Liquid Research Articles

Numerical evaluation of orientation averages and its application to molecular physics.

In molecular physics, it is often necessary to average over the orientation of molecules when calculating observables, in particular when modeling experiments in the liquid or gas phase. Evaluated in terms of Euler angles, this is closely related to integration over two- or three-dimensional unit spheres, a common problem discussed in numerical analysis. The computational cost of the integration depends significantly on the quadrature method, making the selection of an appropriate method crucial for the feasibility of simulations. After reviewing several classes of spherical quadrature methods in terms of their efficiency and error distribution, we derive guidelines for choosing the best quadrature method for orientation averages and illustrate these with three examples from chiral molecule physics. While Gauss quadratures allow for achieving numerically exact integration for a wide range of applications, other methods offer advantages in specific circumstances. Our guidelines can also be applied to higher-dimensional spherical domains and other geometries. We also present a Python package providing a flexible interface to a variety of quadrature methods.

Being Smarter, Azobenzene-Containing Biomaterial Showing Triple Stimuli-Responsive Phase Change Property to Light, Humidity and Force at Room Temperature.

Multiple stimuli-responsiveness is an attractive property that is studied in physical chemistry and materials chemistry. While, multiple stimuli-responsive phase change in an isothermal way is rarely addressed for functional materials at room temperature. In this study, one azobenzene-containing surfactant AZO is designed for the fabrication of triple stimuli-responsive phase change biomaterial (Alg-AZO) through the electrostatic complexation with natural alginate. Thanks to the photoisomerization ability, molecular flexibility and hydrophilicity of AZO, together with the tailoring effect of alginate on AZO, Alg-AZO could perform reversible isothermal phase transition between liquid crystalline and isotropic liquid states under the stimuli of either light or humidity at room temperature. Furthermore, the humidity-induced isotropic state can also fast transit to ordered state under shear force, owing to the π-π interactions between planar trans-AZO in Alg-AZO material. With good biocompatibility, self-healing property and in vivo wound healing promoting capacity that is promoted by light, humidity and force, Alg-AZO would be suitable for working as a new smart biomaterial in biological and biomedical areas. This work provides a designing strategy for gaining multiple stimuli-responsive smart materials based on biomacromolecules, and also opening a new opportunity for gaining self-healing biomaterials capable of working in various conditions.

Acceptorless Dehydrogenation of Alcohols and Polyols Over Cu‐Based Catalysts Prepared by NaBH4 Reduction

AbstractFor the first time, oxide (TiO2, CeO2, ZnO, Al2O3) supported Cu catalysts, prepared by the aqueous reduction method using sodium borohydride, were employed for the acceptorless dehydrogenation of 2‐octanol and various C4–C8 polyols. The method used to prepare the catalysts enabled the formation of small Cu particles in the range of 14–36 nm, depending on the point of the zero charge of the support. We showed that the conversion increased with Cu surface area, where Cu/TiO2 led to the highest conversion of 2‐octanol (>99.9%). The selectivity depends on the support and conversion. Up to 80% conversion, the selectivity to 2‐octanone was between 83% and 90% when using Cu/TiO2. In this study, we also report for the first time the acceptorless dehydrogenation of 1,3‐butanediol, 2,3‐butanediol, 1,2‐pentanediol, and 1,5‐pentanediol in liquid phase. While metal active sites promoted the dehydrogenation reaction, the presence of acidic and basic sites favored the formation of by‐products, mainly resulting from dehydration reactions, pinacol rearrangements, and aldol and retro‐aldol condensations. In addition to value‐added chemicals, all the reactions also released molecular hydrogen.

Microstructures and properties of a novel cemented carbide prepared using a Co–Ni–Cu multiprincipal element alloy as the binder

