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Depletion interactions are thought to significantly contribute to the organization of intracellular structures in the crowded cytosol. The strength of depletion interactions depends on physical parameters such as the depletant number density and the depletant size ratio. Cells are known to dynamically regulate these two parameters by varying the copy number of proteins of a wide distribution of sizes. However, mammalian cells are also known to keep the total protein mass density remarkably constant, to within 0.5% throughout the cell cycle. We thus ask how the strength of depletion interactions varies when the total depletant mass is held fixed, a.k.a. fixed-mass depletion. We answer this question via scaling arguments, as well as by studying depletion effects on networks of reconstituted semiflexible actin in silico and in vitro. We examine the maximum strength of the depletion interaction potential U∗ as a function of q, the size ratio between the depletant and the matter being depleted. We uncover a scaling relation U∗ ∼ qζ for two cases: fixed volume fraction φ and fixed mass density ρ. For fixed volume fraction, we report ζ < 0. For the fixed mass density case, we report ζ > 0, which suggests that the depletion interaction strength increases as the depletant size ratio is increased. To test this prediction, we prepared our filament networks at fixed mass concentrations with varying sizes of the depletant molecule poly(ethylene glycol) (PEG). We characterize the depletion interaction strength in our simulations via the mesh size. In experiments, we observe two distinct actin network morphologies, which we call weakly bundled and strongly bundled. We identify a mass concentration where different PEG depletant sizes lead to weakly bundled or strongly bundled morphologies. For these conditions, we find that the mesh size and intra-bundle spacing between filaments across the different morphologies do not show significant differences, while the dynamic light scattering relaxation time and storage modulus between the two states do show significant differences. Our results demonstrate the ability to tune actin network morphology and mechanics by controlling depletant size and give insights into depletion interaction mechanisms under the fixed-depletant-mass constraint relevant to living cells. [ABSTRACT FROM AUTHOR]

In the interstellar medium, diols and other prebiotic molecules adsorb onto icy mantles surrounding dust grains. Water in the ice may affect the reactivity and photoionization of these diols. Ethylene glycol (EG), 1,2-propylene glycol, and 1,3-propylene glycol clusters with water clusters were used as a proxy to study these interactions. The diol–water clusters were generated in a continuous supersonic molecular beam, photoionized by synchrotron-based vacuum ultraviolet light from the Advanced Light Source, and subsequently detected by reflectron time-of-flight mass spectrometry. The appearance energies for the detected clusters were determined from the mass spectra, collected at increasing photon energy. Clusters of both diol fragments and unfragmented diols with water were detected. The lowest energy geometry optimized conformers for the observed EG–water clusters and EG fragment–water clusters have been visualized using density functional theory (DFT), providing insight into hydrogen bonding networks and how these affect fragmentation and appearance energy. As the number of water molecules clustered around EG fragments (m/z 31 and 32) increased, the appearance energy for the cluster decreased, indicating a stabilization by water. This trend was supported by DFT calculations. Fragment clusters from 1,2-propylene glycol exhibited a similar trend, but with a smaller energy decrease, and no trend was observed from 1,3-propylene glycol. We discuss and suggest that the reactivity and photoionization of diols in the presence of water depend on the size of the diol, the location of the hydroxyl group, and the number of waters clustered around the diol. [ABSTRACT FROM AUTHOR]

Glass formation and reorientational motions are widespread but often-neglected features of deep eutectic solvents although both can be relevant for the technically important ionic conductivity at room temperature. Here, we investigate these properties for two mixtures of ethylene glycol and ZnCl2, which were recently considered superior electrolyte materials for application in zinc-ion batteries. For this purpose, we employed dielectric spectroscopy performed in a broad temperature range, extending from the supercooled state at low temperatures up to the liquid phase around room temperature and beyond. We find evidence for a relaxation process arising from dipolar reorientation dynamics, which reveals the clear signatures of glassy freezing. This freezing also governs the temperature dependence of the ionic dc conductivity. We compare the obtained results with those for deep eutectic solvents that are formed by the same hydrogen-bond donor, ethylene glycol, but by two different salts, choline chloride and lithium triflate. The four materials reveal significantly different ionic and reorientational dynamics. Moreover, we find varying degrees of decoupling of rotational dipolar and translational ionic motions, which can partly be described by a fractional Debye–Stokes–Einstein relation. The typical glass-forming properties of these solvents strongly affect their room-temperature conductivity. [ABSTRACT FROM AUTHOR]

Using deuteron spin-lattice and spin-spin relaxometry, the reorientational dynamics of ethaline (choline chloride/ethylene glycol) and reline (choline chloride/urea) are studied in a component-selective, isotope-edited manner over a wide temperature range, thereby complementing previous work on glyceline (choline chloride/glycerol). Differences in the hydrogen bond propensities effectuate that in reline and glyceline, the choline ions move faster than the hydrogen bond donors, glycerol and urea; in ethaline, the ethylene glycol molecules are reorienting faster. For glyceline and reline, the increase in the corresponding time scale ratio indicates a pronounced strengthening of the glycerol and urea networks upon cooling, while in ethaline, the time scale ratio remains essentially constant. For the three deep eutectic solvents, a comparison of the present component-selective results with the dielectric time constants shows that the latter are primarily sensitive to the dynamics of the respective hydrogen bond donors. In a Walden-type plot, the reorientation rates, selectively determined for the hydrogen bond donors and acceptors, are compared with their conductivity and fluidity, revealing that the dynamics of the choline ions relate most directly to the charge transport. [ABSTRACT FROM AUTHOR]

This study explores application of poly (ethylene glycol) (PEG)‐based hydrogel to improve the antifouling properties and performance of polyphenylsulfone (PPSU) membrane. The modification of PPSU membrane was performed via coating different ratio of polydopamine (PDA) to 3‐(aminopropyl)triethoxysilane (APTES) as interlayer on surface of PPSU membrane followed by grafting of PEG‐NH2 hydrogel. The as‐prepared membranes were characterized and results confirmed the successful coating of interlayer and hydrogel. The performance of as‐prepared membranes was measured using pure water flux, humic acid (HA), and bovine serum albumin (BSA) separation. The PDA‐APTES (50:50) was selected as the optimal interlayer to graft hydrogel with respect to their superior effect on properties of resultant membrane. The permeate flux and HA rejection increased from 35.2 LMH and 55% for pristine PPSU membrane to 83 LMH and 96% for optimal membrane. For optimal membrane the flux recovery ratio (FRR) value of 96% and 93% determined for BSA and HA separation, respectively. Chemical stability examined and the results confirmed that the hydrogel‐coated membrane was more stable in acidic media compared with alkali media. In summary, the simultaneous presence of the interlayer and the grafted hydrogel had a great impact on the morphology, performance, anticlogging properties, and acid resistance of the modified membranes. [ABSTRACT FROM AUTHOR]

Ethylene glycol (EG) is a widely used material, but its vapor is harmful to human health already in low concentrations. Thus, highly sensitive EG gas sensors are urgently needed. Herein, a series samples of ZnO and carbon dots (CDs) were synthesized at different ratios through a simple mechanical grinding method. The senor made using ZnO/CDs2 exhibits an ultra-high response (Ra/Rg) to 100 ppm EG up to 2798, 1378 and 467, and extremely low detection limit as low as 21 ppb, 13 ppb and 2 ppb, under UV light, visible light, and infrared light, respectively, as well as excellent repeatability and long-term stability. Especially, under UV light irradiation, the response of ZnO/CDs2 to 100 ppm EG is 24 times that of pure ZnO (Ra/Rg = 114.7), and more than 71 times that of 9 other gases. The outstanding gas sensing performance of ZnO/CDs2 can be attributed to the excellent light response ability of CDs at first, which greatly enriches the electron concentration in ZnO/CDs under light irradiation. Furthermore, the photo-induced electron transfer (PET) property of CDs and the p-n heterojunction formed at the interface between ZnO and CDs play a key role in rapid electron transport and transfer, avoiding a large number of electron hole recombination. [ABSTRACT FROM AUTHOR]

