Distilled water and aqueous fullerene nanofluids having concentrations of 0.02, 0.2, and 0.4 vol % and titania (titanium dioxide, TiO2) nanofluids of 0.0002, 0.002, and 0.02 vol % were analyzed for heat transfer characteristics. Quenching mediums were stirred at impeller speeds of 0, 500, 1,000, and 1,500 RPMs in a typical Tensi agitation system. During the quenching process, a metal probe made of ISO 9950 Inconel was used to record the temperature history. The inverse heat conduction method was used to calculate the spatial and temporal heat flux. The nanofluid rewetting properties were measured and matched to those of distilled water. The maximum mean heat flux was 3.26 MW/m2, and the quickest heat extraction was 0.2 vol % fullerene nanofluid, according to the results of the heat transfer investigation.
Graphene oxide (GO)-incorporated poly(methyl methacrylate) (PMMA) nanocomposites (PMMA-GO) have demonstrated a wide range of outstanding mechanical, electrical, and physical characteristics. It is of interest to review the synthesis of PMMA-GO nanocomposites and their applications as multifunctional structural materials. The attention of this review is to focus on the radical polymerization techniques, mainly bulk and emulsion polymerization, to prepare PMMA-GO polymeric nanocomposite materials. This review also discusses the effect of solvent polarity on the polymerization process and the types of surfactants (anionic, cationic, nonionic) and initiator used in the polymerization. PMMA-GO nanocomposite synthesis using radical polymerization-based techniques is an active topic of study with several prospects for considerable future improvement and a variety of possible emerging applications. The concentration and dispersity of GO used in the polymerization play critical roles to ensure the functionality and performance of the PMMA-GO nanocomposites.
Piezoelectric material transducers can work as an actuator or sensor. Generally, the actuator will be used to repair the structure, and the sensor will be used to find the health condition. In the last two decades, piezoelectric actuators have shown the capacity to lower and control the shear stress concentration and joint edge peel in adhesively bonded joint systems. Hence, this paper aims at reviewing the application of piezoelectric actuators in damaged structures and adhesively bonded combined systems based on three different repair investigation methods: analytical, numerical, and experimental. Moreover, the study also explores the delamination control of composite material beams and some other studies using a piezoelectric actuator. The specific aim of this work is to determine scientific challenges and future opportunities for considering piezoelectric materials in damaged structure investigations for novice researchers.
Switching to renewable, carbon-neutral sources of energy is urgent and critical for climate change mitigation. Despite how hydrogen production by electrolyzing water can enable renewable energy storage, current technologies unfortunately require rare and expensive platinum group metal electrocatalysts, which limit their economic viability. Transition metal dichalcogenides (TMDs) are low-cost, earth-abundant materials that possess the potential to replace platinum as the hydrogen evolution catalyst for water electrolysis, but so far, pristine TMDs are plagued by poor catalytic performances. Defect engineering is an attractive approach to enhance the catalytic efficiency of TMDs and is not subjected to the limitations of other approaches like phase engineering and surface structure engineering. In this minireview, we discuss the recent progress made in defect-engineered TMDs as efficient, robust, and low-cost catalysts for water splitting. The roles of chalcogen atomic defects in engineering TMDs for improvements to the hydrogen evolution reaction (HER) are summarized. Finally, we highlight our perspectives on the challenges and opportunities of defect engineering in TMDs for electrocatalytic water splitting. We hope to provide inspirations for designing the state-of-the-art catalysts for future breakthroughs in the electrocatalytic HER.
