Solvent Research Articles

Removal of encapsulant ethylene-vinyl acetate for recycling of photovoltaic modules: Hansen solubility parameters analysis

Delamination of photovoltaic modules is crucial for the recovery of solar cell materials. In this article, we investigate the swelling of ethylene-vinyl acetate (EVA) using various organic solvents at a temperature range between 25 to 55°C. The swelling of the encapsulant EVA caused by the interaction of organic solvents aids in the separation of glass, solar cell, and Tedlar layer in the recycling of photovoltaic modules. Further, we quantify the interactions between the encapsulant EVA and the organic solvents by the solvent weight ratio and solvent volume ratio of EVA. The quantification of interactions between encapsulant EVA and various organic solvents is used to estimate the Hansen solubility parameters of encapsulant EVA. The temperature-dependent variation of physical properties of organic solvents and their effect on encapsulant EVA swelling are described. Organic solvents retained in encapsulant EVA matrix after drying at room temperature can be viewed as a method to reduce emissions of volatile organic compounds during recycling. Additionally, our experiments suggest that d-limonene, xylene, and toluene are the most effective solvents for delamination of end-of-life photovoltaic modules for recycling.

Surface polarity modulation enables high-performance polyamide membranes for separation of polar/non-polar organic solvent mixtures

Achieving highly selective separation of organic mixtures is crucial to modern fine chemicals and pharmaceutical industries. The membrane-based organic solvent reverse osmosis (OSRO) technology is expected to break through this barrier. The key to achieving the separation of organic mixed liquids is to design the OSRO membrane as needed based on the physical and chemical properties of the target separation solvent. However, this poses a huge challenge to traditional OSRO membranes. In this work, we report composite polyamide (PA) OSRO membranes with ultrahigh polar/non-polar organic mixture selectivity. The surface polarity of the composite PA membrane is increased by coating a layer of Fe3+/tannic acid (Fe3+/TA) layer on the surface of the PA membrane. The enhanced surface polarity increases the interaction difference between polar and non-polar solvents and the membrane. And a polarization layer is formed on the membrane surface, which weakens the concentration polarization effect on the membrane surface. Under high-concentration feed liquid (the mass ratio of methanol/hexane is 7:3), the separation factor of the prepared membrane reaches 218, which is the highest value of all OSRO membranes reported so far. For the first time, we establish a partial flux analysis for the OSRO process. This analysis unravels the pressure, concentration dependence, and sensitivity of separation performance. It provides novel insights into the design of high-performance OSRO membranes.

All-solution-processed perovskite-quantum-dot light-emitting diodes through effective synergistic combination of orthogonal solvent and electron transport material

Perovskite quantum dots (PQDs) have shown great promise for use in photovoltaic devices, due to their ability to offer advantages such as tunability of visible light and efficient light emission. This study demonstrates the successful utilization of a triazine-based PO-T2T (2,4,6-Tris[3(diphenylphosphenyl)phenyl]-1,3,5-triazine; PO-T2T) as the electron transport layer (ETL) through an all-solution process. To improve the structural and optical characterization of CsPbBr3 and CsPbI3 QDs, three organic solvents, namely chlorobenzene, methyl acetate, and ethyl acetate, were selected to find an effective orthogonal solvent for PO-T2T. The all-solution processed devices incorporating PO-T2T and Methyl acetate (MeOAc) demonstrated impressive external quantum efficiencies of 5.57% for CsPbBr3 and 1.60% for CsPbI3 QDs. Notably, these devices also achieved the highest maximum luminance among all-solution processed PQDs-LEDs, with values of 33334 cd m–2 for CsPbBr3 and 224 cd m–2 for CsPbI3 QDs.