In this study, a novel nanocomposite material consisting of Bi 2 O 3 and Bi 2 MoO 6 , named as Bi 2 O 3 @Bi 2 MoO 6 , was successfully fabricated by co-precipitation method in ethylene glycol solvent. Morphological analysis of the heat-treated sample at 400 °C for 12 h in Ar atmosphere (Bi 2 O 3 @Bi 2 MoO 6 _400 °C) showed that it contained nano-sized particles of Bi 2 O 3 and Bi 2 MoO 6 ; in addition, an amorphous phase along with a crystalline structure was also observed. When used as an anode for Li-ion batteries (LIBs), Bi 2 O 3 @Bi 2 MoO 6 _400 °C anode exhibits excellent electrochemical properties such as high Coulombic efficiency, high specific capacity, excellent capacity retention, and outstanding rate capacity. Specifically, the Bi 2 O 3 @Bi 2 MoO 6 _400 °C anode presented a reversible capacity of 786 mAh g−1 at the beginning cycle at 0.1 A g−1 and retained about 90 % of the charging capacity value after 80 cycles. The advanced electrochemical properties of the nanocomposite anode are related to the combination of many aspects such as nanostructure, existence of amorphous phase, and pseudo-behaviour of metal-based components. The structural stability and electrochemical performance of the anode material, therefore, are improved. These results demonstrate Bi 2 O 3 @Bi 2 MoO 6 _400 °C as a promising material for establishing high-performance LIB anodes. [Display omitted] • Bi 2 O 3 @Bi 2 MoO 6 powders are prepared by a facile method. • Bi 2 O 3 @Bi 2 MoO 6 powders contain amorphous and crystalline phases. • Bi 2 O 3 @Bi 2 MoO 6 materials possess nanostructures (from 20 nm to 50 nm). • Bi 2 O 3 @Bi 2 MoO 6 _400 °C anode displays high initial coulombic efficiency (>80 %). • Bi 2 O 3 @Bi 2 MoO 6 _400 °C anode shows a reversible capacity of 701 mAh g−1 after 80 cycles. [ABSTRACT FROM AUTHOR]

In this study, poly(lactic acid)‐poly(ethylene glycol)‐tetra‐n‐butylammonium hydrogen sulfate (PLA‐PEG‐HS) electrospun mats were fabricated by electrospinning as effective wound dressings against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli), which are the most prevalent species of gram‐positive and gram‐negative bacteria, respectively. PLA is a polymer with high biocompatibility and biodegradability, but its structure is fragile. Therefore, we aimed to improve its structural properties using PEG as a plasticizer and to provide antibacterial properties with HS salt. The nanofibers characterized using differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, thermal gravimetric analysis (TGA), and drying time tests. The addition of HS eliminated the beads in the PLA‐PEG nanofiber and improved the homogeneity of the fiber distribution. Concerning this result, when the liquid absorption capacity (LAC) test was evaluated, PLA‐PEG‐HS nanofiber production was achieved with the highest rate of 480.95%. The thermal properties of nanofibers increased with the addition of HS. Cytotoxicity test results of PLA‐PEG‐HS wound dressings showed high cell viability of 129.05% in L292 mouse fibroblast cells at the end of the 24th hour. PLA‐PEG‐HS nanofibers with 99.99% antibacterial activity against tow bacteria. Considering the modern wound dressing requirements, antibacterial wound dressing production has been successfully achieved. [ABSTRACT FROM AUTHOR]

Propylene glycol is a potential fuel additive with high oxygen-contained. Propylene glycol has two isomers, 1,2-propylene glycol and 1,3-propylene glycol. In order to comprehend the combustion behavior of propylene glycol, the autoignition properties were investigated experimentally behind reflected shock waves. The Ignition delay times were obtained at the temperature range of 1100–1550 K, pressures of 2, 4 and 10 atm, equivalence ratios of 0.5, 1.0 and 2.0, as well as fuel concentrations of 1.0% and 1.5%. The effects of temperature, pressure, fuel and oxygen concentrations on the ignition delay time were studied, and the corresponding quantitative relationships were obtained through linear regression analysis. A detailed oxidation mechanism of propylene glycol was proposed and verified by ignition data and species profiles. Kinetic analyses were carried out to investigate the propylene glycol oxidation. Pathway analysis indicated that H-abstraction reactions are the main consumption channels of propylene glycol. Rate of production analysis illustrated that H-abstraction reactions by H and OH radicals dominate the fuel consumption. Sensitivity analysis confirmed that besides H-abstraction reactions, C–C bond dissociation reactions express strong promoting effects on fuel ignition. Comparisons of the ignition delay time of propylene glycol, ethylene glycol and propanol were conducted. [ABSTRACT FROM AUTHOR]

Upconversion nanoparticles (UCNPs) have been used as a potential nanocarrier for photosensitizers (PSs), which have demonstrated a great deal of promise in achieving an effective photodynamic therapy (PDT) for deep-seated tumors. However, overcoming biological barriers to achieve mitochondria-targeted PDT remains a major challenge. Herein, CD44- and mitochondria-targeted photodynamic nanosystems were fabricated through the self-assembly of hyaluronic acid-conjugated-methoxy poly(ethylene glycol)-diethylenetriamine-grafted-(chlorin e6-dihydrolipoic acid-(3-carboxypropyl)triphenylphosphine bromide) polymeric ligands (HA-c-mPEG-Deta-g-(Ce6-DHLA-TPP)) and NaErF4:Tm@NaYF4 core–shell UCNPs (termed CMPNs). The CMPNs presented ideal physiological stability, a good drug loading capacity and an improved capacity for the generation of singlet oxygen (1O2) based on the FRET mechanism. Significantly, confocal images revealed that CMPNs not only facilitated cellular uptake through CD44-receptor-targeted endocytosis, subsequently enabling rapid evasion from endo-lysosomal sequestration, but also specifically targeted mitochondria, ultimately inducing a profound disruption of mitochondrial membrane potential, which triggered apoptosis upon laser irradiation, thereby significantly enhancing the therapeutic effect. Furthermore, in vitro antitumor experiments further confirmed the substantial enhancement in cancer cell killing efficiency achieved by treating with CMPNs upon near-infrared (NIR) laser irradiation. This innovative approach holds promise for the development of NIR-laser-activated photodynamic nanoagents specifically designed for mitochondria-targeted PDT, thus addressing the limitations of the current PDT treatments. [ABSTRACT FROM AUTHOR]

The Registration, Evaluation, Authorization, and Restriction of Chemicals (REACH) legislation in Europe has limited the use of certain materials in the manufacturing of tattoo inks; in particular, Pigment Blue 15:3 and Pigment Green 7 have been banned for the use in tattoo inks and permanent makeups and all labels must include an accurate list of ingredients. This study analyzed green and blue inks from five different manufacturers distributed to the European market, all of which claim to be REACH compliant. Nine out of ten inks analyzed were found to not be compliant and four contained banned material. The polymorph of Pigment Blue 15 found in four inks was unable to be determined. The majority of inks showed labeling inaccuracies, including the addition of unlisted poly(ethylene glycol) and propylene glycol. This study highlights issues around REACH compliance of tattoo inks on the European market and the need for manufacturing protocols to ensure accurate labeling. [ABSTRACT FROM AUTHOR]

