Showing papers on "Ethylene glycol published in 2023"

Prioritizing Hetero‐Metallic Interfaces via Thermodynamics Inertia and Kinetics Zincophilia Metrics for Tough Zn‐Based Aqueous Batteries

Abstract: Poor thermodynamic stability and sluggish electrochemical kinetics of metallic Zn anode in aqueous solution greatly hamper its practical application. To solve such problems, to date, various zincophilic surface modification strategies are developed, which can facilitate reversible Zn plating/stripping behavior. However, there is still a lack of systematic and fundamental understanding regarding the metrics of thermodynamics inertia and kinetics zincophilia in selecting zincophilic sites. Herein, hetero‐metallic interfaces are prioritized for the first time via optimizing different hetero metals (Fe, Co, Ni, Sn, Bi, Cu, Zn, etc.) and synthetic solvents (ethanol, ethylene glycol, n‐propanol, etc.). Specifically, both theoretical simulations and experimental results suggest that this Bi@Zn interface can exhibit high efficiency owing to the thermodynamics inertia and kinetics zincophilia. A best practice for prioritizing zincophilic sites in a more practical metric is also proposed. As a proof of concept, the Bi@Zn anode delivers ultralow overpotential of ≈55 mV at a high rate of 10 mA cm−2 and stable cycle life over 4700 cycles. The elaborated “thermodynamics inertia and kinetics metalphilia” metrics for hetero‐metallic interfaces can benchmark the success of other metal‐based batteries.

Molecular Engineering of pH-Responsive NIR Oxazine Assemblies for Evoking Tumor Ferroptosis via Triggering Lysosomal Dysfunction.

Abstract: Ferroptosis, a newly discovered form of regulated cell death, is emerging as a promising approach to tumor therapy. However, the spatiotemporal control of cell-intrinsic Fenton chemistry to modulate tumor ferroptosis remains challenging. Here, we report an oxazine-based activatable molecular assembly (PTO-Biotin Nps), which is capable of triggering the lysosomal dysfunction-mediated Fenton pathway with excellent spatiotemporal resolution via near-infrared (NIR) light to evoke ferroptosis. In this system, a pH-responsive NIR photothermal oxazine molecule was designed and functionalized with a tumor-targeting hydrophilic biotin-poly(ethylene glycol) (PEG) chain to engineer well-defined nanostructured assemblies within a single-molecular framework. PTO-Biotin Nps possesses a selective tropism to lysosome accumulation inside tumor cells, accommodated by its enhanced photothermal activity in the acidic microenvironment. Upon NIR light activation, PTO-Biotin Nps promoted lysosomal dysfunction and induced cytosolic acidification and impaired autophagy. More importantly, photoactivation-mediated lysosomal dysfunction via PTO-Biotin Nps was found to markedly enhance cellular Fenton reactions and evoke ferroptosis, thereby improving antitumor efficacy and mitigating systemic side effects. Overall, our study demonstrates that the molecular engineering approach of pH-responsive photothermal oxazine assemblies enables the spatiotemporal modulation of the intrinsic ferroptosis mechanism, offering a novel strategy for the development of metal-free Fenton inducers in antitumor therapy.

Selective Ethylene Glycol Oxidation to Formate on Nickel Selenide with Simultaneous Evolution of Hydrogen

Abstract: There is an urgent need for cost‐effective strategies to produce hydrogen from renewable net‐zero carbon sources using renewable energies. In this context, the electrochemical hydrogen evolution reaction can be boosted by replacing the oxygen evolution reaction with the oxidation of small organic molecules, such as ethylene glycol (EG). EG is a particularly interesting organic liquid with two hydroxyl groups that can be transformed into a variety of C1 and C2 chemicals, depending on the catalyst and reaction conditions. Here, a catalyst is demonstrated for the selective EG oxidation reaction (EGOR) to formate on nickel selenide. The catalyst nanoparticle (NP) morphology and crystallographic phase are tuned to maximize its performance. The optimized NiS electrocatalyst requires just 1.395 V to drive a current density of 50 mA cm−2 in 1 m potassium hydroxide (KOH) and 1 m EG. A combination of in situ electrochemical infrared absorption spectroscopy (IRAS) to monitor the electrocatalytic process and ex situ analysis of the electrolyte composition shows the main EGOR product is formate, with a Faradaic efficiency above 80%. Additionally, C2 chemicals such as glycolate and oxalate are detected and quantified as minor products. Density functional theory (DFT) calculations of the reaction process show the glycol‐to‐oxalate pathway to be favored via the glycolate formation, where the CC bond is broken and further electro‐oxidized to formate.

