Glycol Research Articles

Electrical conductivity of Ni ferrite nanofluids: An experimental study on the effects of temperature, volume fraction, and base fluid

This study investigates the electrical conductivity of NiFe2O4 nanofluids in water and ethylene glycol (EG) as base fluids, aiming to understand how varying volume fractions (φ= 0 %, 0.1 %, 0.25 %, 0.45 %, 0.7 %, and 1 %) and temperatures (20–70°C) influence electrical conductivity. NiFe2O4 nanoparticles were synthesized using the chemical co-precipitation method and characterized through X-ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), and Energy Dispersive Spectroscopy (EDS). The results revealed that at 70°C, the electrical conductivity of NiFe2O4-water nanofluid increased by 1100 % within the volume fraction range of 0–1 %. For NiFe2O4-EG nanofluid, the increase in electrical conductivity was even more significant, reaching 1235 % within the same volume fraction range. Similarly, at a 1 % volume fraction within the temperature range of 20–70°C, the electrical conductivity of NiFe2O4-water nanofluid increased by 136 %, while for NiFe2O4-EG nanofluid, it was 370 %. These findings indicate that both temperature and volume fraction significantly enhance the electrical conductivity of the nanofluids, with a more pronounced effect observed in the NiFe2O4-EG nanofluid compared to the NiFe2O4-water nanofluid. The study validated Shen et al.'s model for electrical conductivity in nanofluids, contrasting with Maxwell's model. The novelty of this work lies in the comprehensive analysis of the electrical conductivity behavior of these nanofluids, which has not been extensively reported in the literature. These findings have potential applications in heat transfer enhancement and magnetic-targeted drug delivery.

Silylation-Driven Volatility Enhancement in Mononuclear Calcium, Magnesium, and Barium Complexes with Monomethyl or Silyl Ether and Bis(diketonate).

Magnesium, calcium, and barium heteroleptic complexes were synthesized by the substitution reaction of the bis(trimethylsilyl)amide of Mg(btsa)2·DME, Ca(btsa)2·DME, and Ba(btsa)2·2DME with an ethereal group and hfac ligands (btsa = bis(trimethylsilyl)amide, DME = dimethoxyethane). The compounds Mg(dts)(hfac)2 (1), Ca(dts)(hfac)2 (2), Mg(dmts)(hfac)2 (3), Ca(dmts)(hfac)2 (4), and Ba(dmts)(hfac)2 (5) were fabricated and analyzed using various techniques, including Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analyses, and elemental analysis (dts = 2,2-dimethyl-3,6,9-trioxa-2-siladecane, dmts = 2,2-dimethyl-3,6,9,12-tetraoxa-2-silatridecane, hfac = hexafluoroacetylacetonate). The structures of complexes 2, 4, and 5 were confirmed using single-crystal X-ray crystallography; all complexes display monomeric structures. All compounds underwent trimethylsilylation of the coordinating ethereal alcohols (meeH and tmgeH) in the presence of HMDS as byproducts because of their increasing acidity originating from the electron-withdrawing hfac ligands. (meeH = 2-(2-methoxyethoxy)ethan-1-ol, tmgeH = tri(ethylene glycol) monoethyl ether, HMDS = hexamethyldisilazane).

Plant-based therapies for urolithiasis: a systematic review of clinical and preclinical studies.

Urolithiasis, the formation of kidney stones, is a common and severe condition. Despite advances in understanding its pathophysiology, affordable treatment options are needed worldwide. Hence, the interest is in herbal medicines as alternative or supplementary therapy for urinary stone disease. This review explores the use of plant extracts and phytochemicals in preventing and treating urolithiasis. Following PRISMA standards, we systematically reviewed the literature on PubMed/Medline, focusing on herbal items evaluated in in vivo models, in vitro studies, and clinical trials related to nephrolithiasis/urolithiasis. We searched English language publications from January 2021 to December 2023. Studies assessing plant extracts and phytochemicals' therapeutic potential in urolithiasis were included. Data extracted included study design, stone type, plant type, part of plant used, solvent type, main findings, and study references. A total of 64 studies were included. Most studies used ethylene glycol to induce hyperoxaluria and nephrolithiasis in rat models. Various extraction methods were used to extract bioactive compounds from different plant parts. Several plants and phytochemicals, including Alhagi maurorum, Aerva lanata, Dolichos biflorus, Cucumis melo, and quercetin, demonstrated potential effectiveness in reducing stone formation, size, and number. Natural substances offer an alternative or supplementary approach to current treatments, potentially reducing pain and improving the quality of life for urolithiasis patients. However, further research is needed to clarify their mechanisms of action and optimize their therapeutic use. The potential of plant-based therapies in treating urolithiasis is promising, and ongoing research is expected to lead to treatment advancements benefiting patients globally.