Exploring the electrochemical performance of metal/metal oxide nanoparticle composites is vital for enhancing the charge storage capability of supercapacitors. Herein, electrodes coated with ZnO/CoO x are fabricated by soaking cotton fabric seeded with 2-methylimidiazole in an ethylene glycol–based solution containing Zn and Co salts. The use of cotton fabric can reduce textile industrial waste while achieving high capacitance and sustainable energy for wearable electronics. In addition, the three-dimensional network of conductive flexible carbon derived from cotton fabric facilitates rapid ion transport kinetics at interlayers. The concentrations of Zn and Co salts are varied to produce ZnO/CoO x samples and determine the optimal salt ratio for superior electrochemical performance. The optimal sample exhibits a capacitance of 1.95 F cm−2 at 5 mA cm−2 and an energy density of 725 μWh·cm−2 over a wide potential window of 1.6 V. The long-term stability test results of the symmetric cells indicate 94 % capacitance retention after 12,000 charge–discharge cycles, emphasizing the advantages of mixed metallic oxides with cellulose-derived carbon fabric for supercapacitor electrodes. This study offers valuable insights into the fabrication of high-performance, flexible, and binder-free supercapacitor electrodes as a scalable alternative for practical applications. [ABSTRACT FROM AUTHOR]

The paper production industry annually produces approximately 50 million tons of lignin, an intermediate product. While lignin has the potential for producing valuable chemicals and energy materials, an effective method for its conversion is yet to be developed. This study aims to establish a sustainable and environmentally friendly approach for electrochemically synthesizing valuable compounds from lignin with using natural deep eutectic solvents as electrolytes. The study used cyclic voltammetry (CV) for the electrochemical depolymerization of Kraft lignin, examining the effects of different scan numbers on depolymerization and the resulting lignin derivatives. Observed changes in the depolymerization peak current of lignin were reported as the number of scans increased. Choline chloride: Lactic acid (CC:LA), Choline chloride: Ethylene glycol (CC:EG), and Lactic acid:1,2-propanediol (LA:PR) were used as green electrolytes. Syringaldehyde was found to be the major compound obtained by this method. As a result of statistical analysis performed using The Grey Relations Analysis method, it was determined that the conditions that utilized Kraft lignin with the highest added value involved performing five cycles of CV scans with the CC:LA electrolyte. CV scans in DES environments increased the yield of lignin-derived phenolic compounds. [ABSTRACT FROM AUTHOR]

We explored the potential value of the alcohol dehydrogenase (ADH) inhibitor isovaleramide (ISO) in the treatment of acute ethylene glycol (EG) poisoning‐induced acute kidney injury. Sprague–Dawley rats were divided into the control, EG, EG + ISO (10 mg/kg) and EG + ISO (20 mg/kg) groups. It is found that ISO intervention significantly reduced the ADH activity in liver tissue by using visible spectrophotometry, inhibited the in vivo metabolism of EG by using gas chromatography, lowered the levels of toxic metabolites glycolic acid and oxalic acid by using high‐performance liquid chromatography and decreased the expression of kidney injury markers serum creatinine (sCr), KIM‐1, neutrophil gelatinase‐associated lipocalin (NGAL) and liver fatty acid‐binding protein (L‐FABP) by ELISA. Additionally, Western blotting results showed that ISO down‐regulated the expression of apoptotic factors Bax and cleaved caspase‐3 in the kidneys and upregulated the expression of antiapoptotic factor Bcl‐2. Pizzolato staining and polarized light microscopy results revealed the reduced deposition of calcium oxalate crystals in the kidney tubules. Using haematoxylin and eosin (H&E), periodic acid‐Schiff (PAS) and Masson staining, we found attenuated kidney tissue pathological injury. Finally, ISO significantly reduced the mortality rate. In conclusion, ISO has the potential to be a valuable drug for the treatment of EG poisoning‐induced acute kidney injury. [ABSTRACT FROM AUTHOR]

Poly (ethylene glycol dimethacrylate-1,2-ethanedithiol) (P(EDGMA-EDT)) and poly (ethylene glycol dimethacrylate-3,6-dioxy-1,8-octanedithiol) (P(EDGMA-DODT)) are excellent solid polymer electrolytes synthesized experimentally. The coordination structure, redox properties, and modification design of P(EDGMA-EDT)-LiTFSI and P(EDGMA-DODT)-LiTFSI are investigated by density functional theory. The theoretical simulation of infrared spectra and the coordination structure information show that the ester carbonyl group in P(EDGMA-EDT) and the ester carbonyl group and ether oxygen in P(EDGMA-DODT) interact with Li+ ions. Li+ ion coordination numbers in these two electrolytes are 4 and 5; thioether and ester groups in polymers are their redox active sites, respectively. Modified sulfone oxide P(EDGMA-EDT)2-SO2 and P(EDGMA-DODT)2-SO2 cannot only maintain the reduction stability but also greatly improve the oxidation potential. LiPF6, LiDFBOP, and LiBF3Cl are good candidates for sulfone-based polymers. The electron-withdrawing groups (− 4Br, − 4Cl, − 4F, − NO2, and − CN) substitution can improve the oxidation potential of P(EDGMA-EDT) but have little effect on the oxidation potential of P(EDGMA-DODT) and reduce the reduction stability of both polymers. These findings provide theoretical guidance for the coordination structure as well as the molecular design of solid electrolytes containing ester groups and thioether. [ABSTRACT FROM AUTHOR]

In the present work, flexible polymeric nanocomposite film of poly(vinyl alcohol)/poly(ethylene glycol) (PVA–PEG) blend filled with aluminum (Al)-doped zinc oxide (AZO) nanoparticles has been successfully synthetized and characterized. The solution casting technique was used to prepare pure PVA–PEG polymeric blend and polymeric blend nanocomposite (PNC) films filled with different concentrations of AZO nanoparticles. The morphological, structural and optical properties of AZO NPs and PNC films were investigated using different techniques such as X-ray diffraction (XRD) scanning electron microscopy (SEM), transmission electron microscopy (TEM) spectroscopy and UV–VIS–NIR spectrophotometer. The XRD results shows that nanoparticles are well distributed in the host blend matrix. TEM observation reveals an average particle size about 49 nm. The contact angle analysis was carried out for PNC films to investigate the effect of AZO filling upon the nanocomposite water wettability. Loading PNC with nanopowder AZO influences their electrical optical properties. The addition of AZO nanoparticles in the polymeric blend reduces its band gap and increases its DC electrical conductivity. The antibacterial activity of the prepared nanocomposite films was tested against various pathogenic bacteria including two types of gram-positive bacteria (Staphylococcus aureus (S. aureus) and Bacillus) and two types of gram-negative bacteria (Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli)). The assay results suggested that the pure blend film has no activity against all types of bacteria. While filled PNC films exhibit a significant antibacterial activity against S. aureus, Bacillus and P. aeruginosa bacteria, they have no any activity against E. coli bacteria. This activity is improved with increasing the filler concentrations in blend matrix. Finally, the obtained results suggest that the prepared PNC films can be a potential multifunctional candidate for different applications, especially optoelectronic devices and biomedical uses. [ABSTRACT FROM AUTHOR]

This study investigates the encapsulation and controlled release of perfume within micellar systems. We explored how perfume‐surfactant interactions and micelle structure influence fragrance delivery. Two mixed‐micelle systems, one with branched‐tail and the other with linear‐tail surfactants, were subjected to varying perfume concentrations, dilution, and time. Using small‐angle neutron scattering (SANS), gas chromatography‐mass spectrometry (GC‐MS), and statistical analysis, we determined that micelle size and shape are significantly affected by perfume content and dilution. While both systems exhibited similar trends, the branched‐tail system uniquely formed a lamellar phase at higher perfume levels. Our findings reveal a strong correlation between micelle geometry and headspace perfume concentration, highlighting the role of surfactant tail structure. This research provides fundamental insights into perfume‐micelle interactions, with potential applications in materials science and active ingredient delivery. [ABSTRACT FROM AUTHOR]