A Co–Ni–Cu multiprincipal element alloy (MPEA) powder was successfully synthesized through coprecipitation. Results of energy dispersive spectroscopy (EDS) and X-ray fluorescence spectroscopy (XRF) revealed nearly equal atomic ratios for Co, Ni, and Cu in the Co–Ni–Cu MPEA powder. Moreover, X-ray diffraction (XRD) confirmed a single-phase face-centered cubic (fcc) structure in the Co–Ni–Cu MPEA powder. To explore the differences in microstructure and mechanical properties, we compared a novel WC–2Co–2Ni–2Cu cemented carbide, utilizing the Co–Ni–Cu MPEA as a binder, with conventional WC–6Co and WC–3Co–3Ni cemented carbides prepared via liquid phase sintering. This comparison was conducted using scanning electron microscopy, XRD, and mechanical properties testing. Observations revealed that the surfaces of WC grains in WC–2Co–2Ni–2Cu and WC–6Co appeared smooth and flat, while those in WC–3Co–3Ni exhibited roughness with numerous terraces. In addition, the average grain size was 0.96, 1.14, and 1.22 μm in WC–2Co–2Ni–2Cu, WC–6Co, and WC–3Co–3Ni, respectively. Notably, the Co–Ni–Cu MPEA inhibited WC grain growth. WC–2Co–2Ni–2Cu (1388 HV30) exhibited hardness similar to that of WC–6Co (1406 HV30) but the highest fracture toughness (9.04 MPa∙m1/2), while WC–3Co–3Ni (1332 HV30) presented the lowest hardness. Bending strength values were recorded at 2406 MPa for WC–2Co–2Ni–2Cu, 2816 MPa for WC–6Co, and 2645 MPa for WC–3Co–3Ni, with WC–6Co exhibiting the highest bending strength. Considering their microstructures, physical properties, and mechanical properties comprehensively, the novel cemented carbides exhibited only slightly reduced bending strength compared to conventional counterparts. Thus, the Co–Ni–Cu MPEA binder demonstrates promising potential as a replacement for the conventional Co metal binder.

Experimental Study on the Impact of Sorption-Desorption on Nitrate Isotopes

Nitrate pollution is a global environmental problem, and mean nitrate levels have risen by an estimated 36% in global waterways since 1990. Tracing nitrate sources is important for water quality management, and nitrate isotopes (δ15N-NO3− and δ18O-NO3−) are commonly used for this purpose because of the different isotopic compositions of different sources. However, the impact of nitrate sorption on matrix and desorption from matrix on N and O isotopic composition of nitrate in liquid phase has not been well clarified. To explore the mechanism for the changes in nitrate concentration and isotopes in liquid phase during sorption and desorption, this study took a shale sample (enriched in clay minerals and commonly exposed in the Earth), conducted a series of laboratory experiments for nitrate sorption and desorption, and studied the impact of sorption and desorption on nitrate N and O isotopic composition in liquid phase. The results showed that the shale sample exhibited a rapid sorption and desorption rate for nitrate in the surface water samples, with the nitrate concentration in the solution decreasing from 14.3 mg/L to 4.1 mg/L within 5 min. The sorption data fit the Langmuir model better than that of the Freundlich model. The maximum possible sorption (Qmax) for the shale sample was estimated to be 46 μg/g. Preliminary laboratory experiments showed that changes in δ15N-NO3− values were not obvious, and changes in δ18O-NO3− values in liquid phase were minor during sorption and desorption of the shale sample, suggesting that nitrogen isotopic fractionation can be neglected, and the sorption of nitrate by the shale sample has a very limited impact on the distribution of nitrate isotopes in liquid phase. However, the impact of nitrate desorption on the nitrate isotopes in liquid phase depends on the isotopic composition of exchangeable nitrate in the solid phase, which may be related to antecedent water–rock interactions. This study provides important information for elucidating the evolution mechanism of nitrate and its isotopic compositions following sorption-desorption, and is conducive to revealing the nitrogen cycle law in the environment.

Two-group interfacial area concentration model for dispersed gas-liquid flows in large-diameter pipes

Interfacial area concentration (IAC) plays a critical role in heat and mass transfers between gas and liquid phases through the interfaces. As interfacial area increases, mass and heat transfers between phases increase. Hence, a reliable IAC estimation is important for two-phase flow numerical simulations to conduct engineering designs and safety analyses. Gas bubbles show different behavior according to their shapes and sizes. Based on the size, gas bubbles can be classified into two groups that show different characteristics, such as IAC. Hence, two-group modeling helps to achieve a general approach for estimating the IAC in bubbly to beyond-bubbly flow regimes. Available models in the literature use empirical correlations to obtain group one and group two void fractions. These empirical approaches are not reliable for different flow conditions. In addition, these models are usually complex with several empirical constants. This study aims to develop a two-group area-averaged IAC model for upward vertical dispersed flows through large-diameter pipes. In addition, this study proposes using a general approach based on the two-group drift-flux model to calculate two-group void fractions rather than applying empirical correlations. The models are evaluated using 156 two-group measured data points in dispersed flow conditions through large-diameter pipes. The resulting prediction errors for group one and group two IAC models are 24.1 % and 34.2 %, and the errors for group one and group two void fraction predictions are 22.8 % and 25.6 %, respectively.

