Ternary Solvent Research Articles

Synthesis of Raspberry-like PMMA Particles In a Ternary Solvent Mixture with Binary Initiators.

There is continuing interest in the synthesis of raspberry-like polymer particles, among which most of the reports have tended to focus on polymer composite particles, while there are relatively few examples of polymer particles with a single component. In this study, raspberry-like poly(methyl methacrylate)(PMMA) particles were synthesized by a one-step method in a ternary solvent mixture with binary initiators. The effects of different polymerization parameters, including the solvent composition, the initiator composition, the stabilizer component, the polymerization temperature, the stirring rate, and the nature of the monomer, on the morphology and size of the resulting particles were studied. A plausible mechanism for raspberry-like particle formation was suggested based on the monitoring data of the polymerization kinetics. The raspberry-like PMMA particles have a high dispersion stability in a salty aqueous environment.

A novel ternary hydrophobic deep eutectic solvent over a wide pH range for lithium recovery

Owing to the crucial role of lithium (Li) in green technology and energy storage, the global demand for Li is constantly increasing. This article provides a new strategy for recovering Li using ternary hydrophobic deep eutectic solvent (HDES). The novel HDES was composed of 2-thiophenyltrifluoroacetone (HTTA), trioctylphosphine oxide (TOPO), and N,N-diethyldecanamide (DDA), and exhibited high efficiency and selectivity for extracting Li from aqueous solutions. This study systematically evaluated the effect of the initial aqueous pH on the Li extraction efficiency, revealing the stable performance of HDES in the pH range 3–13. Compared to the highly alkaline environment required for Li extraction, the pH characteristics of the HDES provide a wider range of applications and a more environmentally friendly alternative. The HDES exhibited rapid extraction kinetics, achieving equilibrium within 10 min and maintaining phase stability without emulsification. The main mechanism of selective Li extraction is the electrostatic interaction between Li(I) and TTA. The interactions between Li(I) and both TOPO and DDA were confirmed by Fourier transform infrared (FT-IR) spectroscopy, thereby improving the selectivity and extraction efficiency. The countercurrent extraction process demonstrated an impressive Li extraction rate of 98.704 % and a Li(I)/Na(I) separation factor of 10643.14 with industrial Li2CO3 mother liquor, highlighting the application potential of the ternary HDES. The excellent performance of the HDES over a wide pH range provides more opportunities for its application, and its high efficiency, selectivity, and environmental characteristics may promote Li recovery.

Use of a rugged mid-infrared spectrometer for in situ process analysis of liquids

The widespread application of mid-infrared (MIR) spectroscopy for process monitoring is currently limited by the poor transmission of MIR light through fibre optics. In this work, the performance of a novel and robust MIR spectrometer has been evaluated for practical deployment in a pilot plant or production environment. The spectrometer utilises a Sagnac interferometer design containing no moving parts and is directly attached to an attenuated total reflectance probe, eliminating the need for fibre optics. The quantitative performance of the spectrometer for the in situ analysis of ternary solvent mixtures was assessed. The predictions obtained by partial least squares were accurate (root mean square error of prediction of < 1% w/w) and comparable to those of a benchmark Michelson-based spectrometer with a fibre-coupled probe, which is more amenable to process development in a laboratory or pilot plant. Calibration transfer between the two spectrometers was performed using the spectral space transformation method to mimic the scenario of the scale-up of a process from the laboratory to pilot scale or from a pilot plant to production scale, where the two different MIR instruments might be deployed. The ability to perform in situ reaction monitoring with the robust Sagnac-based spectrometer was then demonstrated. Spectra acquired during an esterification reaction were resolved using multivariate curve resolution, to produce concentration profiles of each component. These results demonstrate the suitability of this rugged spectrometer for quantitative in situ monitoring of liquid processes, opening up new opportunities for process monitoring in the MIR region.

A Universal Ternary Solvent System of Surface Passivator Enables Perovskite Solar Cells with Efficiency Exceeding 26.