Intracellular Gelation-Mediated Living Bacteria for Advanced Biotherapeutics in Mouse Models.

Despite its significant potential in various disease treatments and diagnostics, microbiotherapy is consistently plagued by multiple limitations ranging from manufacturing challenges to in vivo functionality. Inspired by the strategy involving nonproliferating yet metabolically active microorganisms, we report an intracellular gelation approach that can generate a synthetic polymer network within bacterial cells to solve these challenges. Specifically, poly(ethylene glycol dimethacrylate) (PEGDA, 700 Da) monomers are introduced into the bacterial cytosol through a single cycle of freeze-thawing followed by the initiation of intracellular free radical polymerization by UV light to create a macromolecular PEGDA gel within the bacterial cytosol. The molecular crowding resulting from intracytoplasmic gelation prohibits bacterial division and confers robust resistance to simulated gastrointestinal fluids and bile acids while retaining the ability to secrete functional proteins. Biocompatibility assessments demonstrate that the nondividing gelatinized bacteria are effective in alleviating systemic inflammation triggered by intravenous Escherichia coli injection. Furthermore, the therapeutic efficacy of gelatinized Lactobacillus rhamnosus in colitis mice provides additional support for this approach. Collectively, intracellular gelation indicates a universal strategy to manufacture next-generation live biotherapeutics for advanced microbiotherapy.

Characterization of Iron Oxide Nanotubes Obtained by Anodic Oxidation for Biomedical Applications—In Vitro Studies

To improve the biocompatibility and bioactivity of biodegradable iron-based materials, nanostructured surfaces formed by metal oxides offer a promising strategy for surface functionalization. To explore this potential, iron oxide nanotubes were synthesized on pure iron (Fe) using an anodic oxidation process (50 V–30 min, using an ethylene glycol solution containing 0.3% NH4F and 3% H2O, at a speed of 100 rpm). A nanotube layer composed mainly of α-Fe2O3 with diameters between 60 and 70 nm was obtained. The effect of the Fe-oxide nanotube layer on cell viability and morphology was evaluated by in vitro studies using a human osteosarcoma cell line (SaOs-2 cells). The results showed that the presence of this layer did not harm the viability or morphology of the cells. Furthermore, cells cultured on anodized surfaces showed higher metabolic activity than those on non-anodized surfaces. This research suggests that growing a layer of Fe oxide nanotubes on pure Fe is a promising method for functionalizing and improving the cytocompatibility of iron substrates. This opens up new opportunities for biomedical applications, including the development of cardiovascular stents or osteosynthesis implants.

From Ethylene Glycol to Glycolic Acid: Electrocatalytic Conversion on Pt-Group Metal Surfaces.

Ethylene glycol (EG) is one of the most attractive platform molecules derived from biomass and waste plastics. Thus, the selective electrooxidation of ethylene glycol (EGOR) into value-added chemicals (especially glycolic acid (GA)) can promote its recycling and upgrading. However, the understanding of the EG-to-GA process on Pt-group metal (PGM) electrodes is far limited now. It has been shown that the Pt and Pd electrodes could show considerable EGOR activity but not Rh and Ir electrodes. Meanwhile, EGOR mainly produces the glycolate, oxalate, and formate on Pt and Pd electrodes, whereas it can obtain minute amounts of glycolate and oxalate on Rh and Ir electrodes. Impressively, the selectivity of glycolate on Pt and Pd electrodes can be over 85% (apparent Faradaic efficiency) in alkaline media, although the stability should be further improved through interfacial tuning and/or engineering. This work might deepen the fundamental understanding of the EGOR process on the nature of PGM electrodes.