Entropy generation and forced convection analysis of ethylene glycol/MWCNTs-Fe3O4 non-Newtonian nanofluid in a wavy microchannel with hydrophobic surfaces on

Abstract: A three-dimensional simulation has been conducted to study the impact of the hydrophobicity of surfaces on heat transfer, hydrodynamics, and entropy generation of a non-Newtonian nanofluid in a wavy microchannel. The hybrid nanofluid is composed of ethylene glycol/MWCNTs-Fe3O4, and the wavy surface is under a constant heat flux. The main parameters that have been studied in this research are 10≤ Re ≤150, 1.25% ≤ φ ≤1.8%, and 0 ≤ β* ≤0.1. The effects of the mentioned parameters during the research on velocity and temperature distribution, forced convection, pressure drop, and entropy generation have been investigated in detail. The outcomes indicated that using hydrophobic boundary conditions leads to an increase in heat transfer and a decrease in pressure losses, which is useful for the efficiency of cooling systems. The results also show that although increasing the volume fraction of nano-additives and Reynolds number leads to an increment in cooling, they also increase the pressure drop. The PEC and relative entropy generation results are studied for finding the optimized points.

Peristaltic pumping of Boron Nitride-Ethylene Glycol nanofluid through a complex wavy micro-channel under the effect of induced magnetic field and double diffusive

Abstract: The main objective of this work is to present a comprehensive study that scrutinize the influence of DD convection and induced magnetic field on peristaltic pumping of Boron Nitride-Ethylene Glycol nanofluid flow through a vertical complex irregular microchannel. Experimental study showed that the nanofluid created by suspending Boron Nitride particles in a combination of Ethylene Glycol exhibited non-Newtonian characteristics. Further, the Carreau's fluid model provides accurate predictions about the rheological properties of BN-EG nanofluid. In order to imitate complicated peristaltic wave propagation conditions, sophisticated waveforms are forced at the walls. The essential properties of Brownian motion and thermophoresis phenomena are also included in simulating of heat equation as well as viscous dissipation. Mathematical simulation is performed by utilizing the lubrication approach. The resulting nonlinear coupled differential equation system is solved numerically using the built-in command (ND Solve function) in the Mathematica program. Numerical and pictorial evidence is used to illustrate the importance of various physiological features of flow quantities. The major findings demonstrated that the thermal resistance is observed to rise as the Soret and Dufour numbers increase, while the dissolvent concentration and nanoparticles volume fraction have the opposite effect.

Phase Morphology, Mechanical, and Thermal Properties of Calcium Carbonate-Reinforced Poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide) Bioplastics

Abstract: Poly(L-lactide) (PLLA) is a promising candidate as a bioplastic because of its non-toxicity and biodegradability. However, the low flexibility of PLLA limits its use in many applications. Poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide) (PLLA-b-PEG-b-PLLA) block copolymer is of interest for bioplastic applications due to its superior flexibility compared to PLLA. The aim of this work is to modify PLLA-b-PEG-b-PLLA using a low-cost calcium carbonate (CaCO3) filler to improve material properties compared to PLLA/CaCO3 composites. The addition of CaCO3 enhanced the crystallinity and thermal stability for the PLLA-b-PEG-b-PLLA matrix but not for the PLLA matrix, as determined by differential scanning calorimetry (DSC), X-ray diffractometry (XRD), and thermogravimetric analysis (TGA). Phase morphology investigation using scanning electron microscopy (SEM) revealed that the interfacial adhesion between PLLA-b-PEG-b-PLLA and CaCO3 was stronger than between PLLA and CaCO3. Additionally, tensile testing was carried out to determine the mechanical properties of the composites. With the addition of CaCO3, the tensile stress and Young’s modulus of the PLLA-b-PEG-b-PLLA matrix were increased, whereas these properties of the PLLA matrix were significantly decreased. Thus, CaCO3 shows great promise as an inexpensive filler that can induce nucleation and reinforcing effects for PLLA-b-PEG-b-PLLA bioplastics.