Surface passivation is a vital approach to improve the photovoltaic performance of perovskite solar cells (PSCs), in which the passivator solvent is an inevitable but easy-ignored factor on passivation effects. Herein, a universal ternary solvent system of surface passivators is proposed through comprehensively considering the solubility and selective perovskite dissolution of the solvent to maximize the passivation effect. Tetrahydrothiophene 1-oxide (THTO) is selected as the passivation promoter by comparing the binding energy with perovskite and the ability to distort the perovskite lattice among various aprotic polar solvent molecules, which can facilitate the passivator's reaction with perovskite and achieve sufficient passivation on perovskite surface. Besides, chlorobenzene (CB) is used as the diluting agent to minimize the amount of isopropanol (IPA), inhibiting the additional solvent-induced defects. As a result, the planar PSCs achieve a power conversion efficiency (PCE) of 26.05%, (certificated 25.66%). Besides, the unencapsulated devices exhibit enhanced stability, which can maintain 95.23% and 95.68% of their initial PCE after 2000h of storage in ambient air and 800h of light-soaking in N2-glovebox. Moreover, this ternary solvent system also exhibits a well applicability and reliability in different passivator such as PEAI, BAI, and so on.

Binary and Ternary Deep Eutectic Solvents for Methylene Green Electropolymerization on Multiwalled Carbon Nanotubes: Optimization, Characterization and Application.

Choline chloride (ChCl) based binary and ternary deep eutectic solvents (DES) were evaluated for methylene green electropolymerization with oxalic acid (OA) and ethylene glycol (EG) as hydrogen bond donors. Binary DES ChCl : OA in molar ratios 1 : 1 and 2 : 1 and ChCl : EG 1 : 2 and ternary DES (tDES) in different molar ratios and percentages of water were evaluated. The highest polymer growth was in ChCl : OA : EG-tDES with 13% added water, that had a lower viscosity and higher ionic conductivity when associated with HCl as dopant. This enhanced the formation of more cation radicals and, consequently, more polymer formation. The PMG/MWCNT/GCE-tDES sensor was successfully applied to the simultaneous determination of 5-aminosalicylic acid (5-ASA) and acetaminophen (APAP) by differential pulse voltammetry in the concentration range 1 μM-200 μM, with detection limits of 0.37 μM and 0.49 μM for 5-ASA and APAP, respectively. The sensor demonstrated good repeatability, reproducibility and stability, and was successfully applied in pharmaceutical formulations.

Enhanced Nanocellulose Production from Cotton and Textile Waste Using Binary and Ternary Natural Deep Eutectic Solvents

Enhanced Nanocellulose Production from Cotton and Textile Waste Using Binary and Ternary Natural Deep Eutectic Solvents

Phase-separated solvothermal high yields recovery of lithium and cobalt cathode precursors from end-of-life LiCoO2 lithium-ion batteries

Lithium-ion batteries (LIBs) recycling is one of the most urgent challenges affecting this technological sector. Indeed, their continuously growing production and demand is already leading to the creation of large volumes of end-of-life LIBs (EoL-LIBs). At the same time, the growing demand for LIBs is not sustainable from the point of view of supply of the critical raw materials needed to produce the essential components of LIBs. The development of efficient and sustainable recycling strategies provides a solution to these two urgent issues. Here we propose a new ternary deep eutectic solvent (DES) composition based on choline chloride, citric acid, and ethylene glycol in molar ratio 1:1:1 for the reductive degradation of LiCoO2 cathode. The optimized leaching process (5g of DES for 100 mg of black mass for 30 min at 140 °C) leads to the full degradation of the cathode with extraction yields above 97% for both Li and Co. Simple electrochemical tests confirm irreversible DES degradation, making its recovery and reuse impractical. We demonstrate that a subsequent thermal treatment, using DES as a sacrificial agent, allows to separate and recover Co3O4 and LiCl with adequate purity to be exploited for LiCoO2 resynthesis. As a proof of concept, a new batch of LiCoO2 is synthesized and used for new cells’ assembly. The performance of the resynthesized material is comparable with that of the commercial benchmark material, demonstrating the possibility of a full closed-loop recycling route.

Precursor Ink Engineering to Implement Vacuum Extraction Method for Scalable Production of Perovskite Solar Cells.

Engineering perovskite precursor ink to widen the processing window is crucial to obtaining uniform, compact, and pinhole-free perovskite films at scale using industrially relevant solution coating techniques. Here, we introduce a ternary solvent system and systematically investigate the impacts of coordinating solvents, N-methyl-2-pyrrolidone (NMP) and N,N'-dimethylpropyleneurea (DMPU), on the physical properties of the slot-die-coated perovskite films and on the corresponding device performance. Tailoring NMP and DMPU concentrations in the precursor ink allows us to control the perovskite intermediate phase formation and widen the processing window, enabling the reproducible production of perovskite films with high photoelectrical quality at scale. Using the optimized precursor ink, we demonstrate slot-die-coated perovskite minimodules with power conversion efficiencies of 19 and 16% on 56 and 100 cm2 substrates, respectively.

