive hydrophobic layer for the same purpose, exhibited typical FET characteristics and were applicable to various application environments. The research findings and experiences presented in this paper will provide important references to related societies for the design, fabrication, and application of liquid-gated graphene FETs. [ABSTRACT FROM AUTHOR]

The rheology control of water-based drilling fluids at ultra-high temperatures has been one of the major challenges in deep or ultra-deep resource exploration. In this paper, the effects of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonimide) (ILA), 1-ethyl-3-methylimidazolium tetrafluoroborate (ILB) and N-methyl, butylpyrrolidinium bis(trifluoromethanesulfonimide) (ILC) on the rheological properties and filtration loss of polymer-based slurries at ultra-high temperatures (200 °C and 240 °C) are investigated by the American Petroleum Institute (API) standards. The results show that ionic liquids with different structures could improve the high-temperature rheological properties of polymer-based drilling fluids. The rheological parameter value (YP/PV) of the polymer-based slurry formulated with ILC is slightly higher than that with ILA at the same concentration, while the YP/PV value of the polymer-based slurry with ILA is slightly higher than that with ILB, which is consistent with the TGA thermal stability of ILA, ILB, and ILC; the thermal stability of ILC with pyrrolidine cations is higher than that of ILA with imidazole cations, and the thermal stability of ILA with bis(trifluorosulfonyl)amide anions is higher than that of ILB with tetrafluoroborate anions. Cation interlayer exchange between organic cation and sodium montmorillonite can improve the rheological properties of water-based drilling fluids. And meantime, the S=O bond in bis(trifluorosulfonyl)amide ions and the hydroxyl group of sodium montmorillonite may form hydrogen bonds, which also may increase the rheological properties of water-based drilling fluids. ILA, ILB, and ILC cannot reduce the filtration loss of polymer-based drilling fluids at ultra-high temperatures. [ABSTRACT FROM AUTHOR]

Polysaccharides are formed by a long chain of monosaccharides, with the main function of promoting energetic and structural reserves for plants and animals. They can be applied as a base of electrolytes, using ionic liquids (ILs) as a solvent base. The study of electrolytes is an emerging field, as they are applied as secondary batteries, fuel cells, solar cells, supercapacitors and chemical sensors. They operate stably under extreme conditions, maintaining their high thermal stability. Furthermore, their low cost and environmentally safe character, compared to conventional electrolytes, have attracted considerable attention in the scientific field. ILs are composed entirely of ions and could be potentially applied as solvents. As electrolytes, ILs are environmentally friendly, and their use in combination with polysaccharides leads to a synergic effect. In the present study, a systematic review was performed of all papers published from 2014 to 2022 regarding ILs and polysaccharides through a search of three databases. Due to the large number of results found, only papers about electrolytes were considered and the main findings described. This study allows for easy identification of the most relevant fields of study with respect to ILs and polysaccharides, as well as the main gaps to be explored in the literature. [ABSTRACT FROM AUTHOR]

With the rapid development of science, technology, and the economy of human society, the emission problem of gas pollutants is becoming more and more serious, which brings great pressure to the global ecological environment. At the same time, the natural resources that can be exploited and utilized on Earth are also showing a trend of exhaustion. As an innovative and environmentally friendly material, functionalized ionic liquids (FILs) have shown great application potential in the capture, separation, and resource utilization of gaseous pollutants. In this paper, the synthesis and characterization methods of FILs are introduced, and the application of FILs in the treatment and recycling of gaseous pollutants is discussed. The future development of FILs in this field is also anticipated, which will provide new ideas and methods for the treatment and recycling of gaseous pollutants and promote the process of environmental protection and sustainable development. [ABSTRACT FROM AUTHOR]

Zinc-ion batteries are promising candidates for large-scale energy storage. The side reactions of the hydrogen evolution reaction (HER) and zinc dendrite growth are major challenges for developing high-performance zinc-ion batteries. In this paper, a supramolecular gel electrolyte (BLO-ILZE) was self-assembled in an ionic liquid (EMIMBF4) with zinc tetrafluoroborate (Zn(BF4)2) on the separator in situ to obtain a gel electrolyte used in zinc-ion batteries. BLO-ILZE is demonstrated to significantly enhance conductivity over a broad temperature range between −70 and 100 °C. Interestingly, through testing and fitting, it is found that the supramolecular gel electrolyte satisfies the liquid state law over a wide temperature range, and even achieves high conductivity (2.12 mS cm−1) at −40 °C. It is equivalent to the conductivity of aqueous zinc-ion batteries (ZnSO4/H2O) at −10 °C, which is 2.33 mS cm−1. Moreover, the supramolecular gel electrolyte can effectively inhibit the HER, thus exhibiting a longer lifetime in Zn/Zn cells for 3470 h at 1 mA cm−2 compared to the aqueous zinc-ion batteries with the Zn(BF4)2 aqueous electrolyte (400 h at 1 mA cm−2). The assembled V2O5/BLO-ILZE/Zn full cells also showed cycling performance, with 5000 cycles at 0.5 mA g−1 at room temperature, a capacity of 98%, and a coulombic efficiency of about 100%. [ABSTRACT FROM AUTHOR]