Charge storage in electrochemical double-layer capacitors (EDLCs) is via the adsorption of electrolyte counterions in their positive and negative electrodes under an applied potential. This study investigates the EDLC-type charge storage in carbon nanotubes (CNT) electrodes in aqueous acidic (NaHSO4), basic (NaOH), and neutral (Na2SO4) electrolytes of similar cations but different anions as well as similar anions but different cations (Na2SO4 and Li2SO4) in a two-electrode Swagelok-type cell configuration. The physicochemical properties of ions, such as mobility/diffusion and solvation, are correlated with the charge storage parameters. The neutral electrolytes offer superior charge storage over the acidic and basic counterparts. Among the studied ions, SO4 2- and Li+ showed the most significant capacitance owing to their larger solvated ion size. The charge stored by the anions and cations follows the order SO4 2- > HSO4 - > OH- and Li+ > Na+, respectively. Consequently, the CNT//Li2SO4//CNT cell displayed outstanding charge storage indicators (operating voltage ∼0-2 V, specific capacitance ∼122 F·g-1, specific energy ∼67 W h·kg-1, and specific power ∼541 W·kg-1 at 0.5 A·g-1) than the other cells, which could light a red light-emitting diode (2.1 V) for several minutes. Besides, the CNT//Li2SO4//CNT device showed exceptional rate performance with a capacitance retention of ∼95% at various current densities (0.5-2.5 A·g-1) after 6500 cycles. The insights from this work could be used to design safer electrochemical capacitors of high energy density and power density.
Adsorbates coverage plays a crucial role in a catalysis reaction. In hydrodeoxygenation (HDO), which involves high hydrogen pressure, hydrogen coverage on the surface may affect the adsorption of other adsorbates. The HDO is used in green diesel technology to produce clean and renewable energy from organic compounds. This motivates us to study the hydrogen coverage effect on methyl formate adsorption on MoS2 as a model case of the actual HDO. We calculate the methyl formate adsorption energy as a function of hydrogen coverage using density functional theory (DFT) and then comprehensively analyze the physical origin of the results. We find that methyl formate can have several adsorption modes on the surface. The increased hydrogen coverage can stabilize or destabilize these adsorption modes. However, finally, it leads to convergence at high hydrogen coverage. We extrapolated the trend further and concluded that some adsorption modes might not exist at high hydrogen coverage, while others remain.
This work presents the effect of hydrogen sulfide gas on the phase behavior of both methane gas hydrate formation and CO2 gas hydrate formation. For this, the thermodynamic equilibrium conditions for various gas mixtures containing CH4/H2S and CO2/H2S are initially found by simulation using PVTSim software. These simulated results are compared using an experimental approach and the available literature. Then, the thermodynamic equilibrium conditions generated by simulation are used for generating Hydrate Liquid-Vapor-Equilibrium (HLVE) curves to understand the phase behavior of gases. Further, the effect of hydrogen sulfide on the thermodynamic stability of methane and carbon dioxide hydrates was studied. It was clearly observed from the results that an increase in H2S composition in the gas mixture decreases the stability of CH4 and CO2 hydrates.
Primary amoebic meningoencephalitis and granulomatous amoebic encephalitis are distressing infections of the central nervous system caused by brain-eating amoebae, namely, Naegleria fowleri and Acanthamoeba spp., respectively, and present mortality rates of over 90%. No single drug has been approved for use against these infections, and current therapy is met with an array of obstacles including high toxicity and limited specificity. Thus, the development of alternative effective chemotherapeutic agents for the management of infections due to brain-eating amoebae is a crucial requirement to avert future mortalities. In this paper, we synthesized a conducting polymer-based nanocomposite entailing polyaniline (PANI) and molybdenum disulfide (MoS2) and explored its anti-trophozoite and anti-cyst potentials against Acanthamoeba castellanii and Naegleria fowleri. The intracellular generation of reactive oxygen species (ROS) and ultrastructural appearances of amoeba were also evaluated with treatment. Throughout, treatment with the 1:2 and 1:5 ratios of PANI/MoS2 at 100 μg/mL demonstrated significant anti-amoebic effects toward A. castellanii as well as N. fowleri, appraised to be ROS mediated and effectuate physical alterations to amoeba morphology. Further, cytocompatibility toward human keratinocyte skin cells (HaCaT) and primary human corneal epithelial cells (pHCEC) was noted. For the first time, polymer-based nanocomposites such as PANI/MoS2 are reported in this study as appealing options in the drug discovery for brain-eating amoebae infections.