A green extraction technology of lignocellulose from cassava residue by mechanical activation-assisted ternary deep eutectic solvent

Lignocellulose (LC) is a natural polymer material that holds immense potential for various applications. However, extracting LC from biomass wastes with high-starch content has been challenging due to low selectivity and yield. In this study, LC was prepared from cassava residue (CR) via a combination of mechanical activation pretreatment and a citric acid (CA)-enhanced ternary deep eutectic solvent (TDES) consisting of choline chloride (ChCl), lactic acid (LA), and CA. The mechanical activation reduces the size of CR, greatly promoting the removal ability for starch, lignin and hemicellulose using TDES, and thus improving yield and selectivity of LC through this method. The CA esterified LC to prevent its excessive hydrolysis and increased a significantly higher LC content (82.52 wt%) compared to mechanical activation only and DES without CA, increasing by 6.97 times and 1.26 times, respectively. The extraction temperature significantly affected the structure, composition, thermal stability of LC and the properties of recovered TDES. The LC extracted at 90 °C (LC-90) had the highest cellulose content (82.52 wt%), crystallinity index (44.82 %), and higher degradation temperature (339.7 °C). The properties of the recovered TDES and extraction mechanism were analyzed. This study provides a strategy for the high-value utilization of biomass waste.

Novel ternary deep eutectic solvents pretreatment of corn stalk to realize high-value utilization

The high-valued utilization of biomass components through pretreatment technology can effectively alleviate the pressure of energy and environment. In this study, a ternary deep eutectic solvent (TDES) was prepared by using glycolic acid (GA) and ethylene glycol (EG) as double hydrogen donors and benzyl trimethyl ammonium chloride (TMBAC) as hydrogen acceptor. The corn stalk was separated by TDES to obtain cellulose-rich solid residue and low-condensed lignin. Moreover, the solid residue was converted into bio-oil by rapid pyrolysis, and the low-condensed lignin was converted into fluorescent lignin by grafting luminol for information encryption. The results showed that under the pretreatment condition of 150℃ for 3 h, TDES with the molar ratio of 1:1:2 had a lignin removal ratio of 90.60 %, and the yield of levoglucosan obtained from solid residue pyrolysis bio-oil reached 36.38 %. Furthermore, TDES prevented lignin from forming a C-C polycondensation structure and endowed it with polyhydroxy properties, which was beneficial to graft luminolto enhance the fluorescence intensity efficiently. The high-intensity fluorescent grafted lignin was used for information encryption of various materials. The mechanism of TDES pretreatment and luminol grafting were explored, and the mass balance of corn stalk during pretreatment was described. This study provides a green, environmentally friendly, and efficient pretreatment process for the high-value utilization of biomass.

Efficient β-carotene recovery from surfactant-based aqueous solutions: Advancing from experimental to process simulation

β-carotene is a carotenoid present in the human diet with numerous functions in the body. This work suggests a new platform for efficiently recovering this bioactive compound from aqueous solutions. For the first time, a ternary deep eutectic solvent (DES) is proposed to promote phase separation in aqueous solutions of non-ionic surfactants (Triton X-102 and Tween 20). The influence of temperature on the miscibility regions was investigated from 298.15 K to 308.15 K as a preliminary step. The obtained phase diagrams at three temperatures were accurately correlated using four empirical equations. The extraction capacity of these novel combinations was analysed by means of the Tie-Lines (TL) and their derived magnitudes: Tie-Line Length (TLL) and Slope (S). The reliability of the TLs was ascertained through three empirical equations. Analysis of the data showed that more than 99 % of the model carotene could be extracted using ChCl:U:Gly from a Triton X-102 aqueous solution at 308.15 K. Process simulation using SuperPro Designer confirmed that an effective and sustainable process for recovering β-carotene from algal biomass can be designed using a simple approach.