This paper focuses on the development of electroplating on 150 mm wafer level for microsystem technology applications from 1-Ethyl-3-methylimidazolium chloride (EMImCl) with Aluminumtrichloride (AlCl3). The deposition was carried out on 150 mm wafers with Au or Al seed layers deposited by physical vapor deposition (PVD). The electrodeposition was carried out using pattern plating. On the Au seed layer, bipolar pulse plating was applied. Compared to the Au seed layer, the electrodeposition on the Al seed layer was favorable, with lower current densities and pulsing frequencies. Utilizing the recurrent galvanic pulses and avoiding ionic liquid convection, inhomogeneities lower than 15% were achieved with a laboratory plating cell. One major aspect of this study was the removal of the native Al oxide prior to deposition. It was investigated on the chip and wafer levels using either current- or potential-controlled removal pulses. This process step was affected by the plasma treatment of the wafer, thus the surface free energy, prior to plating. It turned out that a higher surface free energy hindered proper oxide removal at a potential of 3 V. The theory of oxide breakdown based on electrostriction force via the electrical field was applied to discuss the findings and to derive conclusions for future plating experiments. [ABSTRACT FROM AUTHOR]

Hydrometallurgical gold recovery processes play a pivotal role in the gold mining industry, contributing to more than 90% of global gold production. Among the array of techniques available, the Merrill–Crowe process, adsorption, ion exchange, and solvent extraction are central in extracting gold from leach solutions. While the Merrill–Crowe process and gold complex adsorption onto activated carbon represent historical cornerstones, their inherent limitations have prompted the emergence of more recent innovations in ion exchange and solvent extraction, offering enhanced selectivity, control, and sustainability. The evolution of modern organic chemistry has significantly influenced the progress of ion exchange technology, mainly through the introduction of advanced polymer matrix synthetic resins. At the same time, novel solvents tailored to gold complex interactions have revitalized ion exchange and solvent extraction. Introducing ionic liquids and deep eutectic solvents has also added a new dimension to efforts to improve gold extraction metallurgy. This paper reviews these cutting-edge developments and their potential to revolutionize the hydrometallurgical gold recovery process, addressing the pressing need for improved efficiency and environmental responsibility. [ABSTRACT FROM AUTHOR]

In this paper, we report on the use of amorphous lignin, a waste by-product of the paper industry, for the production of high performance carbon fibers (CF) as precursor with improved thermal stability and thermo-mechanical properties. The precursor was prepared by blending of lignin with polyacrylonitrile (PAN), which was previously dissolved in an ionic liquid. The fibers thus produced offered very high thermal stability as compared with the fiber consisting of pure PAN. The molecular compatibility, miscibility, and thermal stability of the system were studied by means of shear rheological measurements. The achieved mechanical properties were found to be related to the temperature-dependent relaxation time (consistence parameter) of the spinning dope and the diffusion kinetics of the ionic liquids from the fibers into the coagulation bath. Furthermore, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical tests (DMA) were utilized to understand in-depth the thermal and the stabilization kinetics of the developed fibers and the impact of lignin on the stabilization process of the fibers. Low molecular weight lignin increased the thermally induced physical shrinkage, suggesting disturbing effects on the semi-crystalline domains of the PAN matrix, and suppressed the chemically induced shrinkage of the fibers. The knowledge gained throughout the present paper allows summarizing a novel avenue to develop lignin-based CF designed with adjusted thermal stability. [ABSTRACT FROM AUTHOR]

The ability to efficiently separate CO2 from other light gases using membrane technology has received a great deal of attention due to its importance in applications such as improving the efficiency of natural gas and reducing greenhouse gas emissions. A wide range of materials has been employed for the fabrication of membranes. This paper highlights the work carried out to develop novel advanced membranes with improved separation performance. We integrated a polymerizable and amino acid ionic liquid (AAIL) with zeolite to fabricate mixed matrix membranes (MMMs). The MMMs were prepared with (vinylbenzyl)trimethylammonium chloride [VBTMA][Cl] and (vinylbenzyl)trimethylammonium glycine [VBTMA][Gly] as the polymeric support with 5 wt% zeolite particles, and varying concentrations of 1-butyl-3-methylimidazolium glycine, [BMIM][Gly] (5–20 wt%) blended together. The membranes were fabricated through photopolymerization. The extent of polymerization was confirmed using FTIR. FESEM confirmed the membranes formed are dense in structure. The thermal properties of the membranes were measured using TGA and DSC. CO2 and CH4 permeation was studied at room temperature and with a feed side pressure of 2 bar. [VBTMA][Gly]-based membranes recorded higher CO2 permeability and CO2/CH4 selectivity compared to [VBTMA][Cl]-based membranes due to the facilitated transport of CO2. The best performing membrane Gly-Gly-20 recorded permeance of 4.17 GPU and ideal selectivity of 5.49. [ABSTRACT FROM AUTHOR]

Due to the unique properties of room temperature ionic liquids (RTILs), most researchers' interest in RTIL-based electrolytes in electric double-layer capacitors (EDLCs) stems from molecular simulations, which are different from experimental scientific research fields. The knowledge of RTIL-based electrolytes in EDLCs began with a supposition obtained from the results of molecular simulations of molten salts. Furthermore, experiments and simulations were promoted and developed rapidly on this topic. In some instances, the achievements of molecular simulations are ahead of even those obtained from experiments in quantity and quality. Molecular simulations offer more information on the impacts of overscreening, quasicrowding, crowding, and underscreening for RTIL-based electrolytes than experimental studies, which can be helpful in understanding the mechanisms of EDLCs. With the advancement of experimental technology, these effects have been verified by experiments. The simulation prediction of the capacitance curve was in good agreement with the experiment for pure RTILs. For complex systems, such as RTIL–solvent mixtures and RTIL mixture systems, both molecular simulations and experiments have reported that the change in capacitance curves is not monotonous with RTIL concentrations. In addition, there are some phenomena that are difficult to explain in experiments and can be well explained through molecular simulations. Finally, experiments and molecular simulations have maintained synchronous developments in recent years, and this paper discusses their relationship and reflects on their application. [ABSTRACT FROM AUTHOR]