The effectiveness of CO2-enhanced oil recovery (EOR) is strongly dependent on the CO2-oil minimum miscible pressure (MMP) value, which can be estimated using various methods. In this study, interfacial tension (IFT) and slim-tube tests were used to estimate the MMP value. Experimental results indicated that the IFT test had a higher MMP value than the slim-tube test. Particularly, the outcomes of IFT and the slim-tube tests differed slightly, i.e., 0.7% and 4.3% at 60 and 66 °C, respectively. Furthermore, the current work also compares MMP data gathered using visual observation and equation of state (EOS) simulation. The MMP estimated by EOS is higher but close to the IFT and slim-tube recovery factor method, where all results are within the 1650-1700 psi and 1700-1800 psi visual observation ranges at 60 and 66 °C, respectively. However, MMP deviations concerning the slim-tube test and EOS were consistent at different temperatures. This study offers an alternative to estimate and evaluate CO2-oil MMP for EOR applications accurately and efficiently.
Carcinoma of the lungs is among the most menacing forms of malignancy and has a poor prognosis, with a low overall survival rate due to delayed detection and ineffectiveness of conventional therapy. Therefore, drug delivery strategies that may overcome undesired damage to healthy cells, boost therapeutic efficacy, and act as imaging tools are currently gaining much attention. Advances in material science have resulted in unique nanoscale-based theranostic agents, which provide renewed hope for patients suffering from lung cancer. Nanotechnology has vastly modified and upgraded the existing techniques, focusing primarily on increasing bioavailability and stability of anti-cancer drugs. Nanocarrier-based imaging systems as theranostic tools in the treatment of lung carcinoma have proven to possess considerable benefits, such as early detection and targeted therapeutic delivery for effectively treating lung cancer. Several variants of nano-drug delivery agents have been successfully studied for therapeutic applications, such as liposomes, dendrimers, polymeric nanoparticles, nanoemulsions, carbon nanotubes, gold nanoparticles, magnetic nanoparticles, solid lipid nanoparticles, hydrogels, and micelles. In this Review, we present a comprehensive outline on the various types of overexpressed receptors in lung cancer, as well as the various targeting approaches of nanoparticles.
Steelmaking industrial waste, that is, silicomanganese fume (SMF), is one of the byproducts obtained during the steelmaking process in an electric submerged arc furnace at 1500 °C. Millions of tons of such wastes are generated yearly and used in different applications such as road construction, cement mortar, recycling into sinter plant, and so forth. In this study, the application of SMF in the drilling operations was investigated by employing SMF as a bridging material (BM) in water-based drilling fluid (WBF). The SMF samples were collected and dry-sieved, and then, the retained particles on each mesh were examined for elemental analysis. Thereafter, a battery of tests was performed using the WBF-SMF system comprising different SMF grades and mixed grades to investigate their bridging performance. The commercial BM (marble) was used as a reference fluid (WBF-marble system) for comparative investigation. The bridging performance of WBF-SMF and WBF-marble systems was tested and compared at 190 °F and 300 psi testing conditions using 10, 12, 20, and 50 μm ceramic discs. The processing techniques have shown that raw SMF does not require prolonged processing steps like the other waste material requires. All the SMF grades have shown homogenous chemical composition in oxides of manganese, silicon, sulfur, calcium, magnesium, and iron. Moreover, the WBF-SMF system have shown substantial improvement in bridging and sealing performance with average 47, 42, 84, and 75% superior fluid loss performance against 10, 12, 20, and 50 μm ceramic discs, respectively, compared to the WBF-marble system. While comparing the filter cake thickness, the WBF-SMF system has deposited a filter cake with more than 50% reduction in thickness compared to the WBF-marble system for different ceramic-disc sizes. Consequently, this study has introduced SMF as a novel BM with a unique particle size distribution that can be used in WBFs to plug formation pores effectively. In addition, this waste material (SMF) has been investigated as an economical, effortless, readily available, and high-performance material compared to other commonly used BMs.