Activation of muscle amine functional groups using eutectic mixture to enhance tissue adhesiveness of injectable, conductive and therapeutic granular hydrogel for diabetic ulcer regeneration

Herein, Polydopamine-modified microgels and microgels incorporated with superficial epoxy groups were synthesized and applied as precursors for the fabrication of four granular hydrogels. To enhance the tissue adhesiveness, a ternary deep eutectic solvent was synthesized to activate the muscle amine functional groups facilitating the formation of robust NC bonds at ambient conditions. At a certain shear rate of 10 s−1, hydrogel DMG displayed a viscosity of 9×103 Pa/s, representing the highest complex viscosity among the tested hydrogels primarily driven by quinone groups in PDA which enhanced reversible interactions, thereby increasing particle cohesion. Moreover, the intersection point escalating from about 4×103 to approximately 9×104 as the concentration of DMG increased from 0 % (for MG) to 70% (7D3MG) by weight. There was a decrease in adhesion strength from 0.45 ± 0.08 N in MG to 0.39 ± 0.16 N, 0.35± 0.18 N, and 0.33 ± 0.15 N for 3D7MG, 7D3MG, and DMG respectively, suggesting that MG was capable of forming numerous covalent bonds, thereby enhancing its adhesion to the substrate. The type of eutectic mixture affected the electrical conductivity and a very important point was the changes in resistance value with time. For MG catalyzed by [DES]AZG, the resistance increased only by 1.3 % (from 3.37 to 3.81 kΩ) at day 3 and 37.09 % (from 3.37 to 4.62 kΩ) at day 5. The 3D7MG hydrogel exhibited superior therapeutic efficacy toward diabetic wound regeneration. The proliferation index value for 3D7MG-[DES]AZG and 3D7MG-[DES]AG were calculated 42.3 % and 58.6 %, respectively, while the control group exhibited a lower value of 37.8 %.

Environmentally stable, Adhesive, Self-healing, Stretchable and Transparent Gelatin based Eutectogels for Self-Powered Humidity Sensors

Intrinsic environmental and stability limitations of hydrogels have inhibited their practical applications as a flexible wearable device due to water evaporation or freezing in complex environments such as low temperatures and arid environments. In this work, a multifunctional gelatin based ionic conductive eutectogel with double network structure is designed via ternary deep eutectic solvent (DES) (acrylic acid (AA), choline chloride (ChCl) and ethylene glycol (EG)). In this system, the introduction of ethylene glycol (EG) can be used to dissolve gelatin. The resulting DESG eutectogel exhibited excellent adhesion, mechanical robustness, anti-freeze, anti-drying, and self-healing. Interestingly, the DESG gels showed high humidity sensitivity in a wide humidity detection range (11 %–83 %), which can be assembled as a self-powdered humidity sensor to monitor human mouth and nose breathing. This work is expected to bring new prospect to construct high performance humidity sensors using gelatin based humidity-responsive materials for a wide range of potential applications in respiratory diagnostics, sleep monitoring, electronic skin and wearable electronics.

Synergistic ternary deep eutectic solvents: An archetype for sustainable and eco-conscious Li and Co recovery from spent batteries

The development of sustainable materials for energy is a critical challenge in the pursuit of a circular economy. This study presents an innovative approach for recycling lithium-ion batteries (LIBs) using a novel, sustainable deep eutectic solvent (DES) composed of glycine, ascorbic acid, and water. This natural, chloride-free ternary DES leverages the biocompatible and eco-friendly properties of its constituents, achieving exceptional leaching efficiency of 99.1 % for lithium and 97.9 % for cobalt under optimized conditions. A multifaceted methodology integrating advanced factorial design, kinetic modeling, and machine learning was employed to refine the process parameters and enhance leaching efficiency. The extraction kinetics were predominantly governed by endothermic surface reactions, characterized by activation energies of 81.5 kJ/mol for Co and 110.9 kJ/mol for Li. An ensemble neural network model accurately predicted the extraction with an R2 > 0.95, demonstrating the robustness of the computational approach. The DES exhibited excellent recyclability over five cycles, thereby emphasizing its potential for practical industrial applications in the field of sustainable materials management. This approach facilitated the selective recovery of high-purity lithium oxalate and cobalt oxalate, underscoring the efficiency and environmental benefits of the process. DFT calculations provided insights into the extraction mechanism, revealing the crucial role of hydrogen bonding and synergistic effects of the DES components. This pioneering study not only advances LIB recycling but also establishes a comprehensive, quantitatively validated framework, paving the way for future innovations in sustainable materials management and supporting global efforts towards a circular economy in energy storage.