Manufacturers of hydraulic fluids invest a lot of effort and resources in improving their physico-chemical properties, with the goal of getting as close as possible to the properties of an ideal hydraulic fluid. It should be non- flammable, environmentally friendly, sustainable and should have excellent physical and chemical properties. After decades of development in the field of ionic liquids and the search for an ionic liquid suitable for use in hydraulic systems, ionic hydraulic liquids are now already in industrial use, especially on devices that operate in harsh and risky operating conditions. Since ionic hydraulic fluids are a completely new type of hydraulic fluid, one of the issues is their compatibility with the materials present in the hydraulic components, including all the seals. This paper refers to the process of testing the compatibility of hydraulic seal materials with different types of ionic hydraulic fluids according to the standardized percentages and recommendations, with emphasis on changes in the swell, shrinkage and hardness of the seals. The presented results are a useful guide for selecting suitable seal materials in case of using high-tech ionic hydraulic fluids. [ABSTRACT FROM AUTHOR]

Curcumin (or diferuloylmethane), a component of Curcuma longa L. rhizomes, displays various biological and pharmacological activities. However, it is poorly bioavailable and unstable in physiological pH. In this review, we cover papers published between 2019 and 2023 on the synthesis and biological activities of more stable and effective curcumin analogs known as monoketone curcuminoids (MKCs) or "monocarbonyl curcuminoids." Recent advances in Claisen–Schmidt condensation, the standard procedure to synthesize MKCs, including the use of ionic liquids, are addressed. MKCs' antimicrobial, anticancer, antioxidant, and antiparasitic actions, as well as other less common MKC biological and pharmacological activities, have been shown to be similar or higher than curcumin. The promising biological and pharmacological activities, combined with the attractive synthetic aspects (e.g., good yields and an easiness of product isolation) to obtain MKCs, make this class of compounds an interesting prospect for further antimicrobial, anticancer, and antiparasitic drug discovery. [ABSTRACT FROM AUTHOR]

To further our understanding of the change in association between lignin and carbohydrates after kraft pulping, isotope-labeled kraft pulp (KP) was prepared using 13 C and D double-isotope-labeled wheat straw, and it was subjected to enzymatic hydrolysis and ionic liquid treatment to explore the linkages between lignin and carbohydrate complexes in wheat straw. Isotope abundance determination showed that 13 C and D abundances in the experimental groups were substantially higher than those in the control group, indicating that the injected exogenous coniferin-[α- 13 C], coniferin-[γ- 13 C], and d-glucose-[6-D 2 ] were effectively absorbed and metabolized during wheat internode growth. Solid-state CP/MAS 13 C-NMR spectroscopy showed that lignin was mainly linked to polysaccharides via acetal, benzyl ether, and benzyl ester bonds. Kraft pulp (KP) from the labeled wheat straw was degraded by cellulase. The obtained residue was fractionated using the ionic liquid DMSO/TBAH to separate the cellulose-lignin complex (KP-CLC) and xylan-lignin complex (KP-XLC). X-ray diffractometer determination showed that the KP-CLC regenerated cellulose type II from type I after the ionic liquid conversion. The 13 C-NMR spectrum of Ac-En-KP-CLC showed that the cellulose-lignin complex structure was chemically bonded between the lignin and cellulose through acetal and benzyl ether bonds. The 13 C-NMR spectrum of En-KP-XLC showed a lignin-hemicellulose complex structure, wherein lignin and xylan were chemically bonded by benzyl ether and acetal bonds. These results indicate that the cross-linking between lignin and carbohydrates exists in lignocellulosic fibers even after kraft pulping.

For over two decades, ionic liquids have been among the most exciting lubrication topics. Ionic liquids were investigated by using them as neat lubricants and lubricity-enhancing additives. However, new and unique features were revealed by introducing new ionic liquids. This paper compares the tribological properties of two ionic liquids with the same trihexyltetradecylphosphonium [P 6,6,6,14] cation and different anions—dicyanamide [DCN] and bis(2,4,4-trimethylpentyl)phosphinate. The widely investigated 1-Butyl-3-methylimidazolium hexafluorophosphate [BMIM] [PF6] ionic liquid was used as a reference. The lubricity was comprehensively investigated using two testing modes: reciprocation in a ball-on-plate tribometer and continuous sliding in a ball-on-disc tribometer. The tests were performed at temperatures of 30 and 80 °C. The friction, wear, and film thickness were evaluated, and a worn surface analysis was conducted. It was found that in the case of reciprocation, anion has a significant effect on the lubricity. The difference was particularly evident when the results at two temperatures were compared. The ability to build a low-friction tribo-film was suggested as the primer source of lubricity. In the case of continuous sliding, the differences were not as noticeable. In this case, viscosity was assigned to be the leading property. [ABSTRACT FROM AUTHOR]