Current ionic polymer–metal composite (IPMC) actuators have severe actuation drawbacks (i.e. low force output and poor stability), hampering their applications. To address these issues, poly(ethylene glycol)‐grafted graphene oxide (PEG‐GO) is synthesized and incorporated into a Nafion matrix, thus producing a PEG‐GO hybrid Nafion film with better physiochemical properties for fabricating a high‐performance, low‐cost IPMC actuator. The modification of PEG to GO not only prevents GO agglomeration and sedimentation, but also avoids loss of PEG in water. Driven by a 0.2 Hz, 2.5 V electric field, the hybrid IPMC actuator exhibits superior electromechanical behaviors, i.e. a swing angle of 110.3°, a blocking force of 6.89 mN and a stable working time of 485 s, respectively increasing by 92%, 209% and 294% when compared to a pure Nafion actuator. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

Hierarchically porous biphasic calcium phosphate (BCP) ceramics with triply periodic minimal surface structure and porous framework have been fabricated by digital light processing (DLP) using dual-phase Pickering emulsion as the paste. The pristine hydroxyapatite and β-tricalcium phosphate particles were separately modified by dispersant firstly to obtain photosensitive Pickering emulsion with suitable rheological properties and stability for DLP printing. The porous structure has been well regulated by dispersant content, and ethylene glycol content. The resulting BCP ceramics exhibited a hierarchical pore structure consisting of interconnected micropores ranging from 1.13 μm to 8.98 μm and model-designed pores of nearly 500 μm, demonstrating excellent compressive strength of 4.83 MPa at a porosity of 60 %. In vitro biological experiments revealed that rat bone marrow mesenchymal stem cells exhibited good proliferation and adhesion ability on the BCP bio-scaffolds, thereby enhancing their application potential in bone regenerative medicine. [ABSTRACT FROM AUTHOR]

As a class of predominantly used cathode interlayers (CILs) in organic solar cells (OSCs), perylene‐diimide (PDI)‐based polymers exhibit intriguing characteristics of excellent charge transporting capacity and suitable energy levels. Despite that, PDI‐based CILs with satisfied film‐forming ability and adequate solvent resistance are rather rare, which not only limits the further advance of OSC performances but also hinders the practical use of PDI CILs. Herein, we designed and synthesized two non‐conjugated PDI polymers for achieving high power conversion efficiency (PCE) in diverse types of OSCs. The utilization of oligo (ethylene glycol) (OEG) linkage enhanced the n‐doping effect of PDI polymers, leading to an improved ability of the CIL to reduce work function and improve electron transporting capability. Moreover, the introduction of the non‐ionic OEG chain effectively improve the wetting property and solvent resistance of PDI polymers, so the PPDINN CIL can withstand diverse processing conditions in fabricating different OSCs, including conventional, inverted and blade‐coated devices. The binary OSC with conventional structure using PPDINN CIL showed a PCE of 18.6 %, along with an improved device stability. Besides, PPDINN is compatible with the large‐area blade‐coating technique, and a PCE of 16.6 % was achieved in the 1‐cm2 OSC where a blade‐coated PPDINN was used. [ABSTRACT FROM AUTHOR]

The glycolysis of PET represents a pivotal approach to achieving high-value utilization following its disposal. However, an efficient and cost-effective catalyst is required. This study reports on the use of a titanium isophthalate (Ti-IPA) catalyst for PET depolymerization. Ti-IPA was prepared using isophthalic acid and titanate as raw materials via a one-pot method. The study investigated the effects of different titanium sources and solvent types on Ti-IPA. The optimal conditions for the glycolysis reaction were determined using response surface methodology, and the 0.86% Ti-IPA catalyst provided a BHET yield of 84.86% for a reaction lasting 3.15 h at 194 °C with 12.8 mL ethylene glycol. Finally, a comparative analysis of the catalytic performance of Ti-IPA revealed that it is a promising novel catalyst with significant commercial potential. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The development of simple, accurate, responsive, and selective antimicrobial drug analysis platforms is extremely important for biomedical research. Developing a novel electrode material that possesses low detection limit, high sensitivity, and stability continues to be a difficult undertaking. Here, vanadium tungstate nanostones (VWNs) were synthesized by utilizing facile sonochemical method with the aid of urea and ethylene glycol for application in electrochemical sensing of antibiotic drug nitrofurantoin (NFT). Using a distinct analytical methods, the structural and morphological characteristics of the as‐prepared transducer material were described. Further, electrochemical behaviour of modified electrode were analysed using cyclic voltammetry and liner sweep voltammetry. Under the optimal conditions VWNs/GCE electrode exhibited superior electrocatalytic activity towards NFT with linear range (20–160 μM), limit of detection (0.019 μM) with better sensitivity (0.69 μM−1 cm−2). The modified electrode demonstrated remarkable repeatability, reproducibility, and excellent stability, indicating its potential as an electrocatalyst. Ultimately, the suggested electrode was used to measure FLT in real samples like tap water and NFT capsule. [ABSTRACT FROM AUTHOR]

This work reports the effects of potassium bromide (KBr) on the electrodeposition of manganese on copper from a DES consisting of a stoichiometric 1:2 mix of choline chloride and ethylene glycol (Ethaline 200). The speciation of MnCl2.4H2O in Ethaline 200 has been investigated using UV–vis spectroscopy, in particular with regard to the addition of KBr to the plating bath, for which no apparent change in the Mn species was noted. This said, the physical properties of the manganese deposits themselves were found to have been considerably improved in comparison to when KBr was omitted from the bath; indeed, the actual adhesion of Mn was achieved for the first time on a copper substrate, somewhat remarkably producing a coating of some considerable thickness. Given its clear electrochemical behavior of the Mn liquid were subsequently determined via cyclic voltammetry method. A reduction in the peak current of Mn was noted on addition of KBr. The mechanism of Mn deposition has been examined via chronocoulometry and chronoamperometry. Surface analyses of Mn deposits have been conducted via SEM/EDX, AFM, and XRD, from which improvements to the Mn surface coatings in depositions performed from an electrolyte containing 0.1 M KBr were noted. [ABSTRACT FROM AUTHOR]

Extrusion‐based 3D printing technology is currently demonstrating considerable potential in the field of tissue engineering scaffolds, enabling the construction of in vitro models with complex structures and functions using a wide range of biomaterials and cells at a low cost. In recent years, researchers have spent considerable effort developing novel bio‐inks and employing a greater variety of cell sources to enhance biological compatibility and functionality. However, the majority of current bio‐ink materials are unprintable due to their low viscosity and long curing time, as well as insufficient shape fidelity before the secondary cross‐linking process. The study aims to bridge this gap by optimizing the material ratios and predicting the printing process before work. This article presents new strategies for the design, fabrication, and analysis of a new composite bio‐ink material. The optimal ink ratios are verified by a design of experiments (DOE) experimental design and evaluation metrics for printing printability (Pr) values. A machine learning model is used to predict the ink printing area and determine the printing process parameters. The influence mechanism of ink materials with different concentrations of poly (ethylene glycol) diacrylate (PEGDA) ratios on printed fibers is investigated. Finally, the optimal results are used as an example to demonstrate the printability of multilayer stents. Thus, the design approach allows for the rapid and cost‐effective exploration of novel ink ratios, while also providing higher fidelity and more accurate process metrics for the fabrication of tissue structures with multidimensional variables. [ABSTRACT FROM AUTHOR]