Environmental-friendly extraction of di(2-ethylhexyl) phthalate from poly(vinyl chloride) using liquefied dimethyl ether

Poly(vinyl chloride) (PVC) is one of the most widely used plastics. However, a major challenge in recycling PVC is that there is no economical method to separate and remove its toxic phthalate plasticizers. This research made a breakthrough by extracting PVC with liquefied dimethyl ether (DME) and successfully separating the plasticizer components. Nearly all (97.1 %) of the di(2-ethylhexyl) phthalate plasticizer was extracted within 30 min by passing liquefied DME (285 g) through PVC at 25 °C. The compatibility of PVC with organic solvents, including liquefied DME, was derived theoretically from their Hansen solubility parameters (HSP), and actual dissolution experiments were conducted to determine the optimal PVC solvents. A liquefied DME mixture was used to dissolve PVC, and the extract was diluted with ethanol to precipitate the dissolved PVC. We demonstrated that liquefied DME is a promising method for producing high quality recycled products and that the process retains the fundamental properties of plasticizers and PVC without inducing degradation or depolymerization. Because of its low boiling point, DME can be easily separated from the solute after extraction, allowing for efficient reuse of the solvent, extracted plasticizer, and PVC. DME does not require heat and produces little harmful wastewater, which significantly reduces the energy consumption of the plasticizer additive separation process.

Soft-Hard segments regulated framework of Nitrogen-Doped reduced graphene oxide aerogel for efficient adsorption of pollutants

Graphene aerogel (GA) is recognized for its high porosity, rendering it a promising candidate for water treatment applications. However, its reuse potential is hampered due to inherent limitations. To address this, the present study introduces a nitrogen-doped graphene aerogel (NGA) developed by integrating polydopamine soft segments and polyaniline hard segments into the GA matrix. This approach promotes the formation of a cohesive and durable 3D network by bridging reduced graphene oxide (rGO) nanosheets, with the hard segments of polyaniline interposed among rGO layers to mitigate significant restacking, thereby enhancing surface area and adsorption sites. NGA demonstrates remarkable properties including strength (67 kPa), reversible compressibility under 64 % strain, low density (12.26 mg/cm3), and thermal stability (Tdecomposition = 679.6 °C in air), which collectively enhance its adsorption capacity and recyclability. This study further examines the influence of various factors such as pH, adsorbates (dyes and organic solvents), initial concentration, and cycle times on the aerogel’s adsorption efficacy. Additionally, simulation outcomes reveal that NGA’s adsorption kinetics and thermodynamics align more closely with the endothermic pseudo-first-order kinetic model, indicative of predominant physical adsorption mechanisms. Given its superior adsorption capabilities for pollutants, NGA holds significant promise for application in water treatment.

Solvent-free Approaches towards the Synthesis of Therapeutically Important Heterocycles

Abstract: The development of synthetic methodologies to obtain a diverse range of heterocyclic scaffolds has been a very attractive area of research due to their vast therapeutic importance. Conventional approaches that require the use of organic solvents, which are generally flammable, toxic, and not ecofriendly, are replaced either with greener alternatives or by completely avoiding their use. In literature, several solvent-free methods have already been reported for the synthesis of vast varieties of organic compounds. This review focuses on the solvent-free methods developed for the synthesis of different types of nitrogen and oxygen heterocycles which have exhibited diverse therapeutic applications.

Alkanediol–hexafluoroisopropanol amphiphilic supramolecular solvent: Fabrication, characterization, and application potential for doping control of hormones and metabolic modulators in human urine