The Amperometric Gas Sensor (AGS) uses an electrode as the transducer element which converts its signal into a current from the electrochemical reaction of analytes taking place at the electrode surface. Many attempts to improve AGS performance, such as modifying the working electrode, applying a particular gas-permeable membrane, and selecting the proper electrolyte, etc., have been reported in the scientific literature. On the other hand, in the materials community, atomic gold has gained much attention because its physicochemical properties dramatically differ from those of gold nanoparticles. This paper provides an overview of the use of atomic gold in AGSs, both in a bulky AGS and a miniaturized AGS. In the miniaturized AGS, the system must be redesigned; for example, the aqueous electrolyte commonly used in a bulky AGS cannot be used due to volatility and fluidity issues. A Room Temperature Ionic Liquid (RTIL) can be used to replace the aqueous electrolyte since it has negligible vapor pressure; thus, a thin film of RTIL can be realized in a miniaturized AGS. In this paper, we also explain the possibility of using RTIL for a miniaturized AGS by incorporating a quartz crystal microbalance sensor. Several RTILs coated onto modified electrodes used for isomeric gas measurement are presented. Based on the results, the bulky and miniaturized AGS with atomic gold exhibited a higher sensor response than the AGS without atomic gold. [ABSTRACT FROM AUTHOR]

Ionic liquids (ILs) are molten organic salts consisting of organic cations and weakly coordinating organic/inorganic anions at room temperature. ILs have excellent physical and chemical properties such as high thermal stability, high combustible temperature, high miscibility with organic compounds and so on, making them good candidates for high performance lubricants and lubricant additives. The functional designability of ILs makes them novel lubrication materials that can break through the bottleneck of the active control of friction and lubrication. This paper firstly briefly introduces how to design the physical and chemical properties of the ILs required for different friction conditions by bonding specific cations with anions. Then, the lubrication mechanisms of ILs as base lubricants and additives for oils and water are focused on. The correlation between the structure of ILs and the lubrication results are established, which can guide the structural design of ILs in different applications. The response behaviors of friction characteristics under external electric fields are analyzed, which can provide a theoretical basis for the intelligent control of friction based on ILs. [ABSTRACT FROM AUTHOR]

The unique properties of ionic liquids (ILs), such as structural tunability, good solubility, chemical/thermal stability, favorable biocompatibility, and simplicity of preparation, have led to a wide range of applications in the pharmaceutical and biomedical fields. ILs can not only speed up the chemical reaction process, improve the yield, and reduce environmental pollution but also improve many problems in the field of medicine, such as the poor drug solubility, product crystal instability, poor biological activity, and low drug delivery efficiency. This paper presents a systematic and concise analysis of the recent advancements and further applications of ILs in the pharmaceutical field from the aspects of drug synthesis, drug analysis, drug solubilization, and drug crystal engineering. Additionally, it explores the biomedical field, covering aspects such as drug carriers, stabilization of proteins, antimicrobials, and bioactive ionic liquids. [ABSTRACT FROM AUTHOR]

Recent advances in nucleation and crystal growth have revolutionized our understanding and control of crystallization processes. This paper highlights key developments in this field and the processes and technologies involved in its continuous growth. Advanced computational models have allowed for precise prediction of nucleation rates and crystal morphologies, facilitating the rational design of materials with desired properties. Innovative strategies have also emerged, enabling enhanced control over crystal growth kinetics and crystallographic orientations. Process intensification strategies, including microreactors and membrane crystallization, enhance nucleation rates and crystal growth. Advances in the potential-driven growth of metal crystals from ionic liquids, including protic ionic liquids (PILs) and solvate ionic liquids (SILs), are discussed. Lastly, current research gaps and future prospects in the field of nucleation and crystal formation are highlighted. The integration of cutting-edge experimental techniques, computational modeling, and novel strategies will drive the understanding of nucleation and crystal growth processes, allowing for the development of materials with tailored properties and enhanced functionality across multiple disciplines. [ABSTRACT FROM AUTHOR]

Given their safety and efficiency in protecting protein integrity, polysorbates (PSs) have been the most widely used excipients for the stabilization of protein therapeutics for years. In recent decades, however, there have been numerous reports about visible or sub-visible particles in PS-containing biotherapeutic products, which is a major quality concern for parenteral drugs. Alternative excipients that are safe for parenteral administration, efficient in protecting different protein drugs against various stress conditions, effective in protein stabilization in high-concentrated liquid formulations, stable under the storage conditions for the duration of the product's shelf-life, and compatible with other formulation components and the primary packaging are highly sought after. The aim of this paper is to review potential alternative excipients from different families, including surfactants, carbohydrate- and amino acid-based excipients, synthetic amphiphilic polymers, and ionic liquids that enable protein stabilization. For each category, important characteristics such as the ability to stabilize proteins against thermal and mechanical stresses, current knowledge related to the safety profile for parenteral administration, potential interactions with other formulation components, and primary packaging are debated. Based on the provided information and the detailed discussion thereof, this paper may pave the way for the identification or development of efficient excipients for biotherapeutic protein stabilization. [ABSTRACT FROM AUTHOR]