Electrocatalytic Upcycling of Biomass and Plastic Wastes to Biodegradable Polymer Monomers and Hydrogen Fuel at High Current Densities

Abstract: Transformation of biomass and plastic wastes to value-added chemicals and fuels is considered an upcycling process that is beneficial to resource utilization. Electrocatalysis offers a sustainable approach; however, it remains a huge challenge to increase the current density and deliver market-demanded chemicals with high selectivity. Herein, we demonstrate an electrocatalytic strategy for upcycling glycerol (from biodiesel byproduct) to lactic acid and ethylene glycol (from polyethylene terephthalate waste) to glycolic acid, with both products being as valuable monomers for biodegradable polymer production. By using a nickel hydroxide-supported gold electrocatalyst (Au/Ni(OH)2), we achieve high selectivities of lactic acid and glycolic acid (77 and 91%, respectively) with high current densities at moderate potentials (317.7 mA/cm2 at 0.95 V vs RHE and 326.2 mA/cm2 at 1.15 V vs RHE, respectively). We reveal that glycerol and ethylene glycol can be enriched at the Au/Ni(OH)2 interface through their adjacent hydroxyl groups, substantially increasing local concentrations and thus high current densities. As a proof of concept, we employed a membrane-free flow electrolyzer for upcycling triglyceride and PET bottles, attaining 11.2 g of lactic acid coupled with 9.3 L of H2 and 13.7 g of glycolic acid coupled with 9.4 L of H2, respectively, revealing the potential of coproduction of valuable chemicals and H2 fuel from wastes in a sustainable fashion.

Numerical solution of an electrically conducting spinning flow of hybrid nanofluid comprised of silver and gold nanoparticles across two parallel surfaces

Abstract: The analysis of the energy transport mechanism received much attention from scientists and researchers. Conventional fluids like vegetable oils, water, ethylene glycol, and transformer oil play a vital role in numerous industrial activities. In certain industrial operations, the low heat conductivity of base fluids causes significant difficulties. This inevitably led to the advancement of critical aspects of nanotechnology. The tremendous significance of nanoscience is in improving the thermal transfer process in different heating transmitting equipment. Therefore, the MHD spinning flow of hybrid nanofluid (HNF) across two permeable surfaces is reviewed. The HNF is made of silver (Ag) and gold (Au) nanoparticles (NPs) in the ethylene glycol (EG). The modeled equations are non-dimensionalized and degraded to a set of ODEs through similarity substitution. The numerical procedure parametric continuation method (PCM) is used to estimate the 1st order set of differential equations. The significances of velocity and energy curves are derived versus several physical parameters. The results are revealed through Tables and Figures. It has been determined that the radial velocity curve declines with the varying values of the stretching parameter, Reynold number, and rotation factor while improving with the influence of the suction factor. Furthermore, the energy profile enhances with the rising number of Au and Ag-NPs in the base fluid.

A ‘print–pause–print’ protocol for 3D printing microfluidics using multimaterial stereolithography