A novel amphiphilic supramolecular solvent (SUPRAS) was developed by hexafluoroisopropanol (HFIP)-induced self-assembly of 1,2-hexanediol in an aqueous matrix. Its application potential in multiclass determination was assessed by extracting from urine 10 prohibited hormones and metabolic modulators (log P from 2.38 to 7.57) listed by the World Anti-Doping Agency (WADA). This SUPRAS is stably formed across a wide pH range (2–12) and is unaffected by salt concentrations (<10 % g mL−1 of NaCl), and it has a higher density than water. The dehydration and hydrogen bonding ability of HFIP, as well as hydrophobic interactions between alkanediols, dominates the formation of the SUPRAS. The nanostructure of the SUPRAS, composed of 1,2-hexanediol, HFIP, and a high content of water (>25 %, w/w), forms large spherical micellar aggregates (10–100 μm) that exhibit amphiphilic properties. A 1,2-hexanediol-HFIP SUPRAS-based liquid-phase microextraction (LPME) method for detection of selected prohibited drugs in urine coupled with liquid chromatography–tandem mass spectrometry (LC-MS/MS) was established, optimized, and validated. The method showed fast extraction time (30 s of vortex) and low solvent consumption (160 μL of organic solvent). Under the optimal conditions (7 % g mL−1 of 1,2-hexanediol, 10 % v/v of HFIP), the SUPRAS achieved high extraction efficiencies (>80 %) and an enrichment factor of 6.0, with minimal matrix effects for all analytes due to its high amphiphilicity and large surface area. The method demonstrated excellent linearity (R ≥ 0.9909), with method limits of detection ranging from 0.018 to 0.18 ng mL−1 and method limits of quantitation ranging from 0.060 to 0.60 ng mL−1, which are well below the minimum required performance levels set by authorities. Furthermore, the intra- and inter-day relative recoveries for spiked human urine samples varied in the ranges of 90.3 %–121 % and 88.1–119 %, respectively, with relative standard deviations less than 13 % and 19 %, respectively. This SUPRAS-based LPME method proves to be simple, highly efficient, and eco-friendly, and it has promising potential for multiclass determination in doping control.

Enantioselective liquid-liquid extraction of 2-cyclohexylmandelic acid enantiomers using chiral ionic liquids.

Obtaining optically pure compounds in an eco-friendly and cost-efficient manner plays an important role in human health and pharmaceutical industry. Racemic separation using multistage stereoselective liquid-liquid extraction has become one of the most practical and effective approach to access homochiral enantiomers. Currently, chiral ionic liquids (CILs) with structural designability have become a promising chiral additive and enable them as adjustable candidates for racemic separation. Herein, a high-effective stereoselective liquid-liquid extraction process composed of imidazolium cations and amino acid-derived anions as the chiral additive was established for racemic 2-cyclohexylmandelic acid (CHMA) separation. We have systematically investigated the choice of organic solvent, concentration of CIL, extraction temperature, and the pH of aqueous phase. For three-stage stereoselective extraction, the maximum enantiomeric excess (e.e.) for CHMA was reached up to 40.6%. Furthermore, the mechanism of steric effect and stereoselective capacity between the CILs and racemic CHMA was discussed and simulated. We envision that the work will facilitate the development of CILs in multistage liquid-liquid extraction and promote the large-scale production of optically pure enantiomers.

Synthesis of Cd (II), Fe (III), Cu (II), and Cr (VI) complexes of Schiff bases and their antibacterial activities

Schiff base and the metal derivatives have been utilized in numerous areas of the economy. Synthesis and antibacterial activities of Cd (II), Cr (VI), Cu (II), and Fe (III) complexes of Schiff bases were evaluated in this work. Complexes synthesized were Bis(1-phenyl-3-methyl-4-Phenyl acetyl 5-pyrazolone)Cadmium (II) (Cd(HPMPP)2), Tris(1-phenyl-3-methyl-4-benzoyl-5-pyrazolone)Iron(III)(Fe(HPMBP)3), Bis(1-phenyl-3-methyl-4-phenylacetyl-5-pyrazolone)Copper (II) (Cu(HPMPP)2), Hexakis(1-phenyl-3-methyl-4-palmitoyl-5-pyrazolone)Chromium (VI) (Cr(HPMPP)6), and Tris(1-phenyl-3-methyl-4- palmitoyl-5-pyrazolone)Iron (III) (Fe(HPMPP)3). The physical state, colour, and melting point of these complexes were determined using appropriate analytical techniques. Results showed that all the complexes were crystalline in nature; their colours were variable, while their melting points were sharp. The solubility of these complexes in deionized water, acetone, methanol, and ethanol was also carried out. The outcome revealed that all the metal complexes were insoluble in deionized water, Cr(HPMPP)6 was soluble in acetone, methanol, and ethanol. However, the solubility of other metal complexes in the organic solvents used was variable. The antibacterial activities of these metal complexes at different concentrations were also tested against distilled water, E. coli, S. aureus, B. subtillus, and S. typhi. The results showed that, antimicrobial activity of these complexes against distilled water was negative whereas, the bacterial growth of all the bacteria was inhibited by the complexes though at different rates. The inhibition rate of microorganisms was inversely proportional to the concentration of the complexes. The antibacterial activities of Cd(HPMPP)2 and Cr(HPMPP)6 were outstanding against the growth of all the bacteria. Thus, a proper processing of these complexes might result in excellent antibacterial drugs. However, more studies on the mode of action of these complexes against microorganisms and their toxicity should be done in order to establish their potentials for pharmaceutical applications.