Preparation of nanoporous poly (L-lactic acid) microspheres with controllable morphology via thermally-induced phase separation

This article describes a facile method to prepare nanoporous poly (l-lactic acid) microspheres via a thermally-induced phase separation method with controllable diameters. It was found that the morphology and diameter of PLLA microspheres were easily controlled by adjusting solvent ratio, quenching temperature, and PLLA concentrations. The results revealed that by using a ternary solvent system consisting of 1,3-dioxolane as a good solvent, 2-butanone as mid-solvent, and water as a poor solvent, the diameter of PLLA microspheres can be easily controlled by changing the ratio of 1,3-dioxolane and water. The diameter of PLLA microspheres prepared ranged from 28.8 ± 5.9 μm to 63.8 ± 12.5 μm. Moreover, the evolution of PLLA spherulitic structures grown from polymer solution was confirmed as well through varying solvent ratios and PLLA concentrations. The presence of water as a non-solvent governed the phase separation mechanism of the phase separation process. At the same time, the diameter of the spherulites is affected by the ratio of 1,3-dioxolane controlling the polymer crystallization process in the polymer-rich region. Interestingly, the surface of these spherulites contains nanopores due to the stacking of lamellar crystals of PLLA during polymer crystallization which contributed to its superhydrophobicity and superoleophilicity. Hence, the prepared PLLA spherulites were utilized as PLLA microspheres with nanoporous surfaces for the adsorption and removal of oil in oil/water and oil-in-water emulsion. This facile method provides a novel pathway to prepare nanoporous PLLA microspheres with controllable diameters for eco-friendly oil/water and oil-in-water separation applications.

Absorption-Desorption Characteristics of the Synthesized Deep Eutectic Solvents for Carbon Dioxide Capture

The development of an environmentally friendly CO2 absorbent with significant energy utilization which can be an alternative to CO2 capture by an ethanolamine solution is presently an obligatory issue. In this work, binary and ternary deep eutectic solvents (DESs) were prepared according to their CO2 absorption/desorption performances. A series of DESs comprise different hydrogen bonding donor (HBD)- acceptor (HBA) pairs as CO2 capturing solvents; HBAs include choline chloride (ChCl) and tetrabutylammonium bromide (TBAB), and selected amines are represented as HBDs and include monoethanolamine (MEA), diethanolamine (DEA), and triethanolamine (TEA). Binary DESs synthesized of ChCl/MEA, ChCl/DEA, ChCl/TEA, TBAB/MEA, TBAB/DEA, and TBAB/TEA in a CO2 absorption cell at a mole ratio of 1:4. While selected amidines were represented as super-based (SB) and included 1,5-Diazabicyclo [4.3.0] non-5-ene (DBN) and 1,8-Diazabicyclo [5.4.0] undec-7-ene (DBU). The ternary DESs were prepared by adding DBN or DBU to the binary DESs system in a (1:4:3) molar ratio. CO2 absorption experiments were attained at atmospheric pressure and a temperature of 30 °C using 15 vol.% CO2 with 85 vol.% N2. On the other hand, the regeneration process for DESs was conducted at 90 oC. Binary DES synthesized from ChCl/MEA gives a higher absorption rate of CO2 of 0.0177 mole/kg. min, CO2 absorption loading of 2.9092 mole CO2/kg solvent, cyclic loading of 2.0001 mole CO2/kg solvent, and a regeneration efficiency of 68.75%. The synthesis DESs showed a better performance compare with a common Ionic liquids.

Investigation of the extraction efficiency and antioxidant capacity of deep eutectic solvent-enhanced Paeonia lactiflora

Study has demonstrated that Paeonia lactiflora contains a significant number of polyphenolic compounds; however, there is little research literature focus on phenolic acids in Paeonia lactiflora. In this study, an ultrasound-assisted extraction method based on ternary DESs was developed for the extraction of biologically active polyphenols in Paeonia lactiflora. The results indicated that the ternary solvent composed of choline chloride, DL-lactic acid, and 1,2-propanediol in a molar ratio of 1:4:2 achieved a superior extraction of polyphenols than that of conventional solvents and other ternary solvents. Subsequently, the response surface method was used to optimize the selected parameters of solid–liquid ratio, extraction time, and temperature for the extraction of phenolic by the DES, and the optimal extraction conditions were as follows: a solid–liquid ratio of 1:13.8 g/mL, an extraction time of 47.5 min, and an extraction temperature of 34.5 °C, with a total polyphenol yield of 79.77 mg/g, which is 1.09 times that of the traditional solvent. Furthermore, the extract of Paeonia lactiflora obtained through the DES method exhibited promising in vitro antioxidant activity and reducing ability. Studies have shown that DES is an efficient and environmentally friendly extraction solvent for extracting polyphenols from natural products, providing a new direction for the development and industrial production of Paeonia lactiflora.