In this paper, three imidazolium-based ionic liquids, viz., 1-butyl-3-undecyl imidazolium bromide ([BUIm]Br), 1-butyl-3-octyl imidazolium bromide ([BOIm]Br), and 1-butyl-3-hexadecyl imidazolium bromide ([BCIm]Br), were synthesized. Three novel microemulsions systems were constructed and then were used to recover Pd (II) from cyanide media. Key extraction parameters such as the concentration of ionic liquids (ILs), equilibration time, phase ratio (R A/O ), and pH were evaluated. The [BUIm]Br/n-heptane/n-pentanol/sodium chloride microemulsion system exhibited a higher extraction percentage of Pd (II) than the [BOIm]Br/n-heptane/n-pentanol/sodium chloride and [BCIm]Br/n-heptane/n-pentanol/sodium chloride microemulsion systems. Under the optimal conditions (equilibrium time of 10 min and pH 10), the extraction percentages of these metals were all higher than 98.5% when using the [BUIm]Br/n-heptane/n-pentanol/sodium chloride microemulsion system. Pd(CN) 4 2- was separated through a two-step stripping procedure, in which Fe (III) and Co (III) were first separated using KCl solution, then Pd(CN) 4 2- was stripped using KSCN solution (separation factors of Pd from Fe and Co exceeded 10 3 ). After five extraction-recovery experiments, the recovery of Pd (II) through the microemulsion system remained over 90%. The Pd (II) extraction mechanism of the ionic liquid [BUIm]Br was determined to occur via anion exchange, as shown by spectral analysis (UV, FTIR), Job's method, and DFT calculations. The proposed process has potential applications for the comprehensive treatment of cyanide metallurgical wastewater.

Ionic liquids (ILs) have presented excellent behaviors in the separation of azeotropes in extractive distillation. However, the intrinsic molecular nature of ILs in the separation of azeotropic systems is not clear. In this paper, Fourier-transform infrared spectroscopy (FTIR) and theoretical calculations were applied to screen the microstructures of ethyl propionate-n-propanol-1-ethyl-3-methylimidzolium acetate ([EMIM][OAC]) systems before and after azeotropy breaking. A detailed vibrational analysis was carried out on the v (C=O) region of ethyl propionate and v (O-D) region of n-propanol- d 1 . Different species, including multiple sizes of propanol and ethyl propionate self-aggregators, ethyl propionate-n-propanol interaction complexes, and different IL-n-propanol interaction complexes, were identified using excess spectroscopy and confirmed with theoretical calculations. Their changes in relative amounts were also observed. The hydrogen bond between n-propanol and ethyl propionate/[EMIM][OAC] was detected, and the interaction properties were also revealed. Overall, the intrinsic molecular nature of the azeotropy breaking was clear. First, the interactions between [EMIM][OAC] and n-propanol were stronger than those between [EMIM][OAC] and ethyl propionate, which influenced the relative volatilities of the two components in the system. Second, the interactions between n-propanol and [EMIM][OAC] were stronger than those between n-propanol and ethyl propionate. Hence, adding [EMIM][OAC] could break apart the ethyl propionate-n-propanol complex (causing the azeotropy in the studied system). When x ([EMIM][OAC]) was lower than 0.04, the azeotropy still existed mainly because the low IL could not destroy the whole ethyl propionate-n-propanol interaction complex. At x (IL) > 0.04, the whole ethyl propionate-n-propanol complex was destroyed, and the azeotropy disappeared.

The current review work focuses on recent developments in the exploration of electroactive nanofluids, ionanofluids, and ionic liquids acting as liquid electrodes. The nanofluids used for this purpose are composed of organic or aqueous electrolytes as base fluids with the addition of nanoparticles in pure, oxidized, or hybrid forms. On the other hand, the ionic liquids are formed by adding a solution, which can be an acid, a base, or a salt, in water. The electrochemical properties, such as electrical conductivity and capacitance, of these innovative fluids are discussed thoroughly, along with their influencing factors, such as the nature and concentration of the included nanoparticles, the type of base fluids, and the operating temperature. Moreover, this overview summarizes the fundamental applications of electroactive nanofluids, ionanofluids, and ionic liquids in various possible flow-cell configurations and electrolysis methods, along with the associated feasibility factors. Additionally, this survey of scientific papers on the matter enabled the listing and evaluation of general aspects related to the usage of electroactive nanofluids, ionanofluids, and ionic liquids. Finally, it addresses the main problems associated with such types of fluids and outlines the primary prospects for further research and utilization of electroactive nanofluids, ionanofluids, and ionic liquids in diverse scientific and technological fields. [ABSTRACT FROM AUTHOR]

Nicotinic acid (NA) is a heteroaromatic carboxylic acid mainly used as feed, in breakfast cereals, and as a beverage additive. Moreover, it is used as an anti-pellagra drug and as an ingredient in multivitamin supplements. It is manufactured using the Lonza process from 3-ethyl-3-methylpyridyne as a raw material using HNO3 as the oxidant agent. However, the use of such an oxidant is connected with greenhouse gases, thus making the technology non-ecological. Another industrial process is oxidative ammonolysis of 3-picoline followed by hydrolysis of a reaction intermediate to NA. This paper presents the results of research on the selective oxidation of 3-picoline with oxygen to NA. Bromide organic salts, including ionic liquids, N-hydroxyphtalimide, and cobalt(II) salts, were used as the catalysts. The reaction was carried out with acetic acid (AcOH) as a solvent. The bromide salts imidazolium bromide, quaternary ammonium bromide, and quaternary phosphonium bromide were used. They also fill the role of corrosion inhibitors caused by the acidic and highly oxidative reaction environment. [ABSTRACT FROM AUTHOR]