Study on the swelling of macromolecular geological organic matter with hydrocarbons and heteroatomic compounds

In this study, we conducted swelling experiments on eleven macromolecular geological organic materials using five types of organic solvents. Our primary objective was to investigate the absorption capacity of different solid organic materials in organic fluids and analyze the influence of their chemical structures. The samples utilized in this research included solid bitumen, kerogen, and coal samples from various basins. The chemical structure of the samples was assessed using solid-state 13C nuclear magnetic resonance (NMR), while X-ray diffraction (XRD) was employed to monitor any detect the structural changes during the swelling process. Our findings reveal that macromolecular geological organic compounds demonstrate a preferential expulsion of saturated hydrocarbons, followed by polycyclic aromatic hydrocarbons, upon interaction with liquid organic matter. The sulfur-containing compounds in solid organic matter demonstrated higher solubility than hydrocarbon compounds, while the solubility of oxygen-containing compounds varied based on the structure of the aliphatic chain and the proportion of oxygen atoms. This research, introduces LA [= Lac × Aac] as a new parameter to assess the combination of aliphatic chain length [Lac] and [Aac] abundance in solid organic matter. Furthermore, XRD testing revealed that the chemical structure unit of heteroatom compounds in solid organic matter consists of amorphous carbon, primarily composed of aliphatic chains. In this study, we evaluated the retention capacity of various macromolecular geological organic matter for both hydrocarbons and heteroatomic compounds. Additionally, the extent of swelling was investigated, providing theoretical support to diverse fields including organic petrology, petroleum geology, coal geology, and organic geochemistry.

Assessing Environmental Impact: Organosolv Extraction of Cellulose Pulp from Wood Waste

In the upcoming years, the paper industry is expected rely on containerboard for packaging, with approximately 80% of it being made from recycled fibers by 2020. Creating a new supply chain for fibers could help mitigate possible shortages. In this context, wood waste emerges as a valuable resource with the potential to serve as a plentiful and cost-effective reservoir for generating new materials, as cellulose fibers. This study presents an assessment of the environmental impact associated with the organosolv extraction of cellulose pulp from wood waste based on a previous in lab study conducted by the authors. The increasing demand for sustainable materials has prompted exploration into alternative methods for cellulose pulp production, with a focus on minimizing environmental footprint. Organosolv extraction, a promising technique, involves the use of organic solvents and acid catalysts to break down lignocellulosic biomass, resulting in high-quality cellulose pulp production. To evaluate the environmental implications of this process, a comprehensive life cycle assessment (LCA) approach was adopted. The LCA framework considers all stages of the organosolv extraction process, from wood waste collection to cellulose pulp manufacture, using a gate-to-gate approach. The functional unit for assessment is set as one ton of cellulose pulp. The dataset utilized for the LCA comprises primary data obtained from laboratory experiments, complemented by secondary data sourced from literature and the Ecoinvent life cycle inventory database. Furthermore, sensitivity analysis was conducted to assess the influence of key parameters on the environmental performance of the organosolv extraction process, with a focus on variations in energy consumption to identify potential areas for optimization and improvement. In summary, this study emphasizes the environmental aspects of utilizing organosolv extraction for cellulose pulp production from wood waste. Further research is warranted to explore energy consumption during the organosolv process for obtaining more precise data and optimizing the process. This could be achieved through pilot-scale experiments or utilizing process simulation software.

Adhesive Zwitterionic Poly(ionic liquid) with unprecedented Organic Solvent Resistance.