3D‐Printed Hydrogel Filter for Biocatalytic CO2 Capture

AbstractInnovative scalable CO2 capture technologies are urgently needed to combat the climate crisis. Reactive absorption in alkaline liquids, an essential process for capturing CO2 at atmospheric pressure, requires high gas–liquid contact and fast reaction kinetics. To meet these needs, self‐supporting hydrogel CO2 gas–liquid contactors (or simply “CO2 filters”) containing the CO2 selective catalyst carbonic anhydrase (CA) are developed using the direct ink writing additive manufacturing approach. The multifunctional filters are composed of semi‐interpenetrating polymer network hydrogels (IPNHs) of poly (ethylene glycol) diacrylate/poly (ethylene oxide) (PEG‐DA/PEO) upon photocuring during 3D printing. Formulations with PEG‐DA levels of 30–60 wt% are sufficiently homogeneous and reactive to produce coherent grids. Based on operational parameters, a 56 wt% PEG‐DA formulation is selected to continuously print self‐supporting 3D stacked cylindrical grids, with or without enzymes in ink. The resulting enzyme‐laden IPHN filters deliver ≈3 times higher CO2 capture efficiency than the no‐enzyme control filters in a laboratory‐scale absorption column test. However, the enhancement effect decreases significantly within 2 d of operation, likely due to burst release of enzymes caused by the flowing solution. Covalent crosslinking of CA near the surface, which can improve durability and CO2 capture performance, will be evaluated in future studies.

Effect of Viscosity and Air Gap within the Spinneret on the Morphology and Mechanical Properties of Hollow-Fiber Polymer Membranes for Separation Performance.

Hollow-fiber membranes for nanofiltration were prepared from the blending of Poly (ethylene glycol) (PEG) with Poly (vinyl chloride) (PVC) with different PEG molecular weights (400 and 4000 g/mol) and PVC via a dry/wet spinning process. In the spinning process, the effects of air gap, wind-up speed, dope extrusion rate, and bore extrusion rate were examined. In addition, the different lengths of the center tube, which acted as the inner-side fiber diameter during the preparation of hollow-fiber membranes, were studied. This research was investigated in order to observe the morphological, dielectric, and dynamic mechanical thermal properties to identify a suitable preparation of a hollow-fiber membrane for feasible applications. The morphology of the PVC-580 blended PEG-400 5 weight percent hollow-fiber membrane was seen to have a dense skin on both the inner and outer fiber surface, along with a suitable dope viscosity. Moreover, it offered finger-like substructures that could provide a high applicable feed-stream permeability and selectivity. Finger-like substructures were present on the near inner fiber surface at the controlled center-tube length of 0.3 cm, more so than at the center tube of 1 cm. This was because the solvent and non-solvent in the lumen tube exchanged more quickly than they did in the coagulant bath. The effect of the wind-up speed during the spinning process was significantly influenced by an affordable hollow fiber that can be indicated by the drawing ratio (λ). It was found that the drawing ratio of 3.3 showed a thickness thinner than 2.6 and 2.0, respectively. In summary, a controlled wind-up speed, an acceptable dope viscosity, and-most importantly-an agglomerated time resulted in membrane preparation.

Mitigating the Effects of Persistent Antipolymer Immune Reactions in Nanomedicine: Evaluating Materials-Based Approaches Using Molecular Imaging.