Ionic liquids are used in various fields due to their unique physical properties and are widely utilized as reaction solvents in the field of synthetic organic chemistry. We have previously proposed a new organic synthetic method in which the catalyst and reaction reagents are supported on ionic liquids. This method has various advantages, such as the ability to reuse the reaction solvent and catalyst and its facile post-reaction treatment. In this paper, we describe the synthesis of an ionic liquid-supported anthraquinone photocatalyst and the synthesis of benzoic acid derivatives using this system. This synthesis of benzoic acid derivatives via the cleavage of vicinal diols by an ionic liquid-supported anthraquinone photocatalyst is an environmentally friendly process, and furthermore, it has a simple post-reaction process, and the catalyst and solvent can both be reused. To the best of our knowledge, this is the first report on the synthesis of benzoic-acid derivatives via the cleavage of vicinal diols using light and an ionic-liquid-supported catalyst.

The paper presents the preparation of new ionic liquids based on hexamethylenetetramine with bis(trifluoromethanesulfonyl)imide and dicyanamide anion, which were characterized in detail in terms of their purity (Ion Chromatography) and thermal properties (Differential Scanning Calorimetry), as well as stability. The obtained substances were used to develop curing systems with ethylene glycol, which were successfully tested for their application with bisphenol A diglycidyl ether molecule. In addition, the curing process and its relationship to the structure of the ionic liquid are characterized in detail. The research showed that hexamethylenetetramine-based new ionic liquids can be successfully designed using well-known and simple synthetic methods-the Delepine reaction. Moreover, attention was paid to their stability, related limitations, and the application of hexamethylenetetramine-based ionic liquids in epoxy-curing systems.

In this paper, we investigate different current collector materials for in situ deposition of lithium using a slurry-based β -Li3PS4 electrolyte layer with a focus on transferability to industrial production. Therefore, half-cells with different current collector materials (carbon-coated aluminum, stainless steel, aluminum, nickel) are prepared and plating/stripping tests are performed. The results are compared in terms of Coulombic efficiency (CE) and overvoltages. The stainless steel current collector shows the best performance, with a mean efficiency of η mean , SST = 98 % ; the carbon-coated aluminum reaches η mean , Al + C = 97 % . The results for pure aluminum and nickel indicate strong side reactions. In addition, an approach is tested in which a solvate ionic liquid (SIL) is added to the solid electrolyte layer. Compared to the cell setup without SIL, this cannot further increase the CE; however, a significant reduction in overvoltages is achieved. [ABSTRACT FROM AUTHOR]

This research paper investigates the tribological performance of diamond-like carbon (DLC) coatings doped with rare earth metals (europium and gadolinium) as well as pure DLC lubricated with ionic liquid additives (trihexyltetradecylphosphonium bis(2-ethylhexyl) phosphate {[P66614][DEHP]} and 1-ethyl-3-methylimidazolium diethyl phosphate {[EMIM][DEP]}) in Polyalphaolefin 8 (PAO8). The study aims to examine the effect of temperature on the interaction between the coatings and additives by conducting tribological experiments using a block-on-disk setup at temperatures of 60 °C, 80 °C, and 100 °C. The primary objective is to evaluate the performance of doped DLC coatings compared to pure DLC coatings with ionic liquid additives in the lubricant in boundary lubrication conditions at various high working temperature environments. The experiments reveal that doped DLC coatings with ionic liquid additives exhibit superior tribological performance compared to pure DLC coatings. The rare earth metal dopants play a positive role in the formation of a tribofilm on the surface of the coatings as it interacts with ionic liquids, resulting in a lower coefficient of friction (CoF). Temperature influences the performance of the coatings and additives. The CoF increases with temperature for pure DLC coatings, while for doped DLC coatings it was significantly less. These findings highlight the influence of temperature on the tribological behavior of DLC coatings. Overall, this study contributes valuable insights into the impact of rare earth metal dopants and ionic liquid additives on the tribological performance of DLC coatings under different temperature conditions. The results demonstrate the potential of utilizing doped DLC coatings with ionic liquid additives as an effective approach to enhance the performance of mechanical systems. [ABSTRACT FROM AUTHOR]

This review summarizes the recent advances in preparing cellulose hydrogels via ionic liquid-based processes and the applications of regenerated cellulose hydrogels/iongels in electrochemical materials, separation membranes, and 3D printing bioinks. Cellulose is the most abundant natural polymer, which has attracted great attention due to the demand for eco-friendly and sustainable materials. The sustainability of cellulose products also depends on the selection of the dissolution solvent. The current state of knowledge in cellulose preparation, performed by directly dissolving in ionic liquids and then regenerating in antisolvents, as described in this review, provides innovative ideas from the new findings presented in recent research papers and with the perspective of the current challenges. [ABSTRACT FROM AUTHOR]