The resistance of adhesives to organic solvents is of paramount importance in diverse industries. Unfortunately, many currently available adhesives exhibit either weak intermolecular chain interactions, resulting in insufficient resistance to organic solvents, or possess a permanent covalent crosslinked network, impeding recyclability. This study introduces an innovative approach to address this challenge by formulating zwitterionic poly(ionic liquid) (ZPIL) derivatives with robust dipole-dipole interactions, incorporating sulfonic anions and imidazolium cations. Due to its unique dynamic and electrostatic self-crosslinking structure, the ZPIL exhibits significant adhesion to various substrates and demonstrates excellent recyclability even after multiple adhesion tests. Significantly, ZPIL exhibits exceptional adhesion stability across diverse non-polar and polar organic solvents, including ionic liquids, distinguishing itself from non-ionic polymers and conventional poly(ionic liquid)s. Its adhesive performance remains minimally affected even after prolonged exposure to soaking conditions. The study presents a promising solution for the design of highly organic solvent-resistant materials for plastics, coatings, and adhesives. This article is protected by copyright. All rights reserved.

Superhydrophobic Highly Flexible Triple-Network Polyorganosiloxane-Based Aerogels for Thermal Insulation, Oil-Water Separation, and Strain/Pressure Sensing.

Polyvinylpolymethylsiloxane (PVPMS)/polydimethylsiloxane (PDMS) copolymer aerogels were synthesized via consecutive radical polymerization and cohydrolytic polycondensation of vinylmethyldimethoxysilane and dimethyldimethoxysilane, followed by supercritical drying or ambient pressure drying. The resultant PVPMS/PDMS copolymer aerogels exhibit a highly porous, tunable triple-network structure consisting of interlinked hydrocarbon polymers, PVPMS and PDMS. These aerogels display superhydrophobicity (151°), low density (109 mg cm-3), low thermal conductivity (29.8 mW m-1 K-1), and adjustable pore structure. The combination of good machinability, low thermal conductivity, excellent compressive elasticity and bending flexibility, and efficient organic solvent adsorption gives these aerogels broad application prospects in thermal insulation and oil-water separation. In addition, PVPMS/PDMS/carbon nanotube (CNT) composite aerogels were obtained by incorporating the conductive CNTs, followed by vacuum drying. The resultant PVPMS/PDMS/CNT composite aerogel exhibits high sensitivity with a broad pressure sensing range in strain and pressure sensing applications.

Cation-Modified Poly(vinyl alcohol) Film to Optimize the Bistability of Transparent Electrophoretic Display Based on Charge Adsorption Behavior in Nonpolar Solvent.

Electrophoretic displays (EPDs) utilize the electrophoretic particles in electronic ink (e-ink) to display different color states with bistability. Bistability of EPDs is achieved by placing colloidal particles in a highly viscous solvent to keep the distribution of colloidal particles stable without sustaining the external field, so it only consumes power when updating the image. The feature of low power consumption makes it suitable for applications such as advertising boards, price tags, etc. Apart from these applications, recent research on lateral-driving EPDs extends its applications to smart windows, privacy control, and so on. However, achieving bistability by simply increasing the viscosity of solvent is inefficient in the case of lateral driving operation. Therefore, it is deserving to have intensive study on the mechanism of bistability from other aspects. Herein, we propose a mechanism to investigate the charge adsorption behavior on the electrode to affect the bistability of particles, which is based on the "Stern layer adsorption/desorption" model. Based on the above mechanism, we further fabricated a hexadecyl trimethylammonium bromide (CTAB)/poly(vinyl alcohol) (PVA) composite film on the electrode to improve the bistability of lateral-driving EPD by reducing the diffusion current caused by unabsorbed charges. This developed lateral-driving EPD can significantly improve the bistability, which is enhanced from 40 s to 7 min, an increase by a factor of approximately 10. This work gives a way to consider the bistability of colloidal particles in nonpolar solvent.

Histone demethylase KDM4A mediating macrophage polarization: A potential mechanism of trichloroethylene induced liver injury.