Enhancing the catalytic performance of non-noble Ni catalysts in the selective hydrogenation of furfural to furfuryl alcohol (FA) in terms of furfural conversion, selectivity, and good recyclability is challenging. Here, spherical nickel phyllosilicate catalysts (Ni_PS) with fibrous-like structures are prepared via a modified sol-gel method with Ni loadings of 2-30 wt %. Upon exposure to air, all the reduced Ni_PS catalysts exhibit more than 80% Ni0/Niphyllosilicate species on the surface, whereas a large portion of Ni oxide species (>55%) is presented on the impregnated catalyst. The Ni2+ species in nickel phyllosilicate catalysts are active and highly stable during reduction, reaction, and regeneration, yielding stable catalytic performance for multiple recycle tests in furfural hydrogenation to FA. Furfural conversion over the Ni_PS catalysts increased monotonically with increasing Ni loading without an FA selectivity drop. The presence of both metallic Ni0 and Niphyllosilicate also produces a synergistic promotional effect for FA formation.
Herein, a novel and environmentally benign solid catalyst was fabricated by grafting WO3 active species onto the ZnCo2O4@CeO2 support for efficient levulinic acid production from corncob waste biomass. The morphological, compositional, and textural properties of the designed catalyst were investigated using different characterization techniques to identify suitable catalyst formulation with enhanced catalytic activity and stability. The results demonstrated that WO3 active species were successfully loaded with uniform distribution onto the support to develop a robust catalyst with both acidic and basic sites. The experimental investigation showed that among the catalysts, WO3(10 wt %)/ZnCo2O4@CeO2 exhibited the best catalytic activity, providing a maximum levulinic acid yield of 78.49% at the optimal conditions of 6 wt % catalyst dosage, reaction temperature of 180 °C, and reaction time of 200 min. The presence of an optimum number of both acid and base active sites on the catalyst surface could lead to the highest catalytic activity of the synthesized catalyst. Finally, the reusability investigation indicated that the synthesized catalyst possessed sufficient recyclability of up to four times for the levulinic acid production from the selected biomass with negligible drop in the catalytic activity.
Extensive application of metal powder, particularly in nanosize could potentially lead to catastrophic dust explosion, due to their pyrophoric behavior, ignition sensitivity, and explosivity. To assess the appropriate measures preventing accidental metal dust explosions, it is vital to understand the physicochemical properties of the metal dust and their kinetic mechanism. In this work, explosion severity of aluminum and silver powder, which can be encountered in a passivated emitter and rear contact (PERC) solar cell, was explored in a 0.0012 m3 cylindrical vessel, by varying the particle size and powder concentration. The P max and dP/dt max values of metal powder were demonstrated to increase with decreasing particle size. Additionally, it was found that the explosion severity of silver powder was lower than that of aluminum powder due to the more apparent agglomeration effect of silver particles. The reduction on the specific surface area attributed to the particles' agglomeration affects the oxidation reaction of the metal powder, as illustrated in the thermogravimetric (TG) curves. A sluggish oxidation reaction was demonstrated in the TG curve of silver powder, which is contradicted with aluminum powder. From the X-ray photoelectron spectroscopy (XPS) analysis, it is inferred that silver powder exhibited two reactions in which the dominant reaction produced Ag and the other reaction formed Ag2O. Meanwhile, for aluminum powder, explosion products only comprise Al2O3.
The low-temperature sintering of (Bi0.5Na0.5)TiO3-based ceramics can be achieved by sintering aid CuO. Piezoelectric ceramics (1 - x)[0.90(Bi0.5Na0.5)TiO3 - 0.10SrTiO3] - xCuO (BNT-ST-Cu) with x = 0, 0.01, 0.02, 0.03, and 0.04 were prepared through the mixed oxide route. A tetragonal structure was indexed for the undoped sample. Its structure was found to be changed to a pseudocubic when Cu was added. For undoped Cu samples, the sintering temperature (T s) for sufficient densification was 1160 °C. However, T s was reduced to 1090-1120 °C for Cu-added specimens. Field emission scanning electron microscopy (FE-SEM) showed a uniform and dense grain morphology for all samples. The maximum dielectric constant temperature (T m) was decreased with the doping concentration of Cu and applied frequency. The strain was increased with Cu concentration and had the maximum value of 500 pm/V for the sample x = 0.02 with symmetric and slim strain loops.