Nature of Topological Phase Transition of Kitaev Quantum Spin Liquids

We investigate the nature of the topological quantum phase transition between the gapless and gapped Kitaev quantum spin liquid phases away from the exactly solvable point. The transition is driven by anisotropy of the Kitaev couplings. At the critical point, the two Dirac points of the gapless Majorana modes merge, resulting in the formation of a semi-Dirac point with quadratic and linear band touching directions. We derive an effective Gross-Neveu-Yukawa-type field theory that describes the topological phase transition in the presence of additional magnetic interactions. We obtain the infrared scaling form of the propagator of the dynamical Ising order parameter field and perform a renormalization-group analysis. The universality of the transition is found to be different from that of symmetry-breaking phase transitions of semi-Dirac electrons. However, as in the electronic case, the Majorana fermions acquire an anomalous dimension, indicative of the breakdown of the fractionalized quasiparticle description. Published by the American Physical Society 2024

Monitoring a batch crystallization process by acoustic emission

Crystallization is regarded as an important unit operation for separation and purification, as well as the production of solid particles with specified end-use properties. However, it is still difficult to control or to optimize the crystallization process due to the complexity of the coupled phenomena taking place simultaneously in the liquid and solid phases. In order to overcome such drawback, different analytical technologies have been implemented in the literature for monitoring (in situ, at best) the key crystallization parameters, e.g. solute concentration and crystal size distribution, which in turn enhances the comprehension about this operation. In our work, a multi-probe monitoring system composed of acoustic emission, ATR-FTIR and imaging probes was applied to the crystallization of a model system (an aqueous solution of adipic acid) in a semi-batch crystallizer. The crystallization was carried out under two different feed rates and under vacuum or atmospheric pressure. The goal was to demonstrate the usefulness of the multi-probe system for monitoring the crystallization process and to study the influence of the process (stirring rotation speed, cooling speed, etc.) on the acoustic emission. As a matter of fact, the multi-probe system tracked information about the dissolved adipic acid in the liquid phase with the ATR-FTIR spectrometry, while the crystal size, shape and number were monitored with the help of the imaging probe (with image treatment methods). The acoustic emission probes were used to detect the beginning of crystallization and the phenomena of crystal growth and agglomeration

Selective leaching of lithium from mixed spent lithium iron phosphate powder

In recent years, lithium iron phosphate (LFP) batteries have been widely used in the electric vehicle industry. The recycling of spent LFP will be propitious to conserving resources and alleviating the environmental risks it poses. In this study, a selective extraction method for lithium from spent LFP was proposed using nitric acid. Lithium leached into the liquid phase, while P and Fe remained in the leaching residue. Under the conditions of 120°C, HNO3/Li molar ratio of 2, and time of 2h, the leaching efficiency of lithium reached 99.5%, with a selectivity reaching 82.1%. Initially, LFP was decomposed to liberate Li, Fe, and P in the liquid phase. Subsequently, ferrous ions were oxidized to trivalent, high-valent iron ions re-precipitated as FePO4·2H2O. Thermodynamic calculations indicate that the temperature and pH value of the extraction system have significant influence on both the oxidation and reprecipitation steps. An imbalance of Fe/P ratio (<1) in the raw material hinders the selectivity of lithium extraction, and supplementing this portion of Fe can enhance the selectivity to over 90%. Additionally, LiCO3 and anhydrous FePO4 were effectively regenerated from the leachate and residue. This study provides a novel approach for the recycling of spent LFP and probably contributes to the sustainability of the lithium ion battery industry.