Recycled ionic liquid vs. deep eutectic solvent in cellulose nanocrystals production: Characterization, techno-economic analysis, and life cycle assessment

Three scenarios involving aqueous mixtures of neoteric solvents have been evaluated as solvents and catalysts for the cellulose hydrolysis reaction to obtain CNC in high yields (>70%). The scenarios considered were: scenario 1 (S1) involves a recyclable ionic liquid dilution of [Hmim][(HSO4)(H2SO4)]/H2O (64 wt% IL); scenario 2 (S2) another recyclable dilution of [Hmim][(HSO4)(H2SO4)]//H2O (80 wt% IL) and scenario 3 (S3) a non-recyclable ternary deep eutectic solvent (60 wt% DES: choline chloride: oxalic acid/30 wt% PA/10 wt% water). Experimental analysis, techno-economic, and life cycle analysis (LCA) indicate that S1 emerges as a suitable scenario among the three analyzed. S1 demonstrated the highest competitiveness, with a lower raw material cost per gram of CNC produced (US$0.81/g) and lower environmental contributions concerning climate change and fossil fuel depletion, accounting mainly for its recyclability. Therefore, the recyclable dilution of 64 wt% IL used in S1 appears to be the most viable option for sustainable and environmentally conscious CNC production. Besides, the physicochemical properties of the CNC were revealed: aspect ratio range 7–8, high dispersion stability related to zeta potential > −40 mV, good crystallinity range 50–80%, and thermal stability with Tonset> 300 °C. These results guided towards a scenario with crucial advantages: a diluted IL that retains its acidity after reuse cycles by a facile recovery process, maintaining high CNC production performance and providing low environmental impacts.

Molecularly Imprinted Polyaniline as Solid‐Phase Material for the Extraction of UV Filters From Waters

ABSTRACTSolid‐phase extraction (SPE) using a polyaniline molecularly imprinted polymer (PANI@MIP) is optimized for the extraction of benzophenone‐4 (BP4) from aqueous matrices. First, the three main variables influencing the washing step of the SPE method—type, composition, volume, and percolation flow rate of the washing solvent—were investigated. The optimal conditions for the washing step using the new PANI@MIP‐SPE for maximum retention of BP4 and elimination of interfering molecules (benzophenone‐3 [BP3] and benzophenone [BP]) were determined as follows: 1.25 mL acetonitrile/acetic acid/hexane (45/05/50 v/v/v) as wash solvent at a flow rate of 1 mL min−1. A multiple linear regression model was validated using Student's t‐test to identify the most significant variables affecting this step, including the type and volume of each eluent solvent and the volume of the ternary mixture solvents. The reliability of the model was further confirmed by analysis of variance (ANOVA) and Fisher's F‐test at α = 0.05. The extraction recoveries of the target analyte exceeded 92% over the range of concentrations (from 0.1 to 120 mg L−1), and the maximum retention capacity of PANI@MIP‐SPE was 600 µg g−1, in contrast to 50 µg g−1 for PANI@NIP‐SPE.

Ca2+/ethanol driven in-situ integration of tough, antifreezing and conductive silk fibroin/polyacrylamide hydrogels for wearable sensors and electronic skin

Integrating high strength, flexibility, biocompatibility, adhesion, and freezing resistance into conductive hydrogels for developing wearable electronic devices has consistently posed significant challenges in relevant research fields. Inspired by the silk dissolution behavior, a robust, flexible, antifreezing, and conductive silk fibroin/polyacrylamide (SF/PAM) hydrogel was synthesized in a CaCl2-ethanol–water (Ca2+/E/W) ternary solvent via a one-pot photogelation process. The gelation of SF and AM was enhanced by the ternary solvent, attributed to the inhibitory effects of Ca2+ ions and alcohols on hydrogen bond formation. The SF/PAM hydrogels based on Ca2+/E/W exhibited desirable mechanical properties (stretching: 800 % strain and 120 kPa stress; compression: 80 % strain and 334.0 kPa stress), excellent recoverability after deformation, high ion conductivity (2.4 S·cm−1) and strain sensitivity (gauge factor: ∼2.0), and low-temperature tolerance (−60 °C). These hydrogels were assembled into various wearable electronic devices, such as strain sensors, electronic skin, and electrodes, for detecting multiple physiological parameters, including joint activities, bioelectrical signals, and subtle movements like finger and wrist rotation, heartbeat, and vocal cord vibrations, demonstrating significant potential in flexible electronic applications.