In this study, the classification, composition, preparation methods, and performance parameters of deep eutectic solvents (DESs) and their recent applications in natural product extraction, drug delivery systems, trace metal determination, nanomaterial synthesis, and electrochemistry are systematically summarised through the literature of recent decades, using DESs and applications as keywords. The hydrogen bond acceptors (HBA) of DESs are mainly quaternary ammonium salts (e.g., choline chloride) or amphoteric ions (e.g., betaine); the hydrogen bond donors (HBD) are mostly compounds such as urea, polyols, and sugars. Their melting points are related to hydrogen bonding, their polarities are higher than most ionic liquids, and their viscosities are generally in the range of 0.01–5 Pa·s. Compared with traditional organic solvents and conventional ionic liquids, DESs have higher solubility, with their ability to dissolve metal oxides and insoluble drugs, and have good biodegradability. DESs have high extraction rates in flavonoids and phenols, can increase drug solubility in drug delivery systems, can effectively extract and perform pre-concentration of metals in trace metal determination, can synthesise new nanomaterial, and can be used as electrolytes for electrochemical reactions in electrochemistry. This paper collates the relevant literature on the physicochemical properties and multi-field applications of DESs, which provides a deeper understanding of DESs and looks forward to the future development of DESs [ABSTRACT FROM AUTHOR]

Dye-sensitized solar cells have been under development for the last three decades but are yet to see the market. This has been attributed to stability issues of the electrolyte in the cell. Electrolytes can be liquid, quasi-solid, or solid. Liquid electrolytes were the first to be developed and, therefore, have been subject to radical revisions in both composition and applicability. They have shown the best power conversion efficiencies but have poor thermal stability. Although quasi-solid and solid-state electrolytes were developed to overcome these stability issues, they too have their limits. The aim of this paper is to explore the development of liquid electrolytes, outlining the current state of the technology and considering their potential in the photovoltaic market. [ABSTRACT FROM AUTHOR]

Some traditional acidic ionic liquids (AILs) have shown great catalytic potential in esterification; meanwhile, the design and application of more new AILs are expected at present.Tropine-based functionalized acidic ionic liquids (FAILs) were synthesized to realize esterification catalysis for the first time; with aspirin synthesis as the template reaction, key influences on the substrate conversion and product yield of the synthesis, such as IL type, ratio of salicylic acid to acetic anhydride, temperature, reaction time and amount of IL, were investigated. The new tropine-based FAILs exhibited excellent performance in catalytic synthesis of aspirin with 88.7% yield and 90.8% selectivity. Multiple recovery and re-usage of N-(3-propanesulfonic acid) tropine is the cation, and p -toluenesulfonic acid is the anion. ([Trps][OTs]) shows satisfactory results. When [Trps][OTs] was used to catalyze different esterification reactions, it also showed good results. The above studies proved that ionic liquid [Trps][OTs] could serve as an ideal green solvent for esterification reaction, which serves as a suitable substitute for current catalysts., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

The increasing concentration of CO 2 in the atmosphere is related to global climate change. Carbon capture, utilization, and storage (CCUS) is an important technology to reduce CO 2 emissions and to deal with global climate change. The development of new materials and technologies for efficient CO 2 capture has received increasing attention among global researchers. Ionic liquids (ILs), especially functionalized ILs, with such unique properties as almost no vapor pressure, thermal- and chemical-stability, non-flammability, and tunable properties, have been used in CCUS with great interest. This paper focuses on the development of functionalized ILs for CO 2 capture in the past decade (2012~2022). Functionalized ILs, or task-specific ILs, are ILs with active sites on cations or/and anions. The main contents include three parts: cation-functionalized ILs, anion-functionalized ILs, and cation-anion dual-functionalized ILs for CO 2 capture. In addition, classification, structures, and synthesis of functionalized ILs are also summarized. Finally, future directions, concerns, and prospects for functionalized ILs in CCUS are discussed. This review is beneficial for researchers to obtain an overall understanding of CO 2 -philic ILs. This work will open a door to develop novel IL-based solvents and materials for the capture and separation of other gases, such as SO 2 , H 2 S, NOx, NH 3 , and so on.

The biodegradation of wood and wood products caused by fungi is recognized as one of the most significant problems worldwide. To extend the service life of wood products, wood is treated with preservatives, often with inorganic compounds or synthetic pesticides that have a negative impact on the environment. Therefore, the development of new, environmentally friendly wood preservatives is being carried out in research centers around the world. The search for natural, plant, or animal derivatives as well as obtaining synthetic compounds that will be safe for humans and do not pollute the environment, while at the same time present biological activity is crucial in terms of environmental protection. The review paper presents information in the literature on the substances and chemical compounds of natural origin (plant and animal derivatives) and synthetic compounds with a low environmental impact, showing antifungal properties, used in research on the ecological protection of wood. The review includes literature reports on the potential application of various antifungal agents including plant extracts, alkaloids, essential oils and their components, propolis extract, chitosan, ionic liquids, silicon compounds, and nanoparticles as well as their combinations.

In this paper, an environmentally friendly inertial motion sensor is investigated, modelled, and characterized as an accelerometer. The sensor is obtained by using bacterial cellulose (BC) as a base biopolymer. BC is then impregnated with ionic liquids. Electrodes are realized by a conducting polymer, in a typical three-layer structure. The sensor works in a cantilever configuration and produces an open voltage signal as the result of a flexing deformation. A model is proposed for the transduction phenomenon. The composite mechano-electric transduction capability is exploited for realizing the accelerometer. Results of the chemical and transduction characterization of the accelerometer are reported. Finally, experimental evidence of the possible nature of the transduction phenomenon is given. [ABSTRACT FROM AUTHOR]