Thermal conductivity measurements of liquid ethane and ethane + propane binary mixtures

Based on the transient hot-wire apparatus, the thermal conductivity of ethane was measured in the temperature range of 146–247 K and pressure < 14 MPa in the liquid phase. The thermal conductivity of ethane + propane binary mixture was measured in the temperature range of 156–288 K and pressure < 25 MPa in the liquid phase. The mole fractions of ethane in binary systems are 0.198, 0.525, and 0.736. The deviation between experimental results and REFPROP calculation falls within 3 % of ethane and mixture. Subsequently, the previous established thermal conductivity model, derived from dimensional analysis, was employed to predict the thermal conductivity of n-alkanes mixture. The mixture critical parameters were obtained first by the mixing rules, and the thermal conductivity of the mixture were calculated. Comparisons were made between the experimental data of ethane and the previously constructed n-alkane model, resulting in an average absolute relative deviation (AARD) of 4.42 %. Similarly, the experimental data of the ethane + propane mixture was compared with the mixture prediction model proposed in this study, yielding an AARD of 1.92 %. The relative deviation between experimental data and model calculations demonstrates good consistency.

Influence of the gas phase on a large-scale bubble column fluid dynamics: Gas holdup, flow regime transitions, and bubble size distributions

We present the results of an experimental study of a large-diameter bubble column operating in batch mode with air or CO2 as the gas phase and water as the liquid phase. The bubble column has an inner diameter of 0.24 m and is 5.3 m in height. The superficial gas velocity varied between 0.0037 m/s and 0.0233 m/s. The experimental investigation consists of gas holdup measurements and image analysis. Flow regime transitions were detected by gas holdup measurements, and image analysis was used to investigate the bubble size distributions. The results suggest that the homogeneous flow regime is stabilized when CO2 is used as the gas phase. The gas holdup is higher for the CO2-water system at fixed superficial gas velocity, especially in the heterogeneous flow regime. In the homogeneous flow regime, the mean bubble diameter and the fraction of large bubbles are lower for the CO2-water system, explaining the higher gas holdup.

Small-angle X-ray scattering analysis of poly(amic acid) dispersed in a liquid matrix to understand the size control of polyimide nanoparticles.

Poly(amic ‍acid) ‍nanoparticles ‍prepared ‍by ‍‍precipitation ‍polymerization with a dispersant were evaluated by small-angle X-ray scattering (SAXS) and field-emission scanning electron microscopy (FE-SEM). The particle size evaluation of poly(amic acid) nanoparticles in the liquid phase by SAXS was performed to gain insight into the size control of poly(amic acid) nanoparticles, and showed good agreement with visual observation by FE-SEM, explaining the effect of the dispersant in obtaining polyimide nanoparticles with small particle size. This indicates that the particle size is maintained without change during the solvent evaporation process. The polyamide nanoparticles controlled by the dispersant effect maintained their size after imidization, and polyimide nanoparticles with a minimum radius of about 60 nm were prepared.

Hydrogen peroxide—a promising oxidizer for rocket engines: physical and chemical properties: decomposition in the liquid phase

Hydrogen peroxide—a promising oxidizer for rocket engines: physical and chemical properties: decomposition in the liquid phase

Construction of the technological process and design development of a multifunctional unit for processing vital soybeans with ultrasound. Feasibility of water-crude suspension

Cereals and legumes have a porous structure, being an inert carrier during mass exchange processes; they contain voids in the form of pores and stomata, on the surface of which there are foreign extractable substances in a solid state, in particular, trypsin and urease inhibitor proteins. These substances, due to their harmful effect on the final product, are subject to removal by extraction. One of the methods for inactivating anti-nutritional substances is ultrasonic treatment of soybeans.The article discusses the technology of inactivating inhibitors that worsen food and protein value of vital soybeans. The developed technology was aimed at dissolving a solid substance - soybean inhibitor protein in a liquid, carried out due to molecular diffusion, intensifying the processes of mass transfer and mass return. When creating a suspension by mixing the solid (crushed soybean grain) and liquid (water) phases, water molecules, which are a solvent, penetrate under the action of capillary forces into the pores and stomata of the treated body, begin to penetrate. On this basis, technological directions of research have been established, a sequence has been built and the physical essence of operations has been substantiated, consisting of four main ones - grinding soybean grain, creating a “water-soybean” suspension, ultrasonic (US) treatment of soybeans, drying. As a result of the conducted research, optimal technological parameters have been established for intensifying the process of inactivation of anti-nutritional substances contained in native soybeans: the degree of grinding of soybean grains is 0.5-1.0 mm; the ratio of water-soy suspension (1:1). The efficiency of the developed technological process will be factors affecting the quality of the resulting products, the duration and energy intensity of the process, resource conservation, simplicity of design and low cost of manufacture, the possibility of automation.