Abstract: Methods to make microfluidic chips using 3D printers have attracted much attention because these simple procedures allow rapid fabrication of ready-to-use products from digital 3D designs with minimal human intervention. Printing high-resolution chips that are simultaneously transparent, biocompatible and contain regions of dissimilar materials is an ongoing challenge. Transparency allows for the optical inspection of specimens containing cells and labeled biomolecules inside the chip. Being able to use different materials for different layers in the product increases the number of potential applications. In this 'print-pause-print' protocol, we describe detailed strategies for fabricating transparent biomicrofluidic devices and multimaterial chips using stereolithographic 3D printing. To print transparent biomicrofluidic chips, we developed a transparent resin based on poly(ethylene glycol) diacrylate (PEG-DA) (average molecular weight: 250 g/mol, PEG-DA-250) and a smooth chip surface technique achieved using glass. Cells can be successfully cultured and visualized on PEG-DA-250 prints and inside PEG-DA-250 microchannels. The multimaterial potential of the technique is exemplified using a molecular diffusion device that comprises parts made of two different materials: the channel walls, which are water impermeable, and a porous barrier structure, which is permeable to small molecules that diffuse through it. The two materials were prepared from two different molecular-weight PEG-DA-based printing resins. Alignment of the two dissimilar material structures is performed automatically by the printer during the printing process, which only requires a simple pause step to exchange the resins. The procedure takes less than 1 h and can facilitate chip-based applications including biomolecule analysis, cell biology, organ-on-a-chip and tissue engineering.

Preparation and Characterization of Electrospun Poly(lactic acid)/Poly(ethylene glycol)–b–poly(propylene glycol)–b–poly(ethylene glycol)/Silicon Dioxide Nanofibrous Adsorbents for Selective Copper (II) Ions Removal from Wastewater

Abstract: The problem of industrial wastewater containing heavy metals is always a big concern, especially Cu2+, which interprets the soil activity in farmland and leaves a negative impact on the environment by damaging the health of animals. Various methods have been proposed as countermeasures against heavy-metal contaminations, and, as a part of this, an electrospun nanofibrous adsorption method for wastewater treatment is presented as an alternative. Poly(lactic acid) (PLA) is a biopolymer with an intrinsic hydrophobic property that has been considered one of the sustainable nanofibrous adsorbents for carrying adsorbate. Due to the hydrophobic nature of PLA, it is difficult to adsorb Cu2+ contained in wastewater. In this study, the hydrophilic PLA/poly(ethylene glycol)-poly(propylene glycol)-poly(ethylene glycol) (PEG-PPG-PEG) nanofibrous adsorbents with different silicon dioxide (SiO2) concentrations were successfully prepared by electrospinning. A hydrophilic group of PEG-PPG-PEG was imparted in PLA by the blending method. The prepared PLA/PEG-PPG-PEG/SiO2 nanofibrous adsorbents were analyzed with their morphological, contact angle analysis, and chemical structure. The Cu2+ adsorption capacities of the different PLA/PEG-PPG-PEG/SiO2 nanofibrous adsorbents were also investigated. The adsorption results indicated that the Cu2+ removal capacity of PLA/PEG-PPG-PEG/SiO2 nanofibrous adsorbents was higher than that of pure ones. Additionally, as an affinity nanofibrous adsorbent, its adsorption capacity was maintained after multiple recycling processes (desorption and re-adsorption). It is expected to be a promising nanofibrous adsorbents that will adsorb Cu2+ for wastewater treatment.

Extraction of Bioactive Compounds from C. vulgaris Biomass Using Deep Eutectic Solvents

Abstract: C. vulgaris microalgae biomass was employed for the extraction of valuable bioactive compounds with deep eutectic-based solvents (DESs). Particularly, the Choline Chloride (ChCl) based DESs, ChCl:1,2 butanediol (1:4), ChCl:ethylene glycol (1:2), and ChCl:glycerol (1:2) mixed with water at 70/30 w/w ratio were used for that purpose. The extracts’ total carotenoid (TCC) and phenolic contents (TPC), as well as their antioxidant activity (IC50), were determined within the process of identification of the most efficient solvent. This screening procedure revealed ChCl:1,2 butanediol (1:4)/H2O 70/30 w/w as the most compelling solvent; thus, it was employed thereafter for the extraction process optimization. Three extraction parameters, i.e., solvent-to-biomass ratio, temperature, and time were studied regarding their impact on the extract’s TCC, TPC, and IC50. For the experimental design and process optimization, the statistical tool Response Surface Methodology was used. The resulting models’ predictive capacity was confirmed experimentally by carrying out two additional extractions under conditions different from the experimental design.