Poly(ethylene glycol) (PEG) is a hydrophilic polymer ubiquitously used in both medical and nonmedical goods. Recent debate surrounding the observed stimulation of immune responses against PEG has spurred the development of materials that may be suitable replacements for this common polymeric component. The underlying view is that these alternative materials with comparable physicochemical properties can overcome the unfavorable and unpredictable effects of antibody-mediated clearance by being chemically, and therefore antigenically, distinct from PEG. However, this hypothesis has not been thoroughly tested in any defined manner, and the immune response observed against PEG has not been rigorously investigated within the context of these emerging materials. Consequently, it remains unclear whether immunity-mediated discrimination between polymeric entities even occurs in vivo and, if this is the case, how it may be exploited. In this study, we utilize positron emission tomography-computed tomography molecular imaging in mice immunized to develop specific antibody responses to PEG and an alternative polymer in order to visualize and quantify the influence of antipolymer antibodies on the biodistribution of synthetic polymers in vivo as a function of immunization status. Under the conditions of this experiment, mice could be primed to exhibit both innate and adaptive immunity to all of the polymer systems to which they were exposed. We demonstrate that alternating between chemically disparate polymers is a viable approach to extend their efficacy when antipolymer humoral immune responses arise.

Facilitating Formate Selectivity via Optimizing eg* Band Broadening in NiMn Hydroxides for Ethylene Glycol Electro‐Oxidation

Ethylene glycol electro‐oxidation reaction (EGOR) on nickel‐based hydroxides (Ni(OH)2) represents a promising strategy for generating value‐added chemicals, i.e. formate and glycolate, and coupling water‐electrolytic hydrogen production. The high product selectivity was one of the most significant area of polyols electro‐oxidation process. Yet, developing Ni(OH)2‐based EGOR electrocatalyst with highly selective product remains a challenge due to the unclear cognition about the EGOR mechanism. Herein, Mn‐doped Ni(OH)2 catalysts were utilized to investigate the EGOR mechanism. Experimental and calculation results reveal that the electronic states of eg* band play an important role in the catalytic performance and the product selectivity for EGOR. Broadening the eg* band could effectively enhance the adsorption capacity of glyoxal intermediates. On the other hand, this enhanced adsorption could lead to reduced side reactions associated with glycolate formation, simultaneously promoting the cleavage of C‐C bonds. Consequently, the selectivity for formate was notably augmented by these enhancements. This work offers new insights into the regulation of catalyst electronic states for improving polyol electrocatalytic activity and product selectivity.

Bioresorbable Polyester Coatings with Antifouling and Antimicrobial Properties for Prevention of Biofilm Formation in Early Stage Infections on Ti6Al4V Hard-Tissue Implants.

Implants made from titanium are used as prostheses because of their biocompatibility and their mechanical properties close to those of human bone. However, the risk of bacterial infection is always a major concern during surgery, and the development of biofilm can make these infections difficult to treat. A promising strategy to mitigate against bacterial infections is the use of antifouling and antimicrobial coatings, where bioresorbable polymers can play an important role due to their controlled degradability and sustained drug release, as well as excellent biocompatibility. In the present study, poly(d,l-lactide) (PDLLA) and poly[d,l-lactide-co-methyl ether poly(ethylene glycol)] (PDLLA-PEG) were studied, varying the PEG content (20-40% w/w) to analyze the effectiveness of PEG as an antifouling molecule. In addition, silver sulfadiazine (AgSD) was used as an additional antimicrobial agent with a concentration ≤5% w/w and incorporated into the PEGylated polymers to create a polymer with both antifouling and antimicrobial properties. Polymers synthesized were applied using spin coating to obtain homogeneous coatings to protect samples made from titanium/aluminum/vanadium (Ti6Al4V). The polymer coatings had a smoothing effect in comparison to that of the uncoated material, decreasing the contact area available for bacterial colonization. It was also noted that PEG addition into the polymeric chain developed amphiphilic materials with a decrease in contact angle from the most hydrophobic (Ti6Al4V) to the most hydrophilic PDLLA-PEG (60/40), highlighting the increase in water uptake contributing to the hydration layer formation, which confers the antifouling effect on the coating. This study demonstrated that the addition of PEG above 20% w/w and AgSD above 1% w/v into the formulation was able to decrease bacterial adherence against clinically relevant biofilm former strains Staphylococcus aureus and Pseudomonas aeruginosa.

Clinical applications of a novel poly-L-lactic acid microsphere and hyaluronic acid suspension for facial depression filling and rejuvenation.