The influence of bromine substitution and linking groups on the phase behaviour of light-responsive rod-like molecules

The effect of aromatic core bromination as well as different linking groups on the phase behaviour of light-responsive rod-like liquid crystalline materials is reported. For this purpose, two new series of laterally brominated rod-like molecules are designed and synthesized. The two series have three benzene rings connected using different linking groups either azo or ester units with different directions. Both series have pentyloxy chain at one end and an octyl chain at the other end in the first group or an octyloxy chain in the second group of materials. Additional lateral bromine substituent was inserted at ortho position with respect to the pentyloxy chain. The molecular self-assembly of the new materials was investigated using polarized optical microscope (POM), differential scanning calorimetry (DSC) and X-Ray diffraction (XRD). Depending on the type of the terminal chain (octyl or octyloxy) at one end and nature of the linking groups nematic phases as well as smectic C phases are observed, with variable temperature ranges. Interestingly, the nematic phases were found to exhibit cybotactic clusters with tilted SmC or orthogonal SmA structure (NCybC or NCybA) with wide temperature ranges. Finally, the isothermal photo switching because of cis–trans photoisomerization was investigated in solution as well as between different liquid crystal phases. This report could be of interest for optical information storage device applications.

Synthesis of uniform spherical silver powder without dispersants in a confined impinging-jet reactor

Sliver powder is the most common and extensively utilized precious metal powder in electronics, primarily for electronic paste. Herein, micron-sized spherical silver powder was synthesized via a liquid phase reduction method employing silver nitrate as the source of silver and ascorbic acid as the reducing agent in a confined impinging jet reactor (CIJR). The impact of the molar ratio between silver nitrate and ascorbic acid, the flow rate, and the temperature on the particle size of silver powder was investigated. The optimal process conditions for silver powder are as follows: maintain a molar ratio of 1:1 and control the feeding rate at 10ml/min while operating at 50 ° C. The confined impinging jet reactor offers enhanced control over reaction conditions during the synthesis of silver powder, surpassing the capabilities of traditional batch reactors. The aforementioned optimized methodology was employed to successfully synthesize uniform and spherical silver powder (with an aspect ratio approaching 1) in the low Reynolds number jet, resulting in an average particle size of d50 = 0.83 μm and a standard deviation of 0.07, without the addition of dispersant. The synthesis method presented here improves the performance of silver powder, simplifies the production process, reduces energy consumption, and minimizes waste generation. These advances yield significant environmental and economic benefits. In the future, with the continuous development and optimization of microreactor technology, this synthesis method is anticipated to play a more prominent role in the commercial-scale production and application of micrometer-sized silver powder.

A Differential Protein Study on Bronchoalveolar Lavage Fluid at Different Stages of Silicosis.

In this study, by comparing the difference in protein expression in bronchoalveolar lavage fluid between silicosis patients in different stages and healthy controls, the pathogenesis of pneumoconiosis was discussed, and a new idea for the prevention and treatment of pneumoconiosis was provided. The lung lavage fluid was pretreated by 10 K ultrafiltration tube, Agilent 1100 conventional liquid phase separation, strong cation exchange column (SCX) HPLC pre-separation, and C18 reverse phase chromatography desalting purification, and protein was labeled with isotope. GO, KEGG pathway, and PPI analysis of differential proteins were conducted by bioinformatics, and protein types and corresponding signal pathways were obtained. Thermo Q-Exactive mass spectrometry identified 943 proteins. T-test analysis was used to evaluate the different significance of the results, and the different protein of each group was obtained by screening with the Ratio≥1.2 or Ratio≤0.83 and P<0.05. We found that there are 16 kinds of protein throughout the process of silicosis. There are different expressions of protein in stages Ⅲ/control, stages Ⅱ/control, stage Ⅰ/control, stages Ⅲ/ stages Ⅱ, stages Ⅲ/ stage Ⅰ and stages Ⅱ/ stage Ⅰ groups. The results of ontology enrichment analysis of total differential protein genes show that KEGG pathway enrichment analysis of differential protein suggested that there were nine pathways related to silicosis. The main biological changes in the early stage of silicosis are glycolysis or gluconeogenesis, autoimmunity, carbon metabolism, phagocytosis, etc., and microfibril-associated glycoprotein 4 may be involved in the early stage of silicosis. The main biological changes in the late stage of silicosis are autoimmunity, intercellular adhesion, etc. Calcium hippocampus binding protein may participate in the biological changes in the late stage of silicosis. It provides a new idea to understand the pathogenesis of silicosis and also raises new questions for follow-up research.