ZnO and black TiO2 have been selected as the most efficient materials for organic pollution abatement due to their increased efficiency when compared to other materials. However, the concept of green chemistry makes it desirable to design green synthesis approaches for their production. In this study, black TiO2 was synthesized using an environmentally safe synthetic technique with glycerol as a reductant. ZnO was prepared by using ionic-liquid-based microwave-assisted extracts of Polygonum minus. To investigate the materials' potential to photodegrade organic pollutants, methylene blue (MB) and phenol were chosen as model organic pollutants. Both materials were found to exhibit spherical morphologies and a mesoporous structure and were efficient absorbers of visible light. ZnO exhibited electron-hole pair recombination lower than that of black TiO2. Black TiO2 was discovered to be an anatase phase, whereas ZnO was found to have a hexagonal wurtzite structure. In contrast to black TiO2, which had a surface area of 239.99 m2/g and a particle size of 28 nm, ZnO had a surface area of 353.11 m2/g and a particle size of 32 nm. With a degradation time of 60 min, ZnO was able to eliminate 97.50% of the 40 mg/L MB. Black TiO2, on the other hand, could reduce 90.0% of the same amount of MB in 60 min. When tested for phenol degradation, ZnO and black TiO2 activities were reduced by nearly 15 and 25%, respectively. A detailed examination of both ZnO and black TiO2 materials revealed that ZnO has more potential and versatility for the degradation of organic pollutants under visible light irradiation.
The degradation of organic dye pollutants is a critical environmental issue that has garnered significant attention in recent years. To address this problem, we investigated the potential of CaCrO4 chromite (CCO) as a photocatalyst for the degradation of cationic and anionic dye solutions under sunlight irradiation. CaCrO4 was synthesized via a sol-gel auto-combustion route and sintered at 900 °C. The Rietveld refined XRD profile confirmed the zircon-type structure of CaCrO4 crystallized in the tetragonal unit cell with I41/amd space group symmetry. The surface morphology of the sample was investigated by field emission scanning electron microscopy (FESEM), which revealed the polyhedral texture of the grains. Energy-dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) studies were carried out to analyze the elemental composition and chemical states of the ions present in the compound. Fourier transform infrared (FT-IR) spectroscopy analysis revealed the vibrational modes corresponding to the tetrahedral and dodecahedral metal oxide bonds. The optical band gap was approximated to be in the range of 1.928 eV by using the Tauc relation. The CaCrO4 catalyst with different contents (5, 20, 35, and 50 mg) was investigated for its photocatalytic performance for the degradation of RhB dye solution under sunlight irradiation using a UV-Vis spectrometer over the experimental wavelength range of 450-600 nm. The degradation efficacy increased from 70.630 to 93.550% for 5-35 mg and then decreased to 68.720% for 50 mg in 140 min under visible light illumination. The comparative study demonstrates that a higher degradation rate was achieved for cationic than anionic dyes in the order RhB > MB > MO. The highest deterioration (93.80%) was achieved for the RhB dye in 140 min. Equilibrium and kinetic studies showed that the adsorption process followed the Langmuir isotherm and pseudo-second-order models, respectively. The maximum adsorption capacity of 21.125 mg/g was observed for the catalyst concentration of 35 mg. From the cyclic test, it has been observed that the synthesized photocatalyst is structurally and morphologically stable and reusable. The radical trapping experiment demonstrated that superoxide and hydroxyl radicals were the primary species engaged in the photodegradation process. A possible mechanism for the degradation of RhB has been proposed. Hence, we conclude that CaCrO4 can be used as an efficient photocatalyst for the remediation of organic dye pollutants from the environment.