Trichloroethylene (TCE) is a commonly used organic solvent in industry. Our previous studies have found that TCE can cause liver injury accompanied by macrophage polarization, but the specific mechanism is unclear. The epigenetic regulation of macrophage polarization is mainly focused on histone modification. Histone lysine demethylase 4A (KDM4A) is involved in the activation of macrophages. In this study, we used a mouse model we investigated the role of KDM4A in the livers of TCE-drinking mice and found that the expression of KDM4A, M1-type polarization indicators, and related inflammatory factors in the livers of TCE-drinking mice. In the study, BALB/c mice were randomly divided into four groups: 2.5 mg/mL TCE dose group and 5.0 mg/mL TCE dose group, the vehicle control group, and the blank control group. We found that TCE triggered M1 polarization of mouse macrophages, characterized by the expression of CD11c and robust production of inflammatory cytokines. Notably, exposure to TCE resulted in markedly increased expression of KDM4A in macrophages. Functionally, the increased expression of KDM4A significantly impaired the expression of H3K9me3 and H3K9me2 and increased the expression of H3K9me1. In addition, KDM4A potentially represents a novel epigenetic modulator, with its upregulation connected to β-catenin activation, a signal critical for the pro-inflammatory activation of macrophages. Furthermore, KDM4A inhibitor JIB-04 treatment resulted in a decrease in β-catenin expression and prevented TCE-induced M1 polarization and the expression of the pro-inflammatory cytokines TNF-α and IL-1β. These results suggest that the association of KDM4A and Wnt/β-catenin cooperatively establishes the activation and polarization of macrophages and global changes in H3K9me3/me2/me1. Our findings identify KDM4A as an essential regulator of the polarization of macrophages and the expression of inflammatory cytokines, which might serve as a potential target for preventing and treating liver injury caused by TCE.

Sodium Hypochlorite Pentahydrate as a Chlorinating Reagent: Application to the Tandem Conversion of β,γ-Unsaturated Carboxylic Acids to α,β-Unsaturated Lactones

Sodium hypochlorite pentahydrate (NaClO·5H2O, 1) has recently been employed in organic synthesis as an oxidant for alcohols, sulfides, glycols, etc. In most of these reactions, however, reagent 1 functions just as a simple oxidant, and the variations of the reactions have not been well explored. In this study, we report another useful and fascinating reaction, in which reagent 1 functions as a green chlorinating reagent toward β,γ-unsaturated carboxylic acid (2). When substrate 2 was stirred at room temperature with 1 (2 eq) in acetonitrile for 1 h, α,β-unsaturated lactone (3) was obtained in moderate yields (up to 62%). The same reaction proceeded in various organic and aqueous solvents as well. When excess reagent 1 was employed, lactone 3 was further oxidized to the corresponding epoxide (4) for some cases. The conversion is initiated by electrophilic attack of HOCl to the C=C bond of 2 to generate a chloronium ion intermediate, which is cyclized to β-chlorolactone (5) and then 3 through the elimination of HCl. The usefulness of 1 as a chlorinating reagent was further demonstrated in the electrophilic substitution of activated aromatic compounds.

A Kinetic and Mechanistic Study of Ir (III)-Catalyzed Oxidation of Methionine by HCF (III) in an Aqueous Alkaline Medium