Rapid discovery of natural antioxidants in Hypericum japonicum: Dual roles of the liquid phase mobile phase as extraction and separation solvent

Hypericum japonicum is a traditional folk medicine with various bioactivities such as hepatoprotective, antioxidant, and anti-tumorous. The antioxidant effect of H. japonicum is one of the most prominent effects due to its responsibility for many of its activities. To clarify active natural substance, the antioxidant properties of H. japonicum were preliminarily assessed by ferric reducing–antioxidant power (FRAP), 2,2-azino-bis-3-ethylbenzothiazoline-6-sulphonic acid (ABTS) and Oxygen radical absorbance capacity (ORAC), as well as superoxide dismutase (SOD). Then, a straightforward and effective method named online liquid extraction-high performance liquid chromatography combined with ABTS antioxidant assay and mass spectrometry (OLE-HPLC-ABTS/Q-TOF-MS) was developed to swiftly and directly discover the antioxidants in H. japonicum. Using mobile phase as extraction and separation reagent, coupled with online activity analysis and compounds identification by high-resolution MS, the online system enables rapid screening of natural antioxidant bioactives from complex mixture. By using it, a total of 9 compounds including flavonoids and phenolic acids characterized by retention time, precise mass, and fragmentation ions in MS/MS spectra showed antioxidant action. Finally, the antioxidant and SOD activity of main found active compounds were validated by in vitro experiment assay and molecular docking. In summary, these results suggested that H. japonicum could be considered as a potential source of natural antioxidants, and the online integrated system might become a promising candidate for the natural antioxidants discovery in the future.

Abnormal resistivity behavior of Co–Cu alloys and responsible metastable liquid phase separation

The electrical resistivity of Co-Cu alloys with Cu content of 10, 20, 30, 40, 50, 60, 70, 80, and 90 at.% was measured in the temperature range from 1400 to 2100K. The experiments were performed during of heating and subsequent cooling of the samples. For alloys with Cu content of 30, 40, 60, 70, 80, and 90 at.%, a bend in the cooling curve specific to the liquid-liquid phase separation (LLPS) process was observed. LLPS is shown when the melt is undercooled to the binodal temperature T∗. The phase transition model of LLPS was proposed for to theoretically determine the temperatures T∗. The LLPS model demonstrates the possibility of percolation phenomena occurring in Cu-Co heterogeneous melts rich in cobalt. The LLPS model shows good agreement with experimental data and the abnormal resistivity behavior of Co–Cu alloys.

A paradigm for natural eutectic solvents based on fatty acids: Molecular interactions and toxicological considerations

In this work, we present experimental and molecular modeling results on archetypal hydrophobic natural deep eutectic solvents (NADES) based on fatty acids (octanoic and dodecanoic acid) and menthol, a representative monoterpenoid. Our goal is to provide a multiscale characterization to enhance the understanding of this field by studying these selected archetypical mixtures. We examine their liquid state properties, intermolecular forces, nanoscopic arrangements, toxicity, and environmental impact.The computational study integrates quantum chemistry, molecular dynamics (both all-atom and coarse-grained approaches), and thermodynamic modeling (COSMO-RS approach) to analyze the fluids and their interactions with biological entities, such as proteins and plasma membranes. The experimental characterization focuses on elucidating intermolecular interactions and liquid phase dynamics using NMR spectroscopy, visible and UV resonance Raman spectroscopy (UVRR). Notably, this is the first report of UVRR data on NADES.Additionally, we simulate the effect of the molecular moieties forming the solvents on biological targets—specifically, protein and cell membrane models –. This in silico analysis aims to rationalize and predict their potential toxicity.Overall, our experimental findings and in silico simulations contribute to a deeper understanding of these novel solvents in terms of their network of interactions. Additionally, they highlight the potential impact on biological targets, providing new data to accurately define the eco-friendliness of type V DES and their suitability as sustainable alternatives to traditional molecular solvents.