Ventilation Air Methane (VAM) refers to the release of fugitive methane (CH4) emissions into the atmosphere during underground coal mining operations. Growing concerns regarding the greenhouse effects of CH4 have led to a worldwide effort in developing efficient and cost-effective methods of capturing CH4. Among these, absorption-based processes, particularly those using Ionic Liquids (ILs) are appealing due to their advantages over conventional methods. In this study, the solubility of CH4 in various ILs, expressed by Henry's law constant, is first reviewed by examining a wide range of experimental techniques. This is followed by a review of thermodynamic modelling tools such as the extended Henry's law model, extended Pitzer's model, Peng–Robinson (PR) equation of state, and Krichevsky−Kasarnovsky (KK) equation of state as well as computational (Artificial Neural Network) modelling approaches. The comprehensive analysis presented in this paper aims to provide a deeper understanding of the factors that significantly influence the process of interest. Furthermore, the study provides a critical examination of recent advancements and innovations in CH4 capture by ILs. ILs, in general, have a higher selectivity for methane compared to conventional solvents. This means that ILs can remove methane more effectively from VAM, resulting in a higher purity of the recovered methane. Overall, ILs offer several advantages over conventional solvents for the after treatment of VAM. They are more selective, less volatile, have a wider temperature range, are chemically stable, and can be made from renewable materials. As a result of their many advantages, ILs are becoming increasingly popular for the after treatment of VAM. They offer a more sustainable, efficient, and safe alternative to conventional solvents, and they are likely to continue gaining market share in the coming years. [ABSTRACT FROM AUTHOR]

Cellulose nanocrystals (CNCs) are nanoscale particles made from cellulose. They have many unique properties such as being lightweight, stiff, and renewable, making them promising for a variety of applications in a wide range of industries, including materials science, energy storage, and biomedicine. In this paper, a two-stage (swelling-SA-catalyzed) method including IL pretreatment and solid acid hydrolysis process was developed to extract CNCs with high purity and good thermal stability from microcrystalline cellulose (MCC). In the first stage, the swelling of MCC in ionic liquid was studied with the assistance of ultrasonication, and it was found that the amorphous regions became more disordered while the crystalline areas were selectively retained under the conditions of 30 min of reaction time, 45 °C of temperature, 2% of ionic liquid water content and 1:4 mass ratio of cellulose to ionic liquid. CNCs were extracted using solid acid hydrolysis, with a 45 wt% solid acid to cellulose ratio and a 5.0 h hydrolysis process at 45 °C. The morphology, crystallinity, surface characteristics and thermo stability of the sample were characterized by atomic force microscopy (AFM), X-ray diffraction (XRD) and thermogravimetric analysis (TGA), respectively. Results demonstrated the highly thermostable CNCs were successful extracted with rodlike shape of 300 ± 100 nm in length and 20 ± 10 nm in width. Solid acid recovery and reuse were also studied, revealing a promising candidate that can reduce the environmental impact associated with chemical products. [ABSTRACT FROM AUTHOR]

As a new and promising compression technology for hydrogen gas, the ionic liquid compressor inherits the advantages of the ionic liquid and the hydraulic system. The liquid density is one of the key parameters influencing the fluid flow field, the sloshing of the bulk liquid, and the movement of droplets generated during the compressor operation. An appropriate selection of the liquid density is important for the compressor design, which would improve the thermodynamic performance of the compressor. However, the density of the ionic liquid varied significantly depending on the specific combination of the cation and anions. This paper proposed the methodology to select the optimal liquid density used in the ionic liquid compressor for hydrogen storage. The gas-liquid interaction in the compression chamber is analysed through numerical simulations under varied liquid density values. Results found that the increase in the liquid density promoted the detachment of the ionic liquid from the cylinder cover during the suction procedure and the contact of the bulk liquid on the compressor cover when the gas is compressed in the cylinder during the compression procedure. Both the droplet size and the dimension of the derived gas vortex decreased when the liquid density increased. The lowest mass transfer of hydrogen through the outlet was obtained at the density of 1150 kg/m3. The density of the ionic liquid from 1300 to 1450 kg/m3 is suggested to the hydrogen compressor, taking into account the transient two-phase flow characteristics, the mass transfer, and the total turbulent kinetic energy. [ABSTRACT FROM AUTHOR]

In recent years, hard turning has been found to be a well-known substitute for traditional grinding for acquiring the finish quality of hardened steel without sacrificing productivity. There are many issues that should be carefully understood and dealt with to attain efficacious performance in hard turning. This article discusses modern manufacturing challenges with a focus on analyzing the current state of the art of the hard turning process in terms of ensuring more environmentally friendly manufacturing through the use of greener cooling methods such as dry, wet/flood cooling, the minimum quantity of lubricant (MQL), high-pressure jet cooling, solid lubricant, nanofluids, ionic liquids (ILs), cryogenic cooling, and hybrid cooling. Nanofluids combined with the MQL system were found to be the superior cooling technique in comparison to dry, wet/flood, and MQL. Cryo-machining also provided superior performance by limiting the cutting temperature during hard turning. The performance of hybrid cooling (MQL + cryogenic) seems to have been superior to MQL and cryogenic coolant alone because it combined the benefits of lubrication and cooling from MQL and cryogenic systems, respectively. The addition of ILs to base fluids or nanofluids improves the thermal properties of the mixed fluid, resulting in better surface quality, lower tool wear, and longer tool life. Furthermore, the purpose of this study is to summarize the various LCA software used for analyzing the sustainability of the hard turning process. Overall, this paper can serve as a resource for researchers and manufacturers working in the field of sustainable machining. [ABSTRACT FROM AUTHOR]