Oil palm trunk (OPT) represents one of the five main oil palm biomass wastes with high carbon content that can be economically converted to a large surface area, porous activated carbon (AC) adsorbent to treat palm oil mill effluent wastewater in Indonesia and Malaysia. In the first portion of this work, the design of the experiment was used to determine the optimum set of synthesis parameters required to maximize the iodine number of AC [i.e., Brunauer-Emmett-Teller (BET) specific surface area indicator] prepared from OPT via chemical activation route using H3PO4. The iodine numbers of AC and AC yield were probed as the impregnation ratio, the activation time, and the activation temperature were varied in the range of 0.28-3.47, 5.68-69.32 min, and 379-521 °C, respectively. An impregnation ratio of 2.29, an activation time of 6 min, and an activation temperature of 450 °C were identified as the optimum set of synthesis parameters. In the second portion of the work, the AC synthesized using the optimum parameters were then characterized and tested as an adsorbent for tannin. N2 sorption results revealed that the AC exhibits type IV isotherm, that is, contains micropores and mesopores and displays a relatively high BET specific surface area of 1657 m2 g-1. Adsorption equilibria isotherms for tannin adsorption onto the AC were collected at three different pH of 2, 4, and 6 and were nonlinearly fitted using Langmuir and Freundlich isotherm models, where the Langmuir isotherm gave better fitting than Freundlich. The higher adsorption capacity at lower pH can be explained in terms of the absence of electrostatic repulsion interaction between the AC surface and the tannic acid species as suggested by the point of zero charges (pHpzc) of 4.8 and an increasing ionization of tannic acid with pH rise between 4 and 7. Adsorption kinetics data were also obtained at four different pH of 2, 4, 6, and 8 where the nonlinear pseudo-first-order model best fitted the kinetic at pH of 2 and the nonlinear pseudo-second-order model represented the kinetic best at the remaining higher pH, which suggests that tannin adsorption onto AC occurred by physisorption at pH of 2 and by chemisorption at pH of 4, 6, and 8.
In this study, geopolymer originating from locally industrial byproducts as red mud (RM) was successfully prepared in the presence of different loadings of rice husk ash (RHA) used for the adsorption of methylene blue (MB) in wastewater. During geopolymerization, various mixing amounts between RM and RHA were conducted when the weight ratio of binder solution/activated alkali-metal solution (Na2SiO3/ NaOH 7 M) was 2.5 and the curing temperature was set at 60 °C for 24 h. As a result, the surface area value of the prepared geopolymer composited with RHA at 0 and 60% was increased from 19.2 to 29.5 m2/g, while the BJH pore size of the prepared geopolymer was reduced to 6.68 and 5.76 nm, respectively. In the dye removal test, higher additions of RHA in the RM-geopolymer maintained better retention of the MB ion due to the increase in the adsorption binding site. The maximum uptake amount of dyes performed at pH 8 was changed from 6.59 to 10.74 mg/g, while RHA was from 0 to 60% after 180 min of immersion in MB solution. The adsorption isotherms well obeyed the Langmuir model, as the relative coefficient R2 was 0.999. Based on these, the initial agricultural waste as RHA and industrial byproducts as RM were valued as functional materials used for dye treatment in wastewater.
Rice husk ash (RHA), a low-cost biomaterial, was utilized to form bio-oil from pyrolysis in a batch-stirred reactor, followed by its upgradation using the RHA catalyst. In the present study, the effect of temperature (ranging from 400 to 480 °C) on bio-oil production produced from RHA was studied to obtain the maximum bio-oil yield. Response surface methodology (RSM) was applied to investigate the effect of operational parameters (temperature, heating rate, and particle size) on the bio-oil yield. The results showed that a maximum bio-oil output of 20.33% was obtained at 480 °C temperature, 80 °C/min heating rate, and 200 μm particle size. Temperature and heating rate positively impact the bio-oil yield, while particle size has little effect. The overall R2 value of 0.9614 for the proposed model proved in good agreement with the experimental data. The physical properties of raw bio-oil were determined, and 1030 kg/m3 density, 12 MJ/kg calorific value, 1.40 cSt viscosity, 3 pH, and 72 mg KOH/g acid value were obtained, respectively. To enhance the characteristics of the bio-oil, upgradation was performed using the RHA catalyst through the esterification process. The upgraded bio-oil stemmed from a density of 0.98 g/cm3, an acid value of 58 mg of KOH/g, a calorific value of 16 MJ/kg, and a viscosity 10.5 cSt, respectively. The physical properties, GC-MS and FTIR, showed an improvement in the bio-oil characterization. The findings of this study indicate that RHA can be used as an alternative source for bio-oil production to create a more sustainable and cleaner environment.