The cryopreservation of cell lines such as primordial germ cells and germ cells is a promising strategy to conserve and reconstitute endangered or commercially important species in aquaculture. In Mexico, the northwest region is the center of the country's most significant fishing and aquaculture production. However, most of the species used in capture fishing are overexploited. Despite this, protocols for the cryopreservation of germ cells are non-existent. Therefore, this work aimed to establish a protocol of isolation, identification, and cryopreservation of germ cells in two species, totoaba (Totoaba macdonaldi) and yellowtail amberjack (Seriola lalandi). Three concentrations of trypsin (0.25%, 0.3%, and 0.5%) were tested for gonadal dissociation. The 0.3% trypsin concentration was the best because it presented the most significant number of viable cells, with 14.35 x 105 for totoaba and 2.96 x 105 for yellowtail amberjack. The immunohistochemistry identification of germ cells in both species was positive for vasa, with 33.30% for totoaba and 34.20% for yellowtail amberjack. The cryoprotectant used was ethylene glycol (1.5 M or 2 M). The ideal temperature for the cryopreservation of gonadal tissue was different for each species, -1°C/min for totoaba and -5°C/min for yellowtail amberjack with 58.42% and 63.48% viable cells after thawing, respectively, with ethylene glycol 1.5 M being the best for both species. The non-controlled rate was the most effective technique to freeze the cell suspension, with 4.20 ± 1.09 x 105/mL viable cells for totoaba and 7.31 ± 2.25 x 105/mL for yellowtail amberjack. In conclusion, the results of the isolation, identification, and cryopreservation protocols for germ cells in totoaba and yellowtail amberjack obtained in this work are the first report for fish species from northwest Mexico, opening the door for the generation of cryobanking of germ cells. Finally, this work would help conserve endangered species and be an alternative to conserving species of commercial importance in aquaculture. [ABSTRACT FROM AUTHOR]

Recently, cases of antifreeze poisoning in companion animals, particularly cats, have surged in the Republic of Korea. Ethylene glycol (EG), the toxic primary component of antifreeze, is metabolized into glycolic acid (GA), leading to severe metabolic acidosis, acute kidney injury, and death. Traditional detection methods, although effective, are often time-consuming owing to complex sample preparation. This study involved a novel analytical method utilizing GC-MS for EG and LC-MS/MS for GA detection, which streamlined the detection process by eliminating the need for derivatization. The method was validated for accuracy and reliability, enabling the rapid and precise identification of EG and GA in biological samples. This study also included the successful application of this method in a case where initial exposure to antifreeze was not apparent, which highlighted the effectiveness of this method in diagnosing poisoning even in cases where clinical history is unclear. The development of this rapid diagnostic approach addresses the urgent need for the efficient detection of antifreeze poisoning, improving animal welfare and supporting forensic investigations. [ABSTRACT FROM AUTHOR]

Diversity in solvent selection bestows the organic gel with appealing characteristics embracing antidrying, anti‐icing, and antifouling abilities. However, organic gel, subjected to the "toxic" inherent property of solvent, is not able to be manipulated on skin. Herein, introducing the hydrogel layer amid organic gel and skin is envisaged to realize application of organic gel on skin. Hydrogel, inserted as the medium layer, works for the coupling role between skin and organic gel, also avoids the direct contact of organic gel toward skin. First, hydrogel system composed of acrylic acid is fabricated, meanwhile organic gel is prepared employing 2‐hydroxyethyl methacrylate, ethylene glycol (EG) as solvent. Organic gel is able to adhere to hydrogel by hydrogen bonding resulting from carboxyl groups of polyacrylic acid chains and hydroxyl groups occurring on 2‐hydroxyethyl methacrylate or EG. Additionally, hydrogen bonding enables the hydrogel to be firmly attached to skin, thus organic gel/hydrogel/skin assembly is produced. The further application of organic gel is exploited by incorporating stimuli‐responsive dyes including spiropyran and rhodamine derivative. [ABSTRACT FROM AUTHOR]

The escalating demand for plastics has resulted in a surge of plastic waste worldwide, posing a monumental environmental challenge. To address this issue, a versatile photo‐oxidative degradation method applicable to seven distinct polymer families is proposed, comprising poly(isobutyl vinyl ether) (PIBVE), poly(2,3‐dihydrofuran) (PDHF), poly(vinyl acetate) (PVAc), poly(n‐butyl acrylate) (PBA), poly(methyl acrylate) (PMA), poly(vinyl chloride) (PVC), poly(dimethyl acrylamide) (PDMA), poly(ethylene oxide) (PEO), poly(oligo(ethylene glycol) methyl ether acrylate) (PEGMEA), and even poly(methyl methacrylate) (PMMA). This method employs photo‐mediated hydrogen atom transfer (HAT) followed by oxidation to promote polymer degradation. This reaction is carried out under aerobic condition in the presence of iron trichloride (FeCl3) as a photocatalyst in combination with low‐intensity purple light irradiation. The process can degrade up to 97% of the polymer in less than 3 h. This degradation process can be easily controlled by switching the light off, which allows for precise modulation of the degradation rate, enhancing the effectiveness of the method. Overall, this method provides a sustainable method for degrading various polymer types with low energy input. [ABSTRACT FROM AUTHOR]

The constant improvement of stereolithography (SL) in terms of achievable resolution and printing time has sparked high expectations that SL will enable the rapid prototyping of truly microfluidic chips with features below 100 µm. However, most commercial high‐resolution stereolithography devices are based on Digital Light Processing (DLP) and thus sacrifice lateral printing size for resolution. Consequently, even 10 years after the advent of microstereolithography there is no commercialized 3D printing system that can effectively fulfill all the demands to replace soft lithography for microfluidic prototyping. In this work, for the first time, This study demonstrates that a commercial laser‐based stereolithography device is capable of manufacturing microfluidic chips with embedded channels smaller than 100 µm with a footprint of 7.24 × 0.3 cm2. A chip fabricated in poly(ethylene glycol) diacrylate (PEGDA) that can readily be used for fluid mixing, is presented in this study. This research shows that the accessibility of high‐resolution chips with footprints of several cm2, using laser‐based stereolithography, enables the manufacturing of truly microfluidic systems with high impact on prototyping and manufacturing. [ABSTRACT FROM AUTHOR]

Ideonella sakaiensis is a bacterium that can degrade and consume polyethylene terephthalate (PET), a plastic material that was previously considered non‐biodegradable. The degradation of PET requires two enzymes, namely poly (ethylene terephthalate) hydrolase (PETase) and mono (2‐hydroxyethyl) terephthalate hydrolase (MHETase), which break down PET into terephthalate (TPA) and ethylene glycol (EG), which serve as carbon sources for the bacterium. Previous studies have focused on the enzymatic properties, structure, and mechanism of action of PETase and MHETase. However, the regulation of PETase and MHETase gene expression has not been investigated. This study identified a protein that binds to the MHETase promoter DNA, MHETase gene‐regulating protein (MRP) in I. sakaiensis. PET or TPA induced the expression of PETase and MHETase genes. Furthermore, the induction of the MHETase gene was abolished by the deletion of the mrp gene, while the expression of the PETase gene was maintained. In addition, the genes involved in TPA metabolism were not induced in the mrp mutant. Furthermore, the growth of the PET and TPA deteriorated due to mrp mutation. Also, MRP binds to the promoter regions of the MHETase gene and TPA metabolizing genes, but not to the PETase gene promoter. These results suggest that MRP is a transcription factor that activates MHETase and TPA‐metabolizing genes. [ABSTRACT FROM AUTHOR]