Solvothermal Synthesis of Calcium Hydroxyapatite via Hydrolysis of Alpha-Tricalcium Phosphate in the Presence of Different Organic Additives

Abstract: In this study, the effects of sodium lauryl sulfate and various amino acids (DL-aspartic acid, dodecanedioic acid, and suberic acid) on the formation of calcium-deficient hydroxyapatite via hydrolysis of α-tricalcium phosphate (α-TCP) were investigated; moreover, a combined effect of these additives and ethylene glycol as a synthesis medium was also estimated. The hydrolysis reaction was performed in solutions containing different concentrations of additives in aqueous and mixed aqueous–organic media under solvothermal conditions. It was demonstrated that the nature and the concentration of organic additives influence the phase purity and morphology of the final product. Higher concentrations of sodium lauryl sulfate and dodecanedioic acid induced the formation of impurities in addition to hydroxyapatite, while aspartic and suberic acid did not affect the phase purity. The morphology of the samples varied from plate- to rod-like depending on the concentrations of specific organic additive.

Investigation on ethylene glycol and glycerol mixture concentration dependent optical, dielectric, electrical, rheological, and thermophysical properties of EG+Gly/ZnO semiconductor nanofluids

Abstract: Wide energy bandgap metal oxide nanomaterials containing semiconductor nanofluids (SNFs) are technologically established as advanced multifunctional materials for progress in high performance soft condensed devices. Therefore, to strengthen this field of materials, the present study reports in detail the optical, dielectric, electrical, rheological, and thermophysical properties of the SNFs based on ethylene glycol (EG) and glycerol (Gly) mixture of an entire concentration range (Gly volume fractions; 0.00, 0.25, 0.50, 0.75, and 1.00) with a fixed amount of zinc oxide (ZnO) semiconductor nanomaterial (0.05 wt%). These green-formulated EG + Gly/ZnO SNF materials showed a longer stability of the suspended nanoparticles in the highly viscous hydrogen bonded base fluid and exhibited an increase in absorbance with the decrease wavelength of visible range photons and the ZnO electronic transition at about 3.2 eV energy of ultraviolet radiations. Dielectric measurements over the 20 Hz–1 MHz range of these SNFs, at 298.15 K, explained a dominant contribution of the electrode and interfacial polarization processes at low frequencies and the molecular dipole polarization of static permittivity about 40 at the higher frequencies. Electrode polarization and conductivity relaxation times enhanced exponentially when the Gly concentration increased in the EG + Gly base fluid which governs the electrical conductivity decrement from 0.79 to 0.04 μS/cm for these SNFs. The rheological study explained the Newtonian characteristics of EG + Gly/ZnO nanofluids with their base fluid mixture concentration controllable dynamic viscosity in the wide range of 17–702 mPa s, at 298.15 K. The density, refractive index, ultrasound velocity, prominent acoustic parameters, and thermal conductivity are determined and discussed to explore the solid-liquid interaction and interfaces formed in these innovative SNF materials.

Molecular Self-Assembled Ether-Based Polyrotaxane Solid Electrolyte for Lithium Metal Batteries.

Abstract: Poly(ethylene oxide) has been widely investigated as a potential separator for solid-state lithium metal batteries. However, its applications were significantly restricted by low ionic conductivity and a narrow electrochemical stability window (<4.0 V vs Li/Li+) at room temperature. Herein, a novel molecular self-assembled ether-based polyrotaxane electrolyte was designed using different functional units and prepared by threading cyclic 18-crown ether-6 (18C6) to linear poly(ethylene glycol) (PEG) via intermolecular hydrogen bond and terminating with hexamethylene diisocyanate trimer (HDIt), which was strongly confirmed by local structure-sensitive solid/liquid-state nuclear magnetic resonance (NMR) techniques. The designed electrolyte has shown an obviously increased room-temperature ionic conductivity of 3.48 × 10-4 S cm-1 compared to 1.12 × 10-5 S cm-1 without assembling polyrotaxane functional units, contributing to the enhanced cycling stability of batteries with both LiFePO4 and LiNi0.8Co0.15Al0.05O2 cathode materials. This advanced molecular self-assembled strategy provides a new paradigm in designing solid polymer electrolytes with demanded performance for lithium metal batteries.