Poly L-lactic acid (PLLA) can stimulate fibrous tissue regeneration to exert a filling effect. However, severe inflammatory reactions and unsatisfactory effects remain a concern. Herein, we describe the mechanism of action, efficacy, and safety of PLLA microspheres in suspension (PLLA-b-PEG/HA) for facial contouring and soft tissue augmentation. PLLA-b-PEG/HA, ssynthesized by copolymerization with ethylene glycol, were suspended in hyaluronic acid (HA). Physiological verification was performed using scanning electron microscopy and X-ray computed tomography. PLLA-b-PEG/HA were subcutaneously injected into the dorsal region of 4-month-old rabbits. Ultrasound assessed volumetric capacity at 3 days and 1, 2, 4, and 12 weeks. The inflammatory response, collagen production, and HA degradation were evaluated. A retrospective case series of 10 patients who received PLLA-b-PEG/HA injections was conducted to assess long-term efficacy and safety. PLLA-b-PEG exhibited a spherical structure with a smooth surface (20-45 μm diameter). In rabbits, implant site volume increased within 4 weeks, gradually decreasing thereafter. Fibrous capsules, microvessel density, and new collagen fiber formation progressively increased at 4, 12, and 26 weeks after injection. Clinical data demonstrated significant improvements in face contouring at months 3 and 12 after injection. All patients showed improved internal contours based on the Global Aesthetic Improvement Scale. After 12 months, 90% of the patients retained good shaping and support effects with minimal adverse reactions. PLLA-b-PEG/HA demonstrated superior biocompatibility and facial regeneration potential, with outstanding dual collagen-stimulating properties. The clinical efficacy and safety of PLLA-b-PEG/HA have been validated and established as a promising therapeutic option.

Red Blood Cell-Like Poly(ethylene glycol) Particles: Influence of Particle Stiffness on Biological Behaviors.

Cell-like particles represent a category of synthetic particles designed to emulate the structures or functions of natural cells. Herein, we present the assembly of cell-like poly(ethylene glycol) (PEG) particles with different stiffnesses and shapes via replication of animal cells and investigate the impact of particle stiffness on their biological behaviors. As a proof of concept, we fabricate red blood cell-like and spherical PEG particles with varying cross-linking densities. A systematic exploration of their properties, encompassing morphology, stiffness, deformability, and biodistribution, reveal the vital influence of particle stiffness on in vivo fate, elucidating its role in governing the traversal of capillaries and the dynamic interactions with phagocytic cells.

Detection and adsorption of florfenicol in milk using bifunctional carbon dot-doped molecularly imprinted polymers.

Detection of florfenicol (FF) residues in animal-derived foods, as one of the most widely used antibiotics, is critically important to food safety. The fluorescent molecularly imprinted polymer (MIP) was synthesized by surface-initiated atom transfer radical polymerization technique with poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) microspheres, 4-vinylpyridine, ethylene glycol dimethacrylate, and FF as the matrix, functional monomer, crosslinker, and template molecule, respectively. Meanwhile, N-S co-doped carbon dot (CD) was synthesized with triammonium citrate and thiourea as precursors under microwave irradiation at 400W for 2.5min and then integrated into FF-MIP to obtain CD@FF-MIP. For comparison, non-imprinted polymer (NIP) without FF was also prepared. The adsorption capacity of CD@FF-MIP to FF reached 53.1mgg-1, which was higher than that of FF-MIP (34.7mgg-1), whereas the adsorption capacity of NIP was only 17.3mgg-1. The adsorption equilibrium of three materials was reached within 50min. Particularly, CD@FF-MIP exhibited an excellent fluorescence quenching response to FF in the concentration range of 3-50 µmolL-1. As a result, CD@FF-MIP was successfully utilized to extract FF in milk samples, which were analyzed by high-performance liquid chromatography. The standard recoveries were 95.8%-98.2%, and the relative standard deviation was 1.6%-4.2%. The method showed the advantages of simple operation, high sensitivity, excellent selectivity, and low cost, and also demonstrated a great application prospect in food detection.

Facilitating Formate Selectivity via Optimizing eg* Band Broadening in NiMn Hydroxides for Ethylene Glycol Electro-Oxidation.