Biomass feedstock ethylene glycol (EG) can be anodically oxidized to the high‐value glycolic acid (GA), which is widely considered as one critical raw material of biodegradable plastics. Developing low‐cost electrocatalyst to economically produce GA with high selectivity still meeting challenges. Herein, a non‐precious Co‐Ni bimetal catalysts are developed for controllable electrooxidizing EG to GA (EGOR). Through regulating the generation of key intermediate (CH2OH‐CO*) on the low‐cost catalyst surface, a successive electrooxidation from EG to GA has been achieved with high selective (96.3%) and conversion rate (>85%) at current density of 150 mA cm−2, which is on par with the reported precious metal catalysts. Through coupling with hydrogen evolution reaction (EGOR‐HER), 2.759 mmol H2 and 7.48 mmol of GA are generated at 80 mA cm−2, which also can save 27% energy comparing with a water splitting system. The synergistic effect between Co and Ni in the bimetallic catalyst has been exploited: high‐valent CoOOH sites catalyzed the generation of CH2OH‐CO* and reduce the energy barrier during GA formation; Whereas, Ni sites can effectively facilitate the formation of CoOOH and improve the adsorption of EG. [ABSTRACT FROM AUTHOR]

Two novel ibuprofen cystamine salts (IBU‐CYS 1 and IBU‐CYS 2) are synthesized by coupling the anion of ibuprofen with cystamine dihydrochloride in 1 : 1 and 2 : 1 ratio to improve the solubility and bioavailability of ibuprofen. The salts are characterized by 1H NMR, FT‐IR and UV‐Vis spectroscopy, differential scanning calorimetry (DSC), thermogravimetry (TGA, DTA) and X‐ray diffraction measurements. IBU‐CYS 1 and IBU‐CYS 2 show higher solubility (6.11 and 7.81 mg/mL) compared to ibuprofen (0.04 mg/mL) in water. IBU‐CYS2 was encapsulated into 2‐hydroxyethyl methacrylate: poly (ethylene glycol) acrylate hydrogels for enhanced delivery. The in vitro studies in PBS (pH 7.4) indicate that the salts are effective in relieving inflammatory responses induced by lipopolysaccharide in RAW264.7 macrophage cells (nitrite inhibition percentages of IBU‐CYS 1, IBU‐CYS 2 and ibuprofen: approximately 34.29, 27.03 and 31.50 respectively) while indicating no cytotoxicity. Therefore, these salts may be promising candidates for the development of effective formulations of this drug. [ABSTRACT FROM AUTHOR]

Cellulose nanocrystal (CNC)‐reinforced composites are gaining commercial attention on account of their high strength and sustainable sourcing. Grafting polymers to the CNCs in these composites has the potential to improve their properties, but current solution‐based synthesis methods limit their production at scale. Utilizing dynamic hindered urea chemistry, a new method for the melt‐functionalization of cellulose nanocrystals has been developed. This method does not require toxic solvents during the grafting step and can achieve grafting densities competitive with state‐of‐the‐art solution‐based grafting methods. Using cotton‐sourced, TEMPO‐oxidized CNCs, multiple molecular weights of poly(ethylene glycol) (PEG) as well as dodecane, polycaprolactone, and poly(butyl acrylate) were grafted to the CNC surface. With PEG‐grafted nanoparticles, grafting densities of 0.47 chains nm−2 and 0.10 chains nm−2 were achieved with 2000 and 10,000 g mol−1 polymer chains respectively, both of which represent significant improvements over previous reports for solution‐based PEG grafting onto CNCs. [ABSTRACT FROM AUTHOR]

Functional polyvinylethylene glycols (PVEGs) with pendent vinyl groups were synthesized by Pd/B synergistic catalysts and their structures were characterized by 1H NMR and FT‐IR. The photopolymerization of the obtained PVEGs with multifunctional thiols in the presence of a photoinitiator proceeded smoothly via thiol‐ene photo‐click reaction to give a series of crosslinked materials by the variation of the molecular weight of PVEGs and a ratio of thiols and enes. The curing behavior was studied by FT‐IR and the properties of crosslinked materials were characterized by the test of gel content, swelling ratio, and water absorption. The dynamic mechanical analysis, mechanical properties, thermogravimetry, and surface properties of the crosslinked materials were investigated and the performance of coating for the crosslinked film materials was also characterized. The crosslinked film materials can be further functionalized by post‐crosslinking modification through thiol‐ene photo‐click reaction. [ABSTRACT FROM AUTHOR]

Homopolymers and alternating copolymers of conjugated molecules exhibit impressive performance in electronic devices. Despite the well‐established procedures, the synthesis of alternating copolymers using three monomers is not as easy as random copolymers. Besides facile synthesis, the random copolymers can match the performance of alternating copolymers in electronic devices. Herein, random copolymers are designed and synthesized comprising thienoisoindigo (TIIG), diketopyrrolopyrrole (DPP), and thiophene. The DPP monomers installed with various side chains including branched alkyl chain, branched alkyl chain with ester functionality, linear oligo ethylene glycol, and siloxane terminated alkyl chain are incorporated into the polymers (P1, P2, P3, and P4, respectively). All the thermally stable, low bandgap random copolymers exhibited strong H‐type aggregation in thin film. The relationship between thin film microstructure originating from diverse side chains and the charge transport in organic field effect transistors (OFETs) is investigated. All the random copolymers exhibited predominantly p‐type charge transport and a maximum hole mobility of 2 × 10−2 cm2 V−1s−1 is observed for P3. The packing of all the polymers is examined theoretically by density functional theory (DFT) and compared with experimental values obtained from grazing incident X‐ray diffraction (GIXRD). [ABSTRACT FROM AUTHOR]

The significance of the present article is to enhance the thermal management and energy efficiency of complex engineering infrastructures such as energy storage systems, modern electric vehicles, thermal insulations, heavy‐duty machinery, and production units. This research aims to understand the intricate relationship between the thermal conductivity performance of ternary (SiO2+Fe2O3+TiO2+H2O+C2H6O2${\mathrm{SiO}}_2 + {\mathrm{Fe}}_2{{\mathrm{O}}}_3 + {\mathrm{TiO}}_2 + {\mathrm{H}}_2{\mathrm{O}} + {{\mathrm{C}}}_2{{\mathrm{H}}}_6{{\mathrm{O}}}_2$) hybrid nanomaterial and entropy generation to optimize material design and efficacy. A synergetic combination of three distinct nanomaterials silicon dioxide, ferric oxide, and titanium oxide with ethylene glycol and water in the ratio 3:2 as a base solvent is comprised of contributing unique thermophysical properties. To elucidate the impact of this hybrid composition on thermal conductivity, various factors are analyzed. The advanced computational technique of Artificial intelligent feed‐forward neural network (AIFFNN) is utilized. The problem governed the system of PDEs, which is transformed into ODEs by dimensionless similarity. Adams method provided the dataset which is filtered and embedded into Marquardt–Levenberg Algorithm (LMA). The study examines the role of nanomaterial constituents, morphology, and boundary conditions on thermal performance and entropy generation. Graphical analysis of velocity, temperature, and entropy is provided with respect to varying parameters, including surface absorption (λ), magnetic strength (Tesla M), radiation parameter (Rd), Brownian motion (Br), and Eckert number (Ec). The findings have practical significance for optimizing material design in engineering and industrial applications. [ABSTRACT FROM AUTHOR]