Introduction: The kinetic study of Ir (III) chloride-catalyzed oxidation of methionine by hexacyanoferrate (abbreviated as HCF) III ions in aqueous alkaline medium was performed spectrophotometrically at constant ionic strength of 0.5 moldm-3 and temperature of 35±0.10C. Method: The progress of the reaction was found to be first-order rate dependence kinetics with respect to [HCF (III)], [OH-], and [IrCl3]. The rate of reaction was found to decrease with an increased concentration of methionine. The ionic strength of the reaction mixture showed a positive salt effect on the reaction rate. Different activation parameters were also evaluated by studying the reaction at four different temperatures. The stoichiometry of the reaction showed Methionine: HCF (III) = 1:4. Result: The oxidation product of the reaction was found to be methionine sulphone, which was identified by an organic solvent method and IR Spectroscopy. Further, a suitable mechanism was proposed to explain all the experimental results. Conclusion: It is assumed that the reaction proceeded through complex formation between substrate (abbreviated) and iridium trichloride. A rate law was derived, which verified the results. CH3-S-(CH2)2-CH (NH2)-COO- + 4HCF (III) Ir (III), H2O CH3-SO2-(CH2)2-CH- (NH2)-COO- + 4HCF (II) result: 1.Methionine sulphone was found to be the main product of oxidation was identified using an organic solvent method and IR Spectroscopy. A suitable mechanism has been proposed to explain all the experimental results. It is assumed that reaction proceeds through complex formation between substrate (abbreviated) and iridium trichloride. A rate law has been derived which verifies the results. CH3 –S-(CH2)2-CH (NH2) – COO- + 4HCF (III) □(→┴(Ir(III),H2O) ) CH3-SO2-(CH2)2-CH (NH2)-COO- + 4HCF (II) 2. Degradation kinetic is anticipated to follow the first order kinetics at lower concentration. 3. The catalytic system can be recycled and reused without loss of activity. 4. The anticipated easy recovery of catalyst from the reaction mixture shows another positive signigficance.

Sonoprocesses for sustainable textile processing and nanofinishing: a review

The textile sector is widely acknowledged as one of the most environmentally damaging sectors globally, primarily due to its high consumption of water and energy, utilization of chemicals, and the discharge of waste water containing a complex mixture of hazardous substances. The incorporation of nanotechnology, particularly through wet processes involving nano finishes, while enhancing textile functionality, further exacerbates these environmental concerns. Consequently, the exploration and promotion of sustainable methodologies are imperative across all wet treatments in textile processing. Among the potential solutions, sonoprocesses stand out as a promising avenue for mitigating resource consumption, and supporting environmentally friendly synthesis and application of nanomaterials to textiles. Sonoprocesses offer the advantage of carrying processes at low temperature and pressure, and the use of aqueous media instead of organic solvents. This comprehensive review delves into the multifaceted applications of sonoprocesses within the textile realm, with a specific emphasis on the synthesis and application of nanomaterials to textiles. Discussing the diverse applications of sonoprocesses, this study will pave the way for the integration of these techniques within the textile industry, ultimately aiming for widespread adoption on a commercial scale. This will help in promoting sustainable practices and reducing the ecological footprint of the textile sector.

Extraction of Dual‐Switch Fluorescent Nanosheets from Asphaltenes under Ambient Conditions

AbstractAsphaltene, often regarded as an undesirable by‐product of petroleum processing, possesses abundant reserves but limited market value. In this study, a simple and environmentally friendly solvent extraction method is conducted under ambient conditions to convert low‐value asphaltene into high‐value asphaltene‐based fluorescent carbon nanosheets (a‐FCS). This approach yields dual‐switch a‐FCS capable of emitting orange‐red fluorescence in solid‐state or water environment and exhibiting blue‐to‐yellow fluorescence in organic solvents. Moreover, the redshift observed in the fluorescence emission wavelength in the solvent is attributed to its intrinsic self‐assembly behavior, which becomes more pronounced with increasing concentration. Upon introduction to water, hydrophobic interactions induce the aggregation of a‐FCS. This aggregation triggers the orange‐red fluorescence by restricting intramolecular rotation on the surface, a phenomenon facilitated by the entanglement of aliphatic chains from asphaltene molecules. This unique property makes them applicable in anti‐counterfeiting and determination of ethanol content in aqueous solution.

Comments Regarding “Solubility determination and thermodynamic model analysis of L-α-glyceryl phosphorylcholine in different organic solvents of 278.15–323.15 K”

A polemic is given regarding several of the calculated curve-fit parameters that Zhou and coworkers reported in their published paper. The calculated curve-fit parameters for the Combined Nearly Ideal Binary Solvent/Redlich-Kister, Jouyban-Acree-van’t Hoff, Sun and modified Apelblat models were found to give mole fraction solubilities that exceeded unity. Our analysis also found that the mean relative absolute percent deviations provided by the authors were significantly underestimated.