Ethylene glycol electro-oxidation reaction (EGOR) on nickel-based hydroxides (Ni(OH)2) represents a promising strategy for generating value-added chemicals, i.e. formate and glycolate, and coupling water-electrolytic hydrogen production. The high product selectivity was one of the most significant area of polyols electro-oxidation process. Yet, developing Ni(OH)2-based EGOR electrocatalyst with highly selective product remains a challenge due to the unclear cognition about the EGOR mechanism. Herein, Mn-doped Ni(OH)2 catalysts were utilized to investigate the EGOR mechanism. Experimental and calculation results reveal that the electronic states of eg* band play an important role in the catalytic performance and the product selectivity for EGOR. Broadening the eg* band could effectively enhance the adsorption capacity of glyoxal intermediates. On the other hand, this enhanced adsorption could lead to reduced side reactions associated with glycolate formation, simultaneously promoting the cleavage of C-C bonds. Consequently, the selectivity for formate was notably augmented by these enhancements. This work offers new insights into the regulation of catalyst electronic states for improving polyol electrocatalytic activity and product selectivity.

Tuning Mechanical Properties, Swelling, and Enzymatic Degradation of Chitosan Cryogels Using Diglycidyl Ethers of Glycols with Different Chain Length as Cross-Linkers.

Cross-linking chitosan at room and subzero temperature using a series of diglycidyl ethers of glycols (DEs)-ethylene glycol (EGDE), 1,4-butanediol (BDDE), and poly(ethylene glycol) (PEGDE) has been investigated to demonstrate that DEs can be a more powerful alternative to glutaraldehyde (GA) for fabrication of biocompatible chitosan cryogels with tunable properties. Gelation of chitosan with DEs was significantly slower than with GA, allowing formation of cryogels with larger pores and higher permeability, more suitable for flow-through applications and cell culturing. Increased hydration of the cross-links with increased DE chain length weakened intermolecular hydrogen bonding in chitosan and improved cryogel elasticity. At high cross-linking ratios (DE:chitosan 1:4), the toughness and compressive strength of the cryogels decreased in the order EGDE > BDDE > PEGDE. By varying the DE chain length and concentration, permeable chitosan cryogels with elasticity moduli from 10.4 ± 0.8 to 41 ± 3 kPa, toughness from 2.68 ± 0.5 to 8.3 ± 0.1 kJ/m3, and compressive strength at 75% strain from 11 ± 2 to 33 ± 4 kPa were fabricated. Susceptibility of cryogels to enzymatic hydrolysis was identified as the parameter most sensitive to cross-linking conditions. Weight loss of cryogels increased with increased DE chain length, and degradation rate of PEGDE-cross-linked chitosan decreased 612-fold, when the cross-linker concentration increased 20-fold.

Thermal, Morphological, Mechanical, and Biodegradation Properties of Poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide)/High-Density Polyethylene Blends.

Polymer blends of poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide) (PLLA-PEG-PLLA) and high-density polyethylene (HDPE) with different blend ratios were prepared by a melt blending method. The thermal, morphological, mechanical, opacity, and biodegradation properties of the PLLA-PEG-PLLA/HDPE blends were investigated and compared to the PLLA/HDPE blends. The blending of HDPE improved the crystallization ability and thermal stability of the PLLA-PEG-PLLA; however, these properties were not improved for the PLLA. The morphology of the blended films showed that the PLLA-PEG-PLLA/HDPE blends had smaller dispersed phases compared to the PLLA/HDPE blends. The PLLA-PEG-PLLA/HDPE blends exhibited higher flexibility, lower opacity, and faster biodegradation and bioerosion in soil than the PLLA/HDPE blends. Therefore, these PLLA-PEG-PLLA/HDPE blends have a good potential for use as flexible and partially biodegradable materials.