Porous liquids (PLs) are a new type of fluid sorbent investigated mainly for the separation of gas mixtures. Here, we explore their application to the separation of miscible liquids, using MEG/water (MEG=monoethylene glycol) and EtOH/water as proof‐of‐principle. Recovery of used MEG is industrially important but its extraction into conventional solvents from water is difficult. PLs ZIF‐8@PDMS (PL1, PDMS=polydimethylsilicone) or ZIF‐8@sesame oil (PL2) each consisting of 25 wt % of the hydrophobic microporous material ZIF‐8 dispersed in PDMS or sesame oil respectively, were formulated and found to be exceedingly physically stable to sedimentation. A 5 nm PEEK membrane was used to provide a permeable barrier between the PL and the alcohol/water phase. MEG was selectively extracted through the membrane from approximately 50 : 50 wt % MEG/water mixtures into the PL phase and this procedure could be applied repeatedly. It was effective for MEG/water mixtures as dilute as 3 : 97 wt %. The PL could also be regenerated (80 °C at 0.01 bar) and re‐used, suggesting its potential for continuous, cyclic extraction. Furthermore, PL3 (silicalite‐1@PDMS) was effective in selective alcohol extraction from beverages. It shows potential for lowering the alcohol concentration in gin or wine due to its excellent chemical stability and nontoxicity. Overall, we show that the enhanced adsorption properties of PLs due the presence of empty pores, which provides unusually high gas solubilities, also makes them, in principle, applicable to liquid‐liquid separations. [ABSTRACT FROM AUTHOR]

Chemocatalytic conversion of cellulose to ethanol provides an alternative route for biofuel production with a theoretical carbon yield of 100%; however, it faces significant challenges of high catalyst cost and poor catalyst stability. In this work, we report a new strategy to decrease the use of expensive noble metals, by decorating mononuclear NbOx on a low-Pt Pt/WOx catalyst surface. The resulting 0.1Nb/0.5Pt/WOx catalyst gave rise to an ethanol yield of 33.7% together with an ethylene glycol yield of 21.8%, and the noble metal efficiency reached 25.90 gethanol gPt−1 h−1, an increase by a factor of 2–10 compared to those in the literature. Moreover, the catalyst stability was significantly enhanced by the decoration of mononuclear NbOx, allowing for recycling at least 7 times without obvious activity decay. Characterization revealed that Pt was highly dispersed at subnanometer and single atom scales, and modification with mononuclear NbOx facilitated hydrogen spillover and created more oxygen vacancies on the WOx surface upon hydrogen reduction, thus generating a higher density of Brønsted acid sites. This effect not only favored cellulose conversion to ethylene glycol but also promoted the hydrogenolysis of ethylene glycol to ethanol. [ABSTRACT FROM AUTHOR]

Monodisperse biodegradable polymer microspheres show broad applications in drug delivery and other fields. In this study, we developed an effective method that combines microfluidics with interfacial instability to prepare monodispersed poly(lactic-co-glycolic acid)-b-polyethylene glycol (PLGA-PEG)/poly(lactic-co-glycolic acid) (PLGA) microspheres with tailored surface morphology. By adjusting the mass ratio of PLGA-PEG to PLGA, the concentration of stabilizers and the type of PLGA, we generated microspheres with various unique folded morphologies, such as "fishtail-like", "lace-like" and "sponge-like" porous structures. Additionally, we demonstrated that risperidone-loaded PLGA-PEG/PLGA microspheres with these folded morphologies significantly enhanced drug release, particularly in the initial stage, by exhibiting a logarithmic release profile. This feature could potentially address the issue of delayed release commonly observed in sustained-release formulations. This study presents a straightforward yet effective approach to construct precisely engineered microspheres offering enhanced control over drug release dynamics. [ABSTRACT FROM AUTHOR]

Indacaterol, a β2 agonist prescribed for long-term management of patients with chronic obstructive pulmonary disease and asthma. In this study the first MISPE cartridges was developed using indacaterol as a template for its selective extraction from rat lung tissues, enabling precise pharmacokinetic evaluation at the drug's site of action. A molecular imprinting polymer was synthesized using indacaterol as a template, methacrylic acid as a functional monomer and ethylene glycol dimethacrylate as a cross-linker with a molar ratio (1: 4: 20). The polymer was characterized by a high binding capacity of 9840 ± 0.86 and high selectivity with an imprinting factor of 4.53 ± 0.12. The synthesized polymer was utilized as a sorbent in solid-phase extraction to purify and extract indacaterol from lung tissue matrix. The optimum molecularly imprinted solid-phase extraction (MISPE) conditions were 20.0 mg of molecular imprinting polymer and non-imprinting polymer, acetonitrile as the loading solvent, acetonitrile: water (20: 80; by volume) as the washing solvent, and methanol: acetic acid (90: 10; by volume) as the eluting solvent. A pharmacokinetic study was performed for indacaterol in rat lungs using the synthesized and optimized MISPE cartridge as a tool for sample purification. These parameters were determined in the lung tissues of rats emphasizing the local exposure of indacaterol to its target organ. The Cmax and Tmax were 51.020 ± 2.810 µg mL− 1 and 0.083 ± 0.001 h, respectively. The AUC 0−24 and AUC0 − inf were 175.920 ± 1.053 and 542.000 ± 5.245 µg h mL− 1, respectively. The elimination rate constant was 0.014 ± 0.00012 h− 1 and the half-life time was 48.510 ± 0.012 h. This study successfully developed and optimized MISPE cartridges using indacaterol as a template, enabling precise pharmacokinetic evaluation in rat lung tissues. The cartridges demonstrated high binding capacity and selectivity, providing crucial insights into the local exposure of indacaterol at its site of action. [ABSTRACT FROM AUTHOR]

Chemocatalytic conversion of cellulose to ethanol provides an alternative route for biofuel production with a theoretical carbon yield of 100%; however, it faces significant challenges of high catalyst cost and poor catalyst stability. In this work, we report a new strategy to decrease the use of expensive noble metals, by decorating mononuclear NbOx on a low-Pt Pt/WOx catalyst surface. The resulting 0.1Nb/0.5Pt/WOx catalyst gave rise to an ethanol yield of 33.7% together with an ethylene glycol yield of 21.8%, and the noble metal efficiency reached 25.90 gethanol gPt−1 h−1, an increase by a factor of 2–10 compared to those in the literature. Moreover, the catalyst stability was significantly enhanced by the decoration of mononuclear NbOx, allowing for recycling at least 7 times without obvious activity decay. Characterization revealed that Pt was highly dispersed at subnanometer and single atom scales, and modification with mononuclear NbOx facilitated hydrogen spillover and created more oxygen vacancies on the WOx surface upon hydrogen reduction, thus generating a higher density of Brønsted acid sites. This effect not only favored cellulose conversion to ethylene glycol but also promoted the hydrogenolysis of ethylene glycol to ethanol. [ABSTRACT FROM AUTHOR]

The bioconversion of cellulose and the transformation of glycerol can yield various diols, aligning with environmental sustainability goals by reducing dependence on fossil fuels, lowering raw material costs, and promoting sustainable development. However, in the selective hydrogenolysis of glycerol to ethylene glycol (EG) and 1,2-propylene glycol (1,2-PG), challenges such as low selectivity of catalytic systems, poor stability, limited renewability, and stringent reaction conditions remain. The production of diols from cellulose involves multiple reaction steps, including hydrolysis, isomerization, retro-aldol condensation, hydrogenation, and dehydration. Consequently, the design of highly efficient catalysts with multifunctional active sites tailored to these specific reaction steps remains a significant challenge. This review aims to provide a comprehensive overview of the selective regulation of catalysts for producing EG and 1,2-PG from cellulose and glycerol. It discusses the reaction pathways, process methodologies, catalytic systems, and the performance of catalysts, focusing on active site characteristics. By summarizing the latest research in this field, we aim to offer a detailed understanding of the state-of-the-art in glycerol and cellulose conversion to diols and provide valuable guidance for future research and industrial applications. Through this review, we seek to clarify the current advancements and selective control strategies in diol production from glycerol or cellulose, thereby offering critical insights for future investigations and industrial scale-up. [ABSTRACT FROM AUTHOR]