Effect of Solvothermal Time to Characteristics and Performance of Photocatalyst Bismuth‐Rich Oxyiodide for Dye Decolorization

AbstractThis study aims to explore how altering solvothermal duration influences the characteristics of the resulting products, spanning crystal structure, band gap energy, morphology, and photocatalytic performance. Bismuth‐rich oxyiodide was synthesized via the solvothermal method by dissolving Bi(NO3)3 ⋅ 5H2O and KI in ethylene glycol. The mixture underwent heating in a Teflon autoclave stainless steel at 120 °C for durations of 6, 12, 24, and 48 hours. Analysis using FTIR revealed the presence of Bi−O and I−O bonds. Diffractograms indicated that all products exhibited traits of Bi4O5I2, with slight traces of Bi5O7I. Distinct band gap energies were observed across the solvothermal durations: 2 eV for 6 hours, 2.08 eV for 12 hours, and 1.89 eV for both 24 and 48 hours, delineating temporal nuances in product properties. Noteworthy, the morphology of the 12 hour variant revealed surface pores, indicative of intricate structural features. Notably, the 12 hour product exhibited the pinnacle of photocatalytic efficacy in methyl orange decolorization under UV light. Furthermore, investigations into photocatalyst mass variations and the inclusion of additional dyes, such as rhemazol black B, further elucidated the robust photocatalytic potential inherent in the B12 variant.

Effect of Different Shapes of Nanoparticles on Mixed Convective Nanofluid Flow in a Darcy-Forchhiemer Porous Medium

The nanofluid has diverse applications in industries, engineering, and medicine due to its greater thermal characteristics. However, various factors such as the shape and size of nanoparticles, the base fluid, the porous medium, the quadratic drag force, and the viscous dissipation have significant effects on the flow and heat transfer characteristics of nanofluids. Therefore, it is crucial to study the influence of these factors. In this paper, a theoretical investigation is conducted to analyze the mechanisms of thermal conductivities of different shapes of nanoparticles, such as platelet, cylinder, brick and blade on the mixed convective nanofluid flow in a vertical channel saturated with porous medium. Consider ethylene glycol and water as base fluids for the nanoparticles, including copper, aluminum oxide, titanium oxide, silver, and iron oxide. A thin, movable baffle plate of negligible thickness is inserted in the channel and made into double passages. To define the porous matrix, the Darcy-Brinkaman-Forchhiemer model is used, and to define the nanofluid, the Tiwari and Das model is used. Robin boundary conditions are considered for the channel flow. The differential transform method (DTM) is applied to solve non-linear governing equations with inertia, and the perturbation method is applied to solve the problem without inertia. Velocity and temperature cantors are shown graphically using MATLAB and MATHEMATICA. The obtained values by DTM and the perturbation method are well validated and shown graphically. The Nusselt number was evaluated and tabulated for all governing parameters. The objective of this article is to investigate the effect of nonspherical shapes of nanoparticles, the base fluid, the inertial forces of the porous medium, and the buoyancy force on the thermal characteristics of flow and heat transfer of nanofluids. The main findings of this problem are that the optimum velocity and temperature cantor are found for platelet-shaped water-based silver nanofluid.

Synthesis and reaction mechanism of high injected electron concentration and low work function [Ca24Al28O64]4+:(4e-) by Sol-gel method combined with spark plasma sintering

The high injected electron concentration and low work function C12A7:e- was successfully prepared by the sol-gel method combined with spark plasma sintering(SPS) using calcium nitrate, aluminum nitrate, citric acid, and ethylene glycol as raw materials. By analyzing the morphology of carbon and its role in the reactive synthesis, we reveal the reaction synthesis mechanism of C12A7:e- under the SPS. The analysis shows that C12A7:e- started to be generated at 800 °C. During the SPS reaction sintering process, carbon atoms from citric acid and ethylene glycol were excited by a pulsed current at high temperature, forming the carbon ions C22- and C (gas). Both act as reducing agents and react with the free oxygen ions O2- in the C12A7 cage cavity to form gaseous CO or CO2, enabling electrons to be injected into the cage cavity, thus generating C12A7:e-. Meanwhile, the graphene oxide (GO) formed on the surface of C12A7:e- grain is produced by the precursor of sol-gel synthesis in the high temperature oxidation environment, which will be conducive to improving the stability of C12A7: e- in air and high temperature oxidation resistance.