Poly(ethylene glycol 1,4-cyclohexanedimethylene isosorbide terephthalate) (PEICT) copolymers synthesized from isosorbide (ISB), 1,4-cyclohexanedimethanol (CHDM), ethylene glycol (EG) and terephthalic acid (PTA) via polycondensation are a class of heat-resistant bio-based polyesters. The content of biomass-sourced ISB has an important influence on the various properties of the terpolymers but lacks detailed study. Herein, we synthesized a series of amorphous terpolyesters with different contents of ISB by melt polycondensation of ISB, CHDM, EG and PTA in a 30 L reactor, and investigated the effect of ISB content on the thermal, mechanical, optical and rheological properties. As the content of ISB increasing, the complex viscosities of terpolyesters were increased and the intrinsic viscosities were decreased. The tensile strength was increased from 45.1 MPa for poly(ethylene glycol 1,4-cyclohexanedimethylene terephthalate) (PCTG)to 48.1 MPa for PEI13.2CTandthe Tg was increased from 83.5 °C for PCTG (ISB 0 mol%) to 98.8 °C for PEI13.2CT (ISB 13.2 mol%). All the values of Td,5%, and Td,max of the terpolyesters were higher than 395 °C and 425 °C. [ABSTRACT FROM AUTHOR]

Smart polymers undergo significant physical or chemical changes in response to stimuli like temperature and pH. Achieving a narrow molecular weight distribution is crucial for their sensitivity. Reversible addition–fragmentation chain transfer (RAFT) in ionic liquids is an effective method for synthesizing such polymers due to its favorable kinetics and environmental benefits. Most studies use imidazolium ionic liquids, while pyridinium ionic liquids are less common despite their easy synthesis. This study reports the first successful RAFT copolymerization of di(ethylene glycol) methyl ether methacrylate (DEGMEMA) and methyl methacrylate in N‐hexylpyridinium hexafluorophosphate ([HPY][PF6]). Both linear and hyperbranched copolymers (Mn > 25,000) with narrow molecular weight distribution were synthesized, showing observable temperature responses and biocompatibility. The linear copolymers had a desirable dispersity (Ð) of less than 1.10, while the hyperbranched copolymer had a Ð of 2.034. The lower critical solution temperatures (LCSTs) of the copolymers were close to or below the LCST of PDEGMEMA (26°C). This study indicates that pyridinium ionic liquids can be explored as a suitable solvent for synthesizing methacrylate‐based smart polymers. [ABSTRACT FROM AUTHOR]

Liquefied hydrogen has a high energy density, so it is suitable for railways that require a lot of energy and use fuel for a long time. In this paper, the effects of changes in hydrogen inlet flow rate, outlet pressure conditions, and ethylene glycol water (EGW) flow rate in liquefied hydrogen heat exchangers for locomotives on hydrogen outlet temperature, EGW outlet temperature, hydrogen pressure-drop, hydrogen outlet density, hydrogen outlet flow velocity, and EGW freezing possible range were analyzed through computational analysis. Increasing the inlet flow rate of EGW increased the outlet temperature of EGW and hydrogen, and showed a greater effect in reducing the freezing possible range than increasing the outlet temperature of hydrogen. Increasing the hydrogen outlet pressure increased the hydrogen and EGW outlet temperature and had a greater effect on the increase in the hydrogen outlet temperature than the decrease in the freezing possible range. [ABSTRACT FROM AUTHOR]

In the study, a new strategy is presented to make PLGA (poly lactic‐co‐glycolic acid) and POEGMEMA (poly(oligo(ethylene glycol) methyl ether methacrylate)) based biodegradable and biocompatible tissue scaffold via a new physical cross‐linking method. The advantage of brushed structure of POEGMEMA polymer and the hydrophobic character of PLGA polymer is taken to make physically entangled network in aqueous media. The hydrophobic nature of PLGA allows to get scaffolds even at low ratio of PLGA (25%, w/w) when using POEGMEMA (yield: 86%). This strategy gives robust polymeric networks in aqueous media without using chemical reactions through high hydrophilic polymer content. Scaffolds with high POEGMEMA ratio (75%, w/w) show two times higher water uptake ratio (≈300%) and two times lower compression strength (19 kPa) compared to the ones with lower POEGMEMA content (50%, w/w). They also show desired degradation profiles in various aqueous solutions. While the scaffolds prepared with 25% and 50% PLGA are almost stable in first 20 days, they completely degrade in 40–50 days. Both scaffold formulations (25% PLGA‐75% POEGMEMA and 50% PLGA‐50% POEGMEMA) have similar proliferative properties for fibroblast cells. The scaffolds also do not show toxicity compared to control group according to live‐dead assay. [ABSTRACT FROM AUTHOR]

The sluggishness of the complementary oxygen evolution reaction (OER) is reckoned as one of the major drawbacks in developing an energy‐efficient green hydrogen‐producing electrolyzer. An array of organic molecule oxidation reactions, operational at a relatively low potential, have been explored as a substitute for the OER. Glycerol oxidation reaction (GOR) has emerged as a leading alternative in this context because glycerol, a waste of biodiesel manufacturing, has become ubiquitous and accessible due to the significant growth in the biodiesel sector in recent decades. Additionally, the GOR generates several value‐added organic compounds following oxidation that enhance the cost viability of the overall electrolysis reaction. In this study, a low‐cost, room temperature operable, and energy‐efficient synthetic methodology has been developed to generate unique two‐dimensional CuO nanosheets (CuO NS). This CuO NS material was embedded on a carbon paper electrode, which showcased excellent glycerol electro‐oxidation performance operational at a moderately low applied potential. Formic acid is the major product of this CuO NS‐driven GOR (Faradaic efficiency ~80 %), as it is formed primarily via the glyceraldehyde oxidation pathway. This CuO NS material was also active for oxidizing other abundant alcohols like ethylene glycol and diethylene glycol, albeit at a relatively poor efficiency. Therefore, this robust CuO NS material has displayed the potential to be used in large‐scale electrolyzers functioning with HER/GOR reactions. [ABSTRACT FROM AUTHOR]

Automakers are focusing on lightweight vehicles to address fuel economy and emission challenges and are using high-performance materials such as 2K PU-based joints as alternatives to cast iron, steel, and other metals. This study was conducted with the aim of expanding the application of 2K PU and enhancing its compatibility with steel substrates, which are commonly used in the automotive manufacturing industry, through the use of O-I hybrid nanoparticles containing alkoxysilane groups as additives in the 2K PU formulation. At the same time, the simplified process introduced and examined in this study demonstrates its feasibility for industrial-scale applications; the process offers notable advantages in reducing workload and curing time by eliminating cumbersome surface pretreatment steps before applying the 2K PU layer. Two types of commercial SB PU and EB PU were selected to study the mechanism by which O-I hybrid NPs enhance adhesion when integrated directly into the 2K PU formulation. We optimized various input parameters through practical work and modeling using the response surface method. These parameters included the amounts of AFAP precursor, APTES, and butylene glycol (BG) and the mixing ratio of O-I hybrid NPs in the formulations of two commercial PUs. The results show that O-I hybrid NPs significantly enhance adhesion, increasing performance on stainless surfaces by up to 2.35 times compared to pristine EB and SB PU. Notably, the SB PU's performance can improve up to 2.5 times according to the RSM predictions, highlighting the substantial impact of O-I hybrid NPs. [ABSTRACT FROM AUTHOR]